Human landing catches provide a useful measure of protective efficacy for the evaluation of volatile pyrethroid spatial repellents

Parasites & Vectors volume 16, Article number: 90 (2023) Cite this article

774 Accesses

1 Citations

2 Altmetric

Metrics details

The human landing catch (HLC) method, in which human volunteers collect mosquitoes that land on them before they can bite, is used to quantify human exposure to mosquito vectors of disease. Comparing HLCs in the presence and absence of interventions such as repellents is often used to measure protective efficacy (PE). Some repellents have multiple actions, including feeding inhibition, whereby mosquitoes may be unable to bite even if they land on a host. A comparison was made between the PE of the volatile pyrethroid spatial repellent (VPSR) transfluthrin determined using a landing method (HLC) and a biting method (allowing the mosquitoes that landed to blood-feed) to evaluate whether HLC is a suitable method for the estimation of the personal PE of a VPSR.

A fully balanced, two-arm crossover design study was conducted using a 6 × 6 × 2-m netted cage within a semi-field system. Hessian strips (4 m × 0.1 m) treated with a 5-, 10-, 15-, or 20-g dose of transfluthrin were evaluated against a paired negative control for three strains of laboratory-reared Anopheles and Aedes aegypti mosquitoes. Six replicates were performed per dose using either the landing or the biting method. The number of recaptured mosquitoes was analysed by negative binomial regression, and the PEs calculated using the two methods were compared by Bland–Altman plots.

For Anopheles, fewer mosquitoes blood-fed in the biting arm than landed in the landing arm (incidence rate ratio = 0.87, 95% confidence interval 0.81–0.93, P < 0.001). For Ae. aegypti, biting was overestimated by around 37% with the landing method (incidence rate ratio = 0.63, 95% confidence interval 0.57–0.70, P = 0.001). However, the PEs calculated for each method were in close agreement when tested by the Bland Altman plot.

The HLC method led to underestimation of mosquito feeding inhibition as a mode of action of transfluthrin, and there were species- and dose-dependent differences in the relationship between landing and biting. However, the estimated PEs were similar between the two methods. The results of this study indicate that HLC can be used as a proxy for personal PE for the evaluation of a VPSR, especially when the difficulties associated with enumerating blood-fed mosquitoes in a field setting are taken into consideration.

Appropriate and effective vector control tools are integral components of mosquito-borne disease control programs worldwide [1]. However, incomplete coverage and poor compliance of vector control interventions remain major challenges in the control of malaria [2] and arbovirus vectors [3]. In addition, some malaria and arbovirus vector species are not completely controlled by current insecticidal tools because they are either behaviourally resistant (they avoid contact with insecticides through outdoor biting or resting, or biting during the day) or physiologically resistant (they can survive contact with an insecticide) [4, 5]. The most efficient vectors of malaria and arboviruses are highly adapted to humans (synanthropic) and are therefore most commonly encountered around human dwellings, either indoors [6] or in the peridomestic space [7]. The former has been a major target location for malaria control for the last three decades through the use of insecticide-treated nets and indoor residual spraying [8], but targeting indoor spaces only is insufficient for the elimination of malaria in many sub-Saharan Africa regions [9]. Therefore, also targeting the peridomestic space with vector control interventions for outdoor biting mosquitoes is more effective as a strategy because many people in these regions spend an extensive amount of time outdoors for domestic activities, where they are unprotected against biting mosquitoes, which may explain residual malaria transmission in these areas [10]. Ideally, novel control interventions deployed in the peridomestic space should prevent bites and kill mosquitoes to provide both personal and community protection for users and non-users of the space [11]. The efficacy of volatile pyrethroid spatial repellents (VPSRs) as a means of protection against mosquitoes in the peridomestic space remains an unanswered research question, and robust methods for their evaluation in this setting are needed.

The semi-field system (SFS) was developed to evaluate the efficacy of vector control tools in a controlled disease-free environment [12]. This bioassay provides a convenient alternative method for the evaluation of vector control tools, and avoids some of the difficulties associated with field trials, such as variation in mosquito density, and the size and layout of houses [13]. SFS has been used to demonstrate the efficacy of VPSRs [14, 15] through the measurement of multiple outcomes, including blood-feeding inhibition, delayed resumption of feeding (disarming), delayed mortality, deterrence and fecundity reduction [16]. However, to maximize the precision of measurement of some endpoints, such as blood-feeding inhibition and delayed mortality, it is necessary to recapture all of the mosquitoes that may be encountered during an intervention. The Ifakara large ambient chamber test (I-LACT) is a large cage fitted inside an SFS with an area that approximates that of a typical peridomestic space, and was designed to improve the recapture of released mosquitoes. Outdoor vector control tools with multiple actions that impact mosquito feeding, and induce sublethal incapacitation or delayed mortality, may be more accurately assessed by using the I-LACT.

The human landing catch (HLC) method is a procedure whereby human volunteers catch mosquitoes that land on them before they bite, by using a mouth aspirator [17]. This procedure is usually used to estimate the protective efficacy (PE) of bite prevention interventions, such as repellents [18,19,20]. Repellents, particularly volatile pyrethroids, exhibit various modes of action, including interference with mosquito olfaction so that not all mosquitoes that land on a host are able to bite. Thus, HLC may underestimate the full PE of a bite-prevention intervention that modulates mosquito host perception [21] or blood-feeding behaviour [22]. Therefore, a comparison of PE of the VPSR transfluthrin was conducted in an I-LACT using either HLC (hereafter ‘landing’) or by allowing mosquitoes to freely interact with a volunteer and blood-feed on them (hereafter ‘biting’).

The I-LACT in which the experiment was conducted is a polyester net cage measuring 6 × 6 × 2 m fixed inside an SFS located at the Ifakara Health Institute, Bagamoyo-Kingani, Tanzania (Fig. 1). The I-LACT dimensions represent the approximate size of the peridomestic space around rural Tanzanian homes, where most domestic activity occurs [23]. This bioassay was designed to ensure the maximum recovery of released mosquitoes for the evaluation of vector control tools. Preliminary experiments have shown that the recapture rate for the I-LACT is approximately 90%, whereas that of the standard SFS compartment is approximately 60%. The lower recapture rate in the SFS is due to its high roof and textured surfaces, which make it difficult to reach and see all released mosquitoes. The sides and roof of the I-LACT are made of polyester netting, to allow airflow, both floor and netting are white coloured to facilitate mosquito collection after exposure as mosquitoes can be easily seen against the white background. The compartment is sealed with a zip to prevent mosquito escape, and is kept free of mosquito predators through daily clearing of spiders and the use of sugar baits spiked with boric acid to minimize scavenging ants. The I-LACT enables controlled experiments with the simultaneous release of multiple laboratory mosquito strains to be carried out. In addition, as laboratory-reared mosquitoes are disease-free, conducting these experiments with blood-feeding endpoints is considered safe. For the experiment reported here, two I-LACTs were used, one for the treatments and one for the controls.

