PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of malarjBioMed CentralBiomed Central Web Sitesearchsubmit a manuscriptregisterthis articleMalaria JournalJournal Front Page
 
Malar J. 2008; 7: 38.
Published online 2008 February 28. doi:  10.1186/1475-2875-7-38
PMCID: PMC2267806

An experimental hut evaluation of Olyset® nets against anopheline mosquitoes after seven years use in Tanzanian villages

Abstract

Background

Long-lasting insecticidal nets (LLINs) are advocated by WHO for protection against malaria. Of the three brands of LLINs currently approved by WHO, Olyset® is the only one currently granted full recommendation. With this type of LLIN, the insecticide (permethrin) is incorporated into the polyethylene fibre during manufacture and diffuses from the core to the surface, thereby maintaining surface concentrations. It has not been determined for how long Olyset nets remain protective against mosquitoes in household use.

Methods

Examples of Olyset nets, which had been in use in Tanzanian villages for seven years, were tested in experimental huts against naturally entering Anopheles gambiae and Anopheles funestus mosquitoes. Performance was compared with new Olyset nets, conventionally treated ITNs (either newly treated with alphacypermethrin or taken from local villages after 1.5 years of use) and untreated nets. All nets were artificially holed except for the seven-year Olyset nets, which had developed holes during prolonged domestic use.

Results

Anopheles funestus and An. gambiae in NE Tanzania are susceptible to pyrethroids. The new Olyset nets caused high mortality against An. funestus (73.9%) and An. gambiae (62.7%) in experimental huts. The seven-year Olyset nets caused 58.9% mortality against An. funestus and 40.0% mortality against An. gambiae. The freshly treated alphacypermethrin nets also caused high mortality against An. funestus (70.6%) and An. gambiae (72.0%); this decreased to 58.4% and 69.6% respectively after 1.5 years of use. The new Olyset nets inhibited blood-feeding by 40–50%. The 7 year Olyset nets showed no feeding inhibition over that shown by the untreated nets. The alphacypermethrin treated nets failed to inhibit blood-feeding after 1.5 years of use. However iHhhdn laboratory tunnel tests samples of all types of treated net including the 7 year Olyset inhibited blood-feeding by more than 95%.

Conclusion

After seven years of use Olyset nets were still strongly insecticidal. Mosquito mortality decreased by only 20–35% over this period. However, Olyset would not provide personal protection after seven years unless it was in good condition and all holes fully repaired.

Background

Long-lasting insecticidal nets (LLINs) in which the insecticide treatment is intended to last for the lifetime of the net are advocated by the World Health Organization for protection against malaria [1]. LLINs have in recent years come to dominate the institutional net-buying market [2,3]. Of the 3 brands of LLIN currently approved by the WHO Pesticide Evaluation Scheme, Olyset® (Sumitomo Chemical Co., Ltd, Japan) is the longest established and is the only LLIN to be granted full, as opposed to interim, recommendation [3,4]. With this brand of LLIN, the pyrethroid insecticide (permethrin) is incorporated into the polyethylene fibre during manufacture and diffuses gradually from the core to the surface. Surface concentrations are regenerated after removal of permethrin by washing or general use [4-6]. Olyset nets are manufactured with a 4 mm mesh which is considerably larger than the 1.5 mm of most bed nets; the larger mesh has the advantage of allowing more ventilation for the sleeper. Olyset has been in use in some Tanzanian villages for several years and according to cone bioassay tests retains insecticidal activity for at least seven years [7].

