Crampton J M, Hill S M
Wolfson Unit of Molecular Genetics, Liverpool School of Tropical Medicine, U.K.
Parassitologia. 1993 Jul;35 Suppl:31-4.
The correct identification of the mosquito vectors of malaria is essential to determine the vectorial significance of the different species within species complexes and to optimise vector control programmes. A number of methods are available including cytogenetic analysis, isoenzyme characterisation, and mating incompatibility. We describe here the development of a simplified DNA probe methodology for the identification of malaria vector specimens, with particular emphasis on the identification of mosquitoes of the Anopheles gambiae complex, which includes the most important vectors of malaria in Africa. The method incorporates the use of a simple 'squash-blot' sample preparation, synthetic oligonucleotide probes, non-radioactive labelling and detection systems, cheap and stable reagents, and all processes are carried out at room temperature without the need for equipment. Identification of up to 300 specimens (larvae, pupae or adults) per day is possible by a single worker using this simple technique and costs $0.02-$0.04 per specimen.
正确识别疟疾的蚊媒对于确定物种复合体中不同物种的媒介重要性以及优化媒介控制计划至关重要。有多种方法可供使用,包括细胞遗传学分析、同工酶特征鉴定和交配不相容性。我们在此描述一种用于鉴定疟疾媒介标本的简化DNA探针方法的开发,特别强调冈比亚按蚊复合体蚊子的鉴定,该复合体包括非洲最重要的疟疾媒介。该方法采用简单的“压片-印迹”样品制备、合成寡核苷酸探针、非放射性标记和检测系统、廉价且稳定的试剂,并且所有过程均在室温下进行,无需设备。一名工作人员使用这种简单技术每天可鉴定多达300个标本(幼虫、蛹或成虫),每个标本成本为0.02-0.04美元。