Skip to main content
Download PDF

Protecting migratory farmers in rural Tanzania using eave ribbons treated with the spatial mosquito repellent, transfluthrin

Malaria Journal volume 18, Article number: 414 (2019) Cite this article

Abstract

Background

Many subsistence farmers in rural southeastern Tanzania regularly relocate to distant farms in river valleys to tend to crops for several weeks or months each year. While there, they live in makeshift semi-open structures, usually far from organized health systems and where insecticide-treated nets (ITNs) do not provide adequate protection. This study evaluated the potential of a recently developed technology, eave ribbons treated with the spatial repellent transfluthrin, for protecting migratory rice farmers in rural southeastern Tanzania against indoor-biting and outdoor-biting mosquitoes.

Methods

In the first test, eave ribbons (0.1 m × 24 m each) treated with 1.5% transfluthrin solution were compared to untreated ribbons in 24 randomly selected huts in three migratory communities over 48 nights. Host-seeking mosquitoes indoors and outdoors were monitored nightly (18.00–07.00 h) using CDC light traps and CO2-baited BG malaria traps, respectively. The second test compared efficacies of eave ribbons treated with 1.5% or 2.5% transfluthrin in 12 huts over 21 nights. Finally, 286 farmers were interviewed to assess perceptions about eave ribbons, and their willingness to pay for them.

Results

In the two experiments, when treated eave ribbons were applied, the reduction in indoor densities ranged from 56 to 77% for Anopheles arabiensis, 36 to 60% for Anopheles funestus, 72 to 84% for Culex, and 80 to 98% for Mansonia compared to untreated ribbons. Reduction in outdoor densities was 38 to 77% against An. arabiensis, 36 to 64% against An. funestus, 63 to 88% against Culex, and 47 to 98% against Mansonia. There was no difference in protection between the two transfluthrin doses. In the survey, 58% of participants perceived the ribbons to be effective in reducing mosquito bites. Ninety per cent were willing to pay for the ribbons, the majority of whom were willing to pay but less than US$2.17 (5000 TZS), one-third of the current prototype cost.

Conclusions

Transfluthrin-treated eave ribbons can protect migratory rice farmers, living in semi-open makeshift houses in remote farms, against indoor-biting and outdoor-biting mosquitoes. The technology is acceptable to users and could potentially complement ITNs. Further studies should investigate durability and epidemiological impact of eave ribbons, and the opportunities for improving affordability to users.

Background

Malaria control has gained significant momentum in the past decade due to key interventions, including insecticide-treated nets (ITNs), indoor residual spraying (IRS), prompt diagnosis, improved chemotherapy and chemoprophylaxis, and health education [1,2,3]. However, the progress observed since 2000 has begun stagnating. The 2018 World Health Organization (WHO) Report indicated an increase in malaria cases in several African countries compared to the previous year [4]. This situation has been attributed to multiple challenges, such as increased propensity of malaria mosquitoes to bite outdoors and in early evenings, as well as resistance to common public health insecticides, notably pyrethroids [5,6,7,8]. Other challenges include high costs of alternative protective measures and sub-optimal user compliance. Complementary technologies are therefore required to ensure that current gains are maintained [9], but also to accelerate efforts towards set global targets [10].

Evidence suggests that improving house designs reduces the burden of vector-borne diseases [11,12,13,14]. Since 2000, economic transitions have led to rapid improvement of housing in Africa, including the doubling of families living in houses made of finished materials and with proper sanitation [15]. An increasing number of African houses now have concrete or brick walls, corrugated iron or tiled roofs, as well as screened windows and eave spaces [15]. Unfortunately, many migratory communities, such as pastoralists and seasonal rice farmers, have not benefitted from these house improvements due to low income levels and competing priorities.

In rural southeastern Tanzania where subsistence rice cultivation is a common economic activity, families often relocate to their farms in distant river valleys for weeks or months (usually between January and June), to tend to their crops, only returning to their main residential homes at the end of the farming season. In most cases, parents bring with them their children below school age. While at the farms, these families usually dwell in temporary structures (Fig. 1), leaving them disproportionately more exposed to mosquito bites than the rest of the population [16]. In some of these structures, use of standard prevention tools, such as ITNs, is also compromised [16]. Affordable alternatives are therefore necessary to sustainably protect these communities from potential infectious and nuisance arthropod bites.

Fig. 1
figure 1

Examples of makeshift housing structures that the migratory farmers use when they go to the farms in the distant river valleys

Full size image

Interventions, such as larval source management, insecticide-treated clothes, blankets and hammocks, as well as topical repellents, may constitute alternatives for such communities [9], but could be affected by poor regular compliance, high costs and poor access [17,18,19,20,21,22]. Passive spatial repellent products may offer a practical alternative. Examples include hessian materials treated with the spatial repellent, transfluthrin, which can provide long-lasting protection due to high retention of transfluthrin by the hessian fabric [23,24,25,26]. Such products typically protect more than one individual by deterring mosquitoes, inhibiting blood-feeding and killing vectors [27,28,29,30,31], without requiring any external energy sources or re-application of active ingredient [23, 32,33,34]. They can also be delivered in a variety of formats for use both indoors and outdoors. Recent studies in Tanzania used the same fabric to create transfluthrin-treated eave ribbons, which when fitted along open eave spaces of houses can effectively prevent mosquito bites both indoors and outdoors [35, 36].

This current study evaluated efficacy of transfluthrin-treated eave ribbons in protecting rural migratory farmers in their semi-open hut structures in distant rice fields in the Kilombero Valley, southeastern Tanzania. The study also assessed perceptions and willingness to pay for this tool by farmers.

