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利用液滴数字 PCR 进行疟蚊现场监测的超灵敏疟疾检测系统。

Ultrasensitive malaria detection system for Anopheles mosquito field surveillance using droplet digital PCR.

机构信息

Department of Parasitology, National Institute of Infectious Diseases, Toyama, Shinjuku-ku, Tokyo, Japan.

Department of Legal Medicine, Graduate School of Medical and Dental Science, Niigata University, Asahimachi, Chuo-ku, Niigata, Japan.

出版信息

Parasitol Int. 2024 Aug;101:102891. doi: 10.1016/j.parint.2024.102891. Epub 2024 Mar 26.

DOI:10.1016/j.parint.2024.102891
PMID:38537686
Abstract

Malaria remains a significant global public health concern, with a recent increase in the number of zoonotic malaria cases in Southeast Asian countries. However, limited reports on the vector for zoonotic malaria exist owing to difficulties in detecting parasite DNA in Anopheles mosquito vectors. Herein, we demonstrate for the first time that several Anopheles mosquitoes contain simian malaria parasite DNA using droplet digital PCR (ddPCR), a highly sensitive PCR method. An entomological survey was conducted to identify simian malaria vector species at Phra Phothisat Temple (PPT), central Thailand, recognized for a high prevalence of simian malaria in wild cynomolgus macaques. A total of 152 mosquitoes from six anopheline species were collected and first analyzed by a standard 18S rRNA nested-PCR analysis for malaria parasite which yielded negative results in all collected mosquitoes. Later, ddPCR was used and could detect simian malaria parasite DNA, i.e. Plasmodium cynomolgi, in 25 collected mosquitoes. And this is the first report of simian malaria parasite DNA detection in Anopheles sawadwongporni. This finding proves that ddPCR is a powerful tool for detecting simian malarial parasite DNA in Anopheles mosquitoes and can expand our understanding of the zoonotic potential of malaria transmission between monkeys and humans.

摘要

疟疾仍然是一个重大的全球公共卫生关注问题,最近东南亚国家的动物源性疟疾病例数量有所增加。然而,由于难以在按蚊媒介中检测寄生虫 DNA,有关动物源性疟疾媒介的报告有限。在此,我们首次使用高灵敏度的 PCR 方法——数字液滴 PCR(ddPCR)证明,几种按蚊中含有灵长类疟原虫 DNA。在泰国中部的 Phra Phothisat 寺(PPT)进行了一项昆虫学调查,以确定灵长类疟疾病媒的种类,该寺的野生食蟹猕猴中灵长类疟疾的患病率很高。从六个按蚊种共采集了 152 只蚊子,首先通过标准的 18S rRNA 巢式 PCR 分析进行疟疾寄生虫检测,所有采集的蚊子均呈阴性结果。后来,使用 ddPCR 可以检测到 25 只采集的蚊子中的灵长类疟原虫 DNA,即食蟹猴疟原虫。这是首次在按蚊 sawadwongporni 中检测到灵长类疟原虫 DNA 的报告。这一发现证明,ddPCR 是检测按蚊中灵长类疟原虫 DNA 的有力工具,可以扩展我们对猴与人之间疟疾传播的人畜共患病潜力的认识。

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