References
- Epidemiol. Infect. v.105 Molecular characterization of trimethoprim resistance in Shigella sonnei in Sicily Agodi, A.;C. Jones;E. J. Threlfall;M. D'Angelo;M. Marranzano https://doi.org/10.1017/S0950268800047610
- Biochem. Biophys. Res. Bommun. v.58 R-factor trimethoprim resistance mechanism: An insusceptible target site Amyes, S. G. B.;J. T. Smith https://doi.org/10.1016/0006-291X(74)90380-5
- Current Protocols in Molecular Biology Ausubel, F. M.;R. Brent;R. E. Kingston;D. D. Moore;J. G. Seidman;J. A. Smith;K. Struhl
- J. Bacteriol. v.125 Transposition of a deoxyribonucleic acid sequence encoding trimethoprim and streptomycin resistance from R483 to other replicons Barth, P. T.;N. Datta;R. W. Hedges;N. J. Grinter
- Nucleic Acids Res. v.7 A rapid alkaline extraction procedure for screening recombinant plasmid DNA Birnboim, I. C.;J. Doly https://doi.org/10.1093/nar/7.6.1513
- Escherichia, Shigella, and Salmonella(7th ed.) Manual of Clinical Microbiology Bopp, C. A.;F. W. Brenner;J. G. Wells;N. A. Strockbine;P. R. Murray(ed.);E. J. Baron(ed.);M. A. Pfaller(ed.);F. C. Tenover(ed.);R. H. Yolken(ed.)
- J. Infect. Dis. v.159 Dissemination of trimethoprim-resistant clones of Shigella sonnei in Bulgaria Bratoeva, M. P.;J. F. John Jr. https://doi.org/10.1093/infdis/159.4.648
- Antimicrob. Agents Chemother. v.43 Detection of a streptomycin/spectinomycin adenylyltransferase gene (aadA) in Enterococcus faecalis Clark, N. C.;Ø. Olsvik;J. M. Swenson;C. A. Spiegel;F. C. Tenover https://doi.org/10.1093/jac/43.1.157
- Nucleic Acids Res. v.11 The nucleotide sequence of the trimethoprim-resistant dihydrofolate reductase gene harboured by Tn7 Fling, M. E.;C. Richards https://doi.org/10.1093/nar/11.15.5147
- Antimicrob. Agents Chemother. v.42 High-level resistance to trimethoprim in clinical isolates of Campylobacter jejuni by acquisition of foreign genes (dfr1 and dfr9) expressing drug-insensitive dihydrofolate reductases Gibrel, A.;O. Skold
- Epidemiol. Infect. v.104 Trimethoprim resistance gene in Shigella dysenteriae 1 isolates obtaines from widely scattered locations of Asia Haider, K.;A. Chatkaeomorakot;B. A. Kay;K. A. Talukder;D. N. Taylor;P. Echeverria;D. A. Sack https://doi.org/10.1017/S0950268800059380
- Drug Resist. Updates v.1 Antibiotic resistance in gram-negative bacteria: The role of gene cassettes and integrons Hall, R. M.;C. M. Collis https://doi.org/10.1016/S1368-7646(98)80026-5
- J. Infect. Dis. v.161 Increase of trimethoprim resistance among Shigella species, 1975-1988: Analysis of resistance mechanisms Heikkila, E.;A. Siitonen;M. Jahkola;M. Fling;L. Sundstrom;P. Huovinen https://doi.org/10.1093/infdis/161.6.1242
- Antimicrob. Agents Chemother. v.35 Analysis of genetic localization of the type 1 trimethoprim resistance gene from Escherichia coli isolated in Finland Hikkila, E.;L. Sundstrom;M. Skurnik;P. Huovinen https://doi.org/10.1128/AAC.35.8.1562
- Antimicrob. Agents Chemother. v.37 A novel dihydrofolate reductase cassette inserted in an integron borne on a Tn21-like element Heikkila, E.;M. Skurnik;L. Sundstrom;P. Huovinen https://doi.org/10.1128/AAC.37.6.1297
- J. Antimicrob. Chemother. v.25 The emergence and mechanisms of trimethoprim resistance in Escherichia coli isolated from outpatients in Finland Hikkila, E.;O. V. Renkonen;R. Sunila;P. Uurasmaa;P. Huovinen https://doi.org/10.1093/jac/25.2.275
- J. Microbiol. Biotechnol. v.10 Analysis of the genome of Symbiobacterium toebii by pulsed-field gel electrophoresis Hong, S. P.;J. H. Park;Y. S. Kim;H. J. Hwang;S. K. Rhee;S. G. Lee;M. H. Sung;N. Esaki
- Antimicrob. Agents Chemother. v.31 Trimethoprim resistance Huovinen, P. https://doi.org/10.1128/AAC.31.10.1451
- Antimicrob. Agents Chemother. v.39 Trimethoprim and sulfonamide resistance Huovinen, P.;L. Sundstrom;G. Swedberg;O. Skold https://doi.org/10.1128/AAC.39.2.279
- J. Antimicrob. Chemother. v.47 The prevalence of trimethoprim-resistance-conferring dihydrofolate reductase genes in urinary isolates of Escherichia coli in Korea Lee, J. C.;J. Y. Oh;J. W. Cho;J. C. Park;J. M. Kim;S. Y. Seol;D. T. Cho https://doi.org/10.1093/jac/47.5.599
- APMIS v.109 Antimicrobial resistance of Shigella sonnei in Korea during the last two decades Lee, J. C.;J. Y. Oh;K. S. Kim;Y. W. Jeong;J. W. Cho;J. C. Park;S. Y. Seol;D. T. Cho https://doi.org/10.1034/j.1600-0463.2001.090307.x
- J. Microbiol. Biotechnol. v.9 Antibacterial activity of antimycolic miconazole against methicillin-resistant Staphyolococcus aureus Lee, S. H.;C. J. Kim