In contrast to this finding, a study of Olyset carried out after two years of household use produced bioassay mortality rates that fell below the threshold set by WHOPES for LLIN [8]. Simple cone bioassay tests in which mosquitoes are exposed to treated netting in plastic containers for a few minutes do not reliably measure operational effectiveness, and interpretation of mortality data is confounded when the insecticide under test shows repellent as well as toxic activity [9]. Permethrin is well known for its excito-repellent activity [10]. Probably the best way to estimate operational effectiveness of LLIN after an interval in the field is to retrieve the nets from householders and to re-evaluate the nets under the realistic but controlled conditions offered by experimental huts since this technique is able to measure in a realistic way what proportion of mosquitoes are inhibited from entering the room with a person sleeping in the net, the proportion of mosquitoes inhibited from biting and feeding, and the proportion killed by the net. In experimental hut trials, volunteers take it in turns to sleep under the nets in the presence of host-seeking mosquitoes, alternating the test net with new LLIN/ITN (positive control) or untreated nets (negative control), and in this way relative protectiveness is demonstrated. In the study reported here some of the Olyset nets reported in Tami et al [7], which had been in use for seven years in Tanzanian villages, were tested in experimental huts against naturally entering Anopheles gambiae and Anopheles funestus mosquitoes. The effectiveness of these Olyset nets was examined relative to that of new Olyset nets, untreated control nets and conventional ITNs treated with alphacypermethrin (either newly treated or taken from local villages after 1.5 years of use).

Materials and Methods

Study area and experimental huts

Four veranda trap huts were constructed according to a basic design first described by Smith [11] with substitution of concrete for wooden floors. Surrounding each of the huts is a 10 cm wide moat filled with water to prevent scavenging ants from entering. The working principle of these huts has been described by Smith & Webley [12] and Curtis et al [13]. The huts are situated at Zeneti village in Muheza district, north-east Tanzania (5°13'S and 38°39'E, altitude 193 m). Anopheles gambiae s.s. and An. funestus are the predominant mosquito species in the area [14].Anopheles funestus is responsible for most of the dry season transmission of Plasmodium falciparum, and An. gambiae s.s. is responsible for wet season transmission.

Bed nets and treatments

The Olyset nets were formerly distributed in the villages of Mbwawa, Kibaha district [15] and Mvumi, Dodoma district [16] in 1994–1995, and were retrieved in July 2002 for laboratory evaluation by Tami et al [7]. Two of the nets were stored in plastic bags at room temperature until June 2005 and then tested in experimental huts at Zeneti. The new Olyset nets were obtained from Sumitomo Chemicals.

The alphacypermethrin nets were treated at a rate of 20 mg/m2 and distributed to houses in Kilulu village near Muheza in October 2003. No re-treatment was carried out. Five nets were retrieved in June 2005 after 20 months of use. The new alphacypermethrin nets were treated at a rate of 20 mg/m2.

Nets had six 4 cm diameter holes cut on sides and ends to simulate the condition of worn or torn nets. The 7 year Olyset already had a comparable number of holes as a result of prolonged domestic use. Five nets per treatment arm were prepared for testing in the huts except that only two seven-year Olyset nets were available for use in huts.

Experimental hut evaluation

The evaluation was run over 60 days between 20 June and 3 September 2005. The five treatments (including the untreated control net) were rotated through each of the four huts twice using a Latin square design. A treatment was allocated to a hut for five consecutive nights before being rotated to another hut. A different net was used on each of the five nights of the rotation. With five treatments and four huts, it was necessary for 1 treatment to drop out of the evaluation during each rotation. Two volunteers from Zeneti village slept in each hut between 19:30 and 6:30 hours. Sleepers were rotated between huts on successive nights in order to reduce the effect of variation in individual attractiveness to mosquitoes. Likewise, the direction of the two open verandas was routinely exchanged with the treatment rotation in order to minimise the potential confounding factor of preferential escape in one or other direction. Huts were cleaned and left to air for at least one night between each five day rotation.

Mosquitoes were collected in the morning at 07:00 from inside the net, the window (exit) traps as well as from the ceiling, walls and floor of the veranda and inside the room. The collected mosquitoes were kept in paper cups and brought to the field laboratory for species identification, determination of gonotrophic condition, and mortality counts. All live mosquitoes were held in paper cups supplied with 10% glucose solution and held for 24 hours after which delayed mortality was scored.

