ORIGINAL RESEARCH article
Volume 10 - 2019 | https://doi.org/10.3389/fmicb.2019.00624
Impacts of Duck-Origin Parvovirus Infection on Cherry Valley Ducklings From the Perspective of Gut Microbiota
- 1Key Laboratory of Animal Disease and Human Health of Sichuan Province, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China
- 2Laboratory of Experimental Animal Disease Model, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China
Duck-origin goose parvovirus (D-GPV) is the causative agent of beak atrophy and dwarfism syndrome (BADS), characterized by growth retardation, skeletal dysplasia, and persistent diarrhea. However, the pathogenic mechanism of D-GPV remains undefined. Here, we first reported the gut microbiome diversity of D-GPV infected Cherry Valley ducks. In the investigation for the influence of D-GPV infection on gut microbiota through a period of infection, we found that D-GPV infection caused gut microbiota dysbiosis by reducing the prevalence of the dominant genera and decreasing microbial diversity. Furthermore, exfoliation of the intestinal epithelium, proliferation of lymphocytes, up-regulated mRNA expression of pro-inflammatory TNF-α, IL-1β, IL-6, IL-17A, and IL-22 and down-regulated mRNA expression of anti-inflammatory IL-10 and IL-4 occurred when D-GPV targeted in cecal epithelium. In addition, the content of short chain fatty acids (SCFAs) in cecal contents was significantly reduced after D-GPV infection. Importantly, the disorder of pro-inflammatory and anti-inflammatory cytokines was associated with the decrease of SCFAs-producing bacteria and the enrichment of opportunistic pathogens. Collectively, the decrease of SCFAs and the enrichment of pathogen-containing gut communities promoted intestinal inflammatory injury. These results may provide a new insight that target the gut microbiota to understand the progression of BADS disease and to research the pathogenic mechanism of D-GPV.
The diverse array of host characteristics can be influenced by the gut microbiota, including nutrition and metabolism, innate and adaptive immunity, mucus composition, proliferation and differentiation of enterocyte, and resistance to pathogen colonization (Hooper et al., 2012; Tremaroli and Bäckhed, 2012; Kim et al., 2016). There are several billions of bacteria, including pathogenic and non-pathogenic species, the commensal and the opportunistic bacteria, present in poultry intestines where is one of the primary sites of exposure to pathogens (Adegunloye, 2006). The commensal bacteria could cause pathology after translocation through the mucosa or under the condition of immunodeficiency, even though most of the bacteria are symbiotic (Marchetti et al., 2008; Glavan et al., 2016). Significant shifts in the microbiota are one of the characteristics of acute mucosal infections, a phenomenon known as dysbiosis (Spor et al., 2011). Furthermore, the infections of gastrointestinal tract can also promote expansion of commensal bacteria with pro-inflammatory potential which can directly exacerbate the pathological process (Egan et al., 2011). Thus, infections can threaten the homeostatic relationship between the host and its gut microbiota in this highly reactive environment. Considering the potential relationships between the gut microbiota and viral infection (Wilks and Golovkina, 2012; Lynch, 2014) and the vital roles of the gut microbiota in regulating the immunity and inflammatory disease (Nobuhiko et al., 2013; Sun et al., 2015). It is vitally important to understand how the composition of the gut microbiota alters as a consequence of Duck-origin Parvovirus (D-GPV) infection and the meanings of these alterations on the pathogenic mechanism of pathogen.
Duck-origin Parvovirus, a novel Goose Parvovirus, is the pathogen of the beak atrophy and dwarfism syndrome (BADS), and has been emerging as a severe threat to the health of duck flocks since 2015 in China (Chen et al., 2015). D-GPV was highly pathogenic to mule ducks and Cherry Valley ducks, and all experimentally infected ducks exhibited atrophic beak, projecting tongue, remarkable growth retardation, skeletal dysplasia and diarrhea similar to naturally infected ducks (Chen H. et al., 2016; Ning et al., 2018). Due to the significant growth retardation, BADS has caused great economic losses to China. Here, we reported an isolate of D-GPV (QH-L01) isolated from Cherry Valley ducks with BADS, a distinct GPV variant strain, which was most closely related to SYG26-35 GPV strains (Chen et al., 2017). Notably, the gastrointestinal abnormalities of diarrhea, weight loss and malnutrition have been observed in BADS ducks. However, the reason of gastrointestinal abnormalities symptoms caused by D-GPV infection is still unclear. Furthermore, there are currently no researches on how D-GPV affects gut microbiota or intestinal health.
To date, the influence of D-GPV infection on gut microbiota of Cherry Valley ducks has not been previously reported. In this study, the cecal microbiota of Cherry Valley ducks were analyzed in order to determine whether potential associations exist between the gut microbiota and gastrointestinal abnormalities after D-GPV infection in a typical industry growth period. Our study would provide the initial basis for understanding the interaction between D-GPV and gut microbiota of Cherry Valley duck.
Materials and Methods
Duck-Origin Parvovirus and Experimental Animals
The D-GPV strain, QH-L01, was originally isolated from the liver of the Cherry Valley duckling flock with BADS in Sichuan province, China (Chen et al., 2017). Forty 2-day-old Cherry Valley ducklings free of specific maternal antibodies were obtained from the breeding facility of the Institute of Poultry Sciences in Sichuan Agricultural University, China. Referring to our previous study (Chen et al., 2017), the titer of QH-L01 was calculated at 106.54 EID50/0.2 mL for intramuscular challenge.
Forty Cherry Valley ducklings, 2-day-old and free from specific maternal antibodies, were randomly allocated into infection group and control group, housed in isolated animal houses and supplied commercial forage of ducklings (TONGWEI Co., Ltd., China) and water ad libitum. The commercial forage for ducklings mainly included 20% protamine, 3.9% crude fiber, 1.1% calcium, and 0.5% phosphorus as detailed in Supplementary Table S1. Twenty ducklings of infection group were inoculated with D-GPV QH-L01 at 106.54 EID50/0.2 mL through intramuscular injection at 2 days of age. Twenty ducklings of control group were inoculated with an equivalent volume of sterile phosphate buffered saline (PBS). Daily clinical symptoms and body weight were monitored, and ten ducklings from infection and control groups were euthanized and autopsied at 6 and 15 days post infection (dpi) until the experiments were completed, respectively. Animal experimentation protocols were approved by the Institutional Animal Care and Use Committee of Sichuan Agricultural University, following the guidelines on animal experiments under the permit No.DY-S20164037.
