Skip to main content

Creating mosquito-free outdoor spaces using transfluthrin-treated chairs and ribbons



Residents of malaria-endemic communities spend several hours outdoors performing different activities, e.g. cooking, story-telling or eating, thereby exposing themselves to potentially-infectious mosquitoes. This compromises effectiveness of indoor interventions, notably long-lasting insecticide-treated nets (LLINs) and indoor residual spraying (IRS). This study characterized common peri-domestic spaces in rural south-eastern Tanzania, and assessed protective efficacy against mosquitoes of hessian fabric mats and ribbons treated with the spatial repellent, transfluthrin, and fitted to chairs and outdoor kitchens, respectively.


Two hundred households were surveyed, and their most-used peri-domestic spaces physically characterized. Protective efficacies of locally-made transfluthrin-emanating chairs and hessian ribbons were tested in outdoor environments of 28 households in dry and wet seasons, using volunteer-occupied exposure-free double net traps. CDC light traps were used to estimate host-seeking mosquito densities within open-structure outdoor kitchens. Field-collected Anopheles arabiensis and Anopheles funestus mosquitoes were exposed underneath the chairs to estimate 24 h-mortality. Finally, The World Health Organization insecticide susceptibility tests were conducted on wild-caught Anopheles from the villages.


Approximately half (52%) of houses had verandas. Aside from these verandas, most houses also had peri-domestic spaces where residents stayed most times (67% of houses with verandas and 94% of non-veranda houses). Two-thirds of these spaces were sited under trees, and only one third (34.4%) were built-up. The outdoor structures were usually makeshift kitchens having roofs and partial walls. Transfluthrin-treated chairs reduced outdoor-biting An. arabiensis densities by 70–85%, while transfluthrin-treated hessian ribbons fitted to the outdoor kitchens caused 77–81% reduction in the general peri-domestic area. Almost all the field-collected An. arabiensis (99.4%) and An. funestus (100%) exposed under transfluthrin-treated chairs died. The An. arabiensis were susceptible to non-pyrethroids (pirimiphos methyl and bendiocarb), but resistant to pyrethroids commonly used on LLINs (deltamethrin and permethrin).


Most houses had actively-used peri-domestic outdoor spaces where exposure to mosquitoes occurred. The transfluthrin-treated chairs and ribbons reduced outdoor-biting malaria vectors in these peri-domestic spaces, and also elicited significant mortality among pyrethroid-resistant field-caught malaria vectors. These two new prototype formats for transfluthrin emanators, if developed further, may constitute new options for complementing LLINs and IRS with outdoor protection against malaria and other mosquito-borne pathogens in areas where peri-domestic human activities are common.


Since 2000, malaria morbidity and mortality have tremendously declined in sub-Saharan Africa [1,2,3,4], though the recent evidence suggests that such gains are starting to stagnate [3,4,5]. Most of the gains observed between 2000 and 2015 were estimated to have been contributed by the existing core indoor vector control interventions, i.e. insecticide-treated nets (ITNs) and indoor residual spraying (IRS) [2, 6,7,8]. Long-lasting insecticide-treated nets (LLINs) and IRS are effective against indoor-biting and indoor-resting mosquitoes, but are less effective against outdoor-biting mosquitoes, which are important vectors of residual malaria transmission [9,10,11,12]. It has been estimated that the Anopheles bites not preventable by LLINs could be causing up to 10 million additional malaria cases annually [12]. As a result, LLINs and IRS require complimentary interventions to achieve the 2030 global targets of reducing malaria burden by at least 90% and elimination in 35 endemic countries [13].

In many malaria-endemic communities, people spend several hours cooking, eating and socializing outdoors in the early evenings before they go to sleep, and also in the early mornings after they wake up [14], when malaria vectors may be active and mediating transmission [11]. Some of these outdoor activities, as well as sleeping outdoors [15], are partly attributable to warm climate [16], but they also have strong cultural determinants [17]. The importance of outdoor malaria transmission, and associated outdoor human activities, are now well-established [9, 10, 14, 17]. However, there are still gaps regarding appropriate interventions to address these gaps. The characteristics of the peri-domestic spaces where households conduct outdoor activities remain poorly documented, despite being essential for designing, creating and testing interventions to complement LLINs and IRS by protecting such outdoor spaces.

Several intervention options have been proposed as candidates for closing these malaria transmission gaps [18]. Examples include: (a) outdoor-baited traps [19, 20], (b) attractive targeted sugar baits [21], (c) pyrethroid-treated clothing [22, 23], zooprophylaxis [24] and repellents [25] among others. Topical repellents applied on human skin are widely available for personal protection in some areas. However, commercial formulations of government-sectioned scale-up campaigns of such topical repellents are limited because they protect only individual users [26], have low user compliance rates and acceptance [27,28,29], and have only short-term efficacy [30]. They are also expensive for repeated use by the low-income populations at greatest risk.

In contrast, spatial repellents are volatile insecticides that diffuse into the air as vapour, and may protect multiple people within the surrounding space against outdoor-biting malaria vectors [31,32,33,34,35]. In recent years, several versions and delivery formats have been developed, which allow wide-area protection of multiple persons without repeated application for several months [31,32,33,34, 36, 37]. In particular, a wide range of transfluthrin emanator prototypes based on treated hessian fabric products have been recently developed that protect indoor and outdoor spaces for several months without repeated reapplication [31,32,33,34, 36, 37]. Transfluthrin also has additional properties beyond just spatial repellency that include toxicity to mosquitoes, and incapacitation that prevents blood-feeding, which could contribute to community-wide mass effects, even for non-users [37, 38].

Improved understanding of the peri-domestic spaces coupled with new interventions that can be effective in such spaces, could potentially address current challenges related with exposure to outdoor-biting exposure and transmission risk. This study was, therefore, aimed at addressing two key knowledge gaps by: (a) characterizing the common peri-domestic spaces used by communities in rural south-eastern Tanzania for various outdoor activities, and, (b) assessing the protective efficacies of two recently-developed hessian-based transfluthrin-emanator prototypes, specifically transfluthrin-treated chairs and transfluthrin-treated hessian ribbons wrapped around outdoor kitchens, against outdoor-biting malaria vectors and other pathogens-carrying mosquitoes in those peri-domestic spaces.


Study area

The study was implemented in Lupiro village (8.385° S, 36.670° E) (Fig. 1), in the Kilombero valley, south-eastern Tanzania. Households were selected from four sub-villages namely: (a) Ndoro; (b) Libaratula; (c) Mabatini and (d) Lupiro Kati. Most residents here were peasants, cultivating rice, maize and other crops. Houses have brick or mud walls, and metal (corrugated iron sheets) or grass-thatched roofs. Annual rainfall is 1200–1600 mm, and temperatures range between 20.0 and 32.6 °C [39, 40]. Principal malaria vectors in this area are Anopheles funestus and Anopheles arabiensis with the former contributing over 80% of transmission [41]. Both An. arabiensis and An. funestus populations in the area have been shown to be resistant to multiple public health insecticides including pyrethroids, carbamates and organochlorides [41,42,43]. LLINs are the main malaria prevention method, most of which are distributed by the government [44].

Fig. 1
figure 1

Illustration of the location of Ulanga and Kilombero districts in the map of Tanzania (a), the location of Lupiro village in Ulanga district (b) and household location in Lupiro village showing both surveyed and those did not (c)

Characterization of the peri-domestic spaces

Two hundred (200) households were surveyed, including 50 from each sub-village (Fig. 1), selected via stratified random sampling. Data were collected using electronic tablets using KoboCollect™, an open access software programmed using Open Data Kit (ODK) [45]. Trained research teams were assigned to each sub-village. Written informed consent was obtained from each of the 200 households. For each household, the peri-domestic spaces were observed directly to characterize them physically based on use, physical site and whether they were built-up or not. Digital pictures were taken of the different peri-domestic environments. The research team also administered survey questions to the household heads to capture: (a) identification information such as age, (b) education level, (c) socio-economic data including source of income, possession of radio, television, cell phone among others, (d) information on peri-domestic spaces such as presence of other peridomestic spaces apart from veranda, and (e) their usage, presence of peri-domestic spaces if the house had no veranda and their usage.

The peri-domestic spaces were classified as either: (a) built-up spaces attached to the main houses, i.e. veranda extensions; (b) built-up spaces not attached to the main houses, e.g. separate kitchens, and (c) non-built-up or other peri-domestic spaces commonly used for various outdoor activities. The outdoor built up structures were also characterized based on the roofing and wall types.

Transfluthrin-treated chairs and hessian ribbons

For the dry season experiment, six identical chairs made of wood and metal frame were constructed by a local carpenter while for the wet season experiment 15 chairs were made (Fig. 2a, b). The chairs were fitted underneath with four standardized hessian fabric mats: two measuring 42 cm × 43 cm and fitted underneath the right and left sides of the chair and other two measuring 20 cm × 33 cm, which were fitted underneath the middle part of the chair (Fig. 2c). These mats were made by a local seamstress at the Ifakara Health Institute fabrication facility (the MozzieHouse). The hessian mats had been treated in emulsified solutions containing 2% transfluthrin (Bayer AG, Germany), prepared as previously described [31, 33].

Fig. 2
figure 2

Design and prototyping of the wooden chairs at the local carpentry (a), overview of the prototyped chair (b), fitting transfluthrin-treated hessian mat underneath the chair (c), one transfluthrin-treated chair with the DN-Mini trap positioned 0.5 m (d), two transfluthrin-treated chairs with DN-Mini trap installed 0.5 m (e); and outdoor kitchen fitted with transfluthrin-treated sisal ribbon with DM-Mini trap positioned 1.2 m (f)

Similarly, the hessian ribbons were prepared as previously described by Mmbando et al. [36]. Each ribbon had 15 cm width and 10 m length, and were also made locally at the MozzieHouse. More detailed descriptions of the hessian ribbons have previously been published by Ogoma et al. [31] and Mmbando et al. [36]. The ribbons were also treated in a 2% emulsified solution of transfluthrin as previously described [36].

Assessing protective efficacies of transfluthrin-treated chairs and ribbons

This assessment was conducted in two seasons: dry and wet seasons, between September to October 2019 and between January to February 2020 as dry and wet seasons, respectively. Following the characterization of the peri-domestic spaces as described above, eight households with outdoor kitchens were selected for a small-scale assessment of protective efficacies of the two candidate interventions in the dry season. The houses were paired and assigned as follows: (a) a control arm, where neither transfluthrin-treated chairs nor transfluthrin-treated ribbons were used, (b) a treatment arm where one transfluthrin-treated chair was used, (c) a second treatment arm where two transfluthrin-treated chairs were used, and (d) a third treatment arm where transfluthrin-treated hessian ribbons were used around the outdoor kitchens. In each arm, two houses were enrolled.

One consenting adult male volunteer was assigned to each household, to sit inside the exposure-free miniaturized double nets trap (DN-Mini) [46] from 1900 to 2300 h. The volunteer spent 45 min each hour retrieving all host-seeking mosquitoes caught in the DN-Mini while attempting to bite him. For the households with transfluthrin-emanating chairs, the DN-Mini was installed 0.5 m from the chairs (Fig. 2d, e). For households with transfluthrin-treated hessian ribbons, the ribbon was fitted 1.3 m above ground (Fig. 2f) onto the outdoor kitchens. CDC light traps [47] were suspended inside these makeshift kitchens to collect host-seeking mosquitoes nightly, while DN-Mini traps were set beside the kitchens to assess biting risk in the general peri-domestic space (Fig. 2f).

Each treatment arm was initially located in two houses per experimental night, but was rotated between the houses using a 4 × 4 Latin square design over 32 experimental nights, so that each treatment or control arm was tested at each of the eight houses four times. The primary outcome was number of mosquitoes of different species caught in the DN-Mini or the CDC light traps per house per night. All treated materials were carefully shifted between the houses to avoid any contamination during the rotations. As the experiments were conducted outdoors with enough airflow, there was no need to break for wash out. Instead, a control set up was used to monitor mortality of mosquitoes as described in the sub-section below. Each morning the collected mosquitoes were sorted and identified using morphological keys [48]. In the wet season, 20 households were enrolled making five households in each arm for other 32 nights. The same procedure was adopted as described in dry season.

