Significance of fermentative modification of aminoglycosides in development of resistance in bacteria | CMAC

Significance of fermentative modification of aminoglycosides in development of resistance in bacteria

Clinical Microbiology and Antimicrobial Chemotherapy. 1999; 1(1):40-50

​ Reshedko G.K.
Section
Antimicrobial Resistance
Type
Journal article
Publication
Clinical Microbiology and Antimicrobial Chemotherapy. 1999; 1(1):40-50
  • 1. Вакуленко С.Б. Бактериальные ферменты, инактивирующие аминогликозидные антибиотики и кодирующие их гены //Антибиотики.–1992.– № 4.–С.49 –54.
  • 2. Вакуленко С.Б. Методы гибридизации нуклеиновых кислот: использование для детекции и изучения распространения генов лекарственной устойчивости // Антибиотики.– 1992.– № 3.–С.44 –50.
  • 3. Решедько Г.К. Фармакодинамическое обоснование повышения эффективности аминогликозидов при лечении грам (–) госпитальных инфекций:Автореф. дис.... канд.мед.наук.– Смоленск,1997.– 22 с.
  • 4. Таисова А.С. Ферменты, инактивирующие аминогликозиды: современное состояние проблемы //Антибиотики.– 1990.– № 6.–С.51 –55.
  • 5. Bryan L.E. General mechanisms of resistance to antibiotics //J.Antimicrob.Chemother.– 1988.– Vol.22.– P.1 –15.
  • 6. Clarke A.J., Francis D., Keenleyside W.J. The prevalence of gentamicin 2 .N acetyltransferase in the Proteeae and its role in the O acetylation of peptidoglycan //FEMS Microbiol Lett.– 1996.– Vol.145.– P.201 –207.
  • 7. Coleman K.et al. Bacterial resistance mechanisms as therapeutic targets //J.Antimicrob.Chemother.– 1994.– Vol.33.– P.1091 –1116.
  • 8. Comez Lus R., Rivera M., Bobey D. Chromosomal origin of acetyltansferase AAC(6') specifying amikacin resistance in Serratia marcescens //Microbiologia Sem.– 1987.– Vol.3.– P.185 –194.
  • 9. Elisha B.G., Steiyn L.M. High level kanamycin resistance associated with the hyperoroduction of AAC(3)-II and a generalised reduction in the accumulation of aminoglycosides in Acinetobacter spp.//J.Antimicrob.Chemother. –1994.– Vol.34.– P.457 –464.
  • 10. Garcia Agata M.I., Alarcon T., Lopez Brea M. Emergence of resistant isolates of Acinetobacter calcoaceticus – A.baumannii complex in a Spanish hospital over a five year period //Eur.J.Clin.Microbiol.Infect.Dis.– 1996. –Vol.15.– P.512 –515.
  • 11. Gaynes R., Groisman E., Lerner S. Isolation, characteriza tion and cloning of a plasmid borne gene encoding a phos photransferase that confers high level amikacin resistance in enteric bacilli //Antimicrob.Agents Chemother.– 1988.– Vol.32.– P.1379 –1384.
  • 12. Glupczynski Y., MacGillavry G., Yourassowsky E. Epidemiology of aminoglycoside resistance in hospitals using netilmicin as sole aminoglycoside: a long term surveilance study //Scientific Symposium.– Sorrento,Italy. –1987.– P.51 –54.
  • 13. Gould I.M. Risk factors for acquisition of multiply drugresistant gram negative bacteria //Eur. J. Clin. Microbiol. Infect. Dis.–1994.– Vol.13 –suppl.1.– P.30 –38.
  • 14. Harrell L.R., Evans L.B. Anaerobic resistance of clinical isolates of Staphylococcus aureus to aminoglysides // Antimicrob.Agents Chemother.–1978.– Vol.14.– P.927 –929.
