- Open Access
Monitoring mosquitoes in urban Dar es Salaam: Evaluation of resting boxes, window exit traps, CDC light traps, Ifakara tent traps and human landing catches
© Govella et al; licensee BioMed Central Ltd. 2011
- Received: 29 November 2010
- Accepted: 21 March 2011
- Published: 21 March 2011
Ifakara tent traps (ITT) are currently the only sufficiently sensitive, safe, affordable and practical method for routine monitoring host-seeking mosquito densities in Dar es Salaam. However, it is not clear whether ITT catches represent indoors or outdoors biting densities. ITT do not yield samples of resting, fed mosquitoes for blood meal analysis.
Outdoors mosquito sampling methods, namely human landing catch (HLC), ITT (Design B) and resting boxes (RB) were conducted in parallel with indoors sampling using HLC, Centers for Disease Control and Prevention miniature light traps (LT) and RB as well as window exit traps (WET) in urban Dar es Salaam, rotating them thirteen times through a 3 × 3 Latin Square experimental design replicated in four blocks of three houses. This study was conducted between 6th May and 2rd July 2008, during the main rainy season when mosquito biting densities reach their annual peak.
The mean sensitivities of indoor RB, outdoor RB, WET, LT, ITT (Design B) and HLC placed outdoor relative to HLC placed indoor were 0.01, 0.005, 0.036, 0.052, 0.374, and 1.294 for Anopheles gambiae sensu lato (96% An. gambiae s.s and 4% An. arabiensis), respectively, and 0.017, 0.053, 0.125, 0.423, 0.372 and 1.140 for Culex spp, respectively. The ITT (Design B) catches correlated slightly better to indoor HLC (r2 = 0.619, P < 0.001, r2 = 0.231, P = 0.001) than outdoor HLC (r2 = 0.423, P < 0.001, r2 = 0.228, P = 0.001) for An. gambiae s.l. and Culex spp respectively but the taxonomic composition of mosquitoes caught by ITT does not match those of the indoor HLC (χ2 = 607.408, degrees of freedom = 18, P < 0.001). The proportion of An. gambiae caught indoors was unaffected by the use of an LLIN in that house.
The RB, WET and LT are poor methods for surveillance of malaria vector densities in urban Dar es Salaam compared to ITT and HLC but there is still uncertainty over whether the ITT best reflects indoor or outdoor biting densities. The particular LLIN evaluated here failed to significantly reduce house entry by An. gambiae s.l. suggesting a negligible repellence effect.
- Lymphatic Filariasis
- Mass Drug Administration
- Light Trap
- Human Landing Catch
In urban Dar es Salaam, Tanzania the principal malaria vectors are species of An. gambiae complex and An. funestus. Culex spp, is also present in larger numbers , causing appreciable nuisance and is known to transmit Lymphatic Filariasis [2–6]. Human infection with Wuchereria bancrofti was generally thought to be increasing in urban African communities due to rapid urbanization coupled with inadequate sanitary facilities which provide ideal breeding habitats  for mosquitoes in the Culex pipiens complex (Culex pipiens L Culex quinquefasciatus,) , which is a major vector of lymphatic filariasis in South Asia, East Africa and Americas particularly in urban areas [3, 9–14]. Although recent global effort to eliminate the filarial infections through mass drug administration (MDA) has reversed this trend to some degree [15–17], it is becoming increasingly clear that elimination of filariasis transmission is unlikely to be achieved by MDA alone [5, 18] so vector control remains an option to be considered that will necessitate routine monitoring of vector densities.
In its initial stages, routine monitoring of adult mosquito densities by the Dar es Salaam Urban Malaria Control program (UMCP) was only possible with the laborious, uncomfortable, requiring intensive supervision and potentially hazardous human landing catch (HLC) for several years [1, 19]. The Dar es Salaam Urban Malaria Control program relies on weekly application of larvicides to all potential breeding habitats observed by community-based staff assigned to defined areas of approximately 0.6 km2[19–21]. In order to enable effective management of routine larvicide application activities, the adult mosquito surveillance system for this programme needs to report mosquito densities at correspondingly high spatial and temporal resolution. This prompted development and evaluation of a safe, sensitive, cheap, practical and affordable alternative to HLC that allows intensive and extensive monitoring of malaria vectors. A series of Ifakara Tent Trap (ITT) designs have been tried and the B design has proven efficacious  and effective  in terms of both number and species composition of mosquitoes caught. It is also cost-effective relative to other sampling methods in terms of cost per mosquito trapped . The B design exposed human subjects to mosquito bites while emptying the large trap chamber [22, 23], this model has since been modified to circumvent this problem, but the new design (C) was not available at the time of this study . The ITT appears to be the most promising method for routine surveillance of biting densities of host-seeking mosquitoes in this setting and may be useful in a variety of African settings.
While monitoring host-seeking mosquito densities are an essential part of understanding disease, samples of resting mosquitoes  are also required to enable assessment of host feeding patterns through blood meal analysis [26–28]. The proportion of blood meals that each vector species obtains from humans is a critical determinant of, not only transmission intensity, but also the efficacy of interventions targeted at humans or the houses they live in [29–35]. Sample of resting mosquitoes for blood meal analyses are therefore important for selecting appropriate control strategies, particularly as vector population composition may become dominated by zoophagic species once high coverage by insecticide-treated nets [36–38] or indoor residual spraying [39–41] is achieved. ITT and HLC both primarily sample host-seeking mosquitoes [22–24] so either resting collection techniques [42–44] or window exit traps (WET)  are required to effectively characterize the feeding behaviours of vector mosquitoes that are relevant to intervention efficacy and selection.
