Molecular detection and phylogenetic analysis of lumpy skin disease virus from outbreaks in Uganda 2017-2018.


Journal

BMC veterinary research
ISSN: 1746-6148
Titre abrégé: BMC Vet Res
Pays: England
ID NLM: 101249759

Informations de publication

Date de publication:
21 Feb 2020
Historique:
received: 12 09 2019
accepted: 14 02 2020
entrez: 23 2 2020
pubmed: 23 2 2020
medline: 29 10 2020
Statut: epublish

Résumé

Lumpy skin disease (LSD) is an infectious viral disease of cattle caused by a Capripoxvirus. LSD has substantial economic implications, with infection resulting in permanent damage to the skin of affected animals which lowers their commercial value. In Uganda, LSD is endemic and cases of the disease are frequently reported to government authorities. This study was undertaken to molecularly characterize lumpy skin disease virus (LSDV) strains that have been circulating in Uganda between 2017 and 2018. Secondly, the study aimed to determine the phylogenetic relatedness of Ugandan LSDV sequences with published sequences, available in GenBank. A total of 7 blood samples and 16 skin nodule biopsies were screened for LSDV using PCR to confirm presence of LSDV nucleic acids. PCR positive samples were then characterised by amplifying the GPCR gene. These amplified genes were sequenced and phylogenetic trees were constructed. Out of the 23 samples analysed, 15 were positive for LSDV by PCR (65.2%). The LSDV GPCR sequences analysed contained the unique signatures of LSDV (A11, T12, T34, S99, and P199) which further confirmed their identity. Sequence comparison with vaccine strains revealed a 12 bp deletion unique to Ugandan outbreak strains. Phylogenetic analysis indicated that the LSDV sequences from this study clustered closely with sequences from neighboring East African countries and with LSDV strains from recent outbreaks in Europe. It was noted that the sequence diversity amongst LSDV strains from Africa was higher than diversity from Eurasia. The LSDV strains circulating in Uganda were closely related with sequences from neighboring African countries and from Eurasia. Comparison of the GPCR gene showed that outbreak strains differed from vaccine strains. This information is necessary to understand LSDV molecular epidemiology and to contribute knowledge towards the development of control strategies by the Government of Uganda.

Sections du résumé

BACKGROUND BACKGROUND
Lumpy skin disease (LSD) is an infectious viral disease of cattle caused by a Capripoxvirus. LSD has substantial economic implications, with infection resulting in permanent damage to the skin of affected animals which lowers their commercial value. In Uganda, LSD is endemic and cases of the disease are frequently reported to government authorities. This study was undertaken to molecularly characterize lumpy skin disease virus (LSDV) strains that have been circulating in Uganda between 2017 and 2018. Secondly, the study aimed to determine the phylogenetic relatedness of Ugandan LSDV sequences with published sequences, available in GenBank.
RESULTS RESULTS
A total of 7 blood samples and 16 skin nodule biopsies were screened for LSDV using PCR to confirm presence of LSDV nucleic acids. PCR positive samples were then characterised by amplifying the GPCR gene. These amplified genes were sequenced and phylogenetic trees were constructed. Out of the 23 samples analysed, 15 were positive for LSDV by PCR (65.2%). The LSDV GPCR sequences analysed contained the unique signatures of LSDV (A11, T12, T34, S99, and P199) which further confirmed their identity. Sequence comparison with vaccine strains revealed a 12 bp deletion unique to Ugandan outbreak strains. Phylogenetic analysis indicated that the LSDV sequences from this study clustered closely with sequences from neighboring East African countries and with LSDV strains from recent outbreaks in Europe. It was noted that the sequence diversity amongst LSDV strains from Africa was higher than diversity from Eurasia.
CONCLUSION CONCLUSIONS
The LSDV strains circulating in Uganda were closely related with sequences from neighboring African countries and from Eurasia. Comparison of the GPCR gene showed that outbreak strains differed from vaccine strains. This information is necessary to understand LSDV molecular epidemiology and to contribute knowledge towards the development of control strategies by the Government of Uganda.

