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Insecticide-impregnated netting as a potential tool for long-lasting control of the leishmaniasis vector Lutzomyia longipalpis in animal shelters

Parasites & Vectors volume 6, Article number: 133 (2013) Cite this article

Abstract

Background

Leishmaniasis remains a serious neglected disease, with more than 350 million people potentially at risk worldwide. Control strategies often rely on spraying residual insecticides to target populations of the sand fly vectors that transmit Leishmania parasites when blood-feeding. These programmes are often difficult to sustain effectively, as sand fly resting sites must be resprayed on a regular basis. Here, we investigate whether application of insecticide-impregnated netting to a surface could act as an alternative to residual spraying for controlling the American visceral leishmaniasis vector Lutzomyia longipalpis.

Methods

Female L. longipalpis from our laboratory colony were exposed for 1 h to three treatments applied to plywood surfaces: 2% permethrin-impregnated netting (Olyset®), 20 mg a.i.m-2 micro-encapsulated lambda-cyhalothrin (Demand CS®) and a no-treatment control. We compared the speed at which these treatments acted, by measuring the percentage of sand flies killed both immediately after exposure to the treatment for 1 hour, as well as the number that had died 24 h after the 1 hour exposure. We repeated the experiment at 6 and 12 months following application to test the effectiveness of each treatment over time.

Results

When first applied, the lambda-cyhalothrin killed more sand flies in the first hour than the permethrin-impregnated netting. However, the effectiveness of the lambda-cyhalothrin diminished over time, so that there was no difference between the two treatments at 12 months. Both killed more sand flies than the control. When measured 24 h following exposure, both test treatments had killed close to 100% of sand flies when first applied, but while the lethal effect of the netting was maintained at close to 100% over 12 months, the effectiveness of the residual insecticide diminished to approximately 80% after 6 months.

Conclusions

The results of these initial laboratory experiments indicate that covering surfaces with insecticide impregnated netting material may provide a longer-lasting solution for killing sand flies than residual spraying. Field trials are needed to identify the feasibility of treating surfaces with netting or similar impregnated materials as part of a control program. In targeting L. longipalpis, the greatest benefits may be seen in treating animal sheds with netting, where these sand flies aggregate in large numbers, and which can be difficult to treat repeatedly by conventional spraying.

Background

Leishmaniasis remains a serious neglected disease, with more than 350 million people at potential risk worldwide, and an estimated 50 000 deaths per year [1]. Infection by the etiologic agents, protozoan parasites of the genus Leishmania (Kinetoplastida: Trypanosomatidiae), can lead to severe disfigurement (cutaneous and mucocutaneous leishmaniasis), and can be fatal if left untreated (visceral leishmaniasis). As there is currently no effective human vaccine [2], strategies that aim to control leishmaniasis most often target infected animal reservoirs, through culling (which is unpopular and often ineffective [3]), or populations of the sand fly vectors (Diptera: Psychodidae), which transmit the disease [4–6]. Approximately 70 species of sand fly have been identified as vectors of leishmaniasis [7], and although ecology and feeding behaviour vary between species, transmission always occurs through blood-feeding by female sand flies on an infected animal or human host.

Sand fly control programmes often rely on spraying potential resting sites (for example, animal or human houses) with residual insecticides [5]. While regular spraying can offer some protection to human populations from infection [8], such strategies are often difficult to sustain effectively, particularly in rural communities, where there may be large numbers of potential resting sites that must be visited and resprayed on a regular basis (for example, once every six months in endemic areas [9]). Spraying also requires training to be conducted effectively, in order to ensure that the correct concentration of insecticide is applied to kill sand flies, while minimizing exposure to sub-lethal amounts which might promote the onset of resistance [10, 11]. In Brazil, where over 90% of visceral leishmaniasis cases in South America occur, insecticide is applied only after a human case has been identified because of the logistics associated with spraying [12].

