The genetic feature and virulence determinant of highly virulent community-associated MRSA ST338-SCCmec Vb in China

Ye Jin1, Wangxiao Zhou1, Zhidong Yin2

  • 1State 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, People's Republic of China.

Insights

ST338, a variant of ST59 community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA), emerged in 1991. ST338 strains possess key virulence factors but lack certain adhesion factors, showing reduced nasal colonization and similar virulence to other CA-MRSA.

Area of Science:

  • Microbiology
  • Genetics
  • Epidemiology

Background:

  • ST59 is the dominant community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) pathotype in China.
  • ST338 is a less-studied variant of ST59 CA-MRSA.

Purpose of the Study:

  • To investigate the epidemiology, genetic characteristics, and virulence of ST338 CA-MRSA strains.
  • To understand the evolutionary origins and pathogenicity of ST338.

Main Methods:

  • Phylogenetic analysis and time estimation to determine ST338's evolutionary history.
  • Genomic analysis to identify virulence factors and adhesion factors.
  • In vitro and in vivo experiments (mice models) to assess colonization and virulence.

Main Results:

  • Phylogenetic analysis suggests ST338 evolved from ST59 around 1991.
  • ST338 strains share similar virulence factor profiles, including genomic islands νSaα, νSaγ, SaPI, hla, and psm, but lack specific adhesion factors (clfA, clfB, eap, cna, icaD).
  • ST338 exhibited weaker nasal colonization than CA-MRSA MW2, and both PVL-positive and PVL-negative strains showed comparable virulence in mouse models, dependent on toxin gene upregulation.

Conclusions:

  • ST338 represents a distinct, highly virulent lineage of CA-MRSA.
  • Its pathogenicity is linked to specific virulence factor expression rather than mobile genetic elements like ΦSa2.
  • Findings offer insights into the emergence and virulence of this novel ST338-SCCmec Vb clone.

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