Role of bacterial antioxidant defense in their resistance to bact | 59996
Journal of Infectious Diseases & Preventive Medicine

Journal of Infectious Diseases & Preventive Medicine
Open Access

ISSN: 2329-8731

Role of bacterial antioxidant defense in their resistance to bactericidal antibiotics

Virtual Meet on Emerging Diseases 2021 & Structural Biology 2021

October 22, 2021 WEBINAR

A. C. Matin

University of California, USA

Keynote: J Infect Dis Preve Med

Abstract :

Sigma S (ss) controls the synthesis of resistance proteins in stationary pathogenic bacteria [(e.g., Escherichia coli (UPEC)]. Deletion of the rpoS gene rendered E. coli more sensitive to bactericidal antibiotics (BAs): gentamicin, nnorfloxacin and ampicillin. Proteomic analysis implicated a weakened antioxidant defense (AD). Use of the psfiA genetic reporter, 3-(p-hydroxyphenyl) fluorescein (HPF) dye, and Amplex Red showed that BAs generated more oxidative stress (OS) in the mutant. Co-administration of the antioxidant N-acetyl cysteine (NAC) and treatment under anaerobic conditions decreased drug lethality of the mutant, further indicating AD involvement. The greater OS in this strain results from impaired capacity to quench endogenous ROS, e.g., respiration linked electron leakage. Infection by UPEC in mice showed that AD was important for UPEC antibiotic reistance also in vivo. Disruption of AD by eliminating quencher proteins, or those of pentose phosphate pathway (which provides NADPH for quenching oxygen radicals) also generated greater OS and killing by BAs. Thus, BAs kill stationary-phase bacteria also by generating OS, and targeting AD can therefore enhance their efficacy. Using bioinformatics, small molecule compounds were identified towards this end, and initial results have given promising results. In space flights, astronauts often suffer from UPEC infection. The EcAMSat mission, using a highly sophisticated microfluidic system showed that UPEC missing ss had increased sensitivity to gentamicin also in space. We have also developed method for determining resistance at single cell level. Together, these results promise to provide powerful means to combat bacterial antibiotic resistance.

Biography :

A. C. Matin obtained his PhD from University of California. He served as a group leader at State University of Groningen, The Netherlands before joining Stanford, where he has been full professor for several years. He has served on several professional pannels and editorial boards and is recipient of many awards. He is an elected fellow of American Academy of Microbiology.

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