Salud Pública de México

In vitro antimicrobial susceptibility in clinical isolates of Enterococcus species** We acknowledge the partial support of Pharmacia and Upjohn, Kalamazoo, Mich. (Dr. Susana Suárez).

In vitro antimicrobial susceptibility in clinical isolates of Enterococcus species** We acknowledge the partial support of Pharmacia and Upjohn, Kalamazoo, Mich. (Dr. Susana Suárez).


Ernesto Calderón-Jaimes, MC, MSP,(1) José Luis Arredondo-García, MC,(2) Felipe Aguilar-Ituarte, MC,(2,3) Pilar García-Roca, QFB.(1)

(1) Departamento de Inmunoquímica y Biología Celular, Hospital Infantil de México Federico Gómez, México, D.F., México.
(2) Unidad de Investigación Clínica, Instituto Nacional de Pediatría, México, D.F., México.
(3) Departamento de Infectología, Hospital Infantil de México Federico Gómez, México, D.F., México.


Objectivo. Describir la actividad antimicrobiana de varios antibióticos, contra 97 cepas de Enterococcus spp., consideradas como aislamientos clínicamente significativos. Material y métodos. En un estudio prospectivo de dos años, (enero de 1998 a diciembre de 1999) hecho en el Instituto Nacional de Pediatría en la Ciudad de México, se procesaron 97 cepas de Enterococcus (60 de Enterococcus faecalis y 37 de Enterococcus faecium, contra 11 antibióticos. La prueba de susceptibilidad se elaboró con agar, de acuerdo con los estándares del Comité Nacional para el Laboratorio Clínico (NCCLS). Todos los aislamientos fueron probados para determinar la resistencia elevada en contra de b-lactámicos, aminoglucósidos y glicopéptidos. Asimismo, se determinó el fenotipo de resistencia hacia la vancomicina. Se evaluaron diferencias de proporciones con X2 o prueba exacta de Fisher. Resultados. La resistencia en general hacia los antibióticos probados fue 17/97 (17.5%) a penicilina, ampicilina, amoxicilina-clavulanato e imipenem. No se encontró resistencia elevada ni presencia de producción de b-lactamasas; 74/97 (48.4%) fueron resistentes a eritromicina, 60% resistentes a ciprofloxacina, 31/97 (32%) resistentes a gentamicina y 55/97 (56.7%) resistentes a estreptomicina. Siete cepas fueron resistentes a vancomicina, todas ellas E. faecium; 5/7 con el fenotipo A y 2/7 con el fenotipo B. Todas las cepas aisladas fueron susceptibles al linezolid. La diferencia en la susceptibilidad antimicrobiana entre las especies fue significativa. Conclusiones. La resistencia antimicrobiana múltiple de Enterococcus spp. es un problema real y es necesaria su vigilancia. El laboratorio de microbiología es la primera línea de defensa en contra de la diseminación de enterococos con resistencia múltiple en el ambiente hospitalario. Todas las cepas aisladas deberían ser probadas en contra de ampicilina, estreptomicina, gentamicina y glicopéptidos.


Objective. To describe the antimicrobial activity of several antimicrobial agents against 97 clinical significant isolates of Enterococcus spp. Material and Methods. During a 2-year prospective study at Instituto Nacional de Pediatria (National Institute of Pediatrics) in Mexico City. Ninety seven strains of Enterococcus spp. (60 E. faecalis and 37 E. faecium) were tested against 11 antibiotics. Susceptibility tests were performed with agar, according to the standards of the sNational Committee for Clinical Laboratory Standards (NCCLS). Isolates were screened for high-level resistance (HLR) to β-lactams, aminoglycosides, glycopeptides and other antibiotics, as well as for vancomycin-phenotypes. Differences between proportions were evaluated with X2 of Fisher exact fest. Results. Overall resistance rates to the antibiotics tested were: 17/97 (17.5%) to penicillin, ampicillin, amoxicillin-clavulanate and imipenem. There was neither HLR nor β-lactamase production; 74/97 (48.4%) were resistant to erythromycin; 60% to ciprofloxacin; 31/97 (32%) to gentamicin, and 55/97 (56.7%) to streptomycin. Seven strains were vancomycin-resistant enterococci (VRE), all of them identified as E. faecium; 5/7 with Van A and 2/7 with Van B phenotypes. All the isolates were susceptible to linezolid. The difference in susceptibility among species was significant.  Conclusions. Mutidrug-resistant enterococci is a real problem and continuous surveillance is necessary. The microbiology laboratory is the first line of defense against the spread of multiantibiotic-resistan enterococci in the hospital environment. All the strains recovered should be tested for susceptibility to ampicillin, streptomycin, gentamicin and glycopeptides.


