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Differential role of gpaB and sidA gene expressions in relation to virulence in Aspergillus species from patients with invasive aspergillosis

The virulence genes in invasive aspergillosis (IA) have not been analyzed adequately. The present study was designed to evaluate the expression of gpaB and sidA genes, which are important virulence genes in Aspergillus spp. from bronchoalveolar lavage (BAL) samples. Direct examination and culture on...

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Autores principales: Ghods, Nayereh, Falahati, Mehraban, Roudbary, Maryam, Farahyar, Shirin, Shamaei, Masoud, Pourabdollah, Mahin, Seif, Farhad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6066728/
https://www.ncbi.nlm.nih.gov/pubmed/29452846
http://dx.doi.org/10.1016/j.bjm.2017.10.003
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author Ghods, Nayereh
Falahati, Mehraban
Roudbary, Maryam
Farahyar, Shirin
Shamaei, Masoud
Pourabdollah, Mahin
Seif, Farhad
author_facet Ghods, Nayereh
Falahati, Mehraban
Roudbary, Maryam
Farahyar, Shirin
Shamaei, Masoud
Pourabdollah, Mahin
Seif, Farhad
author_sort Ghods, Nayereh
collection PubMed
description The virulence genes in invasive aspergillosis (IA) have not been analyzed adequately. The present study was designed to evaluate the expression of gpaB and sidA genes, which are important virulence genes in Aspergillus spp. from bronchoalveolar lavage (BAL) samples. Direct examination and culture on Czapek Agar and Sabouraud Dextrose Agar media were performed for 600 BAL specimens isolated from patients with possible aspergillosis. A Galactomannan ELISA assay was also carried out. The expression levels of the gpaB and sidA genes in isolates were analyzed using quantitative real-time PCR (qRT-PCR). We identified 2 species, including Aspergillus flavus (A. flavus) and Aspergillus fumigatus (A. fumigatus) in 25 positive samples for invasive aspergillosis as validated using GM-ELISA. A. flavus is the main pathogen threatening transplant recipients and cancer patients worldwide. In this study, A. flavus had low levels of the gpaB gene expression compared to A. fumigatus (p = 0.006). The highest sidA expression was detected in transplant recipients (p = 0.05). There was no significant correlation between sidA expression and underlying disease (p = 0.15). The sidA and gpaB gene expression patterns may provide evidence that these virulence genes play important roles in the pathogenicity of Aspergillus isolates; however, there are several regulatory genes responsible for the unexpressed sidA and gpaB genes in the isolates.
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spelling pubmed-60667282018-08-01 Differential role of gpaB and sidA gene expressions in relation to virulence in Aspergillus species from patients with invasive aspergillosis Ghods, Nayereh Falahati, Mehraban Roudbary, Maryam Farahyar, Shirin Shamaei, Masoud Pourabdollah, Mahin Seif, Farhad Braz J Microbiol Bacterial and Fungal Pathogenesis The virulence genes in invasive aspergillosis (IA) have not been analyzed adequately. The present study was designed to evaluate the expression of gpaB and sidA genes, which are important virulence genes in Aspergillus spp. from bronchoalveolar lavage (BAL) samples. Direct examination and culture on Czapek Agar and Sabouraud Dextrose Agar media were performed for 600 BAL specimens isolated from patients with possible aspergillosis. A Galactomannan ELISA assay was also carried out. The expression levels of the gpaB and sidA genes in isolates were analyzed using quantitative real-time PCR (qRT-PCR). We identified 2 species, including Aspergillus flavus (A. flavus) and Aspergillus fumigatus (A. fumigatus) in 25 positive samples for invasive aspergillosis as validated using GM-ELISA. A. flavus is the main pathogen threatening transplant recipients and cancer patients worldwide. In this study, A. flavus had low levels of the gpaB gene expression compared to A. fumigatus (p = 0.006). The highest sidA expression was detected in transplant recipients (p = 0.05). There was no significant correlation between sidA expression and underlying disease (p = 0.15). The sidA and gpaB gene expression patterns may provide evidence that these virulence genes play important roles in the pathogenicity of Aspergillus isolates; however, there are several regulatory genes responsible for the unexpressed sidA and gpaB genes in the isolates. Elsevier 2018-02-03 /pmc/articles/PMC6066728/ /pubmed/29452846 http://dx.doi.org/10.1016/j.bjm.2017.10.003 Text en © 2018 Sociedade Brasileira de Microbiologia. Published by Elsevier Editora Ltda. 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 Bacterial and Fungal Pathogenesis
Ghods, Nayereh
Falahati, Mehraban
Roudbary, Maryam
Farahyar, Shirin
Shamaei, Masoud
Pourabdollah, Mahin
Seif, Farhad
Differential role of gpaB and sidA gene expressions in relation to virulence in Aspergillus species from patients with invasive aspergillosis
title Differential role of gpaB and sidA gene expressions in relation to virulence in Aspergillus species from patients with invasive aspergillosis
title_full Differential role of gpaB and sidA gene expressions in relation to virulence in Aspergillus species from patients with invasive aspergillosis
title_fullStr Differential role of gpaB and sidA gene expressions in relation to virulence in Aspergillus species from patients with invasive aspergillosis
title_full_unstemmed Differential role of gpaB and sidA gene expressions in relation to virulence in Aspergillus species from patients with invasive aspergillosis
title_short Differential role of gpaB and sidA gene expressions in relation to virulence in Aspergillus species from patients with invasive aspergillosis
title_sort differential role of gpab and sida gene expressions in relation to virulence in aspergillus species from patients with invasive aspergillosis
topic Bacterial and Fungal Pathogenesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6066728/
https://www.ncbi.nlm.nih.gov/pubmed/29452846
http://dx.doi.org/10.1016/j.bjm.2017.10.003
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