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pmid:36233441

COVID-19 Salivary Protein Profile: Unravelling Molecular Aspects of SARS-CoV-2 Infection.

Eduardo Esteves · Vera M Mendes · Bruno Manadas · Rafaela Lopes · Liliana Bernardino · Maria José Correia · Marlene Barros · Ana Cristina Esteves · Nuno Rosa

Journal of clinical medicine · 2022 doi:10.3390/jcm11195571

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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COVID-19 Salivary Protein Profile: Unravelling Molecular Aspects of SARS-CoV-2 Infection.
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10.3390/jcm11195571
pmid
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Eduardo Esteves
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Vera M Mendes
[2]
Bruno Manadas
[3]
Rafaela Lopes
[4]
Liliana Bernardino
[5]
Maria José Correia
[6]
Marlene Barros
[7]
Ana Cristina Esteves
[8]
Nuno Rosa
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Journal of clinical medicine
year
2022
abstract
COVID-19 is the most impacting global pandemic of all time, with over 600 million infected and 6.5 million deaths worldwide, in addition to an unprecedented economic impact. Despite the many advances in scientific knowledge about the disease, much remains to be clarified about the molecular alterations induced by SARS-CoV-2 infection. In this work, we present a hybrid proteomics and in silico interactomics strategy to establish a COVID-19 salivary protein profile. Data are available via ProteomeXchange with identifier PXD036571. The differential proteome was narrowed down by the Partial Least-Squares Discriminant Analysis and enrichment analysis was performed with FunRich. In parallel, OralInt was used to determine interspecies Protein-Protein Interactions between humans and SARS-CoV-2. Five dysregulated biological processes were identified in the COVID-19 proteome profile: Apoptosis, Energy Pathways, Immune Response, Protein Metabolism and Transport. We identified 10 proteins (KLK 11, IMPA2, ANXA7, PLP2, IGLV2-11, IGHV3-43D, IGKV2-24, TMEM165, VSIG10 and PHB2) that had never been associated with SARS-CoV-2 infection, representing new evidence of the impact of COVID-19. Interactomics analysis showed viral influence on the host immune response, mainly through interaction with the degranulation of neutrophils. The virus alters the host's energy metabolism and interferes with apoptosis mechanisms.
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A Kruskal–Wallis test was performed to select the proteins statistically different between the COVID+ and COVID- samples. Dunn’s test of multiple comparisons, with Benjamini–Hochberg p-value adjustment, was performed to determine in which comparisons statistical differences were observed. The Mann–Whitney test was used for the binary comparisons.
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A Kruskal–Wallis test was performed to select the proteins statistically different between the COVID+ and COVID- samples. Dunn’s test of multiple comparisons, with Benjamini–Hochberg p-value adjustment, was performed to determine in which comparisons statistical differences were observed. The Mann–Whitney test was used for the binary comparisons.
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Five dysregulated biological processes were identified in the COVID-19 proteome profile: Apoptosis, Energy Pathways, Immune Response, Protein Metabolism and Transport.
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Five dysregulated biological processes were identified in the COVID-19 proteome profile: Apoptosis, Energy Pathways, Immune Response, Protein Metabolism and Transport.
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COVID-19 salivary protein profile: unravelling molecular aspects of SARS-COV-2 infection
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A Kruskal–Wallis test was performed to select the proteins statistically different between the COVID+ and COVID- samples. Dunn’s test of multiple comparisons, with Benjamini–Hochberg p-value adjustment, was performed to determine in which comparisons statistical differences were observed. The Mann–Whitney test was used for the binary comparisons.
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Complete file
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