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A comparison of aerosol and intragastric routes of infection with Listeria spp

Published online by Cambridge University Press:  15 May 2009

P. Bracegirdle
Affiliation:
Division of Pathology, Public Health Laboratory Service, Centre for Applied Microbiology and Research, Porton Down, Salisbury, Wiltshire SP4 OJG
A. A. West
Affiliation:
Division of Pathology, Public Health Laboratory Service, Centre for Applied Microbiology and Research, Porton Down, Salisbury, Wiltshire SP4 OJG
M. S. Lever
Affiliation:
Division of Pathology, Public Health Laboratory Service, Centre for Applied Microbiology and Research, Porton Down, Salisbury, Wiltshire SP4 OJG
R. B. Fitzgeorge
Affiliation:
Division of Pathology, Public Health Laboratory Service, Centre for Applied Microbiology and Research, Porton Down, Salisbury, Wiltshire SP4 OJG
A. Baskerville
Affiliation:
Division of Pathology, Public Health Laboratory Service, Centre for Applied Microbiology and Research, Porton Down, Salisbury, Wiltshire SP4 OJG
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Aerosol infection (AI) of Porton outbreak mice with Listeria species, exhibiting varying degrees of virulence, was compared with gastric intubation (GI) on the basis of numbers of deaths. 50% lethal dose (LD50) and pattern of listerial infection. The AI route appeared to be more sensitive, efficient and consistent than GI in that it required 105 fewer micro-organisms to obtain infection and death then ensued within 4 days, with GI deaths usually occurring on day 7. All the virulent strains tested caused 100% mortality by AI, while virulent and avirulent strains were indistinguishable by GI. Bacterial counts in the livers and spleens of infected mice were consistent with the relative virulence of the infectious agent using AI but not in GI mice. There were higher numbers of micro-organisms and more widespread lesions in the organs of AI mice than in GI. Results indicate that AI is an accurate in vivo indicator of virulence in listeria and using AI, bacterial counts in the liver and spleen could replace LD50 tests, thereby reducing the number of animals required for in vivo virulence testing.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1994

References

REFERENCES

McLauchlin, J. Listeria monocytogenes, recent advances in the taxonomy and epidemiology of listeriosis in humans. J Appl Bact 1987; 63: 111.CrossRefGoogle ScholarPubMed
Rocourt, J, Seeliger, HPR. Distribution des espéces du genre Listeria. Zentralb Bakteriol Parasitenkd Infektionskr Hyg Abt 1, Orig A. 1985; 259; 317–30.Google ScholarPubMed
Schlech, WF, Lavigne, PM, Bortolussi, RA et al. , Epidemic listeriosis. Evidence for transmission by food. N Engl J Med 1983; 308: 203–6.CrossRefGoogle ScholarPubMed
Fleming, DW, Coehi, SL, MacDonald, KL et al. , Pasteurised milk as a vehicle of infection in an outbreak of listeriosis. N Engl J Med 1985: 312: 404–7.CrossRefGoogle Scholar
Linnan, MJ, Mascola, L, Lou, XD. et al. Epidemic listeriosis associated with Mexican-style cheese. N Engl J Med 1988; 319: 823–8.CrossRefGoogle ScholarPubMed
Bille, J. Epidemiology of human listeriosis in Europe, with special reference to the Swiss outbreak. In: Miller, JL.Somkuti, GA, eds. Foodborne listeriosis. Society for Industrial Microbiology. New York: Elsevier Science Publishing. Inc. 1990: 71–4.Google Scholar
Farber, JM, Peterkin, PI. Listeria monocytogenes, a food-borne pathogen. Microbiol Rev 1991; 55: 476511.CrossRefGoogle ScholarPubMed
Audurier, A, Pardon, P, Marly, J, Lantier, F. Experimental infection of mice with Listeria monocytogenes and L. innocua. Ann Microbiol (Paris) 1980; 131B: 4757.Google Scholar
Herbert, D. The chemical composition of microorganisms as a function of their environment. In: Meynell, GG.Gooder, H. eds. Microbial reaction to environment. Symposium of the Society of General Microbiology. Cambridge: Cambridge University Press. 1961: 391416.Google Scholar
Baskerville, A, Fitzgeorge, RB, Broster, M, Hambleton, P, Dennis, PJ. Experimental transmission of Legionnaires' disease by exposure to aerosols of Legionella pneumophila. Lancet 1981; ii: 1389–90.CrossRefGoogle Scholar
Reed, LJ, Muench, H. A simple method of estimating fifty per cent endpoints. Am J Hyg 1938; 27: 493–7.Google Scholar
Kautter, DA, Silverman, SJ, Roessler, WG, Drawdy, JF. Virulence of Listeria monocytogenes for experimental animals. J Infect Dis 1963; 112: 167–80.CrossRefGoogle ScholarPubMed
Gaillard, JL, Berche, P, Sansonetti, P. Transposon mutagenesis as a tool to study the role of haemolysin in the virulence of Listeria monocytogenes. Infect Immun 1986: 52: 50–5.CrossRefGoogle Scholar
Kathariou, S, Metz, P, Hof, H, Goebel, W. Tn916-induced mutations in the haemolysin determinant affecting the virulence of L. monocytogenes. J Bacteriol 1987; 169: 1291–7.CrossRefGoogle Scholar
Hof, H, Hefner, P. Pathogenicity of Listeria monocytogenes in comparison to other Listeria species. Infection 1988: 16 Suppl 2: S1414.CrossRefGoogle ScholarPubMed
Seeliger, HPR. Listeriosis. 2nd edn.Basel: Karger. 1961: 142.Google Scholar
Schlech, WF. New perspectives on the gastrointestinal mode of transmission in invasive Listeria monocytogenes infection. Clin Invest Med 1984; 7: 321–4.Google ScholarPubMed
Al-Ghazali, MR, Al-Azawi, SK. L. monocytogenes contamination of crops grown on soil treated with sewage sludge cake. J Appl Bacteriol 1990: 69: 642–7.CrossRefGoogle ScholarPubMed