A Novel Multiplexed Enzyme-Linked Immunosorbent Assay for the Detection of IgG Seroreactivity to Cytomegalovirus (CMV) UL144.


Journal

Journal of clinical microbiology
ISSN: 1098-660X
Titre abrégé: J Clin Microbiol
Pays: United States
ID NLM: 7505564

Informations de publication

Date de publication:
19 07 2021
Historique:
pubmed: 3 6 2021
medline: 6 8 2021
entrez: 2 6 2021
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 34076473
doi: 10.1128/JCM.00964-21
pmc: PMC8373222
doi:

Substances chimiques

Antibodies, Viral 0
Immunoglobulin G 0
Membrane Glycoproteins 0
UL144 ORF protein, Human herpesvirus 5 0
Viral Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0096421

Références

PLoS One. 2011 Jan 10;6(1):e15949
pubmed: 21264339
J Immunol Methods. 2012 Oct 31;384(1-2):148-51
pubmed: 22732194
J Clin Microbiol. 2005 Jan;43(1):25-9
pubmed: 15634946
Vaccine. 2016 Sep 7;34(39):4643-4644
pubmed: 27506498
Clin Infect Dis. 2006 Nov 1;43(9):1143-51
pubmed: 17029132
Nat Rev Immunol. 2003 Jan;3(1):36-50
pubmed: 12511874
Clin Vaccine Immunol. 2009 Feb;16(2):288-90
pubmed: 19038783
J Clin Virol. 2017 Nov;96:99-104
pubmed: 29035763
Proc Natl Acad Sci U S A. 2005 Jan 25;102(4):1116-21
pubmed: 15647361
J Virol. 1996 Jan;70(1):78-83
pubmed: 8523595
Clin Vaccine Immunol. 2010 May;17(5):836-9
pubmed: 20219875
J Infect Dis. 2017 May 15;215(10):1523-1526
pubmed: 28431127
Am J Obstet Gynecol. 2000 Aug;183(2):476-82
pubmed: 10942490
J Virol. 2013 Apr;87(8):4261-71
pubmed: 23365437
EMBO J. 2006 Sep 20;25(18):4390-9
pubmed: 16932746
J Biol Chem. 1997 May 30;272(22):14029-32
pubmed: 9162022
MethodsX. 2017 Mar 30;4:153-165
pubmed: 28417081
J Infect Dis. 2002 Oct 15;186(8):1057-64
pubmed: 12355354
J Virol. 2008 May;82(9):4250-6
pubmed: 18287226
Front Cell Infect Microbiol. 2020 Jun 26;10:275
pubmed: 32670891
Proc Natl Acad Sci U S A. 2005 Sep 13;102(37):13218-23
pubmed: 16131544
J Immunol. 1999 Jun 15;162(12):6967-70
pubmed: 10358135
J Infect Dis. 2020 Mar 5;221(Suppl 1):S74-S85
pubmed: 32134488
Sci Transl Med. 2016 Oct 26;8(362):362ra145
pubmed: 27797961
J Infect Dis. 2006 Aug 15;194(4):464-73
pubmed: 16845629
J Virol. 1999 Dec;73(12):10040-50
pubmed: 10559318
J Clin Microbiol. 2010 Nov;48(11):3956-62
pubmed: 20810771

Auteurs

H Miller (H)

Department of Pediatrics, Division of Infectious Disease, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

P Simpson (P)

Department of Pediatrics, Division of Quantitative Health Sciences, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

M Forman (M)

Department of Pathology, Johns Hopkins University, Baltimore, Maryland, USA.

A Prigan (A)

Department of Pathology, Children's Wisconsin, Milwaukee, Wisconsin, USA.

S Kehl (S)

Department of Pathology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

B Mesich (B)

Department of Clinical Pathology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

M Faron (M)

Department of Clinical Pathology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

N Ledeboer (N)

Department of Clinical Pathology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

R Arav-Boger (R)

Department of Pediatrics, Division of Infectious Disease, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

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