Evidence map›Paper›PMID 26408175›Full record

ArticleVeterinary research2015

Assessment of population genetic structure in the arbovirus vector midge, Culicoides brevitarsis (Diptera: Ceratopogonidae), using multi-locus DNA microsatellites.

Maria G Onyango, Nigel W Beebe, David Gopurenko, Glenn Bellis, Adrian Nicholas, Moses Ogugo, Appolinaire Djikeng, Steve Kemp, Peter J Walker, Jean-Bernard Duchemin

Abstract read
In one paragraph

Article in Veterinary research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

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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

10 authors.

Maria G OnyangoCSIRO Health & Biosecurity Australian Animal Health Laboratory, 5 Portalington Road, Geelong, Victoria, 3220, Australia. Maria.Onyango@csiro.au.
Nigel W BeebeSchool of Biological Sciences, The University of Queensland, St Lucia, Queensland, 4072, Australia. Nigel.Beebe@csiro.au.
David GopurenkoNSW Department of Primary Industries, Wagga Wagga Agricultural Institute, PMB, Wagga Wagga, New South Wales, 2650, Australia. david.gopurenko@dpi.nsw.gov.au.
Glenn BellisNorthern Australia Quarantine Strategy, 1 Pederson Road, Marrara, Northern Territory, 0812, Australia. glenn.bellis@agriculture.gov.au.
Adrian NicholasGraham Centre for Agricultural Innovation, Locked Bag 588, Wagga Wagga, New South Wales, 2678, Australia. Adrian.nicholas@dpi.nsw.gov.au.
Moses OgugoInternational Livestock Research Institute, P.O. Box 30709, 00100, Nairobi, Kenya. M.ogugo@cgiar.org.
Appolinaire DjikengInternational Livestock Research Institute, P.O. Box 30709, 00100, Nairobi, Kenya. A.Djikeng@cgiar.org.
Steve KempInternational Livestock Research Institute, P.O. Box 30709, 00100, Nairobi, Kenya. s.kemp@cgiar.org.
Peter J WalkerCSIRO Health & Biosecurity Australian Animal Health Laboratory, 5 Portalington Road, Geelong, Victoria, 3220, Australia. Peter.Walker@csiro.au.
Jean-Bernard DucheminCSIRO Health & Biosecurity Australian Animal Health Laboratory, 5 Portalington Road, Geelong, Victoria, 3220, Australia. Jean-Bernard.Duchemin@csiro.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bluetongue virus (BTV) is a major pathogen of ruminants that is transmitted by biting midges (Culicoides spp.). Australian BTV serotypes have origins in Asia and are distributed across the continent into two distinct episystems, one in the north and another in the east. Culicoides brevitarsis is the major vector of BTV in Australia and is distributed across the entire geographic range of the virus. Here, we describe the isolation and use of DNA microsatellites and gauge their ability to determine population genetic connectivity of C. brevitarsis within Australia and with countries to the north. Eleven DNA microsatellite markers were isolated using a novel genomic enrichment method and identified as useful for genetic analyses of sampled populations in Australia, northern Papua New Guinea (PNG) and Timor-Leste. Significant (P < 0.05) population genetic subdivision was observed between all paired regions, though the highest levels of genetic sub-division involved pair-wise tests with PNG (PNG vs. Australia (FST = 0.120) and PNG vs. Timor-Leste (FST = 0.095)). Analysis of multi-locus allelic distributions using STRUCTURE identified a most probable two-cluster population model, which separated PNG specimens from a cluster containing specimens from Timor-Leste and Australia. The source of incursions of this species in Australia is more likely to be Timor-Leste than PNG. Future incursions of BTV positive C. brevitarsis into Australia may be genetically identified to their source populations using these microsatellite loci. The vector's panmictic genetic structure within Australia cannot explain the differential geographic distribution of BTV serotypes.

Indexed as

Genetic VariationMicrosatellite RepeatsAnimalsAustraliaBluetongue virusCeratopogonidaeDNAGenetics, PopulationInsect VectorsPapua New GuineaTimor-LesteDNA

Identifiers

PMID26408175
PMCPMC4582633

What OpenQuestion holds

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Registered trials

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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.