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Evaluation of commercial probiotic lactic cultures against biofilm formation by Cronobacter sakazakii

BACKGROUND/AIMS: Cronobacter sakazakii, an emergent pathogen is considered as a major concern to infants and neonates fed on reconstituted powdered infant milk formula. In conjunction with many other factors, biofilm forming capacity adds to its pathogenic potential. In view of the facts that infant...

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Autores principales: Jamwal, Anubhav, Sharma, Kavita, Chauhan, Rajni, Bansal, Saurabh, Goel, Gunjan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association for the Study of Intestinal Diseases 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6505092/
https://www.ncbi.nlm.nih.gov/pubmed/30508474
http://dx.doi.org/10.5217/ir.2018.00106
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author Jamwal, Anubhav
Sharma, Kavita
Chauhan, Rajni
Bansal, Saurabh
Goel, Gunjan
author_facet Jamwal, Anubhav
Sharma, Kavita
Chauhan, Rajni
Bansal, Saurabh
Goel, Gunjan
author_sort Jamwal, Anubhav
collection PubMed
description BACKGROUND/AIMS: Cronobacter sakazakii, an emergent pathogen is considered as a major concern to infants and neonates fed on reconstituted powdered infant milk formula. In conjunction with many other factors, biofilm forming capacity adds to its pathogenic potential. In view of the facts that infants are at highest risk to C. sakazakii infections, and emerging antibiotic resistance among pathogens, it is imperative to evaluate probiotic cultures for their efficacy against C. sakazakii. Therefore, pure probiotic strains were isolated from commercial probiotic products and tested for their antimicrobial and anti-biofilm activities against C. sakazakii. METHODS: A total of 6 probiotic strains were tested for their antibiotic susceptibility followed by antimicrobial activity using cell-free supernatant (CFS) against C. sakazakii. The inhibitory activity of CFS against biofilm formation by C. sakazakii was determined using standard crystal violet assay and microscopic observations. RESULTS: All the probiotic strains were sensitive to ampicillin, tetracycline, vancomycin and carbenicillin whereas most of the strains were resistant to erythromycin and novobiocin. Four of the 6 probiotic derived CFS possessed antimicrobial activity against C. sakazakii at a level of 40 μL. A higher biofilm inhibitory activity (>80%) was observed at initial stages of biofilm formation with weaker activity during longer incubation upto 48 hours (50%–60%). CONCLUSIONS: The study indicated the efficacy of isolated commercial probiotics strains as potential inhibitor of biofilm formation by C. sakazakii and could be further explored for novel bioactive molecules to limit the emerging infections of C. sakazakii.
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spelling pubmed-65050922019-05-20 Evaluation of commercial probiotic lactic cultures against biofilm formation by Cronobacter sakazakii Jamwal, Anubhav Sharma, Kavita Chauhan, Rajni Bansal, Saurabh Goel, Gunjan Intest Res Original Article BACKGROUND/AIMS: Cronobacter sakazakii, an emergent pathogen is considered as a major concern to infants and neonates fed on reconstituted powdered infant milk formula. In conjunction with many other factors, biofilm forming capacity adds to its pathogenic potential. In view of the facts that infants are at highest risk to C. sakazakii infections, and emerging antibiotic resistance among pathogens, it is imperative to evaluate probiotic cultures for their efficacy against C. sakazakii. Therefore, pure probiotic strains were isolated from commercial probiotic products and tested for their antimicrobial and anti-biofilm activities against C. sakazakii. METHODS: A total of 6 probiotic strains were tested for their antibiotic susceptibility followed by antimicrobial activity using cell-free supernatant (CFS) against C. sakazakii. The inhibitory activity of CFS against biofilm formation by C. sakazakii was determined using standard crystal violet assay and microscopic observations. RESULTS: All the probiotic strains were sensitive to ampicillin, tetracycline, vancomycin and carbenicillin whereas most of the strains were resistant to erythromycin and novobiocin. Four of the 6 probiotic derived CFS possessed antimicrobial activity against C. sakazakii at a level of 40 μL. A higher biofilm inhibitory activity (>80%) was observed at initial stages of biofilm formation with weaker activity during longer incubation upto 48 hours (50%–60%). CONCLUSIONS: The study indicated the efficacy of isolated commercial probiotics strains as potential inhibitor of biofilm formation by C. sakazakii and could be further explored for novel bioactive molecules to limit the emerging infections of C. sakazakii. Korean Association for the Study of Intestinal Diseases 2019-04 2018-12-03 /pmc/articles/PMC6505092/ /pubmed/30508474 http://dx.doi.org/10.5217/ir.2018.00106 Text en © Copyright 2019. Korean Association for the Study of Intestinal Diseases. All rights reserved. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jamwal, Anubhav
Sharma, Kavita
Chauhan, Rajni
Bansal, Saurabh
Goel, Gunjan
Evaluation of commercial probiotic lactic cultures against biofilm formation by Cronobacter sakazakii
title Evaluation of commercial probiotic lactic cultures against biofilm formation by Cronobacter sakazakii
title_full Evaluation of commercial probiotic lactic cultures against biofilm formation by Cronobacter sakazakii
title_fullStr Evaluation of commercial probiotic lactic cultures against biofilm formation by Cronobacter sakazakii
title_full_unstemmed Evaluation of commercial probiotic lactic cultures against biofilm formation by Cronobacter sakazakii
title_short Evaluation of commercial probiotic lactic cultures against biofilm formation by Cronobacter sakazakii
title_sort evaluation of commercial probiotic lactic cultures against biofilm formation by cronobacter sakazakii
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6505092/
https://www.ncbi.nlm.nih.gov/pubmed/30508474
http://dx.doi.org/10.5217/ir.2018.00106
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