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Use of signature-tagged mutagenesis to identify virulence determinants in Haemophilus ducreyi responsible for ulcer formation

机译:使用标记标签的诱变方法鉴定杜克伊嗜血杆菌中导致溃疡形成的毒力决定因素

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摘要

Elucidating the molecular mechanisms responsible for chancroid, a genital ulcer disease caused by Haemophilus ducreyi, has been hampered in part by the relative genetic intractability of the organism. A whole genome screen using signature-tagged mutagenesis in the temperature-dependent rabbit model (TDRM) of H. ducreyi infection uncovered 26 mutants with a presumptive attenuated phenotype. Insertions in two previously recognized virulence determinants, hgbA and lspA1, validated this genome scanning technique. Database interrogation allowed assignment of 24 mutants to several functional classes, including transport, metabolism, DNA repair, stress response and gene regulation. The attenuated virulence for a 3 strain with a mutation in hicB was confirmed by individual infection in the TDRM. The results from this preliminary study indicate that this high throughput strategy will further the understanding of the pathogenesis of H. ducreyi infection
机译:阐明造成类固醇(一种由杜克氏嗜血杆菌引起的生殖器溃疡疾病)的分子机制,已部分地因该生物的相对遗传难治性而受到阻碍。一个完整的基因组筛选使用签名标记的诱变在温度依赖性兔模型(TDRM)的杜克氏杆菌感染中发现了26个突变体,它们具有假定的减毒表型。插入两个先前公认的毒力决定因素,hgbA和lspA1,验证了这种基因组扫描技术。通过数据库查询,可以将24个突变体分配到几个功能类别,包括运输,代谢,DNA修复,应激反应和基因调控。 hicB突变的3株毒力减弱,这是通过TDRM中的个体感染证实的。这项初步研究的结果表明,这种高通量策略将进一步了解杜克氏杆菌感染的发病机理

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