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Detection of Genotype-Specific Antibody Responses to Glycoproteins B and H in Primary and Non-Primary Human Cytomegalovirus Infections by Peptide-Based ELISA

Authors :
Chiara Fornara
Marica De Cicco
Andrew J. Davison
Daniela Cirasola
Daniele Lilleri
Loretta Fiorina
Nicolás M. Suárez
Federica Zavaglio
Giuseppe Gerna
Source :
Viruses, Vol 13, Iss 399, p 399 (2021), Viruses, Volume 13, Issue 3
Publication Year :
2021
Publisher :
MDPI AG, 2021.

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 = 6/7) 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.

Details

ISSN :
19994915
Volume :
13
Database :
OpenAIRE
Journal :
Viruses
Accession number :
edsair.doi.dedup.....7f9da52afd49d75f69db078086fa99cd
Full Text :
https://doi.org/10.3390/v13030399