2019
DOI: 10.3389/fcimb.2019.00062
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The AI-2/luxS Quorum Sensing System Affects the Growth Characteristics, Biofilm Formation, and Virulence of Haemophilus parasuis

Abstract: Haemophilus parasuis (H. parasuis) is a kind of opportunistic pathogen of the upper respiratory tract of piglets. Under certain circumstances, virulent strains can breach the mucosal barrier and enter the bloodstream, causing severe Glässer's disease. Many virulence factors are found to be related to the pathogenicity of H. parasuis strain, but the pathogenic mechanism remains unclear. LuxS/AI-2, as a kind of very important quorum sensing system, affects the growth characteristics, biofilm formation, antibioti… Show more

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Cited by 56 publications
(51 citation statements)
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“…Anginosus , as well as acid resistance and transcription of many virulence genes in Sc. Agalactiae , are also reported to be controlled by AI‐2‐based QS, making QS inhibition an interesting antibacterial strategy (Ma et al., 2017; Wang et al., 2015; Yadav et al., 2018; Zhang et al., 2019; Zhao, Xue, Shang, Sun, & Sun, 2010). Here, we take V. harveyi as a typical example to explain this AI‐2‐based QS system (Martin‐Rodriguez et al, 2015).…”
Section: Bacterial Toxinsmentioning
confidence: 99%
“…Anginosus , as well as acid resistance and transcription of many virulence genes in Sc. Agalactiae , are also reported to be controlled by AI‐2‐based QS, making QS inhibition an interesting antibacterial strategy (Ma et al., 2017; Wang et al., 2015; Yadav et al., 2018; Zhang et al., 2019; Zhao, Xue, Shang, Sun, & Sun, 2010). Here, we take V. harveyi as a typical example to explain this AI‐2‐based QS system (Martin‐Rodriguez et al, 2015).…”
Section: Bacterial Toxinsmentioning
confidence: 99%
“…The UKD fragment obtained in this way was then inserted into a pk18mobsacB plasmid with BamHI and SalI restriction enzymes to generate the recombinant plasmid pk18crp-UKD. The recombinant plasmid was introduced into HPS5 by the nature transformation method as previously described (Zhang et al, 2012b(Zhang et al, , 2019Wang et al, 2013) with some modifications. Briefly, 20 µl of cAMP (8 mM) was added to 20 µl wild-type suspension in logarithmic phase (OD 600 value at 0.9).…”
Section: Construction and Verification Of Crp Mutant Strainmentioning
confidence: 99%
“…Finally, the cells were incubated at 37 • C for 24-48 h. To verify the construction results of the crp mutant, the UKD sequence, kanamycin resistance cassette gene, and crp gene were amplified and then verified by sequencing. The growth characteristics of the wild-type and crp mutant strains were measured (Wang et al, 2017;Zhang et al, 2019). The wild-type and crp mutant strains were cultured in 5 ml fresh T/V/S medium overnight and then diluted with the same medium until the OD 600 value had reached 0.4.…”
Section: Construction and Verification Of Crp Mutant Strainmentioning
confidence: 99%
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