TY - JOUR
T1 - Relationship between iga nephropathy and porphyromonas gingivalis; red complex of periodontopathic bacterial species
AU - Nagasawa, Yasuyuki
AU - Nomura, Ryota
AU - Misaki, Taro
AU - Ito, Seigo
AU - Naka, Shuhei
AU - Wato, Kaoruko
AU - Okunaka, Mieko
AU - Watabe, Maiko
AU - Fushimi, Katsuya
AU - Tsuzuki, Kenzo
AU - Matsumoto-Nakano, Michiyo
AU - Nakano, Kazuhiko
N1 - Funding Information:
Funding: This work was supported by JSPS KAKENHI Grant Numbers JP17K09721, JP19K10098, JP20K10225 and 21K08242.
Publisher Copyright:
© 2021 by the authors. Li-censee MDPI, Basel, Switzerland.
PY - 2021/12/1
Y1 - 2021/12/1
N2 - IgA nephropathy (IgAN) has been considered to have a relationship with infection in the tonsil, because IgAN patients often manifest macro hematuria just after tonsillitis. In terms of oral-area infection, the red complex of periodontal bacteria (Porphyromonas gingivalis (P. gingivalis), Trep-onema denticol (T. denticola) and Tannerella forsythia (T. forsythia)) is important, but the relationship between these bacteria and IgAN remains unknown. In this study, the prevalence of the red complex of periodontal bacteria in tonsil was compared between IgAN and tonsillitis patients. The path-ogenicity of IgAN induced by P. gingivalis was confirmed by the mice model treated with this bac-terium. The prevalence of P. gingivalis and T. forsythia in IgAN patients was significantly higher than that in tonsillitis patients (p < 0.001 and p < 0.05, respectively). A total of 92% of tonsillitis patients were free from red complex bacteria, while only 48% of IgAN patients had any of these bacteria. Nasal administration of P. gingivalis in mice caused mesangial proliferation (p < 0.05 at days 28a nd 42; p < 0.01 at days 14 and 56) and IgA deposition (p < 0.001 at day 42 and 56 after administration). Scanning-electron-microscopic observation revealed that a high-density Electron-Dense Deposit was widely distributed in the mesangial region in the mice kidneys treated with P. gingivalis. These findings suggest that P. gingivalis is involved in the pathogenesis of IgAN.
AB - IgA nephropathy (IgAN) has been considered to have a relationship with infection in the tonsil, because IgAN patients often manifest macro hematuria just after tonsillitis. In terms of oral-area infection, the red complex of periodontal bacteria (Porphyromonas gingivalis (P. gingivalis), Trep-onema denticol (T. denticola) and Tannerella forsythia (T. forsythia)) is important, but the relationship between these bacteria and IgAN remains unknown. In this study, the prevalence of the red complex of periodontal bacteria in tonsil was compared between IgAN and tonsillitis patients. The path-ogenicity of IgAN induced by P. gingivalis was confirmed by the mice model treated with this bac-terium. The prevalence of P. gingivalis and T. forsythia in IgAN patients was significantly higher than that in tonsillitis patients (p < 0.001 and p < 0.05, respectively). A total of 92% of tonsillitis patients were free from red complex bacteria, while only 48% of IgAN patients had any of these bacteria. Nasal administration of P. gingivalis in mice caused mesangial proliferation (p < 0.05 at days 28a nd 42; p < 0.01 at days 14 and 56) and IgA deposition (p < 0.001 at day 42 and 56 after administration). Scanning-electron-microscopic observation revealed that a high-density Electron-Dense Deposit was widely distributed in the mesangial region in the mice kidneys treated with P. gingivalis. These findings suggest that P. gingivalis is involved in the pathogenesis of IgAN.
KW - IgA nephropathy
KW - Infection
KW - Mouse
KW - Oral bacteria
KW - Periodontal bacteria
KW - Porphy-romonas gingivalis
KW - Tonsil
UR - http://www.scopus.com/inward/record.url?scp=85120158116&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85120158116&partnerID=8YFLogxK
U2 - 10.3390/ijms222313022
DO - 10.3390/ijms222313022
M3 - Article
C2 - 34884826
AN - SCOPUS:85120158116
SN - 1661-6596
VL - 22
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 23
M1 - 13022
ER -