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Biofilm-Formation in Clonally Unrelated Multidrug-Resistant Acinetobacter baumannii Isolates

This study analyzed the genotype, antibiotic resistance, and biofilm formation of Acinetobacter baumannii strains and assessed the correlation between biofilm formation, antibiotic resistance, and biofilm-related risk factors. A total of 207 non-replicate multi-drug-resistant A. baumannii strains we...

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Autores principales: Alamri, Aisha M., Alsultan, Afnan A., Ansari, Mohammad A., Alnimr, Amani M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460364/
https://www.ncbi.nlm.nih.gov/pubmed/32748817
http://dx.doi.org/10.3390/pathogens9080630
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author Alamri, Aisha M.
Alsultan, Afnan A.
Ansari, Mohammad A.
Alnimr, Amani M.
author_facet Alamri, Aisha M.
Alsultan, Afnan A.
Ansari, Mohammad A.
Alnimr, Amani M.
author_sort Alamri, Aisha M.
collection PubMed
description This study analyzed the genotype, antibiotic resistance, and biofilm formation of Acinetobacter baumannii strains and assessed the correlation between biofilm formation, antibiotic resistance, and biofilm-related risk factors. A total of 207 non-replicate multi-drug-resistant A. baumannii strains were prospectively isolated. Phenotypic identification and antimicrobial susceptibility testing were carried out. Isolate biofilm formation ability was evaluated using the tissue culture plate (TCP), Congo red agar, and tube methods. Clonal relatedness between the strains was assessed by enterobacterial repetitive intergenic consensus-PCR genotyping. Of the 207 isolates, 52.5% originated from an intensive care unit setting, and pan resistance was observed against ceftazidime and cefepime, with elevated resistance (99–94%) to piperacillin/tazobactam, imipenem, levofloxacin, and ciprofloxacin. alongside high susceptibility to tigecycline (97.8%). The Tissue culture plate, Tube method, and Congo red agar methods revealed that 53.6%, 20.8%, and 2.7% of the strains were strong biofilm producers, respectively, while a significant correlation was observed between biofilm formation and device-originating respiratory isolates (p = 0.0009) and between biofilm formation in colonized vs. true infection isolates (p = 0.0001). No correlation was detected between antibiotic resistance and biofilm formation capacity, and the majority of isolates were clonally unrelated. These findings highlight the urgent need for implementing strict infection control measures in clinical settings.
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spelling pubmed-74603642020-09-02 Biofilm-Formation in Clonally Unrelated Multidrug-Resistant Acinetobacter baumannii Isolates Alamri, Aisha M. Alsultan, Afnan A. Ansari, Mohammad A. Alnimr, Amani M. Pathogens Article This study analyzed the genotype, antibiotic resistance, and biofilm formation of Acinetobacter baumannii strains and assessed the correlation between biofilm formation, antibiotic resistance, and biofilm-related risk factors. A total of 207 non-replicate multi-drug-resistant A. baumannii strains were prospectively isolated. Phenotypic identification and antimicrobial susceptibility testing were carried out. Isolate biofilm formation ability was evaluated using the tissue culture plate (TCP), Congo red agar, and tube methods. Clonal relatedness between the strains was assessed by enterobacterial repetitive intergenic consensus-PCR genotyping. Of the 207 isolates, 52.5% originated from an intensive care unit setting, and pan resistance was observed against ceftazidime and cefepime, with elevated resistance (99–94%) to piperacillin/tazobactam, imipenem, levofloxacin, and ciprofloxacin. alongside high susceptibility to tigecycline (97.8%). The Tissue culture plate, Tube method, and Congo red agar methods revealed that 53.6%, 20.8%, and 2.7% of the strains were strong biofilm producers, respectively, while a significant correlation was observed between biofilm formation and device-originating respiratory isolates (p = 0.0009) and between biofilm formation in colonized vs. true infection isolates (p = 0.0001). No correlation was detected between antibiotic resistance and biofilm formation capacity, and the majority of isolates were clonally unrelated. These findings highlight the urgent need for implementing strict infection control measures in clinical settings. MDPI 2020-08-02 /pmc/articles/PMC7460364/ /pubmed/32748817 http://dx.doi.org/10.3390/pathogens9080630 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Alamri, Aisha M.
Alsultan, Afnan A.
Ansari, Mohammad A.
Alnimr, Amani M.
Biofilm-Formation in Clonally Unrelated Multidrug-Resistant Acinetobacter baumannii Isolates
title Biofilm-Formation in Clonally Unrelated Multidrug-Resistant Acinetobacter baumannii Isolates
title_full Biofilm-Formation in Clonally Unrelated Multidrug-Resistant Acinetobacter baumannii Isolates
title_fullStr Biofilm-Formation in Clonally Unrelated Multidrug-Resistant Acinetobacter baumannii Isolates
title_full_unstemmed Biofilm-Formation in Clonally Unrelated Multidrug-Resistant Acinetobacter baumannii Isolates
title_short Biofilm-Formation in Clonally Unrelated Multidrug-Resistant Acinetobacter baumannii Isolates
title_sort biofilm-formation in clonally unrelated multidrug-resistant acinetobacter baumannii isolates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7460364/
https://www.ncbi.nlm.nih.gov/pubmed/32748817
http://dx.doi.org/10.3390/pathogens9080630
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