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A Novel Multiplexed Enzyme-Linked Immunosorbent Assay for the Detection of IgG Seroreactivity to Cytomegalovirus (CMV) UL144.
Miller, H; Simpson, P; Forman, M; Prigan, A; Kehl, S; Mesich, B; Faron, M; Ledeboer, N; Arav-Boger, R.
Afiliação
  • Miller H; Department of Pediatrics, Division of Infectious Disease, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
  • Simpson P; Department of Pediatrics, Division of Quantitative Health Sciences, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
  • Forman M; Department of Pathology, Johns Hopkins University, Baltimore, Maryland, USA.
  • Prigan A; Department of Pathology, Children's Wisconsin, Milwaukee, Wisconsin, USA.
  • Kehl S; Department of Pathology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
  • Mesich B; Department of Clinical Pathology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
  • Faron M; Department of Clinical Pathology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
  • Ledeboer N; Department of Clinical Pathology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
  • Arav-Boger R; Department of Pediatrics, Division of Infectious Disease, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
J Clin Microbiol ; 59(8): e0096421, 2021 07 19.
Article em En | MEDLINE | ID: mdl-34076473
Infection with human cytomegalovirus (CMV) is common and may have grave consequences in transplant recipients and congenitally infected children. Diagnosis of CMV infection is based on detection of specific antibodies and molecular assays. The incorporation of CMV serological assays into diagnostic algorithms requires careful evaluation and interpretation. Very few serological assays measure CMV infection by a specific strain. We developed an enzyme-linked immunosorbent assay (ELISA) using CMV-encoded UL144 as the antigen. UL144 encodes three major genotypes, A, B, and C, and recombinants. The ELISA was developed with the three UL144 proteins and optimized as a multiplex assay. Sera from 55 positive and 59 negative CMV IgG, determined by the clinical microbiology laboratory, were used for evaluation and optimization. A cutoff optical density (OD) that distinguishes UL144 antibody-positive from antibody-negative sera was established. UL144 A, B, C, and combinations of these antigens were detected in sera. An assay threshold of 0.1 was established and, from a total of 303 sera, the overall sensitivity, specificity, and positive and negative predictive values of the multiplex ELISA were 86.72% (95% confidence interval [CI] 79.59% to 92.07%), 96.57% (92.69% to 98.73%), 94.40% (88.45% to 97.38%), and 91.60% (87.50% to 94.44%), respectively. The inter- and intraassay median coefficients of variation were 0.06 (interquartile range [IQR] 0.56, 0.2) and 0.171 (IQR 0.038, 0.302), respectively. No cross-reactivity was observed with HSV-positive CMV-negative sera. This ELISA gives simple and reproducible results for detection of anti-CMV UL144 IgG. It may assist in differentiating natural infection from CMV vaccines that lack UL144, and may provide an important tool for epidemiological studies of CMV strains.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por Citomegalovirus / Citomegalovirus Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Child / Humans Idioma: En Revista: J Clin Microbiol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por Citomegalovirus / Citomegalovirus Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Child / Humans Idioma: En Revista: J Clin Microbiol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos