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多态性能力肽不会限制肺炎链球菌中的重组。

Polymorphic competence peptides do not restrict recombination in Streptococcus pneumoniae.

机构信息

Department of Biology, Emory University, Program in Population Biology, Ecology, and Evolution, USA.

出版信息

Mol Biol Evol. 2010 Mar;27(3):694-702. doi: 10.1093/molbev/msp287. Epub 2009 Nov 25.

Abstract

Understanding the factors that limit recombination in bacteria is critical in order to better understand and assess its effects on genetic variation and bacterial population genetic structure. Transformation in the naturally competent bacterium, Streptococcus pneumoniae, is regulated by a polymorphic competence (com) apparatus. It has been suggested that polymorphic types, called pherotypes, generate and maintain subpopulation genetic structure within this species. We test predictions stemming from this hypothesis using a cosmopolitan sample of clinical pneumococcal isolates. We sequenced the locus encoding the peptide that induces competence (comC) to assign clones to each known pherotype class and then used multilocus sequence typing to determine whether there is significant genetic differentiation between pherotypes subgroups. We find two dominant pherotypes within our sample, and both are maintained at high frequencies (CSP1 74%, CSP2 26%). Our analyses fail to detect significant genetic differentiation between pherotype groups and find strong evidence, from a coalescent analysis, for interpherotype recombination. In addition, our analyses indicate that positive selection may account for the maintenance of the fixed polymorphism in this locus (comC). Altogether, these results fail to support the prediction that the polymorphism in the competence system acts to limit recombination within S. pneumoniae populations. We discuss why this result is expected given the mechanism underlying transformation and outline a scenario to explain the evolution of polymorphism in the competence system.

摘要

了解限制细菌重组的因素对于更好地理解和评估其对遗传变异和细菌群体遗传结构的影响至关重要。自然感受态细菌肺炎链球菌的转化受多态性感受态(com)装置调控。有人认为,称为表型的多态类型在该物种内产生和维持亚种群遗传结构。我们使用具有世界性的临床肺炎球菌分离株的样本测试了该假设的预测。我们对编码诱导感受态的肽(comC)的基因座进行测序,将克隆分配给每个已知的表型类,然后使用多位点序列分型来确定表型亚群之间是否存在显著的遗传分化。我们在样本中发现了两种主要的表型,并且它们都保持着高频率(CSP1 为 74%,CSP2 为 26%)。我们的分析未能检测到表型组之间存在显著的遗传分化,并且从合并分析中发现了强有力的证据表明表型间存在重组。此外,我们的分析表明,正选择可能解释了该基因座(comC)固定多态性的维持。总之,这些结果未能支持这样的预测,即感受态系统中的多态性会限制肺炎链球菌种群内的重组。我们讨论了为什么在转化的机制下,这一结果是可以预期的,并概述了一个解释感受态系统多态性进化的情景。

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