期刊文献+

组合处理对双菌种生物被膜的清除和杀灭效果 被引量:1

Removal effect and killing efficacy of combination treatments on dual-species biofilms
下载PDF
导出
摘要 该研究建立了食源性病原菌(液化沙雷菌S1和腐生葡萄球菌S2)双菌种生物被膜研究模型,采用微孔板法和MTT法检测单一、组合处理方式对双菌种生物被膜的清除和杀灭效果。研究发现,采用24孔板37℃于TSB培养基中培养24 h可获得稳定的液化沙雷菌-腐生葡萄球菌双菌种生物被膜,组合处理方式优于单一处理效果,处理顺序的不同也会影响生物被膜的清除和杀灭效果,1%Na OH处理20 min再用0.3%Na Cl O处理20 min清除效果最好,双菌种生物被膜的量由1.11(OD595 nm)减少至0.08(OD595 nm),杀灭率达95.73%。 The study mainly focused on the establishment of a dual-species biofilm model formed by two foodbome pathogenic bacteria Serratia lique- faciens S1 and Staphylococcus saprophyticus S2. Microtitor-plate method and MTT assay were used to measure the removal effect and killing effica- cy of single or combination treatments on dual-species biofilm formation. The results showed that the stable dual-species biofilms, consisting of S. liquefaciens S1 and S. saprophyticus S2, could be obtained in tryptone soy broth (TSB) at 37 ℃ for 24 h. The effects of combined treatments were better than single treatments. Moreover, in combined treatments, the removal effect and killing efficacy were also influenced by treatment orders. Results indicated that when the dual-species biofilms were treated with 1% NaOH for 20 min firstly and then disposed with 0.3% NaC10 for another 20 min, the removal effects of biofilms were better than that under other conditions, while the dual-species biofilms quantity decreased from 1.11 (OD595MM) to 0.08 (OD595MM) and the killing efficacy reached to 95.73%.
出处 《中国酿造》 CAS 北大核心 2017年第9期19-24,共6页 China Brewing
基金 国家自然科学基金资助项目(31371716)
关键词 双菌种生物被膜 液化沙雷菌 腐生葡萄球菌 组合处理 dual-species biofilms Serratia liquefaciens Staphylococcus saprophyticus combination treatment
  • 相关文献

参考文献4

二级参考文献100

  • 1陈秋云,韩北忠,李春雷.金黄色葡萄球菌生物被膜在不锈钢表面的形成及其对二氧化氯的敏感性[J].中国农业大学学报,2004,9(4):10-13. 被引量:25
  • 2张志强,田志刚.MTT法检测NK和LAK活性的方法学探讨[J].中国实验临床免疫学杂志,1994,6(3):12-16. 被引量:39
  • 3Gaetti-Jardim E Jr, Marcelino SL, Feitosa AC, Romito GA, Avila-Campos MJ. Quantitative detection of periodonto- pathic bacteria in atherosclerotic plaques from coronary arteries. J Med Microbio12009; 58:1568 1575.
  • 4AI-Ahmad A, Wunder A, Auschill TM, et al. The in vivo dynamics of Streptococcus spp., Actinomyces naeslundii, Fusobacterium nuc[eatum and Veillonella spp. in dental plaque biofilm as analysed by five-colour multiplex fluorescence in situ hybridization. J Med Microbiol 2007; 56: 681-687.
  • 5Malic S, Hill KE, ttayes A, et al. Detection and identifi- cation of specific bacteria in wound biofilms using peptide nucleic acid fluorescent in situ hybridization (PNA FISH). Microbiology 2009; 155:2603-2611.
  • 6Perry-O'Keefe H, Stender H, Broomer A, et al. Filter-based PNA in situ hybridization for rapid detection, identification and enumeration of specific micro-organisms. J Appl Microbio12001; 90:180-189.
  • 7Oosterhof JJ, Buijssen KJ, Busscher HJ, van der Laan BF, van der Mei HC. Effects of quaternary ammonium silane coatings on mixed fimgal and bacterial biofilms on tracheo- esophageal shunt prostheses. Appl Environ Microbiol 2006; 72: 3673-3677.
  • 8Yang L, Haagensen JA, Jelsbak L, et al. In situ growth rates and biofilm development of Pseudomonas aeruginosa popu- lations in chronic lung infections. J Bacteriol 2008; 190: 2767-2776.
  • 9Tyson GW, Chapman J, Hugenholtz P, et al. Community structure and metabolism through reconstruction of microbial genomes from the environment. Nature 2004; 428: 37-43.
  • 10Yergeau E, Lawrence JR, Waiser M J, Korber DR, Greer CW Metatranscriptomic analysis of the response of river biofilms to pharmaceutical products, using anonymous DNA micro- arrays. ApplEnviron Microbiol2010; 76: 5432-5439.

共引文献132

同被引文献14

引证文献1

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部