Table 1.
Elucidated mechanisms and targets of QSI in AHL-mediated QS systems.
| QS inhibitor | Mode of action | Inhibition target: protein, AHL or bacteria | Reference |
|---|---|---|---|
| Sinefungin, butyryl-SAM and MTA | AHL synthesis inhibition | RhlI protein of P. aeruginosa. | [75] |
| Compound J8-C8 | AHL synthesis inhibition | TofI protein of B. glumae. | [76] |
| Tannic acid; trans-cinnamaldehyde | AHL synthesis inhibition | RhlI protein of P. aeruginosa. | [77] |
| Triclosan | AHL synthesis inhibition | Enoyl-ACP reductase (FabI) of P. aeruginosa. | [74] |
| Antibiotic amikacin | AHL synthesis inhibition | CviI of C. violaceum. | [78] |
| Thioether compound JKR-1 | AHL synthesis inhibition | CepI of B. cenocepecia. | [73] |
| Lactonase AiiA from Bacillus sp. Strain 240B1 | QQ enzyme/AHL inactivation | AHLs from Erwinia carotovora. | [84] |
| Lactonase AhlS from Solibacillus silvestris | QQ enzyme/AHL inactivation | C10-HSL. | [97] |
| Lactonase PPH from Mycobacterium tuberculosis | QQ enzyme/AHL inactivation | AHLs secreted by E. amylovora (C6-oxo-HSL). | [85] |
| Enzyme moLRP (marine-originated lactonase-related protein) | QQ enzyme/AHL inactivation | Low- to medium-chain AHLs, like C4-HSL and C6-oxo-HSL. | [82] |
| Penicillin acylase from Streptomyces lavendulae | QQ enzyme/AHL degradation | Long-chain AHLs, mainly C10-HSL, C12-HSL and C14-HSL. | [98] |
| Acylase from Actinoplanes utahensis | QQ enzyme/AHL degradation | Long-chain AHLs, mainly C8-HSL, C10-HSL, and C12-HSL. | [98] |
| Acylase APTM01 from Pseudoalteromonas tetraodonis | QQ enzyme/AHL degradation | Long-chain AHLs, mainly C10-HSL, C12-HSL and 3-oxo-C12-HSL. | [86] |
| Antibodies RS2-1G9 | AHL sequestration | Inhibition of 3-oxo-C12-HSL of P. aeruginosa. | [87] |
| Analogs of 3-oxo-C12-HSL | Inhibition of response regulator | TraR protein of Agrobacterium tumefaciens. | [88] |
| Halogenated furanones | Inhibition of response regulator | Destabilization of LuxR. | [91,99] |
| Furanones | Inhibition of response regulator | Destabilizing LasR of P. aeruginosa, promoting its degradation. | [95] |
| Chlorolactone compound | Inhibition of response regulator | Competition with C6-HSL for binding site of CviR from C. violaceum. | [96] |