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天然大片段缺失与中国近期新出现的禽腺病毒 4 新型基因型的毒力增强无关。

The Natural Large Genomic Deletion Is Unrelated to the Increased Virulence of the Novel Genotype Fowl Adenovirus 4 Recently Emerged in China.

机构信息

State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute of Chinese Academy of Agricultural Sciences, Harbin 150001, China.

Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Disease and Zoonoses, Yangzhou 225009, China.

出版信息

Viruses. 2018 Sep 13;10(9):494. doi: 10.3390/v10090494.

DOI:10.3390/v10090494
PMID:30217040
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6165077/
Abstract

Since 2015, severe hydropericardium-hepatitis syndrome (HHS), caused by a highly pathogenic fowl adenovirus 4 (FAdV-4), emerged in China. In our previous study, the FAdV-4 has been identified as a novel genotype with a unique 1966-bp nucleotide deletion (1966Del) between open reading frame 42 and 43. In this study, the natural 1966Del was frequently identified among 17 clinical isolates and other reported Chinese clinical strains. To investigate the relationship between 1966Del and the increased virulence of the novel FAdV-4, a CRISPR/Cas9 operating platform for FAdV-4 was developed for the first time in this study. Based on this platform, a Re1966 strain was rescued, inserted the relative 1966Del sequence of a nonpathogenic strain KR5. In the pathogenicity study, the Re1966 strain retained high virulence for specific-pathogen-free chickens, similar to the parental wild-type HLJFAd15, although the survival time of chickens infected with Re1966 was much longer. Therefore, the natural 1966Del was identified as a non-essential site for the increased virulence of the emerged novel FAdV-4. Although further research on the virulence-determining region or point within the genome of the novel FAdV-4 is needed, the CRISPR/Cas9 operating platform for the novel FAdV-4 was developed and successfully applied to edit the genomic DNA for the first time, and it provides a novel powerful tool for both basic virology studies and vaccine vector development of FAdVs.

摘要

自 2015 年以来,一种由高致病性禽腺病毒 4(FAdV-4)引起的严重心包炎-肝炎综合征(HHS)在中国出现。在我们之前的研究中,已鉴定出 FAdV-4 为一种新型基因型,其在开放阅读框 42 和 43 之间具有独特的 1966 个核苷酸缺失(1966Del)。在本研究中,在 17 个临床分离株和其他报道的中国临床株中经常发现天然 1966Del。为了研究 1966Del 与新型 FAdV-4 毒力增加之间的关系,本研究首次开发了用于 FAdV-4 的 CRISPR/Cas9 操作平台。基于该平台,拯救了 Re1966 株,并插入了非致病性菌株 KR5 的相对 1966Del 序列。在致病性研究中,Re1966 株对 SPF 鸡保持高致病性,与亲本野生型 HLJFAd15 相似,尽管感染 Re1966 的鸡的存活时间要长得多。因此,天然 1966Del 被鉴定为新型 FAdV-4 毒力增加的非必需位点。尽管需要进一步研究新型 FAdV-4 基因组中决定毒力的区域或位点,但已开发出用于新型 FAdV-4 的 CRISPR/Cas9 操作平台,并首次成功应用于编辑基因组 DNA,为基础病毒学研究和 FAdV 疫苗载体开发提供了一种新的强大工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6851/6165077/bdfba37688fa/viruses-10-00494-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6851/6165077/536f559f4520/viruses-10-00494-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6851/6165077/a3abcc2ba1b1/viruses-10-00494-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6851/6165077/67cba618b44d/viruses-10-00494-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6851/6165077/1aa3077c9386/viruses-10-00494-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6851/6165077/704a275ddff9/viruses-10-00494-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6851/6165077/bdfba37688fa/viruses-10-00494-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6851/6165077/536f559f4520/viruses-10-00494-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6851/6165077/a3abcc2ba1b1/viruses-10-00494-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6851/6165077/67cba618b44d/viruses-10-00494-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6851/6165077/1aa3077c9386/viruses-10-00494-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6851/6165077/704a275ddff9/viruses-10-00494-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6851/6165077/bdfba37688fa/viruses-10-00494-g006.jpg

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