The WET has been found useful for monitoring malaria vector density trends in Southern Africa [45, 46], Equatorial Guinea  and for vectors of Japanese encephalitis  in Korea. However, their sensitivity is likely to be site-specific and strongly influenced by house design. Resting boxes were found to be highly selective in sampling specific mosquito species in coastal areas of the United States of America , but have also shown potential for monitoring Culex quinquefasciatus and Aedes aegypti in urban Brazil .
This article therefore presents an assessment of a number of mosquito trapping methods compared with HLC catches in Dar es Salaam, including the widely used Centers for Disease Control and Prevention miniature Light Trap (LT) and the WET design commonly used in programmatic contexts, in a rigorous formal comparison for the first time in this urban setting. We also assessed whether catches with the B design of the ITT best represent the indoor or outdoor fractions of mosquito populations because, although this device is placed outdoors, it does resemble a small house and requires the mosquito to enter it so it may selectively sample indoor-biting mosquitoes.
This study was conducted at Mchikichini and Jangwani wards situated along the edge of Msimbazi River Valley in urban Dar es Salaam, the largest and most economically important city in Tanzania. The city is located at the shores of Indian Ocean coast with humid and hot climatic condition . There are classically two rainy seasons: a main rainy season from March to June and a shorter, less intense rainy season from October to December .
Dar es Salaam is also the home of the UMCP, a community-based vector control programme which primarily implements locally-supervised larviciding applied on a weekly basis at the neighbourhood level with vertical oversight from the city council [1, 19–21, 23, 51–56]. An. gambiae sibling species can grow from egg to adult in one week or less [33, 57] so the adult mosquito surveillance system for this programme needs to be, not only affordable and practical , but also both spatially and temporally intensive to detect coverage gaps as they occur on such fine geographic scales as neighbourhoods, housing clusters and even individual plots [20, 21] on a weekly or even daily basis [19, 58]. The need for sensitive adult malaria mosquito surveillance in this setting is compounded by low levels of local malaria transmission and correspondingly sparse vector populations that mediate it.
Transmission of malaria in urban Dar es Salaam is generally low with an entomologic inoculation rate of about one or less infectious bite per person per year , corresponding to the approximate limit of detection of malaria transmission by most entomological surveillance systems . Members of the Anopheles gambiae complex (An. gambiae sensu stricto, An. arabiensis, An. merus) and An. funestus are the primary malaria vector in this setting, with An. gambiae s.s. and An. arabiensis being most important . While the nightly biting peak of An. gambiae s.s. in Dar es Salaam is consistent with that of classical reports , recent observations show that this vector species, together with An. arabiensis, tends to bite predominantly outdoors [1, 60].
Resting boxes (RB)
Resting boxes made of cardboard with one open end and black cotton cloth lined inside them , were each placed indoor in a room occupied by a person and outdoor in a shaded area. Mosquitoes caught were retrieved from the boxes using a hand-held aspirator from 8.00 am to 9.00 am on the morning following each sampling night.
Window exit trap (WET)
Centers for Disease Control and Prevention miniature light traps (LT)
CDC miniature light traps (model 512) with inflorescent bulbs were each hung inside a house near an occupied bed covered with either an untreated net or a long lasting insecticidal net (LLIN), with one block in each location assigned to the two types of nets to test for the effect of net treatment upon LT trap efficiency. The Permanet 2.0® brand of LLIN was used. The trap was hung approximately 150 cm from the floor surface and placed with the pan touching one side of the net at the end where the occupant's feet lay .
Ifakara tent trap (ITT Design B)
The B design of the ITT was placed approximately 5 m outside the house with a team member sleeping inside it and mosquitoes were collected in the morning as previously described [22, 23]. The C design of ITT  was not used because it had not been developed and evaluated at the time.
Human landing catch (HLC)
To conduct HLC, each adult male collector exposed his lower limbs and collected the mosquitoes when they landed on his legs with an aspirator [1, 27, 44, 62, 63]. HLC was conducted by a single catcher at each station for 45 minutes each hour, allowing 15 minutes break for rest. To obtain full hourly biting densities, the catches for each hour were therefore divided by 0.75 . Collections were conducted both indoors and outdoors in accordance with the experimental design described below.
Processing of Samples
All Anopheles mosquitoes caught were sorted and morphologically identified  with the aid of a stereomicroscope in the field. A total of 1180 An. gambiae s.l from all traps, were stored in tubes with desiccated silica for subsequent identification to sibling species level by polymerase chain reaction . All Culex were counted, categorized as male or female and discarded.
Sensitivity differences among trapping methods
Data analyses were computed using SPSS version 16.0 for Microsoft Windows (SPSS Inc., Chicago IL). Generalized estimating equations (GEE) were employed to assess the influence of trap type upon mosquito catches by treating house as subject variable with trap type-indoor/outdoor assignment combination and date as within-subject variables. Catches for female An. gambiae s.l. and Culex spp, were each treated as the dependent variable in separately fitted models. Normal distribution with a natural logarithm link function and exchangeable working correlation matrix were selected for these dependent variables. In the first place for fitting to the catches of An. gambiae s.l., all trap types were included in the model, but yielded inestimable parameter values for both indoor and outdoor resting boxes so these two methods were thereafter removed from the fitted dataset.
The distribution of mosquito taxa among sampling methods and correlation of the catches
Trap type may affect taxonomic composition of mosquito catches  so the influence of trapping method upon the distribution of mosquitoes was analyzed by χ2 test . Comparison of multiple pair-wise Pearson correlation tests using logarithmically transformed data (log10 (x+1) for An. gambiae s.l. and log10 (x) for Culex spp of female catches aggregated by date was used to test whether the catches by the ITT best represent the indoor or outdoor biting catches.
