Heat stress as a manageable risk factor to mitigate pneumonia in lambs

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The paper by Goodwin et al (2004 Goodwin, KA, Jackson, R, Brown, C, Davies, PR, Morris, RS and Perkins, NR. 2004. Pneumonic lesions in lambs in New Zealand: patterns of prevalence and effects on production. New Zealand Veterinary Journal, 52: 175–9. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar]) which appeared in the August 2004 issue of the New Zealand Veterinary Journal highlighted the prevalence and costs to the sheep industry of pneumonia in lambs. The costs are considerable, and the article begs the question, “what can sheep farmers do to reduce the effects of pneumonia in lambs?”     

Demodex spp. infestation and suspected demodicosis of alpacas (Vicugna pacos) in New Zealand

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Ectoparasites known to cause skin lesions in alpacas (Vicugna pacos) include the mites Sarcoptes scabiei, Chorioptes bovis and Psoroptes spp., and the lice Microthoracius mazzai and Bovicola breviceps (Cicchino et al. 1998 Cicchino, AC, Munoz, Cobenas ME, Bulman, GM, Diaz, JC and Laos, A. 1998. Identification of Microthoracius mazzai (Phthiraptera: Anoplura) as an economically important parasite of alpacas. Journal of Medical Entomology, 35: 922–930.  [Google Scholar]; Foster et al. 2007 Foster, A, Jackson, A and D'alterio, GL. 2007. Skin diseases of South American camelids. In Practice, 29: 216–223. [Crossref], [Web of Science ®] , [Google Scholar]). Occasionally, Demodex spp. infestations have been reported or mentioned as incidental fi ndings in llamas (Lama glama) (Atlee et al. 1997 Atlee, BA, Stannard, AA, Fowler, ME, Willemse, T, Ihrke, PJ and Olivry, T. 1997. The histology of the normal llama skin. Veterinary Dermatology, 8: 165–176. [Crossref], [Web of Science ®] , [Google Scholar]) and alpacas (Foster et al. 2007 Foster, A, Jackson, A and D'alterio, GL. 2007. Skin diseases of South American camelids. In Practice, 29: 216–223. [Crossref], [Web of Science ®] , [Google Scholar]). So far, only Sarcoptes scabiei (McKenna et al. 2005 McKenna, PB, Hill, FI and Gillett, R. 2005. Sarcoptes scabiei infection on an alpaca (Lama pacos. New Zealand Veterinary Journal, 53: 213–213. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar]), Chorioptes bovis (Arthur 1997 Arthur, DG. 1997. Diseases of lamoids in New Zealand. Surveillance, 24(1): 29–30.  [Google Scholar], non-peer reviewed) and Bovicola breviceps (Palma et al. 2006 Palma, RL, McKenna, PB and Aitken, P. 2006. Confirmation of the occurrence of the chewing louse Bovicola (Lepikentron) breviceps (Insecta: Phthiraptera: Trichodectidae) on alpacas (Lamas pacos) in New Zealand. New Zealand Veterinary Journal, 54: 253–254. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar]) have been recorded on lamoids in New Zealand. Here, we report the first record of Demodex spp. infestation of an alpaca in New Zealand.     

Neospora caninum infection in an aborted bovine foetus in Brazil

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Neospora caninum is an apicomplexan protozoan parasite first reported in dogs (Bjerkås et al., 1984 Bjerkås, I, Mohn, SF and Presthus, J. 1984. Unidentified cyst-forming sporozoan causing encephalomyelitis and myositis in dogs. Zeitschrift für Parasitenk, 70: 271–274. [Crossref], [PubMed], [Web of Science ®] , [Google Scholar]; Dubey et al., 1988a Dubey, JP, Carpenter, JL, Speer, CA, Topper, MJ and Uggla, A. 1988a. Newly recognized fatal protozoan disease of dogs. Journal of the American Veterinary Medical Association, 192: 1269–1285. [PubMed], [Web of Science ®] , [Google Scholar], Dubey et al., 1988b Dubey, JP, Hattel, AL, Lindsay, DS and Topper, MJ. 1988b. Neonatal Neospora caninum infection in dogs: Isolation of the causative agent and experimental transmission. Journal of the American Veterinary Medical Association, 193: 1259–1263.  [Google Scholar]) and subsequently recognised as a cause of bovine abortion (Dubey and Lindsay, 1993 Dubey, JP and Lindsay, DS. 1993. Neosporosis. Parasitology Today, 9: 452–458.  [Google Scholar]). Natural N. caninum infections have been reported in other animal species including the goat, sheep, horse and deer (Dubey and Lindsay, 1996 Dubey, JP and Lindsay, DS. 1996. A review of Neospora caninum and neosporosis. Veterinary Parasitology, 67: 1–59. [Crossref], [PubMed], [Web of Science ®] , [Google Scholar]). The dog was recently identified as definitive host of the parasite (McAllister et al., 1998 McAllister, MM, Dubey, JP, Lindsay, DS, Jolley, WR, Wills, RA and McGuire, AM. 1998. Dogs are definitive hosts of Neosporu caninum. International Journal for Parasitology, 28: 1473–1478. [Crossref], [PubMed], [Web of Science ®] , [Google Scholar]). Neospora caninum has a worldwide distribution (Barber et al., 1995 Barber, JS, Holmdahl, OJM, Owen, MR, Uggla, A and Trees, AJ. 1995. Characterization of the first European isolate of Neosporu caninum (Dubey, Carpenter,Speer, Topper and Uggla). Parasitology, 111: 563–568.  [Google Scholar]; Duivenvoorden, 1995 Duivenvoorden, J. 1995. Neospora abortions in eastern Ontario dairy herds. Canadian Veterinary Journal, 36: 623–623.  [Google Scholar]; Jardine and Wells, 1995 Jardine, JE and Wells, BH. 1995. Bovine neosporosis in Zimbabwe. Veterinary Record, 137: 223–223.  [Google Scholar]; Stenlund et al., 1997 Stenlund, S, Bjorkman, C, Holmdahl, OJM, Kindahl, H and Uggla, A. 1997. Characterization of a Swedish bovine isolate of Neospora caninum. Parasitology Research, 83: 214–219.  [Google Scholar]; Thornton et al., 1991 Thornton, RN, Thompson, EJ and Dubey, JP. 1991. Neospora abortion in New Zealand cattle. New Zealand Veterinary Journal, 39: 129–133. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar]; Umemura et al., 1992 Umemura, T, Shiraki, K, Morita, T, Shimada, A, Haritani, M, Kobayashi, M and Yamagata, S. 1992. Neosporosis in a dog: The first case report in Japan. Journal of the Veterinary Medical Science, 54: 157–159.  [Google Scholar]) but the presence of N. caninum in Brazil has not been confirmed.     

Re: Regional variations in the nematode worm populations of breeding ewes in New Zealand

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The paper by Hervé et al (2003) Hervé, M, McAnulty, RW, Logan, CM and Sykes, AR. 2003. Regional variations in the nematode worm populations of breeding ewes in New Zealand. New Zealand Veterinary Journal, 51: 159–164. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar] which appeared in the August 2003 issue of the New Zealand Veterinary Journal reported on regional differences in the relative proportions of nematode parasite species cultured from faecal samples collected from ewes during lactation.     

Prevalence of Neospora antibodies in New Zealand dairy cattle and dogs

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Neospora caninum is a major cause of disease in cattle and dogs, manifesting with abortions in cattle, and hind limb paresis in mostly young dogs ⁽¹⁾ Dubey, JP and Lindsay, DS. 1996. A review of Neospora caninum and neosporosis. Veterinary Parasitology, 67: 1–59. [Crossref], [PubMed], [Web of Science ®] , [Google Scholar]. Previous reports from New Zealand suggest that around 30% of bovine abortions may be due to Neospora ⁽²⁾ Thornton, RN, Thompson, EJ and Dubey, JP. 1991. Neospora abortion in New Zealand cattle. New Zealand Veterinary Journal, 39: 129–133. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar] ⁽³⁾ Thornton, R. 1992. Bovine abortions — Laboratory diagnosis 1991. Surveillance, 19: 24–24.  [Google Scholar] and that about 40% of recently aborted dairy cows have antibodies against Neospora ⁽⁴⁾ Reichel, MP and Drake, JM. 1996. The diagnosis of Neospora abortions in cattle. New Zealand Veterinary Journal, 44: 151–154. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar].     

