Fibrotic sequelae in pulmonary paracoccidioidomycosis : histopathological aspects in balb/c mice infected with viable and non-viable paracoccidioides brasiliensis propagules

ABSTRACT: Patients with paracoccidioidomycosis often present pulmonary fibrosis and exhibit important respiratory limitations. Based on an already established animal model, the contribution of viable and non-viable P. brasiliensis propagules to the development of fibrosis was investigated. BALB/c ma...

Full description

Autores:
Cock Botero, Ana María
Cano Restrepo, Luz Elena
Vélez Báez, Diana
Aristizabal Bernal, Beatriz Helena
Trujillo Pérez, Judith
Restrepo Moreno, Ángela
Tipo de recurso:
Article of investigation
Fecha de publicación:
2000
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/29423
Acceso en línea:
http://hdl.handle.net/10495/29423
Palabra clave:
Fibrosis Pulmonar
Pulmonary Fibrosis
Esporas Fúngicas
Spores, Fungal
Paracoccidioides brasiliensis
Rights
openAccess
License
https://creativecommons.org/licenses/by-nc-sa/4.0/
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network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv Fibrotic sequelae in pulmonary paracoccidioidomycosis : histopathological aspects in balb/c mice infected with viable and non-viable paracoccidioides brasiliensis propagules
title Fibrotic sequelae in pulmonary paracoccidioidomycosis : histopathological aspects in balb/c mice infected with viable and non-viable paracoccidioides brasiliensis propagules
spellingShingle Fibrotic sequelae in pulmonary paracoccidioidomycosis : histopathological aspects in balb/c mice infected with viable and non-viable paracoccidioides brasiliensis propagules
Fibrosis Pulmonar
Pulmonary Fibrosis
Esporas Fúngicas
Spores, Fungal
Paracoccidioides brasiliensis
title_short Fibrotic sequelae in pulmonary paracoccidioidomycosis : histopathological aspects in balb/c mice infected with viable and non-viable paracoccidioides brasiliensis propagules
title_full Fibrotic sequelae in pulmonary paracoccidioidomycosis : histopathological aspects in balb/c mice infected with viable and non-viable paracoccidioides brasiliensis propagules
title_fullStr Fibrotic sequelae in pulmonary paracoccidioidomycosis : histopathological aspects in balb/c mice infected with viable and non-viable paracoccidioides brasiliensis propagules
title_full_unstemmed Fibrotic sequelae in pulmonary paracoccidioidomycosis : histopathological aspects in balb/c mice infected with viable and non-viable paracoccidioides brasiliensis propagules
title_sort Fibrotic sequelae in pulmonary paracoccidioidomycosis : histopathological aspects in balb/c mice infected with viable and non-viable paracoccidioides brasiliensis propagules
dc.creator.fl_str_mv Cock Botero, Ana María
Cano Restrepo, Luz Elena
Vélez Báez, Diana
Aristizabal Bernal, Beatriz Helena
Trujillo Pérez, Judith
Restrepo Moreno, Ángela
dc.contributor.author.none.fl_str_mv Cock Botero, Ana María
Cano Restrepo, Luz Elena
Vélez Báez, Diana
Aristizabal Bernal, Beatriz Helena
Trujillo Pérez, Judith
Restrepo Moreno, Ángela
dc.contributor.researchgroup.spa.fl_str_mv Micología Médica y Experimental
dc.subject.decs.none.fl_str_mv Fibrosis Pulmonar
Pulmonary Fibrosis
Esporas Fúngicas
Spores, Fungal
topic Fibrosis Pulmonar
Pulmonary Fibrosis
Esporas Fúngicas
Spores, Fungal
Paracoccidioides brasiliensis
dc.subject.proposal.spa.fl_str_mv Paracoccidioides brasiliensis
description ABSTRACT: Patients with paracoccidioidomycosis often present pulmonary fibrosis and exhibit important respiratory limitations. Based on an already established animal model, the contribution of viable and non-viable P. brasiliensis propagules to the development of fibrosis was investigated. BALB/c male mice, 4-6 weeks old were inoculated intranasally either with 4x106 viable conidia (Group I), or 6.5x106 fragmented yeast cells (Group II). Control animals received PBS. Six mice per period were sacrificed at 24, 48, 72h (initial) and 1, 2, 4, 8, 12 and 16 weeks post-challenge (late). Paraffin embedded lungs were sectioned and stained with H&E, trichromic (Masson), reticulin and Grocott´s. During the initial period PMNs influx was important in both groups and acute inflammation involving 34% to 45% of the lungs was noticed. Later on, mononuclear cells predominated. In group I, the inflammation progressed and granulomas were formed and by the 12th week they fussed and became loose. Thick collagen I fibers were observed in 66.6% and 83.3% of the animals at 8 and 12 weeks, respectively. Collagen III, thick fibers became apparent in some animals at 4weeks and by 12 weeks, 83% of them exhibited alterations in the organization and thickness of these elements. In group II mice, this pattern was different with stepwise decrease in the number of inflammatory foci and lack of granulomas. Although initially most animals in this group had minor alterations in thin collagen I fibers, they disappeared by the 4th week. Results indicate that tissue response to fragmented yeast cells was transitory while viable conidia evoked a progressive inflammatory reaction leading to granuloma formation and to excess production and/or disarrangement of collagens I and III; the latter led to fibrosis.
