IPA-3: An Inhibitor of Diadenylate Cyclase of Streptococcus suis with Potent Antimicrobial Activity

• Published in: Antibiotics (Basel) Vol. 11; no. 3; p. 418
• Main Authors: Li, Haotian, Li, Tingting, Zou, Wenjin, Ni, Minghui, Hu, Qiao, Qiu, Xiuxiu, Yao, Zhiming, Fan, Jingyan, Li, Lu, Huang, Qi, Zhou, Rui
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 21.03.2022; MDPI
• Subjects: Antibiotics; antimicrobial; Antimicrobial activity; Antimicrobial agents; Antimicrobial resistance; Bacteria; Binding sites; Biofilms; Chromatography; cyclic diadenylate monophosphate; diadenylate cyclase; Drug resistance; E coli; Enzymatic activity; Gram-positive bacteria; Health risks; High performance liquid chromatography; high-throughput screening; Homeostasis; inhibitor; Inhibitors; IPA-3; Kinases; Liquid chromatography; Meningitis; Molecular docking; Physiology; Proteins; Public health; Screening; Streptococcus infections; Streptococcus suis; Therapeutic targets; Virulence; antimicrobial; diadenylate cyclase; inhibitor; Streptococcus suis; high-throughput screening; IPA-3; cyclic diadenylate monophosphate
• ISSN: 2079-6382; 2079-6382
• DOI: 10.3390/antibiotics11030418

Antimicrobial resistance (AMR) poses a huge threat to public health. The development of novel antibiotics is an effective strategy to tackle AMR. Cyclic diadenylate monophosphate (c-di-AMP) has recently been identified as an essential signal molecule for some important bacterial pathogens involved in various bacterial physiological processes, leading to its synthase diadenylate cyclase becoming an attractive antimicrobial drug target. In this study, based on the enzymatic activity of diadenylate cyclase of Streptococcus suis (ssDacA), we established a high-throughput method of screening for ssDacA inhibitors. Primary screening with a compound library containing 1133 compounds identified IPA-3 (2,2′-dihydroxy-1,1′-dinapthyldisulfide) as an ssDacA inhibitor. High-performance liquid chromatography (HPLC) analysis further indicated that IPA-3 could inhibit the production of c-di-AMP by ssDacA in vitro in a dose-dependent manner. Notably, it was demonstrated that IPA-3 could significantly inhibit the growth of several Gram-positive bacteria which harbor an essential diadenylate cyclase but not E. coli, which is devoid of the enzyme, or Streptococcus mutans, in which the diadenylate cyclase is not essential. Additionally, the binding site in ssDacA for IPA-3 was predicted by molecular docking, and contains residues that are relatively conserved in diadenylate cyclase of Gram-positive bacteria. Collectively, our results illustrate the feasibility of ssDacA as an antimicrobial target and consider IPA-3 as a promising starting point for the development of a novel antibacterial.