This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Krause, K. M.
Right arrow Articles by Benton, B. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Krause, K. M.
Right arrow Articles by Benton, B. M.

 Previous Article  |  Next Article 

Antimicrobial Agents and Chemotherapy, July 2008, p. 2647-2652, Vol. 52, No. 7
0066-4804/08/$08.00+0     doi:10.1128/AAC.01398-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

In Vitro Activity of Telavancin against Resistant Gram-Positive Bacteria{triangledown}

Kevin M. Krause, Marika Renelli, Stacey Difuntorum, Terry X. Wu, Dmitri V. Debabov,{dagger} and Bret M. Benton*

Theravance, Inc., South San Francisco, California 94080

Received 29 October 2007/ Returned for modification 5 February 2008/ Accepted 16 April 2008


arrow
ABSTRACT
 
The in vitro activity of telavancin was tested against 743 predominantly antimicrobial-resistant, gram-positive isolates. Telavancin was highly active against methicillin-resistant staphylococci (MIC90, 0.5 to 1 µg/ml), streptococci (all MICs, ≤0.12 µg/ml), and VanB-type enterococci (all MICs, ≤2 µg/ml). Time-kill studies demonstrated the potent bactericidal activity of telavancin.


arrow
TEXT
 
The pervasiveness of multidrug-resistant, gram-positive bacteria in the hospital setting and their increasing occurrence in the community present a significant challenge for the management of serious infections (1, 10, 11). The worldwide prevalence of methicillin-resistant Staphylococcus aureus (MRSA) and methicillin-resistant coagulase-negative staphylococci (MRCoNS) poses a particular threat (2, 6, 10, 11).

Telavancin, an investigational, multivalent lipoglycopeptide active against gram-positive pathogens, has been evaluated in phase 3 clinical trials for the treatment of complicated skin and skin structure infections (cSSSI) and hospital-acquired pneumonia (G. R. Corey, M. E. Stryjewski, W. D. O'Riordan, V. G. Fowler, Jr., A. Hopkins, M. M. Kitt, and S. L. Barriere, presented at the 14th Annual Meeting of the Infectious Diseases Society of America, Torono, Canada, 12 to 15 October 2006; E. Rubinstein, G. R. Corey, M. E. Stryjewski, H. W. Boucher, R. N. Daly, F. C. Genter, S. L. Barriere, M. M. Kitt, and H. D. Friedland, presented at the 18th European Congress of Clinical Microbiology and Infectious Diseases, Barcelona, Spain, 19 to 22 April 2008).

Preliminary surveillance studies have documented the in vitro activity of telavancin against gram-positive pathogens, including MRSA and CoNS, with reduced susceptibility to glycopeptides and other resistant gram-positive species (5, 7-9, 13). In this report, we describe the results of broth microdilution susceptibility testing of telavancin and comparator agents against a diverse collection of multiresistant gram-positive bacteria including MRSA, MRCoNS, streptococci, including multidrug-resistant Streptococcus pneumoniae (MDRSP), and vancomycin-resistant enterococci (VRE). Time-kill kinetic studies were also performed with representative drug-resistant isolates to further profile the bactericidal activity of telavancin.

A total of 743 gram-positive clinical isolates collected globally between 1998 and 2006 were assembled for this study. Clinical isolates of MRSA (n = 98) were obtained from patients with cSSSI, bacteremia, endocarditis, osteomyelitis, or foreign body infections. Other clinical isolates included 91 MRCoNS, 131 S. pneumoniae isolates, 203 β-hemolytic streptococci, 8 viridans group streptococci, and 212 VRE. Five reference strains (including three quality control strains and two type strains used for time-kill studies) were also tested.

Telavancin was prepared by Theravance, Inc. (South San Francisco, CA). All other antibiotics for MIC testing were supplied independently by TREK Diagnostic Systems (Cleveland, OH). Comparator agents for time-kill studies included vancomycin (Sigma Chemical Co., St. Louis, MO) and linezolid (Zyvox; Pfizer). Susceptibility tests were performed by reference broth microdilution methodology as defined by the CLSI using frozen form panels prepared by TREK Diagnostic Systems (Cleveland, OH) (3). MICs for all streptococci were determined in panels supplemented with 2 to 5% lysed horse blood. Vancomycin and teicoplanin MIC results were used to define the resistance determinants of VRE. S. pneumoniae strains exhibiting concurrent resistance to at least three of the following agents were defined as MDRSP: cefuroxime, penicillin, tetracycline, erythromycin, or trimethoprim-sulfamethoxazole.

