Truman Richard, Fontes Amanda B, De Miranda Antonio B, Suffys Philip, Gillis Thomas
NHDP at LSU, P.O. Box 25072, Baton Rouge, LA 70894, USA.
J Clin Microbiol. 2004 Jun;42(6):2558-65. doi: 10.1128/JCM.42.6.2558-2565.2004.
It has not been possible to distinguish different strains of Mycobacterium leprae according to their genetic sequence. However, the genome contains several variable-number tandem repeats (VNTR), which have been used effectively in strain typing of other bacteria. To determine their suitability for differentiating M. leprae, we developed PCR systems to amplify 5 different VNTR loci and examined a battery of 12 M. leprae strains derived from patients in different regions of the United States, Brazil, Mexico, and the Philippines, as well as from wild armadillos and a sooty mangabey monkey. We found diversity at four VNTR (D = 0.74), but one system (C(16)G(8)) failed to yield reproducible results. Alleles for the GAA VNTR varied in length from 10 to 16 copies, those for AT(17) varied in length from 10 to 15 copies, those for GTA varied in length from 9 to 12 copies, and those for TA(18) varied in length from 13 to 20 copies. Relatively little variation was seen with interspecies transfer of bacilli or during short-term passage of strains in nude mice or armadillos. The TA(18) locus was more polymorphic than other VNTR, and genotypic variation was more common after long-term expansion in armadillos. Most strain genotypes remained fairly stable in passage, but strain Thai-53 showed remarkable variability. Statistical cluster analysis segregated strains and passage samples appropriately but did not reveal any particular genotype associable with different regions or hosts of origin. VNTR polymorphisms can be used effectively to discriminate M. leprae strains. Inclusion of additional loci and other elements will likely lead to a robust typing system that can be used in community-based epidemiological studies and select clinical applications.
根据麻风分枝杆菌的基因序列来区分不同菌株是不可能的。然而,该基因组包含几个可变数目串联重复序列(VNTR),这些序列已有效地用于其他细菌的菌株分型。为了确定它们是否适合区分麻风分枝杆菌,我们开发了PCR系统来扩增5个不同的VNTR位点,并检测了一组12株麻风分枝杆菌,这些菌株来自美国、巴西、墨西哥和菲律宾的不同地区的患者,以及野生犰狳和一只黑掌卷尾猴。我们在四个VNTR位点发现了多样性(D = 0.74),但一个系统(C(16)G(8))未能产生可重复的结果。GAA VNTR的等位基因长度从10到16个拷贝不等,AT(17)的等位基因长度从10到15个拷贝不等,GTA的等位基因长度从9到12个拷贝不等,TA(18)的等位基因长度从13到20个拷贝不等。在细菌的种间转移或菌株在裸鼠或犰狳中的短期传代过程中,观察到的变异相对较少。TA(18)位点比其他VNTR位点多态性更高,并且在犰狳中长期传代后基因型变异更常见。大多数菌株基因型在传代过程中保持相当稳定,但泰国-53菌株表现出显著的变异性。统计聚类分析适当地分离了菌株和传代样本,但没有揭示任何与不同地区或宿主来源相关的特定基因型。VNTR多态性可有效地用于区分麻风分枝杆菌菌株。纳入更多位点和其他元素可能会产生一个强大的分型系统,可用于基于社区的流行病学研究和特定的临床应用。