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Prediction of antimicrobial resistance in clinical Campylobacter jejuni isolates from whole-genome sequencing data

Campylobacter jejuni is recognised as the leading cause of bacterial gastroenteritis in industrialised countries. Although the majority of Campylobacter infections are self-limiting, antimicrobial treatment is necessary in severe cases. Therefore, the development of antimicrobial resistance (AMR) in...

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Autores principales: Dahl, Louise Gade, Joensen, Katrine Grimstrup, Østerlund, Mark Thomas, Kiil, Kristoffer, Nielsen, Eva Møller
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979593/
https://www.ncbi.nlm.nih.gov/pubmed/32974772
http://dx.doi.org/10.1007/s10096-020-04043-y
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author Dahl, Louise Gade
Joensen, Katrine Grimstrup
Østerlund, Mark Thomas
Kiil, Kristoffer
Nielsen, Eva Møller
author_facet Dahl, Louise Gade
Joensen, Katrine Grimstrup
Østerlund, Mark Thomas
Kiil, Kristoffer
Nielsen, Eva Møller
author_sort Dahl, Louise Gade
collection PubMed
description Campylobacter jejuni is recognised as the leading cause of bacterial gastroenteritis in industrialised countries. Although the majority of Campylobacter infections are self-limiting, antimicrobial treatment is necessary in severe cases. Therefore, the development of antimicrobial resistance (AMR) in Campylobacter is a growing public health challenge and surveillance of AMR is important for bacterial disease control. The aim of this study was to predict antimicrobial resistance in C. jejuni from whole-genome sequencing data. A total of 516 clinical C. jejuni isolates collected between 2014 and 2017 were subjected to WGS. Resistance phenotypes were determined by standard broth dilution, categorising isolates as either susceptible or resistant based on epidemiological cutoffs for six antimicrobials: ciprofloxacin, nalidixic acid, erythromycin, gentamicin, streptomycin, and tetracycline. Resistance genotypes were identified using an in-house database containing reference genes with known point mutations and the presence of resistance genes was determined using the ResFinder database and four bioinformatical methods (modified KMA, ABRicate, ARIBA, and ResFinder Batch Upload). We identified seven resistance genes including tet(O), tet(O/32/O), ant(6)-Ia, aph(2″)-If, blaOXA, aph(3′)-III, and cat as well as mutations in three genes: gyrA, 23S rRNA, and rpsL. There was a high correlation between phenotypic resistance and the presence of known resistance genes and/or point mutations. A correlation above 98% was seen for all antimicrobials except streptomycin with a correlation of 92%. In conclusion, we found that WGS can predict antimicrobial resistance with a high degree of accuracy and have the potential to be a powerful tool for AMR surveillance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10096-020-04043-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-79795932021-04-05 Prediction of antimicrobial resistance in clinical Campylobacter jejuni isolates from whole-genome sequencing data Dahl, Louise Gade Joensen, Katrine Grimstrup Østerlund, Mark Thomas Kiil, Kristoffer Nielsen, Eva Møller Eur J Clin Microbiol Infect Dis Original Article Campylobacter jejuni is recognised as the leading cause of bacterial gastroenteritis in industrialised countries. Although the majority of Campylobacter infections are self-limiting, antimicrobial treatment is necessary in severe cases. Therefore, the development of antimicrobial resistance (AMR) in Campylobacter is a growing public health challenge and surveillance of AMR is important for bacterial disease control. The aim of this study was to predict antimicrobial resistance in C. jejuni from whole-genome sequencing data. A total of 516 clinical C. jejuni isolates collected between 2014 and 2017 were subjected to WGS. Resistance phenotypes were determined by standard broth dilution, categorising isolates as either susceptible or resistant based on epidemiological cutoffs for six antimicrobials: ciprofloxacin, nalidixic acid, erythromycin, gentamicin, streptomycin, and tetracycline. Resistance genotypes were identified using an in-house database containing reference genes with known point mutations and the presence of resistance genes was determined using the ResFinder database and four bioinformatical methods (modified KMA, ABRicate, ARIBA, and ResFinder Batch Upload). We identified seven resistance genes including tet(O), tet(O/32/O), ant(6)-Ia, aph(2″)-If, blaOXA, aph(3′)-III, and cat as well as mutations in three genes: gyrA, 23S rRNA, and rpsL. There was a high correlation between phenotypic resistance and the presence of known resistance genes and/or point mutations. A correlation above 98% was seen for all antimicrobials except streptomycin with a correlation of 92%. In conclusion, we found that WGS can predict antimicrobial resistance with a high degree of accuracy and have the potential to be a powerful tool for AMR surveillance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10096-020-04043-y) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-09-24 2021 /pmc/articles/PMC7979593/ /pubmed/32974772 http://dx.doi.org/10.1007/s10096-020-04043-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Dahl, Louise Gade
Joensen, Katrine Grimstrup
Østerlund, Mark Thomas
Kiil, Kristoffer
Nielsen, Eva Møller
Prediction of antimicrobial resistance in clinical Campylobacter jejuni isolates from whole-genome sequencing data
title Prediction of antimicrobial resistance in clinical Campylobacter jejuni isolates from whole-genome sequencing data
title_full Prediction of antimicrobial resistance in clinical Campylobacter jejuni isolates from whole-genome sequencing data
title_fullStr Prediction of antimicrobial resistance in clinical Campylobacter jejuni isolates from whole-genome sequencing data
title_full_unstemmed Prediction of antimicrobial resistance in clinical Campylobacter jejuni isolates from whole-genome sequencing data
title_short Prediction of antimicrobial resistance in clinical Campylobacter jejuni isolates from whole-genome sequencing data
title_sort prediction of antimicrobial resistance in clinical campylobacter jejuni isolates from whole-genome sequencing data
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979593/
https://www.ncbi.nlm.nih.gov/pubmed/32974772
http://dx.doi.org/10.1007/s10096-020-04043-y
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