Antibodies Recognizing Yersinia enterocolitica Lipopolysaccharides of Various Chemotypes in Synovial Fluids From Patients With Juvenile Idiopathic Arthritis

Author:

Kasperkiewicz Katarzyna1ORCID,Świerzko Anna S.2ORCID,Michalski Mateusz2,Eppa Łukasz2,Skurnik Mikael34ORCID,Żuber Zbigniew56ORCID,Cedzyński Maciej2ORCID

Affiliation:

1. Institute of Biology, Biotechnology, And Environmental Protection, Faculty of Natural Sciences, The University of Silesia in Katowice, Jagiellońska 28, 40-032 Katowice, Poland

2. Laboratory of Immunobiology of Infections, Institute of Medical Biology, Polish Academy of Sciences, Lodowa 106, PL 93-232 Łódź, Poland

3. Department of Bacteriology and Immunology, Medicum, Human Microbiome Research Program, Faculty of Medicine, University of Helsinki, Haartmaninkatu 3, 00290 Helsinki, Finland

4. Division of Clinical Microbiology, HUS LAB, University of Helsinki and Helsinki University Hospital, 00290 Helsinki, Finland

5. Pediatrics Clinic, Faculty of Medicine and Health Sciences, Andrzej Frycz Modrzewski Krakow University, Gustawa Herlinga-Grudzińskiego 1, 30-705 Kraków, Poland

6. Department of Rheumatology, St Louis Voivodeship Specialist Children’s Hospital, Cracow, Poland

Abstract

Yersinia enterocolitica O:3 (YeO3) is considered to be associated with reactive arthritis (ReA), and its lipopolysaccharide (LPS) has been detected in synovial fluids from patients. Interestingly, YeO3 wild-type LPS was processed by host cells, resulting in truncated LPS molecules presenting the core region. Previously, we reported the immunogenicity but not adjuvanticity of YeO3 LPSs of wild (S) type, Ra, Rd, or Re chemotypes in mice. Here, we demonstrate the presence of YeO3 LPS chemotype-specific antibodies in all analyzed synovial fluids (SF) from patients with juvenile idiopathic arthritis (JIA). Interestingly, the high titer of antibodies specific for the Kdo-lipid A region was found in most tested SF. In contrast, only a few were positive for antibodies recognizing O-specific polysaccharides. Western blot analysis revealed the presence of antibodies reacting with fast-migrating LPS fractions and enterobacterial common antigen (ECA) in synovial fluid samples. Our data also suggest the importance of LPS-associated ECA for the antigenicity of endotoxin. Furthermore, we confirmed in vitro that Yersinia LPS processing leads to the exposure of its core region and enhanced potency of complement lectin pathway activation.

Funder

The National Science Centre

Publisher

Hindawi Limited

Subject

Immunology,General Medicine,Immunology and Allergy

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