Next Article in Journal
Role of CARD Region of MDA5 Gene in Canine Influenza Virus Infection
Next Article in Special Issue
Nipah Virus: Past Outbreaks and Future Containment
Previous Article in Journal
Barriers to Hepatitis B Screening and Prevention for African Immigrant Populations in the United States: A Qualitative Study
Previous Article in Special Issue
Antivirals Against Chikungunya Virus: Is the Solution in Nature?
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Editorial

Special Issue “Emerging Viruses: Surveillance, Prevention, Evolution, and Control”

by
Jônatas Santos Abrahão
1,* and
Luciana Barros de Arruda
2,*
1
Laboratório de Vírus, Instituto de Ciências Biológicas, Departamento de Microbiologia, Universidade Federal de Minas Gerais, Belo Horizonte 31270-901, MG, Brazil
2
Departamento de Virologia, Instituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-902, RJ, Brazil
*
Authors to whom correspondence should be addressed.
Submission received: 9 March 2020 / Accepted: 9 March 2020 / Published: 11 March 2020
(This article belongs to the Special Issue Emerging Viruses: Surveillance, Prevention, Evolution and Control)
Emerging viruses represent a major concern for public health offices. Climate changes, the international migration of people and products, deforestation, and other anthropogenic activities (and their consequences) have been historically and continuously related to the emerging and re-emerging of new viruses, triggering an increasing number of notified outbreaks, epidemics, and pandemics. In this very popular Special Issue (Emerging Viruses: Surveillance, Prevention, Evolution, and Control), we are proud to have received a total of 70 manuscript submissions, with an acceptance rate 54.29% (38 papers) from colleagues from different parts of the world, working on a wide range of topics.
The deadline for this Special Issue concurred with the emergence of a new human pathogen, the coronavirus SARS-CoV-2, which is spreading in dozens of countries around the world, reinforcing the impact of emerging viruses in public health and the global economy. Interestingly, a considerable number of articles discussing diversity, transmission, and pathogenesis of human and animal infection by respiratory viruses, including coronaviruses, draws the attention of those who follow this issue. Coronaviruses, in particular, are addressed in three papers. Kandeil et al. [1] demonstrate a high seroprevalence of MERS coronavirus in adult dromedary camels from Asia and Africa, and Alsaadi et al. [2] characterize a fusion peptide in the spike protein of MERS-CoV. Avian coronaviruses are also addressed in the article from Fan et al. [3], which reveals the changes in genetic diversity, dominant genotypes, and selection pressure on the bronchitis virus (IBV) circulating in yellow chickens in China.
A few papers access genetic and pathogenic features of avian influenza viruses, which have caused important outbreaks of different bird species and serious losses to the poultry industry, besides being associated to sporadic human infections. Yeo et al. [4] present the characterization of a novel avian influenza A (H2N9) from a wild duck in Korea. Song et al. [5] isolate H5N6 isolates from waterfowls in China, which appear to be multi-reassortant among different genotypes of avian influenza viruses. They demonstrate relevant host–virus features in chickens and mice, including systemic replication and contact transmission between chickens, and upregulation of PRR in different organs in chicken and mice. Mei et al. [6] also reveal that goose-origin H5N6 avian influenza viruses have different pathogenicity and transmissibility in chickens. Yu et al. [7] present a comparative analysis between highly and low pathogenic H7N9 AIV strains. They show that both virus isolates were shed through respiratory and digestive routes in inoculated chickens and could be transmitted to naïve animals; however, the emerging H7N9 highly-pathogenic avian influenza presents a stronger pathogenicity and transmissibility. Sun et al. [8] present data on the H9N2 avian influenza viruses currently circulating in South China and Song et al. [9] compare biological and genetic features of three H9N2 avian influenza in chicken and mice models, showing that different isolates may have distinct replication and transmissibility efficiencies.