  • 15. Jacoby G.A., Blaser M.J., Santanam P. Appearence of amikacin and tobramycin resistance due to 4'-aminoglycoside nucleotidyltransferase [ANT(4')-II ] in Gram negative pathogens //Atimicrob.Agents Chemother.–1990. –Vol.34.– P.2381 –2386.
  • 16. Johnson A.P.et al.Gentamicin resistance in clinical isolates of Escherichia coli encoded by genes of veterinary origin //J.Med.Microbiol.–1994.– Vol.40.– P.221 – 226.
  • 17. Kazama H., Kizu K., Iwasaki M. A new gene, aadA2b, encoding an aminoglycoside adenylyltransferase, AAD(3'')(9), isolated from integron InC in Pseudomonas aeruginosa //Microbios.– 1996.– Vol.86.– P.77 –83.
  • 18. Lambert T., Gerbaud G. Structural relationship between the genes encoding 3'-aminoglycoside phosphotransferases in Campylobacter and in gram positive cocci.// Ann.Inst.Pasteur /Microbiol.–1985.– Vol.136B.– P.135 – 150.
  • 19. Lambert T., Gerbaud G., Galimand M., Courvalin P. Characterization of Acinetobacter haemolyticus aac(6')-Ig gene encoding an aminoglycoside 6'-N-acetyltransferase which modifies amikacin //Antimicrob. Agents. Chemother.– 1993.– Vol.37.– P.2093 –2100.
  • 20. Landuyt H.W.V., Boelaert J., Glibert B., Gordts B. Surveillance of aminoglycoside resistance //Amer.J.Med.– 1986.– Vol.80,suppl.6B.– P.76 –81.
  • 21. LeBlanc D.J., Lee L.N., Inamine J.M. Cloning and nucleotide sequence analysis of a spectinomycin adenyltransferase AAD(9) determinant from Enterococcus faecalis //Atimicrob.Agents Chemother.– 1991.– Vol.35. –P.1804 –1810.
  • 22. Lovering A.M., White L.O., Reeves D.S. AAC(1): a new aminoglycoside acetylating enzyme modifying the C1 aminogroup of apramycin //J.Antimicrob.Chemother.– 1987.– Vol.20.– P.803 –813.
  • 23. Lovering A.M., Bywater M.J., Holt H.A. et al. Resistance of bacterial pathogens to four aminoglycosides and six other antibacterials and prevalence of aminoglycoside modifying enzymes,in 20 UK centres //J.Antimicrob. Chemother.– 1988.– Vol.22.– P.823 –839.
  • 24. Meyer J.R., Nies B.A., Wiedemann B. Amicacin resistance mediated by multiresistance transposon Tn 2424.// J.Bacteriol.–1983.– Vol.155.– P.755 –760.
  • 25. Miller G.H. and aminoglycoside resistance study groups. Increasing complexity of aminoglycoside resistance mechanisms in gram negative bacteria //APUA Newsletter.– 1994.– Vol.12.
  • 26. Miller G.H., Sabatelli F.J., Hare R.S.et al. The most frequent aminoglycoside resistance mechanisms – changes with time and geographic area:a reflection of aminoglycoside usage patterns?//Clin.Infect.Dis.–1997.– Vol.24, suppl.1.– P.S46 –S62.
  • 27. Miller G.H., Sabatelli F.J., Naples L. The utilization of aminoglycoside resistance phenotypes for the determina tion of aminoglycoside resistance mechanisms. Schering Plough research institute,1995.– 43 p.
  • 28. Rather P.N., Mierzwa R., Hare R.S et al.. Cloning and DNA sequence analysis of an aac(3)–Vb gene from Serratia marcescens //Antimicrob.Agents Chemother.– 1992.– Vol.36.– P.2222 –2227.
  • 29. Rather P.N., Miller G.H., Shaw K.J. Genetic analysis of bacterial acetyltransferases:identification of amino acidsdetermining the specificities of the aminoglycoside 6'-N-acetyltransferase Ib and Iia proteins //J.Bacteriol.– 1992.– Vol.174.– P.3196 –3203.
