Skip to main content
Antimicrobial Agents and Chemotherapy logoLink to Antimicrobial Agents and Chemotherapy
. 1986 Dec;30(6):817–822. doi: 10.1128/aac.30.6.817

Intergeneric and interspecies gene exchange in gram-positive cocci.

D R Schaberg, M J Zervos
PMCID: PMC180600  PMID: 3028249

Full text

PDF
817

Selected References

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

  1. Archer G. L., Dietrick D. R., Johnston J. L. Molecular epidemiology of transmissible gentamicin resistance among coagulase-negative staphylococci in a cardiac surgery unit. J Infect Dis. 1985 Feb;151(2):243–251. doi: 10.1093/infdis/151.2.243. [DOI] [PubMed] [Google Scholar]
  2. Archer G. L., Johnston J. L. Self-transmissible plasmids in staphylococci that encode resistance to aminoglycosides. Antimicrob Agents Chemother. 1983 Jul;24(1):70–77. doi: 10.1128/aac.24.1.70. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Banai M., LeBlanc D. J. Streptococcus faecalis R plasmid pJH1 contains an erythromycin resistance transposon (Tn3871) similar to transposon Tn917. J Bacteriol. 1984 Jun;158(3):1172–1174. doi: 10.1128/jb.158.3.1172-1174.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bougueleret L., Bieth G., Horodniceanu T. Conjugative R plasmids in group C and G streptococci. J Bacteriol. 1981 Feb;145(2):1102–1105. doi: 10.1128/jb.145.2.1102-1105.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Buu-Hoï A., Bieth G., Horaud T. Broad host range of streptococcal macrolide resistance plasmids. Antimicrob Agents Chemother. 1984 Feb;25(2):289–291. doi: 10.1128/aac.25.2.289. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Buu-Hoï A., Horodniceanu T. Conjugative transfer of multiple antibiotic resistance markers in Streptococcus pneumoniae. J Bacteriol. 1980 Jul;143(1):313–320. doi: 10.1128/jb.143.1.313-320.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Clewell D. B., An F. Y., White B. A., Gawron-Burke C. Streptococcus faecalis sex pheromone (cAM373) also produced by Staphylococcus aureus and identification of a conjugative transposon (Tn918). J Bacteriol. 1985 Jun;162(3):1212–1220. doi: 10.1128/jb.162.3.1212-1220.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Clewell D. B. Plasmids, drug resistance, and gene transfer in the genus Streptococcus. Microbiol Rev. 1981 Sep;45(3):409–436. doi: 10.1128/mr.45.3.409-436.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Cohen M. L., Wong E. S., Falkow S. Common R-plasmids in Staphylococcus aureus and Staphylococcus epidermidis during a nosocomial Staphylococcus aureus outbreak. Antimicrob Agents Chemother. 1982 Feb;21(2):210–215. doi: 10.1128/aac.21.2.210. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Collatz E., Carlier C., Courvalin P. The chromosomal 3',5"-aminoglycoside phosphotransferase in Streptococcus pneumoniae is closely related to its plasmid-coded homologs in Streptococcus faecalis and Staphylococcus aureus. J Bacteriol. 1983 Dec;156(3):1373–1377. doi: 10.1128/jb.156.3.1373-1377.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Courvalin P. M., Carlier C., Chabbert Y. A. Plasmid-linked tetracycline and erythromycin resistance in group D "streptococcus". Ann Inst Pasteur (Paris) 1972 Dec;123(6):755–759. [PubMed] [Google Scholar]
  12. Courvalin P., Carlier C., Collatz E. Plasmid-mediated resistance to aminocyclitol antibiotics in group D streptococci. J Bacteriol. 1980 Aug;143(2):541–551. doi: 10.1128/jb.143.2.541-551.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Courvalin P., Ounissi H., Arthur M. Multiplicity of macrolide-lincosamide-streptogramin antibiotic resistance determinants. J Antimicrob Chemother. 1985 Jul;16 (Suppl A):91–100. doi: 10.1093/jac/16.suppl_a.91. [DOI] [PubMed] [Google Scholar]
