Abstract
The gut microbiome plays an essential role in the immune system of invertebrates and vertebrates. Pre and pro-biotics could enhance the shrimp immune system by increasing the phenoloxidase (PO), prophenoloxidase (ProPO), and superoxide dismutase activities. During viral infection, the host immune system alteration could influence the gut microbiome composition and probably lead to other pathogenic infections. Since the JAK/STAT pathway is involved in white spot syndrome virus (WSSV) infection, we investigated the intestine immune genes of STAT-silenced shrimp. During WSSV infection, expression levels of PmVago1, PmDoral, and PmSpätzle in PmSTAT-silenced shrimp were higher than normal. In addition, the transcription levels of antimicrobial peptides, including crustinPm1, crustinPm7, and PmPEN3, were higher in WSSV-challenged PmSTAT-silenced shrimp than the WSSV-infected normal shrimp. Meanwhile, PmSTAT silencing suppressed PmProPO1, PmProPO2, and PmPPAE1 expressions during WSSV infection. The microbiota from four shrimp tested groups (control group, WSSV-infected, PmSTAT-silenced, and PmSTAT-silenced infected by WSSV) was significantly different, with decreasing richness and diversity due to WSSV infection. The relative abundance of Bacteroidetes, Actinobacteria, and Planctomycetes was reduced in WSSV-challenged shrimp. However, at the species level, P. damselae, a pathogen to human and marine animals, significantly increased in WSSV-challenged shrimp. In constrast, Shewanella algae, a shrimp probiotic, was decreased in WSSV groups. In addition, the microbiota structure between control and PmSTAT-silenced shrimp was significantly different, suggesting the importance of STAT to maintain the homeostasis interaction with the microbiota.
Similar content being viewed by others
Introduction
The gut microbiome plays an essential role in the organism’s growth, development, and immunity1,2,3. In addition, the gut microbiome improves the immune response, nutrient absorption, and homeostasis maintenance4,5. It is generally accepted, for different organisms, that a higher diversity of the microbiota is associated with a healthy host condition. However, in shrimps, there are examples of low and high diversities associated with diseases6,7, so the direct association of lower diversity with the disease is still under discussion8,9. For example, Cornejo-Granados et al., (2017), found increased Aeromonas taiwanensis, Simiduia agarivorans, and Photobacterium angustum, which could be disease-specific bacteria during the early development of acute hepatopancreatic necrosis disease (AHPND) in Litopenaeus vannamei. Furthermore, AHPND reduced the Shannon diversity index of L. vannamei stomachs, where Vibrio and Candidatus Bacilloplasma were predominant populations, by 53.6%6. In addition, at the genus level, Photobacterium, Propionigenium, and Arcobacter were significantly increased, while Candidatus, Bacilloplasma, and Flavobacterium decreased in WSSV-infected L. vannamei10.
Moreover, pre- and probiotic diets can improve the gut microbiome and benefit the shrimp’s health. For example, L. vannamei fed with a Lactobacillus plantarum mixed diet improved the activities of phenoloxidase (PO), prophenoloxidase (ProPO), and superoxide dismutase (SOD), as well as increased the clearance efficiency of Vibrio alginolyticus and V. harveyi11,12. Furthermore, L. vannamei fed with probiotic Clostridium butyricumhas improved the expression of the host immune-related genes, including ProPO, lipopolysaccharide and β-1,3-glucan binding protein, lysozyme, crustin, and SOD which might enrich the beneficial bacteria such as Bacillus, Clostridium, Lachmoclostridium, Lachnospiraceae, and Lactobacillus13. This finding supported that the microbiome plays a vital role in the training and developing of the shrimp’s innate immune system. In contrast, the immune system controls the maintenance of host-microbe symbiosis14.
Shrimp immunity plays an essential role in microorganism invasion and balances host-microbe symbiosis. Like other invertebrates, pattern-recognition proteins (PRPs) act as an invading censor and activate intracellular signaling, stimulating humoral immune responses15. Shrimp humoral responses are the front-line defense against pathogens. Several signaling immune pathways are involved depending on the type of pathogen16. The Toll, immune deficiency (IMD), and JAK/STAT pathways regulate the immune response of invertebrates17. The Toll pathway responds to Gram-positive bacteria with Lys-type peptidoglycan, fungi, and some viruses such as white spot syndrome virus (WSSV)18,19,20,21. The microbial inducer-PRP complex activates the proteolytic cascade, resulting in the active Spätzle activating the Toll receptor20. The activated Toll receptor leads three cytoplasmic proteins, MyD88, Tube, and Pelle, to form the heterotrimeric complex. The activated Pelle can dissociate the Castus-Dorsal complex by phosphorylation22. The free Dorsal named NF-ƘB transcription factor translocates into the nucleus and up-regulates antimicrobial peptide (AMP) genes23,24. Meanwhile, the IMD pathway acts against Gram-negative bacteria, some Gram-positive Bacilli with the mesodiaminopimelic acid-type (DAP-type) PNGs, and some RNA viruses such as the yellow head virus (YHV)25,26,27. The pathogens were recognized by membrane-bound PRPs and stimulated IMD cascade through TAK1, TAB1, and TAB2 to activate IKK/Relish branches28,29,30,31,32. In shrimp, IKKβ and IKKε have been identified33,34.
The JAK/STAT pathway is activated when the secreted cytokine molecule interacts with JAK/STAT receptor. Then, JAK is activated and introduced to STAT activation by phosphorylation. The active STAT translocates into the nucleus and promotes the transcription of antiviral and immune genes35,36,37. In shrimp, it has been proven that the JAK/STAT pathway could be controlled by the IRF-Vago-JAK/STAT pathway manner, which is similar to the IRF-IFN-JAK/STAT pathway axis of vertebrates38. However, WSSV could hijack the JAK/STAT pathway by activating STAT to promote transcription of WSSV immediate-early gene 1 (IE1) and late gene envelope protein 28 (VP28) during WSSV infection16,39. The LvDOME, JAK/STAT receptor, or LvSTAT silenced shrimp showed reduced WSSV copy numbers and mortality during WSSV infection16,39,40,41,42. So far, there is no study on the gut microbiome of PmSTAT-silenced shrimp.
In vertebrates, the gut microbiome composition and host gene expression are associated. For example, Germ-free mice have lower Cytochrome P450 3a subfamily and transporter genes than normal mice, causing a decrease in the detoxification capability of the germ-free host43. In zebrafish, the expression of the hepatocyte nuclear factor 4A was suppressed by the microbiome, leading to the inhibition of host inflammatory pathways44. This suggests that lacking host transcription factors impacts the expression of downstream genes and microbiome structure. However, the relationship between immunity and gut microbiome in shrimp is unclear.
In this study, we investigate the shrimp gut microbiome, shrimp immunity, and immune-related genes during WSSV infection in PmSTAT-silenced shrimp to fulfill the understanding of host–pathogen-microbiome interactions. Understanding of host-WSSV-microbiome interactions might provide an improved WSSV prevention strategy and the knowledge of bacterial changes associated with a viral infection in a PmSTAT-silenced host.
