Background
Despite considerable efforts to control malaria, the disease remains one of the most pressing public health issues across sub-Saharan Africa. In 2006, there were about 250 million malaria cases [
1]. In 2008, there were an estimated 880,000 deaths from malaria [
2,
3]. Insecticide-treated nets (ITNs) significantly reduce malaria-related morbidity and mortality [
4], and are increasingly utilized in sub-Saharan Africa. In Côte d'Ivoire, ITN coverage is low (<10%), with the majority of nets being considered as 'untreated' as there is evidence that the insecticide used for re-treatment is often not applied within the recommended six months time frame [
4]. In resource-constrained settings, such as Côte d'Ivoire, the relatively short period those insecticides remain effective on a conventionally treated net (CTN) is an important obstacle to sustaining high coverage rates of ITNs.
Long-lasting insecticidal nets (LLINs) were developed as a more sustainable solution to the problems encountered with CTNs and are currently expected to retain biological activity for at least 20 standard World Health Organization (WHO) washes under laboratory conditions and three years of use under field conditions. There are two types of technology for manufacturing LLINs: incorporating the insecticide into polyethylene or polypropylene yarn or coating the insecticide onto polyester. PermaNet® 2.0 is a WHO recommended polyester LLIN coated with the pyrethroid deltamethrin to a target dose of 55 mg/m2 (±25%). This net has been tested in multiple laboratories and field sites. PermaNet® 3.0 was designed to give increased bio-efficacy against pyrethroid-resistant malaria vectors; it is made from two types of fabric; deltamethrin coated on the polyester sides of the net and a synergist piperonyl butoxide (PBO) incorporated with deltamethrin in the polyethylene roof. The target dose of deltamethrin in the sides of PermaNet® 3.0 is 85 mg/m2 (±25%).
Pyrethroid resistance can be caused by high frequency of kdr and/or enhanced metabolic mechanisms in
Anopheles gambiae s.s. These types of mechanisms are widespread in West Africa and in some cases have been shown to reduce the efficacy of treated nets [
5,
6]. It is therefore essential that new LLINs that are efficient against insecticide-resistant malaria vectors are developed. The goal of this study was to evaluate the efficacy of PermaNet
® 3.0 against insecticide-resistant
An. gambiae s.s,
Culex sp and susceptible
Mansonia sp in experimental huts in Côte d'Ivoire using washed and unwashed nets.
Mansoni a was included during this study as it presents a significant biting nuisance in Côte d'Ivoire [
7,
8].
Methods
Study area and experimental huts
The experimental hut station was located at Yaokoffikro, near Bouaké in central Côte d'Ivoire, where 18 experimental huts are available for the assessment of new insecticide formulations. Six experimental huts, built with bricks coated in cement, were refurbished before starting the trial. Mosquito vector abundance at the field site is dominated by
An. gambiae s.s and
Culex sp; the majority of the
An. gambiae s.s. population is represented by the S form (90%) and M form (10%) at low frequency, with high kdr frequencies (94%) combined with a lower frequency of P450-based metabolic resistance [
9,
10].
The huts were situated near rice and vegetable fields in two rows with a five-meter gap between huts. The style of the hut was typical of the region, made from concrete bricks, with a corrugated iron roof, a ceiling of thick polyethylene sheeting, and a concrete base surrounded by a water-filled channel to prevent entry of ants [
11]. Mosquito access was via 4 window slits constructed from pieces of plywood, fixed at an angle to create a tunnel with a 1 cm wide gap. Mosquitoes had to fly upward to enter through the gap and downwards to exit; this limited exodus though the aperture enabling the majority of entering mosquitoes to be retained. A veranda trap made of polyethylene sheeting and screening mesh measuring 2 m long, 1.5 m wide, and 1.5 m high, projected from the back wall of each hut. Movement of mosquitoes between hut and veranda was unimpeded. All huts were thoroughly cleaned before the trial. Sheets were laid over the floor each night to facilitate the collection of mosquitoes from the floor each morning.
