Volume 20, Number 10—October 2014
Increased Pyrethroid Resistance in Malaria Vectors and Decreased Bed Net Effectiveness, Burkina Faso
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|EID||Toé KH, Jones CM, N’Fale S, Ismail HM, Dabiré RK, Ranson H. Increased Pyrethroid Resistance in Malaria Vectors and Decreased Bed Net Effectiveness, Burkina Faso. Emerg Infect Dis. 2014;20(10):1691-1696. https://dx.doi.org/10.3201/eid2010.140619|
|AMA||Toé KH, Jones CM, N’Fale S, et al. Increased Pyrethroid Resistance in Malaria Vectors and Decreased Bed Net Effectiveness, Burkina Faso. Emerging Infectious Diseases. 2014;20(10):1691-1696. doi:10.3201/eid2010.140619.|
|APA||Toé, K. H., Jones, C. M., N’Fale, S., Ismail, H. M., Dabiré, R. K., & Ranson, H. (2014). Increased Pyrethroid Resistance in Malaria Vectors and Decreased Bed Net Effectiveness, Burkina Faso. Emerging Infectious Diseases, 20(10), 1691-1696. https://dx.doi.org/10.3201/eid2010.140619.|
Malaria control is dependent on insecticides. Increases in prevalence of insecticide resistance in malaria vectors across Africa are well-documented. However, few attempts have been made to quantify the strength of this resistance and link it to the effectiveness of control tools. Using quantitative bioassays, we show that in Burkina Faso pyrethroid resistance in Anopheles gambiae mosquitoes has increased in intensity in recent years and now exceeds 1,000-fold. In laboratory assays, this level of resistance renders insecticides used to impregnate bed nets ineffective. Thus, the level of personal and community protection afforded by long-lasting insecticide-treated net campaigns will probably be reduced. Standardized methods are needed to quantify resistance levels in malaria vectors and link these levels to failure of vector control methods.
Long-lasting insecticide–treated bed nets (LLINs) have been shown repeatedly to provide protection against malaria transmission in Africa and reduce childhood mortality rates by ≈20% (1). Distribution of LLINs has increased over the past decade, and an estimated 54% of households at risk for malaria in sub-Saharan Africa have ≥1 LLIN. This factor has been a major contributor in reducing malaria incidence; the estimated malaria mortality rate for Africa has decreased by ≈49% since 2000 (2). These advances are now threatened by rapid selection and spread of resistance to insecticides in malaria vectors (3). Resistance to pyrethroids, the only class of insecticides available for use on LLINs, is now widespread in Anopheles gambiae and An. funestus mosquitoes, the major malaria vectors (4).
To standardize monitoring for insecticide resistance, the World Health Organization (WHO) has developed simple bioassays that use filter papers impregnated with insecticide at a predefined diagnostic dose. A population is described as resistant to an insecticide if a mortality rate >90% is observed in these tests (5). These assays are useful for detecting resistance when it first appears in the population. However, these assays do not provide any information on the strength of this resistance. This information is crucial for assessing the likely effect of this resistance on effectiveness of vector control tools. The Global Plan for Insecticide Resistance Management in Malaria Vectors (3) recommends that all malaria-endemic countries monitor insecticide resistance in local vectors. However, because the correlation between results of diagnostic dose assays and control effectiveness remains undefined, simple detection of resistance in a mosquito population is not sufficient evidence to implement a change in insecticide policy.
In this study, we used variants of WHO assays and bottle assays of the Centers for Disease Control and Prevention (CDC) (Atlanta, GA, USA) to quantify the level of pyrethroid resistance in a population of An. gambiae mosquitoes from Burkina Faso over a 3-year period. A high level of resistance was observed. The lack of comparator data from across Africa makes it impossible to conclude whether the pyrethroid resistance levels seen in Burkina Faso are atypical. However, these data should raise concerns for malaria control across Africa because we demonstrate that this level of resistance is causing operational failure of the insecticides used in LLINs.
The study site was in Vallée de Kou (Bama) in southwestern Burkina Faso, ≈25 km from the city of Bobo-Dioulasso. It consists of 7 small villages (area 1,200 hectares) and has been a major rice cultivation site since the 1970s. The area is surrounded by cotton-, rice-, and vegetable-growing areas in which insecticide use is intensive (6). Multiple rounds of collections of third and fourth instar Anopheles spp. larvae were performed in a 1-km2 radius from village 7 during June–July 2011, October 2011, June 2012, and July–October 2013. Mosquitoes from each collection round were pooled and reared to adults in insectaries at the Institut de Recherche en Sciences de la Sante/Centre Muraz in Bobo-Dioulasso or the Centre National de Recherche et de Formation sur le Paludisme (CNRFP) in Ouagadougou. Species were identified for a subset of mosquitoes from each collection round by using the Sine 200 PCR (7).
