您的位置:山东大学 -> 科技期刊社 -> 《山东大学学报(医学版)》

山东大学学报 (医学版) ›› 2018, Vol. 56 ›› Issue (7): 28-32.doi: 10.6040/j.issn.1671-7554.0.2018.013

• • 上一篇    

人参皂苷对金黄色葡萄球菌生物被膜形成的影响

安继红1,吕维玲1,张永州1,韩姗姗1,刘强2   

  1. 河南大学淮河医院 1.临床药学室;2. 检验科, 河南 开封 475000
  • 发布日期:2022-09-27
  • 通讯作者: 安继红. E-mail:phm416@126.com
  • 基金资助:
    河南省高等学校重点科研项目(17A310001)

Effects of ginsenosides on the biofilm formation of Staphylococcus aureus

AN Jihong1, L(¨overU)Weiling1, ZHANG Yongzhou1, HAN Shanshan1, LIU Qiang2   

  1. 1. Clinical Pharmacy;
    2. Clinical Laboratory, Huaihe Hospital of Henan University, Kaifeng 475000, Henan, China
  • Published:2022-09-27

摘要: 目的 探讨人参皂苷Rh2单体对金黄色葡萄球菌(S.aureus)生物被膜形成的影响。 方法 通过96孔细胞培养板构建S.aureus生物被膜,探讨Rh2对生物被膜形成的影响;通过RNA提取及实时荧光定量PCR检测,探讨Rh2对S.aureus黏附素相关基因表达量的影响;将Rh2与抗生素环丙沙星(CIP)、庆大霉素(GEN)和万古霉素(VAN)联用,采用96孔细胞培养板结合结晶紫染色法探讨其与抗生素之间是否存在协同抑制生物被膜形成的能力。 结果 Rh2对S.aureus浮游菌的增殖无影响,但5 μg/mL的Rh2能显著降低S.aureus生物被膜的形成量(P<0.05),且具有剂量依赖性;10 μg/mL的Rh2能显著抑制S.aureus黏附相关基因icaA、icaCicaD的表达(P均<0.05);此外,10 μg/mL的Rh2可显著促进亚抑菌浓度CIP、GEN和VAN抑制S.aureus生物被膜的形成能力(P均<0.01)。 结论 人参皂苷Rh2单体能通过抑制S.aureus黏附相关基因icaA、icaCicaD的表达而抑制其生物被膜的形成,并能显著促进CIP、GEN和VAN抑制S.aureus生物被膜形成的能力。

关键词: 金黄色葡萄球菌, 人参皂苷, Rh2, 生物被膜, 协同作用

Abstract: Objective To investigate the effect of ginsenoside Rh2 on the biofim formation of Staphylococcus aureus(S.aureus). Methods The biofilm was constructed by using 96-well cell culture plate to study the effect of Rh2 on the biofilm formation of S.aureus, and the effect of Rh2 on the expression of adhesin-related genes of S.aureus was evaluated by RNA extraction and real-time quantitative PCR. The combination of 96-well cell culture plate with crystal violet staining was used to explore the synergistic antibiofilm effects of Rh2 in combination with ciprofloxacin(CIP), gentamicin(GEN)and vancomycin(VAN). Results Rh2 had no effect on the cell growth of S.aureus, while could significantly reduce the biofilm formation(P<0.05)at the concentration of 5 μg/mL. Rh2(10 μg/mL)could significantly inhibit the gene expressions of icaA, icaC and icaD(P<0.05), and promote the inhibitory effects of CIP, GEN and VAN on S.aureus biofilm formation(P<0.05). Conclusion Ginsenoside Rh2 can inhibit the biofilm formation of S. aureus by inhibiting the expressions of adhesion-related genes icaA, icaC and icaD. Rh2 can also promote the inhibitory effects of CIP, GEN and VAN on the biofilm formation of S.aureus.

