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TALEN 技术在抗鼠巨细胞病毒潜伏感染中的潜在应用

Potential Application of TALENs against Murine Cytomegalovirus Latent Infections.

机构信息

Department of Neurosurgery, Mackay Memorial Hospital, Taipei 10449, Taiwan.

Department of Medicine, Mackay Medicine College, New Taipei City 25245, Taiwan.

出版信息

Viruses. 2019 May 3;11(5):414. doi: 10.3390/v11050414.

DOI:10.3390/v11050414
PMID:31058862
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6563206/
Abstract

Cytomegalovirus (CMV) infections are still a global health problem, because the latent viruses persist in humans and cause recurring disease. Currently, there are no therapies for CMV latent infections and the therapies for active infections are limited by side effects and other problems. It is impossible to eradicate latent viruses in animals. HCMV (human CMV) is specific to human diseases; however, it is difficult to study HCMV due to its host specificity and long life cycle. Fortunately, MCMV (murine CMV) provides an excellent animal model. Here, three specific pairs of transcription activator-like effector nuclease (TALEN) plasmids (MCMV1-2, 3-4, and 5-6) were constructed to target the MCMV M80/80.5 sequence in order to test their efficacy in blocking MCMV lytic replication in NIH3T3 cell culture. The preliminary data showed that TALEN plasmids demonstrate specific targeting and cleavage in the MCMV M80/80.5 sequence and effectively inhibit MCMV growth in cell culture when the plasmid transfection is prior to the viral infection. The most specific pairs of TALEN plasmids (MCMV3-4) were further used to confirm the negative regulation of latent MCMV replication and gene expression in Balb/c mice. The injection of specific TALEN plasmids caused significant inhibition in the copy number level of immediately early gene (ie-1) DNA in five organs of mice, when compared with the controls. The result demonstrated that TALENs potentially provide an effective strategy to remove latent MCMV in animals.

摘要

巨细胞病毒 (CMV) 感染仍然是一个全球性的健康问题,因为潜伏的病毒在人体内持续存在并导致反复发作的疾病。目前,尚无针对 CMV 潜伏感染的治疗方法,而针对活跃感染的治疗方法则受到副作用和其他问题的限制。在动物体内,潜伏病毒无法被根除。人巨细胞病毒 (HCMV) 是人类疾病的特异性病毒;然而,由于其宿主特异性和长生命周期,研究 HCMV 非常困难。幸运的是,鼠巨细胞病毒 (MCMV) 提供了一个优秀的动物模型。在这里,构建了三对特定的转录激活样效应物核酸酶 (TALEN) 质粒 (MCMV1-2、3-4 和 5-6),以靶向 MCMV M80/80.5 序列,以测试它们在阻断 NIH3T3 细胞培养物中 MCMV 裂解复制中的功效。初步数据表明,TALEN 质粒在 MCMV M80/80.5 序列中具有特异性靶向和切割作用,并且在质粒转染先于病毒感染时,有效地抑制细胞培养物中的 MCMV 生长。最特异的 TALEN 质粒对 (MCMV3-4) 进一步用于确认潜伏性 MCMV 复制和基因表达在 Balb/c 小鼠中的负调控。与对照组相比,特异性 TALEN 质粒的注射导致小鼠五个器官中立即早期基因 (ie-1) DNA 的拷贝数水平显著抑制。结果表明,TALENs 可能为去除动物体内潜伏性 MCMV 提供了一种有效的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a282/6563206/42b70d46cdf5/viruses-11-00414-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a282/6563206/e418781bf545/viruses-11-00414-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a282/6563206/4a4414be034b/viruses-11-00414-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a282/6563206/6288e840c88d/viruses-11-00414-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a282/6563206/d85052694c21/viruses-11-00414-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a282/6563206/485699107501/viruses-11-00414-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a282/6563206/e54bd0a3b91f/viruses-11-00414-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a282/6563206/42b70d46cdf5/viruses-11-00414-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a282/6563206/e418781bf545/viruses-11-00414-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a282/6563206/4a4414be034b/viruses-11-00414-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a282/6563206/6288e840c88d/viruses-11-00414-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a282/6563206/d85052694c21/viruses-11-00414-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a282/6563206/485699107501/viruses-11-00414-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a282/6563206/e54bd0a3b91f/viruses-11-00414-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a282/6563206/42b70d46cdf5/viruses-11-00414-g007.jpg

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