Bauer J, Andersen A B, Kremer K, Miörner H
Department of Mycobacteriology, Statens Serum Institut, Copenhagen, Denmark.
J Clin Microbiol. 1999 Aug;37(8):2602-6. doi: 10.1128/JCM.37.8.2602-2606.1999.
Mycobacterium tuberculosis complex strains cultured in Denmark have been analyzed by IS6110 restriction fragment length polymorphism (RFLP) on a routine basis from 1992 and onwards. Due to the influx of immigrants with tuberculosis, the number of strains harboring only one to five copies of IS6110 has increased steadily. Since the discriminatory power of IS6110 fingerprinting for such strains is poor, we have performed additional genotyping of all low-copy-number strains by the recently described PCR-based method known as spoligotyping. A total of 311 clinical strains were typed: 14 Mycobacterium bovis BCG, 48 M. bovis, and 249 M. tuberculosis strains. Spoligotyping correctly differentiated M. bovis and M. bovis BCG from M. tuberculosis strains, but it did not differentiate M. bovis from M. bovis BCG. All M. bovis BCG strains exhibited identical spoligotype patterns. The discriminatory power of spoligotyping of low-copy-number M. tuberculosis strains was higher than that of IS6110 fingerprinting. Based on RFLP typing solely, 83% of the low-copy-number M. tuberculosis strains were found to form part of a cluster, and 75% were found to form a cluster on the basis of spoligotyping. When the two techniques were combined, the amount of clustering decreased to 55%. The combination of these two techniques might be valuable in studying the epidemiology of M. tuberculosis strains harboring few copies of the IS6110 element.
自1992年起,丹麦对培养的结核分枝杆菌复合群菌株常规进行IS6110限制性片段长度多态性(RFLP)分析。由于结核病移民的涌入,仅携带1至5个IS6110拷贝的菌株数量稳步增加。由于IS6110指纹图谱对这类菌株的鉴别能力较差,我们采用最近描述的基于PCR的spoligotyping方法对所有低拷贝数菌株进行了额外的基因分型。共对311株临床菌株进行了分型:14株牛型结核分枝杆菌卡介苗、48株牛型结核分枝杆菌和249株结核分枝杆菌菌株。Spoligotyping能正确区分牛型结核分枝杆菌和牛型结核分枝杆菌卡介苗与结核分枝杆菌菌株,但不能区分牛型结核分枝杆菌和牛型结核分枝杆菌卡介苗。所有牛型结核分枝杆菌卡介苗菌株均表现出相同的spoligotype模式。低拷贝数结核分枝杆菌菌株的spoligotyping鉴别能力高于IS6110指纹图谱。仅基于RFLP分型,发现83%的低拷贝数结核分枝杆菌菌株属于一个簇,基于spoligotyping则为75%。当两种技术结合使用时,聚类数量降至55%。这两种技术的结合可能对研究携带少量IS6110元件拷贝的结核分枝杆菌菌株的流行病学有价值。