Enterococci are normal inhabitants of the gastroin testinal tract and part of the normal intestinal flora. They are not particularly pathogenic organisms in humans. Despite their lack of pathogenicity, enterococci have emerged as significant nosocomial pathogens.1-9 Enterococci are also commonly recovered from infections of the abdomen, the pelvis, the biliary tract and wounds. Polymicrobial flora is common in these sites. Enterococci cause infections of other sites less frequently, for example, in bone, joints and the meninges.3,4,10-13

Progress in medical technology, such as the use of various intravascular access devices, magnified the impact of organisms of relatively low virulence, such as enterococci.13 Of critical importance is the intensive use of broad-spectrum antibiotics in hospitals, which fosters a selective pressure favoring the growth of intrinsically drug-resistant commensal organisms like enterococci.6,14-18

Resistance to a number of antimicrobial drugs is characteristic of the genus Enterococcus, although some species are more intrinsically resistant than others.

The role of enterococci as a cause of infections has become increasingly important, not only because of their documented pathogenic potential, but also because of the increasing antimicrobial resistance of some strains, especially resistance to vancomycin (VRE).14 Increasing use of parenteral third-generation cephalosporins and vancomycin for the treatment of intravascular device-related infections might have a role in developing enterococcal resistance.6 Observations of vancomycin-resistant strains have revealed the presence of several different phenotypes of glycopeptide resistance.17

A number of newly-acquired mechanisms of resistance have emerged or become more frequent in Enterococcus species during the past decade, including high-level aminoglycoside resistance, beta-lactamase production, high-level ampicillin resistance, and vancomycin resistance. In United States hospitals, enterococci have become the second most common nosocomial pathogen overall, according to Nationwide Surveillance data.10,19 In our study, 97 isolates from pediatric patients with Enterococcus species considered as clinically significant strains, were tested against several antimicrobials, to determine the in vitro activity of each agent as well as the phenotype in those with VRE.

Material y Métodos

From January 1998 to December 1999, a 2-year prospective study was carried out at Instituto Nacional de Pediatria (National Institute of Pediatrics), a teaching and referral third-level hospital in Mexico City. Only serious infections were included in the study: endocarditis (n=4); primary bacteremia (unknown source) (n=23); catheter- related bacteremia (24); empyema (4); urosepsis (9); meningitis and /or ventriculitis (11); intrabdominal infection (3); and deep surgical wound infection (abscess) (19).

Clinical definition. Clinical significant bacteremia or infection due to Enterococcus spp., was defined by isolation of either species from > 2 blood cultures or from a single blood culture, if there was a clinically apparent and /or culture-positive source of infection. Bacterial strains. A total of 97 isolates were collected, 60 of them were Enterococcus faecalis and 37 were Enterococcus faecium. All of them were stored in doublestrength skim milk (Difco,Labs. Detroit, Mich.) at -70° C.

Enterococcal isolates were identified using driedovernight gram-positive combination panels in the MicroScan WalkAway 96 Instrument (Dade MicroScan, Inc., West Sacramento, CA). Species identification was confirmed by conventional microbiological testing.20,21

Prior to testing for susceptibility, isolates were thawed and subcultured twice to ensure purity and viability. Antimicrobials were supplied from the manufacturers as laboratory powders of known potency; stock solutions were prepared as recommended by the manufacturers. Antimicrobial used were: Penicillin G potassium, ampicillin and amoxicillin-clavulanate, imipenem, erythromycin, streptomycin, gentamicin, ciprofloxacin, teicoplanin, vancomycin and linezolid.

Antimicrobial susceptibility testing. The minimal inhibitory concentration (MIC) was determined in duplicate by the broth microdilution method in Mueller-Hinton broth (Difco, Mexico City, Mexico) supplemented with 10 mg of MgCl2/l and 20 mg of CaCl2/l., with a final inoculum of 1.5 X 105 CFU/ml, as recommended by the National Committee for Clinical Laboratory standards (NCCLS).22 All plates were incubated at 35° C for 24 h in ambient air before determination of Minimal Inhibitory Concentration (MIC) values. The plates were visually read. NCCLS breakpoints were used to interpret MIC data.22 Appropriate quality control was performed by use of Enterococcus faecalis ATCC-29212 (vancomycin susceptible). Linezolid is an investigational drug. NCCLS considered strains with a MIC > 2 µg/ml as susceptible, those with a MIC=4 µg/ml as intermediate, and those with a MIC > 8 µg/ml as resistant.23

Screening for beta-lactamase production was done using Cefinase disk methodology (a chromogenic substrate nitrocefin, Cefinase, BBL, Microbiology Systems, Cockeysville, MD).

High-level aminoglycoside resistance (HLAR). All the strains with a MIC > 64 µg/ml to gentamicin and streptomycin were used to screen for HLAR. Those strains suspected to be HLAR were confirmed by broth tube dilution using brain-heart infusion broth with 500 and 1000 µg/ml concentrations of gentamicin, as well as with 1000 and 2000 µg/ml concentrations of streptomycin.

Phenotypes. The Van A phenotype include enterococci  resistant to high levels of  vancomycin (MIC > 64/ml) and teicoplanin (MIC
> 8 µg/ml). This resistance is vancomycin- and/or teicoplanin- inducible.18 Van B organisms are resistant to a range of vancomycin concentrations, from 4 to > 1024 µg/ml; they typically retain their susceptibility to teicoplanin. This resistance is also inducible by vancomycin but not by teicoplanin.18 Differences between proportions were evaluated with the X2 or Fisher exact test (as appropriate).


A total of 97 clinical isolates of Enterococcus spp. (60 E. faecalis and 37 E. faecium) were collected, identified, and analyzed over a 24-month study period.

Table I shows the in vitro activity of antimicrobial agents that were tested according to different species.

ß-lactam resistance. 5/60 (8.3%) E. faecalis and 27/37 (73.0%) E. faecium were resistant (overall 32/97; 33%) to penicillin; 2/60 (3.3%) E. faecalis and 15/37 (40.5%) E. faecium were resistant (overall 17/97, 17.5%) to ampicillin and amoxicillin-clavulanate; 15/97 (15.4%) –all of them E. faecium– were resistant to imipenem. Resistance between species against ß-lactams was significant. There was neither high-level penicillin resistance nor ß-lactamase production among the clinical strains tested.

High-level aminoglycoside resistance. Fifthteen of sixty (25.0%) E. faecalis and 16/37 (43.3%) E. faecium were resistant (overall 31/97; 32%) to gentamicin; 32/60 (53.4 %) E. faecalis and 23/37 (62.1%) E. faecium were resistant (overall 55/97; 56.7%) to streptomycin. Resistance to aminoglycosides between species was significant. Vancomicin-resistant enterococci. Seven strains were resistant to vancomycin, all of them E. faecium; 5 of 7 strains were also resistant to teicoplanin. All E. faecalis strains were susceptible to vancomycin and teicoplanin.

Phenotypes. Five of seven VRE isolates exhibited the Van A phenotype, and 2/7 exhibited the phenotype Van B. Other antimicrobials. Erythromycin inhibited more than 50% of all strains at or below their respective susceptible breakpoint concentrations. More than 60% of the strains tested were resistant to ciprofloxacin. Notably, 100% of all the isolates tested were inhibited by <4 µg/ml of linezolid.


Enterococci are not generally regarded as highly virulent bacterial pathogens, however, resistance to many antimicrobial drugs complicates the treatment of enterococcal infections. Acquired resistance to high concentrations of ampicillin, aminoglycoside, and glycopeptide antibiotics, specifically vancomycin, has exacerbated this problem.6,8,13,14,18,24,25

In the last decade enterococci have become recognized as leading causes of nosocomial bacteremia, surgical wound infections, and urinary tract infections.

Two types of enterococci cause infections: a) those originating from patients´native flora, which are unlikely to possess resistance beyond that intrinsic to the genus, and to be spread between patients from bed to bed, and b) isolates that possess multiple antibiotic resistance traits and are capable of nosocomial transmission. The therapeutic challenge of multiple-drug resistance enterococci has brought their role as important nosocomial pathogens into sharper focus.

Although E. faecium strains are resistant to ampicillin, aminoglycosides, and glycopeptides more than E. faecalis strains, the relative proportion of infections caused by these species has not dramatically changed in recent years.14

Different patterns of resistance have been informed from many countries.18 That information is scarce in Mexico, particularly in pediatric patients.26,27 In this study the activity of several antimicrobial agents against 97 clinical isolates is reported.

Considerable resistance of E. faecium isolates to most of the antibiotics tested was demonstrated during the study period.

The results of this study confirm that E. faecalis strains resistant to ampicillin and vancomycin are uncommon; in contrast, E. faecium strains resistant to vancomycin (7/ 37 strains) and ampicillin (15/37 strains), increased alarmingly. This observation is similar to those reported by other authors.13,14,28-30

At least for E. feacalis and E. falcium against penicillin, ampicillin and imipenem.

High-level resistance to aminoglycosides is a real problem, this resistance overcomes the synergy of killing combination therapy. Ampicillin and vancomycin are not bactericidal unless combined with an aminoglycoside.10,12,18 High-level gentamicin resistance is most often associated with high-level resistance to all alternative aminoglycosides.

Since enterococcal resistance to gentamicin and streptomycin occurs by different mechanisms, it is important to test susceptibility to both agents. Enterococci with HLR to streptomycin are susceptible to gentamicin. Gentamicin resistance is a good predictor of resistance to other aminoglycosides; also, ampicillin resistance is a predictor of imipenem resistance.31-33

Glycopeptide-resistance in Enterococcus spp. (7/97 or 7.2%) is higher than that found by Miranda and cols.; 5 /235 (2.12%) in E.faecalis and E.faecium strains.26 Those isolates confirm the various levels of resistance to vancomycin and teicoplanin.

In this study, five of seven isolates of E. faecium were phenotype Van A and the other 2 were phenotype Van B. It is useful to identify which species are vancomycin-resistant in enterococcal isolates. Identification of Van A organisms has implications for treatment and infection control.34,35

Other studies on VRE clinical isolates found that most were Van A phenotype strains of E. faecium; they were associated with outbreaks in special wards with immunocompromised patients on long term antimicrobial regimens, with extended lengths of stay and higher severity of illness scores.36-38

Several limitations of the data from this study make firm conclusions problematic. First, all of the microorganisms tested came from a single institution. Second, a relatively small number of E. faecium and E. faecalis were tested; it is possible that these strains might represent only a few clones. Third, no species other than E. faecalis and E. faecium were included.

Once vancomycin-resistant enterococci are established in the hospital environment, their frequent resistance to multiple antibiotics make it difficult to avoid further selective pressure in their favor. Enterococcal infections tend to occur in more debilitated or seriously ill hospitalized patients. Mortality in patients with VRE bacteremia may reach 60-70%. 3,14 From 1989 through 1997, the percentage of infections caused by VRE increased from 0.4 to 23.2 % among patients in the intensive care unit (ICU), and from 0.3 to 15.4% among patients not in the ICU.2

Because most enterococci are resistant to the bactericidal activity of ß-lactam and glycopeptide antibiotics, bactericidal synergy between one of these antibiotics and an aminoglycoside is needed to treat most serious enterococcal infections. The synergistic bactericidal effect between aminoglycosides and ß-lactam or glycopeptide antibiotics is lost if there is highlevel resistance to either class of drug. The increasing use of parenteral vancomycin for the treatment of intravascular device-related infections might have a role in enterococcal resistance.

Treatment of multidrug-resistant enterococci is under an investigational new drug program for treatment of patients with life-threatening infection due to vancomycin-resistant E. faecium bacteremia. There has been a considerable effort to develop alternative agents; for example, dalfopristin-quinupristin is a streptogramin antibiotic that has been studied in the treatment of infections due to vancomycin-resistant E. faecium. Other investigational agents with activity in vitro against Enterococcus spp. susceptible or resistant to glycopeptides include the oxazolidinones. These are a new class of synthetic antibiotics with good antienterococcal activity and are different from any other class. Mechanisms of resistance that affect antibiotics in current clinical use do not affect the activities of oxazolidinones. Linezolid is one of the investigational agents.39,40 In this study linezolid showed excellent activity against multiantibiotic-resistant enterococci. Clinical efficacy and safety studies are needed to determine its real utility. Linezolid has recently been approved by the Food and Drug Administration.

The microbiology laboratory is the first line of defense against the spread of multiantibiotic-resistant enterococci in the hospital environment. Cooperation and communication between the laboratory and the infection control program is essential in recognizing enterococci-resistant isolates from colonization and infection. All of the strains recovered should be tested for susceptibility to ampicillin, streptomycin, gentamicin, and glycopeptides.

