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PtpA and PknG Proteins Secreted by Mycobacterium avium subsp. paratuberculosis are Recognized by Sera from Patients with Rheumatoid Arthritis: A Case–Control Study

Authors Bo M, Erre GL, Bach H, Slavin YN, Manchia PA, Passiu G, Sechi LA

Received 26 June 2019

Accepted for publication 9 October 2019

Published 3 December 2019 Volume 2019:12 Pages 301—308

DOI https://doi.org/10.2147/JIR.S220960

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Colin Mak

Peer reviewer comments 2

Editor who approved publication: Dr Ning Quan


Marco Bo,1 Gian Luca Erre,2 Horacio Bach,3 Yael N Slavin,3 Piera Angela Manchia,4 Giuseppe Passiu,2 Leonardo A Sechi1

1Department of Biomedical Sciences, Section of Microbiology and Virology, University of Sassari, Sassari 07100, Italy; 2Department of Clinical and Experimental Medicine, Azienda Ospedaliero-Universitaria di Sassari, UOC di Reumatologia, Sassari 07100, Italy; 3Division of Infectious Diseases, Faculty of Medicine, The University of British Columbia, Vancouver, BC V6H 3Z6, Canada; 4Centro Trasfusionale, AOU Sassari, Sassari, Italy

Correspondence: Leonardo A Sechi
Department of Biomedical Sciences, University of Sassari, Viale San Pietro 43 B, Sassari 07100, Italy
Tel +39 079228462
Email sechila@uniss.it

Purpose: Rheumatoid arthritis (RA) can result from complex interactions between the affected person’s genetic background and environment. Viral and bacterial infections may play a pathogenetic role in RA through different mechanisms of action. We aimed to evaluate the presence of antibodies (Abs) directed against two proteins of Mycobacterium avium subsp. paratuberculosis (MAP) in sera of RA subjects, which are crucial for the survival of the pathogen within macrophages. Moreover, we analyzed the correlation of immune response to both proteins with the following homologous peptides: BOLF1305–320, MAP_402718–32 and IRF5424–434 to understand how the synergic role of Epstein–Barr virus (EBV) and MAP infection in genetically predisposed subjects may lead to a possible deregulation of interferon regulatory factor 5 (IRF5).
Materials and methods: The presence of Abs against protein tyrosine phosphatase A (PtpA) and protein kinase G (PknG) in sera from Sardinian RA patients (n=84) and healthy volunteers (HCs, n=79) was tested by indirect ELISA.
Results: RA sera showed a remarkably high frequency of reactivity against PtpA in comparison to HCs (48.8% vs 7.6%; p<0.001) and lower but statistically significant responses towards PknG (27.4% vs 10.1%; p=0.0054). We found a significant linear correlation between the number of swollen joints and the concentrations of antibodies against PtpA (p=0.018). Furthermore, a significant bivariate correlation between PtpA and MAP MAP_402718–32 peptide has been found, suggesting that MAP infection may induce a secondary immune response through cross-reaction with IRF5 (R2=0.5).
Conclusion: PtpA and PknG are strongly recognized in RA which supports the hypothesis that MAP infection may be involved in the pathogenesis of RA.

Keywords: Mycobacterium avium subsp. paratuberculosis, PtpA, PknG, virulence factors, rheumatoid arthritis, immune response

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