Zoonoses

References

1. Webster J. R. Wild brown rats (Rattus norvegicus) as a zoonotic risk on farms in England and Wales. Commun Dis Rep Rev 1996; 6:R46–R49
   [Google Scholar]
2. Bignall J. Hantaviruses: the rodents take revenge. Lancet 1995; 345:1564
   [Google Scholar]
3. Nelson G. S. Parasitic zoonoses. In England P. T., Sher A. (eds) The biology of parasitism New York: Alan Liss Inc; 198813–41
   [Google Scholar]
4. Rosner F. Rabies in the Talmud. Med Hist 1974; 18:198–200
   [Google Scholar]
5. Wilkinson L. The development of the virus concept as reflected in corpora of studies on individual pathogens: 4. Rabies. Two millenian of ideas and conjecture on the aetiology of a virus disease. Med Hist 1977; 21:15–31
   [Google Scholar]
6. Celsus De medicina (English translation by Spencer W. G.). London: W. Heinemann; 193838
   [Google Scholar]
7. Pasteur L. Methode pour provenir la rage après. Compte Rendu Hebd Sèanc Acad Sci Paris 1885; 101:765–774
   [Google Scholar]
8. World Health Organization Zoonoses Technical Report Series; 1959 No. 169 Geneva: WHO;
   [Google Scholar]
9. Schnurrenberger P. R., Grigor J. K., Walker J. F., Martin R. J. The zoonosis-prone veterinarian. J Am Vet Med Assoc 1978; 173:373–376
   [Google Scholar]
10. Evans M. R., Gardner D. Cryptosporidiosis outbreak associated with an educational farm holiday. Commun Dis Rep Rev 1996; 6:R50–R51
    [Google Scholar]
11. Dawson A., Griffin R., Fleetwood A., Barrett N. J. Farm visits and zoonoses. Commun Dis Rep Rev 1995; 5:R81–R86
    [Google Scholar]
12. Nelson G. S., Teesdale C., Highton R. B. The role of animals as reservoirs of bilharziasis in Africa. In Wolstenholme G. E. W., O’Connor M. (eds) Ciba Foundation Symposium on Bilhar-ziasis London: Churchill; 1962127–149
    [Google Scholar]
13. Nelson G. S. More than a hundred years of parasitic zoonoses: with special reference to trichinosis and hydatid disease. J Comp Pathol 1988; 98:135–153
    [Google Scholar]
14. Jenner E. An enquiry into the causes and effects of Variolae vaccinae. London: Sampson Low; 1798
    [Google Scholar]
15. Nelson G. S. Zooprophylaxis with special reference to schistosomiasis and filariasis. In Soulsby E. J. L. (ed) Parasitic zoonoses: clinical and experimental studies London: Academic Press; 1974273–285
    [Google Scholar]
16. Downie A. W., Taylor-Robinson C. H., Caunt A. E., Nelson G. S., Manson-Bahr P. E. C., Mathews T. C. H. Tanapox: a new disease caused by a pox virus. BMJ 1971; 1:363–368
    [Google Scholar]
17. Henderson B. E., Cheshire P. P., Kirya G. B., Lule M. Immunologic studies with yellow fever and selected African Group B arboviruses in rhesus and vervet monkeys. Am J Prop Med Hyg 1970; 19:110–118
    [Google Scholar]
18. Andrews C. H. The natural history of viruses. London: Weidenfield and Nicholson; 1967
    [Google Scholar]
19. Gordon Smith C. E. The distribution of antibodies to Japanese encephalitis, dengue, and yellow fever viruses in five rural communities in Malaya. Trans R Soc Trop Med Hyg 1958; 52:237–252
    [Google Scholar]
20. Garrett L. The coming plague: newly emerging diseases in a world out of balance. London: Virago Press; 1995750
    [Google Scholar]
21. Hackett C. J., Guthet T. Some important aspects of yaws eradication. Bull Med Hlth Org 1956; 15:869–874
    [Google Scholar]
22. Innes J. R. East African International Leprosy Specialist Annual Report 1951. Nairobi: Government Printer; 1952
    [Google Scholar]
23. Nelson G. S. Leprosy in the West Nile District of Uganda: an epidemiological study with special reference to the distribution of leprosy in Africa. Trans R Soc Trop Med Hyg 1958; 52:176–185
    [Google Scholar]
24. Chaussinaud R. La Lepre, Paris, L’Expansion Scientifique Francais; 1950
25. Fernandez J. M. M. The early reaction induced by lepromin. Int J Lep 1940; 8:1–14
    [Google Scholar]
26. Uganda Buruli Group BCG vaccination against Mycobacterium ulcerans infection (Buruli ulcer). First result of a trial in Uganda. Lancet 1969; 1:111–115
    [Google Scholar]
27. Wolf R. H., Gormus B. J., Martin L. N. Experimental leprosy in three species of monkey. Science 1985; 227:529–531
    [Google Scholar]
28. Lumpkin L. R., Cox G. F., Wolf J. E. Leprosy in five armadillo handlers. J Am Acad Dermatol 1983; 9:899–903
    [Google Scholar]
29. Hatta M., van Beers S. M., Madjid B., Djumadi A., de Wit M. Y. L., Klaster P. R. Distribution and persistence of Mycobacterium leprae nasal carriage among a population in which leprosy is endemic in Indonesia. Trans R Soc Trop Med Hyg 1995; 89:381–385
    [Google Scholar]
30. Khonde N., Pepin J., Niyongenga T., Milord F., De Wals P. Epidemiological evidence for immunity following Trypanosoma bruce gambiense sleeping sickness. Trans R Soc Trop Med Hyg 1995; 89:607–611
    [Google Scholar]
31. Heisch R. B., McMahon J. P., Manson-Bahr P. E. C. The isolation of Trypanosoma rhodesiense from a bushbuck. BMJ 1958; 2:1203–1204
    [Google Scholar]
32. Wall P. G., Morgan D., Lamden K. A case control study of infection with an epidemic strain of multi-resistant Salmonella typhimurium DTI04 in England and Wales. Commun Dis Rep CDR Wkly 1994; 4:R130–R135
