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New Strategy for Rapid Diagnosis and Characterization of Fungal Infections: The Example of Corneal Scrapings

PURPOSE: The prognosis of people infected with Fungi especially immunocompromised depends on rapid and accurate diagnosis to capitalize on time administration of specific treatments. However, cultures produce false negative results and nucleic-acid amplification techniques require complex post-ampli...

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Autores principales: Goldschmidt, Pablo, Degorge, Sandrine, Che Sarria, Patricia, Benallaoua, Djida, Semoun, Oudy, Borderie, Vincent, Laroche, Laurent, Chaumeil, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388096/
https://www.ncbi.nlm.nih.gov/pubmed/22768289
http://dx.doi.org/10.1371/journal.pone.0037660
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author Goldschmidt, Pablo
Degorge, Sandrine
Che Sarria, Patricia
Benallaoua, Djida
Semoun, Oudy
Borderie, Vincent
Laroche, Laurent
Chaumeil, Christine
author_facet Goldschmidt, Pablo
Degorge, Sandrine
Che Sarria, Patricia
Benallaoua, Djida
Semoun, Oudy
Borderie, Vincent
Laroche, Laurent
Chaumeil, Christine
author_sort Goldschmidt, Pablo
collection PubMed
description PURPOSE: The prognosis of people infected with Fungi especially immunocompromised depends on rapid and accurate diagnosis to capitalize on time administration of specific treatments. However, cultures produce false negative results and nucleic-acid amplification techniques require complex post-amplification procedures to differentiate relevant fungal types. The objective of this work was to develop a new diagnostic strategy based on real-time polymerase-chain reaction high-resolution melting analysis (PCR-HRM) that a) detects yeasts and filamentous Fungi, b) differentiates yeasts from filamentous Fungi, and c) discriminates among relevant species of yeasts. METHODS: PCR-HRM detection limits and specificity were assessed with a) isolated strains; b) human blood samples experimentally infected with Fungi; c) blood experimentally infected with other infectious agents; d) corneal scrapings from patients with suspected fungal keratitis (culture positive and negative) and e) scrapings from patients with suspected bacterial, viral or Acanthamoeba infections. The DNAs were extracted and mixed with primers diluted in the MeltDoctor® HRM Master Mix in 2 tubes, the first for yeasts, containing the forward primer CandUn (5'CATGCCTGTTTGAGCGTC) and the reverse primer FungUn (5'TCCTCCGCTT ATTGATATGCT) and the second for filamentous Fungi, containing the forward primer FilamUn (5'TGCCTGTCCGAGCGTCAT) and FungUn. Molecular probes were not necessary. The yields of DNA extraction and the PCR inhibitors were systematically monitored. RESULTS: PCR-HRM detected 0.1 Colony Forming Units (CFU)/µl of yeasts and filamentous Fungi, differentiated filamentous Fungi from yeasts and discriminated among relevant species of yeasts. PCR-HRM performances were higher than haemoculture and sensitivity and specificity was 100% for culture positive samples, detecting and characterizing Fungi in 7 out 10 culture negative suspected fungal keratitis. CONCLUSIONS: PCR-HRM appears as a new, sensitive, specific and inexpensive test that detects Fungi and differentiates filamentous Fungi from yeasts. It allows direct fungal detection from clinical samples and experimentally infected blood in less than 2.30 h after DNA extraction.
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spelling pubmed-33880962012-07-05 New Strategy for Rapid Diagnosis and Characterization of Fungal Infections: The Example of Corneal Scrapings Goldschmidt, Pablo Degorge, Sandrine Che Sarria, Patricia Benallaoua, Djida Semoun, Oudy Borderie, Vincent Laroche, Laurent Chaumeil, Christine PLoS One Research Article PURPOSE: The prognosis of people infected with Fungi especially immunocompromised depends on rapid and accurate diagnosis to capitalize on time administration of specific treatments. However, cultures produce false negative results and nucleic-acid amplification techniques require complex post-amplification procedures to differentiate relevant fungal types. The objective of this work was to develop a new diagnostic strategy based on real-time polymerase-chain reaction high-resolution melting analysis (PCR-HRM) that a) detects yeasts and filamentous Fungi, b) differentiates yeasts from filamentous Fungi, and c) discriminates among relevant species of yeasts. METHODS: PCR-HRM detection limits and specificity were assessed with a) isolated strains; b) human blood samples experimentally infected with Fungi; c) blood experimentally infected with other infectious agents; d) corneal scrapings from patients with suspected fungal keratitis (culture positive and negative) and e) scrapings from patients with suspected bacterial, viral or Acanthamoeba infections. The DNAs were extracted and mixed with primers diluted in the MeltDoctor® HRM Master Mix in 2 tubes, the first for yeasts, containing the forward primer CandUn (5'CATGCCTGTTTGAGCGTC) and the reverse primer FungUn (5'TCCTCCGCTT ATTGATATGCT) and the second for filamentous Fungi, containing the forward primer FilamUn (5'TGCCTGTCCGAGCGTCAT) and FungUn. Molecular probes were not necessary. The yields of DNA extraction and the PCR inhibitors were systematically monitored. RESULTS: PCR-HRM detected 0.1 Colony Forming Units (CFU)/µl of yeasts and filamentous Fungi, differentiated filamentous Fungi from yeasts and discriminated among relevant species of yeasts. PCR-HRM performances were higher than haemoculture and sensitivity and specificity was 100% for culture positive samples, detecting and characterizing Fungi in 7 out 10 culture negative suspected fungal keratitis. CONCLUSIONS: PCR-HRM appears as a new, sensitive, specific and inexpensive test that detects Fungi and differentiates filamentous Fungi from yeasts. It allows direct fungal detection from clinical samples and experimentally infected blood in less than 2.30 h after DNA extraction. Public Library of Science 2012-07-02 /pmc/articles/PMC3388096/ /pubmed/22768289 http://dx.doi.org/10.1371/journal.pone.0037660 Text en Goldschmidt et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Goldschmidt, Pablo
Degorge, Sandrine
Che Sarria, Patricia
Benallaoua, Djida
Semoun, Oudy
Borderie, Vincent
Laroche, Laurent
Chaumeil, Christine
New Strategy for Rapid Diagnosis and Characterization of Fungal Infections: The Example of Corneal Scrapings
title New Strategy for Rapid Diagnosis and Characterization of Fungal Infections: The Example of Corneal Scrapings
title_full New Strategy for Rapid Diagnosis and Characterization of Fungal Infections: The Example of Corneal Scrapings
title_fullStr New Strategy for Rapid Diagnosis and Characterization of Fungal Infections: The Example of Corneal Scrapings
title_full_unstemmed New Strategy for Rapid Diagnosis and Characterization of Fungal Infections: The Example of Corneal Scrapings
title_short New Strategy for Rapid Diagnosis and Characterization of Fungal Infections: The Example of Corneal Scrapings
title_sort new strategy for rapid diagnosis and characterization of fungal infections: the example of corneal scrapings
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388096/
https://www.ncbi.nlm.nih.gov/pubmed/22768289
http://dx.doi.org/10.1371/journal.pone.0037660
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