Results
PmSTAT dsRNA successfully suppressed PmSTAT transcript and lower WSSV IE1
P. monodon intestines were collected from PBS-injected, PmSTAT-silenced, WSSV-challenged, and PmSTAT-silenced + WSSV challenged groups. Each group contained three replicates (n = 3), and each replicate was a pool of three shrimp intestines. From those, the DNA and total RNA were extracted using typical protocols. After that, quantitative real-time RT-PCR was performed to examine PmSTAT silencing efficiency and WSSV IE1 transcription levels. The PmSTAT expression levels in the shrimp intestines were successfully suppressed in PmSTAT dsRNA injection groups. Meanwhile, transcription levels of the IE1 gene in the intestines of PmSTAT knockdown shrimps were significantly lower than normal shrimps challenged by WSSV (Fig. 1A). This implied that PmSTAT knockdown reduced WSSV infection.
Effect of PmSTAT silencing on immune relate genes
The total RNA of P. monodon intestines was extracted and subjected to qRT-PCR to investigate the expression of immune-related genes, including JAK/STAT, Toll, IMD, cytokine, phenol oxidase, and antimicrobial peptide. The transcription levels of Vago, an IFN-like antiviral cytokine, responded to PmSTAT silencing and WSSV challenge (Fig. 1B). The Vago1 was strongly up-regulated in PmSTAT dsRNA, PmSTAT dsRNA + WSSV and WSSV challenged group. It is worth noting that the expression level of Vago1 in PmSTAT dsRNA + WSSV shrimp was significantly higher than that in PmSTAT dsRNA and WSSV-challenged group. In contrast, Vago4 was up-regulated in normal shrimp infected by WSSV but down-regulated in PmSTAT-silenced shrimp infected by WSSV. As shown in Fig. 1B, PmSTAT silencing significantly enhanced Vago5 transcription level, but the WSSV challenge reduced Vago5 transcripts in both normal and PmSTAT-depleted shrimp.
In PmSTAT-silenced shrimp, the expression levels of the JAK/STAT genes, including PmDOME and PmJAK, were decreased. In constrast, their expression levels were increased upon WSSV infection (Fig. 1C). Regarding the Toll pathway, silencing of PmSTAT enhanced the PmSpätzle expression level more than two-fold, compared to normal shrimp but showed fewer effects on the transcription levels of MyD88, Castus, and Dorsal. The expression level of PmSpätzle in PmSTAT-silenced shrimp was dropped upon WSSV infection (Fig. 1C). Meanwhile, the transcription levels of Relish, a transcription factor in the IMD pathway, in normal and PmSTAT-silenced shrimp slightly increased in response to WSSV infection (Fig. 1C). In this work, the expression level of the inhibitor of kappa B kinase, which plays an essential role in the IKK-NF-ƘB signaling cascade, was also investigated. The expression level of PmIKKβ was increased in response to PmSTAT depletion and WSSV infection (Fig. 1C). PmIKKε1 transcript was increased in both non-infected and WSSV-infected PmSTAT-silenced shrimp, compared to the normal shrimp, while PmIKKε2 transcript was decreased.
Antimicrobial peptides, including crustinPm1, crustinPm7, and peneaidin3, responded to PmSTAT dsRNA. At the same time, the WSSV infection strongly suppresed them (Fig. 1D). Meanwhile, transcription levels of phenol oxidase cascade, including ProPO1, ProPO2, and phenol oxidase activating enzyme 1 (PPAE1), were significantly suppressed by either PmSTAT dsRNA or WSSV. However, PPAE2 expression was promoted by the WSSV challenge (Fig. 1E).
Shrimp intestinal microbiome
A total of 1,544,254 sequences were obtained from 12 libraries, consisting of 4 conditions in triplicate (PBS, PmSTAT dsRNA, PmSTAT dsRNA + WSSV, and WSSV). The average sequencing read was 128,687 per sample, ranging from 101,376 to 162,622. The operational taxonomic units (OTUs) were assigned to a 97% sequence similarity. The reads assigned to OTUs (without singletons and low abundance OTUs (0.005%)) ranged from 60,557 (46.66%) to 94,696 (75.07%), which averaged read were 66,909.33 (49.12%), 82,021.00 (57.14%), 83,628.67 (69.93%) and 74,944.00 (60.82%) in PBS, PmSTAT dsRNA, WSSV, and PmSTAT dsRNA + WSSV, respectively (Supplementary Information, Tables S1and S2). The percentage of the classified taxonomic level is shown in Table S3. The classified percentage ranged from 45.26% to 91.84% at the genus level. Each condition shared 151 genera and 69 species in common. Meanwhile, the unique bacteria found in species levels in each condition, including PBS, PmSTAT dsRNA, PmSTAT dsRNA + WSSV, and WSSV, were 49, 41, 13, and 20, respectively (Supplementary Information, Fig. S1).
The dominant phyla in all samples were Proteobacteria, followed by Bacteroidetes, Actinobacteria, and Planctomycetes (Fig. 2A). However, the relative abundance of phyla Bacteroidetes, Actinobacteria, and Planctomycetes were reduced in WSSV and PmSTAT silenced intestine. Interestingly, Proteobacteria was significantly increased in WSSV-challenged shrimp (P < 0.01). The rest of the phyla, including Bacteroidetes, Actinobacteria, Planctomycetes, Firmicutes, Verrucomicrobia, GN02 (Gracilibacteria), Chloroflexi, and TM (Saccharibacteria), were significantly reduced in WSSV challenged and also in the PmSTAT dsRNA + WSSV intestine. The highest relative abundance was Photobacterium at the genus level, followed by Vibrio and Shewanella (Fig. 2B). The Photobacterium was increased in both WSSV-challenged shrimps. Meanwhile, the relative abundance of Vibrio was similar in all conditions, and P. damselae was significantly increased in both WSSV-challenged shrimps (Fig. 2C). The Linear discriminant analysis effect size (LEfSe) analysis showed that the most LDA scores in each condition, including PBS, PmSTAT dsRNA, WSSV and PmSTAT dsRNA + WSSV was genera Cohesibacter, Shewanella, Roseivirga and Marivita, respectively (Fig. S2). Moreover, potential shrimp probiotics were identified in our samples following the previously reported method45. Overall, the relative abundance considering all potential probiotics was not significantly different between the four conditions (Supplementary Information, Fig. S4). The potential probiotics with abundance in our samples at the genus level were Bdellovibrio, Phaeobacter, Pseudoalteromonas, Rhodobacter, Shewanella, Streptomyces, and Vibrio. While at the species level, we found Phaeobacter sp. DCSW07, Shewanella algae, and Vibrio hepatarius (Supplementary Information, Fig. S5). Interestingly, when we analyzed the abundance of each of the potential probiotic species separately, we found that Shewanella algae significantly increased in PmSTAT dsRNA compared to all other three conditions. On the contrary, S. algae were depleted in the WSSV group (Fig. 2D); however, the differences were insignificant.
The alpha diversity metrics were calculated to investigate the difference between richness (Chao1 and the observed species index) and diversity (Phylogenetic diversity (PD) and Shannon diversity index) among groups (Table 1, Rarefaction curves are shown in Fig. S6). The unchallenged groups (PBS and PmSTAT silenced shrimp) showed higher richness and diversity. Contrarily, the challenged groups (PmSTAT silencing with WSSV and WSSV infected) showed lower richness and diversity. Overall, species richness and diversity were reduced in WSSV challenged shrimps and different from the PBS and PmSTAT silencing shrimps which were similar.
