- Open Access
Cotton pest management practices and the selection of pyrethroid resistance in Anopheles gambiae population in Northern Benin
© Yadouleton et al; licensee BioMed Central Ltd. 2011
- Received: 6 December 2010
- Accepted: 13 April 2011
- Published: 13 April 2011
Pyrethroid insecticides, carbamate and organophosphate are the classes of insecticides commonly used in agriculture for crop protection in Benin. Pyrethroids remain the only class of insecticides recommended by the WHO for impregnation of bed nets. Unfortunately, the high level of pyrethroid resistance in Anopheles gambiae s.l., threatens to undermine the success of pyrethroid treated nets. This study focuses on the investigation of agricultural practices in cotton growing areas, and their direct impact on larval populations of An. gambiae in surrounding breeding sites.
The protocol was based on the collection of agro-sociological data where farmers were subjected to semi-structured questionnaires based on the strategies used for crop protection. This was complemented by bioassay tests to assess the susceptibility of malaria vectors to various insecticides. Molecular analysis was performed to characterize the resistance genes and the molecular forms of An. gambiae. Insecticide residues in soil samples from breeding sites were investigated to determine major factors that can inhibit the normal growth of mosquito larvae by exposing susceptible and resistant laboratory strains.
There is a common use by local farmers of mineral fertilizer NPK at 200 kg/ha and urea at 50 kg/hectare following insecticide treatments in both the Calendar Control Program (CCP) and the Targeted Intermittent Control Program (TICP). By contrast, no chemicals are involved in Biological Program (BP) where farmers use organic and natural fertilizers which include animal excreta.
Susceptibility test results confirmed a high resistance to DDT. Mean mortality of An. gambiae collected from the farms practicing CCP, TICP and BP methods were 33%, 42% and 65% respectively. An. gambiae populations from areas using the CCP and TICP programs showed resistance to permethrin with mortality of 50% and 58% respectively. By contrast, bioassay test results of An. gambiae from BP areas gave a high level of susceptibility to permethrin with an average mortality of 94%.
Molecular analysis identified An. gambiae s.s, and An. arabiensis with a high predominance of An. gambiae s.s (90%). The two molecular forms, M and S, were also determined with a high frequency of the S form (96%).
The Kdr gene seemed the main target- site resistance mechanism detected in CCP, TICP, and BP areas at the rates ranging from 32 to 78%. The frequency of ace-1R gene was very low (< 0.1).
The presence of inhibiting factors in soil samples under insecticide treatments were found and affected negatively in delaying the development of An. gambiae larval populations.
This research shows that Kdr has spread widely in An. gambiae, mainly in CCP and TICP areas where pyrethroids are extensively used. To reduce the negative impact of pesticides use in cotton crop protection, the application of BP-like programs, which do not appear to select for vector resistance would be useful. These results could serve as scientific evidence of the spread of resistance due to a massive agricultural use of insecticides and contribute to the management of pesticides usage on cotton crops hence reducing the selection pressure of insecticides on An. gambiae populations.
- Indoor Residual Spraying
- Malaria Vector
- Breeding Site
- Pyrethroid Resistance
- Biological Program
Malaria remains a major public health problem in Africa. It is reported to be the most significant cause of morbidity and mortality, resulting in a critical loss of working days .
More than 2 billion people in the world are at risk of contracting malaria and one million deaths are recorded yearly of which 90% occur in Sub-Saharan Africa . In Benin, malaria is still the most important disease leading to 67% consultations in local health centres . The strategy of the National Malaria Control Programme (NMCP) is based on effective case management and vector control with Insecticide-Treated Nets (ITN) and Indoor Residual Spraying (IRS).The development of new insecticides for public health use is limited and requires enormous capital and time, making industry reluctant to embark on such ventures. Novel compounds or alternatives are to be sought in the agricultural pesticide pipeline. Several reports have recently shown evidence that the main African malaria vector, Anopheles gambiae s.l., has developed a high level of resistance to pyrethroid insecticides as well as to other classes of public health insecticides. While resistance is now spreading throughout Sub-Saharan Africa, reports from Benin and the West African region indicated the highest recorded frequencies of the resistance genes [3–6].