Assessing mortality effects of the transfluthrin-treated chairs on mosquitoes

This assay was done using three different groups of mosquitoes, as follows: (a) field-collected An. arabiensis and An. funestus of unknown age, which are known to be pyrethroid resistant in this setting [41,42,43], (b) laboratory-reared An. arabiensis from a pyrethroid-susceptible colony of local origin, and (c) laboratory-reared Aedes aegypti from a pyrethroid-susceptible colony of local origin [49].

The wild-caught An. arabiensis females were collected using a separate set of eight DN-Mini traps [46] set outdoors at households without any transfluthrin treatments. Eight consenting adult male volunteers were involved in these collections each night from 1900 h to 0100 h. As population densities of An. funestus in this study area were very low, CDC light traps were used to collect adult females of this species from another village (Tulizamoyo (− 8.3669, 36.7336)) approximately 30 km away.

Each morning captured mosquitoes were sorted and An. arabiensis and An. funestus females separated in two cages containing 100 mosquitoes per species (four cages in total). Since the Anopheles gambiae sensu lato (s.l.) in this area are known to consist exclusively of An. arabiensis [33], no molecular identification was required. Similarly, since indoor collections of An. funestus s.l. have consistently been found to be > 90% An. funestus sensu stricto [50], it was assumed that these were the dominant species in the collections. The separated mosquitoes were kept at a field insectary (average temperature: 26.75 ± 0.09 °C; relative humidity: 73.26 ± 0.46%) for acclimatization for at least 20 h before testing the next evening.

For the tests, two chairs were placed within open verandas of two separate houses. One of the chairs was fitted underneath with transfluthrin-treated hessian mats, while the other was fitted with an untreated hessian mat (control). The caged mosquitoes were placed underneath each chair overnight (1900 h to 0700 h). A simple water moat was used to prevent ants from eating the mosquitoes. Each morning, the cages were returned to the field insectary and monitored for further 12 h, totaling 24 h of observation since start of exposure. This procedure was repeated 10 times (totaling 1140 mosquitoes) for field-collected An. arabiensis and five times (totaling 490 mosquitoes) for field-collected An. funestus tested in control and treated arms.

Similar tests were conducted using cages containing 100 laboratory-reared An. arabiensis or 100 laboratory-reared Ae. aegypti. Since Ae. aegypti mosquitoes are active during the day, they were exposed from 0800 to 1900 h each day, as opposed to the Anopheles mosquitoes, which were exposed at night. Percentage mortality of mosquitoes was calculated for each species separately as a proportion of total exposed.

Testing susceptibility of local malaria vector populations to common public health pesticides

In order to determine phenotypic resistance status of local mosquito populations to common pesticides, standard discriminatory tests were performed using standard WHO susceptibility bioassays [51]. Since transfluthrin is a pyrethroid, the tests also provided indication of how the transfluthrin-based interventions evaluated here (transfluthrin-treated chairs and transfluthrin-treated hessian ribbons) evaluated here would perform against wild pyrethroid-resistant mosquito populations. The susceptibility tests were done for: (a) 0.1% bendiocarb, a carbamate; (b) 4.0% dichlorodiphenyltrichloroethane (DDT), an organochloride; (c) 0.25% pirimiphos methyl, an organophosphate, (d) 0.75% permethrin, a type I pyrethroid; and (e) 0.05% deltamethrin, a type II pyrethroid.

Female An. arabiensis mosquitoes were collected from nearby rice fields as larvae, and reared to emergence at Ifakara Health Institute vector biology laboratory, the VectorSphere. The susceptibility tests were done using 3-day old adult females, using at least 100 mosquitoes per test (25 per replicate), with at least 4 replicates as described in the recent WHO guidelines [51].

Data analysis

The survey data was summarized in ODK analysis module [45] to generate descriptive statistics of peri-domestic spaces and their usage. Data on efficacy of the transfluthrin-treated chairs and ribbons was analysed using R open-source statistical software [52], primarily using generalized linear mixed-effects models [53], each time modelling the numbers of mosquitoes of a given species caught as a function of the treatments (fixed factors), and fitting the data onto Poisson distributions. Volunteer ID, day and house ID were included as random factors in the models.


Characteristics of households

The demographic characteristics of household heads, and physical characteristics of all the 200 houses visited are summarized in Table 1. Most of the household heads were female (128/200). The main construction materials were bricks for the walls (153/200) and corrugated iron sheets for the roofs (140/200). Full details are found in Table 1.

Table 1 Characteristics of the study participants and their houses in 200 surveyed households in Lupiro village, Ulanga District, south-eastern Tanzania

Characteristics of the peri-domestic spaces

Table 2 provides a summary of the physical characteristics of peri-domestic spaces where residents spent time outdoors in the evenings before bedtime. Of the 200 households observed, 52% (103/200) had built-up veranda (Fig. 3a), while 48% (97/200) did not have these verandas.

Table 2 Peridomestic space characteristic of the households surveyed in Lupiro village, Ulanga district, south-eastern Tanzania
Fig. 3
figure 3

Illustration of houses with veranda extension physically characterized during survey (a), houses with built-up peridomestic space away from the main house commonly used for cooking (b) and houses with non-built-up peridomestic space physically characterized as under the tree (c)

It was also observed that other than these verandas (Fig. 3a), most houses had additional peri-domestic spaces where members congregated. Of the 103 that had verandas, 69 (67%) also had other active peri-domestic spaces, of which 23 were built-up structures and 46, were non-built up. These structures all had at least physical roofing, and 70% of them also had no wall. Two thirds of the built-up structures were used as outdoor kitchens (60% used for cooking) as shown in Fig. 3b. Many of the non-built structures (63%) were sited under trees (Fig. 3c), while 35% were in open spaces. The peri-domestic spaces were used for multiple activities, e.g. cooking, eating, socializing among others.