The differences in intestinal microbial communities among groups were analyzed by beta diversity. Principal coordinate analysis (PCoA) based on unweighted UniFrac distances exhibited that all samples formed four significantly separated clusters (ANOSIM p = 0.001) (Fig. 3A). The distances in the PCoA are shown in Fig. 3A. Thus, we quantitatively determined the centroids for each group of samples and then calculated the distance between the centroids for all the treatments (Table 2). With this analysis, we found several behaviors: First, the most extended separations of the distances between the control (PBS) and all the treatments suggested that the microbiota of all conditions differed significantly from that of the control. Second, the distance of PmSTAT dsRNA was more significant Vs. WSSV (0.537) and Vs. PmSTAT dsRNA Vs PmSTAT dsRNA + WSSV (0.495), suggesting that the PmSTAT dsRNA microbiota significantly differed from the WSSV and PmSTAT dsRNA + WSSV. Third, the smaller distance between all comparisons was between WSSV Vs. PmSTAT dsRNA + WSSV (0.334), suggesting that the microbiota between those two conditions was more similar than the other group comparisons. This also suggested that the most substantial effect on the microbiota composition caused by WSSV infection, rather than PmSTAT dsRNA depletion.
Similar clusters were also observed in the UPGMA tree of unweighted UniFrac distances, in which all WSSV-infected shrimps formed one hand of the three, in which the WSSV-infected shrimps clustered separately from the PmSTAT with WSSV (Fig. 3B). Contrarily, the non-infected shrimps created another hand (Fig. 3B), in which the PBS shrimps were separated from the PmSTAT-silenced shrimps. These findings agreed with the positions observed between the four groups in the unweighted PCoA (Fig. 3A).
Discussion
Gut microorganisms are essential in host functions, including development, nutrition, immunity, and disease resistance. However, host-pathogen interaction is still unclear. Therefore, we investigated the intestinal bacterial and immune-related transcription profile. Shrimp intestines were collected from WSSV unchallenged and challenged. In addition, we also investigated those profiles in suppressed JAK/STAT, an antiviral pathway in shrimps.
Changes in bacteria composition during WSSV infection may influence the expression of shrimp immunity. In mosquitoes, Vago function as an IFN-like antiviral cytokine. The transcription levels of LvVago4 and LvVago5 were up-regulated in WSSV-challenged hemocyte species38. Unlike the hemocyte, the transcription level of PmVago4 was slightly up-regulated, and PmVago5 was dramatically down-regulated in WSSV challenged intestine. However, PmVago5 was induced in PmSTAT dsRNA shrimp (Fig. 1B). Meanwhile, PmVago1 was strongly up-regulated by either PmSTAT dsRNA or WSSV challenged. It has been reported that LvTCF, a main downstream effector of Wnt signaling, regulates LvVago1. During WSSV infection in L. vannamei hemocytes, the transcription levels of LvTCF were increased. However, WSSV produced WSV083 to promote the degradation of LvTCF via the ubiquitin-proteasome pathway, which suppressed transcription levels of LvVago146. Furthermore, LvIRF, an interferon regulatory factor, regulates the transcription levels of LvVago4 and LvVago5. In L. vannamei hemocytes, the expression of LvVago4 and LvVago5 were inhibited in LvIRF-silenced shrimp. Moreover, cumulative mortality and WSSV copy numbers were increased in LvVago4- or LvVago5-silenced shrimp38. Unlike L. vannamei hemocytes, PmSTAT silencing promoted transcription levels of PmVago1 and PmVago5 in the P. monodon intestine (Fig. 1B). Meanwhile, WSSV infection strongly induced the expression of PmVago1 and slightly induced the expression of PmVago5 (Fig. 1B). Moreover, suppression of PmSTAT reduced WSSV copy numbers and promoted the transcription levels of PmVago1 (Fig. 1A and B). This suggests that PmVago1 might be the immunity frontline against WSSV in the intestine, unlike hemocytes.
Figure 1C showed that PmSTAT silencing decreased the transcription levels of PmDOME and PmJAK. When PmSTAT-silenced shrimp were challenged by WSSV, the expression of PmDOME and PmJAK was increased, suggesting that WSSV infection altered the JAK/STAT pathway. Since the Dome functionally reduced the WSSV copy number (e.g., replication), presumably, it should be increased when STAT is inhibited. However, the effect of down-regulation of PmDome in the PmSTAT-silenced intestine could suggest novel functions that need more studies.
The expression of PmDorsal, a transcription factor in the Toll pathway, and PmSpätzle were promoted in the PmSTAT dsRNA group (Fig. 1C). Two WSSV microRNA named WSSV-miRNA-N13 and WSSV-miRNA-N23 were identified47. They suppressed the expression of MjDorsal, resulting in the inhibition of MjALF expression. In this study, PmSTAT dsRNA promoted expression of PmDorsal in WSSV-challenged shrimp (Fig. 1C). Previous study has demonstrated that crustinPm1 is controlled through the Toll signaling pathway while crustinPm7 is mediated via both Toll and Imd pathways48. Meanwhile, Lvpenaeidin3a is regulated through the Toll pathway49. The transcription levels of crustinPm1, crustinPm7, and Pmpenaeidin3 were increased in PmSTAT silenced shrimp, while in WSSV-challenged, they were dramatically decreased (Fig. 1D). The ProPO system is one of the important shrimp immunities50. P. monodon hemocyte is the primary cell that express the proteins of this system, while the intestine could not sense transcription in PCR51,52. The PmProPO1, PmProPO2, and PmPPAE1 were expressed in low levels (Fig. 1E) and dramatically suppressed in WSSV-challenged shrimp. Interestingly, PmPPAE2 was strongly promoted in WSSV-challenged shrimp. The ProPO and PPAE are important to PO activity. Single or double ProPO silencing decreased PO activity. However, there were no significant differences in PO activity between single or double ProPO silencing52. Similar results were shown in single or double PPAE silencing. Moreover, single PPAE silencing promoted the expression of other PPAE53. The strongly enhancing PmPPAE2 might result from dramatically suppressed PmPPAE1 by WSSV. However, the expression of PmPPAE2 was not enhanced in PmSTAT silencing during WSSV infection. Thus, the PmSTAT may be necessary to transcript PmPPAE2.
The antimicrobial peptides, including crustinPm1, crustimPm7, and PEN3, were strongly promoted in PmSTAT-silenced and PmSTAT-silenced + WSSV groups and significantly suppressed in WSSV-infected group (Fig. 1D). A previous study suggested that LvPEN3 could inhibit WSSV virion internalization into hemocytes54. Furthermore, FmPEN3 could hinder the growth of Micrococcus lysodeikticus55. The stimulation of the host immune system by RNAi could be beneficial to prevent animals from pathogen invasion.
Suppression of PmSTAT affected transcription levels of many genes, regardless of WSSV infection. PmVago1 and PmVago5 were significantly up-regulated in PmSTAT-silenced shrimp (Fig. 1B). PmSTAT silencing also promoted the expression of Spätzle (Fig. 1C), crustinPm1, crustinPm7, and PEN3 (Fig. 1D). PmVago1, crustinPm1, crustinPm7, and PEN3 remained significantly up-regulated in PmSTAT-silenced shrimp upon WSSV infection, suggesting that these genes may play a key role against WSSV in PmSTAT-silenced shrimp. Furthermore, our results showed that PmVago1 and PPAE2 were up-regulated up to 8- and 12-fold during WSSV infection, respectively (Fig. 1B and 1E). Thus, PmVago1 and PPAE2 could be considered biomarkers for WSSV infection.
The dominant bacteria phyla were Proteobacteria in all shrimp conditions (Fig. 2A). This is similar to previous studies in many crustaceans, including Callinectes sapidus, Eriocheir sinensis, Macrobrachium nipponense, Penaeus monodon, Litopenaeus vannamei and copepod species56,57,58,59,60. However, the Proteobacteria population was significantly increased in WSSV-challenged shrimps, similar to the shift of intestinal microbiota reported in E. sinensis and L. vannamei10,56. Additionally, these phyla were the most abundant and increased in shrimps with AHPND60. At the genus level, the abundance of Photobacterium was significantly increased in WSSV-challenged P. monodon, which is similar to the observed in WSSV and AHPND-challenged L. vannamei10,60 (Fig. 2B). At the species level, P. damselae was the most abundant in WSSV-infected shrimp, and P. damselae subsp. damselae has been associated with massive mortality of cultured L. vannamei61. Moreover, P. damselae subsp. damselae is also associated with infections in marine animals, including turbot (Psetta maxima), rainbow trout (Oncorhynchus mykiss), ovate pompano (Trachinotus ovatus), eel (Anguilla reinhardtii), sea bream (Sparus aurata), and mud crab (Scylla paramamosain)62,63,64,65,66. The P. damselae subsp. damselae infecting S. paramamosain and L. vannamei showed hepatopancreatic tubules were necrotic61,66. The mortality of P. damselae subsp. damselae infecting L. vannamei depended on bacterial infection dosage61. Therefore, it is possible that P. damselae subsp. damselae might be an opportunistic pathogen in shrimp during the WSSV invasion. Moreover, the probiotic bacteria, S. algae, was increased in PmSTAT dsRNA compared to PBS and two WSSV groups (Fig. 2D). In L. vannamei juveniles, S. algae was fed as a probiotic for 60 days, improving shrimp body weight and transcription levels of β-1,3-glucan-binding protein (LGBP) which boosted survival rate against V. parahaemolyticus67. In addition, the LvLGBP dsRNA-treated L. vannamei caused shrimp to be more susceptible to V. parahaemolyticus or WSSV68. Furthermore, rPmLGBP improved the in vitro phenoloxidase (PO) activity of hemocyte suspensions18.
The interaction between bacteria inside the community is complex. For example, the genome sequencing of S. algae, isolated in France, revealed bacteriocins and antimicrobial peptides69. The S. algae was increased, while P. damselae subsp. damselae was decreased in PmSTAT-silenced shrimp (Fig. 2C and 2D). The antimicrobial peptides in the Toll pathway, including crustinPm1, crustimPm7, and PEN3, were strongly promoted in PmSTAT-silenced groups and significantly suppressed in the WSSV infected group (Fig. 1D). Thus, these antimicrobial peptides could reduce the population of P. damselae subsp. damselae in PmSTAT-deprived shrimp, giving an advantage in defense against WSSV. These antimicrobial peptides, however, did not kill or inhibit the probiotic S. algae (Fig. 2D).
The WSSV-challenged shrimp (PmSTAT dsRNA + WSSV and WSSV) revealed low richness and diversity (Table 1). Likewise, the bacterial diversity was reduced in shrimp with white feces syndrome (WFS) challenged with V. harveyi7,70. Moreover, the intestines of healthy shrimps also have lower diversity than diseased shrimps with AHPND60. Notably, no changes in microbial diversity in shrimps infected with WSSV and cotton shrimp-like disease were reported10,71. Thus the association of greater diversity with better host health in shrimps is, until now, under discussion8, and more studies are necessary to understand the role of the microbial ecosystem in health and disease in aquatic organisms. The UPGMA clustering and PCoA analysis using the unweighted UniFrac distances revealed clusters separating the PBS and WSSV-challenged shrimps (Fig. 3). A similar separation of the microbiota from the control by WSSV infection was also observed in L. vannamei10. Interestingly the microbiota changes were minimal when we compared the PmSTAT silencing and STAT silencing + WSSV (Fig. 2 and Table 2). This suggests that changes in the microbiota by the PmSTAT silencing were independent of the WSSV infection.
In a murine model, respiratory viral infections induce secondary bacterial infections. The antiviral immune responses induced by influenza are associated with changes in the microbiota in the respiratory and gastrointestinal tract72. The inflammation of the tissues promotes the secretion of type I and II interferons (IFNs), increasing Proteobacteria and Bacteroidetes in the gut73,74. Meanwhile, the depletion of type I IFN-alpha/beta receptor in mice improved clearance of secondary Streptococcus pneumoniae infection during influenza infection75. However, virus infection also promotes probiotic bacteria. For example, Lactobacillales were enriched in HIV patients76. Moreover, bacteria diversity in HIV patients was higher than in the seronegative group77, suggesting that the host immune response shifts the host microbiome. Understanding the interaction between host–pathogen-microbiome could improve strategies to prevent diseases.
Taken together, the shift of immune and immune-related genes could change the bacteria composition in the shrimp intestine, demonstrating the importance of host-microbiota interactions in understanding the diseases. Interestingly, only silencing the PmSTAT caused drastic effects on the microbiota structure compared to the PBS (Fig. 3A), suggesting the importance of the host gene expression to maintain the homeostasis interaction with the microbiota. However, there are limited examples of this relationship in aquatic animals. For instance, in kuruma shrimp (Marsupenaeus japonicus) the silencing of CTL33 expression led directly to intestinal dysbiosis, tissue damage, and shrimp death78, suggesting a fine regulation through the evolution of the intestinal microbiota homeostasis in invertebrates. In this regard, it has also been observed that scallop antimicrobial peptides and proteins are implicated in maintaining microbial homeostasis and are critical molecules in orchestrating host-microbiota interactions79. Our work opens the possibility of using gene silencing to understand the relationship between shrimp microbiota and the host in the absence and diseases.
Methods
This study was conducted under the ethical principles and guidelines according to the animal use protocol 1923021 approved by Chulalongkorn University Animal Care and Use Committee (CU-ACUC). The biosafety guidelines were reviewed and approved by the Institutional Biosafety Committee of Chulalongkorn University (SC-CU-IBC-004–2018). This study was carried out in compliance with the ARRIVE guidelines.
In vitro double-stranded RNA PmSTAT synthesis
Primer pairs used in this experiment are shown in Supplementary Information, Table S439. P. monodon hemocyte cDNA was amplified using PmSTAT DNA fragment containing T7 promotor in the following conditions: 94 °C for 3 min (denaturation), followed by 35 cycles of 94 °C for 30 s, 60 °C for 30 s and 72 °C for 30 s, and a final extension at 72 °C for 10 min. The PCR products were analyzed by 2% agarose gel electrophoresis and were purified from the agarose gel using GeneHlow™ Gel/PCR kit (Geneaid). The purified PCR products were then used as a template for in vitro transcription using T7 RiboMAX™ Express Large-Scale RNA Production System (Promega) according to the manufacturer’s protocol.
PmSTAT silencing shrimp
The black tiger shrimp, P. monodon, of average 3.12 ± 0.17 g bodyweight, were obtained from Charoen Pokphand Farm in Chanthaburi Province, Thailand. Shrimp were acclimated in 120L tanks at ambient temperature and maintained in aerated water with a salinity of 20 ppt for at least one week before beginning the experiments. P. monodon was injected twice with PmSTAR dsRNA (10 µg per g shrimp) at 0 and 16 h after the first injection. Shrimp’s intestines were collected at 24 h post-second injection. Total RNA was extracted using Tissue Total RNA mini kit (Favorgen, Taiwan). The first-strand cDNA was synthesized using the first-strand cDNA Synthesis Kit (Thermo Fisher, USA) according to manufacturer’s protocol. The knockdown efficiency was measured by qRT-PCR using EF-1α as internal control and calculated by the 2−∆∆CT method80.