Photograph and diagram showing the semi-field system with an Ifakara large ambient chamber test (I-LACT; 6 × 6 × 2 m) in each compartment

Four strains of laboratory-reared mosquitoes were used in the experiments: the fully pyrethroid-susceptible Anopheles gambiae sensu stricto (s.s.) Ifakara strain; the pyrethroid-resistant (knock-down resistance; KDR) Anopheles gambiae s.s. Kisumu strain; the pyrethroid-resistant (metabolic resistance) Anopheles funestus FUMOZ strain; and the pyrethroid-susceptible Aedes aegypti Bagamoyo strain (Table 1). Colonies of these strains are maintained according to MR4 guidelines [24]. The larvae are fed on TetraMin fish flakes (Tetra, UK), and adults on 10% sugar ad libitum; females are membrane-fed cow's blood for egg production. The colonies are maintained under approximately 12-h:12-h light:dark (natural light) at 27 ± 5 °C and 70 ± 30% relative humidity (RH).

Nulliparous 3–8 day-old mosquitoes were used for the experiments. Mosquitoes were selected by placing a hand near to their cage, and those that attempted to aggressively bite were aspirated into paper cups. When two mosquito strains of similar morphology were released simultaneously, red fluorescent pigment (Swada, Cheshire, UK) was used to mark the individuals of one of the strains so that the strains could be distinguished between. Mosquitoes were marked by dusting the mesh lid of the cup with a brush to create a cloud of pigment that was deposited onto the mosquitoes. After marking, the mosquitoes were aspirated into 10 × 10 × 10-cm release cages. The mosquitoes were transferred from the insectary to the SFS in a black cloth bag to prevent them from being damaged by the wind. Aedes mosquitoes were sugar starved for 12 h and Anopheles mosquitoes for 6 h prior to commencement of the experiments, to maximise their avidity without inducing excess mortality. Before each experiment, the mosquitoes were acclimatized for 45 min in the corridor of the SFS, which is separated from the experimental space by polyurethane sheeting to prevent the mosquitoes from coming into contact with the tested insecticides.

Physiological susceptibility tests for transfluthrin were conducted for each mosquito strain before the start of semi-field experiments. The tests were performed using tube test bioassays following World Health Organization (WHO) guidelines [25]. As there is no recommended discriminating dose of transfluthrin for testing the susceptibility status of these mosquitoes, transfluthrin-impregnated papers at the doses proposed by Sukkanon et al. [26] were used. Five serial dilutions of emulsifiable concentrate (EC) were prepared by mixing with acetone and silicone oil in individual Falcon tubes. The concentrations of EC transfluthrin were 0.00125%, 0.0025%, 0.005%, 0.01%, 0.02%, 0.04%, 0.08% and 0.1% for Anopheles, and 0.003125%, 0.00625%, 0.125%, 0.025%, 0.05% and 0.1% for Ae. aegypti. Whatman grade 1 filter papers (12 × 15 cm; Whatman International, Banbury, UK) were prepared by impregnation with the concentrations of EC transfluthrin. For each filter paper, 2 ml of diluted EC transfluthrin was used. The impregnated papers were air-dried in the shade at ambient temperature, then wrapped in aluminium foil and refrigerated at 4 °C before use in the tests that were carried out on the same day. The papers were destroyed after the experiment.

One hundred and fifty non-blood-fed, 3–5-day-old mosquitoes were exposed to the transfluthrin-treated paper or to the control for 1 h. The mosquitoes were then provided with 10% sucrose solution and maintained at approximately 27 °C and 80% RH for the determination of 24 h mortality. Each dilution was tested four times.

The discriminating concentration (DC) for Anopheles (Table 4) was used to test the susceptibility status of An. gambiae (Kisumu strain; KDR) and An. funestus (FUMOZ strain). The same procedure was used as in the susceptibility test, and the same numbers of mosquitoes were exposed to the transfluthrin-treated paper as per the obtained DC.

Hessian sacks (made from fibre of Corchorus olitorius) were purchased locally, washed using detergent powder (OMO) and water, and dried under direct sunlight. A concentration series of EC transfluthrin (Bayothrin EC; Bayer, Monheim am Rhein, Germany) was prepared. Eave-positioned targeted insecticide (EPTI) emanators comprising 4 m × 0.1 m strips of hessian treated with 5 g, 10 g, 15 g, or 20 g of transfluthrin [27] were used for the experiments with Anopheles. For Aedes mosquitoes, freestanding transfluthrin passive emanators (FTPEs) [28] comprising 5 m × 0.1 m hessian strips treated with the same four doses of transfluthrin were used. Negative controls were prepared in the same way with water.

A fully balanced cross-over dose–response experiment was conducted using two I-LACT chambers of the SFS, one for the treatment and one for the control, whereby mosquitoes could interact with the human volunteers (Fig. 2). As previous experiments did not show any difference in the numbers of mosquitoes collected between the chambers, the treated and untreated emanators were fixed to the respective chambers for the duration of the experiment to avoid any potential contamination. Each experimental day, one replicate for biting and one for landing was conducted with the same volunteers. A replicate comprised 1 h of exposure to either the treatment (transfluthrin) or the negative control. To simulate an outdoor peridomestic setting, biting or landing was conducted 2 m from the end inside the I-LACT (Fig. 3). Four doses of transfluthrin-treated emanators (5 g, 10 g, 15 g and 20 g) were evaluated consecutively. Each dose was tested for six replicates, after which the emanator with the next highest concentration of transfluthrin was used.

