Next Article in Journal
From Multiplex Serology to Serolomics—A Novel Approach to the Antibody Response against the SARS-CoV-2 Proteome
Next Article in Special Issue
Bovine Parainfluenza Virus Type 3 (BPIV3) Enters HeLa Cells via Clathrin-Mediated Endocytosis in a Cholesterol- and Dynamin-Dependent Manner
Previous Article in Journal
A Novel Immunofluorescence Assay for the Rapid Serological Detection of SARS-CoV-2 Infection
Previous Article in Special Issue
Liver-Derived Cell Transfection Model Efficacy for HBV Genotype B Replication/Transcription Is Determined by Complex Host Transcription Factor Network
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Viruses
Volume 13
Issue 5
10.3390/v13050748
viruses-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Host Factors That Control Mosquito-Borne Viral Infections in Humans and Their Vector

by
Chasity E. Trammell
1,2 and
Alan G. Goodman
1,3,*
1
School of Molecular Biosciences, College of Veterinary Medicine, Washington State University, Pullman, WA 99163, USA
2
NIH Protein Biotechnology Training Program, Washington State University, Pullman, WA 99164-6240, USA
3
Paul G. Allen School for Global Health, College of Veterinary Medicine, Washington State University, Pullman, WA 99164, USA
*
Author to whom correspondence should be addressed.
Viruses 2021, 13(5), 748; https://0-doi-org.brum.beds.ac.uk/10.3390/v13050748
Submission received: 25 March 2021 / Revised: 13 April 2021 / Accepted: 22 April 2021 / Published: 24 April 2021
(This article belongs to the Special Issue Host Factors in Viral Infections)
Browse Figures
Versions Notes

Abstract

:
Mosquito-borne viral infections are responsible for a significant degree of morbidity and mortality across the globe due to the severe diseases these infections cause, and they continue to increase each year. These viruses are dependent on the mosquito vector as the primary means of transmission to new vertebrate hosts including avian, livestock, and human populations. Due to the dynamic host environments that mosquito-borne viruses pass through as they are transmitted between vector and vertebrate hosts, there are various host factors that control the response to infection over the course of the pathogen’s life cycle. In this review, we discuss these host factors that are present in either vector or vertebrate models during infection, how they vary or are conserved between hosts, and their implications in future research pertaining to disease prevention and treatment.

1. Introduction

Vector-borne diseases pose a significant global health burden. Global climate changes have enabled various arthropod vectors to expand into previously uninhabitable regions which increases potential exposure to at-risk populations [1,2]. In particular, mosquito populations have expanded, and this has resulted in increasing occurrence of mosquito-borne disease [3,4], notably viruses such as West Nile virus (WNV), dengue virus (DENV), Zika virus (ZIKV), and chikungunya virus (CHIKV) [5]. While mosquitoes are also responsible for transmission of hazardous parasitic diseases such as plasmodia and filariasis parasites, their role as transmitters of viral pathogens is of particular interest to epidemiologists and infectious disease monitoring groups. Recent reports by the World Health Organization (WHO) have indicated a steady or downward trend of global malaria cases [6], while viral cases have appeared to increase in both frequency and severity [5,7,8]. This has resulted in the WHO to designate DENV and related mosquito-borne viruses as significant concerns that need to be addressed at the global level in 2020 [9].
Mosquito-borne viruses utilize the mosquito as a natural reservoir for replication and vector for transmission into vertebrate populations. Depending on the virus, transmission can occur in both sylvatic and urban settings during the bloodmeal between mosquito and vertebrate hosts such as primates, birds, and humans [10,11]. Once infected, some vertebrate hosts are unable to clear acute infection and can develop viremia which results in infectious virions circulating in the blood and lymphatic fluid. This would, in turn, result in potential virus transmission from vertebrate to mosquito in subsequent bloodmeals [10]. The transmission cycle between mosquito and vertebrate populations requires constant monitoring to identify new infections in each host type as this would indicate active viral transmission within a community or region.
Viruses that undergo this transmission cycle encounter various environmental and host factors as virions move between mosquito and vertebrate hosts. Immune responses to mosquito-borne viruses vary between vector and vertebrate hosts as the sophistication and complexity in the cellular environment vary between species. This does not, however, mean that there are no evolutionarily conserved responses that are shared between organisms. In fact, at the level of innate immunity, there are many shared antiviral mechanisms that are conserved between species. In the following review, we provide a summary of conserved host factors responsible for initiating antiviral responses against mosquito-borne viruses in mosquito and human systems, how these factors vary between organisms, and how these responses provide a foundational understanding for future vector control and therapeutic research.

2. Mosquito Antiviral Immunity

Mosquito-borne viruses utilize multiple mosquito species as the primary means of transmission into higher-level vertebrate species such as birds and mammals. While these viruses can be transmitted within a vertebrate population by routes such as blood transfusion [12,13], sexual transmission [14], or in utero transmission [15], the mosquito is the predominate means of transmission and is responsible for a majority of disease cases within a community. Mosquitoes acquire a viral infection during the bloodmeal exchange from an infected vertebrate, but there is evidence suggesting vertical transmission of certain viruses such as ZIKV from female mosquitoes to eggs [16,17]. Once the virus-containing bloodmeal is ingested and digested in the midgut, the virus escapes the midgut and systemically infects distal tissues including the ovaries, fat body, and salivary glands [18]. As viremia is reached in the mosquito, the saliva becomes infected with high levels of infectious virions that induces activation of chemosensory-related genes that affects feeding behavior [19]. Once the salivary glands become infected, the mosquito becomes a competent vector for future virus transmission during subsequent bloodmeals. Mosquitoes can be co-infected with different viruses simultaneously without compromising vector competence or survival, such as Aedes aegypti infected with DENV, ZIKV, and CHIKV; the mosquito can then transmit these viruses simultaneously [20,21].
From the initial digestion of the virus-containing bloodmeal to transmission, the mosquito initiates different cellular responses to control the virus without affecting host survival. Physical tissue barriers are present along the mosquito digestive tract, and the virus must pass through this barrier in order to become systemic. Then, the virus reaches the salivary glands and ovaries for horizontal and vertical transmission, respectively. Broad and specific antiviral immune signaling responses are also crucial to reduce a virus’s ability to establish itself within the mosquito. The antiviral barriers involved in protecting mosquitoes from mortality due to viral infection are generally well conserved across genera such as Culex and Aedes.

2.1. Innate Immune Responses in the Mosquito

The mosquito, like other invertebrate species, lacks the canonical adaptive immune system found in more complex vertebrate species such as humans [10]. Instead, mosquitoes utilize response pathways that are heavily conserved across metazoa and are critical in the insect immune system and innate immunity. As opposed to the development of immunological memory via the adaptive immune system, the innate immune system involves recognition of pathogen-associated molecular patterns (PAMPs) by pattern recognition receptors (PRRs) that activate immune signaling pathways which ultimately: (1) induces transcription of downstream antiviral effector proteins, or (2) recruits immune cells that can initiate cellular and humoral signaling to localized infection. The primary focus of innate immune signaling is to initiate an immediate response to infection that aims to clear and keep the virus localized. The innate immune system has been heavily dissected and studied in the context of mammalian systems, the Drosophila melanogaster model organisms, and mosquito species to varying degrees. Taken together, the role and significance of innate immune signaling against mosquito-borne viruses are a well-established and continuously growing field of study.
One of the more significant defense responses against a multitude of viral infections in the mosquito is the RNA interference (RNAi) pathway (Figure 1A). RNAi signaling is a heavily conserved pathway across invertebrate and vertebrate organisms and is involved in regulating gene expression [22]. In invertebrate organisms, the RNAi pathway also functions as an antiviral response pathway that is activated by nucleic acids that are the by-products of the replicative process during viral infection [23,24,25]. Specifically, viral nucleic acids such as double-stranded RNA (dsRNA) are detected by the endoribonuclease Dicer-2 which binds to and cleaves the larger dsRNA into smaller RNA duplexes [26,27]. R2D2 then binds to the small RNA duplexes, and the protein–viral nucleic acid complex is loaded into the RNA-induced silencing complex (RISC) [28]. Once associated with RISC, the effector proteins AGO2 and p400 bind to specific sequences within the viral mRNA target to cleave bound viral nucleic acids [29,30,31]. The purpose of this degradation of viral nucleic acids is to clear the intracellular virus before viral replication proteins can hijack the host translational machinery and generate more infectious virion copies. The importance of this pathway has been demonstrated against flaviviruses such as DENV2 and WNV in Aedes and Culex mosquitoes, respectively [32,33,34], and ZIKV and WNV in D. melanogaster [35,36]. RNAi is also important in controlling viral replication and mosquito survival against alphaviruses such as Sindbis virus (SINV) [37] and Semliki Forest virus (SFV) [38]. While RNAi is present in higher-level organisms such as humans, the extent and importance of its role as an antiviral immune regulator remain unclear and it is not yet defined as an antiviral mechanism in mosquito-borne viral infections [39,40,41].
Another important signaling response involved in mosquito antiviral immunity is the JAK/STAT pathway (Figure 1B). Similar to RNAi, JAK/STAT is linked to various host processes beyond immunity including cellular division, maintenance, and regeneration [43,44], along with regulating oogenesis in insect species [45,46]. Unlike the RNAi pathway, however, the functional role of JAK/STAT as a cellular and antiviral regulator is well conserved between vertebrate and invertebrate hosts [47,48] and is associated with responding to various viral infections including WNV [49], ZIKV [50,51], and DENV [52,53,54]. JAK/STAT is an effector response pathway that activates an intracellular signaling cascade and induces downstream antiviral genes in response to infection [55]. Upon infection, the extracellular ligand unpaired (Upd) is secreted [56,57] and binds to the receptor domeless (dome) expressed on neighboring hemocytes or related immune cells [58]. Binding results in the activation of the intracellular Janus kinase hopscotch (hop) [59] and phosphorylation of transcription factor STAT [60,61]. Phosphorylation then induces the dimerization and nuclear import of STAT to promote transcription of downstream antiviral effectors such as vir-1 [55] and TotM [56]. Vago is a secreted cytokine that activates JAK/STAT signaling in Cx. quinqufasciatus, and Vago is induced in a Dicer-2-dependent manner [62]. JAK/STAT signaling is conserved between invertebrate and vertebrate species as well as its functional role in an innate immune response to viral infections. In humans, JAK/STAT signaling is partially involved in the generation of type-I interferon (IFN)-stimulated responses and has been shown to be active in the presence of ZIKV [63], WNV [64], and Japanese encephalitis virus (JEV) [65]. Since Vago restricts WNV in Cx. quinqufasciatus, its role as an antiviral secreted cytokine is similar to that of mammalian IFN [62].
The Toll and IMD pathways, while primarily associated with antibacterial and antifungal immunity, have also been implicated in antiviral protection within the mosquito and insect models (Figure 1C,D) [66,67]. The Toll pathway is important for defense against Gram-positive bacterial and fungal infections [68,69], whereas IMD is important against Gram-negative bacteria [70,71]. The mechanistic events involved in Toll and IMD signaling have been heavily dissected using the D. melanogaster model, and the pathways are evolutionarily conserved in Aedes and Culex mosquitoes. Toll signaling is initiated when the ligand Spätzle binds to the Toll receptor to activate adaptor proteins MyD88, Tube, and kinase Pelle to induce a phosphorylation cascade that activates degradation of the regulatory factor Cactus following its phosphorylation [72,73,74]. Once Cactus is degraded, the transcription factors Dif and Dorsal are able to translocate into the nucleus to induce transcription of downstream antimicrobial peptides (AMPs) and response genes [75]. The IMD pathway is activated by DAP-type peptidoglycans recognized by peptidoglycan recognition proteins (PGRP-LC) which act as transmembrane receptors that induce a series of phosphorylation and cleavage events in the cytosol. These intracellular events ultimately result in induction of downstream AMPs and response genes [76]. Binding to PGRP-LC induces the formation of a signaling complex composed of the proteins IMD, Fadd, and Dredd [70,77,78]. Dredd cleaves IMD which recruits the Tab2/Tak1 protein complex that induces the phosphorylation and cleavage of the transcription factor Relish (Rel) [79,80,81]. Caspar acts as a negative regulator of IMD by targeting Dredd-mediated cleavage [82]. Cleavage of Rel results in the nuclear translocation of the N-terminus of Rel to induce transcription of effector genes responsible for regulating AMPs and other immune response elements [78,83]. The Toll and IMD pathways have been heavily dissected in the context of antibacterial and antifungal immunity but have also been linked to humoral and cellular antiviral responses in the insect system. For example, Ae. aegypti knocked down for Cactus and Caspar by RNAi exhibited increased Toll and IMD immune signaling during DENV infection and reduced viral replication [84,85]. Toll and JAK/STAT signaling has also been shown to be induced during ZIKV infection in Ae. aegypti [51]. In addition, WNV infection in Culex pipiens induces Toll signaling in addition to the canonical RNAi and JAK/STAT pathways [86]. It is also important to note that each pathway is involved in hemocytes’ functional role as circulating immune cells against insect-specific [55,87,88,89] and vector-borne viruses such as DENV and ZIKV [51,52,84,86,90]. Finally, Toll and IMD signaling is conserved in the human immune system as the Toll-like receptor (TLR) signaling pathway [91] and NF-kB/TNF signaling pathways [92], respectively. Both TLRs and NF-kB/TNF signaling pathways have been linked as critical defense mechanisms against various RNA viruses including WNV [93,94,95,96].

2.2. Physical Barriers in the Mosquito

Mosquitoes primarily become infected through ingestion of a bloodmeal containing a virus. Due to this infection route, virions undergo various environmental pressures and conditions as they move from the midgut to distal tissues such as the salivary glands and ovaries which are involved in horizontal and vertical transmission, respectively. The physical barriers that the viruses overcome in order to reach viremia conditions are a significant component in the mosquito’s response to infection. Comparatively, the physical barriers involved in the mosquitoes’ and humans’ response in infection vary significantly as the different organ systems and cellular pressures encountered would utilize different host factors to respond to viral infection.
Perhaps the most significant tissue functioning as a physical barrier in preventing viremia in the mosquito is the midgut, the organ responsible for the digestion of an ingested bloodmeal and absorbance of essential nutrients [97]. The virus must first overcome the midgut infection barrier, which is when the virus moves from the gut lumen to the midgut epithelial cells. Upon infecting and replicating in the midgut epithelial cells, the virus then passes the midgut escape barrier and basal lamina to disseminate into the hemocoel [97,98]. Once the virus breaches the midgut, virions enter the hemocoel and induce activation of humoral immune responses such as melanization [99] to limit dissemination [100]. Failure to keep infection localized results in viremia that systemically infects distal tissues such as the fat body, hemocytes, and salivary glands [19,101,102]. It is at this point when the virus reaches, modulates signaling events, and establishes itself in the salivary glands that the mosquito becomes a competent vector for virus transmission in future bloodmeals. The dissemination rate into midgut epithelial cells varies between virus and mosquito species as JEV disseminates faster in Culex mosquitoes when compared to DENV2 dissemination in Aedes [103,104]. Dissemination rates are also enhanced based on the frequency of subsequent bloodmeals, regardless of whether they are infected or not, due to the digestive impact on the midgut integrity and permeability [16,105,106].
For a virus to reach the blood–lymphatic system and become systemic, virions must overcome the physical and chemical barriers of skin tissue, in addition to avoiding immune cells. These differences in how viremia is achieved in the vector and mammalian hosts pose as a potential target for vector control intervention. The different cellular environments that the virus is exposed to during dissemination in the mosquito and human hosts implies that targeted therapeutics would have varying degrees of success. For example, recent studies have demonstrated that targeting signaling events involved in digestive and nutritional acquisition may prime mosquitoes for viral infection and reduce viral replication and the likelihood of transmission to subsequent hosts [49,107,108,109]. This is evident in the implementation of using Wolbachia, an endosymbiont present in various insect and arthropod species, as a means of vector control due to its established effect on reducing vector competence and viral replication in mosquito populations [52,110,111]. Additionally, stimulating the insulin/IGF-1 signaling pathway has been shown to reduce infection in mosquito vectors [49,107,108]. While targeting nutritional and digestive events may be effective in limiting viral activity in the mosquito, targeting similar processes in humans or other vertebrates may not be as effective as the virus would not undergo the same cellular pressures. In the case of insulin/ IGF-1 signaling, in which insulin has a broad effect on transcriptional activity beyond immune signaling, it may be possible to implement similar insulin-dependent strategies for both by targeting different insulin targeted-downstream host factors [109,112,113,114].

2.3. Variability between Mosquito Species and Viruses

Specific virus transmissions are generally linked to certain mosquito genera or species. For example, Aedes mosquitoes are primarily associated with hemorrhagic- or arthritic-inducing viruses such as DENV, CHIKV, and yellow fever virus (YFV) transmission, whereas Culex mosquitoes are associated with encephalitic viruses such as WNV, JEV, and St. Louis encephalitis virus (SLEV). Each genus’s geographic range does overlap to a certain degree with significant overlap within the Northern and Southern tropics, but each genus does possess a certain unique range as habitation becomes more polar within Africa and Southeast Asia [3,4,115,116]. There is also evidence of specific genus activity within the Northern and Southern tropics based on present environmental pressures such as elevation, population density, and available nutritional sources [2,117]. This correlates to disease incidence within these areas as well as expansion of mosquito populations within the regions [7,118].
Current studies have primarily focused on how specific mosquito species respond to viral infection without comparison to how other species may respond to the same pathogen. ZIKV and Rift Valley fever virus (RVFV), for example, are able to infect both Aedes and Culex mosquitos but to differing levels of success depending on the species and virus strain [119,120,121]. Research thus far as indicated that certain immune signaling and physical barriers play an important role in antiviral responses, but there is limited understanding as to how multiple canonical or novel signaling pathways may interact with one another to achieve the most effective immune response. While there is still much to discover regarding how different mosquito populations respond to and regulate the multitude of arboviruses that pose a threat to human populations, new studies are beginning to compare the related and unique host factors within mosquito populations and how they may lead to either broad or mosquito-specific intervention targets.

3. Human Antiviral Immunity

Mosquito-borne viruses pose a global health threat as they can be transmitted to humans with limited therapeutics or preventatives available. Unlike the mosquito vector, vertebrate hosts have evolved to possess two forms of immunity: the innate immune response, which is heavily conserved across species as previously discussed, and the adaptive immune response. The latter form of immunity is responsible for specific and long-lasting immunological memory associated with humoral and cellular immune responses. In the context of immune responses during an active viral infection, both branches of host immunity are involved and impact disease morbidity, mortality, and long-term immunity. Many of the host factors and signaling pathways present in the mosquito are also conserved in humans (Table 1). Specifically, the innate immune response pathways previously discussed are present to some orthologous or functional degree. Variability between mosquito and human host factors active during viral infections primarily exists in the form of physical defense barriers and adaptive immune responses.

3.1. Transmission and Physical Barriers in Human Hosts

The human host initiates an immediate immune response following a mosquito bloodmeal in which the virus-infected saliva is ejected from the mosquito hypopharynx into the skin epidermis. The saliva contains various host-derived salivary factors that can enhance viral transmission and reduce pro-inflammatory responses initiated by the human host [122,123,124]. This includes various mosquito-derived factors including anticoagulants [125] and deregulators that disrupt recruitment of immune cells such as macrophages and neutrophils [126,127,128,129]. Ultimately, these salivary factors result in enhanced cell infection and viral replication that assists in viral dissemination [130]. Virions infect local resident cell populations including keratinocytes [131], dermal dendritic cells (DCs), and Langerhans cells (Figure 2A) [132]. DCs are responsible for movement of a virus into the local lymph node where replication and viremia are induced [132]. Permissive tissues typically vary between virus type but include the spleen (DENV, RVFV), liver (YFV, WNV), and neuronal tissue (ZIKV, JEV), amongst others. This tissue tropism coincides with the disease manifestation caused by each virus.

3.2. Innate and Adaptive Immune Responses in the Human Host

Innate immune responses to viral infection in the human host involve both conserved responses present in the mosquito as well as more effective, specific responses evolved in vertebrate organisms. Specifically, the innate immune signaling pathways previously discussed within the mosquito are functionally present in humans in the forms of more evolutionarily advanced responses that can act both independently and cross-talk with other pathways (Table 1). Local immune cells induce expression of pro-inflammatory cytokines and type I interferon (IFN) responses including IFN-α and IFN-β [133]. Induction of IFN and downstream antiviral response genes are regulated by PRRs such as the RIG-I-like receptors (RLR), TLRs, and cGAS/STING that regulate transcription factors such as NF-kB and IRF3, which then stimulates JAK/STAT signaling to induce IFN-stimulated genes (ISG) [141]. This cytokine-mediated signaling indicates the presence of active infection and results in the recruitment of immune cells (Figure 2A) [64,65]. Proper function of these response elements is critical for host survival [142,143]. The NS5 protein expressed by WNV [144], ZIKV [145], DENV [146], JEV [65], and YFV [147] has shown to mediate host immune evasion as an antagonist to IFN signaling which results in enhanced viral replication (Figure 2A). CHIKV NS2 also functions as an antagonist of IFN signaling by inhibiting activation of JAK/STAT [148].
In addition to the innate immune signaling conserved across species, vertebrate organisms have an evolved adaptive immune system to more effectively respond to infection. Components of the adaptive immune system make up the foundation of what is referred to as immune memory by developing established B and T cell populations that can more effectively and specifically recognize, neutralize, and degrade infectious virions during and in subsequent infections. DCs and macrophages act as antigen-presenting cells and link innate and adaptive immune responses to induce expression of pro-inflammatory cytokines and chemokines and recruitment of cell populations involved in the cell-mediated response including NK cells [134,135] and neutrophils [127,136]. As infection progresses, IgG-secretory B cells and CD8+ T cell populations develop to effectively neutralize and inhibit further viral replication (Figure 2B) [137,138,139,140]. While the host factors involved in innate immune signaling are conserved between mosquitoes and humans, the adaptive immune response has evolved its own unique subset of host factors to enhance host immunity against viral pathogens (Table 1).

