Potential involvement of Streptococcus mutans possessing collagen binding protein Cnm in infective endocarditis

Ryota Nomura, Masatoshi Otsugu, Masakazu Hamada, Saaya Matayoshi, Noboru Teramoto, Naoki Iwashita, Shuhei Naka, Michiyo Matsumoto-Nakano, Kazuhiko Nakano

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

Streptococcus mutans, a significant contributor to dental caries, is occasionally isolated from the blood of patients with infective endocarditis. We previously showed that S. mutans strains expressing collagen-binding protein (Cnm) are present in the oral cavity of approximately 10–20% of humans and that they can effectively invade human umbilical vein endothelial cells (HUVECs). Here, we investigated the potential molecular mechanisms of HUVEC invasion by Cnm-positive S. mutans. The ability of Cnm-positive S. mutans to invade HUVECs was significantly increased by the presence of serum, purified type IV collagen, and fibrinogen (p < 0.001). Microarray analyses of HUVECs infected by Cnm-positive or -negative S. mutans strains identified several transcripts that were differentially upregulated during invasion, including those encoding the small G protein regulatory proteins ARHGEF38 and ARHGAP9. Upregulation of these proteins occurred during invasion only in the presence of serum. Knockdown of ARHGEF38 strongly reduced HUVEC invasion by Cnm-positive S. mutans. In a rat model of infective endocarditis, cardiac endothelial cell damage was more prominent following infection with a Cnm-positive strain compared with a Cnm-negative strain. These results suggest that the type IV collagen–Cnm–ARHGEF38 pathway may play a crucial role in the pathogenesis of infective endocarditis.

Original languageEnglish
Article number19118
JournalScientific reports
Volume10
Issue number1
DOIs
Publication statusPublished - Dec 1 2020

ASJC Scopus subject areas

  • General

Fingerprint Dive into the research topics of 'Potential involvement of Streptococcus mutans possessing collagen binding protein Cnm in infective endocarditis'. Together they form a unique fingerprint.

Cite this