Flow chart showing the various iterations of the experiments conducted in this study

Schematic representation of the I-LACT used for the experiments. a Setup of the experiment with transfluthrin-impregnated eave-positioned targeted insecticide (EPTI) strips against Anopheles mosquitoes. b Setup of the experiment with freestanding transfluthrin passive emanators (FTPE) against Aedes aegypti

Two male volunteers aged 25–40 years were recruited by written informed consent. The volunteers were non-smokers and non-alcohol drinkers, and did not use perfumed cosmetics prior to the experiment to minimize heterogeneity in their attraction to mosquitoes [29]. To standardize the area available to the mosquitoes for biting (knees and ankles), the volunteers wore closed shoes and a bug jacket (Fig. 3). The volunteers were rotated between compartments (treatments) after each experimental day (one day for landing and the following day for biting) to account for differential attractiveness to mosquitoes between individuals [30]. Temperature and humidity were recorded inside one of the I-LACT using a Tiny Tag Gemini Data Logger (Chichester, West Sussex, UK). To ensure transfluthrin vaporization, the experiments were conducted at temperatures above 23 ºC [31].

On each experimental day, the treatment and control were allocated to one of the two chambers of the I-LACT 45 min before the experiment commenced, to allow emanation of the transfluthrin to have started before the experiment began. The experiment started when the volunteer sat down on the chair and the mosquitoes were released into the chamber of the I-LACT from the release cages, which were opened by pulling a string (Fig. 3).

The primary outcome was recaptured mosquitoes, which was measured as number of HLC with the landing method, and number of blood-fed mosquitoes with the biting method. The secondary outcome was PE, which was measured by comparison of the number of recaptured mosquitoes relative to those of the corresponding control.

To simulate placement on an eave, the EPTIs were mounted at the top of metal stands measuring 1.6 × 1.6 × 2 m, which were placed inside the cage at 2 m from the volunteer who was seated in front of the cage (Fig. 3). A total of 60 mosquitoes comprising 20 mosquitoes of each of three strains—pyrethroid-resistant An. gambiae s.s. (Kisumu strain; KDR), pyrethroid-susceptible An. gambiae s.s. (Ifakara strain), and An. funestus (FUMOZ strain)—were released per replicate (Fig. 2). On each day of the experiment, one replicate (using the landing or biting method) was conducted between 1830 and 1930 hours, followed by a second replicate, which was conducted between 2030 and 2130 hours. The methods, i.e. landing or biting, were alternated after every three replicates, to ensure that possible differences in host-seeking response of the mosquitoes due to their circadian rhythms could be accounted for.

Two FTPE were positioned on the ground at 2.5-m distance either side of the volunteer and at 2 m from the back of the chamber (Fig. 3). Fifty pyrethroid-susceptible Ae. aegypti mosquitoes (Bagamoyo strain) were then released into the chamber (Fig. 2). A total of three replicates for the biting experiment and three for the landing method were conducted over 3 consecutive days, between 0630 and 0730 hours for the former and between 0830 and 0930 hours for the latter. This order was switched for the remaining 3 experimental days, with the landing method conducted first to control for temporal bias when comparing the results of the two methods, which could have been affected by temperature and mosquito circadian rhythm.

On each day of the experiments, one volunteer was assigned to either the treatment or the control chamber. During the experiments, the volunteer sat on a chair and the mosquitoes were allowed to fly freely and feed in the area between the knee and the ankle [32]. At the end of the period of exposure, the mosquitoes were collected from within the netting chamber for 45–60 min. All knocked-down and resting mosquitoes were located (head torches were used for this at night) and aspirated from the floor and walls of the I-LACT chamber, using mouth aspirators, and then placed in paper cups, with no more than 25 mosquitoes per cup to minimize the mortality that can occur when mosquitoes interact with one another at high densities. The mosquitoes were immediately transported to the insectary and scored as fed or unfed.

On each day of the experiments, one volunteer was assigned to either the treatment or the control chamber. Volunteers assigned to the control were not allowed to enter the treated compartment for any reason before the experiment commenced. The volunteers gently aspirated the mosquitoes that landed on them in the area between the knee and ankle by using mouth aspirators (HLC method). These mosquitoes were placed into a paper cup; a fresh cup was used after every 15-min collection period. After each 15-min collection period, the paper cups were placed in a sealed plastic container to avoid exposure of the mosquitoes to transfluthrin; thus, the mosquitoes were effectively removed from the experiment upon collection. The experiment ended after 1 h, and any remaining mosquitoes were collected by aspiration and placed into cups. All the cups containing mosquitoes were transported to the insectary for counting and recording other data. Head torches were worn to locate and collect Anopheles mosquitoes when experiments were conducted in the evening.

Data from the WHO susceptibility tests are reported as the mean percentage 24-h mortality of the four replicates. Probit regression analysis was used to calculate the DC for transfluthrin from the lethal dose (LD) required to kill 99% of mosquitoes (LD99), where the DC is equivalent to 2 × LD99.

Analyses of the experimental data were done in Stata 14 (Stata Corp) statistical software [33]. Descriptive analyses were conducted to generate the mean proportion of fed or landed mosquitoes with the respective 95% confidence interval (CI), which are presented in the graphs.

To compare biting and landing in the treatment and control, the number of mosquitoes caught using HLC in the landing experiment and the number of mosquitoes that fed in the biting experiment were merged to create a single variable named ‘recaptured’. Recaptured mosquitoes were modelled using negative binomial probability distributions with the logit link function. The collection method (landing vs biting), treatment, dose, volunteer, and mosquito species were treated as independent categorical fixed effects. Temperature and humidity were added to the model as continuous variables. The PE were calculated from the relative risk (RR), using the formula (1 − RR).

Also, the comparison of biting and landing mosquitoes at different doses was assessed using negative binomial probability distributions with the logit link function. The number of fed or landed mosquitoes, treatment, dose, volunteer, and mosquito species were treated as independent categorical fixed effects. Temperature and humidity were added to the model as continuous variables. The PE were calculated from the RR using the formula (1 − RR).

Additionally, for comparison between the biting and landing methods, Bland–Altman plots were used to assess the agreement of the PE measured by the two collection methods and to examine any systematic difference (fixed bias) between the measurements [26].

A clear dose–response was observed for mortality (Table 2). The final DC for each species was obtained by doubling the estimated LD99 (Table 3). The DC for An. gambiae (Ifakara strain) was 0.290%, while for Ae. aegypti it was 0.068%. An. gambiae (Kisumu strain: KDR) and An. funestus (FUMOZ strain) from the laboratory were fully susceptible to transfluthrin at DC 0.29% (> 98% mortality; Table 4).

During the experiments with Anopheles mosquitoes, the average temperature was 25.5 °C (24.5–27 °C) and the average RH 70.2% (61.7–76.1%). For the experiments with Aedes mosquitoes, the average temperature was 27.1 °C (25.7–28.5 °C) and the average RH 90.0% (89.0–90.8%). We were unable to measure the airflow inside the I-LACT chamber with the anemometer located at the site.