Sampling
Shrimp were divided into four groups, PBS-injected, PmSTAT-silenced, WSSV-challenged, and PmSTAT-silenced combined with WSSV-challenged. Shrimp were cultured in 20L tanks (1 tank per group) at ambient temperature and maintained in aerated water with a salinity of 20 ppt. Each group contained nine shrimp. In the PmSTAT silenced groups, shrimp were injected with PmSTAT dsRNA 10 µg per gram shrimp body weight, and then after 16 h, they were injected with the same amount of dsRNA. Meanwhile, PBS was injected into the shrimp control set. Approximately 6 × 106 viral copies of WSSV (quantification described in Fernando et al.81) were injected 24 h after the 2nd PmSTAT dsRNA injection. Shrimp’s intestines were collected at 24 h post-WSSV challenge and immediately processed DNA and RNA extraction. Each group contained nine shrimps, and each replicate was pooled from 3 shrimp intestines.
Total RNA and quantitative real-time PCR
Total RNA was isolated by the Tissue Total RNA mini kit (Favorgen, Taiwan) according to the manufacturer’s protocol. An equal amount of total RNA (500 ng) from each sample was used for cDNA synthesis using First-strand cDNA Synthesis Kit (Thermo Fisher). Quantitative real-time RT-PCR using specific primer pair (Supplementary Table 4) for PmSTAT and WSSV immediate-early gene 1 (IE1) was employed to confirm the PmSTAT silencing efficiency, WSSV-challenged and immune-related gene response during WSSV infection by qRT-PCR. Real-time RT-PCR was carried out using an equal amount of cDNAs (2 µl of tenfold diluted cDNA) in the iCycler iQTM Real-Time detection system and the Luna® Universal qPCR Master Mix (Bio-Rad, USA). The qRT-PCR conditions were 95 °C for 30 s, followed by 40 cycles of 95 °C for 5 s and 55 °C for 10 s. The qRT-PCR was done in triplicate. The fold difference of mRNA transcription was calculated by 2−∆∆CT method.
Statistical analysis was carried out using the IBM SPSS Statistics 22 program with one-way ANOVA followed by a post hoc test (Tukey’s). The result differences were considered significant at P < 0.05.
Sample preparation for microbiome study
Total DNA from the intestines was isolated for microbiota study. To this end, the intestines of nine shrimps have been collected from each treatment group, pooling three intestines as a single sample. The DNA of whole intestines was extracted using the DNA by Quick-DNA Fecal/Soil Microbe Miniprep Kit (Zymo Research, USA). The Qubit™ dsDNA HS (Invitrogen, USA) assay was performed to quantify the DNA concentration. The DNA integrity was confirmed using 1% agarose gel electrophoresis. The V3-V4 regions were amplified from genomic DNA using the following conditions: 95 °C for 3 min (denaturation), followed by 25 cycles of 95 °C for 30 s, 55 °C for 30 s, and 72 °C for 30 s, and a final extension at 72 °C for 5 min. The PCR product was analyzed using 2% agarose gel by electrophoresis and purified using Ampure XP beads (Bechman Coulter). All purified amplicon samples were mixed in equal concentrations and sequenced on the Illumina Miseq sequencing platform using 250 base pair (bp) paired-end (PE) chemistry.
Microbiome analysis
The results from sequencing were filtered and analyzed by Quantitative Insights Into Microbial Ecology (QIIME (version 1.8), http://qiime.org/index.html) as previously reported (Caporaso et al., 2010). The filtered sequences were assigned to the same operational taxonomic units (OTUs) with 97% similarity to the Green Genes reference sequence collection. Therefore, the taxonomic information was assigned to the Green Genes reference database. The OTUs at family, genera, and species levels were subjected to a LEfSe analysis to obtain the significantly different taxonomies among treatments with a significant level (alpha) of 0.05 and the LDA threshold > 2. For all data, statistical significance was set at p < 0.05. Alpha diversity index, including Chao1, Observed species, Phylogenetic diversity (PD), and Shannon diversity index, were calculated via QIIME to estimate diversity within the samples. The significant difference in alpha diversity index between groups was carried out using the IBM SPSS Statistics 22 program with one-way ANOVA followed by a post hoc test (Tukey’s). The result differences were considered significant at P < 0.01. Unweight UniFrac distances were calculated using the QIIME program and visualized using PCoA analysis to estimate the beta diversity. In addition, UPGMA (Unweighted Pair Group Method with Arithmetic mean) was analyzed by QIIME using the beta diversity distance matrix to compare between conditions. Finally, Anosim was performed to measure the differences in the bacterial profiles between groups. The resulting P-value indicated a significant difference between the two groups (P-value < 0.01). The distance between centroids of the PCoA (Fig. 3A) was determined with R using the "usedist" package and the matrix obtained of the beta diversity analysis with the unweighted UniFrac distances.
To find the presence of probiotics in our microbiome samples, we followed the analysis used by Ochoa-Romo et al.45. First, we obtained a new BIOM file from the joined sequences and clustered it with a 97% identity level against the Silva132 database. This database was used because it contains the reference of most probiotic bacteria. Afterward, the relative abundance of 70 probiotics taxa was extracted from the BIOM file using the summarize_taxa_throught_plots.py and an in-house script. Lastly, the Wilcoxon test was performed to determine the significant differential abundance of probiotics among tested groups.
Data availability
All data generated or analysed during this study are included in this published article and its supplementary information file.
Abbreviations
- Pm :
-
Penaeus monodon
- WSSV:
-
White spot syndrome virus
References
Bikel, S. et al. Combining metagenomics, metatranscriptomics and viromics to explore novel microbial interactions: Towards a systems-level understanding of human microbiome. Comput. Struct. Biotechnol. J. 13, 390–401. https://doi.org/10.1016/j.csbj.2015.06.001 (2015).
Ringø, E. et al. Effect of dietary components on the gut microbiota of aquatic animals. A never-ending story?. Aquac. Nutr. 22, 219–282. https://doi.org/10.1111/anu.12346 (2015).
Tzuc, J. T., Escalante, D. R., Rojas Herrera, R., Gaxiola Cortes, G. & Ortiz, M. L. Microbiota from Litopenaeus vannamei: Digestive tract microbial community of pacific white shrimp (Litopenaeus vannamei). Springerplus 3, 280. https://doi.org/10.1186/2193-1801-3-280 (2014).
Hooper, L. V. & Macpherson, A. J. Immune adaptations that maintain homeostasis with the intestinal microbiota. Nat. Rev. Immunol. 10, 159–169. https://doi.org/10.1038/nri2710 (2010).
Hooper, L. V., Midtvedt, T. & Gordon, J. I. How host-microbial interactions shape the nutrient environment of the mammalian intestine. Annu. Rev. Nutr. 22, 283–307. https://doi.org/10.1146/annurev.nutr.22.011602.092259 (2002).
Chen, W. Y., Ng, T. H., Wu, J. H., Chen, J. W. & Wang, H. C. Microbiome dynamics in a shrimp grow-out pond with possible outbreak of acute hepatopancreatic necrosis disease. Sci. Rep. 7, 9395. https://doi.org/10.1038/s41598-017-09923-6 (2017).
Hou, D. et al. Intestinal bacterial signatures of white feces syndrome in shrimp. Appl. Microbiol. Biotechnol. 102, 3701–3709. https://doi.org/10.1007/s00253-018-8855-2 (2018).
