Comparative transcriptomics of Aspergillus fumigatus strains upon exposure to human airway epithelial cells

Autor: Scott G. Filler, Julie C. Dunning Hotopp, Tonya N. Watkins, Tracy H. Hazen, Matthew Chung, Vincent M. Bruno, Hong Liu
Jazyk: angličtina
Rok vydání: 2018
Předmět:
Spores
0301 basic medicine
Respiratory System
RNA-Seq
Aspergillus fumigatus
Af293
Transcriptome
Pathogenesis
Tissue culture
Gene Expression Regulation
Fungal

2.1 Biological and endogenous factors
2.2 Factors relating to the physical environment
Lung
biology
General Medicine
Spores
Fungal

CEA10
3. Good health
Fungal
Infectious Diseases
Phenotype
Host-Pathogen Interactions
Respiratory
Systems Microbiology: Transcriptomics
Proteomics
Networks

Infection
Sequence Analysis
Biotechnology
1.1 Normal biological development and functioning
030106 microbiology
Genes
Fungal

Microbiology
03 medical and health sciences
Genetics
Short Paper
Humans
Gene
Epithelial Cells
biology.organism_classification
In vitro
Emerging Infectious Diseases
030104 developmental biology
Gene Expression Regulation
Genes
Cell culture
A549 Cells
Alveolar Epithelial Cells
Pulmonary Aspergillosis
RNA-seq
airway epithelial cells
Zdroj: Watkins, TN; Liu, H; Chung, M; Hazen, TH; Hotopp, JCD; Filler, SG; et al.(2018). Comparative transcriptomics of Aspergillus fumigatus strains upon exposure to human airway epithelial cells. MICROBIAL GENOMICS, 4(2). doi: 10.1099/mgen.0.000154. UCLA: Retrieved from: http://www.escholarship.org/uc/item/4271m3bp
Microbial Genomics
Microbial genomics, vol 4, iss 2
DOI: 10.1099/mgen.0.000154.
Popis: Aspergillus fumigatus is an opportunistic, ubiquitous, saprophytic mould that can cause severe allergic responses in atopic individuals as well as life-threatening infections in immunocompromised patients. A critical step in the establishment of infection is the invasion of airway epithelial cells by the inhaled fungi. Understanding how A. fumigatus senses and responds to airway cells is important to understand the pathogenesis of invasive pulmonary aspergillosis. Here, we analysed the transcriptomes of two commonly used clinical isolates, Af293 and CEA10, during infection of the A549 type II pneumocyte cell line in vitro. We focused our RNA-seq analysis on the core set of genes that are present in the genomes of the two strains. Our results suggest that: (a) A. fumigatus does not mount a conserved transcriptional response to airway epithelial cells in our in vitro model and (b) strain background and time spent in the tissue culture media have a greater impact on the transcriptome than the presence of host cells. Our analyses reveal both common and strain-specific transcriptional programmes that allow for the generation of hypotheses about gene function as it pertains to pathogenesis and the significant phenotypic heterogeneity that is observed among A. fumigatus isolates.
Databáze: OpenAIRE