Detection of inducible and constitutive clindamycin resistance among Staphylococcus aureus isolates in a tertiary care hospital, Eastern India

Introduction: Clindamycin is an excellent drug for skin and soft tissue Staphylococcus aureus infections, but resistance mediated by inducible macrolide-lincosamide-streptogramin B (iMLS B ) phenotype leads to in vivo therapeutic failure even though they may be in vitro susceptible in Kirby-Bauer di...

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Main Authors: Subasini Majhi, Muktikesh Dash, Dharitri Mohapatra, Ashoka Mohapatra, Nirupama Chayani
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-07-01
Series:Avicenna Journal of Medicine
Subjects:
Online Access:http://www.thieme-connect.de/DOI/DOI?10.4103/2231-0770.184066
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spelling doaj-97392d6ad17546f3b9c934215e4ea8c92021-08-09T23:49:58ZengWolters Kluwer Medknow PublicationsAvicenna Journal of Medicine2231-07702249-44642016-07-010603758010.4103/2231-0770.184066Detection of inducible and constitutive clindamycin resistance among Staphylococcus aureus isolates in a tertiary care hospital, Eastern IndiaSubasini Majhi0Muktikesh Dash1Dharitri Mohapatra2Ashoka Mohapatra3Nirupama Chayani4Department of Microbiology, Sriram Chandra Bhanj Medical College and Hospital, Cuttack, Utkal University, Bhubaneswar, Odisha, IndiaDepartment of Microbiology, Sriram Chandra Bhanj Medical College and Hospital, Cuttack, Utkal University, Bhubaneswar, Odisha, IndiaDepartment of Microbiology, Sriram Chandra Bhanj Medical College and Hospital, Cuttack, Utkal University, Bhubaneswar, Odisha, IndiaDepartment of Microbiology, All India Institute of Medical Sciences, Bhubaneswar, Odisha, IndiaDepartment of Microbiology, Sriram Chandra Bhanj Medical College and Hospital, Cuttack, Utkal University, Bhubaneswar, Odisha, IndiaIntroduction: Clindamycin is an excellent drug for skin and soft tissue Staphylococcus aureus infections, but resistance mediated by inducible macrolide-lincosamide-streptogramin B (iMLS B ) phenotype leads to in vivo therapeutic failure even though they may be in vitro susceptible in Kirby-Bauer disk diffusion method. Objective: The study was aimed to detect the prevalence of iMLS B phenotype among S. aureus isolates by double disk approximation test (D-test) in a tertiary care hospital, Eastern India. Materials and Methods: A total of 209 consecutive S. aureus isolates were identified by conventional methods and subjected to antimicrobial susceptibility testing by Kirby-Bauer disk diffusion method. Erythromycin-resistant isolates were tested for D-test. Results: From 1282 clinical specimens, 209 nonrepeated S. aureus isolates were obtained. Majority of isolates 129 (61.7%) were methicillin-resistant S. aureus (MRSA). There was statistically significant difference between outpatients 60.1% and inpatients 39.9% (P < 0.0001). From 209 S. aureus isolates, 46 (22%) were D-test positive (iMLS B phenotype), 41 (19.6%) were D-test negative (methicillin sensitive [MS] phenotype), and 37 (17.7%) were constitutively resistant (constitutive macrolide-lincosamide-streptogramin B phenotype). The incidence of inducible, constitutive, and MS phenotype was higher in MRSA isolates compared to MS S. aureus (MSSA). The constitutive clindamycin resistance difference between MSSA and MRSA isolates were found to be statistically significant (P = 0.0086). Conclusion: The study revealed 22% of S. aureus isolates were inducible clindamycin resistant, which could be easily misidentified as clindamycin susceptible in Kirby-Bauer disk diffusion method. Therefore, clinical microbiology laboratory should routinely perform D-test in all clinically isolated S. aureus to guide clinicians for the appropriate use of clindamycin.http://www.thieme-connect.de/DOI/DOI?10.4103/2231-0770.184066constitutive macrolide-lincosamide-streptogramin b phenotyped-testinducible macrolide-lincosamide-streptogramin b phenotypemethicillin-resistant staphylococcus aureussensitive methicillin phenotypemethicillin-sensitive staphylococcus aureusstaphylococcus aureus
collection DOAJ
language English
