Mulamba Charles, Irving Helen, Riveron Jacob M, Mukwaya Louis G, Birungi Josephine, Wondji Charles S
Vector Biology Department, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool L3 5QA, UK.
Parasit Vectors. 2014 Feb 17;7:71. doi: 10.1186/1756-3305-7-71.
Although the An. funestus group conceals one of the major malaria vectors in Africa, little is known about the dynamics of members of this group across the continent. Here, we investigated the species composition, infection rate and susceptibility to insecticides of this species group in Uganda.
Indoor resting blood-fed Anopheles adult female mosquitoes were collected from 3 districts in Uganda. Mosquitoes morphologically belonging to the An. funestus group were identified to species by PCR. The sporozoite infection rates were determined by TaqMan and a nested PCR. Susceptibility to major insecticides was assessed using WHO bioassays. The potential role of four candidate resistance genes was assessed using qRT-PCR.
An. funestus s.s. and An. parensis, were the only members of the An. funestus group identified. Both species were sympatric in Masindi (North-West), whereas only An. parensis was present in Mityana (Central) and Ntungamo (South-West). The Plasmodium falciparum infection detected in An. parensis (4.2%) by TaqMan could not be confirmed by nested PCR, whereas the 5.3% infection in An. funestus s.s. was confirmed. An. parensis was susceptible to most insecticides, however, a moderate resistance was observed against deltamethrin and DDT. In the sympatric population of Masindi, resistance was observed to pyrethroids (permethrin and deltamethrin) and DDT, but all the resistant mosquitoes belonged to An. funestus s.s. No significant over-expression was observed for the four P450 candidate genes CYP6M7, CYP9K1, CYP6P9 and CYP6AA4 between deltamethrin resistant and control An. parensis. However, when compared with the susceptible FANG An. funestus s.s strain, the CYP9K1 is significantly over-expressed in An. parensis (15-fold change; P < 0.001), suggesting it could play a role in the deltamethrin resistance.
The contrasting infection rates and insecticide susceptibility profiles of both species highlights the importance of accurate species identification for successful vector control programs.
虽然冈比亚按蚊种群隐藏着非洲主要的疟疾传播媒介之一,但对该种群成员在非洲大陆的动态了解甚少。在此,我们调查了乌干达该蚊种组的物种组成、感染率及对杀虫剂的敏感性。
从乌干达3个地区收集室内吸血后静止的成年雌性按蚊。通过聚合酶链反应(PCR)将形态上属于冈比亚按蚊种群的蚊子鉴定到物种。使用TaqMan和巢式PCR测定子孢子感染率。使用世界卫生组织(WHO)生物测定法评估对主要杀虫剂的敏感性。使用定量逆转录聚合酶链反应(qRT-PCR)评估4个候选抗性基因的潜在作用。
冈比亚按蚊指名亚种和帕氏按蚊是鉴定出的冈比亚按蚊种群仅有的成员。这两个物种在马辛迪(西北)同域分布,而在米蒂亚纳(中部)和恩通加莫(西南)仅存在帕氏按蚊。通过TaqMan在帕氏按蚊中检测到的恶性疟原虫感染率(4.2%)无法通过巢式PCR得到证实,而冈比亚按蚊指名亚种5.3%的感染率得到了证实。帕氏按蚊对大多数杀虫剂敏感,然而,观察到对溴氰菊酯和滴滴涕有中度抗性。在马辛迪的同域种群中,观察到对拟除虫菊酯类(氯菊酯和溴氰菊酯)和滴滴涕有抗性,但所有抗性蚊子都属于冈比亚按蚊指名亚种。在溴氰菊酯抗性和对照帕氏按蚊之间,4个细胞色素P450候选基因CYP6M7、CYP9K1、CYP6P9和CYP6AA4未观察到显著的过表达。然而,与敏感的FANG冈比亚按蚊指名亚种品系相比,CYP9K1在帕氏按蚊中显著过表达(变化15倍;P<0.001),表明它可能在溴氰菊酯抗性中起作用。
两个物种截然不同的感染率和杀虫剂敏感性概况凸显了准确的物种鉴定对成功的病媒控制项目的重要性。