Of 97 houses that did not have veranda extensions, 91 (93.8%) had active peri-domestic spaces, of which 32 had built up structures with roofs, and also walls in one-third of the cases. Of the non-built structures, 42% were under trees. Common uses of these spaces were similar, i.e. resting, cooking, eating.

Overall collected mosquitoes

In the dry season, the total number of mosquitoes collected was 4960, including 2604 Culex spp.; 2264 Anopheles gambiae s.l.; 80 Anopheles coustani; 6 An. funestus; 4 Mansonia spp.; and 2 Coquilettidia mosquitoes. Polymererase chain reaction (PCR) was conducted on 81 samples of An. gambiae s.l. to distinguish between sibling species. Of the 90.1% (73/81) successfully amplified in the PCR assays, all (100%) were identified as An. arabiensis. In the wet season the total number of mosquitoes collected was 14,303, including 12,224 Culex spp.; 1978 An. gambiae s.l.; 42 An. funestus; 37 Mansonia spp.; 15 Ae. aegypti; 6 An. coustani; and 1 Anopheles pharoensis. No molecular assay was conducted to identify mosquito species in this particular season.

Efficacy of transfluthrin-treated chairs and transfluthrin-treated hessian ribbons against outdoor-biting mosquitoes in the peri-domestic spaces

Findings on protective efficacy of the two interventions are summarized in Tables 3 and 4. Using two transfluthrin-treated chairs significantly reduced outdoor-biting An. arabiensis mosquitoes by 76% (Relative rate (RR) = 0.24, 95% confidence interval, CI 0.19–0.29, P < 0.001) and by 85% (RR = 0.15, 95% CI 0.12–0.18, P < 0.001) in dry and wet seasons, respectively. Using one transfluthrin-treated chair also significantly reduced An. arabiensis mosquitoes, in this case by 70% (RR = 0.30, 95% CI 0.25–0.37, P < 0.001) and by 75% (RR = 0.25, 95% CI 0.20–0.31, P < 0.001) in dry and wet seasons. When the densities of Culex mosquitoes were assessed, both the two-chair and one-chair interventions significantly reduced outdoor-biting, achieving 52% (RR = 0.48, CI 0.37–0.63, P < 0.001) and 58% (RR = 0.42, 95% CI 0.31–0.56, P < 0.001) protection, in dry and wet seasons, respectively. In the wet season, both the two-chair and one-chair interventions significantly reduced outdoor-biting, achieving 51% (RR = 0.49, CI 0.43–0.56, P < 0.001) and 40% (RR = 0.60, 95% CI 0.53–0.68, P < 0.001) protection.

Table 3 Comparison of nightly outdoor biting per person between houses with or without transfluthrin-treated chairs or ribbons (dry season)
Table 4 Comparison of nightly outdoor biting per person between houses with or without transfluthrin-treated chairs or ribbons (wet season)

Fitting the transfluthrin-treated hessian ribbons around the outdoor kitchens reduced outdoor-biting An. arabiensis by 81% in the area immediately outside this kitchen enclosure (RR = 0.19, 95% CI 0.16–0.24, P < 0.001), and by 43% (RR = 0.57, CI 0.32–1.03, P = 0.065) inside the enclosures in the dry season. In the wet season, transfluthrin-treated hessian ribbons reduced outdoor-biting An. arabiensis by 77% in the area immediately outside this kitchen enclosure (RR = 0.23, 95% CI 0.18–0.28, P < 0.001). The ribbons also reduced outdoor-biting Culex by 68% (RR = 0.32, CI 0.24–0.43, P < 0.001) near the enclosures and by 77% (RR = 0.23, CI 0.12–0.43, P < 0.001) within the enclosures in the dry season. In the wet season, the ribbons also reduced outdoor-biting Culex by 36% (RR = 0.64, CI 0.56–0.72, P < 0.001) near the enclosures and by 48% (RR = 0.52, CI 0.32–0.86, P < 0.001) within the enclosures.

Mortality of field-collected or laboratory-reared mosquitoes exposed to transfluthrin-treated chairs

Findings on induced mortality of mosquitoes exposed to transfluthrin-treated chairs are summarized in Table 5. When field-collected An. arabiensis females and An. funestus females were exposed underneath the transfluthrin-treated chairs, 99.4% and 100% of them died within 24 h, respectively. All (100%) of the laboratory-reared An. arabiensis or laboratory-reared Ae. aegypti mosquitoes exposed also died when exposed underneath the transfluthrin-treated chairs. Mortality of the mosquitoes exposed to untreated chairs however remained low (5.2% for field-collected An. arabiensis, 0.0% for field-collected An. funestus, 0.1% for laboratory-reared An. arabiensis and 1.1% for laboratory-reared Ae. aegypti).

Table 5 Comparison of induced mortality to mosquitoes exposed to house with or without transfluthrin-treated chairs

Insecticide resistance status of mosquitoes in a study area

Results of the WHO resistance tests are summarized in Table 6. The field populations of An. arabiensis were fully susceptible to bendiocarb (100% mortality), pirimiphos methyl (100% mortality) and DDT (98.8% mortality). However, they were resistant to both permethrin (94.7% mortality) and deltamethrin (80.3% mortality).

Table 6 Show insecticide resistant status in Anopheles arabiensis mosquitoes to difference insecticides at Lupiro village


Several studies in tropical settings have documented that many people stay active outdoors in early evenings before they go indoors and then sleep under bed nets [14, 16, 17]. Those studies also characterized the actual activities that people were involved in outdoors. To our knowledge, this current study is the first to characterize the peri-domestic spaces used by household members in a malaria-endemic setting for various outdoor activities.

The key finding was that most houses had active peri-domestic spaces (veranda extensions, open general areas and makeshift kitchens) where household members performed different activities, usually unprotected from potentially-infectious mosquitoes before they went indoors. In some of the peri-domestic spaces, residents constructed structures for cooking, eating and socializing, but these too were often open and not protective against mosquito bites (Fig. 3b).

