Jamrozy Dorota, Coll Francesc, Mather Alison E, Harris Simon R, Harrison Ewan M, MacGowan Alasdair, Karas Andreas, Elston Tony, Estée Török M, Parkhill Julian, Peacock Sharon J
The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK.
London School of Hygiene and Tropical Medicine, London, WC1E 7HT, UK.
BMC Genomics. 2017 Sep 4;18(1):684. doi: 10.1186/s12864-017-4065-z.
Horizontal transfer of mobile genetic elements (MGEs) that carry virulence and antimicrobial resistance genes mediates the evolution of methicillin-resistant Staphylococcus aureus, and the emergence of new MRSA clones. Most MRSA lineages show an association with specific MGEs and the evolution of MGE composition following clonal expansion has not been widely studied.
We investigated the genomes of 1193 S. aureus bloodstream isolates, 1169 of which were MRSA, collected in the UK and the Republic of Ireland between 2001 and 2010. The majority of isolates belonged to clonal complex (CC)22 (n = 923), which contained diverse MGEs including elements that were found in other MRSA lineages. Several MGEs showed variable distribution across the CC22 phylogeny, including two antimicrobial resistance plasmids (pWBG751-like and SAP078A-like, carrying erythromycin and heavy metal resistance genes, respectively), a pathogenicity island carrying the enterotoxin C gene and two phage types Sa1int and Sa6int. Multiple gains and losses of these five MGEs were identified in the CC22 phylogeny using ancestral state reconstruction. Analysis of the temporal distribution of the five MGEs between 2001 and 2010 revealed an unexpected reduction in prevalence of the two plasmids and the pathogenicity island, and an increase in the two phage types. This occurred across the lineage and was not correlated with changes in the relative prevalence of CC22, or of any sub-lineages within in.
Ancestral state reconstruction coupled with temporal trend analysis demonstrated that epidemic MRSA CC22 has an evolving MGE composition, and indicates that this important MRSA lineage has continued to adapt to changing selective pressure since its emergence.
携带毒力和抗菌抗性基因的移动遗传元件(MGEs)的水平转移介导了耐甲氧西林金黄色葡萄球菌的进化以及新的耐甲氧西林金黄色葡萄球菌克隆的出现。大多数耐甲氧西林金黄色葡萄球菌谱系显示出与特定MGEs的关联,并且克隆扩增后MGEs组成的进化尚未得到广泛研究。
我们研究了2001年至2010年间在英国和爱尔兰共和国收集的1193株金黄色葡萄球菌血流分离株的基因组,其中1169株为耐甲氧西林金黄色葡萄球菌。大多数分离株属于克隆复合体(CC)22(n = 923),其中包含多种MGEs,包括在其他耐甲氧西林金黄色葡萄球菌谱系中发现的元件。几种MGEs在CC22系统发育中显示出可变分布,包括两个抗菌抗性质粒(pWBG751样和SAP078A样,分别携带红霉素和重金属抗性基因)、一个携带肠毒素C基因的致病岛以及两种噬菌体类型Sa1int和Sa6int。使用祖先状态重建在CC22系统发育中鉴定出这五种MGEs的多次获得和丢失。对2001年至2010年间这五种MGEs的时间分布分析显示,两种质粒和致病岛的流行率意外下降,而两种噬菌体类型的流行率增加。这在整个谱系中都有发生,并且与CC22或其任何亚谱系的相对流行率变化无关。
祖先状态重建与时间趋势分析表明,流行的耐甲氧西林金黄色葡萄球菌CC22具有不断演变的MGEs组成,并表明这个重要的耐甲氧西林金黄色葡萄球菌谱系自出现以来一直在持续适应不断变化的选择压力。