Analysis

The numbers of mosquitoes in the two verandah traps were multiplied by two to adjust for the unrecorded escapes through the other two verandahs which are left unscreened to allow routes for entry of wild mosquitoes via the gaps under the eaves [11-13].

The data was double entered and analysed to show the effect of each treatment in terms of:

• Insecticide-induced exiting: percentage of the total mosquito collection from verandah and exit traps in a treatment hut relative to the control.

• Blood feeding inhibition: percentage of unfed mosquitoes from a treatment hut relative to the control.

• Overall mortality: total number of mosquitoes found dead 24 hours after collection.

Assessment of outcome variables between treatments relative to the control was analysed using logistic regression for proportional data and non-parametric tests for numeric data using STATA® statistical analysis software package version 8 (Stata corporation, Collage Station TX, USA, 2003).

Contact bioassays

Before subjecting the treated nets to experimental hut evaluation, contact bioassays were carried out according to WHOPES guidelines [17]. Susceptible laboratory-reared An. gambiae (Kisumu strain) were exposed in batches of five to treated or untreated netting in WHO cones for three minutes, after which they were held for 24 hours for mortality scoring.

Tunnel tests

These were carried out in apparatus designed to simulate experimental hut conditions [18]. The tunnel is a glass cuboid measuring 60 cm long, 25 cm high and 25 cm wide, with three chambers (release, middle and baited). The test netting sample has nine evenly spaced 1 cm diameter holes and is fixed on a cardboard frame and placed at the separation between the middle and the baited (guinea pig) chamber. The partition between release and middle chamber has a single 10 cm diameter hole which is intended to prevent mosquitoes contacting the treated netting before starting bait-seeking flights.

Test mosquitoes were c. 100 non-blood fed, 4–6 days old, insectary-reared An. gambiae (Kisumu strain) or Culex quinquefasciatus (Masimbani strain). These were introduced into the releasing chamber of the tunnel at 18:00 and recovered at 06:00 the next morning. The cage was maintained at 26°C and 80% relative humidity. In the morning mosquitoes were removed and numbers scored separately from each chamber for estimation of penetration, blood feeding and mortality rates. Mosquitoes were held with sugar solution for a further 24 h before scoring delayed mortality.

Resistance tests

Samples of adult An. gambiae and An. funestus collected from the experimental hut site were tested for resistance status on permethrin 0.75% or deltamethrin 0.05% papers in WHO test kits according to WHOPES guidelines (17). Time taken for 50% and 90% knockdown of mosquitoes (KDT50 and KDT90) and 95% confidence intervals were determined by probit analysis using the computer program PoloPlus (Version1.0, LeOra Software).

Ethical clearance

Informed consent was obtained from all volunteers recruited to the experimental hut study. The study was approved by ethics committees of LSHTM and NIMR (Ref: NIMR/HQ/R.8a/Vol. X/86).

Results

Resistance tests

Wild caught An. gambiae and An. funestus from Zeneti village were fully susceptible to permethrin 0.75% and deltamethrin 0.05% test papers (Table (Table11).

Table 1
Susceptibility of wild Anopheles from Zeneti village to Permethrin and Deltamethrin

Experimental hut trial

The total number of mosquitoes collected during 60 nights was 1,108, consisting of An. gambiae (32.1%), An. funestus (59.5%) and Cx. quinquefasciatus (8.4%). The mean number caught per night was 18.5, consisting of 17 Anopheles and 1.5 Culex mosquitoes. A summary of results for An. gambiae and An. funestus is shown in Tables Tables22 and and3.3. Cx. quinquefasciatus were too few in number to provide meaningful conclusions.

Table 2
Comparison of Olyset and alphacypermethrin treated nets against Anopheles gambiae in experimental huts.
Table 3
Comparison of Olyset and alphacypermethrin treated nets against Anopheles funestus in experimental huts.

In experimental hut trials, where all treatments are presented simultaneously, comparison between the mean numbers collected from untreated control and treated huts are used to give estimates of the deterrent or spatial repellent effects of pyrethroid treatments. In the present trial where the number of treatments exceeded the number of huts available, these estimates could not be reliably made because treatments took it in turn to drop out and there were changes in the population of mosquitoes entering the huts during the course of the trial.

