Intestinal Microbial Dysbiosis in Beagles Naturally Infected with Canine Parvovirus
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Canine parvoviral enteritis (PVE) is an important intestinal disease of the puppies; however, the potential impact of the canine parvovirus (CPV) on the gut microbiota has not been investigated. Therefore, the aim of this study was to evaluate the gut microbial shifts in puppies naturally infected with CPV. Fecal samples were collected from healthy dogs and those diagnosed with PVE at 4, 6, 8, and 12 weeks of age. The distal gut microbiota of dogs was characterized using Illumina MiSeq sequencing of the bacterial 16S rRNA genes. The sequence data were analyzed using QIIME with an Operational Taxonomic Unit definition at a similarity cutoff of 97%. Our results showed that the CPV was associated with significant microbial dysbiosis of the intestinal microbiota. Alpha diversity and species richness and evenness in dogs with PVE decreased compared to those of healthy dogs. At the phylum level, the proportion of Proteobacteria was significantly enriched in dogs with PVE while Bacteroidetes was significantly more abundant in healthy dogs (p < 0.05). In dogs with PVE, Enterobacteriaceae was the most abundant bacterial family accounting for 36.44% of the total bacterial population compared to only 0.21% in healthy puppies. The two most abundant genera in healthy dogs were Prevotella and Lactobacillus and their abundance was significantly higher compared to that of dogs with PVE (p < 0.05). These observations suggest that disturbances of gut microbial communities were associated with PVE in young dogs. Evaluation of the roles of these bacterial groups in the pathophysiology of PVE warrants further studies.
Abstract
Canine parvoviral enteritis (PVE) is an important intestinal disease of the puppies; however, the potential impact of the canine parvovirus (CPV) on the gut microbiota has not been investigated. Therefore, the aim of this study was to evaluate the gut microbial shifts in puppies naturally infected with CPV. Fecal samples were collected from healthy dogs and those diagnosed with PVE at 4, 6, 8, and 12 weeks of age. The distal gut microbiota of dogs was characterized using Illumina MiSeq sequencing of the bacterial 16S rRNA genes. The sequence data were analyzed using QIIME with an Operational Taxonomic Unit definition at a similarity cutoff of 97%. Our results showed that the CPV was associated with significant microbial dysbiosis of the intestinal microbiota. Alpha diversity and species richness and evenness in dogs with PVE decreased compared to those of healthy dogs. At the phylum level, the proportion of Proteobacteria was significantly enriched in dogs with PVE while Bacteroidetes was significantly more abundant in healthy dogs (p < 0.05). In dogs with PVE, Enterobacteriaceae was the most abundant bacterial family accounting for 36.44% of the total bacterial population compared to only 0.21% in healthy puppies. The two most abundant genera in healthy dogs were Prevotella and Lactobacillus and their abundance was significantly higher compared to that of dogs with PVE (p < 0.05). These observations suggest that disturbances of gut microbial communities were associated with PVE in young dogs. Evaluation of the roles of these bacterial groups in the pathophysiology of PVE warrants further studies.
참고문헌 (39)
- Nandi S, "Canine parvovirus : current perspective", Indian J. Virol, 21, pp.31~44 (2010)
- Kilian E, "Long-term effects of canine parvovirus infection in dogs", PLoS One, 13, pp.e0192198~ (2018)
- Sime TA, "Parvoviral myocarditis in a 5-week-old Dachshund", J. Vet. Emerg. Crit. Care, 25, pp.765~769 (2015)
- Tress B, "Bacterial microbiome of the nose of healthy dogs and dogs with nasal disease", PLoS One, 12, pp.e0176736~ (2017)
- Guevarra RB, "Piglet gut microbial shifts early in life : causes and effects", J. Anim. Sci. Biotechnol, 10, pp.1~ (2019)
- Song ES, "Comparison of Fecal Microbiota between German Holstein Dairy Cows with and without Left-Sided Displacement of the Abomasum", J. Clin. Microbiol, 54, pp.1140~1143 (2016)
- Kim HB, "Salmonella in Swine: Microbiota Interactions", Ann. Rev. Anim. Biosci, 5, pp.43~63 (2017)
- Handl S, "Massive parallel 16S rRNA gene pyrosequencing reveals highly diverse fecal bacterial and fungal communities in healthy dogs and cats", FEMS Microbiol. Ecol, 76, pp.301~310 (2011)
- Hooda S, "Current state of knowledge : the canine gastrointestinal microbiome", Anim. Health Res. Rev, 13, pp.78~88 (2012)
- Omori M, "Fecal microbiome in dogs with inflammatory bowel disease and intestinal lymphoma", J. Vet. Med. Sci, 79, pp.1840~1847 (2017)
- Kalenyak K, "Comparison of the intestinal mucosal microbiota in dogs diagnosed with idiopathic inflammatory bowel disease and dogs with food-responsive diarrhea before and after treatment", FEMS Microbiol. Ecol, 94(2), pp.1093~ (2018)[DOI]
- Song YG, "Comparative analysis of the reproductive tract microbial communities in female dogs with and without pyometra through the 16S rRNA gene pyrosequencing", Jpn. J. Vet. Res, 65, pp.193~200 (2017)
- Guevarra RB, "The dynamics of the piglet gut microbiome during the weaning transition in association with health and nutrition", J. Anim. Sci. Biotechnol, 9, pp.54~ (2018)
- Hanshew AS, "Minimization of chloroplast contamination in 16S rRNA gene pyrosequencing of insect herbivore bacterial communities", J. Microbiol. Methods, 95, pp.149~155 (2013)
- 김태윤, "Whole-Body Microbiota of Sea Cucumber (Apostichopus japonicus) from South Korea for Improved Seafood Management", Journal of Microbiology and Biotechnology, 27(10), pp.1753~1762 (2017), 한국미생물·생명공학회
- 최성미, "Difference in the Gut Microbiome between Ovariectomy-Induced Obesity and Diet-Induced Obesity", Journal of Microbiology and Biotechnology, 27(12), pp.2228~2236 (2017), 한국미생물·생명공학회
- Schloss PD, "Introducing mothur : Open-Source, Platform-Independent, Community-Supported Software for Describing and Comparing Microbial Communities", Appl. Environ. Microbiol, 75, pp.7537~7541 (2009)
- 김대호, "Metagenomic Approach to Identifying Foodborne Pathogens on Chinese Cabbage", Journal of Microbiology and Biotechnology, 28(2), pp.227~235 (2018), 한국미생물·생명공학회
- 김대호, "Analysis of Microbiota in Bellflower Root, Platycodon grandiflorum, Obtained from South Korea", Journal of Microbiology and Biotechnology, 28(4), pp.551~560 (2018), 한국미생물·생명공학회
- Caporaso JG, "QIIME allows analysis of high-throughput community sequencing data", Nature Methods, 7, pp.335~336 (2010)
- Parks DH, "STAMP : statistical analysis of taxonomic and functional profiles", Bioinformatics, 30, pp.3123~3124 (2014)
- Segata N, "Metagenomic biomarker discovery and explanation", Genome Biol, 12(6), pp.R60~ (2011)
- Luna LG, "Manual of histologic staining methods of the Armed Forces Institute of Pathology", pp.158~160 (1968), McGraw-Hill
- 김보라, "Deciphering Diversity Indices for a Better Understanding of Microbial Communities", Journal of Microbiology and Biotechnology, 27(12), pp.2089~2093 (2017), 한국미생물·생명공학회
- Moon HS, "Comparison of the pathogenicity in three different Korean canine parvovirus 2(CPV-2)isolates", Vet. Microbiol, 131, pp.47~56 (2008)
- Yildiz S, "Influenza A virus infection impacts systemic microbiota dynamics and causes quantitative enteric dysbiosis", Microbiome, 6(1), pp.9~ (2018)
- Rowan-Nash AD, "Cross-Domain and Viral Interactions in the Microbiome", Microbiol. Mol. Biol. Rev, 83(1), pp.e00044-18~ (2019)
- Zaneveld JR, "Stress and stability : applying the Anna Karenina principle to animal microbiomes", Nat. Microbiol, 2, pp.17121~ (2017)
- Vazquez-Baeza Y, "Dog and human inflammatory bowel disease rely on overlapping yet distinct dysbiosis networks", Nat. Microbiol, 1, pp.16177~ (2016)
- Suchodolski JS, "The fecal microbiome in dogs with acute diarrhea and idiopathic inflammatory bowel disease", PLoS One, 7, pp.e51907~ (2012)
- Jia J, "Investigation of the faecal microbiota associated with canine chronic diarrhoea", FEMS Microbiol. Ecol, 71, pp.304~312 (2010)
- Hullar MAJ, "The canine gut microbiome is associated with higher risk of gastric dilatation-volvulus and high risk genetic variants of the immune system", PLoS One, 13, pp.e0197686~ (2018)
- Petersen C, "Defining dysbiosis and its influence on host immunity and disease", Cell Microbiol, 16, pp.1024~1033 (2014)
- Suchodolski JS, "16S rRNA gene pyrosequencing reveals bacterial dysbiosis in the duodenum of dogs with idiopathic inflammatory bowel disease", PLoS One, 7, pp.e39333~ (2012)
- Guard BC, "HORSE SPECIES SYMPOSIUM: Canine intestinal microbiology and metagenomics:From phylogeny to function", J. Anim. Sci, 94, pp.2247~2261 (2016)
- Suchodolski JS, "Analysis of bacterial diversity in the canine duodenum, jejunum, ileum, and colon by comparative 16S rRNA gene analysis", FEMS Microbiol. Ecol, 66, pp.567~578 (2008)
- Heilmann RM, "Fecal markers of inflammation, protein loss, and microbial changes in dogs with the acute hemorrhagic diarrhea syndrome (AHDS)", J. Vet. Emerg. Crit. Care, 27, pp.586~589 (2017)
- Cassmann E, "Alterations of the Ileal and Colonic Mucosal Microbiota in Canine Chronic Enteropathies", PLoS One, 11, pp.e0147321~ (2016)
- Carding S, "Dysbiosis of the gut microbiota in disease", Microb. Ecol. Health Dis, 26, pp.26191~ (2015)
