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

被引:45
|
作者
Brunker, Kirstyn [1 ,2 ,3 ]
Marston, Denise A. [3 ]
Horton, Daniel L. [3 ,4 ]
Cleaveland, Sarah [1 ,2 ]
Fooks, Anthony R. [3 ]
Kazwala, Rudovick [5 ]
Ngeleja, Chanasa [6 ]
Lembo, Tiziana [1 ,2 ]
Sambo, Maganga [7 ]
Mtema, Zacharia J. [7 ]
Sikana, Lwitiko [7 ]
Wilkie, Gavin [8 ]
Biek, Roman [1 ,2 ]
Hampson, Katie [1 ,2 ]
机构
[1] Univ Glasgow, Inst Biodivers Anim Hlth & Comparat Med, Glasgow G12 8QQ, Lanark, Scotland
[2] Univ Glasgow, Boyd Orr Ctr Populat & Ecosystem Hlth, Glasgow G12 8QQ, Lanark, Scotland
[3] Anim & Plant Hlth Agcy, Weybridge KT15 3NB, Surrey, England
[4] Univ Surrey, Sch Vet Med, Guildford GU2 7XH, Surrey, England
[5] Sokoine Univ Agr, Dept Vet Med & Publ Hlth, Morogoro, Tanzania
[6] Tanzania Vet Lab Agcy, Dar Es Salaam, Tanzania
[7] Ifakara Hlth Inst, Ifakara, Tanzania
[8] Univ Glasgow, MRC Ctr Virus Res, Glasgow G61 1QH, Lanark, Scotland
基金
英国惠康基金; 英国医学研究理事会;
关键词
RNA virus; phylodynamics; zoonoses; endemic; rabies; translocation;
D O I
10.1093/ve/vev011
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 humanmediated 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.
引用
收藏
页数:11
相关论文
共 50 条
  • [31] Whole-genome re-sequencing
    Bentley, David R.
    CURRENT OPINION IN GENETICS & DEVELOPMENT, 2006, 16 (06) : 545 - 552
  • [32] Whole-Genome Sequencing in Healthy People
    Lindor, Noralane M.
    Thibodeau, Stephen N.
    Burke, Wylie
    MAYO CLINIC PROCEEDINGS, 2017, 92 (01) : 159 - 172
  • [33] Identification and Whole-Genome Sequencing of a Monkeypox Virus Strain Isolated in Israel
    Cohen-Gihon, Inbar
    Israeli, Ofir
    Shifman, Ohad
    Erez, Noam
    Melamed, Sharon
    Paran, Nir
    Beth-Din, Adi
    Zvi, Anat
    MICROBIOLOGY RESOURCE ANNOUNCEMENTS, 2020, 9 (10):
  • [34] Whole-Genome Sequencing in Primary Care
    Vassy, J. L.
    Christensen, K. D.
    Schonman, E. F.
    Blout, C. L.
    Robinson, J. O.
    Krier, J. B.
    Diamond, P. M.
    Lebo, M.
    Machini, K.
    Azzariti, D. R.
    Dukhovny, D.
    Bates, D. W.
    MacRae, C. A.
    Murray, M. F.
    Rehm, H. L.
    McGuire, A. L.
    Green, R. C.
    ANNALS OF INTERNAL MEDICINE, 2017, 167 (03) : I20 - I20
  • [35] Whole-genome sequencing for HCM screening
    Fernandez-Ruiz I.
    Nature Reviews Cardiology, 2018, 15 (10) : 582 - 582
  • [36] Whole-genome sequencing of the UK Biobank
    Halldorsson, Bjarni, V
    Stefansson, Kari
    NATURE, 2022,
  • [37] Whole-Genome Sequencing in Personalized Therapeutics
    Cordero, P.
    Ashley, E. A.
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2012, 91 (06) : 1001 - 1009
  • [38] Whole-genome sequencing diagnostics for newborns
    Louisa Flintoft
    Nature Reviews Genetics, 2012, 13 (11) : 758 - 758
  • [39] Whole-Genome Sequencing in Outbreak Analysis
    Gilchrist, Carol A.
    Turner, Stephen D.
    Riley, Margaret F.
    Petri, William A., Jr.
    Hewlett, Erik L.
    CLINICAL MICROBIOLOGY REVIEWS, 2015, 28 (03) : 541 - 563
  • [40] PennCNV in whole-genome sequencing data
    Lima, Leandro de Araujo
    Wang, Kai
    BMC BIOINFORMATICS, 2017, 18