Related Experiment Video
Updated: May 1, 2026

An Improved and High Throughput Respiratory Syncytial Virus RSV Micro-neutralization Assay
Published on: January 26, 2019
A respiratory syncytial virus (RSV) vaccine based on parainfluenza virus 5 (PIV5)
Shannon I Phan1, Zhenhai Chen1, Pei Xu2
1Department of Infectious Diseases, University of Georgia, Athens, GA 30602, United States.
Insights
Parainfluenza virus 5 (PIV5) shows promise as a vaccine vector for respiratory syncytial virus (RSV). PIV5-based vaccines expressing RSV F or G proteins protected mice against RSV challenge without worsening lung pathology.
Area of Science:
- Virology
- Immunology
- Vaccinology
Background:
- Human respiratory syncytial virus (RSV) causes severe respiratory illness and hospitalizations, particularly in infants, with no current vaccine.
- Parainfluenza virus 5 (PIV5), a harmless paramyxovirus, is explored as a vaccine vector.
- Developing effective RSV vaccines is a critical public health need.
Purpose of the Study:
- To assess the efficacy of PIV5 as a vaccine vector for respiratory syncytial virus (RSV).
- To evaluate PIV5 expressing RSV F or G proteins as potential single-dose vaccines.
Main Methods:
- Generated two recombinant PIV5 viruses expressing RSV A2 strain fusion (F) or attachment glycoprotein (G).
- Administered single-dose vaccinations of F-PIV5 or G-PIV5 to BALB/c mice.
- Assessed RSV-specific antibody responses and lung pathology after RSV A2 challenge.
Main Results:
- Both F-PIV5 and G-PIV5 induced RSV antigen-specific antibody responses in mice.
- Antibody profiles (IgG2a/IgG1 ratios) resembled those from wild-type RSV A2 infection.
- Vaccinated mice showed no exacerbated lung lesions upon RSV A2 challenge compared to RSV-immunized controls.
- Both F and G PIV5 vaccines conferred protective immunity against RSV challenge.
Conclusions:
- PIV5 is a viable platform for developing vector-based vaccines against RSV.
- PIV5-expressing RSV F or G proteins can induce protective immunity and are safe in a mouse model.
- Further development of PIV5-based RSV vaccines is warranted.
Abstract:
Human respiratory syncytial virus (RSV) is a leading cause of severe respiratory disease and hospitalizations in infants and young children. It also causes significant morbidity and mortality in elderly and immune compromised individuals. No licensed vaccine currently exists. Parainfluenza virus 5 (PIV5) is a paramyxovirus that causes no known human illness and has been used as a platform for vector-based vaccine development. To evaluate the efficacy of PIV5 as a RSV vaccine vector, we generated two recombinant PIV5 viruses - one expressing the fusion (F) protein and the other expressing the attachment glycoprotein (G) of RSV strain A2 (RSV A2). The vaccine strains were used separately for single-dose vaccinations in BALB/c mice. The results showed that both vaccines induced RSV antigen-specific antibody responses, with IgG2a/IgG1 ratios similar to those seen in wild-type RSV A2 infection. After challenging the vaccinated mice with RSV A2, histopathology of lung sections showed that the vaccines did not exacerbate lung lesions relative to RSV A2-immunized mice. Importantly, both F and G vaccines induced protective immunity. Therefore, PIV5 presents an attractive platform for vector-based vaccines against RSV infection.
More Related Videos
Related Concept Videos
Rous Sarcoma Virus (RSV) and Cancer
RSV is a retrovirus that contains two copies of a plus-strand RNA genome. Its genome consists of four main open...
Rous Sarcoma Virus (RSV) and Cancer
Influenza
Pneumonia I: Introduction
Risk Factors
Various factors influence the likelihood of developing pneumonia. Age plays a crucial role, with infants, children under two, and individuals over 65 at increased risk due to their...
Pneumonia I: Introduction
Viral Meningitis

