Klin Farmakol Farm. 2013;27(3-4):101-105

Effect of Pseudomonas aeruginosa resistance on antibiotic therapy

Milan Kolář, Miroslava Htoutou Sedláková, Markéta Šenkyříková, Vojtěch Hanulík, Pavel Honig
Ústav mikrobiologie, LF UP a FN Olomouc

Pseudomonas aeruginosa strains are among very important bacterial pathogens, particularly in the case of nosocomial infections. The frequency

of this species as a causative agent of infections, including life-threatening ones, is increasing, and so is its resistance to the effect

of antibiotic therapy. The aim of the present paper was to determine the resistance of Pseudomonas aeruginosa to antibiotics and to analyze

the group of meropenem-resistant isolates. In the period from 1 January 2008 to 30 June 2013, a total of 11,342 strains of Pseudomonas

aeruginosa were isolated from the clinical material of patients hospitalized in the Olomouc University Hospital and another 1,341 strains

were isolated in the case of patients from the Olomouc Military Hospital. Resistance to antimicrobial agents was assessed using the standard

dilution micromethod. In 57 meropenem-resistant strains of Pseudomonas aeruginosa, the production of metallo-beta-lactamases, serine

carbapenemases, and AmpC enzymes was determined by means of both phenotype and genotype methods. An increasing frequency of

Pseudomonas aeruginosa strains resistant to meropenem and piperacillin with tazobactam was demonstrated. In a number of isolates,

sensitivity only to colistin and amikacin remained preserved. The production of metallo-beta-lactamases and serin carbapenemases was

not confirmed, and resistance to meropenem is particularly related to the production of AmpC and the loss of the cell wall porins.

Keywords: Pseudomonas aeruginosa, infection, treatment

Published: December 1, 2013  Show citation

ACS AIP APA ASA Harvard Chicago Chicago Notes IEEE ISO690 MLA NLM Turabian Vancouver
Kolář M, Htoutou Sedláková M, Šenkyříková M, Hanulík V, Honig P. Effect of Pseudomonas aeruginosa resistance on antibiotic therapy. Klin Farmakol Farm. 2013;27(3-4):101-105.
Download citation

