Barrier screens: a method to sample blood-fed and host-seeking exophilic mosquitoes
© Burkot et al.; licensee BioMed Central Ltd. 2013
Received: 5 December 2012
Accepted: 31 January 2013
Published: 5 February 2013
Determining the proportion of blood meals on humans by outdoor-feeding and resting mosquitoes is challenging. This is largely due to the difficulty of finding an adequate and unbiased sample of resting, engorged mosquitoes to enable the identification of host blood meal sources. This is particularly difficult in the south-west Pacific countries of Indonesia, the Solomon Islands and Papua New Guinea where thick vegetation constitutes the primary resting sites for the exophilic mosquitoes that are the primary malaria and filariasis vectors.
Barrier screens of shade-cloth netting attached to bamboo poles were constructed between villages and likely areas where mosquitoes might seek blood meals or rest. Flying mosquitoes, obstructed by the barrier screens, would temporarily stop and could then be captured by aspiration at hourly intervals throughout the night.
In the three countries where this method was evaluated, blood-fed females of Anopheles farauti, Anopheles bancroftii, Anopheles longirostris, Anopheles sundaicus, Anopheles vagus, Anopheles kochi, Anopheles annularis, Anopheles tessellatus, Culex vishnui, Culex quinquefasciatus and Mansonia spp were collected while resting on the barrier screens. In addition, female Anopheles punctulatus and Armigeres spp as well as male An. farauti, Cx. vishnui, Cx. quinquefasciatus and Aedes species were similarly captured.
Building barrier screens as temporary resting sites in areas where mosquitoes were likely to fly was an extremely time-effective method for collecting an unbiased representative sample of engorged mosquitoes for determining the human blood index.
The importance of a mosquito species as a vector of human disease is determined by multiple parameters including the human blood index (HBI). The HBI is the proportion of blood-fed, resting mosquitoes that contain human blood in their stomachs compared to the total number of mosquitoes which feed on any host species. Accurate estimates of the HBI for a species depends on collecting an unbiased sample of resting, blood-fed mosquitoes of that species. For highly endophilic species that rest for prolonged periods inside houses, it is relatively easy and straightforward to collect large numbers of engorged mosquitoes inside houses. However, HBI estimates based solely on collections of indoor-resting mosquitoes, even for endophilic mosquitoes, are biased towards human-fed mosquitoes, as such collections ignore the portion of the population that will have fed outdoors and be more likely to have fed on other available host species. Accurate HBI estimates require unbiased samples of the entire mosquito population that has recently fed (i.e., those that feed and rest inside houses as well as those that feed and rest outside).
Exophilic mosquito species are common throughout the malaria-endemic world[3–5]. For exophilic vectors, capturing an adequate and representative sample of blood-fed specimens is even more challenging as they tend to be dispersed over large areas and utilize a large number of potential resting sites. The challenge is magnified when the number of adult vectors is limited, as finding engorged resting mosquitoes outdoors requires considerable time and effort to acquire even a small sample of blood-fed mosquitoes. To enhance the prospects of finding blood-fed mosquitoes outside houses, artificial resting sites, such as clay pots and resting boxes may be provided or pits dug to attract engorged females. However, artificial resting sites may harbour relatively few blood-fed, resting mosquitoes since the artificial sites provided must compete with the greater number of available natural resting sites[7, 8].
