168
Views
4
CrossRef citations to date
0
Altmetric
Research Article

Gene Transfer in the GI Tract and Oral Cavity

Pages 73-80 | Published online: 11 Jul 2009

References

  • Trieu-Cuot P, Carlier C, Martin P, Courvalin P. Plasmid transfer by conjugation from Escherichia coli to Gram-posi-tive bacteria. FEMS Microbiol Lett 1987; 8: 289–94.
  • Heinemann JA, Sprague GF Jr. Bacterial conjugative plas-mids mobilise DNA transfer between bacteria and yeast. Nature 1989; 340: 205–9.
  • Mullany P, Wilks M, Puckey L, Tabaqchali S. Gene cloning in Clostridium difficile using Tn9/6 as a shuttle conjugative transposon. Plasmid 1994; 31: 320–3.
  • Lanka E, Wilkins BM. DNA processing reactions in bacterial conjugation. Annu Rev Biochem 1995; 64: 141–69.
  • Wang A, Macrina FL. Streptococcal plasmid pIP501 has a functional oriT site. J Bacteriol 1995; 177: 4199–206.
  • Jaworski DD, Clewell DB. A functional origin of transfer (oriT) on the conjugative transposon Tn9/6. J Bacteriol 1995; 177: 6644–51.
  • Climo MW, Sharma VK, Archer GL. Identification and characterisation of the origin of transfer (oriT) and a gene(-nes) encoding a single stranded endonuclease on the staphylo-coccal plasmid pG01. J Bacteriol 1996; 178: 4975–83.
  • Crellin PK, Rood JI. Tn4451 from Clostridium perfringens is a mobilisable transposon that encodes the functional Mob protein, TnpZ. Mol Microbiol 1998; 27: 631–42.
  • Lyras D, Stone C, Huggins AS, Crellin PK, Bannam TL, Rood JI. Chloramphenicol resistance in Clostridium difficile is encoded on Tn4453 transposons that are closely related to Tn445/ from Clostridium perfringens. Antimicrob Agents Chemother 1998; 23: 784–6.
  • Flannagan SE, Zitzow LA, Su YA, Clewell DB. Nucleotide sequence of the 18 kb conjugative transposon Tn9/6 from Enterococcus faecalis. Plasmid 1994; 32: 350–4.
  • Smith CJ, Tribbble GD, Bayley DP. Genetic elements of Bacteroides species: a moving story. Plasmid 1998; 40: 12–29.
  • Zatyka M, Thomas CM. Control of genes for conjugative transfer of plasmids and other mobile elements. FEMS Mi-crobiol Rev 1998; 21: 291–319.
  • Clewell DB, Flannagan SE. The conjugative transposons of Gram-positive bacteria. In: Clewell DB, ed. Bacterial conjuga-tion. New York: Plenum Press, 1993: 369–93.
  • Salyers AA, Shoemaker NB, Stevens AM, Lhing-Yew L. Conjugative transposons: an unusual and diverse set of inte-grated gene transfer elements. Microbiol Rev 1995; 59: 579–90.
  • Wang H, Roberts AP, Lyras D, Rood JI, Wilks M, Mullany P. Characterisation of the ends and target sites of the novel conjugative transposon Tn5397 from Clostridium difficile: ex-cision and circularisation is mediated by the large resolvase TndX J Bacteriol 2000; 182: 3775–83.
  • Rice LB. Tn9/6 family of conjugative transposons and dis-semination of antimicrobial resistance determinants. Antimi-crob Agents Chemother 1998; 42: 1871–7.
  • Charpentier E, Gerbaud G, Courvalin P. Conjugative mobili-sation of the rolling circle plasmid pIP823 from Listeria monocytogenes BM4293 among Gram-positive and Gram-negative bacteria. J Bacteriol 1999; 181: 3368–74.
  • Hacker J, Blum-Oehler G, Miihldorfer I, Tschdpe H. Patho-genicity islands of virulent bacteria: structure, function and impact on microbial evolution. Mol Microbiol 1997; 23: 1087–9.
  • Lindsay JA, Ruzin A, Ross HF, Kurepina N, Novick RP. The gene for toxic shock toxin is carried by a family of mobile pathogenicity islands in Staphylococcus aureus. Mol Microbiol 1998; 29: 527–43.
  • Recchia GD, Hall RM. Origins of the mobile gene cassettes found in integrons. Trends Microbiol 1997; 5: 389–94.
  • Mullany P, Panen M, Wilks M, Tabaqchali S. A Group II intron in a conjugative transposon from the Gram-positive bacterium, Clostridium difficile. Gene 1996; 174: 145–50.
  • Yeo CC, Tham JM, Yap MWC, Poh CL. Group II intron from Pseudomonas alcaligenes NCIB 9867 (P25X): Entrap-ment in plasmid RP4 and sequence analysis. Microbiology 1997; 143: 2833–40.
  • Huang C-C, Narita M, Yamagata T, Itoh Y, Endo G. Structure analysis of a class II transposon encoding the mercury resistance of the Gram-positive bacterium Bacillus megaterium MB1, a strain isolated from Minamata Bay, Japan. Gene 1999; 234: 361–9.
  • Mills DA, McKay LL, Dunny GM. Splicing of a group II intron involved in the conjugative transfer of pRS01 in Lacto-cocci. J Bacteriol 1996; 178: 3531–8.
  • Shearman C, Godon JJ, Gasson M. Splicing of a group II intron in a functional transfer gene of Lactococcus laais. Mol Microbiol 1996; 21: 45–53.
