Mziray Shabani Ramadhani, Githinji George, de Laurent Zaydah R, Mbelele Peter M, Mohammed Khadija S, Wadugu Boaz D, Grundy Brian S, Heysell Scott K, Mpagama Stellah G, Chilongola Jaffu O
Department of Biochemistry and Molecular Biology, KCMC University, Moshi P.O. Box 2240, Tanzania.
Kibong'oto Infectious Diseases Hospital, Kilimanjaro P.O. Box 12, Tanzania.
Pathogens. 2025 Jun 19;14(6):601. doi: 10.3390/pathogens14060601.
Outbreaks of infectious diseases contribute significantly to morbidity and mortality in resource-limited settings, yet the capacity to identify their etiology remains limited. We aimed to characterize microbes and antimicrobial resistance (AMR) genes in Tanzanian children affected by an acute febrile illness (AFI) outbreak using metagenomic next-generation sequencing (mNGS). A cross-sectional study was conducted on archived blood samples from children who presented with AFI between 2018 and 2019. Total nucleic acids were extracted from 200 µL of blood, and complementary DNA (cDNA), along with enriched pathogenic DNA, was sequenced using the Illumina MiSeq platform. mNGS data were analyzed using CZ-ID Illumina mNGS bioinformatics pipeline v7.0. Results were obtained from 25 participants (mean age: 11.6 years; SD ± 5), of whom 36% had a moderate to high-grade fever. The following five potential microbial causes of AFI were identified: (n = 19), (n = 2), (n = 2), (n = 1) and (n = 1), with being the most prevalent. Twelve AMR genes were detected, including , , , and harbored most of the AMR genes previously associated with resistance to commonly used antibiotics. mNGS offers a promising complementary approach to conventional diagnostics for identifying pathogens and AMR profiles in vulnerable populations.
在资源有限的环境中,传染病爆发对发病率和死亡率有重大影响,但识别其病因的能力仍然有限。我们旨在使用宏基因组下一代测序(mNGS)对受急性发热性疾病(AFI)爆发影响的坦桑尼亚儿童中的微生物和抗菌药物耐药性(AMR)基因进行特征分析。对2018年至2019年期间出现AFI的儿童的存档血样进行了一项横断面研究。从200微升血液中提取总核酸,并使用Illumina MiSeq平台对互补DNA(cDNA)以及富集的致病DNA进行测序。使用CZ-ID Illumina mNGS生物信息学管道v7.0分析mNGS数据。结果来自25名参与者(平均年龄:11.6岁;标准差±5),其中36%有中度至高度发热。确定了以下五种AFI的潜在微生物病因:(n = 19),(n = 2),(n = 2),(n = 1)和(n = 1),其中最为普遍。检测到12个AMR基因,包括,,,和,这些基因包含了以前与对常用抗生素耐药相关的大多数AMR基因。mNGS为在弱势群体中识别病原体和AMR谱提供了一种有前景的补充传统诊断方法。