Evidence map›Paper›PMID 29110670›Full record

ArticleMalaria journal2017

Indoor and outdoor malaria vector surveillance in western Kenya: implications for better understanding of residual transmission.

Teshome Degefa, Delenasaw Yewhalaw, Guofa Zhou, Ming-Chieh Lee, Harrysone Atieli, Andrew K Githeko, Guiyun Yan

Abstract read
In one paragraph

Article in Malaria journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

97 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Teshome DegefaDepartment of Medical Laboratory Sciences, College of Health Sciences, Jimma University, Jimma, Ethiopia.ORCID 0000-0002-3518-2372
Delenasaw YewhalawDepartment of Medical Laboratory Sciences, College of Health Sciences, Jimma University, Jimma, Ethiopia.
Guofa ZhouProgram in Public Health, College of Health Sciences, University of California at Irvine, Irvine, CA, 92697, USA.
Ming-Chieh LeeProgram in Public Health, College of Health Sciences, University of California at Irvine, Irvine, CA, 92697, USA.
Harrysone AtieliCentre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Andrew K GithekoCentre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Guiyun YanProgram in Public Health, College of Health Sciences, University of California at Irvine, Irvine, CA, 92697, USA. guiyuny@uci.edu.

Funding

Vector Biology of Invasive Anopheles stephensi in Rural to Urban Landscapes in EthiopiaU19AI129326 · NIAID · UNIVERSITY OF CALIFORNIA-IRVINE · PI Delenasaw Yewhalaw · 2017 to 2026
$19.9M
Ecology of African Highland MalariaR01AI050243 · NIAID · UNIVERSITY OF CALIFORNIA-IRVINE · PI YAN, GUIYUN · 2001 to 2018
$8.8M
Research Training in Mosquito Genomics and Bioinformat*D43TW001505 · FIC · UNIVERSITY OF CALIFORNIA-IRVINE · PI Guiyun Yan · 2000 to 2026
$6.0M
FIC NIH HHS D43 TW001505NIAID NIH HHS R01 AI050243NIAID NIH HHS U19 AI129326
6 · The paper itself

Abstract

backgroundThe widespread use of indoor-based malaria vector control interventions has been shown to alter the behaviour of vectors in Africa. There is an increasing concern that such changes could sustain residual transmission. This study was conducted to assess vector species composition, feeding behaviour and their contribution to indoor and outdoor malaria transmission in western Kenya.

methodsAnopheles mosquito collections were carried out from September 2015 to April 2016 in Ahero and Iguhu sites, western Kenya using CDC light traps (indoor and outdoor), pyrethrum spray catches (PSCs) (indoor) and pit shelters (outdoor). Species within Anopheles gambiae s.l. and Anopheles funestus s.l. were identified using polymerase chain reaction (PCR). Enzyme-linked immunosorbent assay (ELISA) was used to determine mosquito blood meal sources and sporozoite infections.

resultsA total of 10,864 female Anopheles mosquitoes comprising An. gambiae s.l. (71.4%), An. funestus s.l. (12.3%), Anopheles coustani (9.2%) and Anopheles pharoensis (7.1%) were collected. The majority (61.8%) of the anopheline mosquitoes were collected outdoors. PCR result (n = 581) revealed that 98.9% An. arabiensis and 1.1% An. gambiae s.s. constituted An. gambiae s.l. in Ahero while this was 87% An. gambiae s.s. and 13% An. arabiensis in Iguhu. Of the 108 An. funestus s.l. analysed by PCR, 98.1% belonged to An. funestus s.s. and 1.9% to Anopheles leesoni. The human blood index (HBI) and bovine blood index (BBI) of An. arabiensis was 2.5 and 73.1%, respectively. Anopheles gambiae s.s. had HBI and BBI of 50 and 28%, respectively. The HBI and BBI of An. funestus was 60 and 22.3%, respectively. Forage ratio estimate revealed that An. arabiensis preferred to feed on cattle, An. gambiae s.s. showed preference for both human and cattle, while An. funestus preferred human over other hosts. In Ahero, the sporozoite rates for An. arabiensis and An. funestus were 0.16 and 1.8%, respectively, whereas in Iguhu, the sporozoite rates for An. gambiae s.s. and An. funestus were 2.3 and 2.4%, respectively. In Ahero, the estimated indoor and outdoor entomological inoculation rate (EIR) was 108.6 infective bites/person/year (79.0 from An. funestus and 29.6 from An. arabiensis) and 43.5 infective bites/person/year (27.9 from An. arabiensis and 15.6 from An. funestus), respectively. In Iguhu, the estimated indoor and outdoor EIR was 24.5 infective bites/person/year (18.8 from An. gambiae s.s. and 5.7 from An. funestus) and 5.5 infective bites/person/year (all from An. gambiae s.s.), respectively.

conclusionAnopheles gambiae s.s. showed an increasing tendency to feed on cattle. Anopheles arabiensis was highly zoophagic, whereas An. funestus showed anthropophagic behaviour. While the majority of malaria transmission occurred indoor, the magnitude of outdoor transmission was considerably high. Additional control tools that complement the existing interventions are required to control residual transmission.

Indexed as

EnvironmentEpidemiological MonitoringAnimalsAnophelesBiotaEnzyme-Linked Immunosorbent AssayFeeding BehaviorFemaleHumansKenyaMalariaMaleMosquito VectorsPolymerase Chain ReactionBehaviorKenyaMalaria vectorsResidual transmissionSurveillance

Identifiers

PMID29110670
PMCPMC5674686

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.