Okura Masatoshi, Osawa Ro, Iguchi Atsushi, Arakawa Eiji, Terajima Jun, Watanabe Haruo
Department of Bioscience, Graduate School of Science and Technology, Kobe University, Rokko-dai 1-1, Nada-ku, Kobe, 657-8501, Japan.
J Clin Microbiol. 2003 Oct;41(10):4676-82. doi: 10.1128/JCM.41.10.4676-4682.2003.
A total of 54 Vibrio parahaemolyticus strains including pandemic O3:K6 strains and newly emerged O4:K68, O1:K25, O1:K26, and O1:K untypeable strains (collectively referred to as the "pandemic group") were examined for their pulsed-field gel electrophoresis (PFGE) and arbitrarily primed PCR (AP-PCR) profiles and for the presence or absence of genetic marker DNA sequences, toxRS/new or orf8, that had been reported elsewhere to be specific for the pandemic group. Both PFGE and AP-PCR analyses indicated that all strains of the pandemic group formed a distinct genotypic cluster, suggesting that they originated from the same clone. In addition to the pandemic group, four O3:K6 strains that did not possess the thermostable direct hemolysin (tdh) gene also belonged to this cluster and possessed the toxRS/new sequence. However, three O3:K6 strains that clearly belonged to the pandemic group by PFGE and AP-PCR did not possess the orf8 sequence. The evidence suggests that neither the toxRS/new nor the orf8 sequence is a reliable gene marker for definite identification of the pandemic group. We therefore developed a novel multiplex PCR assay specific for the pandemic group. The assay successfully distinguished pandemic group strains from other V. parahaemolyticus strains by yielding two distinct PCR products for tdh (263 bp) and the toxRS/new sequence (651 bp).
共检测了54株副溶血性弧菌,包括大流行的O3:K6菌株以及新出现的O4:K68、O1:K25、O1:K26和O1:K不可分型菌株(统称为“大流行组”),分析了它们的脉冲场凝胶电泳(PFGE)和随机引物PCR(AP-PCR)图谱,以及是否存在已在其他地方报道的对大流行组具有特异性的遗传标记DNA序列toxRS/new或orf8。PFGE和AP-PCR分析均表明,大流行组的所有菌株形成了一个独特的基因型簇,表明它们起源于同一克隆。除大流行组外,4株不具有耐热直接溶血素(tdh)基因的O3:K6菌株也属于该簇并拥有toxRS/new序列。然而,3株通过PFGE和AP-PCR明确属于大流行组的O3:K6菌株却不具有orf8序列。证据表明,toxRS/new序列和orf8序列都不是用于明确鉴定大流行组的可靠基因标记。因此,我们开发了一种针对大流行组的新型多重PCR检测方法。该检测方法通过产生tdh(263 bp)和toxRS/new序列(651 bp)这两种不同的PCR产物,成功地区分了大流行组菌株与其他副溶血性弧菌菌株。