Distinct infection process of SARS‐CoV‐2 in human bronchial epithelial cell lines. Issue 11 (14th July 2020)
- Record Type:
- Journal Article
- Title:
- Distinct infection process of SARS‐CoV‐2 in human bronchial epithelial cell lines. Issue 11 (14th July 2020)
- Main Title:
- Distinct infection process of SARS‐CoV‐2 in human bronchial epithelial cell lines
- Authors:
- Liao, Yun
Li, Xueqi
Mou, Tangwei
Zhou, Xiaofang
Li, Dandan
Wang, Lichun
Zhang, Ying
Dong, Xingqi
Zheng, Huiwen
Guo, Lei
Liang, Yan
Jiang, Guorun
Fan, Shengtao
Xu, Xingli
Xie, Zhongping
Chen, Hongbo
Liu, Longding
Li, Qihan - Other Names:
- Luo Guangxiang (George) guestEditor.
Ly Hinh guestEditor.
Gao Shou‐Jiang guestEditor. - Abstract:
- Abstract: Coronavirus disease 2019, caused by severe acute respiratory syndrome coronavirus‐2 (SARS‐CoV‐2), leads to a series of clinical symptoms of respiratory and pulmonary inflammatory reactions via unknown pathologic mechanisms related to the viral infection process in tracheal or bronchial epithelial cells. Investigation of this viral infection in the human bronchial epithelial cell line (16HBE) suggests that SARS‐CoV‐2 can enter these cells through interaction between its membrane‐localized S protein with the angiotensin‐converting enzyme 2 molecule on the host cell membrane. Further observation indicates distinct viral replication with a dynamic and moderate increase, whereby viral replication does not lead to a specific cytopathic effect but maintains a continuous release of progeny virions from infected cells. Although messenger RNA expression of various innate immune signaling molecules is altered in the cells, transcription of interferons‐α (IFN‐α), IFN‐β, and IFN‐γ is unchanged. Furthermore, expression of some interleukins (IL) related to inflammatory reactions, such as IL‐6, IL‐2, and IL‐8, is maintained at low levels, whereas that of ILs involved in immune regulation is upregulated. Interestingly, IL‐22, an IL that functions mainly in tissue repair, shows very high expression. Collectively, these data suggest a distinct infection process for this virus in respiratory epithelial cells, which may be linked to its clinicopathological mechanism. Highlights:Abstract: Coronavirus disease 2019, caused by severe acute respiratory syndrome coronavirus‐2 (SARS‐CoV‐2), leads to a series of clinical symptoms of respiratory and pulmonary inflammatory reactions via unknown pathologic mechanisms related to the viral infection process in tracheal or bronchial epithelial cells. Investigation of this viral infection in the human bronchial epithelial cell line (16HBE) suggests that SARS‐CoV‐2 can enter these cells through interaction between its membrane‐localized S protein with the angiotensin‐converting enzyme 2 molecule on the host cell membrane. Further observation indicates distinct viral replication with a dynamic and moderate increase, whereby viral replication does not lead to a specific cytopathic effect but maintains a continuous release of progeny virions from infected cells. Although messenger RNA expression of various innate immune signaling molecules is altered in the cells, transcription of interferons‐α (IFN‐α), IFN‐β, and IFN‐γ is unchanged. Furthermore, expression of some interleukins (IL) related to inflammatory reactions, such as IL‐6, IL‐2, and IL‐8, is maintained at low levels, whereas that of ILs involved in immune regulation is upregulated. Interestingly, IL‐22, an IL that functions mainly in tissue repair, shows very high expression. Collectively, these data suggest a distinct infection process for this virus in respiratory epithelial cells, which may be linked to its clinicopathological mechanism. Highlights: SARS‐CoV‐2 does not lead to a specific cytopathic effect in 16HBE cells, but maintains continuous release of progeny virions from infected cells. During infection, IL‐22, an interleukin that functions mainly in tissue repair, showed very high expression. … (more)
- Is Part Of:
- Journal of medical virology. Volume 92:Issue 11(2020)
- Journal:
- Journal of medical virology
- Issue:
- Volume 92:Issue 11(2020)
- Issue Display:
- Volume 92, Issue 11 (2020)
- Year:
- 2020
- Volume:
- 92
- Issue:
- 11
- Issue Sort Value:
- 2020-0092-0011-0000
- Page Start:
- 2830
- Page End:
- 2838
- Publication Date:
- 2020-07-14
- Subjects:
- ACE2 -- human bronchial epithelial cell line (16HBE) -- IL‐22 -- SARS‐CoV‐2 (COVID‐19)
Virology -- Periodicals
616 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1096-9071 ↗
http://www.interscience.wiley.com/jpages/0146-6615 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jmv.26200 ↗
- Languages:
- English
- ISSNs:
- 0146-6615
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5017.095000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 20936.xml