Non–blood fed An. gambiae female mosquitoes (3–5 days old) were tested with 5 insecticides in 4 insecticide classes: 0.75% permethrin (type I pyrethroid) and 0.05% deltamethrin (type II pyrethroid); 4% DDT (organochlorine); 0.1% bendiocarb (carbamate); and 1% fenitrothion (organophosphate) by using WHO susceptibility tests (8). Each batch of insecticide-impregnated papers was tested against mosquitoes of the An. gambiae Kisumu laboratory strain (insecticide-susceptible) at the CNRFP bioassay laboratory for quality control. Approximately 100 mosquitoes (4 replicates of 25 mosquitoes) were used per test (5). The average mortality rate and binomial confidence interval were calculated per insecticide (9).
In 2011 and 2012, the 50% lethality time (LT50) for the VK7 strain of An. gambiae mosquitoes was determined by varying the length of exposure time (60–600 min). The mean mortality rate was recorded per time point, and the LT50 was estimated by fitting a logistic regression model by using logit-transformed probabilities (10) in R statistical software (http://www.r-project.org).
In 2013, CDC bottle bioassays were used to quantify the level of resistance to deltamethrin. Glass 250-mL bottles were coated with different concentration of deltamethrin ranging from 3.125 μg/mL to 125 μg/mL at CNRFP. Bottles were prepared according to CDC guidelines (11). Female mosquitoes (3–5 days) were aspirated into bottles for 1 h and subsequently transferred to insecticide-free paper cups for 24 h of observation. Four to six replicates were performed for each concentration and for the control bottles (impregnated with acetone). Equivalent age mosquitoes of the Kisumu strain were exposed to various insecticide concentrations (range 0.001 μg/mL–0.5 μg/mL). The 50% lethal dose (LD50) was determined by using R statistical software.
A subset of LLINs that were distributed during the 2010 national distribution campaign were collected directly from houses in 2012; householders were given a new LLIN as a replacement. Only nets reportedly washed ≤5 times were included in the study. New net samples of the same type were also obtained from the population or from local markets. Six types of nets were tested: PermaNet 2.0 (deltamethrin coated on polyester; Vestergaard, Lausanne, Switzerland); Interceptor (α-cypermethrin coated on polyester; BASF, Florham Park, NJ, USA); DawaPlus (deltamethrin coated on polyester; TANA Netting Ltd., Bangkok, Thailand); NetProtect (deltamethrin incorporated into polyethylene; BESTNET, Kolding, Denmark); PermaNet 3.0 (deltamethrin coated on polyester with strengthened border side panels and deltamethrin and piperonyl butoxide incorporated into a polyethylene roof; Vestergaard); and Olyset (permethrin incorporated into polyethylene; Sumitomo Chemical Co., Ltd., Osaka, Japan)..
Cone bioassays were performed according to WHO procedures (12) by using non–blood fed VK7 mosquitoes (3–5 days old) (obtained from larvae collection during October–December 2012) and Kisumu strain mosquitoes. Approximately 60 mosquitoes were assessed per net by using net samples from 2 sides and the top (20 mosquitoes/net sample). Mosquitoes were exposed to the insecticide for 3 min. Knockdown was recorded after 60 min, and the mortality rate was determined 24 h later. Mortality rates after exposure to each net were compared for wild-type and laboratory susceptible (laboratory raised) mosquitoes by using the Fisher exact test.
High-performance liquid chromatography was used to measure the insecticide content of 12 nets. Triplicate samples were tested from each net, and insecticide was extracted from five 8-cm2 disks for each sample by vortexing them in acetone. A 10-μL aliquot was injected onto a reverse-phase, 250 mm, C18 column (Acclaim 120; Dionex, Sunnyvale, CA, USA). Separation was achieved by using a mobile phase of methanol/water (90:10 vol/vol) and at flow rate of 1 mL/min. Pyrethroid elution was monitored by absorption at 232 nm and quantified by peak integration (Chromeleon; Dionex). The quantity of pyrethroid insecticide was determined from a standard curve established with known concentration of pyrethroid insecticide.