A longer-lasting solution for killing sand flies, which does need to be reapplied with the same frequency as residual spraying, could dramatically reduce the cost of leishmaniasis control programmes, facilitating their adoption by disease control agencies. Insecticide-treated bed nets (ITNs) offer a cost-effective alternative to residual spraying, offering personal protection from nuisance insects [13], mosquito vectors of malaria [14] and sand fly vectors of cutaneous leishmaniasis [15, 16]. In Brazil, trials of deltamethrin-impregnated bed nets have demonstrated important entomological effects associated with their use, reducing the landing rate of the American visceral leishmaniasis (AVL) vector Lutomyia longipalpis on humans, and increasing sand fly mortality, compared to untreated nets [15]. However, as a consequence of the crepuscular feeding activity of L. longipalpis, nets used in this way in practice offer limited protection against AVL as more than 50% of bites occur in the early evening, before householders are sleeping under nets [17].

An alternative to using insecticide-releasing materials such as bednets could be to apply the netting to surfaces where sand flies rest, as a direct alternative to residual spraying. Modern long-lasting insecticide netting (LLIN) can withstand washing and will release insecticide for a number of years (e.g. up to 5 for some formulations), without the need for retreatment [18]. If suitably effective at killing L. longipalpis, deployment of such nets as a means of delivering insecticide, at lethal dosage levels without the need for complex training and validation of dosage levels, at sand fly resting sites could be more cost-effective than repeated spraying with residual insecticides. However, while LLINs are now recommended for use in malaria vector control programmes [18] their effectiveness in killing L. longipalpis, and their longevity compared to conventional insecticides for L. longipalpis control, has not been ascertained under controlled conditions.

The aim of this study was to determine whether LLIN could be used as an effective direct replacement for residual insecticide spraying as a means of killing L. longipalpis. The lethal effect of permethrin-impregnated netting against female L. longipalpis was compared with that of a micro-encapsulated formulation of lambda-cyhalothrin, an insecticide recommended for use for L. longipalpis control in Brazil [12], designed to provide long-lasting residual control of insect pests [19]. Our goal was not to compare directly between the two chemical insecticides used in the LLIN and the micro-encapsulated spray, which are present at different concentrations, but rather to determine which of these two products, already marketed for use in protecting against blood-feeding insects, would provide a longer-lasting solution for killing Lutzomyia longipalpis at sand fly resting sites.

To assess the relative longevity of these two insecticide delivery methods, we compared their effectiveness both shortly after their application to a wooden surface, and again after periods of six and twelve months. To test for differences in the speed at which these insecticide treatments act, their lethal effect was measured on a group of sand flies after they had been exposed to a treated surface for 1 hour (immediate effect) and again on the same group of sand flies after a period of 24 h had elapsed since their initial exposure (delayed effect).

Methods

Surface treatment

Insecticides were applied to 80 mm × 80 mm sections of 10 mm-thick marine plywood (Homebase Limited, Buckinghamshire, UK). For netting treatments, a single layer of blue Olyset® (Sumitomo Chemical Co. Ltd., Tokyo, Japan) netting, consisting of woven polyester hexagons (3 mm approximate diameter) impregnated with 2% permethrin, was secured over the entire surface using drawing pins. For residual insecticide treatment, surfaces were treated with a 20 mg a.i.m-2 solution of microencapsulated lambda-cyhalothrin (Demand CS®; BASF PLC, Cheshire, UK), using a paintbrush and allowed to dry for 24 h. This insecticide formulation was chosen as previous studies have demonstrated its relatively long-lasting efficacy against sand flies compared to non-microencapsulated formulations of other insecticides [8], and a similar formulation has been shown to kill L. longipalpis in the field at this concentration [20, 21]. The concentration applied is that recommended by the manufacturer for use against mosquitoes, and is not dissimilar to that endorsed by the Brazilian health authorities for sand fly control (30 mg a.i.m-2, [12]). This product therefore most likely represents the strongest possible competitor for comparison against insecticide impregnated materials for long-lasting control of sand flies. A third category of surfaces were left untreated as controls.

