Evan Mathenge
University of Nairobi
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Malaria Journal | 2008
Ulrike Fillinger; Khadija Kannady; George William; Michael J Vanek; Stefan Dongus; Dickson Nyika; Yvonne Geissbühler; Prosper P Chaki; Nico J Govella; Evan Mathenge; Burton H. Singer; Hassan Mshinda; Steven W. Lindsay; Marcel Tanner; Deo Mtasiwa; Marcia C. Castro; Gerry F. Killeen
BackgroundAs the population of Africa rapidly urbanizes, large populations could be protected from malaria by controlling aquatic stages of mosquitoes if cost-effective and scalable implementation systems can be designed.MethodsA recently initiated Urban Malaria Control Programme in Dar es Salaam delegates responsibility for routine mosquito control and surveillance to modestly-paid community members, known as Community-Owned Resource Persons (CORPs). New vector surveillance, larviciding and management systems were designed and evaluated in 15 city wards to allow timely collection, interpretation and reaction to entomologic monitoring data using practical procedures that rely on minimal technology. After one year of baseline data collection, operational larviciding with Bacillus thuringiensis var. israelensis commenced in March 2006 in three selected wards.ResultsThe procedures and staff management systems described greatly improved standards of larval surveillance relative to that reported at the outset of this programme. In the first year of the programme, over 65,000 potential Anopheles habitats were surveyed by 90 CORPs on a weekly basis. Reaction times to vector surveillance at observations were one day, week and month at ward, municipal and city levels, respectively. One year of community-based larviciding reduced transmission by the primary malaria vector, Anopheles gambiae s.l., by 31% (95% C.I. = 21.6–37.6%; p = 0.04).ConclusionThis novel management, monitoring and evaluation system for implementing routine larviciding of malaria vectors in African cities has shown considerable potential for sustained, rapidly responsive, data-driven and affordable application. Nevertheless, the true programmatic value of larviciding in urban Africa can only be established through longer-term programmes which are stably financed and allow the operational teams and management infrastructures to mature by learning from experience.
BMC Infectious Diseases | 2006
Gerry F. Killeen; Japhet Kihonda; Edith Lyimo; Fred R Oketch; Maya E. Kotas; Evan Mathenge; Joanna Schellenberg; Christian Lengeler; Thomas Smith; Chris Drakeley
BackgroundAfrican malaria vectors bite predominantly indoors at night so sleeping under an Insecticide-Treated Net (ITN) can greatly reduce malaria risk. Behavioural adaptation by mosquitoes to increasing ITN coverage could allow vector mosquitoes to bite outside of peak sleeping hours and undermine efficacy of this key malaria prevention measure.MethodsHigh coverage with largely untreated nets has been achieved in the Kilombero Valley, southern Tanzania through social marketing programmes. Direct surveys of nightly biting activity by An. gambiae Giles were conducted in the area before (1997) and after (2004) implementation of ITN promotion. A novel analytical model was applied to estimate the effective protection provided by an ITN, based on published experimental hut trials combined with questionnaire surveys of human sleeping behaviour and recorded mosquito biting patterns.ResultsAn. gambiae was predominantly endophagic and nocturnal in both surveys: Approximately 90% and 80% of exposure occurred indoors and during peak sleeping hours, respectively. ITNs consistently conferred >70% protection against exposure to malaria transmission for users relative to non-users.ConclusionAs ITN coverage increases, behavioural adaptation by mosquitoes remains a future possibility. The approach described allows comparison of mosquito biting patterns and ITN efficacy at multiple study sites and times. Initial results indicate ITNs remain highly effective and should remain a top-priority intervention. Combined with recently developed transmission models, this approach allows rapid, informative and cost-effective preliminary comparison of diverse control strategies in terms of protection against exposure before more costly and intensive clinical trials.
Journal of Medical Entomology | 2001
Evan Mathenge; John E. Gimnig; Margarette S. Kolczak; Maurice Ombok; Lw Irungu; William A. Hawley
Abstract The impact of permethrin-treated bednets on the feeding and house entering/exiting behavior of malaria vectors was assessed in two studies in western Kenya. In one study, matched pairs of houses were allocated randomly to receive bednets or no bednets. Exiting mosquitoes were collected in Colombian curtains hung around half of each house; indoor resting mosquitoes were collected by pyrethrum spray catches. The number of Anopheles gambiae Giles and An. arabiensis Patton estimated to have entered the houses was unaffected by the presence of bednets; Anopheles funestus Giles was less likely to enter a house if bednets were present. Anopheles gambiae and An. funestus were less likely to obtain a blood meal and significantly more likely to exit houses when bednets were present. No difference was detected in An. arabiensis rates of blood feeding and exiting. In a second experiment, hourly night biting collections were done on 13 nights during the rainy season to assess whether village-wide use of permethrin-treated bednets caused a shift in the time of biting of malaria vectors. A statistically significant shift was detected in the biting times of An. gambiae s.l., although the observed differences were small. No change was observed in the hourly distribution of An. funestus biting. Our study demonstrated that, at least in the short-term, bednets reduced human-vector contact and blood feeding success but did not lead to changes in the biting times of the malaria vectors in western Kenya.
Malaria Journal | 2002
Bart G. J. Knols; Basilio N. Njiru; Evan Mathenge; Wolfgang R Mukabana; John C. Beier; Gerry F. Killeen
BackgroundThe development and implementation of innovative vector control strategies for malaria control in Africa requires in-depth ecological studies in contained semi-field environments. This particularly applies to the development and release of genetically-engineered vectors that are refractory to Plasmodium infection. Here we describe a modified greenhouse, designed to simulate a natural Anopheles gambiae Giles ecosystem, and the first successful trials to complete the life-cycle of this mosquito vector therein.MethodsWe constructed a local house, planted crops and created breeding sites to simulate the natural ecosystem of this vector in a screen-walled greenhouse, exposed to ambient climate conditions, in western Kenya. Using three different starting points for release (blood-fed females, virgin females and males, or eggs), we allowed subsequent stages of the life-cycle to proceed under close observation until one cycle was completed.ResultsCompletion of the life-cycle was observed in all three trials, indicating that the major life-history behaviours (mating, sugar feeding, oviposition and host seeking) occurred successfully.ConclusionThe system described can be used to study the behavioural ecology of laboratory-reared and wild mosquitoes, and lends itself to contained studies on the stability of transgenes, fitness effects and phenotypic characteristics of genetically-engineered disease vectors. The extension of this approach, to enable continuous maintenance of successive and overlapping insect generations, should be prioritised. Semi-field systems represent a promising means to significantly enhance our understanding of the behavioural and evolutionary ecology of African malaria vectors and our ability to develop and evaluate innovative control strategies. With regard to genetically-modified mosquitoes, development of such systems is an essential prerequisite to full field releases.
Malaria Journal | 2006
W Richard Mukabana; Khadija Kannady; G Michael Kiama; Jasper N Ijumba; Evan Mathenge; Ibrahim Kiche; Gamba Nkwengulila; Leonard E. G. Mboera; Deo Mtasiwa; Yoichi Yamagata; Ingeborg van Schayk; Bart G. J. Knols; Steven W. Lindsay; Marcia C. Castro; Hassan Mshinda; Marcel Tanner; Ulrike Fillinger; Gerry F. Killeen
BackgroundIntegrated vector management (IVM) for malaria control requires ecological skills that are very scarce and rarely applied in Africa today. Partnerships between communities and academic ecologists can address this capacity deficit, modernize the evidence base for such approaches and enable future scale up.MethodsCommunity-based IVM programmes were initiated in two contrasting settings. On Rusinga Island, Western Kenya, community outreach to a marginalized rural community was achieved by University of Nairobi through a community-based organization. In Dar es Salaam, Tanzania, Ilala Municipality established an IVM programme at grassroots level, which was subsequently upgraded and expanded into a pilot scale Urban Malaria Control Programme with support from national academic institutes.ResultsBoth programmes now access relevant expertise, funding and policy makers while the academic partners benefit from direct experience of community-based implementation and operational research opportunities. The communities now access up-to-date malaria-related knowledge and skills for translation into local action. Similarly, the academic partners have acquired better understanding of community needs and how to address them.ConclusionUntil sufficient evidence is provided, community-based IVM remains an operational research activity. Researchers can never directly support every community in Africa so community-based IVM strategies and tactics will need to be incorporated into undergraduate teaching programmes to generate sufficient numbers of practitioners for national scale programmes. Academic ecologists at African institutions are uniquely positioned to enable the application of practical environmental and entomological skills for malaria control by communities at grassroots level and should be supported to fulfil this neglected role.