The development of pyrethroid resistance in the primary malaria vectors, An. gambiae s.l. and An. funestus is a serious concern. In the last decade, the emergence of resistance in populations of An. gambiae to common classes of insecticides used in public health has been reported in many African countries including Kenya , Côte d'Ivoire , Benin [10–14], Niger , Burkina Faso [16, 17], Mali, Nigeria , South Africa , and Cameroun . In the 1960s, the role of selective treatment with organochlorines (OC) in agriculture on resistance of An. gambiae was observed in Mali . Evidence of an association between agricultural use of insecticides and the emergence of resistance in malaria vectors has been repeatedly reported. In Côte d'Ivoire and Burkina Faso, N'Guessan et al. reported that the level of vector resistance to pyrethroid insecticides increased during the cotton growing season. Higher frequencies of kdr alleles were observed in the more intensely farmed cotton production areas of Côte d'Ivoire . In Bukina-Faso, a survey of kdr alleles in An. gambiae field populations showed also a higher frequency of kdr alleles in older cotton areas with a decreasing gradient to non treated areas .
Cotton crop protection represents 90% of the insecticide use in West Africa. The control strategies implemented against cotton pest especially Helicoverpa armigera required a regular repeated applications of insecticides during the cotton plant growing cycle. As recommended by the Institut National des Recherches Agronomiques du Benin (INRAB), six consecutive treatments are applied at two weeks interval to protect the crop against bollworms, leafworms and sucking pests. These insecticides are essentially composed of pyrethroids (PYs), organophosphates (OPs) which are also the main classes used in public health and a cyclodiene. The majority of cotton farms observed in northern Benin are located in the upland landscape while the lowland covers the major mosquito breeding sites. Thus run-off has been assumed to be the mechanism by which insecticides from agricultural sites reach malaria vector breeding sites, where they exert a huge selection pressure on larval stages of An. gambiae s.l. The main malaria vector An. gambiae breeds in puddles, stagnant pools and various sites around or within the lowland. During the rainy season, insecticide residues are washed downwards into mosquito breeding sites thus affecting larval population . According to Akogbeto et al. in Benin, insecticide treatments against cotton pests are applied twice a month, for a timeframe of three consecutive months (between July and October) each year. These treatment periods coincide with the rainy season and correspond to the period of high mosquito densities. The evidence supports the hypothesis that breeding sites contamination is the result of the coincidence of agricultural pesticide application and seasonal rainfall/runoff.
Alternatively, integrated pest and vector management (IPVM) strategies based on the rational use of chemical protection, has undoubtedly reduced the negative impact of pesticides on humans, and their environment, including the breeding sites of malaria vectors.
This study aimed to assess the impact of control strategies used against cotton pests (relative amount of insecticide) on the frequency and spread of insecticide resistance in An. gambiae populations. The study, conducted in northern Benin, compared the BP cotton cultivation sites (absence of pesticides use) with the CCP and TICP cotton cultivation sites where insecticides are extensively used. The study focused on the investigation of agricultural practices using pesticides for the control of cotton pests and their impact on the insecticide susceptibility of An. gambiae populations from surrounding breeding sites.
Cotton pests control strategies
The Calendar Control Program (CCP) is based on the conventional treatment which systematically uses the full dosage of insecticides.
The Targeted Intermittent Control Program (TICP) is based on two steps of crop protection [26, 27]. The first steps is a protection which follows a conventional pesticide application schedule (every 14 days from the appearance of floral organs), but only the half dose of insecticide are usually applied. The second step includes a modification of the first treatment meaning that the half-dose left over during the earlier observation made the day before treatment would suggest that the pest populations exceed the economic thresholds of damage. The program was established five years ago.
In the biological control program (BP), no chemical is used for plant protection. That program started over the past five years.
The area of the farms applying CCP and TICP was about 4 hectares and usually farmers ploughed sometime individually or work in groups of farmers' organizations. However, in BP sites of 1 hectare, farmers worked under the supervision of technicians from the Beninese Organization for Organic Farming Promotion (OBEPAP) who assisted in the implementation and the survey of good agricultural practices on organic cotton. These areas were characterised by a continual production of cotton crop.
the CCP around Parakou (2°62 E, 9°33 N), Kandi (2°95 E, 11°16 N) and Banikoara (2°59 E, 11°31 N). This pest management program started thirty years ago and was the main strategy against pest control used by more than 95% of the cotton farmers.
the TICP around N'dali (2°70 E, 9°84 N), Kandi (3°08 E, 11°27 N) and Banikoara (2°41 E, 11°31 N) started five years ago and applied by 4% of cotton farmers.
the BP around Kandi (2°92 E, 11°09 N) and Banikoara (2°52 E, 11°29 N) started five years ago and practiced by 1% of cotton farmers.