  14. Dowd G., Cafferkey M., Dougan G. Gentamicin and methicillin resistant Staphylococcus aureus in Dublin hospitals: molecular studies. J Med Microbiol. 1983 May;16(2):129–138. doi: 10.1099/00222615-16-2-129. [DOI] [PubMed] [Google Scholar]
  15. Dunny G. M., Birch N., Hascall G., Clewell D. B. Isolation and characterization of plasmid deoxyribonucleic acid from Streptococcus mutans. J Bacteriol. 1973 Jun;114(3):1362–1364. doi: 10.1128/jb.114.3.1362-1364.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. El-Solh N., Bouanchaud D. H., Horodniceanu T., Roussel A., Chabbert Y. A. Molecular studies and possible relatedness between R plasmids from groups B and D streptococci. Antimicrob Agents Chemother. 1978 Jul;14(1):19–23. doi: 10.1128/aac.14.1.19. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Engel H. W., Soedirman N., Rost J. A., van Leeuwen W. J., van Embden J. D. Transferability of macrolide, lincomycin, and streptogramin resistances between group A, B, and D streptococci, Streptococcus pneumoniae, and Staphylococcus aureus. J Bacteriol. 1980 May;142(2):407–413. doi: 10.1128/jb.142.2.407-413.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Forbes B. A., Schaberg D. R. Transfer of resistance plasmids from Staphylococcus epidermidis to Staphylococcus aureus: evidence for conjugative exchange of resistance. J Bacteriol. 1983 Feb;153(2):627–634. doi: 10.1128/jb.153.2.627-634.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Franke A. E., Clewell D. B. Evidence for a chromosome-borne resistance transposon (Tn916) in Streptococcus faecalis that is capable of "conjugal" transfer in the absence of a conjugative plasmid. J Bacteriol. 1981 Jan;145(1):494–502. doi: 10.1128/jb.145.1.494-502.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Gibson E. M., Chace N. M., London S. B., London J. Transfer of plasmid-mediated antibiotic resistance from streptococci to lactobacilli. J Bacteriol. 1979 Jan;137(1):614–619. doi: 10.1128/jb.137.1.614-619.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Goering R. V., Ruff E. A. Comparative analysis of conjugative plasmids mediating gentamicin resistance in Staphylococcus aureus. Antimicrob Agents Chemother. 1983 Sep;24(3):450–452. doi: 10.1128/aac.24.3.450. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Gonzalez C. F., Kunka B. S. Plasmid transfer in Pediococcus spp.: intergeneric and intrageneric transfer of pIP501. Appl Environ Microbiol. 1983 Jul;46(1):81–89. doi: 10.1128/aem.46.1.81-89.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Groves D. J. Interspecific relationships of antibiotic resistance in Staphylococcus sp.: isolation and comparison of plasmids determining tetracycline resistance in S. aureus and S. epidermidis. Can J Microbiol. 1979 Dec;25(12):1468–1475. doi: 10.1139/m79-227. [DOI] [PubMed] [Google Scholar]
  24. Hershfield V. Plasmids mediating multiple drug resistance in group B streptococcus: transferability and molecular properties. Plasmid. 1979 Jan;2(1):137–149. doi: 10.1016/0147-619x(79)90012-x. [DOI] [PubMed] [Google Scholar]
  25. Horaud T., Le Bouguenec C., Pepper K. Molecular genetics of resistance to macrolides, lincosamides and streptogramin B (MLS) in streptococci. J Antimicrob Chemother. 1985 Jul;16 (Suppl A):111–135. doi: 10.1093/jac/16.suppl_a.111. [DOI] [PubMed] [Google Scholar]
  26. Horodniceanu T., Bougueleret L., El-Solh N., Bouanchaud D. H., Chabbert Y. A. Conjugative R plasmids in Streptococcus agalactiae (group B). Plasmid. 1979 Apr;2(2):197–206. doi: 10.1016/0147-619x(79)90038-6. [DOI] [PubMed] [Google Scholar]
