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Infectivity assessment of porcine endogenous retrovirus using high-throughput sequencing technologies
Ken Kono1, Kiyoko Kataoka1, Yuzhe Yuan2
1Division of Cell-Based Therapeutic Products, National Institute of Health Sciences, Kanagawa, Japan.
Summary
Porcine endogenous retrovirus (PERV) infectivity risk in xenotransplantation can be assessed using high-throughput sequencing. This method accurately predicts PERV infection risk before using porcine products in humans.
Area of Science:
- Xenotransplantation research
- Virology
- Genomics
Background:
- Xenogenic cell-based therapies, like porcine islet cells for diabetes, face challenges due to porcine endogenous retrovirus (PERV).
- PERV transmission from pigs to humans is a concern for xenotransplantation safety.
- Current methods like PCR may inaccurately assess PERV infection risk.
Purpose of the Study:
- To evaluate the infectivity of PERVs using high-throughput sequencing.
- To develop a reliable method for assessing PERV infection risk in xenotransplantation.
- To determine if genomic sequencing can predict PERV infectivity in human cells.
Main Methods:
- High-throughput sequencing of porcine genomes.
- RNA sequencing of PERV-infected human and porcine cells.
- Mapping sequencing reads to PERV sequences.
- Analyzing normalized read counts to predict infectivity.
Main Results:
- High-throughput sequencing identified PERV sequences in the porcine genome.
- Normalized read counts mapped to PERV regions accurately predicted PERV infectivity.
- This method proved useful for risk assessment prior to xenotransplantation.
Conclusions:
- High-throughput sequencing offers a reliable method for assessing PERV infectivity.
- This approach can mitigate risks associated with xenotransplantation using porcine products.
- Accurate PERV risk evaluation is crucial for the safety of xenotransplantation therapies.

