Development and evaluation of mosquito-electrocuting traps as alternatives to the human landing catch technique for sampling host-seeking malaria vectors
© Maliti et al. 2015
Received: 22 October 2015
Accepted: 2 December 2015
Published: 15 December 2015
The Erratum to this article has been published in Malaria Journal 2016 15:558
The human landing catch (HLC) is the gold standard method for sampling host-seeking malaria vectors. However, the HLC is ethically questionable because it requires exposure of humans to potentially infectious mosquito bites.
Two exposure-free methods for sampling host-seeking mosquitoes were evaluated using electrocuting surfaces as potential replacements for HLC: (1) a previously evaluated, commercially available electrocuting grid (CA-EG) designed for killing flies, and (2) a custom-made mosquito electrocuting trap (MET) designed to kill African malaria vectors. The MET and the CA-EG were evaluated relative to the HLC in a Latin Square experiment conducted in the Kilombero Valley, Tanzania. The sampling consistency of the traps across the night and at varying mosquito densities was investigated. Estimates of the proportion of mosquitoes caught indoors (Pi), proportion of human exposure occurring indoors (πi), and proportion of mosquitoes caught when most people are likely to be indoors (Pfl) were compared for all traps.
Whereas the CA-EG performed poorly (<10 % of catch of HLC), sampling efficiency of the MET for sampling Anopheles funestus s.l. was indistinguishable from HLC indoors and outdoors. For Anopheles gambiae s.l., sampling sensitivity of MET was 20.9 % (95 % CI 10.3–42.2) indoors and 58.5 % (95 % CI 32.2–106.2) outdoors relative to HLC. There was no evidence of density-dependent sampling by the MET or CA-EG. Similar estimates of Pi were obtained for An. gambiae s.l. and An. funestus s.l. from all trapping methods. The proportion of mosquitoes caught when people are usually indoors (Pfl) was underestimated by the CA-EG and MET for An. gambiae s.l., but similar to the HLC for An. funestus. Estimates of the proportion of human exposure occurring indoors (πi) obtained from the CA-EG and MET were similar to the HLC for An. gambiae s.l., but overestimated for An. funestus.
The MET showed promise as an outdoor sampling tool for malaria vectors where it achieved >50 % sampling sensitivity relative to the HLC. The CA-EG had poor sampling sensitivity outdoors and inside. With further modification, the MET could provide an efficient and safer alternative to the HLC for the surveillance of mosquito vectors outdoors.
KeywordsMosquito electrocuting trap Human landing catch Mosquito behaviour Vector sampling tools Outdoor biting Malaria Anopheles arabiensis Anopheles gambiae s.l. Anopheles funestus s.l.
Efforts to control malaria rely heavily on the application of long-lasting insecticidal nets (LLINs) which are the major strategy to protect humans against bites from mosquito vectors in African homes . Rapid increases in the coverage of LLINs over the past decade have been associated with substantial declines in major African vector species . A parallel decline in malaria infection rates in people has been reported in several places, as has a decrease in malaria mortality in infants and adults . However, the widespread use of these vector control measures may be triggering changes in the ecology and genetics of mosquito populations that could threaten their continued effectiveness [4–7].
Insecticide resistance is increasingly reported in areas where LLINs are widely used [8–11]. There are also concerns that LLINs may be selecting for behavioural changes within malaria vectors that allow them to shift their biting to times and places where people are not protected, which can be defined as ‘behavioural avoidance’ [7, 12–16]. These changes in feeding behaviours could arise either due to shifts in malaria vector species composition from dominance by highly endophilic and anthropophilic species (e.g., An. gambiae s.s.) towards those with more exophilic and zoophilic tendencies such as Anopheles arabiensis . Additionally, it has been hypothesized that selection from LLINs could generate within-species behavioural adaptations [13, 15, 18, 19]. The ability to monitor if and how rapidly mosquito behaviour is changing in response to control measures is crucial for assessment of the continued effectiveness of LLINs and indoor residual spraying (IRS) strategies [20–23].
One of the most important and widely used techniques to study the host-seeking behaviour of mosquitoes is the human landing catch (HLC) technique. This technique is regarded as the gold standard tool for sampling host-seeking malaria vectors [24, 25]. The HLC is widely used for a range of purposes, including estimation of entomological exposure rates [26–29], evaluation of vector control measures [30, 31] and for studying mosquito vector behaviour and ecology [16, 26–28, 32, 33]. Although the HLC provides a realistic estimate of the number of mosquito bites that humans are exposed to, this technique has numerous drawbacks. The most notable is ethical concerns raised by requiring the participating human subjects to expose their legs to attract mosquitoes. The aim is for participants to capture mosquitoes landing on them before they bite, but this is not always possible and could generate some risk of exposure to infection [26, 34, 35]. To minimize exposure risk it is recommended that HLC participants use malaria prophylaxis . Whilst it has been shown this precautionary measure can reduce infection risk in HLC participants to below that experienced in the community in some settings , it is unlikely to be effective in areas of high drug resistance, and/or where mosquitoes carry other pathogens (e.g., dengue, filariasis) that pose infection risks . These problems highlight the need for a more efficient, representative and ethical alternative sampling method for investigation of mosquito biting densities and behaviour.
Previous attempts have been made to develop exposure-free sampling tools for collecting indoor or outdoor biting mosquitoes. These techniques include but are not limited to the bed net trap , tent traps [39–41], the CDC light traps , and the mosquito magnet (MM) trap [43–45]. While these methods have shown promise in some settings, most have limitations that restrict their large-scale application, and/or bias collection towards mosquito species with particular phenotypes that may misrepresent the community of mosquitoes attracted to people . Recently, there has been renewed interest in exploring the use of electrocuting surfaces as a means of sampling malaria vectors [47–49]. This approach was originally developed for trapping tsetse flies outdoors , but later adapted to sample mosquitoes drawn towards a host odour source [51, 52]. This trap works by placing a live host in a sealed tent and piping their odour out to an electrocuting net (E-Net) approximately 10 m away that kills mosquitoes on contact. Such E-Nets have already shown promise when used to investigate host species’ preferences and odour responses of the African vector species [51, 52]. As a potential improvement, the use of commercially available ‘bug-zapping’ devices, which can sample insects in the immediate proximity of a host has been explored with some promise, indicating they can achieve a relative sampling efficiency of up to 50 % of the HLC in one study . However, given these devices were developed for large flies, their suitability for trapping African malaria vectors is unclear. Further work is required to develop an electrocuting trap that is optimized for malaria vectors, can meet the performance of the HLC, is suitable for use inside and outdoors, can be used safely in close proximity of humans, and is durable under field conditions. Here, a mosquito electrocuting trap (MET) was designed, developed and field-tested. This trap was custom designed to sample host-seeking African malaria vectors, with the aim of meeting all performance targets defined above.
