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Dysregulation of Key Proteinases in Aspergillus Fumigatus Induced by Blood Platelets



Arghavan B1 ; Shafiee M2, 3 ; Hashemi SJ1 ; Khodavaisy S1 ; Hosseinkhan N4 ; Didehdar M5 ; Getso M1, 6 ; Ayatollahi A7 ; Rezaie S1
Authors
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Authors Affiliations
  1. 1. Department of Medical Parasitology andMycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Department of Medical Laboratory Sciences, Khomein University of Medical Sciences, Khomein, Iran
  3. 3. Stem CellResearch Center, Golestan University of Medical Sciences, Gorgan, Iran
  4. 4. Endocrine Research Center, Institute of Endocrinology and Metabolism, Iran University of Medical Sciences, Tehran, Iran
  5. 5. Department of Parasitology andMycology, School of Medicine, Arak University of Medical Sciences, Arak, Iran
  6. 6. Department of Medical Microbiology and Parasitology, College of Health Sciences, Bayero University, Kano, Nigeria
  7. 7. Laboratory Sciences Research Center, Golestan University of Medical Sciences, Gorgan, Iran

Source: Reports of Biochemistry and Molecular Biology Published:2021

Abstract

Background: Aspergillus fumigatus is the most common species causing invasive aspergillosis (IA), a life- threatening infection with more than 80% mortality. Interactions between A. fumigatus and human blood platelets lead to intravascular thrombosis and localized infarcts. To better understand A. fumigatus pathogenesis, we aimed to analyze the genetic basis of interactions between the pathogen and blood platelets.Methods: A bioinformatic pipeline on microarray gene expression dataset, including analysis of differentially expressed genes (DEGs) using Limma R package and their molecular function, as well as biological pathways identification, was conducted to find the effective genes involved in IA. In the wet phase, the gene expression patterns following fungal exposure to blood platelets at 15, 30, 60, and 180 min were evaluated by quantitative reverse transcriptase-PCR analysis.Results: Three genes encoding aspartic endopeptidases including (Pep1), (Asp f 13), and (P-glucanase) were the standing candidates. The invasion-promoting fungal proteinase-encoding genes were down- regulated after 30 min of hyphal incubation with blood platelets, and then up-regulated at 60 and 180 min, although only Pep1 was greater than the control at the 60and 180 min time points. Also, the same genes were downregulated in more the clinical isolates relative to the standard strain CBS 144.89.Conclusions: Our findings delineate the possible induction of fungal-encoded proteinases by blood platelets. This provides a new research line into A. fumigatus ’ molecular pathogenesis. Such insight into IA pathogenesis might also guide researchers toward novel platelet-based therapies that involve molecular interventions, especially in IA patients. © 2021, Reports of Biochemistry & Molecular Biology .All Rights Reserved.