3.3. Impacts on Morbidity and Mortality

Following a successful immune response, humans are typically able to clear viral infection and generate some protective immunity for potential future infections. There is evidence, however, indicating that even upon clearing an active infection, certain host factors can greatly influence the outcome of future infections against the same or related mosquito-borne viruses. Perhaps the most significant example is the phenomenon known as antibody-dependent enhancement (ADE). ADE is a result of a prior infection generating antibodies that, upon subsequent infections with a similar or related virus, enhances viral entry, replication, and the likelihood of severe disease [149]. This permits partially bound virion–antibody complexes to bind to Fc receptors present on immune cells to mediate increased entry, mass virion replication, and premature release of virions [150,151,152]. DENV is the best example of mosquito-borne virus ADE as subsequent infection with a different serotype [152] or ZIKV [153] may result in this increased viral uptake in immune cells and an increased likelihood of presenting symptoms associated with disease such as hemorrhagic fever or neurological damage. This, in turn, is followed by greater disease severity and risk of mortality [154,155,156]. ADE is a significant concern in the production and implementation of DENV vaccines and as such has caused delays in their effective development and implementation to the general public [157].
Dysfunctional insulin signaling in humans is linked to impaired immunity to mosquito-borne viruses. Diabetic individuals are more prone to developing severe disease symptoms and mortality against ZIKV [158], WNV [159,160], and DENV [161]. Previously medical professionals thought this was due to an overall reduction in host signaling and regulatory processes, but now studies have begun to identify that such viruses impact and target components of insulin signaling to cause disease pathology. The NS4A and NS4B proteins expressed on ZIKV reduce AKT-mTOR signaling, which is targeted in insulin treatment and causes destruction of neuronal tissues that is a hallmark of disease [114]. While the effect that insulin has on human immunity during arboviral infection is still a relatively unexplored field, it may be an ideal candidate for future disease intervention that could be applied at the vector level as well.
Co-infection with multiple arboviruses poses different effects between human and mosquito hosts. While humans may present with more severe clinical symptoms or competing viral replication [162], mosquitoes co-infected with different viruses experience little obvious hazardous phenotypes [20,21] and may even enhance viral replication and the likelihood of transmission [163]. Whether this is due to variability in host factors or viral replication mechanisms is still under investigation, but this phenomenon does present another example in which mosquito and human immune responses to arboviruses vary at the molecular level due to available host factors.

4. Outlook

As evident in the gradual increase in the number and severity of clinical cases as well as the expansion of mosquito activity across the globe, the looming threat that mosquito-borne viruses pose is of significant concern and must be addressed at both the vector and clinical levels. Understanding the host immune responses and how they are varied between organisms is an important step in identifying more effective targets for vector control and therapeutics. More importantly, understanding how the responses are similar between mosquito-borne viruses is of great value as it permits research in broad or virus-specific targeting. As summarized in Table 1, the host factors involved during viral infection in mosquitoes and humans are well conserved with some variability regarding host physical barriers and adaptive immunity.
Further investigation is required into identifying and evaluating the importance of certain antiviral immune responses in both humans and mosquitoes. For example, vector-control mechanisms such as the endosymbiont Wolbachia, while reducing viral load in mosquitoes infected with ZIKV and DENV [110,111], may be pro-viral for other related viruses such as WNV [164]. This indicates that there may be virus-specific variations among related pathogens that result in potential, broad antiviral preventatives being less effective. This is also the case in humans as responses that are important against one virus may be insignificant or detrimental for another [157]. One example of a potential cross-species antiviral target, as previously discussed, is how insulin/IGF-1 signaling regulates mosquito and human immunity. Since this pathway possesses a broad effect on homeostatic activity in both organisms, insulin-mediated immunity may be achieved by targeting different downstream host factors or pathways. While studies into insulin-mediated arboviral immunity are not well established in humans, there is an established effect of dysfunctional insulin signaling on patient survival and virus activity for ZIKV and WNV [114,160]. Research in and implementation of more effective antivirals in both mosquitoes and humans are necessary and require a greater understanding regarding the conserved and differing host factors that respond to these zoonotic infections.

Author Contributions

C.E.T. wrote the manuscript in consultation with A.G.G. All authors have read and agreed to the published version of the manuscript.

Funding

Research in the Goodman Lab is supported by NIH/NIAID Grant R01 AI139051 to A.G.G. C.E.T. is supported by the NIH/NIGMS pre-doctoral fellowship T32 GM008336 and a fellowship from the Poncin Scholarship Fund.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data sharing not applicable.

Acknowledgments

We thank S. Allen Whiles and Y.B. Rodger for critical review of this manuscript.

