Application of Hybridization Chain Reaction/CRISPR-Cas12a for the Detection of SARS-CoV-2 Infection

Author:

Sagoe Kate Obaayaa1ORCID,Kyama Mutinda Cleophas2,Maina Naomi3,Kamita Moses4ORCID,Njokah Muturi3,Thiong’o Kelvin5,Kanoi Bernard N.4ORCID,Wandera Ernest Apondi46,Ndegwa Davies7,Kinyua Dickson Mwenda89,Gitaka Jesse4

Affiliation:

1. Department of Molecular Biology and Biotechnology, Pan African University Institute for Basic Sciences, Technology and Innovation (PAUSTI), Nairobi P.O. Box 62000-00200, Kenya

2. Department of Medical Laboratory Science, College of Health Sciences, Jomo Kenyatta University of Agriculture & Technology, Nairobi P.O. Box 62000-00200, Kenya

3. Department of Biochemistry, College of Health Sciences, Jomo Kenyatta University of Agriculture & Technology, Nairobi P.O. Box 62000-00200, Kenya

4. Directorate of Research and Innovation, Mount Kenya University, Thika P.O. Box 342-01000, Kenya

5. Center for Biotechnology Research and Development, Kenya Medical Research Institute, Nairobi P.O. Box 54840-00200, Kenya

6. Center for Virus Research, Kenya Medical Research Institute, Nairobi P.O. Box 54840-00200, Kenya

7. Department of Medical Laboratory Sciences, Kenya Medical Training College, Nairobi P.O. Box 30195-00100, Kenya

8. Department of Physical Sciences, Meru University of Science & Technology, Meru P.O. Box 972-60200, Kenya

9. Department of Pure and Applied Sciences, Kirinyaga University, Kerugoya P.O. Box 143-10300, Kenya

Abstract

Globally, the emergence of the coronavirus disease (COVID-19) has had a significant impact on life. The need for ongoing SARS-CoV-2 screening employing inexpensive and quick diagnostic approaches is undeniable, given the ongoing pandemic and variations in vaccine administration in resource-constrained regions. This study presents results as proof of concept to use hybridization chain reaction (HCR) and clustered regularly interspaced short palindromic repeats (CRISPR)/Cas12a complex for detecting SARS-CoV-2. HCR hairpin probes were designed using the NUPACK web-based program and further used to amplify the SARS-CoV-2 N gene in archived nasopharyngeal samples. The results were visualized using agarose gels and CRISPR Cas12a-based lateral flow strips. The assay was evaluated using the gold standard, real-time polymerase chain reaction (RT-PCR), as recommended by the World Health Organization (WHO). The results show the comparative efficiency of HCR to RT-PCR. This study shows that HCR and CRISPR are viable alternatives for diagnosing SARS-CoV-2 in samples.

Funder

African Union through the Pan African University Institute for Basic Sciences, Technology, and Innovation

National Research Fund, Kenya

Publisher

MDPI AG

Subject

Clinical Biochemistry

Reference44 articles.

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