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dc.contributor.authorCamacho, Juan 
dc.contributor.authorNegredo, Anabel 
dc.contributor.authorCarrilero, Bartolomé
dc.contributor.authorSegovia, Manuel
dc.contributor.authorMoreno, Antonio
dc.contributor.authorPozo Sanchez, Francisco 
dc.contributor.authorEchevarria, Juan Emilio 
dc.contributor.authorEchevarria, Jose Manuel 
dc.contributor.authorSánchez-Seco, María Paz 
dc.contributor.authorTarrago Asensio, David 
dc.date.accessioned2023-11-17T10:14:53Z
dc.date.available2023-11-17T10:14:53Z
dc.date.issued2023-11
dc.identifier.citationInfect Dis Ther. 2023 Nov;12(11):2621-2630.es_ES
dc.identifier.issn2193-8229es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/16690
dc.description.abstractIntroduction: We report the case of a fatal hemorrhagic varicella primary infection in an immunocompetent man and whole-genome characterization of the virus for the investigation of biomarkers of virulence. Case: A 38-year-old patient born in Nigeria presented to the emergency department with abdominal pain and subsequently developed fatal hemorrhagic disease without skin rash. Extensive laboratory tests including serology and PCR for arenaviruses, bunyaviruses and ebolaviruses were negative. Varicella-zoster virus (VZV) PCR of sera, liver and spleen tissue samples from autopsy revealed the presence of VZV DNA. Primary infection by varicella-zoster virus with hemorrhagic manifestations was diagnosed after virological testing. The VZV genome was sequenced using a mWGS approach. Bioinformatic analysis showed 53 mutations across the genome, 33 of them producing non-synonymous variants affecting up to 14 genes. Some of them, such as ORF11 and ORF 62, encoded for essential functions related to skin or neurotropism. To our knowledge, the mutations reported here have never been described in a VZV causing such a devastating outcome. Discussion: In immunocompetent patients, viral factors should be considered in patients with uncommon symptoms or severe diseases. Some relevant mutations revealed by using whole genome sequencing (WGS) directly from clinical samples may be involved in this case and deserves further investigation. Conclusion: Differential diagnosis of varicella-zoster virus in immunocompetent adults should be considered among patients with suspected VHF, even if the expected vesicular rash is not present at admission and does not arise thereafter. Whole genome sequencing of strains causing uncommon symptoms and/or mortality is needed for epidemiological surveillance and further characterization of putative markers of virulence. Additionally, this report highlights the recommendation for a VZV vaccination policy in non-immunized migrants from developing countries.es_ES
dc.description.sponsorshipThis work was supported by a grant from Instituto de Salud Carlos III. Project code MPY1372/12. The journal’s Rapid Service fee was paid by Consorcio Centro de Investigación en Red (CIBER). The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.es_ES
dc.language.isoenges_ES
dc.publisherSpringer es_ES
dc.type.hasVersionVoRes_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.subjectHemorrhagic feveres_ES
dc.subjectMetagenomic whole genome sequencing (mWGS)es_ES
dc.subjectSingle-nucleotide polymorphism (SNP)es_ES
dc.subjectVaricella-zoster viruses_ES
dc.subjectVaricella-zoster virus cell tropismes_ES
dc.subjectVaricella-zoster virus cladeses_ES
dc.subjectVaricella-zoster virus mutationses_ES
dc.subjectVaricella-zoster virus virulencees_ES
dc.titleMutations in Coding and Non-Coding Regions in Varicella-Zoster Virus Causing Fatal Hemorrhagic Fever Without Rash in an Immunocompetent Patient: Case Reportes_ES
dc.typeresearch articlees_ES
dc.rights.licenseAtribución-NoComercial 4.0 Internacional*
dc.identifier.pubmedID37870692es_ES
dc.format.volume12es_ES
dc.format.number11es_ES
dc.format.page2621-2630es_ES
dc.identifier.doi10.1007/s40121-023-00884-0es_ES
dc.contributor.funderInstituto de Salud Carlos III es_ES
dc.contributor.funderCentro de Investigación Biomédica en Red - CIBERINFEC (Enfermedades Infecciosas) es_ES
dc.contributor.funderCentro de Investigación Biomédica en Red - CIBERESP (Epidemiología y Salud Pública) es_ES
dc.description.peerreviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1007/s40121-023-00884-0es_ES
dc.identifier.journalInfectious diseases and therapyes_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/MPY1372/12es_ES


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