Protein nutrition of dairy cattle

Abstract

In the June 1998 issue of the New Zealand Veterinay Journal, a clinical review was published focusing on aspects of the protein nutrition of dairy cattle (Westwood et al., 1998 Westwood, CT,, Lean, IJ, and Kellaway, RC. 1998. Indications and implications for testing milk urea in dairy cattle: A quantitative review. Part 1. Dietary protein sources and metabolism. New Zealand Veterinary Journal, 46: 87–96. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar]). The authors wrote: “Most species of rumen bacteria can use ammonia for growth, but some, particularly bacteria which ferment cell wall carbohydrates, use or have obligate requirements for amino acids and peptides (Russel et al., 1992 Russel, JB,, O’Connor, JD,, Fox, DG,, Soest, PJ, van and Sniffen, CJ. 1992. A net carbohydrate and protein system for evaluating cattle diets. I. Ruminal fermentation. Journal of Animal Science, 70: 3551–61. [PubMed], [Web of Science ®] , [Google Scholar])”.     

A mass screening programme of angus cattle for the mannosidosis genotype — A prototype programme for control of inherited diseases in animals

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Recent research has shown that the gene frequency for mannosidosis (pseudolipidosis) may approximate 0.05 in pedigree Angus herds (Jolly, unpublished data). As epidemiological studies suggest an equal frequency in commercial non-pedigree herds, the disease is elf economic importance to the national beef industry. Mannosidosis is an inherited lysosomal storage disease associated with a defect in catabolism, of the heterosaccharide fractioln of glycoproteins (Whittem and Walker, 1957 Donnelly, W. J. C., Sheahan, B. J. and Rogers, T. A. 1973a. GM₁ gangliosidosis in Friesian calves. J. Path., 111: 173–179.  [Google Scholar]; Jolly 1971 Donnelly, W. J. C., Sheahan, B. J. and Kelly, M. 1973b. Bet α-galactosidase deficiency in GM₁ gangliosidosis of Friesian calves. Res. vet. Sci., 15: 139–141.  [Google Scholar]; Hocking et al., 1972 Hocking, J. D., Jolly, R. D. and Batt, R. D. 1972. Deficiency of α-mannosidase in Angus cattle. Biochem. J., 128: 69–78.  [Google Scholar]; Phillips et al., 1974 Jolly, R. D. 1971. The pathology of the central nervous system in pseudolipidosis of Argus cattle. J. Path., 103: 113–121.  [Google Scholar]). Whereas animals with mannosidosis have negligible tissue sand plasma levels of α-mannosidase, heterozygotes having one normal gene and one defective gene have approximately half the normal level of enzyme in their tissues and plasma. This observation forms the basis for a control programme in which heterozygotes are identified by their plasma α-mannosidase 1evels (Jolly et al., 1973 Jolly, R. D., Tse, C. A. and Greenway, R. M. 1973. Plasma α-mannosidase activity as a means of detecting mannosidosis heterozygotes. N.Z. vet. J., 21: 64–69. [Taylor &; Francis Online] , [Google Scholar], 1974a Jolly, R. D., Thompson, K. G., Tse, C. A., Munford, R. E. and Merrall, M. 1974a. Identification of mannosidosis heterozygotes — factors affecting normal plasma α-mannosidase levels. N.Z. vet. J., 22: 155–162. [Taylor &; Francis Online] , [Google Scholar], b Jolly, R. D., Thompson, K. G. and Tse, C. A. 1974b. Evaluation of a mass screening programme for identification of mannosidosis heterozygotes in Angus cattle. N.Z. vet. J., 22: 185–190. [Taylor &; Francis Online] , [Google Scholar]).     

