Zhewei Sun, Jinhong Chen, Chunhong Liu, Yueru Tian, Fuqi Ai, Jiaying Du, Wangxiao Zhou, Wenjun Cao, Ming Guan, Baixing Ding
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The ST764 clone and two subclones of ST22-PT hypervirulent clone have developed an extensive quinolone-resistant (eQR) phenotype, conferring additional resistance to advanced quinolones due to the accumulation of four mutations in gyrA (S84L and either S85P, E88K, or E88G) and parC (S80F and either E84K or E84G). These ST764- and ST22-PT-eQR isolates were highly transmissible and showed increased resistance to other commonly used antimicrobials, posing potential high-risk clones. The eQR phenotype may be inherent to the ST764 lineage, which emerged in the late 1980s, coinciding with the widespread fluoroquinolone usage. 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引用次数: 0
摘要
背景:耐甲氧西林金黄色葡萄球菌(MRSA)是引起耳部感染的主要病原体。然而,基因组流行病学和影响社区中耳感染相关MRSA (EIA-MRSA)传播的决定因素仍然未知。方法:2020-2021年,从中国上海不同家庭门诊患者中收集105株EIA-MRSA分离株并进行测序。通过抗菌药敏试验、核心基因组MLST和系统动力学分析来表征EIA-MRSA的传播。结果:喹诺酮类药物耐药性被确定为EIA-MRSA传播的危险因素(OR 9, [95% CI 3-31])。ST764克隆和ST22-PT高毒克隆的两个亚克隆已经发展出广泛的喹诺酮耐药(eQR)表型,由于gyrA (S84L和S85P、E88K或E88G)和parC (S80F和E84K或E84G)中四个突变的积累,赋予了对高级喹诺酮类药物的额外耐药性。这些ST764-和ST22-PT-eQR分离株具有高度传染性,并且对其他常用抗菌素的耐药性增强,构成潜在的高风险克隆。eQR表型可能是ST764谱系所固有的,该谱系出现于20世纪80年代末,与氟喹诺酮类药物的广泛使用相一致。ST22-PT-eQR亚克隆于2017年左右出现,并正在积累抗性基因。结论:对eQR高危克隆保持警惕是至关重要的,特别是收敛性的ST22-PT-eQR亚克隆,其积累了抗性和毒力特征,具有耳部感染的风险。临床试验号:不适用。
Genomic insights into the spread of methicillin-resistant Staphylococcus aureus involved in ear infections.
Background: Methicillin-resistant Staphylococcus aureus (MRSA) is a major pathogen causing ear infections. However, genomic epidemiology and determinants influencing transmission of ear infections associated MRSA (EIA-MRSA) in community remain unknown.
Methods: In 2020-2021, 105 EIA-MRSA isolates were collected and sequenced from outpatients across different households in Shanghai, China. Antimicrobial susceptibility testing, core genome MLST, and phylodynamic analyses were conducted to characterize EIA-MRSA dissemination.
Results: Quinolone resistance was identified as a risk factor for EIA-MRSA spread (OR 9, [95% CI 3-31]). The ST764 clone and two subclones of ST22-PT hypervirulent clone have developed an extensive quinolone-resistant (eQR) phenotype, conferring additional resistance to advanced quinolones due to the accumulation of four mutations in gyrA (S84L and either S85P, E88K, or E88G) and parC (S80F and either E84K or E84G). These ST764- and ST22-PT-eQR isolates were highly transmissible and showed increased resistance to other commonly used antimicrobials, posing potential high-risk clones. The eQR phenotype may be inherent to the ST764 lineage, which emerged in the late 1980s, coinciding with the widespread fluoroquinolone usage. The ST22-PT-eQR subclones emerged in around 2017 and are accumulating resistance genes.
Conclusion: Vigilance is crucial for eQR high-risk clones, particularly the convergent ST22-PT-eQR subclones that accumulate resistance and virulence traits, posing risks for ear infections.
期刊介绍:
BMC Infectious Diseases is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of infectious and sexually transmitted diseases in humans, as well as related molecular genetics, pathophysiology, and epidemiology.