  • Cousineau B, Smith D, Lawrence-Cavanagh S, Mueller JE, Yang J, Mills D, Manias D, Dunny G, Lambowitz AM, Belfort M. Retrohoming of a bacterial group II intron: mobil-ity via complete reverse splicing, independent of homologous recombination. Cell 1998; 94: 451–62.
  • McDougal LK, Tenover FC, Lee LN, Kamile J, Patterson JE, Jorgensen JH, LeBlanc DJ. Detection of Tn917-like sequences within a Tn916-like conjugative transposon (1n3872) in ery-thromycin-resistant isolates of Streptococcus pneumoniae An-timicrob Agents Chemother 1998; 42: 2312–8.
  • Rice LB, Carias LL. Transfer of Tn5385, a composite multire-sistance chromosomal element from Enterococcus faecalis. J Bacteriol 1998; 180: 714–21.
  • Shoemaker NB, Salyers AA Facilitated transfer of IncPI3 R751 derivatives from the chromosome of Bacteroides uni-fotmis to Escherichia coli recipients by a conjugative Bac-teroides tetracycline resistance element. J Bacteriol 1987; 169: 3160–7.
  • Gyles C, Falkow S, Rollins L. In vivo transfer of an Es - cherichia coli enterotoxin plasmid possessing genes for drug resistance. Am J Vet Res 1978; 39: 1438–41.
  • Doucet-Populaire F, Trieu-Cuot P, Dosbaa I, Andremont A, Courvalin P. Conjugal transfer of plasmid DNA from En-terococcus faecalis to Escherichia coli in digestive tracts of gnotobiotic mice. Antimicrob Agents Chemother 1992; 35: 185–7.
  • Pappenheimer AM Jr, Murphy JR Studies on the molecular epidemiology of diphtheria. Lancet 1983; 2: 923–6.
  • Roberts AP, Pratten J, Wilson M, Mullany P. Transfer of a conjugative transposon, Tn5397 in a model oral biofdm. FEMS Microbiol Lett 1999; 177: 63–6.
  • Mel SF, Mekalanos JJ. Modulation of horizontal gene trans-fer in pathogenic bacteria by in vivo signals. Cell 1996; 87: 795–8.
  • Dunny G, Yuhasz M, Ehrenfeld E. Genetic and physiological analysis of conjugation in Streptococcus faecalis. J Bacteriol 1982; 151: 855–9.
  • Celli J, Trieu-Cuot P. Circularisation of Tn916 is required for expression of the transposon-encoded transfer functions: characterisation of long tetracycline-inducable transcripts reading through the attachment site. Mol Microbiol 1998; 28: 103–17.
  • Droge M, Puhler A, Selbitschka W. Horizontal gene transfer in terrestrial and aquatic habitats as assessed by microcosm and field studies. Biol Fert Soils 1999; 29: 221–54.
  • Teuber M, Perreten V, Wirsching F. Antibiotikumresistente bakterien: eine neue dimension in der lebensmittel-mikrobi-ologie. Lebensmittel-Technologie 1996; 29: 182–99.
  • Segal G, Shuman HA. Intracellular multiplication and human macrophage killing by Legionella pneumophila are inhibited by conjugal components of IncQ plasmids RSF1010. Mol Microbiol 1998; 30: 197–208.
  • Shoemaker NB, Salyers AA. Dnase resistant transfer of chro-mosomal cat and tet insertions by filter mating in pneumococ-cus. Plasmid 1980; 3: 80–7.
  • Waldor MK, Tschape H, Mekalanos JJ. A new type of conjugative transposons encodes resistance to sulfamethoxa-zole, trimethoprim and streptomycin in Vibrio cholerae 0139. J Bacteriol 1996; 178: 4157–65.
  • Stevens AM, Shoemaker NB, Salyers AA. Tetracycline regu-lation of genes on Bacteroides conjugative transposons. J Bacteriol 1993; 175: 6134–41.
  • Cooper AJ, Shoemaker NB, Salyers AA. The erythromycin resistance gene from the Bacteroides conjugative transposon TcrEmr 7853 is nearly identical to ermG from Bacillus sphaeri-cus. Antimicrob Agents Chemother 1996; 40: 506–8.
  • Shoemaker NB, Salyers AA. A cryptic 65-kilobase pair trans-poson-like element isolated from Bacteroides uniformus has homology with Bacteroides conjugal tetracycline resistance elements. J Bacteriol 1990; 172: 1694–702.
  • Wren B, Mullany P, Clayton C, Tabaqchali S. Molecular cloning and genetic analysis of chloramphenicol acetyltrans-ferase determinant from Clostridium difficile. Antimicrob Agents Chemother 1988; 32: 1213–7.
  • Ayoubi P, Kilic OA, Vijayakumar MN. Tn5253, the pneumo-coccal (cat tet) BM6001 element is a composite structure of two conjugative transposons, Tn525/ and Tn5252. J Bacteriol 1991; 173: 1617–22.
  • Oskam L, Hillenga DJ, Venema G, Bron S. The integrated state of the rolling-circle plasmid pTB913 in the composite Bacillus plasmid pTB19. Mol Gen Genet 1992; 233: 462–8.
  • Salyers AA, Shoemaker NB. Resistance gene transfer in anaerobes: new insights, new problems. Clin Infect Dis 1996; 23 (Suppl): S36–43.