Identifiants

pubmed: 32085763
doi: 10.1186/s12917-020-02288-5
pii: 10.1186/s12917-020-02288-5
pmc: PMC7035724
doi:

Substances chimiques

Receptors, Chemokine 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

66

Références

J Gen Virol. 2009 Aug;90(Pt 8):1967-1977
pubmed: 19339476
Front Microbiol. 2016 Jun 29;7:1022
pubmed: 27446057
Vet Rec. 1990 Dec 1;127(22):549-50
pubmed: 2281596
Antiviral Res. 2013 May;98(2):261-5
pubmed: 23428671
Transbound Emerg Dis. 2017 Jun;64(3):729-745
pubmed: 26564428
Transbound Emerg Dis. 2018 Jun;65(3):916-920
pubmed: 29363284
Antiviral Res. 2015 Jul;119:28-35
pubmed: 25907637
J Virol Methods. 1998 Sep;74(1):1-7
pubmed: 9763122
Onderstepoort J Vet Res. 2005 Jun;72(2):153-64
pubmed: 16137133
PLoS One. 2018 Dec 12;13(12):e0207480
pubmed: 30540759
Virol J. 2010 Sep 21;7:245
pubmed: 20854693
Virol J. 2012 Jan 20;9:25
pubmed: 22264255
Transbound Emerg Dis. 2018 Feb;65(1):240-243
pubmed: 28239954
J Virol Methods. 2017 Nov;249:48-57
pubmed: 28837841
BMC Vet Res. 2019 Jul 8;15(1):236
pubmed: 31286926
Transbound Emerg Dis. 2016 Dec;63(6):e288-e295
pubmed: 25754131
Prev Vet Med. 2018 Dec 5;:
pubmed: 30553537
BMC Vet Res. 2018 Jun 1;14(1):174
pubmed: 29859091
Vet World. 2018 Aug;11(8):1150-1158
pubmed: 30250377
Transbound Emerg Dis. 2012 Feb;59(1):40-8
pubmed: 21749675
Transbound Emerg Dis. 2008 Sep;55(7):299-307
pubmed: 18503511
Vet Microbiol. 2017 Mar;201:78-84
pubmed: 28284627
Zentralbl Veterinarmed B. 1982 Feb;29(1):31-6
pubmed: 7090644
Prev Vet Med. 2017 Nov 1;147:100-107
pubmed: 29254706
J Virol. 2001 Aug;75(15):7122-30
pubmed: 11435593

Auteurs

Sylvester Ochwo (S)

College of Veterinary Medicine, Animal resources and Biosecurity, Makerere University, P.O.BOX 7062, Kampala, Uganda.

Kimberly VanderWaal (K)

College of Veterinary Medicine, University of Minnesota, 1365 Gortner Avenue St. Paul, MN, Minneapolis, MN, 55108, USA.

Christian Ndekezi (C)

College of Veterinary Medicine, Animal resources and Biosecurity, Makerere University, P.O.BOX 7062, Kampala, Uganda.

Joseph Nkamwesiga (J)

College of Veterinary Medicine, Animal resources and Biosecurity, Makerere University, P.O.BOX 7062, Kampala, Uganda.

Anna Munsey (A)

College of Veterinary Medicine, University of Minnesota, 1365 Gortner Avenue St. Paul, MN, Minneapolis, MN, 55108, USA.

Sarah Gift Witto (SG)

College of Veterinary Medicine, Animal resources and Biosecurity, Makerere University, P.O.BOX 7062, Kampala, Uganda.

Noelina Nantima (N)

Ministry of Agriculture Animal Industry & Fisheries, Berkley Ln, Entebbe, Uganda.

Franklin Mayanja (F)

Ministry of Agriculture Animal Industry & Fisheries, Berkley Ln, Entebbe, Uganda.

Anna Rose Ademun Okurut (ARA)

Ministry of Agriculture Animal Industry & Fisheries, Berkley Ln, Entebbe, Uganda.

David Kalenzi Atuhaire (DK)

College of Veterinary Medicine, Animal resources and Biosecurity, Makerere University, P.O.BOX 7062, Kampala, Uganda.

Frank Norbert Mwiine (FN)

College of Veterinary Medicine, Animal resources and Biosecurity, Makerere University, P.O.BOX 7062, Kampala, Uganda. fmwiine@gmail.com.

Articles similaires

Genome, Chloroplast Phylogeny Genetic Markers Base Composition High-Throughput Nucleotide Sequencing
Robotic Surgical Procedures Animals Humans Telemedicine Models, Animal

Odour generalisation and detection dog training.

Lyn Caldicott, Thomas W Pike, Helen E Zulch et al.
1.00
Animals Odorants Dogs Generalization, Psychological Smell
Animals TOR Serine-Threonine Kinases Colorectal Neoplasms Colitis Mice

Classifications MeSH