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携带 qacA 基因的质粒 p_8N_qac(MN687830.1)从金黄色葡萄球菌到大肠杆菌 C600 的共轭转移:传播洗必泰耐药性的潜在机制。

Conjugative transfer of plasmid p_8N_qac(MN687830.1) carrying qacA gene from Staphylococcus aureus to Escherichia coli C600: potential mechanism for spreading chlorhexidine resistance.

机构信息

Universidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas, São Paulo, São Paulo, Brazil.

Universidade de São Paulo, Faculdade de Medicina, Instituto de Medicina Tropical de São Paulo, São Paulo, São Paulo, Brazil.

出版信息

Rev Inst Med Trop Sao Paulo. 2021 Dec 6;63:e82. doi: 10.1590/S1678-9946202163082. eCollection 2021.

Abstract

The methicillin resistant Staphylococcus aureus (MRSA) is recognized by its ability to acquire and transferring resistance genes through interspecies conjugative plasmids. However, transference of plasmids from Gram-positive cocci to Gram-negative bacilli is not well characterized. In this report, we describe the transfer of a conjugative plasmid carrying qacA from MRSA to Escherichia coli C600. We performed a conjugation experiment using a chlorhexidine resistant MRSA isolate (ST-105/SCCmec type III) carrying the gene qacA and qacC as the donor and a chlorhexidine susceptible E. coli C600 isolate as the receptor. Transconjugants were selected using MacConkey agar plates containing chlorhexidine in concentrations ranging from 0.25 to 16 g.L-1. To genotypically confirm the transfer of the resistance gene, the transconjugants were screened by Polymerase Chain Reaction (PCR) and submitted to Sanger's sequencing. MRSA isolates successfully transferred the chlorhexidine resistance gene (qacA) to the recipient E. coli strain C600. The E. coli transconjugant exhibited an important reduction of chlorhexidine susceptibility, with MICs increasing from ≤ 0.25 to ≥ 16 g.L-1 after conjugation. The qacA gene was detected by PCR as well as in the Sanger's sequencing analysis of DNA from transconjugant plasmids. To the best of our knowledge, this is the first report of the plasmid p_8N_qac(MN687830.1) carrying qacA and its transfer by conjugation from a MRSA to an E. coli. These findings increase concerns on the emergence of resistance dissemination across the genus and emphasizes the importance of continuous antiseptic stewardship.

摘要

耐甲氧西林金黄色葡萄球菌(MRSA)通过种间共轭质粒获得和转移耐药基因而被识别。然而,革兰氏阳性球菌到革兰氏阴性杆菌的质粒转移尚未得到很好的描述。在本报告中,我们描述了携带 qacA 的可共轭质粒从 MRSA 转移到大肠杆菌 C600 的情况。我们使用携带 qacA 和 qacC 基因的耐洗必泰的 MRSA 分离株(ST-105/SCCmec 型 III)作为供体和耐洗必泰的大肠杆菌 C600 分离株作为受体进行了共轭实验。使用含有从 0.25 到 16 g.L-1 浓度的洗必泰的麦康凯琼脂平板选择转导体。为了通过聚合酶链反应(PCR)和提交 Sanger 测序来遗传确认抗性基因的转移,对转导体进行了筛选。MRSA 分离株成功地将洗必泰抗性基因(qacA)转移到了受体大肠杆菌菌株 C600 中。大肠杆菌转导体对洗必泰的敏感性显著降低,在共轭后 MIC 从≤0.25 增加到≥16 g.L-1。qacA 基因通过 PCR 以及转导体质粒的 Sanger 测序分析的 DNA 检测到。据我们所知,这是第一个报道携带 qacA 的质粒 p_8N_qac(MN687830.1)及其从 MRSA 到大肠杆菌的共轭转移的报告。这些发现增加了对耐药性在属间传播的出现的担忧,并强调了持续进行防腐剂管理的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7496/8660028/40488b5db1e3/1678-9946-rimtsp-63-S1678-9946202163082-gf01.jpg

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