Intestinal short-chain fatty acids spatially regulate the antibiotic tolerance and virulence of avian pathogenic Escherichia coli

IF 4.2 1区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE Poultry Science Pub Date : 2025-04-01 Epub Date: 2025-02-20 DOI:10.1016/j.psj.2025.104917
Chong Ling , Lulu Ren , Yaru Song, Qingyun Cao, Hui Ye, Zemin Dong, Changming Zhang, Dingyuan Feng, Jianjun Zuo, Weiwei Wang
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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.
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肠道短链脂肪酸在空间上调控禽致病性大肠杆菌的抗生素耐受性和毒力
禽致病性大肠杆菌(APEC)是严重威胁家禽生产、食品安全和公共卫生的重要病原体。目前,由于APEC具有相当大的毒力因子和对抗生素的高度不敏感,其感染难以预防和控制。短链脂肪酸(SCFAs)是肠道益生菌的主要代谢物,被认为部分通过抑制肠道有害细菌的活性来维持肠道健康。然而,scfa对APEC活动的影响及其潜在机制尚不清楚。在这项研究中,我们模拟了鸡回肠(i-SCFA)和盲肠(c-SCFA)中scfa的浓度,以研究它们对APEC生长、毒力因子表达和抗生素耐受性的影响。结果表明,i-SCFA处理激活了APEC毒力基因的表达,而c-SCFA处理抑制了APEC生长、毒力基因表达和氨苄西林耐受性。此外,我们观察到APEC对scfa和等ph无机酸(盐酸)的不同反应机制,这可能与scfa的部分解离特性和膜穿透特性有关。此外,scfa对APEC细胞外和细胞内H+传感基因的表达具有空间(肠段特异性)影响,其中i-SCFA促进和c-SCFA抑制其表达,特别是细胞内pH稳态调节基因tnaA。已知tnaA编码色氨酸酶,色氨酸酶催化色氨酸转化为吲哚,吲哚是细菌重要的细胞外信号分子。进一步的研究表明,吲哚的加入逆转了c-SCFA对APEC毒力基因表达和氨苄西林耐受性的抑制作用。综上所述,本研究表明,SCFAs可能通过破坏细胞内pH稳态和干扰色氨酸代谢,在空间上调节APEC的生长、毒力基因表达和抗生素耐受性。
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来源期刊
Poultry Science
Poultry Science 农林科学-奶制品与动物科学
CiteScore
7.60
自引率
15.90%
发文量
0
审稿时长
94 days
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.
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