- Nature v.297 Unique insertion site of Tn7 in the E. coli chromosome Liechtenstein, C.;S. Brenner https://doi.org/10.1038/297601a0
- Brazil. J. Clin. Microbiol. v.35 Molecular epidemiology of multiple antibiotic-resistant Shigella flexneri in Fortaleza Lima, A. A. M.;J. J. C. Sidrim;N. L. Lima;W. Titlow;M. E. Evans;R. N. Greenberg
- J. Clin. Microbiol. v.33 Analysis of clonal relationships among isolates of Shigella sonnei by different molecular typing methods Liu, P. Y.;Y. Z. Lau;B. S. Hu;J. M. Shyr;Z. Y. Shi;W. S. Tsai;Y. H. Lin;C. Y. Tseng
- Microbiol. Immunol. v.42 Epidemiologic study of Shigella sonnei from sequential outbreaks and sporadic cases using different typing techniques Matsumoto, M.;Y. Suzuki;M. Saito;N. Ishikawa;M. Ohta
- Epidemiol. Infect. v.110 rRNA gene restriction patterns and biotypes of Shigella sonnei Nastasi, A.;S. Pignato;C. Mammina;G. Giammanco https://doi.org/10.1017/S0950268800050640
- Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aetobically(4th ed.) Approved standard M7-A4. National Committee for Clinical Laboratory Standards National Committee for Clinical Laboratory Standards
- Communicable Disease Monthly Report v.1 The frequency of shigellosis in Korea during the period 1985 to 1989 National Institute of Health in Korea
- Communicable Disease Monthly Report v.9 The frequency of shigellosis in Korea -1998. 8-10 National Institute of Health in Korea
- J. Clin. Microbiol. v.37 Typing and characterization of mechanisms of resistance of Shigella spp. isolated from feces of children under 5 years of age from Ifakara, Tanzania Navia, M. M.;L. Capitano;J. Ruiz;M. Vargas;H. Urassa;D. Schellemberg;J. Gascon;J. Vila
- J. Clin. Microbiol. v.32 Genetic variability and molecular typing of Shigella sonnei strains isolated in Canada Preston, M. A.;A. A. Borczyk
- Microbiol. v.141 Gene cassettes: A new class of mobile element Recchia, G. D.;R. M. Hall https://doi.org/10.1099/13500872-141-12-3015
- Molecular Cloning: A Laboratory Manual(2nd ed.) Sambrook, J.;E. F. Fritsch;T. Maniatis
- J. Microbiol. Biotechnol. v.11 Characterization of a cell line HFH-T2, producing viral particles, from primary human fetal hepatocytes in fected with Hepatitis B virus Shim, J. K.;D. W. Kim;T. H. Chung;J. K. Kim;J. I. Suh;C. Park;Y. C. Lee;T. W. Chung;E. Y. Song;C. H. Kim
- J. Bacteriol. v.155 Identification of the type I trimethoprim-resistant dihydrofolate reductase specified by the Escherichia coli R-plasmid R483: Comparison with prokaryotic and eukaryotic dihydrofolate reductases Simonsen, C. C.;E. Y. Chen;A. D. Levinson
- Antimicrob. Agents Chemother. v.27 Plasmid-borne or chromosomally mediated resistance by Tn7 is the most sommon response to ubiquitous use of trimethoprim Steen, R.;O. Skold https://doi.org/10.1128/AAC.27.6.933
- Antibiot. Chemother. v.9 Inocular replicating apparatus for routine testing of bacterial susceptibility to antibiotics Steers, E.;E. L. Flotz;B. S. Gravis;J. Riden
- Antimicrob. Agents Chemother. v.34 The dhfrl trimethoprim resistance gene of Tn7 can be found at specific sites in other genetic surroundings Sundstrom, L.;O. Skold https://doi.org/10.1128/AAC.34.4.642
- Antimicrob. Agents Chemother. v.31 Novel type of plasmid-borne resistance to trimethoprim Sundstrom, L.;T. Vinayagamoorthy;O. Skold https://doi.org/10.1128/AAC.31.1.60
- J. Clin. Microbiol. v.33 Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: Criteria for bacterial strain typing Tenover, F. C.;R. D. Arbeit;R. V. Goering;P. A. Mickelsen;B. E. Murray;D. H. Persing;B. Swaminathan
- Antimicrob. Agents Chemother. v.42 Class 1 integron-borne multiple-antibiotic resistance carried by IncFI and IncL/M plasmids in Salmonella enterica serotype Typhimurium Tosini, F.;P. Visca;I. Luzzi;A. M. Dionisi;C. Pezzella;A. Petrucca;A. Carattoli
- J. Antimicrob. Chemother. v.33 Genetic structures associated with spread of the type Ia trimethoprim-resistant dihydrofolate reductase gene amongst Escherichia coli strains isolated in the Nottingham area of the United Kingdom Towner, K. J.;A. Brennan;Y. Zhang;C. A. Holtham;J. L. Brough;G. I. Carter https://doi.org/10.1093/jac/33.1.25
- Antimicrob. Agents Chemother. v.38 Antimicrobial resistance of Shigella isolates causing traveler's diarrhea Vila, J.;J. Gascon;S. Abdalla;J. Gomez;F. Marco;A. Moreno;M. Corachan;T. Jimenez de Anta https://doi.org/10.1128/AAC.38.11.2668