Isolation and characterization of novel Streptomyces strain from Algeria and its in-vitro antimicrobial properties against microbial pathogens

Background: The constant development of microbial resistance to the traditional antimicrobial agents and the emergence of new infectious diseases justify the urgent need for new effective antimicrobial molecules. However, the irrational use of antibiotics increases microbial resistance dramatically...

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Main Authors: Fatima Zohra Djebbah, Larbi Belyagoubi, Djamel Eddine Abdelouahid, Farid Kherbouche, Naif Abdullah Al-Dhabi, Mariadhas Valan Arasu, Balasubramani Ravindran
Format: Article
Language:English
Published: Elsevier 2021-11-01
Series:Journal of Infection and Public Health
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1876034121003099
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author Fatima Zohra Djebbah
Larbi Belyagoubi
Djamel Eddine Abdelouahid
Farid Kherbouche
Naif Abdullah Al-Dhabi
Mariadhas Valan Arasu
Balasubramani Ravindran
author_facet Fatima Zohra Djebbah
Larbi Belyagoubi
Djamel Eddine Abdelouahid
Farid Kherbouche
Naif Abdullah Al-Dhabi
Mariadhas Valan Arasu
Balasubramani Ravindran
author_sort Fatima Zohra Djebbah
collection DOAJ
description Background: The constant development of microbial resistance to the traditional antimicrobial agents and the emergence of new infectious diseases justify the urgent need for new effective antimicrobial molecules. However, the irrational use of antibiotics increases microbial resistance dramatically and along with that the frequency of mortality associated with infections is higher. Therefore, to combat the antimicrobial resistance, the screening of compounds with novel chemical structures is essential. This study intended to determine the antimicrobial potential of Streptomyces GLD22 strain isolated from Algeria. Methods: The characterization of Streptomyces strain GLD22 was performed by physiological, biochemical and molecular tests. The antimicrobial activity was tested by the well diffusion method and the minimum inhibitory concentration value calculation were performed using broth micro dilution technique. The extracellular metabolites profiling was done using GC–MS. Results: Physiological, biochemical and phylogenetic analysis confirmed that the strain GLD22 showed maximum identity towards Streptomyces species. The extra cellular metabolites revealed their antimicrobial activity at 1 mg/ml for Klebsiella pneumoniae, Pseudomonas aeruginosa and Escherichia coli, whereas Staphylococcus aureus, Bacillus cereus and Bacillus subtilis documented 0.5, 1 and 1 mg/ml respectively. GC–MS analysis confirmed that 2-tert-butyl-4,6-bis(3,5-di-tert-butyl-4-hydroxybenzyl) phenol, Dibutyl phthalate and Cyclo(leucyloprolyl) were the major drug molecules present in the extract. Conclusion: The novel Streptomyces strain GLD22 recovered from the Gueldaman cave of Algeria showed better antimicrobial activity towards both Gram positive and Gram negative pathogens. Interestingly, the MIC values were comparable with the standard drug molecules. In addition, the identification of active metabolites present in the crude extracts was an advantage.