In response to biases associated with sampling blood-fed, resting mosquitoes, a novel sampling tool was designed based on a hypothesis that engorged mosquitoes might be intercepted and captured when transiting between blood feeding and resting sites. This hypothesis was based on observations by Giglioli and Gillies and Wilkes about the flight patterns of anophelines. Giglioli reported that Anopheles melas entered villages in corridors and at altitudes less than five feet (1.53 m) and that their flight could be diverted by fences. Gillies and Wilkes confirmed that most mosquitoes fly at low altitudes when crossing open terrain although anophelines will modify the height of their flight when they encounter obstacles. It followed that obstacles could be constructed, not to divert flying mosquitoes, but to impede their flight sufficiently to allow capture. For blood-laden mosquitoes, any structure encountered between the host and sites for resting might be sufficient to provide a temporary rest stop for the mosquito. Barrier screens constructed of durable mesh material (shade cloth) are inexpensive, easily constructed, and easily searched for resting mosquitoes from which they can be collected. As an artificially constructed resting site or flight barrier, a screen provides an additional significant advantage over a solid structure in that the mesh is permeable and would permit mosquitoes to follow both visual and olfactory cues to sources of blood meals, oviposition and resting sites. Upon encountering the barrier screen, mosquitoes might then stop, thereby facilitating their discovery and capture. Placement of a barrier screen between likely oviposition/resting sites and potential blood meal sources would enable the capture of both blood-fed mosquitoes seeking a resting site to develop their eggs, as well as recently emerged mosquitoes that have completed egg-laying and/or are searching for a blood meal. Comparisons of blood meal, parity and gravid status of mosquitoes captured on each side of such a screen would provide insight into directional and temporal behaviour patterns.
This initial evaluation of barrier screens as a novel sampling tool to collect exophilic mosquitoes was conducted in three countries in the southwest Pacific (Indonesia, the Solomon Islands and Papua New Guinea). The current paper presents the results of pilot studies to optimise the use and placement of barrier screens and to describe the physiological state of the mosquitoes captured. In this region the primary malaria and lymphatic filariasis vectors are exophilic, including An. sundaicus, An. vagus, An. kochi, An.s annularis, An. tessellatus and the members of the An. punctulatus group[3, 11, 12]. Previous HBI estimates for the An. punctulatus group required years of effort to collect a sufficient number of blood-fed, resting specimens for blood source identification. This was primarily due to the difficulty of finding mosquitoes resting amongst the thick vegetation that serve as the usual resting sites for these mosquitoes[6, 13]. Thus, only a limited number of studies have documented the host blood meal sources in the members of this group in the Solomon Islands[14–16] and Papua New Guinea[13, 16–22], the most recent of which was published 16 years ago.
The experiments involved sampling mosquitoes from the barrier screens or by using human landing catch (HLC) in all three sites. All mosquito catches were conducted between 1800 h and 0600 h, and the catches for each hourly interval were stored in separate collection cups. Regarding sampling resting mosquitoes from the barrier screens, this process was conducted by manually searching the barrier screen and collecting any resting mosquitoes with a mouth aspirator (Figure1C and F). Each side of the barrier screen was searched for approximately 20mins each hour. The catches for each side of the barrier screen were stored in separate collection cups. To collect host-seeking mosquitoes HLC were conducted outdoors. This involved volunteers sitting with their legs and feet exposed and catching mosquitoes with a mouth aspirator that were attracted and seeking a blood meal; HLC collections were also made hourly from 1800 h to 0600 h. All mosquitoes were morphologically identified to sex and species then visually classified as being unfed, partially fed, fully fed or gravid. The morphological keys used to identify the mosquito specimens were O'Connor and Soepanto in Indonesia, Belkin in the Solomon Islands, and Lee in Papua New Guinea. Species identifications were confirmed by molecular analyses (see Laboratory analyses below). The collection details for each mosquito were recorded, including trap type and hour of capture.
A 32 m long barrier screen of polyvinylchloride-coated polyester shade cloth was constructed (Figure1A,B) and evaluated in Sukaraja village in the Lampung District (Rajabasa subdistrict) of southern Sumatra in western Indonesia between 25 August and 1 September 2010. Mosquitoes were collected from the barrier screen over eight nights. The location of mosquitoes was recorded for each mosquito (e.g., <0.5 m; 0.5 to <1.0 m; >1 m above the ground). Domestic animals that might serve as potential host blood meal sources were recorded. After the mosquito processing was complete, unfed female anophelines were dissected for parity status. Additionally, HLC was performed on the same nights as the barrier screen collections at 6 outdoor stations.
Concurrent with barrier screen collections, HLC were conducted from 1800 h to 0600 h at 6 outdoor stations. Mosquitoes were held in individual containers by hour of collection and numbers recorded.
