Home LiteratureArticle Details
PMID: 231182 Published · ppublish English Journal Article

Amplification of chloramphenicol resistance transposons carried by phage P1Cm in Escherichia coli.

Molecular & general genetics : MGG ·Vol. 176 ·No. 2 ·1979-10-03 ·Pages 209-19

Meyer J, Iida S

Abstract

We have characterized a number of P1Cm phages which contain the resistance genes to chloramphenicol and fusidic acid as IS1-flanked Cm transposons. Restriction cleavage and electron microscopic analysis showed that these Cm transposons were carried as monomers (M) or tandem dimers (D). Lysogens of P1Cm (D) are more resistant to chloramphenicol than those of its P1Cm (M) presumably as a result of an increased gene dosage. Amplification of the Cm transposons to tandem multimers was frequently observed in P1Cm (D) lysogens grown in the presence of high concentrations of chloramphenicol or fusidic acid and was also detected in P1Cm (M) lysogens. The degree of amplification varied in different clones which suggests that cells containing spontaneously amplified Cm transposons were selected by high doses of the antibiotics. The dimeric as well as the amplified Cm transposons carried in P1Cm lysogens grown in the absence of chloramphenicol displayed considerable stability. Mechanisms for the amplification of the IS1-flanked transposons are discussed.

MeSH Terms
Chloramphenicol/pharmacology Coliphages/genetics DNA Restriction Enzymes DNA Transposable Elements Escherichia coli/genetics Fusidic Acid/pharmacology Gene Amplification Genetic Linkage Microscopy, Electron R Factors Recombination, Genetic
Chemicals
DNA Transposable Elements Fusidic Acid Chloramphenicol DNA Restriction Enzymes
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Meyer J
Iida S
References (25)
25 references, click to expand
  1. Rearrangements of genetic material in Escherichia coli as observed on the bacteriophage P1 plasmid.
    Cold Spring Harb Symp Quant Biol. 1979;43 Pt 2:1197-208 PMID: 385224
  2. Plaque forming specialized transducing phage P1: isolation of P1CmSmSu, a precursor of P1Cm.
    Mol Gen Genet. 1977 Jun 24;153(3):259-69 PMID: 895711
  3. Plasmid-determined fusidic acid resistance in the Enterobacteriaceae.
    J Gen Microbiol. 1974 Jul;83(0):191-6 PMID: 4606912
  4. Properties of an autonomous r-determinant from R100.1.
    Cold Spring Harb Symp Quant Biol. 1979;43 Pt 2:1223-31 PMID: 385225
  5. Nucleotide sequence of bacteriophage fd DNA.
    Nucleic Acids Res. 1978 Dec;5(12):4495-503 PMID: 745987
  6. Repetition of tetracycline resistance determinant genes on R plasmid pRSD1 in Escherichia coli.
    Mol Gen Genet. 1979 Jan 10;168(2):173-84 PMID: 377009
  7. Mapping of the resistance genes of the R plasmid NR1.
    Mol Gen Genet. 1978 Jan 17;158(3):217-24 PMID: 146819
  8. DRUG RESISTANCE OF ENTERIC BACTERIA. IV. ACTIVE TRANSDUCING BACTERIOPHAGE P1 CM PRODUCED BY THE COMBINATION OF R FACTOR WITH BACTERIOPHAGE P1.
    J Bacteriol. 1964 Nov;88:1266-76 PMID: 14234780
  9. DNA of bacteriophage PM2: a closed circular double-stranded molecule.
    Proc Natl Acad Sci U S A. 1969 Aug;63(4):1164-8 PMID: 5260915
  10. Mapping of the drug resistance genes carried by the r-determinant of the R100.1 plasmid.
    Mol Gen Genet. 1977 Nov 29;157(1):17-23 PMID: 340913
  11. Plaque-forming transducing bacteriophage P1 derivatives and their behaviour in lysogenic conditions.
    Virology. 1976 Jan;69(1):191-205 PMID: 1108412
  12. Physical mapping of BglII, BamHI, EcoRI, HindIII and PstI restriction fragments of bacteriophage P1 DNA.
    Mol Gen Genet. 1977 Jun 24;153(3):311-24 PMID: 895712
  13. Dissociation and reassociation of RTF and r-determinants of the R-factor NR1 in Proteus mirabilis.
    Nat New Biol. 1971 Nov 10;234(45):40-3 PMID: 4942895
  14. Multiple physical differences in the genome structure of functionally related bacteriophages P1 and P7.
    Mol Gen Genet. 1979 Jun 20;173(3):249-61 PMID: 289897
  15. Electron microscope heteroduplex studies of sequence relations among bacterial plasmids: identification and mapping of the insertion sequences IS1 and IS2 in F and R plasmids.
    J Bacteriol. 1975 May;122(2):764-75 PMID: 1092668
  16. Tandem genetic duplications in phage and bacteria.
    Annu Rev Microbiol. 1977;31:473-505 PMID: 334045
  17. Occurrence of insertion sequence (IS) regions on plasmid deoxyribonucleic acid as direct and inverted nucleotide sequence duplications.
    J Bacteriol. 1975 May;122(2):776-81 PMID: 1092669
  18. The insertion element IS1 is a natural constituent of coliphage P1 DNA.
    Plasmid. 1978 Jun;1(3):357-65 PMID: 372970
  19. Plasmid-determined tetracycline resistance in Streptococcus faecalis: evidence for gene amplification during growth in presence of tetracycline.
    Proc Natl Acad Sci U S A. 1975 May;72(5):1720-4 PMID: 807914
  20. EcoRI restriction endonuclease map of the composite R plasmid NR1.
    J Bacteriol. 1976 Jul;127(1):619-36 PMID: 776943
  21. Some properties of the chloramphenicol resistance transposon Tn9.
    Mol Gen Genet. 1979 Oct 3;176(2):221-31 PMID: 393954
  22. Transition of the R factor NR1 and Proteus mirabilis: level of drug resistance of nontransitioned and transitioned cells.
    J Bacteriol. 1975 Jul;123(1):56-68 PMID: 1095563
  23. Acquisition of a determinant for chloramphenicol resistance by coliphage lambda.
    Proc Natl Acad Sci U S A. 1975 Dec;72(12):5041-5 PMID: 1061090
  24. Nucleotide sequence of an insertion element, IS1.
    Proc Natl Acad Sci U S A. 1978 Feb;75(2):615-9 PMID: 273224
  25. Formation, induction, and curing of bacteriophage P1 lysogens.
    Virology. 1972 Jun;48(3):679-89 PMID: 4555608
Article Info
Journal
Molecular & general genetics : MGG
Abbr.
Mol Gen Genet
ISSN
0026-8925
Published
1979-10-03
Pages
209-19
Language
English
Region
Germany
NLM ID
0125036
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]