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dc.contributor.authorValero Rello, Anna
dc.contributor.authorHenares Bonilla, Desirée
dc.contributor.authorAcosta Argueta, Lesly María
dc.contributor.authorJané Checa, Mireia
dc.contributor.authorGodoy Garcia, Pere
dc.contributor.authorMuñoz Almagro, Carmen
dc.contributor.otherUniversitat Politècnica de Catalunya. Departament d'Estadística i Investigació Operativa
dc.date.accessioned2019-02-13T12:56:16Z
dc.date.available2019-02-13T12:56:16Z
dc.date.issued2019-01-01
dc.identifier.citationValero , A. [et al.]. Validation and implementation of a diagnostic algorithm for DNA Detection of Bordetella pertussis, B. parapertussis, and B-holmesii in a Pediatric Referral Hospital in Barcelona, Spain. "Journal of clinical microbiology", 1 Gener 2019, vol. 57, núm. 1, p. e01231-1-e01231-8.
dc.identifier.issn0095-1137
dc.identifier.urihttp://hdl.handle.net/2117/129052
dc.description.abstractThis study aimed to validate a comprehensive diagnostic protocolbased on real-time PCR for the rapid detection and identification ofBordetella per-tussis,Bordetella parapertussis, andBordetella holmesii, as well as its implementationin the diagnostic routine of a reference children’s hospital. The new algorithm in-cluded a triplex quantitative PCR (qPCR) targeting IS481gene (inB. pertussis,B. hol-mesii, and someBordetella bronchisepticastrains), pIS1001(B. parapertussis-specific)andrnaseP as the human internal control. Two confirmatory singleplex tests forB.pertussis(ptxA-Pr) andB. holmesii(hIS1001) were performed if IS481was positive. An-alytical validation included determination of linear range, linearity, efficiency, preci-sion, sensitivity, and a reference panel with clinical samples. Once validated, the newalgorithm was prospectively implemented in children with clinical suspicion ofwhooping cough presenting to Hospital Sant Joan de Deu (Barcelona, Spain) over12 months. Lower limits of detection obtained were 4.4, 13.9, and 27.3 genomicequivalents/ml of sample for IS481(onB. pertussis), pIS1001and hIS1001, and 777.9forptxA-Pr. qPCR efficiencies ranged from 86.0% to 96.9%. Intra- and interassay vari-abilities were 3% and 5%, respectively. Among 566 samples analyzed,B. pertus-sis,B. holmesii, andB. parapertussiswere detected in 11.1%, 0.9% (only in females 4 years old), and 0.2% of samples, respectively. The new algorithm proved to be auseful microbiological diagnostic tool for whooping cough, demonstrating a low rateof other non-pertussis Bordetellaspecies in our surveilled area
dc.language.isoeng
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Spain
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.subject.lcshAlgorithms
dc.subject.lcshDNA
dc.subject.otherB. holmesii
dc.subject.otherB. parapertussis
dc.subject.otherBordetella pertussis
dc.subject.otherreal-time PCR
dc.subject.otherwhooping cough
dc.titleValidation and implementation of a diagnostic algorithm for DNA Detection of Bordetella pertussis, B. parapertussis, and B-holmesii in a Pediatric Referral Hospital in Barcelona, Spain
dc.typeArticle
dc.subject.lemacAlgorismes
dc.subject.lemacADN
dc.contributor.groupUniversitat Politècnica de Catalunya. ADBD - Anàlisi de Dades Complexes per a les Decisions Empresarials
dc.identifier.doi10.1128/JCM.01231-18
dc.description.peerreviewedPeer Reviewed
dc.relation.publisherversionhttps://jcm.asm.org/content/57/1/e01231-18
dc.rights.accessOpen Access
local.identifier.drac23663638
dc.description.versionPostprint (author's final draft)
local.citation.authorValero , A.; Henares, D.; Acosta, L.; Jané, M.; Godoy, P.; Muñoz, C.
local.citation.publicationNameJournal of clinical microbiology
local.citation.volume57
local.citation.number1
local.citation.startingPagee01231-1
local.citation.endingPagee01231-8


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