Field experiments were conducted at Lupiro village (−8.38 S, 36.67 E) located in the Kilombero Valley of southern Tanzania. This village is situated in a malaria-endemic region where the most recent estimate of entomological inoculation rate (EIR) was 33.9 infectious bites per person per year . Historically An. gambiae s.s. was the most abundant member of the An. gambiae s.l. species complex in the Kilombero Valley . However in conjunction with the increasing coverage of insecticide-treated bed nets (ITNs) in this area over the last decade [55, 56], An. gambiae s.s. has almost virtually disappeared and its sibling species An. arabiensis now constitutes >98 % of the species complex in most areas [57–59]. Anopheles funestus is the only other important vector species in the area .
This experiment was conducted using a series of experimental huts designed to imitate the typical design of local houses in the study area . Experimental huts dimensions were 6.5 m long × 3.5 m wide × 2 m high, with a 20-cm wide gap between the top of walls and roof to simulate the open eaves found in most local houses. Trapping stations were set up inside each hut and at an associated outdoor point approximately 10 m away. For outdoor stations, tents were used to provide roofing that protected the traps and collectors from rain (Fig. 1). A 3 × 3 Latin square design was used in which each of the three trapping methods was randomly assigned to one of three experimental huts on each night. On each night, collections were conducted at paired indoor and outdoor trapping stations. Over consecutive nights, the three trapping methods were trialled at each hut to complete a full rotation in 3 days. Seven rounds of trapping were conducted over 21 trapping nights between March and May 2012. The first two rounds were conducted in a group of three experimental huts defined as A, B and C (at site 1), and the remaining five rounds were conducted in a different group of experimental huts (defined D, E and F) which were situated approximately 200 m from the first.
Trapping was conducted from 19.00 to 07.00 hours. During each hour, volunteers spent 45 min passively sitting in a trap (MET or CA-EG) or actively collecting mosquitoes (HLC, Fig. 1d), with the remaining 15 min used as a break. Collectors moved to a different trap or position every hour throughout the night to minimize bias due to variation in their relative attractiveness to mosquitoes. At the end of each hour, MET and CA-EG traps were checked and trapped mosquitoes were removed by mouth aspirators or forceps and placed in labelled cups. On the following morning, mosquitoes from all the three trapping methods were sorted using morphological keys to identify their genera and gender. Female mosquitoes visually identified as belonging to a malaria vector group (An. gambiae s.l. or An. funestus s.l.) were individually stored in Eppendorf tubes with silica gel. Anopheles gambiae s.l. were later analysed using the polymerase chain reaction (PCR) technique to identify their species identity .
All statistical analyses were carried out using the R statistical software version 2.15. Generalized linear mixed models (GLMMs)  were used to assess variation in mosquito vector abundance between trap types. Mosquito abundance data were highly overdispersed and thus modelled as following a negative binomial distribution using the generalized linear mixed model automatic differentiation model builder (glmmADMB) package . Here, trap type was fitted as the primary main effect of interest, and experimental night and hut as random effects. The relative sampling efficiency of the novel trap types relative to the HLC was estimated by computing the ratio of the predicted nightly abundance of vectors from these statistical models.
To test whether there was any systematic increase or decrease in the sampling efficiency of the CA-EG or MET relative to the HLC over the course of a night (e.g., perhaps due to battery decline), a model was constructed in which the fraction of the hourly catch occurring either in CA-EG or MET (e.g., ‘novel trap’/(‘novel trap + HLC’) was defined as the response variable, and trapping hour (defined as being ‘1’ on the first hour, and increasing through the night to 12 as the last hour) fitted as a continuous fixed effect, with experimental night added as a random effect. Here, the proportion of mosquitoes caught by a novel method (CA-EG or MET) out of the total caught from this method and the HLC, was modelled using a GLMM using a logit link function.
Additional analysis was conducted to test whether the relative performance of the novel trap types was density dependent. Density dependence was investigated using the Bland–Altman method which assesses the reliability of two measures via regression analysis of the relationship between their difference and their mean , where non-linearity in this relationship indicates density dependence (see Additional file 1). Values of R adj 2 obtained from these analyses can be interpreted as an estimate of the proportion of deviation from perfect linear correlation due to density dependence rather than random error (with a high value indicating support for density dependence). The precision of the R adj 2 estimate was gauged by estimating its 95 % confidence interval as the 2.5th and 97.5th centiles from 10,000 bootstrap replicates.
Finally, analyses were conducted to assess if the three focal trapping methods varied in their prediction of key mosquito vector behaviours and their related human exposure outcomes . The predictors of malaria vector type of behaviour that were analysed here are the proportion of mosquitoes that were caught feeding indoors (Pi), the proportion of mosquitoes that were caught feeding when most people were indoors (Pfl), and the proportion of human exposure that occurs indoors (πi) [49, 68–70]. The proportion of mosquitoes that were caught indoors (Pi) was calculated by dividing the total number of mosquitoes caught indoors by the total number caught outdoors and indoors over 12 h of the night: I19→07 h/(I19→07 h + O19→07 h) , where I and O, respectively, represent mosquitoes collected indoors and outdoors, and subscripts indicate the start and the end time of the sampling period. The calculation of Pfl and πi requires definition of the period of the night when most people (>50 %) are expected to be indoors and sleeping. This time period was previously estimated for the community living in Lupiro village as 21.00–05.00 . Therefore, the proportion of mosquitoes caught when most people were likely to be indoors (Pfl) was calculated as follows: (I21→05 h + O21→05 h)/(I19→06 h + O19→06 h) . The proportion of human exposure that occurs indoors (πi) was calculated by dividing the number of mosquitoes caught indoors during the period that most people are inside (21.00–05.00) by itself plus the number of mosquito caught outdoors outside of the sleeping hours (I21→05 h)/(I21→05 h + O19,20,06 h) . Binary estimates of Pi, Pfl and πi were estimated using GLMMs with a binomial distribution and a logit link function . In these models, trap type was fitted as a fixed effect, and experimental night as a random effect.