The annual mean rainfall recorded was about 1,300 mm yearly and characterized by a Sudanian climate with one rainy season (middle of May to October) and one dry season (November-May).
KAP Study on the use of insecticides in cotton farms
To generate adequate information on the use of insecticide on cotton fields, Knowledge Attitude-Practice (KAP) surveys were organized in the study sites. In each site, leaders of farmer's organizations were interviewed using semi-structured questionnaires that focused on the treatment strategies, and the use of insecticides in the farms. Further, qualitative data was collected through direct observations, in-depth interviews and focus group discussions.
Mosquito larvae were collected during the rainy season as well as before and during the period of insecticide treatments. The treatment periods started from July to October. During pest control, insecticide residues contaminate mosquito breeding sites whereby they diffuse into the water applying a selection pressure on mosquito larvae. Larvae were collected in the breeding sites of each site and transported to the laboratory of the Centre de Recherche Entomologique de Cotonou, Benin (CREC) for resistance testing. The adults were tested after emergence. A laboratory susceptible strain of An. gambiae Kisumu was used as a reference strain to compare the susceptibility levels of the field populations.
Insecticide susceptibility tests
Mosquitoes collected were assayed using WHO discriminating dosages of four insecticides: permethrin (0.75%), DDT (4%), deltamethrin (0.05%) and bendiocarb (0.1%). Four batches of 25 unfed females, aged 2-5 days, were exposed to the diagnostic doses of insecticide treated papers for 1 hour. The twenty five females of An. gambiae were introduced into each tube and monitored at different time intervals (10, 15, 20, 30, 45, 60 minutes) the number "knocked-down" recorded. After one hour exposure, mosquitoes were transferred into holding tubes and provided with cotton wools wet with a 10% honey solution. Mortalities were recorded after 24 hours and the susceptibility status of the population was graded according to the WHO protocol . Dead and surviving mosquitoes from this bioassay were separately kept in Carnoy solution at -20°C for further molecular analysis.
All An. gambiae s.l. were identified to species using PCR  and as M and S forms by PCR-RFLP . To detect the presence of Kdr mutation in the samples collected from each study site, polymerase chain reaction diagnostic test for detection of kdr "Leu-phe" genes was carried out on An. gambiae mosquitoes from each study site as described by Martinez-Torres et al. .The PCR-RFLP diagnostic test was used to detect the presence of G119S gene (Ace.1 gene) as described by Weill et al. .
Screening of pesticide residues in soil from agricultural settings
This investigation was performed using indirect bioassays focused on factors which can affect the normal growth of mosquito larvae in cotton breeding sites. The hatching rates of An. gambiae eggs and the larval survival during rearing period were assessed in artificial breeding sites made of soil samples collected from different cotton areas. The pyrethroid-susceptible Kisumu strain and the resistant VKPER strain were used to test the presence of insecticide residues in the soil samples by means of mortality rates after exposure. The testing method was based on an artificial breeding site made of a mixture of soil from cotton sites (BP, TICP and CCP programs) and CREC soil used as a control. 100 g of each soil was weight and mixed in 1,000 ml of water. 200 eggs of the susceptible Kisumu strain were placed in each artificial breeding site and compared with 200 eggs of VKPER.
Larvae in all artificial breeding sites were fed with similar quantity and type of food (well ground cat biscuits mixed with yeast powder). Daily observation was done in order to record the number and the instars of larvae. This experiment was replicated three times per month.
The resistant status of mosquito samples was determined according to the WHO criteria :
Mortality rates is > 97%: the population was considered fully susceptible
Mortality rates ranged between 80 > × < 97%: resistance suspected in the population
Mortality rates < 80%, the population was considered resistant to the tested insecticides.
