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首页> 外文期刊>Microbial drug resistance: MDR : Mechanisms, epidemiology, and disease >Analysis on distribution and genomic diversity of high-level antiseptic resistance genes qacA and qacB in human clinical isolates of Staphylococcus aureus.
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Analysis on distribution and genomic diversity of high-level antiseptic resistance genes qacA and qacB in human clinical isolates of Staphylococcus aureus.

机译:人类金黄色葡萄球菌临床分离株中高水平抗药性耐药基因qacA和qacB的分布和基因组多样性。

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摘要

High-level antiseptic resistance of Staphylococcus aureus is mediated by multidrug efflux pumps encoded by qacA and qacB genes. We investigated distribution and genomic diversity of these antiseptic resistance genes in a total of 522 clinical strains of S. aureus isolated recently in a Japanese hospital. The qacA/B gene was detected in 32.6% of methicillin-resistant S. aureus (MRSA) and 7.5% of methicillin-susceptible S. aureus (MSSA), whereas the low-level resistance gene smr, which was examined simultaneously, was detected at lower frequencies in both MRSA (3.3%) and MSSA (5.9%). Epidemiologic typing of S. aureus isolates suggested that higher prevalence of qacA/B in MRSA may be due to spread of a single predominant MRSA strain carrying qacA/B in the hospital. Restriction fragment length polymorphism (RFLP) analysis indicated higher prevalence of the qacB-type gene (59.3%) than the qacA-type gene (40.7%) among the qacA/B genes detected. Nucleotide sequencing analysis revealed the presence of two genetic variants in qacA (V1 and V2) and four variants in qacB (V1-V4) that differ from the qacA prototype in pSK1 by 1-5 nucleotides and 7-9 nucleotides, respectively. Although most strains with qacA-V1, qacA-V2, qacB-V3, and qacB-V4 showed high-level resistance to ethidium bromide (EB)(MIC > 100 microg/ml), all of the S. aureus isolates carrying qacB-V1 and qacB-V2 showed lower MICs of EB and some monovalent cationic antiseptic substances. By analysis of the genomic organization of the qacA/B downstream region, divergent forms of this region rearranged with an insertion of IS256 or IS257 were found primarily for qacB. The downstream region of qacA-V1 was suggested to be an evolutionary origin for other divergent forms. These findings indicated that both qacA and qacB are prevalent in recent clinical isolates, especially in MRSA, and these genes consist of variable genetic variants that may be responsible for different resistance levels against antiseptic substances.
机译:金黄色葡萄球菌的高水平抗药性是由qacA和qacB基因编码的多药外排泵介导的。我们调查了最近在日本一家医院分离的总共522株金黄色葡萄球菌临床菌株中这些抗菌素耐药基因的分布和基因组多样性。在耐甲氧西林的金黄色葡萄球菌(MRSA)和耐甲氧西林的金黄色葡萄球菌(MSSA)中检测到qacA / B基因,检出了同时检测的低水平抗性基因smr(占32.6%)。 MRSA(3.3%)和MSSA(5.9%)的频率较低。金黄色葡萄球菌分离株的流行病学分型表明,qacA / B在MRSA中的较高流行可能是由于携带qacA / B的单个主要MRSA菌株在医院中传播所致。限制性片段长度多态性(RFLP)分析表明,在检测到的qacA / B基因中,qacB型基因(59.3%)的发生率高于qacA型基因(40.7%)。核苷酸测序分析表明,qacA中存在两个遗传变异(V1和V2),而qacB中存在四个遗传变异(V1-V4),它们与pSK1中的qacA原型分别相差1-5个核苷酸和7-9个核苷酸。尽管大多数带有qacA-V1,qacA-V2,qacB-V3和qacB-V4的菌株均表现出对溴化乙锭(EB)的高水平抗性(MIC> 100 microg / ml),但所有带有qacB- V1和qacB-V2显示出EB和一些单价阳离子防腐剂的MIC较低。通过分析qacA / B下游区域的基因组组织,发现该区域以IS256或IS257插入重排的不同形式主要是针对qacB。 qacA-V1的下游区域被认为是其他趋异形式的进化起源。这些发现表明,qacA和qacB都在最近的临床分离株中普遍存在,尤其是在MRSA中,并且这些基因由可变的遗传变异体组成,这些变异体可能导致对防腐剂的不同耐药水平。

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