Rapid, Multispecies Detection of SARS-CoV-2 Antibodies via a Meta-Surface Plasmon Resonance Biosensor

Author:

Zhao Ya12,Li Rui3,Liu Zuqing1,Zhou Hanlin4,Yang Jingyu1,Zhang Shaoran2,Huang Liping34ORCID,Liu Gang L3ORCID,Zhang Qiang156ORCID,Jin Meilin125ORCID

Affiliation:

1. College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, China

2. National Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China

3. College of Life Science and Technology, Huazhong University of Science and Technology, 1037 Luo Yu Road, Wuhan 430074, China

4. Liangzhun (Shanghai) Industrial Co. Ltd., 1582 Gu Mei Road, Shanghai 200233, China

5. Hubei Jiangxia Laboratory, Wuhan 430200, China

6. College of Biomedicine and Health, Huazhong Agricultural University, Wuhan 430070, China

Abstract

Public health concerns have been raised by numerous reports of severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) and its variations infecting a range of animals. Wildlife reservoirs may facilitate the evolution of viral types capable of causing human infection in the future. Therefore, epidemiological monitoring of animals in close contact with humans is necessary. Yet, infection symptoms are not obvious in most animals, which leads to a short nucleic acid test-detection period and limits the application of this method in animals. The use of virus- and pseudovirus-based neutralizing antibody detection techniques is restricted to establishments with elevated biosafety standards. Traditional enzyme-linked immunosorbent assays (ELISA) do not offer multispecies detection and are time-consuming and labor-intensive. This work developed a polyethyleneimine-gold nanoparticle meta-surface plasmon resonance biosensor system-based multispecies SARS-CoV-2 antibody detection platform that is fast, sensitive, has a high throughput, and is fully automated. The test can be done in 30 min and specificity is up to 100% for detection in cats, dogs, and minks. Moreover, the coincidence rate was up to 99.36% (313/315) for the detection of pseudovirus in clinical and immune sera. Additionally, this method’s detection sensitivity in cat, dog, and mink serum is 2,048, 1,024, and 4,096 times, which is much better than indirect ELISA and comparable to indirect immunofluorescence assays. An efficient method for COVID-19 epidemiology screening in animal serum will be made available by this platform.

Funder

Science and Technology Program of Hubei Province

Publisher

Hindawi Limited

Subject

General Veterinary,General Immunology and Microbiology,General Medicine

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