Huws S A, Edwards J E, Kim E J, Scollan N D
Institute of Grassland and Environmental Research (IGER), Plas Gogerddan, Aberystwyth, SY23 3EB, UK.
J Microbiol Methods. 2007 Sep;70(3):565-9. doi: 10.1016/j.mimet.2007.06.013. Epub 2007 Jun 30.
Efficient profiling of eubacterial diversity within complex communities requires that primers are specific for eubacterial 16S rRNA. Specificity of published primers against eubacterial and archaeal 16S rRNA as well as protozoal and fungal 18S rRNA was assessed in silico. The specificity and sensitivity of the V3 and V6-V8 (F968gc and R1401) Denaturing Gradient Gel Electrophoresis (DGGE) primers was subsequently verified using rumen-derived samples. An assessment of the effects of employing touchdown PCR cycling conditions was also made. For DGGE profiling of eubacteria within rumen samples, primers F968gc and R1401 proved the most specific and sensitive providing that touchdown PCR is not used.
对复杂群落中的真细菌多样性进行高效分析,要求引物对真细菌16S rRNA具有特异性。通过计算机模拟评估已发表引物针对真细菌和古细菌16S rRNA以及原生动物和真菌18S rRNA的特异性。随后使用瘤胃来源的样本验证了V3和V6-V8(F968gc和R1401)变性梯度凝胶电泳(DGGE)引物的特异性和敏感性。还评估了采用降落PCR循环条件的效果。对于瘤胃样本中真细菌的DGGE分析,引物F968gc和R1401在不使用降落PCR的情况下被证明是最具特异性和敏感性的。