Day 1 :
Keynote Forum
Tony Velkov
University of Melbourne, Australia
Keynote: From breast cancer to antimicrobial: Combating extremely-resistant Gram-negative superbugs using novel combinations of polymyxin B with selective estrogen receptor modulators
Time : 9:30 am-10:30
Biography:
Tony Velkov is a principal research fellow & NHMRC CDF Level 2 Industry fellow. He is currently pursuing his research as an associate professor in Pharmacology & Therapeutics in the University of Melbourne.
Abstract:
Novel therapeutic approaches are urgently needed to combat nosocomial infections caused by Extremely Drug Resistant (XDR) superbugs. This study aimed to investigate the synergistic antibacterial activity of polymyxin B in combination with Selective Estrogen Receptor Modulators (SERMs) against problematic Gram-negative pathogens. In vitro synergistic antibacterial activity of polymyxin B and the SERMs Tamoxifen, Raloxifene and Toremifene was assessed using the micro dilution checkerboard and static time-kill assays against a panel of Gram-negative isolates. Polymyxin B and the SERMs were ineffective when used as monotherapy against polymyxin-resistant (MIC≥8 mg/L) Pseudomonas aeruginosa, Klebsiella pneumoniae and Acinetobacter baumannii. However, when used in combination, clinically relevant concentrations of polymyxin B and SERMs displayed synergistic killing against the polymyxin-resistant P. aeruginosa, K. pneumoniae and A. baumannii isolates as demonstrated by a ≥2-3 log10 decrease in bacterial count (CFU/ml) after 24 hours. The combination of polymyxin B with Toremifene demonstrated very potent antibacterial activity against P. aeruginosa biofilms in an artificial sputum media assay. Moreover, polymyxin B combined with Toremifene synergistically induced cytosolic GFP release, cytoplasmic membrane depolarization, permeabilizing activity in a nitrocefin assay and an increase of cellular reactive oxygen species from P. aeruginosa cells. Additionally, scanning and transmission electron micrographs showed that polymyxin B in combination with Toremifene causes distinctive damage to the outer membrane of P. aeruginosa cells, compared to treatments with each compound per se. In conclusion, the combination of polymyxin B and SERMs illustrated a synergistic activity against XDR Gram-negative pathogens including highly polymyxin-resistant P. aeruginosa isolates and represents a novel combination therapy strategy for the treatment of infections due to problematic XDR Gram-negatives.
Keynote Forum
Ahmet Katı
University of Health sciences, Turkey
Keynote: Biosynthesis of silver nanoparticles and their versatile antimicrobial properties
Time : 11:00-12:00
Biography:
Ahmet Katı is currently working as an assistant professor in University of Health sciences, Turkey. He was an industrial microbiologist and working as a Research Scientist in Hayat Kimya R&D Center. He is head of Biotechnology research laboratory, coordinating multidisciplinary studies with other internal R&D teams. He is an expert about preservatives which are using household cleaners and cosmetic products. He received a PhD degree in Biotechnology from Yeditepe University, Istanbul. His research area is focusing on industrial enzymes, preservatives, biocidal products and regulations, developing new antimicrobial agents and probiotics.
Abstract:
- Human Virology and Infectious Diseases | Viral Oncology | Antibiotics, Antimicrobials and Chemotherapy | Infection and Immunity | Biofuels and Petroleum Microbiology | Biofilms Formation | Antimicrobial Drugs
Location: Renaissance polat Istanbul Hotel
Chair
Ahmet Kati
University of Health Sciences, Turkey
Session Introduction
Lina M Elsalem,
Jordan University of Science & Technology, Jordan
Title: Synergistic effects of antimicrobial peptide WLBU2 combined with antibiotics against multidrug-resistant bacteria associated with wound infections
Biography:
Lina M Elsalem has completed her PhD in Pharmacology from Faculty of Life Sciences at University of Bradford, UK. She is currently working as an Assistant Professor in the Department of Pharmacology at Faculty of Medicine, Jordan University of Science and Technology.
Abstract:
Microbial resistance against conventional antibiotics is considered as a substantial health and economic burden to any health care system. Accordingly, research in the antimicrobial field has been directed toward the development of new agents such as the engineered cationic amphipathic peptide WLBU2. The aims of this study are: To evaluate the antimicrobial effects of WLBU2 against multi-drug resistant strains of bacteria including Gram-negative Enterobacter cloacae (ESBL+ve) and Gram-positive Methicillin-resistant Staphylococcus aureus (MRSA) and to assess whether synergistic effects can be achieved upon combination treatment of WLBU2 with conventional antibiotics. Clinical isolates of Enterobacter cloacae (ESBL+ve) and MRSA (n=30 for each) were obtained from wound infections in microbiology laboratories of the Jordanian Royal Medical Services. The Minimum Inhibitory Concentration (MIC) for WLBU2 and conventional antibiotics were determined using the microbroth dilution assay, according to CLSI-2017 guidelines. The antibiotics Ceftazidime, Ciprofloxacin and Ceftriaxone were used for Enterobacter cloacae (ESBL+ve), while MRSA was treated with Oxacillin and Erythromycin. The Fractional Inhibitory Concentration (FIC) index was utilized to determine the relationship between antimicrobial agents upon combination of sub-inhibitory concentration of WLBU2 with conventional antibiotics. The MIC for WLBU2 against Enterobacter cloacae (ESBL+ve) and MRSA ranged from (1.5 to 12.5) μg/ml and (0.78125 to 6.25) μg/ml, respectively. Synergistic and additive effects were achieved in Enterobacter cloacae (ESBL+ve) upon combination treatment with Ceftazidime (n=7/30, 17/30), Ciprofloxacin (n=9/30, 17/30) and Ceftriaxone (n=10/30, 17/30) respectively. Regarding MRSA, synergistic and additive effects were obtained with Erythromycin- WLBU2 treatment (n=2/30 and 10/30, respectively), while only additive effects were observed with Oxacillin- WLBU2 combination (n=14/30). Our data reveal that WLBU2 is a potent peptide with antimicrobial activity against Enterobacter cloacae (ESBL+ve) and MRSA. Our findings also support the development of WLBU2 in combination with conventional antibiotics with potential application for treatment of multidrug resistant bacteria associated with wound infections.
Biography:
Samia Hamma-Faradji is a teacher & researcher in the University of Bejaia, Algeria.
Abstract:
Mounira Kara Ali
Boumardes University, Algeria
Title: Kinetic models and parameters estimation study of bioethanol production from inulin using P. caribbica
Biography:
Abstract:
Miyanou Rosales-Hurtado
Université de Nîmes, France
Title: Synthesis of new analogs of diaminopimelic acid (DAP) and lysine
Biography:
Abstract:
Melike Tepe
Gebze Technical University, Turkey
Title: Antibacterial effects of deoxsyhikonin produced by hairy root culture
Biography:
Abstract:
- Clinical Microbiology | Bacterial and Viral Vaccines | Medical Virology, Clinical and Diagnostic Virology | Diagnosis and Treatment of Infectious Diseases | Bacterial and Viral Vaccines | Vector Borne and Zoonotic Infectious Diseases
Location: Renaissance polat Istanbul Hotel
Chair
Hsiu-Jung Lo
National Health Research Institutes, Taiwan
Session Introduction
Zohra Benfodda
Université De Nîmes, France
Title: Rational design, synthesis and antimicrobial properties of thiophene derivatives that inhibit bacterial histidine kinases
Biography:
Abstract:
Biography:
Negar Zarif Zargarian Talasaz is a research student in Dr. Masih Daneshvari Hospital, Iran