Lack of association between amino acid sequences of the bovine leukemia virus envelope and varying stages of infection in dairy cattle

2020 ◽  
Vol 278 ◽  
pp. 197866
Author(s):  
Fernando Cerón Téllez ◽  
Ana Silvia González Méndez ◽  
Jorge Luis Tórtora Pérez ◽  
Elizabeth Loza-Rubio ◽  
Hugo Ramírez Álvarez
2021 ◽  
Vol 91 (3) ◽  
pp. 237-247
Author(s):  
Feray Alkan ◽  
◽  
Ilke Karayel-Hacioglu ◽  
Selda Duran Yelken ◽  
Nuvit Coskun

Bovine leukemia virus (BLV) infection is widespread worldwide and causes significant economic losses in the livestock industry. In this study, to identify the genotypes and to investigate the molecular characterization of BLV strains, we analyzed 25 BLV strains from cattle housed in six herds located in several Turkish geographical regions. Phylogenetic analysis, based on a partial or full-length sequence of the env gp51 gene of BLVs, showed that all Turkish BLVs belonged to genotype 1. The alignment of the deduced amino acid sequences demonstrated fourteen amino acid substitutions in different regions of the env gp51. This study updates our knowledge of BLV in Turkey. Further studies are needed to understand the molecular epidemiology and implement a comprehensive BLV control program in Turkey.


Animals ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1404
Author(s):  
Ali Sakhawat ◽  
Marzena Rola-Łuszczak ◽  
Zbigniew Osiński ◽  
Nazia Bibi ◽  
Jacek Kuźmak

The objective of this study was to determine the true seroprevalence of bovine leukemia virus (BLV) infection in dairy cattle from Pakistan at the animal and herd-level. We tested 1380 dairy cattle from 451 herds and 92 water buffalo. The sera were tested by ELISA and the results were analyzed using Bayesian inference. The median posterior estimate of the herd level true BLV prevalence was 1.4%, with a 95% credible interval (CI) 0.7–3.1, whereas the median posterior estimate of the within-farm true seroprevalence was 3.8% with a 95% CI 2.8–4.8. All 92 sera collected from water buffalo were negative. Several risk factors potentially associated with seropositivity to BLV infections in Pakistan were analyzed using logistic regression model based on calculation of an odds ratio (OR). The study showed an association between seropositivity and medium herd (≥50) size (OR = 23.57, 95% CI: 3.01–103.48). Common housing of indigenous cattle with exotic-breed cattle (OR = 0.67, 95% CI: 06–2.35) or housing indigenous or their crossbred cattle with exotic-breed cattle (OR = 0.95, 95% CI: 0.14–3.01) had no effect on the BLV seroprevalence. Similarly, common housing of cattle and water buffalo was not risk factor for increased BLV seropositivity (OR = 27.10, 95% CI: 0.63–119.34).


Virology ◽  
1989 ◽  
Vol 169 (1) ◽  
pp. 27-33 ◽  
Author(s):  
Daniel Portetelle ◽  
Dominique Couez ◽  
Claudine Bruck ◽  
Richard Kettmann ◽  
Marc Mammerickx ◽  
...  

1977 ◽  
Vol 63 (5) ◽  
pp. 407-413
Author(s):  
Domenico Rutili ◽  
Maurizio Severini ◽  
Luigi Rampichini ◽  
Francesco Titoli ◽  
Umberto Chicchini

In order to find suitable diagnostic procedures to use in an epidemiologic survey for the detection of animals infected with the bovine leukemia virus (BLV), the authors conducted an investigation on 262 Friesian dairy cattle. The results of hematologic, serologic, and electron microscopic examinations are reported. Evaluation of the results demonstrated the validity of the immunodiffusion and immunofluorescence tests and the opportunity for their use in conjunction with examination of the blood picture. From the data reported it would appear useful to extend the investigation to the herds without history of lymphosarcoma.


2019 ◽  
Vol 31 (4) ◽  
pp. 568-571
Author(s):  
Masataka Akagami ◽  
Shoko Oya ◽  
Yuki Kashima ◽  
Satoko Seki ◽  
Yoshinao Ouchi ◽  
...  

The European Community’s leukosis key (EC key) is a well-known hematologic method for detecting bovine leukemia virus (BLV) infection in dairy cattle. The key identifies infected cattle with persistent lymphocytosis via a combination of lymphocyte count (LC) and age. Using the EC key to identify BLV-infected Japanese black (JB) cattle is problematic, however, given the inherently lower LCs of JB cattle compared to dairy cattle. We analyzed the LC in BLV-positive and -negative JB cattle and estimated LC cutoff values by age using receiver operating characteristic curve analysis. Among the 716 JB blood samples collected, 452 (63%) JB cattle were confirmed as BLV-positive by an antibody ELISA for ≥1-y-old cattle and by real-time PCR for <1-y-old cattle. The cutoff values for the LC in each age group were calculated as 6.3 × 109/L for <1 y, 5.9 × 109/L for 1 to <2 y, 5.5 × 109/L for 2 to <3 y, 4.5 × 109/L for 3 to <6 y, 4.3 × 109/L for 6 to ≤10 y, and 3.7 × 109/L for >10 y. The sensitivity and specificity of the estimated cutoff values were 0.49 (95% confidence interval: 0.44–0.53) and 0.81 (0.75–0.85), whereas those of the EC key were 0.20 (0.16–0.24) and 0.99 (0.97–1.00). Our LC cutoff values for screening JB cattle for BLV infection appear to be preferable to those of the EC key.


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