tetano
Editor, Senior Moderator
Clin Proteomics
. 2022 Dec 17;19(1):46.
doi: 10.1186/s12014-022-09386-6.
Proteomic profiling of end-stage COVID-19 lung biopsies
Juergen Gindlhuber[SUP] #[/SUP][SUP] 1 [/SUP], Tamara Tomin[SUP] #[/SUP][SUP] 2 [/SUP], Florian Wiesenhofer[SUP] 3 4 [/SUP], Martin Zacharias[SUP] 1 [/SUP], Laura Liesinger[SUP] 1 [/SUP], Vadim Demichev[SUP] 5 [/SUP], Klaus Kratochwill[SUP] 3 4 [/SUP], Gregor Gorkiewicz[SUP] 1 [/SUP], Matthias Schittmayer[SUP] 6 [/SUP], Ruth Birner-Gruenberger[SUP] 7 8 [/SUP]
Affiliations
Abstract
The outbreak of a novel coronavirus (SARS-CoV-2) in 2019 led to a worldwide pandemic, which remains an integral part of our lives to this day. Coronavirus disease (COVID-19) is a flu like condition, often accompanied by high fever and respiratory distress. In some cases, conjointly with other co-morbidities, COVID-19 can become severe, leading to lung arrest and even death. Although well-known from a clinical standpoint, the mechanistic understanding of lethal COVID-19 is still rudimentary. Studying the pathology and changes on a molecular level associated with the resulting COVID-19 disease is impeded by the highly infectious nature of the virus and the concomitant sampling challenges. We were able to procure COVID-19 post-mortem lung tissue specimens by our collaboration with the BSL-3 laboratory of the Biobanking and BioMolecular resources Research Infrastructure Austria which we subjected to state-of-the-art quantitative proteomic analysis to better understand the pulmonary manifestations of lethal COVID-19. Lung tissue samples from age-matched non-COVID-19 patients who died within the same period were used as controls. Samples were subjected to parallel accumulation-serial fragmentation combined with data-independent acquisition (diaPASEF) on a timsTOF Pro and obtained raw data was processed using DIA-NN software. Here we report that terminal COVID-19 patients display an increase in inflammation, acute immune response and blood clot formation (with concomitant triggering of fibrinolysis). Furthermore, we describe that COVID-19 diseased lungs undergo severe extracellular matrix restructuring, which was corroborated on the histopathological level. However, although undergoing an injury, diseased lungs seem to have impaired proliferative and tissue repair signalling, with several key kinase-mediated signalling pathways being less active. This might provide a mechanistic link to post-acute sequelae of COVID-19 (PASC; "Long COVID"). Overall, we emphasize the importance of histopathological patient stratification when interpreting molecular COVID-19 data.
Keywords: COVID-19; Extracellular matrix; Lung; Proteomics; SARS-CoV-2; Signaling.
. 2022 Dec 17;19(1):46.
doi: 10.1186/s12014-022-09386-6.
Proteomic profiling of end-stage COVID-19 lung biopsies
Juergen Gindlhuber[SUP] #[/SUP][SUP] 1 [/SUP], Tamara Tomin[SUP] #[/SUP][SUP] 2 [/SUP], Florian Wiesenhofer[SUP] 3 4 [/SUP], Martin Zacharias[SUP] 1 [/SUP], Laura Liesinger[SUP] 1 [/SUP], Vadim Demichev[SUP] 5 [/SUP], Klaus Kratochwill[SUP] 3 4 [/SUP], Gregor Gorkiewicz[SUP] 1 [/SUP], Matthias Schittmayer[SUP] 6 [/SUP], Ruth Birner-Gruenberger[SUP] 7 8 [/SUP]
Affiliations
- PMID: 36526981
- DOI: 10.1186/s12014-022-09386-6
Abstract
The outbreak of a novel coronavirus (SARS-CoV-2) in 2019 led to a worldwide pandemic, which remains an integral part of our lives to this day. Coronavirus disease (COVID-19) is a flu like condition, often accompanied by high fever and respiratory distress. In some cases, conjointly with other co-morbidities, COVID-19 can become severe, leading to lung arrest and even death. Although well-known from a clinical standpoint, the mechanistic understanding of lethal COVID-19 is still rudimentary. Studying the pathology and changes on a molecular level associated with the resulting COVID-19 disease is impeded by the highly infectious nature of the virus and the concomitant sampling challenges. We were able to procure COVID-19 post-mortem lung tissue specimens by our collaboration with the BSL-3 laboratory of the Biobanking and BioMolecular resources Research Infrastructure Austria which we subjected to state-of-the-art quantitative proteomic analysis to better understand the pulmonary manifestations of lethal COVID-19. Lung tissue samples from age-matched non-COVID-19 patients who died within the same period were used as controls. Samples were subjected to parallel accumulation-serial fragmentation combined with data-independent acquisition (diaPASEF) on a timsTOF Pro and obtained raw data was processed using DIA-NN software. Here we report that terminal COVID-19 patients display an increase in inflammation, acute immune response and blood clot formation (with concomitant triggering of fibrinolysis). Furthermore, we describe that COVID-19 diseased lungs undergo severe extracellular matrix restructuring, which was corroborated on the histopathological level. However, although undergoing an injury, diseased lungs seem to have impaired proliferative and tissue repair signalling, with several key kinase-mediated signalling pathways being less active. This might provide a mechanistic link to post-acute sequelae of COVID-19 (PASC; "Long COVID"). Overall, we emphasize the importance of histopathological patient stratification when interpreting molecular COVID-19 data.
Keywords: COVID-19; Extracellular matrix; Lung; Proteomics; SARS-CoV-2; Signaling.