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Matsuoka, Daiki Department of Pediatric Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Suehara, Kana Department of Pediatric Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Naka, Shuhei Department of Pediatric Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Kaken ID publons researchmap
Misaki, Taro Division of Nephrology, Seirei Hamamatsu General Hospital
Nagasawa, Yasuyuki Department of General Internal Medicine, Hyogo Medical University
Ito, Seigo Department of Internal Medicine, Japan Self-Defense Force Iruma Hospital
Suehiro, Yuto Department of Pediatric Dentistry, Graduate School of Dentistry, The University of Osaka
Nomura, Ryota Department of Pediatric Dentistry, Graduate School of Biomedical and Health Sciences, Hiroshima University
Nakano, Kazuhiko Department of Pediatric Dentistry, Graduate School of Dentistry, The University of Osaka
Matsumoto-Nakano, Michiyo Department of Pediatric Dentistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Kaken ID
Abstract
Background: The present study was conducted to examine the interaction between collagen-binding protein (Cnm) of Streptococcus mutans and immunoglobulin (IgA) to clarify the possible involvement in IgA nephropathy (IgAN) development.
Methods: The binding of Cnm to human immunoglobulins was examined using an enzyme-linked immunosorbent assay. A nephritis-induced rat model was employed to confirm the localization of Cnm.
Results: IgA1 showed significantly greater binding ability to Cnm than to other bacterial surface proteins, and Cnm showed significantly greater binding ability to IgA1 than to other immunoglobulins. In rats administered Cnm, IgA deposition was observed in the glomerular mesangial region. Furthermore, biotin-labeled Cnm was observed in the same region as IgA deposition in the Cnm group.
Conclusions: Taken together, it is considered that following invasion into the bloodstream, Cnm binds to and forms a complex with IgA1, leading to deposition of IgA1 in renal glomeruli.
Keywords
bacterial surface proteins
collagen-binding protein
human immunoglobulins
IgA nephropathy
Streptococcus mutans
Published Date
2026-01-07
Publication Title
Frontiers in Cellular and Infection Microbiology
Volume
volume15
Publisher
Frontiers Media SA
Start Page
1673581
ISSN
2235-2988
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© 2026 Matsuoka, Suehara, Naka, Misaki, Nagasawa, Ito, Suehiro, Nomura, Nakano and Matsumoto-Nakano.
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DOI
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Related Url
isVersionOf https://doi.org/10.3389/fcimb.2025.1673581
License
https://creativecommons.org/licenses/by/4.0/
Citation
Matsuoka D, Suehara K, Naka S, Misaki T, Nagasawa Y, Ito S, Suehiro Y, Nomura R, Nakano K and Matsumoto-Nakano M (2026) Binding of IgA1 and surface-expressed collagen-binding protein of Streptococcus mutans contributes to IgA nephropathy pathogenesis. Front. Cell. Infect. Microbiol. 15:1673581. doi: 10.3389/fcimb.2025.1673581
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