Yu Jigui, Lin Jisheng, Kim Kyung-Hyo, Benjamin William H, Nahm Moon H
Department of Pathology, University of Alabama at Birmingham, BBRB 614, 1530 Third Avenue South, Birmingham, AL 35294-2170, USA.
Clin Vaccine Immunol. 2011 Nov;18(11):1900-7. doi: 10.1128/CVI.05312-11. Epub 2011 Sep 7.
Streptococcus pneumoniae expresses more than 90 capsule types, and currently available pneumococcal vaccines are designed to provide serotype-specific protection. Consequently, serotyping of pneumococcal isolates is important for determining the serotypes to be included in pneumococcal vaccines and to monitor their efficacy. Yet serotyping of pneumococcal isolates has remained a significant technical challenge. By multiplexing many assays, we have now developed a simple yet comprehensive serotyping assay system that can not only identify all known pneumococcal serotypes but also subdivide nontypeable (NT) isolates into those with or without the conventional capsule locus. We have developed this assay system to require only six key reagents: two are used in one multiplex inhibition-type immunoassay, and four are required in two multiplex PCR-based assays. The assay system is largely automated by a seamless combination of monoclonal antibody-based and PCR-based multiplex assays using the flow cytometric bead array technology from Luminex. The assay system has been validated with a panel of pneumococci expressing all known pneumococcal serotypes and was found to be easily transferable to another laboratory.
肺炎链球菌可表达90多种荚膜类型,目前可用的肺炎球菌疫苗旨在提供血清型特异性保护。因此,对肺炎球菌分离株进行血清分型对于确定肺炎球菌疫苗中包含的血清型以及监测其疗效至关重要。然而,对肺炎球菌分离株进行血清分型仍然是一项重大的技术挑战。通过多重检测,我们现已开发出一种简单而全面的血清分型检测系统,该系统不仅可以识别所有已知的肺炎球菌血清型,还可以将不可分型(NT)分离株细分为具有或不具有传统荚膜位点的分离株。我们开发的这种检测系统仅需要六种关键试剂:两种用于一种多重抑制型免疫检测,另外四种用于两种基于多重PCR的检测。该检测系统通过使用Luminex的流式细胞术微球阵列技术,将基于单克隆抗体的多重检测和基于PCR的多重检测无缝结合,实现了很大程度的自动化。该检测系统已通过一组表达所有已知肺炎球菌血清型的肺炎球菌进行了验证,并且发现很容易转移到另一个实验室。