Net treatment and washing procedures
The conventionally-treated nets (CTNs) were dipped and washed alongside the LLINs at the Liverpool School of Tropical Medicine (LSTM) according to standard WHO procedures described below. The standardized WHO recommended washing method used is not meant to simulate washing procedures in real-life, but allows comparisons with other studies using this format of washing.
Conventionally-treated nets washed to just before exhaustion
Untreated polyester nets were treated with K-O TAB® (deltamethrin 1% corresponding to a dose of 25 mg/m2) following the manufacturer's instructions (Bayer Environmental Sciences). The point of exhaustion was determined by treating one net and performing WHO cone bioassays after each wash, until reaching the exhaustion point, defined as the last wash for which the net still causes ≥80% mortality or ≥ 95% knockdown (KD). After the sixth wash, the mortality rate against the standard susceptible An. gambiae s.s. Kisumu strain was under 80% and the KD rate was below 95%. Consequently, five nets were treated with K-O TAB® and washed five times. After the fifth wash the mortality and the KD rates of the dipped nets were ≥80% and ≥ 95%, respectively, compared to those recorded with the unwashed CTN, hence the targeted dose of the dipped net was assumed to be approximately 25 mg/m2.
Washing procedure
Before each washing of each net (LLINs and CTNs), 20 g of "Savon de Marseille" (Unilever) was added to 10 l of de-chlorinated water and fully dissolved for 30 minutes. Each net was washed, immersed in the soap solution and manually agitated by hand (with protection by gloves) for 10 minutes at approximately 20 rotations per minute. Nets were then rinsed twice in fresh tap water and dried horizontally in shade. The nets were stored at ambient temperature between washes; CTNs were washed five times and PermaNet® 2.0 and PermaNet® 3.0 were washed 20 times with a one day interval between washes.
Bioassays
Insecticide-susceptible An. gambiae s.s. used in bioassays were from a Kisumu strain established at Institut Pierre Richet. Insecticide-resistant An. gambiae s.s adults were obtained from larval collections from natural breeding sites in Yaokoffikro and then transported to the laboratory for rearing to adults. All larvae were provided a diet of Tetra Mikromin fish food until adult emergence. All mosquito rearing and bioassays were performed under ambient environmental conditions.
Cone bioassays were performed at the beginning and at the end of the trial. Susceptible and resistant An. gambiae s.s strains were tested separately. Batches of 5-6 unfed, 2-5 day old female An. gambiae s.s. including the standard susceptible Kisumu strain and a wild insecticide-resistant adult mosquitoes were placed inside the WHO cone and exposed simultaneously and in a similar manner to different parts of the unwashed and washed nets (the roof and the sides) for three minutes before being transferred from cones to holding containers. The number of mosquitoes knocked down was then recorded 60 minutes after exposure and the final mortality was recorded 24 hours post-exposure. Survivors were maintained on 10% honey solution. An untreated net was used as a negative control.
WHO susceptibility tests were performed on 3-5 day old unfed wild-caught pyrethroid-resistant females reared from larval collections, using standard WHO test kits and protocols for adult mosquitoes [
12]. In brief, papers impregnated with 0.05% deltamethrin, 0.75% permethrin and 4% DDT were sourced from WHO. Batches of 20--25 females were exposed to impregnated papers in WHO test tubes for 1 h with at least four replicates per bioassay and concurrent negative controls with corresponding insecticide-free papers. Knockdown (KD) was recorded after 60 min and mosquitoes were transferred to holding containers with access to a 10% honey solution. Mortality was recorded after 24 h.
Volunteer sleepers, rotation and mosquito collection
Preliminary results showed no significant difference in attractiveness of different huts as there was no statistical difference between the mean number of mosquitoes collected in huts after sleepers rotation (P = 0.05). The following 6 treatment arms were tested:
Five nets were used for each treatment arm with each net being tested on one night during each week. Holes were not cut in the nets for ethical reasons as requested by the National Malaria Control Programme. Treatment arms were rotated among the huts each week, according to a pre-established Latin square design. Five adult male volunteers slept in the huts from 20:00 to 05:00 h each night and were rotated randomly among huts each night of the study. At the end of each week the huts were cleaned and aired to avoid potential contamination.
