A chromosomal mutation is superior to a plasmid-encoded mutation for plasmid fitness cost compensation.

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences
PLoS Biology Pub Date : 2024-12-02 eCollection Date: 2024-12-01 DOI:10.1371/journal.pbio.3002926
Rosanna C T Wright, A Jamie Wood, Michael J Bottery, Katie J Muddiman, Steve Paterson, Ellie Harrison, Michael A Brockhurst, James P J Hall
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引用次数: 0

Abstract

Plasmids are important vectors of horizontal gene transfer in microbial communities but can impose a burden on the bacteria that carry them. Such plasmid fitness costs are thought to arise principally from conflicts between chromosomal- and plasmid-encoded molecular machineries, and thus can be ameliorated by compensatory mutations (CMs) that reduce or resolve the underlying causes. CMs can arise on plasmids (i.e., plaCM) or on chromosomes (i.e., chrCM), with contrasting predicted effects upon plasmid success and subsequent gene transfer because plaCM can also reduce fitness costs in plasmid recipients, whereas chrCM can potentially ameliorate multiple distinct plasmids. Here, we develop theory and a novel experimental system to directly compare the ecological effects of plaCM and chrCM that arose during evolution experiments between Pseudomonas fluorescens SBW25 and its sympatric mercury resistance megaplasmid pQBR57. We show that while plaCM was predicted to succeed under a broader range of parameters in mathematical models, chrCM dominated in our experiments, including conditions with numerous recipients, due to a more efficacious mechanism of compensation, and advantages arising from transmission of costly plasmids to competitors (plasmid "weaponisation"). We show analytically the presence of a mixed Rock-Paper-Scissors (RPS) regime for CMs, driven by trade-offs with horizontal transmission, that offers one possible explanation for the observed failure of plaCM to dominate even in competition against an uncompensated plasmid. Our results reveal broader implications of plasmid-bacterial evolution for plasmid ecology, demonstrating the importance of specific compensatory mutations for resistance gene spread. One consequence of the superiority of chrCM over plaCM is the likely emergence in microbial communities of compensated bacteria that can act as "hubs" for plasmid accumulation and dissemination.

在质粒适应度成本补偿方面,染色体突变优于质粒编码突变。
质粒是微生物群落中水平基因转移的重要载体,但会给携带质粒的细菌带来负担。这种质粒适合度成本被认为主要是由染色体和质粒编码的分子机制之间的冲突引起的,因此可以通过补偿突变(CMs)来减少或解决潜在的原因。CMs可以出现在质粒(即plaCM)或染色体(即chrCM)上,对质粒成功和随后的基因转移有不同的预测影响,因为plaCM还可以降低质粒受体的适应成本,而chrCM可以潜在地改善多个不同的质粒。在这里,我们建立了一个理论和一个新的实验系统来直接比较荧光假单胞菌SBW25及其同域抗汞巨质粒pQBR57在进化实验中产生的plaCM和chrCM的生态效应。我们表明,虽然plaCM在数学模型中被预测在更广泛的参数范围内取得成功,但chrCM在我们的实验中占主导地位,包括有许多受体的条件,这是由于更有效的补偿机制,以及将昂贵的质粒传播给竞争对手(质粒“武器化”)所带来的优势。通过分析,我们展示了cm的混合石头剪刀布(RPS)机制的存在,这是由水平传输的权衡驱动的,这为plaCM在与未补偿质粒竞争中未能占据主导地位提供了一种可能的解释。我们的研究结果揭示了质粒细菌进化对质粒生态的广泛影响,证明了抗性基因传播的特定补偿性突变的重要性。chrCM优于plaCM的一个结果是,可能在微生物群落中出现补偿细菌,这些细菌可以作为质粒积累和传播的“枢纽”。
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
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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