All infected ducklings were identified as positive infection by PCR analysis of cloacal swabs as described in our previous study (Luo et al., 2019). The unilateral caeca (cecal tissue and contents) of each animal were removed aseptically, and stored at -80°C until they were processed for total cecal microbial DNA analyses. The one-half of another unilateral caeca tissue and contents were collected and stored at -80°C for RNA isolation and the analysis of short-chain fatty acids (SCFAs). The remaining half of unilateral caeca samples from each ducks was fixed in 4% paraformaldehyde and embedded in paraffin wax, then cut into 5 μm thick sections. Sections were stained with hematoxylin and eosin (H&E) and detected virus antigen with immunohistochemical (IHC) staining.
Bacterial DNA Isolation
Bacterial DNA was extracted for broad-range amplification and sequence analysis of bacterial 16S rRNA genes as detailed in Supplementary Materials. In brief, bacterial DNA was extracted from cecum and its contents using the Fast DNA SPIN extraction kits (MP Biomedicals, Santa Ana, CA, United States), following the manufacturer’s instructions. The quantity and quality of extracted DNAs were measured using a NanoDrop ND-1000 spectrophotometer (Thermo Fisher Scientific, Waltham, MA, United States) and agarose gel electrophoresis, respectively.
Bacterial 16S rRNA Gene Sequencing
Bacterial communities of cecal contents and mucosa-adherent bacteria were determined by Illumina MiSeq sequencing of 16S rRNA genes V3–V4 region, and the caeca samples were collected from D-GPV-infected ducks and healthy control ducks at 6 dpi and 15 dpi, respectively. The bacterial V3–V4 region of 16S rRNA genes was amplified using the forward primer 338F (5′-ACTCCTACGGGAGGCAGCA-3′) and the reverse primer 806R (5′-GGACTACHVGGGTWTCTAAT-3′). After purifying the PCR amplicons followed by the quantification of DNA concentration, amplicons were pooled in equal amounts, and pair-end 2 × 300bp sequencing was performed using the Illlumina MiSeq platform with MiSeq Reagent Kit v3 at Shanghai Personal Biotechnology Co., Ltd (Shanghai, China). The sequencing data were deposited into the Sequence Read Archive (SRA) of NCBI (Accession No. SRP182571). The Quantitative Insights Into Microbial Ecology (QIIME, v1.8.0) pipeline was employed to process the sequencing data, as previously described (Caporaso et al., 2010). After quality filters, the remaining high-quality sequences were clustered into operational taxonomic units (OTUs) at 97% sequence identity by UCLUST and as detailed in Supplementary Materials.
Determination of SCFAs in Cecum
The SCFAs of cecal contents were extracted by the method as described by Baere et al. (2013) with slight modification. Weight 1 g of cecal contents samples were used to dilute at ratio 1:4 to 1:8 (w/v) in sterile distilled water. After vortex mixing for 1 min followed by centrifuge at 5,000 ×g for 10 min, the SCFAs-containing supernatant was filtered through cellulose acetate membrane with a pore size of 0.22 μm. SCFAs analyses were carried out by using HPLC as described by Hudafaujan et al. (2010) method.
Immunohistochemical and Histopathological Analyses
All procedures of IHC staining were performed following the previously described protocols (Chen et al., 2009). Rabbit monoclonal antibody against GPV VP3 protein (Beijing Bioss Biotechnology Co., Ltd., China) was diluted in 1:200, as the primary antibody. After incubating with the primary antibody overnight at 4°C followed by washing three times with PBS, the sections were incubated with mouse anti-rabbit secondary antibody (Biotin-Streptavidin HRP Detection Systems, Boster Biological Technology Co., Ltd., China) for 30 min at 37°C. The positive staining cells appeared dark-brown, denoting the existence of D-GPV antigen, while the negative staining cells were blue under light microscope (Nikon 80i). Caeca samples of the proximal ileum were concurrently stained with H&E prior to catching under a light microscope to assess the histopathology. Ten complete structures of the villus height and crypt depth of every sample were measured using Image-Pro Plus 6.0 (Media Cybernetics, Silver Spring, MD, United States), and the villus height and crypt depth (V/C) ratios were calculated.
RNA Preparation and Quantitative RT-PCR
Total RNA was isolated from selected cecum using RNAiso Plus reagent [Takara Biomedical Technology (Beijing) Co., Ltd]. Complementary DNA (cDNA) was synthesized using PrimeScriptTM RT reagent Kit with gDNA Eraser (Perfect Real Time) [Takara Biomedical Technology (Beijing) Co., Ltd] in accordance with the manufacturer’s instructions. Real-time PCR reactions was performed with final concentrations of 2 × TB Green Premix DimerEraser [Takara Biomedical Technology (Beijing) Co., Ltd], and 0.3 μM forward and reverse primers in 25 μL, using the following conditions: 95°C for 30 s; 40 cycles of 95°C (5 s) and 60°C (30 s) in the Bio-Rad CFX96 Real-Time Detection System (Bio-Rad, United States). The PCR products were detected and monitored by direct measurement of the fluorescence intensity. All measurements were performed in triplicate.
For analysis, target gene expression of each sample was normalized to the house-keeping gene, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), following a previously described protocol (Nair et al., 2011). The 2-ΔΔCT method was used to analyze the results of the qPCR. Sequences of primers used for qRT-PCR specific for cytokines of ducks, were shown in Table 1, including pro-inflammatory TNF-α, IL-1β, IL-6, IL-17A, and IL-22, as well as anti-inflammatory IL-10 and IL-4. Results were expressed as mean ± SEM.
Statistical and Bioinformatics Analysis
The SPSS software package 20.0 (SPSS v. 16, SPSS Inc., Chicago, IL, United States) was used for the statistical calculations in this study. After confirming the normal distribution of variables by the Shapiro–Wilk test, two-tailed Student’s t-test and the post hoc ANOVA was performed to analyze the variables of normal distribution, and means were considered significantly different at a P < 0.05, and summary of P-values for multiple comparisons are presented as P < 0.01 and P < 0.05. When data was not normally distributed it was log-transformed.
The QIIME (v1.8.0) and R packages (v3.2.0) were employed to process the sequence data. OTU-level alpha diversity indices, such as Chao1 richness estimator, ACE metric, Shannon diversity index, and Simpson index, were calculated using the OTU table in QIIME (Hughes et al., 2001). The beta diversity analysis, which utilized UniFrac distance metrics to investigate the structural variation of microbial communities across samples, and visualized via principal coordinate analysis (PCoA) and unweighted pair-group method with arithmetic means (UPGMA) hierarchical clustering, was conducted with R software. LEfSe (Linear discriminant analysis effect size) was performed to detect differentially abundant taxa across groups using the default parameters. Spearman rank correlation tests were performed to evaluate associations between two variables, and P-values were adjusted for false discovery rate according to Bonferroni and Hochberg procedure (Benjamini and Hochberg, 1995).