Exiting rates

The overnight exiting rates of An. gambiae ranged from 91.1% in the untreated control to 98.3% in the huts with the new Olyset nets. Tables Tables22 and and33 show estimates of the proportions induced to exit by the insecticide relative to those which would have exited without insecticide stimulation. All insecticide treatments led to higher exiting rates and this was statistically significant for Olyset and 1.5 year alphacypermethrin treatments against An. gambiae. The overnight exiting rate of An. funestus from the control huts was similar to that shown by An. gambiae. Only the alphacypermethrin treatments induced exiting rates of An. funestus that were significantly greater that the control.

Blood feeding

The blood feeding rates through holed, untreated netting were c.30% in both An. gambiae and An. funestus. Insecticide-induced inhibition of blood feeding ranged between 40% and 50% in the presence of new Olyset nets and between 68% and 72% in the presence of new alphacypermethrin treated nets. The blood-feeding rates through the household-used alphacypermethrin nets were less than through the untreated nets, but the differences were not significant. There was no reduction in blood feeding through the seven-year Olyset nets relative to the untreated nets. Very few mosquitoes were collected from inside any of the treated nets indicating that few penetrated the holes or through the larger mesh of the Olyset nets.

Mortality

The new alphacypermethrin nets induced high rates of mortality against An. gambiae and An. funestus. A difference in mortality rate between the new and the 1.5 year alphacypermethrin treatments was evident in the An. funestus results but not in the An. gambiae results. The new Olyset also scored high mortality. After seven years of use the Olyset nets were still very insecticidal; mortality of An. funestus was only 20% lower and mortality of An. gambiae was 36% lower relative to the new Olyset nets.

The local Cx. quinquefasciatus are highly resistant to pyrethroids, and too few were collected in the huts (100 mosquitoes in 60 nights) to draw major conclusions. Only 33% (7/21) were killed by the new Olyset nets and only 15% (3/20) were killed by the seven-year Olyset. The mortality rates with alphacypermethrin were 25% (4/16) for the new treatment and 6.9% (2/29) for the 1.5 year treatment.

Cone bioassays

Anopheles gambiae (KISUMU) showed knockdown rates ranging from 56%–88% and mortality rates ranging from 84–99% after 3 min exposure to samples of treated netting (Table (Table4).4). Exposure to the 7 year Olyset induced a mortality rate (89%) similar to that induced by the fresh alphacypermethrin treatment. The locally collected Cx. quinquefasciatus Masimbani strain is highly resistant to pyrethroids and few mosquitoes were killed by any of the treatments, whether old or newly treated.

Table 4
Summary of cone bioassay tests on nets collected from the field. 100 adult females were tested on each treatment.

Tunnel tests

All treatments reduced the numbers of An. gambiae penetrating the holed netting (Table (Table5).5). A greater proportion of An. gambiae penetrated the seven-year Olyset netting than penetrated the new Olyset netting. Passage of the pyrethroid resistant Cx. quinquefasciatus through the netting was less inhibited by the insecticide treatments than was the passage of susceptible An. gambiae. Generally, the permethrin in Olyset was more inhibitory to passage than the alphacypermethrin treatments were.

Table 5
Summary of tunnel test studies on the five types of net.

Blood-feeding in An. gambiae was almost fully inhibited by the Olyset and alphacypermethrin treatments. Blood-feeding rates in Cx. quinquefasciatus were inhibited more by the permethrin of Olyset than by alphacypermethrin; feeding rates were higher in tests with the older treatments.

More than 95% An. gambiae were killed by the new Olyset and new alphacypermethrin treatments. Significantly smaller proportions were killed by the treatments which had been used in households; nevertheless 56.6% An. gambiae did succumb to the seven-year Olyset treatment. Very few of the pyrethroid resistant Cx. quinquefasciatus were killed by either alphacypermethrin or Olyset.

