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Value of multiplex PCR for detection of antimicrobial resistance in samples retrieved from patients with orthopaedic infections
BACKGROUND: The performance of multiplex PCR (mPCR) for detection of antimicrobial resistance from clinical isolates is unknown. We assessed the ability of mPCR to analyse resistance genes directly from clinical samples. Patients with orthopedic infections were prospectively included. Phenotypical a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155317/ https://www.ncbi.nlm.nih.gov/pubmed/32290833 http://dx.doi.org/10.1186/s12866-020-01741-7 |
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author | Sigmund, Irene Katharina Renz, Nora Feihl, Susanne Morgenstern, Christian Cabric, Sabrina Trampuz, Andrej |
author_facet | Sigmund, Irene Katharina Renz, Nora Feihl, Susanne Morgenstern, Christian Cabric, Sabrina Trampuz, Andrej |
author_sort | Sigmund, Irene Katharina |
collection | PubMed |
description | BACKGROUND: The performance of multiplex PCR (mPCR) for detection of antimicrobial resistance from clinical isolates is unknown. We assessed the ability of mPCR to analyse resistance genes directly from clinical samples. Patients with orthopedic infections were prospectively included. Phenotypical and genotypical resistance was evaluated in clinical samples (synovial and sonication fluid) where identical pathogens were identified by culture and mPCR. RESULT: A total of 94 samples were analysed, including 60 sonication fluid and 34 synovial fluid samples. For coagulase-negative staphylococcus strains, mPCR detected resistance to oxacillin in 10 of 23 isolates (44%) and to rifampin in none of 6 isolates. For S. aureus isolates, detection rate of oxacillin and rifampin-resistance was 100% (2/2 and 1/1, respectively). Fluoroquinolone-resistance was confirmed by mPCR in all 3 isolates of Enterobacteriaceae, in enterococci resistance to aminoglycoside-high level was detected in 1 of 3 isolates (33%) and in streptococci resistance to macrolides/lincosamides in none of 2 isolates. The overall sensitivity for different pathogens and antimicrobials was 46% and specificity 95%, the median concordance was 80% (range, 57–100%). Full agreement was observed for oxacillin in S. aureus, vancomycin in enterococci, carbapenems/cephalosporins in Enterobacteriaceae and rifampin in Cutibacterium species. CONCLUSION: The overall sensitivity for detection of antimicrobial resistance by mPCR directly from clinical samples was low. False-negative mPCR results occurred mainly in coagulase-negative staphylococci, especially for oxacillin and rifampin. However, the specificity of mPCR was high and a positive result reliably predicted antimicrobial resistance. Including universal primers in the PCR test assay may improve the detection rate but requires additional sequencing step. TRIAL REGISTRATION: www.clinicaltrials.gov No. NCT02530229, registered at 21 August 2015 (retrospectively registered). |
format | Online Article Text |
id | pubmed-7155317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71553172020-04-20 Value of multiplex PCR for detection of antimicrobial resistance in samples retrieved from patients with orthopaedic infections Sigmund, Irene Katharina Renz, Nora Feihl, Susanne Morgenstern, Christian Cabric, Sabrina Trampuz, Andrej BMC Microbiol Research Article BACKGROUND: The performance of multiplex PCR (mPCR) for detection of antimicrobial resistance from clinical isolates is unknown. We assessed the ability of mPCR to analyse resistance genes directly from clinical samples. Patients with orthopedic infections were prospectively included. Phenotypical and genotypical resistance was evaluated in clinical samples (synovial and sonication fluid) where identical pathogens were identified by culture and mPCR. RESULT: A total of 94 samples were analysed, including 60 sonication fluid and 34 synovial fluid samples. For coagulase-negative staphylococcus strains, mPCR detected resistance to oxacillin in 10 of 23 isolates (44%) and to rifampin in none of 6 isolates. For S. aureus isolates, detection rate of oxacillin and rifampin-resistance was 100% (2/2 and 1/1, respectively). Fluoroquinolone-resistance was confirmed by mPCR in all 3 isolates of Enterobacteriaceae, in enterococci resistance to aminoglycoside-high level was detected in 1 of 3 isolates (33%) and in streptococci resistance to macrolides/lincosamides in none of 2 isolates. The overall sensitivity for different pathogens and antimicrobials was 46% and specificity 95%, the median concordance was 80% (range, 57–100%). Full agreement was observed for oxacillin in S. aureus, vancomycin in enterococci, carbapenems/cephalosporins in Enterobacteriaceae and rifampin in Cutibacterium species. CONCLUSION: The overall sensitivity for detection of antimicrobial resistance by mPCR directly from clinical samples was low. False-negative mPCR results occurred mainly in coagulase-negative staphylococci, especially for oxacillin and rifampin. However, the specificity of mPCR was high and a positive result reliably predicted antimicrobial resistance. Including universal primers in the PCR test assay may improve the detection rate but requires additional sequencing step. TRIAL REGISTRATION: www.clinicaltrials.gov No. NCT02530229, registered at 21 August 2015 (retrospectively registered). BioMed Central 2020-04-14 /pmc/articles/PMC7155317/ /pubmed/32290833 http://dx.doi.org/10.1186/s12866-020-01741-7 Text en © The Author(s) 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Sigmund, Irene Katharina Renz, Nora Feihl, Susanne Morgenstern, Christian Cabric, Sabrina Trampuz, Andrej Value of multiplex PCR for detection of antimicrobial resistance in samples retrieved from patients with orthopaedic infections |
title | Value of multiplex PCR for detection of antimicrobial resistance in samples retrieved from patients with orthopaedic infections |
title_full | Value of multiplex PCR for detection of antimicrobial resistance in samples retrieved from patients with orthopaedic infections |
title_fullStr | Value of multiplex PCR for detection of antimicrobial resistance in samples retrieved from patients with orthopaedic infections |
title_full_unstemmed | Value of multiplex PCR for detection of antimicrobial resistance in samples retrieved from patients with orthopaedic infections |
title_short | Value of multiplex PCR for detection of antimicrobial resistance in samples retrieved from patients with orthopaedic infections |
title_sort | value of multiplex pcr for detection of antimicrobial resistance in samples retrieved from patients with orthopaedic infections |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155317/ https://www.ncbi.nlm.nih.gov/pubmed/32290833 http://dx.doi.org/10.1186/s12866-020-01741-7 |
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