Wampande Eddie M, Mupere Ezekiel, Debanne Sara M, Asiimwe Benon B, Nsereko Mary, Mayanja Harriet, Eisenach Kathleen, Kaplan Gilla, Boom Henry W, Gagneux Sebastien, Joloba Moses L
Department of Medical Microbiology, College of Health Sciences, Makerere University, Kampala, Uganda.
BMC Infect Dis. 2013 Oct 17;13:484. doi: 10.1186/1471-2334-13-484.
Previous studies have shown that Mycobacterium tuberculosis (MTB) Uganda family, a sub-lineage of the MTB Lineage 4, is the main cause of tuberculosis (TB) in Uganda. Using a well characterized patient population, this study sought to determine whether there are clinical and patient characteristics associated with the success of the MTB Uganda family in Kampala.
A total of 1,746 MTB clinical isolates collected from 1992-2009 in a household contact study were genotyped. Genotyping was performed using Single Nucleotide Polymorphic (SNP) markers specific for the MTB Uganda family, other Lineage 4 strains, and Lineage 3, respectively. Out of 1,746 isolates, 1,213 were from patients with detailed clinical data. These data were used to seek associations between MTB lineage/sub-lineage and patient phenotypes.
Three MTB lineages were found to dominate the MTB population in Kampala during the last two decades. Overall, MTB Uganda accounted for 63% (1,092/1,746) of all cases, followed by other Lineage 4 strains accounting for 22% (394/1,746), and Lineage 3 for 11% (187/1,746) of cases, respectively. Seventy-three (4 %) strains remained unclassified. Our longitudinal data showed that MTB Uganda family occurred at the highest frequency during the whole study period, followed by other Lineage 4 strains and Lineage 3. To explore whether the long-term success of MTB Uganda family was due to increased virulence, we used cavitary disease as a proxy, as this form of TB is the most transmissible. Multivariate analysis revealed that even though cavitary disease was associated with known risk factors such as smoking (adjusted odds ratio (aOR) 4.8, 95% confidence interval (CI) 3.33-6.84) and low income (aOR 2.1, 95% CI 1.47-3.01), no association was found between MTB lineage and cavitary TB.
The MTB Uganda family has been dominating in Kampala for the last 18 years, but this long-term success is not due to increased virulence as defined by cavitary disease.
先前的研究表明,结核分枝杆菌(MTB)乌干达家族是MTB谱系4的一个亚谱系,是乌干达结核病(TB)的主要病因。本研究利用特征明确的患者群体,试图确定在坎帕拉与MTB乌干达家族成功相关的临床和患者特征。
对1992年至2009年在一项家庭接触者研究中收集的1746株MTB临床分离株进行基因分型。分别使用针对MTB乌干达家族、其他谱系4菌株和谱系3的单核苷酸多态性(SNP)标记进行基因分型。在1746株分离株中,1213株来自有详细临床数据的患者。这些数据用于寻找MTB谱系/亚谱系与患者表型之间的关联。
在过去二十年中,发现三种MTB谱系在坎帕拉的MTB群体中占主导地位。总体而言,MTB乌干达家族占所有病例的63%(1092/1746),其次是其他谱系4菌株占22%(394/1746),谱系3占11%(187/1746)。73株(4%)菌株仍未分类。我们的纵向数据显示,在整个研究期间,MTB乌干达家族出现的频率最高,其次是其他谱系4菌株和谱系3。为了探究MTB乌干达家族的长期成功是否归因于毒力增强,我们以空洞性疾病作为替代指标,因为这种形式的结核病传染性最强。多变量分析显示,尽管空洞性疾病与吸烟(调整后的优势比(aOR)4.8,95%置信区间(CI)3.33 - 6.84)和低收入(aOR 2.1,95%CI 1.47 - 3.01)等已知风险因素相关,但未发现MTB谱系与空洞性结核病之间存在关联。
在过去18年中,MTB乌干达家族在坎帕拉一直占主导地位,但这种长期的成功并非归因于空洞性疾病所定义的毒力增强。