Key words: Staphylococcus aureus, Ginsenosides, Rh2, Biofilm, Synergistic effect

中图分类号: 

  • R378.1+1
[1] Tong SY, Davis JS, Eichenberger E, et al. Staphylococcus aureus infections: epidemiology, pathophysiology, clinical manifestations, and management[J]. Clin Microbiol Rev, 2015, 28(3): 603-661.
[2] Bhattacharya M, Wozniak DJ, Stoodley P, et al. Prevention and treatment of Staphylococcus aureus biofilms[J]. Expert Rev Anti Infect Ther, 2015, 13(12): 1499-516.
[3] Lister JL, Horswill AR. Staphylococcus aureus biofilms: recent developments in biofilm dispersal[J]. Front Cell Infect Microbiol, 2014, 4: 178. doi:10.3389/fcibm.2014.00178.
[4] McCarthy H, Rudkin JK, Black NS, et al. Methicillin resistance and the biofilm phenotype in Staphylococcus aureus[J]. Front Cell Infect Microbiol, 2015, 5:1. doi:10.3389/fcimb.2015.00001.
[5] Zhang J, Sun Y, Wang Y, et al. Non-antibiotic agent ginsenoside 20(S)-Rh2 enhanced the antibacterial effects of ciprofloxacin in vitro and in vivo as a potential NorA inhibitor[J]. Eur J Pharmacol, 2014, 740: 277-284. doi:10.1016/j.ejphar.2014.07.020.
[6] Sherstha L, Kayama S, Sasaki M, et al. Inhibitory effects of antibiofilm compound 1 against Staphylococcus aureus biofilms[J]. Microbiol Immunol, 2016, 60(3): 148-159.
[7] Mirzaee M, Najar-Peerayeh S, Behmanesh M, et al. Relationship between adhesion genes and biofilm formation in vancomycin-intermediate Staphylococcus aureus clinical isolates[J]. Curr Microbiol, 2015, 70(5): 665-670.
[8] Moradali MF, Ghods S, Rehm BH. Pseudomonas aeruginosa lifestyle: a paradigm for adaptation, survival, and persistence[J]. Front Cell Infect Microbiol, 2017, 7: 39. doi:10.3389/fcimb.2017.00039.
[9] 黄月云,夏婷,赵成国,等.人参皂苷Rh2和Rg3抗肿瘤作用研究进展[J].实用中医药杂志, 2016, 32(8): 846-847.
[10] Lee DG, Jang SI, Kim YR, et al. Anti-proliferative effects of ginsenosides extracted from mountain ginseng on lung cancer[J]. Chin J Integr Med, 2016, 22(5): 344-352.
[11] Han S, Jeong AJ, Yang H, et al. Ginsenoside 20(S)-Rh2 exerts anti-cancer activity through targeting IL-6-induced JAK2/STAT3 pathway in human colorectal cancer cells[J]. J Ethnopharmacol, 2016, 194: 83-90. doi:10.1016/j.jep.2016.08.039.
[12] Li H, Huang N, Zhu W, et al. Modulation the crosstalk between tumor-associated macrophages and non-small cell lung cancer to inhibit tumor migration and invasion by ginsenoside Rh2[J]. BMC Cancer, 2018, 18(1): 579.
[13] Tong-Lin Wu T, Tong YC, Chen IH, et al. Induction of apoptosis in prostate cancer by ginsenoside Rh2[J]. Oncotarget, 2018, 9(13): 11109-11118.
[14] Xu R, Peng Y, Wang M, et al. Effects of broad-spectrum antibiotics on the metabolism and pharmacokinetics of ginsenoside Rb1: a study on rats’ gut microflora influenced by lincomycin[J]. J Ethnopharmacol, 2014,158(Pt A): 338-344.
