Overcoming Data Bottlenecks in Genomic Pathogen Surveillance.
WGS
antimicrobial resistance
bioinformatics
metadata
whole genome sequencing
Journal
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213
Informations de publication
Date de publication:
01 12 2021
01 12 2021
Historique:
entrez:
1
12
2021
pubmed:
2
12
2021
medline:
16
3
2022
Statut:
ppublish
Résumé
Performing whole genome sequencing (WGS) for the surveillance of antimicrobial resistance offers the ability to determine not only the antimicrobials to which rates of resistance are increasing, but also the evolutionary mechanisms and transmission routes responsible for the increase at local, national, and global scales. To derive WGS-based outputs, a series of processes are required, beginning with sample and metadata collection, followed by nucleic acid extraction, library preparation, sequencing, and analysis. Throughout this pathway there are many data-related operations required (informatics) combined with more biologically focused procedures (bioinformatics). For a laboratory aiming to implement pathogen genomics, the informatics and bioinformatics activities can be a barrier to starting on the journey; for a laboratory that has already started, these activities may become overwhelming. Here we describe these data bottlenecks and how they have been addressed in laboratories in India, Colombia, Nigeria, and the Philippines, as part of the National Institute for Health Research Global Health Research Unit on Genomic Surveillance of Antimicrobial Resistance. The approaches taken include the use of reproducible data parsing pipelines and genome sequence analysis workflows, using technologies such as Data-flo, the Nextflow workflow manager, and containerization of software dependencies. By overcoming barriers to WGS implementation in countries where genome sampling for some species may be underrepresented, a body of evidence can be built to determine the concordance of antimicrobial sensitivity testing and genome-derived resistance, and novel high-risk clones and unknown mechanisms of resistance can be discovered.
Identifiants
pubmed: 34850839
pii: 6447014
doi: 10.1093/cid/ciab785
pmc: PMC8634317
doi:
Substances chimiques
Anti-Bacterial Agents
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
S267-S274Subventions
Organisme : Medical Research Council
ID : MR/L00464X/1
Pays : United Kingdom
Investigateurs
Harry Harste
(H)
Mihir Kekre
(M)
Dawn Muddyman
(D)
Ben Taylor
(B)
Nicole Wheeler
(N)
Sophia David
(S)
Alejandra Arevalo
(A)
Maria Fernanda Valencia
(M)
Erik C D Osma Castro
(ECD)
Geetha Nagaraj
(G)
Vandana Govindan
(V)
Akshata Prabhu
(A)
D Sravani
(D)
M R Shincy
(MR)
Steffimole Rose
(S)
Kundur N Ravishankar
(KN)
Anderson O Oaikhena
(AO)
Jolaade J Ajiboye
(JJ)
Erkison Ewomazino Odih
(E)
Marietta L Lagrada
(ML)
Polle Krystle V Macaranas
(PKV)
Agnettah M Olorosa
(AM)
Elmer M Herrera
(EM)
Ali Molloy
(A)
John Stelling
(J)
Carolin Vegvari
(C)
Informations de copyright
© The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America.
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