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Updated: May 3, 2026

Developing a Salivary Antibody Multiplex Immunoassay to Measure Human Exposure to Environmental Pathogens
Published on: September 12, 2016
Scedosporium prolificans immunomes against human salivary immunoglobulin A
Aize Pellon1, Andoni Ramirez-Garcia2, Aitziber Antoran1
1Department of Immunology, Microbiology and Parasitology, Faculty of Science and Technology, University of the Basque Country (UPV/EHU), Leioa 48940, Bizkaia, Spain.
Abstract:
The filamentous fungus Scedosporium prolificans is an emerging multidrug resistant pathogen related to serious infections mainly affecting immunocompromised individuals. Considering that it is frequently isolated from anthropic environments and penetrates mainly through the airways, the human mucosal immune system may play an important protective role against S. prolificans. To advance in the search for biomarkers and targets both for diagnosis and treatment, we analysed the S. prolificans immunomes recognized by human salivary Immunoglobulin A. Using indirect immunofluorescence, it was observed that conidia were strongly recognized, while hyphae were not. By 2-D immunoblotting and peptide mass fingerprinting, 25 immunodominant antigens in conidia and 30 in hyphae were identified. These included catalase, putative glyceronetransferase, translation elongation factor-1α, serine/threonine protein kinase, putative superoxide dismutase, putative mitochondrial cyclophilin 1 and peptidyl-prolyl cis-trans isomerase in conidiospores, and putative Hsp60, ATP synthase β chain, 40S ribosomal protein S0, citrate synthase and putative ATP synthase in hyphae. The functional study showed that metabolism - and protein fate - related enzymes were the most abundant antigens in conidia, whereas metabolism - , translation - , or energy production - related enzymes were in hyphae. The immunogenic proteins identified are proposed as candidates for the development of novel diagnostic tools or therapeutic strategies.
Insights
Scedosporium prolificans infections are a growing concern, especially for immunocompromised individuals. Researchers identified key fungal proteins recognized by human saliva, offering potential for new diagnostic and treatment strategies against this resistant pathogen.
Area of Science:
- Mycology
- Immunology
- Infectious Diseases
Background:
- Scedosporium prolificans is an emerging, multidrug-resistant fungal pathogen causing severe infections, particularly in immunocompromised individuals.
- Its prevalence in anthropic environments and airway penetration suggest a critical role for the human mucosal immune system in defense.
- Identifying S. prolificans antigens is crucial for developing diagnostic and therapeutic tools.
Purpose of the Study:
- To analyze the immunomes of S. prolificans recognized by human salivary Immunoglobulin A (IgA).
- To identify specific S. prolificans antigens that can serve as biomarkers or therapeutic targets.
- To understand the immune response against different fungal structures (conidia and hyphae).
Main Methods:
- Indirect immunofluorescence to assess recognition of fungal structures by salivary IgA.
- 2-D immunoblotting and peptide mass fingerprinting to identify specific antigens.
- Functional analysis of identified antigens to determine their roles.
Main Results:
- Conidia of S. prolificans were strongly recognized by salivary IgA, while hyphae were not.
- 25 immunodominant antigens were identified in conidia and 30 in hyphae.
- Antigens included enzymes related to metabolism, protein fate, translation, and energy production, such as catalase, elongation factor-1α, and ATP synthase.
Conclusions:
- The identified immunogenic proteins are potential candidates for novel diagnostic tools.
- These antigens may also serve as targets for developing new therapeutic strategies against S. prolificans infections.
- Understanding the IgA-mediated immune response provides insights into host defense mechanisms.
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