Holt, C. C., Bass, D., Stentiford, G. D. & van der Giezen, M. Understanding the role of the shrimp gut microbiome in health and disease. J. Invertebr. Pathol. 186, 107387. https://doi.org/10.1016/j.jip.2020.107387 (2021).
Cornejo-Granados, F., Gallardo-Becerra, L., Leonardo-Reza, M., Ochoa-Romo, J. P. & Ochoa-Leyva, A. A meta-analysis reveals the environmental and host factors shaping the structure and function of the shrimp microbiota. PeerJ 6, e5382. https://doi.org/10.7717/peerj.5382 (2018).
Wang, J. et al. White spot syndrome virus (WSSV) infection impacts intestinal microbiota composition and function in Litopenaeus vannamei. Fish Shellfish Immunol. 84, 130–137. https://doi.org/10.1016/j.fsi.2018.09.076 (2019).
Chiu, C. H., Guu, Y. K., Liu, C. H., Pan, T. M. & Cheng, W. Immune responses and gene expression in white shrimp, Litopenaeus vannamei, induced by Lactobacillus plantarum. Fish Shellfish Immunol. 23, 364–377. https://doi.org/10.1016/j.fsi.2006.11.010 (2007).
Kongnum, K. & Hongpattarakere, T. Effect of Lactobacillus plantarum isolated from digestive tract of wild shrimp on growth and survival of white shrimp (Litopenaeus vannamei) challenged with Vibrio harveyi. Fish Shellfish Immunol. 32, 170–177. https://doi.org/10.1016/j.fsi.2011.11.008 (2012).
Duan, Y. et al. Changes in the intestine microbial, digestive, and immune-related genes of Litopenaeus vannamei in response to dietary probiotic Clostridium butyricum supplementation. Front. Microbiol. 9, 2191. https://doi.org/10.3389/fmicb.2018.02191 (2018).
Zheng, D., Liwinski, T. & Elinav, E. Interaction between microbiota and immunity in health and disease. Cell Res. 30, 492–506. https://doi.org/10.1038/s41422-020-0332-7 (2020).
Wang, X. W. & Wang, J. X. Pattern recognition receptors acting in innate immune system of shrimp against pathogen infections. Fish Shellfish Immunol. 34, 981–989. https://doi.org/10.1016/j.fsi.2012.08.008 (2013).
Chen, W. Y. et al. WSSV infection activates STAT in shrimp. Dev. Comp. Immunol. 32, 1142–1150. https://doi.org/10.1016/j.dci.2008.03.003 (2008).
Li, F. & Xiang, J. Signaling pathways regulating innate immune responses in shrimp. Fish Shellfish Immunol. 34, 973–980. https://doi.org/10.1016/j.fsi.2012.08.023 (2013).
Amparyup, P., Sutthangkul, J., Charoensapsri, W. & Tassanakajon, A. Pattern recognition protein binds to lipopolysaccharide and beta-1,3-glucan and activates shrimp prophenoloxidase system. J. Biol. Chem. 287, 10060–10069. https://doi.org/10.1074/jbc.M111.294744 (2012).
Wang, P. H. et al. The shrimp NF-kappaB pathway is activated by white spot syndrome virus (WSSV) 449 to facilitate the expression of WSSV069 (ie1), WSSV303 and WSSV371. PLoS One 6, e24773. https://doi.org/10.1371/journal.pone.0024773 (2011).
Wang, P. H. et al. Molecular cloning, characterization and expression analysis of two novel tolls (LvToll2 and LvToll3) and three putative Spatzle-like toll ligands (LvSpz1-3) from Litopenaeus vannamei. Dev. Comp. Immunol. 36, 359–371. https://doi.org/10.1016/j.dci.2011.07.007 (2012).
Huang, X., Wang, W. & Ren, Q. Dorsal transcription factor is involved in regulating expression of crustin genes during white spot syndrome virus infection. Dev. Comp. Immunol. 63, 18–26. https://doi.org/10.1016/j.dci.2016.05.006 (2016).
Hetru, C. & Hoffmann, J. A. NF-kappaB in the immune response of Drosophila. Cold Spring Harb. Perspect. Biol. 1, a000232. https://doi.org/10.1101/cshperspect.a000232 (2009).
Huang, X. D. et al. Identification and functional study of a shrimp dorsal homologue. Dev. Comp. Immunol. 34, 107–113. https://doi.org/10.1016/j.dci.2009.08.009 (2010).
Li, C. Y. & Song, Y. L. Proline-rich domain of penaeidin molecule exhibits autocrine feature by attracting penaeidin-positive granulocytes toward the wound-induced inflammatory site. Fish Shellfish Immunol. 29, 1044–1052. https://doi.org/10.1016/j.fsi.2010.08.020 (2010).
Visetnan, S., Supungul, P., Hirono, I., Tassanakajon, A. & Rimphanitchayakit, V. Activation of PmRelish from Penaeus monodon by yellow head virus. Fish Shellfish Immunol. 42, 335–344. https://doi.org/10.1016/j.fsi.2014.11.015 (2015).
Jearaphunt, M. et al. Shrimp serine proteinase homologues PmMasSPH-1 and -2 play a role in the activation of the prophenoloxidase system. PLoS One 10, e0121073. https://doi.org/10.1371/journal.pone.0121073 (2015).
Udompetcharaporn, A. et al. Identification and characterization of a QM protein as a possible peptidoglycan recognition protein (PGRP) from the giant tiger shrimp Penaeus monodon. Dev. Comp. Immunol. 46, 146–154. https://doi.org/10.1016/j.dci.2014.04.003 (2014).
Lan, J. F. et al. Characterization of an immune deficiency homolog (IMD) in shrimp (Fenneropenaeus chinensis) and crayfish (Procambarus clarkii). Dev. Comp. Immunol. 41, 608–617. https://doi.org/10.1016/j.dci.2013.07.004 (2013).
Feng, N., Wang, D., Wen, R. & Li, F. Functional analysis on immune deficiency (IMD) homolog gene in Chinese shrimp Fenneropenaeus chinensis. Mol. Biol. Rep. 41, 1437–1444. https://doi.org/10.1007/s11033-013-2988-2 (2014).
Wang, S. et al. Identification and functional characterization of the TAB2 gene from Litopenaeus vannamei. Fish Shellfish Immunol. 46, 206–216. https://doi.org/10.1016/j.fsi.2015.06.024 (2015).
Wang, S. et al. Shrimp TAB1 interacts with TAK1 and p38 and activates the host innate immune response to bacterial infection. Mol. Immunol. 88, 10–19. https://doi.org/10.1016/j.molimm.2017.05.016 (2017).
Wang, S. et al. Identification and characterization of transforming growth factor beta-activated kinase 1 from Litopenaeus vannamei involved in anti-bacterial host defense. Fish Shellfish Immunol. 52, 278–288. https://doi.org/10.1016/j.fsi.2016.03.149 (2016).
Wang, P. H. et al. The shrimp IKK-NF-kappaB signaling pathway regulates antimicrobial peptide expression and may be subverted by white spot syndrome virus to facilitate viral gene expression. Cell Mol. Immunol. 10, 423–436. https://doi.org/10.1038/cmi.2013.30 (2013).
Qiu, W. et al. Litopenaeus vannamei NF-kappaB is required for WSSV replication. Dev. Comp. Immunol. 45, 156–162. https://doi.org/10.1016/j.dci.2014.02.016 (2014).
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 5, 441–450. https://doi.org/10.1016/s1534-5807(03)00244-2 (2003).
Barillas-Mury, C., Han, Y. S., Seeley, D. & Kafatos, F. C. Anopheles gambiae Ag-STAT, a new insect member of the STAT family, is activated in response to bacterial infection. EMBO J. 18, 959–967. https://doi.org/10.1093/emboj/18.4.959 (1999).
Boutros, M., Agaisse, H. & Perrimon, N. Sequential activation of signaling pathways during innate immune responses in Drosophila. Dev. Cell 3, 711–722. https://doi.org/10.1016/s1534-5807(02)00325-8 (2002).
Li, C. et al. Activation of Vago by interferon regulatory factor (IRF) suggests an interferon system-like antiviral mechanism in shrimp. Sci. Rep. 5, 15078. https://doi.org/10.1038/srep15078 (2015).
Wen, R., Li, F., Li, S. & Xiang, J. Function of shrimp STAT during WSSV infection. Fish Shellfish Immunol. 38, 354–360. https://doi.org/10.1016/j.fsi.2014.04.002 (2014).
Liu, W. J., Chang, Y. S., Wang, A. H., Kou, G. H. & Lo, C. F. White spot syndrome virus annexes a shrimp STAT to enhance expression of the immediate-early gene ie1. J. Virol. 81, 1461–1471. https://doi.org/10.1128/JVI.01880-06 (2007).
Liu, L.-K. et al. A cytokine receptor domeless promotes white spot syndrome virus infection via JAK/STAT signaling pathway in red claw crayfish Cherax quadricarinatus. Dev. Comp. Immunol. 111, 103749. https://doi.org/10.1016/j.dci.2020.103749 (2020).
Yan, M. et al. Identification of a JAK/STAT pathway receptor domeless from pacific white shrimp Litopenaeus vannamei. Fish Shellfish Immunol. 44, 26–32. https://doi.org/10.1016/j.fsi.2015.01.023 (2015).
Fu, Z. D., Selwyn, F. P., Cui, J. Y. & Klaassen, C. D. RNA-Seq profiling of intestinal expression of xenobiotic processing genes in germ-free mice. Drug Metab. Dispos. Biological Fate Chem. 45, 1225–1238. https://doi.org/10.1124/dmd.117.077313 (2017).
Davison, J. M. et al. Microbiota regulate intestinal epithelial gene expression by suppressing the transcription factor hepatocyte nuclear factor 4 alpha. Genome Res. 27, 1195–1206. https://doi.org/10.1101/gr.220111.116 (2017).
Ochoa-Romo, J. P. et al. Agavin induces beneficial microbes in the shrimp microbiota under farming conditions. Sci. Rep. 12, 6392. https://doi.org/10.1038/s41598-022-10442-2 (2022).
Wang, C. et al. Phosphorylation of shrimp Tcf by a viral protein kinase WSV083 suppresses Its antiviral effect. Front Immunol. 12, 698697. https://doi.org/10.3389/fimmu.2021.698697 (2021).
Ren, Q. et al. Two white spot syndrome virus microRNAs target the dorsal gene to promote virus infection in Marsupenaeus japonicus shrimp. J Virol 91, e02261-e2216. https://doi.org/10.1128/JVI.02261-16 (2017).
Arayamethakorn, S., Supungul, P., Tassanakajon, A. & Krusong, K. Characterization of molecular properties and regulatory pathways of CrustinPm1 and CrustinPm7 from the black tiger shrimp Penaeus monodon. Dev. Comp. Immunol 67, 18–29. https://doi.org/10.1016/j.dci.2016.10.015 (2017).
Hou, F. et al. RNAi knock-down of shrimp Litopenaeus vannamei Toll gene and immune deficiency gene reveals their difference in regulating antimicrobial peptides transcription. Dev. Comp. Immunol. 44, 255–260. https://doi.org/10.1016/j.dci.2014.01.004 (2014).
Amparyup, P., Charoensapsri, W. & Tassanakajon, A. Prophenoloxidase system and its role in shrimp immune responses against major pathogens. Fish Shellfish Immunol. 34, 990–1001. https://doi.org/10.1016/j.fsi.2012.08.019 (2013).
Charoensapsri, W., Amparyup, P., Hirono, I., Aoki, T. & Tassanakajon, A. Gene silencing of a prophenoloxidase activating enzyme in the shrimp, Penaeus monodon, increases susceptibility to Vibrio harveyi infection. Dev. Comp. Immunol. 33, 811–820. https://doi.org/10.1016/j.dci.2009.01.006 (2009).
Amparyup, P., Charoensapsri, W. & Tassanakajon, A. Two prophenoloxidases are important for the survival of Vibrio harveyi challenged shrimp Penaeus monodon. Dev. Comp. Immunol. 33, 247–256. https://doi.org/10.1016/j.dci.2008.09.003 (2009).
Pang, Z., Kim, S. K., Yu, J. & Jang, I. K. Distinct regulation patterns of the two prophenoloxidase activating enzymes corresponding to bacteria challenge and their compensatory over expression feature in white shrimp (Litopenaeus vannamei). Fish Shellfish Immunol. 39, 158–167. https://doi.org/10.1016/j.fsi.2014.04.026 (2014).
Xiao, B. et al. Penaeidins restrict white spot syndrome virus infection by antagonizing the envelope proteins to block viral entry. Emerg. Microbes Infect. 9, 390–412. https://doi.org/10.1080/22221751.2020.1729068 (2020).
Wu, B., Zhang, C., Qin, X., Shi, L. & Zhao, M. Identification and function of penaeidin 3 and penaeidin 5 in Fenneropenaeus merguiensis. Fish Shellfish Immunol. 89, 623–631. https://doi.org/10.1016/j.fsi.2019.04.032 (2019).
Ding, Z. F., Cao, M. J., Zhu, X. S., Xu, G. H. & Wang, R. L. Changes in the gut microbiome of the Chinese mitten crab (Eriocheir sinensis) in response to white spot syndrome virus (WSSV) infection. J. Fish Dis. 40, 1561–1571. https://doi.org/10.1111/jfd.12624 (2017).
Givens, C. E., Burnett, K. G., Burnett, L. E. & Hollibaugh, J. T. Microbial communities of the carapace, gut, and hemolymph of the Atlantic blue crab Callinectes sapidus. Mar. Biol. 160, 2841–2851. https://doi.org/10.1007/s00227-013-2275-8 (2013).
Gerdts, G. et al. The microbiome of north Sea copepods. Helgol. Mar. Res. 67, 757–773. https://doi.org/10.1007/s10152-013-0361-4 (2013).
Tzeng, T. D. et al. Effects of host phylogeny and habitats on gut microbiomes of oriental river prawn (Macrobrachium nipponense). PLoS One 10, 0132860. https://doi.org/10.1371/journal.pone.0132860 (2015).
Cornejo-Granados, F. et al. Microbiome of pacific whiteleg shrimp reveals differential bacterial community composition between wild, aquacultured and AHPND/EMS outbreak conditions. Sci. Rep. 7, 11783. https://doi.org/10.1038/s41598-017-11805-w (2017).
Wang, Z. et al. A novel research on isolation and characterization of Photobacterium damselae subsp. damselae from pacific white shrimp, Penaeus vannamei, displaying black gill disease cultured in China. J. Fish Dis. 43, 551–559. https://doi.org/10.1111/jfd.13153 (2020).