    [Google Scholar]
33. Fone D. L., Barker R. M. Associations between human and farm animal infections with Salmonella typhimurium DTI04 in Hertfordshire. Commun Dis Rep CDR Rev 1994; 4:R136–140
    [Google Scholar]
34. Harris N. V., Weiss N. S., Nolan C. M. The role of poultry and meats in the etiology of Campylobacter jejuni/coli enteritis. Am J Publ Health 1986; 76:407–411
    [Google Scholar]
35. Klein B. S., Vergeront J. M., Blaser M. J. Campylobacter infection associated with raw milk. An outbreak of gastroenteritis due to Campylobacter jejuni and thermotolerant Campylobacter fetus subsp fetus. JAMA 1986; 255:361–364
    [Google Scholar]
36. Humphrey T. J., Henley A., Lanning D. G. The colonization of broiler chickens with Campylobacter jejuni: some epidemiological investigations. Epidemiol Inject 1993; 110:601–607
    [Google Scholar]
37. Hood A. M., Pearson A. D., Shahamat M. The extent of surface contamination of retailed chickens with Campylobacter jejuni serogroups. Epidemiol Inject 1988; 100:17–25
    [Google Scholar]
38. de Boer E., Hahné M. Cross-contamination with Campylobacter jejuni and Salmonella species from raw chicken products during food preparation. J Food Protect 1990; 53:1067–1068
    [Google Scholar]
39. Humphrey T. J. Food poisoning - a change in patterns?. Vet Ann 1991; 31:32–37
    [Google Scholar]
40. Bemdtson E., Tiremo M., Engvall A. Distribution and numbers of Campylobacter in newly slaughtered broiler chickens and hens. Int J Food Microbiol 1992; 15:45–50
    [Google Scholar]
41. Kapperud G., Skjerve E., Bean N. H., Ostrofif S. M., Lassen J. Risk factors for sporadic Campylobacter infections: results of a case-control study in Southeastern Norway. J Clin Microbiol 1992; 30:3117–3121
    [Google Scholar]
42. Humphrey T. J., Lanning D. G., Mead G. C. Inhibition of Campylobacter jejuni in vitro by broiler chicken caecal contents. Vet Rec 1989; 125:272–273
    [Google Scholar]
43. Humphrey T. J., Beckett P. Campylobacter jejuni in dairy cows and raw milk. Epidemiol Infect 1987; 98:263–269
    [Google Scholar]
44. Hutchinson D. N., Bolton F. J., Hinchliffe P. M. Evidence of udder excretion of Campylobacter jejuni as the cause of a milk-borne Campylobacter outbreak. J Hyg 1985; 94:205–215
    [Google Scholar]
45. Humphrey T. J., Hart R. J. C. Campylobacter and salmonella contamination of unpasteurized cows’ milk on sale to the public. J Appl Bacteriol 1988; 65:463–467
    [Google Scholar]
46. Gill K. P., Bates P. G., Lander K. P. The effect of pasteurization on the survival of Campylobacter species in milk. Brit Vet J 1981; 137:378–384
    [Google Scholar]
47. Rodrigue D. C., Tauxe R. V., Rowe B. International increase in Salmonella enteritidis: a new pandemic?. Epidemiol Infect 1990; 105:21–27
    [Google Scholar]
48. Rampling A., Upson R., Ward L. R., Anderson J. R., Peters E., Rowe B. Salmonella enteritidis phage type 4 infection of broiler chickens: a hazard to public health. Lancet 1989; 2:436–438
    [Google Scholar]
49. Cowden J. M., Lynch D., Joseph C. A. Case-control study of infections with Salmonella enteritidis phage type 4 in England. BMJ 1989; 299:771–773
    [Google Scholar]
50. Hoop R. K., Pospischil A. Bacteriological, serological, histological and immuno-histochemical findings in laying hens with naturally acquired Salmonella enteritidis phage type 4 infection. Vet Rec 1993; 133:391–393
    [Google Scholar]
51. Keller L. H., Benson C. E., Krotec K., Eckroade R. J. Salmonella enteritidis colonization of the reproductive tract and forming and freshly laid eggs of chicken. Inject Immun 1995; 63:2443–2449
    [Google Scholar]
52. Humphrey T. J., Whitehead A. Egg age and the growth of Salmonella enteritidis PT4 in egg contents. Epidemiol Infect 1993; 111:209–219
    [Google Scholar]
53. Humphrey T. J., Whitehead A. The growth of Salmonella enteritidis PT4 in egg contents: influence of egg storage conditions. Int J Food Microbiol 1996 (in press)
    [Google Scholar]
54. Anonymous Eggs and salmonella - the facts. British Egg Industry Council; London: 1992
    [Google Scholar]
55. Anonymous Council of the European Communities Directive 29/117/EEC. 17 December 1992
56. Anonymous Salmonella in animal and poultry production 1994. London: MAFF; 1995
    [Google Scholar]
57. Anonymous Report on verocytotoxin-producing Escherichia coli. London: ACMSF; 1995
    [Google Scholar]
58. Orskov F., Orskov I., Villar J. A. Cattle as reservoir of verotoxin-producing Escherichia coli O157:H7. Lancet 1987; 2:276
    [Google Scholar]
59. Chapman P. A., Siddons C. A., Wright D. J., Norman P., Fox J., Crick E. Cattle as a source of verocytotoxigenic Escherichia coli O157. Vet Rec 1992; 131:323–324
    [Google Scholar]
60. Chapman P. A., Siddons C. A., Wright D. J., Norman P., Fox J., Crick E. Cattle as a possible source of verocytotoxin- producing Escherichia coli O157 infections in man. Epidemiol Infect 1993; 111:439–449
    [Google Scholar]
