Evidence map›Paper›PMID 27494934›Full record

ArticleParasites & vectors2016

Onchocerciasis transmission in Ghana: the human blood index of sibling species of the Simulium damnosum complex.

Poppy H L Lamberton, Robert A Cheke, Martin Walker, Peter Winskill, J Lee Crainey, Daniel A Boakye, Mike Y Osei-Atweneboana, Iñaki Tirados, Michael D Wilson, Anthony Tetteh-Kumah and 3 more

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 20 citations in OpenAlex.

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  7. Molecular Identification ofThe American journal of tropical medicine and hygiene · 2017
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 9 institutions in 5 countries.

Poppy H L LambertonLondon Centre for Neglected Tropical Disease Research, Department of Infectious Disease Epidemiology, School of Public Health, Faculty of Medicine (St Mary's campus), Imperial College London, Norfolk Place, London, W2 1PG, UK.
Robert A ChekeLondon Centre for Neglected Tropical Disease Research, Department of Infectious Disease Epidemiology, School of Public Health, Faculty of Medicine (St Mary's campus), Imperial College London, Norfolk Place, London, W2 1PG, UK.
Martin WalkerLondon Centre for Neglected Tropical Disease Research, Department of Infectious Disease Epidemiology, School of Public Health, Faculty of Medicine (St Mary's campus), Imperial College London, Norfolk Place, London, W2 1PG, UK.
Peter WinskillMRC Centre for Outbreak Analysis and Modelling. Department of Infectious Disease Epidemiology, School of Public Health, Faculty of Medicine (St Mary's campus), Imperial College London, Norfolk Place, London, W2 1PG, UK.
J Lee CraineyInstituto Leônidas e Maria Deane, Fundação Oswaldo Cruz, Rua Terezina 476, Adrianopolis, AM, 69057-070, Manaus, Brazil.
Daniel A BoakyeNoguchi Memorial Institute for Medical Research, University of Ghana, Legon, PO Box LG581, Accra, Ghana.
Mike Y Osei-AtweneboanaDepartment of Environmental Biology and Health, Water Research Institute, Council for Scientific and Industrial Research, PO Box M32, Accra, Ghana.
Iñaki TiradosDepartment of Vector Biology, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, L3 5QA, UK.
Michael D WilsonNoguchi Memorial Institute for Medical Research, University of Ghana, Legon, PO Box LG581, Accra, Ghana.
Anthony Tetteh-KumahGhana Health Service, P.O. Box MB-190, Accra, Ghana.
Sampson OtooNoguchi Memorial Institute for Medical Research, University of Ghana, Legon, PO Box LG581, Accra, Ghana.
Rory J PostSchool of Natural Sciences and Psychology, Liverpool John Moores University, Byrom Street, Liverpool, L3 3AH, UK.
María-Gloria BasañezLondon Centre for Neglected Tropical Disease Research, Department of Infectious Disease Epidemiology, School of Public Health, Faculty of Medicine (St Mary's campus), Imperial College London, Norfolk Place, London, W2 1PG, UK. m.basanez@imperial.ac.uk.
University of Ghana · GHImperial College London · GBLondon Centre for Neglected Tropical Disease Research · GBCouncil for Scientific and Industrial Research · GHFundação Oswaldo Cruz · BRGhana Health Service · GHLiverpool John Moores University · GBLiverpool School of Tropical Medicine · GBMedway School of Pharmacy · GB

Funding

Wellcome TrustWellcome Trust 085133/Z/08/ZWellcome Trust 092677/Z/10/ZWellcome Trust 105614/Z/14/Z
6 · The paper itself

Abstract

backgroundVector-biting behaviour is important for vector-borne disease (VBD) epidemiology. The proportion of blood meals taken on humans (the human blood index, HBI), is a component of the biting rate per vector on humans in VBD transmission models. Humans are the definitive host of Onchocerca volvulus, but the simuliid vectors feed on a range of animals and HBI is a key indicator of the potential for human onchocerciasis transmission. Ghana has a diversity of Simulium damnosum complex members, which are likely to vary in their HBIs, an important consideration for parameterization of onchocerciasis control and elimination models.

methodsHost-seeking and ovipositing S. damnosum (sensu lato) (s.l.) were collected from seven villages in four Ghanaian regions. Taxa were morphologically and molecularly identified. Blood meals from individually stored blackfly abdomens were used for DNA profiling, to identify previous host choice. Household, domestic animal, wild mammal and bird surveys were performed to estimate the density and diversity of potential blood hosts of blackflies.

resultsA total of 11,107 abdomens of simuliid females (which would have obtained blood meal(s) previously) were tested, with blood meals successfully amplified in 3,772 (34 %). A single-host species was identified in 2,857 (75.7 %) of the blood meals, of which 2,162 (75.7 %) were human. Simulium soubrense Beffa form, S. squamosum C and S. sanctipauli Pra form were the most anthropophagic (HBI = 0.92, 0.86 and 0.70, respectively); S. squamosum E, S. yahense and S. damnosum (sensu stricto) (s.s.)/S. sirbanum were the most zoophagic (HBI = 0.44, 0.53 and 0.63, respectively). The degree of anthropophagy decreased (but not statistically significantly) with increasing ratio of non-human/human blood hosts. Vector to human ratios ranged from 139 to 1,198 blackflies/person.

conclusionsDNA profiling can successfully identify blood meals from host-seeking and ovipositing blackflies. Host choice varies according to sibling species, season and capture site/method. There was no evidence that HBI is vector and/or host density dependent. Transmission breakpoints will vary among locations due to differing cytospecies compositions and vector abundances.

Indexed as

AdolescentAdultAnimalsBloodChildChild, PreschoolFeeding BehaviorFemaleGhanaHumansInfantInsect VectorsMaleMiddle AgedOnchocerca volvulusOnchocerciasisHost choiceHost-seeking vectorsHuman blood indexOnchocerca volvulusOvipositing vectorsSimulium damnosum (sensu lato)Vector abundance

Identifiers

PMID27494934
PMCPMC4975878
OpenAlexW2479374960

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.