Time-kill experiments were performed according to CLSI (formerly NCCLS) defined methodology (12) for seven isolates: MRSA MED 2028 (osteomyelitis isolate), MRSA MED 1805 (bloodstream isolate), methicillin-resistant S. epidermidis (MRSE) ATCC 35984 (American Type Culture Collection, Manassas, VA), MDRSP MED 1090 (Massachusetts General Hospital, Boston, MA), Streptococcus agalactiae MED 2038 and Streptococcus pyogenes MED 2040 (both cSSSI isolates) (G. R. Corey et al., presented at the 14th Annual Meeting of the Infectious Diseases Society of America, Torono, Canada, 12 to 15 October 2006), and VanB-type vancomycin-resistant Enterococcus faecalis ATCC 51575 (American Type Culture Collection).

The MIC profiles of telavancin and comparator agents against all tested isolates are summarized in Table 1. Based upon MIC90 comparisons, telavancin was among the most-active agents tested against clinical strains of MRSA (MIC90 = 0.5 µg/ml); all isolates were inhibited by ≤1 µg/ml telavancin. Concurrent resistance to comparators had no effect on telavancin activity. Telavancin MICs for two daptomycin-nonsusceptible isolates (daptomycin MICs of 4 and 8 µg/ml) were 0.5 and 0.25 µg/ml. Based upon MIC90 comparisons, daptomycin and quinupristin-dalfopristin were as potent as telavancin, followed by teicoplanin, vancomycin, gentamicin, and linezolid. Trimethoprim-sulfamethoxazole was the most-active agent tested against these strains.


View this table:
[in this window]
[in a new window]

  		TABLE 1. In vitro activity of telavancin against resistant staphylococci, streptococci, and enterococci

The telavancin MIC90 against 74 MRSE and 17 other CoNS that were also resistant to methicillin was 1 µg/ml. Based on MIC90 comparisons, telavancin was more potent against this group of organisms than were vancomycin (MIC90 = 2 µg/ml) and teicoplanin (MIC90 = 16 µg/ml). Telavancin MICs against 16 teicoplanin nonsusceptible MRCoNS ranged from 0.25 to 0.5 µg/ml.

All streptococci were highly susceptible to telavancin, including penicillin-intermediate and -resistant S. pneumoniae and MDRSP (MIC90 = 0.03 µg/ml for all), group A and group B streptococci (MIC90 = 0.06 µg/ml), and viridans group streptococci (MIC range, 0.015 to 0.06 µg/ml). All streptococci were inhibited by ≤0.12 µg/ml of telavancin. The activities of telavancin (MIC90 = 0.03 µg/ml), vancomycin (MIC90 = 0.5 µg/ml), linezolid (MIC90 = 1 µg/ml), and telithromycin (MIC90 = 0.5 µg/ml) against all tested streptococci were unaffected by resistance to other agents, including the activities against MDRSP isolates with concurrent resistance to penicillin, erythromycin, trimethoprim-sulfamethoxazole, cefuroxime, and tetracycline. Some strains of MDRSP tested in this study were also nonsusceptible to other agents, including levofloxacin (5% nonsusceptible; MIC90 = 1 µg/ml), clindamycin (27% nonsusceptible; MIC90 = >0.25 µg/ml), and ceftriaxone (23% nonsusceptible; MIC90 = 2 µg/ml).

Telavancin activity against all 212 tested VRE covered a broad MIC range (0.06 to 32 µg/ml). Based upon MIC90 comparisons, telavancin was at least 32- and 8-fold more active than vancomycin and teicoplanin, respectively, against all tested enterococci. A bimodal distribution of telavancin MICs was observed (Fig. 1). All 32 VanB-type isolates were inhibited by ≤2 µg/ml telavancin and displayed susceptibility (MIC90 = 2 µg/ml) comparable to that reported for vancomycin-sensitive enterococci (7, 8). Telavancin MICs were elevated against VanA-type VRE (MIC50/90 = 8 and 16 µg/ml). Daptomycin and linezolid were the most-active agents tested against the 212 VRE with respective MIC90s of 4 and 2 µg/ml. Quinupristin-dalfopristin was one of the most-active agents against vancomycin-resistant Enterococcus faecium, with an MIC90 of 1 µg/ml.