Ethical approval was obtained from the Institutional Review Board of the Ifakara Health Institute (Reference number IHI/IRB/A.50) and the Medical Research Coordination Committee of the National Institute for Medical Research, Tanzania (Reference number NIMR/HQ/R.8a/Vol. IX/801.) All volunteers recruited in this work were given informed consent forms with details of the procedures, explanation of their right to withdraw at any time, potential risks, and mitigation plan. All participants read and signed the forms before taking part in the work. All participants were provided with malaria prophylaxis, Malarone (250 mg atovaquone and 100 mg proguanil hydrochloride, GlaxoSmithKline) before and during the experiments to prevent malaria infection.
A summary of the total number of mosquito genera and species caught by different sampling methods in this study
Total per trapping method
An. gambiae s.l.
An. funestus s.l.
Predicted sampling efficiency of the novel traps (per night) relative to the HLC gold standard
Relative sampling efficiency (95 % CI)
An. gambiae s.l.
An. funestus s.l.
Sampling consistency across the night
Sampling consistency across varying mosquito densities
Quantification of density dependence using the Bland–Altman method
Adjusted R2 (95 % CI)
An. gambiae s.l.
−9 (−11, 35)
−6 (−11, 27)
−1 (−9, 44)
−3 (−9, 36)
An. funestus s.l.
−11 (−11, 16)
−9 (−11, 34)
−1 (−9, 62)
−11 (−11, 40)
Metrics of mosquito behaviour and human biting exposure distribution
Indicators of malaria vector biting behaviour and human exposure metrics (Pi, Pfl and πi) as estimated by each of the three traps for Anopheles gambiae s.l. and Anopheles funestus s.l.
Proportion caught indoors (Pi)
Proportion caught when most people are indoors (Pfl)
Proportion of human exposure occurring indoors (πi)
Estimate (95 % CI)
Estimate (95 % CI)
Estimate (95 % CI)
An. gambiae s.l.
An. funestus s.l.
The electrocuting traps were less consistent with the HLC when used to estimate other human exposure indicators. The HLC predicted that approximately 98 % of An. gambiae s.l. attempted to feed during hours when most people would be indoors (Pfl, Table 4), which was underestimated at 68 % (z = 9.27, p < 0.001, Table 4) and 40 % (z = −12.91, p < 0.001, Table 4) by the MET and CA-EG, respectively. Predictions were less variable for An. funestus s.l., where Pfl was estimated to be ~70–75 % by the MET and HLC, respectively (z = −1.34, p = 0.18, Table 4), but underestimated as 65 % by the CA-EG (z = −2.62, p = 0.009, Table 4). It is noted that values of Pfl were underestimated in all scenarios where the novel trap type (CA-EG or MET) had a lower sampling sensitivity inside than outside. The MET somewhat underestimated the proportion of human exposure occurring indoors (πi = 36 %) in comparison to the HLC for An. gambiae s.l. (43 %), a difference of borderline statistical significance (z = −2.04, p = 0.04). Estimates of πi for An. gambiae s.l. as obtained from the CA-EG and HLC were indistinguishable (43–46 %, z = 0.77, p = 0.44, Table 4). Both the MET (z = 4.21, p < 0.001) and CA-EG (z = 5.23, p < 0.001) overestimated πi for An. funestus s.l. (73–80 % Table 4) compared to the HLC (55 %, Table 4).
In this study, the potential of two electrocuting traps, the MET and CA-EG, to provide exposure-free alternatives to the HLC technique for sampling African malaria vectors was evaluated. The HLC generally collected more An. gambiae s.l. than the MET, but capture rates of An. funestus s.l. were similar between these methods. The relative sampling efficiency of the MET was reasonably high (~59 %) when used for An. gambiae s.l. outdoors, but fell to ~20 % relative to the HLC when applied indoors. In contrast, the CA-EG performed poorly relative to the HLC in both indoor and outdoor settings, for An. gambiae s.l. and An. funestus. No evidence of density-dependent sampling was observed in either electrocuting trap. Both the MET and CA-EG tended to have higher performance relative to the HLC outdoors compared to indoors, which contributed to these traps producing somewhat biased estimates of human exposure indices. While estimation of the proportion of mosquitoes caught indoors (Pi) by the electrocuting traps were similar to those estimated by HLC, there was tendency of the MET and CA-EG to underestimate (Pfl) when sampling An. gambiae s.l., and overestimate the proportion of human exposure that occurs indoors (πi) when sampling An. funestus s.l. On balance, the sampling sensitivity of the CA-EG was judged too low to merit further consideration as an alternative to the HLC. However, the MET showed strong promise as an alternative method for exposure-free surveillance of African malaria outdoors outside of houses.
The sampling efficiency of the MET was consistently higher for An. funestus s.l. than for An. gambiae s.l. Possible explanations for this include differential sensitivity of these species to electrocution. Several biological factors are known to influence the electrical conductivity of insects, including their cuticular hydrocarbon composition , body size and water content. Differential electrical conductivity between mosquito species could be expected to be less consequential at higher voltages say 50,000 V as used in  because this voltage would be used with lower currents. The voltage and current combination used in the MET were optimized in laboratory studies to produce a high instant kill rate (>80 %) using An. gambiae s.s. as a model, but may be more efficient at killing An. funestus s.l. A previous study using the CA-EG found that sampling efficiency varied between An. gambiae s.s. and An. arabiensis , thus vector-specific sampling may be a common feature of electrocuting traps as has been documented with other methods, such as CDC light traps .
Both electrocuting traps had higher sampling efficiency when used outside than indoors. The reasons underlying this are unknown but could be due to microclimatic variation  which could modify the functioning of electrocuting traps in outdoor and indoor settings, and/or differences in how vectors host seek in outdoor versus indoor location. For example, factors such as the direction and concentration of host odours and wind movement vary between indoor and outdoor settings , and could lead to differential attractiveness of the traps when used in different places. Humans conducting HLC usually bend to collect mosquitoes landing on their legs as shown in Fig. 1d, blowing carbon dioxide to the legs therefore attracting more mosquitoes when doing HLC compared to MET and CA-EG in which carbon dioxide is blown away (Fig. 1b, c). This phenomenon is expected more pronounced indoors than outdoors where wind may blow away the carbon dioxide and may therefore explain a poorer performance of MET and CA-EG indoors relative to the HLC. HLC may not therefore be a perfect indicator of mosquito-biting activities as the stated phenomenon above may bias its function. Further investigation of the performance of electrocuting traps in a broader range of ecological settings is required, including experiments that involve mechanisms to control the breath of the catchers sitting on the HLC as well as on the MET, perhaps by using a breathing tube which directs the carbon dioxide away from traps or towards the traps to increase sensitivity of both methodologies.