Methods

Study area

The study was conducted in three rice farm areas: Igumbiro, Kikwachu and Kilisa, in Ulanga district, southeastern Tanzania (Fig. 2), from March to July 2018. Annual rainfall and mean daily temperatures in the area range from 1200 to 1800 mm and 20 to 32.6 °C, respectively. The main malaria vectors include Anopheles arabiensis and Anopheles funestus, both of which are resistant to pyrethroids [37,38,39,40], and the latter mediating most of the transmission. ITNs are the main vector control tool in the region, and are often distributed by the Government to the main residential communities [41]. Although compliance to ITN use in farmhouses is high [42], these rice farmers remain at risk of nuisance and potential infective bites before going under a bed net due to the poor housing structures that allow easy entry of mosquitoes.

Fig. 2
figure 2

Map showing the study villages and locations of the migratory farming households that participated in the study

Full size image

A recent cross-sectional survey across residential villages in Kilombero and Ulanga found the prevalence varies between < 1% in peri-urban and > 40% in rural villages that are ~ 20 km away from the rice farms where the study was conducted (Swai et al., unpublished).

Transfluthrin-treated eave ribbons

The eave ribbons were prepared as described by Mmbando et al. [35] and cut to size of 0.1 m wide and 24 m long, so that they could fit all around the farm huts (Fig. 3). Treatment of the eave ribbons also followed published procedures [23, 25, 35]. To achieve 1.5 and 2.5% transfluthrin concentrations, 22.5 ml and 37.5 ml of technical grade transfluthrin stock solution were dissolved in 127.5 ml and 112.5 ml of liquid detergent (Axion®), respectively, and 1350 ml of water added, so that the total volume was always 1500 ml. The control eave ribbons were prepared by soaking the ribbons in a mixture of 150 ml Axion® liquid detergent and 1350 ml water, without any transfluthrin. Thus, for the 1.5 and 2.5% concentrations, the amount of transfluthrin per surface area was 13.73 g/m2 and 22.89 g/m2, respectively.

Fig. 3
figure 3

Selected structures for evaluating the use of transfluthrin-treated eave ribbons installed along the eaves spaces of farm huts for preventing mosquito bites indoors and outdoors

Full size image

Assessing efficacy of 1.5% transfluthrin-treated eave ribbons

Using a randomized cross-over design with a wash period of 2 days between treatments, entomological efficacy of eave ribbons treated with 1.5% transfluthrin solution was evaluated as follows: from each of the three rice farms, 8 huts from consenting rice farmers were recruited, so that there was a total of 24 huts. Of the 8 huts in each village, 4 huts were randomly allocated the transfluthrin-treated eave ribbons, while the remaining 4 received untreated eave ribbons (controls). The eave ribbons were fitted along the eave spaces every evening by trained technicians and removed each morning (Fig. 3). The treatment arms were rotated after every 4 consecutive nights of trapping. The experiment was conducted over a total of 16 nights in each village, during which each hut received both the transfluthrin-treated and control eave ribbons twice.

To minimize cross contamination between the treated and control ribbons, the ribbons were fitted in such a way as to ensure no physical contact with the walls or roof of the hut. In addition, a wash out period of 2 days was implemented between rotations, during which no ribbons were fitted to the huts and no experiments were done. All households participating in the study were provided with a new ITN, i.e., Olyset® net (A to Z Textiles, Arusha, Tanzania), as basic protection during sleeping hours.

Each night, indoor and outdoor mosquito collections were done between 18.00 and 07.00 h using CDC® light traps (CDC-LT) [43] and carbon dioxide-baited BG® malaria traps (BGM) [44, 45], respectively. Each morning, the collected mosquitoes were sorted by sex, and all female mosquitoes were morphologically identified into taxa following taxonomic keys [46, 47], and grouped as blood-fed, unfed or gravid. The female Anopheles were preserved in silica-filled microcentrifuge tubes then processed by polymerase chain reaction (PCR) and enzyme-linked immunosorbent assays (ELISA) to respectively distinguish between sibling species [48,49,50] and detect any Plasmodium infections in the salivary glands [51]. Outdoor temperature and humidity were recorded using Tiny tag® data recorders that were hung away from direct sunlight and rain.

Assessing efficacy of 2.5% transfluthrin-treated eave ribbons

Entomological efficacy of 2.5% transfluthrin-treated eave ribbons was evaluated using a three-by-three Latin-square experimental design with a wash out period of 2 days between treatments. Twelve farm huts from consenting migratory rice farmers in Kilisa village were recruited. Four of the huts received eave ribbons treated with 1.5% transfluthrin solution, another 4 huts received ribbons with 2.5% transfluthrin solution and the remaining 4 were fitted with untreated ribbons (i.e., controls). The ribbons were fitted along the eave spaces as described above, and all huts were provided with new Olyset® nets for basic protection. The treatments were rotated between the huts every week. Unfortunately, due to a government directive for the farmers to vacate the fields, the experiment was terminated after 21 nights only. Mosquitoes were processed and environmental data were collected as described above.

Identification of sibling species, blood meals and Plasmodium infections in malaria vectors

The PCR assays for sibling species of Anopheles gambiae sensu lato (s.l.) were performed as described by Scott et al. [48], while those for An. funestus group were done following Koekemoer et al. [49] and Cohuet et al. [50] techniques. All blood-fed Anopheles mosquitoes were screened for human, bovine, chicken, goat, and dog blood using ELISA [51]. Additionally, all female Anopheles were assessed for Plasmodium circumsporozoite proteins using ELISA (csp-ELISA). To eliminate false positives, which are heat labile, all csp-ELISA positive lysates were boiled for 10 min at 100 °C and re-tested [52].

Assessing community perceptions and their willingness to pay for transfluthrin-treated eave ribbons

A quantitative survey was conducted after completion of the entomological efficacy assays to examine the farmers’ perceptions and willingness to pay for the transfluthrin-treated eave ribbons. A total of 286 individuals from the 3 rice farms were recruited. The actual number of individuals from each farm area was proportional to the population size of the area, thus 10, 114 and 162 individuals were recruited from Igumbiro, Kilisa and Kikwachu, respectively. A list of names of farmers was sought from respective local administrative leaders in the rice farms. These were then entered into Excel, random number generated for each farmer and, following systematic sample selection procedures, farmers were randomly selected and recruited. Since most farmers had already vacated their fields at the time of this survey, the interviews were conducted with the respondents at their main residential homes rather than the farms.

A structured questionnaire was administered to collect information on basic demographic and socio-economic traits. Participants were also asked about the current mosquito control tools used while at the rice farms, how much they spent on mosquito control the previous year, their perceptions of eave ribbons as a control tool, and their willingness to pay for the transfluthrin-treated eave ribbons. Willingness to pay was assessed by asking whether participants were willing to purchase the treated eave ribbons, and amount of money they were willing to spend in Tanzanian shillings (TZS). Before asking these questions, the interviewers showed samples of untreated eave ribbons, and explained to the participants how the eave ribbons function.

Data analysis

Mosquito count data were analysed using Stata® 13 (College Station, TX, USA). The effects of treatment on indoor and outdoor mosquito densities in different study arms were examined using generalized linear mixed effects models (GLMMs) with a negative binomial distribution and log-link function to account for overdispersion of the data. Mosquito densities were modelled as a function of treatment with household ID, day and village as random factors. Protective efficacy of the eave ribbons with different transfluthrin concentrations were calculated from the relative risk (RR) values for the control (C) and treatment (T) arms in the no-intercept model, using the formula (C-T)/C*100. Blood meal sources and Plasmodium infections rates were calculated as percentages of total mosquitoes assayed.

Entomological inoculation rates (EIR), i.e., number of malaria infectious bites per person per given period, were determined by multiplying average nightly biting rates and the proportion of sporozoite positive mosquitoes. The nightly biting rate was calculated by dividing total mosquitoes caught by product of number of households and trap nights. To estimate annual EIR, the daily EIR values were multiplied by 365 nights (annual EIR = nightly biting rate × sporozoite rate × 365). Adjusted EIR were calculated by multiplying estimated EIR by correction factors from previous evaluations comparing CDC-LT and BGM trap catches to actual number of mosquitoes that bite unprotected human volunteers, i.e., in human landing catches [53, 54]. A power calculation with GLM simulation modelling using R statistical software [55, 56] confirmed that both experiments were adequately powered (> 80%) despite the second one running for just 21 days.

The perceptions and willingness to pay for the eave ribbon data was analysed as follows: socio-economic status of individuals was first estimated using principal component analysis (PCA), where household assets, structure, energy and water sources were used to classify individuals among the study population into five quintiles. The purchasing amounts mentioned by the participants were grouped into two categories US$ < 2.17 and ≥ 2.17 [(< 5000 and ≥ 5000 TZS) as per exchange rates of January 2019]. Descriptive analysis was conducted to determine the respondent’s perception of effectiveness, willingness to pay by gender, socio-economic status, education levels, and marital status. Perception of effectiveness was summarized using percentages. Pearson’s Chi square test and Chi square test for trend were used to assess association between socio-economic status, frequencies of willingness to pay and the purchasing amount quoted by the respondents. Finally, associations between socio-economic status and quoted purchasing amount was assessed using multivariate logistic regression analysis controlling for age, education and amount of money spent on malaria control the previous year.

Results

Protective efficacy of eave ribbons treated with 1.5% transfluthrin

A total of 3872 An. arabiensis, 1232 An. funestus, 495 Anopheles coustani, 1200 Anopheles pharoensis, 3780 Culex spp. 2234 Mansonia spp. and 97 Aedes spp. female mosquitoes were caught in the 3 rice farms. Igumbiro village had the highest densities of An. funestus and Culex spp. while Kikwachu and Kilisa had the highest densities of An. arabiensis and Mansonia spp. Kilisa also had the highest densities of Anopheles coustani and Anopheles pharoensis (Table 1).

Table 1 Biting densities of different mosquito species caught in the three study rice farms during the study period
Full size table

Eave ribbons treated with 1.5% transfluthrin reduced indoor densities of An. arabiensis by 56% (p < 0.001), An. funestus by 36% (p < 0.001), Culex spp. by 72% (p < 0.001) and Mansonia spp. by 80% (p < 0.001). The ribbons also reduced outdoor biting for An. arabiensis by 38% (p = 0.034), Culex spp. by 64% (p < 0.001) and Mansonia spp. 47% (p < 0.001), respectively (Table 2). There was no observable protection against An. funestus outdoors. Over the duration of the experiment, the nightly temperatures ranged from 22.5 to 31.9 °C, averaging at 25.2 °C, while percentage relative humidity ranged from 65.6 to 100%, averaging at 91.9%.

Table 2 Protection conferred indoors and outdoors against anopheline and culicine species in all three rice farms when 1.5% transfluthrin-treated eave ribbons were fitted along the eaves of rice farm huts
Full size table

Protective efficacy of eave ribbons treated with 2.5% transfluthrin

In tests comparing the eave ribbons treated with either 1.5 or 2.5% transfluthrin, 899 An. arabiensis, 4781 An. funestus, 379 Culex, 748 Mansonia, and 25 Aedes mosquitoes were caught. Both 1.5 and 2.5% transfluthrin-treated eave ribbons conferred substantial protection indoors and outdoors against all mosquito taxa. The highest protection was 76 to 98% against Mansonia spp. followed by 63 to 88% protection against Culex spp. 72 to 77% against An. arabiensis, and 59 to 64% against An. funestus, compared to untreated control ribbons (Table 3). There was no significant difference in protection offered by the two doses. The nightly temperatures ranged between 18.8 and 30.8 °C, averaging at 23.2 °C, while relative humidity ranged between 53.8 and 100%, averaging at 87.4%.

