Publication:
DiiA is a novel dimorphic cell wall protein of Streptococcus pneumoniae involved in invasive disease

dc.contributor.authorEscolano-Martinez, Maria S
dc.contributor.authorDomenech, Arnau
dc.contributor.authorYuste, Jose Enrique
dc.contributor.authorCercenado, Maria I
dc.contributor.authorArdanuy, Carmen
dc.contributor.authorLiñares, Josefina
dc.contributor.authorde la Campa, Adela G
dc.contributor.authorMartin-Galiano, Antonio Javier
dc.contributor.funderMinisterio de Economía y Competitividad (España)
dc.contributor.funderPlan Nacional de I+D+i (España)
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderMinisterio de Educación (España)
dc.date.accessioned2024-02-02T18:46:26Z
dc.date.available2024-02-02T18:46:26Z
dc.date.issued2016-07
dc.description.abstractObjectives: Many outer multidomain proteins play fundamental virulent roles in an allele-dependent manner. We aimed to investigate the influence of the outer SP1992 protein, here renamed DiiA (Dimorphic invasion-involved A), in pneumococcal disease. Methods: The presence and type of diiA allele was screened by PCR in 560 clinical isolates. Isogenic mutants carrying progressive diiA deletions were constructed and checked in mouse models of infection. DiiA binding to human molecules was carried out by surface plasmon resonance. Results: The diiA gene is exclusive of Streptococcus pneumoniae and included in the core genome. DiiA variants contain one or two imperfect repeats (R1 and R2), an unstructured region and a cell-wall anchor domain. Clonal complexes carrying both repeats were associated with invasive disease, while those carrying R2 preferentially caused non-invasive syndromes in patients with underlying risk factors. Mutants lacking both repeats were less efficient in nasopharyngeal colonization and dissemination from lungs. Moreover, the ΔdiiA defective strain suffered a severe impairment in bacterial proliferation in blood. Purified DiiA bound to collagen and lactoferrin with high affinity. Conclusions: DiiA is a distinctive pneumococcal virulence factor contributing to colonization and long-term invasion in this pathogen.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipA.J.M-G. is the recipient of a Miguel Servet contract from the Spanish Ministry of Economy and Competitiveness. This study was supported by grants BIO2011-25343, BIO2014-55462-R and SAF2012-39444-C02 from the Plan Nacional de I+D+I of the Ministry of Science and Innovation, and by a grant from the Fondo de Investigaciones Sanitarias de la Seguridad Social (PI11/00763). CIBER Enfermedades Respiratorias is an initiative of the Instituto de Salud Carlos III. M.E. was supported by a fellowship from the Formacion de Profesorado Universitario (FPU; Ministry of Education, FPU13/02899).es_ES
dc.format.number1es_ES
dc.format.page71-81es_ES
dc.format.volume73es_ES
dc.identifier.citationJ Infect. 2016 Jul;73(1):71-81.es_ES
dc.identifier.doi10.1016/j.jinf.2016.04.010es_ES
dc.identifier.e-issn1532-2742es_ES
dc.identifier.journalThe Journal of infectiones_ES
dc.identifier.pubmedID27105656es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/17441
dc.language.isoenges_ES
dc.publisherElsevier
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/MINECO//SAF2012-39444-C02-02/ES/COLONIZACION NEUMOCOCICA Y ESTADO DE PORTADOR: BASES MOLECULARES, PROFILAXIS Y MEDIDAS TERAPEUTICAS/es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/MICINN//PI11%2F00763/ES/Estudio multicéntrico de la enfermedad neumocócica invasiva en el adulto: incidencia, epidemiología y caracterización molecular de los clones de S.pneumoniae en la era de la vacuna conjugada 13 valente/es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/MICINN//BIO2011-25343/ES/EL CONTROL DEL NIVEL DEL SUPERENROLLAMIENTO EN STREPTOCOCCUS PNEUMONIAE COMO DIANA DE ANTIMICROBIANOS/es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/MINECO//BIO2014-55462-R/ES/PAPEL DE LAS DNA TOPOISOMERASAS Y DE LAS PROTEINAS DE UNION AL NUCLEOIDE EN LA ORGANIZACION DEL CROMOSOMA DE STREPTOCOCCUS PNEUMONIAE: RESPUESTA A ANTIBIOTICOS Y VIRULENCIA/es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/MECD//FPU13%2F02899/ES/FPU13%2F02899/es_ES
dc.relation.publisherversionhttps://doi.org/10.1016/j.jinf.2016.04.010es_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAdhesinees_ES
dc.subjectGenomicses_ES
dc.subjectHypothetical proteines_ES
dc.subjectInvasiones_ES
dc.subjectVaccinees_ES
dc.subjectVirulence factores_ES
dc.subject.meshAdultes_ES
dc.subject.meshAnimalses_ES
dc.subject.meshBacterial Proteinses_ES
dc.subject.meshCell Walles_ES
dc.subject.meshCollagenes_ES
dc.subject.meshDisease Models, Animales_ES
dc.subject.meshGene Deletiones_ES
dc.subject.meshHumanses_ES
dc.subject.meshLactoferrines_ES
dc.subject.meshMalees_ES
dc.subject.meshMice, Inbred C57BLes_ES
dc.subject.meshPolymerase Chain Reactiones_ES
dc.subject.meshProtein Bindinges_ES
dc.subject.meshStreptococcal Infectionses_ES
dc.subject.meshStreptococcus pneumoniaees_ES
dc.subject.meshSurface Plasmon Resonancees_ES
dc.subject.meshVirulence Factorses_ES
dc.titleDiiA is a novel dimorphic cell wall protein of Streptococcus pneumoniae involved in invasive diseasees_ES
dc.typeresearch articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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