Deleting UL49.5 in duck plague virus causes attachment, entry and spread defects-Reference-Cited by-同舟云学术

Deleting UL49.5 in duck plague virus causes attachment, entry and spread defects

Published:2023-05 Issue: Volume:280 Page:109707
ISSN:0378-1135
Container-title:Veterinary Microbiology
language:en
Short-container-title:Veterinary Microbiology

Author:

Li Chunmei,Wang Mingshu,Cheng Anchun^ORCID,Tian Bin,Huang Juan,Wu Ying,Yang Qiao,Gao Qun,Sun Di,Zhang Shaqiu,Ou Xumin,Mao Sai,Zhao Xinxin,Jia Renyong,Liu Mafeng,Chen Shun,Zhu Dekang

Funder

Earmarked Fund for China Agriculture Research System

Sichuan Veterinary Medicine and Drug Innovation Group of China Agricultural Research System

Publisher

Elsevier BV

Subject

General Veterinary,General Medicine,Microbiology

Reference46 articles.

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3. Herpes simplex virus 1 gN partners with gM to modulate the viral fusion machinery;El Kasmi;J. Virol.,2015

4. The nonessential UL49.5 gene of infectious laryngotracheitis virus encodes an O-glycosylated protein which forms a complex with the non-glycosylated UL10 gene product;Fuchs;Virus Res.,2005

5. In vitro and in vivo relevance of infectious laryngotracheitis virus gJ proteins that are expressed from spliced and nonspliced mRNAs;Fuchs;J. Virol.,2005

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1. Complete Genome Sequence and Construction of an Infectious Bacterial Artificial Chromosome Clone of a Virulent Duck Enteritis Virus Strain XJ;Transboundary and Emerging Diseases;2024-05-17

2. RNA-seq analysis of chlorogenic acid intervention in duck embryo fibroblasts infected with duck plague virus;Virology Journal;2024-03-07

3. N-Linked Glycosylation and Expression of Duck Plague Virus pUL10 Promoted by pUL49.5;Microbiology Spectrum;2023-08-17