- Open Access
Pyrethroid resistance in southern African Anopheles funestus extends to Likoma Island in Lake Malawi
© Hunt et al; licensee BioMed Central Ltd. 2010
- Received: 14 October 2010
- Accepted: 31 December 2010
- Published: 31 December 2010
A mosquito survey was carried out on the island of Likoma in Lake Malawi with a view to collecting baseline data to determine the feasibility of implementing an integrated malaria vector control programme. No vector control interventions are currently being applied on the island apart from the sporadic use of treated and untreated bed nets.
Large numbers of Anopheles funestus were found resting inside houses. WHO susceptibility tests were carried out on wild caught females and 1-5 day old F-1 female progeny. Wild caught females were tested on deltamethrin (77.8% mortality) and bendiocarb (56.4% mortality). Female progeny were tested on deltamethrin (41.4% mortality), permethrin (40.4%), bendiocarb (52.5%), propoxur (7.4%), malathion, fenitrothion, DDT, dieldrin (all 100%) and pirimiphos-methyl (98.9%). The malaria parasite rate was 4.9%. A small number of Anopheles arabiensis were also collected.
This locality is 1,500 km north of the currently known distribution of pyrethroid resistant An. funestus in southern Africa. The susceptibility results mirror those found in southern Mozambique and South African populations, but are markedly different to An. funestus populations in Uganda, indicating that the Malawi resistance has spread from the south.
- Indoor Residual Spray
- Insecticide Resistance
- Gambiae Complex
- Anopheles Funestus
Anopheles funestus is the major malaria vector in southern Africa. Early records of its involvement in malaria transmission give Plasmodium falciparum parasite rates as high as 22% in South Africa . More recently, in Tanzania 11% infection rate was recorded  and 5% in southern Mozambique .
South Africa eradicated An. funestus in the 1950's when an extensive indoor residual spraying (IRS) campaign using DDT was rolled out. In the next 50 years, this vector species was recorded only once during a small malaria outbreak in the northern part of the country . In 1999/2000, however, South Africa experienced its worst malaria outbreak since the introduction of IRS in the 1950's and An. funestus was found once again in northern KwaZulu/Natal, just south of Mozambique [5, 6]. The P. falciparum parasite rate in An. funestus was 5.4% and the mosquitoes were found to be resistant to both pyrethroids and carbamates.
Subsequent research in southern Mozambique showed that the insecticide resistant population of An. funestus extended north of the capital, Maputo [7–9]. Most recently, resistance was found in An. funestus from Chokwe , approximately 200 km north of the capital, where previously this population was found to be susceptible .
The present study provides evidence of insecticide resistance in An. funestus from an island in Lake Malawi that is considerably further north than any previous records of resistance.
Mosquitoes were collected resting inside houses using a hand aspirator. Some samples were used immediately for WHO susceptibility tests while others were packaged and returned to Johannesburg where egg batches were obtained and larvae reared through to F-1 adults.
Wild females were screened for malaria parasite infection using ELISA .
Insecticide susceptibility tests carried out on An. funestus females on Likoma Island.
Insecticide susceptibility tests carried out on 1-5 day old female progeny of An. funestus from Likoma Island.
0.9% Pirimiphos methyl
One hundred and eleven wild An. funestus females of unknown age were tested for insecticide resistance under field conditions with no temperature or humidity control. A total of 6 An. gambiae complex females and over 120 females and ± plusorminus90 males of An. funestus, together with a small collection of An. gambiae larvae, were packaged and transported back to the laboratory in Johannesburg.
A total of 223 An. funestus were subjected to molecular assays including all the wild adults used in the susceptibility tests (n = 111) as well as the live females brought back to the laboratory for egg laying (n = 112). 97.3% were successfully identified as An. funestus s.s. (five specimens did not amplify a PCR product and one specimen was identified as An. funestus-like). All males and females of the An. gambiae complex (wild adults and adults reared from larvae, n = 89) were identified as An. arabiensis.
Of the 81 wild An. funestus females tested for parasite infection, 4.9% were positive for P. falciparum using the ELISA method.
