Publication:
Detection and identification of human parainfluenza viruses 1, 2, 3, and 4 in clinical samples of pediatric patients by multiplex reverse transcription-PCR

dc.contributor.authorAguilar, Jose C.
dc.contributor.authorPerez-Breña, Pilar
dc.contributor.authorGarcía, M L
dc.contributor.authorCruz, N
dc.contributor.authorErdman, D D
dc.contributor.authorEchevarria, Juan Emilio
dc.contributor.funderInstituto de Salud Carlos III
dc.date.accessioned2019-05-31T11:27:28Z
dc.date.available2019-05-31T11:27:28Z
dc.date.issued2000-03
dc.descriptionCorrection. Detection and Identification of Human Parainfluenza Viruses 1, 2, 3, and 4 in Clinical Samples of Pediatric Patients by Multiplex Reverse Transcription-PCR. J Clin Microbiol 2000 Jul;38(7):2805. https://doi.org/10.1128/JCM.38.7.2805-2805.2000
dc.description.abstractWe describe a multiplex reverse transcription-PCR (m-RT-PCR) assay that is able to detect and differentiate all known human parainfluenza viruses (HPIVs). Serial dilution experiments with reference strains that compared cell culture isolation and m-RT-PCR showed sensitivities ranging from 0.0004 50% tissue culture infective dose (TCID(50)) for HPIV type 4B (HPIV-4B) to 32 TCID(50)s for HPIV-3. As few as 10 plasmids containing HPIV PCR products could be detected in all cases. When 201 nasopharyngeal aspirate specimens from pediatric patients hospitalized for lower respiratory illness were tested, m-RT-PCR assay detected 64 HPIVs (24 HPIV-3, 23 HPIV-1, 10 HPIV-4, and 7 HPIV-2), while only 42 of them (21 HPIV-1, 14 HPIV-3, 6 HPIV-2, and 1 HPIV-4 isolates) grew in cell culture. Our m-RT-PCR assay was more sensitive than either cell culture isolation or indirect immunofluorescence with monoclonal antibodies for the detection of HPIV infections. Also, HPIV-4 was more frequently detected than HPIV-2 in this study, suggesting that it may have been underestimated as a lower respiratory tract pathogen because of the insensitivity of cell culture.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipWe are very grateful to Francisco Pozo for help with the cloning experiments and Angel del Pozo for photographic work. This work was supported in part by “Fondo de Investigaciones Sanitarias” grant 98/0310 from the Spanish Ministry of Health.es_ES
dc.format.number3es_ES
dc.format.page1191-5es_ES
dc.format.volume38es_ES
dc.identifier.citationJ Clin Microbiol. 2000 Mar;38(3):1191-5.es_ES
dc.identifier.issn0095-1137es_ES
dc.identifier.journalJournal of clinical microbiologyes_ES
dc.identifier.pubmedID10699020es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/7704
dc.language.isoenges_ES
dc.publisherAmerican Society for Microbiology (ASM)es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/98/0310es_ES
dc.relation.publisherversionhttps://jcm.asm.org/content/38/3/1191.longes_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución-NoComercial-CompartirIgual 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.subject.meshAnimalses_ES
dc.subject.meshCell Linees_ES
dc.subject.meshChildes_ES
dc.subject.meshDNA Primerses_ES
dc.subject.meshDNA, Virales_ES
dc.subject.meshDogses_ES
dc.subject.meshFluorescent Antibody Technique, Indirectes_ES
dc.subject.meshHumanses_ES
dc.subject.meshInhalationes_ES
dc.subject.meshParainfluenza Virus 1, Humanes_ES
dc.subject.meshParainfluenza Virus 2, Humanes_ES
dc.subject.meshParainfluenza Virus 3, Humanes_ES
dc.subject.meshRespirovirus Infectionses_ES
dc.subject.meshRetrospective Studieses_ES
dc.subject.meshReverse Transcriptase Polymerase Chain Reactiones_ES
dc.subject.meshRubulaviruses_ES
dc.subject.meshRubulavirus Infectionses_ES
dc.titleDetection and identification of human parainfluenza viruses 1, 2, 3, and 4 in clinical samples of pediatric patients by multiplex reverse transcription-PCRes_ES
dc.typejournal articlees_ES
dc.type.hasVersionAMes_ES
dspace.entity.typePublication
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relation.isAuthorOfPublication21e182d5-c5af-4b64-b10e-ed2f70a7d735
relation.isAuthorOfPublication5c7d63f5-f2f7-4056-a081-af18221680be
relation.isAuthorOfPublication.latestForDiscovery2dfb3fbb-c70b-4c8d-aa67-59c8eba7895f

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