Identificador persistente para citar o vincular este elemento:
https://accedacris.ulpgc.es/jspui/handle/10553/156441
| Campo DC | Valor | idioma |
|---|---|---|
| dc.contributor.author | Zavaglio, Federica | en_US |
| dc.contributor.author | Fiorina, Loretta | en_US |
| dc.contributor.author | Martel Suárez, Nicolás Alfonso | en_US |
| dc.contributor.author | Fornara, Chiara | en_US |
| dc.contributor.author | De Cicco, Marica | en_US |
| dc.contributor.author | Cirasola, Daniela | en_US |
| dc.contributor.author | Davison, Andrew J. | en_US |
| dc.contributor.author | Gerna, Giuseppe | en_US |
| dc.contributor.author | Lilleri, Daniele | en_US |
| dc.date.accessioned | 2026-01-29T15:32:25Z | - |
| dc.date.available | 2026-01-29T15:32:25Z | - |
| dc.date.issued | 2021 | en_US |
| dc.identifier.issn | 1999-4915 | en_US |
| dc.identifier.uri | https://accedacris.ulpgc.es/jspui/handle/10553/156441 | - |
| dc.description.abstract | Background: Strain-specific antibodies to human cytomegalovirus (HCMV) glycoproteins B and H (gB and gH) have been proposed as a potential diagnostic tool for identifying reinfection. We investigated genotype-specific IgG antibody responses in parallel with defining the gB and gH genotypes of the infecting viral strains. Methods: Subjects with primary (n = 20) or non-primary (n = 25) HCMV infection were studied. The seven gB (gB1-7) and two gH (gH1-2) genotypes were determined by real-time PCR and whole viral genome sequencing, and genotype-specific IgG antibodies were measured by a peptide-based enzyme-linked immunosorbent assay (ELISA). Results: Among subjects with primary infection, 73% (n = 8) infected by gB1-HCMV and 63% (n = 5) infected by gB2/3-HCMV had genotype-specific IgG antibodies to gB (gB2 and gB3 are similar in the region tested). Peptides from the rarer gB4-gB7 genotypes had nonspecific antibody responses. All subjects infected by gH1-HCMV and 86% (n = 6) infected by gH2-HCMV developed genotype-specific responses. Among women with non-primary infection, gB and gH genotype-specific IgG antibodies were detected in 40% (n = 10) and 80% (n = 20) of subjects, respectively. Conclusions: Peptide-based ELISA is capable of detecting primary genotype-specific IgG responses to HCMV gB and gH, and could be adopted for identifying reinfections. However, about half of the subjects did not have genotype-specific IgG antibodies to gB. | en_US |
| dc.language | eng | en_US |
| dc.relation.ispartof | Viruses | en_US |
| dc.source | Viruses [eISSN 1999-4915], v. 13(3) (Marzo 2021) | en_US |
| dc.subject | 32 Ciencias médicas | en_US |
| dc.subject | 320102 Genética clínica | en_US |
| dc.subject.other | Human cytomegalovirus | en_US |
| dc.subject.other | Glycoprotein B | en_US |
| dc.subject.other | Glycoprotein H | en_US |
| dc.subject.other | Genotype | en_US |
| dc.subject.other | Antibody | en_US |
| dc.subject.other | Primary infection | en_US |
| dc.subject.other | Non-primary infection | en_US |
| dc.title | Detection of Genotype-Specific Antibody Responses to Glycoproteins B and H in Primary and Non-Primary Human Cytomegalovirus Infections by Peptide-Based ELISA | en_US |
| dc.type | info:eu-repo/semantics/Article | en_US |
| dc.type | Article | en_US |
| dc.identifier.doi | 10.3390/v13030399 | en_US |
| dc.identifier.issue | 3 | - |
| dc.relation.volume | 13 | en_US |
| dc.investigacion | Ciencias de la Salud | en_US |
| dc.type2 | Artículo | en_US |
| dc.description.numberofpages | 16 | en_US |
| dc.utils.revision | Sí | en_US |
| dc.date.coverdate | Marzo 2021 | en_US |
| dc.identifier.ulpgc | Sí | en_US |
| dc.contributor.buulpgc | BU-MED | en_US |
| dc.description.sjr | 1,463 | |
| dc.description.jcr | 5,818 | |
| dc.description.sjrq | Q1 | |
| dc.description.jcrq | Q2 | |
| dc.description.scie | SCIE | |
| dc.description.miaricds | 10,6 | |
| item.fulltext | Con texto completo | - |
| item.grantfulltext | open | - |
| crisitem.author.dept | GIR IUIBS: Diabetes y endocrinología aplicada | - |
| crisitem.author.dept | IU de Investigaciones Biomédicas y Sanitarias | - |
| crisitem.author.dept | Departamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología | - |
| crisitem.author.orcid | 0000-0001-8429-8374 | - |
| crisitem.author.parentorg | IU de Investigaciones Biomédicas y Sanitarias | - |
| crisitem.author.fullName | Martel Suárez, Nicolás Alfonso | - |
| Colección: | Artículos | |
Los elementos en ULPGC accedaCRIS están protegidos por derechos de autor con todos los derechos reservados, a menos que se indique lo contrario.