Characteristics of the Samples and 16S rRNA Gene Sequence Data
After quality trimming and chimera detection followed sample rarefaction, an average of 45,473 high-quality sequences (range from 47,448 to 54,488) remained. In total, sequences from the cecal microflora could be classified into 43 genera in control group of 6 days (C-6d, n = 8), 47 genera in D-GPV infection group of 6 days (I-6d, n = 9), 60 genera in control group of 15 days (C-15d, n = 10) and 55 genera in D-GPV infection group of 15 days (I-15d, n = 10), respectively. Basic information for samples, including accession numbers, sequencing reads, length distribution statistics of sequence, species accumulation curves, the number of taxa observed, and rank abundance curve are reported in Supplementary Table S2 and Supplementary Figure S1.
D-GPV Infection Reduced the Microbial Diversity and Altered the Structure of Community in the Ceca
Multiple alpha diversity metrics of richness and diversity revealed obvious distinctions among microbial populations at different post-infection time. At 6 dpi, the sample richness and diversity showed no significant difference (P > 0.05) between control group and D-GPV infection group reflected by the abundance index Ace, Chao, and Simpson. However, a significant decrease in diversity reflected by the Shannon analyses from D-GPV infected ducks at 15 dpi (P = 0.042) (Figure 1A). Generally, the alpha diversity metrics of richness (Chao1 and ACE) and diversity (Simpson and shannon) in the microbial populations significantly increased (P < 0.05) with ducks maturing in the case of uninfected. In contrast, there is no significant difference between the two infection groups with ducks maturing. Collectively, these data suggested that the increase of diversity of the microbial populations was blocked with the extension of D-GPV infection time.
Figure 1. D-GPV infection reduced the microbial diversity and altered the structure of community in the ceca. (A) Richness and diversity within caecal microbial from uninfected and D-GPV infected ducks. Values are shown as min to max with the mean value calculated for each groups. Statistical tests were performed using post hoc ANOVA and ns indicated no significant difference. (B) Principal coordinate analysis of unweighted UniFrac distances. Samples are colored by different group— Blue, Control-6 days (C-6d, n = 8); Red, D-GPV infection-6 days (I-6d, n = 9); Green, Control-15 days (C-15d, n = 10); Purple, D-GPV infection-15 days (I-15d, n = 10). Axes are scaled by the percent of variation explained by each principal coordinate. (C) Cluster analysis based on unweighted unifrac distance UPGMA. In order to examine the global differences in bacterial composition between the D-GPV infected ducks and the controls over time, we calculated distances between each sample using the unweighted Unifrac. Samples are colored by different group same as (B).
To uncover relationships based on presence or absence of bacterial groups as well as their phylogenetic relatedness, we performed a Principal coordinates (PCoA) analysis of the samples using the phylogenetic-tree-based Unifrac metric. In unweighted UniFrac PCoA, each sample represents a point in multidimensional space based on the composition of the bacterial population in each sample using PC1, PC2, and PC3 (20.6%, 13.50%, and 8.08%, respectively, of the explained variance), and closeness of two points in the PCoA denotes similar bacterial population composition between the samples (Figure 1B). The samples from 6 dpi were separated from 15 dpi on a distinct PC1 axis of variation (left to right), and the separation effect of D-GPV infection groups from control groups on PC3 axis (bottom to top) was better than that of PC2 axis. The analysis showed distinct clustering of microbial communities associated with D-GPV infection and age (or post-infection times), and suggested the distinction between D-GPV infected and control ducks of major shift in the composition of cecal microbiota.
Analysis of similarities (ANOSIM) based on unweighted UniFrac distances for measuring beta-diversity showed that differences among all pairwise comparisons between different groups was statistically significant (P < 0.01, AMOVA) (Table 2). The result of samples from D-GPV infection groups clustered differently with those from controls was additionally confirmed by Hierarchical clustering of the samples based on the unweighted pair group method with arithmetic mean (UPGMA) using the unweighted UniFrac (Figure 1C).
D-GPV-Associated Alterations in Cecal Microbiota
Interestingly, the effects of D-GPV infection on gut microbes varied with growth and development of ducklings. The Bacteroidetes, Firmicutes, and Proteobacteria were the three most dominant phyla detected within caecum of both controls and D-GPV-infection groups (Figure 1C). As noted before, the diversity and spatial structure of gut microbes changed with D-GPV infected period and ages, which were confirmed in microbial composition of phylum level (Figure 2). In the control groups (C-6d and C-15d), there were no significant differences in the major phyla of Bacteroidetes, Firmicutes, and Proteobacteria between 6 dpi and 15 dpi, while the Actinobacteria (P = 0.004), Tenericutes (P = 0.046) and Verrucomicrobia (P = 0.049) were enriched from 6 dpi to 15 dpi, which was consistent with the increase of alpha diversity among control groups. Although there was no difference in alpha diversity between the two infection groups (I-6d and I-15d), the increase relative abundance of Actinobacteria (P < 0.001) existed in the course of infection (from 6 dpi to 15 dpi). When compared with control group, D-GPV infection significantly increased the relative abundance of Tenericutes (P = 0.043) at 6 dpi and Actinobacteria (P = 0.011) at 15 dpi, but decreased the relative abundance of Firmicutes (P = 0.048) at 15 dpi. Furthermore, the colonization of Verrucomicrobia was observed in control group at 15 dpi, while there was no Verrucomicrobia in D-GPV infection group. Therefore, the decreased Shannon index was related to the decrease of Firmicutes and Verrucomicrobia during D-GPV infection.
Figure 2. Comparison of the relative abundance of the Bacteroidetes, Firmicutes, Proteobacteria, Actinobactria, Tenericutes, and Verrucomicrobia phyla within groups. Values are shown as a fraction of the total bacteria detected within each samples. Lines represent the median value. Statistical tests were performed using post hoc ANOVA and ns indicated no significant difference.