Filaroides infections in wild ferrets (Mustela putorius) and stoats (Mustela erminea)

Abstract

Species of metastrongylid nematodes of the genus Filaroides have been recorded in various hosts throughout the world(1) Anderson, RC. 1978. “No.5. Keys to the genera of the superfamily Metastrongyloidea”. In CIH Keys to the Nematode Parasites of Vertebrates, Edited by: Anderson, RC, Chabaud, AG and Willmott, S. 3–4. Wallingford: CAB International.  [Google Scholar]. In New Zealand, the only known species is Filaroides (= Oslerus) osleri, which occurs in wart-like nodules near the bifurcation of the trachea of the dog(2) Jones, BR, Clark, WT, Collins, GH and Johnstone, AC. 1977. Filuroides osleri in a dog. New Zealand Veterinary Journal, 25: 103–104. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar].     

Cilia and cilia-related disorders

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Among the puzzling aspects of the recently described autosomal recessive polycystic kidney disease (ARPKD) of sheep (Johnstone et al 2005 Johnstone, AC, Davidson, BI, Roe, AR, Eccles, MR and Jolly, RD. 2005. Congenital polycystic kidney disease in lambs. New Zealand Veterinary Journal, 53: 307–314. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar]) is the multiplicity of organ systems affected and the phenotypic variations that occur between the various animal species. It has been shown in studies of other inherited polycystic kidney disease syndromes that the normal gene products of a mutant are likely to be involved in ciliary structure and function. The studies that have led to this recognition can be expected to eventually provide the basis for a better understanding of the functioning of this organelle, and the pathogenesis of lesions in the related diseases.

It is well known that cilia are important in the perception of light, olfactory stimuli and sound and that motile cilia provide cell motility (e.g. sperm) and transport of mucus and other fluids. Recent research has indicated that the involvement of the primary cili-um/basal body complex is of central importance in the detection and cellular response to extracellular movement of fluid, critical phases of embryonic development, cell cycle regulation and maintenance of cell polarity.

Confocal microscopic studies of renal cyst epithelium in ovine ARPKD have shown that only 30% of cells have a cilium and that these are often truncated (McGlashan et al 2005 McGlashan, SR, Poole, CA, Stayner, C, Johnstone, AC, Eccles, MR and Jensen, CG. 2005. “Primary cilia in fibrosis associated with two models of polycystic kidney disease”. In Proceedings of the 45th Annual Conference of the American Society for Cell Biology December 10–14 [Google Scholar]). The observation, although preliminary, strongly supports the argument that the mutant gene in this disease of sheep normally encodes for a protein essential for primary ciliary function.     

Serological evidence of respiratory syncytial virus infection in lambs

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Madam;–The results of field trials of a live parainfluenza virus type3(PI₃)vaccine suggested that(PI₃)might not be the only virus involved in the initiation of outbreaks of pneumonia in lambs in New Zealand,(5 Adair, B.M., McFerran, J.B. and McKillop, E.R. 1982. A sixth species of ovine adenovirus isolated from lambs in New Zealand. Arch. Virol., 74: 269–269. [Crossref] , [Google Scholar])The outbreaks that were not associated with infection with(PI₃)could not be linked to infection with the other ovine respiratory viruses then known to be present in New Zealand (ovine adenovirus type 6 and the ovine variant of bovine adenovirus type 7)((1 Adair, B.M., McFerran, J.B. and McKillop, E.R. 1982. A sixth species of ovine adenovirus isolated from lambs in New Zealand. Arch. Virol., 74: 269–269. [Crossref] , [Google Scholar]),(4 Adair, B.M., McFerran, J.B. and McKillop, E.R. 1982. A sixth species of ovine adenovirus isolated from lambs in New Zealand. Arch. Virol., 74: 269–269. [Crossref] , [Google Scholar]),(5 Adair, B.M., McFerran, J.B. and McKillop, E.R. 1982. A sixth species of ovine adenovirus isolated from lambs in New Zealand. Arch. Virol., 74: 269–269. [Crossref] , [Google Scholar])suggesting that other unrecognised viruses might be involved. Respiratory syncytial virus (RSV) is a major cause of pneumonia in human infants and in cattle.(8 Adair, B.M., McFerran, J.B. and McKillop, E.R. 1982. A sixth species of ovine adenovirus isolated from lambs in New Zealand. Arch. Virol., 74: 269–269. [Crossref] , [Google Scholar])This virus has recently been isolated from a yearling ewe with mild rhinitis(6 Adair, B.M., McFerran, J.B. and McKillop, E.R. 1982. A sixth species of ovine adenovirus isolated from lambs in New Zealand. Arch. Virol., 74: 269–269. [Crossref] , [Google Scholar])and there is serological evidence of infection in adult sheep.(3 Adair, B.M., McFerran, J.B. and McKillop, E.R. 1982. A sixth species of ovine adenovirus isolated from lambs in New Zealand. Arch. Virol., 74: 269–269. [Crossref] , [Google Scholar]),(6 Adair, B.M., McFerran, J.B. and McKillop, E.R. 1982. A sixth species of ovine adenovirus isolated from lambs in New Zealand. Arch. Virol., 74: 269–269. [Crossref] , [Google Scholar])However, there are no reports implicating this virus in outbreaks of pneumonia in lambs, although experimental infection of lambs with a bovine isolate of RSV resulted in reduced pulmonary bacterial clearance leading to secondary pneumonic pasteurellosis.(2 Adair, B.M., McFerran, J.B. and McKillop, E.R. 1982. A sixth species of ovine adenovirus isolated from lambs in New Zealand. Arch. Virol., 74: 269–269. [Crossref] , [Google Scholar])     

