Koekemoer L L, Misiani E A, Hunt R H, Kent R J, Norris D E, Coetzee M
Vector Control Reference Unit, National Institute for Communicable Diseases, NHLS, Private bag X 4, Sandringham, 2131, South Africa.
Bull Entomol Res. 2009 Feb;99(1):41-9. doi: 10.1017/S0007485308006123. Epub 2008 Aug 21.
House-resting Anopheles mosquitoes are targeted for vector control interventions; however, without proper species identification, the importance of these Anopheles to malaria transmission is unknown. Anopheles longipalpis, a non-vector species, has been found in significant numbers resting indoors in houses in southern Zambia, potentially impacting on the utilization of scarce resources for vector control. The identification of An. longipalpis is currently based on classical morphology using minor characteristics in the adult stage and major ones in the larval stage. The close similarity to the major malaria vector An. funestus led to investigations into the development of a molecular assay for identification of An. longipalpis. Molecular analysis of An. longipalpis from South Africa and Zambia revealed marked differences in size and nucleotide sequence in the second internal transcribed spacer (ITS2) region of ribosomal DNA between these two populations, leading to the conclusion that more than one species was being analysed. Phylogenetic analysis showed the Zambian samples aligned with An. funestus, An. vaneedeni and An. parensis, whereas the South African sample aligned with An. leesoni, a species that is considered to be more closely related to the Asian An. minimus subgroup than to the African An. funestus subgroup. Species-specific primers were designed to be used in a multiplex PCR assay to distinguish between these two cryptic species and members of the An. funestus subgroup for which there is already a multiplex PCR assay.
室内栖息的按蚊是病媒控制干预措施的目标;然而,如果没有正确的物种鉴定,这些按蚊对疟疾传播的重要性就不得而知。长须按蚊是一种非病媒物种,在赞比亚南部的房屋内大量被发现栖息于室内,这可能会影响到对稀缺的病媒控制资源的利用。目前,长须按蚊的鉴定是基于经典形态学,利用成虫阶段的次要特征和幼虫阶段的主要特征。它与主要疟疾媒介嗜人按蚊非常相似,这促使人们对开发一种用于鉴定长须按蚊的分子检测方法进行研究。对来自南非和赞比亚的长须按蚊进行的分子分析显示,这两个种群的核糖体DNA的第二内部转录间隔区(ITS2)在大小和核苷酸序列上存在显著差异,从而得出结论,所分析的不止一个物种。系统发育分析表明,赞比亚的样本与嗜人按蚊、瓦内登按蚊和帕伦西斯按蚊聚在一起,而南非的样本与利氏按蚊聚在一起,利氏按蚊被认为与亚洲的微小按蚊亚组的关系比与非洲的嗜人按蚊亚组的关系更密切。设计了物种特异性引物,用于多重PCR检测,以区分这两个隐存物种以及嗜人按蚊亚组的成员,对于嗜人按蚊亚组已经有了一种多重PCR检测方法。