Moreover, consistent with beta diversity, clustering analysis of the top 68 genera highlighted differences in their distributions due to D-GPV infection (Figure 3). To identify the specific bacterial taxa associated with D-GPV infection, the linear discriminant analysis (LDA) effect size (LEfSe) method was used to compare the cecal microbiota of healthy controls and D-GPV-infected ducks. The greatest differences in taxa at 6 dpi and 15 dpi between the two communities were, respectively, displayed by the cladogram representative of the structure of cecal microbiota and the predominant bacteria (Figure 4). Some bacteria in the cecal samples sharply varied from the genus classification level. D-GPV infection significantly reduced the relative abundance of genera Streptococcus, Parabacteroides, Enterococcus, and Pretococcus (LDA >2) and increased the relative abundance of genera Anaeroplasma, Eggerthella, Anaerotruncus, Collinsella, Coprobacillus, and Eubacterium (LDA >2) compared with control group at 6 dpi (Figures 4A,B). Additionally, the significant decrease relative abundance of genera Streptococcus, Parabacteroides, Prevotella, Paraprevotella, Lactobacillus, Barnesiella, Butyricimonas, Faecalibacterium, Ruminococcus, Bulleidia, and Akkermansia (LDA >2) and the significantly increased relative abundance of genera Campylobacter, Anaerofustis, Anaerotruncus, Holdemania, and Marcrococcus (LDA >2) were observed in D-GPV infection group at 15 dpi (Figures 4C,D). These genera contain opportunistic pathogens exhibited enrichment in abundance when infected with D-GPV especially during the early stages of 6 dpi, and there were never detected at high abundances in control samples (Figure 5). Clearly, the D-GPV infection was associated with the aberrant composition of the cecal microbiota, and the effect of D-GPV on the colonization of gut microorganism was more obvious along with the extension of infection time.
Figure 3. Bacterial distribution of the top 50 abundant genus among 37 samples. Double hierarchical dendrogram shows the bacterial distribution. The heatmap plot depicts the relative percentage of each bacterial genus within each sample. The relative values for bacterial family are indicated by color intensity with the legend indicated under the heatmap.
Figure 4. The difference of abundances in taxa between the D-GPV-infected groups and the control groups. (A) Taxonomic cladogram obtained from LEfSe sequence analysis at 6 dpi. Biomarker taxa are highlighted by colored circles and shaded areas. Each circle’s diameter reflects the abundance of that taxa in the community. (B) The taxa whose abundance differed between the D-GPV-infected samples (I-6d) and the healthy control samples (C-6d) at 6 dpi. The cutoff value of ≥2.0 used for the linear discriminant analysis (LDA) is shown. (C) Taxonomic cladogram obtained from LEfSe sequence analysis at 15 dpi. (D) The taxa whose abundance differed between the D-GPV-infected samples (I-15d) and the healthy control samples (C-15d) at 15 dpi.
Figure 5. Relative abundance of Campylobacter, Anaeroplasma, Eggerthella, Anaerotruncus, Holdemania, and Macrococcus in the gut microbiota at different post infection time. Values are shown as a fraction of the total bacteria detected within each samples. Lines represent the median value. Statistical tests were performed using post hoc ANOVA and ns indicated no significant difference.
D-GPV Infection Caused Growth Retardation and Decreased the Concentrations of SCFAs
The D-GPV-infected ducklings were obvious stunted growth (Figure 6A) and severely underweight compared with the control group (P < 0.01) (Figure 6B). Interestingly, no significant association between body weight and the relative abundance of phylum Firmicutes was noted within control and D-GPV infected samples at 6 dpi (P = 0.188) (Figure 6C), whereas a trend toward a positive association between body weight and the relative abundance of phylum Firmicutes was observed at 15 dpi (P = 0.004) (Figure 6D).
Figure 6. (A) Individual comparison between control duck and infected duck. (B) Body weight of control group and D-GVP infection group (P < 0.01 by two-tailed Student’s t-test). (C,D) Association between the relative abundance of Firmicutes and body weight of control samples and D-GPV infected samples at 6 dpi and 15 dpi, respectively. Statistical analysis was performed using the Spearman t-test. (E) Effect of D-GPV infection on SCFAs content in caecum. ∗P < 0.05, ∗∗P < 0.01 by post hoc ANOVA, and ns meant no significant differences.
Additionally, lower concentration of SCFAs was detected in the cecal samples collected from D-GPV-infected ducks by HPLC method. The acetic acids were significantly lower in D-GPV-infection groups at both 6 dpi and 15 dpi, furthermore, propionic acid and butyric acids from infection group were reduced at 15 dpi compared to control groups (Figure 6E).
D-GPV Infection Destroyed the Mucosal Epithelium of the Intestine and Promoted Local Intestinal Inflammation
The distribution of the immunoreactivity for the D-GPV antigen was confirmed, as determined in paraformaldehyde-fixed, paraffin-embedded tissue sections by IHC. The D-GPV antigen was mostly strongly distributed in mucosal epithelium and glandular epithelial cells. The D-GPV antigen was randomly and widely distributed on the surface of epithelia at 6 dpi (Figure 7A). Nevertheless, the antigen was mainly distributed in basal region and basement membrane of epithelial cells and cells of laminae propria at 15 dpi (Figure 7B). Positive virus signals were not detected in control samples (Supplementary Figure S2).
Figure 7. The location of D-GPV antigen and histopathological changes in caecum at 6 dpi and 15 dpi. (A) Positive virus signals were detected on the surface of epithelium cells and glandular epithelial cells at 6 dpi. (B) Positive virus signals were mainly detected in basal base and basement membrane of cells at 15 dpi. (C,D) Histological features in the D-GPV infection group (i) and control group (c) are shown with hematoxylin and eosin staining at 6 dpi and 15 dpi. Necrosis and abscission of mucous epithelial cells are indicated with the black arrow. Proliferation of lymphocytes in laminae propria is indicated with the red arrow. (E) Villus height, crypt depth and the ration of villus height to crypt depth (V/C) in caeca of proximal ileum. Values were means ± standard deviation of three independent experiments (∗P < 0.05, ∗∗P < 0.01 by post hoc ANOVA), and ns meant no significant differences.
Cecal histopathology analysis showed that necrosis and abscission of mucosal epithelial cells were observed in the 9/10 of D-GPV infected samples at 6 dpi and 6/10 of D-GPV infected samples at 15 dpi, as well as 10/10 of infected samples at 6 dpi and 9/10 of infected samples at 15 dpi showed local lymphocytic infiltration in chorioepithelium and laminae propria (Figures 7C,D). Importantly, the villus height of D-GPV infected samples was significantly decreased (P < 0.01) at 6 dpi and 15 dpi, and the crypt depth of D-GPV infected samples was significantly increased (P < 0.01) at 6 dpi (Figure 7E). The ratio of villus height/crypt depth was significantly reduced at 15 dpi (P < 0.05) in the ceca of proximal ileum (Figure 7E). The decreased ratio of height of villus and villus height/crypt depth reduced the absorptive area of the intestine and the mature cell manifold, which suggested that D-GPV weaken the absorbing ability of ceca.
Additionally, the expansion of pro-inflammatory cytokines was observed in D-GPV infection group. The mRNA expressions of pro-inflammatory TNF-α, IL-1β, IL-6, IL-17A, and IL-22 were significantly up-regulated after D-GPV infection, although the expression of IL-22 had no significant difference at 15 dpi. While the mRNA expression of anti-inflammatory IL-10 and IL-4 were down-regulated at 15 dpi (Figures 8A,B).