Caprine arthritis encephalitis

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Caprine arthritis encephalitis (CAE) is a disease of goats of any breed, sex and age, caused by a retrovirus related to, but distinct from, the maedi-visna virus which affects sheep.(4) Gazit, A., Yaniv, A., Divr, M., Perk, K., Irving, S.G. and Dahlberg, J.E. 1983. The caprine arthritis-encephalitis virus is a distinct virus within the lentivirus group. Virology, 124: 192–195.  [Google Scholar] (10) Roberson, Susan M., McGuire, T.C., Klevjer-Anderson, Paula, Gorham, J.R. and Cheevers, W.P. 1982. Caprine arthritis-encephalitis virus is distinct from visna and progressive pneumonia viruses as measured by genome sequency homology. J. Virol., 44: 755–758. [PubMed], [Web of Science ®] , [Google Scholar] Both infections are included among the so-called slow virus diseases which are characterised by a long incubation period, protracted clinical course and persistent infection. Maedi-visna is not present in New Zealand but CAE has been detected in a number of goat flocks.     

Incidence of ryegrass staggers in white rhinoceros (Ceratotherium simum) at Auckland Zoo

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Most perennial ryegrass (Lolium perenne) plants in pastures in New Zealand contain a naturally occurring fungal endophyte, Neotyphodium lolii. Endophyte-infected perennial ryegrass produces alkaloids that vary in concentration during the year. Some alkaloids enhance the persistence and productivity of ryegrass pastures by protecting them against insect attack. However, when other alkaloids are consumed they can reduce animal performance and lead to health problems. The alkaloid lolitrem B, for example, causes the neuromuscular disorder ryegrass staggers (Fletcher et al 1999 Fletcher, LR, Sutherland, BL and Fletcher, CG. 1999. “The impact of endophyte on the health and productivity of sheep grazing ryegrass-based pastures”. In Ryegrass endophyte: an essential New Zealand symbiosis Grassland Research and Practice Series Edited by: Woodfield, DR and Matthew, C. Vol. 7, 11–17.  [Google Scholar]). Clinical symptoms of ryegrass staggers in animals range from slight muscular tremors through to staggering and complete collapse. Severely affected animals create management problems and are prone to accidental death. Outbreaks occur sporadically, particularly in summer and autumn and affect sheep, cattle, deer, horses, llamas (Lama glama) and alpaca (Lama pacos). Lolitrem B appears to be a stable compound, which tends to be concentrated in the leaf sheath at the base of the ryegrass plant and in the seed-heads (di Menna et al 1992 di Menna, ME, Mortimer, PH, Prestidge, RA, Hawkes, AD and Sprosen, JM. 1992. Lolitrem B concentrations, counts of Acremo ni um lolii hyphae, and the incidence of ryegrass staggers in lambs on plots of A. lolii-infected perennial ryegrass. New Zealand Journal of Agricultural Research, 35: 211–217. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar]; Keogh et al 1996 Keogh, RG, Tapper, BA and Fletcher, RH. 1996. Distributions of the fungal endophyte Acremonium lolii, and of the alkaloids lolitrem B and peramine, within perennial ryegrass. New Zealand Journal of Agricultural Research, 39: 121–127. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar]). Hay made from endophyte-infected perennial ryegrass contains large numbers of seed-heads and lolitrem B concentrations can be high, especially if it is made in late summer or autumn and, consequently, animals fed such hay are at risk of developing ryegrass staggers.     

