In vitro antimicrobial effect and mechanism of action of plasma-activated liquid on planktonic Neisseria gonorrhoeae

References

• de Korne-Elenbaas J, Pol A, Vet J, et al. Simultaneous detection of Neisseria gonorrhoeae and fluoroquinolone resistance mutations to enable rapid prescription of oral antibiotics. Sex Transm Dis. 2020;47(4):238–242.
   PubMed Web of Science ®Google Scholar
• Quillin SJ, Seifert HS. Neisseria gonorrhoeae host adaptation and pathogenesis. Nat Rev Microbiol. 2018;16(4):226–240.
   PubMed Web of Science ®Google Scholar
• Wang F, Liu J, Liu H, et al. Evaluation of the accuracy of molecular assays targeting the mutation A2059G for detecting high-level azithromycin resistance in Neisseria gonorrhoeae: a systematic review and meta-analysis. Infect Drug Resist. 2018;12:95–104.
   PubMed Web of Science ®Google Scholar
• Cristillo AD, Bristow CC, Torrone E, et al. Antimicrobial resistance in Neisseria gonorrhoeae: proceedings of the STAR sexually transmitted infection-clinical trial group programmatic meeting. Sex Transm Dis. 2019;46(3):e18–e25.
   PubMed Web of Science ®Google Scholar
• Palmer A, Criss AK. Gonococcal defenses against antimicrobial activities of neutrophils. Trends Microbiol. 2018;26(12):1022–1034.
   PubMed Web of Science ®Google Scholar
• Wang L, Yang X, Yang C, et al. The inhibition effect of cold atmospheric plasma-activated media in cutaneous squamous carcinoma cells. Future Oncol. 2019;15(5):495–505.
   PubMed Web of Science ®Google Scholar
• Govaert M, Smet C, Vergauwen L, et al. Influence of plasma characteristics on the efficacy of cold atmospheric plasma (CAP) for inactivation of Listeria monocytogenes and Salmonella Typhimurium biofilms. Innovative Food Sci Emerg Technol. 2019;52:376–386.
   Web of Science ®Google Scholar
• Guo J, Huang K, Wang X, et al. Inactivation of yeast on grapes by plasma-activated water and its effects on quality attributes. J Food Prot. 2017;80(2):225–230.
   PubMed Web of Science ®Google Scholar
• Smet C, Govaert M, Kyrylenko A, et al. Inactivation of single strains of Listeria monocytogenes and Salmonella Typhimurium planktonic cells biofilms with plasma activated liquid. Front Microbiol. 2019;10:1539.
   PubMed Web of Science ®Google Scholar
• Sun P, Wu H, Bai N, et al. Inactivation of Bacillus subtilis spores in water by a direct-current, cold atmospheric-pressure air plasma microjet. Plasma Process Polym. 2012;9(2):157–164.
   Web of Science ®Google Scholar
• Venezia RA, Orrico M, Houston E, et al. Lethal activity of nonthermal plasma sterilization against microorganisms. Infect Control Hosp Epidemiol. 2008;29(5):430–436.
   PubMed Web of Science ®Google Scholar
• Deng S, Ruan R, Mok CK, et al. Inactivation of Escherichia coli on almonds using nonthermal plasma. J Food Sci. 2007;72(2):M62–M66.
   PubMed Web of Science ®Google Scholar
• Xiao D, Cheng C, Jie S, et al. Characteristics of atmospheric-pressure non-thermal N2 and N2/O2 gas mixture plasma jet. J Appl Phys. 2014;115(3):033303.
   Web of Science ®Google Scholar
• Song B, Wang J, Yan Z, et al. Microfluidics for the rapid detection of Staphylococcus aureus using antibody-coated microspheres. Bioengineered. 2020;11(1):1137–1145.
   PubMed Web of Science ®Google Scholar
• O’Brien J, Wilson I, Orton T, et al. Investigation of the Alamar Blue (resazurin) fluorescent dye for the assessment of mammalian cell cytotoxicity. Eur J Biochem. 2000;267(17):5421–5426.
   PubMedGoogle Scholar
• Ruan Z, Guo Y, Gao J, et al. Control of multidrug-resistant planktonic Acinetobacter baumannii: biocidal efficacy study by atmospheric-pressure air plasma. Plasma Sci Technol. 2018;20(6):176–183.
   Web of Science ®Google Scholar
• Shen J, Sun Q, Zhang Z, et al. Characteristics of DC gas-liquid phase atmospheric-pressure plasma and bacteria inactivation mechanism. Plasma Process Polym. 2015;12(3):252–259.
   Web of Science ®Google Scholar
• Xu Z, Cheng C, Shen J, et al. In vitro antimicrobial effects and mechanisms of direct current air-liquid discharge plasma on planktonic Staphylococcus aureus and Escherichia coli in liquids. Bioelectrochemistry. 2018;121:125–134.
