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Prediction of Phenotypic Antimicrobial Resistance Profiles From Whole Genome Sequences of Non-typhoidal Salmonella enterica

Surveillance of antimicrobial resistance (AMR) in non-typhoidal Salmonella enterica (NTS), is essential for monitoring transmission of resistance from the food chain to humans, and for establishing effective treatment protocols. We evaluated the prediction of phenotypic resistance in NTS from genoty...

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Autores principales: Neuert, Saskia, Nair, Satheesh, Day, Martin R., Doumith, Michel, Ashton, Philip M., Mellor, Kate C., Jenkins, Claire, Hopkins, Katie L., Woodford, Neil, de Pinna, Elizabeth, Godbole, Gauri, Dallman, Timothy J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880904/
https://www.ncbi.nlm.nih.gov/pubmed/29636749
http://dx.doi.org/10.3389/fmicb.2018.00592
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author Neuert, Saskia
Nair, Satheesh
Day, Martin R.
Doumith, Michel
Ashton, Philip M.
Mellor, Kate C.
Jenkins, Claire
Hopkins, Katie L.
Woodford, Neil
de Pinna, Elizabeth
Godbole, Gauri
Dallman, Timothy J.
author_facet Neuert, Saskia
Nair, Satheesh
Day, Martin R.
Doumith, Michel
Ashton, Philip M.
Mellor, Kate C.
Jenkins, Claire
Hopkins, Katie L.
Woodford, Neil
de Pinna, Elizabeth
Godbole, Gauri
Dallman, Timothy J.
author_sort Neuert, Saskia
collection PubMed
description Surveillance of antimicrobial resistance (AMR) in non-typhoidal Salmonella enterica (NTS), is essential for monitoring transmission of resistance from the food chain to humans, and for establishing effective treatment protocols. We evaluated the prediction of phenotypic resistance in NTS from genotypic profiles derived from whole genome sequencing (WGS). Genes and chromosomal mutations responsible for phenotypic resistance were sought in WGS data from 3,491 NTS isolates received by Public Health England’s Gastrointestinal Bacteria Reference Unit between April 2014 and March 2015. Inferred genotypic AMR profiles were compared with phenotypic susceptibilities determined for fifteen antimicrobials using EUCAST guidelines. Discrepancies between phenotypic and genotypic profiles for one or more antimicrobials were detected for 76 isolates (2.18%) although only 88/52,365 (0.17%) isolate/antimicrobial combinations were discordant. Of the discrepant results, the largest number were associated with streptomycin (67.05%, n = 59). Pan-susceptibility was observed in 2,190 isolates (62.73%). Overall, resistance to tetracyclines was most common (26.27% of isolates, n = 917) followed by sulphonamides (23.72%, n = 828) and ampicillin (21.43%, n = 748). Multidrug resistance (MDR), i.e., resistance to three or more antimicrobial classes, was detected in 848 isolates (24.29%) with resistance to ampicillin, streptomycin, sulphonamides and tetracyclines being the most common MDR profile (n = 231; 27.24%). For isolates with this profile, all but one were S. Typhimurium and 94.81% (n = 219) had the resistance determinants bla(TEM-1,) strA-strB, sul2 and tet(A). Extended-spectrum β-lactamase genes were identified in 41 isolates (1.17%) and multiple mutations in chromosomal genes associated with ciprofloxacin resistance in 82 isolates (2.35%). This study showed that WGS is suitable as a rapid means of determining AMR patterns of NTS for public health surveillance.
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spelling pubmed-58809042018-04-10 Prediction of Phenotypic Antimicrobial Resistance Profiles From Whole Genome Sequences of Non-typhoidal Salmonella enterica Neuert, Saskia Nair, Satheesh Day, Martin R. Doumith, Michel Ashton, Philip M. Mellor, Kate C. Jenkins, Claire Hopkins, Katie L. Woodford, Neil de Pinna, Elizabeth Godbole, Gauri Dallman, Timothy J. Front Microbiol Microbiology Surveillance of antimicrobial resistance (AMR) in non-typhoidal Salmonella enterica (NTS), is essential for monitoring transmission of resistance from the food chain to humans, and for establishing effective treatment protocols. We evaluated the prediction of phenotypic resistance in NTS from genotypic profiles derived from whole genome sequencing (WGS). Genes and chromosomal mutations responsible for phenotypic resistance were sought in WGS data from 3,491 NTS isolates received by Public Health England’s Gastrointestinal Bacteria Reference Unit between April 2014 and March 2015. Inferred genotypic AMR profiles were compared with phenotypic susceptibilities determined for fifteen antimicrobials using EUCAST guidelines. Discrepancies between phenotypic and genotypic profiles for one or more antimicrobials were detected for 76 isolates (2.18%) although only 88/52,365 (0.17%) isolate/antimicrobial combinations were discordant. Of the discrepant results, the largest number were associated with streptomycin (67.05%, n = 59). Pan-susceptibility was observed in 2,190 isolates (62.73%). Overall, resistance to tetracyclines was most common (26.27% of isolates, n = 917) followed by sulphonamides (23.72%, n = 828) and ampicillin (21.43%, n = 748). Multidrug resistance (MDR), i.e., resistance to three or more antimicrobial classes, was detected in 848 isolates (24.29%) with resistance to ampicillin, streptomycin, sulphonamides and tetracyclines being the most common MDR profile (n = 231; 27.24%). For isolates with this profile, all but one were S. Typhimurium and 94.81% (n = 219) had the resistance determinants bla(TEM-1,) strA-strB, sul2 and tet(A). Extended-spectrum β-lactamase genes were identified in 41 isolates (1.17%) and multiple mutations in chromosomal genes associated with ciprofloxacin resistance in 82 isolates (2.35%). This study showed that WGS is suitable as a rapid means of determining AMR patterns of NTS for public health surveillance. Frontiers Media S.A. 2018-03-27 /pmc/articles/PMC5880904/ /pubmed/29636749 http://dx.doi.org/10.3389/fmicb.2018.00592 Text en Copyright © 2018 Neuert, Nair, Day, Doumith, Ashton, Mellor, Jenkins, Hopkins, Woodford, de Pinna, Godbole and Dallman. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Neuert, Saskia
Nair, Satheesh
Day, Martin R.
Doumith, Michel
Ashton, Philip M.
Mellor, Kate C.
Jenkins, Claire
Hopkins, Katie L.
Woodford, Neil
de Pinna, Elizabeth
Godbole, Gauri
Dallman, Timothy J.
Prediction of Phenotypic Antimicrobial Resistance Profiles From Whole Genome Sequences of Non-typhoidal Salmonella enterica
title Prediction of Phenotypic Antimicrobial Resistance Profiles From Whole Genome Sequences of Non-typhoidal Salmonella enterica
title_full Prediction of Phenotypic Antimicrobial Resistance Profiles From Whole Genome Sequences of Non-typhoidal Salmonella enterica
title_fullStr Prediction of Phenotypic Antimicrobial Resistance Profiles From Whole Genome Sequences of Non-typhoidal Salmonella enterica
title_full_unstemmed Prediction of Phenotypic Antimicrobial Resistance Profiles From Whole Genome Sequences of Non-typhoidal Salmonella enterica
title_short Prediction of Phenotypic Antimicrobial Resistance Profiles From Whole Genome Sequences of Non-typhoidal Salmonella enterica
title_sort prediction of phenotypic antimicrobial resistance profiles from whole genome sequences of non-typhoidal salmonella enterica
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880904/
https://www.ncbi.nlm.nih.gov/pubmed/29636749
http://dx.doi.org/10.3389/fmicb.2018.00592
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