Iriarte M P, Owen R J
National Collection of Type Cultures, Central Public Health Laboratory, London, UK.
FEMS Immunol Med Microbiol. 1996 Aug;15(1):17-22. doi: 10.1111/j.1574-695X.1996.tb00353.x.
PCR-mediated fingerprinting with combined repetitive and arbitrary DNA primers (ERIC-2 and 1026) was used to type Campylobacter jejuni from a milk-associated outbreak, and from sporadic cases of the same and allied HS serotypes. The 14 outbreak strains had identical or similar DNA band profiles whereas the 25 strains from sporadic infections were more heterogeneous with 18 different DNA profiles. Although PCR-based DNA fingerprints lacked serotype specificity, the method was fast, simple to perform and reproducible, provided defined technical protocols were adhered to precisely. Profiles were highly discriminatory but did not consistently match types based on other molecular methods. We conclude that AP-PCR has demonstrable potential for initial rapid investigation of outbreaks, and when used in conjunction with PFGE analysis of DNA restriction profiles, provides a high resolution strategy for accurately defining subtypes of C. jejuni.
利用结合重复和任意DNA引物(ERIC-2和1026)的PCR介导指纹图谱技术,对一起与牛奶相关的空肠弯曲菌暴发菌株以及相同和相关HS血清型的散发病例菌株进行分型。14株暴发菌株具有相同或相似的DNA条带图谱,而来自散发性感染的25株菌株则更为异质,有18种不同的DNA图谱。尽管基于PCR的DNA指纹图谱缺乏血清型特异性,但该方法快速、操作简单且可重复,前提是要严格遵循既定的技术方案。图谱具有高度的鉴别力,但与基于其他分子方法的类型并不总是匹配。我们得出结论,AP-PCR在暴发的初步快速调查中具有明显潜力,并且与DNA限制性图谱的PFGE分析结合使用时,可为准确界定空肠弯曲菌亚型提供高分辨率策略。