Kong Fanrong, Ma Lin, Gilbert Gwendolyn L
Centre for Infectious Diseases and Microbiology (CIDM), Institute of Clinical Pathology and Medical Research (ICPMR), Westmead, New South Wales, Australia 2Department of Dermatology, Beijing Children's Hospital, Affiliate of Capital University of Medical Sciences, Beijing, PR China.
J Med Microbiol. 2005 Dec;54(Pt 12):1133-1138. doi: 10.1099/jmm.0.46244-0.
Streptococcus agalactiae (group B streptococcus, GBS) is an important cause of sepsis in neonates and their mothers, and the elderly and immunocompromised patients. Ongoing surveillance to monitor GBS serotype distribution is needed to guide the development and assess the feasibility of GBS conjugate vaccines. The authors previously developed a molecular serotype identification method based on serotype-specific PCR and partial sequencing of cps genes. In this study, a novel 10-primer pair multiplex PCR and reverse line blot (mPCR/RLB) hybridization assay was developed for simultaneous detection and serotype identification of all nine GBS serotypes. For all 316 GBS isolates tested the mPCR/RLB results corresponded with those of conventional serotyping and individual serotype-specific PCR, and the method was more convenient and practical than either alternative.
无乳链球菌(B组链球菌,GBS)是新生儿及其母亲、老年人和免疫功能低下患者败血症的重要病因。需要持续监测以监测GBS血清型分布,以指导GBS结合疫苗的开发并评估其可行性。作者先前开发了一种基于血清型特异性PCR和cps基因部分测序的分子血清型鉴定方法。在本研究中,开发了一种新型的10引物对多重PCR和反向线印迹(mPCR/RLB)杂交检测法,用于同时检测和鉴定所有九种GBS血清型。对于所有测试的316株GBS分离株,mPCR/RLB结果与传统血清分型和个体血清型特异性PCR结果一致,且该方法比任何一种替代方法都更方便实用。