publishDate 2000
dc.date.issued.none.fl_str_mv 2000
dc.date.accessioned.none.fl_str_mv 2022-06-28T18:27:31Z
dc.date.available.none.fl_str_mv 2022-06-28T18:27:31Z
dc.type.spa.fl_str_mv Artículo de investigación
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dc.identifier.doi.none.fl_str_mv 10.1590/S0036-46652000000200001
dc.identifier.eissn.none.fl_str_mv 1678-9946
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10.1590/S0036-46652000000200001
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dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Rev. Inst. Med. Trop. São Paulo.
dc.relation.citationendpage.spa.fl_str_mv 66
dc.relation.citationissue.spa.fl_str_mv 2
dc.relation.citationstartpage.spa.fl_str_mv 59
dc.relation.citationvolume.spa.fl_str_mv 42
dc.relation.ispartofjournal.spa.fl_str_mv Revista do Instituto de Medicina Tropical de Sao Paulo
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dc.publisher.spa.fl_str_mv Universidade de São Paulo, Faculdade de Medicina
dc.publisher.place.spa.fl_str_mv Sao Paulo, Brasil
institution Universidad de Antioquia
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spelling Cock Botero, Ana MaríaCano Restrepo, Luz ElenaVélez Báez, DianaAristizabal Bernal, Beatriz HelenaTrujillo Pérez, JudithRestrepo Moreno, ÁngelaMicología Médica y Experimental2022-06-28T18:27:31Z2022-06-28T18:27:31Z20000036-4665http://hdl.handle.net/10495/2942310.1590/S0036-466520000002000011678-9946ABSTRACT: Patients with paracoccidioidomycosis often present pulmonary fibrosis and exhibit important respiratory limitations. Based on an already established animal model, the contribution of viable and non-viable P. brasiliensis propagules to the development of fibrosis was investigated. BALB/c male mice, 4-6 weeks old were inoculated intranasally either with 4x106 viable conidia (Group I), or 6.5x106 fragmented yeast cells (Group II). Control animals received PBS. Six mice per period were sacrificed at 24, 48, 72h (initial) and 1, 2, 4, 8, 12 and 16 weeks post-challenge (late). Paraffin embedded lungs were sectioned and stained with H&E, trichromic (Masson), reticulin and Grocott´s. During the initial period PMNs influx was important in both groups and acute inflammation involving 34% to 45% of the lungs was noticed. Later on, mononuclear cells predominated. In group I, the inflammation progressed and granulomas were formed and by the 12th week they fussed and became loose. Thick collagen I fibers were observed in 66.6% and 83.3% of the animals at 8 and 12 weeks, respectively. Collagen III, thick fibers became apparent in some animals at 4weeks and by 12 weeks, 83% of them exhibited alterations in the organization and thickness of these elements. In group II mice, this pattern was different with stepwise decrease in the number of inflammatory foci and lack of granulomas. Although initially most animals in this group had minor alterations in thin collagen I fibers, they disappeared by the 4th week. Results indicate that tissue response to fragmented yeast cells was transitory while viable conidia evoked a progressive inflammatory reaction leading to granuloma formation and to excess production and/or disarrangement of collagens I and III; the latter led to fibrosis.COL00137098application/pdfengUniversidade de São Paulo, Faculdade de MedicinaSao Paulo, Brasilhttps://creativecommons.org/licenses/by-nc-sa/4.0/http://creativecommons.org/licenses/by-nc-sa/2.5/co/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Fibrotic sequelae in pulmonary paracoccidioidomycosis : histopathological aspects in balb/c mice infected with viable and non-viable paracoccidioides brasiliensis propagulesArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionFibrosis PulmonarPulmonary FibrosisEsporas FúngicasSpores, FungalParacoccidioides brasiliensisRev. Inst. Med. Trop. 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