Next Article in Journal
Regulation of Morphology, Aflatoxin Production, and Virulence of Aspergillus flavus by the Major Nitrogen Regulatory Gene areA
Previous Article in Journal
Knowledge, Attitude and Practice of Malawian Farmers on Pre- and Post-Harvest Crop Management to Mitigate Aflatoxin Contamination in Groundnut, Maize and Sorghum—Implication for Behavioral Change
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Toxins
Volume 11
Issue 12
10.3390/toxins11120717
toxins-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:
Article

PirABVP Toxin Binds to Epithelial Cells of the Digestive Tract and Produce Pathognomonic AHPND Lesions in Germ-Free Brine Shrimp

by
Vikash Kumar
1,2,*,
Lobke De Bels
3,
Liesbeth Couck
3,
Kartik Baruah
4,
Peter Bossier
1,† and
Wim Van den Broeck
3,†
1
Lab of Aquaculture & Artemia Reference Center, Department of Animal Sciences and Aquatic Ecology, Faculty of Bioscience Engineering, Ghent University, 9000 Ghent, Belgium
2
ICAR-Central Inland Fisheries Research Institute (CIFRI), Barrackpore 700120, India
3
Department of Morphology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium
4
Department of Animal Nutrition and Management, Faculty of Veterinary Medicine and Animal Sciences, Swedish University of Agricultural Sciences, 75007 Uppsala, Sweden
*
Author to whom correspondence should be addressed.
†
Shared senior authorship.
Toxins 2019, 11(12), 717; https://0-doi-org.brum.beds.ac.uk/10.3390/toxins11120717
Submission received: 18 November 2019 / Revised: 28 November 2019 / Accepted: 6 December 2019 / Published: 9 December 2019
(This article belongs to the Section Bacterial Toxins)
Browse Figures
Review Reports Versions Notes

Abstract

:
Acute hepatopancreatic necrosis disease (AHPND), a newly emergent farmed penaeid shrimp bacterial disease originally known as early mortality syndrome (EMS), is causing havoc in the shrimp industry. The causative agent of AHPND was found to be a specific strain of bacteria, e.g., Vibrio and Shewanella sps., that contains pVA1 plasmid (63–70 kb) encoding the binary PirAVP and PirBVP toxins. The PirABVP and toxins are the primary virulence factors of AHPND-causing bacteria that mediates AHPND and mortality in shrimp. Hence, in this study using a germ-free brine shrimp model system, we evaluated the PirABVP toxin-mediated infection process at cellular level, including toxin attachment and subsequent toxin-induced damage to the digestive tract. The results showed that, PirABVP toxin binds to epithelial cells of the digestive tract of brine shrimp larvae and produces characteristic symptoms of AHPND. In the PirABVP-challenged brine shrimp larvae, shedding or sloughing of enterocytes in the midgut and hindgut regions was regularly visualized, and the intestinal lumen was filled with moderately electron-dense cells of variable shapes and sizes. In addition, the observed cellular debris in the intestinal lumen of the digestive tract was found to be of epithelial cell origin. The detailed morphology of the digestive tract demonstrates further that the PirABVP toxin challenge produces focal to extensive necrosis and damages epithelial cells in the midgut and hindgut regions, resulting in pyknosis, cell vacuolisation, and mitochondrial and rough endoplasmic reticulum (RER) damage to different degrees. Taken together, our study provides substantial evidence that PirABVP toxins bind to the digestive tract of brine shrimp larvae and seem to be responsible for generating characteristic AHPND lesions and damaging enterocytes in the midgut and hindgut regions.
Keywords:
PirABVP toxins; brine shrimp; digestive tract; sloughing; epithelial cells; necrosis
Key Contribution: The finding is the first of its kind, possibly pointing towards a new insight on the infection process of AHPND-causing PirABVP toxins. The PirABVP toxins binds with midgut and hindgut epithelial cells and induces a characteristic AHPND lesion, which leads to subsequent death of challenged brine shrimp larvae.

1. Introduction

The outbreak of acute hepatopancreatic necrosis disease (AHPND) caused by Vibrio spp. has been particularly devastating in the cultivation of shrimp in a number of countries [1,2,3,4,5]. The shrimp production in AHPND-affected regions has at times dropped considerably (to ~60%) and disease has caused an estimated US $43 billion loss across Asia (China, Malaysia, Thailand, Vietnam) and in Mexico in last 10 years [3,6,7]. The Vibrio spp. becomes virulent by acquiring a 63–70 kb plasmid (pVA1) encoding the binary PirABVP toxins, which consist of two subunits PirAVP and PirBVP, and is homologous to the Photorhabdus luminescens insect-related (Pir) toxins PirA/PirB [8,9]. The PirABVP toxins are the primary virulence factor of AHPND-causing bacteria that mediates AHPND and mortality in shrimp [10]. The binary PirABVP toxins mainly target the hepatopancreas (digestive gland) of shrimp and damage the R (resorptive), B (blister), F (fibrillar), and E (embryonic) cells, resulting in dysfunction and massive mortalities (up to 100%) within 20–30 days of shrimp post-larvae stocking [2,5,11]. Since the impact of these binary toxins are significant in shrimp aquaculture, more research attention is needed to unravel the toxin-mediated infection process at cellular level.
Among the binary PirABVP toxins, PirAVP facilitates target-specific recognition of toxins by binding to certain ligands on the cell membrane and receptors (e.g., monosaccharides like N-acetylgalactosamine (GalNAC) and oligosaccharides), while the PirBVP toxin (containing N-terminal domain, PirBN and C-terminal domain, PirBC), is mainly responsible for cell death via pore formation, and is involved in protein–protein and protein–ligand interactions [3,12,13]. Moreover, together PirAVP and PirBVP toxins form a complex and act synergistically, resulting in increased toxicity of PirABVP toxins on the experimental animals [9,13].
In this study, using a highly controlled gnotobiotic brine shrimp model system, we aimed to investigate the morphological changes in the guts of germ-free brine shrimp larvae during PirABVP toxin challenge. Furthermore, we also unraveled that PirABVP toxins bind to epithelial cells of the digestive tract, induce necrosis, and damage the cellular structure, including the nucleus, mitochondria, junctional complex, rough endoplasmic reticulum (RER), etc., which leads to the subsequent death of challenged brine shrimp larvae. The knowledge gained from this study will facilitate future research which aims at the comparison of the digestive tract morphology after the introduction of anti-AHPND therapy in the culture system.

2. Results

2.1. PirAB Toxin Binds the Digestive Tract and Induces Sloughing of Epithelial Cells in Brine Shrimp (Artemia franciscana) Larvae

Immunohistochemistry using Mab (monoclonal antibody) specific to His6-tagged PirABVP toxins, showed strong immunoreactivity in the epithelium of digestive tract from PirABVP-challenged brine shrimp larvae. The PirABVP immunoreactivity was seen from 12 h post-challenge in close contact with the brush border of the enterocytes (Figure 1C–L). In the intestinal lumen, moderately electron-dense cells of variable shapes and size were observed 12 h post-challenge. Shedding or sloughing of enterocytes in the midgut and hindgut regions was regularly visualized from 12 h post challenge onwards until the end of the experiment (60 h post-challenge) (Figure 1C–L). After 60 h post-challenge, the epithelium was severely damaged in the challenged brine shrimp larvae (Figure 1K,L). Additionally, the remaining cellular components, such as the pyknotic nuclei and lysed cellular membrane, were further detached into the lumen and showed signs of degeneration. Moreover, the digestive tract epithelial cells in the control larvae had a normal appearance with the presence of the nucleus, brush border, and prominent gut lumen (Figure 1A,B). In addition, the Mab specific to the His6-tagged PirABVP toxins bound only to PirABVP toxins and did not show any cross-reactivity to other endogenous cellular histidine.

2.2. PirAB Toxin Induced Accumulation of Cellular Debris in the Digestive Tract Is of Epithelial Cell Origin

To further confirm that PirABVP-induced accumulation of cellular debris in the digestive tracts of brine shrimp contains cells of epithelial origin, cytokeratin-specific polyclonal antibody (Pab) was used to localize the epithelial cells in intestinal lumen. Since the sloughing of enterocytes was observed 12 h post-challenge onwards, 12 and 24 h post challenge brine shrimp larvae samples were used to visualize the changes. The PirABVP toxin-challenged brine shrimp larvae sections treated with anti-keratin antibody (cytokeratin Pab), which form the intermediate-sized filaments in the cytoplasm of epithelial cells [14], gave strong immunoreactive staining in the intestinal lumen, indicating positive signals for epithelial cells in the cellular debris. The cytokeratin Pab immunoreactive signals was observed in the midgut and hindgut of the digestive tract in brine shrimp larvae samples at 12 and 24 h post toxin challenge (Figure 2C–H). Moreover, in the control group larvae (no PirABVP toxin) at 12 and 24 h post experiment, the digestive tract appeared normal, with no accumulation of cellular debris (Figure 2A,B).

2.3. PirAB Toxin Binding Leads to Damage and Necrosis of the Digestive Tract in Brine Shrimp Larvae

Next, to confirm that PirABVP toxins are associated with damage on the digestive tracts of brine shrimp larvae, electron microscopical analysis was performed in the 48 h post-challenge brine shrimp larvae samples. TEM ultrastructural observations showed that digestive tract epithelium composing the enterocytes were damaged to different degrees, with focal to extensive necrosis, in PirABVP toxin-challenged brine shrimp larvae (Figure 3A–D). Furthermore, the analysis showed that epithelial enterocytes in the midgut and hindgut regions were damaged showing nuclear pyknosis, cell vacuolisation, and mitochondrial and rough endoplasmic reticulum (RER) damage to different degrees (Figure 3A–D). Notably, there were rod-shaped bacteria observed in the digestive tracts inside and outside the intestinal lumen of PirABVP toxin-challenged brine shrimp larvae. Since germ-free brine shrimp larvae were used for the analysis, these bacteria were identified as the autoclaved bacterial feed given during the challenge experiment. Apparently, the larvae were unable to digest them because of damage in the digestive tract. Moreover, in the control brine shrimp larvae group, the morphology of the digestive tract epithelial enterocytes appeared normal, with an intact mitochondrion, nucleus, rough endoplasmic reticulum (RER), and intercellular junctions (Figure 4A–F). The data indicated that damage of the digestive tract and accumulation of cellular debris in the intestinal lumen was due to the PirABVP toxin-challenge, which leads to subsequent death of challenged larvae as reported in our previous study [9].

