Tracking arboviruses, their transmission vectors and potential hosts by nanopore sequencing of mosquitoes.


Journal

Microbial genomics
ISSN: 2057-5858
Titre abrégé: Microb Genom
Pays: England
ID NLM: 101671820

Informations de publication

Date de publication:
Jan 2024
Historique:
medline: 22 1 2024
pubmed: 19 1 2024
entrez: 19 1 2024
Statut: ppublish

Résumé

The risk to human health from mosquito-borne viruses such as dengue, chikungunya and yellow fever is increasing due to increased human expansion, deforestation and climate change. To anticipate and predict the spread and transmission of mosquito-borne viruses, a better understanding of the transmission cycle in mosquito populations is needed. We present a pathogen-agnostic combined sequencing protocol for identifying vectors, viral pathogens and their hosts or reservoirs using portable Oxford Nanopore sequencing. Using mosquitoes collected in São Paulo, Brazil, we extracted RNA for virus identification and DNA for blood meal and mosquito identification. Mosquitoes and blood meals were identified by comparing cytochrome c oxidase I (COI) sequences against a curated Barcode of Life Data System (BOLD). Viruses were identified using the SMART-9N protocol, which allows amplified DNA to be prepared with native barcoding for nanopore sequencing. Kraken 2 was employed to detect viral pathogens and Minimap2 and BOLD identified the contents of the blood meal. Due to the high similarity of some species, mosquito identification was conducted using blast after generation of consensus COI sequences using RACON polishing. This protocol can simultaneously uncover viral diversity, mosquito species and mosquito feeding habits. It also has the potential to increase understanding of mosquito genetic diversity and transmission dynamics of zoonotic mosquito-borne viruses.

Identifiants

pubmed: 38240642
doi: 10.1099/mgen.0.001184
pmc: PMC10868619
doi:

Substances chimiques

DNA 9007-49-2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Medical Research Council
ID : MC_PC_15100
Pays : United Kingdom
Organisme : Bill & Melinda Gates Foundation
ID : INV-034540
Pays : United States
Organisme : Medical Research Council
ID : MR/S035362/1
Pays : United Kingdom
Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/M501621/1
Pays : United Kingdom

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Auteurs

Jeremy D Mirza (JD)

Institute of Inflammation and Ageing, University of Birmingham, Birmingham, UK.
Department of Biosciences, University of Birmingham, Birmingham, UK.

Lilian de Oliveira Guimarães (L)

Instituto Pasteur, São Paulo, Brazil.

Sam Wilkinson (S)

Department of Biosciences, University of Birmingham, Birmingham, UK.

Esmenia C Rocha (EC)

Instituto de Medicina Tropical, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.

Mayara Bertanhe (M)

Instituto de Medicina Tropical, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.

Vanessa Christe Helfstein (VC)

Instituto Pasteur, São Paulo, Brazil.

Juliana Telles de-Deus (JT)

Instituto Pasteur, São Paulo, Brazil.

Ingra M Claro (IM)

Instituto de Medicina Tropical, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
MRC Centre for Global Infectious Disease Analysis, Jameel Institute, Imperial College London, London, UK.

Nicola Cumley (N)

Department of Biosciences, University of Birmingham, Birmingham, UK.

Joshua Quick (J)

Department of Biosciences, University of Birmingham, Birmingham, UK.

Nuno R Faria (NR)

MRC Centre for Global Infectious Disease Analysis, Jameel Institute, Imperial College London, London, UK.

Ester C Sabino (EC)

Instituto de Medicina Tropical, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.

Karin Kirchgatter (K)

Instituto Pasteur, São Paulo, Brazil.
Instituto de Medicina Tropical, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.

Nicholas J Loman (NJ)

Department of Biosciences, University of Birmingham, Birmingham, UK.

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Classifications MeSH