Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Duck plague virus Glycoprotein J is functional but slightly impaired in viral replication and cell-to-cell spread

28 Feb 2018

Abstract excerpt

To analyse the function of the duck plague virus (DPV) glycoprotein J homologue (gJ), two different mutated viruses, a gJ deleted mutant ΔgJ and a gJR rescue mutant gJR with US5 restored were generated. All recombinant viruses were constructed by using two-step of RED recombination system implemented on the duck plague virus Chinese virulent strain (DPV CHv) genome cloned into a bacterial artificial chromosome....

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Animal Disease Management and Epidemiology
Share to Herpesvirus Infections and Treatments
Share to Viral gastroenteritis research and epidemiology

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 29511274
DOI: 10.1038/s41598-018-22447-x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 26 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Duck plague virus Glycoprotein J is functional but slightly impaired in viral replication and cell-to-cell spreadPMID 29511274Read ↗

The Pivotal Roles of US3 Protein in Cell-to-Cell Spread and Virion Nuclear Egress of Duck Plague VirusSemantic proximity Read ↗

The LORF5 Gene Is Non-essential for Replication but Important for Duck Plague Virus Cell-to-Cell Spread Efficiently in Host CellsSemantic proximity Read ↗

Evaluation of safety and immunogenicity of duck-plague virus gC/gE double gene deletionSemantic proximity Read ↗

N-glycosylation of envelope glycoprotein gI is crucial for the duck plague virus proliferation and virulenceSemantic proximity Read ↗

Evaluation of the Safety and Immunogenicity of Duck-Plague Virus gE MutantsSemantic proximity Read ↗

Simultaneous Tracking of Capsid, Envelope Protein Localization in Living Cells Infected with Double Fluorescent Duck Enteritis VirusSemantic proximity Read ↗

N-glycosylation of the envelope glycoprotein I is essential for the proliferation and virulence of the duck plague virusSemantic proximity Read ↗

Preliminary study of the UL55 gene based on infectious Chinese virulent duck enteritis virus bacterial artificial chromosome cloneSemantic proximity Read ↗

A Recombinant Duck Plague Virus Containing the ICP27 Deletion Marker Provides Robust Protection in DucksSemantic proximity Read ↗

The 164 K, 165 K, and 167 K residues of VP1 are vital for goose parvovirus proliferation in GEFs based on PCR-based reverse genetics system.Semantic proximity Read ↗

Glycoprotein gH of Pseudorabies Virus is Essential for Penetration and Propagation in Cell Culture and in the Nervous System of MiceSemantic proximity Read ↗

Novel reverse genetics of genotype I and III Japanese encephalitis viruses assembled through transformation associated recombination in yeast: The reporter viruses expressing a green fluorescent protein for the antiviral screening assay.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.