Graphene Oxide Nanoparticles Combined with CRISPR/Cas9 System Enable Efficient Inhibition of Pseudorabies Virus

被引:5
|
作者
Li, Shuojun [1 ]
Sun, Yumei [2 ,3 ]
Du, Moqing [5 ]
Shangguan, Aishao [2 ]
Liu, Zhongzhu [2 ]
Li, Wentao [3 ]
Liu Lina [4 ]
Liu, Wenju [2 ]
Zhang, Shujun [2 ]
Han, Heyou [1 ,5 ]
机构
[1] Huazhong Agr Univ, Coll life Sci & Technol, State Key Lab Agr Microbiol, Wuhan 430070, Peoples R China
[2] Huazhong Agr Univ, Key Lab Agr Anim Genet Breeding & Reprod, Minist Educ, Wuhan 430070, Peoples R China
[3] Huazhong Agr Univ, Sch Anim Sci & Technol, Sch Anim Med, State Key Lab Agr Microbiol, Wuhan 430070, Peoples R China
[4] Guizhou Med Univ, Sch Biol & Engn, Dept Biotechnol, Guiyang 550025, Guizhou, Peoples R China
[5] Huazhong Agr Univ, Coll Sci, State Key Lab Agr Microbiol, Wuhan 430070, Peoples R China
基金
中国国家自然科学基金;
关键词
IMMUNE-SYSTEM; INFECTIONS; BACTERIA;
D O I
10.1021/acs.bioconjchem.2c00570
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe an application where graphene oxide nanoparticles (GONs) enable combined inhibition of Pseudorabies Virus (PRV) through delivery of a CRISPR/Cas9 system for targeted cleaving of a PRV genome and direct interaction with viral particles. The sheeted GONs could load CRISPR plasmid DNA (pDNA) to form a small sized, near-spheroidal GONs-CRISPR complex, which enables CRISPR pDNA efficient intracellular delivery and transient expression under serum conditions. Cell studies showed that GONs-CRISPR could allow rapid cellular uptake, endolysosomes escape, and nucleus transport within 3 h. Virus studies demonstrated that the pure GONs have antiviral activity and GONs-CRISPR could significantly inhibit PRV replication and result in progeny PRV decreasing by approximately 4000 times in infected host cells. Transmission electron microscopy (TEM) imaging showed that GONs-CRISPR could destroy the PRV structures by directly interacting with viral particles. This GONs-based strategy may extend the advanced application of the CRISPR system for antiviral action
引用
收藏
页码:326 / 332
页数:7
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