3. Discussion

Acute hepatopancreatic necrosis disease (AHPND), earlier named as early mortality syndrome (EMS), has been particularly devastating in the cultivation of shrimp, causing massive mortality (up to 100%) within 20–30 days of post-larvae stocking [5,11,15]. Since the AHPND outbreak first appeared in China in 2009, it has spread to Vietnam (2010), Malaysia (2011), Thailand (2012), Mexico (2013), Philippines (2015), South America (2016), Australia (2016), Bangladesh (2019), and USA (2019) [7,8,16,17,18,19]. The causative agent of AHPND was found to be a specific strain of bacteria, including Vibrio parahaemolyticus, V. punensis, V. harveyi, V. owensii, V. campbelli, and Shewanella sp. that contains pVA1 plasmid (63–70 kb), encoding the binary PirAVP and PirBVP toxins [9,20,21,22,23]. Although, the PirABVP toxins were reported as the primary virulence factor of AHPND-causing bacteria that mediates AHPND and mortality in shrimps [9,13], the toxin-mediated infection process at the cellular level still remains unclear. To this end, brine shrimp (Artemia franciscana), an aquatic invertebrate crustacean and a model for crustacean shrimp [24,25,26] was used to develop an infection model for AHPND and investigate the morphological changes in the guts of germ-free brine shrimp larvae during the PirABVP toxin challenge. Subsequent studies were carried out to visualize the PirABVP toxin-binding and early pathogenesis in the digestive tracts of brine shrimp larvae, to evaluate the host–pathogen interaction.
The Photorhabdus insect-related (Pir) toxins were first identified in Photorhabdus luminescens, a bacterium that maintains a symbiotic relationship with entomopathogenic nematodes of the family Heterorhabditidae [27,28]. The PirAB toxins act as binary proteins; they are encoded by the PirA and PirB genes, and both proteins are necessary for oral toxicity in moths and mosquitoes [29,30]. The pathology of Pir oral toxicity in larvae of the moth Plutella xylostella is in the midgut epithelium, and its toxicity results in swelling and shedding of the (apical) epithelial cells [31]. In shrimp aquaculture, the virulent AHPND-causing bacteria containing pVA1 plasmid encodes PirABVP toxin genes, homologous to the insecticidal PirA/PirB toxins’ genes, were absent in all non-AHPND bacterial species [32]. Moreover, as shrimp and insects are both arthropods, the AHPND-affected shrimp have pathological responses similar to the PirAB midgut toxicity in insects [5]. In this study, using the germ-free brine shrimp model system, it was shown that PirABVP toxins bind to gut epithelial tissue, especially midgut and hindgut epithelium and produce pathognomonic AHPND lesions. The study further demonstrates that PirABVP toxins binding induce necrosis and damages the cellular structure of the digestive tract including nucleus, mitochondria, rough endoplasmic reticulum (RER), etc. in the challenged brine shrimp larvae.
It was reported previously that the PirAVP and PirBVP toxins both form a three-domain complex, and act synergistically to produce the characteristic symptoms of AHPND in the shrimp [3,33]. In addition, PirABVP toxins have been reported to induce AHPND, possibly via recognition and binding to certain ligands on the cell membrane and receptor, oligomerization, and pore formation on the cell membrane, that leads to cell death [13]. Our results indicate that PirABVP produce characteristic symptoms of AHPND in brine shrimp larvae. In the PirABVP-challenged brine shrimp larvae, shedding or sloughing of epithelial enterocytes in the midgut and hindgut regions was regularly visualized, and the intestinal lumen was filled with moderately electron-dense cells of variable shapes and sizes (Figure 1C–L). Additionally, as the infection proceeded, the epithelium was severely damaged in the challenged brine shrimp larvae at 60 h post-challenge, and the remaining cellular components were further detached into the lumen, and showed signs of degeneration, such as pyknotic nuclei and lysed cellular membranes (Figure 1K,L). Moreover, the previous studies have documented the specificity of PirABVP toxins attachment, in which PirABVP toxins were reported to bind with epithelial cells of hepatopancreas and induce AHPND in shrimp [3,34]. However, the present study showed that specificity of PirABVP toxins is not very high, and additionally that the attachment is not hepatopancreas-dependent. The PirABVP toxins mainly target epithelial cells of the digestive tract and bind with midgut and hindgut epithelium. To the authors’ knowledge, no ultrastructural findings have been published previously which illustrate this type of interaction, in which a toxin binds to the epithelial cells and induces a characteristic AHPND lesion in the digestive tract, which leads to subsequent death of challenged larvae, as reported in our previous study [9]. Thus, this finding is the first of its kind, possibly pointing towards a new insight on the infection process of AHPND-causing PirABVP toxins.
However, it is hard to generalize that the accumulation of electron-dense cells of variable shapes and sizes in the intestinal lumen of the challenged larvae were PirABVP-induced and of epithelial cell origin, since autoclaved bacterial feed given during the experiment can accumulate and form the cellular mass. Hence, we tried to localize the epithelial cells in intestinal lumen and target keratin groups of fibrous proteins, which form the structural framework of epithelial cells [19,35]. The results indicate that in the PirABVP-challenged brine shrimp larvae, the observed cellular debris in the intestinal lumen are of epithelial cell origin (Figure 2C–H). These observations further indicate that PirABVP toxins bind epithelial enterocytes in the midgut and hindgut and induce sloughing that leads to the production of cellular debris in the intestinal lumen.
Since it is evident that PirABVP toxins produce pathognomonic AHPND lesions and damage the digestive tract of brine shrimp larvae, we further studied the detailed morphology of the digestive tract in brine shrimp larvae [18,36]. The results demonstrate that the PirABVP toxin-challenge produces focal to extensive necrosis and damages epithelial enterocytes in the midgut and hindgut regions, resulting in nuclear pyknosis, cell vacuolisation, and mitochondrial and rough endoplasmic reticulum (RER) damage to different degrees (Figure 3A–D). In addition, autoclaved rod-shaped bacterial cells given as feed during the challenge assay were observed in the digestive tract, inside and outside the intestinal lumen of the PirABVP toxin-challenged brine shrimp larvae. As germ-free brine shrimp larvae were used for the analysis, the results indicate that PirABVP toxins affect the digestive process, and larvae were unable to digest the supplied food. Moreover, the bacterial cells were also observed outside the intestinal lumen, which showed that PirABVP toxins might activate a Cry-like pore-forming domain [13,33] and induce damage of the digestive tract, resulting in the movement of bacterial cells outside of the intestinal lumen (Figure 3A–D).

4. Conclusions

In summary, these data illustrate the PirABVP toxin-mediated infection process and pathogenesis in brine shrimp larvae. Our findings also imply that PirABVP toxins seem to be responsible for generating characteristics of AHPND lesions, and damage epithelial enterocytes in the midgut and hindgut regions of the digestive tract. This in vivo visualization is an easy model that might help to study therapies that aim at toxin production interference.

5. Materials and Methods

5.1. Preparation of Recombinant V. parahaemolyticus PirAVP and PirBVP

The PirAVP plasmid (pET21b PirAVP) and PirBVP plasmid (pET21b PirBVP), obtained from Taiwan, were transformed into E. coli Rosetta (DE3) competent cells and the expression of the recombinant, C-terminal His6-tagged PirAVP and PirBVP proteins, respectively, were induced by the addition of 0.25 µM of iso-propyl thiogalactoside (IPTG) [3]. After expression had proceeded at 16 °C for 16 h, the recombinant proteins were purified with the magneHis™ protein purification system (Promega Corporation, WI, USA). The purified recombinant PirAVP and PirBVP toxins were dialyzed in phosphate buffer solution (PBS) (Honeywell, Grauwmeer, Belgium) and concentrated with amicon® ultra-15 centrifugal filters (Merck Millipore, Overijse, Belgium).

5.2. Detection of Recombinant PirAVP and PirBVP Toxins through SDS-PAGE

Following purification and dialysis, the recombinant PirAVP and PirBVP toxins were collected and immediately preserved at −80 °C for further analysis. Subsequently, the protein was electrophoresed in 4–20% SDS-PAGE gel (BioRad, Belgium), with each lane receiving an equivalent volume (10 µL) of toxin. The gels were then stained with Coomassie Biosafe (BioRad Laboratories) and visualized by a ChemiDoc MP imaging system (BioRad, Nazareth, Belgium) for qualitative analysis of recombinant PirAVP and PirBVP toxins (Figure 5) [9]. The concentration of protein was determined using the Bradford method [37] with bovine serum albumin as the standard.

