期刊文献+

酸性环境对变形链球菌srtA基因表达的影响 被引量:1

Effect of acidic environment on Streptococcus mutans srtA expression
下载PDF
导出
摘要 目的检测酸性环境对变形链球菌初始粘附相关基因srtA表达的影响。方法变形链球菌分别在初始pH为5.5和7.0的条件下培养,提取总RNA,逆转录成cDNA,利用TaqMan实时荧光定量PCR技术检测不同环境条件下变形链球菌初始粘附相关基因srtA的表达。结果酸性环境中高粘附能力变形链球菌srtA基因表达明显上调,低粘附能力菌株的srtA基因表达也升高但不具有统计学意义;中性环境中高粘附能力菌株srtA基因表达明显高于低粘附能力菌株,而在酸性环境中这种差异无统计学意义。结论酸性环境促进变形链球菌srtA基因表达可能是变形链球菌抵抗酸性环境的机制之一;变形链球菌对牙面的粘附力可能与其srtA表达的量有关。 Objective To detect the influence of acidic environment on expression of srtA , the main initial adherence associated gene of S. mutans. Methods Total RNA was extracted from S. mutans after being cultured at initial pH of 5.5 and 7.0 and then reversely transcripted into cDNA. By utilizing TaqMan RT - RCR technique, we checked srtA expression. Results In acidic environment, srtA expression of S. mutans increased, but only the difference of more - adherent strains was significant ; srtA expression of more - adherent S. mutans strains was generally higher than that of less -adherent strains, but the difference in acidic environment was not significant. Conclusion The promotion of srtA expression may be one of the mechanisms underlying S. mutans acid resistance ; There might be some correlation between different expression ofsrtA gene and S. mutans initial adherence.
出处 《现代口腔医学杂志》 CAS CSCD 2009年第3期286-288,共3页 Journal of Modern Stomatology
基金 国家自然科学基金资助项目(30200310) 广东省医学科研基金项目(A2008488) 湛江市科技攻关项目(2008C02001)
关键词 变形链球菌 初始粘附 TaqMan实时荧光定量PCR Streptococcus mutans Initial adherence TaqMan real -time quantitative PCR
  • 相关文献

参考文献13

  • 1Ahn SJ, Ahn SJ, Wen ZT, et al. Characteristics of biofilm formation by Streptococcus mutans in the presence of saliva. Infect Immun,2008,76 (9) :4259 - 4268.
  • 2姜颖,张铁柱,杨锦波,刘天佳,陈坤.酸性环境对变形链球菌黏附力的影响[J].广东牙病防治,2008,16(9):398-399. 被引量:7
  • 3姜颖,张铁柱,杨锦波,刘天佳,王君.酸性环境对变形链球菌spaP基因表达的影响[J].实用口腔医学杂志,2008,24(6):780-783. 被引量:3
  • 4Livak K J, Schmittgen TD. Analysis of relative gene expression data using real - time quantitative PCR and the2 -△△Ct method. Methods,2001,25 (4) :402 - 408.
  • 5Browngardt CM, Wen ZT, Bume RA. RegM is required for optimal fructosyhransferase and glucosyhransferase gene expression in Streptococcus mutans. FEMS Microbiol Letters,2004,240 ( 1 ) : 75 - 79.
  • 6姜颖,张铁柱,杨锦波,刘天佳,陈坤.葡萄糖浓度对变形链球菌spaP基因表达的影响[J].现代口腔医学杂志,2008,22(6):584-587. 被引量:4
  • 7Len ACL, Harry DWS, Jacques NA. Proteome analysis of Streptococcus mutans metabolic phenotype during acid tolerance. Microbiol,2004,150( Pt 5) : 1353 - 1366.
  • 8Len ACL, Harry DWS, Jacques NA. Stress - responsive proteins are upregulated in Streptococcus mutans during acid tolerence. Microbiol, 2004,150(Pt 5) : 1339 - 1351.
  • 9Marraffini LA, Dedent AC, Schneewind O. Sortases and the art of anchoring proteins to the envelopes of gram - positive bacteria. Microbiology & Molecular Biology Reviews, 2006,70 ( 1 ) : 192 - 221.
  • 10Hu P, Bian Z, Fan M, et al. Sec translocase and sortase A are colocalised in a locus in the cytoplasmic membrane of Streptococcus mutans. Arch Oral Biol, 2008,53(2) :150 -154.

二级参考文献31

  • 1杨德琴,刘天佳,亓庆国,付春华,庄姮,李颂.变形链球菌临床株F-ATPase亚基基因uncEBF在mRNA水平的表达[J].实用口腔医学杂志,2005,21(6):737-741. 被引量:4
  • 2姜颖,杨锦波,刘天佳,谭红,黄定明.不同浓度的葡萄糖对变形链球菌初始粘附能力的影响[J].华西口腔医学杂志,2006,24(5):455-457. 被引量:14
  • 3Livak KJ', Schmittgen TD. Analysis of relative gene expression data using real - time quantitative PCR and the 2^-△△Ct method. Methods ,2001, 25 (4) :402 - 408.
  • 4Suzuki Nao, Nakano Y, Yoshida A,et al. Real - time TaqMan PCR for quantifying oral bacteria during biofilm formation. J Clini Microbio,2004,42(8) : 3827 -3830.
  • 5Yoshida A, Suzuki N, Nakano Y, et al. Development of a 5, uuclease - based real - time PCR assay for quantitative detection of cariogenic dental pathogens Streptococcus mutaus and Streptococcus sobrinus. J Clin Microbiol,2003,41(9) :4438 -4441.
  • 6Malinen E, Kassinen A, Rinttila T, et al. Comparison of real - time PCR with SYBR Green Ⅰ or 5, - nuclease assays and dot - blot hybridization with rDNA - targeted oligonucleotide probes in quantification of selected faecal bacteria. Microbio, 2003, 149 ( pt1 ) :269 - 277.
  • 7Banas JA, Potvin HC, Singh RN. The regulation of Streptococcus mutans glucan - binding protein A expression. FEMS Microbiology letters, 1997, 154 (2) :289 - 292.
  • 8Li Y, Bume RA. Regulation of the gtfBC and ftf genes of Streptococcus mutaus in biofilms in response to pH and carbohydrate. Microbiol,2001,147 ( pt10) : 2841 - 2848.
  • 9Browngardt CM, Wen ZT, Bume RA. RegM is required for optimal fructosyltransferase and glucosyltransferase gene expression in Streptococcus mutans. FEMS Micrebiol Letters, 2004,240 ( 1 ) : 75 -79.
  • 10Senadheera MD, Guggenheim B, Spatafora GA, et al. A VicRK signal transduction system in Streptococcus mutans affects gtfBCD, gbpB, and ftf expression, biofilm formation, and genetic competence development. J Bacteriol, 2005,187 (12) :4064 - 4076.

共引文献9

同被引文献1

引证文献1

二级引证文献7

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