Mbugi Erasto V, Katale Bugwesa Z, Streicher Elizabeth M, Keyyu Julius D, Kendall Sharon L, Dockrell Hazel M, Michel Anita L, Rweyemamu Mark M, Warren Robin M, Matee Mecky I, van Helden Paul D, Couvin David, Rastogi Nalin
Department of Biochemistry, Muhimbili University of Health and Allied Sciences, P. O. Box 65001, Dar es Salaam, Tanzania.
Department of Microbiology and Immunology, Muhimbili University of Health and Allied Sciences, P.O. Box 65001, Dar es Salaam, Tanzania.
PLoS One. 2016 May 5;11(5):e0154571. doi: 10.1371/journal.pone.0154571. eCollection 2016.
The aim of this study was to assess and characterize Mycobacterium tuberculosis complex (MTBC) genotypic diversity in Tanzania, as well as in neighbouring East and other several African countries. We used spoligotyping to identify a total of 293 M. tuberculosis clinical isolates (one isolate per patient) collected in the Bunda, Dar es Salaam, Ngorongoro and Serengeti areas in Tanzania. The results were compared with results in the SITVIT2 international database of the Pasteur Institute of Guadeloupe. Genotyping and phylogeographical analyses highlighted the predominance of the CAS, T, EAI, and LAM MTBC lineages in Tanzania. The three most frequent Spoligotype International Types (SITs) were: SIT21/CAS1-Kili (n = 76; 25.94%), SIT59/LAM11-ZWE (n = 22; 7.51%), and SIT126/EAI5 tentatively reclassified as EAI3-TZA (n = 18; 6.14%). Furthermore, three SITs were newly created in this study (SIT4056/EAI5 n = 2, SIT4057/T1 n = 1, and SIT4058/EAI5 n = 1). We noted that the East-African-Indian (EAI) lineage was more predominant in Bunda, the Manu lineage was more common among strains isolated in Ngorongoro, and the Central-Asian (CAS) lineage was more predominant in Dar es Salaam (p-value<0.0001). No statistically significant differences were noted when comparing HIV status of patients vs. major lineages (p-value = 0.103). However, when grouping lineages as Principal Genetic Groups (PGG), we noticed that PGG2/3 group (Haarlem, LAM, S, T, and X) was more associated with HIV-positive patients as compared to PGG1 group (Beijing, CAS, EAI, and Manu) (p-value = 0.03). This study provided mapping of MTBC genetic diversity in Tanzania (containing information on isolates from different cities) and neighbouring East African and other several African countries highlighting differences as regards to MTBC genotypic distribution between Tanzania and other African countries. This work also allowed underlining of spoligotyping patterns tentatively grouped within the newly designated EAI3-TZA lineage (remarkable by absence of spacers 2 and 3, and represented by SIT126) which seems to be specific to Tanzania. However, further genotyping information would be needed to confirm this specificity.
本研究的目的是评估和描述坦桑尼亚以及邻国东非和其他几个非洲国家结核分枝杆菌复合群(MTBC)的基因型多样性。我们使用间隔寡核苷酸分型技术(spoligotyping)对在坦桑尼亚的邦达、达累斯萨拉姆、恩戈罗恩戈罗和塞伦盖蒂地区收集的总共293株结核分枝杆菌临床分离株(每位患者一株分离株)进行鉴定。将结果与瓜德罗普岛巴斯德研究所的SITVIT2国际数据库中的结果进行比较。基因分型和系统地理学分析突出了CAS、T、EAI和LAM MTBC谱系在坦桑尼亚的优势地位。三种最常见的寡核苷酸分型国际类型(SITs)分别是:SIT21/CAS1-Kili(n = 76;25.94%)、SIT59/LAM11-ZWE(n = 22;7.51%)和SIT126/EAI5(暂重新分类为EAI3-TZA)(n = 18;6.14%)。此外,本研究新创建了三种SITs(SIT4056/EAI5,n = 2;SIT4057/T1,n = 1;SIT4058/EAI5,n = 1)。我们注意到,东非-印度(EAI)谱系在邦达更为占优势,马努谱系在恩戈罗恩戈罗分离的菌株中更为常见,而中亚(CAS)谱系在达累斯萨拉姆更为占优势(p值<0.0001)。比较患者的HIV状态与主要谱系时,未发现统计学上的显著差异(p值 = 0.103)。然而,当将谱系分组为主干遗传群(PGG)时,我们注意到与PGG1组(北京、CAS、EAI和马努)相比,PGG2/3组(哈勒姆、LAM、S、T和X)与HIV阳性患者的关联更强(p值 = 0.03)。本研究提供了坦桑尼亚(包含来自不同城市的分离株信息)以及邻国东非和其他几个非洲国家MTBC基因多样性图谱,突出了坦桑尼亚与其他非洲国家在MTBC基因型分布方面的差异。这项工作还强调了暂归为新指定的EAI3-TZA谱系(以间隔区2和3缺失为特征,由SIT126代表)内的间隔寡核苷酸分型模式,该谱系似乎是坦桑尼亚特有的。然而,需要更多的基因分型信息来证实这种特异性。