Doumith Michel, Jacquet Christine, Gerner-Smidt Peter, Graves Lewis M, Loncarevic Semir, Mathisen Tone, Morvan Anne, Salcedo Celia, Torpdahl Mia, Vazquez Julio A, Martin Paul
Laboratoire des Listeria, Centre National de Référence des Listeria, World Health Organisation Collaborating Center for Foodborne Listeriosis, Institut Pasteur, Paris, France.
J Food Prot. 2005 Dec;68(12):2648-50. doi: 10.4315/0362-028x-68.12.2648.
The performance of a multiplex PCR assay that separates the four major serovars of the pathogenic Listeria monocytogenes into four distinct PCR groups was evaluated through a multicenter typing study. Identical panels of 90 Listeria isolates were distributed to five participating laboratories that were blind to the nature of the isolates. Isolates were characterized using the previously standardized protocol. Overall concordance was 96.6 to 100%, sufficient for the assay to be used as an alternative to serotyping and confidently applied in laboratories involved in L. monocytogenes typing.
通过一项多中心分型研究,对一种多重聚合酶链反应(PCR)检测方法的性能进行了评估,该方法可将致病性单核细胞增生李斯特菌的四种主要血清型分为四个不同的PCR组。将90株李斯特菌的相同样本分发给五个参与实验室,这些实验室对菌株的性质并不知情。使用先前标准化的方案对菌株进行鉴定。总体一致性为96.6%至100%,足以使该检测方法用作血清分型的替代方法,并可在参与单核细胞增生李斯特菌分型的实验室中可靠应用。