Papua New Guinea
A 40 m barrier screen was similarly constructed between houses and the surrounding vegetation in Mirap village, Madang Province (Figure2B). The barrier screen was constructed in two 20-m segments for ease of set-up and to allow a 1 m gap for access to the surrounding bush along pre-existing trails. One pair of collectors checked the barrier screen for resting mosquitoes for 10 nights in June 2012. The mosquitoes were captured and stored by hour of collection and side of the barrier screen. Additionally, HLC was performed on the same nights as the barrier screen collections at 2 outdoor stations. Locations of screens and collectors were rotated throughout the village every two nights.
Mosquito species identification of the An. punctulatus group was confirmed by PCR[26, 27]. Sequencing of the ITS2 region was also used to identify species in Indonesia. Host blood meal sources (human, pig, goat, and dog) for Anopheles mosquitoes were identified by PCR using slight modifications of the Kent and Norris method. The PCR reactions were made up of 0.4 μl of each primer, 3.0 mM MgCl2, 1.0 mM dNTPs and 0.5 units of Taq polymerase and each reaction in a final volume of 25 μl.
For the Solomon Islands, statistical differences in the proportion of blood-fed to unfed mosquitoes resting on each side of the barrier screen were compared using a generalized linear model (GLM) with a binomial distribution and a categorical explanatory variable for screen side. The basis of the analysis was a binary dataset constructed with the total number of fed and unfed An. farauti collected on each side of the barrier screen by date. This analysis was conducted using R statistical software (ver.2.14.2).
Ethical approval for the study was obtained from review boards relevant to each study site. For Indonesia approval was granted by the National Institute of Health, Research and Development, Indonesia. For the Solomon Islands, approval was granted by the National Health Research & Ethics Committee (02-05-2011) as well as the James Cook University Human Research Ethics Committee (H4122). For Papua New Guinea, approval was granted by the PNG Institute of Medical Research Institutional Review Board (1116) and the PNG Medical Research Advisory Board (11.21). When the study commenced, permission was obtained from each person who volunteered to conduct HLC. After consenting, each volunteer signed an informed consent form stating their willingness to participate in the study.
Tabular comparison of the density of host-seeking (HLC) and resting mosquitoes (barrier screen) caught in the three study sites: Indonesia, the Solomon Islands and Papua New Guinea
HLC b/p/n (total)
Mean/10 m barrier screen (total)
An. farauti s.s.
PAPUA NEW GUINEA
An. farauti s.s.
When capturing mosquitoes on the barrier screen, it was observed that most (92%) were captured resting <1 m from the ground, and of these mosquitoes 74% were within 50 cm of the ground. All anophelines were collected <1 m from the ground with 73% within 50 cm of the ground. Of the anophelines resting on the barrier screen, 25.5% (11/43) were blood fed, whereas only 6.5% (64/992) and 5.6% (22/395) of Cx. vishnui and Cx. quinquefasciatus were blood fed. Gravid females represented 16.3% (7/43), 2.1% (21/992) and 8.9% (35/395) of anophelines, Cx. vishnui and Cx. quinquefasciatus collected on the barrier screen, respectively.
Goats, chickens, humans, dogs and cats were observed in the vicinity of the barrier screen. Only a small portion of the engorged females were tested for blood meal with PCR. All tested An. sundiacus contained dog blood (n= 2) while all tested An. vagus had fed on goats (n= 3). For Cx. quinquefasciatus, 25%, 50% and 25% of identified blood meals were on goats, dogs and humans, respectively (n= 8 successful PCR reactions where the blood meal host was identified, 5 additional blood meal tests could not be identified). For Cx. vishnui, 59%, 20.5% and 20.5% of identified blood meals were on goats, dogs and humans, respectively (n= 49 successful PCR reactions, 3 could not be identified). The parity rate of the Anopheles spp was high at 86% (24/28) and also for the Culex spp at 71% (89/125).
