Abstract
Human clinical strains of Campylobacter jejuni and Campylobacter fetus subsp. fetus colonized the gastrointestinal tracts of both athymic (nu/nu) and euthymic (+/nu) germfree mice (BALB/c). Viable Campylobacter spp. (10(9) to 10(10) CFU/g [dry weight] of cecum and colon contents) were isolated on day 3 after oral challenge, and similar large numbers of viable cells were evident at several intervals during a 10-month experiment. The stomachs and upper small intestines of nu/nu and +/nu mice that were monoassociated for 224 days with C. jejuni 45100 contained 3 to 4 logs fewer viable bacteria than did their ceca or colons. Athymic mice that were monoassociated for 224 days with C. fetus subsp. fetus had 2 to 3 logs more viable Campylobacter spp. in their upper gastrointestinal tracts than did their +/nu littermates. Large viable populations (approximately 10(9)/g of contents) of C. fetus subsp. fetus were in the ceca and colons of both nu/nu and +/nu mice. All C. jejuni strains used in this study chronically infected the mesenteric lymph nodes of both nu/nu and +/nu mice. C. jejuni strains 24 and INN 73-83, which were cytotoxic for Chinese hamster ovary cells in vitro, were also more frequently isolated from the livers, spleens, and kidneys of nu/nu mice than was the weak cytotoxin-producing strain 45100. Additionally, heat-labile-enterotoxin-producing C. jejuni INN 73-83 was recovered more frequently from the internal organs of monoassociated +/nu mice than were any other Campylobacter spp. tested. Natural gastrointestinal colonization of neonatal nu/nu and +/nu mice (born to Campylobacter-colonized mothers) with Campylobacter spp. appeared to be delayed until approximately 1 to 2 weeks after birth. Conventionalization of C. jejuni 45100-monoassociated BALB/c mice with a complex mouse fecal microflora eliminated viable C. jejuni from the mesenteric lymph nodes by day 14 and from the cecum by day 78. These findings show that the gnotobiotic BALB/c mouse is a new model for studying acute and chronic host-Campylobacter sp. interactions.
Full text
PDF





Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Al-Mashat R. R., Taylor D. J. Production of diarrhoea and dysentery in experimental calves by feeding pure cultures of Campylobacter fetus subspecies jejuni. Vet Rec. 1980 Nov 15;107(20):459–464. doi: 10.1136/vr.107.20.459. [DOI] [PubMed] [Google Scholar]
- Blaser M. J., Duncan D. J., Warren G. H., Wang W. L. Experimental Campylobacter jejuni infection of adult mice. Infect Immun. 1983 Feb;39(2):908–916. doi: 10.1128/iai.39.2.908-916.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blaser M. J., Reller L. B. Campylobacter enteritis. N Engl J Med. 1981 Dec 10;305(24):1444–1452. doi: 10.1056/NEJM198112103052404. [DOI] [PubMed] [Google Scholar]
- Bryner J. H., Foley J. W., Hubbert W. T., Matthews P. J. Pregnant guinea pig model for testing efficacy of Campylobacter fetus vaccines. Am J Vet Res. 1978 Jan;39(1):119–121. [PubMed] [Google Scholar]
- Butzler J. P., Skirrow M. B. Campylobacter enteritis. Clin Gastroenterol. 1979 Sep;8(3):737–765. [PubMed] [Google Scholar]
- Caldwell M. B., Walker R. I., Stewart S. D., Rogers J. E. Simple adult rabbit model for Campylobacter jejuni enteritis. Infect Immun. 1983 Dec;42(3):1176–1182. doi: 10.1128/iai.42.3.1176-1182.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Collins F. M., Carter P. B. Development of delayed hypersensitivity in gnotobiotic mice. Int Arch Allergy Appl Immunol. 1980;61(2):165–174. doi: 10.1159/000232430. [DOI] [PubMed] [Google Scholar]
- Czuprynski C. J., Balish E. Pathogenesis of Listeria monocytogenes for gnotobiotic rats. Infect Immun. 1981 Apr;32(1):323–331. doi: 10.1128/iai.32.1.323-331.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fauchère J. L., Véron M., Lellouch-Tubiana A., Pfister A. Experimental infection of gnotobiotic mice with Campylobacter jejuni: colonisation of intestine and spread to lymphoid and reticulo-endothelial organs. J Med Microbiol. 1985 Oct;20(2):215–224. doi: 10.1099/00222615-20-2-215. [DOI] [PubMed] [Google Scholar]
- Fernández H., Neto U. F., Fernandes F., de Almeida Pedra M., Trabulsi L. R. Culture supernatants of Campylobacter jejuni induce a secretory response in jejunal segments of adult rats. Infect Immun. 1983 Apr;40(1):429–431. doi: 10.1128/iai.40.1.429-431.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Field L. H., Underwood J. L., Berry L. J. The role of gut flora and animal passage in the colonisation of adult mice with Campylobacter jejuni. J Med Microbiol. 1984 Feb;17(1):59–66. doi: 10.1099/00222615-17-1-59. [DOI] [PubMed] [Google Scholar]
- Field L. H., Underwood J. L., Pope L. M., Berry L. J. Intestinal colonization of neonatal animals by Campylobacter fetus subsp. jejuni. Infect Immun. 1981 Sep;33(3):884–892. doi: 10.1128/iai.33.3.884-892.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Firehammer B. D., Myers L. L. Campylobacter fetus subsp jejuni: its possible significance in enteric disease of calves and lambs. Am J Vet Res. 1981 Jun;42(6):918–922. [PubMed] [Google Scholar]
- Fitzgeorge R. B., Baskerville A., Lander K. P. Experimental infection of Rhesus monkeys with a human strain of Campylobacter jejuni. J Hyg (Lond) 1981 Jun;86(3):343–351. doi: 10.1017/s0022172400069096. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guerrant R. L., Lahita R. G., Winn W. C., Jr, Roberts R. B. Campylobacteriosis in man: pathogenic mechanisms and review of 91 bloodstream infections. Am J Med. 1978 Oct;65(4):584–592. doi: 10.1016/0002-9343(78)90845-8. [DOI] [PubMed] [Google Scholar]
- Harvey S. M., Greenwood J. R. Probable Campylobacter fetus subsp. fetus gastroenteritis. J Clin Microbiol. 1983 Nov;18(5):1278–1279. doi: 10.1128/jcm.18.5.1278-1279.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Humphrey C. D., Montag D. M., Pittman F. E. Experimental infection of hamsters with Campylobacter jejuni. J Infect Dis. 1985 Mar;151(3):485–493. doi: 10.1093/infdis/151.3.485. [DOI] [PubMed] [Google Scholar]
- Klipstein F. A., Engert R. F. Properties of crude Campylobacter jejuni heat-labile enterotoxin. Infect Immun. 1984 Aug;45(2):314–319. doi: 10.1128/iai.45.2.314-319.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lee A., O'Rourke J. L., Barrington P. J., Trust T. J. Mucus colonization as a determinant of pathogenicity in intestinal infection by Campylobacter jejuni: a mouse cecal model. Infect Immun. 1986 Feb;51(2):536–546. doi: 10.1128/iai.51.2.536-546.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Madge D. S. Campylobacter enteritis in young mice. Digestion. 1980;20(6):389–394. doi: 10.1159/000198479. [DOI] [PubMed] [Google Scholar]
- Manninen K. I., Prescott J. F., Dohoo I. R. Pathogenicity of Campylobacter jejuni isolates from animals and humans. Infect Immun. 1982 Oct;38(1):46–52. doi: 10.1128/iai.38.1.46-52.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Merrell B. R., Walker R. I., Coolbaugh J. C. Campylobacter fetus ss. Jejuni, a newly recognized enteric pathogen: morphology and intestinal colonization. Scan Electron Microsc. 1981;4:125–131. [PubMed] [Google Scholar]
- Moberg L. J., Sugiyama H. Microbial ecological basis of infant botulism as studied with germfree mice. Infect Immun. 1979 Aug;25(2):653–657. doi: 10.1128/iai.25.2.653-657.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Owens W. E., Berg R. D. Bacterial translocation from the gastrointestinal tract of athymic (nu/nu) mice. Infect Immun. 1980 Feb;27(2):461–467. doi: 10.1128/iai.27.2.461-467.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Prescott J. F., Barker I. K., Manninen K. I., Miniats O. P. Campylobacter jejuni colitis in gnotobiotic dogs. Can J Comp Med. 1981 Oct;45(4):377–383. [PMC free article] [PubMed] [Google Scholar]
- Prescott J. F., Karmali M. A. Attempts to transmit campylobacter enteritis to dogs and cats. Can Med Assoc J. 1978 Nov 4;119(9):1001–1002. [PMC free article] [PubMed] [Google Scholar]
- Pönkä A., Tilvis R., Helle J., Kosunen T. U. Infection with Campylobacter fetus. Scand J Infect Dis. 1984;16(1):127–128. doi: 10.3109/00365548409068419. [DOI] [PubMed] [Google Scholar]
- Ruiz-Palacios G. M., Escamilla E., Torres N. Experimental Campylobacter diarrhea in chickens. Infect Immun. 1981 Oct;34(1):250–255. doi: 10.1128/iai.34.1.250-255.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ruiz-Palacios G. M., Torres J., Torres N. I., Escamilla E., Ruiz-Palacios B. R., Tamayo J. Cholera-like enterotoxin produced by Campylobacter jejuni. Characterisation and clinical significance. Lancet. 1983 Jul 30;2(8344):250–253. doi: 10.1016/s0140-6736(83)90234-9. [DOI] [PubMed] [Google Scholar]
- Sanyal S. C., Islam K. M., Neogy P. K., Islam M., Speelman P., Huq M. I. Campylobacter jejuni diarrhea model in infant chickens. Infect Immun. 1984 Mar;43(3):931–936. doi: 10.1128/iai.43.3.931-936.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Skirrow M. B. Campylobacter enteritis: a "new" disease. Br Med J. 1977 Jul 2;2(6078):9–11. doi: 10.1136/bmj.2.6078.9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Soerjadi-Liem A. S., Snoeyenbos G. H., Weinack O. M. Comparative studies on competitive exclusion of three isolates of Campylobacter fetus subsp. jejuni in chickens by native gut microflora. Avian Dis. 1984 Jan-Mar;28(1):139–146. [PubMed] [Google Scholar]
- Stanton T. B., Savage D. C. Colonization of gnotobiotic mice by Roseburia cecicola, a motile, obligately anaerobic bacterium from murine ceca. Appl Environ Microbiol. 1983 May;45(5):1677–1684. doi: 10.1128/aem.45.5.1677-1684.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SultanDosa A. B., Bryner J. H., Foley J. W. Pathogenicity of Campylobacter jejuni and Campylobacter coli strains in the pregnant guinea pig model. Am J Vet Res. 1983 Nov;44(11):2175–2178. [PubMed] [Google Scholar]
- Taylor D. E., Bryner J. H. Plasmid content and pathogenicity of Campylobacter jejuni and Campylobacter coli strains in the pregnant guinea pig model. Am J Vet Res. 1984 Oct;45(10):2201–2202. [PubMed] [Google Scholar]
- Wadström T., Baloda S. B., Krovacek K., Faris A., Bengtson S., Walder M. Swedish isolates of Campylobacter jejuni/coli do not produce cytotonic or cytotoxic enterotoxins. Lancet. 1983 Oct 15;2(8355):911–911. doi: 10.1016/s0140-6736(83)90893-0. [DOI] [PubMed] [Google Scholar]
- Warner D. P., Bryner J. H. Campylobacter jejuni and Campylobacter coli inoculation of neonatal calves. Am J Vet Res. 1984 Sep;45(9):1822–1824. [PubMed] [Google Scholar]
- Yeen W. P., Puthucheary S. D., Pang T. Demonstration of a cytotoxin from Campylobacter jejuni. J Clin Pathol. 1983 Nov;36(11):1237–1240. doi: 10.1136/jcp.36.11.1237. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yrios J. W., Balish E. Pathogenesis of Campylobacter spp. in athymic and euthymic germfree mice. Infect Immun. 1986 Aug;53(2):384–392. doi: 10.1128/iai.53.2.384-392.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]

