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Molecular Characterization of African Swine Fever Viruses from Outbreaks in Peri-Urban Kampala, Uganda
African swine fever (ASF) is an infectious transboundary disease of domestic pigs and wild swine and is currently the most serious constraint to piggery in Uganda. The causative agent of ASF is a large double-stranded linear DNA virus with a complex structure. There are twenty-four ASFV genotypes de...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6463604/ https://www.ncbi.nlm.nih.gov/pubmed/31057618 http://dx.doi.org/10.1155/2019/1463245 |
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author | Norbert Mwiine, Frank Nkamwesiga, Joseph Ndekezi, Christian Ochwo, Sylvester |
author_facet | Norbert Mwiine, Frank Nkamwesiga, Joseph Ndekezi, Christian Ochwo, Sylvester |
author_sort | Norbert Mwiine, Frank |
collection | PubMed |
description | African swine fever (ASF) is an infectious transboundary disease of domestic pigs and wild swine and is currently the most serious constraint to piggery in Uganda. The causative agent of ASF is a large double-stranded linear DNA virus with a complex structure. There are twenty-four ASFV genotypes described to date; however, in Uganda, only genotypes IX and X have been previously described. Inadequate ASF outbreak investigation has contributed to the delayed establishment of effective interventions to aid the control of ASF. Continuous virus characterization enhances the understanding of ASF epidemiology in terms of viral genome variations, extent, severity, and the potential source of the viruses responsible for outbreaks. We collected samples from pigs that had died of a hemorrhagic disease indicative of ASF. DNA was extracted from all samples and screened with the OIE recommended diagnostic PCR for ASF. Partial B646L (p72), full-length E183L (p54) genes, and CVR region of the P72 gene were amplified, purified, and sequenced. Web-based BLAST and MEGA X software were used for sequence analysis. ASF was confirmed in 10 of the 15 suspected pig samples. Phylogenetic analysis confirmed circulation of genotype IX by both full-length E183 (p54) and partial B646L (p72) gene sequencing. Intragenotypic resolution of the CVR region revealed major deletions in the virus genome, in some isolates of this study. The marked reduction in the number of tetrameric tandem repeats in some isolates of this study could potentially play a role in influencing the virulence of this particular genotype IX in Uganda. |
format | Online Article Text |
id | pubmed-6463604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-64636042019-05-05 Molecular Characterization of African Swine Fever Viruses from Outbreaks in Peri-Urban Kampala, Uganda Norbert Mwiine, Frank Nkamwesiga, Joseph Ndekezi, Christian Ochwo, Sylvester Adv Virol Research Article African swine fever (ASF) is an infectious transboundary disease of domestic pigs and wild swine and is currently the most serious constraint to piggery in Uganda. The causative agent of ASF is a large double-stranded linear DNA virus with a complex structure. There are twenty-four ASFV genotypes described to date; however, in Uganda, only genotypes IX and X have been previously described. Inadequate ASF outbreak investigation has contributed to the delayed establishment of effective interventions to aid the control of ASF. Continuous virus characterization enhances the understanding of ASF epidemiology in terms of viral genome variations, extent, severity, and the potential source of the viruses responsible for outbreaks. We collected samples from pigs that had died of a hemorrhagic disease indicative of ASF. DNA was extracted from all samples and screened with the OIE recommended diagnostic PCR for ASF. Partial B646L (p72), full-length E183L (p54) genes, and CVR region of the P72 gene were amplified, purified, and sequenced. Web-based BLAST and MEGA X software were used for sequence analysis. ASF was confirmed in 10 of the 15 suspected pig samples. Phylogenetic analysis confirmed circulation of genotype IX by both full-length E183 (p54) and partial B646L (p72) gene sequencing. Intragenotypic resolution of the CVR region revealed major deletions in the virus genome, in some isolates of this study. The marked reduction in the number of tetrameric tandem repeats in some isolates of this study could potentially play a role in influencing the virulence of this particular genotype IX in Uganda. Hindawi 2019-04-01 /pmc/articles/PMC6463604/ /pubmed/31057618 http://dx.doi.org/10.1155/2019/1463245 Text en Copyright © 2019 Frank Norbert Mwiine et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Norbert Mwiine, Frank Nkamwesiga, Joseph Ndekezi, Christian Ochwo, Sylvester Molecular Characterization of African Swine Fever Viruses from Outbreaks in Peri-Urban Kampala, Uganda |
title | Molecular Characterization of African Swine Fever Viruses from Outbreaks in Peri-Urban Kampala, Uganda |
title_full | Molecular Characterization of African Swine Fever Viruses from Outbreaks in Peri-Urban Kampala, Uganda |
title_fullStr | Molecular Characterization of African Swine Fever Viruses from Outbreaks in Peri-Urban Kampala, Uganda |
title_full_unstemmed | Molecular Characterization of African Swine Fever Viruses from Outbreaks in Peri-Urban Kampala, Uganda |
title_short | Molecular Characterization of African Swine Fever Viruses from Outbreaks in Peri-Urban Kampala, Uganda |
title_sort | molecular characterization of african swine fever viruses from outbreaks in peri-urban kampala, uganda |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6463604/ https://www.ncbi.nlm.nih.gov/pubmed/31057618 http://dx.doi.org/10.1155/2019/1463245 |
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