Yeh R W, Ponce de Leon A, Agasino C B, Hahn J A, Daley C L, Hopewell P C, Small P M
Department of Medicine, Stanford University School of Medicine, CA 94305, USA.
J Infect Dis. 1998 Apr;177(4):1107-11. doi: 10.1086/517406.
To assess genotype stability in Mycobacterium tuberculosis, DNA genotypes were compared in sequential isolates from 49 patients who had sputum cultures separated by at least 90 days that grew M. tuberculosis. By use of IS6110 and the polymorphic GC-rich sequence (PGRS) as markers, it was found that paired isolates from 14 (29%) of 49 patients showed changes in their DNA genotypes between isolates (12 in IS6110 genotypes and 2 in PGRS genotypes). Changed IS6110 genotypes were confined to strains with 8-14 bands and were not related to the bacterial drug susceptibility, the patients' human immunodeficiency virus serostatus, or adherence to therapy. Although this rate of change complicates the interpretation of molecular epidemiologic studies, it can be exploited to gain additional insight into disease transmission. Furthermore, IS6110-related mutations may be a major source of genetic plasticity in M. tuberculosis and provide insights into the organism's evolution and virulence.
为评估结核分枝杆菌的基因型稳定性,对49例痰培养至少间隔90天且培养出结核分枝杆菌的患者的连续分离株进行了DNA基因型比较。以IS6110和富含GC的多态性序列(PGRS)作为标记,发现49例患者中有14例(29%)的配对分离株在分离株之间显示出DNA基因型的变化(12例IS6110基因型变化和2例PGRS基因型变化)。IS6110基因型的变化仅限于具有8 - 14条带的菌株,且与细菌药敏性、患者的人类免疫缺陷病毒血清状态或治疗依从性无关。虽然这种变化率使分子流行病学研究的解释变得复杂,但它可用于深入了解疾病传播。此外,与IS6110相关的突变可能是结核分枝杆菌遗传可塑性的主要来源,并为该生物体的进化和毒力提供见解。