ABSTRACT
Abstract Bovine respiratory syncytial virus (BRSV) is one of the most relevant agents responsi-ble for respiratory disease in cattle from both dairy and beef farms. BRSV is spread by horizontalcontact causing a constant presence of seropositive animals that favors viral circulation throughout the year. Moreover, reinfections with BRSV are frequent between animals regardless of theirage as BRSV does not confer long-lasting protective immunity. Several studies have demonstrated the circulation of BRSV in cattle from different regions of the world; however, little isknown about the dynamics of BRSV infection in cows before and after they begin lactation. Theaim of this work was to study the dynamics of BRSV neutralizing antibodies from birth up to36 months of age in a closed dairy herd of Argentina specifically around the lactation period. Passive maternal antibodies against BRSV started to decrease monthly and became almost undetectable at 8 months of age. We detected two potential infection points at months 11 and 27after birth, in which 30% and 45% of the animals showed seroconversion, respectively. Specifically, an increase in the proportion of seropositive cows after the start of lactation suggests thatthey became reinfected around the time they began lactating. We demonstrate the importanceof understanding BRSV dynamics in a closed dairy herd to review the vaccination schedule ofthe animals to achieve protection against BRSV infection.
Resumen El virus respiratorio sincitial bovino (Bovine respiratory syncytial virus, [BRSV]) es uno de los principales agentes responsables de la enfermedad respiratoria en bovinos, tanto de tambos como de cría. El virus se transmite horizontalmente y causa la presencia constante de animales seropositivos, lo cual favorece la circulación viral a lo largo del ano. A su vez, las reinfecciones por BRSV son frecuentes entre animales independientemente de su edad, dado que el virus no confiere inmunidad protectora a largo plazo. Numerosos estudios han demostrado la circulación de BRSV en bovinos de diferentes regiones del mundo, sin embargo, poco se conoce acerca de la dinámica de infección en vacas antes y después del inicio de la fase de lactancia. El objetivo de este trabajo fue estudiar la dinámica de anticuerpos neutralizantes anti- BRSV en vacas lecheras desde el nacimiento hasta los 36 meses de vida en un tambo cerrado de Argentina, específicamente, en el período de lactancia. Los anticuerpos pasivos específicos para BRSV comenzaron a declinar mensualmente hasta ser casi indetectables a los 6 meses. Detectamos dos potenciales puntos de infección a los meses 11 y 27 luego del nacimiento, momentos en los que el 30 y el 45% de los animales mostraron seroconversión, respectivamente. El incremento en la proporción de vacas seropositivas luego del comienzo de la lactancia sugiere que estas se reinfectaron en el inicio de dicha etapa. Demostramos la importancia de entender la dinámica de circulación del BRSV en un tambo cerrado, a fin de revisar el esquema de vacunación de los animales para que estén protegidos frente a la posible infección por este virus.
Subject(s)
Animals , Cattle , Respiratory Syncytial Virus, Bovine , Antibodies, Neutralizing , Argentina , Cattle Diseases/virology , Respiratory Syncytial Virus, Bovine/immunologyABSTRACT
Bovine respiratory syncytial virus (BRSV) is one of the causative agents of respiratory disease in cattle all over the world, leading to important economic losses. The aim of this work was to determine the seroprevalence of BRSV in feedlot cattle of Argentina and the risk factors associated with the disease. Results showed a high individual seroprevalence of 78.64% (95% confidence interval adjusted -#91;CI-#93; =66.55-90.75%) against the virus. Positive association was found between the presence of high BRSV neutralizing antibody titers, and the following risk factors: cattle age, source of animals, presence of clinical respiratory signs and herd size. This work contributes to updating the understanding of its epidemiology in Argentinean feedlots and poses the need for reevaluating vaccination strategies against this virus in order to control infection and its impact on productivity.