The percentage of blood-fed female An. farauti captured resting on the barrier screen was 62% (n= 73), with 51% (n= 60) of the total mosquitoes being fully engorged. There was a tendency for more blood-fed An. farauti to be captured on the village side of the barrier screen (65%) compared with the breeding-site side (47%), but this difference was not statistically significant (β=0.632, SE=0.517, p=0.221). Only one gravid An. farauti was collected on the barrier screen. The most abundant potential domestic host blood meal sources present in the village in the vicinity of the barrier screen were humans (n= 64), pigs (n= 11) and dogs, (n= 4). The majority, 97% (n= 68), of blood-fed An. farauti contained human blood including 6% (n= 4) having mixed feeds on humans and pigs. Only 3% (n= 2) of An. farauti had fed solely on pigs.
Papua New Guinea
A total of 449 female mosquitoes were collected from the barrier screen with 50% from the village side. Across all species, of those collected from the village side, 54% were blood fed (n= 144) whereas only 34% were blood fed (n= 63) on the opposite side (furthest from the village). Anopheles farauti was the predominant species, comprising 69% of the catch (n= 311). In addition, Anopheles bancroftii (n= 30), Anopheles longirostris (n= 2), An. punctulatus (n= 3), Aedes spp (n= 54), Culex spp (n= 42), Mansonia spp (n= 2) and Armigeres spp (n= 5) were collected (Table1).
The mean number of An. farauti collected per 10 m barrier screen per night was 7.8 (Table1). By abdominal status these An. farauti were: 59.2% blood fed (n= 184), 40.2% unfed (n= 125) and 0.6% gravid (n= 2) (Table1). The mean nightly, human landing rate for An. farauti during the same period was 20.6/p/n (n= 412) with the major landing collection peak occurring between 1900 h and 2000 h and a secondary peak between 2300 h and midnight (Figure3C). Peak collection time for resting mosquitoes on the barrier screen was between midnight and 0100 h (Figure3D). Anopheles bancroftii, An. longirostris and An. punctulatus were not captured in landing catches during the nights when collections on the barrier screens were undertaken.
The hypothesis that a barrier screen trap can detain mosquitoes sufficiently to allow their collection was validated in all three countries where trialled. The barrier screen was specifically designed for collecting an unbiased sample of outdoor resting mosquitoes to provide specimens for calculating the human blood index. This novel tool could directly replace unproductive and/or biased searches for mosquitoes resting outdoors in vegetation, indoors or in outdoor shelters. The use of barrier screens was more time-effective as a means of collecting resting, blood-engorged members of the An. punctulatus group, when population densities are low, compared to searching natural resting sites. Previous studies in Mebat village, PNG, in which the bush was searched for resting anophelines, found 27 engorged members of the An. punctulatus group during 128 days of searching when the mean nightly human landing rate was 8/p/n. In the same study, only 12 engorged anophelines were collected in Hudini village during 128 search days despite a mean nightly human landing rate of 85/p/n. The use of a barrier screen as a sampling tool for resting mosquitoes was more time effective: in the Solomon Islands over a 14-day period, 70 blood-fed An. farauti were collected even though the human landing rate during this period was only 16.5/p/n; in PNG, 184 engorged An. farauti were captured on the barrier screen in a 10-day period when the human landing catch averaged 20.6/p/n.
Positioning the barrier screen between the hosts and oviposition/resting sites enabled samples of blood-fed mosquitoes to be collected to estimate the HBI as well as to sample mosquitoes questing for blood meals. In Indonesia analyses of the limited numbers of blood meals in anophelines confirmed previous descriptions of An. vagus and An. sundaicus as zoophilic as human blood was not identified in any anopheline collected on the barrier screen. Although only a very limited number of blood-fed anophelines were collected in Indonesia, the results were sufficiently encouraging to continue the experiments in the Solomon Islands and PNG. Blood meal analyses were conducted on An. farauti collected in the Solomon Islands, and at this study site the HBI was very high. Previous literature indicated that An. farauti blood-feeding habits vary from zoophilic to anthropophilic[13, 16–22, 29]. The high HBI recorded in this study may be a function of the relative abundance of humans compared to domestic animals (human, pig, and dog populations in the vicinity of the barrier screen numbered 63, 11 and 4, respectively) and/or an innate preference for feeding on humans.
