Barilar Ivan, Fernando Tatiana, Utpatel Christian, Abujate Cláudio, Madeira Carla Maria, José Benedita, Mutaquiha Claudia, Kranzer Katharina, Niemann Tanja, Ismael Nalia, de Araujo Leonardo, Wirth Thierry, Niemann Stefan, Viegas Sofia
Molecular and Experimental Mycobacteriology, Research Center Borstel, Borstel, Germany; German Center for Infection Research, Partner Site Hamburg-Lübeck-Borstel-Riems, Borstel, Germany.
Instituto Nacional de Saúde, Marracuene, Mozambique.
Lancet Infect Dis. 2024 Mar;24(3):297-307. doi: 10.1016/S1473-3099(23)00498-X. Epub 2023 Nov 10.
In 2021, an estimated 4800 people developed rifampicin-resistant tuberculosis in Mozambique, 75% of which went undiagnosed. Detailed molecular data on rifampicin-resistant and multidrug-resistant (MDR) tuberculosis are not available. Here, we aimed at gaining precise data on the determinants of rifampicin-resistant and MDR tuberculosis in Mozambique.
In this retrospective observational study, we performed whole-genome sequencing of 704 rifampicin-resistant Mycobacterium tuberculosis complex (Mtbc) strains submitted to the National Tuberculosis Reference Laboratory (NTRL) in Maputo, Mozambique, between 2015 and 2021. Phylogenetic strain classification, genomic resistance prediction, and cluster analysis were performed.
Between Jan 1, 2015, and July 31, 2021, 2606 Mtbc isolates with an isoniazid or rifampicin resistance were identified in the NTRL biobank, of which, 1483 (56·9%) were from men, 1114 (42·7%) from women, and nine (0·4%) were unknown. Genome-based drug-resistant prediction classified 704 Mtbc strains as rifampicin resistant. 628 (89%) of the 704 Mtbc strains were classified MDR; of those, 146 (23%) were pre-extensively drug resistant (pre-XDR; additional fluoroquinolone resistance), and 24 (4%) extensively drug resistant (XDR; combined fluoroquinolone and bedaquiline resistance). Overall, 61 (9%) of 704 strains revealed resistance to bedaquiline: five (7%) of 76 rifampicin resistant plus bedaquiline resistant, 32 (7%) of 458 MDR plus bedaquiline resistant, and 24 (100%) of 24 XDR. Prevalence of bedaquiline resistance increased from 3% in 2016 to 14% in 2021. The cluster rate (12 single-nucleotide polymorphism threshold) was 42% for rifampicin-resistant strains, 78% for MDR strains, 94% for pre-XDR strains, and 96% for XDR Mtbc strains. 31 (4%) of 704 Mtbc strains, belonging to a diagnostic escape outbreak strain previously described in Eswatini (group_56), had an rpoB Ile491Phe mutation which is not detected by Xpert MTB/RIF (no other rpoB mutation). Of these, 23 (74%) showed additional resistance to bedaquiline, 13 (42%) had bedaquiline and fluoroquinolone resistance, and two (6%) were bedaquiline, fluoroquinolone, and delamanid resistant.
Pre-XDR resistance is highly prevalent among MDR Mtbc strains in Mozambique and so is bedaquiline resistance; and the frequency of bedaquiline resistance quadrupled over time and was found even in Mtbc strains without fluoroquinolone resistance. Importantly, strains with Ile491Phe mutation were frequent, accounting for 31% (n=10) of MDR plus bedaquiline-resistant strains and 54% (n=13) of XDR Mtbc strains. Given the current diagnostic algorithms and treatment regimens, both the emergence of rifampicin resistance due to Ile491Phe and bedaquiline resistance might jeopardise MDR tuberculosis prevention and care unless sequencing-based technology is rolled out. The potential cross border spread of diagnostic escape strains needs further investigation.
The German Ministry of Health through the Seq_MDRTB-Net project, the Deutsche Forschungsgemeinschaft under Germany's Excellence Strategy Precision Medicine in Inflammation and the Research Training Group 2501 TransEvo, the Leibniz Science Campus Evolutionary Medicine of the Lung, and the German Ministry of Education and Research via the German Center for Infection Research.
2021年,莫桑比克估计有4800人感染了耐利福平结核病,其中75%未被诊断出来。目前尚无关于耐利福平结核病和耐多药结核病的详细分子数据。在此,我们旨在获取莫桑比克耐利福平结核病和耐多药结核病决定因素的精确数据。
在这项回顾性观察研究中,我们对2015年至2021年间提交给莫桑比克马普托国家结核病参考实验室(NTRL)的704株耐利福平结核分枝杆菌复合群(Mtbc)菌株进行了全基因组测序。进行了系统发育菌株分类、基因组耐药性预测和聚类分析。
2015年1月1日至2021年7月31日期间,NTRL生物样本库中鉴定出2606株对异烟肼或利福平耐药的Mtbc分离株,其中1483株(56.9%)来自男性,1114株(42.7%)来自女性,9株(0.4%)性别未知。基于基因组的耐药性预测将704株Mtbc菌株分类为耐利福平。704株Mtbc菌株中有628株(89%)被分类为耐多药;其中,146株(23%)为广泛耐药前期(pre-XDR;额外对氟喹诺酮耐药),24株(4%)为广泛耐药(XDR;对氟喹诺酮和贝达喹啉联合耐药)。总体而言,704株菌株中有61株(9%)对贝达喹啉耐药:76株耐利福平加耐贝达喹啉菌株中有5株(7%),458株耐多药加耐贝达喹啉菌株中有32株(7%),24株XDR菌株中有24株(100%)。贝达喹啉耐药率从2016年的3%上升到2021年的14%。耐利福平菌株的聚类率(单核苷酸多态性阈值为12)为42%,耐多药菌株为78%,广泛耐药前期菌株为94%,XDR Mtbc菌株为96%。704株Mtbc菌株中有31株(4%)属于先前在斯威士兰描述的诊断逃逸暴发菌株(第56组),具有rpoB Ile491Phe突变,Xpert MTB/RIF检测不到该突变(无其他rpoB突变)。其中,23株(74%)对贝达喹啉有额外耐药性,13株(42%)对贝达喹啉和氟喹诺酮耐药,2株(6%)对贝达喹啉、氟喹诺酮和德拉马尼德耐药。
广泛耐药前期在莫桑比克耐多药Mtbc菌株中高度流行,贝达喹啉耐药也是如此;贝达喹啉耐药频率随时间增加了四倍,甚至在无氟喹诺酮耐药的Mtbc菌株中也有发现。重要的是,具有Ile491Phe突变的菌株很常见,占耐多药加耐贝达喹啉菌株的31%(n = 10)和XDR Mtbc菌株的54%(n = 13)。鉴于当前的诊断算法和治疗方案,除非推广基于测序的技术,Ile491Phe导致的利福平耐药和贝达喹啉耐药的出现可能会危及耐多药结核病的预防和治疗。诊断逃逸菌株的潜在跨境传播需要进一步调查。
德国卫生部通过Seq_MDRTB-Net项目、德国卓越战略“炎症中的精准医学”下的德国研究基金会和研究培训小组2501 TransEvo、莱布尼茨科学园区肺部进化医学以及德国教育和研究部通过德国感染研究中心提供资金。