All An. gambiae VK7 mosquitoes collected were the M form, except for those collected during October 2011 and June–July 2013, of which the M form comprised 92% (315/335) and 90% (258/287) of the An. gambiae sensu lato populations, respectively. Susceptibility to 5 insecticides was assessed in adults emerging from VK7 strain larval collections in 3 successive years. An. gambiae mosquitoes remained fully susceptible to fenitrothion and showed a high mortality rate to bendiocarb (86.5% in June 2013) but low mortality rates to DDT (range 0%–3%) and for the pyrethroids deltamethrin and permethrin (range 1%–6%) However, no significant differences were found between results of the 3 successive years (p = 0.055) (Figure 1).
Initially, the strength of resistance was assessed by determining the LT50 for deltamethrin. In July 2011, an LT50 of 1 h 38 min (95% CI 1 h 34 min–1 h 42 min) was obtained but this value increased to 4 h 14 min (95% CI 3 h 53 min–4 h 36 min) in October of the same year (Figure 2), which is a 2.6-fold increase in only 4 months. An accurate LT50 could not be determined for samples collected in June 2012. The longest exposure time of 600 min (10 h) showed a mortality rate of 26% (95% CI 17.85%–35.50%), which extrapolates to an LT50 of 21 h 55 min (95% CI 14 h 3 min–34 h 14 min). The estimated LT50 for the Kisumu strain was <2 min (13). This time equates to resistance ratios in the field population versus the susceptible (laboratory raised) strain of 54- fold, 141-fold, and 730-fold in the 3 successive sampling periods.
Because the resistance level exceeded the threshold at which accurate LT50 levels were obtainable, in 2013, a variation of the CDC bottle bioassays was used to calculate the strength of resistance. Mosquitoes collected in July 2013 had an LD50 of 38.79 μg/mL (95% CI 32.99 μg/mL−46.06 μg/mL). The LD50 estimate for October was lower (21.55 μg/mL, 95% CI 15.77 μg/mL–31.22 µg/mL) and showed greater variation (Figure 3). By comparison, the LD50 for the insecticide-susceptible Kisumu strain calculated by using the same method was 0.021 μg/mL (95% CI 0.015 µg/mL–0.029 µg/mL). This value is equivalent to VK7:Kisumu resistance ratios of 1,847:1 for July and 1,026:1 for October.
The efficacies of 6 types of LLINs distributed as part of the National Malaria Control Program of Burkina Faso were assessed against the Kisumu and VK7 mosquito strains to assess the effect of resistance on LLIN effectiveness in a standardized WHO bioassay. New nets and nets that had been in use in the field for ≈2 years were assessed. Only 4 of 6 new nets showed 100% mortality rates against the Kisumu strain (Figure 4, panel A); a fifth net (Olyset) satisfied only the knockdown criteria. When used nets were tested, only 3 nets (Permanet 2.0, Permanet 3.0, and NetProtect) satisfied the WHO criteria (mortality rate >80% and knockdown rate >95%). When we evaluated the nets against VK7 mosquitoes, none of the nets satisfied the knockdown criteria and mean mortality rates were <50% for all new nets and used LLINs tested; mortality rates were lower for used nets than for all types of new nets (Figure 4, panel B).
Because PermaNet 3.0 nets have the synergist piperonyl butoxide incorporated into the net roof, we compared bioassay data for the roof and sides. Mortality rates were significantly higher when mosquitoes were exposed to the roof of the net when new nets were tested (p = 0.011) but not when used nets were tested (p = 0.20).
Low mortality rates observed in cone bioassays, even against susceptible mosquitoes, led us to investigate the amount of insecticide that could be extracted from LLINs used in the bioassays. Analysis by high-performance liquid chromatography was performed for net types that did not satisfy WHO criteria for susceptible mosquitoes; Permanet 2.0 was used as a control. We included data only for nets in which insecticide was coated onto the surface (rather than incorporated into the fibers) because the acetone extraction method used is not efficient in extracting insecticide from the fibers. In each case, higher levels of insecticide were extracted from new nets than from used nets (p<0.05, by 2-tailed t test) except for DawaPlus, for which the amount of active ingredient was ≈0 for used and new nets (Table 1). Less than 12% of the target concentration of insecticide could be extracted from LLINs that induced a mortality rate <80% in the Kisumu strain. In general, the expected concentration of insecticide was isolated from LLINs, which showed the target mortality rate of 80% for cone bioassays.
