Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1997 Nov;65(11):4642–4651. doi: 10.1128/iai.65.11.4642-4651.1997

Attenuation, persistence, and vaccine potential of an Edwardsiella ictaluri purA mutant.

M L Lawrence 1, R K Cooper 1, R L Thune 1
PMCID: PMC175666  PMID: 9353045

Abstract

In this study, an adenine-auxotrophic strain of Edwardsiella ictaluri was constructed and its virulence, tissue persistence, and vaccine efficacy were evaluated. A clone containing the purA gene was isolated from an E. ictaluri genomic library, sequenced, and shown to have an overall sequence identity of 79.3% at the nucleotide level and 85.7% at the amino acid level with the Escherichia coli purA gene. The cloned E. ictaluri purA gene was mutated by deleting a 598-bp segment of the gene and inserting the kanamycin resistance gene from Tn903 into the gap. The delta purA::Km(r) gene was subcloned into the suicide plasmid pGP704, and the resulting plasmid was used to deliver the modified gene into a virulent strain of E. ictaluri by conjugation. Homologous recombination replaced the chromosomal purA gene with the mutated gene to create an adenine-auxotrophic strain (LSU-E2). Compared to wild-type E. ictaluri, LSU-E2 was highly attenuated by the injection, immersion, and oral routes of exposure. By the injection route, LSU-E2 had a 50% lethal dose (LD50) that was greater than 5 logs10 higher than the LD50 for wild-type E. ictaluri. In a tissue persistence study, LSU-E2 was able to invade channel catfish by the immersion route and persist in internal organs for at least 48 h. Channel catfish that were vaccinated with a single immersion dose of LSU-E2 had mortality significantly lower (P < 0.01) following a wild-type E. ictaluri challenge than that of nonvaccinated fish.

Full Text

The Full Text of this article is available as a PDF (976.6 KB).

Selected References

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

  1. Ahmed Z. U., Sarker M. R., Sack D. A. Protection of adult rabbits and monkeys from lethal shigellosis by oral immunization with a thymine-requiring and temperature-sensitive mutant of Shigella flexneri Y. Vaccine. 1990 Apr;8(2):153–158. doi: 10.1016/0264-410x(90)90139-d. [DOI] [PubMed] [Google Scholar]
  2. BACON G. A., BURROWS T. W., YATES M. The effects of biochemical mutation on the virulence of Bacterium typhosum: the virulence of mutants. Br J Exp Pathol. 1950 Dec;31(6):714–724. [PMC free article] [PubMed] [Google Scholar]
  3. Baselski V. S., Upchurch S., Parker C. D. Isolation and phenotypic characterization of virulence-deficient mutants of Vibrio cholerae. Infect Immun. 1978 Oct;22(1):181–188. doi: 10.1128/iai.22.1.181-188.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bertolini J. M., Cipriano R. C., Pyle S. W., McLaughlin J. J. Serological investigation of the fish pathogen Edwardsiella ictaluri, cause of enteric septicemia of catfish. J Wildl Dis. 1990 Apr;26(2):246–252. doi: 10.7589/0090-3558-26.2.246. [DOI] [PubMed] [Google Scholar]
  5. Bowe F., O'Gaora P., Maskell D., Cafferkey M., Dougan G. Virulence, persistence, and immunogenicity of Yersinia enterocolitica O:8 aroA mutants. Infect Immun. 1989 Oct;57(10):3234–3236. doi: 10.1128/iai.57.10.3234-3236.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Brubaker R. R. Interconversion of Purine Mononucleotides in Pasteurella pestis. Infect Immun. 1970 May;1(5):446–454. doi: 10.1128/iai.1.5.446-454.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Collins L. A., Thune R. L. Development of a Defined Minimal Medium for the Growth of Edwardsiella ictaluri. Appl Environ Microbiol. 1996 Mar;62(3):848–852. doi: 10.1128/aem.62.3.848-852.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. FURNESS G., ROWLEY D. Transduction of virulence within the species Salmonella typhimurium. J Gen Microbiol. 1956 Aug;15(1):140–145. doi: 10.1099/00221287-15-1-140. [DOI] [PubMed] [Google Scholar]
  9. Fields P. I., Swanson R. V., Haidaris C. G., Heffron F. Mutants of Salmonella typhimurium that cannot survive within the macrophage are avirulent. Proc Natl Acad Sci U S A. 1986 Jul;83(14):5189–5193. doi: 10.1073/pnas.83.14.5189. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Garber E. D., Hackett A. J., Franklin R. The Virulence of Biochemical Mutants of Klebsiella Pneumoniae. Proc Natl Acad Sci U S A. 1952 Aug;38(8):693–697. doi: 10.1073/pnas.38.8.693. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Hayashi S., Fujiwara S., Noguchi T. Degradation of uric acid in fish liver peroxisomes. Intraperoxisomal localization of hepatic allantoicase and purification of its peroxisomal membrane-bound form. J Biol Chem. 1989 Feb 25;264(6):3211–3215. [PubMed] [Google Scholar]
  12. Herrero M., de Lorenzo V., Timmis K. N. Transposon vectors containing non-antibiotic resistance selection markers for cloning and stable chromosomal insertion of foreign genes in gram-negative bacteria. J Bacteriol. 1990 Nov;172(11):6557–6567. doi: 10.1128/jb.172.11.6557-6567.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hoiseth S. K., Stocker B. A. Aromatic-dependent Salmonella typhimurium are non-virulent and effective as live vaccines. Nature. 1981 May 21;291(5812):238–239. doi: 10.1038/291238a0. [DOI] [PubMed] [Google Scholar]
  14. Homchampa P., Strugnell R. A., Adler B. Molecular analysis of the aroA gene of Pasteurella multocida and vaccine potential of a constructed aroA mutant. Mol Microbiol. 1992 Dec;6(23):3585–3593. doi: 10.1111/j.1365-2958.1992.tb01794.x. [DOI] [PubMed] [Google Scholar]
  15. Ivánovics G., Marjai E., Dobozy A. The growth of purine mutants of Bacillus anthracis in the body of the mouse. J Gen Microbiol. 1968 Sep;53(2):147–162. doi: 10.1099/00221287-53-2-147. [DOI] [PubMed] [Google Scholar]
  16. Janda J. M., Abbott S. L., Oshiro L. S. Penetration and replication of Edwardsiella spp. in HEp-2 cells. Infect Immun. 1991 Jan;59(1):154–161. doi: 10.1128/iai.59.1.154-161.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Kleckner N., Bender J., Gottesman S. Uses of transposons with emphasis on Tn10. Methods Enzymol. 1991;204:139–180. doi: 10.1016/0076-6879(91)04009-d. [DOI] [PubMed] [Google Scholar]
  18. Kusano T., Takeshima T., Inoue C., Sugawara K. Identification of the purA gene encoding adenylosuccinate synthetase in Thiobacillus ferrooxidans. Curr Microbiol. 1993 Apr;26(4):197–204. doi: 10.1007/BF01577377. [DOI] [PubMed] [Google Scholar]
  19. LEVINE H. B., MAURER R. L. Immunization with an induced avirulent auxotrophic mutant of Pseudomonas pseudomallei. J Immunol. 1958 Nov;81(5):433–438. [PubMed] [Google Scholar]
  20. Leung K. Y., Finlay B. B. Intracellular replication is essential for the virulence of Salmonella typhimurium. Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11470–11474. doi: 10.1073/pnas.88.24.11470. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Li Y., Lovell R. T. Elevated levels of dietary ascorbic acid increase immune responses in channel catfish. J Nutr. 1985 Jan;115(1):123–131. doi: 10.1093/jn/115.1.123. [DOI] [PubMed] [Google Scholar]
  22. Lindberg A. A., Kärnell A., Stocker B. A., Katakura S., Sweiha H., Reinholt F. P. Development of an auxotrophic oral live Shigella flexneri vaccine. Vaccine. 1988 Apr;6(2):146–150. doi: 10.1016/s0264-410x(88)80018-5. [DOI] [PubMed] [Google Scholar]
  23. McCarter L. L. MotX, the channel component of the sodium-type flagellar motor. J Bacteriol. 1994 Oct;176(19):5988–5998. doi: 10.1128/jb.176.19.5988-5998.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. McFarland W. C., Stocker B. A. Effect of different purine auxotrophic mutations on mouse-virulence of a Vi-positive strain of Salmonella dublin and of two strains of Salmonella typhimurium. Microb Pathog. 1987 Aug;3(2):129–141. doi: 10.1016/0882-4010(87)90071-4. [DOI] [PubMed] [Google Scholar]
  25. Miller V. L., Mekalanos J. J. A novel suicide vector and its use in construction of insertion mutations: osmoregulation of outer membrane proteins and virulence determinants in Vibrio cholerae requires toxR. J Bacteriol. 1988 Jun;170(6):2575–2583. doi: 10.1128/jb.170.6.2575-2583.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Mommsen T. P., Hochachka P. W. The purine nucleotide cycle as two temporally separated metabolic units: a study on trout muscle. Metabolism. 1988 Jun;37(6):552–556. doi: 10.1016/0026-0495(88)90170-9. [DOI] [PubMed] [Google Scholar]
  27. Mäntsälä P., Zalkin H. Cloning and sequence of Bacillus subtilis purA and guaA, involved in the conversion of IMP to AMP and GMP. J Bacteriol. 1992 Mar;174(6):1883–1890. doi: 10.1128/jb.174.6.1883-1890.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. 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]
  29. Plumb J. A., Wise M. L., Rogers W. A. Modulary effects of temperature on antibody response and specific resistance to challenge of channel catfish, Ictalurus punctatus, immunized against Edwardsiella ictaluri. Vet Immunol Immunopathol. 1986 Jun;12(1-4):297–304. doi: 10.1016/0165-2427(86)90133-9. [DOI] [PubMed] [Google Scholar]
  30. Roberts M., Maskell D., Novotny P., Dougan G. Construction and characterization in vivo of Bordetella pertussis aroA mutants. Infect Immun. 1990 Mar;58(3):732–739. doi: 10.1128/iai.58.3.732-739.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Sigwart D. F., Stocker B. A., Clements J. D. Effect of a purA mutation on efficacy of Salmonella live-vaccine vectors. Infect Immun. 1989 Jun;57(6):1858–1861. doi: 10.1128/iai.57.6.1858-1861.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Smith B. P., Reina-Guerra M., Stocker B. A., Hoiseth S. K., Johnson E. Aromatic-dependent Salmonella dublin as a parenteral modified live vaccine for calves. Am J Vet Res. 1984 Nov;45(11):2231–2235. [PubMed] [Google Scholar]
  34. Stocker B. A. Auxotrophic Salmonella typhi as live vaccine. Vaccine. 1988 Apr;6(2):141–145. doi: 10.1016/s0264-410x(88)80017-3. [DOI] [PubMed] [Google Scholar]
  35. Straley S. C., Harmon P. A. Growth in mouse peritoneal macrophages of Yersinia pestis lacking established virulence determinants. Infect Immun. 1984 Sep;45(3):649–654. doi: 10.1128/iai.45.3.649-654.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Tatusov R. L., Mushegian A. R., Bork P., Brown N. P., Hayes W. S., Borodovsky M., Rudd K. E., Koonin E. V. Metabolism and evolution of Haemophilus influenzae deduced from a whole-genome comparison with Escherichia coli. Curr Biol. 1996 Mar 1;6(3):279–291. doi: 10.1016/s0960-9822(02)00478-5. [DOI] [PubMed] [Google Scholar]
  37. Waltman W. D., Shotts E. B., Hsu T. C. Biochemical characteristics of Edwardsiella ictaluri. Appl Environ Microbiol. 1986 Jan;51(1):101–104. doi: 10.1128/aem.51.1.101-104.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Wolfe S. A., Smith J. M. Nucleotide sequence and analysis of the purA gene encoding adenylosuccinate synthetase of Escherichia coli K12. J Biol Chem. 1988 Dec 15;263(35):19147–19153. [PubMed] [Google Scholar]
  39. Wong J. G., Hathaway S. C., Paat J. J., Paterson R. W., Steele G. H., Jr Drug-induced meningitis. A case involving trimethoprim-sulfamethoxazole. Postgrad Med. 1994 Nov 1;96(6):117-8, 121,124. [PubMed] [Google Scholar]
  40. de Lorenzo V., Timmis K. N. Analysis and construction of stable phenotypes in gram-negative bacteria with Tn5- and Tn10-derived minitransposons. Methods Enzymol. 1994;235:386–405. doi: 10.1016/0076-6879(94)35157-0. [DOI] [PubMed] [Google Scholar]

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

RESOURCES