Publication:
Comparative Analysis of 2022 Outbreak MPXV and Previous Clade II MPXV

dc.contributor.authorMcGrail, Joseph Patrick
dc.contributor.authorPaniz Mondolfi, Alberto
dc.contributor.authorRamírez, Juan David
dc.contributor.authorVidal, Santiago
dc.contributor.authorGarcía-Sastre, Adolfo
dc.contributor.authorPalacios, Gustavo
dc.contributor.authorSánchez-Seco, María Paz
dc.contributor.authorGuerra, Susana
dc.contributor.funderAgencia Estatal de Investigación (España)
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)
dc.contributor.funderUnión Europea. Fondo Social Europeo (ESF/FSE)
dc.date.accessioned2025-01-10T13:30:21Z
dc.date.available2025-01-10T13:30:21Z
dc.date.issued2024-11
dc.description.abstractThe 2022-2024 outbreak of MPOX is an important worldwide public health issue that has triggered significant concerns in the scientific community. MPOX is caused by monkeypox virus (MPXV) belonging to the Poxviridae family. The study of MPXV presents a multifaceted challenge due to the diverse viral formThis study was supported by ISIDORe consortium and Agencia Estatal de Investigación.s produced by this pathogen. Notably the intracellular mature viruses (MVs) primarily contribute to localized lesions and host-to-host transmission, while the extracellular enveloped viruses (EVs) are associated with systemic infection. Clinically, MPOX manifests as a vesiculopustular rash that initially emerges on the face and trunk, subsequently spreading throughout the body, with heightened severity observed in immunocompromised individuals. Results obtained in this manuscript indicate that the 2022 outbreak MPXV has a significantly slower viral cycle compared with previous Clade II strains, with WRAIR 7-61 being more intermediate and USA 2003 producing highest viral titers. Additionally, proteomic and phospho-proteomic analysis displays differences in protein expression between these three strains. These findings highlight key differences between the current Lineage B.1 MPXV and previous strains. Further studies will be undertaken to demonstrate if these differences are important for the apparent increased human-to-human transmission mechanisms observed in the Clade IIb MPXV outbreak.
dc.description.peerreviewed
dc.description.sponsorshipThis study was supported by ISIDORe consortium, Agencia Estatal de Investigación and FEDER/FSE (PID2023‐146351OB‐I00, PID2020‐117425RB‐C21, PDC2021‐121307‐I00)
dc.format.number11
dc.format.pagee70023
dc.format.volume96
dc.identifier.citationMcGrail JP, Mondolfi AP, Ramírez JD, Vidal S, García-Sastre A, Palacios G, Sanchez-Seco MP, Guerra S. Comparative Analysis of 2022 Outbreak MPXV and Previous Clade II MPXV. J Med Virol. 2024 Nov;96(11):e70023.
dc.identifier.doi10.1002/jmv.70023
dc.identifier.e-issn1096-9071
dc.identifier.issn0146-6615
dc.identifier.journalJournal of medical virology
dc.identifier.pubmedID39466906
dc.identifier.urihttps://hdl.handle.net/20.500.12105/25993
dc.language.isoeng
dc.publisherWiley
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/PID2023‐146351OB‐I00
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/PID2020‐117425RB‐C21
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/PDC2021‐121307‐I00
dc.relation.publisherversionhttps://doi.org/10.1002/jmv.70023
dc.repisalud.centroISCIII::Centro Nacional de Microbiología (CNM)
dc.repisalud.institucionISCIII
dc.rights.accessRightsopen access
dc.rights.licenseAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectClade II
dc.subjectEV
dc.subjectMPOX disease
dc.subjectMPXV
dc.subjectMV
dc.subject.meshDisease Outbreaks
dc.subject.meshGenome, Viral
dc.subject.meshHumans
dc.subject.meshMonkeypox virus
dc.subject.meshMpox (monkeypox)
dc.subject.meshPhylogeny
dc.titleComparative Analysis of 2022 Outbreak MPXV and Previous Clade II MPXV
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication
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