The study also demonstrated that the two simple interventions evaluated, i.e. transfluthrin-emanating chairs and ribbons both considerably reduced outdoor-biting by the important residual malaria vector, An. arabiensis. Furthermore, mosquitoes exposed to the chairs were killed rapidly, indicating that the interventions could offer not just personal or household protection, but also communal protection through mass killing effect, by reducing mosquito density, survival and malaria sporozoite infection prevalence [37].

More than half the households surveyed had veranda extensions with roofed enclosures, mostly used for resting, cooking and eating. All these structures provide opportunities for mounting simple interventions in these spaces such as physical screening and complementary chemical measures like these transfluthrin emanator formats and turning them into mosquito proof areas as they are predominantly used for early-evening human activities, notably resting, cooking and eating.

The findings that transfluthrin-emanating chairs provided useful levels of protection against An. arabiensis and Culex spp. corroborate previous observations with other prototypes in outdoor bars [33]. Even though the prototype (chair) used in this study differs to those used in previous studies (decoration) [33], it emphasizes the potential of these technologies for outdoor protection in such communities. Further research should therefore focus on improvement of the prototypes and optimization of the treatments.

Outdoor kitchens were commonly used for cooking in early evening, and were among the commonest constructed spaces identified in households, regardless of whether they had verandas or not. Early-evening cooking within this space coincides with peak hours of mosquito bites [54], amplifying the likelihood of malaria transmission in these spaces. In this study, the high levels of protection provided against An. arabiensis by the repellent-treated hessian ribbons around these outdoor kitchens is, therefore, encouraging and consistent with previous studies [34], which demonstrated that transfluthrin-treated hessian ribbons protected non-users against An. arabiensis sitting within radius of 5 metres. More recently, transfluthrin-treated ribbons fitted to the eaves of houses prevented both indoor and outdoor-biting mosquitoes [31, 36, 37]. Since the increase in temperature also increases the rate of transfluthrin evaporation, the cooking activity within the kitchen may have increased insecticidal activity of transfluthrin. The effect of temperature was also well described by Ogoma et al. [34]. This high level of protection provided against An. arabiensis by the ribbons may have been positively influenced by cooking activities within these enclosures.

In addition to the substantial protection against An. arabiensis demonstrated in the areas immediately outside the ribbon-fitted kitchen, the catches by CDC light traps placed within the kitchens are reduced, albeit more modestly. This modest reduction may be due to the use of CDC light traps in these open spaces, which may have resulted in exaggerated catches of mosquitoes attracted by the light bulb in the traps. It may also be due to the smoke produced from these kitchens, which may have confounded the results observed on An. arabiensis. Interestingly, this emanator prototype provided much more satisfactory protection against nuisance-causing Culex spp. within the kitchens based on the same CDC light trap catches. It is not clear why such significant reductions observed for Culex spp. were not observed for An. arabiensis, but it is nevertheless encouraging that reduced Culex spp. densities should motivate user acceptance. It is also encouraging that these observations are also broadly consistent with previous studies [31, 32] demonstrating that outdoor use of transfluthrin-treated hessian provided more than 90% protection against both An. gambiae s.l. and Culex spp. mosquitoes [31, 32].

Pyrethroid-treated nets divert host-seeking mosquitoes from humans or kill the mosquitoes attempting to feed on the protected persons [55, 56]. With these modes of action, pyrethroid-treated nets not only provide personal protection (to users), but also communal protection (to both users and non-users) by suppressing vectors population through the mass killing effect [57, 58]. Transfluthrin, used to treat the hessian mats fitted underneath the chairs induced high mortality on caged mosquitoes exposed underneath the experimental chairs (100% in most cases). This implies that the chairs may not only provide personal protection, but also community benefit through mass-killing of mosquitoes, even without the mosquitoes making contact with treated surfaces. This effect was particularly important since the field-collected mosquitoes were from villages where Anopheles populations were pyrethroid-resistant (Table 6).

To date, there is no literature which explains the best exposure time for mosquitoes in transfluthrin-treated material that achieves 50% mortality. However, Ogoma et al. [38, 59] demonstrated that even short exposures of 15 min reduced mosquito blood feeding significantly. In this current study, the selection of exposure time was based on what period a particular mosquito species is active. For the day-biting mosquitoes, a day-time exposure was selected and for night-time biting species a night-time exposure was selected.

Even though excito-repellency effects maximize person protection by chasing mosquitoes away, it may attenuate more important mass killing effects by deterring mosquitoes from making fatal contact with lethal doses of the repellent insecticide itself or with complementary solid-phase insecticides applied as LLINs or IRS [60,61,62]. However, these observations of mortality amongst wild malaria vectors exposed to transfluthrin suggest that mass population suppression could be achieved even without mosquitoes necessarily touching treated surfaces. It is also encouraging that Ogoma et al. [34] demonstrated that transfluthrin-treated emanator provided more than 90% biting reduction against An. arabiensis without any obvious diversion to non-users [34]. Another study by Ogoma et al. [38] also observed that transfluthrin-treated coils could protect non-users within 20 m radius. More recently, Mwanga et al. demonstrated that transfluthrin-treated ribbons fitted to the eave gaps of houses protected volunteers both inside and outside the houses [37].

The spread of pyrethroid resistance in malaria vectors clearly compromises ongoing control and elimination efforts [63,64,65]. This is a key concern since transfluthrin is also a pyrethroid. It is however encouraging that transfluthrin-based interventions tested here killed almost 100% of the wild-caught An. arabiensis and An. funestus exposed to emanated vapour from the chairs, even though local populations of both species are clearly resistant to the conventional solid-phase pyrethoids used for LLINs and IRS [41]. It was surprising that transfluthrin, a pyrethroid, was still efficacious against pyrethroid-resistant malaria mosquitoes. However, given that there is no standard resistance test against transfluthrin, it is difficult to explain as to why transfluthrin demonstrated such high mortality. One possible explanation is the long exposure of up to 12 h underneath the transfluthrin-treated chairs. Tests with PBO have established that the resistance in this area is of metabolic nature, thus it may be helpful that these new interventions are considered as complementary to other interventions, e.g. IRS or LLINs using active ingredients not affected by this form of resistance.

