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Published on: September 21, 2011
Role of Small Hydrophobic Protein of J Paramyxovirus in Virulence
Mathew Abraham1, Nicole Michelle Arroyo-Diaz1, Zhuo Li1
1Department of Infectious Diseases, College of Veterinary Medicine, University of Georgia, Athens, Georgia, USA.
Abstract:
J paramyxovirus (JPV) was first isolated from moribund mice with hemorrhagic lung lesions in Australia in 1972. It is a paramyxovirus classified under the newly proposed genus Jeilongvirus JPV has a genome of 18,954 nucleotides, consisting of eight genes in the order 3'-N-P/V/C-M-F-SH-TM-G-L-5'. JPV causes little cytopathic effect (CPE) in tissue culture cells but severe disease in mice. The small hydrophobic (SH) protein is an integral membrane protein encoded by many paramyxoviruses, such as mumps virus (MuV) and respiratory syncytial virus (RSV). However, the function of SH has not been defined in a suitable animal model. In this work, the functions of SH of JPV, MuV, and RSV have been examined by generating recombinant JPV lacking the SH protein (rJPV-ΔSH) or replacing SH of JPV with MuV SH (rJPV-MuVSH) or RSV SH (rJPV-RSVSH). rJPV-ΔSH, rJPV-MuVSH, and rJPV-RSVSH were viable and had no growth defect in tissue culture cells. However, more tumor necrosis factor alpha (TNF-α) was produced during rJPV-ΔSH infection, confirming the role of SH in inhibiting TNF-α production. rJPV-ΔSH induced more apoptosis in tissue culture cells than rJPV, rJPV-MuVSH, and rJPV-RSVSH, suggesting that SH plays a role in blocking apoptosis. Furthermore, rJPV-ΔSH was attenuated in mice compared to rJPV, rJPV-MuVSH, and rJPV-RSVSH, indicating that the SH protein plays an essential role in virulence. The results indicate that the functions of MuV SH and RSV SH are similar to that of JPV SH even though they have no sequence homology.IMPORTANCE Paramyxoviruses are associated with many devastating diseases in animals and humans. J paramyxovirus (JPV) was isolated from moribund mice in Australia in 1972. Newly isolated viruses, such as Beilong virus (BeiPV) and Tailam virus (TlmPV), have genome structures similar to that of JPV. A new paramyxovirus genus, Jeilongvirus, which contains JPV, BeiPV, and TlmPV, has been proposed. Small hydrophobic (SH) protein is present in many paramyxoviruses. Our present study investigates the role of SH protein of JPV in pathogenesis in its natural host. Understanding the pathogenic mechanism of Jeilongvirus is important to control and prevent potential diseases that may emerge from this group of viruses.
Insights
The small hydrophobic (SH) protein of J paramyxovirus (JPV) is crucial for virulence. This study found JPV SH inhibits tumor necrosis factor alpha (TNF-α) production and apoptosis, essential for JPV pathogenesis in mice.
Area of Science:
- Virology
- Molecular Biology
- Immunology
Background:
- J paramyxovirus (JPV), isolated in 1972, belongs to the proposed Jeilongvirus genus.
- Paramyxoviruses cause significant animal and human diseases.
- The function of the small hydrophobic (SH) protein in JPV pathogenesis remained undefined.
Purpose of the Study:
- To investigate the role of JPV SH protein in viral pathogenesis.
- To determine if heterologous SH proteins (from mumps virus and RSV) can complement JPV SH function.
- To elucidate the mechanisms by which JPV SH influences host immune responses and cell viability.
Main Methods:
- Generation of recombinant JPV (rJPV) lacking SH (rJPV-ΔSH) or expressing heterologous SH proteins (rJPV-MuVSH, rJPV-RSVSH).
- Assessment of viral replication in tissue culture cells.
- Quantification of TNF-α production and apoptosis induction during infection.
- Evaluation of viral attenuation in a mouse model.
Main Results:
- Recombinant viruses were viable with no growth defects in cell culture.
- rJPV-ΔSH infection led to increased TNF-α production and apoptosis compared to wild-type and complemented viruses.
- rJPV-ΔSH exhibited significant attenuation in mice, indicating SH is essential for virulence.
- MuV SH and RSV SH could functionally replace JPV SH, despite lacking sequence homology.
Conclusions:
- JPV SH protein plays a critical role in virulence by inhibiting TNF-α production and apoptosis.
- The functions of SH proteins from different paramyxoviruses are conserved.
- Understanding JPV SH function is vital for controlling emerging Jeilongvirus infections.
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