The knockdown times for 50% and 95% of tested mosquitoes (KdT50 and KdT95) were estimated using a log-time probit model .
The resistance allele frequency at the kdr and Ace- 1 locus was calculated using Genepop software (version 3.3) as described by Raymond and Rousset .
A Fisher's exact test was performed to compare the resistance allele frequency at the kdr and Ace- 1 among the mosquitoes from the different strategies.
An analysis of variance (ANOVA) was performed to compare the percentage of hatching eggs in the different treatments in order to know the impact of insecticide on the normal growth of mosquito larvae in cotton breeding sites.
Knowledge-Attitude -Practice (KAP) investigations
Results from our KAP investigations from June to September 2008 in the cotton growing areas showed a common use by farmers of mineral fertilizer NPK at about 200 kg.ha-1 and urea at about 50 kg.ha-1 in both the CCP and the TICP sites. By contrast, in BP areas, all farmers in this group used organic and natural fertilizers which included animal excreta. In the CCP sites, about 6 pesticide treatments were applied by farmers 45 days after seeding and at two week intervals from flowering. Endosulfan or Tihan® (mixture of spirotetramat + flubendiamide), were sprayed in the first two treatments followed by the mixtures of cyfluthrin + chlorpyrifos ethyl for the 3rd and the 4th treatment and then cypermethrin + dimethoate applied for the last two treatments. In TICP sites, the same treatments at intervals of two weeks were made either at half dose or at a complete full dosage when the threshold of infestation was reached (5 of H. armigera larvae observed on 50 plants). In areas practicing Biological Program, farmers apply a mixture of neem or papaya leaves with added chilli and local soap three times before the harvest.
Resistance to insecticides
A total of 1,313 females of An. gambiae collected from different sites around Parakou, N'dali, Kandi, and Banikoara were exposed to papers impregnated with discriminating doses of permethrin (0.75%), deltamethrin (0.05%), DDT (4%) and bendiocarb (0.1%).
Knockdown times (KdT50 and KdT95) and mortality of Anopheles gambiae s.l. populations from 3 cotton sites after exposure to DDT 4% and permethrin 0.75% and their resistance status
kdT50 [Cl95] (min)
kdT95 [Cl95] (min)
% Mortality [Conf lim 95]
11.0 [8.7 - 17.6]
13.2 [9.4 - 18.2]
An. gambiae s.l
Species and molecular forms identification within Anopheles gambiae complex and the frequency of Kdr and Ace-1R mutations in Anopheles gambiae s.s. in Benin
The kdr genotype was scored for 1,400 individuals (100 mosquitoes consistently failed to amplify). The kdr gene occurred in S forms (Table 2). The highest frequency of Kdr mutation was recorded for the populations from three CCP sites (67-78%) and the lowest (35 and 32%) were found in the populations from BP sites around Kandi and Banikora respectively.
The Ace-1R gene was found at very low frequency ranging (from 0.00 to 0.06) in heterozygote An. gambiae s.s from the three CCP sites (Table 2). Among An. gambiae s.s, there was no mosquito of the M molecular form carrying the ace-1R gene.
The resistance allele frequency at the kdr was significantly higher in areas where farmers used insecticide for pest control (CCP and TICP) than in those no insecticide is not request (BP) (p < 0.05.). However, there is no difference between the resistance allele frequency at the kdr from mosquitoes in CCP and TICP strategies (p > 0.05).
However, a significant difference (P < 0.05) was observed between the emergence of VKPER on artificial sites made of soils from TICP (43%) and CCP (35%) sites and Kisumu which gave 20% emergence on TICP and 13% on CCP.
The information generated during interviews with cotton farmers and the observations made in cotton fields has confirmed a common use of fertilizers and insecticides in cotton fields. Cotton cultivation requires intensive use of pesticides including insecticides belonging to the two main classes recommended for vector control in public health: organophosphates and pyrethroids. In West Africa, pyrethroid-treated bed nets remain one of the effective tools for malaria vector control and it provides personal protection to individuals who sleep under them. When used by the whole community, bed nets protect collectively against infective mosquito bites by a mass killing effect of the vectors .
