Mg. Cormican et al., AVOPARCIN, A GLYCOPEPTIDE USED IN ANIMAL FOODS - ANTIMICROBIAL SPECTRUM AND POTENCY TESTED AGAINST HUMAN ISOLATES FROM THE UNITED-STATES, Diagnostic microbiology and infectious disease, 29(4), 1997, pp. 241-248
Avoparcin is a glycopeptide antimicrobial that is widely used as a gro
wth promoter in animal feeds in portions of Western Europe. Recently,
concern has emerged about the possible contribution of avoparcin use t
o the emergence of glycopeptide resistance in enterococci. Relatively
little information exists on the spectrum of activity and potency of a
voparcin. We studied the activity of avoparcin compared to vancomycin,
teicoplanin, and 3 other antimicrobials against 814 recent human clin
ical isolates, including Staphylococcus spp. (240 strains), Streptococ
cus spp. (90 strains), and Enterococcus spp. (60 strains), using refer
ence susceptibility test methods. Our results indicate that avoparcin
was less potent than either vancomycin or teichoplanin against staphyl
ococci (MIC50, 4 mu g/mL). There was a good correlation of avoparcin M
ICs with the MICs for vancomycin and teichoplanin for most species; ho
wever, the avoparcin MICs for Enterococcus spp. of the vanB phenotype
were quite variable (MIG range, 2 to >16 mu g/mL). For Staphylococcus
haemolyticus, high avoparcin MICs (greater than or equal to 16 mu g/mL
) were associated with oxacillin resistance. These results are relevan
t to the debate concerning the appropriateness of continued use of avo
parcin as a growth promoter in animal husbandry. In particular, avopar
cin as a glycopeptide with limited potency against some staphylococci
seems to represent a theoretically greater risk for selecting glycopep
tide resistance among staphylococci, but may not represent any greater
threat for the selection of resistance in enterococci. (C) 1997 Elsev
ier Science Inc.