Figure 8. Quantitative RT-PCR analysis of the expression of pro-inflammatory TNF-α, IL-1β, IL-6, IL-17A, and IL-22, as well as anti-inflammatory IL-10 and IL-4 in the caecum from control and D-GPV infection groups at 6 dpi (A) and 15 dpi (B).
Relationships Between Cecal Microbiota and the Relative Expression of Cytokines
The correlative relationships among pro-inflammatory and anti-inflammatory cytokine expression and cecal predominant bacterial populations were evaluated in this study (Figure 9). The result showed that the pro-inflammatory TNF-α was significantly and negatively correlated with Streptococcus, Parabacteroides, Fusobacterium and Peptococcus at 6 dpi and also negatively correlated with Butyricicoccus at 15 dpi, while it was significantly and positively correlated with Campylobacter and Collinsella at 6 dpi as well as Collinsella and Megamonas at 15 dpi. Expression of pro-inflammatory IL-1β was significantly and negatively correlated with Collinsella at 6 dpi. Expression of IL-6 was significantly and negatively correlated Streptococcus, Enterococcus and Fusobacterium at 6 dpi as well as Ruminococcus and Prevotella at 15 dpi, however, it was positively associated with Anaeroplasma, Campylobacter and Collinsella at 6dpi. The pro-inflammatory IL-17A was negatively associated with Butyricicoccus, Streptococcus and Fusobacterium while correlated positively with Anaeroplasma at 6 dpi, as well as the Parabacteroides was significantly and negatively correlated with the expression of IL-17A at 15 dpi. The expression of IL-22 correlated negatively with Enterococcus, Fusobacterium and Peptococcus while positively correlated with Coprobacillus, Anaeroplasma, and Campylobacter at 6 dpi. The expression of anti-inflammatory IL-10 correlated positively with Blautia, Akkermansia, and Butyricimonas while it was significantly and negatively correlated with Megamonas at 15 dpi.
Figure 9. Correlogram showing Spearman’s correlations between bacterial genera and cytokine responses in the caecum. Heatmap representing positive (blue shading) and negative (red shading) associations between pro-inflammatory TNF-α, IL-1β, IL-6, IL-17A, and IL-22 and anti-inflammatory IL-10 and IL-4. Only the predominant bacterial genera (relative abundance ≥0.01% in every sample at least one group) for which abundance was significantly associated with inflammatory cytokines expression are presented; Clustering was performed based on genera associations with the inflammatory cytokines. P-values were adjusted for false discovery rate according to Bonferroni and Hochberg procedure. An asterisk indicates a significance correlation between the bacterial taxa and the cytokine in a tissue (∗∗P < 0.01, ∗P < 0.05).
The gut microbiota has profound influences on the normal structural and functional development of the mucosal immune system (Hooper et al., 2012). The poultry gut is important to health, however, little is known about how the complex gut microbiota are affected during viral infection. This study first analyzes the effect of D-GPV infection on gut microbiota of Cherry Valley duck, and provides a new perspective for the study on the waterfowl infectious diseases.
In this study, the caecum was utilized to analyze the gut microbiota, for the role in digestion and the overall health of birds. Based on a preliminary analysis of alpha diversity and beta diversity, all the diversity metrics of microbial populations increased significantly as healthy ducks matured. However, the alpha diversity of the gut microbiota in D-GPV infected ducks was decreased, and the structure and composition of cecal microbiota were different from control ducks. The Bacteroidetes, the Firmicutes, and the Proteobacteria were major bacterial phyla in cecal microbiota of Cherry Valley ducks, as previously described in Pekin ducks (Best et al., 2016). The two most dominant phyla of Firmicutes and Bacteroidetes in different organisms such as birds or mammals play an important role in intestinal microbiota metabolism in most studies (Ley et al., 2008; Kohl, 2012). The Firmicutes, a major phylum in the intestines or feces of many animals, is related to the digestibility of crude forage (Mohd Shaufi et al., 2015). In our study, the D-GPV-infected ducklings showed slight weakness, a loss of appetite, and loose stool excretion. We found that the D-GPV was mainly targeted in intestinal epithelial cells with necrosis and abscission of intestinal epithelial cells and lymphocytic infiltration. Importantly, the shorter intestinal villus and the increased crypt depth in D-GPV infected samples suggested intestinal growth retardation. In addition, a significant positive correlation between body weight and the relative abundance of Firmicutes was observed at 15 dpi. Therefore, we speculated that the intestinal injury and the decreased relative abundance of Firmicutes would inevitably decrease the digestion and absorption of nutrients, which was an important causation of growth retardation and diarrhea in Cherry Valley ducks after D-GPV infection.
Interestingly, we demonstrated a significant perturbation in colonization of SCFAs-producing bacteria during D-GPV infected Cherry Valley ducks. This perturbation was characterized by the decreased relative abundance of the dominance, such as the genus Streptococcus, Faecalibacterium, Lactobacillus, Enterococcus, Bulleidia, and Ruminococcus in Firmicutes phylum and the genus Parabacteroides, Prevotella, and Paraprevotella in Bacteroidetes phylum, accompanying with a decrease in microbial diversity. Meanwhile, D-GPV infection obstructed the colonization of some new bacteria at 15 dpi, for instance, the genus Paraprevotella, Bulleidia, Akkermansia, Butyricimonas, and Barnesiella (in Supplementary Figure S3). Thereinto, the genus Streptococcus was a primary acetic acid producer, and the Lactobacillus, Enterococcus, and Parabacteroide were one of the lactic acid and propionic acid producing bacteria, while the genera Butyricimonas, Prevotella, Ruminococcus, and Faecalibacterium were the major butyric acids producing bacteria. The decreased content of SCFAs was also found in D-GPV infected samples. Accordingly, we speculated that the reduction of SCFAs might be linked to the alterations of SCFAs-producing bacteria in cecal microbiota, which were important members of the endogenous bacteria playing an anti-inflammatory role in intestinal tract (Ménard et al., 2004; Fedorova and Danilenko, 2014; Nicholas and Rudensky, 2014). The interaction of SCFAs and G-protein-coupled receptors (GPR) is one of the important signal between gut microbiota and immune system for regulating the homeostasis and maintaining the balance between immune tolerance to commensals bacteria and immunity to pathogens (Kim et al., 2016). There is now sufficient evidence to indicate that SCFAs play an important role in the maintenance of health and the development of disease. It has been reported that SCFAs can enhance the host defenses against pathogens by activating the G-protein-coupled receptors (GPR) to mediate Regulatory T cell (Tregs) development and induce T helper differentiation (Arpaia et al., 2013; Smith et al., 2013). In addition, SCFAs such as butyrate and propionate suppress the activation of nuclear factor-kappaB (NF-κB) via GPR109A or GPR43 receptors to modulate the gene expression of inflammatory cytokines and suppress gut inflammation (Inan et al., 2000; Singh et al., 2014). Therefore, the decreases of SCFAs and SCFAs-producing bacteria could promote intestinal inflammatory injury in the process of D-GPV infection.
