Seroprevalence and risk factors associated with bovine leukemia virus (BLV) seropositivity in cattle herds from Ecuador / Seroprevalencia y factores de riesgo asociados a la seropositividad al virus de la leucemia bovina (BLV) en explotaciones de producción bovina en Ecuador / Seroprevalência e fatores de risco associados à soropositividade do vírus da leucemia bovina (BLV) em rebanhos bovinos do Equador

Abstract Background: Bovine leukemia virus (BLV) is the causative agent of enzootic bovine leukosis (EBL). This disease mainly affects cattle, causing severe economic losses to producers. Objective: To establish individual and herd seroprevalence and determine the risk factors associated with BLV seropositivity for dairy and dual-purpose cattle herds in Ecuador. Methods: A total of 2,668 serum samples from 386 herds were collected. A questionnaire, including variables related to cattle health, management and the environment was completed by each herd. A commercial blocking enzyme-linked immunosorbent assay (ELISA) test was used to determine seropositivity. A generalized estimating equation model (GEE) was developed to determine the factors associated with BLV seropositivity. Results: Individual seroprevalence of BLV infection in Ecuador was 17.3% (CI95% = 15.86-18.74%). Herd prevalence was 37.8% (CI95% = 33.0-42.6%), and intra-herd prevalence ranged between 12.5 and 100% (median: 37.5%). The risk factors associated with BLV seropositivity were artificial insemination (OR: 2,215; CI95% =1.402-3.501), concrete floors (OR: 2.178; CI95% = 1.217-3.889), presence of wild ruminants (OR: 2.998; CI95% = 1.788-5.027), and sampling season (wet; OR: 1.996; CI95% = 1.140-3.497). Conclusions: Results indicate that BLV is widespread in cattle herds in Ecuador. In addition, the study suggests that a control program to fight BLV infection should focus on controlling the risk factors identified.

Resumen Antecedentes: El virus de la leucosis bovina (BLV) es el principal agente etiológico causante de la leucosis enzoótica bovina (EBL). Esta enfermedad afecta a los bovinos causando grandes pérdidas económicas a los productores. Objetivo: Establecer la seroprevalencia y dispersión del BLV, así como los factores de riesgo asociados a la seropositividad en explotaciones lecheras y de doble propósito en Ecuador. Métodos: Se recolectó un total de 2.668 muestras de suero de 386 explotaciones. Se aplicó un cuestionario que incluyó variables relacionadas con la salud del hato, medidas de manejo, y características ambientales de cada explotación. Para los análisis serológicos se utilizó un test inmunológico ligado a enzimas (ELISA). Para definir los factores de riesgo asociados a la seropositividad a BLV se desarrolló un modelo utilizando ecuaciones de estimación generalizadas (GEE). Resultados: La seroprevalencia de BLV en Ecuador fue de 17,3% (IC95% = 15,86-18,74%). La dispersión fue de 37,8% (IC95%= 33,0-42,6%), y la prevalencia intra-hato alcanzó rangos entre 12,5-100% (media: 37,5%). Los factores de riesgo asociados a la seropositividad a BLV fueron: inseminación artificial (OR: 2,215; IC95% = 1,402-3,501), piso de concreto (OR: 2,178; IC95% = 1,217-3,889), presencia de rumiantes salvajes (OR: 2,998; IC95% = 1,788-5,027), y temporada de muestreo (húmeda; OR: 1,996; IC95% = 1,140-3,497). Conclusiones: Los resultados indican que el BLV se encuentra disperso en las explotaciones de Ecuador. Adicionalmente, se sugiere la implementación de un programa de control para la lucha contra el BLV, debiéndose considerar medidas que se enfoquen al control de los factores de riesgo identificados en esta investigación.

Resumo Antecedentes: O vírus da leucemia bovina (BLV) é o principal agente causador da leucose enzoótica bovina (EBL). Esta doença afeta o gado causando graves prejuízos econômicos aos produtores. Objetivo: Estabelecer a soroprevalência e dispersão do BLV, assim como os fatores de risco associados à soropositividade nas produções leiteiras e de duplo propósito no Equador. Métodos: Um total de 2.668 amostras de soro de 386 explorações foram coletadas. Foi aplicado um questionário que incluía variáveis relacionadas à saúde do rebanho, medidas de manejo e ambiente para cada exploração. Para a análise sorológica foi utilizado um teste imunológico sobre enzimas (ELISA) para determinação da soropositividade. Para definir os fatores de risco associados à soropositividade a BLV, foi utilizado um modelo de equações estimativas generalizadas (GEE). Resultados: A soroprevalência de BLVno Equador é de 17,3% (IC95% = 15,86-18,74%). La dispersão de 37,8% (IC95% = 33,0-42,6%), e a prevalência intra-rebanho alcançou entre 12,5-100% (media: 37,5%). Os fatores de risco associados à soropositividade a BLV foram inseminação artificial (OR: 2,215; IC95% = 1,402-3,501), chão de concreto (OR: 2,178; IC95% = 1,217-3,889), presença de ruminantes selvagens (OR: 2,998; IC95% = 1,788-5,027) e época da amostragem (úmida; OR: 1,996; IC95% = 1,140-3,497). Conclusões: Os resultados indicam que o BLV se encontra disseminado nas explorações no Equador. Adicionalmente, o estudo pode contribuir para a implementação de um programa de controle para a luta contra o BLV, devendo-se considerar ações de controle dos fatores de risco identificados nesta investigação.

Infección experimental en ovinos con el virus de leucosis bovina: dosis mínima de células BLV-FLK y virus libre de células, y actividad neutralizante de anticuerpos naturales / Experimental infection of sheep with Bovine leukemia virus (BLV): Minimum dose of BLV-FLK cells and cell-free BLV and neutralization activity of natural antibodies

Abstract Bovine leukemia virus (BLV) is an important cattle pathogen that causes major economic losses worldwide, especially in dairy farms. The use of animal models provides valuable insight into the pathogenesis of viral infections. Experimental infections of sheep have been conducted using blood from BLV-infected cattle, infectious BLV molecular clones or tumor-derived cells. The Fetal Lamb Kidney cell line, persistently infected with BLV (FLK-BLV), is one of the most commonly used long-term culture available for the permanent production of virus. FLK-BLV cells or the viral particles obtained from the cell-free culture supernatant could be used as a source of provirus or virus to experimentally infect sheep. In this report, we aimed to determine the minimum amount of FLK-BLV cells or cell-free supernatant containing BLV needed to produce infection in sheep. We also evaluated the amount of antibodies obtained from a naturally-infected cow required to neutralize this infection. We observed that both sheep experimentally inoculated with 5000 FLK-BLV cells became infected, as well as one of the sheep receiving 500 FLK-BLV cells. None of the animals inoculated with 50 FLK-BLV cells showed evidence of infection. The cell-free FLK-BLV supernatant proved to be infective in sheep up to a 1:1000 dilution. Specific BLV antibodies showed neutralizing activity as none of the sheep became infected. Conversely, the animals receiving a BLV-negative serum showed signs of BLV infection. These results contribute to the optimization of a sheep bioassay which could be useful to further characterize BLV infection.

Resumen El virus de la leucosis bovina (bovine leukemia virus [BLV]) es un importante agente patógeno del ganado que causa importantes pérdidas económicas en todo el mundo, especialmente en los rodeos lecheros. El uso de modelos animales proporciona información valiosa sobre la patogénesis de las infecciones virales. Se realizaron infecciones experimentales en ovejas usando sangre de bovinos infectados con BLV, clones moleculares de BLV infecciosos o células derivadas de tumores. La línea celular Fetal Lamb Kidney, persistentemente infectada con el BLV (FLK-BLV), es uno de los cultivos a largo plazo más utilizados para la producción permanente de virus. Las células FLK-BLV o las partículas virales obtenidas del sobrenadante del cultivo libre de células podrían usarse como fuente de provirus o de virus para infectar experimentalmente ovejas. En este trabajo, nuestro objetivo fue determinar la cantidad mínima de células FLK-BLV o de sobrenadante libre de células que contiene BLV necesaria para producir infección en ovejas. También evaluamos la cantidad de anticuerpos bovinos anti-BLV necesaria para neutralizar la infección. Observamos que las dos ovejas inoculadas experimentalmente con 5000 células FLK-BLV se infectaron, y que una de las dos ovejas que recibieron 500 células FLK-BLV se infectó. Ninguno de los animales inoculados con 50 células FLK-BLV mostró evidencia de infección. El sobrenadante FLK-BLV libre de células demostró ser infectivo en ovejas hasta la dilución 1:1000. Los anticuerpos BLV específicos mostraron actividad neutralizante, ya que ninguna de las ovejas se infectó. Por el contrario, los animales que recibieron un suero BLV negativo mostraron signos de infección por BLV. Estos resultados contribuyen a la optimización de un bioensayo en ovejas útil para caracterizar la infección por BLV.

Performance assessment of imported ELISA in the serodiagnosis of the enzootic bovine leukosis in herds of Pernambuco state, Brazil / Avaliação do desempenho de ELISA importado no sorodiagnóstico da leucose enzoótica bovina em rebanhos do estado de Pernambuco, Brasil

Enzootic bovine leukosis (EBL) is an infectious disease of cosmopolitan distribution and chronic character caused by a virus of the Retroviridae family, bovine leukemia virus (BLV). The epidemiological situation of EBL in Brazil has motivated studies to improve its diagnosis, based on the recommended serological techniques: agar gel immunodiffusion (AGID) and enzyme-linked immunosorbent assay (ELISA). This study was designed to evaluate the use of imported ELISA for the detection of BLV in dairy herds raised in Pernambuco, Brazil, comparing it to AGID. Blood serum samples from 327 dairy cattle from the state of Pernambuco were tested to AGID and the imported commercial ELISA CHEKIT-Leucose-serum, produced by the IDEXX® laboratory for the diagnosis of EBL. Discarding 25 inconclusive samples from one or both tests, 302 samples were analyzed, being 24.1% positive (73/302) in the AGID and 45% (136/302) in the ELISA, which compared to the AGID, a technique considered standard, presented sensitivity of 98.6%, specificity of 72% and Kappa coefficient of 0.55. The lack of agreement in the diagnostic methods was probably due to the high sensitivity of the ELISA, which makes it possible to detect antibodies even in situations with low serum levels. Although AGID has been shown to be an efficient test so far, in more advanced stages of an EBL control and eradication program, with low prevalence rates, ELISA will present better performance, due to its higher sensitivity, avoiding the permanence of animals that spread the disease in the herds.(AU)

A leucose enzoótica bovina (LEB) é uma doença infecciosa de distribuição cosmopolita e caráter crônico causada por um vírus da família Retroviridae, o vírus da leucemia bovina (VLB). A situação epidemiológica da LEB no Brasil vem motivando estudos para o aprimoramento do seu diagnóstico, tendo como base as técnicas sorológicas recomendadas: imunodifusão em gel de ágar (IDGA) e Enzyme-Linked Immunoabsorbent Assay (ELISA). Este estudo teve como objetivo avaliar o uso de ELISA importado para a detecção do VLB em rebanhos leiteiros criados em Pernambuco, Brasil, comparando-o ao IDGA. Amostras de soro sanguíneo de 327 bovinos leiteiros do estado de Pernambuco foram testadas para IDGA e ELISA comercial importado CHEKIT-Leucose-serum, produzido pelo laboratório IDEXX® para o diagnóstico da LEB. Descartadas 25 amostras inconclusivas de um ou ambos os testes, foram analisadas 302 amostras, sendo 24,1% positivas (73/302) na IDGA e 45% (136/302) no ELISA, que em relação à IDGA, técnica considerada padrão, apresentou sensibilidade de 98,6%, especificidade de 72% e coeficiente Kappa de 0.55. A falta de concordância entre os métodos diagnósticos deveu-se, provavelmente, à elevada sensibilidade do ELISA, que possibilita detectar anticorpos mesmo em situações com baixos teores séricos. Apesar da IDGA se mostrar até o momento um teste eficiente, em etapas mais avançadas de um programa de controle e erradicação da LEB, com baixos índices de prevalência, o ELISA apresentará melhor desempenho, por possuir maior sensibilidade, evitando-se a permanência de animais disseminadores da doença nos rebanhos.​(AU)

El componente racial influencia la resistencia a la infección con el virus de la leucosis bovina / The racial component influences resistance to infection with the bovine leukemia virus

RESUMEN El virus de la leucosis bovina (VLB) es un retrovirus que afecta principalmente el ganado lechero, reduciendo la producción de leche entre el 2,5 y 5%. La raza criolla colombiana Blanco Orejinegro (BON) es una raza rustica, bien adaptada, que ha mostrado resistencia in vitro a las infecciones ocasionadas por los virus de la fiebre aftosa y la estomatitis vesicular, así como las originadas por la bacteria Brucella abortus. El objetivo del presente estudio fue determinar si la raza BON y su cruce con Holstein son resistentes a la infección por el VLB. Se tomaron 124 muestras de sangre (59 Holstein, 40 BON y 25 BON x HOL) del mismo hato, se extrajo el DNA y se realizó una PCR-anidada correspondiente a una región del gen env de VLB. Se obtuvo un fragmento de 444 pb en los animales positivos. La prevalencia molecular del hato fue 33% para VLB. Se encontró diferencia significativa para infección por VLB entre los tres grupos raciales (p < 0,05). El porcentaje de infección fue del 55,9% para la raza Holstien, 5% para las vacas BON y 24% para el cruce BON x HOL; este último presentó una reducción en el porcentaje de infección del 32% respecto a la raza Holstein, lo cual puede ser atribuido a la presencia de genes de resistencia en la raza BON. Se comprobó que el nivel de infección es menor en vacas lecheras del cruce BON x HOL que en la raza lechera Holstein.

ABSTRACT The bovine leukemia virus (BLV) is a retrovirus that primarily affects dairy cattle, reducing milk production between 2.5 and 5%. The Colombian Blanco Orejinegro (BON) is a well-adapted, rustic, creole breed resistant to in vitro infections of Foot-and-mouth disease virus and vesicular stomatitis virus, as well as to Brucella abortus. This study aimed to determine if the crossing of BON and Holstein breeds is resistant to infection by BLV. Blood samples of 124 individuals (59 Holstein, 40 BON, and 25 BON x HOL) of the same herd were taken. The DNA was extracted, and a nested PCR was performed related to a region of the env gene of BLV. A fragment of 444 bp was obtained for positives animals. The molecular in-herd prevalence was 33% for BLV. A significant difference for BLV infection was found among the groups (p<0.05). The infection rate for the Holstein group was 55.9%, for BON cattle 5%, and for BON x HOL cattle 24%. The latter showed a reduction in the infection rate of 32% to the Holstein breed, which can be attributed to the presence of resistance genes in the BON breed. It was found that the level of infection is lower in BON x HOL cattle in contrast with Holstein dairy cows.

Heterogeneity determination of bovine leukemia virus genome in Santa Catarina state, Brazil / Determinação da heterogeneidade do genoma do vírus da leucose enzoótica bovina no estado de Santa Catarina, Brasil

Bovine leukemia virus (BLV) is a member of Retroviridae family, genus Deltaretrovirus, and the main viral agent responsible for economic loses in dairy herds. Some studies have been carried out about BLV genotypes, and at least seven genotypes were found out in samples of different regions of the world. The objective of this study was to identify BLV samples from seropositive dairy cattle in Santa Catarina state, Brazil, using molecular techniques. Blood samples were collected (454) from dairy cattle from 31 different farms, and serology using agar gel immunodiffusion test (AGID) was performed. After that, 191 seropositive samples were submitted to DNA extraction, and in 77 samples the polymerase chain reaction (PCR) for amplification of a 440 bp fragment of the env gene was performed. Nineteen DNA samples were subjected to restriction fragment length polymorphism (RFLP) analysis by digestion of the PCR fragment by five restriction endonucleases - BamHI, HaeIII, Tru9I, TaqI, and MwoI. It was found 42% seropositive animals (191/454) and 68% positives of the farms (21/31). The PCR showed 80.5% (62/77) of animals positive. The RFLP analysis identified five different genotypes dispersed by Santa Catarina state, with the highest prevalence for genotype X (47.4%). Overall, our results identified the viral genotypes present in dairy cattle and the prevalence of new variants in representative farms from Santa Catarina state.(AU)

O bovine leukemia virus (BLV) é um membro da família Retroviridae, gênero Deltaretrovirus, e o principal agente viral causador de perdas econômicas em rebanhos leiteiros. Diversos estudos têm sido feitos sobre os genótipos de BLV, e foram encontrados pelo menos sete em amostras de diferentes partes do mundo. O objetivo deste estudo foi realizar a caracterização molecular de amostras de BLV de bovinos leiteiros soropositivos no estado de Santa Catarina. Foram coletadas 454 amostras de sangue de bovinos de 31 propriedades, e fez-se inicialmente a sorologia por meio do teste de imunodifusão em gel de ágar. Após a sorologia, 191 amostras soropositivas foram então submetidas à extração de DNA, e em 77 amostras se realizou a reação da polimerase em cadeia (PCR), para a amplificação de um fragmento de 440 pb do gene env. Dezenove amostras foram submetidas à análise do polimorfismo dos fragmentos de restrição por digestão do fragmento da PCR por cinco enzimas de restrição: BamHI, HaeIII, Tru9I, TaqI e MwoI. Os resultados obtidos na sorologia apontaram 42% de animais soropositivos (191/454) e 68% de propriedades positivas (21/31). Na PCR, 80,52% (62/77) dos animais apresentaram-se positivos. A análise do polimorfismo dos fragmentos de restrição identificou cinco genótipos circulantes no estado, e a maior prevalência foi observada no genótipo X (47,4%). Este estudo permite-nos conhecer alguns dos genótipos virais presentes em bovinos leiteiros do estado de Santa Catarina, bem como identificar a existência de novas variantes e sua prevalência atual, e os resultados são úteis para futuros estudos epidemiológicos.(AU)

Development of an indirect ELISA based on recombinant capsid protein to detect antibodies to bovine leukemia virus

Abstract Serological testing and culling infected animals are key management practices aiming eradication of bovine leukemia virus infection. Here, we report the development of an indirect ELISA based on BLV recombinant capsid protein (BLVp24r) to detect anti-BLV antibodies in cattle serum. The BLVp24r was expressed in Escherichia coli and purified by affinity chromatography, and then used to set up the ELISA parameters. The Polysorp ® plate coated with 50 ng of antigen/well and bovine serum diluted 1:100 gave the best results during standardization. Using sera from infected and non-infected cattle we set up the cutoff point at 0.320 (OD450 nm) with a sensitivity of 98.5% and specificity of 100.0%. Then, we tested 1.187 serum samples from dairy (736 samples) and beef cattle (451 samples) with unknown status to BLV. We found that 31.1% (229/736) and 9.5% (43/451) of samples amongst dairy and beef cattle, respectively, had IgGs to BLV. The rate of agreement with a commercial competitive ELISA was 84.3% with a κ value of 0.68. Thus, our BLVp24r iELISA is suitable to detect BLV infected animals and should be a useful tool to control BLV infection in cattle.

Development of an indirect ELISA based on recombinant capsid protein to detect antibodies to bovine leukemia virus

Abstract Serological testing and culling infected animals are key management practices aiming eradication of bovine leukemia virus infection. Here, we report the development of an indirect ELISA based on BLV recombinant capsid protein (BLVp24r) to detect anti-BLV antibodies in cattle serum. The BLVp24r was expressed in Escherichia coli and purified by affinity chromatography, and then used to set up the ELISA parameters. The Polysorp ® plate coated with 50 ng of antigen/well and bovine serum diluted 1:100 gave the best results during standardization. Using sera from infected and non-infected cattle we set up the cutoff point at 0.320 (OD450 nm) with a sensitivity of 98.5% and specificity of 100.0%. Then, we tested 1.187 serum samples from dairy (736 samples) and beef cattle (451 samples) with unknown status to BLV. We found that 31.1% (229/736) and 9.5% (43/451) of samples amongst dairy and beef cattle, respectively, had IgGs to BLV. The rate of agreement with a commercial competitive ELISA was 84.3% with a value of 0.68. Thus, our BLVp24r iELISA is suitable to detect BLV infected animals and should be a useful tool to control BLV infection in cattle.

