系统发育宿主范围指数揭示了噬菌体特化和毒力的生态限制。

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Clara Torres-Barceló, Claudine Boyer, Julian R Garneau, Stéphane Poussier, Isabelle Robène, Benoît Moury
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引用次数: 0

摘要

众所周知,噬菌体通常具有有限的宿主范围,靶向细菌物种中的特定菌株,但准确测量它们的特异性仍然具有挑战性。诸如宿主细菌的遗传多样性或种群动态等因素往往被忽视,尽管它们对噬菌体专门化和毒力有潜在的影响。本研究的重点是Ralstonia solanacearum物种复合体(RSSC),它由导致一种主要植物病害的遗传多样性细菌组成。它使用多样化的RSSC噬菌体集合来开发新的宿主范围分析方法,并测试关于噬菌体宿主范围的生态和进化假设。我们引入了一种新的“系统发育宿主范围指数”,该指数采用生态多样性指数来解释细菌宿主的遗传多样性,允许在专家和通才之间沿着连续体对噬菌体进行系统分类。我们提出并提供证据表明,在细菌的CRISPR-Cas免疫系统中,通才噬菌体比专才噬菌体更有可能被代表。我们探索的假设,通才噬菌体可能表现出较低的毒力比专业的,由于潜在的进化权衡之间的宿主范围的宽度和毒力。重要的是,噬菌体毒力和宿主范围之间的对比相关性取决于流行病学背景。在细菌多样性较低的情况下,这种权衡得到了证实,但在细菌多样性较高的情况下,没有发现适应广泛宿主的噬菌体的明显成本。这项研究强调了在噬菌体宿主范围内进行遗传分析和研究生态权衡的必要性,这可以提高噬菌体的基础知识和在生物防治或治疗中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Phylogenetic Host-Range Index Reveals Ecological Constraints in Phage Specialisation and Virulence.

Phages are typically known for having a limited host range, targeting particular strains within a bacterial species, but accurately measuring their specificity remains challenging. Factors like the genetic diversity or population dynamics of host bacteria are often disregarded despite their potential influence on phage specialisation and virulence. This study focuses on the Ralstonia solanacearum species complex (RSSC), which comprises genetically diverse bacteria responsible for a major plant disease. It uses a diversified collection of RSSC phages to develop new host-range analysis methods and to test ecological and evolutionary hypotheses on phage host range. We introduce a new 'phylogenetic host-range index' that employs an ecological diversity index to account for the genetic diversity of bacterial hosts, allowing systematic classification of phages along a continuum between specialists and generalists. We propose and provide evidence that generalist phages are more likely to be represented in CRISPR-Cas immune system of bacteria than specialist phages. We explore the hypothesis that generalist phages might exhibit lower virulence than specialist ones due to potential evolutionary trade-offs between host-range breadth and virulence. Importantly, contrasted correlations between phage virulence and host range depend on the epidemiological context. A trade-off was confirmed in a context of low bacterial diversity, but not in a context of higher bacterial diversity, where no apparent costs were detected for phages adapted to a wide range of hosts. This study highlights the need for genetic analyses in phage host range and of investigating ecological trade-offs that could improve both fundamental phage knowledge and applications in biocontrol or therapy.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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