본문 바로가기 주메뉴 바로가기

제품소개

제품상세페이지

Virongy

[Virongy] Rapid Alpha-Pseudoviruses for Influenza A

Cat-No.



Virongy는 혁신적인 바이러스 연구 및 진단 기술을 개발하는 미국의 바이오기업으로,

바이러스 감염 연구와 치료법 개발을 위한 선도적인 솔루션을 제공합니다.








제품 설명 

 

Rapid Alpha-Pseudoviruses for Influenza A




제품 번호


Strain / Reporter Gene / Size 선택



제품 특징


Rapid Alpha-Pseudovirus for Influenza Virus

Built-to-order alpha-pseudovirus for Influenza viruses (IAV) with the Hemagglutinin (HA), Neuraminidase (NA), Nucleoprotein (NP), Matrix (M1), and Ion Channel (M2).

Applications:

  • IAV pseudovirus transduction of target cells for viral entry and functional studies
  • Rapid Anti-IAV drug screening
  • Rapid Anti-IAV neutralizing antibody screening
  • Determination of seroconversion and seroprotection

A novel rapid hybrid alpha-pseudovirus for Influenza virus (Ha-IAV) and other Orthomyxoviridae viruses are now available at Virongy. Ha-IAV particles are pseudoviruses assembled from the structural proteins of the Influenza virus: Hemagglutinin (HA), Neuraminidase (NA), Nucleoprotein (NP), Matrix (M1), and the Ion Channel (M2). They also encapsulate an alphaviral vector for reporter gene expression. The alpha-pseudoviruses are single-cycle viruses with self-amplifying RNA for rapid quantification of neutralizing antibodies, seroconversion, seroprotection, and entry-inhibiting drugs. These pseudoviruses are BSL-2 safe and ready to use for studying viral entry. Furthermore, we assist our customers in constructing Ha-IAV pseudoviruses at any scale.

  • Seroconversion: The process by which a person develops detectable antibodies in the blood in response to an infection or vaccination. It marks the point at which the immune system begins to produce a measurable immune response, indicating that the body has recognized the pathogen.

  • Seroprotection: The level of antibodies in the bloodstream that is considered sufficient to protect against infection. It is often used as a measure of the effectiveness of a vaccine or immune response, indicating that a person has enough antibodies to prevent illness if exposed to the pathogen. For influenza, a serum neutralization titer of 1:40 or greater at a 50% inhibition of viral infectivity is commonly considered a protected titer

Available Strains: 

  • Influenza A/Brevig-Mission/1/1918(H1N1)
  • Influenza A/California/04/2009(H1N1)
  • Influenza A/Victoria/4897/2022 (H1N1)
  • Influenza A/Darwin/9/2021(H3N2)
  • Influenza A/Thailand/NBL1/2006(H5N1)
  • Influenza A/Texas/37/2024 (H5N1)
  • Influenza A/Jiangsu/1/2013(H7N9)

Need a strain not listed here? Ask us about a custom alpha-pseudovirus for your project. For inquiries, please reach out to us via email: info@virongy.com

To enhance your pseudovirus entry, inquire about receiving a complimentary sample of our proprietary Infectin, which significantly enhances productive viral infection in various host cells, thereby boosting the viral infection rate by 3- to 20-fold.

Background:

Alpha-pseudoviruses are a new tool for research and development. Unlike traditional lentivirus or VSV-based systems, which rely on their respective core structural proteins, our alpha-pseudoviruses contain all the authentic structural components of the influenza virus, including HA, NA, M1, M2, and NP proteins. Providing a more biologically accurate and reliable system for studying seasonal, pandemic, and avian influenza strains. Our new system utilizes an alphaviral vector allowing for rapid and robust quantification of reporter signal (luciferase or GFP) in target cells in as little as 6 hours. With its rapid customization capabilities to emerging threats, enhanced safety profile, and robust performance, the alpha-pseudovirus platform sets a new standard for virology research and pandemic preparedness.

Influenza viruses are enveloped with a segmented, single-stranded negative-sense RNA genome, totaling 13.5 Kb in size, divided into 8 segments that code for 12-14 proteins depending on the strain. These segments vary in size from 890 to 2,341 nt. Virions are typically 80-120 nm in diameter and can take on rounded or filamentous shapes. The virus attaches to host cells via sialic acid receptors using the HA protein and enters the cell through clathrin-mediated endocytosis. Acidification of the endosome triggers fusion of the virus membrane with the vesicle membrane, allowing encapsidated RNA segments to migrate to the nucleus. Replication and transcription of genomic segments follow. The viral RNA polymerase (comprising PB1, PB2, and PA subunits) transcribes one mRNA from each genome segment, initiating transcription by cap-snatching from host cell mRNAs. Viral mRNA is then polyadenylated by the viral polymerase through a poly U track stuttering mechanism. Alternative splicing of MP and NS mRNAs yields mRNA encoding M2 and NEP proteins.  High levels of M1 protein facilitate genome segment export from the nucleus via the NEP protein, then the virus assembly and budding take place at the plasma membrane.




References 


Related links:

Sangsiriwut K, Uiprasertkul M, Payungkorn S, Auewarakul P, Ungchusak K, Chantratit W, Puthavathana P. Full-Genomic Sequences of Highly Pathogenic Avian Influenza H5N1 Virus in Human Tissues Demonstrated Adaptation Change for Growth in MDCK Cell Cultures. Unpublished.

Sangsiriwut K, Uiprasertkul M, Payungkorn S, Auewarakul P, Ungchusak K, Chantratit W, Puthavathana P. Direct Submission. Submitted (30-NOV-2017) Center for Research and Innovation, Faculty of Medical Technology, Mahidol University, 999 Phuttamonthon 4 Rd, Salaya, Nakhon Pathom 73170, Thailand.




Virongy Biosciences의 모든 제품을 만나 보세요!


Products

Virus-Specific Tools

Psedoviruses

Kits and Reagents

Transduction Enhancers

Cell Lines


Services

Viral Neutralization Assay Services

Peptide Synthesis

Vector Synthesis


Virongy Biosciences - Exclusive Distributor in South Korea "Morebio" 한국 독점 대리점 "모아바이오"