For all the experiments and all the mosquito strains, the rate of recapture in the I-LACT was higher than that usually observed for the entire compartment of the SFS. For Anopheles mosquitoes, recapture was 427/480 (89%) in the treatment and 453/480 (95%) in the control. For Ae. aegypti, recapture was 1445/1600 (90%) in the treatment and 1565/1600 (98%) in the control.

In the presence of transfluthrin, fewer female Anopheles mosquitoes (Ifakara, Kisumu and FUMOZ strains) were caught using the biting compared to the landing method [incidence rate ratio (IRR) = 0.82, 95% CI 0.74–0.91, P < 0.0001]. A similar, but less pronounced, difference was seen between the biting and the landing methods for the controls (IRR = 0.90, 95% CI 0.82–0.97, P < 0.001) (Table 5).

With respect to species effects (Fig. 4; Table 5), the overall proportion of mosquitoes caught when they were feeding was lower than that of mosquitoes recaptured by HLC for An. gambiae s.s. (IRR = 0.77, 95% CI 0.63–0.94, P < 0.01) and An. funestus (IRR = 0.75, 95% CI 0.63–0.89, P < 0.001). The data were not significantly different for An. gambiae s.s. (Kisumu strain) (IRR = 0.97, 95% CI 0.80–1.17, P > 0.05).

Proportion of recaptured mosquitoes using the HLC method or the biting method for all species and strains of mosquitoes used in this study

For Ae. aegypti mosquitoes, there was a greater overall difference in the proportion of recaptured mosquitoes between the biting and landing experiments (IRR = 0.63, 95% CI 0.57–0.70, P = 0.001). The results of the landing and biting experiments were significantly different both for the treatment (IRR = 0.56, 95% CI 0.46–0.67, P = 0.01) and the control (IRR = 0.70, 95% CI 0.64–0.76, P = 0.001) (Table 6).

The Bland–Altman plot (Fig. 5) of the PEs showed that there was consistent agreement in the results between the biting and landing methods. For Anopheles mosquitoes, the mean difference was −4.75, and the limits of agreement were between -25.57 and 16.07. While the overall difference in PE measured by landing was similar to that of biting, and there was no systematic bias between the methods, the limits of agreement were wide, indicating that precise estimates of feeding inhibition are not possible with the HLC method. The difference was reduced as the average measured PE of the intervention increased, indicating that the results of the two methods were more similar when the interventions were more efficacious (Fig. 5).

Bland–Altman comparison of protective efficacy determined through landing or biting methods

Overall, a clear dose response in PE was observed for all of the species for both of the methods. A higher PE was determined using the biting method compared to the landing method for An. gambiae s.s., An. funestus and Ae. aegypti; this difference was particularly pronounced for Ae. aegypti at low concentrations of transfluthrin. However, the relative difference decreased at higher transfluthrin concentrations, and when transfluthrin was applied at a dose of 20 g, there was no difference in the calculated PE between the methods for any of the species (Fig. 4).

The HLC method is the gold standard for the measurement of human exposure to vectors, and has been extensively used for the evaluation of different vector control tools [17]. The human landing rate gives an approximation of the number of mosquitoes that could bite one person at a particular time and place [34, 35]. For vector-borne pathogens, vector bites are critical for disease transmission, and these and daily mosquito mortality are the most important parameters for the determination of disease risk through mathematical modelling [36].

There was evidence that transfluthrin induced feeding inhibition, as the difference in biting compared to landing was greater in the transfluthrin arm than in the control arm at the lower doses. However, the PE measured by the landing method and the biting method broadly agreed across all the species and doses tested. Differences between the results of the methods were smallest at the highest (most effective) transfluthrin doses for Ae. aegypti and An. gambiae (Kisumu strain; KDR). While there were differences in the results between the landing and biting experiments, the Bland–Altman plots showed that there was good agreement between the PE measured by each method. We therefore suggest that HLCs are a reasonable proxy for bites, and can be used as a substitute for blood-feeding in field evaluation of transfluthrin to limit the risk of vector-borne disease transmission [37].

A higher proportion of Anopheles mosquitoes were caught with the landing method than with the biting method. This was also consistently the case for Ae. aegypti when the methods were compared across doses of transfluthrin. However, this difference was not as pronounced with An. gambiae Kisumu strain (KDR), which is a pyrethroid-resistant mosquito. However, this resistance does not greatly impact landing behaviour in the setting used here [27], thus, this lack of difference could have been due to chance. Further evaluation of landing versus biting methods are ongoing, using formulated products in semi-field and experimental hut experiments, to see if they confirm the findings of this study. The differences between biting and landing observed for other mosquito vectors in the presence of transfluthrin may be explained by behavioural modifications, in that mosquitoes may land but are inhibited from feeding due to sublethal effects on odour processing. Several studies have reported feeding inhibition induced by volatile pyrethroids [38, 39] and pyrethrum [40], and it has been hypothesized that the former interact with olfactory sensors and thus alter a mosquito's ability to feed [41]. Laboratory studies employing membrane feeding have also shown significant reductions in host-seeking behaviours (landing, probing, and blood-feeding) of Ae. aegypti exposed to transfluthrin passive emanators [42]. A recent study on caged Ae. aegypti, using metofluthrin passive emanators, showed a reduction in mosquito probing rates, used as a proxy for biting, which was dose-dependent [43].

The SFS provides a simulated user environment where the initial evaluation of both outdoors and indoor bite prevention interventions can be performed [44]. However, previous studies have shown that, when the whole compartment of the SFS is used, recapture of the released mosquitoes is below 100% [14, 45,46,47]. When some of the exposed mosquitoes are not recovered, they are therefore not accounted for in the statistical analysis, which may bias the results. The I-LACT was designed for the evaluation of outdoor vector control tools, particularly those with multiple actions beyond reducing mosquito landings, such as feeding inhibition, knock-down, and delayed mortality, in an attempt to address this problem.