Malaria Journal | 2007
Pamela Opiyo; W Richard Mukabana; Ibrahim Kiche; Evan Mathenge; Gerry F. Killeen; Ulrike Fillinger
BackgroundCapacity strengthening of rural communities, and the various actors that support them, is needed to enable them to lead their own malaria control programmes. Here the existing capacity of a rural community in western Kenya was evaluated in preparation for a larger intervention.MethodsFocus group discussions and semi-structured individual interviews were carried out in 1,451 households to determine (1) demographics of respondent and household; (2) socio-economic status of the household; (3) knowledge and beliefs about malaria (symptoms, prevention methods, mosquito life cycle); (4) typical practices used for malaria prevention; (5) the treatment-seeking behaviour and household expenditure for malaria treatment; and (6) the willingness to prepare and implement community-based vector control.ResultsMalaria was considered a major threat to life but relevant knowledge was a chimera of scientific knowledge and traditional beliefs, which combined with socio-economic circumstances, leads to ineffective malaria prevention. The actual malaria prevention behaviour practiced by community members differed significantly from methods known to the respondents. Beside bednet use, the major interventions implemented were bush clearing and various hygienic measures, even though these are ineffective for malaria prevention. Encouragingly, most respondents believed malaria could be controlled and were willing to contribute to a community-based malaria control program but felt they needed outside assistance.ConclusionCulturally sensitive but evidence-based education interventions, utilizing participatory tools, are urgently required which consider traditional beliefs and enable understanding of causal connections between mosquito ecology, parasite transmission and the diagnosis, treatment and prevention of disease. Community-based organizations and schools need to be equipped with knowledge through partnerships with national and international research and tertiary education institutions so that evidence-based research can be applied at the grassroots level.
Malaria Journal | 2005
Evan Mathenge; Gedion O Misiani; David O Oulo; Lw Irungu; Paul N. Ndegwa; Thomas Smith; Gerry F. Killeen; Bart G. J. Knols
BackgroundMosquitoes sampling is an important component in malaria control. However, most of the methods used have several shortcomings and hence there is a need to develop and calibrate new methods. The Mbita trap for capturing host-seeking mosquitoes was recently developed and successfully tested in Kenya. However, the Mbita trap is less effective at catching outdoor-biting Anopheles funestus and Anopheles arabiensis in Madagascar and, thus, there is need to further evaluate this trap in diverse epidemiological settings. This study reports a field evaluation of the Mbita trap in a rice irrigation scheme in KenyaMethodsThe mosquito sampling efficiency of the Mbita trap was compared to that of the CDC light trap and the human landing catch in western Kenya. Data was analysed by Bayesian regression of linear and non-linear models.ResultsThe Mbita trap caught about 17%, 60%, and 20% of the number of An. arabiensis, An. funestus, and culicine species caught in the human landing collections respectively. There was consistency in sampling proportionality between the Mbita trap and the human landing catch for both An. arabiensis and the culicine species. For An. funestus, the Mbita trap portrayed some density-dependent sampling efficiency that suggested lowered sampling efficiency of human landing catch at low densities. The CDC light trap caught about 60%, 120%, and 552% of the number of An. arabiensis, An. funestus, and culicine species caught in the human landing collections respectively. There was consistency in the sampling proportionality between the CDC light trap and the human landing catch for both An. arabiensis and An. funestus, whereas for the culicines, there was no simple relationship between the two methods.ConclusionsThe Mbita trap is less sensitive than either the human landing catch or the CDC light trap. However, for a given investment of time and money, it is likely to catch more mosquitoes over a longer (and hence more representative) period. This trap can therefore be recommended for use by community members for passive mosquito surveillance. Nonetheless, there is still a need to develop new sampling methods for some epidemiological settings. The human landing catch should be maintained as the standard reference method for use in calibrating new methods for sampling the human biting population of mosquitoes.
