Transcriptomic characteristics of bronchoalveolar lavage fluid and peripheral blood mononuclear cells in COVID-19 patients
Circulating in China and 158 other countries and areas, the ongoing COVID-19 outbreak has caused devastating mortality and posed a great threat to public health. However, efforts to identify effectively supportive therapeutic drugs and treatments has been hampered by our limited understanding of hos...
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Published in | Emerging microbes & infections Vol. 9; no. 1; pp. 761 - 770 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Taylor & Francis
01.01.2020
Taylor & Francis Ltd Taylor & Francis Group |
Subjects | |
Online Access | Get full text |
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Abstract | Circulating in China and 158 other countries and areas, the ongoing COVID-19 outbreak has caused devastating mortality and posed a great threat to public health. However, efforts to identify effectively supportive therapeutic drugs and treatments has been hampered by our limited understanding of host immune response for this fatal disease. To characterize the transcriptional signatures of host inflammatory response to SARS-CoV-2 (HCoV-19) infection, we carried out transcriptome sequencing of the RNAs isolated from the bronchoalveolar lavage fluid (BALF) and peripheral blood mononuclear cells (PBMC) specimens of COVID-19 patients. Our results reveal distinct host inflammatory cytokine profiles to SARS-CoV-2 infection in patients, and highlight the association between COVID-19 pathogenesis and excessive cytokine release such as CCL2/MCP-1, CXCL10/IP-10, CCL3/MIP-1A, and CCL4/MIP1B. Furthermore, SARS-CoV-2 induced activation of apoptosis and P53 signalling pathway in lymphocytes may be the cause of patients' lymphopenia. The transcriptome dataset of COVID-19 patients would be a valuable resource for clinical guidance on anti-inflammatory medication and understanding the molecular mechansims of host response. |
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AbstractList | Circulating in China and 158 other countries and areas, the ongoing COVID-19 outbreak has caused devastating mortality and posed a great threat to public health. However, efforts to identify effectively supportive therapeutic drugs and treatments has been hampered by our limited understanding of host immune response for this fatal disease. To characterize the transcriptional signatures of host inflammatory response to SARS-CoV-2 (HCoV-19) infection, we carried out transcriptome sequencing of the RNAs isolated from the bronchoalveolar lavage fluid (BALF) and peripheral blood mononuclear cells (PBMC) specimens of COVID-19 patients. Our results reveal distinct host inflammatory cytokine profiles to SARS-CoV-2 infection in patients, and highlight the association between COVID-19 pathogenesis and excessive cytokine release such as CCL2/MCP-1, CXCL10/IP-10, CCL3/MIP-1A, and CCL4/MIP1B. Furthermore, SARS-CoV-2 induced activation of apoptosis and P53 signalling pathway in lymphocytes may be the cause of patients’ lymphopenia. The transcriptome dataset of COVID-19 patients would be a valuable resource for clinical guidance on anti-inflammatory medication and understanding the molecular mechansims of host response. Circulating in China and 158 other countries and areas, the ongoing COVID-19 outbreak has caused devastating mortality and posed a great threat to public health. However, efforts to identify effectively supportive therapeutic drugs and treatments has been hampered by our limited understanding of host immune response for this fatal disease. To characterize the transcriptional signatures of host inflammatory response to SARS-CoV-2 (HCoV-19) infection, we carried out transcriptome sequencing of the RNAs isolated from the bronchoalveolar lavage fluid (BALF) and peripheral blood mononuclear cells (PBMC) specimens of COVID-19 patients. Our results reveal distinct host inflammatory cytokine profiles to SARS-CoV-2 infection in patients, and highlight the association between COVID-19 pathogenesis and excessive cytokine release such as CCL2/MCP-1, CXCL10/IP-10, CCL3/MIP-1A, and CCL4/MIP1B. Furthermore, SARS-CoV-2 induced activation of apoptosis and P53 signalling pathway in lymphocytes may be the cause of patients' lymphopenia. The transcriptome dataset of COVID-19 patients would be a valuable resource for clinical guidance on anti-inflammatory medication and understanding the molecular mechansims of host response.Circulating in China and 158 other countries and areas, the ongoing COVID-19 outbreak has caused devastating mortality and posed a great threat to public health. However, efforts to identify effectively supportive therapeutic drugs and treatments has been hampered by our limited understanding of host immune response for this fatal disease. To characterize the transcriptional signatures of host inflammatory response to SARS-CoV-2 (HCoV-19) infection, we carried out transcriptome sequencing of the RNAs isolated from the bronchoalveolar lavage fluid (BALF) and peripheral blood mononuclear cells (PBMC) specimens of COVID-19 patients. Our results reveal distinct host inflammatory cytokine profiles to SARS-CoV-2 infection in patients, and highlight the association between COVID-19 pathogenesis and excessive cytokine release such as CCL2/MCP-1, CXCL10/IP-10, CCL3/MIP-1A, and CCL4/MIP1B. Furthermore, SARS-CoV-2 induced activation of apoptosis and P53 signalling pathway in lymphocytes may be the cause of patients' lymphopenia. The transcriptome dataset of COVID-19 patients would be a valuable resource for clinical guidance on anti-inflammatory medication and understanding the molecular mechansims of host response. |
Author | Shi, Mang Hu, Wenjia Tang, Zhidong Zhang, Qi Cao, Liu Wu, Honglong Lin, Yongquan Zhou, Yu Lan, Ke Jiang, Ao Guo, Dong Wang, Dehe Zhang, Meiyuan Chen, Yu Liu, Yingle Liu, Yuan Xiong, Yong Yang, Jiayi Guo, Ming |
Author_xml | – sequence: 1 givenname: Yong surname: Xiong fullname: Xiong, Yong organization: State Key Laboratory of Virology, Department of Infectious Disease, Zhongnan Hospital, Wuhan University – sequence: 2 givenname: Yuan surname: Liu fullname: Liu, Yuan organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 3 givenname: Liu surname: Cao fullname: Cao, Liu organization: The Centre for Infection and Immunity Studies, School of Medicine, Sun Yat-sen University – sequence: 4 givenname: Dehe surname: Wang fullname: Wang, Dehe organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 5 givenname: Ming surname: Guo fullname: Guo, Ming organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 6 givenname: Ao surname: Jiang fullname: Jiang, Ao organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 7 givenname: Dong surname: Guo fullname: Guo, Dong organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 8 givenname: Wenjia surname: Hu fullname: Hu, Wenjia organization: State Key Laboratory of Virology, Department of Infectious Disease, Zhongnan Hospital, Wuhan University – sequence: 9 givenname: Jiayi surname: Yang fullname: Yang, Jiayi organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 10 givenname: Zhidong surname: Tang fullname: Tang, Zhidong organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 11 givenname: Honglong surname: Wu fullname: Wu, Honglong organization: BGI PathoGenesis Pharmaceutical Technology – sequence: 12 givenname: Yongquan orcidid: 0000-0001-6663-731X surname: Lin fullname: Lin, Yongquan organization: BGI PathoGenesis Pharmaceutical Technology – sequence: 13 givenname: Meiyuan surname: Zhang fullname: Zhang, Meiyuan organization: BGI PathoGenesis Pharmaceutical Technology – sequence: 14 givenname: Qi orcidid: 0000-0003-2868-1816 surname: Zhang fullname: Zhang, Qi organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 15 givenname: Mang surname: Shi fullname: Shi, Mang organization: The Centre for Infection and Immunity Studies, School of Medicine, Sun Yat-sen University – sequence: 16 givenname: Yingle surname: Liu fullname: Liu, Yingle organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 17 givenname: Yu surname: Zhou fullname: Zhou, Yu email: yu.zhou@whu.edu.cn organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 18 givenname: Ke surname: Lan fullname: Lan, Ke email: klan@whu.edu.cn organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University – sequence: 19 givenname: Yu orcidid: 0000-0003-1300-4652 surname: Chen fullname: Chen, Yu email: chenyu@whu.edu.cn organization: State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32228226$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Apoptosis Betacoronavirus Bronchoalveolar Lavage Fluid Chemokines - analysis Coronavirus Infections - blood Coronavirus Infections - genetics Coronavirus Infections - immunology Coronaviruses COVID-19 cytokine Cytokines Cytokines - analysis Humans inflammation Lavage Leukocytes, Mononuclear Lymphopenia Pandemics Pneumonia, Viral - blood Pneumonia, Viral - genetics Pneumonia, Viral - immunology RNA-Seq SARS-CoV-2 Severe acute respiratory syndrome coronavirus 2 Signal Transduction Transcriptome transcriptome profiling Tumor Suppressor Protein p53 |
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Title | Transcriptomic characteristics of bronchoalveolar lavage fluid and peripheral blood mononuclear cells in COVID-19 patients |
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