Proteomic profile of vitreous in patients with tubercular uveitis

To elucidate disease-specific host protein profile in vitreous fluid of patients with intraocular inflammation due to tubercular uveitis (TBU). Vitreous samples from 13 patients with TBU (group A), 7 with non-TBU (group B) and 9 with no uveitis (group C) were analysed by shotgun proteomics using Liq...

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Published inTuberculosis (Edinburgh, Scotland) Vol. 126; p. 102036
Main Authors Bansal, Reema, Khan, Mohd M., Dasari, Surendra, Verma, Indu, Goodlett, David R., Manes, Nathan P., Nita-Lazar, Aleksandra, Sharma, Surya P., Kumar, Aman, Singh, Nirbhai, Chakraborti, Anuradha, Gupta, Vishali, Dogra, M.R., Ram, Jagat, Gupta, Amod
Format Journal Article
LanguageEnglish
Published Scotland Elsevier Ltd 01.01.2021
Elsevier Science Ltd
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Summary:To elucidate disease-specific host protein profile in vitreous fluid of patients with intraocular inflammation due to tubercular uveitis (TBU). Vitreous samples from 13 patients with TBU (group A), 7 with non-TBU (group B) and 9 with no uveitis (group C) were analysed by shotgun proteomics using Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS). Differentially expressed proteins (DEPs) were subjected to pathway analysis using WEB-based Gene SeT Analysis Toolkit software. Compared to control groups (B + C combined), group A (TBU) displayed 32 (11 upregulated, 21 downregulated) DEPs, which revealed an upregulation of coagulation cascades, complement and classic pathways, and downregulation of metabolism of carbohydrates, gluconeogenesis, glucose metabolism and glycolysis/gluconeogenesis pathways. When compared to group B (non-TBU) alone, TBU displayed 58 DEPs (21 upregulated, 37 downregulated), with an upregulation of apoptosis, KRAS signaling, diabetes pathways, classic pathways, and downregulation of MTORC1 signaling, glycolysis/gluconeogenesis, and glucose metabolism. This differential protein profile provides novel insights into the molecular mechanisms of TBU and a baseline to explore vitreous biomarkers to differentiate TBU from non-TBU, warranting future studies to identify and validate them as a diagnostic tool in TBU. The enriched pathways generate interesting hypotheses and drive further research.
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Present Address: Booz Allen Hamilton, McLean, VA, USA.
IV: in charge of overall direction and planning, critical revision of the article.
VG: sample collection, critical revision of the article.
RB, MK, DRG: Designed and performed the experiments.
Visiting Professor, University of Gdansk, Gdansk, Poland, EU
SD: processed the experimental data, performed the analysis, supervised the manuscript and designed the figures and tables.
AC: inputs in manuscript writing.
Author contribution statement
MK, NM, AN-L: sample processing, analysis and interpretation.
MRD, JR: critical revision of the article.
Both authors have contributed equally.
All authors discussed the results and contributed to the final manuscript.
SPS, AK, NS: experimental work.
RB: Writing and editing of the manuscript, conducting the proteomics experiment, sample collection, literature search.
AG: Conception or design of the work, sample collection, critical revision of the article, in charge of overall direction and planning, final approval of the version to be published
SL: in charge of overall direction and planning.
ISSN:1472-9792
1873-281X
DOI:10.1016/j.tube.2020.102036