The effect of net type on the indoor versus outdoor distribution of mosquitoes
The only method which yielded sufficient numbers of An. gambiae s.l. and for which both indoor and matching outdoor catches in the same house and night were available was HLC. Comparing the effect of LLINs versus untreated nets upon catches was therefore only possible for this particular method. All mosquitoes caught with HLC in a given house and on a particular night were either caught indoors or outdoors, hence the distributions of An. gambiae s.l. with regards to net type was analyzed by binary logistic regression, treating indoor versus outdoor catches of An. gambiae s.l. as binary outcome.
Ethical clearance and protection of human participant
Ethical approval was obtained from Institutional review board of Ifakara Health Institute in Tanzania (IHI/IRB/No. A50) and Medical Research Coordination Committee of the National Institute of Medical Research in Tanzania (NIMR/HQ/R. 8c/Vol. ii/03) and the Ethics Committee of the Liverpool School of Tropical Medicine in the UK (09.60). Written informed consent describing the potential risks and benefits of the study was obtained from all study participants before commencing the study and re-confirmed on each experimental night. Volunteers were screened for malaria parasites by microscopy during recruitment and on a weekly basis throughout the experiment. Those who were found malaria positive were offered treatment free of charge with Artemether-Lumefantrane (Co-Artem®, Roche, Basel, Switzerland), the recommended first-line treatment for malaria in the United Republic of Tanzania. The untreated net versus LLIN blocks were assigned so that no individual participant who already had a net was provided with an untreated net to replace it: participants lacking a net were provided either an untreated net or an LLIN while individuals with an existing net, untreated or otherwise, were all provided with a free Perma Net® 2.0 LLIN.
Sensitivity of alternative traps relative to indoor human landing catch
Number of mosquitoes caught by different methods and crude estimates of sensitivity relative to indoor human landing catch
Anopheles gambiae s.l.
Resting boxes indoor
Resting boxes out
CDC light trap
Ifakara tent trap
Resting boxes indoor
Resting boxes outdoor
CDC light trap
Ifakara tent trap
Resting boxes indoor
Resting boxes outdoor
CDC light traps
Ifakara tent traps
Resting boxes indoor
Resting boxes outdoor
CDC light traps
Ifakara tent traps
Mosquito sampling sensitivity of alternative traps relative to the indoor human landing catch as determined using generalized estimating equations
Anopheles gambiae s.l.
Resting boxes indoor
Resting boxes outdoor
Window exit trap
0.01 [0.002, 0.034]
CDC light trap
0.02 [0.009, 0.032]
Ifakara tent trap
0.26 [0.208, 0.330]
1.07 [0.851, 1.356]
Resting boxes indoor
0.02 [0.010, 0.026]
Resting boxes outdoor
0.07 [0.020, 0.274]
Window exit trap
0.11 [0.077, 0.166]
CDC light trap
0.50 [0.280, 0.893]
Ifakara tent trap
0.34 [0.256, 0.461]
1.17 [1.077, 1.278]
Sibling species composition of An. gambiae sensu lato
Respectively, 96% (871) and 4% (41) of 912 (7, 10, 22, 94 and 779 Sub sample from RB, WET, LT and HLC respectively) successfully amplified specimens of An. gambiae s.l. were An. gambiae s.s. and An. arabiensis. This implies that the results presented here overwhelmingly reflect the response of An. gambiae s.s. to these traps.
Effect of sampling technique upon taxonomic composition of female mosquito and correlation of catches
Effect of long-lasting insecticidal nets upon mosquito sampling
The effect of treatment on proportion of An. gambiae s.l. sampled indoor and outdoor determined by logistic regression as described in the method sections.
An. gambiae s.l. caught indoor (%)
Long lasting net
1.13 [0.91, 1. 41]
Untreated bed net
Sustained control of pathogen- transmitting mosquitoes requires sensitive and representative surveillance. This study compares a wide range of trapping methods, and demonstrates very poor performance of the RB, WET and LT for sampling adult malaria mosquitoes. This implies that such tools are not appropriate for surveillance and monitoring the impact of mosquito control measures in this urban setting where the UMCP targets relatively sparse populations of Anopheles malaria vectors. These results also confirm the previous observational reports that the LT has very low sensitivity in this urban setting . This cannot be explained by the observation that An. gambiae is exophagic in this setting [1, 60] because the reference HLC method was also conducted indoors. While no particular explanation is obvious for such surprisingly poor performance by LT, we speculate that the light source from the LT, which is thought to play a vital role in attracting mosquitoes , may have competed poorly for the attention of Anopheles in this highly illuminated , urbanized environment.
Some reports have suggested that the RB baited with urine odour are useful  for surveillance of An. arabiensis, the most exophilic  sibling species of the An. gambiae s.l. complex [57, 74] in lower Moshi, Tanzania. However, this conclusion was neither supported by this study nor by a previous effectiveness evaluation in Dar es Salaam  which relied on unbaited RB. While these results are discouraging, it may be possible to improve the sensitivity of the approach by lining the boxes internally either with a sticky surface  or a collapsible collection bag to maximize the catch size, because we observed that mosquitoes which entered the RB often escaped, particularly during retrieval.
