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Molecular characterization and complete genome sequence of avian paramyxovirus type 4 prototype strain duck/Hong
Baibaswata Nayak1, Sachin Kumar, Peter L Collins
1Virginia-Maryland Regional College of Veterinary Medicine, University of Maryland, College Park, Maryland, USA. bnayak@umd.edu
Background:
Avian paramyxoviruses (APMVs) are frequently isolated from domestic and wild birds throughout the world. All APMVs, except avian metapneumovirus, are classified in the genus Avulavirus of the family Paramyxoviridae. At present, the APMVs of genus Avulavirus are divided into nine serological types (APMV 1-9). Newcastle disease virus represents APMV-1 and is the most characterized among all APMV types. Very little is known about the molecular characteristics and pathogenicity of APMV 2-9.
Results:
As a first step towards understanding the molecular genetics and pathogenicity of APMV-4, we have sequenced the complete genome of APMV-4 strain duck/Hong Kong/D3/75 and determined its pathogenicity in embryonated chicken eggs. The genome of APMV-4 is 15,054 nucleotides (nt) in length, which is consistent with the "rule of six". The genome contains six non-overlapping genes in the order 3'-N-P/V-M-F-HN-L-5'. The genes are flanked on either side by highly conserved transcription start and stop signals and have intergenic sequences varying in length from 9 to 42 nt. The genome contains a 55 nt leader region at 3' end. The 5' trailer region is 17 nt, which is the shortest in the family Paramyxoviridae. Analysis of mRNAs transcribed from the P gene showed that 35% of the transcripts were edited by insertion of one non-templated G residue at an editing site leading to production of V mRNAs. No message was detected that contained insertion of two non-templated G residues, indicating that the W mRNAs are inefficiently produced in APMV-4 infected cells. The cleavage site of the F protein (DIPQR downward arrowF) does not conform to the preferred cleavage site of the ubiquitous intracellular protease furin. However, exogenous proteases were not required for the growth of APMV-4 in cell culture, indicating that the cleavage does not depend on a furin site.
Conclusion:
Phylogenic analysis of the nucleotide sequences of viruses of all five genera of the family Paramyxoviridae showed that APMV-4 is more closely related to the APMVs than to other paramyxoviruses, reinforcing the classification of all APMVs in the genus Avulavirus of the family Paramyxoviridae.
Insights
Avian paramyxovirus type 4 (APMV-4) genome sequencing revealed its genetic makeup and pathogenicity. This study enhances understanding of APMV-4, contributing to avian virus research.
Area of Science:
- Virology
- Molecular Biology
- Genomics
Background:
- Avian paramyxoviruses (APMVs) are widespread in avian populations.
- APMVs, excluding avian metapneumovirus, belong to the Avulavirus genus within Paramyxoviridae.
- APMV-1 (Newcastle disease virus) is well-characterized, while APMV 2-9 remain poorly understood.
Purpose of the Study:
- To investigate the molecular genetics and pathogenicity of APMV-4.
- To sequence the complete genome of APMV-4 strain duck/Hong Kong/D3/75.
- To determine the pathogenicity of APMV-4 in embryonated chicken eggs.
Main Methods:
- Whole-genome sequencing of APMV-4 strain duck/Hong Kong/D3/75.
- Analysis of genome structure, including gene order and intergenic sequences.
- Assessment of pathogenicity in embryonated chicken eggs.
- mRNA analysis to study gene editing (V and W mRNA production).
- F protein cleavage site analysis.
Main Results:
- The complete APMV-4 genome is 15,054 nucleotides, adhering to the "rule of six".
- The genome comprises six genes (N-P/V-M-F-HN-L) with conserved regulatory signals.
- APMV-4 exhibits V mRNA editing, with inefficient W mRNA production.
- The F protein cleavage site (DIPQR↓F) does not require furin for cleavage, as exogenous proteases were not needed for cell culture growth.
Conclusions:
- Phylogenetic analysis confirms APMV-4's close relationship to other APMVs within the Avulavirus genus.
- This study provides foundational molecular data for APMV-4.
- The findings contribute to the classification and understanding of avian paramyxoviruses.
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