| Literature DB >> 27619840 |
Yan-Dong Tang1, Ji-Ting Liu2, Tong-Yun Wang1, Tong-Qing An1, Ming-Xia Sun1, Shu-Jie Wang1, Qiong-Qiong Fang1, Lin-Lin Hou1, Zhi-Jun Tian1, Xue-Hui Cai3.
Abstract
Currently, pseudorabies virus (PRV) variant strains are outbreaking in China; these variants belong to genotype II PRV. The traditional Bartha-K61 vaccine has failed to provide complete protection against the emergent variant strains. Therefore, rapid attenuation of current epidemic strains is needed for effective PRV control. In this study, we report a rapid method for editing the PRV genome using the CRISPR-Cas9 system. We developed a triple gE/gI/TK gene-inactivated HeN1 PRV strain, because mice were more susceptible to PRV infection, we then evaluated the attenuation of PRV in the mice and demonstrated that modified PRV was fully attenuated. Furthermore, the attenuated strain also induced immune protection in response to a parental PRV challenge. Overall, we showed that PRVs can be rapidly attenuated using CRISPR-Cas9 technology, which will be critical for PRV control, especially when new variant PRV strains emerge.Entities:
Keywords: Attenuation; CRISPR/Cas9; Pseudorabies virus; Vaccine
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Year: 2016 PMID: 27619840 DOI: 10.1016/j.virusres.2016.09.004
Source DB: PubMed Journal: Virus Res ISSN: 0168-1702 Impact factor: 3.303