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International Journal of Epidemiology | 2013

Consistently high estimates for the proportion of human exposure to malaria vector populations occurring indoors in rural Africa

Bernadette J. Huho; Olivier J. T. Briët; Aklilu Seyoum; Chadwick Sikaala; Nabie Bayoh; John E. Gimnig; Fredros O. Okumu; Diadier Diallo; Salim Abdulla; Thomas Smith; Gerry F. Killeen

Background Insecticide-treated nets (ITNs) and indoor residual spraying (IRS) are highly effective tools for controlling malaria transmission in Africa because the most important vectors, from the Anopheles gambiae complex and the A. funestus group, usually prefer biting humans indoors at night. Methods Matched surveys of mosquito and human behaviour from six rural sites in Burkina Faso, Tanzania, Zambia, and Kenya, with ITN use ranging from 0.2% to 82.5%, were used to calculate the proportion of human exposure to An. gambiae sensu lato and An. funestus s.l. that occurs indoors (πi), as an indicator of the upper limit of personal protection that indoor vector control measures can provide. This quantity was also estimated through use of a simplified binary analysis (πiB) so that the proportions of mosquitoes caught indoors (Pi), and between the first and last hours at which most people are indoors (Pfl) could also be calculated as underlying indicators of feeding by mosquitoes indoors or at night, respectively. Results The vast majority of human exposure to Anopheles bites occurred indoors (πiB = 0.79–1.00). Neither An. gambiae s.l. nor An. funestus s.l. strongly preferred feeding indoors (Pi = 0.40–0.63 and 0.22–0.69, respectively), but they overwhelmingly preferred feeding at times when most humans were indoors (Pfl = 0.78–1.00 and 0.86–1.00, respectively). Conclusions These quantitative summaries of behavioural interactions between humans and mosquitoes constitute a remarkably consistent benchmark with which future observations of vector behaviour can be compared. Longitudinal monitoring of these quantities is vital to evaluate the effectiveness of ITNs and IRS and the need for complementary measures that target vectors outdoors.


Parasites & Vectors | 2012

Human exposure to anopheline mosquitoes occurs primarily indoors, even for users of insecticide-treated nets in Luangwa Valley, south-east Zambia

Aklilu Seyoum; Chadwick Sikaala; Javan Chanda; Dingani Chinula; Alex J. Ntamatungiro; Moonga Hawela; John M Miller; Tanya L. Russell; Olivier J. T. Briët; Gerry F. Killeen

BackgroundCurrent front line malaria vector control methods such as indoor residual spraying (IRS) and long-lasting insecticidal nets (LLINs), rely upon the preference of many primary vectors to feed and/or rest inside human habitations where they can be targeted with domestically-applied insecticidal products. We studied the human biting behaviour of the malaria vector Anopheles funestus Giles and the potential malaria vector Anopheles quadriannulatus Theobald in Luangwa valley, south-east Zambia.MethodsMosquitoes were collected by human landing catch in blocks of houses with either combined use of deltamethrin-based IRS and LLINs or LLINs alone. Human behaviour data were collected to estimate how much exposure to mosquito bites indoors and outdoors occurred at various times of the night for LLIN users and non-users.ResultsAnopheles funestus and An. quadriannulatus did not show preference to bite either indoors or outdoors: the proportions [95% confidence interval] caught indoors were 0.586 [0.303, 0.821] and 0.624 [0.324, 0.852], respectively. However, the overwhelming majority of both species were caught at times when most people are indoors. The proportion of mosquitoes caught at a time when most people are indoors were 0.981 [0.881, 0.997] and 0.897 [0.731, 0.965], respectively, so the proportion of human exposure to both species occuring indoors was high for individuals lacking LLINs (An. funestus: 0.983 and An. quadriannulatus: 0.970, respectively). While LLIN users were better protected, more than half of their exposure was nevertheless estimated to occur indoors (An. funestus: 0.570 and An. quadriannulatus: 0.584).ConclusionsThe proportion of human exposure to both An. funestus and An. quadriannulatus occuring indoors was high in the area and hence both species might be responsive to further peri-domestic measures if these mosquitoes are susceptible to insecticidal products.


Parasites & Vectors | 2013

Eliminating malaria vectors

Gerry F. Killeen; Aklilu Seyoum; Chadwick Sikaala; Amri S Zomboko; John E. Gimnig; Nicodem J. Govella; Michael T. White

Malaria vectors which predominantly feed indoors upon humans have been locally eliminated from several settings with insecticide treated nets (ITNs), indoor residual spraying or larval source management. Recent dramatic declines of An. gambiae in east Africa with imperfect ITN coverage suggest mosquito populations can rapidly collapse when forced below realistically achievable, non-zero thresholds of density and supporting resource availability. Here we explain why insecticide-based mosquito elimination strategies are feasible, desirable and can be extended to a wider variety of species by expanding the vector control arsenal to cover a broader spectrum of the resources they need to survive. The greatest advantage of eliminating mosquitoes, rather than merely controlling them, is that this precludes local selection for behavioural or physiological resistance traits. The greatest challenges are therefore to achieve high biological coverage of targeted resources rapidly enough to prevent local emergence of resistance and to then continually exclude, monitor for and respond to re-invasion from external populations.


