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Generation, Amplification, and Titration of Recombinant Respiratory Syncytial Viruses
Published on: April 4, 2019
Infectious bronchitis-virus-like QX strain transmission, pathogenesis, replication, and host miRNA biogenesis pathway
Asad Khan1,2,3, Iftikhar Ali Khan4, Chao Huang1,2
1Laboratory of Experimental Animal Disease Model, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China.
Abstract:
The infectious bronchitis virus (IBV) is an acute, highly contagious, single-stranded RNA (ssRNA) gammacoronavirus mainly transmitted to chickens through the intranasal route. Positive-sense ssRNA viruses primarily act on mRNA and enhance the replication of viral copies. We identified the nasal entry site of the IBV-QX strain and provided insights into the minimal viral replication in systemic organs. Here is an overview of its entry mechanisms and tropism in systemic organ tissues. It enters the host cells via spike proteins, which bind to highly expressed receptors in respiratory, renal, and gastric epithelial cells. Viral RNA primarily replicates in the host cell environment, where it is directly translated into viral proteins. The precise replication of the IBV-QX strain in gastric epithelial cells was previously unknown. Different IBV strains have varying tropism. For the first time, we revealed the key players involved in the microRNA (miRNA) biogenesis pathway by transfecting gastric cells with the IBV-QX strain. Our findings suggest that the QX strain may bind to angiotensin-converting enzyme-2 (ACE2) receptors by circulating throughout the lymphatic system at the very least and influence the translation of argonaute2 (AGO2), Dicer, exportin5 (XPO5), and Drosha proteins. Taken together, QX viral proteins disrupt host miRNA biogenesis, leading to dysregulated immune and cellular responses that enhance viral replication and systemic spread, thereby enabling cross-organ tropism and multi-system pathogenesis.
Insights
Infectious bronchitis virus (IBV) QX strain enters chickens via nasal passages and replicates in gastric cells. It disrupts host microRNA (miRNA) biogenesis, enhancing viral spread and pathogenesis.
Area of Science:
- Virology
- Immunology
- Molecular Biology
Background:
- Infectious bronchitis virus (IBV) is a contagious ssRNA gammacoronavirus primarily affecting chickens.
- IBV transmits intranasally, impacting host cell mRNA and viral replication.
Purpose of the Study:
- To identify the nasal entry site of the IBV-QX strain.
- To investigate IBV-QX replication in systemic organs, particularly gastric epithelial cells.
- To elucidate the mechanisms of IBV-QX entry and tropism, including its effect on miRNA biogenesis.
Main Methods:
- Identification of IBV-QX nasal entry.
- Analysis of viral replication in respiratory, renal, and gastric tissues.
- Transfection of gastric cells with IBV-QX to study miRNA biogenesis pathway involvement.
Main Results:
- The IBV-QX strain enters host cells via spike proteins binding to ACE2 receptors.
- IBV-QX replicates in gastric epithelial cells, a previously uncharacterized tropism.
- QX viral proteins were found to influence key miRNA biogenesis proteins (AGO2, Dicer, XPO5, Drosha), disrupting host miRNA production.
Conclusions:
- The IBV-QX strain exhibits cross-organ tropism, affecting multiple organ systems.
- Disruption of host miRNA biogenesis by IBV-QX enhances viral replication and systemic spread.
- Understanding IBV-QX pathogenesis provides insights into viral strategies for immune evasion and host manipulation.
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