Conflicts of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

  1. Morin, C.W.; Comrie, A.C. Modeled Response of the West Nile Virus Vector Culex Quinquefasciatus to Changing Climate Using the Dynamic Mosquito Simulation Model. Int. J. Biometeorol. 2010, 54, 517–529. [Google Scholar] [CrossRef] [PubMed]
  2. Kamal, M.; Kenawy, M.A.; Rady, M.H.; Khaled, A.S.; Samy, A.M. Mapping the Global Potential Distributions of Two Arboviral Vectors Aedes Aegypti and Ae. Albopictus under Changing Climate. PLoS ONE 2018, 13, e0210122. [Google Scholar] [CrossRef]
  3. Kraemer, M.U.; Sinka, M.E.; Duda, K.A.; Mylne, A.Q.; Shearer, F.M.; Barker, C.M.; Moore, C.G.; Carvalho, R.G.; Coelho, G.E.; Van Bortel, W.; et al. The Global Distribution of the Arbovirus Vectors Aedes Aegypti and Ae. Albopictus. eLife 2015, 4, e08347. [Google Scholar] [CrossRef]
  4. Leta, S.; Beyene, T.J.; De Clercq, E.M.; Amenu, K.; Kraemer, M.U.G.; Revie, C.W. Global Risk Mapping for Major Diseases Transmitted by Aedes Aegypti and Aedes Albopictus. Int. J. Infect. Dis. 2018, 67, 25–35. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Rosenberg, R.; Lindsey, N.P.; Fischer, M.; Gregory, C.J.; Hinckley, A.J.; Mead, P.S.; Paz-Bailey, G.; Waterman, S.H.; Drexler, N.A.; Kersh, G.J.; et al. Vital Signs: Trends in Reported Vectorborne Disease Cases—United States and Territories, 2004–2016. MMWR Morb. Mortal. Wkly. Rep. 2018, 67. [Google Scholar] [CrossRef] [Green Version]
  6. Guglielmi, G. Malaria Cases Are Falling Worldwide. Nature 2019. [Google Scholar] [CrossRef]
  7. Giovanetti, M.; de Mendonça, M.C.L.; Fonseca, V.; Mares-Guia, M.A.; Fabri, A.; Xavier, J.; de Jesus, J.G.; Gräf, T.; Dos Santos Rodrigues, C.D.; Dos Santos, C.C.; et al. Yellow Fever Virus Reemergence and Spread in Southeast Brazil, 2016–2019. J. Virol. 2019, 94, e01623-19. [Google Scholar] [CrossRef] [PubMed]
  8. Gutiérrez, L.A. PAHO/WHO Data—Dengue Cases | PAHO/WHO. Available online: https://www.paho.org/data/index.php/en/mnu-topics/indicadores-dengue-en/dengue-nacional-en/252-dengue-pais-anoen.html?showall=&start=2 (accessed on 2 March 2021).
  9. Ten Health Issues WHO Will Tackle This Year. Available online: https://www.who.int/emergencies/ten-threats-to-global-health-in-2019 (accessed on 21 January 2019).
  10. Ahlers, L.R.H.; Goodman, A.G. The Immune Responses of the Animal Hosts of West Nile Virus: A Comparison of Insects, Birds, and Mammals. Front. Cell. Infect. Microbiol. 2018, 8. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  11. Gutiérrez-Bugallo, G.; Piedra, L.A.; Rodriguez, M.; Bisset, J.A.; Lourenço-de-Oliveira, R.; Weaver, S.C.; Vasilakis, N.; Vega-Rúa, A. Vector-Borne Transmission and Evolution of Zika Virus. Nat. Ecol. Evol. 2019, 3, 561. [Google Scholar] [CrossRef] [Green Version]
  12. Harrington, T.; Kuehnert, M.J.; Kamel, H.; Lanciotti, R.S.; Hand, S.; Currier, M.; Chamberland, M.E.; Petersen, L.R.; Marfin, A.A. West Nile Virus Infection Transmitted by Blood Transfusion. Transfusion (Paris) 2003, 43, 1018–1022. [Google Scholar] [CrossRef]
  13. Tambyah, P.A.; Koay, E.S.C.; Poon, M.L.M.; Lin, R.V.T.P.; Ong, B.K.C. Dengue Hemorrhagic Fever Transmitted by Blood Transfusion. N. Engl. J. Med. 2008, 359, 1526–1527. [Google Scholar] [CrossRef]
  14. D’Ortenzio, E.; Matheron, S.; de Lamballerie, X.; Hubert, B.; Piorkowski, G.; Maquart, M.; Descamps, D.; Damond, F.; Yazdanpanah, Y.; Leparc-Goffart, I. Evidence of Sexual Transmission of Zika Virus. N. Engl. J. Med. 2016, 374, 2195–2198. [Google Scholar] [CrossRef] [PubMed]
  15. Nguyen, S.M.; Antony, K.M.; Dudley, D.M.; Kohn, S.; Simmons, H.A.; Wolfe, B.; Salamat, M.S.; Teixeira, L.B.C.; Wiepz, G.J.; Thoong, T.H.; et al. Highly Efficient Maternal-Fetal Zika Virus Transmission in Pregnant Rhesus Macaques. PLoS Pathog. 2017, 13, e1006378. [Google Scholar] [CrossRef] [Green Version]
  16. Armstrong, P.M.; Ehrlich, H.Y.; Magalhaes, T.; Miller, M.R.; Conway, P.J.; Bransfield, A.; Misencik, M.J.; Gloria-Soria, A.; Warren, J.L.; Andreadis, T.G.; et al. Successive Blood Meals Enhance Virus Dissemination within Mosquitoes and Increase Transmission Potential. Nat. Microbiol. 2020, 5, 239–247. [Google Scholar] [CrossRef]
  17. Comeau, G.; Zinna, R.A.; Scott, T.; Ernst, K.; Walker, K.; Carrière, Y.; Riehle, M.A. Vertical Transmission of Zika Virus in Aedes Aegypti Produces Potentially Infectious Progeny. Am. J. Trop. Med. Hyg. 2020, 103, 876–883. [Google Scholar] [CrossRef]
  18. Merwaiss, F.; Filomatori, C.V.; Susuki, Y.; Bardossy, E.S.; Alvarez, D.E.; Saleh, M.-C. Chikungunya Virus Replication Rate Determines the Capacity of Crossing Tissue Barriers in Mosquitoes. J. Virol. 2021, 95. [Google Scholar] [CrossRef]
  19. Sim, S.; Ramirez, J.L.; Dimopoulos, G. Dengue Virus Infection of the Aedes Aegypti Salivary Gland and Chemosensory Apparatus Induces Genes That Modulate Infection and Blood-Feeding Behavior. PLoS Pathog. 2012, 8, e1002631. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  20. Göertz, G.P.; Vogels, C.B.F.; Geertsema, C.; Koenraadt, C.J.M.; Pijlman, G.P. Mosquito Co-Infection with Zika and Chikungunya Virus Allows Simultaneous Transmission without Affecting Vector Competence of Aedes Aegypti. PLoS Negl. Trop. Dis. 2017, 11, e0005654. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  21. Rückert, C.; Weger-Lucarelli, J.; Garcia-Luna, S.M.; Young, M.C.; Byas, A.D.; Murrieta, R.A.; Fauver, J.R.; Ebel, G.D. Impact of Simultaneous Exposure to Arboviruses on Infection and Transmission by Aedes Aegypti Mosquitoes. Nat. Commun. 2017, 8, 15412. [Google Scholar] [CrossRef] [PubMed]
  22. Schuster, S.; Miesen, P.; van Rij, R.P. Antiviral RNAi in Insects and Mammals: Parallels and Differences. Viruses 2019, 11, 448. [Google Scholar] [CrossRef] [Green Version]
  23. Saleh, M.-C.; Tassetto, M.; van Rij, R.P.; Goic, B.; Gausson, V.; Berry, B.; Jacquier, C.; Antoniewski, C.; Andino, R. Antiviral Immunity in Drosophila Requires Systemic RNAi Spread. Nature 2009, 458, 346–350. [Google Scholar] [CrossRef]
  24. Mukherjee, S.; Hanley, K.A. RNA Interference Modulates Replication of Dengue Virus in Drosophila Melanogaster Cells. BMC Microbiol. 2010, 10, 127. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Campbell, C.L.; Keene, K.M.; Brackney, D.E.; Olson, K.E.; Blair, C.D.; Wilusz, J.; Foy, B.D. Aedes Aegypti Uses RNA Interference in Defense against Sindbis Virus Infection. BMC Microbiol. 2008, 8, 47. [Google Scholar] [CrossRef] [Green Version]
  26. Lee, Y.S.; Nakahara, K.; Pham, J.W.; Kim, K.; He, Z.; Sontheimer, E.J.; Carthew, R.W. Distinct Roles for Drosophila Dicer-1 and Dicer-2 in the SiRNA/MiRNA Silencing Pathways. Cell 2004, 117, 69–81. [Google Scholar] [CrossRef] [Green Version]
  27. Galiana-Arnoux, D.; Dostert, C.; Schneemann, A.; Hoffmann, J.A.; Imler, J.-L. Essential Function in Vivo for Dicer-2 in Host Defense against RNA Viruses in Drosophila. Nat. Immunol. 2006, 7, 590–597. [Google Scholar] [CrossRef] [PubMed]
  28. Liu, Q.; Rand, T.A.; Kalidas, S.; Du, F.; Kim, H.-E.; Smith, D.P.; Wang, X. R2D2, a Bridge between the Initiation and Effector Steps of the Drosophila RNAi Pathway. Science 2003, 301, 1921–1925. [Google Scholar] [CrossRef] [PubMed]
  29. Okamura, K.; Ishizuka, A.; Siomi, H.; Siomi, M.C. Distinct Roles for Argonaute Proteins in Small RNA-Directed RNA Cleavage Pathways. Genes Dev. 2004, 18, 1655–1666. [Google Scholar] [CrossRef] [Green Version]
  30. Van Rij, R.P.; Saleh, M.-C.; Berry, B.; Foo, C.; Houk, A.; Antoniewski, C.; Andino, R. The RNA Silencing Endonuclease Argonaute 2 Mediates Specific Antiviral Immunity in Drosophila Melanogaster. Genes Dev. 2006, 20, 2985–2995. [Google Scholar] [CrossRef] [Green Version]
  31. McFarlane, M.; Almire, F.; Kean, J.; Donald, C.L.; McDonald, A.; Wee, B.; Lauréti, M.; Varjak, M.; Terry, S.; Vazeille, M.; et al. The Aedes Aegypti Domino Ortholog P400 Regulates Antiviral Exogenous Small Interfering RNA Pathway Activity and Ago-2 Expression. mSphere 2020, 5. [Google Scholar] [CrossRef] [Green Version]
  32. Scott, J.C.; Brackney, D.E.; Campbell, C.L.; Bondu-Hawkins, V.; Hjelle, B.; Ebel, G.D.; Olson, K.E.; Blair, C.D. Comparison of Dengue Virus Type 2-Specific Small RNAs from RNA Interference-Competent and –Incompetent Mosquito Cells. PLoS Negl. Trop. Dis. 2010, 4, e848. [Google Scholar] [CrossRef] [Green Version]
  33. Paradkar, P.N.; Duchemin, J.-B.; Voysey, R.; Walker, P.J. Dicer-2-Dependent Activation of Culex Vago Occurs via the TRAF-Rel2 Signaling Pathway. PLoS Negl. Trop. Dis. 2014, 8, e2823. [Google Scholar] [CrossRef] [Green Version]
  34. Brackney, D.E.; Beane, J.E.; Ebel, G.D. RNAi Targeting of West Nile Virus in Mosquito Midguts Promotes Virus Diversification. PLoS Pathog. 2009, 5, e1000502. [Google Scholar] [CrossRef] [Green Version]
  35. Harsh, S.; Ozakman, Y.; Kitchen, S.M.; Paquin-Proulx, D.; Nixon, D.F.; Eleftherianos, I. Dicer-2 Regulates Resistance and Maintains Homeostasis against Zika Virus Infection in Drosophila. J. Immunol. 2018, 201, 3058–3072. [Google Scholar] [CrossRef] [Green Version]