There were differences in the relative sampling sensitivity of CA-EG as estimated in this study compared to that reported by Majambere et al. . Whereas  estimated the sampling efficiency of the CA-EG to be ~50 % relative to the HLC in indoor and outdoor locations, it was only 6–29 % in this study. One explanation could be variation in how human participants were positioned. In  the human bait lay down and were covered by bed nets which were surrounded by six grid units, in this current study the humans were positioned in a sitting position using four grid units, specifically to replicate the human subject’s position in the HLC technique and thus avoid bias due to differential positioning of the hosts. Enclosing the whole human in the trap as was done by  may have contributed to their higher reported performance of the CA-EG in their study compared to this study. Another difference was that the study by  was conducted in Dar es Salaam where An. gambiae s.s. is the dominant species, compared to An. arabiensis in the Kilombero Valley where this study was set. During preliminary laboratory optimization tests conducted during the development of the MET, An. gambiae s.s. was shown to be somewhat more sensitive to electrocution than An. arabiensis. Thus, the lower performance of the CA-EG in the current study may also be due to differences in malaria vector species composition between sites.
One of the ways to make MET smaller and therefore easy to carry around would be to replace the human bait with an artificial odour delivery system. This step would additionally remove human safety concerns and significantly decrease labour. However, to be able to obtain an alternative trapping tool with sampling efficiency close to the gold standard HLC, this study tried to imitate as much as possible some of the features which make HLC superior to other host-seeking traps. Theoretically, a good host-seeking trap should represent as much as possible human exposure rates to host-seeking mosquitoes that happen in real environment. This can be most realistically achieved with the physical presence of a human close to or within the trap. Therefore, replacing the human bait from the MET would reduce accuracy of the trap because other factors than the human odour, such as visual cues and body heat, are involved in attracting host-seeking mosquitoes [75, 76].
On a few occasions there was evidence of decreasing sensitivity of MET and CA-EG over the sampling night relative to the HLC, but this effect was not consistent between vector species, nor between indoor and outdoor settings. A reduction in the sampling efficiency of CA-EG relative to the HLC over the course of a night was reported in . This was interpreted as a sign of battery drainage through time, which reduced the electrical output. Given that a decline in the relative sensitivity of electrocuting traps was not consistently reported in this study, it is difficult to interpret the patterns of time-dependent trap performance observed here. In addition to battery drainage, other factors, such as a build-up of moisture on traps (especially as occurred in outdoor stations) may have contributed to MET’s low relative performance. The MET output voltage was checked every hour and in some cases it was shown to drop below optimal levels, especially in the later hours of the night. Additionally, there were a few occasions where traps temporarily short-circuited during experiments because opposing wires came into contact, and/or the wooden frames became moist and mildly conductive. Experiments were stopped when there was an obvious cessation of current flow, however, there could have been more minor dips occurring during sampling night that went undetected. Use of a higher-capacity battery coupled to an alarm system to notify if and when there is any dip in electrical output could resolve any issues of variable voltage output through time.
This study shows no strong evidence of density-dependent sampling in either the MET or the CA-EG. However, this study was conducted over 21 consecutive nights in the rainy season when mosquito densities were generally high. Thus, it was not possible to assess density dependence across the full range of mosquito densities that occurs between wet and dry seasons. Additionally, it is noted that the detection of density dependence in trapping studies is sensitive to the type of analysis method used . Several previous studies have assessed density dependency based on analysis of how the proportional catch rate varies with differing mosquito densities across nights [39, 78], whereas others, including the present study, use the Bland–Altman method . The Bland–Altman method was chosen because its use of regression analysis to assess the reliability of two measures is not subject to bias inherent in the binomial, proportional catch approach. It is recommended that future studies to evaluate these trapping methods adopt a similar method so that estimations of density dependence are standardized and comparable.
For any mosquito-sampling tool to successfully replace the HLC, it must be able to give meaningful representation of key mosquito behaviours and associated human exposure risk factors. Here, three such measures were investigated that have been widely used in a number of other studies to assess both human risk and likely degree of protection from LLINs [15, 68–70, 79]. One of the most direct measures of indoor exposure is the proportion of mosquitoes that bite indoors (Pi), for which comparable estimates were obtained from both electrocuting traps and the HLC. However, the proportion of mosquitoes caught when people are usually indoors (Pfl) was underestimated by the CA-EG and MET for An. gambiae s.l., but similar to the HLC for An. funestus. Estimates of the proportion of human exposure occurring indoors (πi) obtained from the CA-EG and MET were similar to the HLC for An. gambiae s.l., but overestimated for An. funestus. This is consistent with results from a previous study  where the CA-EG produced a similar estimate of Pi, but underestimated Pfl for An. arabiensis relative to the HLC. The likely explanation for this bias is the differential sampling efficiency of the electrocuting traps when used indoors versus out. This location-dependent performance would be expected to generate biased estimates of Pfl and the proportion of human exposure predicted to occur indoors.
Historical data for the Kilombero Valley (1999) where this study took place indicates the proportion of An. gambiae s.l. caught indoors (Pi) estimated by HLC was 0.58 ± 0.01 , which is higher than the values of 0.37 ± 0.03 (HLC) and 0.35 ± 0.03 (MET) reported here. These differences may be due to concurrent changes within the An. gambiae s.l. complex that have occurred over this time. Whereas most An. gambiae s.l. were found to be An. gambiae s.s. in 1999  to <1 % in 2009 , this species represents <1 % of the An. gambiae s.l. complex now with the remaining fraction being the more exophilic An. arabiensis. The proportion of human exposure occurring indoors that would otherwise be directly preventable with bed net use (πi) was estimated as 0.43 and 0.55 for An. gambiae s.l. and An. funestus s.l., respectively, using HLC in this study. Assuming that all An. gambiae s.l. in this study were An. arabiensis (based on PCR results of 400 samples which showed all of them were An. arabiensis), these estimates of πi are low compared to that reported in western Kenya , where values of 0.87 and 0.86 were obtained for An. arabiensis and An. funestus s.l., respectively. A more recent study in western Kenya  reported πi values of ~0.64 for major vectors An. gambiae s.l. and An. funestus, which are still higher but closer to the values reported in this setting. Another study in Dar es Salaam estimated πi obtained for An. arabiensis to be 0.53  which is also higher than found in this study. The consistently smaller values of πi reported for both An. gambiae s.l. and An. funestus s.l. here indicates that a lower proportion of human exposure to malaria may be occurring indoors in the Kilombero Valley than in other parts of East Africa, and highlights the particular need for interventions that can control outdoor-biting mosquitoes in this setting.