Insecticide testing

For each replicate, the open face (80 mm diameter) of a 118 ml polystyrene cup (Dart Products Limited, West Midlands, UK) was attached to the treated plywood surface using adhesive tape. Twenty-five 6 day-old female L. longipalpis from a laboratory colony [22], were then introduced via a small hole cut in the base of the cup. The hole was sealed using a cotton wool plug, and the treated surface held vertically for 1 h, after which time the cup was removed in a Nylon cage (18 cm × 18 cm × 18 cm), and the number of sand flies alive and dead counted. The cage containing the remaining sand flies was kept within a humidified polythene bag for 24 h at 27°C, when the numbers of dead and alive flies were again recorded. The period of exposure used was chosen to allow comparison with a previous study that used the same time period in similar bioassays measuring the long term effectiveness of lamba-cyhalothrin against sand flies when applied to internal and external surfaces in the field [8].

Ten replicates were performed for each treatment (netting, insecticide and untreated control), using different sand flies and treated surfaces for each replicate. To assess the relative longevity of each treatment, the same testing procedure was repeated after six and twelve months, with treated surfaces kept free-standing under dry indoor conditions in the UK until they were retested.

Data analysis

The percentage of sand flies killed by the three treatments over time was compared by ANOVA. Firstly, percentage of sand flies killed immediately following 1 h of exposure (number of sand flies killed/number exposed * 100) was entered as the dependent variable, with treatment (control, netting and insecticide) and time since application of treatment (0 months, 6 months and 12 months) entered as factors. An interaction term (treatment by time since treatment) was also included, to test for a potential difference in the way in which the effectiveness of the three treatments changed over time. Where significant effects were found in the two-way ANOVA, an individual one-way ANOVA was used to examine how the effectiveness of each treatment changed with time, with time points compared through Tukey’s post-hoc tests. Similarly, one-way ANOVA and Tukey’s post-hoc tests were used to clarify differences in the effectiveness of each treatment at each time point.

The analysis was then repeated with percentage of sand flies killed after 24 h entered as the dependent variable, to test for differences between the three treatments over time in their effectiveness in killing sand flies over a more prolonged period following exposure. All analyses were performed in R version 2.15.2 [23], and for both full models residuals were approximately normally distributed, indicating an appropriate fit to the data set.

Results

Immediate efficacy of insecticide treatments

Overall, a significant difference was found between the three treatments (control, netting and insecticide) in their effectiveness in killing sand flies within 1 h following exposure (immediate effect) (F2, 81 = 107.6, P <0.001) and the immediate lethal effect of treatment was also found to change over time (F2, 81 = 53.1, P < 0.001). The presence of a significant interaction term (treatment by time since treatment; F4, 81 = 49.4, P <0.001) indicated that, overall, the three treatments differed in how their effectiveness changed over time.

Subsequent analysis revealed that the immediate lethal effect of the control (Figure 1A) and netting treatments (Figure 1B) remained constant, killing on average (mean ± SEM) 0.8% ± 0.3 and 13.5% ±1.3 of exposed sand flies respectively. The effectiveness of the insecticide treatment, however, dropped significantly over time, from 56% ± 3.9 immediately after application to 10.0% ± 2.1 at 6 months, whereafter its effectiveness remained relatively constant up to 12 months (Figure 1C).

Figure 1
figure 1

Immediate efficacy of insecticide treatments. Percentage of sand flies killed immediately following 1 h exposure to plywood surfaces, untreated (control), covered with permethrin-impregnated netting or treated with lambda-cyhalothrin (insecticide). A-C: change in effectiveness of each treatment over time. F-values refer to ANOVA across all three time points, different letters indicate significant differences between time points (Tukey’s post-hoc test). D: comparison of effectiveness of each treatment at each time point. F-values refer to ANOVA across all three categories at each time point; different letters indicate significant differences between categories at each time point. * = P < 0.05, ** = P < 0.01, *** = P < 0.05. NS = Not Significant.

