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Screening and Identification of the First Non-CRISPR/Cas9-Treated Chinese Miniature Pig With Defective Porcine Endogenous Retrovirus pol Genes.

Authors :
Ma Y
Jia J
Fan R
Lu Y
Zhao X
Zhong Y
Yang J
Ma L
Wang Y
Lv M
Yang H
Mou L
Dai Y
Feng S
Zhang J
Source :
Frontiers in immunology [Front Immunol] 2022 Jan 19; Vol. 12, pp. 797608. Date of Electronic Publication: 2022 Jan 19 (Print Publication: 2021).
Publication Year :
2022

Abstract

Pig to human xenotransplantation is considered to be a possible approach to alleviate the shortage of human allografts. Porcine endogenous retrovirus (PERV) is the most significant pathogen in xenotransplantation. We screened for pigs that consistently did not transmit human-tropic replication competent PERVs (HTRC PERVs), namely, non-transmitting pigs. Then, we conducted whole-genome resequencing and full-length transcriptome sequencing to further investigate the sequence characteristics of one non-transmitting pig. Using in vitro transmission assays, we found 5 (out of 105) pigs of the Chinese Wuzhishan minipig inbred line that did not transmit PERV to human cells, i.e., non-transmitting pigs. Whole-genome resequencing and full-length transcriptome sequencing of one non-transmitting pig showed that all of the pol genes were defective at both the genome and transcript levels. We speculate that the defective PERV pol genes in this pig might be attributable to the long-term inbreeding process. This discovery is promising for the development of a strain of highly homozygous and genetically stable pigs with defective PERV pol genes as a source animal species for xenotransplantation.<br />Competing Interests: Authors SF and JY are employed by Grand Life Science and Technology, Ltd. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2022 Ma, Jia, Fan, Lu, Zhao, Zhong, Yang, Ma, Wang, Lv, Yang, Mou, Dai, Feng and Zhang.)

Details

Language :
English
ISSN :
1664-3224
Volume :
12
Database :
MEDLINE
Journal :
Frontiers in immunology
Publication Type :
Academic Journal
Accession number :
35126361
Full Text :
https://doi.org/10.3389/fimmu.2021.797608