The complete genome sequence of Seneca Valley virus svv/ch/zz/2016 and its amplification primers
A whole-genome, Seneca technology, applied in the field of molecular biology, can solve problems such as economic losses and major risks in the market of infected pigs
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Embodiment 1
[0041] Example 1. Primer combination designed for one-step RT-PCR amplification of 7 nucleotide sequence fragments of the whole genome of Seneca Valley virus SVV / CH / ZZ / 2016
[0042] One of the purposes of the present invention is to obtain the whole genome sequence of Seneca Valley virus SVV / CH / ZZ / 2016, so that the molecular genetic evolution trend and epidemic situation of Seneca Valley virus are more comprehensive and comprehensive at the level of the whole genome sequence. Learn systematically for further in-depth research.
[0043] According to the full genome nucleotide sequence of Seneca Valley virus reference strains in NCBI, such as SVA / CH / 01 / 2015 (GenBank: KT321458.1), SVA / CH / 02 / 2015 (GenBank: KX173339.1), SVA / CH / DL / 01 / 2016(GenBank:KX751944.1), SVA / CH / GXI09 / 2016(GenBank:KY038016.1), SVA / CH / LX / 01 / 2016(GenBank:KX751945.1), SVA / CH / ZW / 01 / 2016(GenBank:KX751946.1), SVA / HLJ / CHA / 2016(GenBank:KY419132.1), SVA / CH / FJ / 2017(GenBank:KY747510.1), SVA / CH / HN / 2017(GenBank:KY747511....
Embodiment 2
[0047] Example 2. Obtaining the Whole Genome Sequence of Seneca Valley Virus SVV / CH / ZZ / 2016
[0048] Based on the primer combination obtained in Example 1, the present invention can obtain the whole genome sequence of Seneca Valley virus SVV / CH / ZZ / 2016, and the obtaining method comprises the following steps:
[0049] 1. Extract the total RNA of Seneca Valley virus SVV / CH / ZZ / 2016
[0050] Follow Axyprep TM Body Fluid Viral DNA / RNA Miniprep Kit (purchased from AXYGEN Company) instruction manual, extracting the total RNA of Seneca valley virus SVV / CH / ZZ / 2016 (preservation number: CGMCC 14886), the specific steps are as follows:
[0051] (1) Reagent preparation: Prepare isopropanol containing 1% (V / V) glacial acetic acid in advance; add specified volumes of absolute ethanol to reagent Buffer W1A and Buffer W2 respectively. That is, add 17mL absolute ethanol to 24mL Buffer W1A; add 56mL absolute ethanol to 24mL Buffer W2.
[0052] (2) Take 200uL of the sample to be tested (the ...
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