Bactericidal Activity of a Self-Biodegradable Lysine-Containing Dendrimer against Clinical Isolates of Acinetobacter Genus
The genus consists of Gram-negative obligate aerobic pathogens, including clinically relevant species, such as , which frequently cause hospital infections, affecting debilitated patients. The growing resistance to antimicrobial therapies shown by is reaching unacceptable levels in clinical practice...
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Veröffentlicht in: | International journal of molecular sciences 2021-07, Vol.22 (14), p.7274 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The genus
consists of Gram-negative obligate aerobic pathogens, including clinically relevant species, such as
, which frequently cause hospital infections, affecting debilitated patients. The growing resistance to antimicrobial therapies shown by
is reaching unacceptable levels in clinical practice, and there is growing concern that the serious conditions it causes may soon become incurable. New therapeutic possibilities are, therefore, urgently needed to circumvent this important problem. Synthetic cationic macromolecules, such as cationic antimicrobial peptides (AMPs), which act as membrane disrupters, could find application in these conditions. A lysine-modified cationic polyester-based dendrimer (G5-PDK), capable of electrostatically interacting with bacterial surfaces as AMPs do, has been synthesized and characterized here. Given its chemical structure, similar to that of a fifth-generation lysine containing dendrimer (G5K) with a different
, and previously found inactive against Gram-positive bacterial species and
, the new G5-PDK was also ineffective on the species mentioned above. In contrast, it showed minimum inhibitory concentration values (MICs) lower than reported for several AMPs and other synthetic cationic compounds on
genus (3.2-12.7 µM). Time-kill experiments on
,
, and
ascertained the rapid bactericidal effects of G5-PDK, while subsequent bacterial regrowth supported its self-biodegradability. |
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ISSN: | 1422-0067 1661-6596 1422-0067 |
DOI: | 10.3390/ijms22147274 |