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Phenotypic and genotypic study of macrolide, lincosamide and streptogramin B (MLS(B)) resistance in clinical isolates of Staphylococcus aureus in Tehran, Iran

BACKGROUND: Resistance to antimicrobial agents among Staphylococcus aureus is an increasing problem. Two common genes responsible for resistance to macrolide, lincosamide and streptogramin B (MLS(B)) antibiotics are the ermA and ermC genes. Three resistance phenotypes have been detected to these ant...

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Autores principales: Saderi, Horieh, Emadi, Behzad, Owlia, Parviz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3524716/
https://www.ncbi.nlm.nih.gov/pubmed/21278685
http://dx.doi.org/10.12659/MSM.881386
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author Saderi, Horieh
Emadi, Behzad
Owlia, Parviz
author_facet Saderi, Horieh
Emadi, Behzad
Owlia, Parviz
author_sort Saderi, Horieh
collection PubMed
description BACKGROUND: Resistance to antimicrobial agents among Staphylococcus aureus is an increasing problem. Two common genes responsible for resistance to macrolide, lincosamide and streptogramin B (MLS(B)) antibiotics are the ermA and ermC genes. Three resistance phenotypes have been detected to these antibiotics: strains containing cMLS(B) (constitutive MLS(B)) and iMLS(B) (inducible MLS(B)), which are resistant to macrolide, lincosamide and streptogramin B antibiotics, and MS, which is only resistant to macrolide and streptogramin B antibiotics. The aim of this study was to determine the prevalence of MLS(B) phenotypes and genotypes in erythromycin-resistant strains of S. aureus isolated from patients in 4 university hospitals in Tehran, Iran. MATERIAL/METHODS: S. aureus strains were isolated from various clinical specimens and identified by routine phenotypic methods and PCR for nuc gene. Erythromycin resistance was determined by disk diffusion testing. Prevalence of MLS(B) phenotypes was determined by use of the D-test. ermA and ermC genes were detected by PCR. RESULTS: Altogether, 126 erythromycin-resistant strains of S. aureus were detected. Prevalence of cMLS(B), iMLS(B) and MS resistance phenotypes were 92.8%, 6.4%, and 0.8%, respectively; 60.3% of strains had ermA gene and 54.8% ermC gene; 61 strains (48.4%) contained 2 studied erm genes and 42 strains (33.3%) did not have any studied erm genes. CONCLUSIONS: Due to the high prevalence of clindamycin resistance among S. aureus isolated from patients in Iran, we recommend clindamycin therapy only after proper antimicrobial susceptibility testing.
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spelling pubmed-35247162013-04-24 Phenotypic and genotypic study of macrolide, lincosamide and streptogramin B (MLS(B)) resistance in clinical isolates of Staphylococcus aureus in Tehran, Iran Saderi, Horieh Emadi, Behzad Owlia, Parviz Med Sci Monit Basic Research BACKGROUND: Resistance to antimicrobial agents among Staphylococcus aureus is an increasing problem. Two common genes responsible for resistance to macrolide, lincosamide and streptogramin B (MLS(B)) antibiotics are the ermA and ermC genes. Three resistance phenotypes have been detected to these antibiotics: strains containing cMLS(B) (constitutive MLS(B)) and iMLS(B) (inducible MLS(B)), which are resistant to macrolide, lincosamide and streptogramin B antibiotics, and MS, which is only resistant to macrolide and streptogramin B antibiotics. The aim of this study was to determine the prevalence of MLS(B) phenotypes and genotypes in erythromycin-resistant strains of S. aureus isolated from patients in 4 university hospitals in Tehran, Iran. MATERIAL/METHODS: S. aureus strains were isolated from various clinical specimens and identified by routine phenotypic methods and PCR for nuc gene. Erythromycin resistance was determined by disk diffusion testing. Prevalence of MLS(B) phenotypes was determined by use of the D-test. ermA and ermC genes were detected by PCR. RESULTS: Altogether, 126 erythromycin-resistant strains of S. aureus were detected. Prevalence of cMLS(B), iMLS(B) and MS resistance phenotypes were 92.8%, 6.4%, and 0.8%, respectively; 60.3% of strains had ermA gene and 54.8% ermC gene; 61 strains (48.4%) contained 2 studied erm genes and 42 strains (33.3%) did not have any studied erm genes. CONCLUSIONS: Due to the high prevalence of clindamycin resistance among S. aureus isolated from patients in Iran, we recommend clindamycin therapy only after proper antimicrobial susceptibility testing. International Scientific Literature, Inc. 2011-02-01 /pmc/articles/PMC3524716/ /pubmed/21278685 http://dx.doi.org/10.12659/MSM.881386 Text en © Med Sci Monit, 2011 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.
spellingShingle Basic Research
Saderi, Horieh
Emadi, Behzad
Owlia, Parviz
Phenotypic and genotypic study of macrolide, lincosamide and streptogramin B (MLS(B)) resistance in clinical isolates of Staphylococcus aureus in Tehran, Iran
title Phenotypic and genotypic study of macrolide, lincosamide and streptogramin B (MLS(B)) resistance in clinical isolates of Staphylococcus aureus in Tehran, Iran
title_full Phenotypic and genotypic study of macrolide, lincosamide and streptogramin B (MLS(B)) resistance in clinical isolates of Staphylococcus aureus in Tehran, Iran
title_fullStr Phenotypic and genotypic study of macrolide, lincosamide and streptogramin B (MLS(B)) resistance in clinical isolates of Staphylococcus aureus in Tehran, Iran
title_full_unstemmed Phenotypic and genotypic study of macrolide, lincosamide and streptogramin B (MLS(B)) resistance in clinical isolates of Staphylococcus aureus in Tehran, Iran
title_short Phenotypic and genotypic study of macrolide, lincosamide and streptogramin B (MLS(B)) resistance in clinical isolates of Staphylococcus aureus in Tehran, Iran
title_sort phenotypic and genotypic study of macrolide, lincosamide and streptogramin b (mls(b)) resistance in clinical isolates of staphylococcus aureus in tehran, iran
topic Basic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3524716/
https://www.ncbi.nlm.nih.gov/pubmed/21278685
http://dx.doi.org/10.12659/MSM.881386
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