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Use of SCW4 gene primers in PCR methods for the identification of six medically important Aspergillus species.
Arancia, Silvia; Sandini, Silvia; De Carolis, Elena; Vella, Antonietta; Sanguinetti, Maurizio; Norelli, Sandro; De Bernardis, Flavia.
Afiliación
  • Arancia S; Department of Veterinary Public Health and Food Safety. Istituto Superiore di Sanità, Rome, Italy.
  • Sandini S; Department of Infectious, Parasitic and Immune-Mediated Diseases. Istituto Superiore di Sanità, Rome, Italy.
  • De Carolis E; Institute of Microbiology. Università Cattolica del Sacro Cuore, Rome, Italy.
  • Vella A; Institute of Microbiology. Università Cattolica del Sacro Cuore, Rome, Italy.
  • Sanguinetti M; Institute of Microbiology. Università Cattolica del Sacro Cuore, Rome, Italy.
  • Norelli S; National Centre ONDICO. Istituto Superiore di Sanità, Rome, Italy.
  • De Bernardis F; Department of Infectious, Parasitic and Immune-Mediated Diseases. Istituto Superiore di Sanità, Rome, Italy.
New Microbiol ; 39(4): 274-286, 2016 Oct.
Article en En | MEDLINE | ID: mdl-27455180
ABSTRACT
Aspergillus species are the cause of invasive mold infections in immunocompromised patients Aspergillus fumigatus, A. flavus and A. terreus account for most cases of invasive aspergillosis (IA). As certain species are associated with higher mortality and vary in their resistance to antifungal therapy, diagnosis requires increasingly rapid molecular methods that enable sensitive detection and species discrimination. We have developed PCR and Multiplex PCR assays for the detection of six medically important Aspergillus spp. species DNA in bronchoalveolar lavage (BAL) specimens from hematology and intensive care unit (ICU) patients at risk of IA, using different species and genus-specific PCR primers, selected within the SCW4 gene, encoding a cell wall glucanase of A. fumigatus, similar to mannoprotein Mp65 of Candida albicans. The genus-specific PCR primers were able to amplify only Aspergillus DNAs but not that belonging to other fungal genera tested. The species-specific PCR primers allowed differentiation of each Aspergillus species by the amplicon length produced. The methods described in this study are rapid (less than 4 h), reproducible, simple and specific and demonstrate potential application in the clinical laboratory.
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Banco de datos: MEDLINE Asunto principal: Aspergillus / ADN de Hongos / Reacción en Cadena de la Polimerasa Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: New Microbiol Asunto de la revista: MICROBIOLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Italia
Buscar en Google
Banco de datos: MEDLINE Asunto principal: Aspergillus / ADN de Hongos / Reacción en Cadena de la Polimerasa Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: New Microbiol Asunto de la revista: MICROBIOLOGIA Año: 2016 Tipo del documento: Article País de afiliación: Italia