| Autor: |
Caffrey-Carr, Alayna K., Kowalski, Caitlin H., Beattie, Sarah R., Blaseg, Nathan A., Upshaw, Chanell R., Thammahong, Arsa, Lust, Hannah E., Tang, Yi-Wei, Hohl, Tobias M., Cramer, Robert A., Obar, Joshua J. |
| Zdroj: |
Infection and Immunity; September 2017, Vol. 85 Issue: 12 |
| Abstrakt: |
ABSTRACTHeterogeneity among Aspergillus fumigatusisolates results in unique virulence potential and inflammatory responses. How these isolates drive specific immune responses and how this affects fungally induced lung damage and disease outcome are unresolved. We demonstrate that the highly virulent CEA10 strain is able to rapidly germinate within the immunocompetent lung environment, inducing greater lung damage, vascular leakage, and interleukin 1α (IL-1α) release than the low-virulence Af293 strain, which germinates with a lower frequency in this environment. Importantly, the clearance of CEA10 was consequently dependent on IL-1α, in contrast to Af293. The release of IL-1α occurred by a caspase 1/11- and P2XR7-independent mechanism but was dependent on calpain activity. Our finding that early fungal conidium germination drives greater lung damage and IL-1α-dependent inflammation is supported by three independent experimental lines. First, pregermination of Af293 prior to in vivochallenge drives greater lung damage and an IL-1α-dependent neutrophil response. Second, the more virulent EVOL20 strain, derived from Af293, is able to germinate in the airways, leading to enhanced lung damage and IL-1α-dependent inflammation and fungal clearance. Third, primary environmental A. fumigatusisolates that rapidly germinate under airway conditions follow the same trend toward IL-1α dependency. Our data support the hypothesis that A. fumigatusphenotypic variation significantly contributes to disease outcomes. |
| Databáze: |
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