Full size image

The residual insecticide killed more sand flies at 0 months compared to the netting (Figure 1D). However, as the immediate lethal effect of the insecticide decreased over time, the netting became relatively more effective so that by 12 months, there was no significant difference between the two. Throughout, both micro-encapsulated insecticide and netting treatments killed significantly more sand flies than the no-treatment control (Figure 1D).

Efficacy of insecticide treatments over 24 h

The three treatments differed overall in their lethal effect on sand flies in the 24 h period following exposure (F2, 81 = 1026, P <0.001), and overall their effectiveness was found to change over time since application. As above, the extent to which the effectiveness of each treatment diminished was also found to differ (F2, 81 = 6.6, P <0.001).

In subsequent analyses, the lethal effects of the netting and control treatments were not found to differ over the 12 months following application (Figure 2A, B). The netting killed 98.1% ± 0.6 of sand flies exposed, compared to the control, which killed 2.7% ± 0.6 sand flies exposed within 24 h. The effectiveness of the micro-encapsulated insecticide, however, dropped from 97.2% ± 1.3 immediately after treatment, to 74.0% ± 6.9 and 87.2% ± 2.4 six and twelve months after application respectively (Figure 2C).

Figure 2
figure 2

Efficacy of insecticide treatments over 24 h. Percentage of sand flies killed within 24 h following 1 h exposure to plywood surfaces, untreated (control), covered with permethrin-impregnated netting or treated with lambda-cyhalothrin (insecticide). A-C: change in effectiveness of each treatment over time. F-values refer to ANOVA across all three time points, different letters indicate significant differences between time points (Tukey’s post-hoc test). D: comparison of effectiveness of each treatment at each time point. F-values refer to ANOVA across all three categories at each time point; different letters indicate significant differences between categories at each time point. * = P < 0.05, ** = P < 0.01, *** = P < 0.05. NS = Not Significant.

Full size image

In comparing the three treatments at each time point, both the netting and insecticide killed close to 100% of sand flies exposed within 24 h when first applied, with no difference between the effectiveness of the two treatments (Figure 2D). However, at 6 and 12 months, the netting killed significantly more sand flies than the insecticide. Both treatments killed significantly more sand flies than the control throughout the 12 months of the experiment (Figure 2D).

Discussion

Long-lasting insecticide impregnated netting has not previously been tested as a mechanism for delivering insecticide to kill L. longipalpis. In this laboratory study, Olyset® netting attached to a wooden surface killed as many sand flies as lambda-cyhalothrin within 24 h when first applied, and might therefore be considered as a feasible alternative to residual spraying.

Lambda-cyhalothrin has been shown to be effective in killing sand flies under experimental conditions [8, 10, 20, 21] and is recommended for use by the Brazilian Ministry of Health for leishmaniasis control [12]. It was chosen for comparison in this study because the micro-encapsulated formulation is designed to provide a relatively long-lasting residual effect compared to conventional insecticide formulations [19]. Here, efficacy of the lambda-cyhalothrin treatment declined to 74% over 6 months: a reduction similar to that observed against the cutaneous leishmaniasis vector Lutzomyia verrucarum when sprayed on outside walls in Peru [8]. In comparison, the permethrin-impregnated netting maintained its effectiveness at close to 100% lethality 24 h post exposure for the twelve months of the study. Olyset netting might, therefore, provide a longer-lasting solution for killing L. longipalpis: however, permethrin is not currently used by the Brazilian Ministry of Health for sand fly control [12], and while its efficacy under laboratory conditions is shown here, trials performed using a variety of indoor and outdoor surfaces in Brazil will be needed to confirm its effectiveness in the field. Alternatively, trials could be conducted using long-lasting netting impregnated with deltamethrin [24], an insecticide that is already approved for sand fly control by the Brazilian Government [12].