In Benin, pyrethroids have been extensively introduced in agriculture since 1980s . This factor is probably one of the causes of the selection of strong resistance in An. gambiae to permethrin and DDT, particularly in cotton growing areas. Based on recent results, several authors [8-12; 37] have reported that past and current agricultural use of DDT then pyrethroids for crop protection have led to the selection of resistant mosquitoes through insecticide residues accumulated in breeding sites around cotton growing areas. This hypothesis was recently confirmed by Akogbeto et al. showing indirectly the presence of pesticide residues in soil and water from vegetable farms and other agricultural activities in Benin that delay or reduce the emergence rates of mosquito larvae.
The use of insecticides in households for public health purposes and massive quantities of pesticides in agricultural settings has been highlighted as a key factor contributing to the emergence of vector resistance. A recent report by Yadouleton et al. showed that agricultural practices in urban areas seem to have contributed to the emergence of insecticide resistance in Anopheles populations. Our study in vegetable farming systems in Benin demonstrated that improper use of insecticides to control vegetable pests in urban areas directly exerted a huge selection pressure on mosquito larval populations. The high mortality observed with mosquitoes reared on soils from CCP, TICP sites can be explained by the presence of DDT residues in the soil from those sites and the extensive use of pyrethroids by farmers . Our results showed that the high level of the kdr-west ( Leu-Phe) gene seemed to be the main resistance mechanism and responsible for the decrease of mortality rates to DDT and permethrin and is more of an ongoing process in An. gambiae populations from CCP and TICP sites. The kdr gene in the main malaria vector An. gambiae was found at high frequency in samples from the sites using insecticide (CCP and TICP) than those with no use of insecticide (BP program). The low frequency of Kdr gene in BP localities compared with those from CCP and TICP could be due to the fact that in the past these farmers in BP sites used insecticide to control cotton pests. According to reports by Akogbeto et al, Djogbénou et al, and Yadouleton et al., the presence of Kdr genes in mosquito can be due to external factors that affect mosquitoes as larvae or adults. In 2000, a study in Burkina Faso by Diabate et al. reported higher levels of kdr alleles frequency in An. gambiae collected from cotton-growing areas constantly subjected to insecticide treatments, as compared to the low frequency of kdr recorded in rural areas where farmers are restricted to low or no use of pesticides. Despite the use of insecticide in both CCP and TICP sites, the difference in adult mortality rates between CCP and TICP program can be explained by the fact that CCP program uses more insecticide than TICP program.
This study provides clear evidence of the association between the use of insecticides in agriculture and the widespread emergence of insecticide resistance in Anopheles species.
Indeed, in Benin, insecticide treatments against pests in cotton plantations are carried out twice a month, for an average period time of three months (between July and October) per year. That treatment period during the rainy season correspond with the period of high mosquito densities because Anopheles populations have numerous breeding sites particularly in cultivated areas. As reported by Akogbeto et al, some populations of An. gambiae may lay their eggs in breeding sites containing insecticide residues. These eggs undergo a selection pressure from agricultural pesticides, which leads to the emergence of resistant strains. There is clear evidence on the implication of agricultural use of insecticides in the selection of resistance in the major malaria vectors. Our results agree with the work of Akogbeto et al and confirm once again the impact of the extensive use of insecticides in cotton crop protection on the emergence of insecticide resistance in An. gambiae populations. Moreover, in CCP and TICP program, some farmers used insecticides belonging to the organophosphate classes. Ace-1R gene is the main resistance mechanism of An. gambiae s.l. to organophosphates and carbamates also. The present study, has shown that the ace-1R gene is present at low frequency (ranging from 0.01 to 0.09), but only in CCP and TICP program. However, previous field surveys on An. gambiae s.l. populations of South-Western
Burkina Faso by Djogbenou et al in cotton fields showed that ace-1R gene was the main resistance mechanism in An. gambiae s.l.
However the National Malaria Control Program (NMCP) in Benin has started scaling up Long Lasting Insecticidal Nets (LLINs) and carbamate for Indoor Residual Spraying (IRS) countrywide for malaria control. The challenge to find effective strategies to manage insecticide resistance in Anopheles gambiae remains a high priority and an urgent need particularly in Benin where pyrethroid resistance has been reported with a clear evidence in experimental huts of reduced efficacy of ITNs and IRS . One of the strategies will be to remove pyrethroids from agricultural pest control and leave these classes of insecticides for public health purposes and promote other classes of insecticides such as Spinosad which does not show cross resistance to pyrethroids (i.e. the kdr gene).