References

  1. Viscoli C. EORTC International Antimicrobial Therapy Group. Management of infection in cancer patients. Studies of the EORTC International Antimicrobial Therapy Group (IATG). Eur J Cancer 2002? 38(Supp.4)S: 82-87. Go to original source... Go to PubMed...
  2. Mikulska M, Del Bono V, Raiola AM, et al. Blood stream infections in allogeneic hematopoietic stem cell transplant recipients: reemergence of Gram-negative rods and increasing antibiotic resistance. Biol Blood Marrow Transplant 2009? 15: 47-53. Go to original source... Go to PubMed...
  3. Kolář M, Htoutou Sedláková M, Hanulík V. a pracovní skupina. Multirezistentní gramnegativní bakterie u hematoonkologických nemocných. Postgrad Med 2012? 14(příl.5): 6-10.
  4. Vincent JL, Rello J, Marshall JC, et al. International study of the prevalence and outcomes of infection in intensive care units. JAMA 2009; 302: 2323-2329. Go to original source... Go to PubMed...
  5. Bush K, Jacoby GA. Updated Functional Classification of ?-Lactamases. Antimicrob Agent Chemother 2010; 54: 969-976. Go to original source... Go to PubMed...
  6. Kolář M, Htoutou Sedláková M, Suchánková H, Hanulík V. Vliv selekčního tlaku karbapenemů na bakteriální rezistenci. Klin Mikrobiol Inf Lék 2013; 19: 4-7.
  7. Hanulík V, Uvízl R, Husičková V, Htoutou Sedláková M, Kolář M. Bakteriální původci pneumonií u pacientů v intenzivní péči. Klin Mikrobiol Inf Lék 2011; 17: 134-139.
  8. Khawaja A, Zubairi AB, Durrani FK, Zafar A. Etiology and outcome of severe community acquired pneumonia in immunocompetent adult. BMC Infect Dis 2013; 20: 13-94. Go to original source... Go to PubMed...
  9. Micek ST, Lloyd AE, Ritchie DJ, et al. Pseudomonas aeruginosa bloodstream infection: importance of appropriate initial antimicrobial treatment. Antimicrob Agents Chemother 2005; 49: 1306-1311. Go to original source... Go to PubMed...
  10. Tumbarello M, De Pascale G, Trecarichi EM, et al. Clinical outcomes of Pseudomonas aeruginosa pneumonia in intensive care unit patients. Intensive Care Med 2013; 39: 682-692. Go to original source... Go to PubMed...
  11. Giamarellos-Bourboulis EJ, Papadimitriou E, Galanakis N, et al. Multidrug resistance to antimicrobials as a predominant factor influencing patient survival. Inter J Antimicrob Agents 2006; 27: 476-481. Go to original source... Go to PubMed...
  12. Kolář M. Volba antibiotik v intenzivní péči. Postgrad Med 2012; 14: 510-513.
  13. European Committee on Antimicrobial Susceptibility Testing (EUCAST) documents: Document version 2.0 2012-01-01.; 2012. http://eucast.org/clinical_breakpoints.
  14. Htoutou Sedláková M, Hanulík V, Chromá M, et al. Rezistence enterobakterií ke karbapenemům. Klin Mikrobiol Inf Lék 2011; 17: 12-18.
  15. Lee K, Chong Y, Shin HB, et al. Modified Hodge and EDTA-disk synergy tests to screen metallo-?-lactamase-producing strains of Pseudomonas and Acinetobacter species. Clin Microbiol Infect 2001; 7: 88-91. Go to original source... Go to PubMed...
  16. Htoutou Sedlakova M, Hanulik V, Chroma M, et al. Phenotypic detection of broad-spectrum beta-lactamases in microbiological practice. Med Sci Monit 2011; 17: BR147-152. Go to original source... Go to PubMed...
  17. Queenan AM, Torres-Viera C, Gold HS, et al. SME-type carbapenem-hydrolyzing class A ?-lactamases from geographically diverse Serratia marcescens strains. Antimicrob Agents Chemother 2000; 44: 3035-3039. Go to original source... Go to PubMed...
  18. Radice M, Power P, Gutkind G, et al. First class A carbapenemase isolated from Enterobacteriaceae in Argentina. Antimicrob Agents Chemother 2004; 48: 1068-1069. Go to original source... Go to PubMed...
  19. Aubron C, Poirel L, Ash Ronald J, Nordmann P. Carbapenemase-producing Enterobacteriaceae, U.S. rivers. Emerg Infect Dis 2005; 11: 260-264. Go to original source... Go to PubMed...
  20. Bradford PA, Bratu S, Urban C, et al. Emergence of carbapenem-resistant Klebsiella species possessing the class A carbapenem-hydrolyzing KPC-2 and inhibitor-resistant TEM-30 beta-lactamases in New York City. Clin Infect Dis 2004; 39: 55-60. Go to original source... Go to PubMed...
  21. Weldhagen GF, Prinsloo A. Molecular detection of GES2 extended spectrum beta-lactamase producing Pseudomonas aeruginosa in Pretoria, South Africa. Int J Antimicrob Agents 2004; 24: 35-38. Go to original source... Go to PubMed...
  22. Yan JJ, Hsueh PR, Ko WC, et al. Metallo-?-lactamases in clinical Pseudomonas isolates in Taiwan and identification of VIM-3, a novel variant of the VIM-2 enzyme. Antimicrob Agents Chemother 2001; 45: 2224-2228. Go to original source... Go to PubMed...
  23. Castanheira M, Toleman MA, Jones RN, Schmidt FJ, Walsh TR. Molecular characterization of a beta-lactamase gene, blaGIM-1, encoding a new subclass of metallo-beta-lactamase. Antimicrob Agents Chemother 2004; 48: 4654-4661. Go to original source... Go to PubMed...
  24. Donald HM, Scaife W, Amyes SG, Young HK. Sequence analysis of ARI-1, a novel OXA beta-lactamase, responsible for imipenem resistance in Acinetobacter baumannii 6B92. Antimicrob Agents Chemother 2000; 44: 196-199. Go to original source... Go to PubMed...
  25. Poirel L, Heritier C, Toluen V, Nordmann P. Emergence of oxacillinase-mediated resistance to imipenem in Klebsiella pneumoniae. Antimicrob Agents Chemother 2004; 48: 15-22. Go to original source... Go to PubMed...
  26. Kumar A, Roberts D, Wood KE, et al. Duration of hypotension before initiation of effective antimicrobial therapy is the critical determinant of survival in human septic shock. Crit Care Med 2006; 34: 1589-1596. Go to original source... Go to PubMed...
  27. Kolář M, Htoutou Sedláková M, Suchánková H, Hanulík V. Vliv selekčního tlaku karbapenemů na bakteriální rezistenci. Klin Mikrobiol Inf Lék 2013; 19: 4-7.




Clinical Pharmacology and Pharmacy

Madam, Sir,
please be aware that the website on which you intend to enter, not the general public because it contains technical information about medicines, including advertisements relating to medicinal products. This information and communication professionals are solely under §2 of the Act n.40/1995 Coll. Is active persons authorized to prescribe or supply (hereinafter expert).
Take note that if you are not an expert, you run the risk of danger to their health or the health of other persons, if you the obtained information improperly understood or interpreted, and especially advertising which may be part of this site, or whether you used it for self-diagnosis or medical treatment, whether in relation to each other in person or in relation to others.

I declare:

  1. that I have met the above instruction
  2. I'm an expert within the meaning of the Act n.40/1995 Coll. the regulation of advertising, as amended, and I am aware of the risks that would be a person other than the expert input to these sites exhibited


No

Yes

If your statement is not true, please be aware
that brings the risk of danger to their health or the health of others.