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.

IF 2.1 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Journal of Antibiotics Pub Date : 2024-11-22 DOI:10.1038/s41429-024-00790-8
Yuko Sasaki, Takehiro Matsuo, Yoshihiro Watanabe, Masato Iwatsuki, Yuki Inahashi, Satoshi Nishida, Mariko Naito, Mikio Shoji
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Abstract

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-173αA and OM-173βA in the Ōmura 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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通过新建立的牙龈卟啉单胞菌 IX 型分泌系统功能抑制剂筛选方法鉴定纳诺霉素 A 及其类似物。
牙龈卟啉单胞菌是一种革兰氏阴性厌氧菌,是慢性牙周炎的主要病原体。牙龈卟啉单胞菌有一种 IX 型分泌系统(T9SS),能分泌称为龈肽酶的高度水解蛋白酶,以获取肽作为能量来源。虽然大多数与 T9SS 相关的蛋白已经被鉴定出来,但还没有关于 T9SS 特异性抑制剂的报道。为了筛选 T9SS 抑制剂,我们重点研究并鉴定了一种称为 mC 培养基的最小液体培养基,这种培养基含有牛奶酪蛋白作为唯一的蛋白质来源。我们发现,牙龈脓胞野生型菌株 ATCC 33277 会导致 mC 培养基浑浊而不生长。在 mC 培养基中,一种烷化剂--碘乙酰胺(IAM)(gingipains 的抑制剂)和一种质子源--羰基氰化物 3-氯苯腙(CCCP)(CCCP 可耗散 T9SS 介导的分泌所需的质子动力)可明显抑制浊度的增加。此外,gingipain 缺失突变体和 T9SS 缺失突变体都不会导致 mC 培养基浑浊,这表明 mC 培养基浑浊取决于gingipain 活性和 T9SS。这些结果表明,mC培养基可用于评估牙龈鞘氨醇活性及其功能性T9SS。利用 mC 培养基检测系统,我们发现Ōmura 天然化合物库中的 OM-173αA 和 OM-173βA 以及纳诺霉素 A 可能是 T9SS 抑制剂。这些化合物作为分析 T9SS 的工具和治疗牙周病的潜在药物,还需要进一步研究。
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来源期刊
Journal of Antibiotics
Journal of Antibiotics 医学-免疫学
CiteScore
6.60
自引率
3.00%
发文量
87
审稿时长
1 months
期刊介绍: The Journal of Antibiotics seeks to promote research on antibiotics and related types of biologically active substances and publishes Articles, Review Articles, Brief Communication, Correspondence and other specially commissioned reports. The Journal of Antibiotics accepts papers on biochemical, chemical, microbiological and pharmacological studies. However, studies regarding human therapy do not fall under the journal’s scope. Contributions regarding recently discovered antibiotics and biologically active microbial products are particularly encouraged. Topics of particular interest within the journal''s scope include, but are not limited to, those listed below: Discovery of new antibiotics and related types of biologically active substances Production, isolation, characterization, structural elucidation, chemical synthesis and derivatization, biological activities, mechanisms of action, and structure-activity relationships of antibiotics and related types of biologically active substances Biosynthesis, bioconversion, taxonomy and genetic studies on producing microorganisms, as well as improvement of production of antibiotics and related types of biologically active substances Novel physical, chemical, biochemical, microbiological or pharmacological methods for detection, assay, determination, structural elucidation and evaluation of antibiotics and related types of biologically active substances Newly found properties, mechanisms of action and resistance-development of antibiotics and related types of biologically active substances.
期刊最新文献
Acknowledgments 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. Celludinone C, a new dihydroisobenzofuran isolated from Talaromyces cellulolyticus BF-0307. Discovery of new AMR drugs targeting modulators of antimicrobial activity using in vivo silkworm screening systems. Structure-activity relationship studies of ME1111, a novel antifungal agent for topical treatment of onychomycosis.
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