TY - JOUR
T1 - Mass Spectrometric Analysis of Urine from COVID-19 Patients for Detection of SARS-CoV-2 Viral Antigen and to Study Host Response
AU - Chavan, Sandip
AU - Mangalaparthi, Kiran K.
AU - Singh, Smrita
AU - Renuse, Santosh
AU - Vanderboom, Patrick M.
AU - Madugundu, Anil Kumar
AU - Budhraja, Rohit
AU - McAulay, Kathrine
AU - Grys, Thomas E.
AU - Rule, Andrew D.
AU - Alexander, Mariam P.
AU - O’Horo, John C.
AU - Badley, Andrew D.
AU - Pandey, Akhilesh
N1 - Funding Information:
The authors declare the following competing financial interest(s): A.D.B. is supported by grants from NIAID (grants AI110173 and AI120698), Amfar (#109593), and the Mayo Clinic (HH Shieck Khalifa Bib Zayed Al-Nahyan Named Professorship of Infectious Diseases). A.D.B. is a paid consultant for Abbvie and Flambeau Diagnostics, a paid member of the DSMB for Corvus Pharmaceuticals, Equilium, and Excision Biotherapeutics; has received fees for speaking for Reach MD; owns equity for scientific advisory work in Zentalis and nference; and is the founder and President of Splissen therapeutics. T.E.G. is a consultant for Safe Health Systems, on the scientific advisory board of Dropworks and a founder of Cactus Bio, LLC. J.C.O. reports personal fees from Elsevier, Inc. and personal fees from EBates College, outside the submitted work. S.C., K.K.M., S.S., S.R., P.M.V., A.K.M., R.B., K.M., A.D.R, M.P.A., and A.P. have no conflicts of interest to declare.
Funding Information:
This study was supported by DBT/Wellcome Trust India Alliance Margdarshi Fellowship grant IA/M/15/1/502023 awarded to A.P. and the generosity of Eric and Wendy Schmidt. The sponsors had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; or the decision to submit the manuscript for publication.
Publisher Copyright:
© 2021 American Chemical Society
PY - 2021/7/2
Y1 - 2021/7/2
N2 - SARS-CoV-2 infection has become a major public health burden and affects many organs including lungs, kidneys, the liver, and the brain. Although the virus is readily detected and diagnosed using nasopharyngeal swabs by reverse transcriptase polymerase chain reaction (RT-PCR), detection of its presence in body fluids is fraught with difficulties. A number of published studies have failed to detect viral RNA by RT-PCR methods in urine. Although microbial identification in clinical microbiology using mass spectrometry is undertaken after culture, here we undertook a mass spectrometry-based approach that employed an enrichment step to capture and detect SARS-CoV-2 nucleocapsid protein directly from urine of COVID-19 patients without any culture. We detected SARS-CoV-2 nucleocapsid protein-derived peptides from 13 out of 39 urine samples. Further, a subset of COVID-19 positive and COVID-19 negative urine samples validated by mass spectrometry were used for the quantitative proteomics analysis. Proteins with increased abundance in urine of SARS-CoV-2 positive individuals were enriched in the acute phase response, regulation of complement system, and immune response. Notably, a number of renal proteins such as podocin (NPHS2), an amino acid transporter (SLC36A2), and sodium/glucose cotransporter 5 (SLC5A10), which are intimately involved in normal kidney function, were decreased in the urine of COVID-19 patients. Overall, the detection of viral antigens in urine using mass spectrometry and alterations of the urinary proteome could provide insights into understanding the pathogenesis of COVID-19.
AB - SARS-CoV-2 infection has become a major public health burden and affects many organs including lungs, kidneys, the liver, and the brain. Although the virus is readily detected and diagnosed using nasopharyngeal swabs by reverse transcriptase polymerase chain reaction (RT-PCR), detection of its presence in body fluids is fraught with difficulties. A number of published studies have failed to detect viral RNA by RT-PCR methods in urine. Although microbial identification in clinical microbiology using mass spectrometry is undertaken after culture, here we undertook a mass spectrometry-based approach that employed an enrichment step to capture and detect SARS-CoV-2 nucleocapsid protein directly from urine of COVID-19 patients without any culture. We detected SARS-CoV-2 nucleocapsid protein-derived peptides from 13 out of 39 urine samples. Further, a subset of COVID-19 positive and COVID-19 negative urine samples validated by mass spectrometry were used for the quantitative proteomics analysis. Proteins with increased abundance in urine of SARS-CoV-2 positive individuals were enriched in the acute phase response, regulation of complement system, and immune response. Notably, a number of renal proteins such as podocin (NPHS2), an amino acid transporter (SLC36A2), and sodium/glucose cotransporter 5 (SLC5A10), which are intimately involved in normal kidney function, were decreased in the urine of COVID-19 patients. Overall, the detection of viral antigens in urine using mass spectrometry and alterations of the urinary proteome could provide insights into understanding the pathogenesis of COVID-19.
KW - COVID-19
KW - SARS-CoV-2
KW - coronavirus
KW - mass spectrometry
KW - quantitative proteomic analysis
KW - urine
UR - http://www.scopus.com/inward/record.url?scp=85108897663&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85108897663&partnerID=8YFLogxK
U2 - 10.1021/acs.jproteome.1c00391
DO - 10.1021/acs.jproteome.1c00391
M3 - Article
C2 - 34077217
AN - SCOPUS:85108897663
SN - 1535-3893
VL - 20
SP - 3404
EP - 3413
JO - Journal of Proteome Research
JF - Journal of Proteome Research
IS - 7
ER -