Figure 1
View larger version (6K):
[in this window]
[in a new window]

  		FIG. 1. Distribution of telavancin MICs against VRE. Filled bars, VanB-type isolates; open bars, VanA-type isolates.

Time-kill curve study results for seven strains are presented in Table 2. Telavancin was bactericidal (≥3-log10 inoculum reduction) against all three methicillin-resistant staphylococci by 8 h at ≥2x MIC. Vancomycin was also bactericidal against these strains, with regrowth seen against the MRSE isolate by 24 h at 8x MIC, while linezolid produced a bactericidal effect at 8x MIC against two of the three strains tested by 24 h. Telavancin was bactericidal against all tested streptococci at concentrations ranging from 2x MIC (0.03 µg/ml) for the MDRSP isolate to 8x MIC (0.5 µg/ml) for the S. pyogenes isolate. Vancomycin and linezolid were both bactericidal against two of the three tested streptococci at 8x MIC. Telavancin and linezolid were both bacteriostatic against the VanB E. faecalis isolate, reducing the initial inoculum by 1.1 and 1.0 log10 CFU/ml, respectively, at 8x MIC.


View this table:
[in this window]
[in a new window]

  		TABLE 2. Kill kinetics of telavancin and comparators against resistant gram-positive isolates

Our results confirm the potent in vitro inhibitory and bactericidal activities of telavancin against important and emerging antimicrobial-resistant, gram-positive pathogens. Based upon MIC90 comparisons, telavancin was consistently more active than vancomycin and teicoplanin against all organisms tested and showed potency equal to or greater than daptomycin and linezolid against all strain types except VanA-type VRE. These results, in concert with previously published reports, highlight the potential role of telavancin in the treatment of serious gram-positive infections and support the continued clinical evaluation of this new agent.


arrow
FOOTNOTES
 
* Corresponding author. Mailing address: Theravance, Inc., 901 Gateway Blvd., South San Francisco, CA 94080. Phone: (650) 808-6158. Fax: (650) 808-6186. E-mail: bbenton{at}theravance.com Back

