Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1996 Apr;64(4):1166–1172. doi: 10.1128/iai.64.4.1166-1172.1996

Antigen recognition during progression from acute to chronic infection with a cagA-positive strain of Helicobacter pylori.

H M Mitchell 1, S L Hazell 1, T Kolesnikow 1, J Mitchell 1, D Frommer 1
PMCID: PMC173899  PMID: 8606074

Abstract

We have previously published two reports on acute infection with Helicobacter pylori, one of an adult male and one of a family of four. In the present study, we have isolated H.pylori from each of twin boys in the family and compared these by use of random amplified polymorphic DNA PCR. In addition, we have monitored the antibody response over time of the family and the adult male by Western blotting (immunoblotting) with two different strains of H. pylori as the antigen and by use of a commercial kit. The acutely infected twin boys were infected by an identical strain of H. pylori. The twin boys responded to antigens of 19, 26.5, and 29 kDa 30 days after the initial diagnosis, with recognition of 43-to 49-, 66-, 69-, and 87-kDa antigens by day 63. One twin responded to the CagA antigen on day 63, whereas the other responded on day 857. Antibody to the CagA antigen was not detected by use of the infecting strain, UNSW-RU1. Investigation of UNSW-RU1 revealed the presence of cagA. In two acutely infected adults (one, the father of the boys), the initial response to a 45-kDA antigen was later followed by responses to 19-, 29-, 49-, 60-, 77-, and 84-kDa antigens. Sera from the twins' younger sister, born 17 months after the twins acute episode, indicated that she also had become infected. This report supports intrafamilial transmission of H. pylori. Initial antibody responses in the children were to small-molecular-size antigens; in the adults, the initial responses were to larger-molecular-size antigens. The pattern of the serological response differs according to the antigen used. This has implications in regard to international data comparisons.

Full Text

The Full Text of this article is available as a PDF (378.7 KB).

Selected References

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

  1. Akopyanz N., Bukanov N. O., Westblom T. U., Kresovich S., Berg D. E. DNA diversity among clinical isolates of Helicobacter pylori detected by PCR-based RAPD fingerprinting. Nucleic Acids Res. 1992 Oct 11;20(19):5137–5142. doi: 10.1093/nar/20.19.5137. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. 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]
  3. Bamford K. B., Bickley J., Collins J. S., Johnston B. T., Potts S., Boston V., Owen R. J., Sloan J. M. Helicobacter pylori: comparison of DNA fingerprints provides evidence for intrafamilial infection. Gut. 1993 Oct;34(10):1348–1350. doi: 10.1136/gut.34.10.1348. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Barbosa A. J., Queiroz D. M., Mendes E. N., Rocha G. A., Carvalho A. S., Roquete M. L. Campylobacter pylori associated acute gastritis in a child. J Clin Pathol. 1989 Jul;42(7):779–779. doi: 10.1136/jcp.42.7.779. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Covacci A., Censini S., Bugnoli M., Petracca R., Burroni D., Macchia G., Massone A., Papini E., Xiang Z., Figura N. Molecular characterization of the 128-kDa immunodominant antigen of Helicobacter pylori associated with cytotoxicity and duodenal ulcer. Proc Natl Acad Sci U S A. 1993 Jun 15;90(12):5791–5795. doi: 10.1073/pnas.90.12.5791. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Crabtree J. E., Taylor J. D., Wyatt J. I., Heatley R. V., Shallcross T. M., Tompkins D. S., Rathbone B. J. Mucosal IgA recognition of Helicobacter pylori 120 kDa protein, peptic ulceration, and gastric pathology. Lancet. 1991 Aug 10;338(8763):332–335. doi: 10.1016/0140-6736(91)90477-7. [DOI] [PubMed] [Google Scholar]
  7. Drumm B., Perez-Perez G. I., Blaser M. J., Sherman P. M. Intrafamilial clustering of Helicobacter pylori infection. N Engl J Med. 1990 Feb 8;322(6):359–363. doi: 10.1056/NEJM199002083220603. [DOI] [PubMed] [Google Scholar]
  8. Faulde M., Cremer J., Zöller L. Humoral immune response against Helicobacter pylori as determined by immunoblot. Electrophoresis. 1993 Sep;14(9):945–951. doi: 10.1002/elps.11501401150. [DOI] [PubMed] [Google Scholar]
  9. Frommer D. J., Carrick J., Lee A., Hazell S. L. Acute presentation of Campylobacter pylori gastritis. Am J Gastroenterol. 1988 Oct;83(10):1168–1171. [PubMed] [Google Scholar]
  10. Graham D. Y., Alpert L. C., Smith J. L., Yoshimura H. H. Iatrogenic Campylobacter pylori infection is a cause of epidemic achlorhydria. Am J Gastroenterol. 1988 Sep;83(9):974–980. [PubMed] [Google Scholar]
  11. Hazell S. L., Mitchell H. M., Hedges M., Shi X., Hu P. J., Li Y. Y., Lee A., Reiss-Levy E. Hepatitis A and evidence against the community dissemination of Helicobacter pylori via feces. J Infect Dis. 1994 Sep;170(3):686–689. doi: 10.1093/infdis/170.3.686. [DOI] [PubMed] [Google Scholar]
  12. Kaldor J., Tee W., Nicolacopolous C., Demirtzoglou K., Noonan D., Dwyer B. Immunoblot confirmation of immune response to Campylobacter pyloridis in patients with duodenal ulcers. Med J Aust. 1986 Aug 4;145(3-4):133–135. doi: 10.5694/j.1326-5377.1986.tb113771.x. [DOI] [PubMed] [Google Scholar]
  13. Lee A., Logan S. M., Trust T. J. Demonstration of a flagellar antigen shared by a diverse group of spiral-shaped bacteria that colonize intestinal mucus. Infect Immun. 1987 Mar;55(3):828–831. doi: 10.1128/iai.55.3.828-831.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Malaty H. M., Graham D. Y. Importance of childhood socioeconomic status on the current prevalence of Helicobacter pylori infection. Gut. 1994 Jun;35(6):742–745. doi: 10.1136/gut.35.6.742. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Mendall M. A., Goggin P. M., Molineaux N., Levy J., Toosy T., Strachan D., Northfield T. C. Childhood living conditions and Helicobacter pylori seropositivity in adult life. Lancet. 1992 Apr 11;339(8798):896–897. doi: 10.1016/0140-6736(92)90931-r. [DOI] [PubMed] [Google Scholar]
  16. Mitchell H. M., Bohane T., Hawkes R. A., Lee A. Helicobacter pylori infection within families. Zentralbl Bakteriol. 1993 Sep;280(1-2):128–136. doi: 10.1016/s0934-8840(11)80948-5. [DOI] [PubMed] [Google Scholar]
  17. Mitchell H. M., Li Y. Y., Hu P. J., Liu Q., Chen M., Du G. G., Wang Z. J., Lee A., Hazell S. L. Epidemiology of Helicobacter pylori in southern China: identification of early childhood as the critical period for acquisition. J Infect Dis. 1992 Jul;166(1):149–153. doi: 10.1093/infdis/166.1.149. [DOI] [PubMed] [Google Scholar]
  18. Mitchell J. D., Mitchell H. M., Tobias V. Acute Helicobacter pylori infection in an infant, associated with gastric ulceration and serological evidence of intra-familial transmission. Am J Gastroenterol. 1992 Mar;87(3):382–386. [PubMed] [Google Scholar]
  19. Nwokolo C. U., Bickley J., Attard A. R., Owen R. J., Costas M., Fraser I. A. Evidence of clonal variants of Helicobacter pylori in three generations of a duodenal ulcer disease family. Gut. 1992 Oct;33(10):1323–1327. doi: 10.1136/gut.33.10.1323. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Rocha G. A., Queiroz D. M., Mendes E. N., Barbosa A. J., Lima Júnior G. F., Oliveira C. A. Helicobacter pylori acute gastritis: histological, endoscopical, clinical, and therapeutic features. Am J Gastroenterol. 1991 Nov;86(11):1592–1595. [PubMed] [Google Scholar]
  21. Salmeron M., Desplaces N., Lavergne A., Houdart R. Campylobacter-like organisms and acute purulent gastritis. Lancet. 1986 Oct 25;2(8513):975–976. doi: 10.1016/s0140-6736(86)90625-2. [DOI] [PubMed] [Google Scholar]
  22. Sobala G. M., Crabtree J. E., Dixon M. F., Schorah C. J., Taylor J. D., Rathbone B. J., Heatley R. V., Axon A. T. Acute Helicobacter pylori infection: clinical features, local and systemic immune response, gastric mucosal histology, and gastric juice ascorbic acid concentrations. Gut. 1991 Nov;32(11):1415–1418. doi: 10.1136/gut.32.11.1415. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Tummuru M. K., Cover T. L., Blaser M. J. Cloning and expression of a high-molecular-mass major antigen of Helicobacter pylori: evidence of linkage to cytotoxin production. Infect Immun. 1993 May;61(5):1799–1809. doi: 10.1128/iai.61.5.1799-1809.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. von Wulffen H., Grote H. J., Gatermann S., Löning T., Berger B., Buhl C. Immunoblot analysis of immune response to Campylobacter pylori and its clinical associations. J Clin Pathol. 1988 Jun;41(6):653–659. doi: 10.1136/jcp.41.6.653. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Infection and Immunity are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES