The shedding of a virulent Kabete O strain of rinderpest virus by cattle

A Muguga substrain of the virulent Kabete O strain of rinderpest virus was demonstrated in the ocular, nasal, oral and rectal swabs collected from infected cattle. Ocular shedding was detected at the onset of viraemia and before the onset of clinical signs whilst virus shedding in nasal, oral and rectal discharges appeared at the same time as lesions. It is suggested that virus isolation from ocular and nasal swabs should be considered in the diagnosis of rinderpest in addition to the other methods currently employed, as virus was isolated from swabs collected from dead animals.     

Detection of rinderpest virus antigens in vitro and in vivo by direct immunofluorescence

Cell-culture attenuated and virulent strains of rinderpest virus (RV) were inoculated on to bovine kidney cell cultures. A direct immunofluorescent antibody test detected RV antigens in cell cultures within one to three days after inoculation whereas RV cytopathic effects usually took three to nine days to develop. Cells containing RV antigens were also detected in impression smears and frozen sections of tissues collected from RV infected animals at post mortem examination, and in smears of lymph node biopsies taken from cattle with clinical rinderpest. These techniques may offer additional methods for rapid diagnosis of rinderpest.     

An epidemiological model of rinderpest. II. Simulations of the behaviour of rinderpest virus in populations

Fixed parameters for different hypothetical strains of rinderpest virus (RV) and different susceptible populations are described together with details of their derivation. Simulations were then carried out in a computer model to determine the effects that varying these parameters would have on the behaviour of RV in the different populations. The results indicated that virulent strains of RV are more likely to behave in epidemic fashion whereas milder strains tend towards persistence and the establishment of endemicity. High herd immunity levels prevent virus transmission and low herd immunity levels encourage epidemic transmission. Intermediate levels of immunity assist the establishment of endemicity. The virus is able to persist in large populations for longer than in small populations. Different vaccination strategies were also investigated. In areas where vaccination is inefficient annual vaccination of all stock may be the best policy for inducing high levels of herd immunity. In endemic areas and in herds recovering from epidemics the prevalence of clinically affected animals may be very low. In these situations veterinary officers are more likely to find clinical cases by examining cattle for mouth lesions rather than by checking for diarrhoea or high mortalities.     

Use of the caprinised strain of rinderpest virus for potency testing an attenuated cell culture rinderpest vaccine

The caprinised strain of rinderpest virus was inoculated into goats to produce a challenge stock. These goats were kept with control animals (goats, sheep, calves). In this trial the caprinised strain was shown to have a mild pathogenicity for goats and it spread to one of two contact goats but not from goats to other species. The caprinised strain was then tested on cattle where a febrile reaction was observed. The caprinised strain also did not spread between cattle. The cattle vaccinated with a freeze-dried vaccine produced from the attenuated Kabete RBKO strain on bovine kidney cells were then challenged with the caprinised strain with good results.     

Microelisa test for detecting antibodies to rinderpest virus antigens

Summary A microplate enzyme-linked immunosorbent assay (ELISA) was developed which detected antibodies to a soluble antigen prepared from sonicated rinderpest virus-infected cells. The ELISA detected titres of antibody to the virus in the sera of cattle 3 weeks after immunisation with tissue culture rinderpest virus vaccine which were similar to those detected by the virus neutralisation test. The ELISA test shows potential as a rapid and economic technique for screening large numbers of sera for antibody to rinderpest virus.

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La Prueba Micro-Elisa Para Detectar Anticuerpos Producidos Por Antigenos Del Virus De Rinderpest

Resumen Se utilizó la prueba micro-ELISA para detectar anticuerpos producidos por un antígeno soluble preparado con células sonicadasinfectadas con el virus de rinderpest. La prueba ELISA detectó anticuerpos en el suero de bovinos, 3 semanas después de que éstos fueron inmunizados con la vacuna de rinderpest, preparada ésta en cultivos celulares. Los anticuerpos detectados fueron similares a los estudiados mediante la prueba de neutralización viral. La prueba ELISA se perfila como una técnica rápida y económica para trabajar un número apreciable de muestras de suero con el fin de detectar anticuerpos del virus de rinderpest.

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Un Micro-Test Elisa Pour Deceler Les Anticorps Specifiques Du Vir Us Bovipestique

Résumé Un test immuno-enzymatique (ELISA) a été mis au point déceler les anticorps correspondant à un antigène préparé par traitement aux ultra-sons de cellules infectées. Les titres sériques obtenus par cette méthode dans les sérums de bovins immunisés trois semaines auparavant avec du vaccin de culture cellulaire se sont révélés comparables à ceux obtenus par la méthode classique de séroneutralisation. Le test ELISA apparait comme un moyen rapide et économique pour rechercher les anticorps spécifiques du virus bovipestique dans des sérums en grand nombre.

     

Protection of goats against peste-des-petits-ruminants with attenuated rinderpest virus

Goats vaccinated with attenuated rinderpest were protected from peste-des-petits-ruminants virus for at least 12 months; vaccinated animals were unable to transmit the challenge virus. Before challenge neutralising antibodies were directed primarily against rinderpest but following exposure to peste-des-petits-ruminants, a high antibody level to both viruses was found.     

