Cloning and Sequencing of Full Vp4 Gene of Group A Porcine Rotavirus
Chunfeng Wang
Abstract
Chunfeng Wang
Abstract
The antigenic determinants of Vp4 gene of porcine group A Rotavirus were amplified from cell infected with rotavirus by the reverse transcription-polymerase chain reaction(RT-PCR).The length of full Vp4 gene was 2 331 bp.The products of RT-PCR were ligated with plasmid pGEM-Teasy and transformed to JM109.By the analysis of restriction endonuclease cutting,PCR and sequencing,the recombinant plasmids pGEM-T-Vp4 was constructed.The results of nucleotide and amino acid sequences analysis showed that the experimental rotavirus Vp4 gene has over 99% similarity with the rotavirus Vp4 genes of America strain and Heilongjiang strain,which has a positive open reading frame.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
The antigenic determinants of Vp4 gene of porcine group A Rotavirus were amplified from cell infected with rotavirus by the reverse transcription-polymerase chain reaction(RT-PCR).The length of full Vp4 gene was 2 331 bp.The products of RT-PCR were ligated with plasmid pGEM-Teasy and transformed to JM109.By the analysis of restriction endonuclease cutting,PCR and sequencing,the recombinant plasmids pGEM-T-Vp4 was constructed.The results of nucleotide and amino acid sequences analysis showed that the experimental rotavirus Vp4 gene has over 99% similarity with the rotavirus Vp4 genes of America strain and Heilongjiang strain,which has a positive open reading frame.
Key concepts: Rotavirus, Gene, Biology, Plasmid, Restriction enzyme, Open reading frame, Polymerase chain reaction, Virology