Department of Medical Laboratory Science, University of Calabar, Calabar, Nigeria.
Infect Genet Evol. 2012 Jun;12(4):671-7. doi: 10.1016/j.meegid.2011.08.011. Epub 2011 Aug 22.
This study provides with a first insight on Mycobacterium tuberculosis complex epidemiology and genetic diversity in the Cross River State, Nigeria. Starting with 137 smear positive patients recruited over a period of 12months (June 2008 to May 2009), we obtained 97 pure mycobacterial isolates out of which 81 (83.5%) were identified as M. tuberculosis complex. Genotyping revealed a total of 27 spoligotypes patterns with 10 clusters (n=64% or 79% of clustered isolates, 2-32 isolates/cluster), with patients in the age group range 25-34 years being significantly associated with shared-type pattern SIT61 (p=0.019). Comparison with SITVIT2 database showed that with the exception of a single cluster (SIT727/H1), all other clusters observed were representative of West Africa; the two main lineages involved were LAM10-CAM (n=42/81% or 51.8%) of M. tuberculosis and AFRI_2 sublineage of Mycobacterium africanum (n=27/81% or 33.3%). Subsequent 12-loci MIRU typing resulted in a total of 13 SIT/MIT clusters (n=52 isolates, 2-9 isolates per cluster), with a resulting recent n-1 transmission rate of 48.1%. Available drug-susceptibility testing (DST) results for 58/81 clinical isolates revealed 6/58% or 10.4% cases of multiple drug-resistance (MDR); 5/6 MDR cases were caused by strains belonging to LAM10-CAM lineage (a specific cluster SIT61/MIT266 in 4/6 cases, and an orphan spoligotype pattern in 1/6 case). Additionally, MIT266 was associated with streptomycin resistance (p=0.016). All the six MDRTB isolates were concomitantly resistance to streptomycin and ethambutol; however, 4/6 MDR strains with identical MIRU patterns were characterized by consecutive strain numbers hence the possibility of laboratory cross contamination could not be excluded in 3/4 serial cases. The present preliminary study underlines the usefulness of spoligotyping and 12-loci MIRU-VNTRs to establish a baseline of circulating genotypic lineages of M. tuberculosis complex in Nigeria.
本研究首次提供了尼日利亚十字河州结核分枝杆菌复合群的流行病学和遗传多样性的见解。从 137 名在 12 个月(2008 年 6 月至 2009 年 5 月)期间招募的涂片阳性患者中,我们获得了 97 株纯分枝杆菌分离株,其中 81 株(83.5%)鉴定为结核分枝杆菌复合群。基因分型显示共有 27 种 spoligotype 模式和 10 个克隆群(n=64%或聚类分离株的 79%,每个克隆群 2-32 株),年龄在 25-34 岁之间的患者与共享型模式 SIT61 显著相关(p=0.019)。与 SITVIT2 数据库的比较表明,除了一个单一的克隆群(SIT727/H1)外,观察到的所有其他克隆群均代表西非;涉及的两个主要谱系是 LAM10-CAM(n=42/81%或 51.8%)的结核分枝杆菌和 Mycobacterium africanum 的 AFRI_2 亚谱系(n=27/81%或 33.3%)。随后的 12 个基因座 MIRU 分型总共产生了 13 个 SIT/MIT 克隆群(n=52 株分离株,每个克隆群 2-9 株),最近的 n-1 传播率为 48.1%。对 81 例临床分离株中的 58 株进行的药物敏感性试验(DST)结果显示,6/58%或 10.4%的病例为耐多药(MDR);6 例 MDR 病例中有 5 例是由属于 LAM10-CAM 谱系的菌株引起的(6 例中的 4 例是特定的克隆群 SIT61/MIT266,1 例是孤儿 spoligotype 模式)。此外,MIT266 与链霉素耐药性相关(p=0.016)。所有 6 例 MDRTB 分离株同时对链霉素和乙胺丁醇耐药;然而,4/6 例具有相同 MIRU 模式的 MDR 菌株具有连续的菌株编号,因此在 3/4 例连续病例中不能排除实验室交叉污染的可能性。本初步研究强调了 spoligotyping 和 12 个基因座 MIRU-VNTR 用于建立尼日利亚结核分枝杆菌复合群循环基因谱系基线的有用性。