The trial lasted 12 weeks (from April to July 2009) as the number of mosquitoes collected during the first 6 weeks of the trial was low. Each morning, mosquitoes were collected from the floor, walls and roof of the huts as well as from the exit traps. Collected mosquitoes were transferred to the nearby laboratory and identified to the genus and species level using a determination key [
13], and classified as dead/blood fed, alive/blood fed, dead/unfed, and alive/unfed. Surviving mosquitoes were provided with honey solution and held for 24 h after which delayed mortality was assessed.
The effect of each treatment was expressed relative to the control (untreated net) by assessing the deterrent effect (proportion entering), which shows the dissuasive effect of the treatment arms, the induced exophily (proportion of mosquitoes that exit early through the exit traps, treatment-induced exiting) and mortality rates. The blood feeding rate could not be measured as a standard parameter as the number of blood fed
An. gambiae s.s collected was too low and holes were not included in the nets as per standard WHOPES protocol [
12]. All parameters were reported separately for each treatment.
Ethical considerations
Ethical approval was obtained from the Ministry of Health, Côte d'Ivoire, through the National Malaria Control Programme. Written informed consent was obtained from each volunteer sleeper, who was offered anti-malarial chemotherapy (artesunate plus amodiaquine) free of charge, and their vaccination status against yellow fever was checked before enrolment. Volunteer sleepers were medically supervised throughout the study by qualified medical personnel.
Statistical analysis
Data collected every week were double-entered and cross-checked in Windows Excel 2008. Statistical analysis was carried out with STATA version 9.04 (Stata Corporation; College Station, TX, USA) using a significance level of 5%. Data were collected for 4 mosquito species (or groups of species) caught in huts with six types of net (treatments) over a series of 5 nights before changing the treatment allocation the next week. The data variables measured were: number of mosquitoes caught in the room and on the veranda, number dead either immediately after exposure to the net or 24 hrs post exposure and the number of blood fed mosquitoes.
Three main variables were analysed for each mosquito species:
- total number of each mosquito species caught: calculated as (number in room) + (number on veranda)
- proportion of mosquitoes exiting the room: calculated as (number caught on veranda)/(total number)
- mortality: calculated as (total number dead = immediate + delayed)/(total number)
The blood feeding rate was also calculated (number blood fed/total number), but this has not been included as a standardized parameter because holes were not in the nets for ethical reasons, as explained previously. Mosquito numbers were analysed using Poisson GLM (generalized linear model) with a log link function. This model accounts for the variance heterogeneity seen with count data, especially for very low mosquito counts, and fits a model that is linear on the logarithmic scale (exponential in terms of counts). The ratio of all treatments to control is then compared using this model.
The remaining variables were proportion data, and were analysed using a Binomial GLM with logit link function. This model accounts for variance heterogeneity that depends both on the proportion and total number of mosquitoes of each species observed. It fits a model that is linear on the logistic scale (an S-shaped curve on the proportion scale). It is not straightforward to derive ratios between treatments using this model, but it is possible to derive the odds ratio for any test treatment against the control. An odds ratio of 0.5 or less indicates no difference between the treatments; and between treatment and control; an odds ratio > 0.5 indicates a higher proportion for the test treatment compared to the control.
Two sets of analyses were conducted; the first analysis used the daily data to check whether there was any evidence of significant differences between sleepers. This analysis used the model terms: 'Hut' + 'Week' + 'Sleeper' + 'Treatment', where 'Hut' is a factor labelling huts 1-6, 'Week' is a factor labelling weeks 1-12, 'Sleeper' is a factor labelling Sleepers 1-6 and 'Treatment' is a factor labelling treatments 1-6. Fitting this model in this order means allows means for each hut and week to be removed before looking for differences between Sleepers, and treatment differences are assessed only after removing these other effects.
