Frontiers in Microbiology · 2017 · 192 citations · 28 references
Life SciencesInfectious DiseasesMicrobiologyAntimicrobial ResistanceMedical MicrobiologyMicrobial BiotechnologyAntibacterial TherapyAntibiotic ResistanceAntimicrobial TherapyBacterial BiofilmsBiofilm Formation In InfectionResistance In Gram-negative BacteriaAcinetobacter Baumannii ResistanceAnti-biofilm StrategiesAntimicrobial Drug DevelopmentBacterial Biofilm ControlBiofilm-disrupting AgentsLysozyme ActivityNovel Antibacterial Drug DiscoveryPseudomonas Aeruginosa Resistance
The global increase in multidrug-resistant (MDR) bacteria has led to phage therapy being refocused upon. A novel endolysin, LysPA26, containing a lysozyme-like domain, was screened against Pseudomonas aeruginosa in this study. It had activity against MDR P. aeruginosa without pretreatment with an outer-membrane permeabilizer. LysPA26 could kill up to 4 log units P. aeruginosa in 30 min. In addition, temperature and pH effect assays revealed that LysPA26 had good stability over a broad range of pH and temperatures. Moreover, LysPA26 could kill other Gram-negative bacteria, such as Klebsiella pneumonia, Acinetobacter baumannii and Escherichia coli, but not Gram-positive bacteria. Furthermore, LysPA26 could eliminate P. aeruginosa in biofilm formation. Our current results show that LysPA26 is a new and promising antimicrobial agent for the combat of Gram-negative pathogens.
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