Table 3 Protection conferred indoors and outdoors against anopheline and culicine species in Kilisa rice farms when 1.5 and 2.5% transfluthrin-treated eave ribbons were fitted along the eaves of rice farm huts
Full size table

Malaria vector sibling species and blood meal sources

A total of 4771 An. gambiae s.l. and 6013 An. funestus s.l. mosquitoes underwent species identification by PCR, and blood meal analysis and circumsporozoite protein ELISA assays. All An. gambiae s.l were found to be An. arabiensis (100%), while the An. funestus group consisted of 91.4% An. funestus sensu stricto (s.s.), 2.9% Anopheles rivolurum, 0.9% Anopheles leesoni, and 5.8% unamplified samples. Twenty-three mosquitoes blood-fed were caught (14 An. arabiensis and 9 An. funestus s.s.). Blood meal ELISA revealed that 2 (14%), 5 (36%) and 7 (50%) of the An. arabiensis had fed on human, bovine and goat, respectively, while all An. funestus s.s. had fed on humans.

Plasmodium sporozoite infection rates and malaria transmission intensities

Overall, malaria transmission in the rice farms was low; 14 mosquitoes were found with Plasmodium sporozoites (one An. arabiensis, 13 An. funestus s.s.). Four of the An. funestus were caught outdoors while the rest, including the An. arabiensis, were caught indoors. EIR for An. arabiensis and An. funestus were estimated separately for both indoor and outdoor environments, from the CDC-LT and BGM trap catches, respectively (Table 4). Infection rates were higher in An. funestus than An. arabiensis both indoors and outdoors, and An. funestus was responsible for more than 90% of all transmission occurring in the area. Most transmission occurred indoors, where An. funestus had an annual EIR estimate of 2.33 infectious bites per person per year (ib/p/y) indoors compared to 0.79 ib/p/y outdoors. However, since farmers typically spend no more than half a year in the farms, actual infection intensities would be less than half of these estimates.

Table 4 Infectiousness of Anopheles arabiensis and Anopheles funestus mosquitoes caught indoors and outdoors the rice farms
Full size table

Perception of community members regarding the mosquito bites, malaria and eave ribbons

Of the 286 respondents, 92% were subsistence farmers engaged in crop cultivation, while the rest engaged in multiple activities, such as business and fishing in addition to farming. Age of respondents ranged between 18 and 80 years, with the median age being 38. Most respondents (82%; n = 235) had primary level education and 75% (n = 215) were living with a partner. Only 31% (n = 89) of the respondents’ main residential homes had screened windows, 77% (n = 220) had brick walls, 69% (n = 197) had roofs made of iron sheets, and 27% (n = 78) had modern toilet facilities (flush or improved ventilated pit latrines). Almost three-quarters (72%; n = 206) of the respondents had access to piped water, mostly from communal boreholes.

Over 80% of the respondents reported that malaria is a major concern in the rice farms. Most (90%; n = 257) used bed nets for protection against mosquito bites when at the farms. They also reported using non-residual insecticide sprays (mostly pyrethrum), topical repellents, mosquito coils, and smoke from burning wood. Regarding cost for malaria prevention and treatment per year, about one-quarter of the participants (23%; n = 66) said they incurred no cost, 12% (n = 33) spent less than US$2.17 (5000 TZS), 46% (n = 134) spent between US$2.60 and 4.33 (6000-10,000 TZS), 12% (n = 32) between US$4.77 and 8.66 (11,000-20,000 TZS), and 5% spent more than US$9.11 (> 21,000 TZS).

Nearly two-thirds of participants (60%; n = 172) reported facing challenges in protecting themselves or their families against mosquito bites while at the farms. The commonest challenges included: (a) bed nets having large holes, letting in mosquitoes or mosquitoes biting through the nets; (b) high costs and low access of insecticide sprays and topical repellents; (c) lack of effective outdoor protection tools; and, (d) canned insecticide sprays not lasting long.

Current expenditures on malaria prevention, and people’s willingness to pay for transfluthrin-treated eave ribbons

More than 90% of participants said that they would use and pay for the transfluthrin-treated eave ribbons if available. When asked how much they were willing to pay, 70% (n = 200) stated values less than US$2.17 (5000 TZS) for the intervention, while 23% (n = 66) were willing to pay between US$2.21 and 4.33 (5100–10,000 TZS).

Although there was no evidence for association between socio-economic status and willingness to pay for the ribbons (Fisher’s exact test p = 0.558), socio-economic status strongly influenced whether individuals were willing to pay more or less than a set cut-off of US$2.17 (5000 TZS) (Fisher’s exact test p = 0.016). The least poor were more than three times more likely to be willing to pay above this cut-off [(OR = 3.2; 95% CI (1.2–8.3) p = 0.0139]. In addition, individuals who spent US$ > 2.17 per year on mosquito prevention tools were more likely to pay more for the eave ribbons (Table 5). After adjusting for age, education level and amount of money generally spent on mosquito prevention tools, only individuals who spend US$ > 2.17/year on mosquito prevention were willing to pay US$ > 2.17 for the eave ribbons (Table 5).

Table 5 Factors affecting the amount individuals are willing to pay for the transfluthrin-treated eave ribbons
Full size table

Discussion

In this study, the potential of transfluthrin-treated eave ribbons as a protective measure against disease-transmitting and nuisance-biting mosquitoes was evaluated in rice farms of southeastern Tanzania where seasonal migrant farmers live in poorly constructed makeshift housing. Overall, the study results demonstrate that in addition to ITNs, transfluthrin-treated eave ribbons can be used to reduce densities of indoor-biting and outdoor-biting mosquitoes. Since the experimental controls had untreated eave ribbons, the observed reduction may be attributed to the transfluthrin-treatment, rather than any physical barrier from the hessian fabric. Earlier tests by Mmbando et al. demonstrated that eave ribbons work by both repelling host-seeking mosquitoes and directly killing those that come in contact with the vapours [35].

In particular, the reduction of mosquito bites recorded outdoors show that there is a protective radius offered by the transfluthrin-treated eave ribbons beyond the physical house structure itself [24]. Many Tanzanian families spend long periods of time outdoors in the evenings doing various activities, such as cooking, story-telling or playing (children), which exposes them to potentially infectious bites [57,58,59]. It is evident that transfluthrin-treated eave ribbons offer additional protection in such spaces, thereby complementing ITNs. The observed effects were apparent against the malaria vectors, An. arabiensis and An. funestus, but also non-malaria mosquitoes such as Culex and Mansonia spp. both indoors and outdoors.

The protection against An. funestus, which now dominates malaria transmission in the area, was modest in the first experiment but substantial in the second experiment. This is particularly interesting since both An. funestus and An. arabiensis are also known to be resistant to common public health pesticides including pyrethroids [37,38,39,40, 46]. The farms in Kilisa village in particular had very high densities of An. funestus, most likely because of the more permanent water sources in the area, which favour proliferation of this species [60, 61]. It is here too where efficacy of eave ribbons was highest against this species. The transfluthrin-treated eave ribbons were even more protective against culicines than anophelines (Tables 2 and 3). Considering that culicine species are usually more abundant in the area, resistant to most of the public health chemicals (Matowo et al. unpublished) and regularly enter the house via windows and doors [62], the level of nuisance biting and pathogens transmitted by culicines, such as filarial worms, could be greatly reduced by using transfluthrin-treated eave ribbons. Such applications could certainly extend beyond migratory farming communities. It is however particularly important that this technology is used in addition to, not as a replacement of existing interventions such as ITNs. The lack of evidence of a difference in protection conferred by 1.5 and 2.5% transfluthrin treatments suggest that the lower dose would be preferable. Similar treatment doses have previously shown field efficacy against bites by these vector species in experimental huts built in rural southeastern Tanzania [35].

More than 90% of the indoor and outdoor malaria transmission occurring in the rice farms was mediated by An. funestus. These findings match those of a recent entomological surveillance across villages in Ulanga district, Tanzania, which showed that despite their low numbers, An. funestus mediated more than four-fifths of malaria transmission [41]. The EIR observed in the rice farms was however lower than those observed in residential homes in the same district [41]. This is most probably because the small and transient human population in such migratory farming communities is inadequate to sustain higher malaria transmission intensities, even when environmental conditions in the rice farms support the proliferation of mosquitoes.

The risk of malaria transmission in the rice farms was also higher indoors than outdoors. EIR estimates indoors were 2.33 ib/p/y compared to 0.79 ib/p/y outdoors (for An. funestus). Similar observations that transmission is still mostly indoors despite increasing propensity of outdoor biting is also widely reported elsewhere in southeastern Tanzania [41] and western Kenya [63] where An. funestus and An. arabiensis are the most predominant vector species. Though the number of blood-fed specimen were few, An. funestus had higher human blood index than An. arabiensis, suggesting that even in remote areas where human presence is seasonal, An. funestus remains highly anthropophagic. This not only highlights the importance of improving the use of home-based interventions such as ITNs, but also the need to design better tools to protect such disfranchised communities from infectious bites, thereby accelerating the overall goal of malaria elimination. Given the protective efficacy observed during this study, transfluthrin treated eave ribbons can potentially be used as a complimentary intervention in such settings to protect against mosquito bites occurring inside and within peri-domestic areas when people are not under a bed net.

The majority of rice farmers highlighted malaria as a major health concern, especially while they are in their distant farms. Although bed nets are common, the farmers also used locally available insecticide sprays, topical repellent, mosquito coils, and smoke from burning wood. Mmbando et al. reported that the initial prototypes of the eave ribbons cost about US$7 (16,157 TZS) from production to installation [35]. However, more than two-thirds of participants were willing to purchase the product at less than or equal to US$2.17 (5000 TZS), which is just under one-third of the cost, and only individuals from the upper two socio-economic quintiles were willing to pay more than US$2.17 (5000 TZS). Interestingly, nearly all respondents said they would use the technology if produced and marketed to them. Considering that mass production of the transfluthrin-treated eaves ribbons would lower the price, it is possible that the technology could be made more affordable and therefore accessible for these communities. One limitation of this specific aspect of the study was that the method used for determining community members’ willingness to pay was focused only on prices, thus ignoring other key attributes such as aesthetic concerns and user compliance. It therefore captured only the hypothetical purchasing behaviour, and could be prone to response bias [64].

Future studies should evaluate additional effects of the product, including 24-h mortality of wild pyrethroid-resistant mosquitoes as they enter and leave the human dwellings fitted with the eave ribbons. Such additional benefits could magnify the overall protective efficacy of the technology, and potentially extend it to community benefits, as recently demonstrated in semi-field settings [36]. Additional research questions that should be addressed include: (a) whether such products can divert mosquitoes to non-users as previously demonstrated in areas of sub-optimal coverage [65]; (b) the duration of efficacy, which according to semi-field studies is up to 6 months [23], and could therefore effectively cover the entire farming season; (c) opportunities for engaging local communities to accelerate the adoption of this or other similar interventions to complement ITNs; and, (d) community-wide impact on malaria transmission and burden, when the eave ribbons are used alongside ITNs or other interventions. Fortunately, many of these studies are already planned or are ongoing.

Conclusion

Transfluthrin-treated eave ribbons could be used in addition to ITNs to protect seasonal migratory farmers against both indoor and outdoor infectious and nuisance-biting mosquitoes, while they are at their distant farms. The technology is simple, portable, easy to use, widely acceptable, and can be readily fitted onto the makeshift huts that the farmers construct and use when at their farms. Most importantly, it does not require daily compliance as for bed nets or topical repellents. Most of the malaria transmission in the rice farms occurred indoors and was mediated by An. funestus. Rice farmers in the region showed willingness to use and purchase the eave ribbons as a control measure. There is a need to conduct further studies on longevity of protection conferred by the eave ribbons, epidemiological impacts on malaria and its transmission, as well as appropriate financing models for scale-up.

Availability of data

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Abbreviations

An. :

Anopheles

Spp:

species

BG:

biogents

CO2 :

carbon dioxide

ITN:

insecticide-treated nets

IRS:

indoor residual sprays

g/sq m:

grams per square metre

ml:

millilitres

PCR:

ploymerase chain reaction

ELISA:

Enzyme Linked Immunosorbent Assay

Csp:

cricumsporozoite

TZS:

Tanzanian Shillings

CDC:

Centre of disease control

CDC_LT:

Centre of disease control light traps

US $:

United States of America Dollars

PCA:

principal component analysis

References

  1. Alonso PL, Lindsay SW, Armstrong JR, Conteh M, Hill AG, David PH, et al. The effect of insecticide-treated bed nets on mortality of Gambian children. Lancet. 1991;337:1499–502.