  36. Chotkowski, H.L.; Ciota, A.T.; Jia, Y.; Puig-Basagoiti, F.; Kramer, L.D.; Shi, P.-Y.; Glaser, R.L. West Nile Virus Infection of Drosophila Melanogaster Induces a Protective RNAi Response. Virology 2008, 377, 197–206. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Cirimotich, C.M.; Scott, J.C.; Phillips, A.T.; Geiss, B.J.; Olson, K.E. Suppression of RNA Interference Increases Alphavirus Replication and Virus-Associated Mortality in Aedes Aegypti Mosquitoes. BMC Microbiol. 2009, 9, 49. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  38. Siu, R.W.C.; Fragkoudis, R.; Simmonds, P.; Donald, C.L.; Chase-Topping, M.E.; Barry, G.; Attarzadeh-Yazdi, G.; Rodriguez-Andres, J.; Nash, A.A.; Merits, A.; et al. Antiviral RNA Interference Responses Induced by Semliki Forest Virus Infection of Mosquito Cells: Characterization, Origin, and Frequency-Dependent Functions of Virus-Derived Small Interfering RNAs. J. Virol. 2011, 85, 2907–2917. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  39. Cullen, B.R. Viruses and RNA Interference: Issues and Controversies. J. Virol. 2014, 88, 12934–12936. [Google Scholar] [CrossRef] [Green Version]
  40. Schnettler, E.; Sterken, M.G.; Leung, J.Y.; Metz, S.W.; Geertsema, C.; Goldbach, R.W.; Vlak, J.M.; Kohl, A.; Khromykh, A.A.; Pijlman, G.P. Noncoding Flavivirus RNA Displays RNA Interference Suppressor Activity in Insect and Mammalian Cells. J. Virol. 2012, 86, 13486–13500. [Google Scholar] [CrossRef] [Green Version]
  41. Li, Y.; Lu, J.; Han, Y.; Fan, X.; Ding, S.-W. RNA Interference Functions as an Antiviral Immunity Mechanism in Mammals. Science 2013, 342, 231–234. [Google Scholar] [CrossRef] [Green Version]
  42. BioRender. Available online: https://app.biorender.com/illustrations/edit/604466dd34d48400a7c5f5bb (accessed on 7 March 2021).
  43. Osman, D.; Buchon, N.; Chakrabarti, S.; Huang, Y.-T.; Su, W.-C.; Poidevin, M.; Tsai, Y.-C.; Lemaitre, B. Autocrine and Paracrine Unpaired Signaling Regulate Intestinal Stem Cell Maintenance and Division. J. Cell Sci. 2012, 125, 5944–5949. [Google Scholar] [CrossRef] [Green Version]
  44. Wright, V.M.; Vogt, K.L.; Smythe, E.; Zeidler, M.P. Differential Activities of the Drosophila JAK/STAT Pathway Ligands Upd, Upd2 and Upd3. Cell Signal. 2011, 23, 920–927. [Google Scholar] [CrossRef]
  45. Wittes, J.; Schüpbach, T. A Gene Expression Screen in Drosophila Melanogaster Identifies Novel JAK/STAT and EGFR Targets During Oogenesis. G3 Genes Genomes Genet. 2019, 9, 47–60. [Google Scholar] [CrossRef] [Green Version]
  46. Ghiglione, C.; Devergne, O.; Georgenthum, E.; Carballès, F.; Médioni, C.; Cerezo, D.; Noselli, S. The Drosophila Cytokine Receptor Domeless Controls Border Cell Migration and Epithelial Polarization during Oogenesis. Development 2002, 129, 5437–5447. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Herrera, S.C.; Bach, E.A. JAK/STAT Signaling in Stem Cells and Regeneration: From Drosophila to Vertebrates. Dev. Camb. Engl. 2019, 146. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  48. Levy, D.E. Physiological Significance of STAT Proteins: Investigations through Gene Disruption in Vivo. Cell. Mol. Life Sci. CMLS 1999, 55, 1559–1567. [Google Scholar] [CrossRef]
  49. Ahlers, L.R.H.; Trammell, C.E.; Carrell, G.F.; Mackinnon, S.; Torrevillas, B.K.; Chow, C.Y.; Luckhart, S.; Goodman, A.G. Insulin Potentiates JAK/STAT Signaling to Broadly Inhibit Flavivirus Replication in Insect Vectors. Cell Rep. 2019, 29, 1946–1960.e5. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  50. Harsh, S.; Fu, Y.; Kenney, E.; Han, Z.; Eleftherianos, I. Zika Virus Non-Structural Protein NS4A Restricts Eye Growth in Drosophila through Regulation of JAK/STAT Signaling. Dis. Model. Mech. 2020, 13, dmm040816. [Google Scholar] [CrossRef] [Green Version]
  51. Angleró-Rodríguez, Y.I.; MacLeod, H.J.; Kang, S.; Carlson, J.S.; Jupatanakul, N.; Dimopoulos, G. Aedes Aegypti Molecular Responses to Zika Virus: Modulation of Infection by the Toll and Jak/Stat Immune Pathways and Virus Host Factors. Front. Microbiol. 2017, 8. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  52. Terradas, G.; Joubert, D.A.; McGraw, E.A. The RNAi Pathway Plays a Small Part in Wolbachia-Mediated Blocking of Dengue Virus in Mosquito Cells. Sci. Rep. 2017, 7, 43847. [Google Scholar] [CrossRef] [Green Version]
  53. Jupatanakul, N.; Sim, S.; Angleró-Rodríguez, Y.I.; Souza-Neto, J.; Das, S.; Poti, K.E.; Rossi, S.L.; Bergren, N.; Vasilakis, N.; Dimopoulos, G. Engineered Aedes Aegypti JAK/STAT Pathway-Mediated Immunity to Dengue Virus. PLOS Negl. Trop. Dis. 2017, 11, e0005187. [Google Scholar] [CrossRef] [PubMed]
  54. Souza-Neto, J.A.; Sim, S.; Dimopoulos, G. An Evolutionary Conserved Function of the JAK-STAT Pathway in Anti-Dengue Defense. Proc. Natl. Acad. Sci. USA 2009, 106, 17841–17846. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Dostert, C.; Jouanguy, E.; Irving, P.; Troxler, L.; Galiana-Arnoux, D.; Hetru, C.; Hoffmann, J.A.; Imler, J.-L. The Jak-STAT Signaling Pathway Is Required but Not Sufficient for the Antiviral Response of Drosophila. Nat. Immunol. 2005, 6, 946–953. [Google Scholar] [CrossRef]
  56. Agaisse, H.; Petersen, U.-M.; Boutros, M.; Mathey-Prevot, B.; Perrimon, N. Signaling Role of Hemocytes in Drosophila JAK/STAT-Dependent Response to Septic Injury. Dev. Cell 2003, 5, 441–450. [Google Scholar] [CrossRef] [Green Version]
  57. Harrison, D.A.; McCoon, P.E.; Binari, R.; Gilman, M.; Perrimon, N. Drosophila Unpaired Encodes a Secreted Protein That Activates the JAK Signaling Pathway. Genes Dev. 1998, 12, 3252–3263. [Google Scholar] [CrossRef] [Green Version]
  58. Brown, S.; Hu, N.; Hombría, J.C. Identification of the First Invertebrate Interleukin JAK/STAT Receptor, the Drosophila Gene Domeless. Curr. Biol. CB 2001, 11, 1700–1705. [Google Scholar] [CrossRef]
  59. Binari, R.; Perrimon, N. Stripe-Specific Regulation of Pair-Rule Genes by Hopscotch, a Putative Jak Family Tyrosine Kinase in Drosophila. Genes Dev. 1994, 8, 300–312. [Google Scholar] [CrossRef] [Green Version]
  60. Yan, R.; Small, S.; Desplan, C.; Dearolf, C.R.; Darnell, J.E. Identification of a Stat Gene That Functions in Drosophila Development. Cell 1996, 84, 421–430. [Google Scholar] [CrossRef] [Green Version]
  61. Hou, X.S.; Melnick, M.B.; Perrimon, N. Marelle Acts Downstream of the Drosophila HOP/JAK Kinase and Encodes a Protein Similar to the Mammalian STATs. Cell 1996, 84, 411–419. [Google Scholar] [CrossRef] [Green Version]
  62. Paradkar, P.N.; Trinidad, L.; Voysey, R.; Duchemin, J.-B.; Walker, P.J. Secreted Vago Restricts West Nile Virus Infection in Culex Mosquito Cells by Activating the Jak-STAT Pathway. Proc. Natl. Acad. Sci. USA 2012, 109, 18915–18920. [Google Scholar] [CrossRef] [Green Version]
  63. Wu, Y.; Liu, Q.; Zhou, J.; Xie, W.; Chen, C.; Wang, Z.; Yang, H.; Cui, J. Zika Virus Evades Interferon-Mediated Antiviral Response through the Co-Operation of Multiple Nonstructural Proteins in Vitro. Cell Discov. 2017, 3, 17006. [Google Scholar] [CrossRef]
  64. Keller, B.C.; Fredericksen, B.L.; Samuel, M.A.; Mock, R.E.; Mason, P.W.; Diamond, M.S.; Gale, M. Resistance to Alpha/Beta Interferon Is a Determinant of West Nile Virus Replication Fitness and Virulence. J. Virol. 2006, 80, 9424–9434. [Google Scholar] [CrossRef] [Green Version]
  65. Lin, R.-J.; Liao, C.-L.; Lin, E.; Lin, Y.-L. Blocking of the Alpha Interferon-Induced Jak-Stat Signaling Pathway by Japanese Encephalitis Virus Infection. J. Virol. 2004, 78, 9285–9294. [Google Scholar] [CrossRef] [Green Version]
  66. Valanne, S.; Wang, J.-H.; Rämet, M. The Drosophila Toll Signaling Pathway. J. Immunol. 2011, 186, 649–656. [Google Scholar] [CrossRef] [Green Version]
  67. Myllymäki, H.; Valanne, S.; Rämet, M. The Drosophila Imd Signaling Pathway. J. Immunol. 2014, 192, 3455–3462. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  68. Michel, T.; Reichhart, J.M.; Hoffmann, J.A.; Royet, J. Drosophila Toll Is Activated by Gram-Positive Bacteria through a Circulating Peptidoglycan Recognition Protein. Nature 2001, 414, 756–759. [Google Scholar] [CrossRef]
  69. Lemaitre, B.; Nicolas, E.; Michaut, L.; Reichhart, J.M.; Hoffmann, J.A. The Dorsoventral Regulatory Gene Cassette Spätzle/Toll/Cactus Controls the Potent Antifungal Response in Drosophila Adults. Cell 1996, 86, 973–983. [Google Scholar] [CrossRef] [Green Version]
  70. Leulier, F.; Parquet, C.; Pili-Floury, S.; Ryu, J.-H.; Caroff, M.; Lee, W.-J.; Mengin-Lecreulx, D.; Lemaitre, B. The Drosophila Immune System Detects Bacteria through Specific Peptidoglycan Recognition. Nat. Immunol. 2003, 4, 478–484. [Google Scholar] [CrossRef]
  71. Kaneko, T.; Goldman, W.E.; Mellroth, P.; Steiner, H.; Fukase, K.; Kusumoto, S.; Harley, W.; Fox, A.; Golenbock, D.; Silverman, N. Monomeric and Polymeric Gram-Negative Peptidoglycan but Not Purified LPS Stimulate the Drosophila IMD Pathway. Immunity 2004, 20, 637–649. [Google Scholar] [CrossRef] [Green Version]
  72. Horng, T.; Medzhitov, R. Drosophila MyD88 Is an Adapter in the Toll Signaling Pathway. Proc. Natl. Acad. Sci. USA 2001, 98, 12654–12658. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  73. Tauszig-Delamasure, S.; Bilak, H.; Capovilla, M.; Hoffmann, J.A.; Imler, J.-L. Drosophila MyD88 Is Required for the Response to Fungal and Gram-Positive Bacterial Infections. Nat. Immunol. 2002, 3, 91–97. [Google Scholar] [CrossRef] [PubMed]
  74. Sun, H.; Bristow, B.N.; Qu, G.; Wasserman, S.A. A Heterotrimeric Death Domain Complex in Toll Signaling. Proc. Natl. Acad. Sci. USA 2002, 99, 12871–12876. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  75. Wu, L.P.; Anderson, K.V. Regulated Nuclear Import of Rel Proteins in the Drosophila Immune Response. Nature 1998, 392, 93–97. [Google Scholar] [CrossRef] [PubMed]
  76. Choe, K.-M.; Lee, H.; Anderson, K.V. Drosophila Peptidoglycan Recognition Protein LC (PGRP-LC) Acts as a Signal-Transducing Innate Immune Receptor. Proc. Natl. Acad. Sci. USA 2005, 102, 1122–1126. [Google Scholar] [CrossRef] [Green Version]
