Cornick Jennifer E, Kiran Anmol M, Vivancos Roberto, Van Aartsen Jon, Clarke Jenny, Bevan Edward, Alsahag Mansoor, Alaearts Maaike, Bricio Moreno Laura, Jenkinson Howard F, Nobbs Angela H, Anson James, Kadioglu Aras, French Neil, Everett Dean B
Malawi Liverpool Wellcome Trust Clinical Research Programme, Blantyre, Malawi
Institute of Infection & Global Health, University of Liverpool, Liverpool, United Kingdom.
J Clin Microbiol. 2017 Jun;55(6):1837-1846. doi: 10.1128/JCM.00191-17. Epub 2017 Mar 29.
An 32.2 invasive group A streptococcus (iGAS) outbreak occurred in Liverpool from January 2010 to September 2012. This genotype had not previously been identified in Liverpool, but was responsible for 32% (14/44) of all iGAS cases reported during this time period. We performed a case-case comparison of 32.2 iGAS cases with non-32.2 control iGAS cases identified in the Liverpool population over the same time period to assess patient risk factors for 32.2 iGAS infection. The 32.2 iGAS cases were confined to the adult population. We show that homelessness, intravenous drug use, and alcohol abuse predisposed patients to 32.2 iGAS disease; however, no obvious epidemiological linkage between the patients with 32.2 iGAS could be identified. Comparative whole-genome sequencing analysis of 32.2 iGAS and non-32.2 control isolates was also performed to identify pathogen factors which might have driven the outbreak. We identified 19 genes, five of which had previously been implicated in virulence, which were present in all of the 32.2 iGAS isolates but not present in any of the non-32.2 control isolates. We report that a novel 32.2 genotype emerged in Liverpool in 2010 and identified a specific subset of genes, which could have allowed this novel 32.2 genotype to persist in a disadvantaged population in the region over a 3-year period.
2010年1月至2012年9月,英国利物浦爆发了由A组侵入性链球菌(iGAS)32.2型引起的疫情。此前在利物浦尚未发现这种基因型,但在此期间报告的所有iGAS病例中,它占了32%(14/44)。我们对同期在利物浦人群中确定的32.2型iGAS病例与非32.2型对照iGAS病例进行了病例对照比较,以评估32.2型iGAS感染的患者风险因素。32.2型iGAS病例仅限于成年人群。我们发现,无家可归、静脉注射吸毒和酗酒使患者易患32.2型iGAS疾病;然而,未发现32.2型iGAS患者之间存在明显的流行病学联系。我们还对32.2型iGAS和非32.2型对照分离株进行了全基因组测序比较分析,以确定可能导致疫情爆发的病原体因素。我们鉴定出19个基因,其中5个基因以前与毒力有关,所有32.2型iGAS分离株中都有这些基因,而在任何非32.2型对照分离株中都没有。我们报告,2010年在利物浦出现了一种新的32.2型基因型,并鉴定出一组特定的基因,这些基因可能使这种新出现的32.2型基因型在该地区的弱势人群中持续存在了3年。