Physiology of antibiotics lethality in Mycobacteria

The increasing prevalence and spread of drug-resistant strains of M.tuberculosis has resulted in the rise of MDR-TB and XDR-TB cases around the world. This necessitates the need for a better understanding of current bactericidal antibiotics mode of action so as to increase efficacy of current treatm...

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Main Author: Jin, Frances Xin Er
Other Authors: Kevin Pethe
Format: Final Year Project (FYP)
Language:English
Published: 2016
Subjects:
Online Access:http://hdl.handle.net/10356/67197
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author Jin, Frances Xin Er
author2 Kevin Pethe
author_facet Kevin Pethe
Jin, Frances Xin Er
author_sort Jin, Frances Xin Er
collection NTU
description The increasing prevalence and spread of drug-resistant strains of M.tuberculosis has resulted in the rise of MDR-TB and XDR-TB cases around the world. This necessitates the need for a better understanding of current bactericidal antibiotics mode of action so as to increase efficacy of current treatment regimens and uncover novel drug targets. Here we showed that bactericidal antibiotics mode of action induces a death signature involving cellular metabolism. We demonstrated that co-treatment with respiratory inhibitors such as Carbonyl Cyanide m-chlorophenylhydrazone (CCCP) can exert a rescue effect on the killing mechanism of bactericidal antibiotics. Our results suggest that the presence of the death signature is common for at least two different classes of bactericidal antibiotics, and that there is downstream involvement of cellular metabolism processes such as respiration in antibiotics bactericidal mechanism.
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spelling ntu-10356/671972023-02-28T17:59:46Z Physiology of antibiotics lethality in Mycobacteria Jin, Frances Xin Er Kevin Pethe School of Biological Sciences Michelle Ang Lay Teng DRNTU::Science::Biological sciences::Microbiology::Drug Resistance The increasing prevalence and spread of drug-resistant strains of M.tuberculosis has resulted in the rise of MDR-TB and XDR-TB cases around the world. This necessitates the need for a better understanding of current bactericidal antibiotics mode of action so as to increase efficacy of current treatment regimens and uncover novel drug targets. Here we showed that bactericidal antibiotics mode of action induces a death signature involving cellular metabolism. We demonstrated that co-treatment with respiratory inhibitors such as Carbonyl Cyanide m-chlorophenylhydrazone (CCCP) can exert a rescue effect on the killing mechanism of bactericidal antibiotics. Our results suggest that the presence of the death signature is common for at least two different classes of bactericidal antibiotics, and that there is downstream involvement of cellular metabolism processes such as respiration in antibiotics bactericidal mechanism. Bachelor of Science in Biological Sciences 2016-05-12T08:27:11Z 2016-05-12T08:27:11Z 2016 Final Year Project (FYP) http://hdl.handle.net/10356/67197 en Nanyang Technological University 32 p. application/pdf
spellingShingle DRNTU::Science::Biological sciences::Microbiology::Drug Resistance
Jin, Frances Xin Er
Physiology of antibiotics lethality in Mycobacteria
title Physiology of antibiotics lethality in Mycobacteria
title_full Physiology of antibiotics lethality in Mycobacteria
title_fullStr Physiology of antibiotics lethality in Mycobacteria
title_full_unstemmed Physiology of antibiotics lethality in Mycobacteria
title_short Physiology of antibiotics lethality in Mycobacteria
title_sort physiology of antibiotics lethality in mycobacteria
topic DRNTU::Science::Biological sciences::Microbiology::Drug Resistance
url http://hdl.handle.net/10356/67197
work_keys_str_mv AT jinfrancesxiner physiologyofantibioticslethalityinmycobacteria