在ST1 (BI/NAP1/027) 临床分离物中病毒性和基因组多样性Clostridioides difficile
Qiwen Dong1, Huaiying Lin2, Marie-Maude Allen3
1Department of Medicine, University of Chicago, Chicago, IL 60637, USA; Duchossois Family Institute, University of Chicago, Chicago, IL 60637, USA.
Cell reports
|July 31, 2023
概括
在Clostridioides difficile ST1菌株中,一种特定的基因缺失显著降低了疾病的严重程度,而不会影响殖民. 这一发现可能会提高C. difficile大肠炎的诊断准确性.
科学领域:
- 微生物学 微生物学
- 传染性疾病 传染性疾病
- 基因组学就是基因组学.
背景情况:
- 困难菌通过产生毒素引起大肠炎,但疾病的严重程度各不相同.
- 宿主因素和细菌菌株差异与可变的C. difficile感染严重程度有关.
研究的目的:
- 在小鼠模型中研究23种流行性Clostridioides difficile ST1临床隔离物中的毒性变异.
- 确定导致C. difficile引起的疾病严重程度差异的遗传因素.
主要方法:
- 在小鼠中感染23个C. difficile ST1分离体.
- 评估殖民密度和疾病严重程度.
- 对病毒性和病毒性分离物进行基因组分析,以确定遗传变异.
- 在毒性菌株中删除基因以确认毒性减弱.
主要成果:
- 所有测试的C. difficile分离物以类似的方式殖民小鼠,但表现出不同的疾病严重程度,从致命到恶性.
- 毒性分离物具有cdtR基因中的69个基对删除,该基因调节二进制毒素表达.
- 在一种毒性菌株中删除这种cdtR序列使其变得无毒,并降低了毒素基因转录.
结论:
- 在cdtR基因中的自然缺失减弱了C. difficile ST1的毒性,而不会影响殖民或持久性.
- cdtR基因型可以区分毒性和毒性不良的C. difficile菌株.
- 识别cdtR变异可能会提高C. difficile结肠炎的诊断特异性.
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