[15] Gardner A, Wu W, Thomson S, et al. Molecular basis of altered hERG1 channel gating induced by Ginsenoside Rg3[J]. Mol Pharmacol, 2017, 92(4): 437-450.
[16] Harapanahalli AK, Chen Y, Li J, et al. Influence of adhesion force on icaA and cidA gene expression and production of matrix components in Staphylococcus aureus biofilms[J]. Appl Environ Microbiol, 2015, 81(10): 3369-3378.
[17] Guo P, Lam SL. Unusual structures of TTTA repeats in icaC gene of Staphylococcus aureus[J]. FEBS Lett, 2015, 589(12): 1296-1300.
[18] Castelani L, Pilon LE, Martins T, et al. Investigation of biofilm production and icaA and icaD genes in Staphylococcus aureus isolated from heifers and cows with mastitis[J]. Anim Sci J, 2015, 86(3): 340-344.
[19] Lee SM. Anti-inflammatory effects of ginsenosides Rg5, Rz1, and Rk1: inhibition of TNF-ɑ-induced NF-κB, COX-2, and iNOS transcriptional expression[J]. Phytother Res, 2014, 28(12): 1893-1896.
[20] Abdulamir AS, Jassim SA, Hafidh RR, et al. The potential of bacteriophage cocktail in eliminating Methicillin-resistant Staphylococcus aureus biofilms in terms of different extracellular matrices expressed by PIA, ciaA-D and FnBPA genes[J]. Ann Clin Microbiol Antimicrob, 2015, 14: 49. doi:10.1186/S12941-015-0106-0.
[21] Yu D, Zhao L, Xue T, et al. Staphylococcus aureus autoinducer-2 quorum sensing decreases biofilm formation in an icaR-dependent manner[J]. BMC Microbiol, 2012, 12: 288. doi:10.1186/1471-2180-12-288.
[22] Arciola CR, Campoccia D, Ravaioli S, et al. Polysaccharide intercellular adhesin in biofilm: structural and regulatory aspects[J]. Front Cell Infect Microbiol, 2015, 5: 7. doi:10.3389/fcimb.2015.00007.
[23] Aka ST, Haji SH. Sub-MIC of antibiotic induced biofilm formation of Pseudomonas aeruginosa in the presence of chlorhexidine[J]. Braz J Microbiol, 2015, 46(1): 149-154.
[24] Hathroubi S, Fontaine-Gosselin SÈ, Tremblay YD, et al. Sub-inhibitory concentrations of penicillin G induce biofilm formation by field isolates of Actinobacillus pleuropneumoniae[J]. Vet Microbiol, 2015, 79(3-4): 277-286.
[1] 冯凡,胡晓燕,吴伟芳,孙筱林,孙允东,曹倩,肖颖,闫世坤,史培堃,曾贝妮,周亚滨. 干酪乳酸杆菌代谢物对白假丝酵母菌生物被膜的体外抑菌效果及分子机制[J]. 山东大学学报(医学版), 2017, 55(2): 74-78.
[2] 张晓金1,孙高英1,杨玲玲2,郭元芳1,郝秀玉1,郝建荣1,毕文祥1. 人参皂苷Rb1对NEP基因启动子活性的影响[J]. 山东大学学报(医学版), 2013, 51(10): 42-48.
[3] 董向前1,段丽平1,梁兵1,李树安1,柳波2,詹尔益2,宋精玲3,杨志伟4,晋德光4,马岚青1. 人参皂苷Rg1和Rb1抗肝纤维化的体视学研究[J]. 山东大学学报(医学版), 2012, 50(1): 85-.
[4] 毕少杰1,于晶2,刘婷3,刘明涛4,盛美艳4,李玉4. 济南地区异质性万古霉素中介金葡菌的分离率及方法研究[J]. 山东大学学报(医学版), 2010, 48(6): 41-.
[5] 杨玲玲1 ,张静1 ,崔云燕2 ,胡晓燕1 ,孔峰1 ,崔行1
. 以神经内肽酶为靶点筛选治疗阿尔茨海默症
天然药物的实验研究
[J]. 山东大学学报(医学版), 2009, 47(01): 10-14.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!