As the MET applies high voltage electricity to electrocute mosquitoes, human safety in using this trap is a priority. Two measures were taken to ensure no risk of harm to humans using these traps. First, although the MET used relatively high pulsed DC voltage (600 V DC), resistors were incorporated to limit the current to no more than 10 mA which generates a low power output insufficient to cause harm to a human who momentarily touches them . Similarly, although the CA-EG used higher voltages (800 V AC), resistors were used to limit current flow in this trap to 15 mA. A second measure can be incorporated into future versions of MET to remove even this mild risk of minor electrical sensation on contact by placing a protective barrier of non-conductive material in the inner side of the grids.
This study has demonstrated proof-of-principle that the MET can be used with reasonable efficiency to sample malaria vectors outdoors. The CA-EG performance did not merit further consideration because of its low sampling sensitivity. Whereas the current version of MET may misrepresent some aspects of mosquito behaviour, such as the proportion of human exposure to biting that occurs indoors, it is hypothesized that the sampling sensitivity of MET can be improved specifically by ensuring generation of stable voltage across the night, and by avoiding short circuiting which can be achieved by replacing the semi-conducting wooden frames with non-conducting polyvinyl chloride (PVC). It is recommended further testing of the improved MET in a range of ecological settings to explore its ability to be used as an alternative to the HLC.
DM, NM, NJG, and HMF designed the MET trap. DM and NM constructed the MET trap. DM, HMF, NJG, and KK designed the experiment. DM conducted the field experiment. DM, HMF and PJ conducted data analysis. DM and HMF drafted the manuscript. GFK, HF, NJG, KK, NM, and PJ reviewed the manuscript. All authors read and approved the final manuscript.
We thank the European Union Seventh Framework Programme FP7/2007-2013 for supporting this study through the African Vector New Tools (AvecNet) under the Grant Agreement Number 265660. We acknowledge the University of Glasgow for providing tuition fee waiver to DM. We thank our field technicians: Masoud Kilalangongono, Aniset Kihonda, Tokosa, Kasubiri, and Tumpe Mwandyala. We acknowledge the contribution of a number of field volunteers and the community at Lupiro village. We thank Thomas Wallace and Alistair Torry of the University of Glasgow Bioelectronics Unit for their assistance with constructing parts of the MET trap.
The authors declare that they have no competing interests.
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- Lengeler C. Insecticide-treated bed nets and curtains for preventing malaria. Cochrane Database Syst Rev. 2004;(2):CD000363.Google Scholar
- WHO: World malaria report 2013. Geneva: World Health Organization; 2013.Google Scholar
- WHO: World malaria report 2014. Geneva: World Health Organization; 2014.Google Scholar
- Wondji C, Simard F, Lehmann T, Fondjo E, Same-Ekobo A, Fontenille D. Impact of insecticide-treated bed nets implementation on the genetic structure of Anopheles arabiensis in an area of irrigated rice fields in the Sahelian region of Cameroon. Mol Ecol. 2005;14:3683–93.View ArticlePubMedGoogle Scholar
- Chaves LF, Kaneko A, Taleo G, Pascual M, Wilson ML. Malaria transmission pattern resilience to climatic variability is mediated by insecticide-treated nets. Malar J. 2008;7:100.View ArticlePubMedPubMed CentralGoogle Scholar
- Drake JM, Beier JC. Ecological niche and potential distribution of Anopheles arabiensis in Africa in 2050. Malar J. 2014;13:213.View ArticlePubMedPubMed CentralGoogle Scholar
- Killeen GF, Chitnis N. Potential causes and consequences of behavioural resilience and resistance in malaria vector populations: a mathematical modelling analysis. Malar J. 2014;13:97.View ArticlePubMedPubMed CentralGoogle Scholar
- Jones CM, Toe HK, Sanou A, Namountougou M, Hughes A, Diabate A, et al. Additional selection for insecticide resistance in urban malaria vectors: DDT resistance in Anopheles arabiensis from Bobo-Dioulasso, Burkina Faso. PLoS One. 2012;7:e45995.View ArticlePubMedPubMed CentralGoogle Scholar
- Temu EA, Maxwell C, Munyekenye G, Howard AF, Munga S, Avicor SW, et al. Pyrethroid resistance in Anopheles gambiae, in Bomi County, Liberia, compromises malaria vector control. PLoS One. 2012;7:e44986.View ArticlePubMedPubMed CentralGoogle Scholar
- Ranson H, Abdallah H, Badolo A, Guelbeogo WM, Kerah-Hinzoumbe C, Yangalbe-Kalnone E, et al. Insecticide resistance in Anopheles gambiae: data from the first year of a multi-country study highlight the extent of the problem. Malar J. 2009;8:299.View ArticlePubMedPubMed CentralGoogle Scholar
- Kabula B, Kisinza W, Tungu P, Ndege C, Batengana B, Kollo D, et al. Co-occurrence and distribution of East (L1014S) and West (L1014F) African knock-down resistance in Anopheles gambiae sensu lato population of Tanzania. Trop Med Int Health. 2014;19:331–41.View ArticlePubMedGoogle Scholar
- Pates H, Curtis C. Mosquito behavior and vector control. Annu Rev Entomol. 2005;50:53–70.View ArticlePubMedGoogle Scholar
- Reddy MR, Overgaard HJ, Abaga S, Reddy VP, Caccone A, Kiszewski AE, et al. Outdoor host seeking behaviour of Anopheles gambiae mosquitoes following initiation of malaria vector control on Bioko Island, Equatorial Guinea. Malar J. 2011;10:184.View ArticlePubMedPubMed CentralGoogle Scholar
- Govella NJ, Chaki PP, Killeen GF. Entomological surveillance of behavioural resilience and resistance in residual malaria vector populations. Malar J. 2013;12:124.View ArticlePubMedPubMed CentralGoogle Scholar
- Russell TL, Govella NJ, Azizi S, Drakeley CJ, Kachur SP, Killeen GF. Increased proportions of outdoor feeding among residual malaria vector populations following increased use of insecticide-treated nets in rural Tanzania. Malar J. 2011;10:80.View ArticlePubMedPubMed CentralGoogle Scholar