5.3. Axenic Brine Shrimp Hatching

The gnotobiotic brine shrimp larvae was produced by hatching high-quality cysts axenically (germ-free) following decapsulation and hatching procedures as described by Baruah et al. [38]. Briefly, 200 mg of A. franciscana cysts (EG® type, batch 21452, INVE Aquaculture, Dendermonde, Belgium) were hydrated in 18 mL of distilled water for 1 h. Sterile cysts and larvae were obtained via decapsulation using 660 µL NaOH (32%) and 10 mL NaOCl (50%). During the reaction, 0.2-µm filtered aeration was provided. All manipulation was carried out under a laminar flow hood and all tools were sterilized. The decapsulation was stopped after 2 min by adding 10 mL sterile Na2S2O3 at 10g/L. The decapsulated cysts were washed with filtered autoclaved seawater (FASW) containing 35 g/L of instant ocean® synthetic sea salt (Aquarium Systems, Sarrebourg, France). The cysts were resuspended in a 50 mL tube containing 30 mL FASW and incubated for 24 h on a rotor (4 min−1) at 28 °C with constant illumination of approximately 27 µE/m2 s. After 28 h of incubation, hatched larvae at developmental stage instar II (mouth is opened to ingest particles) were collected, and the axenicity was verified by spread plating (100 µL) as well as by adding (500 µL) of the hatching water on marine agar and marine broth respectively, followed by incubating at 28 °C for 5 days [39]. Experiments started with non-axenic larvae were discarded.

5.4. Brine Shrimp Challenge Assay

The challenge assay was performed according to the method developed by Kumar et al. [8]. Briefly, hatched brine shrimp larvae (at developmental stage II) were collected and group of 10 larvae were transferred to 2 mL sterile eppendorf tubes, containing 1 mL FASW. The earlier study has demonstrated that brine shrimp larvae challenged by immersion with PirAVP+PirBVP toxin mixture (1:1 ratio) at 5.2 µg/100 µL, induce significantly high mortality (up to 70%) at 60 h post-exposure [9]. Hence, in this study, the toxic concentration, i.e., 5.2 µg/100 µL, of recombinant PirAVP+PirBVP toxin mixture (1:1 ratio) were used and exposed to brine shrimp larvae. After feeding (autoclaved bacteria) and addition of the recombinant PirABVP toxins, the eppendorf tubes were put back on the rotor and kept at 28 °C. Subsequently, the larvae samples were collected for immunohistochemical analysis at 0, 12, 24, 36, 48, and 60 h after the addition of recombinant toxins. The brine shrimp larvae that were not challenged with recombinant toxins served as a negative control. The assay was performed in triplicates.

5.5. Light Microscopical Analysis Using Immunohistochemistry

In total, two separate immunohistochemical strategies were carried out to determine the PirABVP toxin toxicity in challenged brine shrimp larvae. Briefly, the brine shrimp larvae, from both the treatment and control group, sampled for immunohistochemistry, were fixed for 12 h in a Davidson’s AFA fixative consisting of 80 mL of 100% ethyl alcohol, 15 mL of 40% formaldehyde, and 5 mL of acetic acid, and subsequently transferred to 70% ethanol [40]. After pre-staining with haematoxylin [Haematoxylin (C.I. 75290), Merck KgaA, Darmstadt, Germany], each larva was oriented in 2.0% agarose (electrophoresis grade, 15510-019, Life technologies, Paisley, Scotland) and processed using tissue processor (STP 120, Thermo Scientific, Belgium) for approximately 22 h, followed by embedding in paraffin using an embedding station (EC350-1 and 350-2, Microm international) [41]. Per treatment and per sampling point, 6 brine shrimp larvae were cut into serial sections (dorsoventral, sagittal, and transverse) of 5 µm thickness using a microtome (HM360, Microm international). Subsequently, the histological sections were collected on 3-aminopropyltriethoxysilane (APES) coated slides and placed onto hot plate (60 °C) for 1 h. Afterwards, the slides were transferred and incubated overnight at 37 °C. The tissue slides were cleared in xylene, hydrated in graded ethanol series and epitope retrieval was performed by heating the slides in citrate buffer for 2.5 min at 700–800 W, and for 10 min at 160 W, followed by 30 min incubation at 4 °C. In the first analysis, the consecutive sections were processed for indirect immunoperoxidase staining using anti-His monoclonal antibody 2D5 (Mab) (Bioss antibodies, USA) specific to His6-tagged PirABVP toxins at 1:1000 dilution, with PBS on each consecutive section. Hydrogen peroxide (Dako REAL peroxidase-blocking solution, S2023) was added to the section (to block the peroxidase activity in tissue) for 5 min, and later the slides were incubated with Dako envision (anti-mouse HRP labelled) (Agilent, Lexington, MA, USA) for 30 min. The peroxidase activity was visualized by incubation with 0.03% DAB (Agilent, Lexington, MA, USA) for 5 min. The tissue slides were counterstained with haematoxylin, dehydrated in graded ethanol series, cleared in xylene, and mounted in permount. Tissue slides were analyzed light microscopically (BX61, Olympus) and positive reactions were seen as brown coloration.
In the second analysis, the PirABVP-induced lesions were investigated for epithelial cell origin. The paraffin-embedded histological sections were cleared in xylene, hydrated in graded ethanol series, and transferred to citrate buffer to boil the tissue for 2.5 min at 700–800 W, 10 min at 160 W, followed by 30 min incubation at 4 °C. The tissue sections were incubated with 30% rabbit serum (blocking) for 30 min. Afterwards, the slides were processed for indirect immunoperoxidase staining using polyclonal anti-cytokeratin 20 antibodies (Pab) (SPM191) (Santa Cruz Biotechnology, USA) at 1:100 dilution with antibody diluent. Later, the sections were incubated with hydrogen peroxide (Dako REAL peroxidase-blocking solution, S2023) for 5 min followed by Dako envision (anti-mouse HRP labelled) (Agilent, Lexington, MA, USA) for 30 min. The peroxidase activity was visualized by incubation with 0.03% DAB (Agilent, Lexington, MA, USA) for 5 min. The preparations were counterstained with haematoxylin, dehydrated in graded ethanol series, cleared in xylene, mounted in permount, and analyzed light microscopically (BX61, Olympus). Similarly, the positive immuno-reactivity was visualized as brown coloration.

