Community-associated MRSA: What makes them special?

被引:295
作者
Otto, Michael [1 ]
机构
[1] NIAID, Pathogen Mol Genet Sect, Lab Human Bacterial Pathogenesis, NIH, Bethesda, MD 20892 USA
关键词
Staphylococcus aureus; MRSA; Community-associated MRSA; Alpha-toxin; Panton-Valentine leukocidin; Phenol-soluble modulin; RESISTANT STAPHYLOCOCCUS-AUREUS; PANTON-VALENTINE LEUKOCIDIN; CATABOLIC MOBILE ELEMENT; ALPHA-HEMOLYSIN; VIRULENCE DETERMINANTS; NASAL CARRIAGE; USA300; TOXIN; SKIN; INFECTION;
D O I
10.1016/j.ijmm.2013.02.007
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
While infections with methicillin-resistant Staphylococcus aureus (MRSA) were traditionally restricted to the hospital setting, novel MRSA strains emerged over the last two decades that have the capacity to infect otherwise healthy people outside of the hospital setting. These community-associated (CA-)MRSA strains combine methicillin resistance with enhanced virulence and fitness. Interestingly, CA-MRSA strains emerged globally and from different backgrounds, indicating that the "trade-off" between maintaining sufficient levels of methicillin resistance and obtaining enhanced virulence at a low fitness cost was achieved on several occasions in convergent evolution. However, frequently this process comprised similar changes. First and foremost, all CA-MRSA strains typically carry a novel type of methicillin resistance locus that appears to cause less of a fitness burden. Additionally, acquisition of specific toxin genes, most notably that encoding Panton-Valentine leukocidin (PVL), and adaptation of gene expression of genome-encoded toxins, such as alpha-toxin and phenol-soluble modulins (PSMs), further contributed to the evolution of CA-MRSA. Finally, the exceptional epidemiological success of the USA300 CA-MRSA clone in particular may have been due to yet another gene acquisition, namely that of the speG gene, which is located on the arginine catabolic mobile element (ACME) and involved in detoxifying harmful host-derived polyamines. Published by Elsevier GmbH.
引用
收藏
页码:324 / 330
页数:7
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