Likewise the weak performance by WET can be possibly partly explained by the architectural of the local houses. Most houses used in this study apart from having open eaves and lacking a ceiling, also had walls separating adjacent rooms which did not reach the roof. It was therefore likely that many mosquitoes which entered a room fixed with WET exited via other rooms without a WET. Nevertheless, without such ready exits, there is also limited opportunity for mosquitoes to enter houses in the first place so there may be a fundamental a limit to how efficacious such exit traps can be outside of experimental huts. Furthermore, variations in housing design are a normal feature of representative mosquito sampling so these disappointing results should be interpreted at face value until proven otherwise. It should also be noted that while this approach has been applied and advocated in a number of programmatic settings [45–47, 76], to our knowledge this is the first time the efficacy of this trapping method has been formally evaluated in comparison with HLC or other standard methods in typical residences rather than in experimental huts.
The correlation results obtained from this study indicated the catches from ITT relate better to those from the indoor rather than outdoor HLC but the taxonomic composition of female mosquitoes caught by ITT does not match those of the indoor HLC and re-analysis of data obtained from the previous study in rural setting , yield contradictory correlation results that although consistent with this study for Culex spp the reverse was observed for the An. gambiae s.l. population, consisting primarily of An. arabiensis, in that study. It therefore remains unclear whether densities measured by ITT best reflect indoor or outdoor catches.
Although, pyrethroid treated bed nets are commonly thought to reduce house entry by An. gambiae s.l. [77–80], the particular LLIN product evaluated in this study failed to significantly deter An. gambiae s.l. from entering local houses. This observation is consistent with experimental hut studies in other parts of Tanzania [64, 65]and Benin . We conclude that, in this urban Tanzanian setting, negligible protection against malaria transmission exposure can be expected for non-users sharing the same house. This observation implies also that the reliability of human landing catches in estimating indoor An. gambiae s.l. catches in this setting is not affected by the presence of this particular brand of LLINs.
We would like to appreciate the residents of Jangwani and Mchikichini, Dar es Salaam for their cooperation throughout the study. Special thanks go to all the mosquito catchers for their commitment to this work. We also thank Doctors Hilary Ranson and Louise Kelly-Hope for their constructive comments on this manuscript. Financial support was provided by the Ifakara Health Institute (Core Funding), the Wellcome Trust (Research Career Development Fellowship number 076806 awarded to GFK) and the Bill & Melinda Gates Foundation through the Malaria Transmission Consortium (Award number 45114), coordinated by Dr. Neil Lobo and Professor Frank Collins at Notre Dame University.
- Geissbühler Y, Chaki P, Emidi B, Govella NJ, Shirima R, Mayagaya V, Mtasiwa D, Mshinda H, Fillinger U, Lindsay SW, Kannady K, Caldas de Castro M, Tanner M, Killeen GF: Interdependence of domestic malaria prevention measures and mosquito-human interactions in urban Dar es Salaam, Tanzania. Malar J. 2007, 6: 126-PubMed CentralView ArticlePubMedGoogle Scholar
- Waynd S, Melrose WD, Durrheim DN, Carron J, Gyspong M: Understanding the community impact of lymphatic filariasis: a review of the sociocultural literature. Bull World Health Org. 2007, 85: 421-500.Google Scholar
- Pedersen EM, Kiama WL, Swai ABM, Kihamia CM, Rwiza H, Kisumku UM: Bancroftian filariasis on Pemba Island, Zanzibar, Tanzania: An update on status in urban and semi-urban communities. Trop Med Int Health. 1999, 4: 295-301. 10.1046/j.1365-3156.1999.00391.x.View ArticlePubMedGoogle Scholar
- Maxwell CA, Curtis CF, Haji H, Kisumku S, Thalib AI, Yahya SA: Control of Bancroftian filariasis by integrating therapy with vector control using polystyrene beads in wet pit latrine. Trans R Soc Trop Med Hyg. 1990, 84: 709-714. 10.1016/0035-9203(90)90158-B.View ArticlePubMedGoogle Scholar
- Bockarie MJ, Pedersen EM, White GB, Michael E: Role of vector control in the global program to eradicate lymphatic filariasis. Ann Rev Entomol. 2009, 54: 469-487. 10.1146/annurev.ento.54.110807.090626.View ArticleGoogle Scholar
- Hotez PJ, Kamath A: Neglected tropical diseases in sub-Saharan Africa: review of their prevalence, distribution and disease burden. PLoS Negl Trop Dis. 2009, 3: e412-10.1371/journal.pntd.0000412.PubMed CentralView ArticlePubMedGoogle Scholar
