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Comprehensive plasma proteomic profiling reveals biomarkers for active tuberculosis

Comprehensive plasma proteomic profiling reveals biomarkers for active tuberculosis
Comprehensive plasma proteomic profiling reveals biomarkers for active tuberculosis

Background: tuberculosis (TB) kills more people than any other infection, and new diagnostic tests to identify active cases are required. We aimed to discover and verify novel markers for TB in nondepleted plasma.


Methods: we applied an optimized quantitative proteomics discovery methodology based on multidimensional and orthogonal liquid chromatographic separation combined with high-resolution mass spectrometry to study nondepleted plasma of 11 patients with active TB compared with 10 healthy controls. Prioritized candidates were verified in independent UK (n = 118) and South African cohorts (n = 203).


Results: we generated the most comprehensive TB plasma proteome to date, profiling 5022 proteins spanning 11 orders-of-magnitude concentration range with diverse biochemical and molecular properties. We analyzed the predominantly low–molecular weight subproteome, identifying 46 proteins with significantly increased and 90 with decreased abundance (peptide FDR ≤ 1%, q ≤ 0.05). Verification was performed for novel candidate biomarkers (CFHR5, ILF2) in 2 independent cohorts. Receiver operating characteristics analyses using a 5-protein panel (CFHR5, LRG1, CRP, LBP, and SAA1) exhibited discriminatory power in distinguishing TB from other respiratory diseases (AUC = 0.81).


Conclusion: we report the most comprehensive TB plasma proteome to date, identifying novel markers with verification in 2 independent cohorts, leading to a 5-protein biosignature with potential to improve TB diagnosis. With further development, these biomarkers have potential as a diagnostic triage test.


FUNDING. Colciencias, Medical Research Council, Innovate UK, NIHR, Academy of Medical Sciences, Program for Advanced Research Capacities for AIDS, Wellcome Centre for Infectious Diseases Research.

Biomarkers/blood, Case-Control Studies, Female, Follow-Up Studies, Gene Regulatory Networks, Humans, Male, Mycobacterium tuberculosis/metabolism, Peru/epidemiology, Prospective Studies, Proteome/analysis, ROC Curve, South Africa/epidemiology, Tuberculosis, Pulmonary/blood
2379-3708
Garay-Baquero, Diana J.
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White, Cory H.
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Walker, Naomi F.
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Tebruegge, Marc
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Schiff, Hannah F.
59bd19d1-4547-4807-941b-cc273f6ebf9b
Ugarte-Gil, Cesar
705952c4-d412-4f77-9226-852f2973e117
Morris-Jones, Stephen
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Marshall, Ben G.
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Manousopoulou, Antigoni
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Adamson, John
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Vallejo, Andres F.
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Bielecka, Magdalena K.
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Wilkinson, Robert J.
efcf7079-ebfa-4270-b7a4-a578ffd91178
Tezera, Liku B.
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Woelk, Christopher H.
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Garbis, Spiros D.
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Elkington, Paul
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et al.
Garay-Baquero, Diana J.
da9136fe-3d47-4d04-8ab3-96bfe17a773c
White, Cory H.
45233a78-f0c9-4696-8aaf-1b2673f83c91
Walker, Naomi F.
e586ffdf-ae4b-46fa-83a1-db72501d17c1
Tebruegge, Marc
2c3dff22-0b5f-48a7-bb36-ce323705f74a
Schiff, Hannah F.
59bd19d1-4547-4807-941b-cc273f6ebf9b
Ugarte-Gil, Cesar
705952c4-d412-4f77-9226-852f2973e117
Morris-Jones, Stephen
e22173b1-826a-4b45-a0c6-40f385e81f24
Marshall, Ben G.
12be7650-0780-4923-8c8d-e26862fe3213
Manousopoulou, Antigoni
4e4b92ba-be65-4dba-a15d-87924c56f08b
Adamson, John
b80c4942-809d-4a94-942c-36c1cf3ae8d9
Vallejo, Andres F.
294fca39-0187-47b4-90ad-cadc7b888830
Bielecka, Magdalena K.
90391ea3-aa1f-4104-a893-568c138718a2
Wilkinson, Robert J.
efcf7079-ebfa-4270-b7a4-a578ffd91178
Tezera, Liku B.
c5598dbf-23a8-4934-96a4-7c783bf9e776
Woelk, Christopher H.
4d3af0fd-658f-4626-b3b5-49a6192bcf7d
Garbis, Spiros D.
7067fd19-50c9-4d42-9611-f370289470bd
Elkington, Paul
60828c7c-3d32-47c9-9fcc-6c4c54c35a15

Garay-Baquero, Diana J., White, Cory H. and Walker, Naomi F. , et al. (2020) Comprehensive plasma proteomic profiling reveals biomarkers for active tuberculosis. JCI Insight, 5 (18), [e137427]. (doi:10.1172/jci.insight.137427).

