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Article Publish Status: FREE
Abstract Title:

Diallyl Disulfide From Garlic Oil InhibitsQuorum Sensing Systems and Corresponding Virulence Factors.

Abstract Source:

Front Microbiol. 2018 ;9:3222. Epub 2019 Jan 7. PMID: 30666240

Abstract Author(s):

Wen-Ru Li, Yong-Kai Ma, Xiao-Bao Xie, Qing-Shan Shi, Xia Wen, Ting-Li Sun, Hong Peng

Article Affiliation:

Wen-Ru Li

Abstract:

Previously, we determined that diallyl disulfide (DADS) from garlic oil can inhibitPAO1 pathogenic factors by inactivating the transcription of key genes from three quorum sensing (QS) systems (,, and) based on the effects of DADS on growth, virulence factor production (elastase, pyocyanin, biofilm, and swarming motility), and RNA transcription (real-time q-PCR). To further investigate the mechanisms underlying the inhibition of the threeQS systems by DADS, high-throughput RNA and proteome sequencing techniques were used to study differences in the transcriptional and proteome expression ofPAO1 following treatment with DADS. The RNA-seq and proteomic data are available via NCBI Gene Expression Omnibus database with accession number GSE118801 and ProteomeXchange with identifier PXD011144, respectively. The experimental results indicated that all key genes of the three QS systems (,, and) ofPAO1 as well as the virulence factors (including exoprotease LasA, elastase LasB, lectin LecA and LecB, pyocyanin biosynthesis, and biofilm formation) regulated by these three QS systems were inhibited. This is consistent with our previous studies on the physiology, biochemistry, and RNA expression oftreated with DADS. Additionally, our results also indicated that bacterial motility, chemotaxis, and two-component systems were inhibited by DADS treatment. All these changes abolish the sensitivity ofPAO1 to environmental stimuli and cause the cells to be in a state of passivation. Further research is needed to determine how QS systems regulate these functions. Our findings could potentially contribute to the treatment and control ofinfection, virulence, and pathogenicity.

Study Type : In Vitro Study

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