While both residual insecticide and netting treatments killed close to 100% of L. longipalpis within 24 h when first applied, the immediate mortality-inducing effect of the netting was significantly weaker than that of the lambda-cyhalothrin, with fewer flies killed immediately following 1 h of exposure. A trade-off may therefore exist between the faster immediate efficacy of the residual insecticide when first applied, and the overall longevity of the netting. The speed at which an insecticide intervention acts may be most important when used for personal protection: for example, as a bed net or bedroom wall covering when flies are in close proximity to the target host, and must be killed before they attempt to blood-feed.

Erecting insecticide impregnated materials as an alternative to residual spraying (for example as curtains) might reduce the number of L. longipalpis resting on walls, and therefore biting rate on humans, for a longer period. It may also be a more acceptable solution to householders concerned with the potential health risks of spraying insecticides indoors in close proximity to humans and domestic animals. Impregnated netting used in this way has been shown to be effective against several endophilic species of sand fly, which readily enter houses in search of a blood meal [25–29]. However, the usefulness of such a strategy against vectors that are more abundant in the peridomestic environment, such as L. longipalpis[30], is unclear [31]. In this instance, greater reductions in local vector populations could more easily be achieved by placing the netting in animal houses where sand flies congregate in the early evening [32]. However, previous trials in Brazil have demonstrated that insecticide-treated cotton sheets (‘targets’) sprayed with lambda-cyhalothrin were relatively poor in controlling L. longipalpis in chicken sheds compared with residual spraying [21]. A relatively large proportion of the internal surface of the animal house might, therefore, have to be treated with the netting for such a strategy to have a significant impact on sand fly numbers in the proximity of human houses, and thereby reduce biting risk and subsequent transmission. Attaching the netting to the internal walls of animal houses using staples or nails, while leaving openings free for domestic animals to enter and exit, may provide the most acceptable means of application for householders. However, the efficacy of this solution in killing L. longipalpis will depend on the availability of solid internal surfaces on which sand flies can alight. Furthermore, sand flies may not remain on insecticide treated surfaces for as long as the 1 h exposure period used in this study, instead being diverted away or immobilized once they come into close proximity with a treated surface [17]. Addition of an attractive bait may be needed to prevent sand flies being displaced to non-treated sites, potentially closer to human habitation [20, 21].

Whether or not insecticide-impregnated materials would be adopted by disease control agencies for use against L. longipalpis would depend in part on their cost compared to insecticides, and the logistics of their implementation and maintenance. Although netting may be more bulky to transport, its deployment would not require either the specialist safety equipment or training needed for insecticide spraying, and it would not have to be replaced as frequently. Further efficiency savings could be made if a suitable insecticide impregnated material could be deployed to protect against mosquito vectors of dengue, and malaria, as well as leishmaniasis-transmitting sand flies. However, while insecticide impregnated linings have been tested against mosquitoes, it appears they are most effective when applied in combination with bed nets or residual spraying [33–36]. They may therefore, be most useful in offering protection against exophilic, exophagic or zoophilic sand flies, where bednets offer little protection against crepuscular feeding, and residual spraying of indoor and outdoor resting sites cannot be maintained effectively.

Conclusion

The results of this laboratory study indicate that LLINs could provide a longer-lasting alternative for controlling numbers of L. longipalpis in animal houses, compared to even the most durable of sprayed-on residual insecticide treatments. Field studies are needed to determine how these nets could most effectively be applied in chicken sheds and other animal shelters, where sand flies congregate in large numbers.

References

  1. WHO Expert Committee: Control of the leishmaniasis: report of a meeting of the WHO expert committee on the control of leishmaniases, Geneva, 22-26 March 2010. Who Tech Rep Ser. 2010, 949: 1-186.

    Google Scholar 

  2. Noazin S, Khamesipour A, Moulton LH, Tanner M, Nasseri K, Modabber F, Sharifi I, Khalil EAG, Bernal IDV, Antunes CMF, Smith PG: Efficacy of killed whole-parasite vaccines in the prevention of leishmaniasis: a meta-analysis. Vaccine. 2009, 27: 4747-4753. 10.1016/j.vaccine.2009.05.084.

    Article  CAS  PubMed  Google Scholar 

  3. Tesh R: Control of zoonotic visceral leishmaniasis - Is it time to change strategies?. AmJTrop Med Hyg. 1995, 52: 287-292.

    CAS  Google Scholar 

  4. Lacerda M: The Brazilian leishmaniasis control program. Mem Inst Oswaldo Cruz. 1994, 89: 489-495. 10.1590/S0074-02761994000300036.

    Article  CAS  PubMed  Google Scholar 

  5. Alexander B, Maroli M: Control of phlebotomine sandflies. Med Vet Entomol. 2003, 17: 1-18. 10.1046/j.1365-2915.2003.00420.x.

    Article  CAS  PubMed  Google Scholar 

  6. Courtenay O, Quinnell RJ, Garcez LM, Shaw JJ, Dye C: Infectiousness in a cohort of Brazilian dogs: Why culling fails to control visceral leishmaniasis in areas of high transmission. J Infect Dis. 2002, 186: 1314-1320. 10.1086/344312.

    Article  PubMed  Google Scholar 

  7. Ready PD: Biology of phlebotomine sand flies as vectors of disease agents. Annu Rev Entomol. 2013, 58: 227-250. 10.1146/annurev-ento-120811-153557.

    Article  CAS  PubMed  Google Scholar 

  8. Davies CR, Llanos-Cuentas EA, Campos P, Monge J, Leon E, Canales J: Spraying houses in the Peruvian Andes with lambda-cyhalothrin protects residents against cutaneous leishmaniasis. Trans R Soc Trop Med Hyg. 2000, 94: 631-636. 10.1016/S0035-9203(00)90214-1.

    Article  CAS  PubMed  Google Scholar 

  9. Picado A, Dash AP, Bhattacharya S, Boelaert M: Vector control interventions for visceral leishmaniasis elimination initiative in South Asia, 2005-2010. Indian J Med Res. 2012, 136: 22-31.

    PubMed Central  PubMed  Google Scholar 

  10. Alexander B, Barros VC, de Souza SF, Barros SS, Teodoro LP, Soares ZR, Gontijo NF, Reithinger R: Susceptibility to chemical insecticides of two Brazilian populations of the visceral leishmaniasis vector Lutzomyia longipalpis (Diptera: Psychodidae). Trop Med Int Health. 2009, 14: 1272-1277. 10.1111/j.1365-3156.2009.02371.x.

    Article  CAS  PubMed  Google Scholar 

  11. Chowdhury R, Huda MM, Kumar V, Das P, Joshi AB, Banjara MR, Akhter S, Kroeger A, Krishnakumari B, Petzold M, Mondal D, Das ML: The Indian and Nepalese programmes of indoor residual spraying for the elimination of visceral leishmaniasis: performance and effectiveness. Ann Trop Med Parasitol. 2011, 105: 31-45. 10.1179/136485911X12899838683124.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  12. Secretaria de Vigilância em Saúde: Manual de Vigilância e Controle da Leishmaniose Visceral. 2006, Brasília: Ministério da Saúde

    Google Scholar 

  13. Lindsay SW, Gibson ME: Bednets revisited- old idea, new angle. Parasitol Today. 1988, 4: 270-272. 10.1016/0169-4758(88)90017-8.

    Article  CAS  PubMed  Google Scholar 

  14. Lengeler C: Insecticide-treated nets for malaria control: real gains. Bull World Health Organ. 2004, 82: 84-

    PubMed Central  PubMed  Google Scholar 

  15. Reyburn H, Ashford R, Mohsen M, Hewitt S, Rowland M: A randomized controlled trial of insecticide-treated bednets and chaddars or top sheets, and residual spraying of interior rooms for the prevention of cutaneous leishmaniasis in Kabul, Afghanistan. Trans R Soc Trop Med Hyg. 2000, 94: 361-366. 10.1016/S0035-9203(00)90104-4.

