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Multiplex PCR Assay for Typing of Staphylococcal Cassette Chromosome Mec Types I to V in Methicillin-resistant Staphylococcus aureus
Published on: September 5, 2013
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.
Abstract:
ST59 is the predominant pathotype of community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) in China. As a variant of ST59, there is relatively little known about the detailed information of ST338. To address this issue, here, we described thirteen ST338 CA-MRSA strains isolated from severe bloodstream infection cases, and focused on their epidemiology, genetic features and virulence potential. Phylogenetic analysis showed the earliest isolated strain of this study is likely a predecessor of recent ST338 lineage (after year of 2014). Furthermore, the phylogenetic reconstruction and time estimation suggested that ST338 evolved from ST59 in 1991. Notably, the carrying patten of virulence factors of all ST338 strains were similar, and the genomic islands νSaα, νSaγ and SaPI and the core virulence factors like hla and psm were detected in ST338 isolates. However, all ST338 isolates lacked some adhesion factors such as clfA, clfB, eap, cna and icaD. Additionally, among these ST338 strains, one PVL-negative ST338 isolate was detected. Experiment on mice nose and human alveolar epithelial cell showed that the nasal colonization ability of ST338 was weaker than that of CA-MRSA MW2. In a mouse bloodstream infection model and skin infection model, PVL+ and PVL- strains had the similar virulence, which was dependent on upregulation of toxin genes rather than the presence of mobile genetic elements such as ΦSa2 carrying PVL. Our findings provide important insight into the epidemiology and pathogenicity of the novel and highly virulent ST338-SCCmec Vb clone.
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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