Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Aug;44(8):1896-1906.
doi: 10.1111/risa.14291. Epub 2024 Mar 15.

Use of a risk assessment tool to determine the origin of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)

Affiliations

Use of a risk assessment tool to determine the origin of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)

Xin Chen et al. Risk Anal. 2024 Aug.

Abstract

The origin of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is contentious. Most studies have focused on a zoonotic origin, but definitive evidence such as an intermediary animal host is lacking. We used an established risk analysis tool for differentiating natural and unnatural epidemics, the modified Grunow-Finke assessment tool (mGFT) to study the origin of SARS-COV-2. The mGFT scores 11 criteria to provide a likelihood of natural or unnatural origin. Using published literature and publicly available sources of information, we applied the mGFT to the origin of SARS-CoV-2. The mGFT scored 41/60 points (68%), with high inter-rater reliability (100%), indicating a greater likelihood of an unnatural than natural origin of SARS-CoV-2. This risk assessment cannot prove the origin of SARS-CoV-2 but shows that the possibility of a laboratory origin cannot be easily dismissed.

Keywords: COVID‐19; SARS‐CoV‐2; origin; pandemic; risk analysis.

PubMed Disclaimer

Similar articles

Cited by

References

REFERENCES

    1. Abdelrahman, Z., Li, M., & Wang, X. (2020). Comparative review of SARS‐CoV‐2, SARS‐CoV, MERS‐CoV, and influenza a respiratory viruses. Frontiers in Immunology, 11, 552909.
    1. Adil, M. T., Rahman, R., Whitelaw, D., Jain, V., Al‐Taan, O., Rashid, F., Munasinghe, A., & Jambulingam, P. (2021). SARS‐CoV‐2 and the pandemic of COVID‐19. Postgraduate Medical Journal, 97(1144), 110–116.
    1. Ahamed, J., & Laurence, J. (2022). Long COVID endotheliopathy: Hypothesized mechanisms and potential therapeutic approaches. The Journal of Clinical Investigation, 132(15), e161167.
    1. Akhtar, Z., Trent, M., Moa, A., Tan, T. C., Fröbert, O., & MacIntyre, C. R. (2023). The impact of COVID‐19 and COVID vaccination on cardiovascular outcomes. European Heart Journal Supplements, 25, (Suppl_A), A42–A49.
    1. Al‐Aly, Z., Xie, Y., & Bowe, B. (2021). High‐dimensional characterization of post‐acute sequelae of COVID‐19. Nature, 594(7862), 259–264.

LinkOut - more resources