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

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 compe...

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Autores principales: Ma, Yuyuan, Jia, Junting, Fan, Rui, Lu, Ying, Zhao, Xiong, Zhong, Yadi, Yang, Jierong, Ma, Limin, Wang, Yanlin, Lv, Maomin, Yang, Haiyuan, Mou, Lisha, Dai, Yifan, Feng, Shutang, Zhang, Jingang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807647/
https://www.ncbi.nlm.nih.gov/pubmed/35126361
http://dx.doi.org/10.3389/fimmu.2021.797608
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author Ma, Yuyuan
Jia, Junting
Fan, Rui
Lu, Ying
Zhao, Xiong
Zhong, Yadi
Yang, Jierong
Ma, Limin
Wang, Yanlin
Lv, Maomin
Yang, Haiyuan
Mou, Lisha
Dai, Yifan
Feng, Shutang
Zhang, Jingang
author_facet Ma, Yuyuan
Jia, Junting
Fan, Rui
Lu, Ying
Zhao, Xiong
Zhong, Yadi
Yang, Jierong
Ma, Limin
Wang, Yanlin
Lv, Maomin
Yang, Haiyuan
Mou, Lisha
Dai, Yifan
Feng, Shutang
Zhang, Jingang
author_sort Ma, Yuyuan
collection PubMed
description 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.
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spelling pubmed-88076472022-02-03 Screening and Identification of the First Non-CRISPR/Cas9-Treated Chinese Miniature Pig With Defective Porcine Endogenous Retrovirus pol Genes Ma, Yuyuan Jia, Junting Fan, Rui Lu, Ying Zhao, Xiong Zhong, Yadi Yang, Jierong Ma, Limin Wang, Yanlin Lv, Maomin Yang, Haiyuan Mou, Lisha Dai, Yifan Feng, Shutang Zhang, Jingang Front Immunol Immunology 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. Frontiers Media S.A. 2022-01-19 /pmc/articles/PMC8807647/ /pubmed/35126361 http://dx.doi.org/10.3389/fimmu.2021.797608 Text en Copyright © 2022 Ma, Jia, Fan, Lu, Zhao, Zhong, Yang, Ma, Wang, Lv, Yang, Mou, Dai, Feng and Zhang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Ma, Yuyuan
Jia, Junting
Fan, Rui
Lu, Ying
Zhao, Xiong
Zhong, Yadi
Yang, Jierong
Ma, Limin
Wang, Yanlin
Lv, Maomin
Yang, Haiyuan
Mou, Lisha
Dai, Yifan
Feng, Shutang
Zhang, Jingang
Screening and Identification of the First Non-CRISPR/Cas9-Treated Chinese Miniature Pig With Defective Porcine Endogenous Retrovirus pol Genes
title Screening and Identification of the First Non-CRISPR/Cas9-Treated Chinese Miniature Pig With Defective Porcine Endogenous Retrovirus pol Genes
title_full Screening and Identification of the First Non-CRISPR/Cas9-Treated Chinese Miniature Pig With Defective Porcine Endogenous Retrovirus pol Genes
title_fullStr Screening and Identification of the First Non-CRISPR/Cas9-Treated Chinese Miniature Pig With Defective Porcine Endogenous Retrovirus pol Genes
title_full_unstemmed Screening and Identification of the First Non-CRISPR/Cas9-Treated Chinese Miniature Pig With Defective Porcine Endogenous Retrovirus pol Genes
title_short Screening and Identification of the First Non-CRISPR/Cas9-Treated Chinese Miniature Pig With Defective Porcine Endogenous Retrovirus pol Genes
title_sort screening and identification of the first non-crispr/cas9-treated chinese miniature pig with defective porcine endogenous retrovirus pol genes
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807647/
https://www.ncbi.nlm.nih.gov/pubmed/35126361
http://dx.doi.org/10.3389/fimmu.2021.797608
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