Commensal Escherichia coli inhibits the growth and modulates the fitness, virulence, and antimicrobial resistance of Salmonella Heidelberg in vitro.

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Microbiology spectrum Pub Date : 2025-10-07 Epub Date: 2025-08-18 DOI:10.1128/spectrum.03336-24
Yasir R Khan, Lekshmi K Edison, Thomas Denagamage, Subhashinie Kariyawasam
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引用次数: 0

Abstract

Nontyphoidal Salmonella (NTS) are major foodborne pathogens primarily transmitted to humans through contaminated poultry products. Increased antimicrobial resistance (AMR) in NTS, including Salmonella Heidelberg (SH), has recently become a public health issue. Current control measures are inadequate, emphasizing the need for novel approaches to mitigate NTS colonization in poultry and contamination of poultry products. We hypothesized that commensal Escherichia coli can reduce antibiotic-resistant NTS colonization in the chicken intestines by modulating the fitness, virulence, and AMR potential of Salmonella. To test this hypothesis, we co-cultured a commensal E. coli strain (EC47-1826) isolated from a commercial broiler chicken and an antibiotic-resistant SH strain (SH18-9079) isolated from the liver of a turkey and analyzed their transcriptomes using RNA-sequencing. Our analysis revealed 4,890 differentially expressed genes in SH when co-cultured with commensal E. coli. After filtering the expression data, we found 193 genes were significantly upregulated, while 202 genes were downregulated. Notably, several genes involved in bacterial growth, pathogenicity and virulence, biofilm formation, metal-ion homeostasis, signal transduction and chemotaxis, stress response, transmembrane transport of xenobiotics, and cellular metabolism were downregulated by as much as 86-folds in SH as compared to the control. Furthermore, this study revealed the downregulation of genes associated with AMR and drug efflux in SH by up to 12 folds. These findings highlight that commensal E. coli may reduce the fitness, persistence, virulence, and AMR dissemination of SH, implying that E. coli strains could be utilized to mitigate antibiotic-resistant SH in poultry, ultimately enhancing food safety.IMPORTANCENTS, commonly transmitted to humans through contaminated poultry meat and eggs, is a frequent cause of foodborne illness. Augmenting the situation, foodborne outbreaks of antibiotic-resistant NTS have become an additional food safety and public health concern. Evaluation of growth changes and transcriptomic profiling of antibiotic-resistant SH and commensal E. coli in a mixed culture of the two will provide insights into the ability of commensal E. coli to reduce SH colonization of chicken intestines and the genes involved in that change. Our study showed that commensal E. coli significantly reduced antibiotic-resistant SH counts and expression of Salmonella genes, which play a vital role in their growth and persistence. This suggests the potential use of commensal E. coli to control antibiotic-resistant SH colonization in poultry, leading to improved food safety through reduced NTS contamination of foods of poultry origin and reduced dissemination of antibiotic-resistant Salmonella to humans via the food chain.

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共生大肠杆菌在体外抑制生长并调节海德堡沙门氏菌的适应性、毒力和耐药性。
非伤寒沙门氏菌(NTS)是主要通过受污染的家禽产品传播给人类的食源性病原体。NTS(包括海德堡沙门氏菌)中抗菌素耐药性(AMR)的增加最近已成为一个公共卫生问题。目前的控制措施是不够的,强调需要新的方法来减轻NTS在家禽中的定植和家禽产品的污染。我们假设共生大肠杆菌可以通过调节沙门氏菌的适应性、毒力和AMR潜力来减少耐药NTS在鸡肠中的定植。为了验证这一假设,我们共培养了一株从商业肉鸡中分离出的共生大肠杆菌菌株(EC47-1826)和一株从火鸡肝脏中分离出的耐抗生素SH菌株(SH18-9079),并使用rna测序分析了它们的转录组。我们的分析显示,当与共生大肠杆菌共培养时,SH中有4890个差异表达基因。筛选表达数据后,我们发现有193个基因显著上调,202个基因下调。值得注意的是,与对照组相比,SH中涉及细菌生长、致病性和毒力、生物膜形成、金属离子稳态、信号转导和趋化性、应激反应、外源物跨膜运输和细胞代谢的一些基因下调了86倍。此外,本研究还揭示了SH中与AMR和药物外排相关的基因下调高达12倍。这些发现强调,共生大肠杆菌可能会降低SH的适应性、持久性、毒力和AMR的传播,这意味着大肠杆菌菌株可以用来减轻家禽中的SH耐药性,最终提高食品安全。重要的是,通常通过受污染的禽肉和禽蛋传播给人类,是食源性疾病的常见原因。使情况进一步恶化的是,耐抗生素NTS的食源性暴发已成为一个额外的食品安全和公共卫生问题。对抗生素耐药SH和共生大肠杆菌在混合培养中的生长变化和转录组学分析的评估,将有助于深入了解共生大肠杆菌减少SH在鸡肠道定植的能力以及参与这种变化的基因。我们的研究表明,共生大肠杆菌显著降低了耐药SH计数和沙门氏菌基因的表达,这对它们的生长和持久性起着至关重要的作用。这表明可能使用共生大肠杆菌来控制耐抗生素SH在家禽中的定植,从而通过减少NTS污染家禽源食品和减少耐抗生素沙门氏菌通过食物链传播给人类来改善食品安全。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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