Genomic epidemiology and carbon metabolism of Escherichia coli serogroup O145 reflect contrasting phylogenies.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 30 01 2020
accepted: 08 06 2020
entrez: 26 6 2020
pubmed: 26 6 2020
medline: 1 9 2020
Statut: epublish

Résumé

Shiga toxin-producing Escherichia coli (STEC) are a leading cause of foodborne outbreaks of human disease, but they reside harmlessly as an asymptomatic commensal in the ruminant gut. STEC serogroup O145 are difficult to isolate as routine diagnostic methods are unable to distinguish non-O157 serogroups due to their heterogeneous metabolic characteristics, resulting in under-reporting which is likely to conceal their true prevalence. In light of these deficiencies, the purpose of this study was a twofold approach to investigate enhanced STEC O145 diagnostic culture-based methods: firstly, to use a genomic epidemiology approach to understand the genetic diversity and population structure of serogroup O145 at both a local (New Zealand) (n = 47) and global scale (n = 75) and, secondly, to identify metabolic characteristics that will help the development of a differential media for this serogroup. Analysis of a subset of E. coli serogroup O145 strains demonstrated considerable diversity in carbon utilisation, which varied in association with eae subtype and sequence type. Several carbon substrates, such as D-serine and D-malic acid, were utilised by the majority of serogroup O145 strains, which, when coupled with current molecular and culture-based methods, could aid in the identification of presumptive E. coli serogroup O145 isolates. These carbon substrates warrant subsequent testing with additional serogroup O145 strains and non-O145 strains. Serogroup O145 strains displayed extensive genetic heterogeneity that was correlated with sequence type and eae subtype, suggesting these genetic markers are good indicators for distinct E. coli phylogenetic lineages. Pangenome analysis identified a core of 3,036 genes and an open pangenome of >14,000 genes, which is consistent with the identification of distinct phylogenetic lineages. Overall, this study highlighted the phenotypic and genotypic heterogeneity within E. coli serogroup O145, suggesting that the development of a differential media targeting this serogroup will be challenging.

Identifiants

pubmed: 32584859
doi: 10.1371/journal.pone.0235066
pii: PONE-D-20-02830
pmc: PMC7316241
doi:

Substances chimiques

Malates 0
Serine 452VLY9402
Carbon 7440-44-0
malic acid 817L1N4CKP

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0235066

Déclaration de conflit d'intérêts

Two of the authors (ALC and GB) are employed by a commercial company, AgResearch Ltd. This does not alter our adherence to PLOS ONE policies on sharing data and materials. The remaining authors have declared that no competing interests exist.

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Auteurs

Rose M Collis (RM)

AgResearch Ltd, Hopkirk Research Institute, Massey University, Palmerston North, New Zealand.
Molecular Epidemiology and Veterinary Public Health Laboratory (mEpiLab), Infectious Disease Research Centre, School of Veterinary Science, Massey University, Palmerston North, New Zealand.

Patrick J Biggs (PJ)

Molecular Epidemiology and Veterinary Public Health Laboratory (mEpiLab), Infectious Disease Research Centre, School of Veterinary Science, Massey University, Palmerston North, New Zealand.
School of Fundamental Sciences, Massey University, Palmerston North, New Zealand.
New Zealand Food Safety Science and Research Centre, Massey University, Palmerston North, New Zealand.

Anne C Midwinter (AC)

Molecular Epidemiology and Veterinary Public Health Laboratory (mEpiLab), Infectious Disease Research Centre, School of Veterinary Science, Massey University, Palmerston North, New Zealand.

A Springer Browne (AS)

Molecular Epidemiology and Veterinary Public Health Laboratory (mEpiLab), Infectious Disease Research Centre, School of Veterinary Science, Massey University, Palmerston North, New Zealand.

David A Wilkinson (DA)

Molecular Epidemiology and Veterinary Public Health Laboratory (mEpiLab), Infectious Disease Research Centre, School of Veterinary Science, Massey University, Palmerston North, New Zealand.
New Zealand Food Safety Science and Research Centre, Massey University, Palmerston North, New Zealand.

Hamid Irshad (H)

Animal Health Programme, National Agricultural Research Centre, Islamabad, Pakistan.

Nigel P French (NP)

Molecular Epidemiology and Veterinary Public Health Laboratory (mEpiLab), Infectious Disease Research Centre, School of Veterinary Science, Massey University, Palmerston North, New Zealand.
New Zealand Food Safety Science and Research Centre, Massey University, Palmerston North, New Zealand.

Gale Brightwell (G)

AgResearch Ltd, Hopkirk Research Institute, Massey University, Palmerston North, New Zealand.
New Zealand Food Safety Science and Research Centre, Massey University, Palmerston North, New Zealand.

Adrian L Cookson (AL)

AgResearch Ltd, Hopkirk Research Institute, Massey University, Palmerston North, New Zealand.
Molecular Epidemiology and Veterinary Public Health Laboratory (mEpiLab), Infectious Disease Research Centre, School of Veterinary Science, Massey University, Palmerston North, New Zealand.

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Classifications MeSH