  27. Horodniceanu T., Buu-Hoï A., Delbos F., Bieth G. High-level aminoglycoside resistance in group A, B, G, D (Streptococcus bovis), and viridans streptococci. Antimicrob Agents Chemother. 1982 Jan;21(1):176–179. doi: 10.1128/aac.21.1.176. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Horodniceanu T., Buu-Hoï A., Le Bouguenec C., Bieth G. Narrow host range of some streptococcal R plasmids. Plasmid. 1982 Sep;8(2):199–206. doi: 10.1016/0147-619x(82)90057-9. [DOI] [PubMed] [Google Scholar]
  29. Iordanescu S., Surdeanu M., Della Latta P., Novick R. Incompatibility and molecular relationships between small Staphylococcal plasmids carrying the same resistance marker. Plasmid. 1978 Sep;1(4):468–479. doi: 10.1016/0147-619x(78)90005-7. [DOI] [PubMed] [Google Scholar]
  30. Jacob A. E., Hobbs S. J. Conjugal transfer of plasmid-borne multiple antibiotic resistance in Streptococcus faecalis var. zymogenes. J Bacteriol. 1974 Feb;117(2):360–372. doi: 10.1128/jb.117.2.360-372.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Jacobs M. R., Koornhof H. J., Robins-Browne R. M., Stevenson C. M., Vermaak Z. A., Freiman I., Miller G. B., Witcomb M. A., Isaäcson M., Ward J. I. Emergence of multiply resistant pneumococci. N Engl J Med. 1978 Oct 5;299(14):735–740. doi: 10.1056/NEJM197810052991402. [DOI] [PubMed] [Google Scholar]
  32. Jaffe H. W., Sweeney H. M., Nathan C., Weinstein R. A., Kabins S. A., Cohen S. Identity and interspecific transfer of gentamicin-resistance plasmids in Staphylococcus aureus and Staphylococcus epidermidis. J Infect Dis. 1980 Jun;141(6):738–747. doi: 10.1093/infdis/141.6.738. [DOI] [PubMed] [Google Scholar]
  33. Jaffe H. W., Sweeney H. M., Weinstein R. A., Kabins S. A., Nathan C., Cohen S. Structural and phenotypic varieties of gentamicin resistance plasmids in hospital strains of Staphylococcus aureus and coagulase-negative staphylococci. Antimicrob Agents Chemother. 1982 May;21(5):773–779. doi: 10.1128/aac.21.5.773. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Khan S. A., Novick R. P. Terminal nucleotide sequences of Tn551, a transposon specifying erythromycin resistance in Staphylococcus aureus: homology with Tn3. Plasmid. 1980 Sep;4(2):148–154. doi: 10.1016/0147-619x(80)90004-9. [DOI] [PubMed] [Google Scholar]
  35. Lacey R. W. Antibiotic resistance plasmids of Staphylococcus aureus and their clinical importance. Bacteriol Rev. 1975 Mar;39(1):1–32. doi: 10.1128/br.39.1.1-32.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. 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]
  37. Lyon B. R., Iuorio J. L., May J. W., Skurray R. A. Molecular epidemiology of multiresistant Staphylococcus aureus in Australian hospitals. J Med Microbiol. 1984 Feb;17(1):79–89. doi: 10.1099/00222615-17-1-79. [DOI] [PubMed] [Google Scholar]
  38. Lyon B. R., May J. W., Skurray R. A. Analysis of plasmids in nosocomial strains of multiple-antibiotic-resistant Staphylococcus aureus. Antimicrob Agents Chemother. 1983 Jun;23(6):817–826. doi: 10.1128/aac.23.6.817. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Lyon B. R., May J. W., Skurray R. A. Tn4001: a gentamicin and kanamycin resistance transposon in Staphylococcus aureus. Mol Gen Genet. 1984;193(3):554–556. doi: 10.1007/BF00382099. [DOI] [PubMed] [Google Scholar]
  40. McDonnell R. W., Sweeney H. M., Cohen S. Conjugational transfer of gentamicin resistance plasmids intra- and interspecifically in Staphylococcus aureus and Staphylococcus epidermidis. Antimicrob Agents Chemother. 1983 Jan;23(1):151–160. doi: 10.1128/aac.23.1.151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Meijers J. A., Winkler K. C., Stobberingh E. E. Resistance transfer in mixed cultures of Staphylococcus aureus. J Med Microbiol. 1981 Feb;14(1):21–39. doi: 10.1099/00222615-14-1-21. [DOI] [PubMed] [Google Scholar]
  42. Murphy E., Phillips S., Edelman I., Novick R. P. Tn554: isolation and characterization of plasmid insertions. Plasmid. 1981 May;5(3):292–305. doi: 10.1016/0147-619x(81)90006-8. [DOI] [PubMed] [Google Scholar]
  43. Murray B. E., Mederski-Samoraj B., Foster S. K., Brunton J. L., Harford P. In vitro studies of plasmid-mediated penicillinase from Streptococcus faecalis suggest a staphylococcal origin. J Clin Invest. 1986 Jan;77(1):289–293. doi: 10.1172/JCI112289. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Naidoo J. Interspecific co-transfer of antibiotic resistance plasmids in staphylococci in vivo. J Hyg (Lond) 1984 Aug;93(1):59–66. doi: 10.1017/s0022172400060939. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Naidoo J., Noble W. C. Transfer of gentamicin resistance between strains of Staphylococcus aureus on skin. J Gen Microbiol. 1978 Aug;107(2):391–393. doi: 10.1099/00221287-107-2-391. [DOI] [PubMed] [Google Scholar]
  46. Novick R. P., Murphy E. MLS-resistance determinants in Staphylococcus aureus and their molecular evolution. J Antimicrob Chemother. 1985 Jul;16 (Suppl A):101–110. doi: 10.1093/jac/16.suppl_a.101. [DOI] [PubMed] [Google Scholar]
  47. Ounissi H., Courvalin P. Classification of macrolide-lincosamide-streptogramin-B-type antibiotic resistance determinants. Ann Microbiol (Paris) 1981 Nov-Dec;132 B(3):441–454. [PubMed] [Google Scholar]
  48. Parisi J. T., Robbins J., Lampson B. C., Hecht D. W. Characterization of a macrolide, lincosamide, and streptogramin resistance plasmid in Staphylococcus epidermidis. J Bacteriol. 1981 Nov;148(2):559–564. doi: 10.1128/jb.148.2.559-564.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Polak J., Novick R. P. Closely related plasmids from Staphylococcus aureus and soil bacilli. Plasmid. 1982 Mar;7(2):152–162. doi: 10.1016/0147-619x(82)90074-9. [DOI] [PubMed] [Google Scholar]
  50. Pérez-Díaz J. C., Vicente M. F., Baquero F. Plasmids in Listeria. Plasmid. 1982 Sep;8(2):112–118. doi: 10.1016/0147-619x(82)90049-x. [DOI] [PubMed] [Google Scholar]
  51. Schaberg D. R., Clewell D. B., Glatzer L. Conjugative transfer of R-plasmids from Streptococcus faecalis to Staphylococcus aureus. Antimicrob Agents Chemother. 1982 Aug;22(2):204–207. doi: 10.1128/aac.22.2.204. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Schaberg D. R., Power G., Betzold J., Forbes B. A. Conjugative R plasmids in antimicrobial resistance of Staphylococcus aureus causing nosocomial infections. J Infect Dis. 1985 Jul;152(1):43–49. doi: 10.1093/infdis/152.1.43. [DOI] [PubMed] [Google Scholar]
  53. Scott D. F., Wood D. O., Brownell G. H., Carter M. J., Best G. K. Aminoglycoside modification by gentamicin-resistant isolates of Staphylococcus aureus. Antimicrob Agents Chemother. 1978 Apr;13(4):641–644. doi: 10.1128/aac.13.4.641. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Shalita Z., Murphy E., Novick R. P. Penicillinase plasmids of Staphylococcus aureus: structural and evolutionary relationships. Plasmid. 1980 May;3(3):291–311. doi: 10.1016/0147-619x(80)90042-6. [DOI] [PubMed] [Google Scholar]
  55. Sjöström J. E., Löfdahl S., Philipson L. Transformation of Staphylococcus aureus by heterologous plasmids. Plasmid. 1979 Oct;2(4):529–535. doi: 10.1016/0147-619x(79)90052-0. [DOI] [PubMed] [Google Scholar]
  56. Smith M. D., Shoemaker N. B., Burdett V., Guild W. R. Transfer of plasmids by conjugation in Streptococcus pneumonias. Plasmid. 1980 Jan;3(1):70–79. doi: 10.1016/s0147-619x(80)90035-9. [DOI] [PubMed] [Google Scholar]
