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. 1997 Feb;65(2):838–842. doi: 10.1128/iai.65.2.838-842.1997

Development of a murine model of chronic Salmonella infection.

S Sukupolvi 1, A Edelstein 1, M Rhen 1, S J Normark 1, J D Pfeifer 1
PMCID: PMC176137  PMID: 9009354

Abstract

The invasive disease caused by Salmonella typhimurium in mice resembles the acute phase of human typhoid fever caused by Salmonella typhi, and experimental murine salmonellosis is a widely used experimental model for systemic salmonellosis. In this paper we demonstrate that murine S. typhimurium infection can also be used to model the development of the chronic carrier state that develops in humans after infection with S. typhi. We describe a virulent variant of S. typhimurium that has decreased expression of AgfA fibers under all environmental conditions studied and that causes a chronic carrier state in BALB/c mice after peroral inoculation. The chronic carrier state is associated with persistence of bacteria in the small intestine, spleen, and liver, and chronic infection continues despite the development of protective immunity to challenge with virulent Salmonella.

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Selected References

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  1. Anderson G. W., Hamblen A. D., Smith H. M. Typhoid Carriers -A Study of Their Disease Producing Potentialities Over a Series of Years as Indicated by a Study of Cases. Am J Public Health Nations Health. 1936 Apr;26(4):396–405. doi: 10.2105/ajph.26.4.396. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Arnqvist A., Olsén A., Normark S. Sigma S-dependent growth-phase induction of the csgBA promoter in Escherichia coli can be achieved in vivo by sigma 70 in the absence of the nucleoid-associated protein H-NS. Mol Microbiol. 1994 Sep;13(6):1021–1032. doi: 10.1111/j.1365-2958.1994.tb00493.x. [DOI] [PubMed] [Google Scholar]
  3. Buchwald D. S., Blaser M. J. A review of human salmonellosis: II. Duration of excretion following infection with nontyphi Salmonella. Rev Infect Dis. 1984 May-Jun;6(3):345–356. doi: 10.1093/clinids/6.3.345. [DOI] [PubMed] [Google Scholar]
  4. Collinson S. K., Clouthier S. C., Doran J. L., Banser P. A., Kay W. W. Salmonella enteritidis agfBAC operon encoding thin, aggregative fimbriae. J Bacteriol. 1996 Feb;178(3):662–667. doi: 10.1128/jb.178.3.662-667.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Collinson S. K., Doig P. C., Doran J. L., Clouthier S., Trust T. J., Kay W. W. Thin, aggregative fimbriae mediate binding of Salmonella enteritidis to fibronectin. J Bacteriol. 1993 Jan;175(1):12–18. doi: 10.1128/jb.175.1.12-18.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Collinson S. K., Emödy L., Müller K. H., Trust T. J., Kay W. W. Purification and characterization of thin, aggregative fimbriae from Salmonella enteritidis. J Bacteriol. 1991 Aug;173(15):4773–4781. doi: 10.1128/jb.173.15.4773-4781.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Doran J. L., Collinson S. K., Burian J., Sarlós G., Todd E. C., Munro C. K., Kay C. M., Banser P. A., Peterkin P. I., Kay W. W. DNA-based diagnostic tests for Salmonella species targeting agfA, the structural gene for thin, aggregative fimbriae. J Clin Microbiol. 1993 Sep;31(9):2263–2273. doi: 10.1128/jcm.31.9.2263-2273.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Edelman R., Levine M. M. Summary of an international workshop on typhoid fever. Rev Infect Dis. 1986 May-Jun;8(3):329–349. doi: 10.1093/clinids/8.3.329. [DOI] [PubMed] [Google Scholar]
  9. Evans D. G., Evans D. J., Jr, Tjoa W. Hemagglutination of human group A erythrocytes by enterotoxigenic Escherichia coli isolated from adults with diarrhea: correlation with colonization factor. Infect Immun. 1977 Nov;18(2):330–337. doi: 10.1128/iai.18.2.330-337.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hammar M., Arnqvist A., Bian Z., Olsén A., Normark S. Expression of two csg operons is required for production of fibronectin- and congo red-binding curli polymers in Escherichia coli K-12. Mol Microbiol. 1995 Nov;18(4):661–670. doi: 10.1111/j.1365-2958.1995.mmi_18040661.x.. [DOI] [PubMed] [Google Scholar]
  11. Hitchcock P. J., Brown T. M. Morphological heterogeneity among Salmonella lipopolysaccharide chemotypes in silver-stained polyacrylamide gels. J Bacteriol. 1983 Apr;154(1):269–277. doi: 10.1128/jb.154.1.269-277.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hormaeche C. E., Pettifor R. A., Brock J. The fate of temperature-sensitive salmonella mutants in vivo in naturally resistant and susceptible mice. Immunology. 1981 Apr;42(4):569–576. [PMC free article] [PubMed] [Google Scholar]
  13. Hornick R. B., Greisman S. E., Woodward T. E., DuPont H. L., Dawkins A. T., Snyder M. J. Typhoid fever: pathogenesis and immunologic control. N Engl J Med. 1970 Sep 24;283(13):686–691. doi: 10.1056/NEJM197009242831306. [DOI] [PubMed] [Google Scholar]
  14. Hughes K. T., Roth J. R. Transitory cis complementation: a method for providing transposition functions to defective transposons. Genetics. 1988 May;119(1):9–12. doi: 10.1093/genetics/119.1.9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Lanata C. F., Levine M. M., Ristori C., Black R. E., Jimenez L., Salcedo M., Garcia J., Sotomayor V. Vi serology in detection of chronic Salmonella typhi carriers in an endemic area. Lancet. 1983 Aug 20;2(8347):441–443. doi: 10.1016/s0140-6736(83)90401-4. [DOI] [PubMed] [Google Scholar]
  16. Levine M. M., Black R. E., Lanata C. Precise estimation of the numbers of chronic carriers of Salmonella typhi in Santiago, Chile, an endemic area. J Infect Dis. 1982 Dec;146(6):724–726. doi: 10.1093/infdis/146.6.724. [DOI] [PubMed] [Google Scholar]
  17. MERSELIS J. G., Jr, KAYE D., CONNOLLY C. S., HOOK E. W. QUANTITATIVE BACTERIOLOGY OF THE TYPHOID CARRIER STATE. Am J Trop Med Hyg. 1964 May;13:425–429. doi: 10.4269/ajtmh.1964.13.425. [DOI] [PubMed] [Google Scholar]
  18. Mastroeni P., Villarreal-Ramos B., Hormaeche C. E. Adoptive transfer of immunity to oral challenge with virulent salmonellae in innately susceptible BALB/c mice requires both immune serum and T cells. Infect Immun. 1993 Sep;61(9):3981–3984. doi: 10.1128/iai.61.9.3981-3984.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Nauciel C., Vilde F., Ronco E. Host response to infection with a temperature-sensitive mutant of Salmonella typhimurium in a susceptible and a resistant strain of mice. Infect Immun. 1985 Sep;49(3):523–527. doi: 10.1128/iai.49.3.523-527.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. O'Callaghan D., Maskell D., Liew F. Y., Easmon C. S., Dougan G. Characterization of aromatic- and purine-dependent Salmonella typhimurium: attention, persistence, and ability to induce protective immunity in BALB/c mice. Infect Immun. 1988 Feb;56(2):419–423. doi: 10.1128/iai.56.2.419-423.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Olsén A., Arnqvist A., Hammar M., Sukupolvi S., Normark S. The RpoS sigma factor relieves H-NS-mediated transcriptional repression of csgA, the subunit gene of fibronectin-binding curli in Escherichia coli. Mol Microbiol. 1993 Feb;7(4):523–536. doi: 10.1111/j.1365-2958.1993.tb01143.x. [DOI] [PubMed] [Google Scholar]
  22. Olsén A., Jonsson A., Normark S. Fibronectin binding mediated by a novel class of surface organelles on Escherichia coli. Nature. 1989 Apr 20;338(6217):652–655. doi: 10.1038/338652a0. [DOI] [PubMed] [Google Scholar]
  23. Schmieger H. Phage P22-mutants with increased or decreased transduction abilities. Mol Gen Genet. 1972;119(1):75–88. doi: 10.1007/BF00270447. [DOI] [PubMed] [Google Scholar]
  24. Sukupolvi S., O'Connor D., Edwards M. F. The traT protein is able to normalize the phenotype of a plasmid-carried permeability mutation of Salmonella typhimurium. J Gen Microbiol. 1986 Aug;132(8):2079–2085. doi: 10.1099/00221287-132-8-2079. [DOI] [PubMed] [Google Scholar]
  25. Thatte J., Rath S., Bal V. Immunization with live versus killed Salmonella typhimurium leads to the generation of an IFN-gamma-dominant versus an IL-4-dominant immune response. Int Immunol. 1993 Nov;5(11):1431–1436. doi: 10.1093/intimm/5.11.1431. [DOI] [PubMed] [Google Scholar]
  26. Wilkinson R. G., Gemski P., Jr, Stocker B. A. Non-smooth mutants of Salmonella typhimurium: differentiation by phage sensitivity and genetic mapping. J Gen Microbiol. 1972 May;70(3):527–554. doi: 10.1099/00221287-70-3-527. [DOI] [PubMed] [Google Scholar]

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