Tuberculous sialoadenitis in a badger

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Tuberculous lesions in the skin of carnivorous species such as the mustelids have often been associated with the contamination of bite wounds inflicted during intra-species conflict (Muirhead et al., 1974 Muirhead, RH, Gallagher, J and Burn, KJ. 1974. Tuberculosis in wild badgers in Gloucestershire: Epidemiology. Veterinary Record, 95: 552–555.  [Google Scholar]; Cheeseman et al., 1988 Cheeseman, CL, Wilesmith, JW, Stuart, FA and Mallinson, PJ. 1988. Dynamics of tuberculosis in a naturally infected badger population. Mammal Review, 18: 61–72.  [Google Scholar]; Clifton-Hadley et al., 1993 Clifton-Hadley, RS, Wilesmith, JW and Stuart, FA. 1993. Mycobacterium bovis in the European badger (Meles meles): Epidemiological findings in tuberculous badgers from a naturally infected population. Epidemiology and Infection, 111: 9–19.  [Google Scholar]; Nolan and Wilesmith, 1994 Nolan, A and Wilesmith, JW. 1994. Tuberculosis in badgers (Meles meles). Veterinary Microbiology, 40: 179–191.  [Google Scholar]; Ragg et al., 1995 Ragg, JR, Waldrup, KA and Moller, H. 1995. The distribution of gross lesions of tuberculosis caused by Mycobacterium bovis in feral ferrets (Mustela furo) from Otago, New Zealand. New Zealand Veterinary Journal, 43: 338–341. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar]; Lugton et al., 1997 Lugton, IW, Wobeser, G, Morris, RS and Caley, P. 1997. Epidemiology of Mycobacterium bovis infection in feral ferrets (Mustela furo) in New Zealand: II. Routes of infection and excretion. New Zealand Veterinary Journal, 45: 151–157. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar]). A strong association between tuberculous tonsillitis and recovery of Mycobacterium bovis from the oral cavity of ferrets (Mustela furo) was reported by Lugton et al. (1997 Lugton, IW, Wobeser, G, Morris, RS and Caley, P. 1997. Epidemiology of Mycobacterium bovis infection in feral ferrets (Mustela furo) in New Zealand: II. Routes of infection and excretion. New Zealand Veterinary Journal, 45: 151–157. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar]). They believed that the recovery of M. bovis from the pharynx was enhanced by the act of swabbing which could damage the oral mucosal epithelium and dislodge infected mucosal macrophages. The authors speculated that tubercle bacilli could enter the oral cavity through disrupted tonsillar epithelium, although they found no evidence of epithelial damage. It is also well established that in many species, infected pulmonary secretions reach the oral cavity and contaminate saliva (Jennings, 1949 Jennings, AR. 1949. The distribution of tuberculous lesions in the dog and cat, with reference to the pathogenesis. Veterinary Record, 61: 380–384.  [Google Scholar]).     

Parainfluenza type 3 virus in cattle with upper respiratory disease

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Parainfluenza type 3(Pl₃) virus has been associated with upper respiratory disease of cattle in many countries (Hoerlein et al., 1959 Bögel, K. 1961. Virologische Undersuchungsbefunde bei Kalbern mit respiratoris-chem Syndrom unter besonderer Berucksichtigung der Parainfluenza 3 Myxovirus. Mh. Tierheilk, 13: 129–129. 162. [Cited by Jolly, R. D., (1967), N.Z. vet. J., 15: 43–4.] [Google Scholar]; Bögel, 1961 Campbell, R. S. F. 1972. “Virus diseases of cattle. Virology and Virus Disease”. In Proc. No. 16 of Course for Veterinarians, 132–132. University of Sydney.  [Google Scholar]; Reisinger, 1962 Carter, Margery E. and Hunter, R. 1970. Isolation of parainfluenza type 3 virus from sheep in New Zealand. N.Z. vet. J., 18: 226–227. [Taylor &; Francis Online] , [Google Scholar]; Jolly and Ditchfield, 1965 Curtis, R. A. and Sutton, R. H. 1972. Chronic granular rhinitis (nasal catarrh) of cattle. N.Z. vet. J., 20: 125–125. [Taylor &; Francis Online] , [Google Scholar]). However, PI₃ virus has not been isolated from cattle with respiratory disease in New Zealand although a serological study found that 89.3% of cows had significant levels of antibody against PI₃ virus (Pastier and Hansen, 1966). In most cases infections are subclinical, and there is little evidence to suggest that PI₃ virus is an important cause of disease in New Zealand cattle (Jolly, 1967 Fastier, L. B. and Hansen, N. F. 1966. The occurrence of antibodies to bovine virus diarrhoea, infectious bovine rhinotracheitis and parainfluenza 3 viruses in sera from New Zealand cattle. N.Z. vet J., 14: 27–32. [Taylor &; Francis Online] , [Google Scholar]). This communication records an outbreak of upper respiratory disease in cattle from which PI₃ virus was isolated.     

Leptospirosis in a lamb

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Recently, we reported on outbreaks of Leptospira interrogans serovar pomona infection in newly weaned lambs(1) Vermunt, JJ, West, DM, Cooke, MM, Alley, MR and Collins-Emerson, J. 1994. Observations on three outbreaks of Leptospira interrogans serovar pomona infection in lambs. New Zealand Veterinary Journal, 42: 133–6. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar]. It was suggested that wet environmental conditions played an important role in the pathogenesis of the disease in that class of sheep. This communication presents observations on another case of ovine leptospirosis, one that occurred under different circumstances, i.e. different season, age and environmental conditions.     

leptospira interrogans serovar hardjo vaccination against leptospira interrogans serovar balcanica infection

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Sir, — Leptospira interrogans serovar balcanica is now recognised as a widespread infection among opossums in New Zealand ⁽²⁾ Hathaway, S. C, Blackmore, D. K. and Marshall, R. B. 1978. The serologic and cultural prevalence of Leptospira interrogans serovar balcanica in opossums (Trichosurus vulpecula) in New Zealand. J. Wild Dis., 14: 345–350. [PubMed], [Web of Science ®] , [Google Scholar] and the possibility of domestic stock acting as accidental hosts has recently been demonstrated. ⁽³⁾ Mackintosh, C. G., Marshall, R. B. and Blackmore, D. K. 1980. Leptospira interrogans serovar balcanica in cattle. N.Z. vet. J., 28: 268–268. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar] With the recent development of hardjo vaccines ⁽¹⁾ Flint, S. H. and Liardet, D. M. 1980. A Trivalent leptospiral vaccine with emphasis on a Leptospira interrogans serovar hardjo component to prevent leptospiruria. N.Z. vet. J., 28: 263–266. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar] ⁽⁴⁾ Marshall, R. B., Broughton, E. S. and Hellstrom, J. S. 1979. Protection of cattle against natural challenge with Leptospira interrogans serovar hardjo using a hardjo - pomona vaccine. N.Z. vet. J., 27: 114–116. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar] for controlling infection with this serovar in the maintenance hosts, stock could be left vulnerable to infection with other prevalent serovars such as balcanica.     

Cobalt deficiency in sheep and diagnostic reference ranges

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In the last 2 years, two papers have been published suggesting that current New Zealand reference criteria for diagnosing cobalt deficiency should be reviewed (Grace et al 2003), and they are conservatively high and lead to the over-diagnosis of vitamin B₁₂ deficiency and ill-thriftiness in sheep (Gruner et al 2004). The comments refer to reference ranges cited by animal health diagnostic laboratories. These reference ranges were derived from the paper by Clark et al (1989 Clark, RG, Wright, DF, Millar, KR and Rowland, JD. 1989. Reference curves to diagnose cobalt deficiency in sheep using liver and serum vitamin B₁₂ levels.. New Zealand Veterinary Journal, 37: 7–11. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar]), which reviewed data from published and unpublished weight gain response trials preceding that date. The review included all published trials in New Zealand and as many unpublished trials that the authors could obtain. They involved serum vitamin B12 data from 54 trials and liver vitamin B₁₂ data from 21 trials. It was stated that more data from trials conducted in autumn were required to reliably determine an autumn response curve. In addition, it was envisaged that as other trial data became available the reference curves could be upgraded (Clark et al 1985 Clark, RG, Wright, DF and Millar, KR. 1985. A proposed new approach and protocol to defining mineral deficiencies using reference curves. Cobalt deficiency in young sheep is used as a model.. New Zealand Veterinary Journal, 33: 1–5. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar]).     

Gastroenteritis and inanition diarrhoea of sheep transported by ship

Abstract

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“Gastroenteritis” of sheep being transported in bulk livestock ships has been reported ⁽¹⁾ Richards, RB, Norris, RT, Dunlop, RH and McQuade, NC. 1989. Causes of death in sheep exported live by sea. Australian Veterinary Journal, 37: 33–38.  [Google Scholar] ⁽²⁾ Black, H. 1989. Live sheep shipments. New Zealand Veterinary Journal, 37: 175–175. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar] ⁽³⁾ Davis, GB. 1989. The live sheep trade. Surveillance, 16(4): 24–26.  [Google Scholar], but still remains a poorly defined disease syndrome.     

Toxoplasmosis in piglets

Abstract

Extract

Ovine toxoplasmosis is of importance in New Zealand where it is recognized as the most common cause of intrauterine infection leading to abortion and stillbirths (Hartley and Boyes, 1964 Hartley, W. J. and Boyes, Betty W. 1964. Incidence of ovine perinatal mortality in New Zealand with particular reference to intrauterine infections. N.Z. vet. J., 12: 33–36. [Taylor &; Francis Online] , [Google Scholar]). Although clinical disease is rare in humans, serological evidence shows a high incidence of subclinical infection with 50% of New Zealand adults over 40 years of age showing positive titres (Manning and Reid, 1956 Manning, J. D. and Reid, J. D. 1956. Toxoplasmosis in New Zealand. A serological survey. N.Z. med. J., 55: 441–447. [PubMed] , [Google Scholar]). There is, however, a paucity of information on the disease incidence in other species in this country. Hartley (1956) Hartley, W. J. 1956. Some observations on canine toxoplasmosis. N.Z. vet. J., 4: 115–118. [Taylor &; Francis Online] , [Google Scholar] has recorded toxoplasmosis in dogs and fowls. Pneumonia in a pig associated with Toxoplasma gondii was described by Shortridge and Smith (1964) Shortridge, E. H. and Smith, B. 1964. Toxoplasmosis in a pig in New Zealand. N.Z. vet. J., 12: 118–120. [Taylor &; Francis Online] , [Google Scholar] while, more recently, Shortridge (1968) Shortridge, E. H. 1968. Toxoplasmosis in cats in New Zealand. N.Z. vet. J., 16: 129–130. [Taylor &; Francis Online] , [Google Scholar] noted two cases of feline toxoplasmosis. This present communication concerns an outbreak of acute toxoplasmosis in several piglets.     

Re: The safety of oral calcium formate

Abstract

A Short Communication was published in the October 2002 issue of the New Zealand Veterinary Journal entitled “An investigation of the safety of oral calcium formate in dairy cows using clinical, biochemical and histopathological parameters” (McIntyre and Weston 2002 McIntyre, LH and Weston, SJ. 2002. An investigation of the safety of oral calcium formate in dairy cows using clinical, biochemical and histopathological parameters. New Zealand Veterinary Journal, 50: 195–198. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar]). It appeared to be comparing results directly withthose of a prior communication (Scott and Van Wijk 2000 Scott, DJ and Van Wijk, N. 2000. Comparison in dairy cattle of mucosal toxicity of calcium formate and calcium chloride in oil. New Zealand Veterinary Journal, 48: 24–26. [Taylor &; Francis Online], [Web of Science ®] , [Google Scholar]).