Identification of nanaomycin A and its analogs by a newly established screening method for functional inhibitors of the type IX secretion system in Porphyromonas gingivalis

被引:0
作者
Sasaki, Yuko [1 ]
Matsuo, Takehiro [1 ]
Watanabe, Yoshihiro [2 ]
Iwatsuki, Masato [2 ]
Inahashi, Yuki [2 ]
Nishida, Satoshi [3 ]
Naito, Mariko [1 ]
Shoji, Mikio [1 ]
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Dept Microbiol & Oral Infect, 1-7-1 Sakamoto, Nagasaki, Nagasaki 8528588, Japan
[2] Kitasato Univ, Omura Satoshi Mem Inst, 5-9-1 Shirokane,Minato Ku, Tokyo 1088641, Japan
[3] Teikyo Univ, Dept Microbiol & Immunol, Sch Med, 2-11-1 Kaga,Itabashi Ku, Tokyo 1738605, Japan
关键词
GLIDING MOTILITY; PROTEIN; GROWTH; STREPTOMYCES; MEMBRANE; STRAIN; MODE;
D O I
10.1038/s41429-024-00790-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Porphyromonas gingivalis, a Gram-negative anaerobic bacterium, is a key pathogen in chronic periodontitis. P. gingivalis has a type IX secretion system (T9SS) that secretes highly hydrolytic proteinases called gingipains for obtaining peptides as an energy source. Although most T9SS-related proteins have been identified, no specific inhibitor of T9SS has been reported. To screen T9SS inhibitors, we focused on and characterized a minimal liquid medium called mC medium that contains milk casein as the sole protein source. We found that P. gingivalis wild-type strain ATCC 33277 caused cloudiness of mC medium without growth. In mC medium, an alkylating agent, iodoacetamide (IAM) that is an inhibitor of gingipains, and a protonophore, carbonyl cyanide 3-chlorophenylhydrazone (CCCP) that dissipates the proton motive force required for T9SS-mediated secretion, clearly inhibited the increase in turbidity. Moreover, neither the gingipain-null mutant nor the T9SS-deficient mutant caused mC medium cloudiness, suggesting that mC medium cloudiness is dependent on gingipain activity and T9SS. These results indicated that mC medium can be used to assess P. gingivalis gingipain activity and its functional T9SS. Using an assay system with mC medium, we discovered that OM-173 alpha A and OM-173 beta A in the & Omacr;mura Natural Compound Library and nanaomycin A were probable T9SS inhibitors. The compounds need to be further investigated as tools for analyzing T9SS and as potential therapeutic agents for periodontal disease.
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页码:90 / 105
页数:16
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