format Article
sources DOAJ
author Subasini Majhi
Muktikesh Dash
Dharitri Mohapatra
Ashoka Mohapatra
Nirupama Chayani
spellingShingle Subasini Majhi
Muktikesh Dash
Dharitri Mohapatra
Ashoka Mohapatra
Nirupama Chayani
Detection of inducible and constitutive clindamycin resistance among Staphylococcus aureus isolates in a tertiary care hospital, Eastern India
Avicenna Journal of Medicine
constitutive macrolide-lincosamide-streptogramin b phenotype
d-test
inducible macrolide-lincosamide-streptogramin b phenotype
methicillin-resistant staphylococcus aureus
sensitive methicillin phenotype
methicillin-sensitive staphylococcus aureus
staphylococcus aureus
author_facet Subasini Majhi
Muktikesh Dash
Dharitri Mohapatra
Ashoka Mohapatra
Nirupama Chayani
author_sort Subasini Majhi
title Detection of inducible and constitutive clindamycin resistance among Staphylococcus aureus isolates in a tertiary care hospital, Eastern India
title_short Detection of inducible and constitutive clindamycin resistance among Staphylococcus aureus isolates in a tertiary care hospital, Eastern India
title_full Detection of inducible and constitutive clindamycin resistance among Staphylococcus aureus isolates in a tertiary care hospital, Eastern India
title_fullStr Detection of inducible and constitutive clindamycin resistance among Staphylococcus aureus isolates in a tertiary care hospital, Eastern India
title_full_unstemmed Detection of inducible and constitutive clindamycin resistance among Staphylococcus aureus isolates in a tertiary care hospital, Eastern India
title_sort detection of inducible and constitutive clindamycin resistance among staphylococcus aureus isolates in a tertiary care hospital, eastern india
publisher Wolters Kluwer Medknow Publications
series Avicenna Journal of Medicine
issn 2231-0770
2249-4464
publishDate 2016-07-01
description Introduction: Clindamycin is an excellent drug for skin and soft tissue Staphylococcus aureus infections, but resistance mediated by inducible macrolide-lincosamide-streptogramin B (iMLS B ) phenotype leads to in vivo therapeutic failure even though they may be in vitro susceptible in Kirby-Bauer disk diffusion method. Objective: The study was aimed to detect the prevalence of iMLS B phenotype among S. aureus isolates by double disk approximation test (D-test) in a tertiary care hospital, Eastern India. Materials and Methods: A total of 209 consecutive S. aureus isolates were identified by conventional methods and subjected to antimicrobial susceptibility testing by Kirby-Bauer disk diffusion method. Erythromycin-resistant isolates were tested for D-test. Results: From 1282 clinical specimens, 209 nonrepeated S. aureus isolates were obtained. Majority of isolates 129 (61.7%) were methicillin-resistant S. aureus (MRSA). There was statistically significant difference between outpatients 60.1% and inpatients 39.9% (P < 0.0001). From 209 S. aureus isolates, 46 (22%) were D-test positive (iMLS B phenotype), 41 (19.6%) were D-test negative (methicillin sensitive [MS] phenotype), and 37 (17.7%) were constitutively resistant (constitutive macrolide-lincosamide-streptogramin B phenotype). The incidence of inducible, constitutive, and MS phenotype was higher in MRSA isolates compared to MS S. aureus (MSSA). The constitutive clindamycin resistance difference between MSSA and MRSA isolates were found to be statistically significant (P = 0.0086). Conclusion: The study revealed 22% of S. aureus isolates were inducible clindamycin resistant, which could be easily misidentified as clindamycin susceptible in Kirby-Bauer disk diffusion method. Therefore, clinical microbiology laboratory should routinely perform D-test in all clinically isolated S. aureus to guide clinicians for the appropriate use of clindamycin.
topic constitutive macrolide-lincosamide-streptogramin b phenotype
d-test
inducible macrolide-lincosamide-streptogramin b phenotype
methicillin-resistant staphylococcus aureus
sensitive methicillin phenotype
methicillin-sensitive staphylococcus aureus
staphylococcus aureus
url http://www.thieme-connect.de/DOI/DOI?10.4103/2231-0770.184066
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