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Evaluation of catalase activity of clinical and environmental isolates of Aspergillus species
BACKGROUND AND OBJECTIVES: Catalases are a good scavenger of H(2)O(2) which degrades hydrogen peroxide into water and oxygen. They are considered as a virulence factor that are present in both spores and hypha of fungi. There is limited data regarding catalase activity in Aspergillus species. This s...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085545/ https://www.ncbi.nlm.nih.gov/pubmed/35664717 http://dx.doi.org/10.18502/ijm.v14i1.8815 |
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author | Gharaghani, Maral Jafarian, Hadis Hatami, Maryam Shabanzadeh, Mahboubeh Zarei Mahmoudabadi, Ali |
author_facet | Gharaghani, Maral Jafarian, Hadis Hatami, Maryam Shabanzadeh, Mahboubeh Zarei Mahmoudabadi, Ali |
author_sort | Gharaghani, Maral |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: Catalases are a good scavenger of H(2)O(2) which degrades hydrogen peroxide into water and oxygen. They are considered as a virulence factor that are present in both spores and hypha of fungi. There is limited data regarding catalase activity in Aspergillus species. This study aimed to assess the mycelial catalase activity of clinical and environmental isolates of Aspergillus niger, A. tubingensis, A. flavus, A. luchuensis, A. piperis and A. terreus. MATERIALS AND METHODS: Briefly, clinical and environmental Aspergillus species were used in the current study. Catalase activity was assessed for both groups of isolates including 13 A. flavus (12 clinical, 1 environmental), 13 A. terreus (8 clinical, 5 environmental), 26 A. tubingensis (13 clinical, 13 environmental), and 44 A. niger (25 environmental, 19 clinical) species. Fungal balls of mycelia were separated from the liquid culture and were crushed using homogenizer. The supernatants were collected and used for a catalase activity assay. RESULTS: Totally, in our study 98 Aspergillus including 45 environmental and 53 clinical isolates were assessed for catalase activity. High catalase activity was detected among environmental Aspergillus species (Mean= 1.62 mU/ml) and the mean of mycelial catalase activity among clinical A. terreus isolates was higher than environmental strains. CONCLUSION: In summary, mycelial catalase activity varied among species and environmental isolates demonstrated higher catalase activity. Totally a significant difference was found between clinical and environmental Aspergillus isolates. |
format | Online Article Text |
id | pubmed-9085545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Tehran University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-90855452022-06-04 Evaluation of catalase activity of clinical and environmental isolates of Aspergillus species Gharaghani, Maral Jafarian, Hadis Hatami, Maryam Shabanzadeh, Mahboubeh Zarei Mahmoudabadi, Ali Iran J Microbiol Original Article BACKGROUND AND OBJECTIVES: Catalases are a good scavenger of H(2)O(2) which degrades hydrogen peroxide into water and oxygen. They are considered as a virulence factor that are present in both spores and hypha of fungi. There is limited data regarding catalase activity in Aspergillus species. This study aimed to assess the mycelial catalase activity of clinical and environmental isolates of Aspergillus niger, A. tubingensis, A. flavus, A. luchuensis, A. piperis and A. terreus. MATERIALS AND METHODS: Briefly, clinical and environmental Aspergillus species were used in the current study. Catalase activity was assessed for both groups of isolates including 13 A. flavus (12 clinical, 1 environmental), 13 A. terreus (8 clinical, 5 environmental), 26 A. tubingensis (13 clinical, 13 environmental), and 44 A. niger (25 environmental, 19 clinical) species. Fungal balls of mycelia were separated from the liquid culture and were crushed using homogenizer. The supernatants were collected and used for a catalase activity assay. RESULTS: Totally, in our study 98 Aspergillus including 45 environmental and 53 clinical isolates were assessed for catalase activity. High catalase activity was detected among environmental Aspergillus species (Mean= 1.62 mU/ml) and the mean of mycelial catalase activity among clinical A. terreus isolates was higher than environmental strains. CONCLUSION: In summary, mycelial catalase activity varied among species and environmental isolates demonstrated higher catalase activity. Totally a significant difference was found between clinical and environmental Aspergillus isolates. Tehran University of Medical Sciences 2022-02 /pmc/articles/PMC9085545/ /pubmed/35664717 http://dx.doi.org/10.18502/ijm.v14i1.8815 Text en Copyright © 2022 The Authors. Published by Tehran University of Medical Sciences https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International license (https://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited. |
spellingShingle | Original Article Gharaghani, Maral Jafarian, Hadis Hatami, Maryam Shabanzadeh, Mahboubeh Zarei Mahmoudabadi, Ali Evaluation of catalase activity of clinical and environmental isolates of Aspergillus species |
title | Evaluation of catalase activity of clinical and environmental isolates of Aspergillus species |
title_full | Evaluation of catalase activity of clinical and environmental isolates of Aspergillus species |
title_fullStr | Evaluation of catalase activity of clinical and environmental isolates of Aspergillus species |
title_full_unstemmed | Evaluation of catalase activity of clinical and environmental isolates of Aspergillus species |
title_short | Evaluation of catalase activity of clinical and environmental isolates of Aspergillus species |
title_sort | evaluation of catalase activity of clinical and environmental isolates of aspergillus species |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085545/ https://www.ncbi.nlm.nih.gov/pubmed/35664717 http://dx.doi.org/10.18502/ijm.v14i1.8815 |
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