Publication:
Identification of Pneumococcal Serotypes by PCR-Restriction Fragment Length Polymorphism.

dc.contributor.authorGarcía-Suárez, María Del Mar
dc.contributor.authorGonzález-Rodríguez, Irene
dc.contributor.authorCima-Cabal, María Dolores
dc.contributor.authorYuste, Jose Enrique
dc.contributor.authorVázquez, Fernando
dc.contributor.authorSantiago, Enrique
dc.contributor.funderUniversity of Oviedo (España)
dc.contributor.funderMinisterio de Educación, Cultura y Deporte (España)
dc.contributor.funderUniversidad Internacional de La Rioja (España)
dc.date.accessioned2021-05-13T14:58:08Z
dc.date.available2021-05-13T14:58:08Z
dc.date.issued2019-11-18
dc.description.abstractStreptococcus pneumoniae shows more than 90 capsular serotypes that can be distinguished by their reactivity against antisera. The main objective of this work was the development of a molecular method for serotyping without the use of antisera. A computer program containing an algorithm was used to search in a database for potentially useful enzymes for Restriction Fragment Length Polymorphism-RFLP typing, in order to maximize the discrimination between different serotypes. DNA sequences of 90 serotypes for the region between dexB and aliA genes were compiled, and a computer screening of restriction enzymes was performed. The wzg-wzh-wzd-wze region and Sse9I restriction predicted unique PCR-RFLP patterns for 39 serotypes and eight serogroups. A second restriction enzyme resolved fragment specific patterns for 25 serotypes. The method was tested with 98 serotype-unknown clinical isolates. PCR-RFLP analysis deduced correct serotypes that were confirmed by Quellung reaction for 78.5% of the isolates.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThis research was funded by University of Oviedo (UNOV-08-MB-3) and Ministerio de Educación y Cultura (MEC-06-BIO2006-1533-C04-02) of Spain and the APC was funded by Universidad Internacional de La Rioja (UNIR).es_ES
dc.format.number4es_ES
dc.format.volume9es_ES
dc.identifier.citationDiagnostics (Basel). 2019; 9(4):196es_ES
dc.identifier.doi10.3390/diagnostics9040196es_ES
dc.identifier.issn2075-4418es_ES
dc.identifier.journalDiagnostics (Basel)es_ES
dc.identifier.pubmedID31752204es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/12955
dc.language.isoenges_ES
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/MEC-06-BIO2006-1533-C04-02es_ES
dc.relation.publisherversionhttps://doi.org/10.3390/diagnostics9040196es_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectPCR-RFLPes_ES
dc.subjectStreptococcus pneumoniaees_ES
dc.subjectSerotypees_ES
dc.titleIdentification of Pneumococcal Serotypes by PCR-Restriction Fragment Length Polymorphism.es_ES
dc.typeresearch articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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