Insecticide resistance in Anopheles arabiensis in Sudan: temporal trends and underlying mechanisms
© Abdalla et al.; licensee BioMed Central Ltd. 2014
Received: 23 December 2013
Accepted: 8 April 2014
Published: 8 May 2014
Malaria vector control in Sudan relies mainly on indoor residual spraying (IRS) and the use of long lasting insecticide treated bed nets (LLINs). Monitoring insecticide resistance in the main Sudanese malaria vector, Anopheles arabiensis, is essential for planning and implementing an effective vector control program in this country.
WHO susceptibility tests were used to monitor resistance to insecticides from all four WHO-approved classes of insecticide at four sentinel sites in Gezira state over a three year period. Insecticide resistance mechanisms were studied using PCR and microarray analyses.
WHO susceptibility tests showed that Anopheles arabiensis from all sites were fully susceptible to bendiocarb and fenitrothion for the duration of the study (2008–2011). However, resistance to DDT and pyrethroids was detected at three sites, with strong seasonal variations evident at all sites. The 1014 F kdr allele was significantly associated with resistance to pyrethroids and DDT (P < 0.001) with extremely high effects sizes (OR > 7 in allelic tests). The 1014S allele was not detected in any of the populations tested. Microarray analysis of the permethrin-resistant population of An. arabiensis from Wad Medani identified a number of metabolic genes that were significantly over-transcribed in the field-collected resistant samples when compared to the susceptible Sudanese An. arabiensis Dongola strain. These included CYP6M2 and CYP6P3, two genes previously implicated in pyrethroid resistance in Anopheles gambiae s.s, and the epsilon-class glutathione-S-transferase, GSTe4.
These data suggest that both target-site mechanisms and metabolic mechanisms play an important role in conferring pyrethroid resistance in An. arabiensis from Sudan. Identification in An. arabiensis of candidate loci that have been implicated in the resistance phenotype in An. gambiae requires further investigation to confirm the role of these genes.
KeywordsAnopheles arabiensis Malaria Insecticide resistance Mechanisms
Sudan, in 2010, accounted for the highest number of malaria cases in the World Health Organization Eastern Mediterranean Region (WHO/EMR), and was responsible for 58% of the total regional malaria cases. The 2007 National Strategic Plan for Malaria in Sudan aimed to reduce morbidity and mortality of malaria by 50% by 2012 (National Malaria Control Programme, unpublished data). The use of long-lasting insecticidal nets (LLINs) and indoor residual spraying (IRS) are the main components of most malaria prevention and control strategies because they are highly effective and have a relatively low cost. Currently there are only four classes of insecticides approved for IRS (pyrethroids, organochlorines, organophosphates and carbamates), and only one class, the pyrethroids, allowed for use on LLINs. Given the importance of insecticide use in malaria vector control, and the continuous development of insecticide resistance in malaria mosquitoes, monitoring the susceptibility of vectors to pyrethroids and the other insecticide classes is essential. Furthermore, it is necessary to identify the resistance mechanisms involved[2, 3] in order to formulate evidence-based resistance management strategies.
Malaria vector control in Sudan has a long history. The main vector control interventions include IRS and the use of LLINs, chemical larviciding of water bodies/breeding sites, environmental management and some, albeit limited, biological control. The Sudanese Ministry of Health (MOH) has provided free distribution of LLINs in Gezira state since 2005.
Insecticide resistance is widespread in the major African vectors belonging to the Anopheles gambiae complex[5–8] and in particular, resistance to pyrethroids has been shown to hamper malaria control programmes. Anopheles arabiensis is the main vector in central Sudan and multiple insecticide resistance has been reported in Sudanese populations of this species. This includes resistance to the organochlorides benzene hexachloride (BHC) and dichlorodiphenyltrichloroethane (DDT), the organophosphate malathion and to various pyrethroids.
The two best understood mechanisms of insecticide resistance in mosquitoes are target site insensitivity and metabolic resistance. Target site insensitivity to pyrethroids and DDT is a result of changes in the neuronal voltage-gated sodium ion channel (VGSC). In An. gambiae s.s., two point mutations at amino acid position 1014 of the VGSC have been described, resulting in either a leucine to phenylalanine (L1014F), or a leucine to serine (L1014S) substitution. Both of these knockdown resistance (kdr) mutations have been shown to be associated with DDT and pyrethroid resistance phenotypes[15–17]. In An. arabiensis, kdr mutations have been found in several widely dispersed locations including Burkina Faso, Tanzania, Uganda and Sudan[12, 18–21].