  57. Stewart G. C., Rosenblum E. D. Genetic behavior of the methicillin resistance determinant in Staphylococcus aureus. J Bacteriol. 1980 Dec;144(3):1200–1202. doi: 10.1128/jb.144.3.1200-1202.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. Tennent J. M., May J. W., Skurray R. A. Multiple antibiotic resistance in Staphylococcus aureus and Staphylococcus epidermidis: plasmids in strains associated with nosocomial infection. Pathology. 1984 Jul;16(3):250–255. doi: 10.3109/00313028409068532. [DOI] [PubMed] [Google Scholar]
  59. Tomich P. K., An F. Y., Clewell D. B. Properties of erythromycin-inducible transposon Tn917 in Streptococcus faecalis. J Bacteriol. 1980 Mar;141(3):1366–1374. doi: 10.1128/jb.141.3.1366-1374.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  60. Townsend D. E., Ashdown N., Greed L. C., Grubb W. B. Transposition of gentamicin resistance to staphylococcal plasmids encoding resistance to cationic agents. J Antimicrob Chemother. 1984 Aug;14(2):115–124. doi: 10.1093/jac/14.2.115. [DOI] [PubMed] [Google Scholar]
  61. Townsend D. E., Bolton S., Ashdown N., Grubb W. B. Transfer of plasmid-borne aminoglycoside-resistance determinants in staphylococci. J Med Microbiol. 1985 Oct;20(2):169–185. doi: 10.1099/00222615-20-2-169. [DOI] [PubMed] [Google Scholar]
  62. Vescovo M., Morelli L., Bottazzi V., Gasson M. J. Conjugal Transfer of Broad-Host-Range Plasmid pAMbeta1 into Enteric Species of Lactic Acid Bacteria. Appl Environ Microbiol. 1983 Sep;46(3):753–755. doi: 10.1128/aem.46.3.753-755.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  63. Vogel L., Nathan C., Sweeney H. M., Kabins S. A., Cohen S. Infections due to gentamicin-resistant Staphylococcus aureus strain in a nursery for neonatal infants. Antimicrob Agents Chemother. 1978 Mar;13(3):466–472. doi: 10.1128/aac.13.3.466. [DOI] [PMC free article] [PubMed] [Google Scholar]
  64. Weinstein R. A., Kabins S. A., Nathan C., Sweeney H. M., Jaffe H. W., Cohen S. Gentamicin-resistant staphylococci as hospital flora: epidemiology and resistance plasmids. J Infect Dis. 1982 Mar;145(3):374–382. doi: 10.1093/infdis/145.3.374. [DOI] [PubMed] [Google Scholar]
  65. Weisblum B., Holder S. B., Halling S. M. Deoxyribonucleic acid sequence common to staphylococcal and streptococcal plasmids which specify erythromycin resistance. J Bacteriol. 1979 Jun;138(3):990–998. doi: 10.1128/jb.138.3.990-998.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  66. Witte W. Transfer of drug-resistance-plasmids in mixed cultures of Staphylococci. Zentralbl Bakteriol Orig A. 1977;237(2-3):147–159. [PubMed] [Google Scholar]
  67. Yag Y., Franke A. E., Clewell D. B. Plasmid-determined resistance to erythromycin: comparison of strains of streptococcus faecalis and streptococcus pyogenes with regard to plasmid hmology and resistance inducibility. Antimicrob Agents Chemother. 1975 Jun;7(6):871–873. doi: 10.1128/aac.7.6.871. [DOI] [PMC free article] [PubMed] [Google Scholar]
  68. Zervos M. J., Dembinski S., Mikesell T., Schaberg D. R. High-level resistance to gentamicin in Streptococcus faecalis: risk factors and evidence for exogenous acquisition of infection. J Infect Dis. 1986 Jun;153(6):1075–1083. doi: 10.1093/infdis/153.6.1075. [DOI] [PubMed] [Google Scholar]
  69. van Embden J. D., Engel H. W., van Klingeren B. Drug resistance in group D streptococci of clinical and nonclinical origin: prevalence, transferability, and plasmid properties. Antimicrob Agents Chemother. 1977 Jun;11(6):925–932. doi: 10.1128/aac.11.6.925. [DOI] [PMC free article] [PubMed] [Google Scholar]
  70. van Embden J. D., Soedirman N., Engel H. W. Transferable drug resistance to group A and group B streptococci. Lancet. 1978 Mar 25;1(8065):655–656. doi: 10.1016/s0140-6736(78)91153-4. [DOI] [PubMed] [Google Scholar]

Articles from Antimicrobial Agents and Chemotherapy are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES