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dc.creatorXirogianni, A.en
dc.creatorTzanakaki, G.en
dc.creatorKaragianni, E.en
dc.creatorMarkoulatos, P.en
dc.creatorKourea-Kremastinou, J.en
dc.date.accessioned2015-11-23T10:54:18Z
dc.date.available2015-11-23T10:54:18Z
dc.date.issued2009
dc.identifier10.1016/j.diagmicrobio.2008.09.017
dc.identifier.issn0732-8893
dc.identifier.urihttp://hdl.handle.net/11615/34704
dc.description.abstractThis study describes the development and evaluation of a multiplex single-tube polymerase chain reaction assay for the simultaneous detection of Haemophilus influenzae, Pseudomonas aeruginosa, Staphylococcus aureus, and Streptococcus spp. used as target species-specific or genus-specific genes. The assay enables the detection of 5 to 50 pg of bacterial DNA. The sensitivity of the assay was evaluated as 100% for R aeruginosa, S. aureus, and Streptococcus spp., and 94.3% for H. influenzae; the specificity was 100% for all 4 microorganisms (positive predictive value, 100%; negative predictive value, 98.2%). The assay permits rapid and accurate detection of these 4 microorganisms in a wide range of clinical samples such as whole blood, cerebrospinal, ear, pleural and ophthalmic fluids, as well as bronchoalveolar lavage and bronchial secretions. (c) 2009 Published by Elsevier Inc.en
dc.sourceDiagnostic Microbiology and Infectious Diseaseen
dc.source.uri<Go to ISI>://WOS:000263212100001
dc.subjectHaemophilus influenzaeen
dc.subjectStreptococcus spp.en
dc.subjectPseudomonas aeruginosaen
dc.subjectStalphylococcus aureusen
dc.subjectMultiplex PCRen
dc.subjectClinical samplesen
dc.subjectBACTERIAL-MENINGITISen
dc.subjectCEREBROSPINAL-FLUIDen
dc.subjectRAPID DETECTIONen
dc.subjectMULTIPLEXen
dc.subjectPCRen
dc.subjectMENINGOCOCCAL DISEASEen
dc.subjectIDENTIFICATIONen
dc.subjectDIAGNOSISen
dc.subjectPNEUMONIAEen
dc.subjectGENEen
dc.subjectAMPLIFICATIONen
dc.subjectInfectious Diseasesen
dc.subjectMicrobiologyen
dc.titleDevelopment of a single-tube polymerase chain reaction assay for the simultaneous detection of Haemophilus influenzae, Pseudomonas aeruginosa, Staphylococcus aureus, and Streptococcus spp. directly in clinical samplesen
dc.typejournalArticleen


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