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Identification of Candidates for a Subunit Vaccine against Extraintestinal Pathogenic Escherichia coli

机译:鉴定针对肠外致病性大肠埃希菌的亚单位疫苗的候选人

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摘要

Extraintestinal pathogenic Escherichia coli (ExPEC) strains cause a large spectrum of infections. The majority of ExPEC strains are closely related to the B2 or the D phylogenetic group. The aim of our study was to develop a protein-based vaccine against these ExPEC strains. To this end, we identified ExPEC-specific genomic regions, using a comparative genome analysis, between the nonpathogenic E. coli strain K-12 MG1655 and ExPEC strains C5 (meningitis isolate) and CFT073 (urinary tract infection isolate). The analysis of these genomic regions allowed the selection of 40 open reading frames, which are conserved among B2/D clinical isolates and encode proteins with putative outer membrane localization. These genes were cloned, and recombinant proteins were purified and assessed as vaccine candidates. After immunization of BALB/c mice, five proteins induced a significant protective immunity against a lethal challenge with a clinical E. coli strain of the B2 group. In passive immunization assays, antigen-specific antibodies afforded protection to naive mice against a lethal challenge. Three of these antigens were related to iron acquisition metabolism, an important virulence factor of the ExPEC, and two corresponded to new, uncharacterized proteins. Due to the large number of genetic differences that exists between commensal and pathogenic strains of E. coli, our results demonstrate that it is possible to identify targets that elicit protective immune responses specific to those strains. The five protective antigens could constitute the basis for a preventive subunit vaccine against diseases caused by ExPEC strains.
机译:肠外致病性大肠杆菌(ExPEC)菌株引起大范围的感染。大多数ExPEC菌株与B2或D系统发生基团密切相关。我们研究的目的是针对这些ExPEC菌株开发基于蛋白质的疫苗。为此,我们使用比较基因组分析在非致病性大肠杆菌K-12 MG1655菌株和ExPEC菌株C5(脑膜炎分离株)和CFT073(尿路感染分离株)之间鉴定了ExPEC特异性基因组区域。通过对这些基因组区域的分析,可以选择40个开放阅读框,这些阅读框在B2 / D临床分离株中是保守的,并编码假定的外膜定位蛋白。克隆了这些基因,纯化了重组蛋白并评估为候选疫苗。免疫BALB / c小鼠后,五种蛋白质诱导了针对B2组临床大肠杆菌菌株致死性攻击的显着保护性免疫。在被动免疫分析中,抗原特异性抗体可保护幼稚小鼠免受致命攻击。这些抗原中的三种与铁获取代谢有关,这是ExPEC的重要毒力因子,另外两种与新的,未表征的蛋白质相对应。由于大肠杆菌的共生和致病菌株之间存在大量遗传差异,因此我们的结果表明,有可能鉴定出引发针对那些菌株的保护性免疫应答的靶标。这五种保护性抗原可以构成针对ExPEC菌株引起的疾病的预防性亚单位疫苗的基础。

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