International Centre of Insect Physiology and Ecology (Icipe), P.O. Box 30772-00100, Nairobi, Kenya.
University of Pretoria Institute for Sustainable Malaria Control, School of Health Systems and Public Health, University of Pretoria, Pretoria, South Africa.
Malar J. 2023 Mar 16;22(1):95. doi: 10.1186/s12936-023-04489-3.
The primary malaria vector-control interventions, indoor residual spraying and long-lasting insecticidal nets, are effective against indoor biting and resting mosquito species. Consequently, outdoor biting and resting malaria vectors might elude the primary interventions and sustain malaria transmission. Varied vector biting and resting behaviour calls for robust entomological surveillance. This study investigated the bionomics of malaria vectors in rural south-east Zambia, focusing on species composition, their resting and host-seeking behaviour and sporozoite infection rates.
The study was conducted in Nyimba District, Zambia. Randomly selected households served as sentinel houses for monthly collection of mosquitoes indoors using CDC-light traps (CDC-LTs) and pyrethrum spray catches (PSC), and outdoors using only CDC-LTs for 12 months. Mosquitoes were identified using morphological taxonomic keys. Specimens belonging to the Anopheles gambiae complex and Anopheles funestus group were further identified using molecular techniques. Plasmodium falciparum sporozoite infection was determined using sandwich enzyme-linked immunosorbent assays.
From 304 indoor and 257 outdoor light trap-nights and 420 resting collection, 1409 female Anopheles species mosquitoes were collected and identified morphologically; An. funestus (n = 613; 43.5%), An. gambiae sensu lato (s.l.)(n = 293; 20.8%), Anopheles pretoriensis (n = 282; 20.0%), Anopheles maculipalpis (n = 130; 9.2%), Anopheles rufipes (n = 55; 3.9%), Anopheles coustani s.l. (n = 33; 2.3%), and Anopheles squamosus (n = 3, 0.2%). Anopheles funestus sensu stricto (s.s.) (n = 144; 91.1%) and Anopheles arabiensis (n = 77; 77.0%) were the dominant species within the An. funestus group and An. gambiae complex, respectively. Overall, outdoor CDC-LTs captured more Anopheles mosquitoes (mean = 2.25, 95% CI 1.22-3,28) than indoor CDC-LTs (mean = 2.13, 95% CI 1.54-2.73). Fewer resting mosquitoes were collected with PSC (mean = 0.44, 95% CI 0.24-0.63). Sporozoite infectivity rates for An. funestus, An. arabiensis and An. rufipes were 2.5%, 0.57% and 9.1%, respectively. Indoor entomological inoculation rates (EIRs) for An. funestus s.s, An. arabiensis and An. rufipes were estimated at 4.44, 1.15 and 1.20 infectious bites/person/year respectively. Outdoor EIRs for An. funestus s.s. and An. rufipes at 7.19 and 4.31 infectious bites/person/year, respectively.
The findings of this study suggest that An. rufipes may play an important role in malaria transmission alongside An. funestus s.s. and An. arabiensis in the study location.
主要的疟疾媒介控制干预措施,包括室内滞留喷洒和长效杀虫剂蚊帐,对室内叮咬和休息的蚊子种类有效。因此,户外叮咬和休息的疟疾媒介可能逃避主要干预措施,并维持疟疾传播。不同的媒介叮咬和休息行为需要强有力的昆虫学监测。本研究调查了赞比亚东南部农村地区疟疾媒介的生物学特性,重点研究了物种组成、它们的休息和宿主寻找行为以及孢子虫感染率。
该研究在赞比亚恩亚姆巴区进行。随机选择的家庭作为每月收集室内蚊子的哨点家庭,使用 CDC 诱蚊灯(CDC-LTs)和除虫菊酯喷雾捕获(PSC),以及仅使用 CDC-LTs 进行 12 个月的户外蚊子收集。使用形态分类学钥匙对蚊子进行识别。属于冈比亚按蚊复合体和致倦库蚊组的标本进一步使用分子技术进行鉴定。使用夹心酶联免疫吸附试验确定恶性疟原虫孢子虫感染情况。
从 304 个室内和 257 个户外灯光诱捕夜和 420 个休息采集中,共收集和鉴定了 1409 只雌性按蚊种蚊子;致倦库蚊(n=613;43.5%)、冈比亚按蚊复合体(n=293;20.8%)、普氏按蚊(n=282;20.0%)、嗜人按蚊(n=130;9.2%)、库蚊(n=55;3.9%)、刺扰伊蚊(n=33;2.3%)和塞内加尔按蚊(n=3;0.2%)。致倦库蚊 s.s.(n=144;91.1%)和阿巴新蚊(n=77;77.0%)分别是致倦库蚊组和冈比亚按蚊复合体中的优势种。总体而言,户外 CDC-LTs 捕获的按蚊数量(均值=2.25,95%CI 1.22-3,28)多于室内 CDC-LTs(均值=2.13,95%CI 1.54-2.73)。用 PSC 收集的休息蚊子较少(均值=0.44,95%CI 0.24-0.63)。致倦库蚊、阿巴新蚊和鲁菲蚊的孢子虫感染率分别为 2.5%、0.57%和 9.1%。致倦库蚊 s.s.、阿巴新蚊和鲁菲蚊的室内昆虫学感染率(EIR)估计分别为 4.44、1.15 和 1.20 个感染性叮咬/人/年。致倦库蚊 s.s.和鲁菲蚊的户外 EIR 分别为 7.19 和 4.31 个感染性叮咬/人/年。
本研究结果表明,在研究地点,鲁菲蚊可能与致倦库蚊 s.s.和阿巴新蚊一起,在疟疾传播中发挥重要作用。