    Article  CAS  PubMed  Google Scholar 

  16. Jalouk L, Al Ahmed M, Gradoni L, Maroli M: Insecticide-treated bednets to prevent anthroponotic cutaneous leishmaniasis in Aleppo Governorate, Syria: results from two trials. Trans R Soc Trop Med Hyg. 2007, 101: 360-367. 10.1016/j.trstmh.2006.07.011.

    Article  CAS  PubMed  Google Scholar 

  17. Courtenay O, Gillingwater K, Gomes PAF, Garcez LM, Davies CR: Deltamethrin-impregnated bednets reduce human landing rates of sandfly vector Lutzomyia longipalpis in Amazon households. Med Vet Entomol. 2007, 21: 168-176. 10.1111/j.1365-2915.2007.00678.x.

    Article  CAS  PubMed  Google Scholar 

  18. WHO: Insecticide-treated mosquito nets: a position statement. 2007, Geneva, Switzerland: World Health Organization

    Google Scholar 

  19. Wege PE, Hoppé MA, Bywater AF, Weeks SD: A microencapsulated formulation of lambda-cyhalothrin In Proceedings of the International Conference on Urban Pests: 19–22. Prague. 1999, 1999: 301-310.

    Google Scholar 

  20. Bray DP, Alves GB, Dorval ME, Brazil RP, Hamilton JG: Synthetic sex pheromone attracts the leishmaniasis vector Lutzomyia longipalpis to experimental chicken sheds treated with insecticide. Parasit Vectors. 2010, 3: 16-10.1186/1756-3305-3-16.

    Article  PubMed Central  PubMed  Google Scholar 

  21. Kelly DW, Mustafa Z, Dye C: Differential application of lambda-cyhalothrin to control the sandfly Lutzomyia longipalpis. Med Vet Entomol. 1997, 11: 13-24. 10.1111/j.1365-2915.1997.tb00285.x.

    Article  CAS  PubMed  Google Scholar 

  22. Bray DP, Bandi KK, Brazil RP, Oliveira AG, Hamilton JGC: Synthetic sex pheromone attracts the leishmaniasis vector Lutzomyia longipalpis (Diptera: Psychodidae) to traps in the field. J Med Entomol. 2009, 46: 428-434. 10.1603/033.046.0303.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  23. R Core Team: R: A language and environment for statistical computing. 2012, Vienna, Austria: R Foundation for Statistical Computing

    Google Scholar 

  24. Das ML, Roy L, Rijal S, Paudel IS, Picado A, Kroeger A, Petzold M, Davies C, Boelaert M: Comparative study of kala-azar vector control measures in eastern Nepal. Acta Trop. 2010, 113: 162-166. 10.1016/j.actatropica.2009.10.012.

    Article  CAS  PubMed  Google Scholar 

  25. Maroli M, Majori G: Permethrin-impregnated curtains against phlebotomine sandflies (Diptera: Psychodidae): laboratory and field studies. Parassitologia. 1991, 33 (Suppl): 399-404.

    PubMed  Google Scholar 

  26. Majori G, Maroli M, Sabatinelli G, Fausto A: Efficacy of permethrin-impregnated curtains against endophilic phlebotomine sandflies in Burkina-Faso. Med Vet Entomol. 1989, 3: 441-444. 10.1111/j.1365-2915.1989.tb00253.x.

    Article  CAS  PubMed  Google Scholar 

  27. Kroeger A, Avila EV, Morison L: Insecticide impregnated curtains to control domestic transmission of cutaneous leishmaniasis in Venezuela: cluster randomised trial. Br Med J. 2002, 325: 810-813. 10.1136/bmj.325.7368.810.

    Article  Google Scholar 

  28. Elnaiem DA, Aboud MA, El Mubarek SG, Hassan HK, Ward RD: Impact of pyrethroid-impregnated curtains on Phlebotomus papatasi sandflies indoors at Khartoum, Sudan. Med Vet Entomol. 1999, 13: 191-197. 10.1046/j.1365-2915.1999.00183.x.

