Englund Stina, Bölske Göran, Johansson Karl Erik
Department of Bacteriology, National Veterinary Institute, SE-751 89 Uppsala, Sweden.
FEMS Microbiol Lett. 2002 Apr 9;209(2):267-71. doi: 10.1111/j.1574-6968.2002.tb11142.x.
The insertion sequence IS900 has been considered specific for Mycobacterium avium subsp. paratuberculosis (M. paratuberculosis) and has, therefore, been used as the target gene for diagnostic PCR of M. paratuberculosis. From a healthy dairy cow we have isolated and characterised a mycobacterium harbouring one copy of a sequence with 94% identity to IS900 at the nucleic acid level. The isolate was shown to be related to Mycobacterium cookii, as assessed by 16S rRNA sequencing. Strong amplifications were obtained with several PCR primers described for detection of IS900. This finding shows the need of alternative PCR systems based on other genes than IS900 to confirm the presence of M. paratuberculosis.
插入序列IS900被认为是副结核分枝杆菌(M. paratuberculosis)所特有的,因此,它被用作副结核分枝杆菌诊断性PCR的靶基因。我们从一头健康的奶牛中分离并鉴定出一种分枝杆菌,该分枝杆菌在核酸水平上含有一个与IS900具有94%同一性的序列拷贝。通过16S rRNA测序评估,该分离株显示与库克分枝杆菌相关。使用几种描述用于检测IS900的PCR引物均获得了强扩增。这一发现表明需要基于IS900以外的其他基因的替代PCR系统来确认副结核分枝杆菌的存在。