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pSK41 样质粒对于粪肠球菌中 Inc18 样 vanA 质粒向金黄色葡萄球菌的体外转移是必需的。

pSK41-like plasmid is necessary for Inc18-like vanA plasmid transfer from Enterococcus faecalis to Staphylococcus aureus in vitro.

机构信息

Division of Healthcare Quality Promotion, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

出版信息

Antimicrob Agents Chemother. 2013 Jan;57(1):212-9. doi: 10.1128/AAC.01587-12. Epub 2012 Oct 22.

Abstract

Vancomycin-resistant Staphylococcus aureus (VRSA) is thought to result from the in vivo conjugative transfer of a vanA plasmid from an Enterococcus sp. to S. aureus. We studied bacterial isolates from VRSA cases that occurred in the United States to identify microbiological factors which may contribute to this plasmid transfer. First, vancomycin-susceptible, methicillin-resistant S. aureus (MRSA) isolates from five VRSA cases were tested for their ability to accept foreign DNA by conjugation in mating experiments with Enterococcus faecalis JH2-2 containing pAM378, a pheromone-response conjugative plasmid. All of the MRSA isolates accepted the plasmid DNA with similar transfer efficiencies (∼10(-7)/donor CFU) except for one isolate, MRSA8, for which conjugation was not successful. The MRSA isolates were also tested as recipients in mating experiments between an E. faecalis isolate with an Inc18-like vanA plasmid that was isolated from a VRSA case patient. Conjugative transfer was successful for 3/5 MRSA isolates. Successful MRSA recipients carried a pSK41-like plasmid, a staphylococcal conjugative plasmid, whereas the two unsuccessful MRSA recipients did not carry pSK41. The transfer of a pSK41-like plasmid from a successful MRSA recipient to the two unsuccessful recipients resulted in conjugal transfer of the Inc18-like vanA plasmid from E. faecalis at a frequency of 10(-7)/recipient CFU. In addition, conjugal transfer could be achieved for pSK41-negative MRSA in the presence of a cell-free culture filtrate from S. aureus carrying a pSK41-like plasmid at a frequency of 10(-8)/recipient CFU. These results indicated that a pSK41-like plasmid can facilitate the transfer of an Inc18-like vanA plasmid from E. faecalis to S. aureus, possibly via an extracellular factor produced by pSK41-carrying isolates.

摘要

耐万古霉素金黄色葡萄球菌(VRSA)被认为是由于肠球菌属中的 vanA 质粒在体内的共轭转移到金黄色葡萄球菌而产生的。我们研究了在美国发生的 VRSA 病例中的细菌分离物,以确定可能有助于这种质粒转移的微生物学因素。首先,通过与含有 pAM378 的粪肠球菌 JH2-2 进行共轭实验,测试了来自 5 例 VRSA 病例的耐万古霉素、耐甲氧西林金黄色葡萄球菌(MRSA)分离物接受外源 DNA 的能力,pAM378 是一种激素反应共轭质粒。除了一个分离物 MRSA8 之外,所有的 MRSA 分离物都以相似的转移效率(约 10(-7)/供体 CFU)接受质粒 DNA,MRSA8 的共轭实验不成功。还将这些 MRSA 分离物作为受体,在与从 VRSA 病例患者中分离的具有 Inc18 样 vanA 质粒的粪肠球菌分离物之间进行共轭实验。3/5 的 MRSA 分离物成功进行了共轭转移。成功的 MRSA 受体携带 pSK41 样质粒,一种葡萄球菌共轭质粒,而两个不成功的 MRSA 受体没有携带 pSK41。从成功的 MRSA 受体中转移 pSK41 样质粒到两个不成功的受体中,导致粪肠球菌中的 Inc18 样 vanA 质粒以 10(-7)/受体 CFU 的频率进行共轭转移。此外,在携带 pSK41 样质粒的金黄色葡萄球菌的无细胞培养滤液存在的情况下,pSK41 阴性的 MRSA 可以实现共轭转移,频率为 10(-8)/受体 CFU。这些结果表明,pSK41 样质粒可以促进粪肠球菌中的 Inc18 样 vanA 质粒向金黄色葡萄球菌的转移,可能是通过携带 pSK41 的分离物产生的细胞外因子。

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