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Development of a screening platform to discover natural products active against SARS-CoV-2 infection using lung organoid models.
Lee, Joo-Eun; Jeong, Se Yun; Li, Zijun; Kim, Hyun-Yi; Kim, Hyun-Woo; Yoo, Min Jeong; Jang, Hee Joo; Kim, Do-Kyun; Cho, Namki; Yoo, Hee Min; Kim, Ki Hyun.
Afiliação
  • Lee JE; College of Pharmacy, Chonnam National University, Gwangju, 61186, Republic of Korea.
  • Jeong SY; School of Pharmacy, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
  • Li Z; College of Pharmacy, Chonnam National University, Gwangju, 61186, Republic of Korea.
  • Kim HY; Biometrology Group, Korea Research Institute of Standards and Science (KRISS), Daejeon, 34113, Republic of Korea.
  • Kim HW; NGeneS Inc., Ansan, 15495, Republic of Korea.
  • Yoo MJ; Korea Zoonosis Research Institute, Jeonbuk National University, Iksan, 54531, Republic of Korea.
  • Jang HJ; School of Pharmacy, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
  • Kim DK; School of Pharmacy, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
  • Cho N; Korea Zoonosis Research Institute, Jeonbuk National University, Iksan, 54531, Republic of Korea.
  • Yoo HM; College of Pharmacy, Chonnam National University, Gwangju, 61186, Republic of Korea.
  • Kim KH; Biometrology Group, Korea Research Institute of Standards and Science (KRISS), Daejeon, 34113, Republic of Korea. hmy@kriss.re.kr.
Biomater Res ; 27(1): 18, 2023 Mar 01.
Article em En | MEDLINE | ID: mdl-36855173
ABSTRACT

BACKGROUND:

Natural products can serve as one of the alternatives, exhibiting high potential for the treatment and prevention of COVID-19, caused by SARS-CoV-2. Herein, we report a screening platform to test the antiviral efficacy of a natural product library against SARS-CoV-2 and verify their activity using lung organoids.

METHODS:

Since SARS-CoV-2 is classified as a risk group 3 pathogen, the drug screening assay must be performed in a biosafety level 3 (BSL-3) laboratory. To circumvent this limitation, pseudotyped viruses (PVs) have been developed as replacements for the live SARS-CoV-2. We developed PVs containing spikes from Delta and Omicron variants of SARS-CoV-2 and improved the infection in an angiotensin-converting enzyme 2 (ACE2)-dependent manner. Human induced pluripotent stem cells (hiPSCs) derived lung organoids were generated to test the SARS-CoV-2 therapeutic efficacy of natural products.

RESULTS:

Flavonoids from our natural product library had strong antiviral activity against the Delta- or Omicron-spike-containing PVs without affecting cell viability. We aimed to develop strategies to discover the dual function of either inhibiting infection at the beginning of the infection cycle or reducing spike stability following SARS-CoV-2 infection. When lung cells are already infected with the virus, the active flavonoids induced the degradation of the spike protein and exerted anti-inflammatory effects. Further experiments confirmed that the active flavonoids had strong antiviral activity in lung organoid models.

CONCLUSION:

This screening platform will open new paths by providing a promising standard system for discovering novel drug leads against SARS-CoV-2 and help develop promising candidates for clinical investigation as potential therapeutics for COVID-19.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article