Discussion

The Olyset nets acquired from the Tanzanian villages after seven years of household use had in the earlier bioassay tests conducted by Tami et al (7) produced results (92% knockdown and 50% mortality) of similar magnitude to the bioassay tests presented here. Tami et al [7] demonstrated that the nets retained 30–40% of the original insecticide content after seven years of household use. The relationship between laboratory bioassay results and field efficacy of nets under household conditions is poorly understood [19,20]. It is not possible to make predictions from bioassay data as to whether the observed insecticidal effect is sufficient to kill mosquitoes or protect against biting in a household or community setting. Only field studies can provide an unequivocal answer, and experimental hut trials are a controlled and objective way to obtain such information. Randomised controlled trials measuring changes in malaria incidence constitute the gold standard for evaluating treated nets but while it would be feasible to run such trials with new LLIN, attempting a controlled trial with 7y old nets or interpreting results 7y after the introduction of new LLINs would be problematic to say the least. Experimental hut trials measuring personal protection or insecticide-induced mosquito mortality are simple, comparatively cheap to undertake and give clear answers about current effectiveness of older nets. The conclusion is that after seven years of household use the Olyset nets had lost only a third of their efficacy against An. gambiae and An. funestus. These results are consistent with those obtained in experimental huts with Olyset net obtained from other communities after three [4] and four years of use [21].

A possible limitation of experimental hut trials is that only a handful of nets can be tested at any one time; WHO recommends testing 5 nets per treatment arm [18]. In the present trial only two 7y Olyset were available for testing but the results for each was consistent with the other and this raises confidence in the results.

This study was carried out in an area of NE Tanzania where An. gambiae and An. funestus are fully susceptible to pyrethroids and Cx. quinquefasciatus is highly resistant [22]. The trial coincided with the end of the rainy season and the start of the dry season when there is a natural succession from An. gambiae to An. funestus. Cx. quinquefasciatus were not abundant at this time but it was still clear, even with the low numbers collected, that the pyrethroid treated nets had little impact on this species in the field (or in laboratory cone or tunnel tests) owing to the resistance expressed in the Culex populations around Muheza [22]. In the present trial, five treatment arms were being tested in four experimental huts and it was therefore necessary to systematically drop each treatment during the course of the rotations. Unfortunately, owing to variation in weekly mosquito abundance it was difficult to estimate with accuracy the existence of spatial repellency (deterrence) since this calculation requires comparison of the number of mosquitoes captured in rooms with different treatments rather than the proportion of mosquitoes affected by a treatment within a particular room (in contrast to the estimates of the proportion of mosquitoes prevented from blood-feeding or the proportion killed). With the benefit of hindsight it is better to reduce the number of treatments or increase the number of huts to match the number of treatments than have individual treatments phase in or out of the trial.

The experimental huts showed that, when new, both alphacypermethrin and Olyset nets provide significant protection against mosquito bites. However, after 1.5 years of use in the case of alphacypermethrin and seven years in the case of Olyset the nets failed to prevent mosquito biting despite still killing many An. gambiae and An. funestus. This observation is not consistent with the results of tunnel tests which showed that the seven-year Olyset net provided a level of protection and blood feeding inhibition similar to the other treatments. Trials by Maxwell et al. with 4y old nets in experimental huts found quite a good reduction in biting [21]. It seems probable that tunnel tests overestimate the field effectiveness of treatments compared to hut trial estimates. In hut trials parts of the sleepers' bodies may touch the sides of the net giving mosquitoes an opportunity to feed through the netting. Olyset net is highly resilient to wear-and-tear but even Olysets can develop holes after seven years, and the comparatively large holes that had developed probably contributed to the high rate of blood feeding. Regular maintenance and repair of holes would help restore protection against mosquito biting, making the nets better tools for personal protection. Extrapolating from the mortality results, it is predicted that were Olysets to be used by the majority of households in the community the overall impact on mosquito population density and longevity should be sufficient to achieve considerable reduction in malaria transmission even after seven years of use. To prevent biting of users, programmes may find it necessary to replace Olyset nets after about 7y. Further studies of the persistence of effectiveness under village conditions are urgently needed.

