Whole genome sequence of Vibrio cholerae directly from dried spotted filter paper.


Journal

PLoS neglected tropical diseases
ISSN: 1935-2735
Titre abrégé: PLoS Negl Trop Dis
Pays: United States
ID NLM: 101291488

Informations de publication

Date de publication:
05 2019
Historique:
received: 21 09 2018
accepted: 25 03 2019
revised: 11 06 2019
pubmed: 31 5 2019
medline: 29 10 2019
entrez: 31 5 2019
Statut: epublish

Résumé

Global estimates for cholera annually approximate 4 million cases worldwide with 95,000 deaths. Recent outbreaks, including Haiti and Yemen, are reminders that cholera is still a global health concern. Cholera outbreaks can rapidly induce high death tolls by overwhelming the capacity of health facilities, especially in remote areas or areas of civil unrest. Recent studies demonstrated that stool specimens preserved on filter paper facilitate molecular analysis of Vibrio cholerae in resource limited settings. Specimens preserved in a rapid, low-cost, safe and sustainable manner for sequencing provides previously unavailable data about circulating cholera strains. This may ultimately contribute new information to shape public policy response on cholera control and elimination. Whole genome sequencing (WGS) recovered close to a complete sequence of the V. cholerae O1 genome with satisfactory genome coverage from stool specimens enriched in alkaline peptone water (APW) and V. cholerae culture isolates, both spotted on filter paper. The minimum concentration of V. cholerae DNA sufficient to produce quality genomic information was 0.02 ng/μL. The genomic data confirmed the presence or absence of genes of epidemiological interest, including cholera toxin and pilus loci. WGS identified a variety of diarrheal pathogens from APW-enriched specimen spotted filter paper, highlighting the potential for this technique to explore the gut microbiome, potentially identifying co-infections, which may impact the severity of disease. WGS demonstrated that these specimens fit within the current global cholera phylogenetic tree, identifying the strains as the 7th pandemic El Tor. WGS results allowed for mapping of short reads from APW-enriched specimen and culture isolate spotted filter papers. This provided valuable molecular epidemiological sequence information on V. cholerae strains from remote, low-resource settings. These results identified the presence of co-infecting pathogens while providing rare insight into the specific V. cholerae strains causing outbreaks in cholera-endemic areas.

Sections du résumé

BACKGROUND
Global estimates for cholera annually approximate 4 million cases worldwide with 95,000 deaths. Recent outbreaks, including Haiti and Yemen, are reminders that cholera is still a global health concern. Cholera outbreaks can rapidly induce high death tolls by overwhelming the capacity of health facilities, especially in remote areas or areas of civil unrest. Recent studies demonstrated that stool specimens preserved on filter paper facilitate molecular analysis of Vibrio cholerae in resource limited settings. Specimens preserved in a rapid, low-cost, safe and sustainable manner for sequencing provides previously unavailable data about circulating cholera strains. This may ultimately contribute new information to shape public policy response on cholera control and elimination.
METHODOLOGY/PRINCIPAL FINDINGS
Whole genome sequencing (WGS) recovered close to a complete sequence of the V. cholerae O1 genome with satisfactory genome coverage from stool specimens enriched in alkaline peptone water (APW) and V. cholerae culture isolates, both spotted on filter paper. The minimum concentration of V. cholerae DNA sufficient to produce quality genomic information was 0.02 ng/μL. The genomic data confirmed the presence or absence of genes of epidemiological interest, including cholera toxin and pilus loci. WGS identified a variety of diarrheal pathogens from APW-enriched specimen spotted filter paper, highlighting the potential for this technique to explore the gut microbiome, potentially identifying co-infections, which may impact the severity of disease. WGS demonstrated that these specimens fit within the current global cholera phylogenetic tree, identifying the strains as the 7th pandemic El Tor.
CONCLUSIONS
WGS results allowed for mapping of short reads from APW-enriched specimen and culture isolate spotted filter papers. This provided valuable molecular epidemiological sequence information on V. cholerae strains from remote, low-resource settings. These results identified the presence of co-infecting pathogens while providing rare insight into the specific V. cholerae strains causing outbreaks in cholera-endemic areas.

Identifiants

pubmed: 31145741
doi: 10.1371/journal.pntd.0007330
pii: PNTD-D-18-01428
pmc: PMC6559667
doi:

Types de publication

Evaluation Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0007330

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 098051
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 206194
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 098051
Pays : United Kingdom

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Angèle H M Bénard (AHM)

Wellcome Trust Sanger Institute, Genome campus, Hinxton United Kingdom.

Etienne Guenou (E)

M.A. SANTE (Meilleur Accès aux Soins de Santé), Yaoundé, Cameroon.
Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.

Maria Fookes (M)

Wellcome Trust Sanger Institute, Genome campus, Hinxton United Kingdom.

Jerome Ateudjieu (J)

M.A. SANTE (Meilleur Accès aux Soins de Santé), Yaoundé, Cameroon.
Department of Public Health, Faculty of Medicine and Pharmaceutical Sciences, University of Dschang, Cameroon Dschang Cameroon.
Clinical Research Unit, Division of Health Operations Research, Ministry of Public Health, N°8, quartier du Lac (Yaoundé III), Cameroon.

Watipaso Kasambara (W)

Ministry of Health, Lilongwe, Malawi.

Matthew Siever (M)

John Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.

Stanislas Rebaudet (S)

Assistance Publique-Hôpitaux de Marseille (APHM), Marseille, France.
Hôpital Européen, Marseille, France.

Jacques Boncy (J)

National Laboratory of Public Health in Haiti (LNSP), Ministry of Public Health and Population, Haiti.

Paul Adrien (P)

Directorate for Epidemiology, Laboratory and Research, Ministry of Public Health and Population, Haiti.

Renaud Piarroux (R)

Sorbonne Université, INSERM, Institut Pierre-Louis d'Epidémiologie et de Santé Publique, APHP, Hôpital Pitié-Salpêtrière, Paris, France.

David A Sack (DA)

John Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.

Nicholas Thomson (N)

Wellcome Trust Sanger Institute, Genome campus, Hinxton United Kingdom.
London School of Hygiene and Tropical Medicine, Keppel St, Bloomsbury, London WC1E 7HT, United Kingdom.

Amanda K Debes (AK)

John Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States of America.

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Classifications MeSH