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Macrolide Resistance Trends in β-Hemolytic Streptococci in a Tertiary Korean Hospital

PURPOSE: Erythromycin-resistant β-hemolytic streptococci (BHS) has recently emerged and quickly spread between and within countries throughout the world. In this study, we evaluate the antimicrobial susceptibility patterns and erythromycin resistance mechanisms of BHS during 2003-2004. MATERIALS AND...

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Autores principales: Uh, Young, Hwang, Gyu Yel, Jang, In Ho, Cho, Hyun Mi, Noh, Song Mi, Kim, Hyo Youl, Kwon, Ohgun, Yoon, Kap Jun
Formato: Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2628142/
https://www.ncbi.nlm.nih.gov/pubmed/17963333
http://dx.doi.org/10.3349/ymj.2007.48.5.773
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author Uh, Young
Hwang, Gyu Yel
Jang, In Ho
Cho, Hyun Mi
Noh, Song Mi
Kim, Hyo Youl
Kwon, Ohgun
Yoon, Kap Jun
author_facet Uh, Young
Hwang, Gyu Yel
Jang, In Ho
Cho, Hyun Mi
Noh, Song Mi
Kim, Hyo Youl
Kwon, Ohgun
Yoon, Kap Jun
author_sort Uh, Young
collection PubMed
description PURPOSE: Erythromycin-resistant β-hemolytic streptococci (BHS) has recently emerged and quickly spread between and within countries throughout the world. In this study, we evaluate the antimicrobial susceptibility patterns and erythromycin resistance mechanisms of BHS during 2003-2004. MATERIALS AND METHODS: The MICs of seven antimicrobials were determined for 204 clinical isolates of BHS from 2003 to 2004. Resistance mechanisms of erythromycin-resistant BHS were studied by the double disk test as well as by polymerase chain reaction (PCR). RESULTS: Compared with our previous study, resistance among Streptococcus pyogenes isolates to a variety of drugs decreased strikingly: from 25.7% to 4.8% in erythromycin; 15.8% to 0% in clindamycin; and 47.1% to 19.0% in tetracycline. The prevalent phenotypes and genotypes of macrolide-lincosamide-streptogramin(B) (MLS(B)) resistance in Streptococcus pyogenes isolates have been changed from the constitutive MLS(B) phenotype carrying erm(B) to the M phenotype with mef(A) gene. In contrast with Streptococcus pyogenes, resistance rates to erythromycin (36.7%), clindamycin (43.1%), and tetracycline (95.4%) in Streptococcus agalactiae isolates did not show decreasing trends. Among the Streptococcus dysgalactiae subsp. equisimilis isolates (Lancefield group C, G), resistance rates to erythromycin, clindamycin, tetracycline and chloramphenicol were observed to be 9.4%, 3.1%, 68.8%, and 9.4%, respectively. CONCLUSION: Continual monitoring of antimicrobial resistance among large-colony-forming BHS is needed to provide the medical community with current data regarding the resistance mechanisms that are most common to their local or regional environments.
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spelling pubmed-26281422009-02-02 Macrolide Resistance Trends in β-Hemolytic Streptococci in a Tertiary Korean Hospital Uh, Young Hwang, Gyu Yel Jang, In Ho Cho, Hyun Mi Noh, Song Mi Kim, Hyo Youl Kwon, Ohgun Yoon, Kap Jun Yonsei Med J Original Article PURPOSE: Erythromycin-resistant β-hemolytic streptococci (BHS) has recently emerged and quickly spread between and within countries throughout the world. In this study, we evaluate the antimicrobial susceptibility patterns and erythromycin resistance mechanisms of BHS during 2003-2004. MATERIALS AND METHODS: The MICs of seven antimicrobials were determined for 204 clinical isolates of BHS from 2003 to 2004. Resistance mechanisms of erythromycin-resistant BHS were studied by the double disk test as well as by polymerase chain reaction (PCR). RESULTS: Compared with our previous study, resistance among Streptococcus pyogenes isolates to a variety of drugs decreased strikingly: from 25.7% to 4.8% in erythromycin; 15.8% to 0% in clindamycin; and 47.1% to 19.0% in tetracycline. The prevalent phenotypes and genotypes of macrolide-lincosamide-streptogramin(B) (MLS(B)) resistance in Streptococcus pyogenes isolates have been changed from the constitutive MLS(B) phenotype carrying erm(B) to the M phenotype with mef(A) gene. In contrast with Streptococcus pyogenes, resistance rates to erythromycin (36.7%), clindamycin (43.1%), and tetracycline (95.4%) in Streptococcus agalactiae isolates did not show decreasing trends. Among the Streptococcus dysgalactiae subsp. equisimilis isolates (Lancefield group C, G), resistance rates to erythromycin, clindamycin, tetracycline and chloramphenicol were observed to be 9.4%, 3.1%, 68.8%, and 9.4%, respectively. CONCLUSION: Continual monitoring of antimicrobial resistance among large-colony-forming BHS is needed to provide the medical community with current data regarding the resistance mechanisms that are most common to their local or regional environments. Yonsei University College of Medicine 2007-10-31 2007-10-31 /pmc/articles/PMC2628142/ /pubmed/17963333 http://dx.doi.org/10.3349/ymj.2007.48.5.773 Text en Copyright © 2007 The Yonsei University College of Medicine http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Uh, Young
Hwang, Gyu Yel
Jang, In Ho
Cho, Hyun Mi
Noh, Song Mi
Kim, Hyo Youl
Kwon, Ohgun
Yoon, Kap Jun
Macrolide Resistance Trends in β-Hemolytic Streptococci in a Tertiary Korean Hospital
title Macrolide Resistance Trends in β-Hemolytic Streptococci in a Tertiary Korean Hospital
title_full Macrolide Resistance Trends in β-Hemolytic Streptococci in a Tertiary Korean Hospital
title_fullStr Macrolide Resistance Trends in β-Hemolytic Streptococci in a Tertiary Korean Hospital
title_full_unstemmed Macrolide Resistance Trends in β-Hemolytic Streptococci in a Tertiary Korean Hospital
title_short Macrolide Resistance Trends in β-Hemolytic Streptococci in a Tertiary Korean Hospital
title_sort macrolide resistance trends in β-hemolytic streptococci in a tertiary korean hospital
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2628142/
https://www.ncbi.nlm.nih.gov/pubmed/17963333
http://dx.doi.org/10.3349/ymj.2007.48.5.773
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