Conclusion

After seven years of regular use, the LLIN Olyset remained highly insecticidal to mosquitoes that came into contact with it under field conditions. Personal protection, as measured by a reduction in blood-feeding rate relative to that of untreated nets, was evident in laboratory tunnel tests but not under field conditions. Personal protection would require all holes to be mended and for occupants to not touch the sides of the netting while sleeping. Further studies on the persistence of effects of LLINs under village conditions are urgently needed.

Abbreviations

LLIN Long-lasting insecticidal net,

WHO World Health Organization,

ITN Insecticide-treated net,

WHOPES World Health Organization Pesticide Evaluation Scheme,

LSHTM London School of Hygiene & Tropical Medicine,

NIMR National Institute of Medical Research,

KCMC Kilimanjaro Christian Medical Centre.

Authors' contributions

RCM supervised the project, carried out the analysis and drafted the manuscript.

SMM managed the project and entomological teams, participated in the design of the study and contributed to drafting the manuscript.

PTT, VM, FSM and WS carried out trial, processed the data and helped to analyse the data.

FWM and CFC contributed to the study design and critically reviewed the manuscript.

CM contributed to the study design and supervision of research, and critically reviewed the manuscript.

MR contributed to study design and data analysis and revised the manuscript.

All authors read and approved the final manuscript.

Acknowledgements

We are grateful to Dr A. Tami for providing the Olyset nets which had been in domestic use for seven years. The construction of experimental huts and the trials of Olyset were supported by the Gates Malaria Partnership.