{triangledown} Published ahead of print on 28 April 2008. Back

{dagger} Present address: NovaBay, Inc., Emeryville, CA 94608. Back


arrow
REFERENCES
 
    1
  1. Baquero, F. 1997. Gram-positive resistance: challenge for the development of new antibiotics. J. Antimicrob. Chemother. 39(Suppl. A):1-6.[Abstract/Free Full Text]
    2. 2
  2. Chambers, H. F. 1997. Methicillin resistance in staphylococci: molecular and biochemical basis and clinical implications. Clin. Microbiol. Rev. 10:781-791.[Abstract]
    3. 3
  3. Clinical and Laboratory Standards Institute. 2006. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically. Approved standard, 7th ed. CLSI document M7-A7. CLSI, Wayne, PA.
    4. 4
  4. Clinical and Laboratory Standards Institute. 2007. Performance standards for antimicrobial susceptibility testing; 15th informational supplement. CLSI document M100-S17. CLSI, Wayne, PA.
    5. 5
  5. Goldstein, E. J., D. M. Citron, C. V. Merriam, Y. A. Warren, K. L. Tyrrell, and H. T. Fernandez. 2004. In vitro activities of the new semisynthetic glycopeptide telavancin (TD-6424), vancomycin, daptomycin, linezolid, and four comparator agents against anaerobic gram-positive species and Corynebacterium spp. Antimicrob. Agents Chemother. 48:2149-2152.[Abstract/Free Full Text]
    6. 6
  6. Hiramatsu, K., L. Cui, M. Kuroda, and T. Ito. 2001. The emergence and evolution of methicillin-resistant Staphylococcus aureus. Trends Microbiol. 9:486-493.[CrossRef][Medline]
    7. 7
  7. Jansen, W. T., A. Verel, J. Verhoef, and D. Milatovic. 2007. In vitro activity of telavancin against gram-positive clinical isolates recently obtained in Europe. Antimicrob. Agents Chemother. 51:3420-3424.[Abstract/Free Full Text]
    8. 8
  8. King, A., I. Phillips, and K. Kaniga. 2004. Comparative in vitro activity of telavancin (TD-6424), a rapidly bactericidal, concentration-dependent anti-infective with multiple mechanisms of action against gram-positive bacteria. J. Antimicrob. Chemother. 53:797-803.[Abstract/Free Full Text]
    9. 9
  9. Leuthner, K. D., C. M. Cheung, and M. J. Rybak. 2006. Comparative activity of the new lipoglycopeptide telavancin in the presence and absence of serum against 50 glycopeptide non-susceptible staphylococci and three vancomycin-resistant Staphylococcus aureus. J. Antimicrob. Chemother. 58:338-343.[Abstract/Free Full Text]
    10. 10
  10. Lowy, F. D. 2003. Antimicrobial resistance: the example of Staphylococcus aureus. J. Clin. Investig. 111:1265-1273.[CrossRef][Medline]
    11. 11
  11. Maranan, M. C., B. Moreira, S. Boyle-Vavra, and R. S. Daum. 1997. Antimicrobial resistance in staphylococci. Epidemiology, molecular mechanisms, and clinical relevance. Infect. Dis. Clin. N. Am. 11:813-849.[CrossRef][Medline]
    12. 12
  12. National Committee for Clinical Laboratory Standards. 1999. Methods for determining bactericidal activity of antimicrobial agents; approved guideline. NCCLS document M26-A. NCCLS, Wayne, PA.
    13. 13
  13. Pace, J. L., K. Krause, D. Johnston, D. Debabov, T. Wu, L. Farrington, C. Lane, D. L. Higgins, B. Christensen, J. K. Judice, and K. Kaniga. 2003. In vitro activity of TD-6424 against Staphylococcus aureus. Antimicrob. Agents Chemother. 47:3602-3604.[Abstract/Free Full Text]

Antimicrobial Agents and Chemotherapy, July 2008, p. 2647-2652, Vol. 52, No. 7
0066-4804/08/$08.00+0     doi:10.1128/AAC.01398-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Kosowska-Shick, K., Clark, C., Pankuch, G. A., McGhee, P., Dewasse, B., Beachel, L., Appelbaum, P. C. (2009). Activity of Telavancin against Staphylococci and Enterococci Determined by MIC and Resistance Selection Studies. Antimicrob. Agents Chemother. 53: 4217-4224 [Abstract] [Full Text]  
  • Lunde, C. S., Hartouni, S. R., Janc, J. W., Mammen, M., Humphrey, P. P., Benton, B. M. (2009). Telavancin Disrupts the Functional Integrity of the Bacterial Membrane through Targeted Interaction with the Cell Wall Precursor Lipid II. Antimicrob. Agents Chemother. 53: 3375-3383 [Abstract] [Full Text]  
  • LaPlante, K. L., Mermel, L. A. (2009). In Vitro Activities of Telavancin and Vancomycin against Biofilm-Producing Staphylococcus aureus, S. epidermidis, and Enterococcus faecalis Strains. Antimicrob. Agents Chemother. 53: 3166-3169 [Abstract] [Full Text]  
  • Charneski, L., Patel, P. N, Sym, D. (2009). Telavancin: A Novel Lipoglycopeptide Antibiotic. The Annals of Pharmacotherapy 43: 928-938 [Abstract] [Full Text]  
  • Hegde, S. S., Difuntorum, S., Skinner, R., Trumbull, J., Krause, K. M. (2009). Efficacy of telavancin against glycopeptide-intermediate Staphylococcus aureus in the neutropenic mouse bacteraemia model. J Antimicrob Chemother 63: 763-766 [Abstract] [Full Text]  

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Krause, K. M.
Right arrow Articles by Benton, B. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Krause, K. M.
Right arrow Articles by Benton, B. M.

Copyright © 2009 by the American Society for Microbiology.   For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»