Usage of chairs cut across different settings, such as normal households, public places, official surroundings used for resting after working hours (Fig. 4). Based on this information, the use of transfluthrin-treated chairs may be rolled out as a complementary vector control strategy even during dengue fever outbreak.

Fig. 4
figure 4

Picture of the first mosquito-free zone established at Ifakara Health Institute in January 2020. The chairs have transfluthrin-treated hessian mats underneath, but are layered with plastic sheeting to prevent rainfall and user contact

One important limitation of this study was that caged mosquitoes were placed underneath the transfluthrin-treated chairs for 12 h. This long-time exposure may well greatly exceed true exposure levels in the field, where mosquitoes can freely fly around and way upon encountering airborne insecticide. Nonetheless, since transfluthrin effects are vapor-mediated, this initial attempt to quantify possible lethal modes of action is encouraging and offers a basis for future improvements in study designs for developing and evaluating these technologies.


Most houses in this rural African context had well-used peri-domestic spaces (veranda extensions, makeshift kitchens and completely open spaces) where members performed different activities before bed time, usually unprotected from potentially-infectious mosquitoes before they went indoors. Both the transfluthrin-emanating chairs and ribbons reduced outdoor exposure to biting malaria vectors in these peri-domestic spaces and also caused significant mortality of caged, field collected malaria vector mosquitoes. The two emanator prototypes still require additional improvements, optimizations and assessments in future studies, but they could potentially constitute new options for outdoor malaria prevention to complement LLINs and IRS in areas where peri-domestic human activities are common.

Availability of data and materials

Not applicable.



Center of disease control


Confidence interval


Generalized linear mixed effects model


Indoor residual spraying


Ifakara Health Institute


Institutional Review Board


Long-lasting insecticidal nets


National Institute for Medical Research


Polymerase chain reaction


Relative rate


  1. WHO. World malaria report 2015. Geneva: World Health Organization; 2015.

    Google Scholar 

  2. 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 

  3. WHO. World malaria report 2018. Geneva: World Health Organization; 2018.

    Google Scholar 

  4. WHO. Word malaria report 2017. Geneva: World Health Organization; 2017.

    Google Scholar 

  5. WHO. World malaria report 2019. Geneva: World Health Organization; 2019.

    Google Scholar 

  6. Noor AM, Kinyoki DK, Mundia CW, Kabaria CW, Mutua JW, Alegana VA, et al. The changing risk of Plasmodium falciparum malaria infection in Africa: 2000–10: a spatial and temporal analysis of transmission intensity. Lancet. 2014;383:1739–47.

    Article  PubMed  PubMed Central  Google Scholar 

  7. O’Meara WP, Mangeni JN, Steketee R, Greenwood B. Changes in the burden of malaria in sub-Saharan Africa. Lancet Infect Dis. 2010;10:545–55.

    Article  PubMed  Google Scholar 

  8. Steketee RW, Campbell CC. Impact of national malaria control scale-up programmes in Africa: magnitude and attribution of effects. Malar J. 2010;9:299.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Govella NJ, Ferguson H. Why use of interventions targeting outdoor biting mosquitoes will be necessary to achieve malaria elimination. Front Physiol. 2012;3:199.

    Article  PubMed  PubMed Central  Google Scholar 

  10. 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.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Durnez L, Coosemans M. Residual transmission of malaria: an old issue for new approaches. In: Manguin S, editor. Anopheles mosquitoes: new insight into malaria vectors. London: IntechOpen; 2013.

    Google Scholar 

  12. Sherrard-Smith E, Skarp JE, Beale AD, Fornadel C, Norris LC, Moore SJ, et al. Mosquito feeding behavior and how it influences residual malaria transmission across Africa. Proc Natl Acad Sci USA. 2019;116:15086–95.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. WHO. Global technical strategy for malaria 2016–2030. Geneva: World Health Organization; 2015.

    Google Scholar 

  14. Monroe A, Moore S, Koenker H, Lynch M, Ricotta E. Measuring and characterizing night time human behaviour as it relates to residual malaria transmission in sub-Saharan Africa: a review of the published literature. Malar J. 2019;18:6.

    Article  PubMed  PubMed Central  Google Scholar 

  15. 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 

  16. Moshi IR, Ngowo H, Dillip A, Msellemu D, Madumla EP, Okumu FO, et al. Community perceptions on outdoor malaria transmission in Kilombero Valley, Southern Tanzania. Malar J. 2017;16:274.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Finda MF, Moshi IR, Monroe A, Limwagu AJ, Nyoni AP, Swai JK, et al. Linking human behaviours and malaria vector biting risk in south-eastern Tanzania. PLoS ONE. 2019;14:e0217414.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Williams YA, Tusting LS, Hocini S, Graves PM, Killeen GF, Kleinschmidt I, et al. Expanding the vector control toolbox for malaria elimination: a systematic review of the evidence. Adv Parasitol. 2018;99:345–79.

    Article  PubMed  Google Scholar 

  19. Homan T, Hiscox A, Mweresa CK, Masiga D, Mukabana WR, Oria P, et al. The effect of mass mosquito trapping on malaria transmission and disease burden (SolarMal): a stepped-wedge cluster-randomised trial. Lancet. 2016;388:1193–201.

    Article  PubMed  Google Scholar 

  20. Okumu FO, Govella NJ, Moore SJ, Chitnis N, Killeen GF. Potential benefits, limitations and target product-profiles of odor-baited mosquito traps for malaria control in Africa. PLoS ONE. 2010;5:e11573.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Müller GC, Beier JC, Traore SF, Toure MB, Traore MM, Bah S, et al. Successful field trial of attractive toxic sugar bait (ATSB) plant-spraying methods against malaria vectors in the Anopheles gambiae complex in Mali, West Africa. Malar J. 2010;9:210.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Crawshaw AF, Maung TM, Shafique M, Sint N, Nicholas S, Li MS, et al. Acceptability of insecticide-treated clothing for malaria prevention among migrant rubber tappers in Myanmar: a cluster-randomized non-inferiority crossover trial. Malar J. 2017;16:92.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Rowland M, Durrani N, Hewitt S, Mohammed N, Bouma M, Carneiro I, et al. Permethrin-treated chaddars and top-sheets: appropriate technology for protection against malaria in Afghanistan and other complex emergencies. Trans R Soc Trop Med Hyg. 1999;93:465–72.