Parasites & Vectors | 2013

Evaluation of alternative mosquito sampling methods for malaria vectors in Lowland South - East Zambia

Chadwick Sikaala; Gerry F. Killeen; Javan Chanda; Dingani Chinula; John M Miller; Tanya L. Russell; Aklilu Seyoum

BackgroundSampling malaria vectors and measuring their biting density is of paramount importance for entomological surveys of malaria transmission. Human landing catch (HLC) has been traditionally regarded as a gold standard method for surveying human exposure to mosquito bites. However, due to the risk of human participant exposure to mosquito-borne parasites and viruses, a variety of alternative, exposure-free trapping methods were compared in lowland, south-east Zambia.MethodsCentres for Disease Control and Prevention miniature light trap (CDC-LT), Ifakara Tent Trap model C (ITT-C), resting boxes (RB) and window exit traps (WET) were all compared with HLC using a 3 × 3 Latin Squares design replicated in 4 blocks of 3 houses with long lasting insecticidal nets, half of which were also sprayed with a residual deltamethrin formulation, which was repeated for 10 rounds of 3 nights of rotation each during both the dry and wet seasons.ResultsThe mean catches of HLC indoor, HLC outdoor, CDC-LT, ITT-C, WET, RB indoor and RB outdoor, were 1.687, 1.004, 3.267, 0.088, 0.004, 0.000 and 0.008 for Anopheles quadriannulatus Theobald respectively, and 7.287, 6.784, 10.958, 5.875, 0.296, 0.158 and 0.458, for An. funestus Giles, respectively. Indoor CDC-LT was more efficient in sampling An. quadriannulatus and An. funestus than HLC indoor (Relative rate [95% Confidence Interval] = 1.873 [1.653, 2.122] and 1.532 [1.441, 1.628], respectively, P < 0.001 for both). ITT-C was the only other alternative which had comparable sensitivity (RR = 0.821 [0.765, 0.881], P < 0.001), relative to HLC indoor other than CDC-LT for sampling An. funestus.ConclusionsWhile the two most sensitive exposure-free techniques primarily capture host-seeking mosquitoes, both have substantial disadvantages for routine community-based surveillance applications: the CDC-LT requires regular recharging of batteries while the bulkiness of ITT-C makes it difficult to move between sampling locations. RB placed indoors or outdoors and WET had consistently poor sensitivity so it may be useful to evaluate additional alternative methods, such as pyrethrum spray catches and back packer aspirators, for catching resting mosquitoes.


Malaria Journal | 2013

The changing burden of malaria and association with vector control interventions in Zambia using district-level surveillance data, 2006-2011.

Mulakwa Kamuliwo; Emmanuel Chanda; Ubydul Haque; Mercy Mwanza-Ingwe; Chadwick Sikaala; Cecilia Katebe-Sakala; Victor Mukonka; Douglas E. Norris; David L. Smith; Gregory E. Glass; William J. Moss

BackgroundMalaria control was strengthened in Zambia over the past decade. The two primary interventions for vector control are indoor residual spraying (IRS) and long-lasting insecticide-treated nets (LLINs). Using passive malaria surveillance data collected from 2006 to 2011 through the Zambian District Health Information System, the associations between increased coverage with LLINs and IRS and the burden of malaria in Zambia were evaluated.MethodsNational passive malaria surveillance data from 2006 to 2011 were analysed. A district-level, random-effects model with Poisson regression was used to explore the association between malaria cases and coverage with LLINs and IRS. Malaria cases and LLINs and IRS coverage were mapped to visualize spatiotemporal variation in malaria for each year.ResultsFrom 2006–2011, 24.6 million LLINs were distributed and 6.4 million houses were sprayed with insecticide. Coverage with LLINs was not uniformly distributed over the study period and IRS was targeted to central and southern districts where malaria transmission was low. LLIN coverage was associated with a reduction in malaria cases, although an increase in the number of malaria cases was reported in some districts over the study period. A high burden of malaria persisted in north-eastern Zambia, whereas a reduction in the number of reported malaria cases was observed in western and southern Zambia.ConclusionEnhanced and targeted interventions in north-eastern Zambia where the burden of malaria remains high, as well as efforts to sustain low malaria transmission in the south-west, will be necessary for Zambia to achieve the national goal of being malaria free by 2030.