Medical and Veterinary Entomology | 2002
Evan Mathenge; Gf Killeen; D. O. Oulo; Lw Irungu; Paul N. Ndegwa; B. G. J. Knols
Abstract An exposure‐free bednet trap (the ‘Mbita trap’) for sampling of Afrotropical malaria vectors was developed during preliminary studies of mosquito behaviour around human‐occupied bednets. Its mosquito sampling efficiency was compared to the CDC miniature light‐trap and human landing catches under semi‐field conditions in a screen‐walled greenhouse using laboratory‐reared Anopheles gambiae Giles sensu stricto (Diptera: Culicidae). When compared in a competitive manner (side by side), the Mbita trap caught 4.1 ± 0.5 times as many mosquitoes as the CDC light‐trap, hung beside an occupied bednet (P < 0.0001) and 43.2 ± 10% the number caught by human landing catches (P < 0.0001). The ratio of Mbita trap catches to those of the CDC light trap increased with decreasing mosquito density. Mosquito density did not affect the ratio of Mbita trap to human‐landing catches. In a non‐competitive comparison (each method independent of the other), the Mbita trap caught 89.7 ± 10% the number of mosquitoes caught by human landing catches (P < 0.0001) and 1.2 ± 0.1 times more mosquitoes than the CDC light trap (P = 0.0008). Differences in Mbita trap performance relative to the human landing catch under non‐competitive vs. competitive conditions were explained by the rate at which each method captured mosquitoes. Such bednet traps do not expose people to potentially infectious mosquito bites and operate passively all night without the need for skilled personnel. This trap is specifically designed to catch host‐seeking mosquitoes only and may be an effective, sensitive, user‐friendly and economic alternative to existing methods for mosquito surveillance in Africa.
Malaria Journal | 2015
Immo Kleinschmidt; Abraham Mnzava; Hmooda Toto Kafy; Charles M. Mbogo; Adam Ismail Bashir; Jude D. Bigoga; Alioun Adechoubou; K. Raghavendra; Tessa Bellamy Knox; Elfatih M Malik; Zinga José Nkuni; Nabie Bayoh; Eric Ochomo; Etienne Fondjo; Celestin Kouambeng; Herman Parfait Awono-Ambene; Josiane Etang; Martin Akogbéto; Rajendra M Bhatt; Dipak Kumar Swain; Teresa Kinyari; Kiambo Njagi; Lawrence Muthami; Krishanthi Subramaniam; John S. Bradley; Philippa West; Achile Massougbodji; Mariam Okê-Sopoh; Aurore Hounto; Khalid A Elmardi
BackgroundProgress in reducing the malaria disease burden through the substantial scale up of insecticide-based vector control in recent years could be reversed by the widespread emergence of insecticide resistance. The impact of insecticide resistance on the protective effectiveness of insecticide-treated nets (ITN) and indoor residual spraying (IRS) is not known. A multi-country study was undertaken in Sudan, Kenya, India, Cameroon and Benin to quantify the potential loss of epidemiological effectiveness of ITNs and IRS due to decreased susceptibility of malaria vectors to insecticides. The design of the study is described in this paper.MethodsMalaria disease incidence rates by active case detection in cohorts of children, and indicators of insecticide resistance in local vectors were monitored in each of approximately 300 separate locations (clusters) with high coverage of malaria vector control over multiple malaria seasons. Phenotypic and genotypic resistance was assessed annually. In two countries, Sudan and India, clusters were randomly assigned to receive universal coverage of ITNs only, or universal coverage of ITNs combined with high coverage of IRS. Association between malaria incidence and insecticide resistance, and protective effectiveness of vector control methods and insecticide resistance were estimated, respectively.ResultsCohorts have been set up in all five countries, and phenotypic resistance data have been collected in all clusters. In Sudan, Kenya, Cameroon and Benin data collection is due to be completed in 2015. In India data collection will be completed in 2016.DiscussionThe paper discusses challenges faced in the design and execution of the study, the analysis plan, the strengths and weaknesses, and the possible alternatives to the chosen study design.
The Open Tropical Medicine Journal | 2008
Fredros O. Okumu; Maya E. Kotas; Japheth Kihonda; Evan Mathenge; Gerry F. Killeen; Sarah J Moore
To monitor malaria transmission, effective sampling methods for host seeking vectors are necessary. The suit- ability of these methods can be determined by field measurements of their trapping efficiencies. We compared the effi- ciencies of the Human Landing Catch (HLC), the Centers for Disease Control light trap (CDC-LT) placed next to occu- pied bednets and the Mbita trap for sampling Anopheles gambiae s.l and Anopheles funestus. The sampling methods were rotated through three houses, each with a human bait, for 8 cycles in a 3 x 3 Latin-square design. Relative to the HLC, the efficiency (and 95% c. i) of the CDC-LT for sampling An. gambiae s.l. was 0.331 (0.237 - 0.460) while that for Mbita trap was 0.031 (0.013 - 0.077). For An. funestus however, the sampling efficiencies were 0.818 (0.611 - 1.096) and 0.022 (0.003-0.165) respectively. We conclude that both the CDC-LT placed next to an occupied bednet and the Mbita trap are less efficient than HLC, the latter being evidently unsuitable for use in the Kilombero Valley.