  77. Georgel, P.; Naitza, S.; Kappler, C.; Ferrandon, D.; Zachary, D.; Swimmer, C.; Kopczynski, C.; Duyk, G.; Reichhart, J.M.; Hoffmann, J.A. Drosophila Immune Deficiency (IMD) Is a Death Domain Protein That Activates Antibacterial Defense and Can Promote Apoptosis. Dev. Cell 2001, 1, 503–514. [Google Scholar] [CrossRef] [Green Version]
  78. Stöven, S.; Silverman, N.; Junell, A.; Hedengren-Olcott, M.; Erturk, D.; Engström, Y.; Maniatis, T.; Hultmark, D. Caspase-Mediated Processing of the Drosophila NF-ΚB Factor Relish. Proc. Natl. Acad. Sci. USA 2003, 100, 5991–5996. [Google Scholar] [CrossRef] [Green Version]
  79. Silverman, N.; Zhou, R.; Stöven, S.; Pandey, N.; Hultmark, D.; Maniatis, T. A Drosophila IκB Kinase Complex Required for Relish Cleavage and Antibacterial Immunity. Genes Dev. 2000, 14, 2461–2471. [Google Scholar] [CrossRef] [Green Version]
  80. Paquette, N.; Broemer, M.; Aggarwal, K.; Chen, L.; Husson, M.; Ertürk-Hasdemir, D.; Reichhart, J.-M.; Meier, P.; Silverman, N. Caspase Mediated Cleavage, IAP Binding and Ubiquitination: Linking Three Mechanisms Crucial for Drosophila NF-ΚB Signaling. Mol. Cell 2010, 37, 172. [Google Scholar] [CrossRef] [Green Version]
  81. Dushay, M.S.; Asling, B.; Hultmark, D. Origins of Immunity: Relish, a Compound Rel-like Gene in the Antibacterial Defense of Drosophila. Proc. Natl. Acad. Sci. USA 1996, 93, 10343–10347. [Google Scholar] [CrossRef] [Green Version]
  82. Kim, M.; Lee, J.H.; Lee, S.Y.; Kim, E.; Chung, J. Caspar, a Suppressor of Antibacterial Immunity in Drosophila. Proc. Natl. Acad. Sci. USA 2006, 103, 16358–16363. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  83. Stöven, S.; Ando, I.; Kadalayil, L.; Engström, Y.; Hultmark, D. Activation of the Drosophila NF-ΚB Factor Relish by Rapid Endoproteolytic Cleavage. EMBO Rep. 2000, 1, 347–352. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  84. Barletta, A.B.F.; Alves, L.R.; Nascimento Silva, M.C.L.; Sim, S.; Dimopoulos, G.; Liechocki, S.; Maya-Monteiro, C.M.; Sorgine, M.H.F. Emerging Role of Lipid Droplets in Aedes Aegypti Immune Response against Bacteria and Dengue Virus. Sci. Rep. 2016, 6. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  85. Xi, Z.; Ramirez, J.L.; Dimopoulos, G. The Aedes Aegypti Toll Pathway Controls Dengue Virus Infection. PLoS Pathog. 2008, 4, e1000098. [Google Scholar] [CrossRef] [PubMed]
  86. Zink, S.D.; Van Slyke, G.A.; Palumbo, M.J.; Kramer, L.D.; Ciota, A.T. Exposure to West Nile Virus Increases Bacterial Diversity and Immune Gene Expression in Culex Pipiens. Viruses 2015, 7, 5619–5631. [Google Scholar] [CrossRef] [Green Version]
  87. Zambon, R.A.; Nandakumar, M.; Vakharia, V.N.; Wu, L.P. The Toll Pathway Is Important for an Antiviral Response in Drosophila. Proc. Natl. Acad. Sci. USA 2005, 102, 7257–7262. [Google Scholar] [CrossRef] [Green Version]
  88. Wang, Z.; Wu, D.; Liu, Y.; Xia, X.; Gong, W.; Qiu, Y.; Yang, J.; Zheng, Y.; Li, J.; Wang, Y.F.; et al. Drosophila Dicer-2 Has an RNA Interference–Independent Function That Modulates Toll Immune Signaling. Sci. Adv. 2015, 1, e1500228. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  89. Costa, A.; Jan, E.; Sarnow, P.; Schneider, D. The Imd Pathway Is Involved in Antiviral Immune Responses in Drosophila. PLoS ONE 2009, 4, e7436. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  90. Nanfack-Minkeu, F.; Mitri, C.; Bischoff, E.; Belda, E.; Casademont, I.; Vernick, K.D. Interaction of RNA Viruses of the Natural Virome with the African Malaria Vector, Anopheles Coluzzii. Sci. Rep. 2019, 9, 6319. [Google Scholar] [CrossRef]
  91. Medzhitov, R.; Preston-Hurlburt, P.; Janeway, C.A. A Human Homologue of the Drosophila Toll Protein Signals Activation of Adaptive Immunity. Nature 1997, 388, 394–397. [Google Scholar] [CrossRef]
  92. Engström, Y.; Kadalayil, L.; Sun, S.C.; Samakovlis, C.; Hultmark, D.; Faye, I. Kappa B-like Motifs Regulate the Induction of Immune Genes in Drosophila. J. Mol. Biol. 1993, 232, 327–333. [Google Scholar] [CrossRef]
  93. Kumar, M.; Belcaid, M.; Nerurkar, V.R. Identification of Host Genes Leading to West Nile Virus Encephalitis in Mice Brain Using RNA-Seq Analysis. Sci. Rep. 2016, 6. [Google Scholar] [CrossRef]
  94. Daffis, S.; Suthar, M.S.; Michael Gale, J.; Diamond, M.S. Measure and Countermeasure: Type I IFN (IFN-α/β) Antiviral Response against West Nile Virus. J. Innate Immun. 2009, 1, 435–445. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  95. Szretter, K.J.; Daffis, S.; Patel, J.; Suthar, M.S.; Klein, R.S.; Gale, M.; Diamond, M.S. The Innate Immune Adaptor Molecule MyD88 Restricts West Nile Virus Replication and Spread in Neurons of the Central Nervous System. J. Virol. 2010, 84, 12125–12138. [Google Scholar] [CrossRef] [Green Version]
  96. Thackray, L.B.; Shrestha, B.; Richner, J.M.; Miner, J.J.; Pinto, A.K.; Lazear, H.M.; Gale, M.; Diamond, M.S. Interferon Regulatory Factor 5-Dependent Immune Responses in the Draining Lymph Node Protect against West Nile Virus Infection. J. Virol. 2014, 88, 11007–11021. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  97. Okuda, K.; de Souza Caroci, A.; Ribolla, P.E.M.; de Bianchi, A.G.; Bijovsky, A.T. Functional Morphology of Adult Female Culex Quinquefasciatus Midgut during Blood Digestion. Tissue Cell 2002, 34, 210–219. [Google Scholar] [CrossRef]
  98. Romoser, W.S.; Wasieloski, L.P.; Pushko, P.; Kondig, J.P.; Lerdthusnee, K.; Neira, M.; Ludwig, G.V. Evidence for Arbovirus Dissemination Conduits from the Mosquito (Diptera: Culicidae) Midgut. J. Med. Entomol. 2004, 41, 467–475. [Google Scholar] [CrossRef] [Green Version]
  99. Rodriguez-Andres, J.; Rani, S.; Varjak, M.; Chase-Topping, M.E.; Beck, M.H.; Ferguson, M.C.; Schnettler, E.; Fragkoudis, R.; Barry, G.; Merits, A.; et al. Phenoloxidase Activity Acts as a Mosquito Innate Immune Response against Infection with Semliki Forest Virus. PLoS Pathog. 2012, 8, e1002977. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  100. Kumar, A.; Srivastava, P.; Sirisena, P.; Dubey, S.K.; Kumar, R.; Shrinet, J.; Sunil, S. Mosquito Innate Immunity. Insects 2018, 9, 95. [Google Scholar] [CrossRef] [Green Version]
  101. Parikh, G.R.; Oliver, J.D.; Bartholomay, L.C. A Haemocyte Tropism for an Arbovirus. J. Gen. Virol. 2009, 90, 292–296. [Google Scholar] [CrossRef]
  102. Girard, Y.A.; Klingler, K.A.; Higgs, S. West Nile Virus Dissemination and Tissue Tropisms in Orally Infected Culex Pipiens Quinquefasciatus. Vector Borne Zoonotic Dis. Larchmt. N. Y. 2004, 4, 109–122. [Google Scholar] [CrossRef]
  103. Mourya, D.T.; Mishra, A.C. Antigen Distribution Pattern of Japanese Encephalitis Virus in Culex Tritaeniorhynchus, C. Vishnui & C. Pseudovishnui. Indian J. Med. Res. 2000, 111, 157–161. [Google Scholar]
  104. Zhang, M.; Zheng, X.; Wu, Y.; Gan, M.; He, A.; Li, Z.; Liu, J.; Zhan, X. Quantitative Analysis of Replication and Tropisms of Dengue Virus Type 2 in Aedes Albopictus. Am. J. Trop. Med. Hyg. 2010, 83, 700–707. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  105. Girard, Y.A.; Popov, V.; Wen, J.; Han, V.; Higgs, S. Ultrastructural Study of West Nile Virus Pathogenesis in Culex Pipiens Quinquefasciatus (Diptera: Culicidae). J. Med. Entomol. 2005, 42, 429–444. [Google Scholar] [CrossRef]
  106. Weaver, S.C.; Scott, T.W.; Lorenz, L.H.; Lerdthusnee, K.; Romoser, W.S. Togavirus-Associated Pathologic Changes in the Midgut of a Natural Mosquito Vector. J. Virol. 1988, 62, 2083–2090. [Google Scholar] [CrossRef] [Green Version]
  107. Xu, J.; Hopkins, K.; Sabin, L.; Yasunaga, A.; Subramanian, H.; Lamborn, I.; Gordesky-Gold, B.; Cherry, S. ERK Signaling Couples Nutrient Status to Antiviral Defense in the Insect Gut. Proc. Natl. Acad. Sci. USA 2013, 110, 15025–15030. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  108. DiAngelo, J.R.; Bland, M.L.; Bambina, S.; Cherry, S.; Birnbaum, M.J. The Immune Response Attenuates Growth and Nutrient Storage in Drosophila by Reducing Insulin Signaling. Proc. Natl. Acad. Sci. USA 2009, 106, 20853–20858. [Google Scholar] [CrossRef] [Green Version]
  109. Drexler, A.L.; Pietri, J.E.; Pakpour, N.; Hauck, E.; Wang, B.; Glennon, E.K.K.; Georgis, M.; Riehle, M.A.; Luckhart, S. Human IGF1 Regulates Midgut Oxidative Stress and Epithelial Homeostasis to Balance Lifespan and Plasmodium Falciparum Resistance in Anopheles Stephensi. PLoS Pathog. 2014, 10, e1004231. [Google Scholar] [CrossRef] [Green Version]
  110. Haqshenas, G.; Terradas, G.; Paradkar, P.N.; Duchemin, J.-B.; McGraw, E.A.; Doerig, C. A Role for the Insulin Receptor in the Suppression of Dengue Virus and Zika Virus in Wolbachia-Infected Mosquito Cells. Cell Rep. 2019, 26, 529–535.e3. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  111. Hedges, L.M.; Brownlie, J.C.; O’Neill, S.L.; Johnson, K.N. Wolbachia and Virus Protection in Insects. Science 2008, 322, 702. [Google Scholar] [CrossRef] [PubMed]
  112. Luckhart, S.; Giulivi, C.; Drexler, A.L.; Antonova-Koch, Y.; Sakaguchi, D.; Napoli, E.; Wong, S.; Price, M.S.; Eigenheer, R.; Phinney, B.S.; et al. Sustained Activation of Akt Elicits Mitochondrial Dysfunction to Block Plasmodium Falciparum Infection in the Mosquito Host. PLoS Pathog. 2013, 9, e1003180. [Google Scholar] [CrossRef] [Green Version]
  113. Altindis, E.; Cai, W.; Sakaguchi, M.; Zhang, F.; GuoXiao, W.; Liu, F.; De Meyts, P.; Gelfanov, V.; Pan, H.; DiMarchi, R.; et al. Viral Insulin-like Peptides Activate Human Insulin and IGF-1 Receptor Signaling: A Paradigm Shift for Host–Microbe Interactions. Proc. Natl. Acad. Sci. USA 2018, 115, 2461–2466. [Google Scholar] [CrossRef] [Green Version]
