Xianzhen Feng, Jianing Zhang, Alan Fernando Rodríguez-Serrano, Jinqing Huang, I-Ming Hsing
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引用次数: 0
Abstract
Effective wound-infection management requires reducing bacterial load and avoiding the formation of bacterial biofilms. In this study, we characterized the structure, composition, and function of mucin extracted from the porcine stomach and demonstrated its pH responsiveness, bacterial load control, and biofilm disruption capabilities. The microstructure of the mucin extract shifts from aggregated to relaxed state and its structure changes from gel to solution as its surrounding pH increases. The deterioration of wounds, characterized, among others, by changes in pH, can be monitored by observing changes in the apparent structural features of the mucin extract, e.g., turbidity. Moreover, the extract displays membrane toxicity against lipid membranes and bacteriostatic effects on both gram-negative and gram-positive bacteria. Notably, the extract also promotes the dispersion of bacterial biofilms after 24 h and 48 h of formation. The biocompatibility, pH responsiveness, and antibiofilm properties of mucin present a novel approach for treating chronic wound infections.
期刊介绍:
ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to:
* Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials.
* Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets.
* Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance.
* Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents.
* Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota.
* Small molecule vaccine adjuvants for infectious disease.
* Viral and bacterial biochemistry and molecular biology.