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PLoS One ; 15(10): e0240012, 2020.
Article in English | MEDLINE | ID: covidwho-881156

ABSTRACT

COVID-19 or severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) appeared throughout the World and currently affected more than 9 million people and caused the death of around 470,000 patients. The novel strain of the coronavirus disease is transmittable at a devastating rate with a high rate of severe hospitalization even more so for the elderly population. Naso-oro-pharyngeal swab samples as the first step towards detecting suspected infection of SARS-CoV-2 provides a non-invasive method for PCR testing at a high confidence rate. Furthermore, proteomics analysis of PCR positive and negative naso-oropharyngeal samples provides information on the molecular level which highlights disease pathology. Samples from 15 PCR positive cases and 15 PCR negative cases were analyzed with nanoLC-MS/MS to identify the differentially expressed proteins. Proteomic analyses identified 207 proteins across the sample set and 17 of them were statistically significant. Protein-protein interaction analyses emphasized pathways like Neutrophil degranulation, Innate Immune System, Antimicrobial Peptides. Neutrophil Elastase (ELANE), Azurocidin (AZU1), Myeloperoxidase (MPO), Myeloblastin (PRTN3), Cathepsin G (CTSG) and Transcobalamine-1 (TCN1) were found to be significantly altered in naso-oropharyngeal samples of SARS-CoV-2 patients. The identified proteins are linked to alteration in the innate immune system specifically via neutrophil degranulation and NETosis.


Subject(s)
Betacoronavirus/genetics , Cell Degranulation/immunology , Coronavirus Infections/immunology , Nasopharynx/virology , Neutrophil Activation/immunology , Neutrophils/immunology , Pneumonia, Viral/immunology , Proteome , Up-Regulation , Adult , COVID-19 , Chromatography, Liquid/methods , Coronavirus Infections/virology , Female , Humans , Male , Middle Aged , Pandemics , Pneumonia, Viral/virology , Protein Interaction Maps , Proteomics/methods , Real-Time Polymerase Chain Reaction , SARS-CoV-2 , Tandem Mass Spectrometry/methods , Young Adult
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