El virus respiratorio sincicial bovino (BRSV) es uno de los agentes causantes de enfermedad respiratoria bovina a nivel mundial, conduciendo a importantes pérdidas económicas. El objetivo de este trabajo fue determinar la seroprevalencia del BRSV en bovinos de engorde a corral de Argentina y estudiar los factores de riesgo asociados. Los resultados mostraron una elevada seroprevalencia individual del 78,64% (IC = 66,55-90,75%) contra el virus. Se encontró una asociación positiva entre la presencia de altos títulos de anticuerpos neutralizantes contra BRSV y los factores de riesgo: edad del ganado, origen de los animales, presencia de signos clínicos respiratorios y el tamaño del rebano. Este trabajo contribuye en gran medida a la comprensión de la epidemiología en los establecimientos de engorde a corral de Argentina y plantea la necesidad de revaluar las estrategias de vacunación contra este virus con el fin de controlar la infección y su impacto en la producción.
Subject(s)
Animals , Cattle , Cattle Diseases , Seroepidemiologic Studies , Respiratory Syncytial Virus, Bovine , Respiratory Syncytial Virus Infections , Argentina/epidemiology , Cattle Diseases/epidemiology , Cattle Diseases/virology , Risk Factors , Respiratory Syncytial Virus Infections/veterinary , Respiratory Syncytial Virus Infections/epidemiology , Antibodies, ViralABSTRACT
Objective. The purpose of this study was to compare the intra-class correlation coefficients (ICC) and design effects (D) estimates adjusted or unadjusted for sensibility (Se) and specificity (Sp) of the diagnostic tests using a Bayesian procedure. Materials and methods. Sera from 232 animals from 44 randomly selected herds, to detect antibodies against parainfluenza-3 virus (PIV3) from non-vaccinated dual-purpose cattle from Colima Mexico, were used. Only 176 animals from 33 herds were used to evaluate the presence of the bovine respiratory syncytial virus (BRSV). Results. The ICC and D values adjusted and unadjusted for PIV3 were 0.33, 2.73, 0.32, and 2.71, respectively. For BRSV the values were 0.31, 2.64, 0.28 and 2.49. Conclusions. The adjusted or unadjusted ICC and D estimates were similar because of the high Se and Sp of the diagnostic tests and the relatively high prevalence of the diseases here studied.
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Subject(s)
Animals , Respiratory Syncytial Virus, BovineABSTRACT
Foram estudados 33 surtos de pneumonia em bovinos jovens na área de influência do Laboratório Regional de Diagnóstico (LRD) da Faculdade de Veterinária da Universidade Federal de Pelotas (UFPel) entre os anos de 2000 e 2011. Foram diagnosticados 18 surtos de pneumonia (54,54%) em bovinos de raças leiteiras, Holandês ou Jersey e 13 surtos (39,39%) em gado de corte ou cruzas de gado de corte. A morbidade variou entre 0,06%-100% e a mortalidade foi de 0,06%-34,6%. A doença ocorreu igualmente em todas as estações do ano e foi mais frequente em bezerros de 1-3 meses totalizando 13 surtos. Sete surtos ocorreram em bovinos entre 4-6 meses, sete entre 7-12 meses e seis surtos ocorreram em bezerros de 1-29 dias. Pneumonia enzoótica pela infecção pelo vírus sincicial respiratório bovino (BRSV) com lesões histológicas de broncopneumonia, pneumonia intersticial e presença de células sinciciais foi mais frequente em bovinos de raças de corte com dez surtos (58,8%); seis surtos dessa enfermidade ocorreram em raças de leite (35,2%). O diagnóstico foi confirmado por imuno-histoquímica em sete casos. Os sinais clínicos da maioria dos casos de pneumonia observados caracterizaram-se por dispneia, emagrecimento, apatia, tremores, bruxismo, desidratação, respiração ruidosa, tosse, corrimento nasal seroso ou mucopurulento, decúbito e morte. As lesões macroscópicas caracterizaram-se por presença de áreas de consolidação vermelho-escuras, edema e enfisema nas regiões crânio-ventrais dos lobos pulmonares cardíaco e apical ou pneumonia intersticial com distribuição difusa, edema e enfisema. Histologicamente, as lesões pulmonares eram variáveis. Broncopneumonia necrossupurativa difusa acentuada com hiperplasia de pneumócitos tipo II e edema intersticial e alveolar foi observada em 15 casos. Os resultados deste trabalho demonstram que as pneumonias são importantes causas de perdas econômicas em bovinos jovens na região de influência do LRD. Deve ser destacado que a pneumonia enzoótica devido a infecção pelo BRSV é importante tanto em bovinos de corte como de leite independente da forma de criação.