- Curtis CF, Feachem RG: Sanitation and Culex pipiens mosquitoes: a brief review. J Trop Med Hyg. 1981, 84: 17-25.PubMedGoogle Scholar
- Smith JL, Fonseca DM: Rapid assay for identification of members of the Culex (Culex) pipiens complex, their hybrids and other sibling species (Diptera: Culicidae). Am J Trop Med Hyg. 2004, 70: 339-345.PubMedGoogle Scholar
- Cantey PT, Rout J, Rao G, Williamson J, Fox LM: Increasing compliance with mass drug administration program for Lymphatic Filariasis in India through education and lymphedema management programs. PLoS Negl Trop Dis. 2010, 4: e728-10.1371/journal.pntd.0000728.PubMed CentralView ArticlePubMedGoogle Scholar
- Raghavan NGS: Epidemiology of filariasis in India. Bull World Health Org. 1957, 16: 553-579.PubMed CentralPubMedGoogle Scholar
- Nathan MB: Bancroftian filariasis in coastal North Trinidad, West Indies: intensity of transmission by Culex quinquefasciatus. Trans R Soc Trop Med Hyg. 1981, 75: 721-730. 10.1016/0035-9203(81)90163-2.View ArticlePubMedGoogle Scholar
- Janousek TE, Lowrie RC: Vector competency of Culex quinquefasciatus (Haitian strain) following infection with Wuchereria bancrofti. Trans R Soc Trop Med Hyg. 1989, 83: 679-680. 10.1016/0035-9203(89)90395-7.View ArticlePubMedGoogle Scholar
- Zhang S, Cheng F, Webber R: A successful control program for lymphatic filariasis in Hubei, China. Trans R Soc Trop Med Hyg. 1994, 88: 510-512. 10.1016/0035-9203(94)90140-6.View ArticlePubMedGoogle Scholar
- Service M, (ed): Medical entomology for students. 2004, Cambridge University Press, 285-ThirdGoogle Scholar
- Malecela MN, Mwingira U, Mwakitalu ME, Kabali C, Michael E, MacKenzie CD: The sharp end- experiences from the Tanzanian programme for the elimination of lymphatic filariasis: notes from the end of the road. Ann Trop Med Parasitol. 2009, 103: 53-57. 10.1179/000349809X12502035776676.View ArticleGoogle Scholar
- Malecela MN, Lazarus W, Mwingira U, Mwakitalu E, Makene C, Kabali C, MacKenzie C: Eliminating LF: A progress report from Tanzania. J Lymphoedema. 2009, 4: 10-12.Google Scholar
- MacKenzie CD, Lazarus WM, Mwakitalu ME, Mwingira U, Malecela MN: Lymphatic filariasis: patients and global elimination programme. Ann Trop Med Parasitol. 2009, 103: 41-51. 10.1179/000349809X12502035776630.View ArticleGoogle Scholar
- Simonsen PE, Pedersen EM, Rwegoshora RT, Malecela MN, Derua YA, Magesa SM: Lymphatic filariasis control in Tanzania: effect of repeated mass drug administration with Ivermectin and Albendazole on infection and transmission. PLoS Negl Trop Dis. 2010, 4: e696-10.1371/journal.pntd.0000696.PubMed CentralView ArticlePubMedGoogle Scholar
- Fillinger U, Kannady K, William G, Vanek MJ, Dongus S, Nyika D, Geissbuhler Y, Chaki PP, Govella NJ, Mathenge EM, Singer BH, Mshinda H, Lindsay SW, Tanner M, Mtasiwa D, Castro MC, Killeen GF: A tool box for operational mosquito larval control; preliminary results and early lessons from the Urban Malaria Control Programme in Dar es Salaam. Malar J. 2008, 7: 20-10.1186/1475-2875-7-20.PubMed CentralView ArticlePubMedGoogle Scholar
- Chaki PP, Govella NJ, Shoo B, Hemed A, Tanner M, Fillinger U, Killeen GF: Achieving high coverage of larval-stage mosquito surveillance: challenges for a community-based mosquito control programme in urban Dar es Salaam, Tanzania. Malar J. 2009, 8: 311-10.1186/1475-2875-8-311.PubMed CentralView ArticlePubMedGoogle Scholar
- Dongus S, Nyika D, Kannady K, Mtasiwa D, Mshinda H, Fillinger U, Drescher AW, Tanner M, Castro MC, Killeen GF: Participatory mapping of target areas to enable operational larval source management to suppress malaria vector mosquitoes in Dar es Salaam, Tanzania. Int J Health Geogr. 2007, 6 (1): 37-10.1186/1476-072X-6-37.PubMed CentralView ArticlePubMedGoogle Scholar
- Govella NJ, Chaki PP, Geissbühler Y, Kannady K, Okumu FO, Charlwood JD, Anderson RA, Killeen GF: A new tent trap for sampling exophagic and endophagic members of the Anopheles gambiae complex. Malar J. 2009, 8: 157-10.1186/1475-2875-8-157.PubMed CentralView ArticlePubMedGoogle Scholar
- Sikulu M, Govella NJ, Ogoma SB, Mpangile J, Kambi SH, Kannady K, Chaki PP, Mukabana WR, Killeen GF: Comparative evaluation of the Ifakara tent trap-B, standardized resting boxes and human landing catch for sampling malaria vectors and other mosquitoes in urban Dar es Salaam, Tanzania. Malar J. 2009, 8: 197-10.1186/1475-2875-8-197.PubMed CentralView ArticlePubMedGoogle Scholar
- Govella NJ, Moore J, Killeen GF: An exposure free tool for monitoring adult malaria mosquito populations. Am J Trop Med Hyg. 2010, 83 (3): 596-600. 10.4269/ajtmh.2010.09-0682.PubMed CentralView ArticlePubMedGoogle Scholar
