From: The prevention strategies of swine viruses related to xenotransplantation
virus | PERV | PCMV | HEV | PCV |
---|---|---|---|---|
Source of the virus | Endogenous | exogenous | exogenous | exogenous |
Detection method | Realtime-PCR, droplet digital PCR | Serological methods, duplex real-time PCR | Serological methods, real-time PCR | multiplex real-time PCR[69] |
Detection sites | Any tissue, organ. | Serological testing performed on blood samples, nucleic acid testing performed on nasal swabs, spleen, kidney. | Nucleic acid testing performed on muscle, urine, serum, and feces samples. | In most tissues and body fluids, with serum and lymphoid tissue being the main sites |
Virus removal from pig | Gene editing | PCMV can be removed with a high probability by early weaning, colostrum deprivation and cesarean derivation | Divide-column breeding, farm disinfection, isolate negative pig groups. | use commercial vaccines. |
Genetically Modified Pigs | Gene-edited pigs with internal PERV copies partially or completely knocked out. | N/A | N/A | N/A |
RNA interference | Anti-PERV shRNA targeting the gag and pol genes [57] | N/A | Targeting the ORF3 gene of HEV GT3. | Target sequence in the Rep gene encoding region [70] |
vaccine | N/A | N/A | vaccine candidates, such as intramuscular vaccine derived from a gt 4 strain, HEV p179 | Commercial vaccines, such as inactivated vaccines, or subunit vaccines based on the ORF2 protein of PCV2. |