Lambisia Arnold W, Mwita Morobe John, Moraa Edidah, Mwarumba Salim, K N Korir Fredrick, Seif Athman Raila, Kiptui Rebecca, Mbee Micheal, Mugo Nelly, Amoth Patrick, Muange Penny, J Houldcroft Charlotte, Barasa Edwine, Mwangangi Joseph, Githinji George, C Holmes Edward, Isabella Ochola-Oyier Lynette, N Agoti Charles
Kenya Medical Research Institute, KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Lighthouse for Christ Eye Centre, Mombasa, Kenya.
Wellcome Open Res. 2025 Mar 31;10:28. doi: 10.12688/wellcomeopenres.23522.2. eCollection 2025.
In early 2024, a surge in acute hemorrhagic conjunctivitis (AHC), also referred as "red eye" disease, was observed in coastal Kenya, prompting the Ministry of Health to issue an outbreak alert. Herein, we investigated the etiology of this outbreak.
Ocular swabs were obtained from 13 individuals presenting with AHC at a Mombasa clinic in early February 2024. Ten of these were analyzed using bacterial cultures, and all 13 using a pan-adenovirus quantitative PCR (qPCR) and metagenomic sequencing. Potential viral etiology was confirmed by a specific qPCR, amplicon sequencing and phylogenetic analysis.
Bacterial cultures yielded no growth except in three samples where non-pathogenic bacteria were detected. All 13 samples were adenovirus qPCR negative. Metagenomic sequencing detected coxsackievirus A24 variant (CA24v) in three of the 13 samples. CV-A24v detections were confirmed by both CV-A24v specific qPCR and amplicon sequencing of an approximately 450 nucleotide long VP4/2 junction genomic region. Phylogenetic analysis of the VP4/2 sequences showed that they were closely related to CV-A24v genotype IV.
The AHC epidemic in coastal Kenya in early 2024 was likely caused by CA24v. Metagenomic sequencing is a powerful tool for identifying potential causative agents of new disease outbreaks.
2024年初,在肯尼亚沿海地区观察到急性出血性结膜炎(AHC)病例激增,AHC也被称为“红眼病”,这促使肯尼亚卫生部发布了疫情警报。在此,我们对此次疫情的病因进行了调查。
2024年2月初,从蒙巴萨一家诊所的13名急性出血性结膜炎患者处采集眼拭子。其中10份样本进行细菌培养分析,所有13份样本均采用泛腺病毒定量PCR(qPCR)和宏基因组测序。通过特异性qPCR、扩增子测序和系统发育分析确定潜在的病毒病因。
除在3份样本中检测到非致病性细菌外,细菌培养均无生长。所有13份样本的腺病毒qPCR检测均为阴性。宏基因组测序在13份样本中的3份中检测到柯萨奇病毒A24变种(CV-A24v)。通过CV-A24v特异性qPCR和对约450个核苷酸长的VP4/2连接基因组区域的扩增子测序,证实了CV-A24v的检测结果。对VP4/2序列的系统发育分析表明,它们与CV-A24v基因型IV密切相关。
2024年初肯尼亚沿海地区的急性出血性结膜炎疫情可能由CV-A24v引起。宏基因组测序是识别新疾病暴发潜在病原体的有力工具。