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Relative infectivity of the SARS-CoV-2 Omicron variant in human alveolar cells.
Kim, Taewoo; Min, Kyoung Il; Yang, Jeong-Sun; Kim, Jun Won; Cho, Junhyung; Kim, Yun Ho; Lee, Jeong Seok; Kim, Young Tae; Kim, Kyung-Chang; Kim, Jeong Yeon; Na, Kwon Joong; Lee, Joo-Yeon; Ju, Young Seok.
  • Kim T; Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon 34141, Republic of Korea.
  • Min KI; Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon 34141, Republic of Korea.
  • Yang JS; Division of Emerging Virus & Vector Research, Center for Emerging Virus Research, National Institute of Health, Korea Disease Control and Prevention Agency, Cheongju 28159, Republic of Korea.
  • Kim JW; Division of Emerging Virus & Vector Research, Center for Emerging Virus Research, National Institute of Health, Korea Disease Control and Prevention Agency, Cheongju 28159, Republic of Korea.
  • Cho J; Division of Emerging Virus & Vector Research, Center for Emerging Virus Research, National Institute of Health, Korea Disease Control and Prevention Agency, Cheongju 28159, Republic of Korea.
  • Kim YH; Department of Thoracic and Cardiovascular Surgery, Seoul National University Hospital, Seoul National University Cancer Research Institute, Seoul 03080, Republic of Korea.
  • Lee JS; Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon 34141, Republic of Korea.
  • Kim YT; GENOME INSIGHT Inc., Daejeon 34051, Republic of Korea.
  • Kim KC; Department of Thoracic and Cardiovascular Surgery, Seoul National University Hospital, Seoul National University Cancer Research Institute, Seoul 03080, Republic of Korea.
  • Kim JY; Division of Emerging Virus & Vector Research, Center for Emerging Virus Research, National Institute of Health, Korea Disease Control and Prevention Agency, Cheongju 28159, Republic of Korea.
  • Na KJ; GENOME INSIGHT Inc., Daejeon 34051, Republic of Korea.
  • Lee JY; Department of Thoracic and Cardiovascular Surgery, Seoul National University Hospital, Seoul National University Cancer Research Institute, Seoul 03080, Republic of Korea.
  • Ju YS; Division of Emerging Virus & Vector Research, Center for Emerging Virus Research, National Institute of Health, Korea Disease Control and Prevention Agency, Cheongju 28159, Republic of Korea.
iScience ; 25(12): 105571, 2022 Dec 22.
Article in English | MEDLINE | ID: covidwho-2105157
ABSTRACT
With the continuous emergence of highly transmissible SARS-CoV-2 variants, the comparison of their infectivity has become a critical issue for public health. However, a direct assessment of the viral characteristic has been challenging because of the lack of appropriate experimental models and efficient methods. Here, we integrated human alveolar organoids and single-cell transcriptome sequencing to facilitate the evaluation. In a proof-of-concept study with four highly transmissible SARS-CoV-2 variants, including GR (B.1.1.119), Alpha (B.1.1.7), Delta (B.1.617.2), and Omicron (BA.1), a rapid evaluation of the relative infectivity was possible. Our system demonstrates that the Omicron variant is 5- to 7-fold more infectious to human alveolar cells than the other SARS-CoV-2 variants at the initial stage of infection. To our knowledge, for the first time, this study measures the relative infectivity of the Omicron variant under multiple virus co-infection and provides new experimental procedures that can be applied to monitor emerging viral variants.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies Topics: Variants Language: English Journal: IScience Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies Topics: Variants Language: English Journal: IScience Year: 2022 Document Type: Article