  114. Liang, Q.; Luo, Z.; Zeng, J.; Chen, W.; Foo, S.-S.; Lee, S.-A.; Ge, J.; Wang, S.; Goldman, S.A.; Zlokovic, B.V.; et al. Zika Virus NS4A and NS4B Proteins Deregulate Akt-MTOR Signaling in Human Fetal Neural Stem Cells to Inhibit Neurogenesis and Induce Autophagy. Cell Stem Cell 2016, 19, 663–671. [Google Scholar] [CrossRef] [Green Version]
  115. Samy, A.M.; Elaagip, A.H.; Kenawy, M.A.; Ayres, C.F.J.; Peterson, A.T.; Soliman, D.E. Climate Change Influences on the Global Potential Distribution of the Mosquito Culex Quinquefasciatus, Vector of West Nile Virus and Lymphatic Filariasis. PLoS ONE 2016, 11, e0163863. [Google Scholar] [CrossRef] [PubMed]
  116. Alaniz, A.J.; Carvajal, M.A.; Bacigalupo, A.; Cattan, P.E. Global Spatial Assessment of Aedes Aegypti and Culex Quinquefasciatus: A Scenario of Zika Virus Exposure. Epidemiol. Infect. 2018, 147. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  117. Muttis, E.; Balsalobre, A.; Chuchuy, A.; Mangudo, C.; Ciota, A.T.; Kramer, L.D.; Micieli, M.V. Factors Related to Aedes Aegypti (Diptera: Culicidae) Populations and Temperature Determine Differences on Life-History Traits with Regional Implications in Disease Transmission. J. Med. Entomol. 2018, 55, 1105–1112. [Google Scholar] [CrossRef]
  118. Miller, M.J.; Loaiza, J.R. Geographic Expansion of the Invasive Mosquito Aedes Albopictus across Panama—Implications for Control of Dengue and Chikungunya Viruses. PLoS Negl. Trop. Dis. 2015, 9, e0003383. [Google Scholar] [CrossRef] [Green Version]
  119. Weger-Lucarelli, J.; Rückert, C.; Chotiwan, N.; Nguyen, C.; Luna, S.M.G.; Fauver, J.R.; Foy, B.D.; Perera, R.; Black, W.C.; Kading, R.C.; et al. Vector Competence of American Mosquitoes for Three Strains of Zika Virus. PLoS Negl. Trop. Dis. 2016, 10, e0005101. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  120. Elizondo-Quiroga, D.; Medina-Sánchez, A.; Sánchez-González, J.M.; Eckert, K.A.; Villalobos-Sánchez, E.; Navarro-Zúñiga, A.R.; Sánchez-Tejeda, G.; Correa-Morales, F.; González-Acosta, C.; Arias, C.F.; et al. Zika Virus in Salivary Glands of Five Different Species of Wild-Caught Mosquitoes from Mexico. Sci. Rep. 2018, 8, 1–7. [Google Scholar] [CrossRef] [Green Version]
  121. Jupp, P.G.; Kemp, A.; Grobbelaar, A.; Lema, P.; Burt, F.J.; Alahmed, A.M.; Al Mujalli, D.; Al Khamees, M.; Swanepoel, R. The 2000 Epidemic of Rift Valley Fever in Saudi Arabia: Mosquito Vector Studies. Med. Vet. Entomol. 2002, 16, 245–252. [Google Scholar] [CrossRef]
  122. Moser, L.A.; Lim, P.-Y.; Styer, L.M.; Kramer, L.D.; Bernard, K.A. Parameters of Mosquito-Enhanced West Nile Virus Infection. J. Virol. 2016, 90, 292–299. [Google Scholar] [CrossRef] [Green Version]
  123. Sun, P.; Nie, K.; Zhu, Y.; Liu, Y.; Wu, P.; Liu, Z.; Du, S.; Fan, H.; Chen, C.-H.; Zhang, R.; et al. A Mosquito Salivary Protein Promotes Flavivirus Transmission by Activation of Autophagy. Nat. Commun. 2020, 11, 260. [Google Scholar] [CrossRef] [Green Version]
  124. Styer, L.M.; Lim, P.-Y.; Louie, K.L.; Albright, R.G.; Kramer, L.D.; Bernard, K.A. Mosquito Saliva Causes Enhancement of West Nile Virus Infection in Mice. J. Virol. 2011, 85, 1517–1527. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  125. Stark, K.R.; James, A.A. Salivary Gland Anticoagulants in Culicine and Anopheline Mosquitoes (Diptera:Culicidae). J. Med. Entomol. 1996, 33, 645–650. [Google Scholar] [CrossRef] [PubMed]
  126. Schneider, B.S.; Soong, L.; Coffey, L.L.; Stevenson, H.L.; McGee, C.E.; Higgs, S. Aedes Aegypti Saliva Alters Leukocyte Recruitment and Cytokine Signaling by Antigen-Presenting Cells during West Nile Virus Infection. PLoS ONE 2010, 5, e11704. [Google Scholar] [CrossRef]
  127. Bai, F.; Kong, K.-F.; Dai, J.; Qian, F.; Zhang, L.; Brown, C.R.; Fikrig, E.; Montgomery, R.R. A Paradoxical Role for Neutrophils in the Pathogenesis of West Nile Virus. J. Infect. Dis. 2010, 202, 1804–1812. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  128. Ben-Nathan, D.; Huitinga, I.; Lustig, S.; van Rooijen, N.; Kobiler, D. West Nile Virus Neuroinvasion and Encephalitis Induced by Macrophage Depletion in Mice. Arch. Virol. 1996, 141, 459–469. [Google Scholar] [CrossRef]
  129. Vogt, M.B.; Lahon, A.; Arya, R.P.; Kneubehl, A.R.; Clinton, J.L.S.; Paust, S.; Rico-Hesse, R. Mosquito Saliva Alone Has Profound Effects on the Human Immune System. PLoS Negl. Trop. Dis. 2018, 12, e0006439. [Google Scholar] [CrossRef]
  130. Pingen, M.; Bryden, S.R.; Pondeville, E.; Schnettler, E.; Kohl, A.; Merits, A.; Fazakerley, J.K.; Graham, G.J.; McKimmie, C.S. Host Inflammatory Response to Mosquito Bites Enhances the Severity of Arbovirus Infection. Immunity 2016, 44, 1455–1469. [Google Scholar] [CrossRef] [Green Version]
  131. Lim, P.-Y.; Behr, M.J.; Chadwick, C.M.; Shi, P.-Y.; Bernard, K.A. Keratinocytes Are Cell Targets of West Nile Virus In Vivo. J. Virol. 2011, 85, 5197–5201. [Google Scholar] [CrossRef] [Green Version]
  132. Johnston, L.J.; King, N.J.C.; Halliday, G.M. Langerhans Cells Migrate to Local Lymph Nodes Following Cutaneous Infection with an Arbovirus. J. Investig. Dermatol. 2000, 114, 560–568. [Google Scholar] [CrossRef] [Green Version]
  133. Samuel, M.A.; Diamond, M.S. Alpha/Beta Interferon Protects against Lethal West Nile Virus Infection by Restricting Cellular Tropism and Enhancing Neuronal Survival. J. Virol. 2005, 79, 13350–13361. [Google Scholar] [CrossRef] [Green Version]
  134. Hershkovitz, O.; Rosental, B.; Rosenberg, L.A.; Navarro-Sanchez, M.E.; Jivov, S.; Zilka, A.; Gershoni-Yahalom, O.; Brient-Litzler, E.; Bedouelle, H.; Ho, J.W.; et al. NKp44 Receptor Mediates Interaction of the Envelope Glycoproteins from the West Nile and Dengue Viruses with NK Cells. J. Immunol. Baltim. Md 1950 2009, 183, 2610–2621. [Google Scholar] [CrossRef] [PubMed]
  135. Zhang, M.; Daniel, S.; Huang, Y.; Chancey, C.; Huang, Q.; Lei, Y.F.; Grinev, A.; Mostowski, H.; Rios, M.; Dayton, A. Anti-West Nile Virus Activity of in Vitro Expanded Human Primary Natural Killer Cells. BMC Immunol. 2010, 11, 3. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  136. Xin, L.; Vargas-Inchaustegui, D.A.; Raimer, S.S.; Kelly, B.C.; Hu, J.; Zhu, L.; Sun, J.; Soong, L. Type I IFN Receptor Regulates Neutrophil Functions and Innate Immunity to Leishmania Parasites. J. Immunol. Baltim. Md 1950 2010, 184, 7047–7056. [Google Scholar] [CrossRef] [Green Version]
  137. Purtha, W.E.; Chachu, K.A.; Virgin, H.W.; Diamond, M.S. Early B-Cell Activation after West Nile Virus Infection Requires Alpha/Beta Interferon but Not Antigen Receptor Signaling. J. Virol. 2008, 82, 10964–10974. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  138. Pinto, A.K.; Daffis, S.; Brien, J.D.; Gainey, M.D.; Yokoyama, W.M.; Sheehan, K.C.F.; Murphy, K.M.; Schreiber, R.D.; Diamond, M.S. A Temporal Role of Type I Interferon Signaling in CD8+ T Cell Maturation during Acute West Nile Virus Infection. PLoS Pathog. 2011, 7, e1002407. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  139. Hong, J.P.; McCarthy, M.K.; Davenport, B.J.; Morrison, T.E.; Diamond, M.S. Clearance of Chikungunya Virus Infection in Lymphoid Tissues Is Promoted by Treatment with an Agonistic Anti-CD137 Antibody. J. Virol. 2019, 93, e01231-19. [Google Scholar] [CrossRef]
  140. Lazear, H.M.; Pinto, A.K.; Ramos, H.J.; Vick, S.C.; Shrestha, B.; Suthar, M.S.; Gale, M.; Diamond, M.S. Pattern Recognition Receptor MDA5 Modulates CD8+ T Cell-Dependent Clearance of West Nile Virus from the Central Nervous System. J. Virol. 2013, 87, 11401–11415. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  141. Akira, S.; Uematsu, S.; Takeuchi, O. Pathogen Recognition and Innate Immunity. Cell 2006, 124, 783–801. [Google Scholar] [CrossRef] [Green Version]
  142. Lazear, H.M.; Govero, J.; Smith, A.M.; Platt, D.J.; Fernandez, E.; Miner, J.J.; Diamond, M.S. A Mouse Model of Zika Virus Pathogenesis. Cell Host Microbe 2016, 19, 720–730. [Google Scholar] [CrossRef] [Green Version]
  143. Shresta, S.; Kyle, J.L.; Snider, H.M.; Basavapatna, M.; Beatty, P.R.; Harris, E. Interferon-Dependent Immunity Is Essential for Resistance to Primary Dengue Virus Infection in Mice, Whereas T- and B-Cell-Dependent Immunity Are Less Critical. J. Virol. 2004, 78, 2701–2710. [Google Scholar] [CrossRef] [Green Version]
  144. Lubick, K.J.; Robertson, S.J.; McNally, K.L.; Freedman, B.A.; Rasmussen, A.L.; Taylor, R.T.; Walts, A.D.; Tsuruda, S.; Sakai, M.; Ishizuka, M.; et al. Flavivirus Antagonism of Type I Interferon Signaling Reveals Prolidase as a Regulator of IFNAR1 Surface Expression. Cell Host Microbe 2015, 18, 61–74. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  145. Grant, A.; Ponia, S.S.; Tripathi, S.; Balasubramaniam, V.; Miorin, L.; Sourisseau, M.; Schwarz, M.C.; Sánchez-Seco, M.P.; Evans, M.J.; Best, S.M.; et al. Zika Virus Targets Human STAT2 to Inhibit Type I Interferon Signaling. Cell Host Microbe 2016, 19, 882–890. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  146. Morrison, J.; Laurent-Rolle, M.; Maestre, A.M.; Rajsbaum, R.; Pisanelli, G.; Simon, V.; Mulder, L.C.F.; Fernandez-Sesma, A.; García-Sastre, A. Dengue Virus Co-Opts UBR4 to Degrade STAT2 and Antagonize Type I Interferon Signaling. PLoS Pathog. 2013, 9, e1003265. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  147. Laurent-Rolle, M.; Morrison, J.; Rajsbaum, R.; Macleod, J.M.L.; Pisanelli, G.; Pham, A.; Ayllon, J.; Miorin, L.; Martinez, C.; tenOever, B.R.; et al. The Interferon Signaling Antagonist Function of Yellow Fever Virus NS5 Protein Is Activated by Type I Interferon. Cell Host Microbe 2014, 16, 314–327. [Google Scholar] [CrossRef] [Green Version]
