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Histological Quantification to Determine Lung Fungal Burden in Experimental Aspergillosis
Published on: March 9, 2018
[Strategy of Aspergillus fumigatus to evade attacks from host--projectile weapons and armor]
Takahito Toyotome1, Akira Watanabe, Aya Iwasaki
1Division of Fungal Infection, Medical Mycology Research Center, Chiba University, Chiba, Japan.
Abstract:
Humans are continually inhaling environmental fungi. When the host immune system is competent, the inhaled fungi are cleared away from the lung by host defense mechanisms. But in immunocompromised individuals, the environmental fungi (e.g., Aspergillus fumigatus) sometimes cause infection. Pathogenic fungi possess various mechanisms to invade the host. A. fumigatus is no exception in possessing several virulence factors and defense mechanisms against host immune attack.One of the virulence factors is secondary metabolite. A. fumigatus produces a variety of secondary metabolites, and the fungal products in culture supernatant have a strong apoptosis-inducing activity to macrophages and alveolar epithelial cells. These data suggest that A. fumigatus is equipped with special projectile weapons for destroying host physical barriers and immunological barriers in lung.The fungal cell wall is an easy target for the host to recognize the pathogen. One of the fungal cell wall components, beta- (1,3) -glucan, is a major fungal PAMP (pathogen-associated molecular pattern), which is recognized by one of the pattern recognition receptors, dectin-1. The interaction induces activation of transcription factors and production of proinflammatory cytokines in the host cell. However, beta-glucan of A. fumigatus is strongly exposed to the surface only during the "swollen-conidia" phase. In the hyphal phase, the fungus is covered with "armor", i.e., other cell wall components to minimize the exposure of the beta-glucan structure. These findings suggest that A. fumigatus evades the recognition and the attack from host by masking beta-glucan. A. fumigatus has clever mechanisms to defend itself and to attack the host immune system.
Insights
Aspergillus fumigatus uses secondary metabolites to damage host cells and masks beta-glucan in its cell wall to evade immune detection. These mechanisms help the fungus cause infection, especially in immunocompromised individuals.
Area of Science:
- Mycology
- Immunology
- Pathogen Biology
Background:
- Environmental fungi, including Aspergillus fumigatus, are inhaled by humans.
- While a competent immune system clears fungi, immunocompromised individuals are susceptible to infections.
- Pathogenic fungi like A. fumigatus possess virulence factors and defense mechanisms to invade hosts.
Purpose of the Study:
- To investigate the virulence factors and immune evasion strategies of Aspergillus fumigatus.
- To understand how A. fumigatus destroys host physical and immunological barriers.
- To elucidate the mechanisms by which A. fumigatus evades host immune recognition.
Main Methods:
- Analysis of secondary metabolites produced by A. fumigatus in culture supernatant.
- Investigation of fungal cell wall composition and beta-glucan exposure during different fungal growth phases.
- Examination of host immune responses, including apoptosis induction and pattern recognition receptor (dectin-1) interaction.
Main Results:
- A. fumigatus secretes secondary metabolites that induce apoptosis in macrophages and alveolar epithelial cells.
- Beta-glucan, a key pathogen-associated molecular pattern (PAMP), is masked by other cell wall components during the hyphal phase.
- This masking of beta-glucan by A. fumigatus hinders recognition by host pattern recognition receptors like dectin-1.
Conclusions:
- A. fumigatus employs secondary metabolites as weapons to breach host defenses.
- The fungus utilizes cell wall modifications to evade immune surveillance, particularly by masking beta-glucan.
- These combined strategies highlight A. fumigatus's sophisticated mechanisms for causing infection in the lung.
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