Abstract
The antimicrobial activity of evernimicin (formerly SCH 27899), a novel oligosaccharide antimicrobial of the everninomicin class, was evaluated against four groups of Gram-positive pathogens: (i) Streptococcus pneumoniae (n = 1452); (ii) methicillin- or oxacillin-resistant Staphylococcus aureus (MRSA) and coagulase-negative staphylococci (MR-CoNS; n = 1427); (iii) enterococci (n = 1517); and (iv) non-pneumococcal streptococci (n = 1388), using the Etest method at each study centre throughout Eastern and Western Europe, Scandinavia, South Africa, Turkey and North America. Comparative MICs were determined for a variety of reference compounds, including vancomycin, quinupristin/dalfopristin, chloramphenicol, penicillin, ampicillin, oxacillin, ceftriaxone and ciprofloxacin. Evernimicin was highly active against all strains tested, with MIC90 values ≤1.0 mg/L, ranging from 0.047 mg/L against S. pneumoniae to 1.0 mg/L against MRSA/MR-CoNS and enterococci. Compared with the reference agents, the MIC90 of evernimicin were lower against all species. Against MRSA and MR-CoNS the MIC90s of evernimicin, quinupristin/dalfopristin and vancomycin (the three most active agents) were 1.0, 1.5 and 3.0 mg/L, respectively. Against all species tested, the relative activities and spectra of these agents were: evernimicin > vancomycin > quinupristin/dalfopristin. The Etest proved to be reliable and reproducible, despite occasional interpretive difficulties caused by observer inexperience. Quality control results were excellent among the 33 participant sites. The results of this in vitro, multicentre, multinational study demonstrate that evernimicin possesses high antimicrobial activity against Gram-positive organisms that compares favourably with established antibacterial treatments and newer agents such as quinupristin/dalfopristin. Further clinical investigations of everninomicin class compounds appear warranted.
| Original language | English |
|---|---|
| Pages (from-to) | 15-25 |
| Number of pages | 11 |
| Journal | Journal of Antimicrobial Chemotherapy |
| Volume | 47 |
| Issue number | 1 |
| State | Published - 2001 |
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All Science Journal Classification (ASJC) codes
- Pharmacology
- Microbiology
Cite this
In vitro Gram-positive antimicrobial activity of evernimicin (SCH 27899), a novel oligosaccharide, compared with other antimicrobials : A multicentre international trial. / Jones, R. N.; Hareb, R. S.; Sabatelli, F. J.; Aldridge, K.; Della-Latta, P.; Ferraro, M. J.; Goering, Richard V.; Hindkler, J.; Bruckner, D.; Jacobs, M.; Jones, R.; Low, D.; Medeiros, A.; Boyce, J.; Murray, B.; Baquero, F.; Costa, D.; Frimodt-Møller, N.; Goossens, H.; Graninger, D.; Gudmundsson, S.; Gur, D.; Huovinen, P.; Kettner, M.; Keuleyen, E.; Klugman, K.; Le Clercq, R.; Patzer, J.; Petrikkos, G.; Lingaas, E.; Nord, C.; Reshedko, G.; Stratchounski, L.; Schindler, J.; Schito, G. C.; Jones, M. E.; Wiedemann, B.; Wise, R.
In: Journal of Antimicrobial Chemotherapy, Vol. 47, No. 1, 2001, p. 15-25.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - In vitro Gram-positive antimicrobial activity of evernimicin (SCH 27899), a novel oligosaccharide, compared with other antimicrobials
T2 - A multicentre international trial
AU - Jones, R. N.
AU - Hareb, R. S.
AU - Sabatelli, F. J.
AU - Aldridge, K.
AU - Della-Latta, P.
AU - Ferraro, M. J.
AU - Goering, Richard V.
AU - Hindkler, J.
AU - Bruckner, D.
AU - Jacobs, M.
AU - Jones, R.
AU - Low, D.
AU - Medeiros, A.
AU - Boyce, J.
AU - Murray, B.
AU - Baquero, F.
AU - Costa, D.
AU - Frimodt-Møller, N.
AU - Goossens, H.
AU - Graninger, D.
AU - Gudmundsson, S.
AU - Gur, D.
AU - Huovinen, P.
AU - Kettner, M.
AU - Keuleyen, E.
AU - Klugman, K.
AU - Le Clercq, R.
AU - Patzer, J.
AU - Petrikkos, G.
AU - Lingaas, E.
AU - Nord, C.
AU - Reshedko, G.
AU - Stratchounski, L.
AU - Schindler, J.
AU - Schito, G. C.
AU - Jones, M. E.
AU - Wiedemann, B.
AU - Wise, R.
PY - 2001
Y1 - 2001
N2 - The antimicrobial activity of evernimicin (formerly SCH 27899), a novel oligosaccharide antimicrobial of the everninomicin class, was evaluated against four groups of Gram-positive pathogens: (i) Streptococcus pneumoniae (n = 1452); (ii) methicillin- or oxacillin-resistant Staphylococcus aureus (MRSA) and coagulase-negative staphylococci (MR-CoNS; n = 1427); (iii) enterococci (n = 1517); and (iv) non-pneumococcal streptococci (n = 1388), using the Etest method at each study centre throughout Eastern and Western Europe, Scandinavia, South Africa, Turkey and North America. Comparative MICs were determined for a variety of reference compounds, including vancomycin, quinupristin/dalfopristin, chloramphenicol, penicillin, ampicillin, oxacillin, ceftriaxone and ciprofloxacin. Evernimicin was highly active against all strains tested, with MIC90 values ≤1.0 mg/L, ranging from 0.047 mg/L against S. pneumoniae to 1.0 mg/L against MRSA/MR-CoNS and enterococci. Compared with the reference agents, the MIC90 of evernimicin were lower against all species. Against MRSA and MR-CoNS the MIC90s of evernimicin, quinupristin/dalfopristin and vancomycin (the three most active agents) were 1.0, 1.5 and 3.0 mg/L, respectively. Against all species tested, the relative activities and spectra of these agents were: evernimicin > vancomycin > quinupristin/dalfopristin. The Etest proved to be reliable and reproducible, despite occasional interpretive difficulties caused by observer inexperience. Quality control results were excellent among the 33 participant sites. The results of this in vitro, multicentre, multinational study demonstrate that evernimicin possesses high antimicrobial activity against Gram-positive organisms that compares favourably with established antibacterial treatments and newer agents such as quinupristin/dalfopristin. Further clinical investigations of everninomicin class compounds appear warranted.
AB - The antimicrobial activity of evernimicin (formerly SCH 27899), a novel oligosaccharide antimicrobial of the everninomicin class, was evaluated against four groups of Gram-positive pathogens: (i) Streptococcus pneumoniae (n = 1452); (ii) methicillin- or oxacillin-resistant Staphylococcus aureus (MRSA) and coagulase-negative staphylococci (MR-CoNS; n = 1427); (iii) enterococci (n = 1517); and (iv) non-pneumococcal streptococci (n = 1388), using the Etest method at each study centre throughout Eastern and Western Europe, Scandinavia, South Africa, Turkey and North America. Comparative MICs were determined for a variety of reference compounds, including vancomycin, quinupristin/dalfopristin, chloramphenicol, penicillin, ampicillin, oxacillin, ceftriaxone and ciprofloxacin. Evernimicin was highly active against all strains tested, with MIC90 values ≤1.0 mg/L, ranging from 0.047 mg/L against S. pneumoniae to 1.0 mg/L against MRSA/MR-CoNS and enterococci. Compared with the reference agents, the MIC90 of evernimicin were lower against all species. Against MRSA and MR-CoNS the MIC90s of evernimicin, quinupristin/dalfopristin and vancomycin (the three most active agents) were 1.0, 1.5 and 3.0 mg/L, respectively. Against all species tested, the relative activities and spectra of these agents were: evernimicin > vancomycin > quinupristin/dalfopristin. The Etest proved to be reliable and reproducible, despite occasional interpretive difficulties caused by observer inexperience. Quality control results were excellent among the 33 participant sites. The results of this in vitro, multicentre, multinational study demonstrate that evernimicin possesses high antimicrobial activity against Gram-positive organisms that compares favourably with established antibacterial treatments and newer agents such as quinupristin/dalfopristin. Further clinical investigations of everninomicin class compounds appear warranted.
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M3 - Article
VL - 47
SP - 15
EP - 25
JO - Journal of Antimicrobial Chemotherapy
JF - Journal of Antimicrobial Chemotherapy
SN - 0305-7453
IS - 1
ER -