Evidence map›Paper›PMID 27774283›Full record

ArticleVirus evolution2015

Elucidating the phylodynamics of endemic rabies virus in eastern Africa using whole-genome sequencing.

Kirstyn Brunker, Denise A Marston, Daniel L Horton, Sarah Cleaveland, Anthony R Fooks, Rudovick Kazwala, Chanasa Ngeleja, Tiziana Lembo, Maganga Sambo, Zacharia J Mtema and 4 more

Open access · goldAbstract read
In one paragraph

Article in Virus evolution, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

44 citing papers in PubMed, 68 citations in OpenAlex.

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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

14 authors at 7 institutions in 2 countries.

Kirstyn BrunkerInstitute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow G12 8QQ, UK; The Boyd Orr Centre for Population and Ecosystem Health, University of Glasgow, Glasgow G12 8QQ, UK; Animal and Plant Health Agency, Weybridge, Woodham Lane, KT15 3NB, UK.
Denise A MarstonAnimal and Plant Health Agency, Weybridge, Woodham Lane, KT15 3NB, UK.
Daniel L HortonAnimal and Plant Health Agency, Weybridge, Woodham Lane, KT15 3NB, UK; School of Veterinary Medicine, University of Surrey, Guildford GU2 7XH, UK.
Sarah CleavelandInstitute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow G12 8QQ, UK; The Boyd Orr Centre for Population and Ecosystem Health, University of Glasgow, Glasgow G12 8QQ, UK.
Anthony R FooksAnimal and Plant Health Agency, Weybridge, Woodham Lane, KT15 3NB, UK.
Rudovick KazwalaDepartment of Veterinary Medicine and Public Health, Sokoine University of Agriculture, Morogoro, United Republic of Tanzania.
Chanasa NgelejaTanzania Veterinary Laboratory Agency, Dar es Salaam, United Republic of Tanzania, Temeke Veterinary, Mandela Road, P.O. BOX 9254.
Tiziana LemboInstitute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow G12 8QQ, UK; The Boyd Orr Centre for Population and Ecosystem Health, University of Glasgow, Glasgow G12 8QQ, UK.
Maganga SamboIfakara Health Institute, Ifakara, United Republic of Tanzania, P.O. Box 53.
Zacharia J MtemaIfakara Health Institute, Ifakara, United Republic of Tanzania, P.O. Box 53.
Lwitiko SikanaIfakara Health Institute, Ifakara, United Republic of Tanzania, P.O. Box 53.
Gavin WilkieMRC Centre for Virus Research, University of Glasgow, Sir Michael Stoker Building, Garscube Campus, 464 Bearsden Road, Glasgow G61 1QH, UK.
Roman BiekInstitute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow G12 8QQ, UK; The Boyd Orr Centre for Population and Ecosystem Health, University of Glasgow, Glasgow G12 8QQ, UK.
Katie HampsonInstitute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow G12 8QQ, UK; The Boyd Orr Centre for Population and Ecosystem Health, University of Glasgow, Glasgow G12 8QQ, UK.
Glasgow Centre for Population Health · GBIfakara Health Institute · TZAnimal and Plant Health Agency · GBUniversity of Glasgow · GBMRC University of Glasgow Centre for Virus Research · GBSokoine University of Agriculture · TZUniversity of Surrey · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Many of the pathogens perceived to pose the greatest risk to humans are viral zoonoses, responsible for a range of emerging and endemic infectious diseases. Phylogeography is a useful tool to understand the processes that give rise to spatial patterns and drive dynamics in virus populations. Increasingly, whole-genome information is being used to uncover these patterns, but the limits of phylogenetic resolution that can be achieved with this are unclear. Here, whole-genome variation was used to uncover fine-scale population structure in endemic canine rabies virus circulating in Tanzania. This is the first whole-genome population study of rabies virus and the first comprehensive phylogenetic analysis of rabies virus in East Africa, providing important insights into rabies transmission in an endemic system. In addition, sub-continental scale patterns of population structure were identified using partial gene data and used to determine population structure at larger spatial scales in Africa. While rabies virus has a defined spatial structure at large scales, increasingly frequent levels of admixture were observed at regional and local levels. Discrete phylogeographic analysis revealed long-distance dispersal within Tanzania, which could be attributed to human-mediated movement, and we found evidence of multiple persistent, co-circulating lineages at a very local scale in a single district, despite on-going mass dog vaccination campaigns. This may reflect the wider endemic circulation of these lineages over several decades alongside increased admixture due to human-mediated introductions. These data indicate that successful rabies control in Tanzania could be established at a national level, since most dispersal appears to be restricted within the confines of country borders but some coordination with neighbouring countries may be required to limit transboundary movements. Evidence of complex patterns of rabies circulation within Tanzania necessitates the use of whole-genome sequencing to delineate finer scale population structure that can that can guide interventions, such as the spatial scale and design of dog vaccination campaigns and dog movement controls to achieve and maintain freedom from disease.

Indexed as

endemicphylodynamicsrabiesRNA virustranslocationzoonoses

Identifiers

PMID27774283
PMCPMC5014479
OpenAlexW2179689535

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.