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Production of Transgenic Pigs Mediated by Pseudotyped Lentivirus and Sperm

Sperm-mediated gene transfer can be a very efficient method to produce transgenic pigs, however, the results from different laboratories had not been widely repeated. Genomic integration of transgene by injection of pseudotyped lentivirus to the perivitelline space has been proved to be a reliable r...

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Autores principales: Zhang, Yongliang, Xi, Qianyun, Ding, Jinghua, Cai, Weiguang, Meng, Fanmin, Zhou, Junyun, Li, Hongyi, Jiang, Qingyan, Shu, Gang, Wang, Songbo, Zhu, Xiaotong, Gao, Ping, Wu, Zhenfang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3335058/
https://www.ncbi.nlm.nih.gov/pubmed/22536374
http://dx.doi.org/10.1371/journal.pone.0035335
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author Zhang, Yongliang
Xi, Qianyun
Ding, Jinghua
Cai, Weiguang
Meng, Fanmin
Zhou, Junyun
Li, Hongyi
Jiang, Qingyan
Shu, Gang
Wang, Songbo
Zhu, Xiaotong
Gao, Ping
Wu, Zhenfang
author_facet Zhang, Yongliang
Xi, Qianyun
Ding, Jinghua
Cai, Weiguang
Meng, Fanmin
Zhou, Junyun
Li, Hongyi
Jiang, Qingyan
Shu, Gang
Wang, Songbo
Zhu, Xiaotong
Gao, Ping
Wu, Zhenfang
author_sort Zhang, Yongliang
collection PubMed
description Sperm-mediated gene transfer can be a very efficient method to produce transgenic pigs, however, the results from different laboratories had not been widely repeated. Genomic integration of transgene by injection of pseudotyped lentivirus to the perivitelline space has been proved to be a reliable route to generate transgenic animals. To test whether transgene in the lentivirus can be delivered by sperm, we studied incubation of pseudotyped lentiviruses and sperm before insemination. After incubation with pig spermatozoa, 62±3 lentiviral particles were detected per 100 sperm cells using quantitative real-time RT-PCR. The association of lentivirus with sperm was further confirmed by electron microscopy. The sperm incubated with lentiviral particles were artificially inseminated into pigs. Of the 59 piglets born from inseminated 5 sows, 6 piglets (10.17%) carried the transgene based on the PCR identification. Foreign gene and EGFP was successfully detected in ear tissue biopsies from two PCR-positive pigs, revealed via in situ hybridization and immunohistochemistry. Offspring of one PCR-positive boar with normal sows showed PCR-positive. Two PCR-positive founders and offsprings of PCR-positive boar were further identified by Southern-blot analysis, out of which the two founders and two offsprings were positive in Southern blotting, strongly indicating integration of foreign gene into genome. The results indicate that incubation of sperm with pseudotyped lentiviruses can incorporated with sperm-mediated gene transfer to produce transgenic pigs with improved efficiency.
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spelling pubmed-33350582012-04-25 Production of Transgenic Pigs Mediated by Pseudotyped Lentivirus and Sperm Zhang, Yongliang Xi, Qianyun Ding, Jinghua Cai, Weiguang Meng, Fanmin Zhou, Junyun Li, Hongyi Jiang, Qingyan Shu, Gang Wang, Songbo Zhu, Xiaotong Gao, Ping Wu, Zhenfang PLoS One Research Article Sperm-mediated gene transfer can be a very efficient method to produce transgenic pigs, however, the results from different laboratories had not been widely repeated. Genomic integration of transgene by injection of pseudotyped lentivirus to the perivitelline space has been proved to be a reliable route to generate transgenic animals. To test whether transgene in the lentivirus can be delivered by sperm, we studied incubation of pseudotyped lentiviruses and sperm before insemination. After incubation with pig spermatozoa, 62±3 lentiviral particles were detected per 100 sperm cells using quantitative real-time RT-PCR. The association of lentivirus with sperm was further confirmed by electron microscopy. The sperm incubated with lentiviral particles were artificially inseminated into pigs. Of the 59 piglets born from inseminated 5 sows, 6 piglets (10.17%) carried the transgene based on the PCR identification. Foreign gene and EGFP was successfully detected in ear tissue biopsies from two PCR-positive pigs, revealed via in situ hybridization and immunohistochemistry. Offspring of one PCR-positive boar with normal sows showed PCR-positive. Two PCR-positive founders and offsprings of PCR-positive boar were further identified by Southern-blot analysis, out of which the two founders and two offsprings were positive in Southern blotting, strongly indicating integration of foreign gene into genome. The results indicate that incubation of sperm with pseudotyped lentiviruses can incorporated with sperm-mediated gene transfer to produce transgenic pigs with improved efficiency. Public Library of Science 2012-04-20 /pmc/articles/PMC3335058/ /pubmed/22536374 http://dx.doi.org/10.1371/journal.pone.0035335 Text en Zhang et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zhang, Yongliang
Xi, Qianyun
Ding, Jinghua
Cai, Weiguang
Meng, Fanmin
Zhou, Junyun
Li, Hongyi
Jiang, Qingyan
Shu, Gang
Wang, Songbo
Zhu, Xiaotong
Gao, Ping
Wu, Zhenfang
Production of Transgenic Pigs Mediated by Pseudotyped Lentivirus and Sperm
title Production of Transgenic Pigs Mediated by Pseudotyped Lentivirus and Sperm
title_full Production of Transgenic Pigs Mediated by Pseudotyped Lentivirus and Sperm
title_fullStr Production of Transgenic Pigs Mediated by Pseudotyped Lentivirus and Sperm
title_full_unstemmed Production of Transgenic Pigs Mediated by Pseudotyped Lentivirus and Sperm
title_short Production of Transgenic Pigs Mediated by Pseudotyped Lentivirus and Sperm
title_sort production of transgenic pigs mediated by pseudotyped lentivirus and sperm
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3335058/
https://www.ncbi.nlm.nih.gov/pubmed/22536374
http://dx.doi.org/10.1371/journal.pone.0035335
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