References

  • WHO A WHO Position Statement. Geneva, WHO; 2007. Global Malaria Programme – Insecticide Treated Mosquito Nets.http://www.who.int/malaria/docs/itn/ITNspospaperfinal.pdf
  • Wise J. Drive to produce more long-lasting insecticidal mosquito nets for malaria. Bull World Health Organ. 2004;82:884–886. [PubMed]
  • Teklehaimanot A, Sachs JD, Curtis C. Malaria control needs mass distribution of insecticidal bednets. Lancet. 2007;369:2143–2146. doi: 10.1016/S0140-6736(07)60951-9. [PubMed] [Cross Ref]
  • N'Guessan R, Darriet F, Doannio JMC, Chandre F, Carnevale P. Olyset ® Net efficacy against pyrethroid-resistant Anopheles gambiae and Culex quinquefasciatus after 3 years' field use in Cote d'Ivoire. Med Vet Entomol. 2001;15:97–104. doi: 10.1046/j.1365-2915.2001.00284.x. [PubMed] [Cross Ref]
  • Gonzales JO, Kroeger A, Avina AI, Pabin E. Wash resistance of insecticide treated materials. Trans R Soc Trop Med Hyg. 2002;96:370–375. doi: 10.1016/S0035-9203(02)90363-9. [PubMed] [Cross Ref]
  • Graham K, Kayedi MH, Maxwell C, Kaur H, Rehman H, Malima R, Curtis CF, Lines JD, Rowland MW. Multi-country field trials comparing wash-resistance of PermaNet and conventional insecticide-treated nets against anopheline and culicine mosquitoes. Med Vet Entomol. 2005;19:72–83. doi: 10.1111/j.0269-283X.2005.00543.x. [PubMed] [Cross Ref]
  • Tami A, Mubyazi G, Talbert A, Mshinda H, Duchon S, Lengeler C. Evaluation of Olyset TM insecticide-treated nets distributed seven years previously in Tanzania. Malar J. 2004;3:19. doi: 10.1186/1475-2875-3-19. [PMC free article] [PubMed] [Cross Ref]
  • Lindblade KA, Dotson E, Hawley WA, Bayoh N, Williamson J, Mount D, Olang G, Vulule J, Slutsker L, Gimnig J. Evaluation of long-lasting insecticidal nets after 2 years of household use. Trop Med Int Health. 2005;10:1141–1150. doi: 10.1111/j.1365-3156.2005.01501.x. [PubMed] [Cross Ref]
  • WHO Report of the Tenth WHOPES Working Group Meeting WHO/HG, Geneva 11–14 December 2006. Review of: Spinosad 0.5% GR & 12% SC, Lambda-cyhalothrin 10% CS, K-O Tab 1-2-3, Interceptor. WHO/CDS/NTD/WHOPES/20071.
  • Lines JD, Myamba J, Curtis CF. Experimental hut trials of permethrin-impregnated mosquito nets and eave curtains against malaria vectors in Tanzania. Med Vet Entomol. 1987;1:37–51. [PubMed]
  • Smith A. A verandah-trap for studying the house-frequenting habits of mosquitoes and for assessing insecticides. I. A description of the verandah-trap hut and of studies on the egress of An. gambiae Giles and Mansonia uniformis Theo. from an untreated hut. Bull Ent Res. 1965;56:161–167. [PubMed]
  • Smith A, Webley DJ. A Verandah-trap hut for studying the house-frequenting habits of mosquitoes and for assessing insecticides. II. The effect of DDT on behaviour and mortality. Bull Ent Res. 1969;59:3–46. [PubMed]
  • Curtis CF, Myamba J, Wilkes TK. Comparison of different insecticides and fabrics for anti-mosquito, bednets and curtains. Med Vet Entomol. 1996;10:1–11. [PubMed]
  • Mboera LEG, Magesa SM. The rise and fall in malaria sporozoite rates in Anopheles gambiae and Anopheles funestus in north-east Tanzania from 1934 to 1999. Annals Trop Med Parasit. 2001;95:325–330. doi: 10.1080/00034980120055526. [PubMed] [Cross Ref]
  • Njunwa KJ, Kilimali VAEB, Marero SM, Msuya FHM, Pilyimo R, Kamuzora D. Permethrin incorporated bednets, 'Olyset net', reduce malaria transmission after twelve months of their use in three villages of Kibaha District, Coast Region, Tanzania. Report from Sumitomo Chemical Co Ltd Japan Dar es Salaam, Tanzania. 1996.
  • Chuih A. Malaria control activities in Mvumi – Dodoma Rural from 1994 to July 1996. District Medical Health Report, Dodoma rural District Dodoma, Tanzania. 1996.
  • WHO Report of the WHO Informal consultation Document WHO/CDS/CPC/MAL/9812. Geneva, WHO; Tests Procedures for Insecticide Resistance Monitoring in Malaria Vectors, Bio-Efficacy and persistence of Insecticides on Treated surfaces.
  • WHO WHO/CDS/NTD/WHOPES/GCDPP/20063. Geneva, WHO; Guidelines for testing mosquito adulticides for indoor residual spraying and treatment of mosquito nets.
  • Corbel V, Chandre F, Brengues C, Akogbeto M, Lardeux F, Hougard JM, Guillet P. Dosage-dependent effects of permethrin-treated nets on the behaviour of Anopheles gambiae and the selection of pyrethroid resistance. Malar J. 2004;3:22. doi: 10.1186/1475-2875-3-22. [PMC free article] [PubMed] [Cross Ref]
  • Hougard JM, Duchon S, Darriet F, Zaim M, Rogier C, Guillet P. Comparative performances, under laboratory conditions, of seven pyrethroid insecticides used for impregnation of mosquito nets. Bull World Health Organ. 2003;5:324–333. [PubMed]
  • Maxwell CA, Myamba J, Magoma J, Rwegoshora RT, Magesa SM, Curtis CF. Tests of Olyset ® nets by bioassay and in experimental huts. J Vect Borne Dis. 2006;43:1–6. [PubMed]
  • Khayrandish A, Wood RJ. A multiple basis for insecticide resistance in a strain of Culex quinquefasciatus from Muheza, studied as resistance declined. Bull Ent Res. 1993;83:75–86.

Articles from Malaria Journal are provided here courtesy of BioMed Central