» Articles » PMID: 35106136

Toxin-like Peptides in Plasma, urine and Faecal samples from COVID-19 Patients

Overview
Journal F1000Res
Date 2022 Feb 3
PMID 35106136
Authors
Affiliations
Soon will be listed here.
Abstract

 SARS-CoV-2 that causes COVID-19 disease and led to the pandemic currently affecting the world has been broadly investigated. Different studies have been performed to understand the infection mechanism, and the involved human genes, transcripts and proteins. In parallel, numerous clinical extra-pulmonary manifestations co-occurring with COVID-19 disease have been reported and evidence of their severity and persistence is increasing. Whether these manifestations are linked to other disorders co-occurring with SARS-CoV-2 infection, is under discussion. In this work, we report the identification of toxin-like peptides in COVID-19 patients by application of the Liquid Chromatography Surface-Activated Chemical Ionization - Cloud Ion Mobility Mass Spectrometry.    Plasma, urine and faecal samples from COVID-19 patients and control individuals were analysed to study peptidomic toxins' profiles. Protein precipitation preparation procedure was used for plasma, to remove high molecular weight proteins and efficiently solubilize the peptide fraction; in the case of faeces and urine, direct peptide solubilization was employed.    Toxin-like peptides, almost identical to toxic components of venoms from animals, like conotoxins, phospholipases, phosphodiesterases, zinc metal proteinases, and bradykinins, were identified in samples from COVID-19 patients, but not in control samples.   The presence of toxin-like peptides could potentially be connected to SARS-CoV-2 infection. Their presence suggests a possible association between COVID-19 disease and the release in the body of (oligo-)peptides almost identical to toxic components of venoms from animals. Their involvement in a large set of heterogeneous extra-pulmonary COVID-19 clinical manifestations, like neurological ones, cannot be excluded. Although the presence of each individual symptom is not selective of the disease, their combination might be related to COVID-19 by the coexistence of the panel of the here detected toxin-like peptides. The presence of these peptides opens new scenarios on the aetiology of the COVID-19 clinical symptoms observed up to now, including neurological manifestations.

Citing Articles

The first report on detecting SARS-CoV-2 inside bacteria of  the human gut microbiome: A case series on asymptomatic family members and a child with COVID-19.

Brogna C, Cristoni S, Petrillo M, Bisaccia D, Lauritano F, Montano L F1000Res. 2024; 11:135.

PMID: 39464247 PMC: 11502994. DOI: 10.12688/f1000research.77421.2.


Who Is the Intermediate Host of RNA Viruses? A Study Focusing on SARS-CoV-2 and Poliovirus.

Brogna C, Bisaccia D, Costanzo V, Lettieri G, Montano L, Viduto V Microorganisms. 2024; 12(4).

PMID: 38674588 PMC: 11051822. DOI: 10.3390/microorganisms12040643.


Recent progress in mass spectrometry-based urinary proteomics.

Joshi N, Garapati K, Ghose V, Kandasamy R, Pandey A Clin Proteomics. 2024; 21(1):14.

PMID: 38389064 PMC: 10885485. DOI: 10.1186/s12014-024-09462-z.


Proteomic Profiling of Urine From Hospitalized Patients With Severe Pneumonia due to SARS-CoV-2 vs Other Causes: A Preliminary Report.

Wilson L, Chang J, Meier S, Ganief T, Ganief N, Oelofse S Open Forum Infect Dis. 2023; 10(10):ofad451.

PMID: 37799131 PMC: 10549212. DOI: 10.1093/ofid/ofad451.


A Pictorial Essay Describing the CT Imaging Features of COVID-19 Cases throughout the Pandemic with a Special Focus on Lung Manifestations and Extrapulmonary Vascular Abdominal Complications.

Brogna B, Bignardi E, Megliola A, Laporta A, La Rocca A, Volpe M Biomedicines. 2023; 11(8).

PMID: 37626610 PMC: 10452395. DOI: 10.3390/biomedicines11082113.


References
1.
Terracciano R, Preiano M, Fregola A, Pelaia C, Montalcini T, Savino R . Mapping the SARS-CoV-2-Host Protein-Protein Interactome by Affinity Purification Mass Spectrometry and Proximity-Dependent Biotin Labeling: A Rational and Straightforward Route to Discover Host-Directed Anti-SARS-CoV-2 Therapeutics. Int J Mol Sci. 2021; 22(2). PMC: 7825748. DOI: 10.3390/ijms22020532. View

2.
Horby P, Lim W, Emberson J, Mafham M, Bell J, Linsell L . Dexamethasone in Hospitalized Patients with Covid-19. N Engl J Med. 2020; 384(8):693-704. PMC: 7383595. DOI: 10.1056/NEJMoa2021436. View

3.
Cheng M, Zhang S, Porritt R, Noval Rivas M, Paschold L, Willscher E . Superantigenic character of an insert unique to SARS-CoV-2 spike supported by skewed TCR repertoire in patients with hyperinflammation. Proc Natl Acad Sci U S A. 2020; 117(41):25254-25262. PMC: 7568239. DOI: 10.1073/pnas.2010722117. View

4.
Schoch C, Ciufo S, Domrachev M, Hotton C, Kannan S, Khovanskaya R . NCBI Taxonomy: a comprehensive update on curation, resources and tools. Database (Oxford). 2020; 2020. PMC: 7408187. DOI: 10.1093/database/baaa062. View

5.
Prasasty V, Radifar M, Istyastono E . Natural Peptides in Drug Discovery Targeting Acetylcholinesterase. Molecules. 2018; 23(9). PMC: 6225273. DOI: 10.3390/molecules23092344. View