Rivas, A. J., Lemos, M. L. & Osorio, C. R. Photobacterium damselae subsp. damselae, a bacterium pathogenic for marine animals and humans. Front. Microbiol. 4, 283. https://doi.org/10.3389/fmicb.2013.00283 (2013).
Pedersen, K., Skall, H. F., Lassen-Nielsen, A. M., Bjerrum, L. & Olesen, N. J. Photobacterium damselae subsp. damselae, an emerging pathogen in danish rainbow trout, Oncorhynchus mykiss (Walbaum), mariculture. J. Fish Dis. 32, 465–472. https://doi.org/10.1111/j.1365-2761.2009.01041.x (2009).
Ketterer, P. J. & Eaves, L. E. Deaths in captive eels (Anguila reinhardtii) due to Photobacterium (Vibrio) damsela. Aust. Vet. J. 69, 203–204. https://doi.org/10.1111/j.1751-0813.1992.tb07528.x (1992).
Zhao, D. H. et al. Characterization of two phenotypes of Photobacterium damselae subsp. damselae isolated from diseased juvenile Trachinotus ovatus Reared in cage mariculture. J. World Aquac. Soc. 40, 281–289. https://doi.org/10.1111/j.1749-7345.2009.00251.x (2009).
Xie, J. et al. First report of Photobacterium damselae subsp damselae infection in the mud crab Scylla paramamosain cultured in China. Aquaculture 530, 735880. https://doi.org/10.1016/j.aquaculture.2020.735880 (2021).
Interaminense, J. A. et al. Effects of dietary Bacillus subtilis and Shewanella algae in expression profile of immune-related genes from hemolymph of Litopenaeus vannamei challenged with Vibrio parahaemolyticus. Fish Shellfish Immunol. 86, 253–259. https://doi.org/10.1016/j.fsi.2018.11.051 (2019).
Phupet, B., Pitakpornpreecha, T., Baowubon, N., Runsaeng, P. & Utarabhand, P. Lipopolysaccharide- and beta-1,3-glucan-binding protein from Litopenaeus vannamei: Purification, cloning and contribution in shrimp defense immunity via phenoloxidase activation. Dev. Comp. Immunol. 81, 167–179. https://doi.org/10.1016/j.dci.2017.11.016 (2018).
Cimmino, T., Olaitan, A. O. & Rolain, J. M. Whole genome sequence to decipher the resistome of Shewanella algae, a multidrug-resistant bacterium responsible for pneumonia, Marseille France. Expert Rev. Anti-infect. Ther. 14, 269–275. https://doi.org/10.1586/14787210.2016.1106936 (2016).
Rungrassamee, W., Klanchui, A., Maibunkaew, S. & Karoonuthaisiri, N. Bacterial dynamics in intestines of the black tiger shrimp and the pacific white shrimp during Vibrio harveyi exposure. J. Invertebr. Pathol. 133, 12–19. https://doi.org/10.1016/j.jip.2015.11.004 (2016).
Zhou, L. et al. Intestinal bacterial signatures of the “cotton shrimp-like” disease explain the change of growth performance and immune responses in pacific white shrimp (Litopenaeus vannamei). Fish Shellfish Immunol. 92, 629–636. https://doi.org/10.1016/j.fsi.2019.06.054 (2019).
Hanada, S., Pirzadeh, M., Carver, K. Y. & Deng, J. C. Respiratory viral infection-induced microbiome alterations and secondary bacterial pneumonia. Front. Immunol. 9, 2640. https://doi.org/10.3389/fimmu.2018.02640 (2018).
Dominguez-Cherit, G. et al. Critically Ill patients with 2009 influenza A(H1N1) in Mexico. JAMA 302, 1880–1887. https://doi.org/10.1001/jama.2009.1536 (2009).
Wang, J. et al. Respiratory influenza virus infection induces intestinal immune injury via microbiota-mediated Th17 cell-dependent inflammation. J. Exp. Med. 211, 2397–2410. https://doi.org/10.1084/jem.20140625 (2014).
Shahangian, A. et al. Type I IFNs mediate development of postinfluenza bacterial pneumonia in mice. J. Clin. Investig. 119, 1910–1920. https://doi.org/10.1172/jci35412 (2009).
Perez-Santiago, J. et al. Gut Lactobacillales are associated with higher CD4 and less microbial translocation during HIV infection. AIDS (London, England) 27, 1921–1931. https://doi.org/10.1097/qad.0b013e3283611816 (2013).
Mutlu, E. A. et al. A compositional look at the human gastrointestinal microbiome and immune activation parameters in HIV infected subjects. Plos Pathog. 10, e1003829. https://doi.org/10.1371/journal.ppat.1003829 (2014).
Zhang, Y. X., Zhang, M. L. & Wang, X. W. C-type lectin maintains the homeostasis of intestinal microbiota and mediates biofilm formation by intestinal bacteria in shrimp. J. Immunol. 206, 1140–1150. https://doi.org/10.4049/jimmunol.2000116 (2021).
Gonzalez, R. et al. Host defense effectors expressed by hemocytes shape the bacterial microbiota from the scallop hemolymph. Front. Immunol. 11, 599625. https://doi.org/10.3389/fimmu.2020.599625 (2020).
Livak, K. J. & Schmittgen, T. D. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods 25, 402–408. https://doi.org/10.1006/meth.2001.1262 (2001).
Mendoza-Cano, F. & Sánchez-Paz, A. Development and validation of a quantitative real-time polymerase chain assay for universal detection of the white spot syndrome virus in marine crustaceans. Virol. J. 10, 186. https://doi.org/10.1186/1743-422x-10-186 (2013).
Acknowledgements
We acknowledge Chulalongkorn University for supporting T.J. via the The Second Century Fund (C2F) and P.L. via the 100th Anniversary Chulalongkorn University Fund for Doctoral Scholarship, the 90th Anniversary of Chulalongkorn University Fund, and the Overseas Research Experience Scholarship for Graduate Student from the Graduate School. This research was funded by Ratchadaphiseksomphot Endowment Fund, Food and Economic Animals (RCU_F_64_005_23), Center of Excellence in Structural and Computational Biology (to K.K) and Center of Excellence for Molecular Biology and Genomics of Shrimp (to A.T.). An additional support came from the Genomics Research Network on Disease Resistance in Shrimp (IRN61W0001). The current study was also funded by DGAPA PAPPIT UNAM IN215520 and CONACYT grant Ciencia-Frontera-2019-263986 to A.O.L. We also thank Juan Manuel Hurtado Ramírez from IBT-UNAM for informatics technical support for server maintenance.
Author information
Authors and Affiliations
Contributions
T.J. and P.L. conducted gene silencing and real-time experiments. T.J. and F.S.L. prepared samples for microbiome study. T.J. and J.P.O. analyzed the microbiome data with help from L.G.B. A.T. provided resources and equipment. A.O.L. supervised T.J. and analyzed the data. K.K. conceived and supervised the project and contribute to data analysis. T.J. wrote the first draft. A.O.L. and K.K. edited the manuscript. All authors reviewed the results and approved the final version of the manuscript.
Corresponding authors
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Jatuyosporn, T., Laohawutthichai, P., Romo, J.P.O. et al. White spot syndrome virus impact on the expression of immune genes and gut microbiome of black tiger shrimp Penaeus monodon. Sci Rep 13, 996 (2023). https://doi.org/10.1038/s41598-023-27906-8
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-023-27906-8
This article is cited by
-
Effects of PmDOME and PmSTAT knockdown on white spot syndrome virus infection in Penaeus monodon
Scientific Reports (2023)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.