    Article  CAS  PubMed  Google Scholar 

  24. Rowland M, Durrani N, Kenward M, Mohammed N, Urahman H, Hewitt S. Control of malaria in Pakistan by applying deltamethrin insecticide to cattle: a community-randomised trial. Lancet. 2001;357:1837–41.

    Article  CAS  PubMed  Google Scholar 

  25. Gupta RK, Rutledge LC. Role of repellents in vector control and disease prevention. Am J Trop Med Hyg. 1994;50:82–6.

    Article  CAS  PubMed  Google Scholar 

  26. Moore SJ, Davies CR, Hill N, Cameron MM. Are mosquitoes diverted from repellent-using individuals to non-users? Results of a field study in Bolivia. Trop Med Int Health. 2007;2:532–9.

    Article  Google Scholar 

  27. Maia MF, Kliner M, Richardson M, Lengeler C, Moore SJ. Mosquito repellents for malaria prevention. Cochrane Database Syst Rev. 2018;2:CD011595.

    PubMed  Google Scholar 

  28. Gryseels C, Uk S, Sluydts V, Durnez L, Phoeuk P, Suon S, et al. Factors influencing the use of topical repellents: implications for the effectiveness of malaria elimination strategies. Sci Rep. 2015;5:16847.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Makungu C, Stephen S, Kumburu S, Govella NJ, Dongus S, Hildon ZJ-L, et al. Informing new or improved vector control tools for reducing the malaria burden in Tanzania: a qualitative exploration of perceptions of mosquitoes and methods for their control among the residents of Dar es Salaam. Malar J. 2017;16:410.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Sangoro O, Kelly AH, Mtali S, Moore SJ. Feasibility of repellent use in a context of increasing outdoor transmission: a qualitative study in rural Tanzania. Malar J. 2014;13:347.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Ogoma SB, Ngonyani H, Simfukwe ET, Mseka A, Moore J, Killeen GF. Spatial repellency of transfluthrin-treated hessian strips against laboratory-reared Anopheles arabiensis mosquitoes in a semi-field tunnel cage. Parasit Vectors. 2012;5:54.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Govella NJ, Ogoma SB, Paliga J, Chaki PP, Killeen G. Impregnating hessian strips with the volatile pyrethroid transfluthrin prevents outdoor exposure to vectors of malaria and lymphatic filariasis in urban Dar es Salaam, Tanzania. Parasit Vectors. 2015;8:322.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  33. 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  CAS  PubMed  PubMed Central  Google Scholar 

  34. 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  CAS  PubMed  PubMed Central  Google Scholar 

  35. Achee NL, Bangs MJ, Farlow R, Killeen GF, Lindsay S, Logan JG, et al. Spatial repellents: from discovery and development to evidence-based validation. Malar J. 2012;11:164.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Mmbando AS, Ngowo H, Limwagu A, Kilalangongono M, Kifungo K, Okumu FO. Eave ribbons treated with the spatial repellent, transfluthrin, can effectively protect against indoor-biting and outdoor-biting malaria mosquitoes. Malar J. 2018;17:368.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Mwanga EP, Mmbando AS, Mrosso PC, Stica C, Mapua SA, Finda MF, et al. Eave ribbons treated with transfluthrin can protect both users and non-users against malaria vectors. Malar J. 2019;18:314.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. 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  CAS  PubMed  PubMed Central  Google Scholar 

  39. Tanzania Meteorological Agency. Accessed 15 Oct 2019.

  40. World Weather Online. Accessed 15 Oct 2019.

  41. Kaindoa EW, Matowo NS, Ngowo HS, Mkandawile G, Mmbando A, Finda M, et al. Interventions that effectively target Anopheles funestus mosquitoes could significantly improve control of persistent malaria transmission in south-eastern Tanzania. PLoS ONE. 2017;12:e0177807.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Lwetoijera DW, Harris C, Kiware SS, Dongus S, Devine GJ, McCall PJ, Majambere S. Increasing role of Anopheles funestus and Anopheles arabiensis in malaria transmission in the Kilombero Valley, Tanzania. Malar J. 2014;13:331.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Matowo NS, Munhenga G, Tanner M, Coetzee M, Feringa WF, Ngowo HS, et al. Fine-scale spatial and temporal heterogeneities in insecticide resistance profiles of the malaria vector, Anopheles arabiensis in rural south-eastern Tanzania. Wellcome Open Res. 2017;2:96.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  44. Renggli S, Mandike R, Kramer K, Patrick F, Brown NJ, McElroy PD, et al. Design, implementation and evaluation of a national campaign to deliver 18 million free long-lasting insecticidal nets to uncovered sleeping spaces in Tanzania. Malar J. 2013;12:85.

    Article  PubMed  PubMed Central  Google Scholar 

  45. KoBoToolbox: Simple, robust and powerful tools for data collection. Accessed 17 Oct 2019.

  46. Limwagu AJ, Kaindoa EW, Ngowo HS, Hape E, Finda M, Mkandawile G, et al. Using a miniaturized double-net trap (DN-Mini) to assess relationships between indoor–outdoor biting preferences and physiological ages of two malaria vectors, Anopheles arabiensis and Anopheles funestus. Malar J. 2019;18:282.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  47. Sudia WD, Chamberlain RW. Battery-operated light trap, an improved model. J Am Mosq Control Assoc. 1988;4:536–8.

    CAS  PubMed  Google Scholar 

  48. Gillies M, Coetzee M. A supplement to the Anophelinae of Africa South of the Sahara. Publ S Afr Inst Med Res. 1987;55:1–143.