Monitoring Anopheles spp. vectors for susceptibility to insecticides is recommended by WHO in all countries that use LLINs or indoor residual spraying for malaria control (3). Most countries in Africa that have implemented resistance monitoring since 2010 have detected pyrethroid resistance in some regions. Many countries have detected resistance to multiple insecticide classes (www.irmapper.com). Ideally, the first detection of resistance should elicit a change in insecticide class as part of a proactive resistance management program. However, because only pyrethroids are currently available for impregnating bed nets, and use of alternative insecticide classes for indoor residual spraying often result in higher program costs (14,15), resistance management options are severely limited. Thus, data obtained from routine resistance monitoring should be sufficient to make evidence-based decisions on insecticide-based vector control strategies. Use of only diagnostic dose assays alone can mask major changes in the strength of resistance. This finding can be seen in the current study, in which no major difference was seen in pyrethroid mortality rates over a 3-year period with a fixed exposure of insecticide. However, when exposure time or concentration was varied, increases in the strength of the resistance were observed.
We used 3 bioassays to quantify the strength of the resistance and link this strength to the effectiveness of current vector control tools. Each of these methods has limitations, which are summarized in Table 2. In this study, we did not use a tunnel test, in which mosquitoes are exposed overnight to a holed net, with a guinea pig as bait, and the mortality rate and blood-feeding inhibition are measured (12). It would be useful to determine if the longer exposure time used in the tunnel test resulted in higher mortality rates, although given the long exposure time required to achieve the LT50 with impregnated papers, it is expected that the LLINs would also fail a tunnel test against the VK7 mosquito population.
There is a need for agreement on a consensus method for resistance monitoring, together with clear guidelines for interpreting the operational value of the results and recommended courses of action. This method would not necessarily replace diagnostic dose assays, which are valuable for detecting the prevalence of resistance in a population, but would instead provide a quantitative estimate of the strength of resistance that is linked to predicted control failure. Such assays are common practice in the agricultural sector and a cross-sectorial approach would be invaluable for improving resistance monitoring in malaria control.
The resistance levels we report in the current study are alarming. Because few studies have attempted to quantify resistance strength in field populations, it is difficult to know if this extreme resistance phenotype is exceptional or symptomatic of the status of pyrethroid resistance in malaria vectors in Africa. Two other studies have used the LT50 method to assess the strength of resistance to pyrethroids in field populations compared with susceptible (laboratory raised) strains. In 2011, deltamethrin resistance ratios of 138-fold were recorded in Tiassalé, Côte d’Ivoire (13) and 292-fold in Jinja, Uganda (16). Thus, to our knowledge, deltamethrin resistance levels of 730-fold in 2012 (estimated by LT50) and >1,000 fold in 2013 (estimated by LD50) reported in the current study are the highest in the published literature.
This level of resistance will almost certainly affect the effectiveness of vector control. We demonstrate that the insecticide resistance of VK7 mosquitoes severely affected the performance of LLINs in standardized laboratory bioassays. In Kenya, pyrethroid-resistant mosquitoes were found resting inside holed LLINs and, when tested by cone bioassays, these LLINs were also found to be ineffective at killing local vectors (17). Linking resistance strength with increases in malaria transmission is currently not possible but is a key priority for further studies. No data on the strength of pyrethroid resistance in An. funestus mosquitoes in southern Africa in 2000 are available. This resistance has been widely accredited with causing control failure that resulted in a dramatic increase in malaria cases (18).
Finally, it is vital to recognize that insecticide resistance is not the only cause of reduced effectiveness of vector control tools. In the current study, we showed that cone bioassays for new and used LLINS were less effective at killing the field-caught An. gambiae mosquitoes than they were against a standard susceptible (laboratory raised) strain, which provided additional evidence for the effect of resistance. However, we also found that 2 brands of the LLINs (Olyset and DawaPlus) showed poor performance against the susceptible mosquito strain, and another LLIN (Interceptor) showed adequate performance only when new nets were used. Although these data were obtained for a small sample set, they are a cause for concern and must be investigated further.
Mr Toé is a doctoral student at the Liverpool School of Tropical Medicine, Liverpool, UK. His research interests are evaluating the distribution, causes, and effects of insecticide resistance in malaria vectors in Africa.
K.H.T., C.M.J., and H.M.I performed the experiments and analyzed the data; C.M.J. and H.R. designed the study; K.H.T., C.M.J., and H.R wrote the manuscript; and S.N. and R.K.D. supervised the field work.
This study was supported by European Union Seventh Framework Programme FP7 (2007–2013) under grant agreement no. 265660 AecNet.
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