Abstract:Quorum sensing (QS) is a mechanism dependent on bacterial density. This coordinated process is mediated by the synthesis and the secretion of signal molecules, called autoinducers (AIs). N-acyl-homoserine lactones (AHLs) are the most common AIs that are used by Gram-negative bacteria and are involved in biofilm formation. Quorum Quenching (QQ) is the interference of QS by producing hydrolyzing enzymes, among other strategies. The main objective of the present study was to identify QS and QQ strains from MBR wa… Show more
“…Many QS signal molecule-degrading microbes have been found in nature, including Gordonia sp. (Soler et al, 2018), Bacillus sp. (Dong et al, 2002;Lee et al, 2002;Ulrich, 2004;Soler et al, 2018;Bhatt et al, 2020), Streptomyces sp.…”
Section: Discussionmentioning
confidence: 99%
“…(Soler et al, 2018), Bacillus sp. (Dong et al, 2002;Lee et al, 2002;Ulrich, 2004;Soler et al, 2018;Bhatt et al, 2020), Streptomyces sp. (Park et al, 2005;Devaraj et al, 2017), Micromonospora sp.…”
Quorum quenching (QQ) is a promising strategy for preventing and controlling quorum sensing (QS)-mediated bacterial infections. It interferes with QS by the inhibition of signal synthesis, the detection of enzyme-catalyzed degradation, and the modification of signals. N-Acyl homoserine lactones (AHLs) represent a family of widely conserved QS signals involved in the regulation of virulence factor production in many Gram-negative bacterial pathogens. In this study, AHL-degrading bacterial strains were isolated, and the most efficient one was evaluated for its potential against QS-mediated pathogens. Results showed that an AHL-degrading bacteria Ochrobactrum intermedium D-2 effectively attenuated maceration produced by the pathogen Pectobacterium carotovorum subsp. carotovorum (Pcc) on radish and potato slices. Strain D-2 exhibited a superior AHL degradation activity and efficiently degraded various AHLs, including N-hexanoyl-L-homoserine lactone (C6HSL), N-(3-oxohexanoyl)-L-homoserine lactone (3OC6HSL), N-(3-oxooctanoyl)-L-homoserine lactone (3OC8HSL), and N-(3-oxododecanoyl)-L-homoserine lactone (3OC12HSL). Analysis of the degradation products of AHL by gas chromatography-mass spectrometry led to the identification of N-cyclohexyl-propanamide and propanamide as the main intermediate products, suggesting that AHL was degraded by hydrolysis. Annotation and analysis of the whole genome sequence of strain D-2 revealed the presence of an AHL-lactonase, termed AidF. Moreover, the application of strain D-2 was able to substantially reduce the disease severity caused by Pcc on host plants. These results reveal the biochemical basis of a highly efficient AHL-degrading bacterial isolate and present the potential to attenuate Pcc virulence through QQ.
“…Many QS signal molecule-degrading microbes have been found in nature, including Gordonia sp. (Soler et al, 2018), Bacillus sp. (Dong et al, 2002;Lee et al, 2002;Ulrich, 2004;Soler et al, 2018;Bhatt et al, 2020), Streptomyces sp.…”
Section: Discussionmentioning
confidence: 99%
“…(Soler et al, 2018), Bacillus sp. (Dong et al, 2002;Lee et al, 2002;Ulrich, 2004;Soler et al, 2018;Bhatt et al, 2020), Streptomyces sp. (Park et al, 2005;Devaraj et al, 2017), Micromonospora sp.…”
Quorum quenching (QQ) is a promising strategy for preventing and controlling quorum sensing (QS)-mediated bacterial infections. It interferes with QS by the inhibition of signal synthesis, the detection of enzyme-catalyzed degradation, and the modification of signals. N-Acyl homoserine lactones (AHLs) represent a family of widely conserved QS signals involved in the regulation of virulence factor production in many Gram-negative bacterial pathogens. In this study, AHL-degrading bacterial strains were isolated, and the most efficient one was evaluated for its potential against QS-mediated pathogens. Results showed that an AHL-degrading bacteria Ochrobactrum intermedium D-2 effectively attenuated maceration produced by the pathogen Pectobacterium carotovorum subsp. carotovorum (Pcc) on radish and potato slices. Strain D-2 exhibited a superior AHL degradation activity and efficiently degraded various AHLs, including N-hexanoyl-L-homoserine lactone (C6HSL), N-(3-oxohexanoyl)-L-homoserine lactone (3OC6HSL), N-(3-oxooctanoyl)-L-homoserine lactone (3OC8HSL), and N-(3-oxododecanoyl)-L-homoserine lactone (3OC12HSL). Analysis of the degradation products of AHL by gas chromatography-mass spectrometry led to the identification of N-cyclohexyl-propanamide and propanamide as the main intermediate products, suggesting that AHL was degraded by hydrolysis. Annotation and analysis of the whole genome sequence of strain D-2 revealed the presence of an AHL-lactonase, termed AidF. Moreover, the application of strain D-2 was able to substantially reduce the disease severity caused by Pcc on host plants. These results reveal the biochemical basis of a highly efficient AHL-degrading bacterial isolate and present the potential to attenuate Pcc virulence through QQ.