The I-LACT has sides composed of netting that serves to equalize the climatic conditions between the inside and the outside of the chamber. Its ground area, 30 m2, represents that of a typical peridomestic space [23], the area within which the tested intervention would be deployed. Furthermore, the I-LACT is large enough to accommodate human volunteers, to allow human-mosquito interaction. This interaction is important as it mimics what happens during host searching, unlike the arm-in-cage experiment in which mosquitoes are placed close to an individual's arm [48], or where mosquitoes are confined to small cages [23] for the assessment of delayed mortality caused by insecticide exposure, which may bias results. For example, when mosquitoes are held in a space close to the emanator, their mortality will increase [49], and will likely be higher than that when they are free to fly away from the source of the insecticide. The I-LACT may also be a useful bioassay for the evaluation of other outdoor vector control tools which lead to multiple responses, including knock-down, mortality, and blood-feeding inhibition during host seeking. It also allows the use of consistently high numbers of disease-free mosquitoes in semi-field experiments to ensure that the statistical power is high.

Around 90% recapture of released mosquitoes was demonstrated with the I-LACT bioassay. This high recapture rate provides an opportunity to fully assess the multiple effects of volatile pyrethroids on exposed mosquitoes. Volatile pyrethroids exert several measurable outcomes on exposed mosquitoes, including repellence [50], blood-feeding inhibition [42], disarming [16], knock-down (sublethal incapacitation) [39], and mortality [39, 51]. Of these outcomes, only repellence can be appropriately evaluated by HLC, as only mosquitoes that land are taken into consideration in the analysis. Other outcomes such as mortality or knock-down may not be fully assessed by HLC [28, 45], as mosquitoes will spend more time in contact with the treated device while blood-feeding, which may increase mortality. Conversely, blood-fed mosquitoes show enhanced survival when exposed to pyrethroids [52]. While these additional endpoints are routinely assessed in experimental hut trials of pyrethroids that are applied to insecticide-treated nets [53] and correlate with the results of clinical trials, guidelines for ambient emanators and mosquito coils [54], as well as spatial repellents [55], mainly focus on mosquito landing. Measuring these additional endpoints is important for understanding the full impact of VPSRs when applied at scale, and may be used for mathematical modelling [56] to better understand target product profiles and entomological correlates of impact.

The importance of multiple endpoints of transfluthrin treatment beyond bite prevention alone was demonstrated in a randomised control trial (RCT) in Indonesia, where there was no significant protection from mosquito landings offered by transfluthrin emanators compared to the control, yet clinical cases of malaria were significantly reduced [57]. These findings suggest that there are some limitations to using only HLC to measure the efficacy of volatile pyrethroids in the field, and further endpoints should be evaluated in RCTs of volatile pyrethroids, including human blood index [58] as a proxy for blood-feeding inhibition, and population survival estimates as a proxy for mortality [59]. A recent cluster-randomised trial of a passive transfluthrin emanator in Iquitos, Peru demonstrated a reduction in arbovirus incidence as well as in Ae. aegypti abundance and proportion of blood-fed mosquitoes [60], suggesting the importance of mortality and blood-feeding inhibition for public health applications of volatile pyrethroids.

The I-LACT was used to carry out a dose–response experiment designed to compare the PEs of different doses of transfluthrin, as determined by using a landing or biting method. A short exposure time was used in the experiments to mimic real life, as mosquitoes are likely to be exposed to a treatment for only a short period of time before their behavioural responses are elicited [41]. There was no interaction between treatment and species, indicating that transfluthrin used at the concentrations in this experiment induced protection against all the mosquito species tested, regardless of their resistance mechanism, in agreement with previous work [27]. The calculated PE was similar between the landing and biting experiments. The findings from this study agree with those from a field study undertaken in Tanzania by Ogoma et al. [31], who showed that hessian strips treated with transfluthrin at doses of between 5 and 15 g reduced the number of mosquito landings in the peridomestic space similarly for several Anopheles vector species. These results indicate that, in an area where mosquitoes bite outdoors, fabric treated with the lower dose could be used to both protect humans from mosquito bites and provide community protection, while maximizing human safety. A consistent PE of 30% over a period of several months achieved with a product with a high compliance of use would confer greater protection than use of a product with a higher PE but a low compliance of use [61].

The PE of around 30% against Ae. aegypti and Anopheles achieved with transfluthrin at the lowest dose of 5 g in the present study was lower than the 60% estimated using hessian strips at the same dosage in a previous experiment, which was conducted using the landing method in the entire SFS compartment [27]. A PE of 60% was replicated in a field and semi-field experiment conducted in Kenya [47]. The difference in the PEs may be explained by the difference in volume between the I-LACT and the semi-field compartment. The volume of the I-LACT into which the mosquitoes were released was 75.6 m3, whereas the larger 1228-m3 volume of each semi-field compartment allowed the mosquitoes to move further away from the source of transfluthrin. Similarly, a study conducted to measure the PE of a topical repellent in the SFS (here considered to be a relatively small volume) and in the field (here considered to be a relatively large volume) reported a higher PE in the field trial [15]. These results indicate that it is likely that the chance of repeated biting by a mosquito in an area with a large volume are reduced because the mosquito may move away from the host after coming into contact with transfluthrin. This also suggests that, in a smaller space, inhibition of landing could be underestimated, and sublethal incapacitation and mortality could be overestimated, as the modes of action are dose dependent, with mortality occurring at higher doses or longer exposure time [22].

The PE was slightly higher for both the landing and biting methods for Aedes mosquitoes compared to Anopheles mosquitoes. These differences in protection may have been partly due to the differences in ambient temperature at the time that the two experiments were conducted. The ambient temperature was slightly lower (25 °C) in the night-time experiment with Anopheles mosquitoes than during the experiment conducted in the morning with Aedes mosquitoes (27 °C). However, these temperatures fall within the range, i.e. 21–30 °C, at which the effect of transfluthrin is optimal [31]. Future experiments should be designed to evaluate the efficacy of transfluthrin-treated emanators at different temperatures, and environmental conditions should always be taken into consideration in the analyses. Although the wind speed inside the SFS could not be measured in the present study because it was below the limit of detection of the anemometer used, it is possible that, under conditions of greater air movement and lower temperature, a lower PE would be achieved using the same type of emanator and dosages as used here. In some studies, more consistent evaporation of a volatile pyrethroid between replicates is achieved through the use of a fan [43], and consistency in the rate of evaporation of a tested pyrethroid is an important consideration for future trials of ambient emanators.

The feeding inhibition of An. gambiae s.s., An. funestus and Ae. aegypti mosquitoes in the presence of transfluthrin was underestimated by the HLC method, and the magnitude of the difference between landing and biting varied among the species and doses of transfluthrin tested in this study. The PE calculated for the landing or biting methods did not show any systematic bias, and was generally in agreement when tested with the Bland–Altman plot, with better agreement at higher concentrations of transfluthrin, which also afforded greater PE. Therefore, either method can be used to assess the personal PE of volatile pyrethroids, with the caveat that results may vary due to the stochasticity inherent to entomological experiments, with greater variability occurring when interventions provide lower efficacy. The findings reported here indicate that HLC can be used as a proxy of personal PE for the evaluation of volatile pyrethroids, especially when the difficulties associated with counting fed mosquitoes in a field setting are taken into account.

All data generated or analysed during this study are included in this published article and its additional file.

Confidence interval

Discriminating concentration

Emulsifiable concentrate

Eave-positioned targeted insecticide

Freestanding transfluthrin passive emanator

Human landing catch

Ifakara large ambient chamber test

Institutional Review Board

Protective efficacy

Relative humidity

Semi-field system

World Health Organization

Wilson AL, Courtenay O, Kelly-Hope LA, Scott TW, Takken W, Torr SJ, et al. The importance of vector control for the control and elimination of vector-borne diseases. PLoS Negl Trop Dis. 2020;14:e0007831.

Article CAS PubMed PubMed Central Google Scholar

World Health Organization. The world malaria report 2021. Geneva: World Health Organization; 2021.

Book Google Scholar

Achee NL, Grieco JP, Vatandoost H, Seixas G, Pinto J, Ching-Ng L, et al. Alternative strategies for mosquito-borne arbovirus control. PLoS Negl Trop Dis. 2019;13:e0006822.

Article PubMed PubMed Central Google Scholar

Russell TL, Govella NJ, Azizi S, Drakeley CJ, Kachur SP, et al. 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.

Article PubMed PubMed Central Google 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.

Article PubMed Google 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.

Article PubMed Google Scholar

Pollard EJM, MacLaren D, Russell TL, Burkot TR. Protecting the peri-domestic environment: the challenge for eliminating residual malaria. Sci Rep. 2020;10:7018.

Article CAS PubMed PubMed Central Google Scholar

Bhatt S, Weiss DJ, Cameron E, Bisanzio D, Mappin B, Dalrymple U, et al. The effect of malaria control on Plasmodium falciparum in Africa between 2000 and 2015. Nature. 2015;526:207–11.

Article CAS PubMed PubMed Central Google Scholar

World Health Organization. World malaria report. Geneva: World Health Organization; 2021.

Google Scholar

Monroe A, Asamoah O, Lam Y, Koenker H, Psychas P, Lynch M, et al. Outdoor-sleeping and other night-time activities in northern Ghana: implications for residual transmission and malaria prevention. Malar J. 2015;14:35.

Article PubMed PubMed Central Google Scholar

Magesa SM, Wilkes TJ, Mnzava AE, Njunwa KJ, Myamba J, Kivuyo MD, et al. Trial of pyrethroid impregnated bednets in an area of Tanzania holoendemic for malaria. Part 2. Effects on the malaria vector population. Acta Tropic. 1991;49:97–108.

Article CAS Google Scholar

Ferguson HM, Ng’habi KR, Walder T, Kadungula D, Moore SJ, Lyimo I, et al. Establishment of a large semi-field system for experimental study of African malaria vector ecology and control in Tanzania. Malar J. 2008;7:158.

Article PubMed PubMed Central Google 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.

Article CAS PubMed PubMed Central Google Scholar

Ogoma SB, Lorenz LM, Ngonyani H, Sangusangu R, Kitumbukile M, et al. An experimental hut study to quantify the effect of DDT and airborne pyrethroids on entomological parameters of malaria transmission. Malar J. 2014;13:131.

Article PubMed PubMed Central Google Scholar

Sangoro O, Lweitojera D, Simfukwe E, Ngonyani H, Mbeyela E, Lugiko D, et al. Use of a semi-field system to evaluate the efficacy of topical repellents under user conditions provides a disease exposure free technique comparable with field data. Malar J. 2014;13:159.

Article PubMed PubMed Central Google Scholar

Denz A, Njoroge MM, Tambwe MM, Champagne C, Okumu F, van Loon JJA, et al. Predicting the impact of outdoor vector control interventions on malaria transmission intensity from semi-field studies. Parasit Vectors. 2021;14:64.

Article PubMed PubMed Central Google 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.

Article PubMed PubMed Central Google Scholar

Andrés M, Lorenz LM, Mbeleya E, Moore SJ. Modified mosquito landing boxes dispensing transfluthrin provide effective protection against Anopheles arabiensis mosquitoes under simulated outdoor conditions in a semi-field system. Malar J. 2015;14:255.

Article PubMed PubMed Central Google Scholar

Mmbando AS, Ngowo HS, Kilalangongono M, Abbas S, Matowo NS, Moore SJ, et al. Small-scale field evaluation of push-pull system against early- and outdoor-biting malaria mosquitoes in an area of high pyrethroid resistance in Tanzania. Wellcome Open Res. 2017;2:112.

Article PubMed PubMed Central Google Scholar

Masalu JP, Finda M, Okumu FO, Minja EG, Mmbando AS, Sikulu-Lord MT, et al. Efficacy and user acceptability of transfluthrin-treated sisal and hessian decorations for protecting against mosquito bites in outdoor bars. Parasit Vectors. 2017;10:197.

Article PubMed PubMed Central Google Scholar

Afify A, Betz JF, Riabinina O, Lahondère C, Potter CJ. Commonly used insect repellents hide human odors from Anopheles mosquitoes. Curr Biol. 2019;29:3669-3680.e3665.

Article CAS PubMed PubMed Central Google Scholar

Bibbs CS, Kaufman PE. Volatile pyrethroids as a potential mosquito abatement tool: a review of pyrethroid-containing spatial repellents. J Integr Pest Manag. 2017;8:21–21.

Article Google Scholar

Masalu JP, Finda M, Killeen GF, Ngowo HS, Pinda PG, Okumu FO. Creating mosquito-free outdoor spaces using transfluthrin-treated chairs and ribbons. Malar J. 2020;19:109.

Article CAS PubMed PubMed Central Google Scholar

MR4: Methods in Anopheles Research Manual. 2019. https://www.beiresources.org/portals/2/MR4/MR4_Publications/Methods%20in%20Anopheles%20Research%202014/2014MethodsinAnophelesResearchManualFullVersionv2tso.pdf. Accessed 01 Mar 2023.

WHO. Standard operating procedure for testing insecticide susceptibility of adult mosquitoes in WHO bottle bioassays. Geneva: World Health Organization; 2022.

