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Studies on the pathogenesis of rinderpest in experimental cattle I. Correlation of clinical signs, viraemia and virus excretion by various routes

Published online by Cambridge University Press:  15 May 2009

B Liess
Affiliation:
East African Veterinary Research Organization, Muguga, P.O. Box 32, Kikuyu, Kenya, East Africa
W Plowright
Affiliation:
East African Veterinary Research Organization, Muguga, P.O. Box 32, Kikuyu, Kenya, East Africa
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A total of twenty-five grade cattle were infected experimentally with a strain of rinderpest virus of moderately high virulence (RGK/1). Three methods of introduction of the virus were employed, i.e. subcutaneous or intranasal inoculation (14 animals) and housing in contact with reacting cattle (11 animals).

A quantitative study of the viraemia and of virus excretion by the nasal, urinary and faecal routes, was made by the inoculation of primary calf kidney cultures. All virological data were related to the onset of pyrexia, the incubation period in inoculated animals being 3–5 days, while in those infected by contact it was 8–11 days. Viraemia preceded the first rise of temperature by as much as 2 days in inoculated animals and 1 day in the contact cases. All animals had viraemia by the 4th day of the disease, but thereafter the percentage of positives declined rapidly, reaching nil by the 9th day.

The case mortality rate was 48 % with the majority of animals dying on the 7th to 10th days after reaction.

Virus was detected in the nasal secretions of some animals on the 2nd day preceding pyrexia. The proportion of nasal excretors rose slowly to reach a maximum of 87·5 % on the 4th day and no positives were detected after the 9th day of fever. The titre of virus in nasal discharges reached high levels, often probably in the region of 105·0 to 106·0 TCD 50/ml.

Urinary excretion of virus began on the 1st day of fever in about 25 % of animals; reaching a maximum of 62·5 % on the 7th day. No virus was recovered from the urine after the 8th day of the disease, the rapid decline in the excretor rate being only partially attributable to the death of severe cases. Urinary titres were relatively low; they seldom exceeded 102·0 TCD 50/ml.

Virus was first recovered from the faeces on the 3rd day of pyrexia. Excretion by this route was not constantly associated with the development of diarrhoea, but the rapid decline which occurred in the excretor rate on the 8th and 9th days was undoubtedly attributable to the death of diarrhoeic individuals which took place at that time. The majority of faecal titres were in the approximate range of 103·0 to 104·0 TCD 50/g. but occasional samples attained ca. 106·0 TCD 50/g.

It was calculated, from the clinical and virological data that cattle can excrete virus, at least by the nasal route, as much as 6 days before the appearance of pathognomonic clinical signs, i.e. oral necrosis and erosion.

Our findings for rinderpest were compared with those of other investigators of this disease and also with the available information on canine distemper and human measles.

We are very grateful for their able technical assistance to Messrs L. W. Rowe, C. S. Rampton and R. F. Staple. Particular thanks are due to Mr C. S. Rampton for his preparation of all the figures. We have received considerable and indispensable help from our junior laboratory staff, especially Mr Francis Ngugi Gachuhi and Mr Joash Adero.

This paper is published by permission of Mr H. R. Binns, C.M.G., O.B.E., the Director of the East African Veterinary Research Organization.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1964

