Validation of Multiplex Serology for human hepatitis viruses B and C, human T-lymphotropic virus 1 and Toxoplasma gondii.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 27 09 2018
accepted: 21 12 2018
entrez: 8 1 2019
pubmed: 8 1 2019
medline: 19 10 2019
Statut: epublish

Résumé

Multiplex Serology is a high-throughput technology developed to simultaneously measure specific serum antibodies against multiple pathogens in one reaction vessel. Serological assays for hepatitis B (HBV) and C (HCV) viruses, human T-lymphotropic virus 1 (HTLV-1) and the protozoan parasite Toxoplasma gondii (T. gondii) were developed and validated against established reference assays. For each pathogen, between 3 and 5 specific antigens were recombinantly expressed as GST-tag fusion proteins in Escherichia coli and tested in Monoplex Serology, i.e. assays restricted to the antigens from one particular pathogen. For each of the four pathogen-specific Monoplex assays, overall seropositivity was defined using two pathogen-specific antigens. In the case of HBV Monoplex Serology, the detection of past natural HBV infection was validated based on two independent reference panels resulting in sensitivities of 92.3% and 93.0%, and specificities of 100% in both panels. Validation of HCV and HTLV-1 Monoplex Serology resulted in sensitivities of 98.0% and 95.0%, and specificities of 96.2% and 100.0%, respectively. The Monoplex Serology assay for T. gondii was validated with a sensitivity of 91.2% and specificity of 92.0%. The developed Monoplex Serology assays largely retained their characteristics when they were included in a multiplex panel (i.e. Multiplex Serology), containing additional antigens from a broad range of other pathogens. Thus HBV, HCV, HTLV-1 and T. gondii Monoplex Serology assays can efficiently be incorporated into Multiplex Serology panels tailored for application in seroepidemiological studies.

Identifiants

pubmed: 30615688
doi: 10.1371/journal.pone.0210407
pii: PONE-D-18-28149
pmc: PMC6322760
doi:

Substances chimiques

Antibodies, Viral 0
Antigens 0
Antigens, Protozoan 0
Antigens, Viral 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0210407

Subventions

Organisme : Wellcome Trust
ID : 109965/Z/15/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 106289/Z/14/Z
Pays : United Kingdom
Organisme : Department of Health
Pays : United Kingdom

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Nicole Brenner (N)

Infections and Cancer Epidemiology, Infection, Inflammation and Cancer Research Program, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Faculty of Biosciences, Heidelberg University, Heidelberg, Germany.

Alexander J Mentzer (AJ)

The Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
Big Data Institute, Li Ka Shing Centre for Health Information and Discovery, University of Oxford, Oxford, United Kingdom.

Julia Butt (J)

Infections and Cancer Epidemiology, Infection, Inflammation and Cancer Research Program, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Kathrin L Braband (KL)

Infections and Cancer Epidemiology, Infection, Inflammation and Cancer Research Program, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Angelika Michel (A)

Infections and Cancer Epidemiology, Infection, Inflammation and Cancer Research Program, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Katie Jeffery (K)

Department of Microbiology, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.

Paul Klenerman (P)

Department of Microbiology, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.
NIHR Biomedical Research Centre, Oxford, United Kingdom.

Barbara Gärtner (B)

Institut für Medizinische Mikrobiologie und Hygiene, Universität des Saarlands, Homburg, Germany.

Paul Schnitzler (P)

Center for Infectious Diseases, Virology, University Hospital of Heidelberg, Heidelberg, Germany.

Adrian Hill (A)

The Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
The Jenner Institute, University of Oxford, Oxford, United Kingdom.

Graham Taylor (G)

Molecular Diagnostic Unit, Imperial College Healthcare NHS Trust, London, United Kingdom.

Maria A Demontis (MA)

Molecular Diagnostic Unit, Imperial College Healthcare NHS Trust, London, United Kingdom.

Edward Guy (E)

Toxoplasma Reference Unit, Public Health Wales Microbiology, Swansea, United Kingdom.

Stephen J Hadfield (SJ)

Toxoplasma Reference Unit, Public Health Wales Microbiology, Swansea, United Kingdom.

Rachael Almond (R)

UK Biobank, Stockport, United Kingdom.

Naomi Allen (N)

UK Biobank, Stockport, United Kingdom.
Nuffield Department of Population Health, Medical Sciences Division, University of Oxford, Oxford, United Kingdom.

Michael Pawlita (M)

Molecular Diagnostics of Oncogenic Infections Division, Infection, Inflammation and Cancer Research Program, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Tim Waterboer (T)

Infections and Cancer Epidemiology, Infection, Inflammation and Cancer Research Program, German Cancer Research Center (DKFZ), Heidelberg, Germany.

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Classifications MeSH