Abstract:Abstract Bacterial biofilm is the leading cause of bacterial drug resistance increases. Staphylococcus epidermidis is an opportunistic pathogen, once it formed the biofilm, it will adhere to the surfaces of medical device and make the diseases recurrent and difficult to cure. Quorum sensing system has been recently regarded as the research target to suppress the bacterial biofilm formation. S-ribosyl homocysteine lyase (LuxS) is the key enzyme for the synthesis of autoinducer-2 (AI-2), they constitute the AI-2/LuxS quorum sensing system in bacteria. In this study, the biofilm formed in the early stage was chosen as the experiment subject, then antisense locked nucleic acid (LNA) technology was used to block the expression of LuxS gene in S. epidermidis AI-2/LuxS quorum sensing system, the inhibitory effect of 2 antisense locked oligonucleotides named LNA81 and LNA352 was compared by the transcription level of LuxS gene, Using real-time PCR measured the relative expression quantity of biofilm formation related genes, including sigma factor B (sigB), intercellular adhesion AB (icaAB), staphylococal accessory regulator A (sarA), accumulation-associated protein (aap), fibrinogen-binding protein (fbe) and autolysin E (atlE). AI-2 signaling molecule activity was measured by Vibrio harveyi bioluminescence assay, and the formation and characteristic parameters of biofilm were analyzed by confocal laser scanning microscope (CLSM) and image structure analyzer (ISA) software. Results showed that between the 2 antisense locked oligonucleotides, LNA81 and LNA352, 100 nmol/L LNA81 mixed with 2.5 μL RNAiMAX transfection reagent exhibited better inhibition in expression of LuxS through targeting LuxS mRNA, it could get a 43% inhibition ratio in LuxS transcription at 6 h. When the transcription of LuxS was inhibited partially, the transcript level of gene sigB and icaAB increased, sarA, aap, fbe and atlE decreased. The activity of AI-2 signaling molecule was decreased in 9 h compared to control group, at the time of 6 h its activity got a minimum, and after 9 h its activity was closed to the control group, this tendency was consistent with the transcript level of gene LuxS which was inhibited to a minimum at 6 h and its inhibition ratio became unsteady after 6 h. Finally, the ability of biofilm formation was decreased, the structure of biofilm was more simple than control group. This study is focus on the regulating effect of AI-2/LuxS quorum sensing system on the early biofilm formation, antisense strategy was used to target LuxS mRNA, which is the critical gene for the formation of AI-2, it not only has the ablity of quorum sensing system but also plays an important role in sulfur metabolism and glycometabolism in bacteria. It can be seen that AI-2 signaling molecule activity and expression of genes involved in biofilm formation were affected when the LuxS gene expression was partial blocked. The biofilm formation is a dynamic process, it is affected by various factors, the changes of above factors were finally resulting in inhibition of the biofilm formation. These results will provide a theoretical basis for the further study on AI-2/LuxS quorum sensing system and its regulatory effects on the biofilm formation in S. epidermidis, they also can provide more potential targets and therapeutic schedule to prevent S. epidermidis infection.
[1]Castelani L, Santos AFS, Miranda MD, et al.2013.Molecular Typing of Mastitis-Causing Staphylococcus aureus Isolated from Heifers and Cows[J].International Journal of Molecular Sciences, 14(2):4326-4333.[2]Lasarre B, Federle MJ.2013.Exploiting quorum sensing to confuse bacterial pathogens[J].Microbiology and Molecular Biology Reviews, 77(1):73-111.[3]夏培元, 史惠卿.2013.AI-2 群体感应系统抑制剂:细菌生物膜感染的潜在新药[J].第三军医大学学报, 35(23):2502-2507.(Xia P Y, Shi H Q.2013.AI-2 quorum sensing inhibitors:potential drug to bacterial biofilm infections[J].Journal of Third Military Medical University, 35(23):2502-2507.)[4]Li YH, Tian XL.2012.Quorum sensing and bacterial social interactions in biofilms [J]. Sensors, 12(3): 2519-2538.[5]Vidal JE, Ludewick HP, Kunkel RM, et al.2011.The LuxS-dependent quorum-sensing system regulates early biofilm formation by Streptococcus pneumoniae strain D39[J].?Infection and Immunity, 79(10): 4050-4060.[6]Ren D, Bedzyk LA, Ye RW, et al.2004.Differential gene expression shows natural brominated furanones interfere with the autoinducer-2 bacterial signaling system of Escherichia coli[J].Biotechnology and Bioengineering, 88(5): 630-642.[7]He Z, ?Liang J, ?Tang Z, ?et al.2015.Role of the?luxS?gene in initial biofilm formation by Streptococcus mutans[J].Journal of Molecular?Microbiology and?Biotechnology, 25(1):60-68.[8]陈伟.2011.细菌QS系统LuxS功能研究进展[J].中国兽医学报, 31(7):1083-1088.(Chen W.2011.Current status on function of bacterial LuxS in quorum sensing system-A[J].Chinese Journal of Veterinary Science, 31(7):1083-1088.)[9]任志明.2010.LuxS 基因在细菌代谢组学中的相关功能研究进展[J].国际口腔医学杂志, 37(6):664-667.(Ren Z M.2010.Research progress of LuxS gene related function on the bacterial metabonomics[J].International Journal of Stomatolpgy, 37(6):664-667.)[10]Tamura K, Stecher G, Peterson D, et al.2013.MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0[J].?Molecular Biology and Evolution, 30:2725-2729.?[11]达飞,侯征, 孟静茹, 等.2013.反义锁核酸阻断耐甲氧西林金黄色葡萄球菌agr 群体感应系统[J].中国生物工程杂志, 33(5):1- 6.(Da F, Hou Z, Meng J R, et al.2013. Blocking methicilli-resistant Streptococcus Aureus Agr quorum sensing system by antisense LNA[J].China Biotechnology, 33(5):1- 6.)[12]胡建娥, 夏云.2011.肽核酸体外抑制铜绿假单胞菌 PAO1生物膜形成的研究[J].第三军医大学学报, 33(3):294-298.(Hu J E, Xia Y.2011.Inhibitory effect of peptide nucleic acid on biofilm formation of Pseudomonas aeruginosa PAO1 in Vitro[J].Journal of Third Military Medical University, 33(3):294-298.)[13]李朋莲, 张志民, 李振玲, 等.2015.siRNA干扰对变形链球菌耐氟菌ffh基因产酸能力的影响[J].口腔医学研究, 31(2):105-108.(Li P L, Zhang Z M, Li Z L, et al.2015.Effect of siRNA interference on the acidogenicity for gene ffh of fluoride resistant Streptococcus mutans[J].Journal of Oral Science Research, 31(2):105-108.)[14]邵圣文, 张智志, 顾红光, 等.2009.RNA干扰铜绿假单胞菌群体感应系统对生物膜影响的研究[J].中国抗生素杂志, 34(3):184-188.(Shao S W, Zhang Z Z, Gu H G, et al.2009.The effect of small interfering RNA against quorum sensing system of Pseudomonas aeruginosa on the biofilm[J].Chinese Journal of Antibiotics, 34(3):184-188.)[15]高山峨, 范长胜, 苑兴卉, 等.2006.表皮葡萄球菌SigB基因调控生物膜合成的研究[J].复旦学报(自然科学版), 45(6):779-790.(Gao S E, Fan C S, Yuan X H, et al.2006. SigB effects on biofilm formation in Staphylococcus epidermidis[J].Journal of FuDan University(Natural Science), 45(6):779-790.)[16]欧元祝, 朱于莉, 陈洁敏, 等.2006.表皮葡萄球菌AtlE蛋白介导生物膜起始黏附的相关机制[J].复旦学报(医学版), 33(5):569-573.(OU Y Z, Zhu Y L, Chen J M, et al.2006.The mechanism of Staphylococcus epidermidis AtlE protein mediating primary attachment of biofilm formation[J].FuDan University Journal of Medical Science, 33(5):569-573.)[17]Pei L, Palma M, Nilsson M, et al.1999.Functional studies of a fibrinogen binding protein from Staphylococcus epidermidis[J].Infection and Immunity, 67(9):4525-4530.[18]李燕, 李冬冬, 陶传敏, 等.2010.表皮葡萄球菌生物被膜相关基因的检测及评价[J].中华医院感染学杂志, 20(4):473-477.(Li Y, Li D D, Tao C M, et al.2010.Detection and evaluation for biofilm formation of Staphylococcus epidermidis and related genes[J].Chinese Journal of Nosocomiology, 20(4):473-477.)[19]Xu L, Li HL, Vuong C, et al.2006.Role of the luxS Quorum-Sensing System in Biofilm Formation and Virulence of Staphylococcus epidermidis[J].Infection and Immunity, 74(1):488-496.