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Expression of a Cryptic Secondary Sigma Factor Gene Unveils Natural Competence for DNA Transformation in Staphylococcus aureus

机译:隐性次级Sigma因子基因的表达揭示了金黄色葡萄球菌DNA转化的自然能力。

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摘要

It has long been a question whether Staphylococcus aureus, a major human pathogen, is able to develop natural competence for transformation by DNA. We previously showed that a novel staphylococcal secondary sigma factor, SigH, was a likely key component for competence development, but the corresponding gene appeared to be cryptic as its expression could not be detected during growth under standard laboratory conditions. Here, we have uncovered two distinct mechanisms allowing activation of SigH production in a minor fraction of the bacterial cell population. The first is a chromosomal gene duplication rearrangement occurring spontaneously at a low frequency [≤10−5], generating expression of a new chimeric sigH gene. The second involves post-transcriptional regulation through an upstream inverted repeat sequence, effectively suppressing expression of the sigH gene. Importantly, we have demonstrated for the first time that S. aureus cells producing active SigH become competent for transformation by plasmid or chromosomal DNA, which requires the expression of SigH-controlled competence genes. Additionally, using DNA from the N315 MRSA strain, we successfully transferred the full length SCCmecII element through natural transformation to a methicillin-sensitive strain, conferring methicillin resistance to the resulting S. aureus transformants. Taken together, we propose a unique model for staphylococcal competence regulation by SigH that could help explain the acquisition of antibiotic resistance genes through horizontal gene transfer in this important pathogen.
机译:长期以来一直存在的问题是,主要的人类病原体金黄色葡萄球菌是否能够发展通过DNA转化的天然能力。我们以前表明,一种新的葡萄球菌次级sigma因子SigH,可能是能力发展的关键组成部分,但由于在标准实验室条件下无法在生长过程中检测到其表达,因此相应的基因似乎是隐秘的。在这里,我们发现了两种不同的机制,可在细菌细胞群的一小部分中激活SigH的产生。首先是染色体基因重复重排以低频[≤10 -5 ]自发发生,从而产生新的嵌合sigH基因的表达。第二个涉及通过上游反向重复序列的转录后调控,有效抑制sigH基因的表达。重要的是,我们首次证明了产生活性SigH的金黄色葡萄球菌细胞能够通过质粒或染色体DNA转化,这需要SigH控制的能力基因的表达。此外,使用来自N315 MRSA菌株的DNA,我们通过自然转化成功地将全长SCCmecII元件转移至对甲氧西林敏感的菌株,从而使甲氧西林对所得的金黄色葡萄球菌转化株具有抗性。综上所述,我们提出了一种独特的SigH葡萄球菌能力调节模型,该模型可以解释这种重要病原体中通过水平基因转移获得抗生素抗性基因。

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