Thirty-three outbreaks involving pneumonia in young cattle diagnosed in the area of influence of the Regional Diagnostic Laboratory (LRD) of the Veterinary School of the Federal University of Pelotas (UFPel) between 2000 and 2011 were studied. Eighteen outbreaks (54.54%) were diagnosed in dairy breeds and Jersey or Holstein and 13 outbreaks (39.39%) in beef cattle or crossbred beef cattle. Morbidity ranged from 0.06% -100% and mortality was 0.06% to 34.61%. The disease occurred in all seasons of year and was more frequent in calves aged 1-3 months (11 outbreaks). Seven outbreaks occurred in cattle between 4-6 months, seven between 6-12 months and six outbreaks occurred in calves 1-30 days. Bovine respiratory disease due to infection with bovine respiratory syncytial virus (BRSV) was more frequent in beef cattle breeds with eight outbreaks (44.44%); six outbreaks of this disease occurred in calves of dairy breeds (33.33%). The diagnosis was confirmed by immunohistochemistry in seven cases. The main clinical signs were characterized by dyspnea, weight loss, lethargy, tremors, bruxism, dehydration, rapid and noisy breathing, coughing, serous or mucopurulent nasal discharge, recumbency and death. Gross lesions were characterized by dark red areas of consolidation, edema and emphysema in cranio-ventral regions of the apical and cardiac lung lobes or diffuse interstitial pneumonia, edema and emphysema. Histologically, lung lesions were variable. Diffuse bronchopneumonia necrotizing with marked hyperplasia of type II pneumocytes and alveolar and interstitial edema was observed in 15 cases. The results of this study demonstrate that pneumonia is an important cause of economic loss in young cattle in the area of influence of the LRD and that enzootic pneumonia due to BRSV infection is important in both beef cattle and milk cattle regardless of husbandry systems.
Subject(s)
Animals , Cattle , Bronchopneumonia/diagnosis , Bronchopneumonia/veterinary , Bovine Respiratory Disease Complex/diagnosis , Pneumonia of Calves, Enzootic , Respiratory Syncytial Virus, BovineABSTRACT
The aim of this work was the cloning of those transmembrane glycoproteins G and F from an isolate bovine respiratory syncytial viruses (BRSV) - a Brazilian isolate of BRSV, named BRSV-25-BR in previous studies, in a prokaryotic system to proceed the sequencing of larger genomic fragments. The nucleotide substitutions were confirmed and these clones may also be used in further studies regarding the biological effects of those proteins in vitro and in vivo.
O objetivo deste trabalho foi a clonagem das glicoproteínas transmembrana G e F de um isolado de vírus respiratório sincicial bovino (BRSV) - um isolado brasileiro denominado BRSV-25-BR- que já demonstrou possuir mutações em regiões altamente conservadas do gene da proteína G - em sistema procariótico, com o intuito de sequenciar fragmentos genômicos maiores. As substituições de nucleotídeos foram confirmadas e tais clones podem ser utilizados em futuros estudos sobre os efeitos biológicos destas proteínas tanto in vitro como in vivo.
