<i>Porphyromonas gingivalis</i> Components/Secretions Synergistically Enhance Pneumonia Caused by <i>Streptococcus pneumoniae</i> in Mice

<i>Streptococcus pneumoniae</i> is an important causative organism of respiratory tract infections. Although periodontal bacteria have been shown to influence respiratory infections such as aspiration pneumonia, the synergistic effect of <i>S. pneumoniae</i> and <i>Porp...

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Main Authors: Teppei Okabe, Yosuke Kamiya, Takeshi Kikuchi, Hisashi Goto, Masayuki Umemura, Yuki Suzuki, Yoshihiko Sugita, Yoshikazu Naiki, Yoshiaki Hasegawa, Jun-ichiro Hayashi, Shotaro Kawamura, Noritaka Sawada, Yuhei Takayanagi, Takeki Fujimura, Naoya Higuchi, Akio Mitani
Format: Article
Language:English
Published: MDPI AG 2021-11-01
Series:International Journal of Molecular Sciences
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Online Access:https://www.mdpi.com/1422-0067/22/23/12704
Description
Summary:<i>Streptococcus pneumoniae</i> is an important causative organism of respiratory tract infections. Although periodontal bacteria have been shown to influence respiratory infections such as aspiration pneumonia, the synergistic effect of <i>S. pneumoniae</i> and <i>Porphyromonas gingivalis</i>, a periodontopathic bacterium, on pneumococcal infections is unclear. To investigate whether <i>P. gingivalis</i> accelerates pneumococcal infections, we tested the effects of inoculating <i>P. gingivalis</i> culture supernatant (PgSup) into <i>S. pneumoniae</i>-infected mice. Mice were intratracheally injected with <i>S. pneumoniae</i> and PgSup to induce pneumonia, and lung histopathological sections and the absolute number and frequency of neutrophils and macrophages in the lung were analyzed. Proinflammatory cytokine/chemokine expression was examined by qPCR and ELISA. Inflammatory cell infiltration was observed in <i>S. pneumoniae</i>-infected mice and <i>S. pnemoniae</i> and PgSup mixed-infected mice, and mixed-infected mice showed more pronounced inflammation in lung. The ratios of monocytes/macrophages and neutrophils were not significantly different between the lungs of <i>S. pneumoniae</i>-infected mice and those of mixed-infected mice. PgSup synergistically increased TNF-α expression/production and IL-17 production compared with <i>S. pneumoniae</i> infection alone. We demonstrated that PgSup enhanced inflammation in pneumonia caused by <i>S. pneumoniae</i>, suggesting that virulence factors produced by <i>P. gingivalis</i> are involved in the exacerbation of respiratory tract infections such as aspiration pneumonia.
ISSN:1661-6596
1422-0067