In addition, some opportunistic pathogens increased in abundance as the disease progressed, including the genera Campylobacter, Anaerofustis, Anaeroplasma, Eggerthella, Anaerotruncus, Holdemania, Macrococcus, Coprobacillus, Collinsella, and Eubacterium present within D-GPV infected ducks especially during the early stages of 6 dpi. Thereinto, the enrichment of Coriobacteriaceae, Coprobacillus, and Mogibacteriaceae have been reported in colorectal cancer of human (Chen et al., 2012; Gao et al., 2014). Furthermore, the genus Campylobacter and Eggerthella were reported to be associated with intestinal inflammation (Spiller et al., 2000; Lau et al., 2004). It was indicative to determine whether the increased abundance of D-GPV infection-related genera could serve as a predisposing cause of gastrointestinal abnormalities symptoms and threat to the health of host. Infiltration of inflammatory cells in multiple organs and decrease of lymphocytes in immune organs have been both reported in D-GPV-infected Cherry valley ducks and mule ducks (Chen H. et al., 2016; Liu et al., 2018). The expansion of the pro-inflammatory cytokines TNF-α, IL-1β, IL-6, IL-17A, and IL-22 is important for the immune responses of infectious individuals (Neurath, 2015; Mcdermott et al., 2016). Furthermore, IL-17A participates in the primary responses to fungi and also bacterial infections and induction of the pro-inflammatory based diseases (Douzandeh-Mobarrez and Kariminik, 2017). TNF-α, IL-1β, IL-6, IL-17A, and IL-22, as the most important pro-inflammatory cytokines, were largely up-regulated in our experimental process of D-GPV infection which played an important role to induce inflammation and the recruitment of leukocytes.
In the correlation analyses, the abundance of SCFAs-producing bacteria such as Streptococcus, Parabacteroides, Enterococcus, Fusobacterium and Peptococcus were negatively associated with the pro-inflammatory TNF-α, IL-6, IL-17A, and IL-22, in particularly, the anti-inflammatory IL-10 was positively related with some butyric acid producing bacteria such as Blautia and Butyricimonas at 15 dpi. Nevertheless, the opportunistic pathogens such as Anaeroplasma, Campylobacter and Collinsella were positively associated with TNF-α, IL-6, IL-17A, and IL-22. Interestingly, it appears that altered population of gut microbiota can be associated with pathologic expression of inflammatory factor. For example, Kamiya et al. revealed that oral administration of SCFAs-producing bacteria (Lactobacillus bulgaricus and Streptococcus thermophiles) results in up-regulation of IL-17A by the Peyer’s patches resident T lymphocytes (Kamiya et al., 2016). Chen J. et al. (2016) also showed the abundance of Collinsella is associated with pathologic expression of IL-17A and deterioration of rheumatoid arthritis. Furthermore, the high levels of Campylobacter jejuni leads to alteration in gut microbiota population and expression of IL-17A, IL-22, and TNF-α in pathologic format (Heimesaat et al., 2016; Rodrigues et al., 2018). A feature of IBD-ulcerative colitis and Crohn’s disease was a change in ’healthy’ microbiota such as Bifidobacterium and Bacteriodes, and a concurrent reduction in SCFAs (Hudafaujan et al., 2010; Chaysavanh et al., 2012). Accordingly, the increase of pro-inflammatory cytokines and decrease of anti-inflammatory cytokines were associated with the decrease of SCFAs-producing bacteria and the enrichment of opportunistic pathogens which could promote the development of intestinal inflammation in D-GPV infection.
The effect on the gut microbiome have been reported in some immunosuppressive virus, such as HIV in human (Lozupone et al., 2013), Marek’s disease virus (MDV) in chicken (Perumbakkam et al., 2014) and canine distemper virus (CDV) in giant panda (Zhao et al., 2017). CD4+ lymphocytes have been reported to help regulate the growth of bacteria within the gut microbiome (Slack et al., 2009). Although the decreased activity of CD4+ lymphocytes is one of the cause of affecting gut microbiota composition and diversity, the function of dendritic cells in using MHC-II to present antigens to activate T cells for sampling gut microbes is mentionable to recognition and regulation of gut microbes (Farache et al., 2013; Bolnick et al., 2015). It is essential in regulating the gut microbiota that adaptive cellular immunity has the ability to modulate flexible responses to host-specific microbial communities by inducing inflammatory immune attacks or tolerance via anti-inflammatory pathways (Sun et al., 2015). It is reported that MHC are associated with GPV infection, and MHC gene is the susceptible gene to GPV (Zhu et al., 2015). To some extent, the alterations of the gut microbiota support the statement that the immune system has a pivotal role in shaping the composition of gut microbiota. Nevertheless, there is no clear evidence that whether D-GPV infection alters the gut microbiota through the suppressing activity of CD4+ lymphocytes or regulating the gene expression of MHC-II. Therefore, the interaction between intestinal mucosal immune response and gut microbiota during D-GPV infection needs further investigation.
In conclusion, the present study provides a new insight for dysbiosis caused by waterfowl parvovirus on the host gut microbiome. D-GPV targeted intestinal epithelial cells and caused the dysbiosis in gut microbiota accompanying with decrease in the content of short chain fatty acids in ceca. Moreover, the results show a correlation among the deletion of some specific SCFAs-producing bacteria, the enrichment of opportunistic pathogens and intestinal inflammatory injury in D-GPV infection. This research sheds light into the correlative new field in the mechanism of D-GPV and a theoretical basis for dysbiosis of this disease.
JX, CH, and ZC designed the experiments. JX, DC, and WL performed the experiments. JX and QL analyzed the data. JX, QL, XL, and DC drafted the manuscript. AC, LT, JF, YO, YG, and WW participated in data interpretation and manuscript editing. All authors reviewed the manuscript and finally approved the publication of the article.
This work was supported by grants from National Key Technology Support Program (2014BAI03B01 to ZC), and basic research program of Sci-tech department of Sichuan Province (2019YJ0426).
