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. 1995 Sep;177(17):5028–5034. doi: 10.1128/jb.177.17.5028-5034.1995

Use of a novel mobilizable vector to inactivate the scrA gene of Streptococcus sobrinus by allelic replacement.

N D Buckley 1, L N Lee 1, D J LeBlanc 1
PMCID: PMC177280  PMID: 7665480

Abstract

The virulence factors of the cariogenic bacterium Streptococcus sobrinus have been difficult to assess because of a lack of tools for the genetic manipulation of this organism. The construction of an Escherichia coli-Streptococcus shuttle vector, pDL289, that can be mobilized into S. sobrinus by the conjugative plasmid pAM beta 1 was described in a previous report. The vector contains pVA380-1 for replication and mobilization in streptococci, the pSC101 replicon for maintenance in E. coli, a kanamycin resistance marker that functions in both hosts, and the multiple cloning site and lacZ from pGEM7Zf(-). pDL289 is stable with or without selection in several species of Streptococcus. In this study, a derivative with a deletion in the minus origin of the pVA380-1 component of pDL289 was constructed. This derivative, pDL289 delta 202, was less stable than pDL289 in Streptococcus gordonii Challis, Streptococcus mutans, and S. sobrinus. Both pDL289 and pDL289 delta 202 were mobilizable by pAM beta 1 into S. sobrinus, with frequencies of 3 x 10(-6) and 1 x 10(-7) transconjugants per recipient CFU, respectively. The cloned scrA gene of S. sobrinus 6715-10 coding for the EIISuc of the sucrose-specific phosphoenolpyruvate phosphotransferase system was interrupted by the insertion of a streptococcal spectinomycin resistance gene active in E. coli and streptococci. The interrupted scrA gene was subcloned into both pDL289 and pDL289 delta 202. Each recombinant plasmid was introduced into the DL1 strain of S. gordonii Challis, which was then used as a recipient for the conjugative transfer of pAM beta 1. The latter plasmid was used to mobilize each recombinant plasmid from S. gordonii Challis DL1 to S. sobrinus 6715-10RF. Subsequently, recombinants derived from a double-crossover event were isolated on the basis of resistance to spectinomycin and susceptibility to kanamycin. Recombinational events were confirmed by Southern hybridization, and the inactivation of the EII Suc in double crossovers was confirmed by phosphotransferase system assays. This is the first report of allelic replacement in S. sobrinus.

