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2006 | 58 | 1 |

Tytuł artykułu

Czestosc koniugacyjnego transferu genow lekoopornosci z ESBL-dodatnich paleczek Enterobacteriaceae izolowanych od chorych z oddzialow pediatrycznych

Warianty tytułu

EN
Conjugative transfer frequency of resistance genes from ESBL-producing Enterobacteriaceae strains isolated from patients hospitalized in pediatric wards

Języki publikacji

PL

Abstrakty

PL
Badania przeprowadzono na 54 szczepach pałeczek z rodziny Enterobacte- riaceae wytwarzających ß-laktamazy typu ESBL, izolowanych od dzieci hospitalizowanych w Akademickim Szpitalu Klinicznym we Wrocławiu. Spośród badanych szczepów 47 (87%) przekazywało plazmidy kodujące ESBL do szczepu biorcy Escherichia coli K12 C600 z częstością 10-5-10-1. Wszystkie kliniczne izolaty oraz uzyskane transkoniuganty były wrażliwe in vitro na karbapenemy oraz norfloksacynę. Stwierdzono wysoki odsetek szczepów opornych na kotrimoksazol (94,4%), gentamicynę (94,4%) i amikacynę (85,2%). Oporność na aminoglikozydy oraz kotrimoksazol była często przekazywana w procesie koniugacji ze szczepów dawców do szczepu biorcy.
EN
The aim of this study was to evaluate the transfer frequency of plasmids encoding extended-spectrum ß-lactamases (ESBLs) from clinical isolates of Enterobacteriaceae to E. coli K12 C600 recipient strain. Additionally, resistance patterns to antimicrobial drugs of the isolates as well as transconjugants were analyzed. Fifty-four clinical strains belonging to the Enterobacteriaceae family were isolated from children hospitalized in Medical University Hospital in Wroclaw. All the strains studied were identified in automatic ATB system using ID32E tests. Besides, they were ESBL-positive as was confirmed by the double-disc synergy test (DDST). The minimal inhibitory concentration (MIC) was determined for twelve selected antibiotics and chemotherapeutics. The majority of the strains (87%) were able to transfer plasmid-mediated ESBL to E. coli K12 C600 recipient strain with a frequencies ranged from 10-5 to 10-1 per donor cell. All the isolates studied as well as their transconjugants were susceptible to imipenem, meropenem and norfloxacin (MIC <1mg/L). On the other hand, these strains displayed high level of resistance (MIC 512 - >1024 mg/L) to cefotaxime, ceftriaxone, gentamycin, amikacin and cotrimoxazole. Genetic markers conferring resistance to aminoglycosides and cotrimoxazole were often co-transferred to recipient strain in conjugation process.

Wydawca

-

Rocznik

Tom

58

Numer

1

Opis fizyczny

s.41-51,tab.,bibliogr.

Twórcy

autor
  • Akademia Medyczna we Wroclawiu, ul.Chalubinskiego 4, 50-368 Wroclaw
autor
autor

Bibliografia

  • 1. Babini GS, Livermore DM. Antimicrobial resistance amongst Klebsiella spp. collected from intensive care units in Southern and Western Europe in 1997-1998. J Antimicrob Chemother 2000; 45: 183-9.
  • 2. Baraniak A, Fielt J, Hryniewicz W i inni. Ceftazidime-hydrolysing CTX-M-15 extended-spectrum beta-lactamase (ESBL) in Poland. JAntimicrob Chemother 2002; 50: 393-6.
  • 3. Bonnet R. Growing group of extended-spectrum ß-lactamases: the CTX-M enzymes. Antimicrob Agents Chemother 2004; 48: 1-14.
  • 4. Gniadkowski M, Palucha A, Grzesiowski P i inni. Outbreak of ceftazidime-resistant Klebsiella pneumoniae in a pediatric hospital in Warsaw, Poland: clonal spread of the TEM-47 extended- spectrum beta-lactamase (ESBL)-producing strain and transfer of a plasmid carrying the SHV-5- like ESBL-encoding gene. Antimicrob Agents Chemother 1998; 42: 3079-85.
  • 5. Gniadkowski M, Schneider I, Palucha A i inni. Cefotaxime-resistant Enterohacteriaceae isolates from a hospital in Warsaw, Poland: identification of a new CTX-M-3 cefotaxime-hydrolyzing ß-lactamase that is closely related to the CTX-M-l/MEN-1 enzyme. Antimicrob Agents Chemother 1998; 42: 827-32.
  • 6. Jacoby GA, Sutton L. Properties of plasmids responsible for production of extended-spectrum ß-lactamases. Antimicrob Agents Chemother 1991; 35: 164-9.
  • 7. Jarlier V, Nicolas MH, Fournier G, Philippon A. Extended broad-spectrum ß-lactamases conferring transferable resistance to newer â-lactam agents in Enterohacteriaceae: hospital prevalence and susceptibility patterns. Rev Infect Dis 1988; 10: 867-78.
  • 8. Knothe H, Shah P, Krcmery V i inni. Transferable resistance to cefotaxime, cefoxitin, cefamandole and cefuroxime in clinical isolates of Klebsiella pneumoniae and Serratia marcescens. Infection 1983; 11: 315-17.
  • 9. Livermore DM. ß-lactamases in laboratory and clinical resistance. Clin Microbiol Rev 1995 ; 8: 557- 84.
  • 10. Livermore DM, Yuan M. Antibiotic resistance and production of extended-spectrum ß-lactamases amongst Klebsiella spp. from intensive care units in Europe. J Antimicrob Chemother 1996; 38: 409-24.
  • 11. Medeiros AA. Evolution and dissemination of ß-lactamases accelerated by generations of ß-lactam antibiotics. Clin Infect Dis 1997; 24: 19-45.
  • 12. Moustaoui N, Soukri A, Elmdaghri N i inni. Molecular biology of extended-spectrum beta-lactama- seproducing Enterohacteriaceae responsible for digestive tract colonization. Hosp Infect 2004; 57: 202-8.
  • 13. Munday CJ, Whitehead GM, Todd NJ i inni. Predominance and genetic diversity of community- and hospital-acquired CTX-M extended-spectrum beta-labtamases in York, UK. JAntimicrob Chemother 2004; 54: 628-33.
  • 14. National Committee for Clinical Laboratory Standards. Performance standards for antimicrobial susceptibility testing, 11"' ed. Informational Supplement M100-S11. NCCLS 2001.Wayne, Pa.
  • 15. Neuwirth C, Siebor E, Lopez J i inni. Outbreak of TEM-24-producing Enterobacter aerogenes in an intensive care unit and dissemination of the extended-spectrum ß-lactamase to other members of the family Enterohacteriaceae. J Clin Microbiol 1996; 34: 76-9.
  • 16. Palucha A, Mikiewicz B, Hryniewicz W i inni. Concurrent outbreaks of extended-spectrum beta- lactamase-producing organisms of the family Enterohacteriaceae in a Warsaw hospital. J Antimicrob Chemother 1999; 44: 489-99.
  • 17. Pena C., Pujol M, Ricart A i inni. Risk factors for faecal carriage of Klebsiella pneumoniae producing extended spectrum beta-lactamase (ESBL-KP) in the intensive care unit. Hosp Infect 1997; 35: 9-16.
  • 18. Radosz-Komoniewska H, Gniadkowski M, Rogal-Zawada D i inni. Incidence of extended-spectrum beta-lactamases in clinical isolates of the family Enterobacteriaceae in a pediatric hospital. Pol J Microbiol 2004; 53: 27-34.
  • 19. Raczkowska, Dolna I, Kowalska-Krochmal В i inni. Wykrywanie beta-laktamaz o rozszerzonym zakresie działania (ESBL) w klinicznych szczepach bakterii Gram-ujemnych. Adv Clin Exp Med 1998, 7: 399-408.
  • 20. Spanu T, Luzzaro F, Perilli M i inni. Occurrence of extended-spectrum ß-lactamases in members of the family Enterobacteriaceae in Italy: implication for resistance to ß-lactams and other antimicrobial drugs. Antimicrob Agents Chemother 2002; 46: 196-202.

Typ dokumentu

Bibliografia

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