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Rapid in-country sequencing of whole virus genomes to inform rabies elimination programmes [version 1; peer review: 2 approved]

Authors :
Kirstyn Brunker
Gurdeep Jaswant
S.M. Thumbi
Kennedy Lushasi
Ahmed Lugelo
Anna M. Czupryna
Fred Ade
Gati Wambura
Veronicah Chuchu
Rachel Steenson
Chanasa Ngeleja
Criselda Bautista
Daria L. Manalo
Ma. Ricci R. Gomez
Maria Yna Joyce V. Chu
Mary Elizabeth Miranda
Maya Kamat
Kristyna Rysava
Jason Espineda
Eva Angelica V. Silo
Ariane Mae Aringo
Rona P. Bernales
Florencio F. Adonay
Michael J. Tildesley
Denise A. Marston
Daisy L. Jennings
Anthony R. Fooks
Wenlong Zhu
Luke W. Meredith
Sarah C. Hill
Radoslaw Poplawski
Robert J. Gifford
Joshua B. Singer
Mathew Maturi
Athman Mwatondo
Roman Biek
Katie Hampson
Source :
Wellcome Open Research, Vol 5 (2020)
Publication Year :
2020
Publisher :
Wellcome, 2020.

Abstract

Genomic surveillance is an important aspect of contemporary disease management but has yet to be used routinely to monitor endemic disease transmission and control in low- and middle-income countries. Rabies is an almost invariably fatal viral disease that causes a large public health and economic burden in Asia and Africa, despite being entirely vaccine preventable. With policy efforts now directed towards achieving a global goal of zero dog-mediated human rabies deaths by 2030, establishing effective surveillance tools is critical. Genomic data can provide important and unique insights into rabies spread and persistence that can direct control efforts. However, capacity for genomic research in low- and middle-income countries is held back by limited laboratory infrastructure, cost, supply chains and other logistical challenges. Here we present and validate an end-to-end workflow to facilitate affordable whole genome sequencing for rabies surveillance utilising nanopore technology. We used this workflow in Kenya, Tanzania and the Philippines to generate rabies virus genomes in two to three days, reducing costs to approximately £60 per genome. This is over half the cost of metagenomic sequencing previously conducted for Tanzanian samples, which involved exporting samples to the UK and a three- to six-month lag time. Ongoing optimization of workflows are likely to reduce these costs further. We also present tools to support routine whole genome sequencing and interpretation for genomic surveillance. Moreover, combined with training workshops to empower scientists in-country, we show that local sequencing capacity can be readily established and sustainable, negating the common misperception that cutting-edge genomic research can only be conducted in high resource laboratories. More generally, we argue that the capacity to harness genomic data is a game-changer for endemic disease surveillance and should precipitate a new wave of researchers from low- and middle-income countries.

Subjects

Subjects :
Medicine
Science

Details

Language :
English
ISSN :
2398502X
Volume :
5
Database :
Directory of Open Access Journals
Journal :
Wellcome Open Research
Publication Type :
Academic Journal
Accession number :
edsdoj.2af14cb359c4b6b8ecac9f516e1e97a
Document Type :
article
Full Text :
https://doi.org/10.12688/wellcomeopenres.15518.1