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. 2011 Apr;55(4):1728-33.
doi: 10.1128/AAC.00862-10. Epub 2011 Jan 31.

In vivo efficacy of the novel aminoglycoside ACHN-490 in murine infection models

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In vivo efficacy of the novel aminoglycoside ACHN-490 in murine infection models

Noe Reyes et al. Antimicrob Agents Chemother. 2011 Apr.

Abstract

Aminoglycosides are broad-spectrum antibiotics with particular clinical utility against life-threatening infections. As resistance to antibiotics, including aminoglycosides, continues to grow, there is a need for new and effective antimicrobial agents. ACHN-490 is a novel aminoglycoside in clinical development with activity against multidrug-resistant Gram-negative and select Gram-positive pathogens. Here we assess the in vivo efficacy of ACHN-490 against a variety of common pathogens in two murine models: the septicemia and neutropenic thigh models. When its activity against a gentamicin-susceptible strain of Escherichia coli was tested in the septicemia model, ACHN-490 improved 7-day survival with a dose-response profile similar to that of gentamicin, with 100% survival seen at doses of 1.6 mg/kg of body weight and above. In animals infected with a gentamicin-susceptible strain of Pseudomonas aeruginosa, treatment with either ACHN-490 or gentamicin led to 100% survival at doses of 16 mg/kg and above in the septicemia model. ACHN-490 was also effective in the neutropenic thigh model, reducing multidrug-resistant Enterobacteriaceae family and methicillin-resistant Staphylococcus aureus strains, as well as broadly susceptible strains, to static levels with dose-dependent activity. Against gentamicin-sensitive Enterobacteriaceae and methicillin-resistant S. aureus, the efficacy of ACHN-490 was comparable to that of gentamicin. However, gentamicin-resistant Enterobacteriaceae strains and those harboring the Klebsiella pneumoniae carbapenemase responded to ACHN-490 but not gentamicin, with static doses ranging from 12 mg/kg to 64 mg/kg for ACHN-490. These results suggest that ACHN-490 has the potential to become a clinically useful agent against drug-resistant pathogens, including Enterobacteriaceae, P. aeruginosa, and methicillin-resistant S. aureus, and support further development of this promising novel aminoglycoside.

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Figures

FIG. 1.
FIG. 1.
Structure of ACHN-490.
FIG. 2.
FIG. 2.
Efficacy of ACHN-490 and comparator aminoglycosides in septicemia model.
FIG. 3.
FIG. 3.
Efficacy of ACHN-490 and comparator antibiotics against Enterobacteriaceae in neutropenic thigh model.
FIG. 4.
FIG. 4.
Efficacy of ACHN-490 and comparator antibiotics against S. aureus in neutropenic thigh model.

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References

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