    Google Scholar 

  49. Kahamba NF, Limwagu AJ, Mapua SA, Msugupakulya BJ, Msaky DS, Kaindoa EW, et al. Habitat characteristics and insecticide susceptibility of Aedes aegypti in the Ifakara area, south-eastern Tanzania. Parasit Vectors. 2020;13:53.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  50. Masalu JP, Okumu FO, Mmbando AS, Sikulu-Lord MT, Ogoma SB. Potential benefits of combining transfluthrin-treated sisal products and long-lasting insecticidal nets for controlling indoor-biting malaria vectors. Parasit Vectors. 2018;11:231.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  51. WHO. Test procedures for insecticide resistance monitoring in malaria vector mosquitoes. 2nd ed. Geneva: World Health Organization; 2018.

    Google Scholar 

  52. R Core Team. R: a language and environment for statistical computing. Vienna: R Foundation for Statistical Computing; 2012. 2018.

  53. Bates D, Mächler M, Bolker B, Walker S. Fitting linear mixed-effects models Usinglme4. J Stat Soft. 2015;67:1.

    Article  Google Scholar 

  54. 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.

    Article  PubMed  PubMed Central  Google Scholar 

  55. Lindsay SW, Adiamah JH, Miller JE, Armstrong JRM. Pyrethroid-treated bednet effects on mosquitoes of the Anopheles gambiae complex in The Gambia. Med Vet Entomol. 1991;5:477–83.

    Article  CAS  PubMed  Google Scholar 

  56. Miller JE, Lindsay SW, Armstrong JRM. Experimental hut trials of bednets impregnated with synthetic pyrethroid or organophosphate insecticide for mosquito control in The Gambia. Med Vet Entomol. 1991;5:465–76.

    Article  CAS  PubMed  Google Scholar 

  57. Carnevale P, Robert V, Boudin C, Halna JM, Pazart L, Gazin P, et al. Control of malaria using mosquito nets impregnated with pyrethroids in Burkina Faso. Bull Soc Pathol Exot. 1988;81:832–46.

    CAS  Google Scholar 

  58. 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 Trop. 1991;49:97–108.

    Article  CAS  PubMed  Google Scholar 

  59. Ogoma SB, Lorenz LM, Ngonyani H, Sangusangu R, Kitumbukile M, Kilalangongono 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  CAS  PubMed  PubMed Central  Google Scholar 

  60. Killeen GF, Chitnis N, Moore SJ, Okumu FO. Target product profile choices for intra-domiciliary malaria vector control pesticide products: repel or kill? Malar J. 2011;10:207.

    Article  PubMed  PubMed Central  Google Scholar 

  61. Killeen GF, Moore SJ. Target product profiles for protecting against outdoor malaria transmission. Malar J. 2012;11:17.

    Article  PubMed  PubMed Central  Google Scholar 

  62. Killeen GF, Seyoum A, Gimnig JE, Stevenson JC, Drakeley CJ, Chitnis N. Made-to-measure malaria vector control strategies: rational design based on insecticide properties and coverage of blood resources for mosquitoes. Malar J. 2014;13:146.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  63. Protopopoff N, Mosha JF, Lukole E, Charlwood JD, Wright A, Mwalimu CD, et al. Effectiveness of a long-lasting piperonyl butoxide-treated insecticidal net and indoor residual spray interventions, separately and together, against malaria transmitted by pyrethroid-resistant mosquitoes: a cluster, randomised controlled, two-by-two factorial design trial. Lancet. 2018;391:1577–88.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  64. Cook J, Tomlinson S, Kleinschmidt I, Donnelly MJ, Akogbeto M, Adechoubou A, et al. Implications of insecticide resistance for malaria vector control with long-lasting insecticidal nets: trends in pyrethroid resistance during a WHO-coordinated multi-country prospective study. Parasit Vectors. 2018;1:550.

    Google Scholar 

  65. Tiono AB, Ouédraogo A, Ouattara D, Bougouma EC, Coulibaly S, Diarra A, et al. Efficacy of Olyset Duo, a bednet containing pyriproxyfen and permethrin, versus a permethrin-only net against clinical malaria in an area with highly pyrethroid-resistant vectors in rural Burkina Faso: a cluster-randomised controlled trial. Lancet. 2018;392:569–80.

    Article  PubMed  Google Scholar 

Download references


We sincerely thank volunteers and technicians involved in this study. Our appreciations also go to laboratory staff at Ifakara Health Institute, Mr. Said Abbasi and Mr. Francis Tumbo who conducted PCR analysis of mosquito samples.


The study was funded by Biotechnology and Biological Sciences Research Council (BBSRC) through Building Out Vector-borne diseases in sub-Saharan Africa: the BOVA Network (Grant number: BOVA007). FOO was also funded by Wellcome Trust Intermediate Fellowship in Public Health and Tropical Medicine (Grant number: WT102350/Z/13/Z) and the Howard Hughes Medical Institute (HHMI)-Gates International Scholarship (Grant number: OPP1099295).

Author information

Authors and Affiliations



JPM, GFK and FOO conceived the idea, helped to obtain the funds, designed and conducted experiments, analysed the data and drafted the manuscript; MF helped in the design of the peri-domestic survey, edited and revised the manuscript; HSN helped on data analysis and edited the manuscript; PGM helped in conducting WHO standard susceptibility test on mosquitoes, edited and revised the manuscript; FOO and GFK edited and revised the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to John P. Masalu.

Ethics declarations

Ethics approval and consent to participate

The study was approved by the Institute Review Board of Ifakara Health Institute IHI/IRB/No: 02-2019 and Medical Research Coordinated Committee of the National Institute for Medical Research of the United Republic of Tanzania (NIMR/HQ/R.8a/Vol.1X/3152). All study participants were recruited after signing informed consent forms.

Consent for publication

This manuscript has been approved for publication by Institute for Medical Research of the United Republic of Tanzania (NIMR/HQ/P.12VOLXXIX/39).

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

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

Rights and permissions

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 The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Masalu, J.P., Finda, M., Killeen, G.F. et al. Creating mosquito-free outdoor spaces using transfluthrin-treated chairs and ribbons. Malar J 19, 109 (2020).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: