» Articles » PMID: 11217866

Emergence of Methicillin-resistant Staphylococcus Aureus with Intermediate Glycopeptide Resistance: Clinical Significance and Treatment Options

Overview
Journal Drugs
Specialty Pharmacology
Date 2001 Feb 24
PMID 11217866
Citations 31
Authors
Affiliations
Soon will be listed here.
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.

Citing Articles

The Functional Study of Response Regulator ArlR Mutants in Staphylococcus Aureus.

Zhou J, Refat M, Guo Y, Zhang J, Jiao M, He W Appl Biochem Biotechnol. 2024; 196(11):7687-7702.

PMID: 38530540 PMC: 11645427. DOI: 10.1007/s12010-024-04919-1.


The ArlS Kinase Inhibitor Tilmicosin Has Potent Anti-Biofilm Activity in Both Static and Flow Conditions.

Wang Z, Wang H, Bai J, Cai S, Qu D, Xie Y Microorganisms. 2024; 12(2).

PMID: 38399660 PMC: 10891534. DOI: 10.3390/microorganisms12020256.


Mechanisms of gram-positive vancomycin resistance (Review).

Selim S Biomed Rep. 2021; 16(1):7.

PMID: 34938536 PMC: 8686198. DOI: 10.3892/br.2021.1490.


Vancomycin Serum Concentration after 48 h of Administration: A 3-Years Survey in an Intensive Care Unit.

Perin N, Roger C, Marin G, Molinari N, Evrard A, Lavigne J Antibiotics (Basel). 2020; 9(11).

PMID: 33182613 PMC: 7698174. DOI: 10.3390/antibiotics9110793.


Strategic Moves of "Superbugs" Against Available Chemical Scaffolds: Signaling, Regulation, and Challenges.

Baral B, Mozafari M ACS Pharmacol Transl Sci. 2020; 3(3):373-400.

PMID: 32566906 PMC: 7296549. DOI: 10.1021/acsptsci.0c00005.


References
1.
RUBIN R, Harrington C, Poon A, Dietrich K, Greene J, Moiduddin A . The economic impact of Staphylococcus aureus infection in New York City hospitals. Emerg Infect Dis. 1999; 5(1):9-17. PMC: 2627695. DOI: 10.3201/eid0501.990102. View

2.
Hershberger E, Aeschlimann J, MOLDOVAN T, Rybak M . 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.... Antimicrob Agents Chemother. 1999; 43(3):717-21. PMC: 89193. DOI: 10.1128/AAC.43.3.717. View

3.
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(8):2557-66. PMC: 179004. DOI: 10.1128/jb.179.8.2557-2566.1997. View

4.
Aeschlimann J, Hershberger E, Rybak M . Analysis of vancomycin population susceptibility profiles, killing activity, and postantibiotic effect against vancomycin-intermediate Staphylococcus aureus. Antimicrob Agents Chemother. 1999; 43(8):1914-8. PMC: 89390. DOI: 10.1128/AAC.43.8.1914. View

5.
Watanakunakorn C . Treatment of infections due to methicillin-resistant Staphylococcus aureus. Ann Intern Med. 1982; 97(3):376-8. DOI: 10.7326/0003-4819-97-3-376. View