Antimicrobial Resistance and Infectious Diseases Research Laboratory, Murdoch University, Murdoch, Western Australia, Australia.
PathWest Laboratory Medicine-WA, Fiona Stanley Hospital, Murdoch, Western Australia, Australia.
PLoS One. 2020 Feb 10;15(2):e0228676. doi: 10.1371/journal.pone.0228676. eCollection 2020.
Production of the Panton-Valentine leukocidin (PVL) by Staphylococcus aureus is mediated via the genes lukS-PV and lukF-PV which are carried on bacteriophage ϕSa2. PVL is associated with S. aureus strains that cause serious infections and clones of community-associated methicillin-resistant S. aureus (CA-MRSA) that have additionally disseminated widely. In Western Australia (WA) the original CA-MRSA were PVL negative however, between 2005 and 2008, following the introduction of eight international PVL-positive CA-MRSA, PVL-positive WA CA-MRSA were found. There was concern that PVL bacteriophages from the international clones were transferring into the local clones, therefore a comparative study of PVL-carrying ϕSa2 prophage genomes from historic WA PVL-positive S. aureus and representatives of all PVL-positive CA-MRSA isolated in WA between 2005 and 2008 was performed. The prophages were classified into two genera and three PVL bacteriophage groups and had undergone many recombination events during their evolution. Comparative analysis of mosaic regions of selected bacteriophages using the Alignments of bacteriophage genomes (Alpha) aligner revealed novel recombinations and modules. There was heterogeneity in the chromosomal integration sites, the lysogeny regulation regions, the defence and DNA processing modules, the structural and packaging modules and the lukSF-PV genes. One WA CA-MRSA (WA518751) and one international clone (Korean Clone) have probably acquired PVL-carrying ϕSa2 in WA, however these clones did not disseminate in the community. Genetic heterogeneity made it impossible to trace the source of the PVL prophages in the other WA clones. Against this background of PVL prophage diversity, the sequence of one group, the ϕSa2USA/ϕSa2wa-st93 group, was remarkably stable over at least 20 years and associated with the highly virulent USA300 and ST93-IVa CA-MRSA lineages that have disseminated globally.
金黄色葡萄球菌产生的潘顿-瓦伦丁白细胞毒素 (PVL) 是由携带噬菌体 ϕSa2 的 lukS-PV 和 lukF-PV 基因介导的。PVL 与引起严重感染的金黄色葡萄球菌菌株有关,与社区获得性耐甲氧西林金黄色葡萄球菌 (CA-MRSA) 的克隆有关,这些克隆已经广泛传播。在西澳大利亚州(WA),最初的 CA-MRSA 是 PVL 阴性的,然而,在 2005 年至 2008 年间,随着 8 种国际 PVL 阳性 CA-MRSA 的引入,发现了 PVL 阳性的 WA CA-MRSA。人们担心来自国际克隆的 PVL 噬菌体正在转移到本地克隆中,因此对历史上 WA 地区 PVL 阳性金黄色葡萄球菌和 2005 年至 2008 年间在 WA 地区分离的所有 PVL 阳性 CA-MRSA 代表的携带 PVL 的 ϕSa2 前噬菌体基因组进行了比较研究。这些前噬菌体被分为两个属和三个 PVL 噬菌体群,并在进化过程中经历了多次重组事件。使用噬菌体基因组比对 (Alpha) 对齐器对选定噬菌体的镶嵌区进行比较分析,揭示了新的重组和模块。在染色体整合位点、溶原调控区、防御和 DNA 处理模块、结构和包装模块以及 lukSF-PV 基因方面存在异质性。一个 WA CA-MRSA(WA518751)和一个国际克隆(韩国克隆)可能在 WA 获得了携带 PVL 的 ϕSa2,但这些克隆并没有在社区中传播。遗传异质性使得无法追踪其他 WA 克隆中 PVL 前噬菌体的来源。在这种 PVL 前噬菌体多样性的背景下,至少 20 年来,一个组,即 ϕSa2USA/ϕSa2wa-st93 组的序列非常稳定,与高度毒力的 USA300 和 ST93-IVa CA-MRSA 谱系有关,这些谱系已经在全球传播。