H1N1 swine influenza features are also addressed in this issue. Song et al. [10] compare phylogenetic and pathogenic features of two swine influenza H1N1 viruses isolated from Shandong. By phylodynamics analyses, Adam et al. [11] suggest an increased selection of influenza H1N1/pdm09 clade 6b residues and other high mortality mutants in India.
Arboviruses represent a hot-topic as well. Maia et al. [12] present the discovery of novel viruses in mosquitoes from Brazilian wetlands, including viruses from nine different families: Iflaviridae, Phenuiviridae, Rhabdoviridae, Flaviviridae, Reoviridae, Chuviridae, Circoviridae, Partitiviridae, and Totiviridae. The natural coinfection of Aedes aegypti by chikungunya and dengue type 2 virus in Brazil is also reported by Aragão et al. [13] The influence of the environment on chikungunya virus transmission in Senegal is revealed by Sow et al. [14]. Barbosa Costa et al. [15] describe a possible silent circulation of the Saint Louis encephalitis virus among humans and equids in Brazil. Rezende et al. [16] present an interesting case of late-relapsing hepatitis after acute yellow fever virus infection. Arbovirus diagnosis, in particular Zika virus diagnosis, is also discussed. Pérez-Olmeda [17] evaluates the performance characteristics of the LIAISON XL Zika Capture IgM II. Versiane et al. [18] describe the identification of B-cell epitopes with potential use to discriminate dengue from zika infections in serological assays.
We received several papers on veterinary viruses. Yu et al. [19] present data on the prevalence and co-infection of fowl adenovirus. Meng et al. [20] identify and characterize a novel fowl adenovirus and perform an immunoprotective evaluation of an inactivated FAdV-4 vaccine. The emergence of avian orthoavulavirus 13 in wild migratory waterfowl in China and related genetic features are presented by Fei et al. [21]. Lu et al. [22] report a novel subtype of bovine hepacivirus in China. Águeda-Pinto et al. [23] present a genetic characterization of a recombinant myxoma virus in the Lepus granatensis. Data on the immunogenicity in rabbits of virus-like particles from a rabbit haemorrhagic disease virus is presented by Miao et al. [24]. Malossi et al. [25] sequence and analyze the genome of different equine infectious anemia viruses, revealing that Brazilian strains share a monophyletic cluster. Sozzi et al. [26] describe the isolation and genome sequencing of a pestivirus from aborted lamb fetuses in Italy. Chen et al. [27] evaluate the genetic diversity of porcine circovirus 3 in China. Morandini et al. [28] report a novel adélie penguin circovirus from Antarctica. Chen et al. [29] present insights on the phylogeny and virulence of porcine reproductive and respiratory syndrome virus variants.
Other relevant research papers are also published. Garry and Garry [30] present in depth proteomics computational analyses on the antennavirus glycoprotein complex. Ribeiro et al. [31] present data on a nymphalid-infecting group I alphabaculovirus. Spitz et al. [32] present relevant data on the first complete genome sequence of hepatitis C virus subtype 2b from Latin America. Silva et al. [33] demonstrate that a given TREX1 polymorphism is associated with higher proviral load, lower inflammatory cytokine levels, and is more frequent in HAM/TSP symptomatic patients infected with HTLV-1. Moutelíková et al. [34] show the emergence of rare bovine–human reassortant DS-1-Like rotavirus A strains in human patients in the Czech Republic. Duarte et al. [35] present the virome of different wild birds and mammals from Brazilian cerrado, showing sequences of members of Adenoviridae, Anelloviridae, Circoviridae, Caliciviridae, and Parvoviridae families, complete or nearly complete genomes of known anelloviruses, circoviruses, and parvoviruses, as well as putative novel species.
At last, we also received reviews on emerging viruses. Martins et al. [36] discuss the existence of antivirals against the chikungunya virus in nature. Wubshet et al. [37] review data on the foot and mouth disease virus in Ethiopia from 2008 to 2018. Judson et al. [38] examine nosocomial transmission of emerging viruses via aerosol-generating medical procedures.
Although this Special Issue was prepared by Viruses in collaboration with the Brazilian Society for Virology, we are very grateful for having received submissions from several countries and hundreds of colleagues. We believe that the success of this Special Issue is the consequence of the great job done by Viruses staff and all authors that decided to submit their research here. On behalf of the Brazilian Society of Virology, thank you!

