Abstract
The emergence of Acinetobacter sp. strains resistant to all antibacterial agents including colistin necessitates the development of new types of antimicrobial agents. Six cationic α-helical frog skin-derived peptides (CPF-AM1, PGLa-AM1, B2RP-ERa, [E4K]alyteserin-1c, [D4K]B2RP and [G4K]XT-7) were selected for this study on the basis of potent growth-inhibitory activity against Gram-negative bacteria and low haemolytic activity against human erythrocytes. All peptides were active against a range of colistin-susceptible [minimum inhibitory concentration (MIC) ≤ 2 μg/mL] and colistin-resistant (MIC ≥ 64 μg/mL) clinical isolates of multidrug-resistant strains of Acinetobacter baumannii and Acinetobacter nosocomialis. The most potent peptides against the colistin-resistant strains were [D4K]B2RP and [E4K]alyteserin-1c (MIC = 4-16 μg/mL for both). The MIC values of these peptides against the colistin-susceptible strains were in the same range. The frog peptides show potential for development into drugs to treat infections caused by pandrug-resistant Gram-negative pathogens.
| Original language | English |
|---|---|
| Pages (from-to) | 317-320 |
| Number of pages | 4 |
| Journal | International Journal of Antimicrobial Agents |
| Volume | 39 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published (in print/issue) - Apr 2012 |
Funding
Funding : This work was supported by a Faculty Support Grant ( NP-10-11/103 ) and a University Research Grant from the United Arab Emirates University (Al-Ain, United Arab Emirates).
| Funders | Funder number |
|---|---|
| United Arab Emirates University |
Keywords
- Acinetobacter baumannii
- Antimicrobial peptide
- Colistin resistance
- Frog skin