{"title":"Intestinal short-chain fatty acids spatially regulate the antibiotic tolerance and virulence of avian pathogenic Escherichia coli","authors":"Chong Ling , Lulu Ren , Yaru Song, Qingyun Cao, Hui Ye, Zemin Dong, Changming Zhang, Dingyuan Feng, Jianjun Zuo, Weiwei Wang","doi":"10.1016/j.psj.2025.104917","DOIUrl":null,"url":null,"abstract":"<div><div>Avian pathogenic <em>Escherichia coli</em> (APEC) represents a key pathogen severely threatening the poultry production, as well as food safety and public health. At present, the infection by APEC is hard to be prevented and controlled, because it possesses considerable virulence factors and high insensitivity to antibiotics. Short-chain fatty acids (SCFAs), the primary metabolites of intestinal probiotics, are considered to contribute to maintain intestinal health partially through inhibiting the activity of detrimental bacteria in gut. However, the effects of SCFAs on APEC activity and the underlying mechanisms remain unclear. In this study, we simulated the concentrations of SCFAs in the ileum (i-SCFA) and cecum (c-SCFA) of chickens to investigate their effects on the growth, virulence factor expression, and antibiotic tolerance of APEC. The results indicated that i-SCFA treatment activated the expression of APEC virulence genes, whereas c-SCFA treatment inhibited APEC growth, virulence gene expression, and ampicillin tolerance. Moreover, we observed different response mechanisms of APEC to SCFAs and the equal-pH inorganic acid (hydrochloric acid), which may be attributable to the partial dissociation property and membrane penetration characteristic of SCFAs. Additionally, SCFAs exhibited spatial (intestinal segment-specific) effects on the expression of extracellular and intracellular H<sup>+</sup> sensing genes in APEC, with i-SCFA promoting and c-SCFA inhibiting their expression, particularly the intracellular pH homeostasis-regulating gene <em>tnaA</em>. It is known that <em>tnaA</em> encodes tryptophanase that catalyzes the conversion of tryptophan into indole, an important extracellular signaling molecule of bacteria. Further investigation revealed that the addition of indole reversed the inhibitory effects of c-SCFA on virulence gene expression and ampicillin tolerance of APEC. In summary, this study demonstrates that SCFAs spatially regulate APEC growth, virulence gene expression and antibiotic tolerance potentially by implicating in the disruption of intracellular pH homeostasis and interference with tryptophan metabolism.</div></div>","PeriodicalId":20459,"journal":{"name":"Poultry Science","volume":"104 4","pages":"Article 104917"},"PeriodicalIF":3.8000,"publicationDate":"2025-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Poultry Science","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0032579125001567","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURE, DAIRY & ANIMAL SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Avian pathogenic Escherichia coli (APEC) represents a key pathogen severely threatening the poultry production, as well as food safety and public health. At present, the infection by APEC is hard to be prevented and controlled, because it possesses considerable virulence factors and high insensitivity to antibiotics. Short-chain fatty acids (SCFAs), the primary metabolites of intestinal probiotics, are considered to contribute to maintain intestinal health partially through inhibiting the activity of detrimental bacteria in gut. However, the effects of SCFAs on APEC activity and the underlying mechanisms remain unclear. In this study, we simulated the concentrations of SCFAs in the ileum (i-SCFA) and cecum (c-SCFA) of chickens to investigate their effects on the growth, virulence factor expression, and antibiotic tolerance of APEC. The results indicated that i-SCFA treatment activated the expression of APEC virulence genes, whereas c-SCFA treatment inhibited APEC growth, virulence gene expression, and ampicillin tolerance. Moreover, we observed different response mechanisms of APEC to SCFAs and the equal-pH inorganic acid (hydrochloric acid), which may be attributable to the partial dissociation property and membrane penetration characteristic of SCFAs. Additionally, SCFAs exhibited spatial (intestinal segment-specific) effects on the expression of extracellular and intracellular H+ sensing genes in APEC, with i-SCFA promoting and c-SCFA inhibiting their expression, particularly the intracellular pH homeostasis-regulating gene tnaA. It is known that tnaA encodes tryptophanase that catalyzes the conversion of tryptophan into indole, an important extracellular signaling molecule of bacteria. Further investigation revealed that the addition of indole reversed the inhibitory effects of c-SCFA on virulence gene expression and ampicillin tolerance of APEC. In summary, this study demonstrates that SCFAs spatially regulate APEC growth, virulence gene expression and antibiotic tolerance potentially by implicating in the disruption of intracellular pH homeostasis and interference with tryptophan metabolism.
期刊介绍:
First self-published in 1921, Poultry Science is an internationally renowned monthly journal, known as the authoritative source for a broad range of poultry information and high-caliber research. The journal plays a pivotal role in the dissemination of preeminent poultry-related knowledge across all disciplines. As of January 2020, Poultry Science will become an Open Access journal with no subscription charges, meaning authors who publish here can make their research immediately, permanently, and freely accessible worldwide while retaining copyright to their work. Papers submitted for publication after October 1, 2019 will be published as Open Access papers.
An international journal, Poultry Science publishes original papers, research notes, symposium papers, and reviews of basic science as applied to poultry. This authoritative source of poultry information is consistently ranked by ISI Impact Factor as one of the top 10 agriculture, dairy and animal science journals to deliver high-caliber research. Currently it is the highest-ranked (by Impact Factor and Eigenfactor) journal dedicated to publishing poultry research. Subject areas include breeding, genetics, education, production, management, environment, health, behavior, welfare, immunology, molecular biology, metabolism, nutrition, physiology, reproduction, processing, and products.