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Analysis of Nucleotide Sequence of Tax, miRNA and LTR of Bovine Leukemia Virus in Cattle with Different Levels of Persistent Lymphocytosis in Russia.
Pluta, Aneta; Blazhko, Natalia V; Ngirande, Charity; Joris, Thomas; Willems, Luc; Kuzmak, Jacek.
Affiliation
  • Pluta A; Department of Biochemistry, National Veterinary Research Institute, 24-100 Pulawy, Poland.
  • Blazhko NV; Research Center Innovations, 630039 Novosibirsk, Russia.
  • Ngirande C; Laboratory of Enzyme Analysis and DNA Technologies, Novosibirsk State Agrarian University, St. Dobrolyubova, 630039 Novosibirsk, Russia.
  • Joris T; Molecular and Cellular Epigenetics (Interdisciplinary Cluster for Applied Genoproteomics, GIGA) and Molecular Biology (TERRA), University of Liège (ULiège), 4000 Liege, Belgium.
  • Willems L; Molecular and Cellular Epigenetics (Interdisciplinary Cluster for Applied Genoproteomics, GIGA) and Molecular Biology (TERRA), University of Liège (ULiège), 4000 Liege, Belgium.
  • Kuzmak J; Department of Biochemistry, National Veterinary Research Institute, 24-100 Pulawy, Poland.
Pathogens ; 10(2)2021 Feb 20.
Article in En | MEDLINE | ID: mdl-33672613
ABSTRACT
Bovine Leukemia Virus (BLV) is the etiological agent of enzootic bovine leucosis (EBL), a lymphoproliferative disease of the bovine species. In BLV-infected cells, the long terminal repeat (LTR), the viral Tax protein and viral miRNAs promote viral and cell proliferation as well as tumorigenesis. Although their respective roles are decisive in BLV biology, little is known about the genetic sequence variation of these parts of the BLV genome and their impact on disease outcome. Therefore, the objective of this study was to assess the relationship between disease progression and sequence variation of the BLV Tax, miRNA and LTR regions in infected animals displaying either low or high levels of persistent lymphocytosis (PL). A statistically significant association was observed between the A(+187)C polymorphism in the downstream activator sequence (DAS) region in LTR (p-value = 0.00737) and high lymphocytosis. Our study also showed that the mutation A(-4)G in the CAP site occurred in 70% of isolates with low PL and was not found in the high PL group. Conversely, the mutations G(-133)A/C in CRE2 (46.7%), C(+160)T in DAS (30%) and A(310)del in BLV-mir-B4-5p, A(357)G in BLV-mir-B4-3p, A(462)G in BLV-mir-B5-5p, and GA(497-498)AG in BLV-mir-B5-3p (26.5%) were often seen in isolates with high PL and did not occur in the low PL group. In conclusion, we found several significant polymorphisms among BLV genomic sequences in Russia that would explain a progression towards higher or lower lymphoproliferation. The data presented in this article enabled the classification between two different genotypes; however, clear association between genotypes and the PL development was not found.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Pathogens Year: 2021 Document type: Article Affiliation country: Poland

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Pathogens Year: 2021 Document type: Article Affiliation country: Poland