- Sougoufara S, Diedhiou SM, Doucoure S, Diagne N, Sembene PM, Harry M, et al. Biting by Anopheles funestus in broad daylight after use of long-lasting insecticidal nets: a new challenge to malaria elimination. Malar J. 2014;13:125.View ArticlePubMedPubMed CentralGoogle Scholar
- Derua YA, Alifrangis M, Hosea KM, Meyrowitsch DW, Magesa SM, Pedersen EM, et al. Change in composition of the Anopheles gambiae complex and its possible implications for the transmission of malaria and lymphatic filariasis in north-eastern Tanzania. Malar J. 2012;11:188.View ArticlePubMedPubMed CentralGoogle Scholar
- Kabbale FG, Akol AM, Kaddu JB, Onapa AW. Biting patterns and seasonality of Anopheles gambiae sensu lato and Anopheles funestus mosquitoes in Kamuli District, Uganda. Parasit Vectors. 2013;6:340.View ArticlePubMedPubMed CentralGoogle Scholar
- Ndiath MO, Mazenot C, Sokhna C, Trape JF. How the malaria vector Anopheles gambiae adapts to the use of insecticide-treated nets by African populations. PLoS One. 2014;9:e97700.View ArticlePubMedPubMed CentralGoogle Scholar
- Russell TL, Beebe NW, Cooper RD, Lobo NF, Burkot TR. Successful malaria elimination strategies require interventions that target changing vector behaviours. Malar J. 2013;12:56.View ArticlePubMedPubMed CentralGoogle Scholar
- Gatton ML, Chitnis N, Churcher T, Donnelly MJ, Ghani AC, Godfray HC, et al. The importance of mosquito behavioural adaptations to malaria control in Africa. Evolution. 2013;67:1218–30.View ArticlePubMedPubMed CentralGoogle Scholar
- Govella NJ, Ferguson H. Why use of interventions targeting outdoor biting mosquitoes will be necessary to achieve malaria elimination. Front Physiol. 2012;3:199.View ArticlePubMedPubMed CentralGoogle Scholar
- Briet OJ, Chitnis N. Effects of changing mosquito host searching behaviour on the cost effectiveness of a mass distribution of long-lasting, insecticidal nets: a modelling study. Malar J. 2013;12:215.View ArticlePubMedPubMed CentralGoogle Scholar
- Magbity EB, Magbity EB, Lines JD, Marbiah MT, David K, Peterson E. How reliable are light traps in estimating biting rates of adult Anopheles gambiae s.l. (Diptera: Culicidae) in the presence of treated bed nets? Bull Entomol Res. 2002;92:71–6.View ArticlePubMedGoogle Scholar
- Lima JB, Rosa-Freitas MG, Rodovalho CM, Santos F, Lourenco-de-Oliveira R. Is there an efficient trap or collection method for sampling Anopheles darlingi and other malaria vectors that can describe the essential parameters affecting transmission dynamics as effectively as human landing catches? A Review. Mem Inst Oswaldo Cruz. 2014;109:685–705.View ArticlePubMedPubMed CentralGoogle Scholar
- Mboera LE. Sampling techniques for adult Afrotropical malaria vectors and their reliability in the estimation of entomological inoculation rate. Tanzan Health Res Bull. 2005;7:117–24.PubMedGoogle Scholar
- Rohani A, Chan ST, Abdullah AG, Tanrang H, Lee HL. Species composition of mosquito fauna in Ranau, Sabah, Malaysia. Trop Biomed. 2008;25:232–6.PubMedGoogle Scholar
- Loaiza JR, Bermingham E, Scott ME, Rovira JR, Conn JE. Species composition and distribution of adult Anopheles (Diptera: Culicidae) in Panama. J Med Entomol. 2008;45:841–51.View ArticlePubMedPubMed CentralGoogle Scholar
- Kilama M, Smith DL, Hutchinson R, Kigozi R, Yeka A, Lavoy G, et al. Estimating the annual entomological inoculation rate for Plasmodium falciparum transmitted by Anopheles gambiae s.l. using three sampling methods in three sites in Uganda. Malar J. 2014;13:111.View ArticlePubMedPubMed CentralGoogle Scholar
- Osse RA, Aikpon R, Gbedjissi GL, Gnanguenon V, Sezonlin M, Govoetchan R, et al. A shift from indoor residual spraying (IRS) with bendiocarb to long-lasting insecticidal (mosquito) nets (LLINs) associated with changes in malaria transmission indicators in pyrethroid resistance areas in Benin. Parasit Vectors. 2013;6:73.View ArticlePubMedPubMed CentralGoogle Scholar
- Malaithong N, Polsomboon S, Poolprasert P, Parbaripai A, Bangs MJ, Suwonkerd W, et al. Human-landing patterns of Anopheles dirus sensu lato (Diptera: Culicidae) in experimental huts treated with DDT or deltamethrin. J Med Entomol. 2010;47:823–32.View ArticlePubMedGoogle Scholar
- Bockarie MJ, Alexander N, Bockarie F, Ibam E, Barnish G, Alpers M. The late biting habit of parous Anopheles mosquitoes and pre-bedtime exposure of humans to infective female mosquitoes. Trans R Soc Trop Med Hyg. 1996;90:23–5.View ArticlePubMedGoogle Scholar
- Yadouleton A, N’Guessan R, Allagbe H, Asidi A, Boko M, Osse R, et al. The impact of the expansion of urban vegetable farming on malaria transmission in major cities of Benin. Parasit Vectors. 2010;3:118.View ArticlePubMedPubMed CentralGoogle Scholar
- Mathenge EM, Misiani GO, Oulo DO, Irungu LW, Ndegwa PN, Smith TA, et al. Comparative performance of the Mbita trap, CDC light trap and the human landing catch in the sampling of Anopheles arabiensis, An. funestus and culicine species in a rice irrigation in western Kenya. Malar J. 2005;4:7.View ArticlePubMedPubMed CentralGoogle Scholar
- Achee NL, Youngblood L, Bangs MJ, Lavery JV, James S. Considerations for the use of human participants in vector biology research: a tool for investigators and regulators. Vector Borne Zoonotic Dis. 2015;15:89–102.View ArticlePubMedPubMed CentralGoogle Scholar
- Gimnig JE, Walker ED, Otieno P, Kosgei J, Olang G, Ombok M, et al. Incidence of malaria among mosquito collectors conducting human landing catches in western Kenya. Am J Trop Med Hyg. 2013;88:301–8.View ArticlePubMedPubMed CentralGoogle Scholar
- Simonsen PE, Pedersen EM, Rwegoshora RT, Malecela MN, Derua YA, Magesa SM. Lymphatic filariasis control in Tanzania: effect of repeated mass drug administration with ivermectin and albendazole on infection and transmission. PLoS Negl Trop Dis. 2010;4:e696.View ArticlePubMedPubMed CentralGoogle Scholar
