Imoli Diana, Maingi John M, Mbae Cecilia, Kavai Susan M, Wairimu Celestine, Mundalo Sheilla, Odityo Georgina, Wairimu Mary, Mekuria Zelalem, Gebreyes Wondwossen, Kariuki Samuel
Centre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
Department of Biochemistry, Microbiology and Biotechnology, Kenyatta University, Nairobi, Kenya.
J Antimicrob Chemother. 2025 Jul 14. doi: 10.1093/jac/dkaf224.
In mid-2021, a global surge in cholera cases was reported. This study characterized Vibrio cholerae O1 isolates obtained from faecal samples of cholera-positive cases during the 2022 cholera outbreak in Kenya.
A total of 202 V. cholerae were confirmed through serogroup and serotype characterization by slide agglutination. Susceptibility testing was done using the Kirby-Bauer disc diffusion method, and ESBL production confirmed using the double-disc synergy test. WGS was performed on Illumina and ONT platforms, followed by bioinformatics analysis.
All the isolates were identified as V. cholerae O1 of Ogawa serotype, with 99% classified as MDR and 98.5% positive for ESBL production. Notably, the isolates were resistant to azithromycin, one of the recommended antibiotics for cholera treatment. MDR was linked to the acquisition of an IncC plasmid (pVCMLK181) carrying seven resistance genes, including mph(A), mph(E) and msr(E), which confer resistance to azithromycin, and the blaPER-7 ESBL gene. Resistance to nalidixic acid was associated with mutations in QRDRs of gyrA and parC. The isolates also carried SXT/R391-like ICE, ICEVchInd5 featuring a 10 kb deletion and mapped to the 7PET-AFR13 lineage. Phylogenetic analysis revealed a close relationship to other highly drug-resistant AFR13 strains reported in Tanzania, Comoros and Mayotte.
The high prevalence of multidrug resistance in cholera isolates emphasizes the need for continuous surveillance to monitor the evolution of MDR V. cholerae O1 strains and calls for consideration of deployment of alternative management and prevention options including oral cholera vaccines and long-term improvement of water, sanitation and hygiene (WASH) infrastructure and practice.
2021年年中,有报告称霍乱病例在全球范围内激增。本研究对2022年肯尼亚霍乱疫情期间从霍乱阳性病例粪便样本中分离出的霍乱弧菌O1菌株进行了特征分析。
通过玻片凝集法对血清群和血清型进行鉴定,共确认了202株霍乱弧菌。采用 Kirby-Bauer 纸片扩散法进行药敏试验,并使用双纸片协同试验确认超广谱β-内酰胺酶(ESBL)的产生。在Illumina和ONT平台上进行全基因组测序(WGS),随后进行生物信息学分析。
所有分离株均被鉴定为小川血清型霍乱弧菌O1,其中99%被归类为多重耐药(MDR),98.5%的菌株ESBL检测呈阳性。值得注意的是,这些分离株对阿奇霉素耐药,而阿奇霉素是推荐用于治疗霍乱的抗生素之一。MDR与获得一个携带七个耐药基因的IncC质粒(pVCMLK181)有关,这些基因包括mph(A)、mph(E)和msr(E),它们赋予对阿奇霉素的耐药性,以及blaPER-7 ESBL基因。对萘啶酸的耐药性与gyrA和parC的喹诺酮耐药决定区(QRDR)突变有关。这些分离株还携带SXT/R391样整合性接合元件(ICE),即ICEVchInd5,其具有10 kb的缺失,并定位于7PET-AFR13谱系。系统发育分析表明,这些菌株与坦桑尼亚、科摩罗和马约特岛报告的其他高度耐药AFR13菌株关系密切。
霍乱分离株中多重耐药的高流行率强调了持续监测以监测MDR霍乱弧菌O1菌株演变的必要性,并呼吁考虑采用替代管理和预防措施,包括口服霍乱疫苗以及长期改善水、环境卫生和个人卫生(WASH)基础设施及实践。