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

Author:

Zhou Wangxiao1,Jin Ye12,Shen Ping13,Chen Weiwei4,Chen Yunbo1,Xiao Yonghong135

Affiliation:

1. State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine , Hangzhou , China

2. Department of General Intensive Care Unit, The Second Affiliated Hospital of Zhejiang University School of Medicine , Hangzhou, Zhejiang , China

3. Department of Structure and Morphology, Jinan Microecological Biomedicine Shandong Laboratory , Jinan, Shandong , China

4. Department of Laboratory Medicine, The First Affiliated Hospital, School of Medicine, Zhejiang University , Hangzhou , China

5. Research Units of Infectious Disease and Microecology, Chinese Academy of Medical Sciences , Beijing , China

Abstract

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.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Research Project of Jinan Microecological Biomedicine Shandong Laboratory

Fundamental Research Funds for the Central Universities

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

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