Subject(s)
Animals , Cattle , Glycoproteins , Protein Splicing , Respiratory Syncytial Virus, BovineABSTRACT
A baixa eficiência de penetração de alguns vírus em células de cultivo pode representar uma dificuldade para o isolamento e a multiplicação viral in vitro. No presente estudo investigou-se o efeito do polietilenoglicol (PEG) na replicação de sete vírus bovinos em células de linhagem de rim bovino (MDBK). A eficiência de penetração e replicação foi mensurada pela contagem do número de placas virais produzidas em tapetes celulares, após adsorção do inóculo viral (100 DICC50 mL-1) com ou sem a adição de PEG a 5 por cento (peso molecular 6.000). A adição de PEG ao inóculo resultou em aumentos significativos do número de placas para o vírus da diarréia viral bovina (BVDV) (aumento de 3,4 vezes), vírus da estomatite vesicular (VSV) (2,2 vezes) e vírus respiratório sincicial bovino (BRSV) (1,5 vezes). A adição de PEG não produziu aumento significativo no número de placas dos herpesvírus bovinos 1, 2 e 5 (BoHV-1, BoHV-2 e BoHV-5). Por outro lado, o PEG produziu uma redução do número de placas (1,4 vezes) produzidas pelo vírus da parainfluenza bovina (bPI-3V). A adição de PEG a 5 por cento também aumentou a sensibilidade de detecção (entre 10 e 100 vezes) do BVDV no soro de três bezerros persistentemente infectados. Para o BRSV, a adição de PEG aumentou em duas vezes a sensibilidade do isolamento viral de secreções nasais de duas ovelhas infectadas experimentalmente. Esses resultados demonstram que o PEG aumenta a eficiência de infecção do BVDV, VSV e BRSV em células de cultivo, podendo ser utilizado para aumentar a sensibilidade de detecção desses vírus em amostras clínicas (isolamento viral) e/ou, para aumentar os títulos de vírus produzidos em cultivo celular.
The low efficiency of penetration of some viruses in cultured cells may represent an obstacle for viral isolation and/or viral multiplication in tissue culture. This study investigated the effect of polyethylene glycol (PEG) on the penetration and replication of seven bovine enveloped viruses in culture cells. Penetration efficiency was measured by counting the number of viral plaques produced in bovine kidney cells (MDBK). The addition of 5 percent PEG (molecular weight 6.000) to the viral inoculum containing 100 TCID50 mL-1 (tissue culture median infectious dosis) of each virus, during adsorption for 2h at 37ºC, resulted in a significant increase in the number of plaques for bovine viral diarrhea virus (BVDV) (increase of 3.4-fold), vesicular stomatitis virus (VSV) (2.2-fold) and bovine respiratory syncytial virus (BRSV) (1.5-fold). The addition of 5 percent PEG to the inoculum of bovine herpesviruses 1, 2 and 5 (BoHV-1, BoHV-2 and BoHV-5) did not increase the number of viral plaques. On the other hand, PEG produced a reduction in the number of plaques by bovine parainfluenza virus (bPI-3V) (1.4-fold). Furthermore, the addition of 5 percent PEG produced a 10- to 1000-fold increase in the sensitivity of BVDV detection in the serum of three persistently infected calves; and doubled the sensitivity of detection of BRSV in nasal secretions of two experimentally infected sheep. These results demonstrate that PEG enhances the efficiency of infection by BVDV, VSV and BRSV in cultured bovine cells and therefore may be used to increase the sensitivity of virus detection in clinical samples (viral isolation), and/or to increase virus titers in cell cultures.
Subject(s)
Animals , Cattle , Polyethylene Glycols/pharmacology , Drug Carriers/pharmacology , Virus Replication , Respiratory Syncytial Virus, Bovine/physiology , Diarrhea Viruses, Bovine Viral/physiologyABSTRACT
An immunoistochemical (IHC) test was developed to detect bovine respiratory syncytial virus (BRSV) in cell cultures and tissues of experimentally infected mice and calves, using a commercial monoclonal antibody (Mab) against human respiratory syncytial virus (HRSV), as a less expensive alternative, instead of producing specific monoclonal antibodies to BRSV. Clinical samples from calves suffering respiratory disease were also submitted to this test. IHC detected BRSV antigens in mouse tracheas (3, 5 and 7 days post-infection) and lungs (5 and 7 days post-infection), and in one of three lungs from experimentally infected calves. Lungs samples from two naturally infected calves were tested and resulted positive for BRSV by the IHC test. These results suggest that this test may be used in the future for diagnosis as well as a useful tool to assess the distribution of BRSV infections in Brazilian herds.