5.6. Transmission Electron Microscopical (TEM) Analysis

The brine shrimp larvae, either challenged (PirABVP toxin) or not-challenged, were fixed in Karnovsky’s fixative for TEM analysis. After overnight fixation at 4 °C, the specimens were washed in sodium cacodylate buffer (pH 7.4) and post fixed for 1 h 30 min in 1% osmium tetroxide. Subsequently, the samples were dehydrated using Leica tissue processor (EM TP, type 709202). After polymerization, the samples got trimmed with the Leica EM TRIM (S4E, type 702601). The semithin sections (1 µm) were cut with glass knives on a Leica Ultramicrotome (EM UC6) and stained with toluidine blue to select and localize the regions of interest. Later, ultrathin sections (90 nm) were cut with a Leica Ultramicrotome (EM UC6) using a diamond knife (DIATOME, ultra 45°; 2.5 mm), and mounted on formvar-coated single slot copper grids (Formvar solution, EMS). The sections were contrasted with uranyl acetate and lead citrate and examined on a transmission electron microscope JEM-1400 Plus (JEOL, Benelux).

Author Contributions

The authors V.K., P.B. and W.V.d.B. conceived, proposed the idea and designed the study. V.K., L.D.B. and L.C. performed the experiments and analyzed the data. V.K. writing-original draft preparation. V.K., L.D.B., L.C., K.B., P.B. and W.V.d.B. writing-review and editing.

Funding

Vikash Kumar is supported by Netaji Subhas international doctoral fellowship from Indian Council of Agricultural Research (ICAR), New Delhi, India.

