Effect of Porphyromonas gingivalis infection on gut dysbiosis and resultant arthritis exacerbation in mouse model

Abstract Background Porphyromonas gingivalis (Pg) infection causes periodontal disease and exacerbates rheumatoid arthritis (RA). It is reported that inoculation of periodontopathogenic bacteria (i.e., Pg) can alter gut microbiota composition in the animal models. Gut microbiota dysbiosis in human h...

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Main Authors: Yuta Hamamoto, Kazuhisa Ouhara, Syuichi Munenaga, Mikio Shoji, Tatsuhiko Ozawa, Jyunzo Hisatsune, Isamu Kado, Mikihito Kajiya, Shinji Matsuda, Toshihisa Kawai, Noriyoshi Mizuno, Tsuyoshi Fujita, Shintaro Hirata, Kotaro Tanimoto, Koji Nakayama, Hiroyuki Kishi, Eiji Sugiyama, Hidemi Kurihara
Format: Article
Language:English
Published: BMC 2020-10-01
Series:Arthritis Research & Therapy
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13075-020-02348-z
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language English
format Article
sources DOAJ
author Yuta Hamamoto
Kazuhisa Ouhara
Syuichi Munenaga
Mikio Shoji
Tatsuhiko Ozawa
Jyunzo Hisatsune
Isamu Kado
Mikihito Kajiya
Shinji Matsuda
Toshihisa Kawai
Noriyoshi Mizuno
Tsuyoshi Fujita
Shintaro Hirata
Kotaro Tanimoto
Koji Nakayama
Hiroyuki Kishi
Eiji Sugiyama
Hidemi Kurihara
spellingShingle Yuta Hamamoto
Kazuhisa Ouhara
Syuichi Munenaga
Mikio Shoji
Tatsuhiko Ozawa
Jyunzo Hisatsune
Isamu Kado
Mikihito Kajiya
Shinji Matsuda
Toshihisa Kawai
Noriyoshi Mizuno
Tsuyoshi Fujita
Shintaro Hirata
Kotaro Tanimoto
Koji Nakayama
Hiroyuki Kishi
Eiji Sugiyama
Hidemi Kurihara
Effect of Porphyromonas gingivalis infection on gut dysbiosis and resultant arthritis exacerbation in mouse model
Arthritis Research & Therapy
Porphyromonas gingivalis
Rheumatoid arthritis
Periodontitis
Citrullinated protein
Dysbiosis
author_facet Yuta Hamamoto
Kazuhisa Ouhara
Syuichi Munenaga
Mikio Shoji
Tatsuhiko Ozawa
Jyunzo Hisatsune
Isamu Kado
Mikihito Kajiya
Shinji Matsuda
Toshihisa Kawai
Noriyoshi Mizuno
Tsuyoshi Fujita
Shintaro Hirata
Kotaro Tanimoto
Koji Nakayama
Hiroyuki Kishi
Eiji Sugiyama
Hidemi Kurihara
author_sort Yuta Hamamoto
title Effect of Porphyromonas gingivalis infection on gut dysbiosis and resultant arthritis exacerbation in mouse model
title_short Effect of Porphyromonas gingivalis infection on gut dysbiosis and resultant arthritis exacerbation in mouse model
title_full Effect of Porphyromonas gingivalis infection on gut dysbiosis and resultant arthritis exacerbation in mouse model
title_fullStr Effect of Porphyromonas gingivalis infection on gut dysbiosis and resultant arthritis exacerbation in mouse model
title_full_unstemmed Effect of Porphyromonas gingivalis infection on gut dysbiosis and resultant arthritis exacerbation in mouse model
title_sort effect of porphyromonas gingivalis infection on gut dysbiosis and resultant arthritis exacerbation in mouse model
publisher BMC
series Arthritis Research & Therapy
issn 1478-6362
publishDate 2020-10-01
description Abstract Background Porphyromonas gingivalis (Pg) infection causes periodontal disease and exacerbates rheumatoid arthritis (RA). It is reported that inoculation of periodontopathogenic bacteria (i.e., Pg) can alter gut microbiota composition in the animal models. Gut microbiota dysbiosis in human has shown strong associations with systemic diseases, including RA, diabetes mellitus, and inflammatory bowel disease. Therefore, this study investigated dysbiosis-mediated arthritis by Pg oral inoculation in an experimental arthritis model mouse. Methods Pg inoculation in the oral cavity twice a week for 6 weeks was performed to induce periodontitis in SKG mice. Concomitantly, a single intraperitoneal (i.p.) injection of laminarin (LA) was administered to induce experimental arthritis (Pg-LA mouse). Citrullinated protein (CP) and IL-6 levels in serum as well as periodontal, intestinal, and joint tissues were measured by ELISA. Gut microbiota composition was determined by pyrosequencing the 16 s ribosomal RNA genes after DNA purification of mouse feces. Fecal microbiota transplantation (FMT) was performed by transferring Pg-LA-derived feces to normal SKG mice. The effects of Pg peptidylarginine deiminase (PgPAD) on the level of citrullinated proteins and arthritis progression were determined using a PgPAD knockout mutant. Results Periodontal alveolar bone loss and IL-6 in gingival tissue were induced by Pg oral infection, as well as severe joint destruction, increased arthritis scores (AS), and both IL-6 and CP productions in serum, joint, and intestinal tissues. Distribution of Deferribacteres and S24-7 was decreased, while CP was significantly increased in gingiva, joint, and intestinal tissues of Pg-inoculated experimental arthritis mice compared to experimental arthritis mice without Pg inoculation. Further, FMT from Pg-inoculated experimental arthritis mice reproduced donor gut microbiota and resulted in severe joint destruction with increased IL-6 and CP production in joint and intestinal tissues. The average AS of FMT from Pg-inoculated experimental arthritis was much higher than that of donor mouse. However, inoculation of the PgPAD knockout mutant inhibited the elevation of arthritis scores and ACPA level in serum and reduced CP amount in gingival, joint, and intestinal tissues compared to Pg wild-type inoculation. Conclusion Pg oral infection affected gut microbiota dysbiosis and joint destruction via increased CP generation.
