详细信息
Modulation of Intestinal Barrier, Inflammatory Response, and Gut Microbiota by Pediococcus pentosaceus zy-B Alleviates Vibrio parahaemolyticus Infection in C57BL/6J Mice ( SCI-EXPANDED收录 EI收录) 被引量:10
文献类型:期刊文献
英文题名:Modulation of Intestinal Barrier, Inflammatory Response, and Gut Microbiota by Pediococcus pentosaceus zy-B Alleviates Vibrio parahaemolyticus Infection in C57BL/6J Mice
作者:Wang, Rundong[1,2,3];Deng, Yijia[1,2];Zhang, Yuhao[1];Li, Xuepeng[2];Sun, Lijun[4];Deng, Qi[4];Liu, Ying[4];Gooneratne, Ravi[5];Li, Jianrong[1,2]
机构:[1]Southwest Univ, Coll Food Sci, Chongqing 400715, Peoples R China;[2]Bohai Univ, Coll Food Sci & Engn, Jinzhou 121013, Peoples R China;[3]Lingnan Normal Univ, Coll Food Sci & Engn, Zhanjiang 524048, Peoples R China;[4]Guangdong Ocean Univ, Coll Food Sci & Technol, Zhanjiang 524088, Peoples R China;[5]Lincoln Univ, Fac Agr & Life Sci, Dept Wine Food & Mol Biosci, Canterbury 7647, New Zealand
年份:2022
卷号:70
期号:6
起止页码:1865
外文期刊名:JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
收录:SCI-EXPANDED(收录号:WOS:000756703000011)、、EI(收录号:20220711632976)、Scopus(收录号:2-s2.0-85124478346)、WOS
基金:This work was supported by the National Key R&D Program of China (2019YFD0901702) , the young innovative program of Guangdong provincial department of education (2019KQNCX072) , and the characteristic innovation project of Guangdong provincial department of education (2020KTSCX071) .
语种:英文
外文关键词:Pediococcus pentosaceus zy-B; protective effect; Vibrio parahaemolyticus; intestinal homeostasis; gut microbiota
外文摘要:Modulation of the intestinal barrier, inflammation, and gut microbiota by Pediococcus pentosaceus zy-B (zy-B) in Vibrio parahaemolyticus (Vp)-infected C57BL/6J mice was studied. Mice intragastrically pretreated with 108 colony-forming units (CFU) zy-B significantly alleviated Vp infection as evidenced by maintaining body weight and reduced disease activity index score and intestine ratio. In addition, zy-B reduced the Vp load in the ileum and cecum, significantly reduced the load in the colon, prevented colonic atrophy, and strengthened mucosal integrity. Mechanistically, zy-B ameliorated intestinal barrier dysfunction by upregulating tight junction protein expression, which in turn reduced the lipopolysaccharide, D-lactic acid (D-LA), and diamine oxidase concentrations and downregulated the cannabinoid receptor 1 (CB1) and CB2 mRNA expressions. Moreover, zy-B systemically reduced inflammation by decreasing interleukin-1 beta (IL-1 beta), interleukin-6 (IL-6), and tumor necrosis factor-alpha levels, and increased interleukin-10 (IL-10), immunoglobulin M (IgM), and immunoglobulin G (IgG) levels in the colon and serum. Furthermore, zy-B markedly altered the gut microbiota composition by enriching Bifidobacterium, Akkermansia, and Lactobacillus in the colon. Overall, zy-B appears to act as a probiotic to alleviate Vp infection by protecting the intestinal barrier, reducing inflammation, and promoting the growth of "beneficial" gut microbiota.
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