首页> 外文期刊>Frontiers in Microbiology >The Changing Pattern of Population Structure of Staphylococcus aureus from Bacteremia in China from 2013 to 2016: ST239-030-MRSA Replaced by ST59-t437
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The Changing Pattern of Population Structure of Staphylococcus aureus from Bacteremia in China from 2013 to 2016: ST239-030-MRSA Replaced by ST59-t437

机译:2013年至2016年中国细菌性金黄色葡萄球菌人口结构的变化模式:用ST59-t437代替ST239-030-MRSA

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To investigate the epidemiology and genetic structure of Staphylococcus aureus bacteremia in China, a total of 416 isolates from 22 teaching hospitals in 12 cities from 2013 and 2016 were characterized by antibiogram analysis, multilocus sequence typing (MLST), spa typing and staphylococcal cassette chromosome mec (SCC mec ) typing. The predominant meticillin-susceptible (MSSA) genotypes in 2013 were ST188 (19.1%), ST7 (8.7%), and ST398 (7.8%), respectively, and they continued to be the main genotypes in 2016. The prevalence of meticillin-resistant S. aureus (MRSA) were 36.5% (66/181) and 36.6% (86/235) in 2013 and 2016, respectively. Interestingly, the susceptibility rates of MRSA to rifampicin and fluoroquinolones increased significantly from 2013 to 2016 ( P < 0.01), and this was associated with changes in genetic structure. ST239-t030-MRSA, the predominant genotype among all MRSAs in 2013 (34.8%), was replaced by ST59-t437-MRSA (15.1%) in 2016. Further analysis revealed that the ST239-t030-MRSA were more resistant to rifampicin, tetracycline and fluoroquinolones than ST59-t437-MRSA ( P < 0.01). To further gain insight into the mechanisms underlying the changes of genetic structure, in vitro competition and fitness measurements were performed. Importantly, ST239-t030-MRSA displayed lower growth rate and lower competitive advantage compared to ST59-t437-MRSA. Together, our findings reveal that fitness advantage of ST59-t437-MRSA over ST239-t030-MRSA may lead to changes in genetic structure and increased susceptibility of MRSA to rifampicin and fluoroquinolones in Chinese patients with S. aureus bacteremia. Our study supports temporal dynamics in MRSA clone diversities, further providing critical insights into the importance of continued monitoring of MRSA.
机译:为调查中国金黄色葡萄球菌菌血症的流行病学和遗传结构,采用抗菌素分析,多位点序列分型(MLST),spa分型和葡萄球菌盒式染色体mec对2013年和2016年来自12个城市的22家教学医院的416种分离株进行了特征分析。 (SCC mec)键入。 2013年,主要的甲氧西林敏感性基因型分别为ST188(19.1%),ST7(8.7%)和ST398(7.8%),并在2016年继续成为主要基因型。耐甲氧西林的流行率2013年和2016年金黄色葡萄球菌(MRSA)分别为36.5%(66/181)和36.6%(86/235)。有趣的是,从2013年到2016年,MRSA对利福平和氟喹诺酮类药物的敏感性显着增加(P <0.01),这与遗传结构的变化有关。 ST239-t030-MRSA是2013年所有MRSA中的主要基因型(34.8%),2016年被ST59-t437-MRSA(15.1%)取代。进一步的分析表明,ST239-t030-MRSA对利福平的耐药性更高,四环素和氟喹诺酮类比ST59-t437-MRSA(P <0.01)。为了进一步了解遗传结构变化的潜在机制,进行了体外竞争和适应性测量。重要的是,与ST59-t437-MRSA相比,ST239-t030-MRSA表现出较低的增长率和较低的竞争优势。总之,我们的发现表明,在中国金黄色葡萄球菌菌血症患者中,ST59-t437-MRSA比ST239-t030-MRSA具有更强的健身优势,可能会导致遗传结构发生变化,并增加MRSA对利福平和氟喹诺酮类药物的敏感性。我们的研究支持MRSA克隆多样性的时间动态,进一步为持续监测MRSA的重要性提供了重要的见解。

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