Evidence map›Paper›PMID 41563283›Full record

ArticleJournal of applied oral science : revista FOB2026

Antigenemia and oral lesions in paracoccidioidomycosis: is there a correlation?

Tatiana Teixeira de Miranda, Eva Burger

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Article in Journal of applied oral science : revista FOB, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Tatiana Teixeira de MirandaUniversidade Federal de Alfenas (UNIFAL-MG), Instituto de Ciências Biomédicas, Departamento de Microbiologia e Imunologia, Alfenas, Minas Gerais, Brasil.ORCID http://orcid.org/0009-0005-7983-7851
Eva BurgerUniversidade Federal de Alfenas (UNIFAL-MG), Instituto de Ciências Biomédicas, Departamento de Microbiologia e Imunologia, Alfenas, Minas Gerais, Brasil.ORCID http://orcid.org/0000-0001-8361-8268

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundParacoccidioidomycosis is a systemic mycosis caused by the dimorphic fungus Paracoccidioides brasiliensis and related species, which are endemic to Latin America. Oral manifestations are highly relevant for diagnosis, representing the primary anatomical site biopsied for confirmation.

objectiveTo investigate whether the virulence of P. brasiliensis influences the levels of circulating antigen in susceptible (B10.A) and resistant (A/Sn) murine models at multiple post-infection time points. The presence of oral lesions and their correlation with antigenemia were also assessed. METHODOLOGY: One-week-old female B10.A and A/Sn mice were inoculated with the P. brasiliensis lineages Pb18 or Pb265, whereas controls received sterile saline. At four, eight, 12, and 16 post-inoculation weeks, sera were collected via sub-axillary plexus incision under anesthesia. Circulating antigen levels were quantified using competitive ELISA. Specific antibody titers were determined by indirect non-competitive ELISA and P. brasiliensis antigens. Intergroup comparisons were performed using two-way ANOVA, followed by multiple comparisons. Oral cavities were visually examined by three independent evaluators to find mulberry stomatitis. Prevalence was expressed as the percentage of affected animals.

resultsSignificant differences in the circulating antigen levels were detected between susceptible mice infected with Pb18 and Pb265 and between susceptible and resistant mice infected with Pb18 16 weeks after inoculation. The highest levels of antibodies were found when both B10.A and A/Sn mice were infected with Pb18. During infection, no mice showed mulberry-like lesions in the oral cavity.

conclusionThe virulence of the infecting P. brasiliensis strain, although not specifically linked to the gp43 antigen, plays a critical role in antigenemia. Despite absent oral lesions-an inherent limitation of this murine model-this study provides relevant insights into the relationship between fungal virulence and circulating antigen levels.

Indexed as

Antigens, FungalParacoccidioidesParacoccidioidomycosisAnalysis of VarianceAnimalsAntibodies, FungalDisease Models, AnimalEnzyme-Linked Immunosorbent AssayFemaleMiceTime FactorsVirulenceAntibodies, FungalAntigens, Fungal

Identifiers

PMID41563283
PMCPMC13123787

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.