  148. Fros, J.J.; Liu, W.J.; Prow, N.A.; Geertsema, C.; Ligtenberg, M.; Vanlandingham, D.L.; Schnettler, E.; Vlak, J.M.; Suhrbier, A.; Khromykh, A.A.; et al. Chikungunya Virus Nonstructural Protein 2 Inhibits Type I/II Interferon-Stimulated JAK-STAT Signaling. J. Virol. 2010, 84, 10877–10887. [Google Scholar] [CrossRef] [Green Version]
  149. Tirado, S.M.C.; Yoon, K.-J. Antibody-Dependent Enhancement of Virus Infection and Disease. Viral Immunol. 2003, 16, 69–86. [Google Scholar] [CrossRef] [PubMed]
  150. Gollins, S.W.; Porterfield, J.S. Flavivirus Infection Enhancement in Macrophages: Radioactive and Biological Studies on the Effect of Antibody on Viral Fate. J. Gen. Virol. 1984, 65 Pt 8, 1261–1272. [Google Scholar] [CrossRef]
  151. Gollins, S.W.; Porterfield, J.S. Flavivirus Infection Enhancement in Macrophages: An Electron Microscopic Study of Viral Cellular Entry. J. Gen. Virol. 1985, 66 Pt 9, 1969–1982. [Google Scholar] [CrossRef]
  152. Dejnirattisai, W.; Jumnainsong, A.; Onsirisakul, N.; Fitton, P.; Vasanawathana, S.; Limpitikul, W.; Puttikhunt, C.; Edwards, C.; Duangchinda, T.; Supasa, S.; et al. Cross-Reacting Antibodies Enhance Dengue Virus Infection in Humans. Science 2010, 328, 745–748. [Google Scholar] [CrossRef] [Green Version]
  153. Charles, A.S.; Christofferson, R.C. Utility of a Dengue-Derived Monoclonal Antibody to Enhance Zika Infection In Vitro. PLoS Curr. 2016, 8. [Google Scholar] [CrossRef]
  154. Kliks, S.C.; Nimmanitya, S.; Nisalak, A.; Burke, D.S. Evidence That Maternal Dengue Antibodies Are Important in the Development of Dengue Hemorrhagic Fever in Infants. Am. J. Trop. Med. Hyg. 1988, 38, 411–419. [Google Scholar] [CrossRef] [PubMed]
  155. Kliks, S.C.; Nisalak, A.; Brandt, W.E.; Wahl, L.; Burke, D.S. Antibody-Dependent Enhancement of Dengue Virus Growth in Human Monocytes as a Risk Factor for Dengue Hemorrhagic Fever. Am. J. Trop. Med. Hyg. 1989, 40, 444–451. [Google Scholar] [CrossRef] [PubMed]
  156. Guzmán, M.G.; Kourí, G.; Valdés, L.; Bravo, J.; Vázquez, S.; Halstead, S.B. Enhanced Severity of Secondary Dengue-2 Infections: Death Rates in 1981 and 1997 Cuban Outbreaks. Rev. Panam. Salud Publica Pan Am. J. Public Health 2002, 11, 223–227. [Google Scholar] [CrossRef] [Green Version]
  157. de Silva, A.M.; Harris, E. Which Dengue Vaccine Approach Is the Most Promising, and Should We Be Concerned about Enhanced Disease after Vaccination? Cold Spring Harb. Perspect. Biol. 2018, 10. [Google Scholar] [CrossRef] [PubMed]
  158. Nielsen, K.K.; Bygbjerg, I.C. Zika Virus and Hyperglycaemia in Pregnancy. Lancet 2016, 387, 1812. [Google Scholar] [CrossRef] [Green Version]
  159. Kumar, M.; Roe, K.; Nerurkar, P.V.; Orillo, B.; Thompson, K.S.; Verma, S.; Nerurkar, V.R. Reduced Immune Cell Infiltration and Increased Pro-Inflammatory Mediators in the Brain of Type 2 Diabetic Mouse Model Infected with West Nile Virus. J. Neuroinflammation 2014, 11, 80. [Google Scholar] [CrossRef] [Green Version]
  160. Kumar, M.; Roe, K.; Nerurkar, P.V.; Namekar, M.; Orillo, B.; Verma, S.; Nerurkar, V.R. Impaired Virus Clearance, Compromised Immune Response and Increased Mortality in Type 2 Diabetic Mice Infected with West Nile Virus. PLoS ONE 2012, 7, e44682. [Google Scholar] [CrossRef]
  161. Lee, I.-K.; Hsieh, C.-J.; Lee, C.-T.; Liu, J.-W. Diabetic Patients Suffering Dengue Are at Risk for Development of Dengue Shock Syndrome/Severe Dengue: Emphasizing the Impacts of Co-Existing Comorbidity(Ies) and Glycemic Control on Dengue Severity. J. Microbiol. Immunol. Infect. Wei Mian Yu Gan Ran Za Zhi 2020, 53, 69–78. [Google Scholar] [CrossRef]
  162. Vogels, C.B.F.; Rückert, C.; Cavany, S.M.; Perkins, T.A.; Ebel, G.D.; Grubaugh, N.D. Arbovirus Coinfection and Co-Transmission: A Neglected Public Health Concern? PLoS Biol. 2019, 17, e3000130. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  163. Chaves, B.A.; Orfano, A.S.; Nogueira, P.M.; Rodrigues, N.B.; Campolina, T.B.; Nacif-Pimenta, R.; Pires, A.C.A.M.; Júnior, A.B.V.; da Costa Paz, A.; da Costa Vaz, E.B.; et al. Coinfection with Zika Virus (ZIKV) and Dengue Virus Results in Preferential ZIKV Transmission by Vector Bite to Vertebrate Host. J. Infect. Dis. 2018, 218, 563–571. [Google Scholar] [CrossRef] [Green Version]
  164. Dodson, B.L.; Hughes, G.L.; Paul, O.; Matacchiero, A.C.; Kramer, L.D.; Rasgon, J.L. Wolbachia Enhances West Nile Virus (WNV) Infection in the Mosquito Culex Tarsalis. PLoS Negl. Trop. Dis. 2014, 8, e2965. [Google Scholar] [CrossRef] [PubMed]
Viruses 13 00748 g001 550
Figure 1. Innate immune signaling in insect and mosquito systems. The innate immune system is heavily conserved across species and involves various signaling pathways induced in response to viral nucleic acids (RNAi) or detection of upstream antiviral effectors (JAK/STAT, Toll, IMD). (A) The RNA interference (RNAi) pathway functions to detect cytosolic dsRNA or DNA that is indicative of viral infection. (B) The JAK/STAT pathway, which is conserved between mosquito and human species, induces transcription of downstream antiviral effector genes. (C) The Toll pathway functions to respond to Gram-positive bacterial and fungal infection and is present in the form of TLR in mammals. (D) The IMD pathway is activated during Gram-negative bacterial infection and is similar to the TNF/NF-kB pathway. Adapted from “Blank Pathway (Linear)”, by BioRender.com (2021). Retrieved from https://app.biorender.com/biorender-templates [42].
Figure 1. Innate immune signaling in insect and mosquito systems. The innate immune system is heavily conserved across species and involves various signaling pathways induced in response to viral nucleic acids (RNAi) or detection of upstream antiviral effectors (JAK/STAT, Toll, IMD). (A) The RNA interference (RNAi) pathway functions to detect cytosolic dsRNA or DNA that is indicative of viral infection. (B) The JAK/STAT pathway, which is conserved between mosquito and human species, induces transcription of downstream antiviral effector genes. (C) The Toll pathway functions to respond to Gram-positive bacterial and fungal infection and is present in the form of TLR in mammals. (D) The IMD pathway is activated during Gram-negative bacterial infection and is similar to the TNF/NF-kB pathway. Adapted from “Blank Pathway (Linear)”, by BioRender.com (2021). Retrieved from https://app.biorender.com/biorender-templates [42].
Viruses 13 00748 g001
Viruses 13 00748 g002 550
Figure 2. Innate and adaptive immune signaling in the human system. Humans defend against viral infections using physical barriers, innate immune signaling, and adaptive immune signaling responses. (A) Innate immune responses occur at physical barriers and involve the secretion of pro-inflammatory cytokines and chemokines by resident immune cells such as macrophages, neutrophils, and dendritic cells [126,127,128,129,131,132,133]. Components of the innate immune system are well conserved in both mosquitoes and humans. (B) The adaptive immune response primarily involves the generation of specialized and specific antibody-producing B cells, NK cells, and CD8+ T cells [134,135,136,137,138,139,140]. The adaptive immune response is a more evolved form of immunity that is unique to vertebrate organisms. Created with BioRender.com [42].
Figure 2. Innate and adaptive immune signaling in the human system. Humans defend against viral infections using physical barriers, innate immune signaling, and adaptive immune signaling responses. (A) Innate immune responses occur at physical barriers and involve the secretion of pro-inflammatory cytokines and chemokines by resident immune cells such as macrophages, neutrophils, and dendritic cells [126,127,128,129,131,132,133]. Components of the innate immune system are well conserved in both mosquitoes and humans. (B) The adaptive immune response primarily involves the generation of specialized and specific antibody-producing B cells, NK cells, and CD8+ T cells [134,135,136,137,138,139,140]. The adaptive immune response is a more evolved form of immunity that is unique to vertebrate organisms. Created with BioRender.com [42].
Viruses 13 00748 g002
Table
Table 1. Host factors involved in responses to mosquito-borne viruses.
Table 1. Host factors involved in responses to mosquito-borne viruses.
RNA InterferenceJAK/STATTollIMD/TNFPhysical BarriersAdaptive Immunity
MosquitoesDicer-2
AGO2
Drosha
R2D2
p400
piwi4
Ppo8		Hop
STAT1
Vago
vir-1		Toll
dMyD88
Dorsal
DIF
Cactus
Spätzle		Relish
Caspar
Fadd
Dredd		Hemocytes
Midgut epithelium		N/A
HumansDicer
AGO
Drosha
TARBP2
Piwi		JAK
STAT1/2
RIG-I
MDA5
IFN-α/β		TLRs
MyD88
NF-kB
IFN-α/β 888IRF7		NF-kB
FAF1
Caspase8/10		Blood–brain barrier
Epidermis
Dermis		B cells
T cells
Italicized factors are unique to the specified host or no ortholog exists in the other host.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Trammell, C.E.; Goodman, A.G. Host Factors That Control Mosquito-Borne Viral Infections in Humans and Their Vector. Viruses 2021, 13, 748. https://0-doi-org.brum.beds.ac.uk/10.3390/v13050748

AMA Style

Trammell CE, Goodman AG. Host Factors That Control Mosquito-Borne Viral Infections in Humans and Their Vector. Viruses. 2021; 13(5):748. https://0-doi-org.brum.beds.ac.uk/10.3390/v13050748

Chicago/Turabian Style

Trammell, Chasity E., and Alan G. Goodman. 2021. "Host Factors That Control Mosquito-Borne Viral Infections in Humans and Their Vector" Viruses 13, no. 5: 748. https://0-doi-org.brum.beds.ac.uk/10.3390/v13050748

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop