» Articles » PMID: 26754835

A New Genotype of Bovine Leukemia Virus in South America Identified by NGS-based Whole Genome Sequencing and Molecular Evolutionary Genetic Analysis

Abstract

Background: Bovine leukemia virus (BLV) is a member of retroviridae family, together with human T cell leukemia virus types 1 and 2 (HTLV-1 and -2) belonging to the genes deltaretrovirus, and infects cattle worldwide. Previous studies have classified the env sequences of BLV provirus from different geographic locations into eight genetic groups. To investigate the genetic variability of BLV in South America, we performed phylogenetic analyses of whole genome and partial env gp51 sequences of BLV strains isolated from Peru, Paraguay and Bolivia, for which no the molecular characteristics of BLV have previously been published, and discovered a novel BLV genotype, genotype-9, in Bolivia.

Results: In Peru and Paraguay, 42.3 % (139/328) and over 50 % (76/139) of samples, respectively, were BLV positive. In Bolivia, the BLV infection rate was up to 30 % (156/507) at the individual level. In Argentina, 325/420 samples were BLV positive, with a BLV prevalence of 77.4 % at the individual level and up to 90.9 % at herd level. By contrast, relatively few BLV positive samples were detected in Chile, with a maximum of 29.1 % BLV infection at the individual level. We performed phylogenetic analyses using two different approaches, maximum likelihood (ML) tree and Bayesian inference, using 35 distinct partial env gp51 sequences from BLV strains isolated from Peru, Paraguay, and Bolivia, and 74 known BLV strains, representing eight different BLV genotypes from various geographical locations worldwide. The results indicated that Peruvian and Paraguayan BLV strains were grouped into genotypes-1, -2, and -6, while those from Bolivia were clustered into genotypes-1, -2, and -6, and a new genotype, genotype-9. Interestingly, these results were confirmed using ML phylogenetic analysis of whole genome sequences obtained by next generation sequencing of 25 BLV strains, assigned to four different genotypes (genotypes-1, -2, -6, and -9) from Peru, Paraguay, and Bolivia. Comparative analyses of complete genome sequences clearly showed some specific substitutions, in both structural and non-structural BLV genes, distinguishing the novel genotype-9 from known genotypes.

Conclusions: Our results demonstrate widespread BLV infection in South American cattle and the existence of a new BLV genotype-9 in Bolivia. We conclude that at least seven BLV genotypes (genotypes-1, -2, -4, -5, -6, -7, and -9) are circulating in South America.

Citing Articles

The Prevalence and Molecular Characterization of Bovine Leukemia Virus among Dairy Cattle in Henan Province, China.

Zhao Y, Zhu X, Zhang Z, Chen J, Chen Y, Hu C Viruses. 2024; 16(9).

PMID: 39339874 PMC: 11437460. DOI: 10.3390/v16091399.


Molecular frequency of bovine leukemia virus in Creole cattle of Eastern Colombia.

Jaimes-Duenez J, Goyeneche-Ortiz E, Tique-Oviedo M, Ortiz-Pineda M, Cardenas-Pinto L, Jimenez-Leano A Vet Anim Sci. 2024; 25:100372.

PMID: 39022766 PMC: 11253674. DOI: 10.1016/j.vas.2024.100372.


Characterization and application of recombinant Bovine Leukemia Virus Env protein.

Tome-Poderti L, Olivero-Deibe N, Carrion F, Portela M, Obal G, Cabrera G Sci Rep. 2024; 14(1):12190.

PMID: 38806566 PMC: 11133380. DOI: 10.1038/s41598-024-62811-8.


Genetic Variability of Bovine Leukemia Virus: Evidence of Dual Infection, Recombination and Quasi-Species.

Pluta A, Rola-Luszczak M, Hoffmann F, Donnik I, Petropavlovskiy M, Kuzmak J Pathogens. 2024; 13(2).

PMID: 38392916 PMC: 10893129. DOI: 10.3390/pathogens13020178.


The Global Epidemiology of Bovine Leukemia Virus: Current Trends and Future Implications.

Lv G, Wang J, Lian S, Wang H, Wu R Animals (Basel). 2024; 14(2).

PMID: 38254466 PMC: 10812804. DOI: 10.3390/ani14020297.


References
1.
Monti G, Frankena K, Engel B, Buist W, Tarabla H, de Jong M . Evaluation of a new antibody-based enzyme-linked immunosorbent assay for the detection of bovine leukemia virus infection in dairy cattle. J Vet Diagn Invest. 2005; 17(5):451-7. DOI: 10.1177/104063870501700507. View

2.
Callebaut I, Voneche V, Mager A, Fumiere O, Krchnak V, Merza M . Mapping of B-neutralizing and T-helper cell epitopes on the bovine leukemia virus external glycoprotein gp51. J Virol. 1993; 67(9):5321-7. PMC: 237931. DOI: 10.1128/JVI.67.9.5321-5327.1993. View

3.
BRUCK C, Mathot S, Portetelle D, Berte C, Franssen J, Herion P . Monoclonal antibodies define eight independent antigenic regions on the bovine leukemia virus (BLV) envelope glycoprotein gp51. Virology. 1982; 122(2):342-52. DOI: 10.1016/0042-6822(82)90234-3. View

4.
Arainga M, Takeda E, Aida Y . Identification of bovine leukemia virus tax function associated with host cell transcription, signaling, stress response and immune response pathway by microarray-based gene expression analysis. BMC Genomics. 2012; 13:121. PMC: 3441221. DOI: 10.1186/1471-2164-13-121. View

5.
Alfonso R, Almansa J, Barrera J . [Serological prevalence and evaluation of the risk factors of bovine enzootic leukosis in the Bogotá savannah and the Ubaté and Chiquinquirá Valleys, Colombia]. Rev Sci Tech. 1998; 17(3):723-32. View