Generation of a SARS-CoV-2-susceptible mouse model using adenovirus vector expressing human angiotensin-converting enzyme 2 driven by an elongation factor 1α promoter with leftward orientation
2024

Creating a Mouse Model for Studying SARS-CoV-2 Infection

Sample size: 6 publication 10 minutes Evidence: high

Author Information

Author(s): Matsumoto Yusuke, Honda Tomoko, Yasui Fumihiko, Endo Akinori, Sanada Takahiro, Toyama Sakiko, Takagi Asako, Munakata Tsubasa, Kono Risa, Yamaji Kenzaburo, Yamamoto Naoki, Saeki Yasushi, Kohara Michinori

Primary Institution: Tokyo Metropolitan Institute of Medical Science

Hypothesis

Can an adenoviral vector expressing human ACE2 create a mouse model that mimics COVID-19 pathology?

Conclusion

The study successfully developed a mouse model that exhibits severe pneumonia similar to human COVID-19 after infection with SARS-CoV-2.

Supporting Evidence

  • The model showed severe pneumonia with significant weight loss in infected mice.
  • Histopathological analysis revealed thickened alveolar walls and inflammatory cell infiltration.
  • Viral replication was confirmed through quantitative real-time RT-PCR.
  • Elevated levels of inflammatory cytokines were observed in the infected mice.
  • Proteomic analysis indicated distinct lung proteomes associated with different SARS-CoV-2 strains.

Takeaway

Researchers made a special mouse that can get sick from the same virus that makes people sick with COVID-19, helping them study the disease better.

Methodology

Mice were inoculated with an adenoviral vector expressing hACE2 and then infected with SARS-CoV-2 to assess disease severity and viral replication.

Potential Biases

Potential bias in the interpretation of results due to the specific mouse strain used.

Limitations

The model may not fully replicate all aspects of human COVID-19 pathology.

Participant Demographics

Specific pathogen-free 7-8-week-old female BALB/c CrSLC mice were used.

Statistical Information

P-Value

<0.05

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.3389/fimmu.2024.1440314

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