topic Porphyromonas gingivalis
Rheumatoid arthritis
Periodontitis
Citrullinated protein
Dysbiosis
url http://link.springer.com/article/10.1186/s13075-020-02348-z
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spelling doaj-deb727fd6e114bc2903d27401e1798542020-11-25T03:33:35ZengBMCArthritis Research & Therapy1478-63622020-10-0122111510.1186/s13075-020-02348-zEffect of Porphyromonas gingivalis infection on gut dysbiosis and resultant arthritis exacerbation in mouse modelYuta Hamamoto0Kazuhisa Ouhara1Syuichi Munenaga2Mikio Shoji3Tatsuhiko Ozawa4Jyunzo Hisatsune5Isamu Kado6Mikihito Kajiya7Shinji Matsuda8Toshihisa Kawai9Noriyoshi Mizuno10Tsuyoshi Fujita11Shintaro Hirata12Kotaro Tanimoto13Koji Nakayama14Hiroyuki Kishi15Eiji Sugiyama16Hidemi Kurihara17Department of Periodontal Medicine, Division of Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima UniversityDepartment of Periodontal Medicine, Division of Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima UniversityDepartment of Periodontal Medicine, Division of Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima UniversityDepartment of Microbiology and Oral Infection, Graduate School of Biomedical Sciences, Nagasaki UniversityDepartment of Immunology, Faculty of Medicine, Academic Assembly, University of ToyamaAntimicrobial Resistance Research Center, National Institute of Infectious Diseases (NIID)Department of Orthodontics and Craniofacial Developmental Biology, Graduate School of Biomedical & Sciences, Hiroshima UniversityDepartment of Periodontal Medicine, Division of Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima UniversityDepartment of Periodontal Medicine, Division of Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima UniversityDepartment of Periodontology, Nova Southeastern University College of Dental MedicineDepartment of Periodontal Medicine, Division of Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima UniversityDepartment of Periodontal Medicine, Division of Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima UniversityDepartment of Clinical Immunology and Rheumatology, Hiroshima University HospitalDepartment of Orthodontics and Craniofacial Developmental Biology, Graduate School of Biomedical & Sciences, Hiroshima UniversityDepartment of Microbiology and Oral Infection, Graduate School of Biomedical Sciences, Nagasaki UniversityDepartment of Immunology, Faculty of Medicine, Academic Assembly, University of ToyamaDepartment of Clinical Immunology and Rheumatology, Hiroshima University HospitalDepartment of Periodontal Medicine, Division of Applied Life Sciences, Institute of Biomedical & Health Sciences, Hiroshima UniversityAbstract Background Porphyromonas gingivalis (Pg) infection causes periodontal disease and exacerbates rheumatoid arthritis (RA). It is reported that inoculation of periodontopathogenic bacteria (i.e., Pg) can alter gut microbiota composition in the animal models. Gut microbiota dysbiosis in human has shown strong associations with systemic diseases, including RA, diabetes mellitus, and inflammatory bowel disease. Therefore, this study investigated dysbiosis-mediated arthritis by Pg oral inoculation in an experimental arthritis model mouse. Methods Pg inoculation in the oral cavity twice a week for 6 weeks was performed to induce periodontitis in SKG mice. Concomitantly, a single intraperitoneal (i.p.) injection of laminarin (LA) was administered to induce experimental arthritis (Pg-LA mouse). Citrullinated protein (CP) and IL-6 levels in serum as well as periodontal, intestinal, and joint tissues were measured by ELISA. Gut microbiota composition was determined by pyrosequencing the 16 s ribosomal RNA genes after DNA purification of mouse feces. Fecal microbiota transplantation (FMT) was performed by transferring Pg-LA-derived feces to normal SKG mice. The effects of Pg peptidylarginine deiminase (PgPAD) on the level of citrullinated proteins and arthritis progression were determined using a PgPAD knockout mutant. Results Periodontal alveolar bone loss and IL-6 in gingival tissue were induced by Pg oral infection, as well as severe joint destruction, increased arthritis scores (AS), and both IL-6 and CP productions in serum, joint, and intestinal tissues. Distribution of Deferribacteres and S24-7 was decreased, while CP was significantly increased in gingiva, joint, and intestinal tissues of Pg-inoculated experimental arthritis mice compared to experimental arthritis mice without Pg inoculation. Further, FMT from Pg-inoculated experimental arthritis mice reproduced donor gut microbiota and resulted in severe joint destruction with increased IL-6 and CP production in joint and intestinal tissues. The average AS of FMT from Pg-inoculated experimental arthritis was much higher than that of donor mouse. However, inoculation of the PgPAD knockout mutant inhibited the elevation of arthritis scores and ACPA level in serum and reduced CP amount in gingival, joint, and intestinal tissues compared to Pg wild-type inoculation. Conclusion Pg oral infection affected gut microbiota dysbiosis and joint destruction via increased CP generation.http://link.springer.com/article/10.1186/s13075-020-02348-zPorphyromonas gingivalisRheumatoid arthritisPeriodontitisCitrullinated proteinDysbiosis