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Related Experiment Video

Updated: May 6, 2026

An In vitro Model to Study Immune Responses of Human Peripheral Blood Mononuclear Cells to Human Respiratory Syncytial Virus Infection
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An In vitro Model to Study Immune Responses of Human Peripheral Blood Mononuclear Cells to Human Respiratory Syncytial Virus Infection

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A Rapid Yeast-Based System for Modifying Respiratory Syncytial Virus.

Mahesh K C1,2, Ilada Thongpan1,2, Namita Bhattarai1,2

  • 1Center for Microbe and Immunity Research, Abigail Wexner Research Institute, Nationwide Children's Hospital, Columbus, OH, USA.

Methods in Molecular Biology (Clifton, N.J.)
|August 29, 2025
PubMed
Summary

Researchers developed a new yeast-based system to quickly create modified respiratory syncytial virus (RSV) strains. This method simplifies genetic engineering for studying RSV infection and developing new therapies.

Keywords:
Copy DNA (cDNA)Homologous recombinationPolymerase chain reaction (PCR)Respiratory syncytial virus (RSV)T7 polymeraseVirus rescue from cDNAYeast-based cDNA assembly

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Generation, Amplification, and Titration of Recombinant Respiratory Syncytial Viruses
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Generation, Amplification, and Titration of Recombinant Respiratory Syncytial Viruses
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Generation, Amplification, and Titration of Recombinant Respiratory Syncytial Viruses

Published on: April 4, 2019

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Area of Science:

  • Virology
  • Molecular Biology
  • Microbiology

Background:

  • Respiratory syncytial virus (RSV) research benefits from genetic modifications for studying viral spread and replication.
  • Previous recombinant systems for RSV genome manipulation were inefficient and time-consuming.
  • Understanding RSV infection in different cell types, including human bronchial epithelial (HBE) cells, is crucial.

Purpose of the Study:

  • To develop an improved and efficient system for constructing and modifying respiratory syncytial virus (RSV) cDNA.
  • To facilitate the rapid generation of RSV mutant viruses for research purposes.

Main Methods:

  • A novel yeast-based cDNA assembly system was employed for RSV genome manipulation.
  • The system streamlines the construction of RSV cDNA clones and modifications.
  • This approach enables the generation of recombinant RSV mutant viruses.

Main Results:

  • The yeast-based system significantly streamlines the construction and modification of RSV cDNA.
  • This methodology allows for the rapid generation of RSV mutant viruses.
  • The system overcomes limitations of previous standard recombinant systems.

Conclusions:

  • The described yeast-based cDNA assembly system offers a faster and more efficient approach for RSV genetic engineering.
  • This advancement will accelerate research into RSV pathogenesis and the development of antiviral strategies.
  • The system enables detailed studies of viral protein function and host-pathogen interactions.