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Antifungal activity of terrestrial Streptomyces rochei strain HF391 against clinical azole -resistant Aspergillus fumigatus

BACKGROUND AND PURPOSE: Actinomycetes have been discovered as source of antifungal compounds that are currently in clinical use. Invasive aspergillosis (IA) due to Aspergillus fumigatus has been identified as individual drug-resistant Aspergillus spp. to be an emerging pathogen opportunities a globa...

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Autores principales: Hadizadeh, S, Forootanfar, H, Shahidi Bonjar, GH, Falahati Nejad, M, Karamy Robati, A, Ayatollahi Mousavi, SA, Amirporrostami, S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Society of Medical Mycology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490309/
https://www.ncbi.nlm.nih.gov/pubmed/28680984
http://dx.doi.org/10.18869/acadpub.cmm.1.2.19
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author Hadizadeh, S
Forootanfar, H
Shahidi Bonjar, GH
Falahati Nejad, M
Karamy Robati, A
Ayatollahi Mousavi, SA
Amirporrostami, S
author_facet Hadizadeh, S
Forootanfar, H
Shahidi Bonjar, GH
Falahati Nejad, M
Karamy Robati, A
Ayatollahi Mousavi, SA
Amirporrostami, S
author_sort Hadizadeh, S
collection PubMed
description BACKGROUND AND PURPOSE: Actinomycetes have been discovered as source of antifungal compounds that are currently in clinical use. Invasive aspergillosis (IA) due to Aspergillus fumigatus has been identified as individual drug-resistant Aspergillus spp. to be an emerging pathogen opportunities a global scale. This paper described the antifungal activity of one terrestrial actinomycete against the clinically isolated azole-resistant A. fumigatus. MATERIALS AND METHODS: Soil samples were collected from various locations of Kerman, Iran. Thereafter, the actinomycetes were isolated using starch-casein-nitrate-agar medium and the most efficient actinomycetes (capable of inhibiting A. fumigatus) were screened using agar block method. In the next step, the selected actinomycete was cultivated in starch-casein- broth medium and the inhibitory activity of the obtained culture broth was evaluated using agar well diffusion method. RESULTS: The selected actinomycete, identified as Streptomyces rochei strain HF391, could suppress the growth of A. fumigatus isolates which was isolated from the clinical samples of patients treated with azoles. This strain showed higher inhibition zones on agar diffusion assay which was more than 15 mm. CONCLUSION: The obtained results of the present study introduced Streptomyces rochei strain HF391 as terrestrial actinomycete that can inhibit the growth of clinically isolated A. fumigatus.
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spelling pubmed-54903092017-07-05 Antifungal activity of terrestrial Streptomyces rochei strain HF391 against clinical azole -resistant Aspergillus fumigatus Hadizadeh, S Forootanfar, H Shahidi Bonjar, GH Falahati Nejad, M Karamy Robati, A Ayatollahi Mousavi, SA Amirporrostami, S Curr Med Mycol Original Article BACKGROUND AND PURPOSE: Actinomycetes have been discovered as source of antifungal compounds that are currently in clinical use. Invasive aspergillosis (IA) due to Aspergillus fumigatus has been identified as individual drug-resistant Aspergillus spp. to be an emerging pathogen opportunities a global scale. This paper described the antifungal activity of one terrestrial actinomycete against the clinically isolated azole-resistant A. fumigatus. MATERIALS AND METHODS: Soil samples were collected from various locations of Kerman, Iran. Thereafter, the actinomycetes were isolated using starch-casein-nitrate-agar medium and the most efficient actinomycetes (capable of inhibiting A. fumigatus) were screened using agar block method. In the next step, the selected actinomycete was cultivated in starch-casein- broth medium and the inhibitory activity of the obtained culture broth was evaluated using agar well diffusion method. RESULTS: The selected actinomycete, identified as Streptomyces rochei strain HF391, could suppress the growth of A. fumigatus isolates which was isolated from the clinical samples of patients treated with azoles. This strain showed higher inhibition zones on agar diffusion assay which was more than 15 mm. CONCLUSION: The obtained results of the present study introduced Streptomyces rochei strain HF391 as terrestrial actinomycete that can inhibit the growth of clinically isolated A. fumigatus. Iranian Society of Medical Mycology 2015-06 /pmc/articles/PMC5490309/ /pubmed/28680984 http://dx.doi.org/10.18869/acadpub.cmm.1.2.19 Text en Copyright© 2015, Published by Mazandaran University of Medical Sciences on behalf of Iranian Society of Medical Mycology and Invasive Fungi Research Center. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial 4.0 International License ( https://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Original Article
Hadizadeh, S
Forootanfar, H
Shahidi Bonjar, GH
Falahati Nejad, M
Karamy Robati, A
Ayatollahi Mousavi, SA
Amirporrostami, S
Antifungal activity of terrestrial Streptomyces rochei strain HF391 against clinical azole -resistant Aspergillus fumigatus
title Antifungal activity of terrestrial Streptomyces rochei strain HF391 against clinical azole -resistant Aspergillus fumigatus
title_full Antifungal activity of terrestrial Streptomyces rochei strain HF391 against clinical azole -resistant Aspergillus fumigatus
title_fullStr Antifungal activity of terrestrial Streptomyces rochei strain HF391 against clinical azole -resistant Aspergillus fumigatus
title_full_unstemmed Antifungal activity of terrestrial Streptomyces rochei strain HF391 against clinical azole -resistant Aspergillus fumigatus
title_short Antifungal activity of terrestrial Streptomyces rochei strain HF391 against clinical azole -resistant Aspergillus fumigatus
title_sort antifungal activity of terrestrial streptomyces rochei strain hf391 against clinical azole -resistant aspergillus fumigatus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490309/
https://www.ncbi.nlm.nih.gov/pubmed/28680984
http://dx.doi.org/10.18869/acadpub.cmm.1.2.19
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