Humoral antibody response in animals infected with virulent rinderpest virus

Summary Humoral antibody responses in cattle or rabbits infected with virulent rinderpest virus or lapinised rinderpest virus respectively were assessed. Rinderpest specific antibodies could be first detected 6 days post-infection. No correlation could be established between antibody response and the course of the disease in infected animals during the early stages of infection. The animals with fatal infection either did not respond or had a transient antibody response. A gradual increase in antibody titre from 7 days post-infection was observed in animals which ultimately recovered.

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Respuesta De Anticuerpos Humorales En Animales Infectados Con Virus Virulento De Rinderpest

Resumen Se llevó a cabo un estudio tendiente a captar la respuesta de anticuerpos humorales en bovinos o conejos infectados con virus virulento de rinderpest o virus lapinizado de rinderpest, respectivamente. Los anticuerpos específicos de rinderpest fueron detectados a partir de los 6 días despues de la inoculación. No se pudo establecer correlación entre la respuesta de anticuerpos y el curso de la enfermedad en animales infectados, durante los estadíos iniciales de la enfermedad. Los animales con infecciones fatales o no respondieron o tuvieron una respuesta humoral débil. Los animales que se recuperaron presentaron un alza progresiva en el nivel de anticuerpos desde los 7 días después de la infección.

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Response Immunitaire Humorale Chez Des Animaux Infectes Par Le Virus De La Peste Bovine

Résumé Les réponses immunitaires de bovines ou lapins infectés respectivement par le virus de la peste bovine virulent ou lapinisé ont été évaluées. Des anticorps spécifiques contre la peste bovine ont pu être décelés 6 jours après l'infection. Aucune corrélation n'a pu être établie entre la réponse immunitaire et l'évolution de la maladie chez les animaux durant les premiers stades de l'infection. Les animaux n'ayant pas survécu soit n'ont pas développé une réponse immunitaire soit l'on présentée mais de façon transitoire. Une augmentation graduelle de taux d'anticorps à partir du 7e jour après l'infection a été observée chez les animaux qui ont fini par guérir.

     

Development and distribution of rinderpest virus antigen in experimentally infected goats

Three goats, experimentally infected with rinderpest virus were examined for the development and distribution of precipitating antigens in various tissues and secretions using the agar gel immunodiffusion test. Virus antigens were detected in ocular secretions and lymph node biopsies from the second to the fourth and fifth days of pyrexia, respectively, but were not detected in nasal secretions. Precipitating antigens were demonstrated in various lymphoid organs, the lung and abomasum of a goat killed on the fourth day of pyrexia. These findings are discussed in relation to the epidemiology of rinderpest in goats in Africa.     

Differentiation of peste des petits ruminants and rinderpest viruses by neutralisation indices using hyperimmune rinderpest antiserum

Summary Six field isolates believed to be rinderpest viruses and 2 known strains of peste des petits ruminants (PPR) viruses were titrated in the presence of normal rabbit serum and with hyperimmune rinderpest antiserum prepared in rabbits. The known PPR viruses had indices less than 10 whereas 4 of the suspect field isolates had indices greater than a hundred. Two suspect field isolates had indices less than 20; both were collected from small ruminant wild life and are probably PPR viruses.

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Diferenciacion De Peste De Los Pequenos Rumiantes Y Virus De Rinderpest Mediante Indices De Neutrilizacion Utilizando Antisueros Hiperinmunes De Rinderpest

Resumen Seis aislamientos de campo sospediosos de Rinderpest y dos cepas conocidas de Peste de los pequeños rumiantes (PPR) fueron titulados en titulados en presencia de suero normal de conejo y suero hiperimmune a Rinderpest, prepardo en conjo. Las cepas concidos de PPR dierond titulos menores de 10, mientras que 4 de los aislamientos sospechosos de Rinderpest dieron titulos mayores de 100. Los 2 aislamientos de campo restantes dieron titulos menores de 20. Ambos fueron aislados de pequenños ruminantes silvestras y probablemente sean virus de PPR.

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Differenciation Des Virus De La Peste Bovine Et De La Peste Des Petits Ruminants Par Les Indices De Neutralisation Utilisant Des Antiserums Hyperimmuns De La Peste Bovine

Résumé La titration de 6 isolats recuellis sur le terrain et considérés comme étant du virus de la peste bovine, et 2 souches connues du virus de la peste des petits ruminants (PPR) ont été titrés en présence de sérum normal de lapin et avec un antisérum hyperimmun de la peste bovine préparé sur lapins. Les virus identifiés PPR avaient des indices inférieurs à 10 alors que 4 des isolats suspects présentaient des indices supérieurs à 100. Deux isolats suspects avaient des indices inférieurs à 20 et tous deux provenaient de petits ruminants sauvages et sont probablement des virus de la PPR.

     

Immune response and protection of cattle and pigs generated by a vaccinia virus recombinant expressing the F protein of rinderpest virus

The immune response of cattle and pigs to a vaccinia recombinant virus containing the fusion (F) protein gene of rinderpest virus was examined. Half the cattle and all the pigs gave humoral response to primary vaccination and all the cattle gave an anamnestic response to a second vaccination 28 days after the primary vaccination. All the cattle after a single or secondary vaccination were completely protected clinically after exposure to a lethal dose of the Saudi 1/81 strain of virus. Prior vaccination with another TK- vaccinia recombinant (VVCAT) suppressed, but did not abrogate, the immune response to the rinderpest F recombinant. The pigs gave a humoral immune response in the absence of any local reaction at the site of vaccination.