The application of single-genome amplification and sequencing in genomic analysis of an attenuated EIAV vaccine.
- Author:
Hua-Mian WEI
1
;
Xue-Feng WANG
;
Shan-Shan WANG
;
Cheng DU
;
Hai-Fang LIU
;
Qiang LIU
;
Jian-Hu ZHOU
Author Information
1. State Key Laboratory of Veterinary Biotechnology, Harbin, China. weihuamian@163.com
- Publication Type:Journal Article
- MeSH:
Calibration;
Cloning, Molecular;
DNA, Complementary;
genetics;
Genome, Viral;
genetics;
Infectious Anemia Virus, Equine;
immunology;
Nucleic Acid Amplification Techniques;
methods;
Polymerase Chain Reaction;
Sequence Analysis;
methods;
Vaccines, Attenuated;
genetics;
Viral Envelope Proteins;
genetics;
Viral Vaccines;
genetics
- From:
Chinese Journal of Virology
2012;28(4):431-438
- CountryChina
- Language:Chinese
-
Abstract:
Our previous studies found that the Chinese attenuated EIAV vaccine was composed of a pool of quasispecies, which showed a complicated diversity called "multi-species". Further determining the viral composition of these species in the vaccine should improve the identification of predominant viruses in the vaccine and facilitate the analysis of in vivo evolution of EIAV and the vaccine. In this study, the comparison of fidelities in amplifying and sequencing the V3 to V5 fragment of EIAV envelope gp90 gene by either a single-genome amplification (SGA) approach or the traditional RT-PCR (bulk PCR) was performed. Results revealed that the diversities were 1.84% and 1.88% for SGA- and bulk PCR-derived sequences, respectively. Futher analysis revealed that beside the sequences highly homologous to those derived by the bulk PCR, nine of 73 sequences derived by SGA contained a deduced amino acid domain that was identical to the corresponding domain in the virulent strain LN40. In addition, sequences with deletion of one predicted amino acid residual was detected by using SGA The presence of these less populated sequences provided additional evidence for the "multi-species" hypothesis for the action mechanism of the EIAV vaccine. Furthermore, based on the analysis of sampling bias, Our results that the difference in copy number of each viral specie in the pool of quasispecies resulted in the inefficiency to amplify viral sequences that were in low population by bulk PCR. Therefore, the sequences amplified by bulk PCR could not correctly represent the composition of quasispecies. As an approach based on the amplification and sequencing single isolated genome, SGA significantly improved the weakness of bulk PCR and appeared its advantage in analysis of EIAV genome composition with high variety.
