Genomic epidemiology reveals geographically structured co-circulation of AFR10 and AFR13 Vibrio cholerae lineages driving cholera outbreaks in Tanzania (2022-2024).

IF 4.5 2区 生物学 Q1 GENETICS & HEREDITY
Ibrahim I Mauki, Reuben Abednego, Lawrence Mapunda, Maria Ezekiely Kelly, Monica Fredrick Francis, Jackson Mushumbusi, Dennis Mrosso Kado, Feliciana Rawile, Boaz Wadugu, Hamisi Swalehe, Modest Benard, Edna Mgimba, Seif Abdul, Ambele Mwafulango, Tolbert Sonda, Calvin Sindato, Paul Kazyoba, Nyambura Moremi
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引用次数: 0

Abstract

Cholera remains a persistent public health challenge in Tanzania, with recurrent outbreaks across multiple regions overwhelming the health systems. Despite the ongoing surveillance to control the transmission, limited genomic characterization of circulating Vibrio cholerae strains has constrained traceability of outbreak sources and transmission dynamics including virulence determinants and antimicrobial resistance profiles to guide clinical and public health interventions. We conducted a genome analysis of 144 archived isolates from 2022 to 2024 cholera outbreaks from 16 regions across Tanzania. Sequencing was performed using Oxford Nanopore platforms. Comprehensive bioinformatics analysis was applied including genome assembly, multi-locus sequence typing, resistance gene detection, virulence profiling and phylogenetic reconstruction. Of 144 isolates, sequencing confirmed 119 to be V. cholerae, of which 109 (91.6%) belonged to sequence type ST69. Phylogenetic analysis identified two distinct transmission lineages: AFR10 (formerly T10) and AFR13 (formerly T13), demonstrating marked geographic stratification. AFR10 isolates clustered predominantly around Lake Tanganyika basin, bordering the Democratic Republic of the Congo and Zambia, whereas AFR13 isolates were widely distributed across different zones of Tanzania. All isolates harboured key virulence genes (ctxA, ctxB, tcpA) and multiple resistance genes conferring resistance to co-trimoxazole and macrolides. The catB gene was found to be silenced in these isolates. Notably, tetracycline resistance genes (tetA/B/C) were absent. The qacEdelta gene was only detected in AFR13 isolates and has been linked to resistance to quaternary ammonium compounds (antiseptics and disinfectants) in Gram-negative bacteria from other studies. These findings demonstrate the co-circulation of two sublineages (AFR10 and AFR13) of the seventh pandemic El Tor lineage with distinct geographic distribution, suggesting both localized persistence and regional circulation. The observed genotypic and phenotypic susceptibility to tetracycline supports the continued use of doxycycline as a first-line therapy in adults. However, the detected macrolide resistance (an alternative treatment for children) and resistance genes associated with reduced susceptibility to antiseptics underscore the need for extensive monitoring. Strengthened national and cross-border genomic surveillance is essential for effective cholera control.

基因组流行病学揭示了AFR10和AFR13霍乱弧菌谱系的地理结构共循环,推动了坦桑尼亚的霍乱暴发(2022-2024)。
在坦桑尼亚,霍乱仍然是一项持续存在的公共卫生挑战,多个地区的反复暴发使卫生系统不堪重负。尽管正在进行监测以控制传播,但循环霍乱弧菌菌株的有限基因组特征限制了疫情来源和传播动态的可追溯性,包括毒力决定因素和抗微生物药物耐药性概况,以指导临床和公共卫生干预。我们对来自坦桑尼亚16个地区的2022年至2024年霍乱暴发的144株存档分离株进行了基因组分析。测序使用Oxford Nanopore平台进行。综合生物信息学分析包括基因组组装、多位点序列分型、抗性基因检测、毒力分析和系统发育重建。144株分离株经测序鉴定为霍乱弧菌119株,其中ST69型109株(91.6%)。系统发育分析确定了两个不同的传播谱系:AFR10(原T10)和AFR13(原T13),显示出明显的地理分层。AFR10分离株主要聚集在与刚果民主共和国和赞比亚接壤的坦噶尼喀湖盆地周围,而AFR13分离株广泛分布在坦桑尼亚的不同地区。所有分离株均含有关键毒力基因(ctxA、ctxB、tcpA)和多重耐药基因,对复方新诺明和大环内酯类药物具有耐药性。在这些分离株中发现catB基因是沉默的。值得注意的是,四环素耐药基因(tetA/B/C)缺失。qacEdelta基因仅在AFR13分离株中检测到,并且与其他研究中革兰氏阴性菌对季铵化合物(防腐剂和消毒剂)的耐药性有关。这些发现表明,第七次大流行El Tor谱系的两个亚谱系(AFR10和AFR13)具有不同的地理分布,这表明既存在局部持久性,也存在区域性循环。观察到的基因型和表型对四环素的易感性支持继续使用强力霉素作为成人一线治疗。然而,检测到的大环内酯类药物耐药性(儿童的一种替代治疗方法)和耐药基因与对防腐剂的易感性降低相关,强调了广泛监测的必要性。加强国家和跨界基因组监测对于有效控制霍乱至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbial Genomics
Microbial Genomics Medicine-Epidemiology
CiteScore
6.60
自引率
2.60%
发文量
153
审稿时长
12 weeks
期刊介绍: Microbial Genomics (MGen) is a fully open access, mandatory open data and peer-reviewed journal publishing high-profile original research on archaea, bacteria, microbial eukaryotes and viruses.
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