Sukkanon C, Bangs MJ, Nararak J, Hii J, Chareonviriyaphap T. Discriminating lethal concentrations for transfluthrin, a volatile pyrethroid compound for mosquito control in Thailand. J Am Mosq Control Assoc. 2019;35:258–66.

Article PubMed Google Scholar

Tambwe MM, Moore S, Hofer L, Kibondo UA, Saddler A. Transfluthrin eave-positioned targeted insecticide (EPTI) reduces human landing rate (HLR) of pyrethroid resistant and susceptible malaria vectors in a semi-field simulated peridomestic space. Malar J. 2021;20:357.

Article CAS PubMed PubMed Central Google Scholar

Tambwe MM, Moore SJ, Chilumba H, Swai JK, Moore JD, Stica C, et al. Semi-field evaluation of freestanding transfluthrin passive emanators and the BG sentinel trap as a "push-pull control strategy" against Aedes aegypti mosquitoes. Parasit Vectors. 2020;13:392.

Article CAS PubMed PubMed Central Google Scholar

Shirai O, Tsuda T, Kitagawa S, Naitoh K, Seki T, Kamimura K, et al. Alcohol ingestion stimulates mosquito attraction. J Am Mosq Control Assoc. 2002;18:91–6.

PubMed Google Scholar

Lindsay SW, Adiamah JH, Miller JE, Pleass RJ, Armstrong JR. Variation in attractiveness of human subjects to malaria mosquitoes (Diptera: Culicidae) in The Gambia. J Med Entomol. 1993;30:368–73.

Article CAS PubMed Google Scholar

Ogoma SB, Mmando AS, Swai JK, Horstmann S, Malone D, Killeen GF. A low technology emanator treated with the volatile pyrethroid transfluthrin confers long term protection against outdoor biting vectors of lymphatic filariasis, arboviruses and malaria. PLoS Negl Trop Dis. 2017;11:e0005455.

Article PubMed PubMed Central Google Scholar

World Health Organization, WHO pesticide evaluation scheme—2013—guidelines for efficacy testing of spatial repellents-annotated. Geneva: World Health Organization; 2013.

Google Scholar

StataCorp. Stata statistical software: release 16. College Station, TX: StataCorp LLC; 2019.

Google Scholar

Schoeler GB, Schleich SS, Manweiler SA, Sifuentes VL. Evaluation of surveillance devices for monitoring Aedes aegypti in an urban area of northeastern Peru. J Am Mosq Control Assoc. 2004;20:6–11.

PubMed Google Scholar

Briët 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.

Article PubMed PubMed Central Google Scholar

Wallace DI, Southworth BS, Shi X, Chipman JW, Githeko AK. A comparison of five malaria transmission models: benchmark tests and implications for disease control. Mal J. 2014;13:268.

Article Google Scholar

Harrington LC, Foy BD, Bangs MJ. Considerations for human blood-feeding and arthropod exposure in vector biology research: an essential tool for investigations and disease control. Vector Borne Zoonotic Dis. 2020;20:807–16.

Article PubMed PubMed Central Google Scholar

Ogoma SB, Ngonyani H, Simfukwe ET, Mseka A, Moore J, Maia MF, et al. The mode of action of spatial repellents and their impact on vectorial capacity of Anopheles gambiae sensu stricto. PLoS ONE. 2014;9:e110433.

Article PubMed PubMed Central Google Scholar

Ritchie SA, Devine GJ. Confusion, knock-down and kill of Aedes aegypti using metofluthrin in domestic settings: a powerful tool to prevent dengue transmission? Parasit Vectors. 2013;6:262.

Article PubMed PubMed Central Google Scholar

Smith A, Hudson EJ, Esozed S. Trials with pyrethrum mosquioto coils against Anopheles gambiae Gillies, Mansonia uniformis Theo. and Culex fatigans Wied. entering verandah-trap huts. Pyrethrum Post 1971:111–115.

Bibbs CS, Kaufman PE. Volatile pyrethroids as a potential mosquito abatement tool: a review of pyrethroid-containing spatial repellents. J Integr Pest Manag. 2017;8:1–10.

Article Google Scholar

McPhatter LP, Mischler PD, Webb MZ, Chauhan K, Lindroth EJ, Richardson AG, et al. Laboratory and semi-field evaluations of two (transfluthrin) spatial repellent devices against Aedes aegypti (L.) (Diptera: Culicidae). US Army Med Dep J 2017:13–22.

Darbro JM, Muzari MO, Giblin A, Adamczyk RM, Ritchie SA, Devine GJ. Reducing biting rates of Aedes aegypti with metofluthrin: investigations in time and space. Parasit Vectors. 2017;10:69.

Article PubMed PubMed Central Google Scholar

Tambwe MM, Swai JK, Moore SJ. Semi-field bioassays for the evaluation of spatial (and topical) arthropod repellents for indoor and outdoor use. In: Coats J, Corona C, Debboun M, editors. Advances in arthropod repellents. Amsterdam: Elsevier; 2021.

Google Scholar

Ponlawat A, Kankaew P, Chanaimongkol S, Pongsiri A, Richardson JH, Evans BP. Semi-field evaluation of metofluthrin-impregnated nets on host-seeking Aedes aegypti and Anopheles dirus. J Am Mosq Control Assoc. 2016;32:130–8.

Article PubMed Google Scholar

Sukkanon C, Tisgratog R, Muenworn V, Bangs MJ, Hii J, Chareonviriyaphap T. Field evaluation of a spatial repellent emanation vest for personal protection against outdoor biting mosquitoes. J Med Entomol. 2021;58:756–66.

Article CAS PubMed Google Scholar

Njoroge MM, Fillinger U, Saddler A, Moore S, Takken W, van Loon JJA, et al. Evaluating putative repellent "push" and attractive "pull" components for manipulating the odour orientation of host-seeking malaria vectors in the peri-domestic space. Parasit Vectors. 2021;14:42.

Article CAS PubMed PubMed Central Google Scholar

Colucci B, Müller P. Evaluation of standard field and laboratory methods to compare protection times of the topical repellents PMD and DEET. Sci Rep. 2018;8:12578.

Article PubMed PubMed Central Google Scholar

Martin NJ, Nam VS, Lover AA, Phong TV, Tu TC, Mendenhall IH. The impact of transfluthrin on the spatial repellency of the primary malaria mosquito vectors in Vietnam: Anopheles dirus and Anopheles minimus. Malar J. 2020;19:9.

