Rat H1 parvovirus infection leads to alterations in gut microbiota.
Animals
Bacteria
/ classification
Cluster Analysis
Cytokines
/ blood
DNA, Bacterial
/ chemistry
DNA, Ribosomal
/ chemistry
Dysbiosis
/ pathology
Gastrointestinal Microbiome
Ileum
/ pathology
Parvoviridae Infections
/ complications
Parvovirus
/ growth & development
Phylogeny
RNA, Ribosomal, 16S
/ genetics
Rats, Wistar
Rodent Diseases
/ microbiology
Sequence Analysis, DNA
Methanobrevibacter
16S rRNA
H1 parvovirus
flatulence
gut microbiota
Journal
Pathogens and disease
ISSN: 2049-632X
Titre abrégé: Pathog Dis
Pays: United States
ID NLM: 101595366
Informations de publication
Date de publication:
01 07 2019
01 07 2019
Historique:
received:
20
05
2019
accepted:
09
10
2019
pubmed:
12
10
2019
medline:
24
4
2020
entrez:
12
10
2019
Statut:
ppublish
Résumé
H1 parvovirus (H1PV) infection in rats is of concern to the research community as infection may compromise rodent-based experiments. The aim of this study was to evaluate the influence of H1PV infection on rat gut microbiota. Inbred Wistar rats were infected with H1PV by routine gavage and clinical signs were recorded. Gross anatomical and histopathological examination of the gut was performed, as was immune cytokine analysis. The cecal contents were also collected for 16S rRNA sequencing. Gross anatomical examination showed distention of the ileum associated with flatulence after infection, while histopathological examination showed hyperemia and inflammatory cell infiltration in the ileum. Upregulation of the interleukin-6 in sera in H1PV infected rats was also detected. The gut microbiota had been significantly changed in H1PV infected rats: there was a reduction in several bacteria species including probiotic bacteria from the genera Parabacteroides and Butyricicoccus, while others were increased, including those from the genera Methanobrevibacter and Syntrophococcus. Taken together, these results demonstrate that chronic H1PV infection in rats leads to gastrointestinal inflammation with flatulence. The gut microbiota alterations were associated with decreased polymorphisms, reduced abundance of probiotic bacteria and increased abundance of methane-producing bacteria.
Identifiants
pubmed: 31603501
pii: 5585884
doi: 10.1093/femspd/ftz058
pii:
doi:
Substances chimiques
Cytokines
0
DNA, Bacterial
0
DNA, Ribosomal
0
RNA, Ribosomal, 16S
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© FEMS 2019.