It will be necessary to study additional E. faecalis and E. faecium strains from different hospitals and, if possible to include less common enterococcal species such as E. gallinarum and E. casseliflavus, which are relatively infrequent causes of human infections but they have intrinsic resistance to low concentrations of vancomycin.


The authors are grateful to Dr. L.E. Espinosa de los Monteros, M. Sc. Norma Velázquez , Dr. Renata Avila, and Esther Lombardo for their technical assistance to store the samples and ensure the purity and viability of strains tested.


1. Schaberg DR, Culver DH, Gaynes RP. Mayor trends in the microbial etiology of nosocomial infection. Am J Med 91;(suppl 3B):72S-75S.
2. Centers for Disease Control and Prevention. Nosocomial enterococci resistant to vancomycin-United States, 1989-1993. MMWR Morb Mortal Wkly Rep 1993;42:597-599.
3. Tornieporth N, Roberts RB, John J, Hafnier A, Riley LW. Risk factors associated with vancomycin-resistant Enterococcus faecium infection or colonization in 145 matched case patients and control patients. Clin Infect Dis 1996;23:767-772.
4. Edmond MB, Ober JF, Dawson JD, Weinbaurri DC, Wenzel RP. Vancomycin- resistant enterococcal bacteremia: Natural history and attributable mortality. Clin Infect Dis 1996;23:1234-1239.
5. Eliopoulos GM. Vancomycin-resistant enterococci: Mechanism and clinical relevance. Infect Dis Clin North Am 1997;11:851-865.
6. Murray BE. The life and times of the enterococcus. Clin Microbiol Rev 1990;3:45-65.
7. Rubin L, Tucci V, Cerenado E, Elioponlos G, Isenberg H. Vancomycinresistant Enterococcus faecium in hospitalized children. Infect Control Hosp Epidemiol 1992;13:700-705.
8. Fridkin SK, Gaynes RP. Antimicrobial resistance in intensive care units. Clin Chest Med 1999;20:303-316.
9. Patterson JE, Sweeney AH, Simms M, Carley N, Mangi R, Sabetta J et al. An analysis of 110 serious enterococcal Infections. Epidemiology, antibiotic susceptibility, and outcome. Medicine 1995;74:191-200.
10. Ross TW. Infectious disease challenge: Vancomycin-resistant enterococcus and staphylococcus. Drug Topics 1998;142:76-83.
11. Murray BE. Vancomycin-resistant enterococci. Am J Med 1997;102: 284-293.
12. Murray BE. Diversity among multidrug-resistant enterococci. Emerg Infect Dis 1998;4:37-47.
13. Gold HS. Vancomycin-resistant enterococci: Mechanisms and clinical observations. Clin Infect Dis 2001;33:210-219.
14. Huycke MM, Sahm DF, Gilmore MS. Multiple-drug resistant enterococci: The nature of the problem and an agenda for the future. Emerg Infect Dis 1998;4:239-249.
15. Hodges TR, Zighelboim-Daum S, Eliopulus GM, Wennerstein CB, Moellering RC. Antimicrobial susceptibility changes in Enterococcus faecalis following various penicillin exposure regimens. Antimicrob Agents Chemother 1992;36:121-125.
16. Moellering RC. Vancomycin-resistant enterococci. Clin Infect Dis 1998;26:1196-1199.
17. Gold HS, Moellering RC. Drug therapy: Antimicrobial-drug resistance. N Engl J Med 1996;335:1445-1454.
18. Centinkaya Y, Falk P, Mayhall CG. Vancomycin-resistant enterococci. Clin Microbiol Rev 2000;13:686-707.
19. Perl TM. The threat of vancomycin resistance. Am J Med. 1999;106: 26S-37S.
20. Facklam RR, Sham DF, Teixeira LM. Enterococcus. En: Murray PR, Baron EJ, Pfaller MA, Tenover FC, Yolken RA, ed. Manual of clinical microbiology.
7th ed. Washington, DC: American Society for Microbiology, 1999:297-305.
21. Facklam RR, Collin MD. Identification of Enterococcus species isolated from human infections by a conventional test scheme. J Clin Microbiol 1989;27:731-734.
22. National Committee for Clinical Laboratory Standards. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically. Approved standard-5th ed. Wayne (PA): NCCLS, 2000; Document M7- A-5, 27.
23. National Committee for Clinical Laboratory Standards. Performance standards for antimicrobial susceptibility testing. Twelfth Informational Supplement. Wayne (PA): NCCLS, 2002; Document M100-S12.
