Hilary Miller, Julia Howard, Juliet Elvy, Patrick Campbell, Trevor Anderson, Sarah Bakker, Alexandra Eustace, Hermes Perez, David Winter, Kristin Dyet
{"title":"从新西兰人类临床病例中分离出的携带 mecC 的金黄色葡萄球菌的基因组流行病学。","authors":"Hilary Miller, Julia Howard, Juliet Elvy, Patrick Campbell, Trevor Anderson, Sarah Bakker, Alexandra Eustace, Hermes Perez, David Winter, Kristin Dyet","doi":"10.1099/acmi.0.000849.v2","DOIUrl":null,"url":null,"abstract":"<p><p>In 2011, a novel methicillin resistance gene, <i>mecC</i>, was described in human and bovine <i>Staphylococcus aureus</i> isolates. <i>mecC-</i>positive <i>S. aureus</i> is most commonly associated with livestock and wildlife populations across Europe and is particularly prevalent in hedgehogs, but only occasionally causes human infections. In this study, we characterize and investigate the origin of two human <i>S. aureus</i> isolates containing <i>mecC</i> genes from New Zealand. The two isolates were identified from patients with severe invasion infections as part of an <i>S. aureus</i> bacteraemia study. Whole-genome sequencing was used to characterize staphylococcal cassette chromosome <i>mec</i> (SCC<i>mec</i>) elements and perform phylogenetic comparisons with publicly available strains from <i>mecC</i>-associated clonal complexes, including isolates from hedgehogs from New Zealand and Europe/United Kingdom (UK), and livestock, wildlife and human isolates from Europe/UK. The two isolates from our study have almost identical SCC<i>mec</i> type XI elements containing a <i>mecC</i> gene. However, this gene contains a premature stop codon, consistent with the methicillin-susceptible phenotype observed for these isolates. Core genome SNP analyses showed that the two isolates are 234 SNPs apart and are most closely related to an isolate obtained from a New Zealand hedgehog. However, there are considerable differences in the <i>mecC</i> mobile element between the human and hedgehog isolates, indicating the presence of an as-yet-unknown reservoir of <i>mecC S. aureus</i> in the New Zealand environment.</p>","PeriodicalId":94366,"journal":{"name":"Access microbiology","volume":"6 9","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11376224/pdf/","citationCount":"0","resultStr":"{\"title\":\"Genomic epidemiology of mecC-carrying Staphylococcus aureus isolates from human clinical cases in New Zealand.\",\"authors\":\"Hilary Miller, Julia Howard, Juliet Elvy, Patrick Campbell, Trevor Anderson, Sarah Bakker, Alexandra Eustace, Hermes Perez, David Winter, Kristin Dyet\",\"doi\":\"10.1099/acmi.0.000849.v2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In 2011, a novel methicillin resistance gene, <i>mecC</i>, was described in human and bovine <i>Staphylococcus aureus</i> isolates. <i>mecC-</i>positive <i>S. aureus</i> is most commonly associated with livestock and wildlife populations across Europe and is particularly prevalent in hedgehogs, but only occasionally causes human infections. In this study, we characterize and investigate the origin of two human <i>S. aureus</i> isolates containing <i>mecC</i> genes from New Zealand. The two isolates were identified from patients with severe invasion infections as part of an <i>S. aureus</i> bacteraemia study. Whole-genome sequencing was used to characterize staphylococcal cassette chromosome <i>mec</i> (SCC<i>mec</i>) elements and perform phylogenetic comparisons with publicly available strains from <i>mecC</i>-associated clonal complexes, including isolates from hedgehogs from New Zealand and Europe/United Kingdom (UK), and livestock, wildlife and human isolates from Europe/UK. The two isolates from our study have almost identical SCC<i>mec</i> type XI elements containing a <i>mecC</i> gene. However, this gene contains a premature stop codon, consistent with the methicillin-susceptible phenotype observed for these isolates. Core genome SNP analyses showed that the two isolates are 234 SNPs apart and are most closely related to an isolate obtained from a New Zealand hedgehog. However, there are considerable differences in the <i>mecC</i> mobile element between the human and hedgehog isolates, indicating the presence of an as-yet-unknown reservoir of <i>mecC S. aureus</i> in the New Zealand environment.</p>\",\"PeriodicalId\":94366,\"journal\":{\"name\":\"Access microbiology\",\"volume\":\"6 9\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11376224/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Access microbiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1099/acmi.0.000849.v2\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Access microbiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1099/acmi.0.000849.v2","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
2011 年,在人和牛的金黄色葡萄球菌分离物中发现了一种新型甲氧西林耐药基因 mecC。mecC 阳性的金黄色葡萄球菌最常见于欧洲的家畜和野生动物,在刺猬中尤为流行,但偶尔也会引起人类感染。在本研究中,我们对新西兰两例含有 mecC 基因的人类金黄色葡萄球菌分离物进行了特征描述和来源调查。作为金黄色葡萄球菌菌血症研究的一部分,这两个分离株是从严重入侵感染的患者身上鉴定出来的。全基因组测序用于鉴定葡萄球菌盒式染色体mec(SCCmec)元件的特征,并与公开发表的mecC相关克隆复合菌株进行系统发育比较,包括来自新西兰和欧洲/英国(UK)刺猬的分离株,以及来自欧洲/英国的家畜、野生动物和人类分离株。我们研究中的两个分离物具有几乎完全相同的包含 mecC 基因的 SCCmec XI 型元件。然而,该基因含有一个过早终止密码子,这与在这些分离株中观察到的对甲氧西林敏感的表型一致。核心基因组 SNP 分析表明,这两个分离株相差 234 个 SNPs,与从新西兰刺猬身上获得的一个分离株关系最为密切。然而,人类和刺猬分离物的 mecC 移动元素存在很大差异,这表明新西兰环境中存在一个尚未知晓的 mecC 金黄色葡萄球菌储库。
Genomic epidemiology of mecC-carrying Staphylococcus aureus isolates from human clinical cases in New Zealand.
In 2011, a novel methicillin resistance gene, mecC, was described in human and bovine Staphylococcus aureus isolates. mecC-positive S. aureus is most commonly associated with livestock and wildlife populations across Europe and is particularly prevalent in hedgehogs, but only occasionally causes human infections. In this study, we characterize and investigate the origin of two human S. aureus isolates containing mecC genes from New Zealand. The two isolates were identified from patients with severe invasion infections as part of an S. aureus bacteraemia study. Whole-genome sequencing was used to characterize staphylococcal cassette chromosome mec (SCCmec) elements and perform phylogenetic comparisons with publicly available strains from mecC-associated clonal complexes, including isolates from hedgehogs from New Zealand and Europe/United Kingdom (UK), and livestock, wildlife and human isolates from Europe/UK. The two isolates from our study have almost identical SCCmec type XI elements containing a mecC gene. However, this gene contains a premature stop codon, consistent with the methicillin-susceptible phenotype observed for these isolates. Core genome SNP analyses showed that the two isolates are 234 SNPs apart and are most closely related to an isolate obtained from a New Zealand hedgehog. However, there are considerable differences in the mecC mobile element between the human and hedgehog isolates, indicating the presence of an as-yet-unknown reservoir of mecC S. aureus in the New Zealand environment.