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A safe, cost-effective, and high-throughput SARS-CoV-2 antigen capture ELISA suitable for large-scale screening in low-resource settings.
Singh, Ashutosh; Sahu, Upasana; Kulkarni, Pratik M; Yadav, Rupali; Bhatia, Sandeep; Murugkar, Harshad Vinayakrao; Hosamani, Madhusudan; Basagoudanavar, Suresh; Sharma, Gaurav Kumar; Gupta, Praveen Kumar; Kumar, Naveen; Sanyal, Aniket; Kumar, Naveen.
Afiliação
  • Singh A; ICAR-National Institute of High Security Animal Diseases, Bhopal 462022, India.
  • Sahu U; ICAR-National Institute of High Security Animal Diseases, Bhopal 462022, India.
  • Kulkarni PM; ICAR-Indian Veterinary Research Institute, Hebbal, Bengaluru 560024, India.
  • Yadav R; ICAR-National Institute of High Security Animal Diseases, Bhopal 462022, India.
  • Bhatia S; ICAR-National Institute of High Security Animal Diseases, Bhopal 462022, India.
  • Murugkar HV; ICAR-National Institute of High Security Animal Diseases, Bhopal 462022, India.
  • Hosamani M; ICAR-Indian Veterinary Research Institute, Hebbal, Bengaluru 560024, India.
  • Basagoudanavar S; ICAR-Indian Veterinary Research Institute, Hebbal, Bengaluru 560024, India.
  • Sharma GK; ICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly 243122, India.
  • Gupta PK; ICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly 243122, India.
  • Kumar N; ICAR-National Research Center for Equines, Hisar 125001, India; ICMR-National Insitute of Virology, Pune 411001, India.
  • Sanyal A; ICAR-National Institute of High Security Animal Diseases, Bhopal 462022, India.
  • Kumar N; ICAR-National Institute of High Security Animal Diseases, Bhopal 462022, India. Electronic address: navyog.yadav84@gmail.com.
J Virol Methods ; 329: 114995, 2024 Sep.
Article em En | MEDLINE | ID: mdl-38972641
ABSTRACT
Diagnostics employing multiple modalities have been essential for controlling and managing COVID-19, caused by SARS-CoV-2. However, scaling up Reverse Transcription-Quantitative Polymerase Chain Reaction (RT-qPCR), the gold standard for SARS-CoV-2 detection, remains challenging in low and middle-income countries. Cost-effective and high-throughput alternatives like enzyme-linked immunosorbent assay (ELISA) could address this issue. We developed an in-house SARS-CoV-2 nucleocapsid capture ELISA, and validated on 271 nasopharyngeal swab samples from humans (n = 252), bovines (n = 10), and dogs (n = 9). This ELISA has a detection limit of 195 pg/100 µL of nucleocapsid protein and does not cross-react with related coronaviruses, ensuring high specificity to SARS-CoV-2. Diagnostic performance was evaluated using receiver operating characteristic curve analysis, showing a diagnostic sensitivity of 67.78 % and specificity of 100 %. Sensitivity improved to 74.32 % when excluding positive clinical samples with RT-qPCR Ct values > 25. Furthermore, inter-rater reliability analysis demonstrated substantial agreement (κ values = 0.73-0.80) with the VIRALDTECT II Multiplex RT-qPCR kit and perfect agreement with the CoVeasy™ COVID-19 rapid antigen self-test (κ values = 0.89-0.93). Our findings demonstrated that the in-house nucleocapsid capture ELISA is suitable for SARS-CoV-2 testing in humans and animals, meeting the necessary sensitivity and specificity thresholds for cost-effective, large-scale screening.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ensaio de Imunoadsorção Enzimática / Sensibilidade e Especificidade / SARS-CoV-2 / COVID-19 Limite: Animals / Humans Idioma: En Revista: J Virol Methods Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Índia País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ensaio de Imunoadsorção Enzimática / Sensibilidade e Especificidade / SARS-CoV-2 / COVID-19 Limite: Animals / Humans Idioma: En Revista: J Virol Methods Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Índia País de publicação: Holanda