The first analyses showed evidence of sleeper effects only for the blood feeding rate, where numbers were so low as to be unreliable. Hence this parameter could not be used as an outcome measure. The analysis of weekly totals was almost identical to the analysis of daily totals. The statistical analysis on the number of blood fed mosquitoes was then done by using the total blood feds of each species with each treatment, which were analysed separately.
A second set of analyses on weekly totals was therefore carried out using the model terms:
The significance of the treatments was assessed using the F-test from analysis of deviance (analogous to ANOVA for continuous data). Predictions for each treatment were obtained with a 95% confidence interval, and the ratio (or odds ratio) with respect to the control treatment was obtained, again with a 95% confidence interval. Finally, the deterrent effect (proportion entering), the induced exophily and mortality rates between treatment arms were compared.
Discussion
The excito-repellency effect of all the treated nets was consistently high (≥ 50%) compared to the control. Mosquitoes were affected by pyrethroid on the nets, corroborating previous findings that pyrethroid-impregnated nets provide an irritant barrier against susceptible and resistant
An. gambiae s.s mosquitoes, due to the excito-repellency and knock-down effects of pyrethroids [
14]. The absence of holes in the nets, for ethical reasons, could have impacted the excito-repellency effect of all the treated nets, as sleepers would be accessible to
An. gambiae s.s,
Culex sp, Mansonia sp and other mosquitoes when under holed nets. Access to a blood meal may then reduce the excito-repellency rate recorded with each net. However, in areas with pyrethroid resistance, such as Benin [
15], Burkina Faso and Cameroon [
6], even when holes were present in the nets, the mortality rates recorded were low (30-40%) whereas in susceptible area such as Tanzania, mortality were above 80% [
16] confirming the fact that mosquitoes resistance to pyrethroid reduced efficacy of nets. Low blood feeding rates were recorded for all treatment arms because nets were tested intact.
Cone bioassays against resistant
An. gambiae s.s showed that the KD rate was > 95% and the mortality was > 80%, only with unwashed PermaNet
® 3.0, although with washed 20x PermaNet
® 3.0 a mortality rate > 80% was recorded against resistant
An. gambiae s.s. Four out of five of the cone bioassays were performed on the polyester sides of washed PermaNet
® 3.0 coated with high dose of deltamethrin (85 mg/m
2). Previous studies conducted in sub-Saharan Africa have shown that the deltamethrin content remained high in the polyester sides of washed PermaNet
® 3.0 even after 20 washes [
6,
17]. Chemical analysis of deltamethrin and PBO content on nets used in this study was not conducted.
The highest mortality rates against
An. gambiae s.s (55.0%) and
Culex sp (51.6%) were recorded with unwashed PermaNet
® 3.0; mortality rates recorded with the other treatment arms were low (less than 40%) and did not differ significantly. The high dose of deltamethrin alone in the side panels of unwashed PermaNet
® 3.0 could explain the significant difference in mortality of resistant
An. gambiae s.s with this net compared to the other treatment arms. A previous study showed that the loss of deltamethrin after washing is very low in the side panels of PermaNet
® 2.0 [
6] where the dose of deltamethrin was initially equal to 55 mg/m
2 (±25%) before washing. That could partially explain why in these studies unwashed and washed PermaNet
® 2.0 performed equally [
17] confirming results reported in this study even if none measurement related to the deltamethrin and PBO doses was done before and after nets washing in the study.