The density of An. farauti captured on the barrier screen paralleled the results of human landing catches with most resting An. farauti captured between 1800 h and 2100 h in the Solomon Islands and before midnight in PNG. These results, coupled with anecdotal observations made during the course of the experiments indicate that the barrier screen does indeed act as a barrier which temporarily detains mosquitoes, opposed to being an artificial resting site. Notably, greater numbers of resting An. farauti captured on the village side of the barrier screen may reflect the willingness of blood-fed An. farauti to rest longer on the barrier screen than mosquitoes questing for blood. Such questing mosquitoes would be more likely to encounter the barrier screen on the oviposition site side but would be expected to fly over or around the barrier screen to continue following cues to the locations of potential blood meals in the village. The success of the barrier screen as a tool for collecting blood-fed mosquitoes provides the baseline for designing detailed experiments to systematically observe individual mosquito resting behaviour as well as to study the population-level feeding behaviour. Of note here that is the observation that most mosquitoes, and particularly anophelines, rest near the ground is consistent with both the observations in The Gambia of Giglioli for Anopheles melas and Damar et al. in Indonesia who reported that Anopheles aconitus, Anopheles subpictus and Anopheles indefinitus rest indoors at a median height of 38 cm above the floor.
Although the experiments were designed to sample female anophelines, the barrier screen also useful for sampling culicine species, with >1,500 specimens of two Culex species being captured during seven nights in Indonesia. In addition, a small number of male Anopheles and Aedes spp were also collected on the barrier screens. Interestingly, most male Aedes were captured on the barrier screen between 0200 h and 0500 h. With further refinements, screens or similar barriers may provide a simple method for sampling the male mosquito population, an area in which far too little is presently known.
The potential use of novel barrier screens as a method for sampling blood-fed mosquitoes seeking resting sites, female mosquitoes questing for blood meals and male mosquitoes, was evaluated in three countries that are well known for their exophilic and exophagic anophelines. Importantly, the technique is largely free of the biases associated with solely collecting mosquitoes resting inside households and is much more effective than searching for outdoor-resting mosquitoes in the natural vegetation. The approach was validated as a means of sampling engorged females for HBI determination and shows promise as an approach to sampling host-seeking female mosquitoes as well as male mosquito populations. It is proposed that barrier screens could replace direct searching of vegetation for collecting outdoor-resting anophelines in many locations.
Barrier screens placed to intercept mosquitoes between blood feeding, resting and ovipositing provide a novel way to sample mosquitoes. These barrier screens are easy and economical to construct and are effective in capturing Anopheles, Culex and Aedes spp including both males and females. Manipulating the locations where barrier screens are placed provides opportunities for capturing mosquitoes to better understand when and where mosquitoes move between host-seeking, egg laying and resting activities.
This work was supported by Grant No. 45114 from the Bill and Melinda Gates Foundation to the Malaria Transmission Consortium for the work in Indonesia and the Solomon Islands. In addition, the support of the National Institutes of Health for the International Center of Excellence in Malaria Research in the Pacific (subawards to James Cook University and the Papua New Guinea Institute of Medical Research; award number SU19AI08986-03) is gratefully acknowledged. Technical assistance when conducting the field collections was provided by Allen Apairamo and John Lodo of the Vector Borne Disease Control Programme, Solomon Islands and Gussy Koimbu and Michelle Katusele of Papua New Guinea Institute of Medical Research. The analysis of blood meal contents with ELISA and PCRs were conducted by Dr Brandyce St. Laurent at the University of Notre Dame, Capt Weng Chow at AMI and Peter Moore at UQ. The authors thank the communities of each study village for their support as well as the support of Albino Bobogare, Director of National Vector Borne Disease Control Programme, Solomon Islands, and Professor Peter Siba, Director of the Papua New Guinea Institute of Medical Research.
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