Acknowledgments

We thank Chu-Fang Lo of National Cheng Kung University, Tainan, Taiwan for providing V. parahaemolyticus PirA plasmid (pET21b PirAVP) and PirB plasmid (pET21b PirBVP). We would like to acknowledge the technical assistant provided by Brigitte Van Moffaert and Anita De Haese. This research was made possible by the support of the UGent TEM Expertise Centre.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Dong, X.; Wang, H.; Xie, G.; Zou, P.; Guo, C.; Liang, Y.; Huang, J. An isolate of Vibrio campbellii carrying the pirVP gene causes acute hepatopancreatic necrosis disease. Emerg. Microbes Infect. 2017, 6, e2. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Dong, X.; Bi, D.; Wang, H.; Zou, P.; Xie, G.; Wan, X.; Yang, Q.; Zhu, Y.; Chen, M.; Guo, C.; et al. pirABvp-Bearing Vibrio parahaemolyticus and Vibrio campbellii pathogens isolated from the Same AHPND-affected pond possess highly similar pathogenic plasmids. Front. Microbiol. 2017, 8, 1–9. [Google Scholar] [CrossRef] [PubMed]
  3. Lee, C.-T.; Chen, I.-T.; Yang, Y.-T.; Ko, T.-P.; Huang, Y.-T.; Huang, J.-Y.; Huang, M.-F.; Lin, S.-J.; Chen, C.-Y.; Lin, S.-S.; et al. The opportunistic marine pathogen Vibrio parahaemolyticus becomes virulent by acquiring a plasmid that expresses a deadly toxin. Proc. Natl. Acad. Sci. USA 2015, 112, 10798–10803. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Li, P.; Kinch, L.N.; Ray, A.; Dalia, A.B.; Cong, Q.; Nunan, L.M.; Camilli, A.; Grishin, N.V.; Salomon, D.; Orth, K. Acute hepatopancreatic necrosis disease-causing Vibrio parahaemolyticus strains maintain an antibacterial type VI secretion system with versatile effector repertoires. Appl. Environ. Microbiol. 2017, 83, e00737–17. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Han, J.E.; Tang, K.F.J.; Tran, L.H.; Lightner, D.V. Photorhabdus insect-related (Pir) toxin-like genes in a plasmid of Vibrio parahaemolyticus, the causative agent of acute hepatopancreatic necrosis disease (AHPND) of shrimp. Dis. Aquat. Organ. 2015, 113, 33–40. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Nunan, L.; Lightner, D.; Pantoja, C.; Gomez-Jimenez, S. Detection of acute hepatopancreatic necrosis disease (AHPND) in Mexico. Dis. Aquat. Organ. 2014, 111, 81–86. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Flegel, T.W. A future vision for disease control in shrimp aquaculture. J. World Aquac. Soc. 2019, 50, 249–266. [Google Scholar] [CrossRef]
  8. Kumar, V.; Baruah, K.; Nguyen, D.V.; Smagghe, G.; Vossen, E.; Bossier, P. Phloroglucinol mediated Hsp70 production in crustaceans: Protection against Vibrio parahaemolyticus in Artemia franciscana and Macrobrachium rosenbergii. Front. Immunol. 2018, 9, 1091. [Google Scholar] [CrossRef] [Green Version]
  9. Kumar, V.; Viet, D.; Baruah, K.; Bossier, P. Probing the mechanism of VP AHPND extracellular proteins toxicity purified from Vibrio parahaemolyticus AHPND strain in germ-free Artemia test system. Aquaculture 2019, 504, 414–419. [Google Scholar] [CrossRef]
  10. Choi, M.; Stevens, A.M.; Smith, S.A.; Taylor, D.P.; Kuhn, D.D. Strain and dose infectivity of Vibrio parahaemolyticus: the causative agent of early mortality syndrome in shrimp. Aquac. Res. 2017, 48, 3719–3727. [Google Scholar] [CrossRef]
  11. Campa-Córdova, A.I.; León-Gallo, A.F.; Romero-Maldonado, A.; Ibarra-Serrano, A.C.; Rosales-Mendoza, S.; Hirono, I.; Angulo, C. Recombinant PirA-like toxin protects shrimp against challenge with Vibrio parahaemolyticus, the aetiological agent of acute hepatopancreatic necrosis disease. J. Fish Dis. 2017, 40, 1725–1729. [Google Scholar] [CrossRef] [PubMed]
  12. Hong, X.; Lu, L.; Xu, D. Progress in research on acute hepatopancreatic necrosis disease (AHPND). Aquac. Int. 2016, 24, 577–593. [Google Scholar] [CrossRef]
  13. Lin, S.J.; Hsu, K.C.; Wang, H.C. Structural insights into the cytotoxic mechanism of Vibrio parahaemolyticus PirAvpand PirBvptoxins. Mar. Drugs 2017, 15, 373. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Pérez-Sánchez, J.; Terova, G.; Simó-Mirabet, P.; Rimoldi, S.; Folkedal, O.; Calduch-Giner, J.A.; Olsen, R.E.; Sitjà-Bobadilla, A. Skin mucus of gilthead sea bream (Sparus aurata L.) protein mapping and regulation in chronically stressed fish. Front. Physiol. 2017, 8, 1–18. [Google Scholar] [CrossRef] [PubMed]
  15. Leung, T.L.F.; Bates, A.E. More rapid and severe disease outbreaks for aquaculture at the tropics: Implications for food security. J. Appl. Ecol. 2013, 50, 215–222. [Google Scholar] [CrossRef]
  16. Shinn, A.P.; Pratoomyot, J.; Griffiths, D.; Jiravanichpaisal, J.; Briggs, M. Asian shrimp production and the economic costs of disease. Asian Fish. Sci. J. 2018, 31S, 29–58. [Google Scholar]
  17. FAO. State of Fisheries and Aquaculture in the World; The Food and Agriculture Organization of the United Nations: Rome, Italy, 2018; ISBN 9789251305621. Available online: http://www.fao.org/3/i9540en/i9540en.pdf (accessed on 9 February 2019).
  18. Tran, L.; Nunan, L.; Redman, R.M.; Mohney, L.L.; Pantoja, C.R.; Fitzsimmons, K.; Lightner, D.V. Determination of the infectious nature of the agent of acute hepatopancreatic necrosis syndrome affecting penaeid shrimp. Dis. Aquat. Organ. 2013, 105, 45–55. [Google Scholar] [CrossRef]
  19. Dong, X.; Wang, H.; Zou, P.; Chen, J.; Liu, Z.; Wang, X.; Huang, J. Complete genome sequence of Vibrio campbellii strain 20130629003S01 isolated from shrimp with acute hepatopancreatic necrosis disease. Gut Pathog. 2017, 9, 1–5. [Google Scholar] [CrossRef]
  20. Liu, L.; Xiao, J.; Xia, X.; Pan, Y.; Yan, S. Draft Genome Sequence of Vibrio owensii Strain SH-14, Which Causes. Genome Announc. 2015, 3, 3354. [Google Scholar] [CrossRef] [Green Version]
  21. Restrepo, L.; Bayot, B.; Arciniegas, S.; Bajaña, L.; Betancourt, I.; Panchana, F.; Reyes Muñoz, A. PirVP genes causing AHPND identified in a new Vibrio species (Vibrio punensis) within the commensal Orientalis clade. Sci. Rep. 2018, 8, 13080. [Google Scholar] [CrossRef]
  22. Wechprasit, P.; Panphloi, M.; Thitamadee, S.; Sritunyalucksana, K.; Prachumwat, A. Complete Genome Sequence of Shewanella sp. Strain TH2012, Isolated from Shrimp in a Cultivation Pond Exhibiting Early Mortality Syndrome. Microbiol. Resour. Announc. 2019, 8, e01703–18. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Roy, S.; Kumar, V.; Bossier, P.; Norouzitallab, P.; Vanrompay, D. Phloroglucinol Treatment Induces Transgenerational Epigenetic Inherited Resistance Against Vibrio Infections and Thermal Stress in a Brine Shrimp (Artemia franciscana) Model. Front. Immunol. 2019, 10, 2745. [Google Scholar] [CrossRef] [Green Version]
  24. Baruah, K.; Huy, T.T.; Norouzitallab, P.; Niu, Y.; Gupta, S.K.; De Schryver, P.; Bossier, P. Probing the protective mechanism of poly-ß-hydroxybutyrate against vibriosis by using gnotobiotic Artemia franciscana and Vibrio campbellii as host-pathogen model. Sci. Rep. 2015, 5, 9427. [Google Scholar] [CrossRef] [PubMed]
  25. Baruah, K.; Duy Phong, H.P.P.; Norouzitallab, P.; Defoirdt, T.; Bossier, P. The gnotobiotic brine shrimp (Artemia franciscana) model system reveals that the phenolic compound pyrogallol protects against infection through its prooxidant activity. Free Radic. Biol. Med. 2015, 89, 593–601. [Google Scholar] [CrossRef]
  26. Norouzitallab, P.; Baruah, K.; Vanrompay, D.; Bossier, P. Teaching Shrimps Self-Defense to Fight Infections. Trends Biotechnol. 2019, 37, 16–19. [Google Scholar] [CrossRef]
  27. Ffrench-Constant, R.H.; Waterfield, N.; Burland, V.; Perna, N.T.; Daborn, P.J.; Bowen, D.; Blattner, F.R. A genomic sample sequence of the entomopathogenic bacterium Photorhabdus luminescens W14: Potential implications for virulence. Appl. Environ. Microbiol. 2000, 66, 3310–3329. [Google Scholar] [CrossRef] [Green Version]
  28. Duchaud, E.; Rusniok, C.; Frangeul, L.; Buchrieser, C.; Givaudan, A.; Taourit, S.; Bocs, S.; Boursaux-Eude, C.; Chandler, M.; Charles, J.F.; et al. The genome sequence of the entomopathogenic bacterium Photorhabdus luminescens. Nat. Biotechnol. 2003, 21, 1307–1313. [Google Scholar] [CrossRef]
  29. Waterfield, N.; Kamita, S.G.; Hammock, B.D.; Ffrench-Constant, R. The Photorhabdus Pir toxins are similar to a developmentally regulated insect protein but show no juvenile hormone esterase activity. FEMS Microbiol. Lett. 2005, 245, 47–52. [Google Scholar] [CrossRef] [Green Version]
  30. Blackburn, M.B.; Farrar, R.R.; Novak, N.G.; Lawrence, S.D. Remarkable susceptibility of the diamondback moth (Plutella xylostella) to ingestion of Pir toxins from Photorhabdus luminescens. Entomol. Exp. Appl. 2006, 121, 31–37. [Google Scholar] [CrossRef]
  31. Ahantarig, A.; Chantawat, N.; Waterfield, N.R.; Ffrench-Constant, R.; Kittayapong, P. PirAB toxin from Photorhabdus asymbiotica as a larvicide against dengue vectors. Appl. Environ. Microbiol. 2009, 75, 4627–4629. [Google Scholar] [CrossRef] [Green Version]
