4.7 Article

Comparative analysis of genomic characteristics, fitness and virulence of MRSA ST398 and ST9 isolated from China and Germany

Journal

EMERGING MICROBES & INFECTIONS
Volume 10, Issue 1, Pages 1481-1494

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/22221751.2021.1951125

Keywords

MRSA; genome; fitness; virulence; pig; ST398; ST9

Funding

  1. National Natural Science Foundation of China [31761133022, 81861138051]
  2. German Research Foundation [SCHW382/11-1]

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Research has shown that MRSA ST9 strains isolated from pigs in China and Germany have evolved independently, while MRSA ST398 strains in these two countries have close evolutionary relationships. Factors contributing to the success of dominant clones like ST9 in China and ST398 in Germany include resistance to common antimicrobial agents, enhanced biofilm formation ability, and resistance to desiccation. Additionally, the presence of the vwb (nu Sa alpha) gene on the genome island may partly explain their colonization fitness in pigs.
Methicillin-resistant Staphylococcus aureus (MRSA) of sequence types ST398 and ST9 are dominant lineages among livestock in Europe and Asia, respectively. Although both STs were commonly found as colonizers of the skin and the mucosal membranes, MRSA ST398, rather than MRSA ST9, has been reported to cause infections in humans and animals. Herein, we comparatively analyzed the genomic characteristics, fitness and virulence of MRSA ST398 and ST9 isolated from pigs in both China (CHN) and Germany (GER) to explore the factors that lead to differences in their epidemics and pathogenicity. We observed that the CHN-MRSA ST9 and the GER-MRSA ST9 have evolved independently, whereas the CHN-MRSA ST398 and GER-MRSA ST398 had close evolutionary relationships. Resistance to antimicrobial agents commonly used in livestock, the enhanced ability of biofilm formation, and the resistance to desiccation contribute to the success of the dominant clones of CHN-MRSA ST9 and GER-MRSA ST398, and the vwb (nu Sa alpha) gene on the genomic island might in part contribute to their colonization fitness in pigs. All MRSA ST398 strains revealed more diverse genome structures, higher tolerance to acids and high osmotic pressure, and greater competitive fitness in co-culture experiments. Notably, we identified and characterized a novel hysA (nu Sa beta) gene, which was located on the genomic island nu Sa beta of MRSA ST398 but was absent in MRSA ST9. The enhanced pathogenicity of the MRSA ST398 strains due to hysA (nu Sa beta) might in part explain why MRSA ST398 strains are more likely to cause infections.

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