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细菌质粒接合介导的肠道水平基因转移模型

Models for Gut-Mediated Horizontal Gene Transfer by Bacterial Plasmid Conjugation.

作者信息

Ott Logan C, Mellata Melha

机构信息

Department of Food Science and Human Nutrition, Iowa State University, Ames, IA, United States.

Interdepartmental Microbiology Graduate Program, Iowa State University, Ames, IA, United States.

出版信息

Front Microbiol. 2022 Jun 30;13:891548. doi: 10.3389/fmicb.2022.891548. eCollection 2022.

DOI:10.3389/fmicb.2022.891548
PMID:35847067
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9280185/
Abstract

The emergence of new antimicrobial resistant and virulent bacterial strains may pose a threat to human and animal health. Bacterial plasmid conjugation is a significant contributor to rapid microbial evolutions that results in the emergence and spread of antimicrobial resistance (AR). The gut of animals is believed to be a potent reservoir for the spread of AR and virulence genes through the horizontal exchange of mobile genetic elements such as plasmids. The study of the plasmid transfer process in the complex gut environment is limited due to the confounding factors that affect colonization, persistence, and plasmid conjugation. Furthermore, study of plasmid transfer in the gut of humans is limited to observational studies, leading to the need to identify alternate models that provide insight into the factors regulating conjugation in the gut. This review discusses key studies on the current models for , , and modeling of bacterial conjugation, and their ability to reflect the gut of animals. We particularly emphasize the use of computational and models that may approximate aspects of the gut, as well as animal models that represent conditions to a greater extent. Directions on future research studies in the field are provided.

摘要

新型抗菌耐药和有毒力的细菌菌株的出现可能对人类和动物健康构成威胁。细菌质粒接合是微生物快速进化的一个重要因素,导致抗菌药物耐药性(AR)的出现和传播。动物肠道被认为是通过质粒等可移动遗传元件的水平交换传播AR和毒力基因的一个重要储存库。由于影响定殖、持久性和质粒接合的混杂因素,在复杂肠道环境中对质粒转移过程的研究受到限制。此外,对人类肠道中质粒转移的研究仅限于观察性研究,因此需要确定替代模型,以深入了解调节肠道中接合作用的因素。本综述讨论了关于细菌接合的体外、体内和计算机建模的当前模型的关键研究,以及它们反映动物肠道情况的能力。我们特别强调使用可能近似肠道情况的计算模型和体外模型,以及在更大程度上代表体内条件的动物模型。本文还提供了该领域未来研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca25/9280185/49f21b5d2886/fmicb-13-891548-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca25/9280185/49f21b5d2886/fmicb-13-891548-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca25/9280185/49f21b5d2886/fmicb-13-891548-g001.jpg

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