  32. Kondo, H.; Tinwongger, S.; Proespraiwong, P.; Mavichak, R.; Unajak, S.; Nozaki, R.; Hirono, I. Draft Genome Sequences of Six Strains of Vibrio parahaemolyticus Isolated from Early Mortality Syndrome/Acute Hepatopancreatic Necrosis Disease Shrimp in Thailand. Genome Announc. 2014, 2, e00221–14. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Lin, S.J.; Chen, Y.F.; Hsu, K.C.; Chen, Y.L.; Ko, T.P.; Lo, C.F.; Wang, H.C.; Wang, H.C. Structural insights to the heterotetrameric interaction between the vibrio parahaemolyticus pirAvp and pirBvp toxins and activation of the cry-like pore-forming domain. Toxins 2019, 11, E233. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Sirikharin, R.; Taengchaiyaphum, S.; Sanguanrut, P.; Chi, T.D.; Mavichak, R.; Proespraiwong, P.; Nuangsaeng, B.; Thitamadee, S.; Flegel, T.W.; Sritunyalucksana, K. Characterization and PCR detection of binary, pir-like toxins from vibrio parahaemolyticus isolates that cause acute hepatopancreatic necrosis disease (AHPND) in shrimp. PLoS ONE 2015, 10, e0126987. [Google Scholar] [CrossRef] [PubMed]
  35. Magin, T.M.; Vijayaraj, P.; Leube, R.E. Structural and regulatory functions of keratins. Exp. Cell Res. 2007, 313, 2021–2032. [Google Scholar] [CrossRef]
  36. Gunasekara, R.A.Y.S.A.; Defoirdt, T.; Rekecki, A.; Decostere, A.; Cornelissen, M.; Sorgeloos, P.; Bossier, P.; Van den Broeck, W. Light and transmission electron microscopy of Vibrio campbellii infection in gnotobiotic Artemia franciscana and protection offered by a yeast mutant with elevated cell wall glucan. Vet. Microbiol. 2012, 158, 337–343. [Google Scholar] [CrossRef]
  37. Bradford, M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 1976, 72, 248–254. [Google Scholar] [CrossRef]
  38. Baruah, K.; Cam, D.T.V.; Dierckens, K.; Wille, M.; Defoirdt, T.; Sorgeloos, P.; Bossier, P. In vivo effects of single or combined N-acyl homoserine lactone quorum sensing signals on the performance of Macrobrachium rosenbergii larvae. Aquaculture 2009, 288, 233–238. [Google Scholar] [CrossRef]
  39. Baruah, K.; Norouzitallab, P.; Roberts, R.J.; Sorgeloos, P.; Bossier, P. A novel heat-shock protein inducer triggers heat shock protein 70 production and protects Artemia franciscana nauplii against abiotic stressors. Aquaculture 2012, 334, 152–158. [Google Scholar] [CrossRef]
  40. Gunasekara, R.A.Y.S.A.; Rekecki, A.; Baruah, K.; Bossier, P.; Van den Broeck, W. Evaluation of probiotic effect of Aeromonas hydrophila on the development of the digestive tract of germ-free Artemia franciscana nauplii. J. Exp. Mar. Biol. Ecol. 2010, 393, 78–82. [Google Scholar] [CrossRef]
  41. Gunasekara, R.A.Y.S.A.; Rekecki, A.; Cornillie, P.; Cornelissen, M.; Sorgeloos, P.; Simoens, P.; Bossier, P.; Van den Broeck, W. Morphological characteristics of the digestive tract of gnotobiotic Artemia franciscana nauplii. Aquaculture 2011, 321, 1–7. [Google Scholar] [CrossRef]
Toxins 11 00717 g001a 550Toxins 11 00717 g001b 550
Figure 1. PirABVP toxins bind to the digestive tract and induce sloughing of epithelial cells in brine shrimp (Artemia franciscana) larvae. Immunohistochemistry of brine shrimp (A. franciscana) larvae after 0, 12, 24, 36, 48, and 60 h post PirABVP toxin challenge. The paraffin sections were treated with anti-his Mab (monoclonal antibody) specific to His-tagged PirAB toxins, then counterstained with haematoxylin. Legend: (1) Gut cells; (2) brush border; (3) gut lumen (A,B): 0 h post-challenge; (C,D): 12 h post-challenge; (E,F): 24 h post-challenge (G,H): 36 h post-challenge; (I,J): 48 h post-challenge; (K,L): 60 h post-challenge. (C,L): PirABVP toxin binds with digestive tract epithelium and induce shedding or sloughing of enterocytes in the midgut and hindgut regions (arrowhead). At 48 h and 60 h post-challenge, epithelium was severely damaged and the remaining cellular components including nuclei were further detached into the lumen and showed signs of degeneration such as pyknotic nuclei and lysed cellular membrane (arrowhead).
Figure 1. PirABVP toxins bind to the digestive tract and induce sloughing of epithelial cells in brine shrimp (Artemia franciscana) larvae. Immunohistochemistry of brine shrimp (A. franciscana) larvae after 0, 12, 24, 36, 48, and 60 h post PirABVP toxin challenge. The paraffin sections were treated with anti-his Mab (monoclonal antibody) specific to His-tagged PirAB toxins, then counterstained with haematoxylin. Legend: (1) Gut cells; (2) brush border; (3) gut lumen (A,B): 0 h post-challenge; (C,D): 12 h post-challenge; (E,F): 24 h post-challenge (G,H): 36 h post-challenge; (I,J): 48 h post-challenge; (K,L): 60 h post-challenge. (C,L): PirABVP toxin binds with digestive tract epithelium and induce shedding or sloughing of enterocytes in the midgut and hindgut regions (arrowhead). At 48 h and 60 h post-challenge, epithelium was severely damaged and the remaining cellular components including nuclei were further detached into the lumen and showed signs of degeneration such as pyknotic nuclei and lysed cellular membrane (arrowhead).
Toxins 11 00717 g001aToxins 11 00717 g001b
Toxins 11 00717 g002 550
Figure 2. PirAB toxin-induced accumulation of cellular debris in the digestive tract are of epithelial cells origin. Immunohistochemistry of brine shrimp (A. franciscana) larvae after 12 and 24 h post PirABVP toxin challenge. The paraffin sections were treated with anti-cytokeratin polyclonal antibody (Pab), specific to keratin group of fibrous proteins in epithelial cells, then counterstained with haematoxylin. (A): 12 h post- experiment, negative control (no PirABVP toxin); (B): 24 h post- experiment, negative control (no PirABVP toxin); (C–E): 12 h post-challenge; (F–H): 24 h post-challenge. (C–H): PirABVP challenge-induced sloughing that leads to accumulation of cellular debris in the intestinal lumen (arrowhead) is of epithelial cell origin.
Figure 2. PirAB toxin-induced accumulation of cellular debris in the digestive tract are of epithelial cells origin. Immunohistochemistry of brine shrimp (A. franciscana) larvae after 12 and 24 h post PirABVP toxin challenge. The paraffin sections were treated with anti-cytokeratin polyclonal antibody (Pab), specific to keratin group of fibrous proteins in epithelial cells, then counterstained with haematoxylin. (A): 12 h post- experiment, negative control (no PirABVP toxin); (B): 24 h post- experiment, negative control (no PirABVP toxin); (C–E): 12 h post-challenge; (F–H): 24 h post-challenge. (C–H): PirABVP challenge-induced sloughing that leads to accumulation of cellular debris in the intestinal lumen (arrowhead) is of epithelial cell origin.
Toxins 11 00717 g002
Toxins 11 00717 g003 550
Figure 3. PirABVP toxin-binding leads to necrosis and damages the digestive tracts of brine shrimp larvae. Transmission electron microscopy (TEM) analysis of brine shrimp (A. franciscana) larvae after 48 h post-PirABVP toxin challenge. (A–D): PirABVP toxin challenge damages epithelial enterocytes and induces focal to extensive necrosis, resulting in the movement of bacterial cells (autoclaved feed) outside of the intestinal lumen. Legend: (1) Autoclaved bacteria feed for brine shrimp larvae; (2) damaged enterocytes with different degrees of focal to extensive necrosis. *Because brine shrimp larvae were too small, before tissue processing and sectioning, the larvae were transferred to 2% agarose which resulted in development of black lines in some TEM figures (A,B).
Figure 3. PirABVP toxin-binding leads to necrosis and damages the digestive tracts of brine shrimp larvae. Transmission electron microscopy (TEM) analysis of brine shrimp (A. franciscana) larvae after 48 h post-PirABVP toxin challenge. (A–D): PirABVP toxin challenge damages epithelial enterocytes and induces focal to extensive necrosis, resulting in the movement of bacterial cells (autoclaved feed) outside of the intestinal lumen. Legend: (1) Autoclaved bacteria feed for brine shrimp larvae; (2) damaged enterocytes with different degrees of focal to extensive necrosis. *Because brine shrimp larvae were too small, before tissue processing and sectioning, the larvae were transferred to 2% agarose which resulted in development of black lines in some TEM figures (A,B).
Toxins 11 00717 g003
Toxins 11 00717 g004 550
Figure 4. Digestive tract in control brine shrimp larvae appeared normal, with intact cellular membranes. Transmission electron microscopy (TEM) analysis of control group brine shrimp (A. franciscana) larvae after 48 h. (A–F): The digestive tract epithelial enterocytes appeared normal with an intact mitochondrion, nucleus, rough endoplasmic reticulum (RER), and intercellular junctions. Legend: (1) nucleus; (2) midgut lumen; (3) midgut enterocytes; (4) tight junction; (5) microvilli; (6) mitochondria; (7) rough endoplasmic reticulum (RER).
Figure 4. Digestive tract in control brine shrimp larvae appeared normal, with intact cellular membranes. Transmission electron microscopy (TEM) analysis of control group brine shrimp (A. franciscana) larvae after 48 h. (A–F): The digestive tract epithelial enterocytes appeared normal with an intact mitochondrion, nucleus, rough endoplasmic reticulum (RER), and intercellular junctions. Legend: (1) nucleus; (2) midgut lumen; (3) midgut enterocytes; (4) tight junction; (5) microvilli; (6) mitochondria; (7) rough endoplasmic reticulum (RER).
Toxins 11 00717 g004
Toxins 11 00717 g005 550
Figure 5. SDS-PAGE analysis of purified V. parahaemolyticus PirAVP and PirBVP toxins. Molecular mass standards (M) in kilodaltons (Protein ladder), Lane 1-PirAVP at 13 kDa, Lane 2-PirBVP at 50 kDa.
Figure 5. SDS-PAGE analysis of purified V. parahaemolyticus PirAVP and PirBVP toxins. Molecular mass standards (M) in kilodaltons (Protein ladder), Lane 1-PirAVP at 13 kDa, Lane 2-PirBVP at 50 kDa.
Toxins 11 00717 g005

