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Characterization of biofilm formed by multidrug resistant Pseudomonas aeruginosa DC-17 isolated from dental caries
The present work reports with the screening of biofilm-producing bacteria from the dental caries. The dental pathogens showed resistance against various antibiotics and biofilm forming ability at various levels. Among the bacterial strain, Pseudomonas aeruginosa DC-17 showed enhanced biofilm product...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569125/ https://www.ncbi.nlm.nih.gov/pubmed/33100852 http://dx.doi.org/10.1016/j.sjbs.2020.07.020 |
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author | Wu, Xiaojuan Al Farraj, Dunia A. Rajaselvam, Jayarajapazham Alkufeidy, Roua M. Vijayaraghavan, Ponnuswamy Alkubaisi, Noorah A. Agastian, P. Alshammari, Maryam K. |
author_facet | Wu, Xiaojuan Al Farraj, Dunia A. Rajaselvam, Jayarajapazham Alkufeidy, Roua M. Vijayaraghavan, Ponnuswamy Alkubaisi, Noorah A. Agastian, P. Alshammari, Maryam K. |
author_sort | Wu, Xiaojuan |
collection | PubMed |
description | The present work reports with the screening of biofilm-producing bacteria from the dental caries. The dental pathogens showed resistance against various antibiotics and biofilm forming ability at various levels. Among the bacterial strain, Pseudomonas aeruginosa DC-17 showed enhanced biofilm production. Extracellular polymeric substance (EPS) was synthesized by the selected bacterial isolate considerably and contributed as the major component of biofilm. EPS composed of eDNA, proteins and lipids. The total protein content of the EPS was found to be 1.928 mg/mL and was the major component than carbohydrate and DNA. Carbohydrate content was 162.3 mg/L and DNA content of EPS was 4.95 μg/mL. These macromolecules interacted in the matrix to develop dynamic and specific interactions to signalling biofilm to differentiating various environments. Also, the isolated bacteria showed resistant against various commercially available antibiotics. The isolates showed more resistance against penicillin (98%) and were sensitive against amoxicillin. Among the factors, temperature, pH and sugar concentration influenced biofilm formation. Biofilm forming ability of the selected bacterial stain was tested at various pH values and alkaline pH was favoured for biofilm production. Biofilm production was found to be maximum at 40 °C and 8% sucrose enhanced biofilm formation. Biofilm formed by P. aeruginosa DC-17 was resistant against various tested antimicrobials and chemicals. |
format | Online Article Text |
id | pubmed-7569125 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-75691252020-10-22 Characterization of biofilm formed by multidrug resistant Pseudomonas aeruginosa DC-17 isolated from dental caries Wu, Xiaojuan Al Farraj, Dunia A. Rajaselvam, Jayarajapazham Alkufeidy, Roua M. Vijayaraghavan, Ponnuswamy Alkubaisi, Noorah A. Agastian, P. Alshammari, Maryam K. Saudi J Biol Sci Original Article The present work reports with the screening of biofilm-producing bacteria from the dental caries. The dental pathogens showed resistance against various antibiotics and biofilm forming ability at various levels. Among the bacterial strain, Pseudomonas aeruginosa DC-17 showed enhanced biofilm production. Extracellular polymeric substance (EPS) was synthesized by the selected bacterial isolate considerably and contributed as the major component of biofilm. EPS composed of eDNA, proteins and lipids. The total protein content of the EPS was found to be 1.928 mg/mL and was the major component than carbohydrate and DNA. Carbohydrate content was 162.3 mg/L and DNA content of EPS was 4.95 μg/mL. These macromolecules interacted in the matrix to develop dynamic and specific interactions to signalling biofilm to differentiating various environments. Also, the isolated bacteria showed resistant against various commercially available antibiotics. The isolates showed more resistance against penicillin (98%) and were sensitive against amoxicillin. Among the factors, temperature, pH and sugar concentration influenced biofilm formation. Biofilm forming ability of the selected bacterial stain was tested at various pH values and alkaline pH was favoured for biofilm production. Biofilm production was found to be maximum at 40 °C and 8% sucrose enhanced biofilm formation. Biofilm formed by P. aeruginosa DC-17 was resistant against various tested antimicrobials and chemicals. Elsevier 2020-11 2020-07-18 /pmc/articles/PMC7569125/ /pubmed/33100852 http://dx.doi.org/10.1016/j.sjbs.2020.07.020 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Wu, Xiaojuan Al Farraj, Dunia A. Rajaselvam, Jayarajapazham Alkufeidy, Roua M. Vijayaraghavan, Ponnuswamy Alkubaisi, Noorah A. Agastian, P. Alshammari, Maryam K. Characterization of biofilm formed by multidrug resistant Pseudomonas aeruginosa DC-17 isolated from dental caries |
title | Characterization of biofilm formed by multidrug resistant Pseudomonas aeruginosa DC-17 isolated from dental caries |
title_full | Characterization of biofilm formed by multidrug resistant Pseudomonas aeruginosa DC-17 isolated from dental caries |
title_fullStr | Characterization of biofilm formed by multidrug resistant Pseudomonas aeruginosa DC-17 isolated from dental caries |
title_full_unstemmed | Characterization of biofilm formed by multidrug resistant Pseudomonas aeruginosa DC-17 isolated from dental caries |
title_short | Characterization of biofilm formed by multidrug resistant Pseudomonas aeruginosa DC-17 isolated from dental caries |
title_sort | characterization of biofilm formed by multidrug resistant pseudomonas aeruginosa dc-17 isolated from dental caries |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569125/ https://www.ncbi.nlm.nih.gov/pubmed/33100852 http://dx.doi.org/10.1016/j.sjbs.2020.07.020 |
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