With the spread of Kdr allele frequency from CCP and TICP programmes, to reduce the emergence of insecticide resistance in An. gambiae population, African governments would be better advised to promote the BP cotton or genetically modified cotton such as Bt Cotton (Bacillus thurengiensis) which require lower pesticide than the cotton with CCP and TICP programme and would permit to suppress the massive use of pyrethroid insecticides.
This work was financially supported by the French government (Corus 6015 project). I am grateful to CREC's staff particularly Sebastien Koudenoukpe and Géraldo Houndéton for technical assistance during laboratory bioassays and field collections.
- WHO: World Malaria Report 2009. 2009, World Health Organzation, GenevaGoogle Scholar
- Ministère de la santé: Annuaire des statistiques sanitaires 2006. 2009, CotonouGoogle Scholar
- Reimer L, Fondjo E, Patchoke S, Diallo B, Lee YNg, Ndjemai HM, Atangana J, Traore SF, Lanzaro G, Cornel AJ: Relationship between kdr mutation and resistance to pyrethroid and DDT insecticides in natural populations of Anopheles gambiae. J Med Entomol. 2008, 45: 260-266. 10.1603/0022-2585(2008)45[260:RBKMAR]2.0.CO;2.View ArticlePubMedGoogle Scholar
- Ramphul U, Boase T, Bass C, Okedi LM, Donnelly MJ, Muller P: Insecticide resistance and its association with target-site mutations in natural populations of Anopheles gambiae from eastern Uganda. Trans R Soc Trop Med Hyg. 2009, 103: 1121-1126. 10.1016/j.trstmh.2009.02.014.View ArticlePubMedGoogle Scholar
- Chandre F, Darrier F, Manga L, Akogbeto M, Faye O, Mouchet J, Guillet P: Status of pyrethroid resistance in Anopheles gambiae sensu lato. Bull World Health Organ. 1999, 77: 230-234.PubMed CentralPubMedGoogle Scholar
- Santolamazza F, Calzetta M, Etang J, Barrese E, Dia I, Caccone A, Donnelly MJ, Petrarca V, Simard F, Pinto J, Torre A: Distribution of knock-down resistance mutations in Anopheles gambiae molecular forms in west and west-central Africa. Malar J. 2008, 7: 74-10.1186/1475-2875-7-74.PubMed CentralView ArticlePubMedGoogle Scholar
- Djènontin A, Sahabi B, Moiroux N, Henry MC, Bousari O, Chabi J, Ossè R, Koudénoukpo S, Corbel V, Akogbéto M, Chandre F: Culicidae diversity, malaria transmission and insecticide resistance alleles in malaria vectors in Ouidah Kpomasse-Tori district from Benin (West Africa): A pre-intervention study. Parasit Vectors. 2010, 3: 83-PubMed CentralView ArticlePubMedGoogle Scholar
- Vulule JM, Beach RF, Atieli FK, Mcallister JC, Brogdon WG, Roberts JM, Mwangi RW, Hawley WA: Elevated oxidase and esterase levels associated with permethrin tolerance in Anopheles gambiae from Kenyan villages using permethrin impregnated nets. Med Vet Entomol. 1999, 13: 239-244. 10.1046/j.1365-2915.1999.00177.x.View ArticlePubMedGoogle Scholar
- Elissa N, Mouchet J, Rivière F, Meunier JY, Yao K: Resistance of Anopheles gambiae s.s. to pyrethroids in Côte d'Ivoire. Ann Soc Belge Méd Trop. 1993, 73: 291-294.Google Scholar
- Akogbéto M, Yakoubou S: Résistance des vecteurs du paludisme vis-à-vis des pyréthrinoïdes utilisés pour l'imprégnation des moustiquaires au Bénin, Afrique de l'Ouest. Bull Soc Pathol Exot. 1999, 92: 123-130.PubMedGoogle Scholar
- Yadouleton AW, Asidi A, Rousseau FD, Braïma J, Agossou CD, Akogbeto MC: Development of vegetable farming: a cause of the emergence of insecticide resistance in populations of Anopheles gambiae in urban areas of Benin. Malar J. 2009, 8: 103-10.1186/1475-2875-8-103.PubMed CentralView ArticlePubMedGoogle Scholar
- Corbel V, N'Guessan R, Brengues C, Chandre F, Djogbenou L, Martin T, Akogbeto M, Hougard JM, Rowland M: Multiple insecticide resistance mechanisms in Anopheles gambiae and Culex quinquefasciatus from Benin, West Africa. Acta Trop. 2007, 101: 207-216. 10.1016/j.actatropica.2007.01.005.View ArticlePubMedGoogle Scholar
- N'Guessan R, Corbel V, Akogbeto M, Rowland M: Reduced efficacy of insecticidetreated nets and indoor residual spraying for malaria control in pyrethroid resistance area, Benin. Emerg infect diseases. 2007, 13: 199-206.View ArticleGoogle Scholar
- Djogbénou L, Dabire R, Diabate A, Kengne P, Akogbeto M, Hougard JM, Chandre F: Identification and Geographic Distribution of the Ace-1R Mutation in the Malaria Vector Anopheles gambiae in South-Western Burkina Faso, West Africa. Am J trop med hyg. 2008, 78: 298-302.PubMedGoogle Scholar
- Czeher C, Labbo R, Arzika I, Duchemin JB: Evidence of increasing Leu-Phe knockdown resistance mutation in Anopheles gambiae from Niger following a nationwide long-lasting insecticide-treated nets implementation. Malar J. 2008, 7: 189-10.1186/1475-2875-7-189.PubMed CentralView ArticlePubMedGoogle Scholar
- Diabate A, Baldet T, Chandre F, Guiguemde RT, Brengues C, Guillet P, Hemingway J, Hougard JM: First report of the kdr mutation in Anopheles gambiae M form from Burkina Faso, West Africa. Parassitologia. 2002, 44: 157-158.PubMedGoogle Scholar
- Diabate A, Baldet T, Chandre F, Akogbéto M, Guiguemde RT, Darriet F, Brengues C, Guillet P, Hemingway J, Graham JS, Hougard JM: The role of agricultural use of insecticides in resistance to pyrethroids in Anopheles gambiae s.l in Burkina Faso. Am J Trop Med Hyg. 2002, 67: 617-622.PubMedGoogle Scholar
- Fanello C, Petrarca V, Torre D, Santolamazza A, Dolo F, Coulibaly G, Alloueche MA, Curtis CG, Toure YT, Coluzzi M: The pyrethroid knock-down resistance gene in the Anopheles gambiae complex in Mali and further indication of incipient speciation within An. gambiae s.s. Insect Mol Biol. 2003, 12: 241-245. 10.1046/j.1365-2583.2003.00407.x.View ArticlePubMedGoogle Scholar
- Awolola TS, Brooke BD, Koekemoer LL, Coetzee M: Resistance of the malaria vector Anopheles gambiae s.s. to pyrethroid insecticides, in south-western Nigeria. Ann Trop Med Parasitol. 2002, 96: 849-852. 10.1179/000349802125002581.View ArticlePubMedGoogle Scholar
- Hargreaves K, Koerkemoer LL, Brooke B, Hunt RH, Mthembu J, Coetzee M: Anopheles funestus resistant to pyrethroid insecticides in South Africa. Med Vet Entomol. 2000, 14: 181-189. 10.1046/j.1365-2915.2000.00234.x.View ArticlePubMedGoogle Scholar
- Etang J, Manga L, Chandre F, Guillet P, Fondjo E, Mimpfoundi R, Toto JC, Fontenille D: Insecticide susceptibility status of Anopheles gambiae s.l. (Diptera: Culicidae) in the Republic of Cameroon. J Med Entomol. 2003, 40: 491-497. 10.1603/0022-2585-40.4.491.View ArticlePubMedGoogle Scholar
- WABI: The cross-border integration of the cotton sub-sector. West African Borders and Integration Network. Coton et Fibres Tropicales. 2003, 112: 54-71.Google Scholar
- N'Guessan F, Darriet P, Guillet P, Carnevalle M, Lamizana T, Corbel V, Chandre F: Resistance to carbosulfan in Anopheles gambiae base on reduced of acethylcholinesterase. Med vet Entomol. 2003, 17: 19-25.View ArticlePubMedGoogle Scholar
- Akogbéto M, Djouaka R, Gazard DA: Screening of pesticide residues in soil and water samples from agricultural settings. Malar J. 2006, 5: 22-PubMed CentralView ArticlePubMedGoogle Scholar
- Akogbéto M, Djouaka R, Noukpo H: Use of agricultural insecticides in Benin. Bull Soc Pathol Exot. 2005, 98: 400-405.PubMedGoogle Scholar
- Deguine JP, Ekukole G, Amiote P: La lutte étagée ciblée: un nouveau programme de protection insecticide en culture cotonnière au Cameroun. Coton et Fibres Tropicales. 1993, 48: 99-119.Google Scholar
- Prudent P, Loko S, Deybe D, Vaissayre M: Factors limiting the adoption of IPM practices by cotton farmers in Benin: a participatory approach. Cambridge University Press. 2006, 10: 10-17.Google Scholar
- WHO: World Malaria Report 2008. 2008, World Health Organzation, GenevaGoogle Scholar
- Scott JA, Brogdon WG, Collins FH: Identification of single specimens of the Anopheles gambiae complex by the polymerase chain reaction. Am J Trop Med Hyg. 1993, 49: 520-529.PubMedGoogle Scholar
- Favia G, Torre D, Bagayoko M, Lanfrancotti M, Sagnon NF, Toure Y, Coluzzi M: Molecular identification of sympatric chromosomal forms of Anopheles gambiae and further evidence of their reproductive isolation. Insect Mol Biol. 1997, 6: 377-383. 10.1046/j.1365-2583.1997.00189.x.View ArticlePubMedGoogle Scholar
- Martinez TD, Chandre F, Williamson MS, Darriet F, Berge JB, Devonshire AL, Guillet P, Pasteur N, Pauron D: Molecular characterization of pyrethroid knockdown resistance (kdr) in the major malaria vector Anopheles gambiae s.s. Insect Mol Biol. 1998, 7: 179-184. 10.1046/j.1365-2583.1998.72062.x.View ArticleGoogle Scholar
- Weill M, Malcolm C, Chandre , Mogensen K, Berthomieu A, Marquine M, Raymond M: The unique mutation in ace-1 giving high insecticide resistance is easily detectable in mosquito vectors. Insect Mol. 2004, 9: 1-7. 10.1111/j.1365-2583.2004.00452.x.View ArticleGoogle Scholar
- WHO: World Malaria Report 1998. 1998, World Health Organzation, GenevaGoogle Scholar
- Finney DJ: Probit analysis. 1971, Cambridge University Press CambridgeGoogle Scholar
- Raymond M, Rousset F: Genepop (version 1.2). A population genetics software exact tests and ecumenicism. Heredity J. 1995, 86: 248-249.Google Scholar
- Henry MC, Assi SB, Rogier C, Dossou-Yovo J, Chandre F, Guillet P, Carnevale P: Protective Efficacy of Lambda-Cyhalothrin Treated Nets in Anopheles gambiae Pyrethroid Resistance areas of Cote d'ivoire. Am J Trop Med Hyg. 2005, 73: 859-864.PubMedGoogle Scholar
- Hargreaves K, Koekemoer LL, Brooke BD, Hunt RH, Mthembu J, Coetzee M: Anopheles funestus resistant to pyrethroid insecticides in South Africa. Med Vet Entomol. 2000, 14: 1-9. 10.1046/j.1365-2915.2000.00234.x.View ArticleGoogle Scholar
- Yadouleton AW, Padonou G, Asidi A, Moiroux N, Sahabi B, Corbel V, N'guessan R, Gbenou D, Yacoubou I, Kinde G, Akogbeto MC: Insecticide resistance status in Anopheles gambiae in southern Benin. Malar J. 2010, 9: 83-10.1186/1475-2875-9-83.PubMed CentralView ArticlePubMedGoogle Scholar
- Akogbéto MC, Padonou G, Gbénou D, Irish S, Yadouleton AW: Bendiocarb, a potential alternative against pyrethroid resistant Anopheles gambiae in Benin,West Africa. Malar J. 2010, 9: 204-PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.