- Pates H, Curtis C: Mosquito behavior and vector control. Ann Rev Entomol. 2005, 50: 53-70. 10.1146/annurev.ento.50.071803.130439.View ArticleGoogle Scholar
- Lefevre T, Gouagna LC, Dabire KR, Elguero E, Fontenille D, Renaud F, Costantini C, Thomas F: Beyond nature and nurture: phenotypic plasticity in blood-feeding behavior of Anopheles gambiae s.s. when humans are not readily accessible. Am J Trop Med Hyg. 2009, 81 (6): 1023-10.4269/ajtmh.2009.09-0124.View ArticlePubMedGoogle Scholar
- Service MW: A critical review of procedures for sampling populations of adult mosquitoes. Bull Entomol Res. 1977, 67: 343-382. 10.1017/S0007485300011184.View ArticleGoogle Scholar
- Lyimo IN, Ferguson HM: Ecological and evolutionary determinants of host species choice in mosquito vectors. Trends Parasitol. 2009, 25 (4): 189-196. 10.1016/j.pt.2009.01.005.View ArticlePubMedGoogle Scholar
- Killeen GF, Smith TA: Exploring the contributions of bed nets, cattle, insecticides and excitorepellency to malaria control: a deterministic model of mosquito host-seeking behaviour and mortality. Trans R Soc Trop Med Hyg. 2007, 101 (9): 867-880. 10.1016/j.trstmh.2007.04.022.PubMed CentralView ArticlePubMedGoogle Scholar
- Killeen GF, Smith TA, Ferguson HM, Mshinda H, Abdulla S, Lengeler C, Kachur SP: Preventing childhood malaria in Africa by protecting adults from mosquitoes with insecticide-treated nets. PLoS Med. 2007, 4: e229-10.1371/journal.pmed.0040229.PubMed CentralView ArticlePubMedGoogle Scholar
- Garrett-Jones C: The human blood index of malarial vectors in relationship to epidemiological assessment. Bull World Health Org. 1964, 30: 241-261.PubMed CentralPubMedGoogle Scholar
- Garrett-Jones C: Prognosis for interruption of malaria transmission through assessment of the mosquito's vectorial capacity. Nature. 1964, 204: 1173-1175. 10.1038/2041173a0.View ArticlePubMedGoogle Scholar
- Gillies MT, DeMeillon B: The Anophelinae of Africa south of the Sahara (Ethiopian zoogeographical region). 1968, Johannesburg: South African Institute for Medical ResearchGoogle Scholar
- MacDonald G: The epidemiology and control of malaria. 1957, London: Oxford University PressGoogle Scholar
- Bruce-Chwatt LJ, (ed): Diagnostic methods in malaria. 1985, London: William Heinemann Medical Books LtdGoogle Scholar
- Bayoh MN, Mathias DK, Odiere MR, Mutuku FM, Kamau L, Gimnig JE, Vulule JM, Hawley WA, Hamel MJ, Walker ED: Anopheles gambiae: historical population decline associated with reginal distribution of insecticide-treated bed nets in Western Nyanza Province, Kenya. Malar J. 2010, 9: 62-10.1186/1475-2875-9-62.PubMed CentralView ArticlePubMedGoogle Scholar
- Russell TL, Lwetoijera DW, Maliti D, Chipwaza B, kihonda J, Charlwood JD, Smith TA, Lengeler C, Mwanyangala MA, Nathan R, Knols BGJ, Takken W, Killeen GF: Impact of promoting longer-lasting insecticide treatment of bed nets upon malaria transmission in a rural Tanzanian setting with pre-existing high coverage of untreated nets. Malar J. 2010, 9: 187-10.1186/1475-2875-9-187.PubMed CentralView ArticlePubMedGoogle Scholar
- Lindblade KA, Gimnig JE, Kamau L, Hawley WA, Odhiambo F, Olang G, Terkuile FO, Vulule JM, Slutsker L: Impact of sustained use of insecticide-treated bednets on malaria vector species distribution and Culicine mosquitoes. J Med Entomol. 2006, 42: 428-432.View ArticleGoogle Scholar
- Gillies MT, Smith A: Effect of a residual house spraying campaign on species balance in Anopheles funestus group: The replacement of Anopheles funestus Giles with Anopheles rivulorum Leeson. Bull Entomol Res. 1960, 51: 248-252. 10.1017/S0007485300057953.View ArticleGoogle Scholar
- Gillies MT: A new species of the Anopheles funestus complex (Diptera: Culicidae) from East Africa. Proc Roy Ent Soc London (B). 1962, 31: 81-86.Google Scholar
- Gillies MT, Furlong M: An investigation into behaviour of Anopheles parensis Gillies at Malindi on coast of Kenya. Bull Entomol Res. 1964, 55: 1-16. 10.1017/S0007485300049221.View ArticleGoogle Scholar
- Kulkarni MA, Kweka E, Nyale E, Lyatuu E, Mosha FW, Chandramohan D, Rau ME, Drakeley C: Entomological evaluation of malaria vectors at different altitudes in Hai district, northeastern Tanzania. J Med Entomol. 2006, 43: 580-588. 10.1603/0022-2585(2006)43[580:EEOMVA]2.0.CO;2.View ArticlePubMedGoogle Scholar
- Anonymous: The 2002 population and housing census general report. 2003, Dar es Salaam, Tanzania: National Bureau of StatisticsGoogle Scholar
- Anonymous: Manual on practical entomology. Part 2. Methods and techniques. 1975, Geneva: World Health Organization No.13Google Scholar
- Mouatcho JC, Hargreaves K, Koekemoer LL, Brooke BD, Oliver SV, Hunt MC: Indoor collections of Anopheles funestus group (Diptera:Culicidae) in sprayed houses in northern KwaZulu-Natal, South Africa. Malar J. 2007, 6: 30-10.1186/1475-2875-6-30.PubMed CentralView ArticlePubMedGoogle Scholar