Determinación de Leucosis Enzoótica Bovina Mediante las Claves Hematológicas de Göttingen y Elisa en Boyacá, Colombia / Enzootic Bovine Leukosis Assessment by Hematology Gottingen Keys and ELISA in Boyacá, Colombia

La Leucosis Enzootica Bovina (LEB) es una enfermedad de distribución mundial que genera grandes pérdidas económicas. Esta enfermedad, afecta principalmente la ganadería de las zonas lecheras y en Colombia no se tienen datos exactos del estado sanitario, ni se han estimado las pérdidas generadas a causa de esta patología. El objetivo fue determinar la presencia de LEB utilizando las claves hematológicas de Göttingen en Toca, Boyacá (Colombia). Se tomaron 243 muestras serológicas a 81 hembras de razas lecheras, seleccionadas al azar en intervalos de dos meses. Posteriormente, las muestras positivas y sospechosas a las claves, fueron procesadas mediante la técnica de ELISA, con el fin de corroborar su seropositividad. Las claves de Göttingen permitieron clasificar, de los 81 ejemplares, cinco muestras positivas y 18 sospechosas, de las cuales las cinco positivas resultaron también positivas a la técnica de ELISA. De los 18 ejemplares sospechosos, cinco resultaron seropositivos. La prevalencia total fue del 13.5 %; para los ejemplares entre 3 y 6 años de edad fue de 25% y para mayores de seis años fue del 6%. Se pudo concluir que el recuento de leucocitos fue de relevancia para el diagnóstico de la LEB. Sin embargo, las técnicas de Göttingen resultan no ser tan específicas para la detección de la enfermedad, por lo cual se recomienda la aplicación de técnicas con una especificidad y una sensibilidad mayor como ELISA y PCR.

Bovine Leukemia Virus (BLV) is an internationally prevalent disease that causes great economic losses. It mainly affects livestock in dairy production areas. Colombia lacks accurate data on the prevalence of BLV and its economic effect. This study aimed to determine the presence of BLV using Göttingen Hematological Keys in Toca, Boyacá (Colombia). A total of 243 serological samples were taken from 81 females of randomly selected dairy breeds at two-month intervals. Subsequently, the positive and suspect samples to the keys were processed by the ELISA technique in order to corroborate their seropositivity. The Göttingen keys allowed researchers to classify, from the 81 specimens, five positive samples and 18 suspicious ones, of which the five positive samples were also positive for the ELISA technique. Of the 18 suspected specimens, five were also seropositive. The total prevalence was 13.5%; for individuals between 3 and 6 years of age the prevalence was 25% and for individuals over 6 years the prevalence was 6%. Researchers concluded that the leukocyte count was relevant for the diagnosis of LEB. However, the Göttingen techniques are unspecific for the detection of the disease, so techniques with greater specificity and sensitivity such as ELISA and PCR yield more accurate results.

Development and evaluation of an immunochromatographic assay using a gp51 monoclonal antibody for the detection of antibodies against the bovine leukemia virus

Infection of cattle with bovine leukemia virus (BLV) has been observed and reported worldwide, including in Korea. The onsite identification of infected cattle would help decreasing and eradicating BLV infections on farms. Here, we present a new immunochromatographic assay that employs monoclonal antibodies (MAbs) for the detection of antibodies against BLV in the field. BLV envelope glycoprotein (gp)51 was expressed in E. coli, and MAbs against recombinant BLV gp51 were generated for the development of an immunochromatographic assay to detect BLV antibodies in cattle. The sensitivity and specificity of the assay were determined by comparing these results with those obtained from a standard enzyme linked immunosorbent assay (ELISA). A total of 160 bovine sera were used to evaluate the new immunochromatographic assay. Using ELISA as a reference standard, the relative specificity and sensitivity of this assay were determined to be 94.7% and 98%, respectively. Because of its high sensitivity and specificity, this BLV antibody detection assay would be suitable for the onsite identification of BLV infection in the field.

Genetic analysis of env and gag gene fragments of bovine leukemia virus identified in cattle from Korea / 대한수의학회지

Bovine leukemia virus (BLV) is the causative agent of enzootic bovine leukosis. This study was conducted to clarify the molecular characteristics of BLVs obtained from a specific region in Korea. Proviral BLVs were detected in anti-BLV antibody-positive blood samples by PCR. Env and gag fragments were sequenced and compared to previously published reference sequences. Analysis of the env gene sequence revealed that the YI strain was highly similar to genotype 1, including United States and Japanese strains. The gag gene sequence had the highest degree of similarity with a Japanese strain.

Enzootic bovine leucosis ­ a case report / Leucose enzoótica bovina ­ relato de caso

Enzootic bovine leucosis is an infectious disease of cattle caused by the bovine leukemia virus that results in lymphoma within target tissues. Cattle might demonstrate four clinicopathological age-related manifestations of the disease: juvenile, adult, thymic, and cutaneous form. This article describes the unusual manifestation of this disease in a 4-yr-old cow. Regional lymph nodes were enlarged during clinical examination. Peripheral and internal lymph nodes, as well as the vagina, uterus, spleen, liver, heart, thoracic vertebrae, eye and the thoracic and abdominal cavities demonstrated lymphoma at necropsy. Bovine enzootic leucosis was confirmed by histopathology and agar gel immunodifusion.

A leucose enzoótica bovina é uma doença infecciosa de bovinos causada pelo vírus da leucemia bovina que produz linfoma em tecidos alvos. Bovinos podem demonstrar quatro manifestações clínico-patológicas da doença relacionadas à idade: forma juvenil, adulta, tímica e cutânea. Esse artigo descreve a manifestação incomum dessa doença em uma vaca de quatro anos de idade. Os linfonodos regionais apresentaram-se aumentados no exame clínico. Linfoma foi observado nos linfonodos periféricos e internos bem como na vagina, útero, baço, fígado, coração, vértebras torácicas, olho e nas cavidades torácica e abdominal durante a necropsia. A leucose enzoótica bovina foi confirmada na histopatologia e pela imunodifusão em gel de ágar.

Proliferação de linfócitos e apoptose de células CD5+ de bovinos infectados pelo vírus da leucose enzoótica bovina / Apoptosis of CD5+ cells and lymphocyte proliferation in bovine leukemia virus-infected dairy cows

Avaliaram-se a proliferação de linfócitos e a apoptose de células CD5+ de bovinos naturalmente infectados pelo vírus da leucose enzoótica bovina. Para tal, 100 vacas da raça Holandesa, em lactação, foram triadas quanto ao sorodiagnóstico para a leucose enzoótica bovina e o perfil hematológico, e 15 foram escolhidos e distribuídos uniformemente entre os três grupos, a saber: animais negativos, animais positivos alinfocitóticos e animais positivos e que manifestaram linfocitose persistente (LP). Para a avaliação da proliferação de linfócitos, procedeu-se ao isolamento das células mononucleares por gradiente de centrifugação, em que 2x10(6) linfócitos por mL foram plaqueados por poço e analisados por citometria de fluxo utilizando-se o fluorocromo CFSE-DA. A apoptose do sangue periférico deu-se utilizando a anexina V-FITC, e para a identificação das células CD5+, utilizaram-se anticorpos monoclonais. Ocorreu menor proliferação de linfócitos nos animais infectados e que manifestavam LP, e menor apoptose de células CD5+ do sangue periférico. Pode-se sugerir que o desenvolvimento da LP, resultante do aumento de linfócitos B, deve-se à redução do processo apoptótico das células CD5+, principal população infectada, e que a maior proliferação linfocitária pode se restringir apenas ao estádio inicial do desenvolvimento da LP.

The purpose of the present trail was to evaluate the lymphocyte proliferation and the apoptosis rates of CD5+ cells in dairy cows infected with bovine leukemia virus (BLV) with distinct lymphocyte profiles in infected animals known as alymphocytotic (AL) and persistent lymphocytosis (PL). A total of 100 Holstein cows were sera tested for bovine leukemia virus through agar gel immunodiffusion (AGID) and enzyme-linked immunosorbent-assay (ELISA). From these animals, 15 cows were selected and divided uniformly in 3 groups (negative, AL, LP). The lymphocyte proliferation was performed using flow cytometric measurement of CFSE-DA dye, where 2x10(6)/mL lymphocytes were plated per well. The apoptosis of CD5+ cells from peripheral blood was performed using the annexin V-FITC to measure the apoptosis rates and the identification of CD5+ was accessed using monoclonal antibodies. Animals from the LP group showed lower lymphocyte proliferation and also lower apoptosis rates of CD5+ cells compared with negative and AL animals. The development of PL which resulted from an increase in B cell count, is due to the decrease in the apoptosis rates of CD5+ cells, and the higher lymphocyte proliferation appears to be limited only in the initial stages of development of LP.

Occurrence of seropositive sheep (Ovis aries) to bovine leukemia virus in Brazil / Ocorrência de ovinos (Ovis aries) soropositivos ao vírus da leucemia bovina no Brasil

Occurrence of seropositive sheep (Ovis aries) to Bovine Leukemia Virus (BLV) by agar-gel immunodiffusion test (AGID) using the antigen gp51 was surveyed for the period 2005-2007. Samples were collected from sheep in the Brazilian states of Rio Grande do Sul, Paraná, São Paulo, Pernambuco, Maranhão, Pará, Bahia, Mato Grosso, Rondônia, and Acre. Two of 35 (5.7%) flocks were seropositive to BLV, and the rate of seropositive animals was 0.077% (two of 2,592). The two seropositive sheep were female, one 13-month old Santa Inês breed and other of unknown age and breed, both from the state of São Paulo. Distribution of BLV in the ovine population studied proved to be a rare event in Brazil.

A ocorrência de ovinos sororreagentes ao vírus da Leucemia Bovina (VLB) pelo teste de imunodifusão em gel de ágar (IDGA) utilizando o antígeno gp51 foi avaliada no período de 2005-2007, em diferentes regiões do Brasil. Amostras foram colhidas de ovinos dos Estados do Rio Grande do Sul, Paraná, São Paulo, Pernambuco, Maranhão, Pará, Bahia, Mato Grosso, Rondônia e Acre. Duas em 35 cabanhas (5,7%) e dois em 2592 ovinos (0,077%) foram soropositivos. Os únicos animais com anticorpos contra o VLB eram fêmeas, uma com 13 meses de idade e da raça Santa Inês e a outra não se conhecia a idade e raça, ambas provenientes do Estado de São Paulo. A distribuição da soropositividade na população estudada demonstrou ser rara a infecção pelo VLB em ovinos no Brasil.

Agar gel immunodiffusion analysis using baculovirus-expressed recombinant bovine leukemia virus envelope glycoprotein (gp51/gp30T-)

Bovine leukemia virus (BLV) envelope glycoprotein (gp51/gp30T-), consisting of BLV gp51 and BLV gp30 that lacked its C-terminal transmembrane domain, was expressed in insect cells under the control of the baculovirus polyhedron promoter. Recombinant BLV gp51/gp30T- secreted from insect cells was determined by immunofluorescence, enzyme-linked immunosorbent and western blot assays using a BLV-specific monoclonal antibody and BLV-positive bovine antibodies. An agar gel immunodiffusion (AGID) test using gp51/gp30T- as the antigen for the detection of BLV antibodies in serum was developed and compared to traditional AGID, which uses wild type BLV antigen derived from fetal lamb kidney cells. AGID with the recombinant BLV gp51/gp30T- was relatively more sensitive than traditional AGID. When the two methods were tested with bovine sera from the field, the recombinant BLV gp51/gp30T- and traditional antigen had a relative sensitivity of 69.8% and 67.4%, respectively, and a relative specificity of 93.3% and 92.3%. These results indicated that the recombinant BLV gp51/gp30T- is an effective alternative antigen for the diagnosis of BLV infection in cattle.

Low numbers of intestinal Shiga toxin-producing E. coli correlate with a poor prognosis in sheep infected with bovine leukemia virus

Healthy ruminants carry intestinal Shiga toxin (Stx)-producing Escherichia coli (STEC). Stx has antiviral activities in vitro and STEC numbers correlate with reduced early viremia in sheep experimentally infected with bovine leukemia virus (BLV). This study assessed the impact of intestinal STEC on BLV-induced disease for one year post-BLV-challenge. High STEC scores (CFU/g feces x frequency of STEC-positive samples) correlated with good health, whereas poor weight gain, distress, and tumor development occurred only among animals with low STEC scores. STEC carriage was associated with increased percentages of B cells in peripheral blood.

Simultaneous presence of bovine papillomavirus and bovine leukemia virus in different bovine tissues: in situ hybridization and cytogenetic analysis

Bovine papillomavirus (BPV) DNA sequences were detected in different tissues, in addition to epithelium. Cytogenetic abnormalities were observed in blood lymphocytes. The presence of more than one virus in a single tissue is a difficult aspect to evaluate, especially when the DNA sequences are detected in tissues that are not specifically targeted by the virus. BPV and bovine leukemia virus (BLV) are clastogenic, causing chromosome aberrations in peripheral blood lymphocytes. In the present study, we investigated the simultaneous presence of DNA sequences of both viruses and the possibility of vertical transmission and compared the types of chromosome aberrations related to viral action. BPV 1, 2, and 4 DNA sequences were found in three females of the herd and in their offspring. BLV DNA sequences were not detected in their progeny. A newborn calf that was negative for BLV infection showed specific chromosome rearrangements possibly related to the effect of infection with BPV.

Establishment of a bovine leukemia virus-free dairy herd in Korea

In view of the high prevalence rate of bovine leukemia virus (BLV)infections in cattle over the entire country, a large dairy farm in Chungnam province was chosen and 'test and segregate' program was instituted. On July 1999, ELISA test was performed on 491 animals on the farm and only 163 cattle (139 adult cows, 18 female and 6 male calves)were BLV-seronegative. From February 2000 through April 2004, the seronegative group was placed in barns 1,500 to 2,000 m from seropositive group and thereafter tested at 3-to 5-month intervals by ELISA. Animals seroconverted in consecutive tests were removed from the seronegative group immediately after the detection of anti-BLV antibodies. The changes in management were aimed at preventing iatrogenic transfer of blood between cattle. Replacement heifers imported from other countries and calves born at the farm were repeatedly tested by ELISA, and only seronegative animals were introduced into the group. As of April 2004, there were 311 cattle in the BLV seronegative group of the farm. Twent y four cows of the initial 139 adult cows were seroconverted in 2000, and no seropositive animals were found since February 2001. Follow up of the group, from which all seropositive cattle were moved to a separate location, revealed no recurrence of BLV infection for three years. The approach in the present study might be valuable for Korean producers who would like to move toward a BLV-negative status.

Flow Cytometric Analysis of Lymphocyte Subpopulations of Cattle Infected with Bovine Leukemia Virus

We examined lymphocyte subpopulations of peripheral blood from BLV infected and noninfected Holstein-Friesian dairy cattle reared in Korea by flow cytometry using monoclonal antibodies specifically reactive with bovine leukocyte differentiation marker. Lymphocyte subpopulations expressing BoCD11b, B-B2, CD5, B, MHC II-DP, MHC II-DQ, and MHC II-DR antigens were significantly abundant in the BLV(+) group than the BLV(-) group (p<0.01). On double staining, subpopulation of B-1a(BoCD5+ BoCD11b+) lymphocytes was significantly increased in leukemic group. However, T-lymphocyte lineage expressing BoCD2, BoCD4, BoCD8, and WC1 antigens was significantly lower than in the BLV(+) group (p<0.01). However the absolute number of T-lymphocytes expressing BoCD2, BoCD4, BoCD8, and WC1 antigens in BLV(+) group remained with in the normal range. Furthermore mean ratio of BoCD4/BoCD8 in the BLV(+) groups was higher than that in the BLV(-) group. Taken together, cellular immune responses did not seem to significantly be decreased in the leukemic cattle.

Levantamento sorológico da infecção pelo vírus da leucose bovina nos rebanhos leiteiros do Estado do Rio Grande do Sul, Brasil / Serological survey of the bovine leukosis virus infection in dairy herds of the Rio Grande do Sul State, Brazil

O vírus da Leucose Enzoótica Bovina (VLB) causa uma infecção persistente em bovinos, sendo responsável por perdas econômicas significativas para a pecuária bovina. O objetivo deste estudo foi determinar a prevalência da infecção pelo VLB no rebanho leiteiro do Estado do Rio Grande do Sul, Brasil e estudar alguns aspectos epidemiológicos da infecção. Um total de 39.799 amostras de soro. coletadas em 4.200 propriedades de 172 municípios, distribuídos em 9 regiões geográficas, foram testadas pela técnica de imunodifusão em gel de ágar (IDGA), com antígeno glicoprotéico (glicoproteína gp 51). Os exames sorológicos revelaram 3.645 (9,2%) amostras positivas. No entanto, a prevalência média do Estado, quando foi considerada aproximadamente 1% da população em cada região, foi de 12,0% (1.295/10.357) e 29,1% (385/1.321) das propriedades apresentaram pelo menos um animal positivo. A prevalência da infecção variou de 2,2% (17,8% das propriedades) em Uruguaiana, a 19,6% (57,8% das propriedades) em São Gabriel. Foram observadas taxas de 15,5% (41.8% das propriedades) na grande Porto Alegre; 9,9% (64,4%) em Pelotas: 19,4% (42,9%) em Bagé; 9,2% (36,2%) na grande Santa Rosa; 12.9% (37,8%) em Erexim; 7,1% (26,5%) em Passo Fundo e 8,0% (33,8%) em Santa Maria. Esses resultados demonstram que a infecção pelo VLB esta amplamente distribuída no rebanho leiteiro do Estado. No entanto, os índices de infecção são relativamente baixos se comparados com índices de outros estados e países e são compatíveis com programas de controle e erradicação.

Bovine leukosis vírus (BLV) is associated with a persistem infection in cattle that is responsible for serious lasses to the livestock industry. The objective of this study was to determine the prevalence and to analyse some epidemiological aspects of the BLV infection in the dairy herd of the Rio Grande do Sul state. A total of 39.799 blood samples, collected in 4,200 herds from 172 counties, distributed in 9 geographic regions, were tested by the agar-gel immunodiffusion test (AGID) with glycoproteic antigen (glycoprotein gp 51). The sorologic tests showed 3,645 (9.2%) positive; however, the prevalence in the state, when considered about 1% of the population in each region was only, 12.0% (1,295/10,357) and 29.1% (385/1,321) of the herds had at least one seropositive animal. The prevalence ranged from 2.2% (17.8% of the herds) in Uruguaiana to l9.6% (57.85% of the herds) in São Gabriel. Prevalences of 15.5% (41.8% of herds) in the Porto Alegre metropolitan area. 9.9% (64.4%) in Pelotas, 19.4% (42.9%) in Bagé, 9.2% (36.2%) in Santa Rosa, 12.9% (37.8%) in Erexim, 7.1% (26.5%) in Passo Fundo and 8% (33.8%) in Santa Maria were observed. These results show that the BLV infection is widely spread within the Rio Grande do Sul dairy herd. Nevertheless, the overall prevalence is still low if compared to other states and countries and may be compatible with control and eradication efforts.