Bovine leukaemia virus infection in New Zealand cattle

Bovine Leukaemia Virus (BLV) infection in New Zealand cattle was investigated. In a national survey of 5000 sera from 500 herds, BLV antibody was not detected. An additional 1062 sera from 140 herds were tested and 3 sera were positive. In the herd of origin of one of these 3 sera, 22.6% of cattle were serologically positive for BLV. Where cases of bovine lymphosarcoma had been diagnosed, 38 of 39 herds tested were negative for BLV antibody. Within the remaining herd, 36% of cows tested were serologically-positive. BLV was isolated from 2 serologically positive cows in this herd.     

Bovine respiratory syncytial virus infection in an ontario cattle herd

Bovine respiratory syncytial virus was recovered from the lung of a six month old calf that died during an outbreak of respiratory disease in a cattle herd in Ontario. Lung tissue removed from the calf at necropsy, performed within two hours of death, was frozen at -70°C prior to virus isolation attempts. Syncytia and intracytoplasmic inclusions were demonstrated both in histological sections of the calf's lung and in stained cell culture preparations infected with the bovine respiratory syncytial virus isolate. Direct fluorescent antibody and virus neutralization tests serologically confirmed the identity of the isolate.     

Equine rhinopneumonitis virus infection in New Zealand

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Sir,—Japanese workers (Matumoto el al., 1965 Matumoto, M., Ishizaki, R. and Shimuzu, T. 1965. Serologic survey of equine rhinopneumonitis virus infection among horses in various countries. Arch, f. Viruslorsch., 15: 609–624.  [Google Scholar]) have examined 388 horse sera from 17 countries including New Zealand and have found evidence of a high incidence of infection with equine rhinopneumonitis virus. The New Zealand material was supplied between 1957 and 1960, by Dr J. D. Manning, then of the National Health Institute, Wellington.     

Bovine viral diarrhoea virus infection in cattle,sheep and goats in northern Tanzania

Virological and serological investigations were carried out in cattle, sheep and goats raised in the northern part of Tanzania in order to explore the possibility of bovine viral diarrhoea (BVD) virus cycling within these animal species. Two noncytopathogenic BVD virus isolates (A4/5/Tan86 and A4/10/Tan86) were obtained from sera sampled from inapparently infected indigenous (zebu) cattle originating from Kiteto district in Arusha region. No BVD virus was isolated from any of the sheep or goat sera. Seroepidemiological investigations revealed widespread prevalence of neutralising antibodies to BVD virus not only in cattle but also in sheep and goats. The seropositive rates are discussed in relation to previous observations in Tanzania and other parts of the world and to the livestock husbandry practices in northern Tanzania.     

Bovine virus diarrhea (BVD)--diagnostic determination of cattle with persistent BVD virus infection

Buffy coats of 1074 cattle were examined for regard to BVD virus using the usual long-termed-cultivation (LTC) in bovine kidney monolayer cell cultures (7 days) whereby 268 carriers could be detected. Serum samples collected simultaneously from the same cattle were examined by means of a short-termed-cultivation (STC) of only two days in stationary macroplate cell cultures. Using this method only 172 carriers were found. Amongst 96 serum samples from animals positive in LTC of buffy coat leucocytes and negative in the STC further 19 cattle were found to be viraemic when the sera were tested by LTC, too. Thus 77 of a total of 268 serum samples (28.7%) taken from viraemic cattle turned out to be negative in the STC as well as the LTC. These results are discussed with regard to the antibody level and the age of the animals. The reduced sensitivity is considered in relation to the favourable time and cost factor. STC of serum samples in connection with the serological results proved to be valuable for the examination of cattle of more than 6 months of age but not for calves below 6 months.     

Neospora abortion in New Zealand cattle

Protozoal abortion in cattle was retrospectively studied by examining material submitted to the Batchelar Animal Health Laboratory in the years 1987-90. Only cases in which foetal brain had been submitted were examined. Histologically, protozoal lesions were seen in the brains of 28% of 320 aborted foetuses. Lesions were also seen in 10% of the hearts and 34% of the placentas examined, but these were not as characteristic as those in the brains. Protozoa, confirmed immunohistochemically as being Neospora caninum-like in two brains, were seen in 5% of aborted foetuses with lesions. No protozoa or associated lesions were seen in 57 late term foetuses or neonatal controls. A farm survey supported the hypothesis that Neospora is an important cause of multiple abortions in cattle. Laboratory and farm data suggested that protozoal abortion was more common in early gestation. No predisposing causes of abortion were found and there was no evidence of point infection of affected herds.     

Bovine leukaemia proviral DNA detection in cattle using the polymerase chain reaction

Bovine leukaemia virus (BLV) is the causative agent in enzootic bovine leukosis a disease occurring worldwide. This virus is normally detected by the agar gel immunodiffusion or ELISA assays which rely on the appearance of antibodies to a major surface protein of the virus, gp51, present in the serum of infected cattle. We have used the polymerase chain reaction, which depends on the amplification of specific DNA sequences as a sensitive assay for the detection of BLV. It was possible to detect proviral DNA in 100 pg of tumour DNA from an infected host using agarose gel electrophoresis followed by ethidium bromide staining. The sensitivity of the assay was increased by two log orders when hybridization analysis, using a BLV proviral DNA probe, was used in combination with amplification of the DNA. Proviral DNA was detected in both lymphocytic and tumour DNA and at all stages of infection in cattle.     

Bovine respiratory syncytial virus infection

Bovine respiratory syncytial virus (BRSV) belongs to the pneumovirus genus within the family Paramyxoviridae and is a major cause of respiratory disease in young calves. BRSV is enveloped and contains a negative sense, single-stranded RNA genome encoding 11 proteins. The virus replicates predominantly in ciliated respiratory epithelial cells but also in type II pneumocytes. It appears to cause little or no cytopathology in ciliated epithelial cell cultures in vitro, suggesting that much of the pathology is due to the host's response to virus infection. RSV infection induces an array of pro-inflammatory chemokines and cytokines that recruit neutrophils, macrophages and lymphocytes to the respiratory tract resulting in respiratory disease. Although the mechanisms responsible for induction of these chemokines and cytokines are unclear, studies on the closely related human (H)RSV suggest that activation of NF-kappaB via TLR4 and TLR3 signalling pathways is involved. An understanding of the mechanisms by which BRSV is able to establish infection and induce an inflammatory response has been facilitated by advances in reverse genetics, which have enabled manipulation of the virus genome. These studies have demonstrated an important role for the non-structural proteins in anti-interferon activity, a role for a virokinin, released during proteolytic cleavage of the fusion protein, in the inflammatory response and a role for the SH and the secreted form of the G protein in establishing pulmonary infection. Knowledge gained from these studies has also provided the opportunity to develop safe, stable, live attenuated virus vaccine candidates.     

Salmonella cholerae-suis from cattle in New Zealand

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Salmonella cholerae-suis is considered to be the most common salmonella found in pigs. Following its first isolation by Salmon and Smith (1885 Salmon, E. and Smith, T. 1885. Report on Swine Plague. Rep. U.S. Bur. anim. Ind., : 184–184.  [Google Scholar]), S. cholerae-suis was thought to be the cause of hog cholera. However, hog cholera is now known to be due to a virus, while S. cholerae-suis is a common secondary invader in this disease.