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Novel SCCmec variants in clonal complex 398 and lineage-specific pseudo-SCCmec identified in ST88 MRSA from invasive bloodstream infections in China

SCCmec公司 流动遗传元素 生物 遗传学 谱系(遗传) 基因 克隆(Java方法) 金黄色葡萄球菌 基因组 微生物学 耐甲氧西林金黄色葡萄球菌 细菌
作者
Wangxiao Zhou,Yue Jin,Ping Shen,Weiwei Chen,Yunbo Chen,Yonghong Xiao
出处
期刊:Journal of Antimicrobial Chemotherapy [Oxford University Press]
卷期号:78 (9): 2366-2375 被引量:2
标识
DOI:10.1093/jac/dkad250
摘要

Abstract Background Methicillin resistance in Staphylococcus aureus is primarily due to the mecA gene found in highly diverse staphylococcal cassette chromosome mec (SCCmec) elements, with an increasing number of variants being continually discovered. Objectives To characterize two novel SCCmec variants identified in clonal complex (CC) 398 strains and lineage-specific pseudo-SCCmec elements in the ST88 clone. Methods WGS and comparative genomic analysis were used to elucidate the SCCmec element diversity of representative isolates. Results The non-typeable 47 kb SCCmec found in the CC398 strain SKLX55795 represents a novel subtype of XIV, showing significant differences in structural organization and genetic content within the joining regions compared with the XIV element from the prototype strain SC792. This unique subtype comprised remnants from various mobile genetic elements that encode antimicrobial resistance genes, ultimately forming a large MDR region. Genome analysis of CC398 strain SKLX61416 revealed the presence of a novel 50 kb composite SCCmec with two distinct domains, carrying the ccr gene complexes 5/8 and containing genes for the detoxification of arsenic and sulphide. Further sequence analysis disclosed that 44.23% (23/52) of ST88 strains in our collection carried a lineage-specific pseudo-SCCmec, termed ΨSCCmecST88. This ΨSCCmecST88 harboured the mec gene complex C2, along with a series of genes associated with heavy metal resistance, but lacked an approximately 28 kb region encompassing the ccr gene complex. Conclusions Our findings provide evidence for the ongoing evolution of SCCmec elements within the CC398 and ST88 clones, underscoring the need for further surveillance to understand the biological significance of these elements.
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