Penney T J, Martin D R, Williams L C, de Malmanche S A, Bergquist P L
ESR Communicable Disease Centre, Porirua, New Zealand.
FEMS Microbiol Lett. 1995 Aug 1;130(2-3):145-9. doi: 10.1111/j.1574-6968.1995.tb07711.x.
Serological typing of the streptococcal M protein has recently been challenged by a number of unique molecular methodologies based on oligonucleotide recognition of allelic variations within the M protein (emm) gene. In these methods, stringent hybridization of an oligonucleotide probe to a polymerase chain reaction amplified emm gene is used as confirmation of specific M type identity. A sample of 17 isolates from 7 previously defined distinct genotypes were tested using a single M1 oligonucleotide probe. Isolates from only three of the genotypes hybridized with the probe. The results demonstrate that a single emm-specific oligonucleotide probe can not identify all members of M type 1, as defined by conventional serotyping using polyclonal antisera.
基于寡核苷酸对M蛋白(emm)基因内等位基因变异的识别,一些独特的分子方法最近对链球菌M蛋白的血清学分型提出了挑战。在这些方法中,寡核苷酸探针与聚合酶链反应扩增的emm基因进行严格杂交,以此作为特定M型身份的确认。使用单个M1寡核苷酸探针检测了来自7个先前定义的不同基因型的17株分离株样本。只有三个基因型的分离株与该探针杂交。结果表明,如使用多克隆抗血清进行的传统血清学分型所定义的那样,单个emm特异性寡核苷酸探针无法识别所有M1型成员。