Bacillus velezensis HBXN2020 alleviates Salmonella Typhimurium-induced colitis by improving intestinal barrier integrity and reducing inflammation

Author:

Wang Linkang123,Wang Haiyan123,Li Xinxin123,Zhu Mengyuan123,Gao Dongyang123,Hu Dayue123,Xiong Zhixuan123,Li Xiangmin123,Qian Ping123

Affiliation:

1. National Key Laboratory of Agricultural Microbiology, Hubei Hongshan Laboratory, Huazhong Agricultural University

2. College of Veterinary Medicine, Huazhong Agricultural University

3. Key Laboratory of Preventive Veterinary Medicine in Hubei Province, the Cooperative Innovation Center for Sustainable Pig Production

Abstract

Bacillus velezensis is a novel species of Bacillus that has been widely investigated because of its broad-spectrum antimicrobial activity. However, most studies on Bacillus velezensis have focused on biocontrol of plant diseases, with few reports on antagonizing Salmonella Typhimurium infections. In this study, Bacillus velezensis HBXN2020 was isolated from healthy black piglets and was found to exhibit broad-spectrum antibacterial activity and robust anti-stress capabilities. Importantly, Bacillus velezensis HBXN2020 did not cause any adverse side effects in mice when administered at various doses (1 × 10 7 , 1 × 10 8 , and 1 × 10 9 CFU) for 14 days. In a Salmonella Typhimurium ATCC14028-induced mice colitis model, either curative or prophylactic, supplementing Bacillus velezensis HBXN2020 spores significantly lowered the levels of Salmonella Typhimurium ATCC14028 in their feces, ileum, cecum, and colon, and the disease activity index (DAI). Importantly, supplementing Bacillus velezensis HBXN2020 spores significantly regulated cytokine levels (TNF-α, IL-1β, IL-6, and IL-10) and maintained the expression of tight junction proteins and mucin protein. More importantly, supplementing Bacillus velezensis HBXN2020 spores also significantly enhanced the homeostasis of colonic microbiota and the abundance of beneficial bacteria. Collectively, Bacillus velezensis HBXN2020 can alleviate bacterial colitis by enhancing intestinal homeostasis and gut barrier integrity and reducing inflammation.

Publisher

eLife Sciences Publications, Ltd

Reference62 articles.

1. Salmonella enterica serovar Typhimurium skills to succeed in the host: virulence and regulation;Clin Microbiol Rev,2013

2. Neu3 neuraminidase induction triggers intestinal inflammation and colitis in a model of recurrent human food-poisoning;Proc Natl Acad Sci U S A,2021

3. Epidemiology and Outcomes of Nontyphoidal Salmonella Bacteremias from England, 2004 to 2015;J Clin Microbiol,2019

4. Invasive Salmonella infections among children in Bintulu, Sarawak, Malaysian Borneo: a 6-year retrospective review;BMC Infect Dis,2019

5. Antimicrobial resistance: A global emerging threat to public health systems;Crit Rev Food Sci Nutr,2017

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