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耐甲氧西林降低了与医疗保健相关的耐甲氧西林金黄色葡萄球菌的毒力,其机制是干扰 agr 群体感应系统。

Methicillin resistance reduces the virulence of healthcare-associated methicillin-resistant Staphylococcus aureus by interfering with the agr quorum sensing system.

机构信息

Department of Biology and Biochemistry, University of Bath, UK.

出版信息

J Infect Dis. 2012 Mar 1;205(5):798-806. doi: 10.1093/infdis/jir845. Epub 2012 Feb 1.

DOI:10.1093/infdis/jir845
PMID:22301683
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3318674/
Abstract

The difficulty in successfully treating infections caused by methicillin-resistant Staphylococcus aureus (MRSA) has led to them being referred to as highly virulent or pathogenic. In our study of one of the major healthcare-associated MRSA (HA-MRSA) clones, we show that expression of the gene responsible for conferring methicillin resistance (mecA) is also directly responsible for reducing the ability of HA-MRSA to secrete cytolytic toxins. We show that resistance to methicillin induces changes in the cell wall, which affects the bacteria's agr quorum sensing system. This leads to reduced toxin expression and, as a consequence, reduced virulence in a murine model of sepsis. This diminished capacity to cause infection may explain the inability of HA-MRSA to move into the community and help us understand the recent emergence of community-associated MRSA (CA-MRSA). CA-MRSA typically express less penicillin-binding protein 2a (encoded by mecA), allowing them to maintain full virulence and succeed in the community environment.

摘要

耐甲氧西林金黄色葡萄球菌(MRSA)引起的感染很难成功治疗,因此被称为高毒力或致病性。在我们对主要的医院获得性耐甲氧西林金黄色葡萄球菌(HA-MRSA)之一的研究中,我们发现导致耐甲氧西林的基因(mecA)的表达也直接导致 HA-MRSA 分泌细胞毒素的能力降低。我们发现,耐甲氧西林诱导细胞壁发生变化,从而影响细菌的agr 群体感应系统。这导致毒素表达减少,进而导致败血症小鼠模型中的毒力降低。这种感染能力的降低可能解释了 HA-MRSA 无法进入社区的原因,并帮助我们理解最近社区获得性耐甲氧西林金黄色葡萄球菌(CA-MRSA)的出现。CA-MRSA 通常表达较少的青霉素结合蛋白 2a(由 mecA 编码),使它们能够保持完全的毒力并在社区环境中成功生存。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4491/3318674/4fe0397c26c2/infdisjir845f05_ht.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4491/3318674/e551c5099e7a/infdisjir845f04_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4491/3318674/4fe0397c26c2/infdisjir845f05_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4491/3318674/2600372c7a91/infdisjir845f01_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4491/3318674/20e16214169d/infdisjir845f02_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4491/3318674/9e95b18cf297/infdisjir845f03_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4491/3318674/e551c5099e7a/infdisjir845f04_lw.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4491/3318674/4fe0397c26c2/infdisjir845f05_ht.jpg

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