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmicb.2019.00624/full#supplementary-material
Arpaia, N., Campbell, C., Fan, X., Dikiy, S., Veeken, J. V. D., Deroos, P., et al. (2013). Metabolites produced by commensal bacteria promote peripheral regulatory T cell generation. Nature 504, 451–455. doi: 10.1038/nature12726
Baere, S. D., Eeckhaut, V., Steppe, M., Maesschalck, C. D., Backer, P. D., Immerseel, F. V., et al. (2013). Development of a HPLC–UV method for the quantitative determination of four short-chain fatty acids and lactic acid produced by intestinal bacteria during in vitro fermentation. J. Pharm. Biomed. Anal. 80, 107–115. doi: 10.1016/j.jpba.2013.02.032
Benjamini, Y., and Hochberg, Y. (1995). Controlling the false discovery rate - a practical and powerful approach to multiple testing. J. R. Stat. Soc. 57, 289–300. doi: 10.1111/j.2517-6161.1995.tb02031.x
Best, A. A., Porter, A. L., Fraley, S. M., and Fraley, G. S. (2016). Characterization of gut microbiome dynamics in developing pekin ducks and impact of management system. Front. Microbiol. 7:2125. doi: 10.3389/fmicb.2016.02125
Bolnick, D. I., Snowberg, L. K., Caporaso, J. G., Lauber, C., Knight, R., and Stutz, W. E. (2015). Major histocompatibility complex class IIb polymorphism influences gut microbiota composition and diversity. Mol. Ecol. 23, 4831–4845. doi: 10.1111/mec.12846
Caporaso, J. G., Kuczynski, J., Stombaugh, J., Bittinger, K., Bushman, F. D., Costello, E. K., et al. (2010). QIIME allows analysis of high-throughput community sequencing data. Nat. Methods 7, 335–336. doi: 10.1038/nmeth.f.303
Chen, B., Xu, J., Huang, C., Liu, W., Yan, D., Chen, J., et al. (2017). Isolation, identification and analysis of VP1 gene of a cherry valley duck-origin parvovirus strain QH-L01. Chin. Vet. Sci. 47, 909–914. doi: 10.16656/j.issn.1673-4696.2017.07.018
Chen, H., Dou, Y., Tang, Y., Zhang, Z., Zheng, X., Niu, X., et al. (2015). Isolation and genomic characterization of a duck-origin GPV-Related parvovirus from cherry valley ducklings in China. PLoS One 10:e0140284. doi: 10.1371/journal.pone.0140284
Chen, H., Dou, Y., Tang, Y., Zheng, X., Niu, X., Yang, J., et al. (2016). Experimental reproduction of beak atrophy and dwarfism syndrome by infection in cherry valley ducklings with a novel goose parvovirus-related parvovirus. Vet. Microbiol. 183, 16–20. doi: 10.1016/j.vetmic.2015.11.034
Chen, J., Wright, K., Davis, J. M., Jeraldo, P., Marietta, E. V., Murray, J., et al. (2016). An expansion of rare lineage intestinal microbes characterizes rheumatoid arthritis. Genome Med. 8:43. doi: 10.1186/s13073-016-0299-7
Chen, S., Cheng, A., Wang, M., Zhu, D., Luo, Q., Liu, F., et al. (2009). Immunohistochemical detection and localization of new type gosling viral enteritis virus in paraformaldehyde-fixed paraffin-embedded tissue. Vet. Immunol. Immunopathol. 130, 226–235. doi: 10.1016/j.vetimm.2009.02.011
Chen, W., Liu, F., Ling, Z., Tong, X., and Xiang, C. (2012). Human intestinal lumen and mucosa-associated microbiota in patients with colorectal cancer. PLoS One 7:e39743. doi: 10.1371/journal.pone.0039743
Douzandeh-Mobarrez, B., and Kariminik, A. (2017). Gut microbiota and IL-17A: physiological and pathological responses. Probiotics Antimicrob. Proteins doi: 10.1007/s12602-017-9329-z [Epub ahead of print].
Egan, C. E., Cohen, S. B., and Denkers, E. Y. (2011). Insights into inflammatory bowel disease using Toxoplasma gondii as an infectious trigger. Immunol. Cell Biol. 90, 668–675. doi: 10.1038/icb.2011.93
Farache, J., Zigmond, E., Shakhar, G., and Jung, S. (2013). Contributions of dendritic cells and macrophages to intestinal homeostasis and immune defense. Immunol. Cell Biol. 91, 232–239. doi: 10.1038/icb.2012.79
Fedorova, I. A., and Danilenko, V. N. (2014). Immunogenic properties of a probiotic component of the human gastrointestinal tract microbiota. Biol. Bull. Rev. 4, 457–466. doi: 10.1134/S2079086414060036
Gao, R. Y., Zhu, Q. C., Wu, W., and Qin, H. L. (2014). Compositional differences in fecal microbiota between rats with colorectal cancer and normal rats. World Chin. J. Digestol. 22, 661–667. doi: 10.11569/wcjd.v22.i5.661
Glavan, T. W., Gaulke, C. A., Rocha, C. S., Sankaranwalters, S., Hirao, L. A., Raffatellu, M., et al. (2016). Gut immune dysfunction through impaired innate pattern recognition receptor expression and gut microbiota dysbiosis in chronic SIV infection. Mucosal Immunol. 9, 677–688. doi: 10.1038/mi.2015.92
Heimesaat, M. M., Grundmann, U., Alutis, M. E., Fischer, A., Göbel, U. B., and Bereswill, S. (2016). The IL-23/IL-22/IL-18 axis in murine Campylobacter jejuni infection. Gut Pathog. 8, 1–14. doi: 10.1186/s13099-016-0106-4
Hudafaujan, N., Abdulamir, A. S., Fatimah, A. B., Anas, O. M., Shuhaimi, M., Yazid, A. M., et al. (2010). The impact of the level of the intestinal short chain fatty acids in inflammatory bowel disease patients versus healthy subjects. Open Biochem. J. 4, 53–58. doi: 10.2174/1874091X01004010053
Hughes, J. B., Hellmann, J. J., Ricketts, T. H., and Bohannan, B. J. (2001). Counting the uncountable: statistical approaches to estimating microbial diversity. Appl. Environ. Microbiol. 67, 4399–4406. doi: 10.1128/aem.67.10.4399-4406.2001
Inan, M. S., Rasoulpour, R. J., and Yin, L. (2000). The luminal short-chain fatty acid butyrate modulates NF-κB activity in a human colonic epithelial cell line. Gastroenterology 118, 724–734. doi: 10.1016/S0016-5085(00)70142-9
Kamiya, T., Watanabe, Y., Makino, S., Kano, H., and Tsuji, N. M. (2016). Improvement of intestinal immune cell function by lactic acid bacteria for dairy products. Microorganisms 5:E1. doi: 10.3390/microorganisms5010001
