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GFP Labelled Newcastle Disease Virus

For research use only. Not intended for any clinical use.
Cat.No.
OTV-009
Description
Newcastle disease virus (NDV) is a non-segmented, single-stranded negative-sense RNA virus which belongs to the genus Avulavirus within the subfamily Paramyxovirinae of the family Paramyxoviridae. NDV can cause diseases in humans. This virus is an engineered recombinant NDV expressing the green fluorescent protein (GFP). It can be used as an efficient tool for studying NDV. This virus should be handled in BSL2 facilities.
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Dry ice
Storage
-80˚C

Background

Case Study

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Newcastle disease virus is an avian paramyxovirus type I of the genus Newcastle disease-like virus of the family Paramyxoviridae. The virus is present in all tissues, organs, body fluids, secretions and excretions of sick birds, with the highest levels of toxins in the brain, spleen and lungs, and the longest duration of toxins in the bone marrow. Newcastle disease virus can enter the body through the digestive tract or respiratory tract, or through the conjunctiva of the eye, injured skin and cloacal mucosa. The virus quickly multiplies at the site of invasion within 24 hours, then enters the blood and spreads throughout the body, causing viremia. At the same time, the virus also causes serious damage to the heart and vascular system, leading to myocardial degeneration and heart failure, thereby causing a high degree of blood circulation disorder. In the respiratory tract, catarrhal inflammation and bleeding mainly occur, causing the trachea to be blocked by exuded mucus, causing severe breathing difficulties. In the later stages of the disease, the virus invades the central nervous system, often causing non-suppurative encephalitis changes, leading to neurological symptoms. GFP is a protein originally derived from the jellyfish Aequorea victoria, which emits bright green fluorescence when exposed to ultraviolet or blue light. Integration of the GFP gene into the NDV genome has enabled researchers to visually track the virus in living cells and organisms, greatly enhancing our understanding of viral replication, transmission, and pathogenesis. This real-time visualization has helped identify the cellular and molecular mechanisms that control viral replication and immune evasion. In addition, GFP-tagged NDV is a valuable tool for the development and evaluation of antiviral drugs and vaccines, enabling precise measurement of viral load and effectiveness of therapeutic interventions.

Interferon regulatory factors (IRFs) play key roles in multiple aspects of immune responses, and IRF1, IRF3, and IRF7 are positive regulators of IFN induction in mammals. However, IRF3, the most critical regulator in mammals, is naturally absent in birds. In this study, we cloned goose IRF1 (GoIRF1) and performed a series of bioinformatics analyses to compare the protein homology of GoIRF1 with IRF1 in other species. Overexpression of GoIRF1 in DF-1 cells induced activation of IFN-β, and this activation was independent of the dose of transfected GoIRF1 plasmid. Overexpression of GoIRF1 in goose embryonic fibroblasts (GEFs) induced the expression of IFNs, proinflammatory cytokines, and IFN-stimulated genes (ISGs). It also inhibited the replication of green fluorescent protein (GFP)-labelled Newcastle disease virus (NDV) (NDV-GFP) and GFP-labelled vesicular stomatitis virus (VSV) (VSV-GFP). These results suggest that GoIRF1 is an important regulator of IFNs, proinflammatory cytokines, and ISGs and plays a role in antiviral innate immunity in geese.

To examine the antiviral effect of GoIRF1, DF-1 cells overexpressing GoIRF1 and normal DF-1 cells were infected with VSV-GFP or NDV-GFP, and fluorescence was measured using a fluorescence microscope. At 14 or 24 h after viral infection, the fluorescence intensities of both VSV-GFP and NDV-GFP in cells overexpressing GoIRF1 were significantly lower than those in control cells (Fig. 1A and B). This result suggests that overexpression of GoIRF1 in DF-1 cells can inhibit the viral replication of VSV-GFP and NDV-GFP. The virus-infected cells were then lysed and collected for Western blot analysis. The GFP protein expression levels of NDV-GFP and VSV-GFP in cells overexpressing GoIRF1 were significantly lower than those in control (transfected with an empty vector) cells.

GoIRF1 inhibits viral yield.Figure 1. GoIRF1 inhibits viral yield. (Lin Z, et al., 2022)

Customer Q&As
What is Newcastle Disease Virus?

A: Newcastle Disease Virus (NDV) is a highly contagious virus that primarily affects birds, particularly poultry. It belongs to the Paramyxoviridae family and is classified as Avian Paramyxovirus Serotype 1 (APMV-1).

Which species are susceptible to Newcastle disease virus?

A: NDV can infect a wide range of bird species, including chickens, turkeys, ducks, geese, and wild birds. In addition to birds, some strains of NDV can also infect mammals, including humans, although human infection is rare and typically mild.

What are the symptoms of Newcastle Disease in birds?

A: Symptoms of Newcastle Disease in birds include respiratory distress, coughing, sneezing, greenish diarrhea, nervous signs like tremors and paralysis, decreased egg production, and high mortality rates.

What is the genome size of Newcastle Disease Virus?

A: The genome of the Newcastle Disease Virus (NDV) is approximately 15,186 nucleotides in length and contains six open reading frames (ORFs) which encode for various viral proteins.

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Customer Reviews
Excellent Product Stability

We're extremely satisfied with the stability of the GFP Labelled NDV. Unlike other labelled viruses we've tried, this one maintains strong fluorescence signal over extended incubation periods.

United States

10/03/2020

User-Friendly Handling

Handling the GFP Labelled Newcastle Disease Virus was straightforward and user-friendly.

Germany

03/31/2024

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