Skip to main content
The American Journal of Pathology logoLink to The American Journal of Pathology
. 1994 Oct;145(4):959–968.

Chronic active hepatitis in mice caused by Helicobacter hepaticus.

J M Ward 1, M R Anver 1, D C Haines 1, R E Benveniste 1
PMCID: PMC1887338  PMID: 7943185

Abstract

Helicobacter infections cause chronic gastroenteritis in humans and several animal species. We recently discovered a new Helicobacter (H. hepaticus) that is the etiological agent of a unique chronic active hepatitis in mice. Natural infection appeared to be acquired early in life in enzootically infected colonies. Liver lesions arose as focal necrosis and focal nonsuppurative inflammation by 1 to 4 months of age in susceptible mouse strains. By 6 to 8 months, extensive liver involvement included hepatocytomegaly, bile ductular (oval cell) hyperplasia, and cholangitis. There was an age-related increase in proliferating cell nuclear antigen hepatocyte nuclear labeling index. The bacteria were usually found within bile canaliculi as determined by ultrastructural evaluation of liver lesions, the Steiner modification of the Warthin-Starry stain and immunohistochemistry with a rabbit antibody to Helicobacter pylori. Naturally infected mice showed an age-related increase in serum IgG antibodies to Helicobacter hepaticus proteins. The disease was experimentally reproduced by intraperitoneal injection of liver suspensions from affected livers or bacteria cultivated in vitro. The earliest lesions of the experimental disease appeared 4 weeks after injection. The course of spontaneous and experimental infection was slow and insidious and resulted in high titers of antibodies to bacterial proteins. This chronic bacterial infection represents a new model of chronic liver disease.

