Transcriptome and the gut microbiome analysis of the impacts of Brucella abortus oral infection in BALB/c mice.


Journal

Microbial pathogenesis
ISSN: 1096-1208
Titre abrégé: Microb Pathog
Pays: England
ID NLM: 8606191

Informations de publication

Date de publication:
Oct 2023
Historique:
received: 10 04 2023
revised: 22 07 2023
accepted: 31 07 2023
medline: 18 9 2023
pubmed: 3 8 2023
entrez: 2 8 2023
Statut: ppublish

Résumé

Brucellosis is a zoonotic infectious disease caused by Brucella spp, which could cause serious economic losses to animal husbandry and threaten human public health. Ingestion of contaminated animal products is a common way to acquire Brucella infection in humans, while research on effect of oral Brucella infection on host gut microbiota and the gene expression in intestinal tissues is limited. In the present study, 16S rRNA sequencing and RNA sequencing were conducted to explore gut microbiota and expression profiles of mRNAs in the colon of BALB/c mice, which were infected by Brucella abortus 2308. The fecal samples were collected at 7 and 28 days post infection to observe changes in the gut microbiota during Brucella infection. In the alpha diversity analysis, significantly increased Chao 1 index was observed at 28 days after Brucella infection. The Bray-Curtis distancebased principal coordinate analysis indicated that the WT group showed a separation from the Brucella infection groups. In addition, analysis of composition of microbes revealed that Prevotellaceae_NK3B31_group were more abundant in 1 week and 4 week infection groups, while Turicibacter was only more abundant in 4 week infection group. Based on the RNA-seq assay, a total of 45 differentially expressed genes were detected between Brucella abortus infection group and control group. Furthermore, KEGG pathway enrichment analysis showed that protein processing in endoplasmic reticulum, Legionellosis, Spliceosome, Hippo signaling pathway and Influenza A were significantly enriched in response to Brucella abortus infection. Our finding will help to improve the knowledge of the mechanisms underlying Brucella infection and may provide novel targets for future treatment of this pathogen infection.

Identifiants

pubmed: 37532208
pii: S0882-4010(23)00311-X
doi: 10.1016/j.micpath.2023.106278
pii:
doi:

Substances chimiques

RNA, Ribosomal, 16S 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106278

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Kun Han (K)

Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100193, China; College of Veterinary Medicine, Northwest A&F University, Yangling, 712100, Shaanxi, China.

Hao Dong (H)

National Institutes for Food and Drug Control, Beijing, 102600, China.

Xiaowei Peng (X)

China Institute of Veterinary Drug Control, Beijing, 102600, China.

Jiali Sun (J)

China Institute of Veterinary Drug Control, Beijing, 102600, China; College of Veterinary Medicine, China Agricultural University, Beijing, 100193, China.

Hui Jiang (H)

Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.

Yu Feng (Y)

China Institute of Veterinary Drug Control, Beijing, 102600, China.

Jiabo Ding (J)

Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100193, China. Electronic address: dingjiabo@126.com.

Sa Xiao (S)

College of Veterinary Medicine, Northwest A&F University, Yangling, 712100, Shaanxi, China. Electronic address: saxiao@nwafu.edu.cn.

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Classifications MeSH