- Mathenge EM, Omweri GO, Irungu LW, Ndegwa PN, Walczak E, Smith TA, et al. Comparative field evaluation of the Mbita trap, the Centers for Disease Control light trap, and the human landing catch for sampling of malaria vectors in western Kenya. Am J Trop Med Hyg. 2004;70:33–7.PubMedGoogle Scholar
- Govella NJ, Chaki PP, Geissbuhler Y, Kannady K, Okumu F, Charlwood JD, et al. A new tent trap for sampling exophagic and endophagic members of the Anopheles gambiae complex. Malar J. 2009;8:157.View ArticlePubMedPubMed CentralGoogle Scholar
- Govella NJ, Moore JD, Killeen GF. An exposure-free tool for monitoring adult malaria mosquito populations. Am J Trop Med Hyg. 2010;83:596–600.View ArticlePubMedPubMed CentralGoogle Scholar
- Krajacich BJ, Slade JR, Mulligan RT, Labrecque B, Kobylinski KC, Gray M, et al. Design and testing of a novel, protective human-baited tent trap for the collection of anthropophilic disease vectors. J Med Entomol. 2014;51:253–63.View ArticlePubMedPubMed CentralGoogle Scholar
- Faye O, Diallo S, Gaye O, Ndir O, Faye O. Comparative efficacy of the use of CDC light traps and humans to sampling anopheles populations. Results obtained in the area of Bignona (Senegal). Bull Soc Pathol Exot. 1992;85:185–9.PubMedGoogle Scholar
- Vezenegho SB, Adde A, Gaborit P, Carinci R, Issaly J, Pommier de Santi V, et al. Mosquito magnet(R) liberty plus trap baited with octenol confirmed best candidate for Anopheles surveillance and proved promising in predicting risk of malaria transmission in French Guiana. Malar J. 2014;13:384.View ArticlePubMedPubMed CentralGoogle Scholar
- Chaves LS, Laporta GZ, Sallum MA. Effectiveness of mosquito magnet in preserved area on the coastal Atlantic rainforest: implication for entomological surveillance. J Med Entomol. 2014;51:915–24.View ArticlePubMedGoogle Scholar
- Sithiprasasna R, Jaichapor B, Chanaimongkol S, Khongtak P, Lealsirivattanakul T, Tiang-Trong S, et al. Evaluation of candidate traps as tools for conducting surveillance for Anopheles mosquitoes in a malaria-endemic area in western Thailand. J Med Entomol. 2004;41:151–7.View ArticlePubMedGoogle Scholar
- James S, Takken W, Collins FH, Gottlieb M. Needs for monitoring mosquito transmission of malaria in a pre-elimination world. Am J Trop Med Hyg. 2014;90:6–10.View ArticlePubMedPubMed CentralGoogle Scholar
- Dugassa S, Lindh JM, Torr SJ, Lindsay SW, Fillinger U. Evaluation of the influence of electric nets on the behaviour of oviposition site seeking Anopheles gambiae s.s. Parasit Vectors. 2014;7:272.View ArticlePubMedPubMed CentralGoogle Scholar
- Dugassa S, Lindh JM, Torr SJ, Oyieke F, Lindsay SW, Fillinger U. Electric nets and sticky materials for analysing oviposition behaviour of gravid malaria vectors. Malar J. 2012;11:374.View ArticlePubMedPubMed CentralGoogle Scholar
- Majambere S, Massue DJ, Mlacha Y, Govella NJ, Magesa SM, Killeen GF. Advantages and limitations of commercially available electrocuting grids for studying mosquito behaviour. Parasit Vectors. 2013;6:53.View ArticlePubMedPubMed CentralGoogle Scholar
- Vale GA. Attractants for controlling and surveying tsetse populations. Trans R Soc Trop Med Hyg. 1974;68:11.View ArticlePubMedGoogle Scholar
- Torr SJ, Della Torre A, Calzetta M, Costantini C, Vale GA. Towards a fuller understanding of mosquito behaviour: use of electrocuting grids to compare the odour-orientated responses of Anopheles arabiensis and An. quadriannulatus in the field. Med Vet Entomol. 2008;22:93–108.View ArticlePubMedGoogle Scholar
- Knols BG, Mboera LE, Takken W. Electric nets for studying odour-mediated host-seeking behaviour of mosquitoes. Med Vet Entomol. 1998;12:116–20.View ArticlePubMedGoogle Scholar
- Russell TL, Lwetoijera DW, Maliti D, Chipwaza B, Kihonda J, Charlwood JD, et al. Impact of promoting longer-lasting insecticide treatment of bed nets upon malaria transmission in a rural Tanzanian setting with pre-existing high coverage of untreated nets. Malar J. 2010;9:187.View ArticlePubMedPubMed CentralGoogle Scholar
- Charlwood JD, Vij R, Billingsley PF. Dry season refugia of malaria-transmitting mosquitoes in a dry savannah zone of east Africa. Am J Trop Med Hyg. 2000;62:726–32.PubMedGoogle Scholar
- Gosoniu L, Vounatsou P, Tami A, Nathan R, Grundmann H, Lengeler C. Spatial effects of mosquito bednets on child mortality. BMC Public Health. 2008;8:356.View ArticlePubMedPubMed CentralGoogle Scholar
- Killeen GF, Smith TA. Exploring the contributions of bed nets, cattle, insecticides and excitorepellency to malaria control: a deterministic model of mosquito host-seeking behaviour and mortality. Trans R Soc Trop Med Hyg. 2007;101:867–80.View ArticlePubMedPubMed CentralGoogle Scholar
- Okumu FO, Moore J, Mbeyela E, Sherlock M, Sangusangu R, Ligamba G, et al. A modified experimental hut design for studying responses of disease-transmitting mosquitoes to indoor interventions: the Ifakara experimental huts. PLoS One. 2012;7:e30967.View ArticlePubMedPubMed CentralGoogle Scholar
- Matowo NS, Moore J, Mapua S, Madumla EP, Moshi IR, Kaindoa EW, et al. Using a new odour-baited device to explore options for luring and killing outdoor-biting malaria vectors: a report on design and field evaluation of the Mosquito Landing Box. Parasit Vectors. 2013;6:137.View ArticlePubMedPubMed CentralGoogle Scholar
- Mayagaya VS, Nkwengulila G, Lyimo IN, Kihonda J, Mtambala H, Ngonyani H, et al. The impact of livestock on the abundance, resting behaviour and sporozoite rate of malaria vectors in southern Tanzania. Malar J. 2015;14:17.View ArticlePubMedPubMed CentralGoogle Scholar
- Lwetoijera DW, Harris C, Kiware SS, Dongus S, Devine GJ, McCall PJ, et al. Increasing role of Anopheles funestus and Anopheles arabiensis in malaria transmission in the Kilombero Valley, Tanzania. Malar J. 2014;13:331.View ArticlePubMedPubMed CentralGoogle Scholar
- PlusZap: Insect control. http://insect-o-cutor.co.uk/telerikfiles/Insect-O-Cutor%20Catalogue%20300112%20-%20PlusZap.pdf (2000).
