2012 ©
             Publication
Journal Publication
Research Title Use of human antimicrobial peptides to combat of multidrug-resistant uropathogenic Escherichia coli causing catheter associated urinary tract infections 
Date of Distribution 7 December 2019 
Conference
     Title of the Conference The 49th National Graduate Research Conference : NGRC 
     Organiser Council of the Graduate Studies Administrators of Thailand (CGAT) 
     Conference Place Nakhon Si Thammarat Rajabhat University, Nakhon Si Thammarat, Thailand 
     Province/State Nakhon Si Thammarat, Thailand 
     Conference Date 6 December 2019 
     To 7 December 2019 
Proceeding Paper
     Volume 2562 
     Issue
     Page 199-210 
     Editors/edition/publisher Asst. Prof. Dr. LADAWAN KAEWSEENUAL 
     Abstract Catheter associated urinary tract infections or CAUTIs are one common type of healthcare associated infections. Uropathogenic Escherichia coli (UPEC) plays the leading role in the pathogenesis of CAUTIs, the main issue that make CAUTIs harder to treat is the increasing of drug-resistant incidence. Therefore, novel antimicrobial agent such as cathelicidin antimicrobial peptide (CAMP) was investigated. The aim of this study was to determine the antimicrobial activity of human CAMP (LL-37), its truncated peptide (LL-31) and D-enantiomer form (D-LL-37, D-LL-31, D-LL-13-31 and D-LL-13-37) against clinical isolates of multidrug-resistant (MDR)-UPEC. Ten MDR-UPEC clinical isolates were collected from patients presented with catheter associated urinary tract infections. Antimicrobial susceptibility of all isolates were tested using micro-broth dilution technique and antimicrobial activity of all peptides and time-kill kinetics of the most effective peptide against MDR-UPEC in planktonic form were determined using colony counting assay. The minimal inhibitory concentrations (MICs) and minimal bactericidal concentrations (MBCs) of ceftriaxone against all MDR-UPEC isolates in planktonic form were equal or greater than 1,024 μg/ml. While 20 μM of LL-37, D-LL-37, LL-31 and D-LL-31 exhibited 100% killing activity against MDR-UPEC within 1 hour. Killing kinetics revealed that 1 μM of D-LL-31 displayed the strongest bactericidal activity which can reach the bacterial endpoint within 1 hour against highly resistant isolate, while D-LL-37 which required 24 hours. Moreover, conventional antibiotic ceftriaxone had no killing antimicrobial effect in higher concentration (15 μM) along 24 hours of incubation period. These results indicate that D-LL-31 might be possible to develop as novel antimicrobial agent against CAUTIs in the future. 
Author
605070021-0 Mr. MATAPON PUTTICHAT [Main Author]
Medicine Master's Degree

Peer Review Status มีผู้ประเมินอิสระ 
Level of Conference ชาติ 
Type of Proceeding Full paper 
Type of Presentation Oral 
Part of thesis true 
Presentation awarding false 
Attach file
Citation 0