Reação em cadeia de Polimerase como uma ferramenta auxiliar para o diagnóstico de Lesões Orais e Maxilofaciais de Aspergilose
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Universidade Federal de Minas Gerais
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Dissertação de mestrado
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Background: 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.
Abstract
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 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.
Assunto
Aspergilose, Proteína C-Reativa, Reação em Cadeia Polimerase, Aspergillus, Diagnóstico, Dissertação Acadêmica
Palavras-chave
aspergillosis, Aspergillus, PCR, Diagnosis