Delaunay Agnès, Dallot Sylvie, Filloux Denis, Dupuy Virginie, Roumagnac Philippe, Jacquot Emmanuel
INRA-Cirad-Montpellier SupAgro, UMR 385 BGPI, Cirad TA A-54K, Montpellier cedex, 34398, France.
Methods Mol Biol. 2015;1302:187-206. doi: 10.1007/978-1-4939-2620-6_15.
The multiplex SNaPshot and the capillary electrophoresis-single-strand conformation polymorphism (CE-SSCP) procedures are here used for rapid and high-throughput description of the molecular variability of viral populations. Both approaches are based on (1) standard amplification of genomic sequence(s), (2) labeled primers or labeled single-stranded DNA, and (3) migration of fluorescent-labeled molecules in capillary electrophoresis system. The SNaPshot technology was used to describe the diversity of 20 targeted single nucleotide polymorphisms (SNPs) selected from alignment of viral genomic sequences retrieved from public database. The CE-SSCP procedure was applied to identify the polymorphisms of two small (<500 bases in length) genomic regions of viral genomes. The different steps of SNaPshot and CE-SSCP setup procedures are presented using Potato virus Y (PVY, Potyvirus) and Plum pox virus (PPV, Potyvirus) RNA viruses as molecular targets, respectively.
多重SNaPshot法和毛细管电泳-单链构象多态性(CE-SSCP)方法在此用于快速、高通量描述病毒群体的分子变异性。这两种方法均基于:(1)基因组序列的标准扩增;(2)标记引物或标记单链DNA;(3)荧光标记分子在毛细管电泳系统中的迁移。SNaPshot技术用于描述从公共数据库检索到的病毒基因组序列比对中选择的20个靶向单核苷酸多态性(SNP)的多样性。CE-SSCP方法用于鉴定病毒基因组两个小的(长度<500个碱基)基因组区域的多态性。分别以马铃薯Y病毒(PVY,马铃薯Y病毒属)和李痘病毒(PPV,马铃薯Y病毒属)RNA病毒作为分子靶点,介绍了SNaPshot和CE-SSCP设置程序的不同步骤。