Acknowledgments

We thank Brazilian Society for Virology board of directors and associated members for all the support during organization and divulgation of this special issue.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Kandeil:, A.; Gomaa, M.; Nageh, A.; Shehata, M.M.; Kayed, A.E.; Sabir, J.S.M.; Abiadh, A.; Jrijer, J.; Amr, Z.; Abi Said, M.; et al. Middle east respiratory syndrome coronavirus (MERS-CoV) in dromedary camels in Africa and Middle East. Viruses 2019, 11, 717. [Google Scholar] [CrossRef] [Green Version]
  2. Alsaadi, E.A.J.; Neuman, B.W.; Jones, I.M. A fusion peptide in the spike protein of mers coronavirus. Viruses 2019, 11, 825. [Google Scholar] [CrossRef] [Green Version]
  3. Fan, W.; Tang, N.; Dong, Z.; Chen, J.; Zhang, W.; Zhao, C.; He, Y.; Li, M.; Wu, C.; Wei, T.; et al. Genetic analysis of avian coronavirus infectious bronchitis virus in yellow chickens in southern china over the past decade: Revealing the changes of genetic diversity, dominant genotypes, and selection pressure. Viruses 2019, 11, 898. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Yeo, S.-J.; Than, D.-D.; Park, H.-S.; Sung, H.W.; Park, H. Molecular characterization of a novel avian influenza a (H2N9) strain isolated from wild duck in Korea in 2018. Viruses 2019, 11, 1046. [Google Scholar] [CrossRef] [Green Version]
  5. Song, Y.; Li, W.; Wu, W.; Liu, Z.; He, Z.; Chen, Z.; Zhao, B.; Wu, S.; Yang, C.; Qu, X.; et al. Phylogeny, pathogenicity, transmission, and host immune responses of four H5N6 avian influenza viruses in chickens and mice. Viruses 2019, 11, 1048. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Mei, K.; Guo, Y.; Zhu, X.; Qu, N.; Huang, J.; Chen, Z.; Zhang, Y.; Zhao, B.; He, Z.; Liao, M.; et al. Different pathogenicity and transmissibility of goose-origin H5N6 avian influenza viruses in chickens. Viruses 2019, 11, 612. [Google Scholar] [CrossRef] [Green Version]
  7. Yu, H.; Zhang, K.; Ye, X.; Wang, W.; Wu, W.; Wang, X.; Guan, Y.; He, Z.; Wang, Y.; Jiao, P. Comparative pathogenicity and transmissibility of the H7N9 highly pathogenic avian influenza virus and the H7N9 low pathogenic avian influenza virus in chickens. Viruses 2019, 11, 1047. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Sun, H.; Lin, J.; Liu, Z.; Yu, Y.; Wu, M.; Li, S.; Liu, Y.; Feng, Y.; Wu, Y.; Li, M.; et al. Genetic, molecular, and pathogenic characterization of the H9N2 avian influenza viruses currently circulating in South China. Viruses 2019, 11, 1040. [Google Scholar] [CrossRef] [Green Version]
  9. Song, Y.; Zhang, Y.; Chen, L.; Zhang, B.; Zhang, M.; Wang, J.; Jiang, Y.; Yang, C.; Jiang, T. Genetic characteristics and pathogenicity analysis in chickens and mice of three H9N2 avian influenza viruses. Viruses 2019, 11, 1127. [Google Scholar] [CrossRef] [Green Version]
  10. Song, Y.; Zhang, Y.; Zhang, B.; Chen, L.; Zhang, M.; Wang, J.; Jiang, Y.; Yang, C.; Jiang, T. Identification, genetic analysis, and pathogenicity of classical swine H1N1 and human-swine reassortant H1N1 influenza viruses from pigs in China. Viruses 2020, 12, 55. [Google Scholar] [CrossRef] [Green Version]
  11. Adam, D.C.; Scotch, M.; MacIntyre, C.R. Phylodynamics of influenza a/H1N1pdm09 in India reveals circulation patterns and increased selection for Clade 6b residues and other high mortality mutants. Viruses 2019, 11, 791. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Maia, L.M.S.; Pinto, A.Z.d.L.; Carvalho, M.S.d.; Melo, F.L.d.; Ribeiro, B.M.; Slhessarenko, R.D. Novel viruses in mosquitoes from Brazilian Pantanal. Viruses 2019, 11, 957. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Aragão, C.F.; Pinheiro, V.C.S.; Nunes Neto, J.P.; Silva, E.V.P.D.; Pereira, G.J.G.; Nascimento, B.L.S.d.; Castro, K.d.S.; Maia, A.M.; Catete, C.P.; Martins, L.C.; et al. Natural infection of Aedes aegypti by Chikungunya and Dengue type 2 virus in a transition area of North-Northeast Brazil. Viruses 2019, 11, 1126. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Sow, A.; Nikolay, B.; Faye, O.; Cauchemez, S.; Cano, J.; Diallo, M.; Faye, O.; Sadio, B.; Ndiaye, O.; Weaver, S.C.; et al. Changes in the transmission dynamic of Chikungunya virus in Southeastern Senegal. Viruses 2020, 12, 196. [Google Scholar] [CrossRef] [Green Version]