Record type: Article

Abstract

Background: tuberculosis (TB) kills more people than any other infection, and new diagnostic tests to identify active cases are required. We aimed to discover and verify novel markers for TB in nondepleted plasma.


Methods: we applied an optimized quantitative proteomics discovery methodology based on multidimensional and orthogonal liquid chromatographic separation combined with high-resolution mass spectrometry to study nondepleted plasma of 11 patients with active TB compared with 10 healthy controls. Prioritized candidates were verified in independent UK (n = 118) and South African cohorts (n = 203).


Results: we generated the most comprehensive TB plasma proteome to date, profiling 5022 proteins spanning 11 orders-of-magnitude concentration range with diverse biochemical and molecular properties. We analyzed the predominantly low–molecular weight subproteome, identifying 46 proteins with significantly increased and 90 with decreased abundance (peptide FDR ≤ 1%, q ≤ 0.05). Verification was performed for novel candidate biomarkers (CFHR5, ILF2) in 2 independent cohorts. Receiver operating characteristics analyses using a 5-protein panel (CFHR5, LRG1, CRP, LBP, and SAA1) exhibited discriminatory power in distinguishing TB from other respiratory diseases (AUC = 0.81).


Conclusion: we report the most comprehensive TB plasma proteome to date, identifying novel markers with verification in 2 independent cohorts, leading to a 5-protein biosignature with potential to improve TB diagnosis. With further development, these biomarkers have potential as a diagnostic triage test.


FUNDING. Colciencias, Medical Research Council, Innovate UK, NIHR, Academy of Medical Sciences, Program for Advanced Research Capacities for AIDS, Wellcome Centre for Infectious Diseases Research.

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Submitted date: 27 February 2020
Accepted/In Press date: 31 July 2020
Published date: 17 September 2020
Keywords: Biomarkers/blood, Case-Control Studies, Female, Follow-Up Studies, Gene Regulatory Networks, Humans, Male, Mycobacterium tuberculosis/metabolism, Peru/epidemiology, Prospective Studies, Proteome/analysis, ROC Curve, South Africa/epidemiology, Tuberculosis, Pulmonary/blood

Identifiers

Local EPrints ID: 446827
URI: http://eprints.soton.ac.uk/id/eprint/446827
ISSN: 2379-3708
PURE UUID: 12e33f9f-1cbb-44d7-8da2-49c401e59f8a
ORCID for Diana J. Garay-Baquero: ORCID iD orcid.org/0000-0002-9450-8504
ORCID for Hannah F. Schiff: ORCID iD orcid.org/0000-0002-0860-1818
ORCID for Liku B. Tezera: ORCID iD orcid.org/0000-0002-7898-6709
ORCID for Spiros D. Garbis: ORCID iD orcid.org/0000-0002-1050-0805
ORCID for Paul Elkington: ORCID iD orcid.org/0000-0003-0390-0613

Catalogue record

Date deposited: 23 Feb 2021 17:33
Last modified: 28 Mar 2024 02:56

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Contributors

Author: Diana J. Garay-Baquero ORCID iD
Author: Cory H. White
Author: Naomi F. Walker
Author: Marc Tebruegge
Author: Hannah F. Schiff ORCID iD
Author: Cesar Ugarte-Gil
Author: Stephen Morris-Jones
Author: Ben G. Marshall
Author: Antigoni Manousopoulou
Author: John Adamson
Author: Andres F. Vallejo
Author: Magdalena K. Bielecka
Author: Robert J. Wilkinson
Author: Liku B. Tezera ORCID iD
Author: Christopher H. Woelk
Author: Spiros D. Garbis ORCID iD
Author: Paul Elkington ORCID iD
Corporate Author: et al.

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