Reação em cadeia de Polimerase como uma ferramenta auxiliar para o diagnóstico de Lesões Orais e Maxilofaciais de Aspergilose

dc.creatorThaís Ellen Chaves Gomes
dc.date.accessioned2024-12-19T15:14:35Z
dc.date.accessioned2025-09-08T23:49:20Z
dc.date.available2024-12-19T15:14:35Z
dc.date.issued2024-08-06
dc.description.abstractAspergillosis is a fungal disease caused by the inhalation of fungal spores of the genus Aspergillus spp. This fungus mainly affects the lungs but can spread and infect the maxillofacial region through the bloodstream or inoculation of the fungus after extraction or endodontic treatment, especially in the upper posterior teeth. The disease has nonspecific clinical manifestations that hinder its early diagnosis. Although the Polymerase Chain Reaction (PCR) technique holds promise as a diagnostic tool for aspergillosis, anatomopathological analysis services do not routinely adopt this method. Therefore, the present study aimed to evaluate the applicability of PCR and standardise the techniques of preparation of biological samples for the detection of the three species: Aspergillus niger, Aspergillus fumigatus and Aspergillus flavus. Six samples of formalin-fixed, paraffin-embedded tissue (FFPE) with a histopathological diagnosis suggestive of aspergillosis were investigated using PCR. As a positive control for the PCR reaction, morphologically and genetically characterized cultures were used, with their sequences deposited at NCBI under accession codes MW837777 (A. fumigatus) and MW837779 (A. niger). The A. flavus culture used is reference RC 2053. Four of the six samples evaluated were positive for Aspergillus spp., of which one was co-infected with A. fumigatus and A. flavus species, while two others were positive only for A. flavus, and one sample was positive only for A. fumigatus. These findings suggest that PCR can be used as an auxiliary method for diagnosing aspergillosis. However, this was a pilot study, and expansion of the sample size and the evaluation of PCR in comparison with other diagnostic tests for aspergillosis are essential to determine the accuracy of the method.
dc.description.sponsorshipCAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
dc.identifier.urihttps://hdl.handle.net/1843/78784
dc.languageeng
dc.publisherUniversidade Federal de Minas Gerais
dc.relationPrograma Institucional de Internacionalização – CAPES - PrInt
dc.rightsAcesso Aberto
dc.subjectAspergilose
dc.subjectProteína C-Reativa
dc.subjectReação em Cadeia Polimerase
dc.subjectAspergillus
dc.subjectDiagnóstico
dc.subjectDissertação Acadêmica
dc.subject.otheraspergillosis
dc.subject.otherAspergillus
dc.subject.otherPCR
dc.subject.otherDiagnosis
dc.titleReação em cadeia de Polimerase como uma ferramenta auxiliar para o diagnóstico de Lesões Orais e Maxilofaciais de Aspergilose
dc.typeDissertação de mestrado
local.contributor.advisor-co1Roberta Rayra Martins Chaves
local.contributor.advisor1Ricardo Santiago Gomez
local.contributor.advisor1Latteshttps://lattes.cnpq.br/5760422122697584
local.creator.Latteshttp://lattes.cnpq.br/2004192020141297
local.description.resumoBackground: Aspergillosis is a fungal disease caused by the inhalation of fungal spores of the genus Aspergillus spp. This fungus mainly affects the lungs but can spread and infect the max illofacial region through the bloodstream or inoculation of the fungus after extraction or endodontic treatment, especially in the upper posterior teeth. The disease has nonspecific clinical manifestations that hinder its early diagnosis. Although the Polymerase Chain Reaction (PCR) technique holds promise as a diagnostic tool for aspergillosis, anatomopathological analysis services do not routinely adopt this method. Objectives: Therefore, the present study aimed to evaluate the applicability of PCR and standardise the techniques of preparation of biological samples for the detection of the Citation: Gomes, T.E.C.; Bastos, V.C.; Boniek, D.; Romañach, M.; Rocha, F.F.; Chaves, R.R.M.; Gomez, R.S. A PCR-Based Approach for Early Diagnosis of Head and Neck Aspergillosis: A Pilot Study. Genes 2024, 15, 1428. https://doi.org/ 10.3390/genes15111428 Academic Editors: Shinya Nishio and Silvia Turroni Received: 14 August 2024 Revised: 20 September 2024 Accepted: 30 October 2024 Published: 31 October 2024 Copyright: © 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/). three species: Aspergillus niger, Aspergillus fumigatus and Aspergillus flavus. Methods: Six samples of formalin-fixed, paraffin-embedded tissue (FFPE) with a histopathological diagnosis suggestive of aspergillosis were investigated using PCR. As a positive control for the PCR reaction, morphologically and genetically characterized cultures were used, with their sequences deposited at NCBI under accession codes MW837777 (A. fumigatus) and MW837779 (A. niger). The A. flavus culture used is reference RC 2053. Results: Four of the six samples evaluated were positive for Aspergillus spp., of which one was co-infected with A. fumigatus and A. flavus species, while two others were positive only for A. flavus, and one sample was positive only for A. fumigatus. Conclusions: These findings suggest that PCR can be used as an auxiliary method for diagnosing aspergillosis. However, this was a pilot study, and expansion of the sample size and the evaluation of PCR in comparison with other diagnostic tests for aspergillosis are essential to determine the accuracy of the method.
local.publisher.countryBrasil
local.publisher.initialsUFMG
local.publisher.programPrograma de Pós-Graduação em Medicina Molecular

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