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Antibiofilm Activity, Compound Characterization, and Acute Toxicity of Extract from a Novel Bacterial Species of Paenibacillus
The effectiveness of many antimicrobial agents is currently decreasing; therefore, it is important to search for alternative therapeutics. Our study was carried out to assess the in vitro antibiofilm activity using microtiter plate assay, to characterize the bioactive compounds using Ultra Performan...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982407/ https://www.ncbi.nlm.nih.gov/pubmed/24790603 http://dx.doi.org/10.1155/2014/649420 |
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author | Alasil, Saad Musbah Omar, Rahmat Ismail, Salmah Yusof, Mohd Yasim |
author_facet | Alasil, Saad Musbah Omar, Rahmat Ismail, Salmah Yusof, Mohd Yasim |
author_sort | Alasil, Saad Musbah |
collection | PubMed |
description | The effectiveness of many antimicrobial agents is currently decreasing; therefore, it is important to search for alternative therapeutics. Our study was carried out to assess the in vitro antibiofilm activity using microtiter plate assay, to characterize the bioactive compounds using Ultra Performance Liquid Chromatography-Diode Array Detection and Liquid Chromatography-Mass Spectrometry and to test the oral acute toxicity on Sprague Dawley rats of extract derived from a novel bacterial species of Paenibacillus strain 139SI. Our results indicate that the crude extract and its three identified compounds exhibit strong antibiofilm activity against a broad range of clinically important pathogens. Three potential compounds were identified including an amino acid antibiotic C(8)H(20)N(3)O(4)P (MW 253.237), phospholipase A2 inhibitor C(21)H(36)O(5) (MW 368.512), and an antibacterial agent C(14)H(11)N(3)O(2) (MW 253.260). The acute toxicity test indicates that the mortality rate among all rats was low and that the biochemical parameters, hematological profile, and histopathology examination of liver and kidneys showed no significant differences between experimental groups (P > 0.05). Overall, our findings suggest that the extract and its purified compounds derived from novel Paenibacillus sp. are nontoxic exhibiting strong antibiofilm activity against Gram-positive and Gram-negative pathogens that can be useful towards new therapeutic management of biofilm-associated infections. |
format | Online Article Text |
id | pubmed-3982407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-39824072014-04-30 Antibiofilm Activity, Compound Characterization, and Acute Toxicity of Extract from a Novel Bacterial Species of Paenibacillus Alasil, Saad Musbah Omar, Rahmat Ismail, Salmah Yusof, Mohd Yasim Int J Microbiol Research Article The effectiveness of many antimicrobial agents is currently decreasing; therefore, it is important to search for alternative therapeutics. Our study was carried out to assess the in vitro antibiofilm activity using microtiter plate assay, to characterize the bioactive compounds using Ultra Performance Liquid Chromatography-Diode Array Detection and Liquid Chromatography-Mass Spectrometry and to test the oral acute toxicity on Sprague Dawley rats of extract derived from a novel bacterial species of Paenibacillus strain 139SI. Our results indicate that the crude extract and its three identified compounds exhibit strong antibiofilm activity against a broad range of clinically important pathogens. Three potential compounds were identified including an amino acid antibiotic C(8)H(20)N(3)O(4)P (MW 253.237), phospholipase A2 inhibitor C(21)H(36)O(5) (MW 368.512), and an antibacterial agent C(14)H(11)N(3)O(2) (MW 253.260). The acute toxicity test indicates that the mortality rate among all rats was low and that the biochemical parameters, hematological profile, and histopathology examination of liver and kidneys showed no significant differences between experimental groups (P > 0.05). Overall, our findings suggest that the extract and its purified compounds derived from novel Paenibacillus sp. are nontoxic exhibiting strong antibiofilm activity against Gram-positive and Gram-negative pathogens that can be useful towards new therapeutic management of biofilm-associated infections. Hindawi Publishing Corporation 2014 2014-03-24 /pmc/articles/PMC3982407/ /pubmed/24790603 http://dx.doi.org/10.1155/2014/649420 Text en Copyright © 2014 Saad Musbah Alasil et al. https://creativecommons.org/licenses/by/3.0/ 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 Alasil, Saad Musbah Omar, Rahmat Ismail, Salmah Yusof, Mohd Yasim Antibiofilm Activity, Compound Characterization, and Acute Toxicity of Extract from a Novel Bacterial Species of Paenibacillus |
title | Antibiofilm Activity, Compound Characterization, and Acute Toxicity of Extract from a Novel Bacterial Species of Paenibacillus
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title_full | Antibiofilm Activity, Compound Characterization, and Acute Toxicity of Extract from a Novel Bacterial Species of Paenibacillus
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title_fullStr | Antibiofilm Activity, Compound Characterization, and Acute Toxicity of Extract from a Novel Bacterial Species of Paenibacillus
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title_full_unstemmed | Antibiofilm Activity, Compound Characterization, and Acute Toxicity of Extract from a Novel Bacterial Species of Paenibacillus
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title_short | Antibiofilm Activity, Compound Characterization, and Acute Toxicity of Extract from a Novel Bacterial Species of Paenibacillus
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title_sort | antibiofilm activity, compound characterization, and acute toxicity of extract from a novel bacterial species of paenibacillus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982407/ https://www.ncbi.nlm.nih.gov/pubmed/24790603 http://dx.doi.org/10.1155/2014/649420 |
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