Kong Y, Cave M D, Zhang L, Foxman B, Marrs C F, Bates J H, Yang Z H
Epidemiology Department, School of Public Health, University of Michigan, 109 S. Observatory Street, Ann Arbor, MI 48109-2029, USA.
J Clin Microbiol. 2006 Nov;44(11):3940-6. doi: 10.1128/JCM.01146-06. Epub 2006 Sep 6.
Regions of difference (RDs) have been described in clinical isolates of Mycobacterium tuberculosis, but the potential epidemiological and clinical relevance of the genotypes of these RDs remains to be investigated. We screened a population-based sample of 648 isolates for the deletion of five RDs, designated RD105, RD181, RD142, RD150, and RD239, using microarray-based hybridization, PCR, and DNA sequencing and assessed the associations between the RD deletions and the clinical characteristics of the patients using chi-square analysis and multivariate logistic regression model. Of the 648 isolates, 18 (2.8%) had the RD239 deletion and 39 (6.0%) had the RD105 deletion. The deletions of RD142, RD150, and RD181 subdivided the isolates with the RD105 deletion into four groups comprising a group with concurrent deletions of RD105, RD181, and RD142 (n = 13); a group with concurrent deletions of RD105, RD181, and RD150 (n = 5); a group with concurrent deletions of RD105 and RD181 (n = 13); and a group with a deletion of RD105 only (n = 8). Extrathoracic tuberculosis is statistically significantly associated with infection with the isolates with concurrent deletions of RD105, RD181, and RD142 (adjusted odds ratio [OR] = 3.05; 95% confidence interval [CI] = 1.58, 5.90) and the isolates with concurrent deletions of RD105, RD181, and RD150 (adjusted OR = 11.09; 95% CI = 4.27, 28.80), after controlling for the previously identified risk factors for extrathoracic tuberculosis (human immunodeficiency virus serostatus, race, gender, and the genotype of the plcD gene). These two combinations of RD deletions have the potential for predicting the clinical presentation of M. tuberculosis infection in the human host.
结核分枝杆菌临床分离株中已发现差异区域(RDs),但这些RDs基因型潜在的流行病学和临床相关性仍有待研究。我们采用基于微阵列的杂交、聚合酶链反应(PCR)和DNA测序技术,对648株基于人群的分离株进行了5种RDs(即RD105、RD181、RD142、RD150和RD239)缺失情况的筛查,并使用卡方分析和多变量逻辑回归模型评估了RDs缺失与患者临床特征之间的关联。在这648株分离株中,18株(2.8%)存在RD239缺失,39株(6.0%)存在RD105缺失。RD142、RD150和RD181的缺失将存在RD105缺失的分离株分为四组,包括同时缺失RD105、RD181和RD142的一组(n = 13);同时缺失RD105、RD181和RD150的一组(n = 5);同时缺失RD105和RD181的一组(n = 13);以及仅缺失RD105的一组(n = 8)。在控制了先前确定的肺外结核危险因素(人类免疫缺陷病毒血清学状态、种族、性别和plcD基因的基因型)后,肺外结核与同时缺失RD105、RD181和RD142的分离株感染在统计学上显著相关(校正比值比[OR] = 3.05;95%置信区间[CI] = 1.58, 5.90),也与同时缺失RD105、RD181和RD150的分离株感染显著相关(校正OR = 11.09;95% CI = 4.27, 28.80)。这两种RDs缺失组合具有预测人类宿主中结核分枝杆菌感染临床表现的潜力。