Thibault Virginie C, Grayon Maggy, Boschiroli Maria Laura, Hubbans Christine, Overduin Pieter, Stevenson Karen, Gutierrez Maria Cristina, Supply Philip, Biet Franck
UR1282, Infectiologie Animale, Santé Publique (IASP-311), INRA Centre de Tours, F-37380 Nouzilly, France.
J Clin Microbiol. 2007 Aug;45(8):2404-10. doi: 10.1128/JCM.00476-07. Epub 2007 May 30.
Mycobacterium avium subsp. paratuberculosis, the etiological agent of paratuberculosis, affects a wide range of domestic ruminants and has been suggested to be involved in Crohn's disease in humans. Most available methods for identifying and differentiating strains of this difficult species are technically demanding and have limited discriminatory power. Here, we report the identification of novel PCR-based typing markers consisting of variable-number tandem repeats (VNTRs) of genetic elements called mycobacterial interspersed repetitive units (MIRUs). Eight markers were applied to 183 M. avium subsp. paratuberculosis isolates from bovine, caprine, ovine, cervine, leporine, and human origins from 10 different countries and to 82 human isolates of the closely related species M. avium from France. Among the M. avium subsp. paratuberculosis isolates, 21 patterns were found by MIRU-VNTR typing, with a discriminatory index of 0.751. The predominant R01 IS900 restriction fragment length polymorphism type, comprising 131 isolates, was divided into 15 MIRU-VNTR types. Among the 82 M. avium isolates, the eight MIRU-VNTR loci distinguished 30 types, none of which was shared by M. avium subsp. paratuberculosis isolates, resulting in a discriminatory index of 0.889. Our results suggest that MIRU-VNTR typing is a fast typing method that, in combination with other methods, might prove to be optimal for PCR-based molecular epidemiological studies of M. avium/M. avium subsp. paratuberculosis pathogens. In addition, presumably identical M. avium subsp. paratuberculosis 316F vaccine strains originating from the Weybridge laboratory and from different commercial batches from Mérial actually differed by one or both typing methods. These results indicate a substantial degree of genetic drift among different vaccine preparations, which has important implications for prophylactic approaches.
副结核分枝杆菌亚种,即副结核病的病原体,可感染多种家养反刍动物,并且有人认为它与人类的克罗恩病有关。大多数现有的用于鉴定和区分这种难培养菌菌株的方法技术要求高且鉴别能力有限。在此,我们报告了基于新型PCR的分型标记的鉴定,这些标记由称为分枝杆菌散布重复单元(MIRU)的遗传元件的可变数目串联重复序列(VNTR)组成。八个标记应用于来自10个不同国家的牛、羊、山羊、鹿、兔和人类来源的183株副结核分枝杆菌亚种分离株,以及来自法国的82株密切相关的鸟分枝杆菌人类分离株。在副结核分枝杆菌亚种分离株中,通过MIRU-VNTR分型发现了21种模式,鉴别指数为0.751。占主导地位的R01 IS900限制性片段长度多态性类型(包括131株分离株)被分为15种MIRU-VNTR类型。在82株鸟分枝杆菌分离株中,八个MIRU-VNTR位点区分出30种类型,没有一种与副结核分枝杆菌亚种分离株共有,鉴别指数为0.889。我们的结果表明,MIRU-VNTR分型是一种快速分型方法,与其他方法结合使用,可能被证明是基于PCR的鸟分枝杆菌/副结核分枝杆菌亚种病原体分子流行病学研究的最佳方法。此外,推测来自韦布里奇实验室和梅里亚不同商业批次的相同副结核分枝杆菌亚种316F疫苗株实际上在一种或两种分型方法上存在差异。这些结果表明不同疫苗制剂之间存在相当程度的基因漂移,这对预防方法具有重要意义。