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Rapid identification of Stenotrophomonas maltophilia by peptide nucleic acid fluorescence in situ hybridization

The objective of this study was to develop a novel peptide nucleic acid (PNA) probe for Stenotrophomonas maltophilia identification by fluorescence in situ hybridization (FISH). The probe was evaluated using 33 human and veterinary clinical S. maltophilia isolates and 45 reference strains representi...

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Detalles Bibliográficos
Autores principales: Hansen, N, Rasmussen, A K I, Fiandaca, M J, Kragh, K N, Bjarnsholt, T, Høiby, N, Stender, H, Guardabassi, L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4184662/
https://www.ncbi.nlm.nih.gov/pubmed/25356348
http://dx.doi.org/10.1002/nmi2.38
Descripción
Sumario:The objective of this study was to develop a novel peptide nucleic acid (PNA) probe for Stenotrophomonas maltophilia identification by fluorescence in situ hybridization (FISH). The probe was evaluated using 33 human and veterinary clinical S. maltophilia isolates and 45 reference strains representing common bacterial species in the respiratory tract. The probe displayed 100% sensitivity and 100% specificity on pure cultures and allowed detection in sputum from cystic fibrosis patients. The detection limit was 10(4) CFU/mL in spiked tracheal aspirate and bronchoalveolar lavage from healthy horses. Altogether the study shows that this species-specific PNA FISH probe facilitates rapid detection of S. maltophilia in biological specimens.