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Isolation and Genetic Analysis of Multidrug Resistant Bacteria from Diabetic Foot Ulcers

Severe diabetic foot ulcers (DFUs) patients visiting Sir Sunderlal Hospital, Banaras Hindu University, Varanasi, were selected for this study. Bacteria were isolated from swab and deep tissue of 42 patients, for examining their prevalence and antibiotic sensitivity. DFUs of majority of the patients...

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Autores principales: Shahi, Shailesh K., Kumar, Ashok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4700134/
https://www.ncbi.nlm.nih.gov/pubmed/26779134
http://dx.doi.org/10.3389/fmicb.2015.01464
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author Shahi, Shailesh K.
Kumar, Ashok
author_facet Shahi, Shailesh K.
Kumar, Ashok
author_sort Shahi, Shailesh K.
collection PubMed
description Severe diabetic foot ulcers (DFUs) patients visiting Sir Sunderlal Hospital, Banaras Hindu University, Varanasi, were selected for this study. Bacteria were isolated from swab and deep tissue of 42 patients, for examining their prevalence and antibiotic sensitivity. DFUs of majority of the patients were found infected with Enterococcus spp. (47.61%), Escherichia coli (35.71%), Staphylococcus spp. (33.33%), Alcaligenes spp. (30.95%), Pseudomonas spp. (30.95%), and Stenotrophomonas spp. (30.95%). Antibiotic susceptibility assay of 142 bacteria with 16 antibiotics belonging to eight classes showed the presence of 38 (26.76%) isolates with multidrug resistance (MDR) phenotypes. MDR character appeared to be governed by integrons as class 1 integrons were detected in 26 (68.42%) isolates. Altogether six different arrays of genes (aadA1, aadB, aadAV, dhfrV, dhfrXII, and dhfrXVII) were found within class 1 integron. Gene cassette dhfrAXVII-aadAV (1.6 kb) was present in 12 (3 Gram positive and 9 Gram negative) isolates and was conserved across all the isolates as evident from RFLP analysis. In addition to the presence of class 1 integron, six β-lactamase resistance encoding genes namely bla(TEM), bla(SHV), bla(OXA), bla(CTX−M−gp1), bla(CTX−M−gp2), and bla(CTX−M−gp9) and two methicillin resistance genes namely mecA and femA and vancomycin resistance encoding genes (vanA and vanB) were identified in different isolates. Majority of the MDR isolates were positive for bla(TEM) (89.47%), bla(OXA) (52.63%), and bla(CTX−M−gp1) (34.21%). To our knowledge, this is the first report of molecular characterization of antibiotic resistance in bacteria isolated from DFUs from North India. In conclusion, findings of this study suggest that class-1 integrons and β-lactamase genes contributed to the MDR in above bacteria.
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spelling pubmed-47001342016-01-15 Isolation and Genetic Analysis of Multidrug Resistant Bacteria from Diabetic Foot Ulcers Shahi, Shailesh K. Kumar, Ashok Front Microbiol Microbiology Severe diabetic foot ulcers (DFUs) patients visiting Sir Sunderlal Hospital, Banaras Hindu University, Varanasi, were selected for this study. Bacteria were isolated from swab and deep tissue of 42 patients, for examining their prevalence and antibiotic sensitivity. DFUs of majority of the patients were found infected with Enterococcus spp. (47.61%), Escherichia coli (35.71%), Staphylococcus spp. (33.33%), Alcaligenes spp. (30.95%), Pseudomonas spp. (30.95%), and Stenotrophomonas spp. (30.95%). Antibiotic susceptibility assay of 142 bacteria with 16 antibiotics belonging to eight classes showed the presence of 38 (26.76%) isolates with multidrug resistance (MDR) phenotypes. MDR character appeared to be governed by integrons as class 1 integrons were detected in 26 (68.42%) isolates. Altogether six different arrays of genes (aadA1, aadB, aadAV, dhfrV, dhfrXII, and dhfrXVII) were found within class 1 integron. Gene cassette dhfrAXVII-aadAV (1.6 kb) was present in 12 (3 Gram positive and 9 Gram negative) isolates and was conserved across all the isolates as evident from RFLP analysis. In addition to the presence of class 1 integron, six β-lactamase resistance encoding genes namely bla(TEM), bla(SHV), bla(OXA), bla(CTX−M−gp1), bla(CTX−M−gp2), and bla(CTX−M−gp9) and two methicillin resistance genes namely mecA and femA and vancomycin resistance encoding genes (vanA and vanB) were identified in different isolates. Majority of the MDR isolates were positive for bla(TEM) (89.47%), bla(OXA) (52.63%), and bla(CTX−M−gp1) (34.21%). To our knowledge, this is the first report of molecular characterization of antibiotic resistance in bacteria isolated from DFUs from North India. In conclusion, findings of this study suggest that class-1 integrons and β-lactamase genes contributed to the MDR in above bacteria. Frontiers Media S.A. 2016-01-05 /pmc/articles/PMC4700134/ /pubmed/26779134 http://dx.doi.org/10.3389/fmicb.2015.01464 Text en Copyright © 2016 Shahi and Kumar. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Shahi, Shailesh K.
Kumar, Ashok
Isolation and Genetic Analysis of Multidrug Resistant Bacteria from Diabetic Foot Ulcers
title Isolation and Genetic Analysis of Multidrug Resistant Bacteria from Diabetic Foot Ulcers
title_full Isolation and Genetic Analysis of Multidrug Resistant Bacteria from Diabetic Foot Ulcers
title_fullStr Isolation and Genetic Analysis of Multidrug Resistant Bacteria from Diabetic Foot Ulcers
title_full_unstemmed Isolation and Genetic Analysis of Multidrug Resistant Bacteria from Diabetic Foot Ulcers
title_short Isolation and Genetic Analysis of Multidrug Resistant Bacteria from Diabetic Foot Ulcers
title_sort isolation and genetic analysis of multidrug resistant bacteria from diabetic foot ulcers
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4700134/
https://www.ncbi.nlm.nih.gov/pubmed/26779134
http://dx.doi.org/10.3389/fmicb.2015.01464
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