- Sanford MR, Demirci B, Marsden CD, Lee Y, Cornel AJ, Lanzaro GC. Morphological differentiation may mediate mate-choice between incipient species of Anopheles gambiae s.s. PLoS One. 2011;6:e27920.View ArticlePubMedPubMed CentralGoogle Scholar
- Mnyone LL, Lyimo IN, Lwetoijera DW, Mpingwa MW, Nchimbi N, Hancock PA, et al. Exploiting the behaviour of wild malaria vectors to achieve high infection with fungal biocontrol agents. Malar J. 2012;11:87.View ArticlePubMedPubMed CentralGoogle Scholar
- Scott JA, Brogdon WG, Collins FH. Identification of single specimens of the Anopheles gambiae complex by the polymerase chain reaction. Am J Trop Med Hyg. 1993;49:520–9.PubMedGoogle Scholar
- Crawley MJ. The R book. Int Stat Rev. 2007;75:425–6.View ArticleGoogle Scholar
- Skaug H, Fournier D, Bolker B, Magnusson A, Nielsen A. glmmADMB: generalized linear mixed models using AD Model Builder. R package version 0.7.0. http://glmmadmbr-forger-project.org (2011).
- Altman DG, Bland JM. Measurement in medicine: the analysis of method comparison studies. The Stat. 1983;32:307–17.Google Scholar
- Seyoum A, Sikaala CH, Chanda J, Chinula D, Ntamatungiro AJ, Hawela M, et al. Human exposure to anopheline mosquitoes occurs primarily indoors, even for users of insecticide-treated nets in Luangwa Valley, South-east Zambia. Parasit Vectors. 2012;5:101.View ArticlePubMedPubMed CentralGoogle Scholar
- Huho B, Briet O, Seyoum A, Sikaala C, Bayoh N, Gimnig J, et al. Consistently high estimates for the proportion of human exposure to malaria vector populations occurring indoors in rural Africa. Int J Epidemiol. 2013;42:235–47.View ArticlePubMedPubMed CentralGoogle Scholar
- Govella NJ, Okumu FO, Killeen GF. Insecticide-treated nets can reduce malaria transmission by mosquitoes which feed outdoors. Am J Trop Med Hyg. 2010;82:415–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Killeen GF, Kihonda J, Lyimo E, Oketch FR, Kotas ME, Mathenge E, et al. Quantifying behavioural interactions between humans and mosquitoes: evaluating the protective efficacy of insecticidal nets against malaria transmission in rural Tanzania. BMC Infect Dis. 2006;6:161.View ArticlePubMedPubMed CentralGoogle Scholar
- Kenneth HL. Cuticular hydrocarbons of locusta, schistocerca, and Periplaneta, and their role in waterproofing. Insect Biochem. 1976;6:457–472.Google Scholar
- Sikaala CH, Killeen GF, Chanda J, Chinula D, Miller JM, Russell TL, et al. Evaluation of alternative mosquito sampling methods for malaria vectors in Lowland South-East Zambia. Parasit Vectors. 2013;6:91.View ArticlePubMedPubMed CentralGoogle Scholar
- Lorenz LM, Keane A, Moore JD, Munk CJ, Seeholzer L, Mseka A, et al. Taxis assays measure directional movement of mosquitoes to olfactory cues. Parasit Vectors. 2013;6:131.View ArticlePubMedPubMed CentralGoogle Scholar
- Carde RT. Multi-cue integration: how female mosquitoes locate a human host. Curr Biol. 2015;25:R793–5.View ArticlePubMedGoogle Scholar
- van Breugel F, Riffell J, Fairhall A, Dickinson MH. Mosquitoes use vision to associate odor plumes with thermal targets. Curr Biol. 2015;25:2123–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Briet OJ, Huho BJ, Gimnig JE, Bayoh N, Seyoum A, Sikaala CH, et al. Applications and limitations of Centers for Disease Control and Prevention miniature light traps for measuring biting densities of African malaria vector populations: a pooled-analysis of 13 comparisons with human landing catches. Malar J. 2015;14:247.View ArticlePubMedPubMed CentralGoogle Scholar
- Sikulu M, Govella NJ, Ogoma SB, Mpangile J, Kambi SH, Kannady K, et al. Comparative evaluation of the Ifakara tent trap-B, the standardized resting boxes and the human landing catch for sampling malaria vectors and other mosquitoes in urban Dar es Salaam, Tanzania. Malar J. 2009;8:197.View ArticlePubMedPubMed CentralGoogle Scholar
- Bayoh MN, Walker ED, Kosgei J, Ombok M, Olang GB, Githeko AK, et al. Persistently high estimates of late night, indoor exposure to malaria vectors despite high coverage of insecticide treated nets. Parasit Vectors. 2014;7:380.View ArticlePubMedGoogle Scholar
- Cooke MK, Kahindi SC, Oriango RM, Owaga C, Ayoma E, Mabuka D, et al. ‘A bite before bed’: exposure to malaria vectors outside the times of net use in the highlands of western Kenya. Malar J. 2015;14:259.View ArticlePubMedPubMed CentralGoogle Scholar
- Clifford DF. Electric shock. The electronics handbook edn. Boca Raton: CRC Press; 2005.Google Scholar