    Article  CAS  PubMed  Google Scholar 

  2. Lengeler C, Snow RW. From efficacy to effectiveness: insecticide-treated bednets in Africa. Bull World Health Organ. 1996;74:325–32.

    CAS  PubMed  PubMed Central  Google Scholar 

  3. Murray CJL, Rosenfeld LC, Lim SS, Andrews KG, Foreman KJ, Haring D, et al. Global malaria mortality between 1980 and 2010: a systematic analysis. Lancet. 2012;379:413–31.

    Article  PubMed  Google Scholar 

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

    Google Scholar 

  5. The malERA Consultative Group on Vector Control. A research agenda for malaria eradication: vector control. PLoS Med. 2011;8:e1000401.

    Article  PubMed Central  Google Scholar 

  6. Okumu F. The paradigm of eave tubes: scaling up house improvement and optimizing insecticide delivery against disease-transmitting mosquitoes. Malar J. 2017;16:207.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Moore SJ. A new perspective on the application of mosquito repellents. Lancet Infect Dis. 2016;16:1093–4.

    Article  PubMed  Google Scholar 

  8. Durnez L, Coosemans M. Residual transmission of malaria: an old issue for new approaches. Anopheles mosquitoes—new insights into malaria vectors. InTechOpen Publ. 2013;21:671–704.

    Google Scholar 

  9. 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 

  10. WHO. Global Malaria Programme. Global technical strategy for malaria, 2016–2030. Geneva: World Health Organization; 2015.

    Google Scholar 

  11. Tusting LS, Willey B, Lines J. Building malaria out: improving health in the home. Malar J. 2016;15:320.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Ogoma SB, Lweitoijera DW, Ngonyani H, Furer B, Russell TL, Mukabana WR, et al. Screening mosquito house entry points as a potential method for integrated control of endophagic filariasis, arbovirus and malaria vectors. PLoS Negl Trop Dis. 2010;4:e773.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Bradley J, Rehman AM, Schwabe C, Vargas D, Monti F, Ela C, et al. Reduced prevalence of malaria infection in children living in houses with window screening or closed eaves on Bioko Island, Equatorial Guinea. PLoS One. 2013;8:e80626.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  14. Lindsay SW, Emerson PM, Charlwood JD. Reducing malaria by mosquito-proofing houses. Trends Parasitol. 2002;18:510–4.

    Article  PubMed  Google Scholar 

  15. Tusting LS, Bisanzio D, Alabaster G, Cameron E, Cibulskis R, Davies M, et al. Mapping changes in housing in sub-Saharan Africa from 2000 to 2015. Nature. 2019;568:391–4.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Swai JK, Finda MF, Madumla EP, Lingamba GF, Moshi IR, Rafiq MY, et al. Studies on mosquito biting risk among migratory rice farmers in rural south-eastern Tanzania and development of a portable mosquito-proof hut. Malar J. 2016;15:564.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Gu W, Utzinger J, Novak RJ. Habitat-based larval interventions: a new perspective for malaria control. Am J Trop Med Hyg. 2008;78:2–6.

    Article  PubMed  Google Scholar 

  18. Chaki PP, Dongus S, Fillinger U, Kelly A, Killeen GF. Community-owned resource persons for malaria vector control: enabling factors and challenges in an operational programme in Dar es Salaam, United Republic of Tanzania. Hum Resour Health. 2011;9:21.

    Article  PubMed  PubMed Central  Google Scholar 

  19. WHO. Interim Position Statement: The role of larviciding for malaria control in sub Saharan Africa. Geneva: World Health Organization; 2013.

    Google Scholar 

  20. 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 

  21. 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 

  22. Chen-Hussey V, Carneiro I, Keomanila H, Gray R, Bannavong S, Phanalasy S, et al. Can topical insect repellents reduce malaria? A cluster-randomised controlled trial of the insect repellent N,N-diethyl-m-toluamide (DEET) in Lao PDR. PLoS ONE. 2013;8:e70664.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. 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 

  24. 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  CAS  Google Scholar 

  25. Govella N, Ogoma S, Paliga J, Chaki P, 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  PubMed  PubMed Central  CAS  Google Scholar 

  26. 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  CAS  Google Scholar 

  27. Wouters W, van den Bercken J. Action of pyrethroids. Gen Pharmacol. 1978;9:387–98.

    Article  CAS  PubMed  Google Scholar 

  28. Kennedy JS. The excitant and repellent effects on mosquitoes of sub-lethal contacts with DDT. Bull Entomol Res. 1947;37:593–607.

    Article  CAS  PubMed  Google Scholar 

  29. Adams ME, Miller TA. Neural and behavioral correlates of pyrethroid and DDT-type poisoning in the house fly, Musca domestica L. Pestic Biochem Physiol. 1980;13:137–47.

    Article  CAS  Google Scholar 

  30. 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  CAS  Google Scholar 

  31. 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  PubMed  PubMed Central  CAS  Google Scholar 

  32. Ogoma SB, Moore SJ, Maia MF. A systematic review of mosquito coils and passive emanators: defining recommendations for spatial repellency testing methodologies. Parasit Vectors. 2012;5:287.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Kawada H, Maekawa Y, Takagi M, Tsuda Y. Trial of spatial repellency of metofluthrin-impregnated paper strip against Anopheles and Culex in shelters without walls in Lombok, Indonesia. J Am Mosq Control Assoc. 2004;20:434–7.

    PubMed  Google Scholar 

  34. Kawada H, Temu EA, Minjas JN, Matsumoto O, Iwasaki T, Takagi M. Field evaluation of spatial repellency of metofluthrin-impregnated plastic strips against Anopheles gambiae complex in Bagamoyo, coastal Tanzania. J Am Mosq Control Assoc. 2008;24:404–9.

