Advanced Detection Method for Dengue NS1 Protein Using Ultrasensitive ELISA with Thio-NAD Cycling

Author:

Chen Po-Kai1,Chang Jyun-Hao1,Ke Liang-Yin2ORCID,Kao Jun-Kai34ORCID,Chen Chang-Hua45,Yang Rei-Cheng36,Yoshimura Teruki7,Ito Etsuro18ORCID,Tsai Jih-Jin91011ORCID

Affiliation:

1. Department of Biology, Waseda University, Tokyo 162-8480, Japan

2. Department of Medical Laboratory Science and Biotechnology, College of Health Sciences, Kaohsiung Medical University, Kaohsiung 80708, Taiwan

3. Frontier Molecular Medical Research Center in Children, Changhua Christian Children’s Hospital, Changhua 50006, Taiwan

4. Department of Post-Baccalaureate Medicine, College of Medicine, National Chung Hsing University, Taichung 402204, Taiwan

5. Changhua Christian Hospital, Changhua 50006, Taiwan

6. Kaohsiung Medical University Chung-Ho Memorial Hospital, Kaohsiung 80756, Taiwan

7. School of Pharmaceutical Sciences, Health Science University of Hokkaido, Hokkaido 061-0293, Japan

8. Graduate Institute of Medicine, Kaohsiung Medical University, Kaohsiung 80708, Taiwan

9. Tropical Medicine Center, Kaohsiung Medical University Hospital, Kaohsiung 80756, Taiwan

10. School of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 80708, Taiwan

11. Division of Infectious Diseases, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung 80756, Taiwan

Abstract

Dengue fever, a mosquito-borne disease in tropical and subtropical climates caused by the dengue virus (DENV), has become a major social and economic burden in recent years. However, current primary detection methods are inadequate for early diagnosis of DENV because they are either time-consuming, expensive, or require training. Non-structural protein 1 (NS1) is secreted during DENV infection and is thus considered a suitable biomarker for the development of an early detection method. In the present study, we developed a detection method for the NS1 protein based on a previously reported thio-NAD cycling ELISA (i.e., ultrasensitive ELISA) and successfully achieved a LOD of 1.152 pg/mL. The clinical diagnosis potential of the detection system was also evaluated by using 85 patient specimens, inclusive of 60 DENV-positive and 25 DENV-negative specimens confirmed by the NAAT method. The results revealed 98.3% (59/60) sensitivity and 100% (25/25) specificity, which was in almost perfect agreement with the NAAT data with a kappa coefficient of 0.972. The present study demonstrates the diagnostic potential of using an ultrasensitive ELISA as a low-cost, easy-to-use method for the detection of DENV compared with NAAT and could be of great benefit in low-income countries.

Funder

Japan Society for the Promotion of Science

Waseda University Grant for Special Research Projects

SPRING from the Japan Science and Technology Agency

National Health Research Institute, Taiwan

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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