ArticleSaudi journal of biological sciences2014
Extensive homologous recombination in classical swine fever virus: A re-evaluation of homologous recombination events in the strain AF407339.
Article in Saudi journal of biological sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 14 citations in OpenAlex.
- A Review of Pseudorabies Virus Variants: Genomics, Vaccination, Transmission, and Zoonotic Potential.Viruses · 2022Review
- Complete genome sequences of classical swine fever virus: Phylogenetic and evolutionary analyses.Frontiers in microbiology · 2022Article
- Porcine reproductive and respiratory syndrome virus genetic variability a management and diagnostic dilemma.Virology journal · 2021Review
- Genetic changes and evolutionary analysis of canine circovirus.Archives of virology · 2021Article
- Recombination shapes African swine fever virus serotype-specific locus evolution.Scientific reports · 2020Article
- Comprehensive codon usage analysis of porcine deltacoronavirus.Molecular phylogenetics and evolution · 2019Article
- Genetic and evolutionary analysis of emerging H3N2 canine influenza virus.Emerging microbes & infections · 2018Article
- Evolution of codon usage in Zika virus genomes is host and vector specific.Emerging microbes & infections · 2016Article
- Genomic analysis of codon usage shows influence of mutation pressure, natural selection, and host features on Marburg virus evolution.BMC evolutionary biology · 2015Article
- Published sequences do not support transfer of oseltamivir resistance mutations from avian to human influenza A virus strains.BMC infectious diseases · 2015Article
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Authors and funding
2 authors at 1 institution in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In this short report, the genome-wide homologous recombination events were re-evaluated for classical swine fever virus (CSFV) strain AF407339. We challenged a previous study which suggested only one recombination event in AF407339 based on 25 CSFV genomes. Through our re-analysis on the 25 genomes in the previous study and the 41 genomes used in the present study, we argued that there should be possibly at least two clear recombination events happening in AF407339 through genome-wide scanning. The reasons for identifying only one recombination event in the previous study might be due to the limited number of available CSFV genome sequences at that time and the limited usage of detection methods. In contrast, as identified by most detection methods using all available CSFV genome sequences, two major recombination events were found at the starting and ending zones of the genome AF407339, respectively. The first one has two parents AF333000 (minor) and AY554397 (major) with beginning and ending breakpoints located at 19 and 607 nt of the genome respectively. The second one has two parents AF531433 (minor) and GQ902941 (major) with beginning and ending breakpoints at 8397 and 11,078 nt of the genome respectively. Phylogenetic incongruence analysis using neighbor-joining algorithm with 1000 bootstrapping replicates further supported the existence of these two recombination events. In addition, we also identified additional 18 recombination events on the available CSFV strains. Some of them may be trivial and can be ignored. In conclusion, CSFV might have relatively high frequency of homologous recombination events. Genome-wide scanning of identifying recombination events should utilize multiple detection methods so as to reduce the risk of misidentification.
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