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A murine inhalation model to characterize pulmonary exposure to dry Aspergillus fumigatus conidia.

Authors
Buskirk-AD; Green-BJ; Lemons-AR; Nayak-AP; Goldsmith-WT; Kashon-ML; Anderson-SE; Hettick-JM; Templeton-SP; Germolec-DR; Beezhold-DH
Source
PLoS One 2014 Oct; 9(10):e109855
NIOSHTIC No.
20045313
Abstract
Most murine models of fungal exposure are based on the delivery of uncharacterized extracts or liquid conidia suspensions using aspiration or intranasal approaches. Studies that model exposure to dry fungal aerosols using whole body inhalation have only recently been described. In this study, we aimed to characterize pulmonary immune responses following repeated inhalation of conidia utilizing an acoustical generator to deliver dry fungal aerosols to mice housed in a nose only exposure chamber. Immunocompetent female BALB/cJ mice were exposed to conidia derived from Aspergillus fumigatus wild-type (WT) or a melanin-deficient (Aalb1) strain. Conidia were aerosolized and delivered to mice at an estimated deposition dose of 1x105 twice a week for 4 weeks (8 total). Histopathological and immunological endpoints were assessed 4, 24, 48, and 72 hours after the final exposure. Histopathological analysis showed that conidia derived from both strains induced lung inflammation, especially at 24 and 48 hour time points. Immunological endpoints evaluated in bronchoalveolar lavage fluid (BALF) and the mediastinal lymph nodes showed that exposure to WT conidia led to elevated numbers of macrophages, granulocytes, and lymphocytes. Importantly, CD8+ IL17+ (Tc17) cells were significantly higher in BALF and positively correlated with germination of A. fumigatus WT spores. Germination was associated with specific IgG to intracellular proteins while Aalb1 spores elicited antibodies to cell wall hydrophobin. These data suggest that inhalation exposures may provide a more representative analysis of immune responses following exposures to environmentally and occupationally prevalent fungal contaminants.
Keywords
Fungi; Models; Exposure-levels; Aerosols; Pulmonary-system; Pulmonary-function; Animals; Laboratory-animals; Histopathology; Lung; Lung-disorders; Lung-function; Inhalation-studies
Contact
Donald H. Beezhold, Allergy and Clinical Immunology Branch, Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Centers for Disease Control and Prevention, Morgantown, W V 26505
CODEN
POLNCL
Publication Date
20141001
Document Type
Journal Article
Email Address
zec1@cdc.gov
Fiscal Year
2015
NTIS Accession No.
NTIS Price
Identifying No.
M112014
Issue of Publication
10
ISSN
1932-6203
NIOSH Division
HELD
Priority Area
Healthcare and Social Assistance; Services
Source Name
Public Library of Science One
State
WV; NC
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