Chen Yan, Chatterjee Som S, Porcella Stephen F, Yu Yun-Song, Otto Michael
Pathogen Molecular Genetics Section, Laboratory of Human Bacterial Pathogenesis, National Institute of Allergy and Infectious Diseases, US National Institutes of Health, Bethesda, Maryland, United States of America.
PLoS One. 2013 Aug 20;8(8):e72803. doi: 10.1371/journal.pone.0072803. eCollection 2013.
In the past decade, community-associated (CA-) infections with methicillin-resistant Staphylococcus aureus (MRSA) have emerged throughout the world. Different CA-MRSA strains dominate in different geographical locations. Many CA-MRSA lineages contain genes coding for the Pantón-Valentine leukocidin. However, the role of this leukotoxin in CA-MRSA pathogenesis is still controversial. The genome sequences of two key PVL-positive CA-MRSA strains (USA300, USA400) have been reported, but we lack information on the more recently found PVL-negative CA-MRSA strains. One such strain is the PVL-negative ST72, the main cause of CA-MRSA infections in Korea. Here, we report the entire genome sequence of CA-MRSA ST72 and analyze its gene content with a focus on virulence factors. Our results show that this strain does not have considerable differences in virulence factor content compared to other CA-MRSA strains (USA300, USA400), indicating that other toxins do not substitute for the lack of PVL in ST72. This finding is in accordance with the notion that differential expression of widespread virulence determinants, rather than the acquisition of additional virulence factors on mobile genetic elements, such as PVL, is responsible for the increased virulence of CA- compared to hospital-associated MRSA.
在过去十年中,耐甲氧西林金黄色葡萄球菌(MRSA)引起的社区相关性(CA-)感染在全球范围内出现。不同的CA-MRSA菌株在不同地理位置占主导地位。许多CA-MRSA谱系含有编码杀白细胞素(Pantón-Valentine leukocidin)的基因。然而,这种白细胞毒素在CA-MRSA发病机制中的作用仍存在争议。已报道了两种关键的PVL阳性CA-MRSA菌株(USA300、USA400)的基因组序列,但我们缺乏关于最近发现的PVL阴性CA-MRSA菌株的信息。其中一种菌株是PVL阴性的ST72,它是韩国CA-MRSA感染的主要原因。在此,我们报告了CA-MRSA ST72的全基因组序列,并重点分析了其毒力因子的基因组成。我们的结果表明,与其他CA-MRSA菌株(USA300、USA400)相比,该菌株在毒力因子组成上没有显著差异,这表明其他毒素不能替代ST72中缺乏的PVL。这一发现与以下观点一致,即与医院相关性MRSA相比,CA-MRSA毒力增加的原因是广泛存在的毒力决定因素的差异表达,而非通过移动遗传元件获得额外的毒力因子,如PVL。