24. Bonten MJ, Slaughter S, Ambergen AW, Hayden MK, van Voorhis J, Nathan C et al. The role of “colonization pressure” in the spread of vancomycin- resistant enterococci: An important infection control variable. Arch Intern Med 1998;158:1127-1132.
25. Palmer SM, Ryback MJ. Vancomycin-resistant enterocci. Pharmacotherapy 1996;16:819-829.
26. Miranda G, Lee L, Kelly C, Solórzano F, Leaños B, Muñoz O et al. Antimicrobial resistance from enterococci in a pediatric hospital. Plasmids in Enterococcus faecalis isolates with high-level gentamicin and streptomycin resistance. Arch Med Res 2001;32:159-163.
27. Sifuentes-Osornio J, Ponce deLeón A, Muñoz-Trejo T, Villalobos-Zapata Y, Ontiveros-Rodríguez C, Gómez-Roldan C. Antimicrobial susceptibility patterns and high-level gentamicin resistance among enterococci isolated in a Mexican tertiary care center. Rev Invest Clin 1996;48:91-96.
28. Pfaller MA, Jones RN, Doern GV, Kugler K, the SENTRY participants Group. Bacterial pathogens isolated from patients with blood stream infections: Frequencies of ocurrence and antimicrobial susceptibility patterns from the SENTRY Antimicrobial Surveillance Program (United States and Canada, 1997). Antimicrob Agents Chemother 1998;42:1762-1770.
29. Sader HS, Jones RN, Gales AC, Winokur P, Kugler KC, Pfaller MA et al. Antimicrobial susceptibility patterns for pathogens isolated from patients in Latin American medical centers with a diagnosis of pneumonia: Analysis of results from the SENTRY. Antimicrobial Surveillance Program (1997), SENTRY Latin American Study Group. Diagn Microbiol Infect Dis 1998;32:289-301.
30. Gales AC, Jones RN, Pfaller MA, Gordon KA, Sader HS, Sampaio J et al. Two-year assessment of the pathogen frequency and antimicrobial resistance patterns among organisms isolated from skin and soft tissue infections in Latin American hospitals: Result from the SENTRY Antimicrobial Surveillance Program,1997-98. Int J Infect Dis 2000;4:75-84.
31. Arthur M, Reynolds PE, Depardieu F, Corvalin P. Mechanisms of glycopeptide resistance in enterococci. J Infect Dis 1996;32:11-16.
32. Ferretti JJ, Gilmore KS, Courvalin P. Nucleotide sequence analysis of the gene specifying the bifunctional 6’-aminoglycoside acetyltransferase
2”-aminoglycoside phosphotransferase enzyme in Streptococcus faecalis and identification and cloning of gene regions specifying the two activities. J Bacteriol 1986;167:631-638.
33. Weinstein MP. Comparative evaluation of penicillin, ampicillin, and imipenem MICs and susceptibility breakpoints for vancomycin-susceptible and vancomycin-resistant Enterococcus faecalis and Enterococcus faecium. J Clin Microbiol 2001;39:2729-2731.
34. Herman DJ, Gerdin DN. Screening and treatment of infections caused by resistant enterococci. Antimicrob Agent Chemother 1991;35:215-219.
35. Quintiliani R, Evers S, Courvalin P. The van B gene confers various levels of self-transferable resistance to vancomycin in enterococci. J Infect Dis 1993;167:1220-1223.
36. Garbutt J. Ventrapragada M, Littenberg B, Mundy LM. Association between resistance to vancomycin and death in cases of Enterococcus faecium bacteremia. Clin Infect Dis 2000;30:466-472.
37. Lautenback E, Bilker WB, Brennan PJ. Enterococcal bacteremia: Ris  factors for vancomycin resistance and predictors of mortality. Infect Control Hosp Epidemiol 1999;20:318-323.
38. Lucas G, Lechtzin N, Puryear W, Yaul, Flexner C, Moore R. Vancomycinresistant and vancomycin-susceptible enterococcal bacteremia: Comparison of clinical features and outcomes. Clin Infect Dis 1998;26:1127-1133.
39. Naskin GA, Siddiqui F, Stosor V, Hacek D, Peterson LR. In vitro activities of linezolid against important gram-positive bacterial pathogens including vancomycin-resistant enterococci. Antimicrob Agents Chemother 1999;43:2059-2062
40. Clement D, Markham A. Linezolid. Drug 2000;59: 815-827.

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