Share and Cite

MDPI and ACS Style

Kumar, V.; Bels, L.D.; Couck, L.; Baruah, K.; Bossier, P.; Broeck, W.V.d. PirABVP Toxin Binds to Epithelial Cells of the Digestive Tract and Produce Pathognomonic AHPND Lesions in Germ-Free Brine Shrimp. Toxins 2019, 11, 717. https://0-doi-org.brum.beds.ac.uk/10.3390/toxins11120717

AMA Style

Kumar V, Bels LD, Couck L, Baruah K, Bossier P, Broeck WVd. PirABVP Toxin Binds to Epithelial Cells of the Digestive Tract and Produce Pathognomonic AHPND Lesions in Germ-Free Brine Shrimp. Toxins. 2019; 11(12):717. https://0-doi-org.brum.beds.ac.uk/10.3390/toxins11120717

Chicago/Turabian Style

Kumar, Vikash, Lobke De Bels, Liesbeth Couck, Kartik Baruah, Peter Bossier, and Wim Van den Broeck. 2019. "PirABVP Toxin Binds to Epithelial Cells of the Digestive Tract and Produce Pathognomonic AHPND Lesions in Germ-Free Brine Shrimp" Toxins 11, no. 12: 717. https://0-doi-org.brum.beds.ac.uk/10.3390/toxins11120717

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