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Selected References

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  1. Anderson D. G., McKay L. L. Simple and rapid method for isolating large plasmid DNA from lactic streptococci. Appl Environ Microbiol. 1983 Sep;46(3):549–552. doi: 10.1128/aem.46.3.549-552.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bartolomé B., Jubete Y., Martínez E., de la Cruz F. Construction and properties of a family of pACYC184-derived cloning vectors compatible with pBR322 and its derivatives. Gene. 1991 Jun 15;102(1):75–78. doi: 10.1016/0378-1119(91)90541-i. [DOI] [PubMed] [Google Scholar]
  3. Birnboim H. C., Doly J. A rapid alkaline extraction procedure for screening recombinant plasmid DNA. Nucleic Acids Res. 1979 Nov 24;7(6):1513–1523. doi: 10.1093/nar/7.6.1513. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Buckley N. D., Lee L. N., LeBlanc D. J. M39 construction of a mobilizable vector for genetic analysis of Streptococcus sobrinus. Dev Biol Stand. 1995;85:399–401. [PubMed] [Google Scholar]
  5. Chen Y. Y., LeBlanc D. J. Genetic analysis of scrA and scrB from Streptococcus sobrinus 6715. Infect Immun. 1992 Sep;60(9):3739–3746. doi: 10.1128/iai.60.9.3739-3746.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Chen Y. Y., Lee L. N., LeBlanc D. J. Sequence analysis of scrA and scrB from Streptococcus sobrinus 6715. Infect Immun. 1993 Jun;61(6):2602–2610. doi: 10.1128/iai.61.6.2602-2610.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Churchward G., Belin D., Nagamine Y. A pSC101-derived plasmid which shows no sequence homology to other commonly used cloning vectors. Gene. 1984 Nov;31(1-3):165–171. doi: 10.1016/0378-1119(84)90207-5. [DOI] [PubMed] [Google Scholar]
  8. Clewell D. B., Yagi Y., Dunny G. M., Schultz S. K. Characterization of three plasmid deoxyribonucleic acid molecules in a strain of Streptococcus faecalis: identification of a plasmid determining erythromycin resistance. J Bacteriol. 1974 Jan;117(1):283–289. doi: 10.1128/jb.117.1.283-289.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Dunny G. M., Brown B. L., Clewell D. B. Induced cell aggregation and mating in Streptococcus faecalis: evidence for a bacterial sex pheromone. Proc Natl Acad Sci U S A. 1978 Jul;75(7):3479–3483. doi: 10.1073/pnas.75.7.3479. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Dunny G. M., Lee L. N., LeBlanc D. J. Improved electroporation and cloning vector system for gram-positive bacteria. Appl Environ Microbiol. 1991 Apr;57(4):1194–1201. doi: 10.1128/aem.57.4.1194-1201.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Ellwood D. C., Hamilton I. R. Properties of Streptococcus mutans Ingbritt growing on limiting sucrose in a chemostat: repression of the phosphoenolpyruvate phosphotransferase transport system. Infect Immun. 1982 May;36(2):576–581. doi: 10.1128/iai.36.2.576-581.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Galli D., Wirth R. Comparative analysis of Enterococcus faecalis sex pheromone plasmids identifies a single homologous DNA region which codes for aggregation substance. J Bacteriol. 1991 May;173(9):3029–3033. doi: 10.1128/jb.173.9.3029-3033.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Gruss A., Ehrlich S. D. The family of highly interrelated single-stranded deoxyribonucleic acid plasmids. Microbiol Rev. 1989 Jun;53(2):231–241. doi: 10.1128/mr.53.2.231-241.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Hayakawa M., Aoki H., Kuramitsu H. K. Isolation and characterization of the sucrose 6-phosphate hydrolase gene from Streptococcus mutans. Infect Immun. 1986 Sep;53(3):582–586. doi: 10.1128/iai.53.3.582-586.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Henikoff S. Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing. Gene. 1984 Jun;28(3):351–359. doi: 10.1016/0378-1119(84)90153-7. [DOI] [PubMed] [Google Scholar]
  16. Inamine J. M., Lee L. N., LeBlanc D. J. Molecular and genetic characterization of lactose-metabolic genes of Streptococcus cremoris. J Bacteriol. 1986 Sep;167(3):855–862. doi: 10.1128/jb.167.3.855-862.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Köhler B., Bjarnason S. Mutans streptococci, lactobacilli and caries prevalence in 11- and 12-year-old Icelandic children. Community Dent Oral Epidemiol. 1987 Dec;15(6):332–335. doi: 10.1111/j.1600-0528.1987.tb01747.x. [DOI] [PubMed] [Google Scholar]
  18. LeBlanc D. J., Chen Y. Y., Lee L. N. Identification and characterization of a mobilization gene in the streptococcal plasmid, pVA380-1. Plasmid. 1993 Nov;30(3):296–302. doi: 10.1006/plas.1993.1063. [DOI] [PubMed] [Google Scholar]
  19. LeBlanc D. J., Crow V. L., Lee L. N., Garon C. F. Influence of the lactose plasmid on the metabolism of galactose by Streptococcus lactis. J Bacteriol. 1979 Feb;137(2):878–884. doi: 10.1128/jb.137.2.878-884.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. LeBlanc D. J., Hassell F. P. Transformation of Streptococcus sanguis Challis by plasmid deoxyribonucleic acid from Streptococcus faecalis. J Bacteriol. 1976 Oct;128(1):347–355. doi: 10.1128/jb.128.1.347-355.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. LeBlanc D. J., Hawley R. J., Lee L. N., St Martin E. J. "Conjugal" transfer of plasmid DNA among oral streptococci. Proc Natl Acad Sci U S A. 1978 Jul;75(7):3484–3487. doi: 10.1073/pnas.75.7.3484. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. LeBlanc D. J., Inamine J. M., Lee L. N. Broad geographical distribution of homologous erythromycin, kanamycin, and streptomycin resistance determinants among group D streptococci of human and animal origin. Antimicrob Agents Chemother. 1986 Apr;29(4):549–555. doi: 10.1128/aac.29.4.549. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. LeBlanc D. J., Lee L. N., Abu-Al-Jaibat A. Molecular, genetic, and functional analysis of the basic replicon of pVA380-1, a plasmid of oral streptococcal origin. Plasmid. 1992 Sep;28(2):130–145. doi: 10.1016/0147-619x(92)90044-b. [DOI] [PubMed] [Google Scholar]
  24. Loesche W. J. Role of Streptococcus mutans in human dental decay. Microbiol Rev. 1986 Dec;50(4):353–380. doi: 10.1128/mr.50.4.353-380.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Lunsford R. D., Macrina F. L. Molecular cloning and characterization of scrB, the structural gene for the Streptococcus mutans phosphoenolpyruvate-dependent sucrose phosphotransferase system sucrose-6-phosphate hydrolase. J Bacteriol. 1986 May;166(2):426–434. doi: 10.1128/jb.166.2.426-434.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Macrina F. L., Wood P. H., Jones K. R. Genetic transformation of Streptococcus sanguis (Challis) with cryptic plasmids from Streptococcus ferus. Infect Immun. 1980 Jun;28(3):692–699. doi: 10.1128/iai.28.3.692-699.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Munro C., Michalek S. M., Macrina F. L. Cariogenicity of Streptococcus mutans V403 glucosyltransferase and fructosyltransferase mutants constructed by allelic exchange. Infect Immun. 1991 Jul;59(7):2316–2323. doi: 10.1128/iai.59.7.2316-2323.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. ORLAND F. J., BLAYNEY J. R., HARRISON R. W., REYNIERS J. A., TREXLER P. C., WAGNER M., GORDON H. A., LUCKEY T. D. Use of the germfree animal technic in the study of experimental dental caries. I. Basic observations on rats reared free of all microorganisms. J Dent Res. 1954 Apr;33(2):147–174. doi: 10.1177/00220345540330020201. [DOI] [PubMed] [Google Scholar]
  29. Poy F., Jacobson G. R. Evidence that a low-affinity sucrose phosphotransferase activity in Streptococcus mutans GS-5 is a high-affinity trehalose uptake system. Infect Immun. 1990 May;58(5):1479–1480. doi: 10.1128/iai.58.5.1479-1480.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Russell R. R., Aduse-Opoku J., Sutcliffe I. C., Tao L., Ferretti J. J. A binding protein-dependent transport system in Streptococcus mutans responsible for multiple sugar metabolism. J Biol Chem. 1992 Mar 5;267(7):4631–4637. [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. Sato Y., Kuramitsu H. K. Sequence analysis of the Streptococcus mutans scrB gene. Infect Immun. 1988 Aug;56(8):1956–1960. doi: 10.1128/iai.56.8.1956-1960.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Sato Y., Poy F., Jacobson G. R., Kuramitsu H. K. Characterization and sequence analysis of the scrA gene encoding enzyme IIScr of the Streptococcus mutans phosphoenolpyruvate-dependent sucrose phosphotransferase system. J Bacteriol. 1989 Jan;171(1):263–271. doi: 10.1128/jb.171.1.263-271.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Slee A. M., Tanzer J. M. Effect of growth conditions on sucrose phosphotransferase activity of Streptococcus mutans. Infect Immun. 1980 Mar;27(3):922–927. doi: 10.1128/iai.27.3.922-927.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Slee A. M., Tanzer J. M. Phosphoenolpyruvate-dependent sucrose phosphotransferase activity in Streptococcus mutans NCTC 10449. Infect Immun. 1979 Jun;24(3):821–828. doi: 10.1128/iai.24.3.821-828.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Slee A. M., Tanzer J. M. Sucrose transport by Streptococcus mutans. Evidence for multiple transport systems. Biochim Biophys Acta. 1982 Nov 22;692(3):415–424. doi: 10.1016/0005-2736(82)90392-3. [DOI] [PubMed] [Google Scholar]
  37. Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
  38. Sreebny L. M. Sugar availability, sugar consumption and dental caries. Community Dent Oral Epidemiol. 1982 Feb;10(1):1–7. doi: 10.1111/j.1600-0528.1982.tb00352.x. [DOI] [PubMed] [Google Scholar]
  39. St Martin E. J., Wittenberger C. L. Characterization of a phosphoenolpyruvate-dependent sucrose phosphotransferase system in Streptococcus mutans. Infect Immun. 1979 Jun;24(3):865–868. doi: 10.1128/iai.24.3.865-868.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Tao L., Sutcliffe I. C., Russell R. R., Ferretti J. J. Transport of sugars, including sucrose, by the msm transport system of Streptococcus mutans. J Dent Res. 1993 Oct;72(10):1386–1390. doi: 10.1177/00220345930720100701. [DOI] [PubMed] [Google Scholar]
  41. Vocke C., Bastia D. Primary structure of the essential replicon of the plasmid pSC101. Proc Natl Acad Sci U S A. 1983 Nov;80(21):6557–6561. doi: 10.1073/pnas.80.21.6557. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Wittenberger C. L., Beaman A. J., Lee L. N. Tween 80 effect on glucosyltransferase synthesis by Streptococcus salivarius. J Bacteriol. 1978 Jan;133(1):231–239. doi: 10.1128/jb.133.1.231-239.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. de Soet J. J., van Loveren C., Lammens A. J., Pavicić M. J., Homburg C. H., ten Cate J. M., de Graaff J. Differences in cariogenicity between fresh isolates of Streptococcus sobrinus and Streptococcus mutans. Caries Res. 1991;25(2):116–122. doi: 10.1159/000261353. [DOI] [PubMed] [Google Scholar]
  44. van Houte J. Bacterial specificity in the etiology of dental caries. Int Dent J. 1980 Dec;30(4):305–326. [PubMed] [Google Scholar]

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