Metabolic resistance is generally associated with three large enzyme families: the cytochrome P450 monooxygenases (CYP450s), carboxyl/cholinesterases (CCEs), and glutathione-S transferases (GSTs). Little information is available on the metabolic resistance mechanisms present in Sudanese An. arabiensis populations although Hemingway[11, 23] did implicate a carboxylesterase gene in resistance to malathion. Recently, Nardini et al. reported that one P450 gene, CYP9L1, showed increased transcription in a Sudanese DDT selected laboratory strain (SENN-DDT) compared to an unselected susceptible strain.
In the present study, we describe the insecticide resistance patterns of An. arabiensis populations from central Sudan over a three year period, and report the principle mechanisms responsible for the observed resistance to pyrethroids and DDT. Results from this study will guide the development of effective insecticide resistance management strategies in Sudan.
This study was carried out in Gezira state in central Sudan. The state is situated in a rich savanna environment. The area has a hot dry summer from April to June with daily temperatures between 32-42°C, and relative humidity of 20%. The rainy season starts in late June and ends in October. Winter is relatively cold and dry and occurs from December to February, with daily temperatures between 15-21°C, and a relative humidity of 30% (Sudan Meteorological Services, 2005, unpublished data).
Anopheles mosquitoes were collected between October 2008 and January 2011. Two rounds of collections were performed every year in each of the four sites to coincide with the two peaks of malaria transmission seasons (October/November - the period towards the end of the wet season; and January - the dry season). Mosquitoes were collected as larvae and transferred to the BNNICD (Blue Nile National Institute for Communicable Diseases) insectary and reared to the adult stage to be used for WHO insecticide susceptibility tests. Samples were taken from multiple breeding sites within a 10 km radius and collections undertaken over several days to minimize the probability of analyzing siblings from a single female.
WHO bioassay tests
Larvae were reared to the adult stage, morphologically identified, and only Anopheles gambiae s.l. non-blood fed, 3–5 day old adult females were used for the insecticide bioassays. Insecticide papers were obtained from the WHO reference centre in Malaysia. Each batch was tested on the insecticide susceptible Kisumu strain of An. gambiae at the Liverpool School of Tropical Medicine before dispatch to Sudan. Five insecticides were tested: 4% DDT (organochlorine), 0.75% permethrin (type I pyrethroid), 0.05% deltamethrin (type II pyrethroid), 0.1% bendiocarb (carbamate) and 1% fenitrothion (organophosphate) according to standard WHO protocols.
Mosquito identification and kdr mutation detection
From each sentinel site and for each insecticide, 30–50 mosquitoes taken from the control exposure as well as 20 specimens that survived exposure and 20 specimens that died, were identified to species level using PCR. The hydrolysis probe/Taqman®-kdr assay was used for the detection of the L1014F and L1014S mutations from pyrethroid/DDT bioassay survivors and dead specimens.
Susceptibility status of mosquito populations was evaluated according to WHO criteria. Mortality greater than 98% indicates susceptibility, mortality less than 98% suggests resistance and needs further investigation, and mortality of 90% or lower confirms insecticide resistance. Mortalities in the control groups were less than 5%, thus no corrections using Abbott’s formula were required. A two sample t-test was used to compare the differences in mortalities between the two different seasons during each year of collection and to check for significant change in mortalities over the three years. Analyses were undertaken for each insecticide using Statistix7 analytical software. Regression analysis was used to compare the kdr allele frequencies over the three years. Allelic association between kdr and resistance, and odds ratios, were calculated in Vassar Stats (http://vassarstats.net/odds2x2.html).
Microarray analysis was performed to test for gene transcription differences between three sample conditions: Wad Medani resistant mosquitoes (survived 120 minute exposure to permethrin, which is equivalent to an LT80), Wad Medani unexposed, and the control DONG (susceptible An. arabiensis strain from Dongola in North Sudan, susceptible to all known insecticides; housed at BNNICD, Sudan and the Botha de Meillon Insectary, National Institute for Communicable Diseases (NICD), South Africa).
For each biological condition, total RNA was extracted from 5 pools of 15, 3 day old unfed female mosquitoes using the Arcturus PicoPure Kit (Life Technologies, Paisley, UK) with an on-column DNase digestion (RNase-Free DNase , Qiagen, UK). Total RNA concentration was measured using a NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, USA) and quality assessed using the Agilent RNA 6000 Nano Assay on an Agilent 2100 Bioanalyzer (Agilent Technologies, Stockport, UK). RNA pools (100 ng total) were labeled separately with Cy3 and/or Cy5 using the Agilent Low Input Quick Amp Labeling Kit (Agilent Technologies) following the manufacturer’s recommendations. Labeled RNA was purified using the RNeasy Mini Kit (Qiagen), eluted in 30 μl water, and quantity and quality determined as above. All samples passed the yield and specific activity thresholds recommended by Agilent. Cy3-labelled cRNA (300 ng) and Cy5-labelled cRNA (300 ng) were combined and hybridised to the AGAM-15 K chip.
The experimental design for microarray comparisons is depicted in Additional file1: Figure S1. Hybridization, washing, scanning and feature extraction were performed according to the manufacturer’s recommendations. Analysis was undertaken in GeneSpring GX 11 (Agilent Technologies) following filtering out of all probes where either red or green signal was not significantly above background. A 2-fold cut-off with probability ≤0.05 (FDR adjusted;) was applied to all features in order to determine significance. All data have been submitted to ArrayExpress (http://www.ebi.ac.uk/miamexpress/) with accession number E-MEXP-3656.
The microarray results were validated by quantitative real-time PCR (qPCR).
Primer sequences used for qPCR validation of CYP6P3 , CYP6Z3 and GSTe4
Superscript III (Invitrogen) was used to produce cDNA for qPCR. All cDNA samples were cleaned using the PCR Purification Kit (Qiagen) prior to use. A 2-fold dilution series of template cDNA was used to produce the required standard curves. All reactions were prepared in triplicate in 20 μl volumes containing 1× Agilent Brilliant III SYBR qPCR Mastermix, 300 nM of each primer, and 1 μl template RNA (100 ng/ul). Reactions were performed using the Agilent MX3005 qPCR system. The cycling conditions were 3 min at 95°C followed by 10s at 95°C, 10s at 60°C (40 cycles). The ΔΔCt method was used for calculation of fold change values.
WHO bioassay tests
High frequencies of permethrin and DDT resistance were observed over the three years of monitoring in the urban agricultural area of Wad Medani, and in Rufaa, the area with low insecticide exposure (Figure 2).
Comparison of the mortalities obtained for each insecticide between the two seasons for each year of monitoring
Oct. –Nov Vs Jan.
Oct. –Nov. Vs Jan.
Oct. –Nov. 2008Vs Jan. 2009
Oct. –Nov. 2008Vs Jan. 2009
Oct. –Nov. 2008 Vs Jan. 2009
Oct. –Nov. 2008 Vs Jan. 2009
Oct. –Nov. 2008 Vs Jan. 2009
Oct. –Nov. 2008 Vs Jan. 2009
Oct. –Nov. 2008 Vs Jan. 2009
Comparison of the mortalities obtained for each insecticide between different year one and three of the study
Year 1 Vs Year 3
Oct. –Nov 2009 VS Oct. –Nov 2010
Year 1 Vs Year 3
Oct. –Nov 2009 VS Oct. –Nov 2010
Year 1 Vs Year 3
Oct. –Nov 2009 VS Oct. –Nov 2010
Detection of kdr
Summary of L1014F kdr genotypes and allele frequencies in alive and dead An. arabiensis exposed to pyrethroid and DDT from all sentinel sites in central Sudan during all 3 years of collection
Number of alleles
Significantly up-regulated ( p < 0.05; FC > 2) detoxification genes in whole genome microarray comparison of Wad Medani resistant vs . Dongola colony
COE09941 - Putative Carboxylesterase
COE09895 - Putative Carboxylesterase
qPCR validated the microarray results for CYP6P3 (microarray FC = 12.45; qPCR FC = 13.35) and for GSTe4 (microarray FC = 2.41; qPCR FC = 3.2). For CYP6Z3, the FC value obtained from microarray analysis (10.39) was lower than that obtained using qPCR (21.35) but was still significant.
Previous studies have shown that insecticide resistance is present in Sudanese vector populations[10–12, 23, 31, 32]. The present study extends this work through evaluation of the resistance status of An. arabiensis over three years of monitoring in areas with different levels of insecticide exposure and explores the difference in resistance patterns between the two different seasons of malaria transmission.
Anopheles arabiensis was the only member of the An. gambiae complex found in Gezira state, as has been demonstrated previously[4, 12, 32, 33]. The field population of An. arabiensis collected from Gezira state was susceptible to bendiocarb (a carbamate) and fenitrothion (organophosphate). Bendiocarb is currently used for IRS in Gezira state. It was first applied for public health purposes in central Sudan in 2007 when An. arabiensis showed strong resistance to the pyrethroid insecticide, permethrin.
Anopheles arabiensis from central Sudan exhibited resistance to permethrin, DDT and deltamethrin. The most resistant population was found in Wad Medani, an urban agricultural site. The presence of multiple insecticide resistance in the study area is consistent with previous studies[12, 31, 32]. There is strong variation in mortality rates between the two different seasons of each year of collection (wet/dry). For example, in Wad Medani, permethrin and DDT resistance during the 2008–2009 rounds of collections was high with mortality rates of 33% and 35.5% respectively during the wet season. During the dry season, the mortality rates increased to 89% and 73.4% for permethrin and DDT respectively. The same trend is observed for deltamethrin where the mortality was 73.2% during the wet season and 100% during the dry season. Such seasonal variations in susceptibility of Anopheles mosquitoes to insecticides have been reported in Burkina Faso, Benin and Chad.
Resistance in the mosquito population to permethrin, and the reduced susceptibility to deltamethrin in Wad Elhadad, a site of intensive LLIN coverage, may have developed as a result of sustained exposure of adult mosquitoes to these insecticides from LLINs. DDT is currently not used in Sudan, however, high levels of resistance were still observed. DDT resistance was strongly associated with the L1014F mutation and it is possible that recent pyrethroid use has selected for this cross-resistance mechanism. As a result, high levels of DDT resistance was observed, even in areas where DDT use had been discontinued for a number of years. Similar results were reported in the same area in previous studies[12, 32]. The kdr allele 1014 F is strongly associated with resistance in these populations. Effects sizes (Odds Ratios) are high; in allelic tests they are similar to the values reported previously for effects sizes of kdr in Ghanaian and Cameroonian An. gambiae.
While 1014 F imparts a dramatic effect on resistance, it does not completely explain the resistance phenotype since many 1014 L homozygotes survive 1 hr exposure to pyrethroids and DDT, suggesting that alternative mechanisms of resistance are operating in this population. This phenomenon has been described before[21, 38, 39].
In order to investigate the metabolic resistance mechanisms involved in the resistance of these field populations, a whole genome microarray approach was used. In comparisons of An. arabiensis from Wad Medani, which survived exposure to permethrin equivalent to an LT80, with the susceptible DONG strain, a large number of genes showed significantly different transcription levels. The most significantly over-transcribed genes were trypsins, chymotrypsins and loci of no known function for which the relationship with resistance is difficult to investigate. A number of detoxification genes were also significantly over-transcribed, including genes with known roles in permethrin metabolism, e.g. CYP6P3 and CYP6M2, both of which have been demonstrated to be capable of metabolising pyrethroids in vitro[40, 41]. In addition to this, CYP6M2 was recently shown to also metabolise DDT. The highest over-transcribed candidate was the glutathione-S-transferase GSTe4 which exhibits >15 fold mRNA expression in the resistant strain. Whilst GSTs have recognised roles in DDT metabolism, they may also be associated with pyrethroid resistance.
No significantly over-transcribed probes were detected in comparisons of Wad Medani resistant samples with unexposed controls from the same site. However, this may be explained by significant effects of 1014 F on resistance since samples for microarray were not matched for kdr status. In addition, there is reduced power to detect gene expression differences in comparisons of resistant samples with unexposed controls since these, by definition, will contain resistant individuals. The high levels of resistance and the importance of both target-site and metabolic processes in the resistance phenotype indicate that continued monitoring of expression of detoxification loci in resistant populations of An. arabiensis is necessary.
Whether the resistance found in central Sudan is due to agricultural usage of chemicals, domestic aerosols/coils/ITNs for personal protection or from malaria vector control activities is difficult to assess as we do not have data on the types or quantities of chemicals used for agriculture or domestic use. What is clear, however, is that resistance has been found at all four study sites, albeit at different frequencies. This endorses the malaria vector control programme’s implementation of a resistance management strategy for central Sudan, as mentioned above, along the lines advocated by the WHO Global Plan for Insecticide Resistance Management.
This study reports strong seasonal variation in the susceptibility levels to pyrethroids and DDT in Gezira state. The results obtained in this study will enable informed choice of insecticides for use in vector control programmes in Gezira state. In addition, the data obtained will provide baseline information needed in the monitoring of the susceptibility of An. arabiensis to the carbamate insecticide bendiocarb currently being used by the vector control programme for indoor residual house spraying.
HA received financial support from the UNICEF/UNDP/World Bank/WHO Special Programme for Research and Training in Tropical Diseases (WHO/TDR). The study was supported by grants from the NHLS-Research Trust (LLK) and the South African Research Chair Initiative of the Department of Science and Technology and the National Research Foundation (MC). We would like to thank Chris Jones and Rodolphe Poupardin (LSTM) for assistance with data analysis.
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