“…Since QQ strategies do not interfere directly with bacterial growth, the probabilities of inducing tolerance or resistance against these mechanisms are lower 37,38 . Previous studies have already reported the successful approach of using QS inhibitors to control different types of bacterial biofilms 35,[39][40][41][42] . Therefore, the confirmation of a possible role of AHL-type QS signals in dental plaque formation would open new perspectives in the prevention and treatment of oral diseases.…”
Acyl homoserine lactones (AHLs), the quorum sensing (QS) signals produced by Gram-negative bacteria, are currently considered to play a minor role in the development of oral biofilm since their production by oral pathogens has not been ascertained thus far. However, we report the presence of AHLs in different oral samples and their production by the oral pathogen Porphyromonas gingivalis. the importance of AHLs is further supported by a very high prevalence of AHL-degradation capability, up to 60%, among bacteria isolated from dental plaque and saliva samples. Furthermore, the widespectrum AHL-lactonase Aii20J significantly inhibited oral biofilm formation in different in vitro biofilm models and caused important changes in bacterial composition. Besides, the inhibitory effect of Aii20J on a mixed biofilm of 6 oral pathogens was verified using confocal microscopy. Much more research is needed in order to be able to associate specific AHLs with oral pathologies and to individuate the key actors in AHL-mediated QS processes in dental plaque formation. However, these results indicate a higher relevance of the AHLs in the oral cavity than generally accepted thus far and suggest the potential use of inhibitory strategies against these signals for the prevention and treatment of oral diseases.
“…Over the last years, interfering with QS bacterial communication systems has been proposed as a promising mechanism to prevent the development of different types of bacterial biofilms [ 11 , 12 , 13 , 14 , 15 ]. Commonly, the term “quorum quenching” (QQ) refers to the enzymatic inactivation of QS processes [ 16 ], while the more general term “quorum sensing inhibition” (QSI) is preferred to describe the chemical disruption of the cell-to-cell communication system caused by QS inhibitory compounds [ 17 ].…”
Section: Introductionmentioning
confidence: 99%
“…Using QQ enzymes that can degrade the AHLs produced by Gram-negative bacteria has been suggested as a novel anti-biofouling strategy [ 25 , 26 , 27 ], and a few studies have evaluated the effect of QQ enzymes on the ecology of multispecies biofilms [ 14 , 28 , 29 , 30 ]. QQ strategies have been successfully applied to control biofouling in membrane bioreactors (MBRs) for wastewater treatment [ 11 , 15 ] and to reduce biocorrosion [ 28 ], as they are associated with deep changes in the microfouling community [ 28 ]. This effect could be observed even in in vitro oral biofilm models dominated by Gram-positive species [ 14 ].…”
Interfering with the quorum sensing bacterial communication systems has been proposed as a promising strategy to control bacterial biofilm formation, a key process in biofouling development. Appropriate in vitro biofilm-forming bacteria models are needed to establish screening methods for innovative anti-biofilm and anti-microfouling compounds. Four marine strains, two Pseudoalteromonas spp. and two Vibrio spp., were selected and studied with regard to their biofilm-forming capacity and sensitivity to quorum sensing (QS) inhibitors. Biofilm experiments were performed using two biofilm cultivation and quantification methods: the xCELLigence® system, which allows online monitoring of biofilm formation, and the active attachment model, which allows refreshment of the culture medium to obtain a strong biofilm that can be quantified with standard staining methods. Although all selected strains produced acyl-homoserine-lactone (AHL) QS signals, only the P. flavipulchra biofilm, measured with both quantification systems, was significantly reduced with the addition of the AHL-lactonase Aii20J without a significant effect on planktonic growth. Two-species biofilms containing P. flavipulchra were also affected by the addition of Aii20J, indicating an influence on the target bacterial strain as well as an indirect effect on the co-cultured bacterium. The use of xCELLigence® is proposed as a time-saving method to quantify biofilm formation and search for eco-friendly anti-microfouling compounds based on quorum sensing inhibition (QSI) strategies. The results obtained from these two in vitro biofilm formation methods revealed important differences in the response of biosensor bacteria to culture medium and conditions, indicating that several strains should be used simultaneously for screening purposes and the cultivation conditions should be carefully optimized for each specific purpose.
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