快速检测志贺毒素2基因的LAMP方法的建立

[1] Rapid and sensi-tive detection of Shiga toxin-producing Escherichia coli from nonen-riched stool specimens by real-time PCR in comparison to enzymeimmunoassay and culture. THOMAS E G,LYNNE M S,JON E R,et al. Journal of Clinical Microbiology . 2009

[2] 产志贺毒素Ⅱ型变异体大肠杆菌LAMP检测方法的建立 [J]. 中国兽医科学, 2011, 41 (03) : 287 - 291

[3] Comparison of im-munomagnetic separation and culture,Reveal TM and VIPTM forthe detection of E.coli O157 in enrichment cultures of naturallycontaminated raw beef,lamb and mixed meat products. CHAPMAN P A,ELLIN M,ASHTON R A. Letterin Applied Microbiology . 2001

[4] Virulence genes of Shiga toxin-producing Escherichia coli isolated from food,animals and humans. MENG J,ZHAO S,DOYLE M P. International Journal of Food Microbiology . 1998

[5] Loop-mediated isothermal amplification of DNA. Notomi T,Okayama H,Masubuchi H, et al. Nucleic Acids Research . 2000

[6] Diarrheagenic Escherichia coli. Nataro JP,Kaper JB. Clinical Microbiology Reviews . 1998

[7] Attaching effacingbacteria in animals. Wales AD,Woodward MJ,Pearson GR. Journal of Comparative Pathology . 2005

[8] Sensitive and rapid de-tection of Vero toxin-producing Escherichia coli using loop-media-ted isothermal amplification. Hara-Kudo Y,Nemoto J,Ohtsuka K,et al. Journal of Medical Microbiology . 2007

[9] EnterohaemorrhagicEscherichia coli in human medicine. KARCH H,TARR P I,BIELASZEWSKA M. International Journal ofMedical Microbiology . 2005

[10] Efficient synthesis of double dye-labeled oligodeoxyribonucleotide probes and their application in a real time PCR assay. Mullah B,Livak K,Andrus A, et al. Nucleic Acids Research . 1998

[1] Rapid and sensi-tive detection of Shiga toxin-producing Escherichia coli from nonen-riched stool specimens by real-time PCR in comparison to enzymeimmunoassay and culture. THOMAS E G,LYNNE M S,JON E R,et al. Journal of Clinical Microbiology . 2009

[2] 产志贺毒素Ⅱ型变异体大肠杆菌LAMP检测方法的建立 [J]. 中国兽医科学, 2011, 41 (03) : 287 - 291

[3] Comparison of im-munomagnetic separation and culture,Reveal TM and VIPTM forthe detection of E.coli O157 in enrichment cultures of naturallycontaminated raw beef,lamb and mixed meat products. CHAPMAN P A,ELLIN M,ASHTON R A. Letterin Applied Microbiology . 2001

[4] Virulence genes of Shiga toxin-producing Escherichia coli isolated from food,animals and humans. MENG J,ZHAO S,DOYLE M P. International Journal of Food Microbiology . 1998

[5] Loop-mediated isothermal amplification of DNA. Notomi T,Okayama H,Masubuchi H, et al. Nucleic Acids Research . 2000

[6] Diarrheagenic Escherichia coli. Nataro JP,Kaper JB. Clinical Microbiology Reviews . 1998

[7] Attaching effacingbacteria in animals. Wales AD,Woodward MJ,Pearson GR. Journal of Comparative Pathology . 2005

[8] Sensitive and rapid de-tection of Vero toxin-producing Escherichia coli using loop-media-ted isothermal amplification. Hara-Kudo Y,Nemoto J,Ohtsuka K,et al. Journal of Medical Microbiology . 2007

[9] EnterohaemorrhagicEscherichia coli in human medicine. KARCH H,TARR P I,BIELASZEWSKA M. International Journal ofMedical Microbiology . 2005

[10] Efficient synthesis of double dye-labeled oligodeoxyribonucleotide probes and their application in a real time PCR assay. Mullah B,Livak K,Andrus A, et al. Nucleic Acids Research . 1998