  15. Barbosa Costa, G.; Marinho, P.E.S.; Vilela, A.P.P.; Saraiva-Silva, A.T.; Crispim, A.P.C.; Borges, I.A.; Dutra, A.G.S.; Lobato, Z.I.P.; dos Reis, J.K.P.; de Oliveira, D.B.; et al. Silent circulation of the Saint Louis encephalitis virus among humans and equids, Southeast Brazil. Viruses 2019, 11, 1029. [Google Scholar] [CrossRef] [Green Version]
  16. Rezende, I.M.; Pereira, L.S.; Fradico, J.R.B.; Pascoal Xavier, M.A.; Alves, P.A.; Campi-Azevedo, A.C.; Speziali, E.; dos Santos, L.Z.M.; Albuquerque, N.S.; Penido, I.; et al. Late-relapsing hepatitis after yellow fever. Viruses 2020, 12, 222. [Google Scholar] [CrossRef] [Green Version]
  17. Pérez-Olmeda, M.; Sánchez-Seco, M.P.; Vázquez, A.; Balfagón, P.; de la Fuente, J.; Murillo, M.Á.; Minguito, T.; de Ory, F. Evaluation of the liaison XL Zika capture IgM II for the diagnosis of Zika virus infections. Viruses 2020, 12, 69. [Google Scholar] [CrossRef] [Green Version]
  18. Versiani, A.F.; Rocha, R.P.; Mendes, T.A.O.; Pereira, G.C.; Coelho dos Reis, J.G.A.; Bartholomeu, D.C.; da Fonseca, F.G. Identification of B-cell epitopes with potential to serologicaly discrimnate Dengue from Zika infections. Viruses 2019, 11, 1079. [Google Scholar] [CrossRef] [Green Version]
  19. Yu, G.; Lin, Y.; Dou, Y.; Tang, Y.; Diao, Y. Prevalence of fowl adenovirus serotype 4 and co-infection by immunosuppressive viruses in fowl with hydropericardium hepatitis syndrome in Shandong province, China. Viruses 2019, 11, 517. [Google Scholar] [CrossRef] [Green Version]
  20. Meng, K.; Yuan, X.; Yu, J.; Zhang, Y.; Ai, W.; Wang, Y. Identification, pathogenicity of novel fowl adenovirus serotype 4 SDJN0105 in shandong, china and immunoprotective evaluation of the newly developed inactivated oil-emulsion FAdV-4 vaccine. Viruses 2019, 11, 627. [Google Scholar] [CrossRef] [Green Version]
  21. Fei, Y.; Liu, X.; Mu, J.; Li, J.; Yu, X.; Chang, J.; Bi, Y.; Stoeger, T.; Wajid, A.; Muzyka, D.; et al. The emergence of avian orthoavulavirus 13 in wild migratory waterfowl in China revealed the existence of diversified trailer region sequences and HN gene lengths within this serotype. Viruses 2019, 11, 646. [Google Scholar] [CrossRef] [Green Version]
  22. Lu, G.; Ou, J.; Zhao, J.; Li, S. Presence of a novel subtype of bovine hepacivirus in china and expanded classification of bovine hepacivirus strains worldwide into 7 subtypes. Viruses 2019, 11, 843. [Google Scholar] [CrossRef] [Green Version]
  23. Águeda-Pinto, A.; Lemos de Matos, A.; Abrantes, M.; Kraberger, S.; Risalde, M.A.; Gortázar, C.; McFadden, G.; Varsani, A.; Esteves, P.J. Genetic characterization of a recombinant myxoma virus in the Iberian hare (Lepus granatensis). Viruses 2019, 11, 530. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Miao, Q.; Qi, R.; Veldkamp, L.; Ijzer, J.; Kik, M.L.; Zhu, J.; Tang, A.; Dong, D.; Shi, Y.; van Oers, M.M.; et al. Immunogenicity in rabbits of virus-like particles from a contemporary rabbit haemorrhagic disease virus type 2 (gi.2/rhdv2/b) isolated in the Netherlands. Viruses 2019, 11, 553. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Malossi, C.D.; Fioratti, E.G.; Cardoso, J.F.; Magro, A.J.; Kroon, E.G.; Aguiar, D.M.d.; Borges, A.M.C.M.; Nogueira, M.F.; Ullmann, L.S.; Araujo, J.P. High genomic variability in equine infectious anemia virus obtained from naturally infected horses in pantanal, Brazil: An endemic region case. Viruses 2020, 12, 207. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Sozzi, E.; Lavazza, A.; Gaffuri, A.; Bencetti, F.C.; Prosperi, A.; Lelli, D.; Chiapponi, C.; Moreno, A. Isolation and full-length sequence analysis of a pestivirus from aborted Lamb fetuses in Italy. Viruses 2019, 11, 744. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Chen, Y.; Xu, Q.; Chen, H.; Luo, X.; Wu, Q.; Tan, C.; Pan, Q.; Chen, J.-L. Evolution and genetic diversity of porcine circovirus 3 in china. Viruses 2019, 11, 786. [Google Scholar] [CrossRef] [Green Version]