   PubMed Web of Science ®Google Scholar
• Duan Q, Jia Y, Qin Y, et al. Narciclasine attenuates LPS-induced acute lung injury in neonatal rats through suppressing inflammation and oxidative stress. Bioengineered. 2020;11(1):801–810.
   PubMed Web of Science ®Google Scholar
• Naïtali M, Kamgang-Youbi G, Herry JM, et al. Combined effects of long-living chemical species during microbial inactivation using atmospheric plasma-treated water. Appl Environ Microbiol. 2010;76(22):7662–7664.
   PubMed Web of Science ®Google Scholar
• Liu J, Yang D, Lin L, et al. Discovery and control of culturable and viable but non-culturable cells of a distinctive Lactobacillus harbinensis strain from spoiled beer. Sci Rep. 2018;8(1):11446.
   PubMedGoogle Scholar
• Joshi SG, Cooper M, Yost A, et al. Nonthermal dielectric-barrier discharge plasma-induced inactivation involves oxidative DNA damage and membrane lipid peroxidation in Escherichia coli. Antimicrob Agents Chemother. 2011;55(3):1053–1062.
   PubMed Web of Science ®Google Scholar
• Yoon SJ, Park JE, Yang JH, et al. OxyR regulon controls lipid peroxidation-mediated oxidative stress in Escherichia coli. J Biochem Mol Biol. 2002;35:297–301.
   PubMedGoogle Scholar
• Lemire JA, Harrison JJ, Turner RJ. Antimicrobial activity of metals: mechanisms, molecular targets and applications. Nat Rev Microbiol. 2013;11:371–384.
   PubMed Web of Science ®Google Scholar
• Liu J, Deng Y, Peters BM, et al. Transcriptomic analysis on the formation of the viable putative non-culturable state of beer-spoilage Lactobacillus acetotolerans. Sci Rep. 2016;6(1):36753.
   PubMedGoogle Scholar
• Liu J, Li L, Peters BM, et al. The viable but nonculturable state induction and genomic analyses of Lactobacillus casei BM-LC14617, a beer-spoilage bacterium. Microbiol Open. 2017;6(5):e00506.
   Google Scholar
• Liu J, Li L, Li B, et al. First study on the formation and resuscitation of viable but nonculturable state and beer spoilage capability of Lactobacillus lindneri. Microb Pathog. 2017;107:219–224.
   PubMed Web of Science ®Google Scholar
• Liu J, Li L, Li B, et al. Study on spoilage capability and VBNC state formation and recovery of Lactobacillus plantarum. Microb Pathog. 2017;110:257–261.
   PubMed Web of Science ®Google Scholar
• Joshi SG, Cooper M, Yost A, et al. Nonthermal dielectric-barrier discharge plasma-induced inactivation involves oxidative DNA damage and membrane lipid peroxidation in Escherichia coli. Antimicrob Agents Chemother. 2011;55(3):1053–1062.
   PubMed Web of Science ®Google Scholar
• Muela A, Seco C, Camafeita E, et al. Changes in Escherichia coli outer membrane subproteome under environmental conditions inducing the viable but nonculturable state. FEMS Microbiol Ecol. 2008;64(1):28–36.
   PubMed Web of Science ®Google Scholar
• Gutteridge JM. Lipid peroxidation and antioxidants as biomarkers of tissue damage. Clin Chem. 1995;41(12 Pt 2):1819–1828.
   PubMed Web of Science ®Google Scholar
• Lefebre M, Valvano M. In Vitro resistance of Burkholderia cepacia complex isolates to reactive oxygen species in relation to catalase and superoxide dismutase production. Reading Microbiology. 2001;1471:97–109.
   PubMedGoogle Scholar
• Zheng M, Wang X, Templeton LJ, et al. DNA microarray-mediated transcriptional profiling of the Escherichia coli response to hydrogen peroxide. J Bacteriol. 2001;183(15):4562–4570.
   PubMed Web of Science ®Google Scholar
• Gong Q, He L, Wang M, et al. Comparison of the TLR4/NFκB and NLRP3 signalling pathways in major organs of the mouse after intravenous injection of lipopolysaccharide. Pharm Biol. 2019;57(1):555–563.
   PubMed Web of Science ®Google Scholar
• Duncan JA, Gao X, Huang MT, et al. Neisseria gonorrhoeae activates the proteinase Cathepsin B to mediate the signaling activities of the NLRP3 and ASC-containing inflammasome. J Immunol. 2009;182(10):6460–6469.
   PubMed Web of Science ®Google Scholar
• Chen J, Zhang F, Yang H, et al. Effect of Neisseria gonorrhoeae infection on the expression of IL-1β and NLRP3 in mononuclear cells. China J Leprosy Skin Dis 2019; 35: 133–135. doi:CNKI:SUN:MALA.0.2019-03-002. ;:. .
   Google Scholar
• Yang X, Yang C, Wang L, et al. Inhibition of basal cell carcinoma cells by cold atmospheric plasma-activated solution and differential gene expression analysis. Int J Oncol. 2020;56(5):1262–1273.
   PubMed Web of Science ®Google Scholar