- Hargreaves K, Hunt RH, Brooke BD, Mthembu J, Weeto MM, Awolola TS, Coetzee M: Anopheles arabiensis and Anopheles quadriannulatus resistance to DDT in South Africa. Med Vet Entomol. 2003, 17: 417-422. 10.1111/j.1365-2915.2003.00460.x.View ArticlePubMedGoogle Scholar
- Sharp BL, Ridl FC, Govender D, Kuklinski J, Kleinschmidt I: Malaria vector control by indoor residual insecticide spraying on the tropical island of Bioko, Equatorial Guinea. Malar J. 2007, 6: 52-10.1186/1475-2875-6-52.PubMed CentralView ArticlePubMedGoogle Scholar
- Chen YK, Chow CY: Methods of sampling populations of the Japanese encephalitis vector mosquitoes in Korea (A preliminary report). Korean J Parasitol. 1969, 7: 25-28. 10.3347/kjp.19220.127.116.11.View ArticleGoogle Scholar
- Crans WJ: Resting boxes as mosquito surveillance tools. Proceeding of the eighty-second annual meeting of the New Jersey mosquito control association: 1989. 1989, New Jersey mosquito biology and control. Center for vector biology, 53-57.Google Scholar
- Barata EAM, Neto FC, Dibo MR, Macoris MLG, barbosa AA, Natal D, Barata JMS, Andriguetti MTM: Capture of culicids in urban areas: evaluation of the resting box method. Rev Saude Publica. 2007, 41: 1-7. 10.1590/S0034-89102007000300008.View ArticleGoogle Scholar
- Mukabana WR, Kannady K, Kiama GM, Ijumba JN, Mathenge EM, Kiche I, Nkwengulila G, Mboera L, Mtasiwa D, Yamagata Y, van Schayk I, Knols BG, Lindsay SW, Caldas de Castro M, Mshinda H, Tanner M, Fillinger U, Killeen GF: Ecologists can enable communities to implement malaria vector control in Africa. Malar J. 2006, 5: 9-10.1186/1475-2875-5-9.PubMed CentralView ArticlePubMedGoogle Scholar
- Geissbühler Y, Kannady K, Chaki PP, Emidi B, Govella NJ, Mayagaya V, Kiama M, Mtasiwa D, Mshinda H, Lindsay SW, Tanner M, Fillinger U, Castro MC, Killeen GF: Microbial larvicide application by a large-scale, community-based program reduces malaria infection prevalence in Urban Dar Es Salaam, Tanzania. PLoS One. 2009, 4: e5107-PubMed CentralView ArticlePubMedGoogle Scholar
- Sattler MA, Mtasiwa D, Kiama M, Premji Z, Tanner M, Killeen GF, Lengeler C: Habitat characterization and spatial distribution of Anopheles sp. mosquito larvae in Dar es Salaam (Tanzania) during an extended dry period. Malar J. 2005, 4: 4-10.1186/1475-2875-4-4.PubMed CentralView ArticlePubMedGoogle Scholar
- Dongus S, Nyika D, kannady K, Mtasiwa D, Mshinda H, Gosoniu L, Drescher AW, Fillinger U, Tanner M, Killeen GF, Castro MC: Urban agriculture and Anopheles habitats in Dar es Salaam, Tanzania. Geospatial Health. 2009, 3: 189-210.View ArticlePubMedGoogle Scholar
- Wang SJ, Lengeler C, Smith TA, Vounatsou P, Cisse G, Tanner M: Rapid urban malaria appraisal (RUMA) III: Epidemiology of urban malaria in the municipality of Yopougon (Abidjan). Malar J. 2006, 5: 28-10.1186/1475-2875-5-28.PubMed CentralView ArticlePubMedGoogle Scholar
- Castro MC, Tsuruta A, Kanamori S, Kannady K, Mkude S: Community-based environmental management for malaria control: evidence from a small-scale intervention in Dar es Salaam, Tanzania. Malar J. 2009, 8: 57-10.1186/1475-2875-8-57.PubMed CentralView ArticlePubMedGoogle Scholar
- Gillies MT, Coetzee M: A supplement to the Anophelinae of Africa South of the Sahara (Afrotropical region). 1987, Johannesburg: South African Medical Research InstituteGoogle Scholar
- Killeen GF, Tanner M, Mukabana WR, Kalongolela MS, Kannady K, Lindsay SW, Fillinger U, Castro MC: Habitat targeting for controlling aquatic stages of malaria vectors in Africa. Am J Trop Med Hyg. 2006, 74: 517-518.PubMedGoogle Scholar
- Beier JC, Killeen GF, Githure J: Entomologic inoculation rates and Plasmodium falciparum malaria prevalence in Africa. Am J Trop Med Hyg. 1999, 61: 109-113.PubMedGoogle Scholar
- Govella NJ, Okumu FO, Killeen GF: Insecticide-treated nets can reduce malaria transmission by mosquitoes which feed outdoors. Am J Trop Med Hyg. 2010, 82: 415-419. 10.4269/ajtmh.2010.09-0579.PubMed CentralView ArticlePubMedGoogle Scholar
- Mboera LEG, Kihonda J, Braks MA, knols BGJ, Braks MA, Knols BG: Influence of Centers for Disease Control light trap position, relative to a human-baited bed net, on catches of Anopheles gambiae and Culex quinquefasciatus in Tanzania. Am J Trop Med Hyg. 1998, 59: 595-596.PubMedGoogle Scholar
- Mboera LEG: Sampling techniques for adult Afrotropical malaria vectors and their reliability in the estimation of entomological inoculation rates. Tanzania Health Res Bull. 2005, 7: 117-124.Google Scholar
- Anonymous: Malaria entomology and vector control. Learner's Guide. 2002, Geneva: World Health Organisation, TrialGoogle Scholar