The results of the first insecticide susceptibility tests, carried out on the island using wild female An. funestus of unknown age, are given in Table 1. Since the controls gave >5% mortality, Abbott's formula  was used to correct the results, giving 77.8% mortality on deltamethrin and 56.4% on bendiocarb. The papers used in the field were tested in the laboratory using a susceptible An. gambiae colony and gave 100% mortality for all samples and replicates (n = 100 for each insecticide).
The second round of insecticide susceptibility tests was carried out in the laboratory at 25°C and 85% RH using 1-5 day old An. funestus females pooled from approximately 120 egg batches. Nine different insecticides from all four classes were tested and the results are given in Table 2.
Unfortunately, the An. arabiensis sample reared from larvae was too small (n = 42 females) to carry out meaningful susceptibility tests.
The marked difference between the deltamethrin susceptibility tests carried out on wild females in the field and those on the laboratory reared, 1-5 day old F-1 progeny (p <0.005), can be explained in two ways. One, high temperatures are known to affect the survival of mosquitoes exposed to insecticides  and this may account for the high mortality in the field samples. Two, An. funestus susceptibility to this sub-class of pyrethroids may be age dependent . Since the survey was carried out in May towards the end of the transmission season, it is likely that the wild-caught females tested in the field were an aging population and were therefore more susceptible to the insecticides. However, Hunt et al.  also report that blood fed, mated, females did not show any decrease in resistance over time, and aging wild populations would all be mated and have taken numerous blood meals.
It is clear from the susceptibility results that a resistance management strategy will have to be devised and implemented in order to control malaria on the island. If pyrethroid treated bed nets are to be distributed widely on Likoma Island, then IRS must be carried out simultaneously with an organophosphate or DDT in order to manage the resistance. Carbamates are unfortunately not an option with such a high frequency of survival. The An. funestus population is fully susceptible to DDT, which raises the possibility of using DDT for IRS perhaps in a rotation with one of the organophosphates.
The most worrying aspect of this survey is the discovery of pyrethroid and carbamate resistance in the An. funestus population approximately 1,500 km north (Figure 1) of its current known distribution at Chokwe in southern Mozambique . The report by Casimiro et al.  on samples collected from central Mozambique in 2006 showed that An. funestus had >95% mortality to pyrethroids and carbamates. The WHO criteria recommend that this percentage of susceptibility requires further investigation, but operationally it is unlikely that a control programme would change its policy based on this frequency of resistance/susceptibility.
Likoma Island in Lake Malawi is just a few kilometres away from Mozambique and presumably the mosquitoes are either blown over by the wind or brought on boats that ply their trade between the island and the mainland. One must assume, therefore, that the An. funestus population in northern Mozambique is also resistant and this has serious implications for current malaria control efforts being undertaken in this region. Since both pyrethroid and carbamate resistance has been found in the Likoma population, mirroring the resistance found in more southerly populations, it can be assumed that the resistance is spreading northwards through the An. funestus populations through gene flow, and not arising as separate genetic mutation events. There are no obvious geographical barriers to gene flow in this region of southern Africa and presumably we can expect the resistance to spread northwards into southern Tanzania and westwards into Zambia and Zimbabwe. The recently reported resistance in An. funestus from Uganda  is obviously different to that observed in southern African populations, based on both susceptibility tests and molecular characterization of the P450 genes [5, 16, 18, 19]. In Uganda, both pyrethroid and DDT resistance was found, with full susceptibility to carbamates, suggesting that this resistance has arisen independently under different selection pressures as suggested by Morgan et al.  based on their molecular data.
This paper highlights the seriousness of the rapid spread of insecticide resistance in An. funestus in southern Africa and the urgent need for resistance management strategies within malaria vector control programmes within the region.
Mr John Chiphwanya and Mrs Doreen Ali of the Malawi National Malaria Control Programme are thanked for support for this project and for assistance with the logistics. Staff and students of the Vector Control Reference Unit are thanked for technical support in the field and the laboratory. The survey was funded by Bayer and the DST/NRF Research Chair grant to MC.
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