Skip to main content
Erschienen in: Drugs 1/2001

01.01.2001 | Current Opinion

Emergence of Methicillin-Resistant Staphylococcus aureus with Intermediate Glycopeptide Resistance

Clinical Significance and Treatment Options

verfasst von: Professor Michael J. Rybak, Ronda L. Akins

Erschienen in: Drugs | Ausgabe 1/2001

Einloggen, um Zugang zu erhalten

Abstract

Methicillin-resistant Staphylococcus aureus is a pathogen that is associated with serious infections that pose a significant risk of morbidity and mortality because of their multidrug resistant nature. Until recently, therapeutic options were limited to vancomycin, making the use of this drug widespread. Unfortunately, the continued application of this drug has led to the emergence of glycopeptide intermediate susceptible S. aureus (GISA). By definition, these organisms demonstrated a vancomycin minimum inhibitory concentration (MIC) of >4 mg/L and <32 mg/L. However, although the mechanism of resistance is not fully elucidated at this time, GISA strains have demonstrated thickened or aggregated cell walls, an increase in penicillin binding proteins and greater autolytic activity. At present, the overall number of reported cases of GISA is relatively low. In most cases, thus far, prolonged courses of vancomycin were reported. A few cases reported monitoring serum vancomycin concentrations but because of limited information, no association with outcome can be made. Whether these GISA strains will become more widespread or evolve into fully glycopeptide resistant strains is unknown at this time. Although there are a number of new agents that possess activity against these pathogens, there is no consensus regarding specific recommendations for treatment. Strict infection control practices, routine screening for resistance and controlled use of antibacterial agents, especially vancomycin, are critical steps in preventing the further development of resistance among staphylococci.
Literatur
1.
Zurück zum Zitat Sahm DF, Marsilio MK, Piazza G. Antimicrobial resistance in key bloodstream bacterial isolates: electronic surveillance with The Surveillance Network Database — USA. Clin Infect Dis 1999; 29: 259–63PubMedCrossRef Sahm DF, Marsilio MK, Piazza G. Antimicrobial resistance in key bloodstream bacterial isolates: electronic surveillance with The Surveillance Network Database — USA. Clin Infect Dis 1999; 29: 259–63PubMedCrossRef
2.
Zurück zum Zitat Sabath LD. Mechanisms of resistance to beta-lactam antibiotics in strains of Staphylococcus aureus. Ann Intern Med 1982; 97: 339–44PubMed Sabath LD. Mechanisms of resistance to beta-lactam antibiotics in strains of Staphylococcus aureus. Ann Intern Med 1982; 97: 339–44PubMed
3.
Zurück zum Zitat Watanakunakorn C. Treatment of infections due to methicillin-resistant Staphylococcus aureus. Ann Intern Med 1982; 97: 376–8PubMed Watanakunakorn C. Treatment of infections due to methicillin-resistant Staphylococcus aureus. Ann Intern Med 1982; 97: 376–8PubMed
4.
Zurück zum Zitat Rubin RJ, Harrington CA, Poon A, et al. The economic impact of Staphylococcus aureus infections in New York City Hospitals. Emerg Infect Dis 1999; 5(1): 9–17PubMedCrossRef Rubin RJ, Harrington CA, Poon A, et al. The economic impact of Staphylococcus aureus infections in New York City Hospitals. Emerg Infect Dis 1999; 5(1): 9–17PubMedCrossRef
5.
Zurück zum Zitat Waldvogel FA. Staphylococcus aureus (including toxic shock syndrome). In: Mandell GL, Bennett JE, Dolin R, editors. Mandell, Douglas and Bennett’s principles and practice of infectious diseases. 4th ed. New York (NY): Churchill Livingstone, 1995: 1754–77 Waldvogel FA. Staphylococcus aureus (including toxic shock syndrome). In: Mandell GL, Bennett JE, Dolin R, editors. Mandell, Douglas and Bennett’s principles and practice of infectious diseases. 4th ed. New York (NY): Churchill Livingstone, 1995: 1754–77
6.
Zurück zum Zitat Sieradzki K, Villari P, Tomasz A. Decreased susceptibilities to teicoplanin and vancomycin among coagulase-negative methicillin-resistant clinical isolates of staphylococci. Antimicrob Agents Chemother 1998; 42: 100–7PubMed Sieradzki K, Villari P, Tomasz A. Decreased susceptibilities to teicoplanin and vancomycin among coagulase-negative methicillin-resistant clinical isolates of staphylococci. Antimicrob Agents Chemother 1998; 42: 100–7PubMed
7.
Zurück zum Zitat Schwalbe RS, Stapleton JT, Gilligan PH. Emergence of vancomycin resistance in coagulase-negative staphylococci. N Engl J Med 1987; 316(13): 927–31PubMedCrossRef Schwalbe RS, Stapleton JT, Gilligan PH. Emergence of vancomycin resistance in coagulase-negative staphylococci. N Engl J Med 1987; 316(13): 927–31PubMedCrossRef
8.
Zurück zum Zitat Smith TL, Pearson ML, Wilcox KR, et al. Emergence of vancomycin resistance in Staphylococcus aureus. N Engl J Med 1999; 340(7): 493–501PubMedCrossRef Smith TL, Pearson ML, Wilcox KR, et al. Emergence of vancomycin resistance in Staphylococcus aureus. N Engl J Med 1999; 340(7): 493–501PubMedCrossRef
9.
Zurück zum Zitat Johnson AP. Intermediate vancomycin resistance in Staphylococcus aureus: a major threat or a minor inconvenience? J Antimicrob Chemother 1998; 42: 289–91PubMedCrossRef Johnson AP. Intermediate vancomycin resistance in Staphylococcus aureus: a major threat or a minor inconvenience? J Antimicrob Chemother 1998; 42: 289–91PubMedCrossRef
10.
Zurück zum Zitat Sieradzki K, Roberts RB, Haber SW, et al. The development of vancomycin resistance in a patient with methicillin-resistant Staphylococcus aureus infection. N Engl J Med 1999; 340(7): 517–23PubMedCrossRef Sieradzki K, Roberts RB, Haber SW, et al. The development of vancomycin resistance in a patient with methicillin-resistant Staphylococcus aureus infection. N Engl J Med 1999; 340(7): 517–23PubMedCrossRef
11.
12.
Zurück zum Zitat Edmond MB, Wenzel RP, Pasculle AW. Vancomycin-resistant Staphylococcus aureus: perspectives on measures needed for control. Ann Intern Med 1996; 124: 329–34PubMed Edmond MB, Wenzel RP, Pasculle AW. Vancomycin-resistant Staphylococcus aureus: perspectives on measures needed for control. Ann Intern Med 1996; 124: 329–34PubMed
13.
Zurück zum Zitat Noble WC, Virani Z, Cree RG, et al. Co-transfer of vancomycin and other resistance genes from Enterococcus faecalis NCTC 12201 to Staphylococcus aureus. FEMS Microbiol Lett 1992; 93: 195–8CrossRef Noble WC, Virani Z, Cree RG, et al. Co-transfer of vancomycin and other resistance genes from Enterococcus faecalis NCTC 12201 to Staphylococcus aureus. FEMS Microbiol Lett 1992; 93: 195–8CrossRef
14.
Zurück zum Zitat Hiramatsu K, Aritaka N, Hanaki H, et al. Dissemination in Japanese hospitals of strains of Staphylococcus aureus heterogeneously resistant to vancomycin. Lancet 1997; 350: 1670–3PubMedCrossRef Hiramatsu K, Aritaka N, Hanaki H, et al. Dissemination in Japanese hospitals of strains of Staphylococcus aureus heterogeneously resistant to vancomycin. Lancet 1997; 350: 1670–3PubMedCrossRef
15.
Zurück zum Zitat Interim guidelines for prevention and control of staphylococcal infection associated with reduced susceptibility to vancomycin. Morb Mortal Wkly Rep 1997; 46(27): 626–8, 635 Interim guidelines for prevention and control of staphylococcal infection associated with reduced susceptibility to vancomycin. Morb Mortal Wkly Rep 1997; 46(27): 626–8, 635
16.
Zurück zum Zitat Geisel R, Schmitz FJ, Thomas L, et al. Emergence of heterogeneous intermediate vancomycin resistance in Staphylococcus aureus in the Dusseldorf area. J Antimicrob Chemother 1999; 43: 846–8PubMedCrossRef Geisel R, Schmitz FJ, Thomas L, et al. Emergence of heterogeneous intermediate vancomycin resistance in Staphylococcus aureus in the Dusseldorf area. J Antimicrob Chemother 1999; 43: 846–8PubMedCrossRef
17.
Zurück zum Zitat Howe RA, Bowker KE, Walsh TR, et al. Vancomycin resistant Staphylococcus aureus. Lancet 1998; 351: 601–2CrossRef Howe RA, Bowker KE, Walsh TR, et al. Vancomycin resistant Staphylococcus aureus. Lancet 1998; 351: 601–2CrossRef
18.
Zurück zum Zitat Marchese A, Balistreri G, Tonoli E, et al. Heterogeneous vancomycin resistance in methicillin-resistant Staphylococcus aureus: strains isolated in a large Italian Hospital. J Clin Microbiol 2000; 38: 866–9PubMed Marchese A, Balistreri G, Tonoli E, et al. Heterogeneous vancomycin resistance in methicillin-resistant Staphylococcus aureus: strains isolated in a large Italian Hospital. J Clin Microbiol 2000; 38: 866–9PubMed
19.
Zurück zum Zitat Soares JJ, Dos S, da Silva-Carvalho MC, et al. Spread of methicillin-resistant Staphylococcus aureus belonging to the Brazilian epidemic clone in a general hospital and emergence of heterogeneous resistance to glycopeptide antibiotics among three isolates. J Hosp Infect 2000; 44: 301–8 Soares JJ, Dos S, da Silva-Carvalho MC, et al. Spread of methicillin-resistant Staphylococcus aureus belonging to the Brazilian epidemic clone in a general hospital and emergence of heterogeneous resistance to glycopeptide antibiotics among three isolates. J Hosp Infect 2000; 44: 301–8
20.
Zurück zum Zitat Reduced susceptibility of staphylococcus to vancomycin: Japan 1996. Morb Mortal Wkly Rep 1997; 46: 624–35 Reduced susceptibility of staphylococcus to vancomycin: Japan 1996. Morb Mortal Wkly Rep 1997; 46: 624–35
21.
Zurück zum Zitat Hiramatsu K, Hanaki H, Yabuta K, et al. Methicillin-resistant Staphylococcus aureus clinical strain with reduced vancomycin susceptibility. J Antimicrob Chemother 1997; 40: 135–6PubMedCrossRef Hiramatsu K, Hanaki H, Yabuta K, et al. Methicillin-resistant Staphylococcus aureus clinical strain with reduced vancomycin susceptibility. J Antimicrob Chemother 1997; 40: 135–6PubMedCrossRef
22.
Zurück zum Zitat Hiramatsu K. The emergence of Staphylococcus aureus with reduced susceptibility to vancomycin in Japan. Am J Med 1998; 104(5A): 7S–10PubMedCrossRef Hiramatsu K. The emergence of Staphylococcus aureus with reduced susceptibility to vancomycin in Japan. Am J Med 1998; 104(5A): 7S–10PubMedCrossRef
23.
Zurück zum Zitat Update: Staphylococcus aureus with reduced susceptibility to vancomycin: United States, 1997. Morb Mortal Wkly Rep 1997; 46(35): 813–15 Update: Staphylococcus aureus with reduced susceptibility to vancomycin: United States, 1997. Morb Mortal Wkly Rep 1997; 46(35): 813–15
24.
Zurück zum Zitat Ploy MC, Grelaud C, Martin C, et al. First clinical isolate of vancomycin-intermediate Staphylococcus aureus in a French hospital. Lancet 1998; 351: 1212PubMedCrossRef Ploy MC, Grelaud C, Martin C, et al. First clinical isolate of vancomycin-intermediate Staphylococcus aureus in a French hospital. Lancet 1998; 351: 1212PubMedCrossRef
25.
Zurück zum Zitat Rotun SS, McMath V, Schoonmaker DJ, et al. Staphylococcus aureus with reduced susceptibility to vancomycin isolated from a patient with fatal bacteremia. Emerg Infect Dis 1999; 5: 147–9PubMedCrossRef Rotun SS, McMath V, Schoonmaker DJ, et al. Staphylococcus aureus with reduced susceptibility to vancomycin isolated from a patient with fatal bacteremia. Emerg Infect Dis 1999; 5: 147–9PubMedCrossRef
26.
27.
Zurück zum Zitat Tenover FC, Lancaster MV, Hill BC, et al. Characterization of staphylococci with reduced susceptibilities to vancomycin and other glycopeptides. J Clin Microbiol 1998; 36: 1020–7PubMed Tenover FC, Lancaster MV, Hill BC, et al. Characterization of staphylococci with reduced susceptibilities to vancomycin and other glycopeptides. J Clin Microbiol 1998; 36: 1020–7PubMed
28.
Zurück zum Zitat Hershberger E, Aeschlimann JR, Moldovan T, et al. Evaluation of bactericidal activities of LY333328, vancomycin, teicoplanin, ampicillin-sulbactam, trovafloxacin, and RP59500 alone or in combination with rifampin or gentamicin against different strains of vancomycin-intermediate Staphylococcus aureus by time-kill curve methods. Antimicrob Agents Chemother 1999; 43: 717–21PubMed Hershberger E, Aeschlimann JR, Moldovan T, et al. Evaluation of bactericidal activities of LY333328, vancomycin, teicoplanin, ampicillin-sulbactam, trovafloxacin, and RP59500 alone or in combination with rifampin or gentamicin against different strains of vancomycin-intermediate Staphylococcus aureus by time-kill curve methods. Antimicrob Agents Chemother 1999; 43: 717–21PubMed
29.
Zurück zum Zitat Akins RL, Rybak MJ. In vitro activities of daptomycin, arbekacin, vancomycin, and gentamicin alone and/or in combination against glycopeptide-intermediate resistant Staphylococcus aureus in an infection model. Antimicrob Chemother 2000; 44: 1925–9CrossRef Akins RL, Rybak MJ. In vitro activities of daptomycin, arbekacin, vancomycin, and gentamicin alone and/or in combination against glycopeptide-intermediate resistant Staphylococcus aureus in an infection model. Antimicrob Chemother 2000; 44: 1925–9CrossRef
30.
Zurück zum Zitat Rybak MJ, Hershberger E, Moldovan T. Comparative in vitro activity of daptomycin versus vancomycin, linezolid, and synercid against methicillin-resistant and susceptible staphylococci, vancomycin-intermediate susceptible Staphylococcus aureus and vancomycin susce [abstract C-146]. Program and abstracts of the 38th Interscience Conference on Antimicrobial Agents and Chemotherapy: 1998 Sep 24–27; San Diego (CA). Washington, DC: American Society for Microbiology, 1998: 110 Rybak MJ, Hershberger E, Moldovan T. Comparative in vitro activity of daptomycin versus vancomycin, linezolid, and synercid against methicillin-resistant and susceptible staphylococci, vancomycin-intermediate susceptible Staphylococcus aureus and vancomycin susce [abstract C-146]. Program and abstracts of the 38th Interscience Conference on Antimicrobial Agents and Chemotherapy: 1998 Sep 24–27; San Diego (CA). Washington, DC: American Society for Microbiology, 1998: 110
31.
Zurück zum Zitat Hanaki H, Kuwahara-Arai K, Boyle-Vavra S et al. Activated cell-wall synthesis is associated with vancomycin resistance in methicillin-resistant Staphylococcus aureus clinical strains MU3 and MU50. J Antimicrob Chemother 1998; 42: 199–209PubMedCrossRef Hanaki H, Kuwahara-Arai K, Boyle-Vavra S et al. Activated cell-wall synthesis is associated with vancomycin resistance in methicillin-resistant Staphylococcus aureus clinical strains MU3 and MU50. J Antimicrob Chemother 1998; 42: 199–209PubMedCrossRef
32.
Zurück zum Zitat Shlaes DM, Shlaes JH, Vincent S, et al. Teicoplanin-resistant Staphylococcus aureus expresses a novel membrane protein and increases expression of penicillin-binding protein 2 complex. Antimicrob Agents Chemother 1993; 37: 2432–7PubMedCrossRef Shlaes DM, Shlaes JH, Vincent S, et al. Teicoplanin-resistant Staphylococcus aureus expresses a novel membrane protein and increases expression of penicillin-binding protein 2 complex. Antimicrob Agents Chemother 1993; 37: 2432–7PubMedCrossRef
33.
Zurück zum Zitat Milewski WM, Boyle-Vavra S, Moreira B, et al. Overproduction of a 37-kilodalton cytoplasmic protein homologous to NAD+-linked D-lactate dehydrogenase associated with vancomycin resistance in Staphylococcus aureus. Antimicrob Agents Chemother 1996; 40: 166–72PubMed Milewski WM, Boyle-Vavra S, Moreira B, et al. Overproduction of a 37-kilodalton cytoplasmic protein homologous to NAD+-linked D-lactate dehydrogenase associated with vancomycin resistance in Staphylococcus aureus. Antimicrob Agents Chemother 1996; 40: 166–72PubMed
34.
Zurück zum Zitat Daum RS, Gupta S, Sabbagh R, et al. Characterization of Staphylococcus aureus isolates with decreased susceptibility to vancomycin and teicoplanin: isolation and purification of a constitutively produced protein associated with decreased susceptibility. J Infect Dis 1992; 166: 1066–72PubMedCrossRef Daum RS, Gupta S, Sabbagh R, et al. Characterization of Staphylococcus aureus isolates with decreased susceptibility to vancomycin and teicoplanin: isolation and purification of a constitutively produced protein associated with decreased susceptibility. J Infect Dis 1992; 166: 1066–72PubMedCrossRef
35.
Zurück zum Zitat Aeschlimann JR, Hershberger E, Rybak MJ. Analysis of vancomycin population susceptibility profiles, killing activity, and postantibiotic effect against vancomycin-intermediate Staphylococcus aureus. Antimicrob Agents Chemother 1999; 43: 1914–18PubMed Aeschlimann JR, Hershberger E, Rybak MJ. Analysis of vancomycin population susceptibility profiles, killing activity, and postantibiotic effect against vancomycin-intermediate Staphylococcus aureus. Antimicrob Agents Chemother 1999; 43: 1914–18PubMed
36.
Zurück zum Zitat Boyle-Vavra S, Berke SK, Lee JC, et al. Reversion of glycopeptide intermediate-resistant Staphylococcus aureus associated with loss of type 5 capsule [session 147. C1 paper 1455]. Program and abstracts of the 39th Interscience Conference on Antimicrobial Agents and Chemotherapy: 1999 Sep 26–29; San Francisco (CA). Washington, DC: American Society for Microbiology, 1999: 132 Boyle-Vavra S, Berke SK, Lee JC, et al. Reversion of glycopeptide intermediate-resistant Staphylococcus aureus associated with loss of type 5 capsule [session 147. C1 paper 1455]. Program and abstracts of the 39th Interscience Conference on Antimicrobial Agents and Chemotherapy: 1999 Sep 26–29; San Francisco (CA). Washington, DC: American Society for Microbiology, 1999: 132
37.
Zurück zum Zitat Aeschlimann JR, Hershberger E, Rybak MJ. Activity of vancomycin administered every 12 hours or as continuous infusion against two clinical strains of vancomycin-intermediate Staphylococcus aureus in an in vitro pharmacodynamic model [abstract A-10]. Program and abstracts of the 38th Interscience Conference on Antimicrobial Agents and Chemotherapy: 1998 Sep 24–27; San Diego (CA). Washington, DC: American Society for Microbiology, 1998: 3 Aeschlimann JR, Hershberger E, Rybak MJ. Activity of vancomycin administered every 12 hours or as continuous infusion against two clinical strains of vancomycin-intermediate Staphylococcus aureus in an in vitro pharmacodynamic model [abstract A-10]. Program and abstracts of the 38th Interscience Conference on Antimicrobial Agents and Chemotherapy: 1998 Sep 24–27; San Diego (CA). Washington, DC: American Society for Microbiology, 1998: 3
38.
Zurück zum Zitat Dudley M, Griffith D, Corcoran E, et al. Pharmacokinetic-pharmacodynamic indices for vancomycin treatment of susceptible and intermediate S. aureus in the neutropenic mouse thigh model [session 198 paper 2031]. Program and abstracts of the 39th Interscience Conference on Antimicrobial Agents and Chemotherapy: 1999 Sep 26–29; San Francisco (CA). Washington, DC: American Society for Microbiology, 1999: 49 Dudley M, Griffith D, Corcoran E, et al. Pharmacokinetic-pharmacodynamic indices for vancomycin treatment of susceptible and intermediate S. aureus in the neutropenic mouse thigh model [session 198 paper 2031]. Program and abstracts of the 39th Interscience Conference on Antimicrobial Agents and Chemotherapy: 1999 Sep 26–29; San Francisco (CA). Washington, DC: American Society for Microbiology, 1999: 49
39.
Zurück zum Zitat Aeschlimann JR, Hershberger E, Rybak MJ. Activity of LY333328, an investigational glycopeptide, against three strains of vancomycin-intermediate Staphylococcus aureus in an in vitro pharmacodynamic infection model [abstract A-135]. Program and abstracts of the 38th Interscience Conference on Antimicrobial Agents and Chemotherapy: 1998 Sep 24–27; San Diego (CA). Washington, DC: American Society for Microbiology, 1998:43 Aeschlimann JR, Hershberger E, Rybak MJ. Activity of LY333328, an investigational glycopeptide, against three strains of vancomycin-intermediate Staphylococcus aureus in an in vitro pharmacodynamic infection model [abstract A-135]. Program and abstracts of the 38th Interscience Conference on Antimicrobial Agents and Chemotherapy: 1998 Sep 24–27; San Diego (CA). Washington, DC: American Society for Microbiology, 1998:43
40.
Zurück zum Zitat Sieradzki K, Tomasz A. Inhibition of cell wall turnover and autolysis by vancomycin in a highly vancomycin-resistant mutant of Staphylococcus aureus. J Bacteriol 1997; 179: 2557–66PubMed Sieradzki K, Tomasz A. Inhibition of cell wall turnover and autolysis by vancomycin in a highly vancomycin-resistant mutant of Staphylococcus aureus. J Bacteriol 1997; 179: 2557–66PubMed
41.
Zurück zum Zitat Sieradzki K, Tomasz A. Suppression of beta-lactam antibiotic resistance in a methicillin-resistant Staphylococcus aureus through synergic action of early cell wall inhibitors and some other antibiotics. J Antimicrob Chemother 1997; 39: Suppl. A: 47–51PubMedCrossRef Sieradzki K, Tomasz A. Suppression of beta-lactam antibiotic resistance in a methicillin-resistant Staphylococcus aureus through synergic action of early cell wall inhibitors and some other antibiotics. J Antimicrob Chemother 1997; 39: Suppl. A: 47–51PubMedCrossRef
42.
Zurück zum Zitat Aeschlimann JR, Hershberger E, Rybak MJ. Pharmacodynamic predictors of activity for ampicillin/sulbactam and trovafloxacin versus vancomycin-intermediate Staphylococcus aureus in an in vitro infection model [abstract A-38]. Program and abstracts of the 38th Interscience Conference on Antimicrobial Agents and Chemotherapy: 1998 Sep 24–27; San Diego (CA). Washington, DC: American Society for Microbiology, 1998: 12 Aeschlimann JR, Hershberger E, Rybak MJ. Pharmacodynamic predictors of activity for ampicillin/sulbactam and trovafloxacin versus vancomycin-intermediate Staphylococcus aureus in an in vitro infection model [abstract A-38]. Program and abstracts of the 38th Interscience Conference on Antimicrobial Agents and Chemotherapy: 1998 Sep 24–27; San Diego (CA). Washington, DC: American Society for Microbiology, 1998: 12
Metadaten
Titel
Emergence of Methicillin-Resistant Staphylococcus aureus with Intermediate Glycopeptide Resistance
Clinical Significance and Treatment Options
verfasst von
Professor Michael J. Rybak
Ronda L. Akins
Publikationsdatum
01.01.2001
Verlag
Springer International Publishing
Erschienen in
Drugs / Ausgabe 1/2001
Print ISSN: 0012-6667
Elektronische ISSN: 1179-1950
DOI
https://doi.org/10.2165/00003495-200161010-00001

Weitere Artikel der Ausgabe 1/2001

Drugs 1/2001 Zur Ausgabe

Adis Drug Evaluation

Fluoxetine