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Biofilm Formation and Detection of Fluoroquinolone- and Carbapenem-Resistant Genes in Multidrug-Resistant Acinetobacter baumannii
Acinetobacter baumannii is an important opportunistic pathogen that shows resistance to cephalosporins, penicillins, carbapenems, fluoroquinolones, and aminoglycosides, the multiresistance being associated with its ability to form biofilms in clinical environments. The aim of this study was to deter...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Hindawi
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6939427/ https://www.ncbi.nlm.nih.gov/pubmed/31929848 http://dx.doi.org/10.1155/2019/3454907 |
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author | Avila-Novoa, María-Guadalupe Solís-Velázquez, Oscar-Alberto Rangel-López, Daniel-Eduardo González-Gómez, Jean-Pierre Guerrero-Medina, Pedro-Javier Gutiérrez-Lomelí, Melesio |
author_facet | Avila-Novoa, María-Guadalupe Solís-Velázquez, Oscar-Alberto Rangel-López, Daniel-Eduardo González-Gómez, Jean-Pierre Guerrero-Medina, Pedro-Javier Gutiérrez-Lomelí, Melesio |
author_sort | Avila-Novoa, María-Guadalupe |
collection | PubMed |
description | Acinetobacter baumannii is an important opportunistic pathogen that shows resistance to cephalosporins, penicillins, carbapenems, fluoroquinolones, and aminoglycosides, the multiresistance being associated with its ability to form biofilms in clinical environments. The aim of this study was to determine biofilm formation and its potential association with genes involved in antibiotic resistance mechanisms of A. baumannii isolates of different clinical specimens. We demonstrated 100% of the A. baumannii isolates examined to be multidrug resistant (MDR), presenting a 73.3% susceptibility to cefepime and a 53.3% susceptibility to ciprofloxacin. All A. baumannii isolates were positive for bla(OXA-51), 33.3% being positive for bla(OXA-23) and ISAba1, and 73.3% being positive for gyrA. We found 86.6% of A. baumannii strains to be low-grade biofilm formers and 13.3% to be biofilm negative; culturing on Congo red agar (CRA) plates revealed that 73.3% of the A. baumannii isolates to be biofilm producers, while 26.6% were not. These properties, combined with the role of A. baumannii as a nosocomial pathogen, increase the probability of A. baumannii causing nosocomial infections and outbreaks as a complication during therapeutic treatments and emphasize the need to control A. baumannii biofilms in hospital environments. |
format | Online Article Text |
id | pubmed-6939427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-69394272020-01-10 Biofilm Formation and Detection of Fluoroquinolone- and Carbapenem-Resistant Genes in Multidrug-Resistant Acinetobacter baumannii Avila-Novoa, María-Guadalupe Solís-Velázquez, Oscar-Alberto Rangel-López, Daniel-Eduardo González-Gómez, Jean-Pierre Guerrero-Medina, Pedro-Javier Gutiérrez-Lomelí, Melesio Can J Infect Dis Med Microbiol Research Article Acinetobacter baumannii is an important opportunistic pathogen that shows resistance to cephalosporins, penicillins, carbapenems, fluoroquinolones, and aminoglycosides, the multiresistance being associated with its ability to form biofilms in clinical environments. The aim of this study was to determine biofilm formation and its potential association with genes involved in antibiotic resistance mechanisms of A. baumannii isolates of different clinical specimens. We demonstrated 100% of the A. baumannii isolates examined to be multidrug resistant (MDR), presenting a 73.3% susceptibility to cefepime and a 53.3% susceptibility to ciprofloxacin. All A. baumannii isolates were positive for bla(OXA-51), 33.3% being positive for bla(OXA-23) and ISAba1, and 73.3% being positive for gyrA. We found 86.6% of A. baumannii strains to be low-grade biofilm formers and 13.3% to be biofilm negative; culturing on Congo red agar (CRA) plates revealed that 73.3% of the A. baumannii isolates to be biofilm producers, while 26.6% were not. These properties, combined with the role of A. baumannii as a nosocomial pathogen, increase the probability of A. baumannii causing nosocomial infections and outbreaks as a complication during therapeutic treatments and emphasize the need to control A. baumannii biofilms in hospital environments. Hindawi 2019-12-20 /pmc/articles/PMC6939427/ /pubmed/31929848 http://dx.doi.org/10.1155/2019/3454907 Text en Copyright © 2019 María-Guadalupe Avila-Novoa et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Avila-Novoa, María-Guadalupe Solís-Velázquez, Oscar-Alberto Rangel-López, Daniel-Eduardo González-Gómez, Jean-Pierre Guerrero-Medina, Pedro-Javier Gutiérrez-Lomelí, Melesio Biofilm Formation and Detection of Fluoroquinolone- and Carbapenem-Resistant Genes in Multidrug-Resistant Acinetobacter baumannii |
title | Biofilm Formation and Detection of Fluoroquinolone- and Carbapenem-Resistant Genes in Multidrug-Resistant Acinetobacter baumannii |
title_full | Biofilm Formation and Detection of Fluoroquinolone- and Carbapenem-Resistant Genes in Multidrug-Resistant Acinetobacter baumannii |
title_fullStr | Biofilm Formation and Detection of Fluoroquinolone- and Carbapenem-Resistant Genes in Multidrug-Resistant Acinetobacter baumannii |
title_full_unstemmed | Biofilm Formation and Detection of Fluoroquinolone- and Carbapenem-Resistant Genes in Multidrug-Resistant Acinetobacter baumannii |
title_short | Biofilm Formation and Detection of Fluoroquinolone- and Carbapenem-Resistant Genes in Multidrug-Resistant Acinetobacter baumannii |
title_sort | biofilm formation and detection of fluoroquinolone- and carbapenem-resistant genes in multidrug-resistant acinetobacter baumannii |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6939427/ https://www.ncbi.nlm.nih.gov/pubmed/31929848 http://dx.doi.org/10.1155/2019/3454907 |
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