Article PubMed PubMed Central Google Scholar

Achee NL, Masuoka P, Smith P, Martin N, Chareonviryiphap T, Polsomboon S, et al. Identifying the effective concentration for spatial repellency of the dengue vector Aedes aegypti. Parasit Vectors. 2012;5:300.

Article PubMed PubMed Central Google Scholar

Salazar FV, Achee NL, Grieco JP, Prabaripai A, Ojo TA, Eisen L, et al. Effect of Aedes aegypti exposure to spatial repellent chemicals on BG-Sentinel™ trap catches. Parasit Vectors. 2013;6:145.

Article CAS PubMed PubMed Central Google Scholar

Machani MG, Ochomo E, Sang D, Bonizzoni M, Zhou G, Githeko AK, et al. Influence of blood meal and age of mosquitoes on susceptibility to pyrethroids in Anopheles gambiae from western Kenya. Malar J. 2019;18:112.

Article PubMed PubMed Central Google Scholar

World Health Organization Pesticide Evaluation Scheme. Guidelines for laboratory and field testing of long-lasting insecticidal nets WHO/HTM/NTD/WHOPES/2013.3. Geneva: World Health Institution; 2013.

Google Scholar

World Health Organization Pesticide Evaluation Scheme. Guidelines for efficacy testing of household insecticide products: mosquito coils, vaporizer mats, liquid vaporizers ambient aerosolsWHO/HTM/NTD/WHOPES/2009.3. Geneva: World health Organization; 2009.

Google Scholar

World Health Organization. Guidelines for efficacy testing of spatial repellents. Geneva: World Health Organisation; 2013.

Google Scholar

Sherrard-Smith E, Ngufor C, Sanou A, Guelbeogo MW, N’Guessan R, Elobolobo E, et al. Inferring the epidemiological benefit of indoor vector control interventions against malaria from mosquito data. Nat Commun. 2022;13:3862.

Article CAS PubMed PubMed Central Google Scholar

Syafruddin D, Asih PBS, Rozi IE, Permana DH, Nur Hidayati AP, Syahrani L, et al. Efficacy of a spatial repellent for control of malaria in Indonesia: a cluster-randomized controlled trial. Am J Trop Med Hyg. 2020;103:344–58.

Article PubMed PubMed Central Google Scholar

Pappa V, Reddy M, Overgaard H, Abaga S, Caccone A. Estimation of the human blood index in malaria mosquito vectors in Equatorial Guinea after indoor antivector interventions. Am J Trop Med Hyg. 2011;84:598.

Article Google Scholar

Matthews J, Bethel A, Osei G. An overview of malarial Anopheles mosquito survival estimates in relation to methodology. Parasit Vectors. 2020;13:233.

Article PubMed PubMed Central Google Scholar

Morrison AC, Reiner RC, Elson WH, Astete H, Guevara C, del Aguila C, et al. Efficacy of a spatial repellent for control of Aedes-borne virus transmission: a cluster randomized trial in Iquitos, Peru. medRxiv. 2021;14:124.

Google Scholar

Kiszewski AE, Darling ST. Estimating a mosquito repellent's potential to reduce malaria in communities. J Vector Borne Dis. 2010;47:217–21.

CAS PubMed Google Scholar

Download references

We would like to thank Frank Tenywa and Athuman Kambagha for establishing the Aedes aegypti mosquito colony in the insectary for experimental use. Bayer Crop Protection kindly donated the transfluthrin used in these experiments. We thank the director general of the National Medical Research Institute for permission to publish this manuscript.

Ifakara Health Institute covered the costs of the experiments. The salaries of MMT, SJM and AS were funded through a grant from the Innovative Vector Control Consortium (IVCC). IVCC would like to acknowledge the Bill and Melinda Gates Foundation and UK Aid as the sources of funding for the push–pull project.

Vector Control Product Testing Unit, Ifakara Health Institute, P.O. Box 74, Bagamoyo, Tanzania

Mgeni Mohamed Tambwe, Ummi Abdul Kibondo, Olukayode Ganiu Odufuwa, Jason Moore, Ahmed Mpelepele, Rajabu Mashauri & Sarah Jane Moore

Department of Epidemiology and Public Health, Swiss Tropical and Public Health Institute, Kreuzstrasse 2, 4123, Allschwill, Basel, Switzerland

Mgeni Mohamed Tambwe, Olukayode Ganiu Odufuwa, Jason Moore & Sarah Jane Moore

University of Basel, Petersplatz 1, 4001, Basel, Switzerland

Mgeni Mohamed Tambwe, Olukayode Ganiu Odufuwa, Jason Moore & Sarah Jane Moore

Telethon Kids Institute, Perth, Australia

Adam Saddler

London School of Hygiene and Tropical Medicine, Keppel Street, London, WC1E 7HT, UK

Olukayode Ganiu Odufuwa

Nelson Mandela African Institution of Science and Technology (NM-AIST), P.O. Box 447, Tengeru, Tanzania

Sarah Jane Moore

You can also search for this author in PubMed Google Scholar

MMT and SJM: conceived and designed the study. MMT and RM: supervised the semi-field experiment, volunteers, and data collection, and performed the susceptibility test. MMT, AS, UAK and SJM: analysed the data. MMT: drafted the manuscript. AS, OGO and SJM: revised the manuscript. MMT and JDM: designed the FTPE and the I-LACT. All the authors read and approved the final manuscript.

Correspondence to Mgeni Mohamed Tambwe.

The volunteers that participated in this experiment were Ifakara Health Institute employees, trained and skilled in mosquito collection. They were recruited voluntarily through written informed consent after the risks and benefits of the study, and their right to withdraw from the study at any point without any consequences, were clearly explained to them. All the mosquitoes used in this experiment were laboratory-reared and free from arboviral diseases. The study was approved by the Ifakara Health Institute Review Board (certificate no. 024-2016) and the National Institute for Medical Research, Tanzania (certificate NIMR/HQ/R.8a/Vol.IX/2381).

The authors declare that they have no competing interests. SJM, UA and OGO conduct contracted product evaluation of various types of vector control tools, including volatile pyrethroids.

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

Tambwe, M.M., Kibondo, U.A., Odufuwa, O.G. et al. Human landing catches provide a useful measure of protective efficacy for the evaluation of volatile pyrethroid spatial repellents. Parasites Vectors 16, 90 (2023). https://doi.org/10.1186/s13071-023-05685-5

Download citation

Received: 12 October 2022

Accepted: 25 January 2023

Published: 07 March 2023

DOI: https://doi.org/10.1186/s13071-023-05685-5

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative