Anwar Farhan, Vedantam Gayatri
School of Animal and Comparative Biomedical Sciences, University of Arizona, Tucson, AZ, 85721, United States.
School of Animal and Comparative Biomedical Sciences, University of Arizona, Tucson, AZ, 85721, United States; Bio5 Institute for Collaborative Research, University of Arizona, Tucson, AZ, 85721, United States; Southern Arizona VA Healthcare System, Tucson, AZ, 85723, United States.
Curr Opin Microbiol. 2022 Apr;66:86-91. doi: 10.1016/j.mib.2022.01.007. Epub 2022 Feb 3.
Clostridioides difficile is a leading cause of the healthcare-associated disease C. difficile infection (CDI), which has an annual US burden of over 200 000 cases. CDI mitigation strategies have been complicated by the emergence, and widespread distribution, of phylogenetically diverse lineages, as well as pathogen recalcitrance to genetic manipulation. In this review, we highlight past and current efforts to elucidate C. difficile surface glycopolymer biology since these molecules are essential for colonization, disease, and immunity elicitation, and may therefore have potential as CDI anti-infective targets.
艰难梭菌是医疗保健相关疾病艰难梭菌感染(CDI)的主要病因,在美国每年有超过20万例病例。系统发育上不同谱系的出现和广泛分布,以及病原体对基因操作的顽固抵抗,使得CDI缓解策略变得复杂。在这篇综述中,我们重点介绍了过去和当前为阐明艰难梭菌表面糖聚合物生物学所做的努力,因为这些分子对于定植、疾病和免疫激发至关重要,因此可能具有作为CDI抗感染靶点的潜力。