肠球菌冗余 pbp5 基因的多样化基因组和流行病学景观:对质粒调动、氨苄西林敏感性和环境相互作用的见解。

IF 8.2 1区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES
Science of the Total Environment Pub Date : 2024-12-20 Epub Date: 2024-11-23 DOI:10.1016/j.scitotenv.2024.177562
Paula Bierge, Miquel Sánchez-Osuna, Bárbara Duarte, Inmaculada Gómez-Sánchez, Mateu Espasa, Ana R Freitas, Luisa Peixe, Oriol Gasch, Oscar Q Pich, Carla Novais
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引用次数: 0

摘要

细菌的基因冗余在提高适应性和加速进化以应对选择性压力(尤其是与环境快速变化相关的压力)方面发挥着至关重要的作用。氨苄青霉素等氨基青霉素类药物是人类和动物肠球菌感染的重要治疗选择,耐药性大多与 pbp5 基因突变或过度表达有关。虽然偶尔有报道称存在多余的 pbp5 基因,但尚未详细探讨其对宿主细菌的益处。在对来自菌血症患者的粪肠球菌进行全基因组测序的过程中,我们发现了一株带有冗余 pbp5 基因的 ST592 菌株(Efm57)。这为我们提供了一个机会,研究不同来源、不同地理区域和不同时间范围内不同肠球菌物种中多个 pbp5 获取基因的普遍性及其影响。对公共数据库中 618 个完整肠球菌基因组的分析表明,3.2% 的肠球菌含有冗余 pbp5 基因,这些基因位于不同流行病学背景的不同物种的染色体或质粒上。这些基因编码的蛋白质与原生拷贝的同源性从 51.1% 到 97.5% 不等。系统发育分析将冗余的 PBP5 氨基酸序列分为三个不同的支系,插入序列(大多类似 IS6)使其最近扩散到具有不同遗传骨架的各种质粒上。pbp5 质粒上存在多种抗生素耐药基因,包括对利奈唑胺(linezolid)产生耐药性的基因,这突出表明它们参与了与其他临床相关抗生素的共同选择和重组事件。共轭实验证实了来自 Efm57 菌株的特定 24 kb pbp5- 质粒的可转移性。该质粒与更高的氨苄青霉素最低抑菌浓度有关,并赋予细菌在 22 °C 下的生长优势。总之,冗余 pbp5 基因在肠球菌属中的广泛分布凸显了重叠生态系统中遗传流动性、环境因素和多重耐药性之间复杂的相互作用,强调了在 "一个健康 "框架内了解这些动态以减少抗生素耐药性传播的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diverse genomic and epidemiological landscapes of redundant pbp5 genes in Enterococcus spp.: Insights into plasmid mobilization, ampicillin susceptibility, and environmental interactions.

Genetic redundancy in bacteria plays a crucial role in enhancing adaptability and accelerating evolution in response to selective pressures, particularly those associated with rapid environmental changes. Aminopenicillins like ampicillin are important therapeutic options for Enterococcus infections in both humans and animals, with resistance mostly associated with pbp5 gene mutations or overexpression. While the occurrence of redundant pbp5 genes has been occasionally reported, the advantages for the host bacteria have not been explored in detail. During a whole-genome sequencing project of Enterococcus faecium from bacteremic patients, we identified an ST592 strain (Efm57) with redundant pbp5 genes. This presented an opportunity to investigate the prevalence and implications of multiple pbp5 acquisitions in diverse Enterococcus species across various sources, geographical regions, and timeframes. The analysis of 618 complete Enterococcus genomes from public databases revealed that 3.2 % harbored redundant pbp5 genes, located on chromosomes or plasmids across different species from diverse epidemiological backgrounds. The proteins encoded by these genes showed homologies ranging from 51.1 % to 97.5 % compared to native copies. Phylogenetic analysis grouped redundant PBP5 amino acid sequences into three distinct clades, with insertion sequences (mostly IS6-like) facilitating their recent spread to diverse plasmids with varying genetic backbones. The presence of multiple antibiotic resistance genes on pbp5-plasmids, including those conferring resistance to linezolid, underscores their involvement in co-selection and recombination events with other clinically-relevant antibiotics. Conjugation experiments confirmed the transferability of a specific 24 kb pbp5-plasmid from the Efm57 strain. This plasmid was associated with higher minimum inhibitory concentrations of ampicillin and conferred bacteria growth advantages at 22 °C. In conclusion, the widespread distribution of redundant pbp5 genes among Enterococcus spp. highlights the complex interplay between genetic mobility, environmental factors, and multidrug resistance in overlapping ecosystems emphasizing the importance of understanding these dynamics to mitigate antibiotic resistance spread within the One Health framework.

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来源期刊
Science of the Total Environment
Science of the Total Environment 环境科学-环境科学
CiteScore
17.60
自引率
10.20%
发文量
8726
审稿时长
2.4 months
期刊介绍: The Science of the Total Environment is an international journal dedicated to scientific research on the environment and its interaction with humanity. It covers a wide range of disciplines and seeks to publish innovative, hypothesis-driven, and impactful research that explores the entire environment, including the atmosphere, lithosphere, hydrosphere, biosphere, and anthroposphere. The journal's updated Aims & Scope emphasizes the importance of interdisciplinary environmental research with broad impact. Priority is given to studies that advance fundamental understanding and explore the interconnectedness of multiple environmental spheres. Field studies are preferred, while laboratory experiments must demonstrate significant methodological advancements or mechanistic insights with direct relevance to the environment.
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