Desenvolveu-se um teste de imunohistoquímica (IHQ) para detecção do vírus respiratório sincicial bovino (BRSV) multiplicado em cultivo celular e em tecidos de camundongos e bezerros infectados experimentalmente, utilizando um anticorpo monoclonal comercial contra o vírus respiratório sincicial humano (HRSV), como uma alternativa para eliminar os custos de produção de anticorpos monoclonais específicos para o BRSV. Amostras clínicas de bezerros com sintomatologia respiratória foram analisadas. A técnica mostrou-se eficiente na detecção de antígenos do BRSV em traquéias (3, 5 e 7 dias pós-infecção) e pulmões (5 e 7 dias pós-infecção) dos camundongos infectados e em uma das três amostras de pulmões dos bezerros infectados experimentalmente. Amostras de pulmões de dois animais com infecção natural foram positivas para BRSV. Conclui-se que o teste de IHQ pode ser usado no diagnóstico das infecções por BRSV e na avaliação da distribuição dessas infecções nos rebanhos bovinos brasileiros.
Subject(s)
Antibodies, Monoclonal/metabolism , Cattle , Immunohistochemistry , Mice , Respiratory Syncytial Virus, Bovine/isolation & purification , Respiratory Syncytial Virus, Human/isolation & purificationABSTRACT
Descreve-se a ocorrência de infecção pelo vírus sincicial respiratório bovino (BRSV) em bezerros descendentes de animais das raças pardo-suíça e holandesa importados da Alemanha, æustria, Suíça e Uruguai, na qual morreram em Alagoas, Brasil, pelo menos 220 cabeças, de 1995 até a presente data. O quadro clínico caracterizou-se por hipertermia, tosse seca, mais tarde dispnéia acentuada e por vezes lacrimejamento; à auscultação havia estertores secos, depois úmidos, com sibilos, muitas vezes audíveis à distância. O exame histológico revelou pneumonia intersticial com formação de células sinciciais, infiltração predominantemente linfocitária com presença de eosinófilos e de corpúsculos de Russel, proliferação de pneumócitos tipo II e leve metaplasia escamosa. Células epiteliais de bronquíolos e células sinciciais marcaram-se positivamente com o anticorpo anti-BRSV. A ocorrência da enfermidade no Sul e agora no Nordeste do Brasil indica a necessidade de se promover um amplo levantamento epidemiológico para se avaliar o grau de perdas e a proporção de animais infectados no país. Lembramos que parte dos animais importados, ao que tudo indica, já estavam infectados nos países de origem, quando desembarcaram em Belém, Pará
Cases of bovine respiratory syncytial virus (BRSV) infection affecting calves in the State of Alagoas, Brazil, are described. At least 220 calves, which were the progeny of Brown Swiss and Holstein Friesian cattle imported from Germany, Austria, and Uruguay, have died from the disease since 1995. Clinical signs included fever, dry cough, serous ocular discharge and, towards the final stages, marked dyspnea. On auscultation there were loud and harsh breathing sounds, and a strong wheezing could be heard from a distance. Histopathology of the lung revealed interstitial pneumonia associated with syncytial cells and infiltration by lymphocytes and eosinophils. A few plasma cells containing Russel bodies in their cytoplasm were also observed. There was hyperplasia of type II pneumocytes and mild squamous metaplasia of the respiratory epithelium. Bronchiolar epithelial cells and syncytial cells were positively stained with anti-BRSV antibody. The finding of BRSV infection in calves in Northeast Brazil plus identical findings already reported from South Brazil, strongly indicate the need for a wide epidemiologic survey in order to evaluate the losses due to BRSV infection and the incidence of infected cattle. There is evidence that at least part of the imported animals involved in this outbreak was already infected on arrival at the port of Belém, in the State of Pará, Brazil.
