Lack of correlation of in vitro amphotericin B susceptibility testing withoutcome in a murine model of Aspergillus infection

Amphotericin B has been the standard therapy for invasive aspergillosis sin ce its introduction in 1957. It is only moderately effective. Many suscepti bility tests have been used but little variation has been noted between str ains. We have studied three strains of Aspergillus fumigatus and one of Asp ergillus terreus in a neutropenic mouse model of invasive aspergillosis and attempted to correlate the variable efficacy in vivo with MICs generated b y over 30 different susceptibility test formats. One strain of A. fumigatus (AF65) and the strain of A. terreus(AT49) were 'resistant' and the remainin g two strains of A. fumigatus (AF210 and AF294) were 'susceptible' in vivo. Only AT49 had elevated MICs of amphotericin (MIC greater than or equal to 2 mg/L) by 41 of 54 in vitro testing systems. With each test format, includ ing Etest, there was no distinction between MICs obtained for AF65, AF210 a nd AF294 (MICs 0.125-64 mg/L depending on the test). Thus despite extensive efforts we have been unable to correlate susceptible test results with in vivo outcome in A. fumigatus but we have with A. terreus, with some test fo rmats. This suggests that, at present, amphotericin B susceptibility testin g of A. fumigatus is of limited clinical value and further work needs to be done to find testing systems that can identify the 'resistance' documented in vivo.