Full text

PDF
968

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Andersen L. P., Espersen F. Immunoglobulin G antibodies to Helicobacter pylori in patients with dyspeptic symptoms investigated by the western immunoblot technique. J Clin Microbiol. 1992 Jul;30(7):1743–1751. doi: 10.1128/jcm.30.7.1743-1751.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Benveniste R. E., Morton W. R., Clark E. A., Tsai C. C., Ochs H. D., Ward J. M., Kuller L., Knott W. B., Hill R. W., Gale M. J. Inoculation of baboons and macaques with simian immunodeficiency virus/Mne, a primate lentivirus closely related to human immunodeficiency virus type 2. J Virol. 1988 Jun;62(6):2091–2101. doi: 10.1128/jvi.62.6.2091-2101.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Blaser M. J. Helicobacter pylori: its role in disease. Clin Infect Dis. 1992 Sep;15(3):386–391. doi: 10.1093/clind/15.3.386. [DOI] [PubMed] [Google Scholar]
  4. Brenes F., Ruiz B., Correa P., Hunter F., Rhamakrishnan T., Fontham E., Shi T. Y. Helicobacter pylori causes hyperproliferation of the gastric epithelium: pre- and post-eradication indices of proliferating cell nuclear antigen. Am J Gastroenterol. 1993 Nov;88(11):1870–1875. [PubMed] [Google Scholar]
  5. Buendia M. A. Hepatitis B viruses and hepatocellular carcinoma. Adv Cancer Res. 1992;59:167–226. doi: 10.1016/s0065-230x(08)60306-1. [DOI] [PubMed] [Google Scholar]
  6. Davis C. P., McAllister J. S., Savage D. C. Microbial colonization of the intestinal epithelium in suckling mice. Infect Immun. 1973 Apr;7(4):666–672. doi: 10.1128/iai.7.4.666-672.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Dunsford H. A., Sell S., Chisari F. V. Hepatocarcinogenesis due to chronic liver cell injury in hepatitis B virus transgenic mice. Cancer Res. 1990 Jun 1;50(11):3400–3407. [PubMed] [Google Scholar]
  8. Eaton K. A., Dewhirst F. E., Radin M. J., Fox J. G., Paster B. J., Krakowka S., Morgan D. R. Helicobacter acinonyx sp. nov., isolated from cheetahs with gastritis. Int J Syst Bacteriol. 1993 Jan;43(1):99–106. doi: 10.1099/00207713-43-1-99. [DOI] [PubMed] [Google Scholar]
  9. Emile J. F., Sebagh M., Féray C., David F., Reynès M. The presence of epithelioid granulomas in hepatitis C virus-related cirrhosis. Hum Pathol. 1993 Oct;24(10):1095–1097. doi: 10.1016/0046-8177(93)90189-n. [DOI] [PubMed] [Google Scholar]
  10. Erlandsen S. L., Chase D. G. Paneth cell function: phagocytosis and intracellular digestion of intestinal microorganisms. II. Spiral microorganism. J Ultrastruct Res. 1972 Nov;41(3):319–333. doi: 10.1016/s0022-5320(72)90072-x. [DOI] [PubMed] [Google Scholar]
  11. Factor V. M., Radaeva S. A. Oval cells--hepatocytes relationships in Dipin-induced hepatocarcinogenesis in mice. Exp Toxicol Pathol. 1993 Aug;45(4):239–244. doi: 10.1016/S0940-2993(11)80399-4. [DOI] [PubMed] [Google Scholar]
  12. Fox J. G., Dewhirst F. E., Tully J. G., Paster B. J., Yan L., Taylor N. S., Collins M. J., Jr, Gorelick P. L., Ward J. M. Helicobacter hepaticus sp. nov., a microaerophilic bacterium isolated from livers and intestinal mucosal scrapings from mice. J Clin Microbiol. 1994 May;32(5):1238–1245. doi: 10.1128/jcm.32.5.1238-1245.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Fox J. G., Edrise B. M., Cabot E. B., Beaucage C., Murphy J. C., Prostak K. S. Campylobacter-like organisms isolated from gastric mucosa of ferrets. Am J Vet Res. 1986 Feb;47(2):236–239. [PubMed] [Google Scholar]
  14. Johnson D. E., Russell R. G., Lockatell C. V., Zulty J. C., Warren J. W., Mobley H. L. Contribution of Proteus mirabilis urease to persistence, urolithiasis, and acute pyelonephritis in a mouse model of ascending urinary tract infection. Infect Immun. 1993 Jul;61(7):2748–2754. doi: 10.1128/iai.61.7.2748-2754.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Kita E., Katsui N., Nishi K., Emoto M., Yanagase Y., Kashiba S. Hepatic lesions in experimental Campylobacter jejuni infection of mice. J Gen Microbiol. 1986 Nov;132(11):3095–3103. doi: 10.1099/00221287-132-11-3095. [DOI] [PubMed] [Google Scholar]
  16. Kita E., Nishikawa F., Kamikaidou N., Nakano A., Katsui N., Kashiba S. Mononuclear cell response in the liver of mice infected with hepatotoxigenic Campylobacter jejuni. J Med Microbiol. 1992 Nov;37(5):326–331. doi: 10.1099/00222615-37-5-326. [DOI] [PubMed] [Google Scholar]
  17. Kita E., Oku D., Hamuro A., Nishikawa F., Emoto M., Yagyu Y., Katsui N., Kashiba S. Hepatotoxic activity of Campylobacter jejuni. J Med Microbiol. 1990 Nov;33(3):171–182. doi: 10.1099/00222615-33-3-171. [DOI] [PubMed] [Google Scholar]
  18. Klaasen H. L., Koopman J. P., Van den Brink M. E., Bakker M. H., Poelma F. G., Beynen A. C. Intestinal, segmented, filamentous bacteria in a wide range of vertebrate species. Lab Anim. 1993 Apr;27(2):141–150. doi: 10.1258/002367793780810441. [DOI] [PubMed] [Google Scholar]
  19. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  20. Lee A., Fox J., Hazell S. Pathogenicity of Helicobacter pylori: a perspective. Infect Immun. 1993 May;61(5):1601–1610. doi: 10.1128/iai.61.5.1601-1610.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Lee A., Gordon J., Dubos R. Enumeration of the oxygen sensitive bacteria usually present in the intestine of healthy mice. Nature. 1968 Dec 14;220(5172):1137–1139. doi: 10.1038/2201137a0. [DOI] [PubMed] [Google Scholar]
  22. Lee A., Phillips M. W., O'Rourke J. L., Paster B. J., Dewhirst F. E., Fraser G. J., Fox J. G., Sly L. I., Romaniuk P. J., Trust T. J. Helicobacter muridarum sp. nov., a microaerophilic helical bacterium with a novel ultrastructure isolated from the intestinal mucosa of rodents. Int J Syst Bacteriol. 1992 Jan;42(1):27–36. doi: 10.1099/00207713-42-1-27. [DOI] [PubMed] [Google Scholar]
  23. Lee A., Phillips M. Isolation and cultivation of spirochetes and other spiral-shaped bacteria associated with the cecal mucosa of rats and mice. Appl Environ Microbiol. 1978 Mar;35(3):610–613. doi: 10.1128/aem.35.3.610-613.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Malo D., Vidal S. M., Hu J., Skamene E., Gros P. High-resolution linkage map in the vicinity of the host resistance locus Bcg. Genomics. 1993 Jun;16(3):655–663. doi: 10.1006/geno.1993.1244. [DOI] [PubMed] [Google Scholar]
  25. Nakamura T., Hayama M., Sakai T., Hotchi M., Tanaka E. Proliferative activity of hepatocytes in chronic viral hepatitis as revealed by immunohistochemistry for proliferating cell nuclear antigen. Hum Pathol. 1993 Jul;24(7):750–753. doi: 10.1016/0046-8177(93)90012-6. [DOI] [PubMed] [Google Scholar]
  26. Negrini R., Lisato L., Zanella I., Cavazzini L., Gullini S., Villanacci V., Poiesi C., Albertini A., Ghielmi S. Helicobacter pylori infection induces antibodies cross-reacting with human gastric mucosa. Gastroenterology. 1991 Aug;101(2):437–445. doi: 10.1016/0016-5085(91)90023-e. [DOI] [PubMed] [Google Scholar]
  27. Okada N., Toriumi W., Sakamoto K., Fujiwara K. Pathologic observations of mouse liver infected with Tyzzer's organisms using immunoperoxidase method. Nihon Juigaku Zasshi. 1986 Feb;48(1):89–98. doi: 10.1292/jvms1939.48.89. [DOI] [PubMed] [Google Scholar]
  28. Paster B. J., Lee A., Fox J. G., Dewhirst F. E., Tordoff L. A., Fraser G. J., O'Rourke J. L., Taylor N. S., Ferrero R. Phylogeny of Helicobacter felis sp. nov., Helicobacter mustelae, and related bacteria. Int J Syst Bacteriol. 1991 Jan;41(1):31–38. doi: 10.1099/00207713-41-1-31. [DOI] [PubMed] [Google Scholar]
  29. Queiroz D. M., Contigli C., Coimbra R. S., Nogueira A. M., Mendes E. N., Rocha G. A., Moura S. B. Spiral bacterium associated with gastric, ileal and caecal mucosa of mice. Lab Anim. 1992 Oct;26(4):288–294. doi: 10.1258/002367792780745760. [DOI] [PubMed] [Google Scholar]
  30. Reddy K. R., Farnum J. B., Thomas E. Acute hepatitis associated with campylobacter colitis. J Clin Gastroenterol. 1983 Jun;5(3):259–262. doi: 10.1097/00004836-198306000-00013. [DOI] [PubMed] [Google Scholar]
  31. Savage D. C., McAllister J. S., Davis C. P. Anaerobic bacteria on the mucosal epithelium of the murine large bowel. Infect Immun. 1971 Oct;4(4):492–502. doi: 10.1128/iai.4.4.492-502.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Schauer D. B., Ghori N., Falkow S. Isolation and characterization of "Flexispira rappini" from laboratory mice. J Clin Microbiol. 1993 Oct;31(10):2709–2714. doi: 10.1128/jcm.31.10.2709-2714.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Scheuer P. J., Ashrafzadeh P., Sherlock S., Brown D., Dusheiko G. M. The pathology of hepatitis C. Hepatology. 1992 Apr;15(4):567–571. doi: 10.1002/hep.1840150402. [DOI] [PubMed] [Google Scholar]
  34. Stanley J., Linton D., Burnens A. P., Dewhirst F. E., Owen R. J., Porter A., On S. L., Costas M. Helicobacter canis sp. nov., a new species from dogs: an integrated study of phenotype and genotype. J Gen Microbiol. 1993 Oct;139(10):2495–2504. doi: 10.1099/00221287-139-10-2495. [DOI] [PubMed] [Google Scholar]
  35. Suzuki M., Miura S., Suematsu M., Fukumura D., Kurose I., Suzuki H., Kai A., Kudoh Y., Ohashi M., Tsuchiya M. Helicobacter pylori-associated ammonia production enhances neutrophil-dependent gastric mucosal cell injury. Am J Physiol. 1992 Nov;263(5 Pt 1):G719–G725. doi: 10.1152/ajpgi.1992.263.5.G719. [DOI] [PubMed] [Google Scholar]
  36. Takagaki Y., Fujiwara K. Bacteremia in experimental Tyzzer's disease of mice. Jpn J Microbiol. 1968 Jun;12(2):129–143. doi: 10.1111/j.1348-0421.1968.tb00377.x. [DOI] [PubMed] [Google Scholar]
  37. Taylor S. L., Dean P. J., Riely C. A. Primary autoimmune cholangitis. An alternative to antimitochondrial antibody-negative primary biliary cirrhosis. Am J Surg Pathol. 1994 Jan;18(1):91–99. [PubMed] [Google Scholar]
  38. Vandamme P., Falsen E., Rossau R., Hoste B., Segers P., Tytgat R., De Ley J. Revision of Campylobacter, Helicobacter, and Wolinella taxonomy: emendation of generic descriptions and proposal of Arcobacter gen. nov. Int J Syst Bacteriol. 1991 Jan;41(1):88–103. doi: 10.1099/00207713-41-1-88. [DOI] [PubMed] [Google Scholar]
  39. WILSON J. W., LEDUC E. H. Role of cholangioles in restoration of the liver of the mouse after dietary injury. J Pathol Bacteriol. 1958 Oct;76(2):441–449. doi: 10.1002/path.1700760213. [DOI] [PubMed] [Google Scholar]
  40. Ward J. M., Collins M. J., Jr, Parker J. C. Naturally occurring mouse hepatitis virus infection in the nude mouse. Lab Anim Sci. 1977 Jun;27(3):372–376. [PubMed] [Google Scholar]
  41. Ward J. M., Fox J. G., Anver M. R., Haines D. C., George C. V., Collins M. J., Jr, Gorelick P. L., Nagashima K., Gonda M. A., Gilden R. V. Chronic active hepatitis and associated liver tumors in mice caused by a persistent bacterial infection with a novel Helicobacter species. J Natl Cancer Inst. 1994 Aug 17;86(16):1222–1227. doi: 10.1093/jnci/86.16.1222. [DOI] [PubMed] [Google Scholar]
  42. Wotherspoon A. C., Doglioni C., Diss T. C., Pan L., Moschini A., de Boni M., Isaacson P. G. Regression of primary low-grade B-cell gastric lymphoma of mucosa-associated lymphoid tissue type after eradication of Helicobacter pylori. Lancet. 1993 Sep 4;342(8871):575–577. doi: 10.1016/0140-6736(93)91409-f. [DOI] [PubMed] [Google Scholar]
  43. Yoshida M. C., Masuda R., Sasaki M., Takeichi N., Kobayashi H., Dempo K., Mori M. New mutation causing hereditary hepatitis in the laboratory rat. J Hered. 1987 Nov-Dec;78(6):361–365. doi: 10.1093/oxfordjournals.jhered.a110416. [DOI] [PubMed] [Google Scholar]

Articles from The American Journal of Pathology are provided here courtesy of American Society for Investigative Pathology

RESOURCES