Suppr超能文献

通过CRISPR/Cas9对chNHE1基因进行精确编辑可产生抗禽白血病病毒J亚群的鸡原始生殖细胞。

Precise Editing of chNHE1 Gene via CRISPR/Cas9 Generates ALV-J-Resistant Chicken Primordial Germ Cell.

作者信息

Zhou Xinyi, Liao Ruyu, Tan Min, Zhang Yu, Wang Haiwei, Zhang Keshan, Wang Qigui, Lan Xi

机构信息

College of Animal Science and Technology, Southwest University, Chongqing 400715, China.

Chongqing Academy of Animal Sciences, Chongqing 402460, China.

出版信息

Animals (Basel). 2025 Jul 9;15(14):2018. doi: 10.3390/ani15142018.

Abstract

Avian leukosis virus subgroup J (ALV-J), an α-retrovirus, mediates infection by binding to the host-specific receptor chNHE1 (chicken sodium-hydrogen exchanger type 1), leading to immunosuppression and tumorigenesis, which severely threatens the sustainable development of the poultry industry. Studies have shown that the tryptophan residue at position 38 (W38) of the chNHE1 protein is the critical site for ALV-J infection. In this study, we employed the CRISPR/Cas9 system to construct a lentiviral vector targeting the W38 site of chNHE1, transfected it into chicken primordial germ cells (PGCs), and validated its antiviral efficacy through ALV-J infection assays, successfully establishing an in vitro gene-editing system for chicken PGCs. The constructed dual lentiviral vector efficiently targeted the W38 site. PGCs isolated from 5.5- to 7-day-old chicken embryos were suitable for in vitro gene editing. Stable fluorescence expression was observed within 24-72 h post-transfection, confirming high transfection efficiency. ALV-J challenge tests demonstrated that no viral env gene expression was detected in transfected PGCs at 48 h or 72 h post-infection, while high env expression was observed in control groups. After 7 days of infection, p27 antigen ELISA tests were negative in transfected groups but positive in controls, indicating that W38-deleted PGCs exhibited strong resistance to ALV-J. This study successfully generated ALV-J-resistant gene-edited PGCs using CRISPR/Cas9 technology, providing a novel strategy for disease-resistant poultry breeding and advancing avian gene-editing applications.

摘要

禽白血病病毒J亚群(ALV-J)是一种α逆转录病毒,通过与宿主特异性受体chNHE1(鸡钠氢交换体1型)结合介导感染,导致免疫抑制和肿瘤发生,严重威胁家禽业的可持续发展。研究表明,chNHE1蛋白第38位的色氨酸残基(W38)是ALV-J感染的关键位点。在本研究中,我们利用CRISPR/Cas9系统构建了靶向chNHE1的W38位点的慢病毒载体,将其转染到鸡原始生殖细胞(PGCs)中,并通过ALV-J感染试验验证其抗病毒效果,成功建立了鸡PGCs的体外基因编辑系统。构建的双慢病毒载体有效地靶向了W38位点。从5.5至7日龄鸡胚中分离的PGCs适合体外基因编辑。转染后24至72小时内观察到稳定的荧光表达,证实转染效率高。ALV-J攻毒试验表明,感染后48小时或72小时,转染的PGCs中未检测到病毒env基因表达,而对照组中观察到高env表达。感染7天后,转染组的p27抗原ELISA检测为阴性,而对照组为阳性,表明缺失W38的PGCs对ALV-J表现出较强的抗性。本研究利用CRISPR/Cas9技术成功培育出抗ALV-J的基因编辑PGCs,为抗病家禽育种提供了新策略,推动了禽类基因编辑应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8c0/12291641/ba41edc59f77/animals-15-02018-g0A1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验