    Article  CAS  PubMed  Google Scholar 

  29. Alexander B, Usma M, Cadena H, Quesada B, Solarte Y, Roa W, Travi B: Evaluation of deltamethrin-impregnated bednets and curtains against phlebotomine sandflies in Valle Del Cauca, Colombia. Med Vet Entomol. 1995, 9: 279-283. 10.1111/j.1365-2915.1995.tb00134.x.

    Article  CAS  PubMed  Google Scholar 

  30. Quinnell R, Dye C: Correlates of the peridomestic abundance of Lutzomyia-Longipalpis (Diptera, Psychodidae) in Amazonian Brazil. Med Vet Entomol. 1994, 8: 219-224. 10.1111/j.1365-2915.1994.tb00502.x.

    Article  CAS  PubMed  Google Scholar 

  31. Kroeger A, Gonzalez M, Ordonez-Gonzalez J: Insecticide-treated materials for malaria control in Latin America: to use or not to use?. Trans R Soc Trop Med Hyg. 1999, 93: 565-570. 10.1016/S0035-9203(99)90048-2.

    Article  CAS  PubMed  Google Scholar 

  32. Morrison A, Ferro C, Pardo R, Torres M, Wilson M, Tesh R: Nocturnal activity patterns of Lutzomyia longipalpis (Diptera, Psychodidae) at an endemic focus of visceral leishmaniasis in Colombia. J Med Entomol. 1995, 32: 605-617.

    Article  CAS  PubMed  Google Scholar 

  33. Kasili S, Kutima H, Mwandawiro C, Ngumbi PM, Anjili CO, Enayati AA: Laboratory and semi-field evaluation of long-lasting insecticidal nets against leishmaniasis vector, Phlebotomus (Phlebotomus) duboscqi in Kenya. J Vector Borne Dis. 2010, 47: 1-10.

    PubMed  Google Scholar 

  34. Brosseau L, Drame PM, Besnard P, Toto J-C, Foumane V, Le Mire J, Mouchet F, Remoue F, Allan R, Fortes F, Carnevale P, Manguin S: Human antibody response to Anopheles saliva for comparing the efficacy of three malaria vector control methods in Balombo, Angola. Plos One. 2012, 7: e44189-10.1371/journal.pone.0044189.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  35. Chandre F, Dabire RK, Hougard J-M, Djogbenou LS, Irish SR, Rowland M, N’guessan R: Field efficacy of pyrethroid treated plastic sheeting (durable lining) in combination with long lasting insecticidal nets against malaria vectors. Parasit Vectors. 2010, 3: 65-10.1186/1756-3305-3-65.

    Article  PubMed Central  PubMed  Google Scholar 

  36. Messenger LA, Miller NP, Adeogun AO, Awolola TS, Rowland M: The development of insecticide-treated durable wall lining for malaria control: insights from rural and urban populations in Angola and Nigeria. Malar J. 2012, 11: 332-10.1186/1475-2875-11-332.

    Article  PubMed Central  PubMed  Google Scholar 

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Acknowledgements

The authors wish to thank Dr P Taylor and Mrs A Underhill for assistance in sand fly rearing. This work was supported by the Welcome Trust.

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  1. Centre for Applied Entomology and Parasitology, Institute for Science and Technology in Medicine, Keele University, Keele, Staffordshire, ST5 5BG, UK

    Daniel Peter Bray & James G C Hamilton

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  1. Daniel Peter Bray
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  2. James G C Hamilton
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Correspondence to Daniel Peter Bray.

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The authors declare that they have no competing interests.

Authors’ contributions

DPB and JGH conceived the study. DPB carried out the study, performed the analysis and drafted the manuscript. Both authors read and approved the final manuscript.

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Bray, D.P., Hamilton, J.G.C. Insecticide-impregnated netting as a potential tool for long-lasting control of the leishmaniasis vector Lutzomyia longipalpis in animal shelters. Parasites Vectors 6, 133 (2013). https://doi.org/10.1186/1756-3305-6-133

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  • DOI: https://doi.org/10.1186/1756-3305-6-133

Keywords

Parasites & Vectors

ISSN: 1756-3305

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