  28. Morandini, V.; Dugger, K.M.; Ballard, G.; Elrod, M.; Schmidt, A.; Ruoppolo, V.; Lescroël, A.; Jongsomjit, D.; Massaro, M.; Pennycook, J.; et al. Identification of a novel Adélie Penguin circovirus at Cape Crozier (Ross Island, Antarctica). Viruses 2019, 11, 1088. [Google Scholar] [CrossRef] [Green Version]
  29. Chen, N.; Ye, M.; Huang, Y.; Li, S.; Xiao, Y.; Li, X.; Li, S.; Li, X.; Yu, X.; Tian, K.; et al. Identification of two porcine reproductive and respiratory syndrome virus variants sharing high genomic homology but with distinct virulence. Viruses 2019, 11, 875. [Google Scholar] [CrossRef] [Green Version]
  30. Garry, C.E.; Garry, R.F. Proteomics computational analyses suggest that the antennavirus glycoprotein complex includes a class I viral fusion protein (α-penetrene) with an internal Zinc-binding domain and a stable signal peptide. Viruses 2019, 11, 750. [Google Scholar] [CrossRef] [Green Version]
  31. Ribeiro, B.M.; dos Santos, E.R.; Trentin, L.B.; da Silva, L.A.; de Melo, F.L.; Kitajima, E.W.; Ardisson-Araújo, D.M.P. A nymphalid-infecting group I alphabaculovirus isolated from the major passion fruit caterpillar pest dione juno juno (lepidoptera: Nymphalidae). Viruses 2019, 11, 602. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  32. Spitz, N.; Barros, J.J.; do Ó, K.M.; Brandão-Mello, C.E.; Araujo, N.M. The first complete genome sequences of hepatitis C virus subtype 2B from latin america: Molecular characterization and phylogeographic analysis. Viruses 2019, 11, 1000. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Silva, D.d.C.; Amoras, E.d.S.G.; Moura, T.C.F.; Lopes, F.T.; Gomes, S.T.M.; Costa, C.A.d.; Sousa, M.S.; Ishak, R.; Vallinoto, A.C.R.; Queiroz, M.A.F. Trex1 531c polymorphism is associated with high proviral load levels in HTLV-1-infected persons. Viruses 2019, 12, 7. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Moutelíková, R.; Sauer, P.; Dvořáková Heroldová, M.; Holá, V.; Prodělalová, J. Emergence of rare bovine–human reassortant DS-1-like rotavirus a strains with g8p genotype in human patients in the Czech Republic. Viruses 2019, 11, 1015. [Google Scholar] [CrossRef] [Green Version]
  35. Duarte, M.A.; Silva, J.M.F.; Brito, C.R.; Teixeira, D.S.; Melo, F.L.; Ribeiro, B.M.; Nagata, T.; Campos, F.S. Faecal virome analysis of wild animals from Brazil. Viruses 2019, 11, 803. [Google Scholar]
  36. Oliveira Silva Martins, D.; de Andrade Santos, I.; Moraes de Oliveira, D.; Riquena Grosche, V.; Carolina Gomes Jardim, A. Antivirals against Chikungunya virus: Is the solution in nature? Viruses 2020, 12, 272. [Google Scholar] [CrossRef] [Green Version]
  37. Wubshet, A.K.; Dai, J.; Li, Q.; Zhang, J. Review on outbreak dynamics, the endemic serotypes, and diversified topotypic profiles of foot and mouth disease virus isolates in Ethiopia from 2008 to 2018. Viruses 2019, 11, 1076. [Google Scholar] [CrossRef] [Green Version]
  38. Judson, S.D.; Munster, V.J. Nosocomial transmission of emerging viruses via aerosol-generating medical procedures. Viruses 2019, 11, 940. [Google Scholar] [CrossRef] [Green Version]

Share and Cite

MDPI and ACS Style

Abrahão, J.S.; de Arruda, L.B. Special Issue “Emerging Viruses: Surveillance, Prevention, Evolution, and Control”. Viruses 2020, 12, 306. https://0-doi-org.brum.beds.ac.uk/10.3390/v12030306

AMA Style

Abrahão JS, de Arruda LB. Special Issue “Emerging Viruses: Surveillance, Prevention, Evolution, and Control”. Viruses. 2020; 12(3):306. https://0-doi-org.brum.beds.ac.uk/10.3390/v12030306

Chicago/Turabian Style

Abrahão, Jônatas Santos, and Luciana Barros de Arruda. 2020. "Special Issue “Emerging Viruses: Surveillance, Prevention, Evolution, and Control”" Viruses 12, no. 3: 306. https://0-doi-org.brum.beds.ac.uk/10.3390/v12030306

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