Subject(s)
Animals , Cattle , Bovine Respiratory Disease Complex/complications , Bovine Respiratory Disease Complex/epidemiology , Bovine Respiratory Disease Complex/prevention & control , Respiratory Syncytial Virus, Bovine/isolation & purificationABSTRACT
São descritas as manifestações clínicas, patológicas, microbiológicos e sorológicos da enfermidade natural causada pelo Vírus Respiratório Sincicial Bovino (BRSV) em uma criação extensiva de bovinos de corte no Rio Grande do Sul. Clinicamente havia tosse crônica e dispnéia intensa frente a exercícios físicos mínimos em dois animais. Os dois foram sacrificados e necropsiados. As alterações macroscópicas eram pulmonares com enfisema alveolar disseminado, focos de atelectasia e espessamento dos septos interlobulares. A imunofluorescência para BRSV em corte de pulmão congelado foi positiva em ambos os casos, sendo negativa para Parainfluenza-3 (PI-3), Diarréia Vírica Bovina (BVDV) e Rinotraqueíte Infecciosa Bovina (BHV). Foi isolado BRSV em cultivo celular de MDBK a partir de um dos animais necropsiados. Nenhuma associação foi detectada através de elisa para detecção de antígeno LPS gênero específico de Chlamydia psittaci no tecido pulmonar. O exame histopatológico evidenciou células sinciciais, enfisema crônico, hipertrofia da camada muscular peribronquiolar e metaplasia escamosa do epitélio bronquial e bronquiolar. O exame sorológico para BRSV evidenciou 79% de soropositivos em uma primeira amostragem na qual havia animais jovens e alguns com tosse. O segundo exame sorológico 6 meses após, proveniente de animais de diferentes faixas etárias, resultou em 17,3% de soropositivos. Este é o primeiro relato de doença causada por BRSV no Brasil
Subject(s)
Animals , Cattle , Disease Outbreaks , Cattle Diseases/epidemiology , Respiratory Syncytial Virus Infections/pathology , Respiratory Syncytial Virus, Bovine , Brazil , Respiratory Syncytial Virus Infections/epidemiology , Respiratory Syncytial Virus Infections/virologyABSTRACT
To investigate the requirements for bovine respiratory syncytial virus (BRSV) cell fusion, the fusion (F), the attachment (G) and the small hydrophobic (SH) glycoproteins were expressed individually or coexpressed, using the vaccinia virus-T7 polymerase transient expression system. The contribution of individual glycoproteins in cell fusion was studied by a reporter gene activation assay. Activation of a reporter gene, beta-galactosidase, was assessed by colorimetric assay of detergent cell lysates or by in situ staining. Quantitative measurements indicated much higher sensitivity compared with analysis of syncytium formation. Our results showed that expression of any individual BRSV envelope gene or coexpression of F + G genes, did not induce significant cell fusion; however, coexpression of F + G + SH genes induced extensive cell fusion. To examine the role of N-linked glycosylation, each of the four potential glycosylation sites were individually removed by mutagenesis. The fusogenic activities of these F glycosylation mutants was examined using the reporter gene activation assay. Our results showed removal of individual carbohydrate chains on F2 subunit had no significant deleterious effects on cell fusion.
Subject(s)
Animals , Cattle , Cell Fusion/physiology , Genes, Reporter , Genes, Viral , Glycosylation , Mutagenesis, Site-Directed , Respiratory Syncytial Virus, Bovine/genetics , Viral Fusion Proteins/chemistryABSTRACT
Comparative studies to evaluate the immunogenic of the local inactivated combined vaccine incorporating IBR,PI-3 and BVD viruses prepared from the local isolates growth in MDBK cell line and inactivated by binary ethyleneimine and adsorbed with 20%. Alhydrogel adjuvant, and the imported inactivated vaccine which contains PI-3, IBR and BVD-MD and respiratory syncytia vaccine [Triangle 4]. The kinetics of immune response are elicited by ELISA Immuno Assay [EIA] and serum neutralization test [SNT] against the same component of the vaccine. The protective capacity of each vaccine was studied by challenge exposure which was performed at one month post vaccination [PV] assured that vaccinated animals resisted infection well. The non vaccinated control infected animal showed a high rate of thermal reaction and viraemia. The results of virus isolation could be confirmed by fluorescent antibody technique. The present data explained a significant higher degree of immunogenicity demonstrated with the local prepared vaccine than the imported against all the same categories of the two vaccines