- Graham K, Kayedi MH, Maxwell C, Kaur H, Rehman H, Malima R, Curtis CF, Lines JD, Rowland MW: Multicountry field trials comparing wash-resistance of PermaNet and conventional insecticide-treated nets against anopheline and culicine mosquitoes. Med Vet Entomol. 2005, 19: 72-83. 10.1111/j.0269-283X.2005.00543.x.View ArticlePubMedGoogle Scholar
- Tungu P, Magesa SM, Maxwell CA, Malima R, Masue D, Sudi W, Myamba J, Pigeon O, Rowland M: Evaluation of PermeNet 3.0 a deltermethrin-PBO combination net against Anopheles gambiae and pyrethroid resistant Culex quinquefasciatus mosquitoes: an experimental hut trial in Tanzania. Malar J. 2010, 9: 21-10.1186/1475-2875-9-21.PubMed CentralView ArticlePubMedGoogle Scholar
- Fettene M, Balkew M, Gimblet C: Utilization, retention and bio-efficacy studies of PermaNet in selected villages in Buie and Fentalie districts of Ethiopia. Malar J. 2009, 8: 114-10.1186/1475-2875-8-114.PubMed CentralView ArticlePubMedGoogle Scholar
- Scott JA, Brogdon WG, Collins FH: Identification of single specimens of Anopheles gambiae complex by polymerase chain reaction. Am J Trop Med Hyg. 1993, 49: 520-529.PubMedGoogle Scholar
- Okumu FO, Madumla EP, John AN, Lwetoijera DW, Sumaye RD: Attracting, trapping and killing disease-transmitting mosquitoes using odor-baited stations-The Ifakara Odor-Baited Stations. Parasit &Vectors. 2010, 3: 12-View ArticleGoogle Scholar
- Kirkwood BR: Essentials of medical statistics. 1988, Oxford: Blackwell scientific publicationGoogle Scholar
- Costantini C, Sagnon NF, Sanogo E, Merzagora L, Colluzi M: Relationship to human biting collections and influence of light and bednets in CDC light-trap catches of West African malaria vectors. Bull Entomol Res. 1998, 88: 503-511. 10.1017/S000748530002602X.View ArticleGoogle Scholar
- Miller TA, Stryker R, Wilkinson RN, Esah S: Influence of moonlight and other environmental factors on the abundance of certain mosquito species in light-trap collections in Thailand. J Med Entomol. 1970, 17: 555-561.View ArticleGoogle Scholar
- Kweka EJ, Mwang'onde BJ, Kimaro E, Msangi S, Massenga CP, Mahande AM: A resting box for outdoor sampling of adult Anopheles arabiensis in rice irrigation schemes of lower Moshi, northern Tanzania. Malar J. 2009, 8: 82-10.1186/1475-2875-8-82.PubMed CentralView ArticlePubMedGoogle Scholar
- White GB: Anopheles gambiae complex and disease transmission in Africa. Trans R Soc Trop Med Hyg. 1974, 68: 279-301. 10.1016/0035-9203(74)90035-2.View ArticleGoogle Scholar
- Coetzee M, Craig M, le Sueur D: Distribution of African malaria mosquitoes belonging to the Anopheles gambiae complex. Parasitol Today. 2000, 16: 74-77. 10.1016/S0169-4758(99)01563-X.View ArticlePubMedGoogle Scholar
- Facchinelli L, Koenraadt CJM, Fanello C, Kijchalao U, Valerio L, Jones JW, Scott TW, Torre A: Evaluation of a sticky trap for collecting Aedes (stegomyia) adults in a dengue-endemic area in Thailand. Am J Trop Med Hyg. 2008, 78: 904-909.PubMedGoogle Scholar
- Ridl FC, Bass C, Torrez M, Govender D, Ramdeen V, Yellot L, Edu AE, Schwabe C, Mohloai P, Maharaj R, Kleinschmeidt I: A pre-intervention study of malaria vector abundance in Rio Muni, Equatorial Guinea: their role in malaria transmission and the incidence of insecticide resistance alleles. Malar J. 2008, 7: 194-10.1186/1475-2875-7-194.PubMed CentralView ArticlePubMedGoogle Scholar
- Miller JE, Lindsay SW, Armstrong JRM: Experimental hut trials of bednet impregnated with synthetic pyrethroid and organophosphate insecticides for mosquito control in The Gambia. Med Vet Entomol. 1991, 5: 465-476. 10.1111/j.1365-2915.1991.tb00575.x.View ArticlePubMedGoogle Scholar
- Lindsay SW, Adiamah JH, Miller JE, Armstrong JRM: Pyrethroid-treated bednet effects on mosquitoes of the Anopheles gambiae complex. Med Vet Entomol. 1991, 5: 477-483. 10.1111/j.1365-2915.1991.tb00576.x.View ArticlePubMedGoogle Scholar
- Lindsay SW, Adiamah JH, Armstrong JRM: The effect of permethrin-impregnated bed nets on house entry by mosquitoes in The Gambia. Bull Entomol Res. 1992, 82: 49-55. 10.1017/S0007485300051488.View ArticleGoogle Scholar
- N'Guessan R, Asidi A, Boko P, Odjo A, Akogbeto M, Pigeon O, Rowland M: An experimental hut evaluation of Permanet 3.0®, a deltamethrin-piperonyl butoxide combination net, against pyrethroid-resistant Anopheles gambiae and Culex quinquefasciatus mosquitoes in southern Benin. Trans R Soc Trop Med Hyg. 2010, 104: 758-765.View ArticlePubMedGoogle Scholar
- Corbel V, Chabi J, Dabire RD, Etang J, Nwane P, Pigeon O, Akogbeto M, Hougard J-M: Field efficacy of a new mosaic long-lasting mosquito net (PermaNet 3.0) against pyrethroid-resistant malaria vectors: A mult centre study in Western and Central Africa. Malar J. 2010, 9: 113-PubMed CentralView ArticlePubMedGoogle Scholar
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