    Article  PubMed  Google Scholar 

  35. 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 

  36. 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  PubMed  PubMed Central  CAS  Google Scholar 

  37. 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  PubMed Central  Google Scholar 

  38. Hunt RH, Brooke BD, Pillay C, Koekemoer LL, Coetzee M. Laboratory selection for and characteristics of pyrethroid resistance in the malaria vector Anopheles funestus. Med Vet Entomol. 2005;19:271–5.

    Article  CAS  PubMed  Google Scholar 

  39. Nkya TE, Akhouayri I, Poupardin R, Batengana B, Mosha F, Magesa S, et al. Insecticide resistance mechanisms associated with different environments in the malaria vector Anopheles gambiae: a case study in Tanzania. Malar J. 2014;13:28.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  40. 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  PubMed  PubMed Central  CAS  Google Scholar 

  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  PubMed  PubMed Central  CAS  Google Scholar 

  42. Hetzel MW, Alba S, Fankhauser M, Mayumana I, Lengeler C, Obrist B, et al. Malaria risk and access to prevention and treatment in the paddies of the Kilombero Valley, Tanzania. Malar J. 2008;7:7.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Mboera LE, Kihonda J, Braks MA, Knols BG. Short report: influence of centers for disease control light trap position, relative to a human-baited bed net, on catches of Anopheles gambiae and Culex quinquefasciatus in Tanzania. Am J Trop Med Hyg. 1998;59:595–6.

    Article  CAS  PubMed  Google Scholar 

  44. Gama RA, da Silva IM, Geier M, Eiras ÁE, da Silva IM, Geier M, et al. Development of the BG-malaria trap as an alternative to human-landing catches for the capture of Anopheles darlingi. Mem Inst Oswaldo Cruz. 2013;108:63–771.

    Article  Google Scholar 

  45. Lima JBP, Rosa-Freitas MG, Rodovalho CM, Santos F, Lourenço-de-Oliveira R. Is there an efficient trap or collection method for sampling Anopheles darlingi and other malaria vectors that can describe the essential parameters affecting transmission dynamics as effectively as human landing catches?—A review. Mem Inst Oswaldo Cruz. 2014;109:685–705.

    Article  PubMed  PubMed Central  Google Scholar 

  46. Gillies MT, Coetzee M. A Supplement to the Anophelinae of the South of the Sahara (Afrotropical Region). Publ South Afr Inst Med Res. 1987;55:1–143.

    Google Scholar 

  47. Edwards F. Mosquitoes of the Ethiopian Region. III. Culicine Adults and Pupae. London: Br Museum (Natural Hist); 1941.

    Google Scholar 

  48. Scott JA, Brogdon WG, Collins FH, Brogdon WG, Scott JA, Brogdon WG, et al. Identification of single specimens of the Anopheles gambiae complex by the polymerase chain reaction. Am J Trop Med Hyg. 1993;49:520–9.

    Article  CAS  PubMed  Google Scholar 

  49. Koekemoer LL, Kamau L, Hunt RH, Coetzee M. A cocktail polymerase chain reaction assay to identify members of the Anopheles funestus (Diptera: Culicidae) group. Am J Trop Med Hyg. 2002;66:804–11.

    Article  CAS  PubMed  Google Scholar 

  50. Cohuet A, Simard F, Toto JC, Kengne P, Coetzee M, Fontenille D. Species identification within the Anopheles funestus group of malaria vectors in Cameroon and evidence for a new species. Am J Trop Med Hyg. 2003;69:200–5.

    Article  CAS  PubMed  Google Scholar 

  51. Beier JC, Perkins PV, Koros JK, Onyango FK, Gargan TP, Wirtz RA, et al. Malaria sporozoite detection by dissection and ELISA to assess infectivity of Afrotropical Anopheles (Diptera: Culicidae). J Med Entomol. 1990;27:377–84.

    Article  CAS  PubMed  Google Scholar 

  52. Durnez L, Van Bortel W, Denis L, Roelants P, Veracx A, Trung HD, et al. False positive circumsporozoite protein ELISA: a challenge for the estimation of the entomological inoculation rate of malaria and for vector incrimination. Malar J. 2011;10:195.

    Article  PubMed  PubMed Central  Google Scholar 

  53. Okumu FO, Kihonda J, Mathenge E, Kotas ME, Moore SJ, Killeen GF. Comparative evaluation of methods used for sampling malaria vectors in the Kilombero Valley, South Eastern Tanzania. Open Trop Med J. 2008;1:51–5.

    Article  Google Scholar 

  54. Batista EPA, Eiras AE, Ngowo H, Opiyo M, Shubis GK, Meza FC, et al. Field evaluation of the BG-Malaria trap for monitoring malaria vectors in rural Tanzanian villages. PLoS ONE. 2018;13:e0205358.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  55. Team RDC. R: A language and environment for statistical computing. Vienna: R Foundation for Statistical Computing; 2013. p. 2014.

    Google Scholar 

  56. Johnson PCD, Barry SJE, Ferguson HM, Müller P. Power analysis for generalized linear mixed models in ecology and evolution. Methods Ecol Evol. 2015;6:133–42.

    Article  PubMed  Google Scholar 

  57. 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 

  58. Dunn CE, Le Mare A, Makungu C. Malaria risk behaviours, socio-cultural practices and rural livelihoods in southern Tanzania: implications for bednet usage. Soc Sci Med. 2011;72:408–17.

    Article  PubMed  Google Scholar 

  59. 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 

  60. Diuk-Wasser MA, Toure MB, Dolo G, Bagayoko M, Sogoba N, Traore SF, et al. Vector abundance and malaria transmission in rice-growing villages in Mali. Am J Trop Med Hyg. 2005;72:725–31.

    Article  PubMed  Google Scholar 

  61. De Gillies MT, Meillon B. The Anophelinae of Africa south of the Sahara (Ethiopian Zoogeographical Region). Publ South Afr Inst Med Res. 1968;54:1–343.

    Google Scholar 

  62. Njie M, Dilger E, Lindsay SW, Kirby MJ. Importance of eaves to house entry by Anopheline, but not culicine, mosquitoes. J Med Entomol. 2009;46:505–10.

    Article  PubMed  Google Scholar 

  63. Degefa T, Yewhalaw D, Zhou G, Lee MC, Atieli H, Githeko AK, et al. Indoor and outdoor malaria vector surveillance in western Kenya: implications for better understanding of residual transmission. Malar J. 2017;16:443.

    Article  PubMed  PubMed Central  Google Scholar 

  64. Breidert C, Hahsler M, Reutterer T. A review of methods for measuring willingness-to-pay. Innov Marketing. 2006;2:1–32.

    Google Scholar 

  65. Maia MF, Kreppel K, Mbeyela E, Roman D, Mayagaya V, Lobo NF, et al. A crossover study to evaluate the diversion of malaria vectors in a community with incomplete coverage of spatial repellents in the Kilombero Valley, Tanzania. Parasit Vectors. 2016;9:451.

    Article  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

We thank all study participants for their readiness to actively participate in this study. Special thanks to Mr Godian Selemani, field volunteer who facilitated smooth running of all project activities. Also, to the supervisors for their guidance during the conduct of the study.

Funding

JKS was funded by Wellcome Trust Masters Fellowship in Public Health (Grant Number: 200086/Z/15/Z). FOO was also funded by a Wellcome Trust Intermediate Fellowship in Public Health & Tropical Medicine (Grant No. WT102350/Z/13/Z), and a Howard Hughes Medical Institute (HHMI)-Gates International Research Scholarship (Grant No. OPP1099295).

Author information

Authors and Affiliations

  1. Environmental Health and Ecological Science Department, Ifakara Health Institute, P.O. Box 53, Ifakara, Tanzania

    Johnson K. Swai, Arnold S. Mmbando, Halfan S. Ngowo, Olukayode G. Odufuwa, Marceline F. Finda, Winifrida Mponzi, Anna P. Nyoni, Deogratius Kazimbaya, Alex J. Limwagu, Rukiyah M. Njalambaha, Saidi Abbasi, Sarah J. Moore, Lena M. Lorenz & Fredros O. Okumu

  2. Institute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow, G12 8QQ, UK

    Halfan S. Ngowo & Fredros O. Okumu

  3. School of Public Health, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa

    Marceline F. Finda & Fredros O. Okumu

  4. Swiss Tropical and Public Health Institute, Socinstrasse. 57, 4002, Basel 4, Switzerland

    Sarah J. Moore

  5. University of Basel, St. Petersplatz 1, 4002, Basel, Switzerland

    Sarah J. Moore

  6. Department of Disease Control, Faculty of Infectious and Tropical Disease, London School of Hygiene and Tropical Medicine, Keppel Street, London, WC1E 7HT, UK

    Joanna Schellenberg & Lena M. Lorenz

  7. School of Life Science and Bioengineering, The Nelson Mandela African, Institution of Science and Technology, P. O. Box 447, Arusha, Tanzania

    Fredros O. Okumu

Authors
  1. Johnson K. Swai
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Arnold S. Mmbando
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Halfan S. Ngowo
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Olukayode G. Odufuwa
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Marceline F. Finda
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Winifrida Mponzi
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Anna P. Nyoni
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Deogratius Kazimbaya
    View author publications

    You can also search for this author in PubMed Google Scholar

  9. Alex J. Limwagu
    View author publications

    You can also search for this author in PubMed Google Scholar

  10. Rukiyah M. Njalambaha
    View author publications

    You can also search for this author in PubMed Google Scholar

  11. Saidi Abbasi
    View author publications

    You can also search for this author in PubMed Google Scholar

  12. Sarah J. Moore
    View author publications

    You can also search for this author in PubMed Google Scholar

  13. Joanna Schellenberg
    View author publications

    You can also search for this author in PubMed Google Scholar

  14. Lena M. Lorenz
    View author publications

    You can also search for this author in PubMed Google Scholar

  15. Fredros O. Okumu
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

FOO JKS ASM conceptualized the idea. FOO JKS and LML designed the study. JKS DK WPM APN and MFF performed collection of data. SA supported laboratory analysis. JKS MFF OGO and HSN analysed the data. AJL created the map. RMN and JKS project administration. LML, SJM, JS and FOO offered scientific supervision. JKS wrote the original manuscript draft. ASM, OGO, HSN, WPM, APN, MFF, SA, SJM, JS, LML and FOO reviewed and revised the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Johnson K. Swai.

Ethics declarations

Ethics approval and consent to participate

Medical Research Coordinating Committee of the National Institute for Medical Research in Tanzania (NIMR/HQ/R.8a/Vol.IX/2476) and the Institutional Review Board of Ifakara Health Institute IHI/IRB/EXT/No: 009-2018 approved the study protocol. Participation in this study was voluntary. Both oral and written consent were sought. Households and participants were recruited only if they willingly agreed to participate and returned a signed written consent form. Additionally, prior to starting the study, permission to carry out the study was obtained from the community leaders in the areas where the study was conducted. Long-lasting insecticide treated nets, i.e. the Olyset® nets were provided to all households participating in the transfluthrin-treated eave ribbons evaluations.

Consent for publication

This manuscript has been approved for publication by the National Institute of Medical Research, Tanzania. Reference number: NIMR/HQ/P.12 VOL XXVII/30.

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 distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Swai, J.K., Mmbando, A.S., Ngowo, H.S. et al. Protecting migratory farmers in rural Tanzania using eave ribbons treated with the spatial mosquito repellent, transfluthrin. Malar J 18, 414 (2019). https://doi.org/10.1186/s12936-019-3048-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12936-019-3048-8

Keywords

Malaria Journal

ISSN: 1475-2875

Contact us