  • 30. Schmitz F.J., Fluit A.C., Gondolf M.et al. The prevalence of amynoglycoside resistance and corresponding resistance genes in clinical isolates of staphylococci from 19 European hospitals //J.Antimicrob.Chemother.–1999. –Vol.43.– P.253 –259.
  • 31. Schmitz F.J., Verhoef L., Fluit A.C., and the SENTRY Participants Group. Prevalence of aminoglycoside resistance in 20 European university hospitals participating in the European SENTRY Antimicrobial surveillance programme //Eur.J.Clin.Microbiol.Infect.Dis.–1999.– Vol.18.– P.414 –421.
  • 32. Shaw K.J., Cramer C.A., Rizzo M.et al. Isolation, characterization, and DNA sequence analysis of an AAC(6')-II gene from Pseudomonas aeruginosa //Atimicrob.Agents Chemother.– 1989.– Vol.33.– P.2052 –2062.
  • 33. Shaw K.J., Hare R.S., Sabatelli F.J. et al. Correlation between aminoglycoside resistance profiles and DNA hybridization of clinical isolates //Antimicrob.Agents Chemother.– 1991.– Vol.35.– P.2253 –2261.
  • 34. Shaw K.J., Munayyer H., Miller G.H. Nucleotide sequence analysis and DNA hybridization studies of the ant(4')-IIa gene from Pseudomonas aeruginosa // Antimicrob.Agents Chemother.–1993.– Vol.37.– P.708 –714.
  • 35. Shaw K.J., Rather P.N., Sabatelli F.J., Mann P.et al. Characterization of the chromosomal aac(6')-Ic gene from Serratia marcescens //Antimicrob.Agents Chemother.– 1992.– Vol.36.– P.1447 –1455.
  • 36. Shaw K.J., Rather P.N., Hare R.S. Miller G.H. Molecular genetics of aminoglycoside resistance genes and familial relationships of the aminoglycoside modifying enzymes//Microbiol.Rev.– 1993.– Vol.57.– P.138 –163.
  • 37. Tait S., Amyes S.G.B. Two different inserts are present in the recombination locus of Tn 21 –like transposons from Acinetobacter spp.//36th ICAAC Conference.– 1996..– Abstr.C 51.
  • 38. The Belgian Ag R study group and Glupczynski Y., Miller G., Sabatelli F. et al. Changes in Aminoglycoside (Ag) Resistance (R) Mechanisms (M) in Belgium over 15 years //36 th ICAAC Conference.– 1996.– Abstr.C 124.
  • 39. The French Ag R M group and Bismuth R., Collatz E., Lambert T.et al. Aminoglycoside (Ag) Resistance (R) Mechanisms (M) in France from ‘89 to ‘93 //36 th ICAAC Conference.– 1996.– Abstr.C 125.
  • 40. Vliegenthart J.S., Ketelaar van Gaalen P.A.G., Van de Klundert J.A.M. Nucleotide sequence of the aacC3 gene, a gentamicin resistance determinant encoding aminoglycoside (3)N acetyltransferase III expressed in Pseudomonas aeruginosa but not in Escherichia coli.// Atimicrob Agents Chemother.– 1991..– Vol..35.– P..892 –897.
  • 41. Wohlleben W., Arnold W., Bissonnette L.et al. On the evolution of the Tn 21 like multiresistance transposons: sequence analysis of the gene (aacCI)for gentamicin acetyltransferase 3-I(AAC(3)-I), another member of the Tn 21 –based expression cassete //Mol.Gen.Genet.– 1989.– Vol.217.– P.202 –208.
  • 42. Wu H.Y., Shaw K.J., Hare R.S., Miller G. Aminoglycoside resistance gene from Citrobacter freundii //36 th ICAAC Conference.– 1996.– Abstr.C 099.
  • 43. Zighelboim Daum S., Moellering R.C.Jr. Mechanisms and significance of antimicrobial resistance in enterococci //Paul Actor et al.eds.Antibiotic inhibition of bacterial cell.–1988.– P.603 –615.
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