The loss of efficacy of washed PermaNet
® in this study could be due to the resistance of
An. gambiae s.s to pyrethroids, as in susceptible area such as Tanzania, the mortality rates recorded are usually above 80% even with washed PermaNet
® 2.0 [
16]. Consequently, washing is considered to be a more important loss mechanism for coated nets than for incorporated nets. Over the course of 20 washes, there was a weak partial loss of activity against the resistant
An. gambiae s.s and
Culex spp with PermaNet
® 3.0 in the experimental hut trial, which was supported by bio-efficacy data indicating a reduction in mortality rates detected via cone bioassays on washed PermaNet 3.0. Probably the loss of deltamethrin after 20 washings in the polyester sides of PermaNet
® 3.0, combined with the high pyrethroid resistance rates in
An. gambiae s.s and
Culex spp explains the low mortality rate recorded with washed PermaNet
® 2.0 and PermaNet
® 3.0. Results from cone bio-assays showed that the mortality rate recorded with 20x washed PermaNet 3.0 in the roof and sides and 20x washed PermaNet 2.0 against resistant
An. gambiae was equal to 86% and 57%, respectively. Similar bioassays results were reported in Ladji, in southern Benin where
An. gambiae s.s M form species were resistant to pyrethroids and DDT, with high frequency of
kdr and metabolic resistance. In Benin, similar mortality rates were observed with
An. gambiae tested in WHO susceptibility kits with deltamethrin (43.9% vs. 45.2%) [
15]. The current study demonstrated that washed and unwashed PermaNet 2.0, washed PermaNet 3.0 and the conventionally-treated washed net (CTN) performed equally, while unwashed PermaNet 3.0 was associated with increased mortality. This is consistent with a recent study carried out in Benin, West Africa, which showed that although unwashed PermaNet
® 3.0 was associated with a higher mortality than unwashed PermaNet 2.0 or unwashed Olyset, once washed, PermaNet 2.0 and 3.0 performed similarly [
15]. In Vietnam where resistance did not seem to be affecting net efficacy, all PermaNet arms were performing slightly better than conventionally treated nets washed until just before exhaustion [
17]. In Burkina Faso, in Vallee du Kou where the
kdr mutation frequency was high (> 80%), results showed a strong reduction of LLIN efficacy. In this area, a significantly higher mortality and blood feeding inhibition was associated with unwashed and washed PermaNet
® 3.0 compared to unwashed and washed PermaNet
® 2.0 [
18].
This study raises concerns that resistance appears to be having an impact on the efficacy of the nets in Ivory Coast (<40% mortality), in southern Benin (40 to < 30% mortality) with deltamethrin lambda-cyhalothrin [
5,
15] treated nets and in Burkina Faso (<40% mortality) [
6] compared to >80% mortality in Tanzania where the vectors are susceptible [
16]. Resistance mechanisms in
Anopheles gambiae from the village of Ladji in Benin include
kdr and metabolic mechanisms [
5,
19]. Resistance due to the involvement of P450s and
kdr[
15,
20] has undermined attempts at malaria control with deltamethrin residual spraying in southern Africa caused by
An. funestus[
21]. Elevated P450 activity in a strain of
An. gambiae from Cameroon has been found to reduce the efficacy of permethrin-treated netting in laboratory tests [
22,
23]. However, recent cone bio-assays performed on PermaNet 2.0 and PermaNet 3.0 after eight months use with metabolic resistant
An. gam b
iae and
Anopheles arabiensis from northern Cameroon showed very high mortality rates (Koudou
et al, unpublished data). Enzyme-based pyrethroid resistance mechanisms, such as elevated esterases and/or P450's, combined mechanisms such as
kdr and metabolic resistance, and other mechanisms such as reduced penetration of insecticide, may be more of an obstacle to the control of malaria vectors in Cote d'Ivoire [
24].
Washing of PermaNet
® 2.0 and PermaNet
® 3.0 did not affect their deterrent effects against resistant
An. gambiae s.s or
Culex sp. However, the deterrent effect, i.e. the reduction in the number of mosquitoes entering the hut, may not be a reliable indicator of ITN efficacy, as within the same geographical area this index has varied considerably with different vectors and nets (including PermaNet
® 2.0) between experiments, e.g. from zero to 70.0% against
kdr-based pyrethroid resistant
An. gambiae s.s[
25,
26].
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
BGK: designed experiments, coordinated field activities, collected and analysed data, wrote and revised the paper; AAK: designed the study and participated in the coordination of the field activities and revised the paper; DM: contributed to the study design and revised the paper; JH: participated in the design of the study and revised the paper. All authors have read and agreed with the contents of the submitted manuscript.