References

REFERENCES

Bindrich, H. (1950). Zur Ausscheidung des Hundestaupevirus mit dem Harn. Exp. vet. Med. 3, 34–8.Google Scholar
Bindrich, H. (1954). Beitrag zum Wesen der Staupevirusinfektion des Hundes und zu ihrer Bekämpfung. Arch. exp. Vet.-Med. 8, 299307.Google Scholar
Burdon-Sanderson, J. (1866). On the nature, progress and symptoms of the cattle plague, and the modes of its propagation. In 3rd Cattle Plague Report, pp. 154.Google Scholar
Curasson, G. (1932). La Peste Bovine. Paris: Vigot Frères.Google Scholar
Curasson, G. (1942). Traité de Pathologie Exotique Vétérinaire et Comparée, 2me ed. Paris: Vigot Frères.Google Scholar
Dulbecco, R. & Vogt, M. (1954). Plaque formation and isolation of pure lines with poliomyelitis viruses. J. exp. Med. 99, 167–83.CrossRefGoogle ScholarPubMed
Edmonds, C. R. & Walker, G. K. (1929). Diseases of Animals in Tropical Countries, 2nd ed. London: Baillière, Tindall and Cox.Google Scholar
Enders, J. F. (1962). Measles virus. Historical review, isolation and behaviour in various systems. Amer. J. Dis. Child. 103, 282–7.CrossRefGoogle ScholarPubMed
Enders, J. F., Katz, S. L. & Medearis, D. N. (1959).Recent advances in knowledge of the measles virus. In Perspectives in Virology, I. Ed. M, Pollard.New York: John Wiley and Sons, Inc. (Quoted by Robbins (1962).)Google Scholar
Gorham, J. R. (1960). Canine distemper (la maladie de Carré). Adv. vet. Sci. 6, 287351.Google Scholar
Gorham, J. R. & Brandley, C. A. (1953). The transmission of distemper among ferrets and mink. Proc. Book Amer. vet. med. Ass., 90th Annu. Meeting, pp. 129–41. (Quoted by Gorham (1960).)Google Scholar
Gresser, I. & Katz, S. L. (1960). Isolation of measles virus from urine. New Engl. J. Med. 263, 452. (Quoted by Enders (1962).)CrossRefGoogle ScholarPubMed
Grist, N. R. (1950). The pathogenesis of measles: review of the literature and discussion of the problem. Glasgow med. J. 31, 431–41.Google ScholarPubMed
Hagan, W. A. & Bruner, D. W. (1957).The Infectious Diseases of Domestic Animals. Ithaca. New York: Comstock Publishing Associates.Google Scholar
Hall, G. N. (1933). Investigations on rinderpest immunization. Thesis, Zürich.Google Scholar
Hornby, H. E. (1926). Studies in rinderpest immunity. II. Methods of infection. Vet. J. 82, 348–55.Google Scholar
Hutyra, F., Marek, J. & Manninger, R. (1946). Special Pathology and Therapeutics of the Diseases of Domestic Animals, 5th ed., vol. I, pp. 256–84. London: Baillière, Tindall and Cox.Google Scholar
Liu, C. & Coffin, D. L. (1957). Studies on canine distemper infection by means of fluoresceinlabelled antibody. I. The pathogenesis, pathology and diagnosis of the disease in experimentally infected ferrets. Virology, 3, 115–31.CrossRefGoogle Scholar
MacOwan, K. D. S. (1956).Annu. Rep. Dep. vet. Serv., Kenya (1955). Nairobi: Government Printer.Google Scholar
Marcet, W. (1866). On the chemical pathology of the cattle plague. In 3rd Cattle Plague Report, pp. 5567d.Google Scholar
Masugi, M. & Minami, G. (1938). A case of measles with giant-cell formation in the respiratory tract, mouth and pharyngeal mucosae. On the inclusions of measles giant cells. Beitr. path. Anat. 101, 483502.Google Scholar
Maurer, F. D., Jones, T. C., Easterday, B. & DeTray, D. E. (1955). The pathology of rinderpest. Proc. Book Amer. vet. med. Ass., 92nd Annu. Meeting, pp. 201–11.Google Scholar
Morley, D., Woodland, M. & Martin, W. J. (1963.) Measles in Nigerian children. J. Hyg., Camb., 61, 115–34.CrossRefGoogle ScholarPubMed
Papp, K. (1937). Fixation du virus morbilleux aux leucocytes du sang dès la période d'incubation de la maladie. Bull. Acad. Méd., Paris, 117, 46. (Quoted by Robbins (1962).)Google Scholar
Plowright, W. (1963 a). Rinderpest. virus. Ann. N.Y. Acad. Sci. 101, 548–63.CrossRefGoogle Scholar
Plowright, W. (1963 b) Some properties of strains of rinderpest virus recently isolated in E. Africa. Res. vet. Sci. 4, 96108.CrossRefGoogle Scholar
Plowright, W., Cruickshank, J. G. & Waterson, A. P. (1962). The morphology of rinderpest virus. Virology, 17, 118–22.CrossRefGoogle ScholarPubMed
Plowright, W. & Ferris, R. D. (1959). Studies with rinderpest virus in tissue culture. I. Growth and cytopathogenicity. J. comp. Path. 69, 152–72.CrossRefGoogle ScholarPubMed
Plowright, W. & Ferris, R. D. (1961). Studies with rinderpest virus in tissue culture. III. The stability of cultured virus and its uses in virus neutralization tests. Arch. ges. Virusforsch. 11, 516–33.CrossRefGoogle Scholar
Plowright, W. & Ferris, R. D. (1962). Studies with rinderpest virus in tissue culture. A technique for the detection and titration of virulent virus in cattle tissues. Res. vet. Sci. 3, 94103.CrossRefGoogle Scholar
Rake, G. (1959). Measles. In Viral and Rickettsial Infections of Man (ed. Rivers, T. M and Horsfall, F. L), 3rd ed., pp. 741–52. London: Pitman Medical Publishing Co. Ltd.Google Scholar
Robbins, F. C. (1962). Measles: clinical features, pathogenesis, pathology and complications. Amer. J. Dis. Child. 103, 266–73.CrossRefGoogle ScholarPubMed
Roberts, G. B. S. & Bain, A. D. (1958). The pathology of measles. J. Path. Bact. 76, 111–18.CrossRefGoogle ScholarPubMed
Rockborn, G. (1957 a). Viraemia and neutralizing antibodies in experimental distemper in dogs. Arch. ges. Virusforsch. 7, 168–82.CrossRefGoogle ScholarPubMed
Rockborn, G. (1957 b). Viraemia and neutralizing antibodies in naturally acquired distemper in dogs. Arch. ges. Virusforsch. 7, 183–90.CrossRefGoogle ScholarPubMed
Rockborn, G. (1958). Further studies on viraemia and neutralizing antibodies in naturally acquired distemper in dogs. Arch. ges. Virusforsch. 8, 111.CrossRefGoogle Scholar
Ruckle, G. & Rogers, K. D. (1957). Studies with measles virus. II. Isolation of virus and immunologic studies in persons who have had the natural disease. J. Immunol. 78, 341–55.CrossRefGoogle ScholarPubMed
Schein, H. & Jacotot, H. (1925.) La séro-infection: vaccination préventive contre la peste bovine. Arch. Insts Pasteur Indochine, no. 1, 4856.Google Scholar
Scott, G. R. & Brown, R. D. (1961). Rinderpest diagnosis with special reference to the agargel double diffusion test. Bull. epiz. Dis. Afr. 9, 83125.Google Scholar
Semsroth, K. H. (1939). Multinucleate epithelial giant cells with inclusion bodies in prodromal measles. Arch. Path. 28, 386389.Google Scholar
Smith, H. A. & Jones, T. C. (1957). Veterinary Pathology. London: Henry Kimpton.Google Scholar
Third Report of the Commissioners Appointed to Inquire into the Origin and Nature, etc. of the Cattle Plague. London: Her Majesty's Stationery Office, 1866. (Referred to elsewhere as the 3rd Cattle Plague Report.)Google Scholar
Thompson, W. R. (1947). Use of moving averages and interpolation to estimate median effective dose. I. Fundamental formulas, estimation of error and relation to other methods. Bact. Rev. 11, 115–45.CrossRefGoogle ScholarPubMed