Cargando…

Phenotypic and genotypic antimicrobial susceptibility patterns of the emerging human respiratory pathogen Mycoplasma amphoriforme isolated from the UK and Denmark

OBJECTIVES: To determine the phenotypic and genotypic antibiotic susceptibility of Mycoplasma amphoriforme isolates recovered from patients in the UK and Denmark. METHODS: Seven isolates of M. amphoriforme were examined for antimicrobial susceptibility to seven antibiotics using the microbroth dilut...

Descripción completa

Detalles Bibliográficos
Autores principales: Day, Jessica, Afshar, Baharak, Rowlands, Richard S, Umer, Taiba S, Windsor, Helena, Paukner, Susanne, Jensen, Jorgen S, Spiller, Owen B, Chalker, Victoria J, Beeton, Michael L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616542/
https://www.ncbi.nlm.nih.gov/pubmed/36048620
http://dx.doi.org/10.1093/jac/dkac293
_version_ 1784820665458622464
author Day, Jessica
Afshar, Baharak
Rowlands, Richard S
Umer, Taiba S
Windsor, Helena
Paukner, Susanne
Jensen, Jorgen S
Spiller, Owen B
Chalker, Victoria J
Beeton, Michael L
author_facet Day, Jessica
Afshar, Baharak
Rowlands, Richard S
Umer, Taiba S
Windsor, Helena
Paukner, Susanne
Jensen, Jorgen S
Spiller, Owen B
Chalker, Victoria J
Beeton, Michael L
author_sort Day, Jessica
collection PubMed
description OBJECTIVES: To determine the phenotypic and genotypic antibiotic susceptibility of Mycoplasma amphoriforme isolates recovered from patients in the UK and Denmark. METHODS: Seven isolates of M. amphoriforme were examined for antimicrobial susceptibility to seven antibiotics using the microbroth dilution assay in line with the CLSI guidelines for mycoplasmas. Each isolate was additionally subjected to WGS to identify resistance-associated mutations. Based on the consensus sequences from the genomic data, PCR primers were designed, and tested, for the amplification of the QRDR within the parC gene. RESULTS: Of the seven isolates investigated, four (57%) were resistant to moxifloxacin (0.5–1 mg/L) and levofloxacin (1–2 mg/L), compared with those that were susceptible (0.03–0.06 and 0.006 mg/L, respectively). Isolate H29 was resistant to five of the seven antibiotics tested: moxifloxacin, 0.5 mg/L; levofloxacin, 2 mg/L; azithromycin, 64 mg/L; erythromycin, 128 mg/L; and clindamycin, 64 mg/L. All isolates were susceptible to tetracycline (0.06 mg/L) and lefamulin (0.001–0.004 mg/L). Mutations from genomic data confirmed the presence of an S89F mutation within the ParC protein among all fluoroquinolone-resistant isolates and an A2059G mutation in the 23S rRNA gene in the macrolide- and lincosamide-resistant isolate H29. CONCLUSIONS: To the best of our knowledge, this is the first time where phenotypic and genotypic resistance data have been paired for M. amphoriforme confirming a correlation between the two. These data suggest the need for focused testing and resistance determination of isolates from high-risk patients given the backdrop of a high prevalence of antimicrobial resistance.
format Online
Article
Text
id pubmed-9616542
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-96165422022-11-01 Phenotypic and genotypic antimicrobial susceptibility patterns of the emerging human respiratory pathogen Mycoplasma amphoriforme isolated from the UK and Denmark Day, Jessica Afshar, Baharak Rowlands, Richard S Umer, Taiba S Windsor, Helena Paukner, Susanne Jensen, Jorgen S Spiller, Owen B Chalker, Victoria J Beeton, Michael L J Antimicrob Chemother Original Research OBJECTIVES: To determine the phenotypic and genotypic antibiotic susceptibility of Mycoplasma amphoriforme isolates recovered from patients in the UK and Denmark. METHODS: Seven isolates of M. amphoriforme were examined for antimicrobial susceptibility to seven antibiotics using the microbroth dilution assay in line with the CLSI guidelines for mycoplasmas. Each isolate was additionally subjected to WGS to identify resistance-associated mutations. Based on the consensus sequences from the genomic data, PCR primers were designed, and tested, for the amplification of the QRDR within the parC gene. RESULTS: Of the seven isolates investigated, four (57%) were resistant to moxifloxacin (0.5–1 mg/L) and levofloxacin (1–2 mg/L), compared with those that were susceptible (0.03–0.06 and 0.006 mg/L, respectively). Isolate H29 was resistant to five of the seven antibiotics tested: moxifloxacin, 0.5 mg/L; levofloxacin, 2 mg/L; azithromycin, 64 mg/L; erythromycin, 128 mg/L; and clindamycin, 64 mg/L. All isolates were susceptible to tetracycline (0.06 mg/L) and lefamulin (0.001–0.004 mg/L). Mutations from genomic data confirmed the presence of an S89F mutation within the ParC protein among all fluoroquinolone-resistant isolates and an A2059G mutation in the 23S rRNA gene in the macrolide- and lincosamide-resistant isolate H29. CONCLUSIONS: To the best of our knowledge, this is the first time where phenotypic and genotypic resistance data have been paired for M. amphoriforme confirming a correlation between the two. These data suggest the need for focused testing and resistance determination of isolates from high-risk patients given the backdrop of a high prevalence of antimicrobial resistance. Oxford University Press 2022-09-01 /pmc/articles/PMC9616542/ /pubmed/36048620 http://dx.doi.org/10.1093/jac/dkac293 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Research
Day, Jessica
Afshar, Baharak
Rowlands, Richard S
Umer, Taiba S
Windsor, Helena
Paukner, Susanne
Jensen, Jorgen S
Spiller, Owen B
Chalker, Victoria J
Beeton, Michael L
Phenotypic and genotypic antimicrobial susceptibility patterns of the emerging human respiratory pathogen Mycoplasma amphoriforme isolated from the UK and Denmark
title Phenotypic and genotypic antimicrobial susceptibility patterns of the emerging human respiratory pathogen Mycoplasma amphoriforme isolated from the UK and Denmark
title_full Phenotypic and genotypic antimicrobial susceptibility patterns of the emerging human respiratory pathogen Mycoplasma amphoriforme isolated from the UK and Denmark
title_fullStr Phenotypic and genotypic antimicrobial susceptibility patterns of the emerging human respiratory pathogen Mycoplasma amphoriforme isolated from the UK and Denmark
title_full_unstemmed Phenotypic and genotypic antimicrobial susceptibility patterns of the emerging human respiratory pathogen Mycoplasma amphoriforme isolated from the UK and Denmark
title_short Phenotypic and genotypic antimicrobial susceptibility patterns of the emerging human respiratory pathogen Mycoplasma amphoriforme isolated from the UK and Denmark
title_sort phenotypic and genotypic antimicrobial susceptibility patterns of the emerging human respiratory pathogen mycoplasma amphoriforme isolated from the uk and denmark
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616542/
https://www.ncbi.nlm.nih.gov/pubmed/36048620
http://dx.doi.org/10.1093/jac/dkac293
work_keys_str_mv AT dayjessica phenotypicandgenotypicantimicrobialsusceptibilitypatternsoftheemerginghumanrespiratorypathogenmycoplasmaamphoriformeisolatedfromtheukanddenmark
AT afsharbaharak phenotypicandgenotypicantimicrobialsusceptibilitypatternsoftheemerginghumanrespiratorypathogenmycoplasmaamphoriformeisolatedfromtheukanddenmark
AT rowlandsrichards phenotypicandgenotypicantimicrobialsusceptibilitypatternsoftheemerginghumanrespiratorypathogenmycoplasmaamphoriformeisolatedfromtheukanddenmark
AT umertaibas phenotypicandgenotypicantimicrobialsusceptibilitypatternsoftheemerginghumanrespiratorypathogenmycoplasmaamphoriformeisolatedfromtheukanddenmark
AT windsorhelena phenotypicandgenotypicantimicrobialsusceptibilitypatternsoftheemerginghumanrespiratorypathogenmycoplasmaamphoriformeisolatedfromtheukanddenmark
AT pauknersusanne phenotypicandgenotypicantimicrobialsusceptibilitypatternsoftheemerginghumanrespiratorypathogenmycoplasmaamphoriformeisolatedfromtheukanddenmark
AT jensenjorgens phenotypicandgenotypicantimicrobialsusceptibilitypatternsoftheemerginghumanrespiratorypathogenmycoplasmaamphoriformeisolatedfromtheukanddenmark
AT spillerowenb phenotypicandgenotypicantimicrobialsusceptibilitypatternsoftheemerginghumanrespiratorypathogenmycoplasmaamphoriformeisolatedfromtheukanddenmark
AT chalkervictoriaj phenotypicandgenotypicantimicrobialsusceptibilitypatternsoftheemerginghumanrespiratorypathogenmycoplasmaamphoriformeisolatedfromtheukanddenmark
AT beetonmichaell phenotypicandgenotypicantimicrobialsusceptibilitypatternsoftheemerginghumanrespiratorypathogenmycoplasmaamphoriformeisolatedfromtheukanddenmark
AT phenotypicandgenotypicantimicrobialsusceptibilitypatternsoftheemerginghumanrespiratorypathogenmycoplasmaamphoriformeisolatedfromtheukanddenmark