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spelling doaj.art-1799a334968d4b0894d4cfda80a43d342022-12-21T21:45:56ZengElsevierJournal of Infection and Public Health1876-03412021-11-01141116711678Isolation and characterization of novel Streptomyces strain from Algeria and its in-vitro antimicrobial properties against microbial pathogensFatima Zohra Djebbah0Larbi Belyagoubi1Djamel Eddine Abdelouahid2Farid Kherbouche3Naif Abdullah Al-Dhabi4Mariadhas Valan Arasu5Balasubramani Ravindran6Laboratoire de Microbiologie Appliquée à l’Agro-alimentaire, Au Biomédical et à l’Environnement (LAMAABE), Département de Biologie, Université Abou Bekr Belkaid, BP 119, Imama, 13000 Tlemcen, Algeria; Corresponding authors.Laboratoire des Produits Naturels (LAPRONA), Département de Biologie, Université Abou Bekr Belkaid, BP 119, Imama, 13000 Tlemcen, AlgeriaLaboratoire de Microbiologie Appliquée à l’Agro-alimentaire, Au Biomédical et à l’Environnement (LAMAABE), Département de Biologie, Université Abou Bekr Belkaid, BP 119, Imama, 13000 Tlemcen, AlgeriaCentre National de Recherches Préhistoriques, Anthropologiqes et Historiques (CNRPAH), 3 rue Franklin Roosevelt, 16000 Alger, AlgeriaDepartment of Botany and Microbiology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia; Corresponding authors.Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi ArabiaDepartment of Environmental Energy and Engineering, Kyonggi University Youngtong-Gu, Suwon, Gyeonggi-Do, 16227, Republic of KoreaBackground: The constant development of microbial resistance to the traditional antimicrobial agents and the emergence of new infectious diseases justify the urgent need for new effective antimicrobial molecules. However, the irrational use of antibiotics increases microbial resistance dramatically and along with that the frequency of mortality associated with infections is higher. Therefore, to combat the antimicrobial resistance, the screening of compounds with novel chemical structures is essential. This study intended to determine the antimicrobial potential of Streptomyces GLD22 strain isolated from Algeria. Methods: The characterization of Streptomyces strain GLD22 was performed by physiological, biochemical and molecular tests. The antimicrobial activity was tested by the well diffusion method and the minimum inhibitory concentration value calculation were performed using broth micro dilution technique. The extracellular metabolites profiling was done using GC–MS. Results: Physiological, biochemical and phylogenetic analysis confirmed that the strain GLD22 showed maximum identity towards Streptomyces species. The extra cellular metabolites revealed their antimicrobial activity at 1 mg/ml for Klebsiella pneumoniae, Pseudomonas aeruginosa and Escherichia coli, whereas Staphylococcus aureus, Bacillus cereus and Bacillus subtilis documented 0.5, 1 and 1 mg/ml respectively. GC–MS analysis confirmed that 2-tert-butyl-4,6-bis(3,5-di-tert-butyl-4-hydroxybenzyl) phenol, Dibutyl phthalate and Cyclo(leucyloprolyl) were the major drug molecules present in the extract. Conclusion: The novel Streptomyces strain GLD22 recovered from the Gueldaman cave of Algeria showed better antimicrobial activity towards both Gram positive and Gram negative pathogens. Interestingly, the MIC values were comparable with the standard drug molecules. In addition, the identification of active metabolites present in the crude extracts was an advantage.http://www.sciencedirect.com/science/article/pii/S1876034121003099ActinomycetesAntimicrobial activityMinimum inhibitory concertationGC–MS
spellingShingle Fatima Zohra Djebbah
Larbi Belyagoubi
Djamel Eddine Abdelouahid
Farid Kherbouche
Naif Abdullah Al-Dhabi
Mariadhas Valan Arasu
Balasubramani Ravindran
Isolation and characterization of novel Streptomyces strain from Algeria and its in-vitro antimicrobial properties against microbial pathogens
Journal of Infection and Public Health
Actinomycetes
Antimicrobial activity
Minimum inhibitory concertation
GC–MS
title Isolation and characterization of novel Streptomyces strain from Algeria and its in-vitro antimicrobial properties against microbial pathogens
title_full Isolation and characterization of novel Streptomyces strain from Algeria and its in-vitro antimicrobial properties against microbial pathogens
title_fullStr Isolation and characterization of novel Streptomyces strain from Algeria and its in-vitro antimicrobial properties against microbial pathogens
title_full_unstemmed Isolation and characterization of novel Streptomyces strain from Algeria and its in-vitro antimicrobial properties against microbial pathogens
title_short Isolation and characterization of novel Streptomyces strain from Algeria and its in-vitro antimicrobial properties against microbial pathogens
title_sort isolation and characterization of novel streptomyces strain from algeria and its in vitro antimicrobial properties against microbial pathogens
topic Actinomycetes
Antimicrobial activity
Minimum inhibitory concertation
GC–MS
url http://www.sciencedirect.com/science/article/pii/S1876034121003099
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