Standardization and Evaluation of an Anti-ZIKV IgM ELISA Assay for the Serological Diagnosis of Zika Virus Infection

Author:

Sirikajornpan Kanittha1,Suntarattiwong Piyarat2,Suwanpakdee Detchvijitr3,Tabprasit Sutchana4,Buddhari Darunee1,Thaisomboonsuk Butsaya1,Klungthong Chonticha1,Poolpanichupatam Yongyuth1,Buathong Rome5,Srikiatkhachorn Anon67,Jones Anthony1,Fernandez Stefan1,Hunsawong Taweewun1

Affiliation:

1. 1Department of Virology, Armed Forces Research Institute of Medical Sciences (AFRIMS), Bangkok, Thailand;

2. 2Pediatrician, Infectious Diseases Unit, Department of Pediatrics, Queen Sirikit National Institute of Child Health, Bangkok, Thailand;

3. 3Department of Pediatrics, Phramongkutklao Hospital, Bangkok, Thailand;

4. 4Research Division, Royal Thai Army-Armed Forces Research Institute of Medical Sciences (RTA-AFRIMS), Bangkok, Thailand;

5. 5Department of Disease Control, Bureau of Epidemiology, Ministry of Public Health, Nonthaburi, Thailand;

6. 6Institute for Immunology and Informatics, University of Rhode Island, Providence, Rhode Island;

7. 7Faculty of Medicine, King Mongkut’s Institute of Technology Ladkrabang, Bangkok, Thailand

Abstract

ABSTRACT. Here, we describe the development of the in-house anti-Zika virus (ZIKV) IgM antibody capture ELISA (in-house ZIKV IgM ELISA) for the detection and diagnosis of acute ZIKV infections. We compared the in-house ZIKV IgM ELISA assay performance against two commercial kits, Euroimmun ZIKV IgM and InBios 2.0 ZIKV IgM ELISA. We tested the assays’ ability to detect anti-ZIKV IgM using a well-defined serum sample panel. This panel included 80 ZIKV negative samples (20 negative, 20 found to be primary dengue virus [DENV][ infections, 20 secondary DENV infections, and 20 Japanese encephalitis virus [JEV] infections) and 67 ZIKV reverse transcriptase–polymerase chain reaction–positive acute serum samples. The OD values were calculated to enzyme immunoassay (EIA) unts by comparing them to weak positive controls. The results demonstrated the high sensitivity (88.06%) and specificity (90.00%) of our in-house ZIKV IgM ELISA and its 89.12% overall percentage agreement. The kappa values were deemed to be within excellent range and comparable to the InBios ZIKV IgM ELISA. Some cross-reactivity was observed among secondary DENV and JEV samples, and to a much lower extent, among primary DENV samples. These data indicate that our in-house ZIKV IgM ELISA is a reliable assay for the detection of anti-ZIKV IgM antibodies in serum.

Publisher

American Society of Tropical Medicine and Hygiene

Subject

Virology,Infectious Diseases,Parasitology

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