Antibiofilm and Anti-��-Lactamase Activities of Burdock Root Extract and Chlorogenic Acid against Klebsiella pneumoniae

Abstract

Small phytochemicals have been successfully adopted as antibacterial chemotherapies and are being increasingly viewed as potential antibiofilm agents. Some of these molecules are known to repress biofilm and toxin production by certain bacterial and yeast pathogens, but information is lacking with regard to the genes allied with biofilm formation. The present study was performed to investigate the inhibitory effect of burdock root extract (BRE) and of chlorogenic acid (CGA; a component of BRE) on clinical isolates of <i>Klebsiella pneumoniae</i>. BRE and CGA exhibited significant antibiofilm activity against <i>K. pneumoniae</i> without inflicting any harm to its planktonic counterparts. In vitro assays supported the β-lactamase inhibitory effect of CGA and BRE while in silico docking showed that CGA bound strongly with the active sites of sulfhydryl-variable-1 β-lactamase. Furthermore, the mRNA transcript levels of two biofilm-associated genes (type 3 fimbriae <i>mrkD</i> and trehalose-6-phosphate hydrolase <i>treC</i>) were significantly downregulated in CGA- and BRE-treated samples. In addition, CGA inhibited biofilm formation by <i>Escherichia coli</i> and <i>Candida albicans</i> without affecting their planktonic cell growth. These findings show that BRE and its component CGA have potential use in antibiofilm strategies against persistent <i>K. pneumoniae</i> infections.