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Inducible Clindamycin Resistance Is More Common in Lancefield groups C and G Streptococci Compared with group A in Clinical Specimens: A Single-center Experience, 2013 to 2016
BACKGROUND: Current susceptibility testing recommendations for β-hemolytic streptococci outline testing for clindamycin resistance, including inducible resistance by a positive D-zone phenotype. However, few studies describe the prevalence of clindamycin resistance among invasive GCS and GGS organis...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630812/ http://dx.doi.org/10.1093/ofid/ofx163.1629 |
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author | Sabin, Arick Hansen, Glen |
author_facet | Sabin, Arick Hansen, Glen |
author_sort | Sabin, Arick |
collection | PubMed |
description | BACKGROUND: Current susceptibility testing recommendations for β-hemolytic streptococci outline testing for clindamycin resistance, including inducible resistance by a positive D-zone phenotype. However, few studies describe the prevalence of clindamycin resistance among invasive GCS and GGS organisms. This study aims to describe the prevalence of clindamycin resistance among GCS/GGS compared with invasive group A streptococci (GAS) during the same period in a large United States health system. METHODS: Streptococcus isolates from blood, tissue, and body fluids (n = 298) recorded from January 1, 2013 to May 1, 2017 were audited using SafetySurveillor® software. Members of the anginosus-group streptococci were excluded. Specimens submitted to the clinical microbiology laboratory were grown in 5% CO(2) on colistin-nalidixic-acid agar, Mueller–Hinton 5% sheep blood agar, and chocolate agar. Cultures positive for β-hemolytic streptococci were identified to the species level via MALDI-TOF MS. Disk diffusion D-zone testing was performed with 0.5 McFarland standards using erythromycin (15 μg) and clindamycin (2 μg) disks 12 mm apart on Mueller–Hinton 5% sheep blood agar plates incubated at 35°C in 5% CO(2) for 20–24 hours. Susceptibilities to penicillin, erythromycin, clindamycin, and vancomycin were recorded per current CLSI breakpoints. RESULTS: A total of n = 212 GCS/GGS isolates were tested, of which n = 61 (28.8%) demonstrated clindamycin resistance; 85.2% were clindamycin resistant via a positive D-zone phenotype compared with 14.8% that were constitutively clindamycin resistant. A total of n = 86 GAS isolates were tested, of which n = 9 (10%) demonstrated clindamycin resistance; 44% reported clindamycin resistance via a positive D-zone phenotype compared with 56% which were constitutively clindamycin resistant. CONCLUSION: Clindamycin resistance among GCS and GGS was present in 24.5% of the isolates tested compared with 10% for GAS. As a proportion of the total number of isolates tested, inducible resistance was 14.5% more frequent among GCS and GGS than was observed for GAS. This study demonstrates a higher proportional level of clindamycin resistance in GCS/GGC compared with GAS infections detected over the same study period. DISCLOSURES: All authors: No reported disclosures. |
format | Online Article Text |
id | pubmed-5630812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56308122017-11-07 Inducible Clindamycin Resistance Is More Common in Lancefield groups C and G Streptococci Compared with group A in Clinical Specimens: A Single-center Experience, 2013 to 2016 Sabin, Arick Hansen, Glen Open Forum Infect Dis Abstracts BACKGROUND: Current susceptibility testing recommendations for β-hemolytic streptococci outline testing for clindamycin resistance, including inducible resistance by a positive D-zone phenotype. However, few studies describe the prevalence of clindamycin resistance among invasive GCS and GGS organisms. This study aims to describe the prevalence of clindamycin resistance among GCS/GGS compared with invasive group A streptococci (GAS) during the same period in a large United States health system. METHODS: Streptococcus isolates from blood, tissue, and body fluids (n = 298) recorded from January 1, 2013 to May 1, 2017 were audited using SafetySurveillor® software. Members of the anginosus-group streptococci were excluded. Specimens submitted to the clinical microbiology laboratory were grown in 5% CO(2) on colistin-nalidixic-acid agar, Mueller–Hinton 5% sheep blood agar, and chocolate agar. Cultures positive for β-hemolytic streptococci were identified to the species level via MALDI-TOF MS. Disk diffusion D-zone testing was performed with 0.5 McFarland standards using erythromycin (15 μg) and clindamycin (2 μg) disks 12 mm apart on Mueller–Hinton 5% sheep blood agar plates incubated at 35°C in 5% CO(2) for 20–24 hours. Susceptibilities to penicillin, erythromycin, clindamycin, and vancomycin were recorded per current CLSI breakpoints. RESULTS: A total of n = 212 GCS/GGS isolates were tested, of which n = 61 (28.8%) demonstrated clindamycin resistance; 85.2% were clindamycin resistant via a positive D-zone phenotype compared with 14.8% that were constitutively clindamycin resistant. A total of n = 86 GAS isolates were tested, of which n = 9 (10%) demonstrated clindamycin resistance; 44% reported clindamycin resistance via a positive D-zone phenotype compared with 56% which were constitutively clindamycin resistant. CONCLUSION: Clindamycin resistance among GCS and GGS was present in 24.5% of the isolates tested compared with 10% for GAS. As a proportion of the total number of isolates tested, inducible resistance was 14.5% more frequent among GCS and GGS than was observed for GAS. This study demonstrates a higher proportional level of clindamycin resistance in GCS/GGC compared with GAS infections detected over the same study period. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2017-10-04 /pmc/articles/PMC5630812/ http://dx.doi.org/10.1093/ofid/ofx163.1629 Text en © The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Sabin, Arick Hansen, Glen Inducible Clindamycin Resistance Is More Common in Lancefield groups C and G Streptococci Compared with group A in Clinical Specimens: A Single-center Experience, 2013 to 2016 |
title | Inducible Clindamycin Resistance Is More Common in Lancefield groups C and G Streptococci Compared with group A in Clinical Specimens: A Single-center Experience, 2013 to 2016 |
title_full | Inducible Clindamycin Resistance Is More Common in Lancefield groups C and G Streptococci Compared with group A in Clinical Specimens: A Single-center Experience, 2013 to 2016 |
title_fullStr | Inducible Clindamycin Resistance Is More Common in Lancefield groups C and G Streptococci Compared with group A in Clinical Specimens: A Single-center Experience, 2013 to 2016 |
title_full_unstemmed | Inducible Clindamycin Resistance Is More Common in Lancefield groups C and G Streptococci Compared with group A in Clinical Specimens: A Single-center Experience, 2013 to 2016 |
title_short | Inducible Clindamycin Resistance Is More Common in Lancefield groups C and G Streptococci Compared with group A in Clinical Specimens: A Single-center Experience, 2013 to 2016 |
title_sort | inducible clindamycin resistance is more common in lancefield groups c and g streptococci compared with group a in clinical specimens: a single-center experience, 2013 to 2016 |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630812/ http://dx.doi.org/10.1093/ofid/ofx163.1629 |
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