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Direct rescue of segmented negative-sense RNA viruses from complementary DNA in monkey kidney Vero cells

09.22.26 | Research Foundation for the State University of New York

This technology enables the direct rescue of segmented negative-sense RNA viruses from complementary DNA in monkey kidney Vero cells, facilitating safer and more efficient live-attenuated vaccine production.

Background :

Segmented negative-sense RNA viruses pose significant challenges for vaccine development due to the complexity of their genomes and the inefficiency of current methods for recovering infectious viruses from complementary DNA. Traditional approaches often rely on tumorigenic baby hamster kidney (BHK) cells, which raise safety concerns for vaccine manufacturing. Additionally, existing transfection technologies struggle to deliver viral cDNA plasmids effectively, limiting the production of live-attenuated vaccines for important pathogens such as the influenza virus, rotavirus, and bunyaviruses.

Technology Overview :

This innovation introduces a novel method to rescue segmented negative-sense RNA viruses directly from complementary DNA (cDNA) plasmids within African green monkey kidney Vero cells, which are a World Health Organization (WHO) acceptable cell substrate for human vaccine manufacturing. The process employs triggered endosome escape technologies to simultaneously deliver viral cDNA plasmids and a bacteriophage T7 DNA-dependent RNA polymerase (DdRp) expression vector. Each viral cDNA plasmid encodes a bacteriophage T7 DdRp promoter that drives transcription of positive-sense antigenomic RNA, which serves as a template for the translation of viral proteins that constitute the viral replication complex. A key novelty is replacing the conventional use of tumorigenic BHK cells with non-cancerous Vero cells, thereby aligning with WHO guidelines for vaccine manufacturing and national regulatory authorities. By modifying existing delivery technologies such as VeroFect, this method improves the uptake and expression of viral components required to generate infectious RNA viruses from cDNA. The approach streamlines the development of live-attenuated vaccines for segmented negative-sense RNA viruses, offering a scalable, regulatory-compliant solution that enables rapid response to emerging viral threats.

Advantages :

• Utilizes non-cancerous Vero cells, reducing the requirement of demonstrating a lack of tumorgenic materials compared to traditional BHK cells.
• Employs triggered endosome escape transfection technique for efficient delivery of viral cDNA plasmids, improving virus recovery rates.
• Supports manufacturing of live-attenuated vaccines for important, segmented negative-sense RNA viruses, including influenza virus, rotavirus, and bunyavirus.
• Reduces reliance on less safe or less efficient cell substrates and transfection methods.
• Enables a scalable, regulatory-friendly platform suitable for human vaccine production.
• Leverages a modified existing technology (VeroFect) to enhance performance without requiring entirely new infrastructure.

Applications :

• Development and production of live-attenuated vaccines targeting segmented negative-sense RNA viruses.
• Research tool for virologists studying viral rescue and replication using cDNA plasmids in non-cancerious cell lines.
• Platform technology for rapid vaccine response against emerging segmented negative-sense RNA virus outbreaks.
• Potential use in improving gene delivery techniques involving RNA virus vectors in the development of candidate vaccines and therapies.
• Commercial vaccine manufacturing that demands high safety and efficiency standards for cell substrates.

Intellectual Property Summary : Patent pending

Stage of Development : Inquire for more information.

Licensing Status : This technology is available for licensing.

About the Research Foundation for the State University of New York:

As the nation's largest research foundation supporting the nation's largest public university system, The Research Foundation for SUNY powers research and innovation to address today's most pressing problems and shape a better future for generations to come. The Research Foundations supports SUNY researchers leading the way globally in AI for the public good, quantum technologies, next-generation semiconductors, biotech and medicine, energy and climate solutions, and more. The Research Foundation for SUNY is a private, nonprofit educational corporation that is tax-exempt under Internal Revenue Code (IRC) Section 501(c)(3). To learn more, please visit us online at rfsuny.org .

About the State University of New York

The State University of New York is the largest comprehensive system of higher education in the United States, and more than 95 percent of all New Yorkers live within 30 miles of any one of SUNY’s 64 colleges and universities. Across the system, SUNY has four academic health centers, five hospitals, four medical schools, two dental schools, a law school, the country’s oldest school of maritime, the state's only college of optometry, 12 Educational Opportunity Centers, over 30 ATTAIN digital literacy labs, and manages one US Department of Energy National Laboratory. In total, SUNY serves about 1.7 million students across its portfolio of credit- and non-credit-bearing courses and programs, continuing education, and community outreach programs. SUNY oversees nearly a quarter of academic research in New York. Research expenditures system-wide are nearly $1.5 billion in fiscal year 2025, including significant contributions from students and faculty. There are more than three million SUNY alumni worldwide, and annually one in three New Yorkers who earn a college degree is a SUNY alum. To learn more about how SUNY creates opportunities, visit suny.edu .

Keywords

Contact Information

Matthew Sheiffer
Research Foundation for the State University of New York
matthew.sheiffer@rfsuny.org

Source

This article is based on a news release from Research Foundation for the State University of New York. BrightSurf curates and republishes science news from research institutions worldwide; the original release is linked below.

How to Cite This Article

APA:
Research Foundation for the State University of New York. (2026, September 22). Direct rescue of segmented negative-sense RNA viruses from complementary DNA in monkey kidney Vero cells. Brightsurf News. https://www.brightsurf.com/news/80E0E4J8/direct-rescue-of-segmented-negative-sense-rna-viruses-from-complementary-dna-in-monkey-kidney-vero-cells.html
MLA:
"Direct rescue of segmented negative-sense RNA viruses from complementary DNA in monkey kidney Vero cells." Brightsurf News, Sep. 22 2026, https://www.brightsurf.com/news/80E0E4J8/direct-rescue-of-segmented-negative-sense-rna-viruses-from-complementary-dna-in-monkey-kidney-vero-cells.html.