Lau, S. K., Woo, P. C., Woo, G. K., Fung, A. M., Wong, M. K., Chan, K. M., et al. (2004). Eggerthella hongkongensis sp. nov. and eggerthella sinensis sp. nov., two novel Eggerthella species, account for half of the cases of Eggerthella bacteremia. Diagn. Microbiol. Infect. Dis. 49, 255–263. doi: 10.1016/j.diagmicrobio.2004.04.012
Liu, R., Hu, Y., Lu, R., Fu, Q., Wan, C., Fu, G., et al. (2018). Aetiology detection and histopathological features of “short break dwarf syndrom” in mule ducks. Chin. J. Vet. Sci. 38, 51–58. doi: 10.16303/j.cnki.1005-4545.2018.01.07
Lozupone, C. A., Li, M., Campbell, T. B., Flores, S. C., Linderman, D., Gebert, M. J., et al. (2013). Alterations in the gut microbiota associated with HIV-1 infection. Cell Host Microbe 14, 329–339. doi: 10.1016/j.chom.2013.08.006
Luo, Q., Chen, B., Xu, J., Ma, W., Lao, C., Li, Y., et al. (2019). Development of a SYBR green II real-time polymerase chain reaction for the clinical detection of the duck-origin goose parvovirus in China. Intervirology 17, 1–7. doi: 10.1159/000495181
Marchetti, G., Bellistrì, G. M., Borghi, E., Tincati, C., Ferramosca, S., Francesca, M. L., et al. (2008). Microbial translocation is associated with sustained failure in Cd4+ T-cell reconstitution in Hiv-infected patients on long-term highly active antiretroviral therapy. Aids 22, 2035–2038. doi: 10.1097/QAD.0b013e3283112d29
Mcdermott, A. J., Falkowski, N. R., Mcdonald, R. A., Pandit, C. R., Young, V. B., and Huffnagle, G. B. (2016). Interleukin-23 (IL-23), independent of IL-17 and IL-22, drives neutrophil recruitment and innate inflammation during clostridium difficile colitis in mice. Immunology 147, 114–124. doi: 10.1111/imm.12545
Ménard, S., Candalh, C., Bambou, J. C., Terpend, K., Cerf-Bensussan, N., Heyman, M., et al. (2004). Lactic acid bacteria secrete metabolites retaining anti-inflammatory properties after intestinal transport. Gut 53, 821–828. doi: 10.1136/gut.2003.026252
Mohd Shaufi, M. A., Sieo, C. C., Chong, C. W., Gan, H. M., and Ho, Y. W. (2015). Deciphering chicken gut microbial dynamics based on high-throughput 16S rRNA metagenomics analyses. Gut Pathog. 7:4. doi: 10.1186/s13099-015-0051-7
Nair, S., Arathy, D. S., Issac, A., and Sreekumar, E. (2011). Differential gene expression analysis of in vitro duck hepatitis B virus infected primary duck hepatocyte cultures. Virol. J. 8, 363–363. doi: 10.1186/1743-422X-8-363
Ning, K., Liang, T., Wang, M., Dong, Y., Qu, S., and Zhang, D. (2018). Pathogenicity of a variant goose parvovirus from short beak and dwarfism syndrome of pekin ducks in goose embryos and goslings. Avian Pathol. 47, 391–399. doi: 10.1080/03079457.2018.1459040
Perumbakkam, S., Hunt, H. D., and Cheng, H. H. (2014). Marek’s disease virus influences the core gut microbiome of the chicken during the early and late phases of viral replication. FEMS Microbiol. Ecol. 90, 300–312. doi: 10.1111/1574-6941.12392
Rodrigues, R. C., Pocheron, A. L., Cappelier, J. M., Tresse, O., and Haddad, N. (2018). An adapted in vitro assay to assess Campylobacter jejuni interaction with intestinal epithelial cells: taking into stimulation with TNFα. J. Microbiol. Methods 149, 67–72. doi: 10.1016/j.mimet.2018.04.020
Singh, N., Gurav, A., Sivaprakasam, S., Brady, E., Padia, R., Shi, H., et al. (2014). Activation of the receptor (Gpr109a) for niacin and the commensal metabolite butyrate suppresses colonic inflammation and carcinogenesis. Immunity 40, 128–139. doi: 10.1016/j.immuni.2013.12.007
Slack, E., Hapfelmeier, S., Stecher, B., Velykoredko, Y., Stoel, M., Lawson, M. A., et al. (2009). Innate and adaptive immunity cooperate flexibly to maintain host-microbiota mutualism. Science 325, 617–620. doi: 10.1126/science.1172747
Smith, P. M., Howitt, M. R., Panikov, N., Michaud, M., Gallini, C. A., Bohloolyy, M., et al. (2013). The microbial metabolites, short chain fatty acids, regulate colonic treg cell homeostasis. Science 341, 569. doi: 10.1126/science.1241165
Spiller, R. C., Jenkins, D., Thornley, J. P., Hebden, J. M., Wright, T., Skinner, M., et al. (2000). Increased rectal mucosal enteroendocrine cells, T lymphocytes, and increased gut permeability following acute campylobacter enteritis and in post-dysenteric irritable bowel syndrome. Gut 47, 804–811. doi: 10.1136/gut.47.6.804
Zhao, N., Li, M., Luo, J., Wang, S., Liu, S., Wang, S., et al. (2017). Impacts of canine distemper virus infection on the giant panda population from the perspective of gut microbiota. Sci. Rep. 7, 39954. doi: 10.1038/srep39954
Keywords: D-GPV, BADS, gut microbiota dysbiosis, intestinal inflammation, SCFAs
Citation: Luo Q, Xu J, Huang C, Lei X, Cheng D, Liu W, Cheng A, Tang L, Fang J, Ou Y, Geng Y and Chen Z (2019) Impacts of Duck-Origin Parvovirus Infection on Cherry Valley Ducklings From the Perspective of Gut Microbiota. Front. Microbiol. 10:624. doi: 10.3389/fmicb.2019.00624
Received: 07 September 2018; Accepted: 12 March 2019;
Published: 28 March 2019.
Edited by:Souvik Ghosh, Ross University School of Veterinary Medicine, Saint Kitts and Nevis
Reviewed by:Felix Ngosa Toka, Ross University School of Veterinary Medicine, Saint Kitts and Nevis
Jakub Kreisinger, Charles University, Czechia
Copyright © 2019 Luo, Xu, Huang, Lei, Cheng, Liu, Cheng, Tang, Fang, Ou, Geng and Chen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Zhengli Chen, firstname.lastname@example.org
†These authors have contributed equally to this work as co-first authors