Table 5.
Summary of the quorum-sensing inhibition methods employed against the ESKAPE organisms and their impact on pathogenicity.
Organism name | Method of disruption of quorum-sensing mechanism | Further details | Targeted quorum sensing system | Major parameters analyzed | Observations | References |
---|---|---|---|---|---|---|
Enterococcus sp. | Gene knockout | Long flanking homology (LFH) PCR was used to generate deletion mutants | LuxS/AI-2 | Proliferation ability after deletion | No significant effect | (Yang et al., 2018) |
Biofilm-forming ability | Decreased | |||||
Chemical inhibitor | Siamycin I | fsr system | Growth of the microbe | Decreased | (Nakayama et al., 2007) | |
Gelatinase activity | Decreased | |||||
GBAP production | Decreased | |||||
Biofilm-forming ability | Decreased | |||||
Staphylococcus aureus | Gene knockout and chemical inhibitor | RIP | agr system | Biofilm-forming ability | Decreased | (Balaban et al., 2007) |
Klebsiella pneumoniae | Chemical Inhibitor | 2′-Hydroxycinnamic acid and 3-methyl-2(5H)-furanone | C6-AHL system | Biofilm-forming ability | Decreased | (Cadavid and Echeverri, 2019) |
Adherence | Decreased | |||||
Gene knockout | “Gene Gorging” method followed by allelic replacement with a kanamycin resistance-encoding gene (Km) was used to generate deletion mutants | LuxS/AI-2 system | Biofilm-forming ability | Decreased | (Chen L et al., 2020) | |
Ability to synthesize lipopolysaccharide (wzm) | Decreased | |||||
Ability to synthesize polysaccharide (pgaA), which is involved in the synthesis of porin | Increased | |||||
Ability to synthesize type 3 fimbriae (mrkA) | No significant effect | |||||
Acinetobacter baumannii | Chemical Inhibitor | Chloroquine, Levamisole, Propranolol, Erythromycin, and Azithromycin | Aba1/AbaR system | Biofilm-forming ability | Decreased | (Seleem et al., 2020) |
Twitching and swarming motilities | Decreased | |||||
Ability to produce proteolytic enzymes | Decreased | |||||
Resistance to oxidative stress | Decreased | |||||
Gene knockout | Cloned plasmid pMo130v was used to generate ΔabaI deletion mutants encompassing regions of the A1S_0109 gene | Aba1/AbaR system | Biofilm-forming ability | Decreased | (Mayer et al., 2020) | |
Surface associated motility | Decreased | |||||
Pseudomonas aeruginosa | Chemical inhibitor | Catechin-7-xyloside (C7X), sappanol and butein | LasR system | Biofilm-forming ability | Decreased | (Zhong et al., 2020) |
Ability to generate pyocyanin | Decreased | |||||
Ability to generate rhamnolipids | Decreased | |||||
Ability to generate elastin | Decreased | |||||
Gene knockout and Chemical Inhibitor | Quercetin | LasI system | Biofilm-forming ability | Decreased | (Ouyang et al., 2020) | |
Adhesion | Decreased | |||||
Swarming motility | Decreased | |||||
RhlI system | Biofilm-forming ability | No direct effect | ||||
LasI/RhlI system | Biofilm-forming ability | Decreased | ||||
Adhesion | Decreased | |||||
Swarming motility | Decreased | |||||
Enterobacter sp. | – | – | – | – | – | – |
"-" denotes insufficient information.