Lasso Peptide Microcin J25 Effectively Enhances Gut Barrier Function and Modulates Inflammatory Response in an Enterotoxigenic Escherichia coli-Challenged Mouse Model

被引:23
作者
Ding, Xiuliang [1 ,2 ]
Yu, Haitao [1 ,2 ]
Qiao, Shiyan [1 ,2 ]
机构
[1] China Agr Univ, Minist Agr, Feed Ind Ctr, State Key Lab Anim Nutr, Beijing 100193, Peoples R China
[2] Beijing Biofeed Addit Key Lab, Beijing 100193, Peoples R China
关键词
enterotoxigenic Escherichia coli; microcin J25; intestinal epithelial barrier; intestinal inflammation; mice; pathogen; mitogen-activated protein kinase; nuclear factor kappa B; ANTIMICROBIAL PEPTIDE; INTESTINAL MORPHOLOGY; DEVELOPING-COUNTRIES; TRAVELERS DIARRHEA; HOST-DEFENSE; MICROBIOTA; EPIDEMIOLOGY; ANTIBACTERIAL; PERMEABILITY; HOMEOSTASIS;
D O I
10.3390/ijms21186500
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bacterial resistance leads to severe public health and safety issues worldwide. Alternatives to antibiotics are currently needed. A promising lasso peptide, microcin J25 (MccJ25), is considered to be the best potential substitute for antibiotics to treat pathogen infection, including enterotoxigenicEscherichia coli(ETEC). This study evaluated the efficacy of MccJ25 in the prevention of ETEC infection. Forty-five female BALB/c mice of clean grade (aged seven weeks, approximately 16.15 g) were randomly divided into three experimental groups as follows: (i) control group (uninfected); (ii) ETEC infection group; (iii) MccJ25 + ETEC group. Fifteen mice per group in five cages, three mice/cage. MccJ25 conferred effective protection against ETEC-induced body weight loss, decrease in rectal temperature and increase in diarrhea scores in mice. Moreover, in ETEC-challenged mice model, MccJ25 significantly improved intestinal morphology, decreased intestinal histopathological scores and attenuated intestinal inflammation by decreasing proinflammatory cytokines and intestinal permeability, including reducing serum diamine oxidase and D-lactate levels. MccJ25 enhanced epithelial barrier function by increasing occludin expression in the colon and claudin-1 expression in the jejunum, ultimately improving intestinal health of host. MccJ25 was further found to alleviate gut inflammatory responses by decreasing inflammatory cytokine production and expression via the activation of the mitogen-activated protein kinase and nuclear factor kappa B signaling pathways. Taken together, the results indicated that MccJ25 protects against ETEC-induced intestinal injury and intestinal inflammatory responses, suggesting the potential application of MccJ25 as an excellent antimicrobial or anti-inflammation agent against pathogen infections.
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页码:1 / 17
页数:17
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