Scientific Reports | 2016

Unexpected diversity of Anopheles species in Eastern Zambia: implications for evaluating vector behavior and interventions using molecular tools

Neil F. Lobo; Brandyce St. Laurent; Chadwick Sikaala; Busiku Hamainza; Javan Chanda; Dingani Chinula; Sindhu M. Krishnankutty; Jonathan D. Mueller; Nicholas A. Deason; Quynh T. Hoang; Heather L. Boldt; Julie Thumloup; Jennifer Stevenson; Aklilu Seyoum; Frank H. Collins

The understanding of malaria vector species in association with their bionomic traits is vital for targeting malaria interventions and measuring effectiveness. Many entomological studies rely on morphological identification of mosquitoes, limiting recognition to visually distinct species/species groups. Anopheles species assignments based on ribosomal DNA ITS2 and mitochondrial DNA COI were compared to morphological identifications from Luangwa and Nyimba districts in Zambia. The comparison of morphological and molecular identifications determined that interpretations of species compositions, insecticide resistance assays, host preference studies, trap efficacy, and Plasmodium infections were incorrect when using morphological identification alone. Morphological identifications recognized eight Anopheles species while 18 distinct sequence groups or species were identified from molecular analyses. Of these 18, seven could not be identified through comparison to published sequences. Twelve of 18 molecularly identified species (including unidentifiable species and species not thought to be vectors) were found by PCR to carry Plasmodium sporozoites - compared to four of eight morphological species. Up to 15% of morphologically identified Anopheles funestus mosquitoes in insecticide resistance tests were found to be other species molecularly. The comprehension of primary and secondary malaria vectors and bionomic characteristics that impact malaria transmission and intervention effectiveness are fundamental in achieving malaria elimination.


Malaria Journal | 2014

Monitoring, characterization and control of chronic, symptomatic malaria infections in rural Zambia through monthly household visits by paid community health workers

Busiku Hamainza; Hawela Moonga; Chadwick Sikaala; Mulakwa Kamuliwo; Adam Bennett; Thomas P. Eisele; John M. Miller; Aklilu Seyoum; Gerry F. Killeen

BackgroundActive, population-wide mass screening and treatment (MSAT) for chronic Plasmodium falciparum carriage to eliminate infectious reservoirs of malaria transmission have proven difficult to apply on large national scales through trained clinicians from central health authorities.MethodologyFourteen population clusters of approximately 1,000 residents centred around health facilities (HF) in two rural Zambian districts were each provided with three modestly remunerated community health workers (CHWs) conducting active monthly household visits to screen and treat all consenting residents for malaria infection with rapid diagnostic tests (RDT). Both CHWs and HFs also conducted passive case detection among residents who self-reported for screening and treatment.ResultsDiagnostic positivity was higher among symptomatic patients self-reporting to CHWs (42.5%) and HFs (24%) than actively screened residents (20.3%), but spatial and temporal variations of diagnostic positivity were highly consistent across all three systems. However, most malaria infections (55.6%) were identified through active home visits by CHWs rather than self-reporting to CHWs or HFs. Most (62%) malaria infections detected actively by CHWs reported one or more symptoms of illness. Most reports of fever and vomiting, plus more than a quarter of history of fever, headache and diarrhoea, were attributable to malaria infection. The minority of residents who participated >12 times had lower rates of malaria infection and associated symptoms in later contacts but most residents were tested <4 times and high malaria diagnostic positivity (32%) in active surveys, as well as incidence (1.7 detected infections per person per year) persisted in the population. Per capita cost for active service delivery by CHWs was US


Malaria Journal | 2014

A cost-effective, community-based, mosquito-trapping scheme that captures spatial and temporal heterogeneities of malaria transmission in rural Zambia

Chadwick Sikaala; Dingani Chinula; Javan Chanda; Busiku Hamainza; Mulenga Mwenda; Isabel Mukali; Mulakwa Kamuliwo; Neil F. Lobo; Aklilu Seyoum; Gerry F. Killeen

5.14 but this would rise to US


Malaria Journal | 2015

Applications and limitations of centers for disease control and prevention miniature light traps for measuring biting densities of African malaria vector populations : a pooled-analysis of 13 comparisons with human landing catches

Olivier J. T. Briët; Bernadette J. Huho; John E. Gimnig; Nabie Bayoh; Aklilu Seyoum; Chadwick Sikaala; Nicodem J. Govella; Diadier Diallo; Salim Abdullah; Thomas Smith; Gerry F. Killeen

10.68 with full community compliance with monthly testing at current levels of transmission, and US


Malaria Journal | 2016

Targeting indoor residual spraying for malaria using epidemiological data: a case study of the Zambia experience

Jessie Pinchoff; David A. Larsen; Silvia Renn; Derek Pollard; Christen M. Fornadel; Mark Maire; Chadwick Sikaala; Chomba Sinyangwe; Benjamin Winters; Daniel J. Bridges; Anna M. Winters

6.25 if pre-elimination transmission levels and negligible treatment costs were achieved.ConclusionMonthly active home visits by CHWs equipped with RDTs were insufficient to eliminate the human infection reservoir in this typical African setting, despite reasonably high LLIN/IRS coverage. However, dramatic impact upon infection and morbidity burden might be attainable and cost-effective if community participation in regular testing could be improved and the substantial, but not necessarily prohibitive, costs are affordable to national programmes.

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Aklilu Seyoum

Liverpool School of Tropical Medicine

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Gerry F. Killeen

Liverpool School of Tropical Medicine

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Dingani Chinula

Liverpool School of Tropical Medicine

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Busiku Hamainza

Zambian Ministry of Health

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Mulakwa Kamuliwo

Zambian Ministry of Health

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John E. Gimnig

Centers for Disease Control and Prevention

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Fredros O. Okumu

University of the Witwatersrand

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Bernadette J. Huho

Swiss Tropical and Public Health Institute

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