salicylates and Gram-Positive-Bacterial-Infections

With the increasing reports of community-acquired and nosocomial infection caused by multidrug-resistant Gram-positive pathogens, there is an urgent need to develop new antimicrobial agents with novel antibacterial mechanisms. Here, we investigated the antibacterial activity of the natural product ginkgolic acid (GA) (15:1), derived from Ginkgo biloba, and its potential mode of action against the Gram-positive bacteria Enterococcus faecalis and Staphylococcus aureus. The MIC values of GA (15:1) against clinical E. faecalis and S. aureus isolates from China were ≤4 and ≤8 μg/mL, respectively, from our test results. Moreover, GA (15:1) displayed high efficiency in biofilm formation inhibition and bactericidal activity against E. faecalis and S. aureus. During its inhibition of the planktonic bacteria, the antibacterial activity of GA (15:1) was significantly improved under the condition of abolishing iron homeostasis. When iron homeostasis was abolished, inhibition of planktonic bacteria by GA (15:1) was significantly improved. This phenomenon can be interpreted as showing that iron homeostasis disruption facilitated the disruption of the functions of ribosome and protein synthesis by GA (15:1), resulting in inhibition of bacterial growth and cell death. Genetic mutation of ferric uptake regulator (Fur) led to GA (15:1) tolerance in

Topics: Animals; Anti-Bacterial Agents; Enterococcus faecalis; Female; Ginkgo biloba; Gram-Positive Bacterial Infections; Homeostasis; Humans; Iron; Mice; Mice, Inbred BALB C; Microbial Sensitivity Tests; Plant Extracts; Salicylates; Staphylococcus aureus

Implanted biomaterials could provide surface for bacterial adherence and formation of biofilm, eventually leading to biomaterial-centered infections (BCIs). In this in vitro study, we examined the biofilm-forming capacity of Enterococcus faecalis on gutta-percha (GP) points under different nutrient status and surface conditioning with saliva and serum.. GP points (n = 420) coated with different root canal sealers (Sealapex or Roth) were conditioned with saliva or serum for 2-, 4-, and 12-week intervals and subsequently were incubated with E. faecalis for 2 weeks under nutrient-rich and nutrient-deprived environments. The biofilm-forming capacity and the nature of biofilm formed on GP were assessed by using a viable cell assay and scanning electron microscopy (SEM).. E. faecalis produced biofilms on GP points (with and without root canal sealers) under both nutrient-rich and nutrient-deprived environments after conditioning with saliva or serum. SEM reflected that the biofilms formed under nutrient-rich conditions were regular, whereas the biofilms formed under nutrient-deprived conditions were irregular and scanty. Under nutrient-deprived conditions, longer conditioning periods in saliva or serum were required for bacterial adherence.. Under the conditions of this study, saliva and serum conditioning of GP points plays an important role in the biofilm formation under tough environmental conditions.

Topics: Bacterial Adhesion; Bacteriological Techniques; Biofilms; Blood; Calcium Hydroxide; Colony Count, Microbial; Culture Media; Enterococcus faecalis; Gram-Positive Bacterial Infections; Gutta-Percha; Humans; Materials Testing; Microscopy, Electron, Scanning; Root Canal Filling Materials; Salicylates; Saliva; Surface Properties; Time Factors; Tooth, Nonvital; Zinc Oxide-Eugenol Cement