Ramstad Silje N, Wasteson Yngvild, Lindstedt Bjørn-Arne, Taxt Arne M, Bjørnholt Jørgen V, Brandal Lin T, Bohlin Jon
Department of Microbiology, Division of Laboratory Medicine, Oslo University Hospital, Oslo, Norway.
Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Front Microbiol. 2021 Sep 8;12:728116. doi: 10.3389/fmicb.2021.728116. eCollection 2021.
Shiga toxin-producing (STEC) may cause severe disease mainly due to the ability to produce Shiga toxins (Stx) encoded on bacteriophages. In Norway, more than 30% of the reported cases with STEC O145:H25 develop hemolytic uremic syndrome (HUS), and most cases, with known travel history, acquired the infection domestically. To describe phage characteristics associated with high virulence, we extracted the Stx2a phage sequences from eight clinical Norwegian O145:H25 STEC to conduct in-depth molecular characterization using long and short read sequencing. The Stx2a phages were annotated, characterized, and compared with previously published Stx2a phages isolated from STEC of different serotypes. The Norwegian O145:H25 Stx2a phages showed high sequence identity (>99%) with 100% coverage. The Stx2a phages were located at the integration site , were approximately 45 kbp long, and harbored several virulence-associated genes, in addition to , such as and . We observed high sequence identity (>98%) and coverage (≥94%) between Norwegian O145:H25 Stx2a phages and publicly available Stx2a phages from O145:H25 and O145:H28 STEC, isolated from HUS cases in the USA and a hemorrhagic diarrhea case from Japan, respectively. However, low similarity was seen when comparing the Norwegian O145:H25 Stx2a phage to Stx2a phages from STEC of other serotypes. In all the Norwegian O145:H25 STEC, we identified a second phage or remnants of a phage (a shadow phage, 61 kbp) inserted at the same integration site as the Stx2a phage. The shadow phage shared similarity with the Stx2a phage, but lacked and harbored effector genes not present in the Stx2a phage. We identified a conserved Stx2a phage among the Norwegian O145:H25 STEC that shared integration site with a shadow phage in all isolates. Both phage and shadow phage harbored several virulence-associated genes that may contribute to the increased pathogenicity of O145:H25 STEC.
产志贺毒素大肠杆菌(STEC)可能引发严重疾病,主要是因为它有能力产生噬菌体编码的志贺毒素(Stx)。在挪威,超过30%的报告的STEC O145:H25病例会发展为溶血性尿毒症综合征(HUS),而且大多数有已知旅行史的病例是在国内感染的。为了描述与高毒力相关的噬菌体特征,我们从8株挪威临床O145:H25 STEC中提取了Stx2a噬菌体序列,使用长读长和短读长测序进行深入的分子特征分析。对Stx2a噬菌体进行注释、特征分析,并与先前发表的从不同血清型的STEC中分离出的Stx2a噬菌体进行比较。挪威O145:H25 Stx2a噬菌体显示出高序列同一性(>99%)且覆盖率为100%。Stx2a噬菌体位于整合位点,长度约为45 kbp,除了[此处原文缺失相关基因信息]外,还含有几个与毒力相关的基因,如[此处原文缺失相关基因信息]和[此处原文缺失相关基因信息]。我们观察到挪威O145:H25 Stx2a噬菌体与分别从美国HUS病例和日本一例出血性腹泻病例中分离出的O145:H25和O145:H28 STEC的公开可用Stx2a噬菌体之间具有高序列同一性(>98%)和覆盖率(≥94%)。然而,将挪威O145:H25 Stx2a噬菌体与其他血清型的STEC的Stx2a噬菌体进行比较时,相似性较低。在所有挪威O145:H25 STEC中,我们在与Stx2a噬菌体相同的整合位点鉴定出了第二种噬菌体或噬菌体残余(一种影子噬菌体,61 kbp)。影子噬菌体与Stx2a噬菌体有相似性,但缺少[此处原文缺失相关基因信息],并含有Stx2a噬菌体中不存在的效应子基因。我们在挪威O145:H25 STEC中鉴定出一种保守的Stx2a噬菌体,在所有分离株中它都与一种影子噬菌体共享整合位点。噬菌体和影子噬菌体都含有几个与毒力相关的基因,这可能导致O145:H25 STEC的致病性增加。