61. Millar L. G., Kaspar C. W. Escherichia coli O157:H7 acid tolerance and survival in apple cider. J Food Protect 1994; 57:460–464
    [Google Scholar]
62. Butler J. C., Peters C. J. Hantaviruses and hantavirus pulmonary syndrome. Clin Infect Dis 1994; 19:387–395
    [Google Scholar]
63. Hart C. A., Bennett M. Hantaviruses: an increasing problem?. Ann Trop Med Parasitol 1994; 88:347–358
    [Google Scholar]
64. Bennett M., Hart C. A. Hantavirus infection. J Med Microbiol 1994; 41:71–73
    [Google Scholar]
65. Groen J. Hantavirus infections in the Netherlands. PhD Thesis Erasmus University; Rotterdam: 1996
    [Google Scholar]
66. Antic D., Lim B. U., Kang C. Y. Nucleotide sequence and coding capacity of the large (L) genomic RNA segment of Seoul 8039 virus, a member of the hantavirus genus. Virus Res 1991; 19:59–66
    [Google Scholar]
67. Elliott R. M. Molecular biology of the Bunyaviridae. J Gen Virol 1990; 71:501–522
    [Google Scholar]
68. Arikawa J., Takashima J., Hashimoto N. Cell fusion by haemorrhagic fever with renal syndrome (HFRS) viruses and its application for titration of virus infectivity and neutralizing antibody. Arch Virol 1985; 86:303–313
    [Google Scholar]
69. Isegawa Y., Tanishita O., Ueda S., Yamanishi K. Association of serine in position 1124 of Hantaan virus glycoprotein with virulence in mice. J Gen Virol 1994; 75:3273–3278
    [Google Scholar]
70. Avsic-Zupanc T., Xiao S.-Y., Stojanovic R., Gligic A., van der Groen G., LeDuc J. W. Characterization of Dobrova virus: a hantavirus from Slovenia, Yugoslavia. J Med Virol 1992; 38:132–137
    [Google Scholar]
71. Antioniades A., Grekas D., Rossi C. A., LeDuc J. W. Isolation of a hantavirus from a severely ill patient with hemorrhagic fever with renal syndrome in Greece. J Infect Dis 1987; 156:1010–1013
    [Google Scholar]
72. Gligic A., Dimkovic N., Xiao S.-Y. Belgrade virus: a new hantavirus causing severe hemorrhagic fever with renal syndrome in Yugoslavia. J Infect Dis 1992; 166:113–120
    [Google Scholar]
73. Kim G. R., Lee Y. T., Park C. H. A new natural reservoir of hantavirus: isolation of hantaviruses from lung tissue of bats. Arch Virol 1994; 134:85–95
    [Google Scholar]
74. Isegawa Y., Fujiwara Y., Ohshima A. Nucleotide sequence of the M genome segment of hemorrhagic fever with renal syndrome virus stain B-1. Nucleic Acids Res 1990; 18:4936
    [Google Scholar]
75. Kariwa H., Yoshizumi S., Arikawa J. Evidence for the existence of Puumala-related viruses among Clethrionomys rufocanus in Hokkaido, Japan. Am J Trop Med Hyg 1995; 53:222–227
    [Google Scholar]
76. Nichol S. T., Spiropoulou C. F., Morzumov S. Genetic identification of a hantavirus associated with an outbreak of acute respiratory illness. Science 1993; 262:914–917
    [Google Scholar]
77. Song J.-W., Baek L.-J., Gajdusek D. C. Isolation of pathogenic hantavirus from white-footed mouse (Peromycus leucopus). Lancet 1994; 344:1637
    [Google Scholar]
78. Torrez-Martinez N., Hjelle B. Enzootic of Bayou hantavirus in rice rats (Oryzomys palustris) in 1983. Lancet 1995; 346:780–781
    [Google Scholar]
79. Rollin P. E., Ksiazek T. G., Elliott L. H. Isolation of Black Creek Canal Virus, a new hantavirus from Sigmodon hispidus in Florida. J Med Virol 1995; 46:35–39
    [Google Scholar]
80. Torrez-Martinez N., Song W., Hjelle B. Nucleotide sequence analysis of the M genomic sequences of E1 Moro Canyon hantavirus: antigenic distinction from Four Comers hantavirus. Virology 1995; 211:336–338
    [Google Scholar]
81. Li D., Schmaljohn A. L., Anderson K., Schmaljohn C. S. Complete nucleotide sequence of the M and S segments of two hantavirus isolates from California: evidence for reassortment in nature among viruses related to hantavirus pulmonary syndrome. Virology 1995; 206:973–983
    [Google Scholar]
82. Plyusnin A., Vapalahti O., Lankinen H. Tula vims: a newly detected hantavirus carried by common voles. J Virol 1994; 68:7833–7839
    [Google Scholar]
83. Gavrilovskaya I. N., Apekina N. S., Myasnikov Y. A. Features of circulation of hemorrhagic fever with renal syndrome (HFRS) among small mammals in the European USSR. Arch Virol 1983; 75:313–316
    [Google Scholar]
84. Weissenbacher M. C., Merani M. S., Hodara V. L. Hantavirus infection in laboratory and wild rodents in Argentina. Medicina (B Aires) 1990; 50:43–46
    [Google Scholar]
85. Tang Y. W., Xu Z. Y., Zhu Z. Y., Tsai T. J. Isolation of haemorrhagic fever with renal syndrome virus from Suncus murinus an insectivore. Lancet 1985; 1:513–514
    [Google Scholar]
86. Groen J., Gerding M. N., Jordans J. G. M., Clement J. P., Nieuwenhuijs J. H. M., Osterhaus A. D. M. E. Hantavirus infections in The Netherlands: epidemiology and disease. Epidemiol Infect 1995; 114:373–383
    [Google Scholar]
87. Luo Z. Z. Isolation of epidemic haemorrhagic fever vims from a cat. Clin J Microbiol Immunol 1985; 5:79–81
    [Google Scholar]
88. Bennett M., Lloyd G., Jones N. Prevalence of antibody to hantavirus in some cat populations in Britain. Vet Rec 1990; 127:548–549
    [Google Scholar]
89. Slonova R. A., Tkachenko E. A., Kushnarev E. L., Dzagurova T. K., Astakova T. I. Hantavirus isolation from birds. Acta Virol 1992; 36:493
    [Google Scholar]
90. Xu Z. Y., Tang T. W., Kan L. Y., Tsai T. F. Cats - source of protection or infection? A case-control study of hemorrhagic fever with renal syndrome. Am J Epidemiol 1987; 126:942–948
    [Google Scholar]
91. Tkachenko E. A., Lee H. W. Etiology and epidemiology of hemorrhagic fever with renal syndrome. Kidney Int 1991; 40: suppl 35S54–S61
    [Google Scholar]
92. Lloyd G., Jones N. Infection of laboratory workers with acquired from immunocytomas propagated in laboratory rats. J Infect 1986; 12:117–125
    [Google Scholar]
93. McKee K. T., Kim G. R., Green D. E., Peters C. J. Hantaan virus infection in suckling mice: virologic and pathologic correlates. J Med Virol 1985; 17:107–117
    [Google Scholar]
94. Groen J., Gerding M., Koeman J. P. A macaque model for hantavirus infection. J Infect Dis 1995; 172:38–44
    [Google Scholar]
95. Ahlm C., Settergren B., Gothefors L., Juto P. Nephropathia epidemica (hemorrhagic fever with renal syndrome) in children: clinical characteristics. Pediatr Infect Dis J 1994; 13:45–49
    [Google Scholar]
96. Schreiber M., Laue T., Wolff C. Hantavirus pulmonary syndrome in Germany. Lancet 1996; 347:336–337
    [Google Scholar]
97. Glass G. E., Watson A. J., LeDuc J. W., Kelen G. D., Quinn T. C., Childs J. E. Infection with rat borne hantavirus in US residents is consistently associated with hypotensive renal disease. J Infect Dis 1993; 167:614–620
    [Google Scholar]
98. Niklasson B., Hellsten G., LeDuc J. Haemorrhagic fever with renal syndrome: a study of sequelae following nephropathia epidemica. Arch Virol 1994; 137:241–247
    [Google Scholar]
99. de Courten M. P., Ksiazek T. G., Rollin P. E., Khan A. S., Daily P. J., Knowles W. C. Seroprevalence study of hantavirus antibodies in Pima Indians with renal disease. J Infect Dis 1995; 171:762–763
    [Google Scholar]
100. Duchin J. S., Koster F. T., Peters C. J. Hantavirus pulmonary syndrome: a clinical description of 17 patients with a newly recognized disease. N Engl J Med 1994; 330:949–955
     [Google Scholar]
101. Zaki S. R., Albers R. C., Greer P. W. Retrospective diagnosis of a 1983 case of fatal hantavirus pulmonary syndrome. Lancet 1994; 343:1037–1038
     [Google Scholar]
102. Moolenaar R. L., Dalton C., Lipman H. B. Clinical features that differentiate hantavirus pulmonary syndrome from three other acute respiratory illnesses. Clin Infect Dis 1995; 21:643–649
     [Google Scholar]
103. Simonsen L., Dalton M. J., Breiman R. F. Evaluation of the magnitude of the 1993 hantavirus outbreak in the Southwestern United States. J Infect Dis 1995; 172:729–733
     [Google Scholar]
104. dos Santos V. M. [Acute respiratory disease caused by Hantavirus Four Corners]. Rev Soc Bras Med Trop 1995; 28:59
     [Google Scholar]
105. Niklasson B., LeDuc J. W. Epidemiology of nephropathia epidemica in Sweden. J Infect Dis 1987; 155:269–276
     [Google Scholar]
106. McKenna P., Clement J., Matthys P., Coyle P. V., McCaughey C. Serological evidence of hantavirus disease in Northern Ireland. J Med Virol 1994; 43:33–38
     [Google Scholar]
107. Zeitz P. S., Butler J. C., Cheek J. E. A case-control study of hantavirus pulmonary syndrome during an outbreak in Southwestern United States. J Infect Dis 1995; 171:864–870
     [Google Scholar]
108. Clement J., Underwood P., Ward J., Pilaski J., LeDuc J. Hantavirus outbreak during military manoeuvres in Germany. Lancet 1996; 347:336
     [Google Scholar]
109. Huggins J. W., Hsiang C. M., Cosgriff T. M. Prospective, double-blind, concurrent, placebo-controlled trial of intravenous ribavirin therapy of hemorrhagic fever with renal syndrome. J Infect Dis 1991; 164:1119–1127
     [Google Scholar]
110. Sayer W. J., Entwhisle G., Uyeno B., Bignall R. C. Cortisone therapy of early epidemic hemorrhagic fever: a preliminary report. Ann Intern Med 1955; 42:839–851
     [Google Scholar]
111. Vapalahti O., Plyusnin A., Vaheri A., Henttonen H. Hantavirus antibodies in European mammalogists. Lancet 1995; 345:1569
     [Google Scholar]
112. Lee H. W., An C. N., Song J. W. Field trial of an inactivated vaccine against hemorrhagic fever with renal syndrome. Arch Virol 1990 Suppl 1:35–47
     [Google Scholar]
113. Baxby D. Poxviruses. In Zuckerman A. J., Banatvala J. E., Pattison J. R. (eds) Principles and practice of clinical virology 3rd edn London: John Wiley; 1994441–466
     [Google Scholar]
114. Baxby D., Bennett M., Getty B. Human cowpox 1969–93: a review based on 54 cases. Br J Dermatol 1994; 131:598–607
     [Google Scholar]
115. Johannesen J. V., Krogh H. K., Solberg I., Dalen A., Wijngaarden H., Johansen B. Human orf. J Cutan Pathol 1975; 2:265–283
     [Google Scholar]
116. Robinson A. J., Petersen G. Y. Orf virus infection of workers in the meat industry. N Z Med J 1983; 96:81–85
     [Google Scholar]
117. Pether J. V. S., Guerrier C. J. W., Jones S. M., Adam A. E., Kingsbury W. N. Giant orf in a normal individual. Br J Dermatol 1986; 115:496–497
     [Google Scholar]
118. Yirrell D. L., Vestey J. P. Human orf infections. J Eur Acad Derm Venereol 1994; 3:451–459
     [Google Scholar]
119. Khodakevich L., Szczeniowski M., Manbu-ma-Disu . The role of squirrels in sustaining monkeypox vims transmission. Trop Geogr Med 1987; 39:115–122
     [Google Scholar]
120. Jezek Z., Fenner F. Human monkeypox. Monographs in Virology. vol 17 Basel: Karger; 1988
     [Google Scholar]
121. Jezek Z., Grab B., Szczeniowski M., Paluku K. M., Mutombo M. Clinico-epidemiological features of monkeypox patients with an animal or human source of infection. Bull World Health Organ 1988; 66:459–464
     [Google Scholar]
122. Jezek Z., Marennikova S. S., Mutombo M., Nakano J. H., Pakuku K. M., Szczeniowski M. Human monkeypox: a study of 2510 contacts of 214 patients. J Infect Dis 1986; 154:551–555
     [Google Scholar]
123. Baxby D. Indications for smallpox vaccination: policies still differ. Vaccine 1993; 11:395–396
     [Google Scholar]
124. Jezek Z., Grab B., Szczeniowski M. V., Paluku K. M., Mutombo M. Human monkeypox: secondary attack rates. Bull World Health Organ 1988; 66:465–470
     [Google Scholar]
125. Esposito J. J., Nakano J. H., Obijeski J. F. Can variola-like viruses be derived from monkeypox virus? An investigation based on DNA mapping. Bull World Health Organ 1985; 63:695–703
     [Google Scholar]
126. Baxby D. Jenner’s smallpox vaccine: the riddle of vaccinia virus and its origin. London: Heinemann Educational Books; 1981
     [Google Scholar]
127. Baxby D. Is cowpox misnamed? A review of 10 human cases. BMJ 1977; 1:1379–1381
     [Google Scholar]
128. Baxby D., Osborne A. D. Antibody studies in natural bovine cowpox. J Hyg 1979; 83:425–428
     [Google Scholar]
129. Crouch A. C., Baxby D., McCracken C. M., Gaskell R. M., Bennett M. Serological evidence for the reservoir host of cowpox virus in British wildlife. Epidemiol Infect 1995; 115:185–191
     [Google Scholar]
130. Bennett M., Gaskell C. J., Baxby D., Gaskell R. M., Kelly D. F., Naidoo J. Feline cowpox vims infection. J Small Anim Pract 1990; 31:167–173
     [Google Scholar]
131. Lewis-Jones M. S., Baxby D., Cefai C., Hart C. A. Cowpox can mimic anthrax. Br J Dermatol 1993; 129:625–627
     [Google Scholar]
132. Pfeifl B., Pullman H., Eis-Hubinger A. M., Gerritzen A., Schneiss K. E., Mayr A. Letale Tierpockeninfektion bei einem Atopiker unter dem Bild einer Variola vera. Hautarzt 1991; 42:293–297 [In German with English Abstract]
     [Google Scholar]
133. Baxby D., Hill B. J. Characteristics of a new poxvirus isolated from Indian buffaloes. Arch Gesamte Virusforsch 1971; 35:70–79
     [Google Scholar]
134. Dumbell K., Richardson M. Virological investigations of specimens from buffaloes affected by buffalopox in Maharashtra State, India between 1985 and 1987. Arch Virol 1993; 128:257–267
     [Google Scholar]
135. Lai S. M., Singh I. P. Buffalopox - a review. Trop Anim Health Prod 1977; 9:107–112
     [Google Scholar]
136. Ghosh T. K., Arora R. R., Sehgel C. L., Ray S. N., Wattal B. L. An investigation of buffalopox outbreak in animals and human beings in Dhulia District [Maharashtra State]. J Commun Dis 1977; 9:93–101
     [Google Scholar]
137. Jezek Z., Arita I., Szczeniowski M., Paluku K. M., , Kalisa Ruti, Nakano J. H. Human tanapox in Zaire: clinical and epidemiological observations on cases confirmed by laboratory studies. Bull World Health Organ 1985; 63:1027–1035
     [Google Scholar]
138. Baxby D. Poxvims infections in domestic animals. In Darai G. (ed) Vims diseases in laboratory and captive animals Boston: Martinus Nijhoff; 198817–35
     [Google Scholar]
139. Madeley C. R. M., Taylor C. ‘Outbreak’?. Lancet 1995; 346: Suppl 27
     [Google Scholar]
140. Blewett D. A., Trees A. J. The epidemiology of ovine toxoplasmosis, with especial respect to control. Br Vet J 1987; 143:128–135
     [Google Scholar]
141. Fleck D. G., Kwantes W. The laboratory diagnosis of toxoplasmosis. Public Health Laboratory Service Monograph 1980; 13:1–20
     [Google Scholar]
142. Blewett D. A. The epidemiology of ovine toxoplasmosis. I. The interpretation of data for the prevalence of antibody in sheep and other species. Br Vet J 1983; 139:537–545
     [Google Scholar]
143. McColm A. A., Hutchinson W. M., Siim J. C. The prevalence of Toxoplasma gondii in meat animals and cats in central Scotland. Ann Trop Med Parasitol 1981; 75:157–164
     [Google Scholar]
144. Jackson M. H., Hutchison W. M., Siim J. C. Prevalence of Toxoplasma gondii in meat animals, cats and dogs in central Scotland. Br Vet J 1987; 143:159–165
     [Google Scholar]
145. Gettings P. M., Stephens G. L., Wills J. M. Prevalence of chlamydia, toxoplasma, toxocara and ringworm in farm cats in south–west England. Vet Rec 1987; 121:213–216
     [Google Scholar]
146. Churcher P. B., Lawton J. H. Predation by domestic cats in an English village. J Zool 1987; 212:439–455
     [Google Scholar]
147. May R. M. Control of feline delinquency. Nature 1988; 332:392–393
     [Google Scholar]
148. Lainson R. The demonstration of Toxoplasma in animals, with particular reference to members of the Mustelidae. Trans R Soc Trop Med Hyg 1957; 51:111–122
     [Google Scholar]
149. Jackson M. H., Hutchison W. M., Siim J. C. Toxoplasmosis in a wild rodent population of central Scotland and a possible explanation of the mode of transmission. J Zool 1986; 209:549–557
     [Google Scholar]
150. Peach W., Fowler J., Hay J. Incidence of Toxoplasma infection in a population of European starlings Sturnus vulgaris from central England. Ann Trop Med Parasitol 1989; 83:173–177
     [Google Scholar]
151. Burg J. L., Grover C. M., Pouletty P., Boothroyd J. C. Direct and sensitive detection of a pathogenic protozoan, Toxoplasma gondii, by polymerase chain reaction. J Clin Microbiol 1989; 27:1787–1792
     [Google Scholar]
152. Dubey J. P., Beattie C. P. Toxoplasmosis of animals and man. Boca Raton, Florida: CRC Press; 1988
     [Google Scholar]
153. Dardé M. L., Bouteille B., Pestre-Alexandre M. Isoenzyme analysis of 35 Toxoplasma gondii isolates and the biology and epidemiological implications. J Parasitol 1992; 78:786–794
     [Google Scholar]
154. Sibley L. D., Boothroyd J. C. Virulent strains of Toxoplasma gondii comprise a single clonal lineage. Nature 1992; 359:82–85
     [Google Scholar]
155. Howe D. K., Sibley L. D. Toxoplasma gondii comprises three clonal lineages: correlation of parasite genotype with human disease. J Infect Dis 1995; 172:1561–1566
     [Google Scholar]
156. Tyzzer E. E. Sporozoan found in the peptic glands of the common mouse. Proc Soc Exp Biol Med 1907; 5:12–13
     [Google Scholar]
157. Tyzzer E. E. Cryptosporidium parvum (sp. nov.), a coccidium found in the small intestine of the common mouse. Archiv Protistenkunde 1912; 26:394–412
     [Google Scholar]
158. O’Donoghue P. J. Cryptosporidium and cryptosporidiosis in man and animals. Int J Parasitol 1995; 25:139–195
     [Google Scholar]
159. Ditrich O., Palkovic L., Sterba J., Prokopic J., Londova J., Giboda M. The first finding of Cryptosporidium baileyi in man. Parasitol Res 1991; 77:44–47
     [Google Scholar]
160. Baxby D., Hart C. A. The incidence of cryptosporidiosis: a two-year prospective survey in a children’s hospital. J Hyg 1986; 96:107–111
     [Google Scholar]
161. Bennett M., Baxby D., Blundell N., Gaskell C. J., Hart C. A., Kelly D. F. Cryptosporidiosis in the domestic cat. Vet Rec 1985; 116:73–74
     [Google Scholar]
162. Mtambo M. M. A., Nash A. S., Blewett D. A., Smith H. V., Wright S. Cryptosporidium infection in cats: prevalence of infection in domestic and feral cats in the Glasgow area. Vet Rec 1991; 129:502–504
     [Google Scholar]
163. Reynolds D. J., Morgan J. H., Chanter N. Microbiology of calf diarrhoea in southern Britain. Vet Rec 1986; 119:34–39
     [Google Scholar]
164. Chalmers R. M., Sturdee A. P., Bull S. A. Miller Rodent reservoirs of Cryptosporidium. In Betts W. B., Casemore D., Fricker C., Smith H., Watkins J. (eds) Protozoan parasites and water Proceedings of a conference held in York, 26–28 September 1994 Cambridge: R Soc Chem;
     [Google Scholar]
165. Webster J. P., Macdonald D. W. Parasites of wild brown rats (Rattus norvegicus) on UK farms. Parasitology 1995; 111:247–255
     [Google Scholar]
166. Smith H. V., Rose J. B. Waterborne Cryptosporidiosis. Parasitol Today 1990; 6:8–12
     [Google Scholar]
167. Ortega Y. R., Sheehy R. R., Cama V. A., Oishi K. K., Sterling C. R. Restriction fragment length polymorphism analysis of Cryptosporidium parvum isolates of bovine and human origin. J Protozool 1991; 38:40S–41S
     [Google Scholar]
168. Morgan U. M., Constantine C., O’Donoghue P., Meloni B. P., O’Brien P. A., Thompson R. C. A. Molecular characterization of Cryptosporidium isolates from humans and other animals using random amplified polymorphic DNA analysis. Am J Trop Med Hyg 1995; 52:559–564
     [Google Scholar]
169. Awad-el-kariem F. M., Robinson H. A., Dyson D. A. Differentiation between human and animal strains of Cryptosporidium parvum using isoenzyme typing. Parasitology 1995; 110:129–132
     [Google Scholar]
170. Meloni B. P., Lymbery A. J., Thompson R. C. A. Genetic characterization of isolates of Giardia duodenalis by enzyme electrophoresis: implications for reproductive biology, population structure, taxonomy, and epidemiology. J Parasitol 1995; 81:368–383
     [Google Scholar]
171. Monis P. T., Mayrhofer G., Andrews R. H., Homan W. L., Limper L., Ey P. L. Molecular genetic analysis of Giardia intestinalis isolates at the glutamate dehydrogenase locus. Parasitology 1996; 112:1–12
     [Google Scholar]
172. Thompson R. C. A., Reynoldson J. A., Mendis A. H. W. Giardia and giardiasis. Adv Parasitol 1993; 32:72–160
     [Google Scholar]
173. Majewska A. C. Successful experimental infections of a human volunteer and Mongolian gerbils with Giardia of animal origin. Trans R Soc Trop Med Hyg 1994; 88:360–362
     [Google Scholar]
174. Faubert G. M. Is giardiasis a true zoonosis? Evidence that giardiasis is a zoonosis. Parasitol Today 1988; 4:66–68
     [Google Scholar]
175. Bemrick W. J., Erlandsen S. L. Giardiasis - is it really a zoonosis?. Parasitol Today 1988; 4:69–71
     [Google Scholar]
176. Burnie A. G., Simpson J. W., Lindsay D., Miles R. S. The excretion of Campylobacter, salmonellae and Giardia lamblia in the faeces of stray dogs. Vet Res Commun 1983; 6:133–138
     [Google Scholar]
177. Simpson J. W., Burnie A. G., Miles R. S., Scott J. L., Lindsay D. I. Prevalence of Giardia and Cryptosporidium infection in dogs in Edinburgh. Vet Rec 1988; 123:445
     [Google Scholar]
178. Sykes T. J., Fox M. T. Patterns of infection with Giardia in dogs in London. Trans R Soc Trop Med Hyg 1989; 83:239–240
     [Google Scholar]
179. Winsland J. K. D., Nimmo S., Butcher P. D., Farthing M. J. G. Prevalence of Giardia in dogs and cats in the United Kingdom: survey of an Essex veterinary clinic. Trans R Soc Trop Med Hyg 1989; 83:791–792
     [Google Scholar]
180. Taylor M. A., Catchpole J., Marshall R. N., Green J. Giardiasis in lambs at pasture. Vet Rec 1993; 133:131–133
     [Google Scholar]
181. Xiao L. Giardia infection in farm animals. Parasitol Today 1994; 10:436–438
     [Google Scholar]
182. Buret A., denHollander N., Wallis P. M., Befus D., Olson M. E. Zoonotic potential of giardiasis in domestic ruminants. J Infect Dis 1990; 162:231–237
     [Google Scholar]
183. Anon Giardiasis and water. Lancet 1980; 1:1176
     [Google Scholar]
184. Thompson R. C. A. Biology and systematics of Echinococcus. In Thomson R. C. A., Lymbery A. J. (eds) Echinococcus and hydatid disease Wallingford: Oxon, CAB International; 19951–50
     [Google Scholar]
185. McManus D. P., Rishi A. K. Genetic heterogeneity within Echinococcus granulosus isolates from different hosts and geographical areas characterized with DNA probes. Parasitology 1989; 99:17–29
     [Google Scholar]
186. Bowles J., McManus D. P. Molecular variation in Echinococcus. Acta Tropica 1993; 53:291–305
     [Google Scholar]
187. Schantz P. M., Chai J., Craig P. S. Epidemiology and control of hydatid disease. In Thomson R. C. A., Lymbery A. J. (eds) Echinococcus and hydatid disease Wallingford, Oxon: CAB International; 1995233–331
     [Google Scholar]
188. Allan J. C., Craig P. S., Garcia Noval J. Coproantigen detection for immunodiagnosis of echinococcosis and taeniasis in dogs and humans. Parasitology 1992; 104:347–356
     [Google Scholar]
189. Walters T. M. H. Hydatid disease in Wales: 1 Epidemiology. Vet Rec 1978; 102:257–259
     [Google Scholar]
190. Clarkson M. J., Walters T. M. H. The growth and development of Echinococcus granulosus of sheep origin in dogs and foxes in Britain. Ann Trop Med Parasitol 1991; 85:53–61
     [Google Scholar]
191. Clarkson M. J. Hydatid disease in Wales: 2 Eradication. Vet Rec 1978; 102:259–261
     [Google Scholar]
192. Chisholm I. L., Mac Vicar M. J., Williams H. Hydatid disease in the Western Isles. J Hyg 1983; 90:19–25
     [Google Scholar]
193. Stallbaumer M. F., Clarkson M. J., Bailey J. W., Pritchard J. E. The epidemiology of hydatid disease in England and Wales. J Hyg 1986; 96:121–127
     [Google Scholar]
194. Palmer S. R., Biffin A. H. B. The changing incidence of human hydatid disease in England and Wales. Epidemiol Infect 1987; 99:693–700
     [Google Scholar]
195. Morris D. L., Clarkson M. J., Stallbaumer M. F., Pritchard J., Jones R. S., Chinnery J. B. Albendazole treatment of pulmonary hydatid cysts in naturally infected sheep: a study with relevance to the treatment of hydatid cysts in man. Thorax 1985; 40:453–458
     [Google Scholar]
196. Morris D. L., Dykes P. W., Marriner S. Albendazole - objective evidence of response in human hydatid disease. JAMA 1985; 253:2053–2057
     [Google Scholar]
197. Todorov T., Mechkov G., Vutova K. Factors influencing the response to chemotherapy in human cystic echinococcosis. Bull World Health Organ 1992; 70:347–358
     [Google Scholar]
198. Wen H., Zhang H. W., Muhmut M., Zou P. F., New R. R., Craig P. S. Initial observation on albendazole in combination with cimetidine for the treatment of human cystic echinococcosis. Ann Trop Med Parasitol 1994; 88:49–52
     [Google Scholar]
199. Yasawy M. I., Al Karawi M. A., Mohamed A. R. E. Combination of praziquantel and albendazole in the treatment of hydatid disease. Trop Med Parasitol 1993; 44:192–194
     [Google Scholar]
200. New R. R. C., Wen H., Craig P. S. Efficacy of albendazole administered orally is improved by encapsulation in liposomes. J Controlled Release 1994; 28:350–351
     [Google Scholar]
201. Heath D. D. Immunology of Echinococcus infections. In Thomson R. C. A., Lymbery A. J. (eds) Echinococcus and hydatid disease Wallingford, Oxon: CAB International; 1995183–199
     [Google Scholar]
202. Dixon J. B., Jenkins P. Immunology of mammalian metacestode infections. I Antigens, protective immunity and immunopathology. Helminthol Abstr 1995; 64:533–542
     [Google Scholar]
203. Dixon J. B., Jenkins P. Immunology of mammalian metacestode infections. II Immune recognition and effector function. Helminthol Abstr 1995; 64:599–613
     [Google Scholar]
204. Anderson E. S. Drug resistance in Salmonella typhimurium and its implications. BMJ 1968; 3:333–339
     [Google Scholar]
205. Report Joint Committee on the Use of Antibiotics in Animal Husbandry and Veterinary Medicine. London: HMSO; 1968
     [Google Scholar]
206. Bates J., Jordens J. Z., Griffiths D. T. Farm animals as a putative reservoir for vancomycin-resistant enterococcal infection in man. J Antimicrob Chemother 1994; 34:507–516
     [Google Scholar]
207. Klare I., Heier H., Claus H., Reissbrodt R., Witte W. VanA-mediated high-level glycopeptide resistance in Enterococcus facium from animal husbandry. FEMS Microbiol Lett 1994; 125:165–171
     [Google Scholar]
208. Robinson T. C., Jackson E. R., Marr A. Mastitis incidence in quarters with different infection status at drying off and calving in two treatment groups. Br Vet J 1988; 144:166–173
     [Google Scholar]
209. Wray C., Todd J. N., Hinton M. Epidemiology of Salmonella typhimurium infection in calves: excretion of S. typhimurium in faeces of calves in different management systems. Vet Rec 1987; 121:293–296
     [Google Scholar]
210. Sojka W. J., Wray C. A survey of drug resistance in Salmonella isolated from animals in England and Wales from 1975 to 1978. Br Vet J 1980; 136:463–477
     [Google Scholar]
211. Wray C., McLaren I. M., Beedell Y. E. Bacterial resistance monitoring of salmonellas isolated from animals, national experience of surveillance schemes in the United Kingdom. Vet Microbiol 1993; 35:313–319
     [Google Scholar]
212. Threlfall E. J., Frost J. A., Ward L. R., Rowe B. Epidemic in cattle and humans of Salmonella typhimurium DT 104 with chromosomally integrated multiple drug resistance. Vet Rec 1994; 134:577
     [Google Scholar]
213. Wray C., Hedges R. W., Shannon K. P., Bradley D. E. Apramycin and gentamicin resistance in Escherichia coli and salmonellas isolated from farm animals. J Hyg 1986; 97:445–456
     [Google Scholar]
214. Piddock L. J. V., Wray C., McCaren I., Wise R. Quinolone resistance in Salmonella spp: veterinary pointers. Lancet 1990; 2:125
     [Google Scholar]
215. Wray C. Some aspects of the occurrence of resistant bacteria in the normal animal flora. J Antimicrob Chemother 1986; 18: Suppl C141–147
     [Google Scholar]
216. Wray C., McLaren I. M., Carroll P. J. Escherichia coli isolated from farm animals in England and Wales between 1986 and 1991. Vet Rec 1993; 133:439–442
     [Google Scholar]
217. Francis P. G., Carroll P. J. Antibiotic resistant patterns of Staphylococcus aureus strains isolated from clinical bovine mastitis. Vet Rec 1986; 118:361–363
     [Google Scholar]
218. Mackie D. P., Logan E. F., Pollock D. A., Rodgers S. P. Antibiotic sensitivity of bovine staphylococcal and coliform mastitis isolates over four years. Vet Rec 1988; 123:515–517
     [Google Scholar]
219. Perrin-Caoullioud I., Martel J. L., Coudert M. Bilan de l’epidemioscerveillance de l’antibioresistance de Staphylococcus aureus en pathologie bovièn. Rev Med Vet 1988; 139:709–718
     [Google Scholar]
220. Noble W. C., Allaker R. P. Staphylococci on the skin of pigs: isolates from two farms with different antibiotic policies. Vet Rec 1992; 130:466–468
     [Google Scholar]
221. Linton A. H. Microbial risks of growth promoter use. In Helmuth R., Bulling E. (eds) Proceedings of the Symposium ‘Criteria and Methods for the Microbiological Evaluation of Growth Promoters in Animal Feed’ Vet Med-Hefte Inst fur Vet-Med des BGA; Berlin: 198558–79
     [Google Scholar]
222. Threlfall E. J., Rowe B., Ferguson J. L., Ward L. R. Increasing incidence of resistance to gentamicin and related aminoglycosides in Salmonella typhimurium phage type 204C in England, Wales and Scotland. Vet Rec 1982; 117:355–357
     [Google Scholar]
223. Chaslus-Dancla E., Glupczynski Y., Gerbaud G., Lagorce M., Lafont J. P., Courvalin P. Detection of apramycin resistant Enterobacteriaceae in hospital isolates. FEMS Microbiol Lett 1989; 61:261–266
     [Google Scholar]
224. Salauze D., Otal I., Gomez-Lus R., Davies J. Aminoglycoside acetyltransferase 3-IV (aac4) and hygromycin B4-1 phosphotransferase (hyph B) in bacteria isolated from human and animal sources. Antimicrob Agents Chemother 1990; 34:1915–1920
     [Google Scholar]
225. Hunter J. E. B., Hart C. A., Shelley J. C., Walton J. R., Bennett M. Human isolates of apramycin-resistant Escherichia coli which contain the gene for the AAC(3)IV enzyme. Epidemiol Infect 1993; 110:253–259
     [Google Scholar]
226. Pohl P., Glupczynski Y., Marin M., Van Robaeys G., Lintermans P., Couturier M. Replicon typing, characterization of plasmids encoding resistance to gentamicin and apramycin in Escherichia coli and Salmonella typhimurium isolated from human and animal sources in Belgium. Epidemiol Infect 1993; 111:229–238
     [Google Scholar]
227. Johnson A. P., Malde M., Woodford N., Cunney R. J., Smyth E. G. Urinary isolates of apramycin-resistant Escherichia coli and Klebsiella pneumoniae from Dublin. Epidemiol Infect 1995; 114:105–112
     [Google Scholar]
228. Report Impact of antibiotic-resistant bacteria. Office of Technology Assessment 1994 Congress of the United States. p 27