dc.contributor.author | Ellafi(, Abaq | |
dc.date.accessioned | 2020-07-07T10:09:37Z | |
dc.date.available | 2020-07-07T10:09:37Z | |
dc.date.issued | 2020-02-25 | |
dc.identifier.uri | http://repository.limu.edu.ly/handle/123456789/1727 | |
dc.description | Antimicrobial resistance (AMR) has been revealed to be a major threat to public health.
Invasive bacterial infections are the leading cause of child mortality and morbidity around
the world [1]. With the growing occurrence of AMR, controlling such bacterial infections
has become more and more challenging. If action is not taken to manage the situation it is
predicated that by 2050 AMR will result in 10 million deaths per year [2]. AMR occurs
when bacteria or other microbes resist the effects of an antibiotic, the microbe becomes
immune and reduces or eliminates the effectiveness of drugs, chemicals, or other agents
that are designed to cure or prevent infections [3]. In general, resistance to antibiotics
occurs by chromosomal mutations or horizontal gene transfer of resistance elements [4].
The aim is to validate the putative synthetic lethal/sick interactions of quinolone resistance
mutations in conditional knockout strain of E. coli. | en_US |
dc.description.abstract | Antimicrobial resistance (AMR) occurs when microbes become resistant to the antibiotics
that are designed to cure them. Genetic interactions or epistasis of AMR mutations play an
important role in determining the predictability and the persistence of AMR. Synthetic
lethality is an example of genetic interactions, whereby when separated two mutations are
viable but when combined are lethal. This validates the putative synthetic lethal/sick
interactions of quinolone resistance mutations in 17 conditional knockout E. coli strains.
The quinolone resistance mutations examined were gyrase A (gyrA) mutations, which
include S83L, D87N or S83L-D87N combined. The results showed that 16/17 knockout
strains showed reduced phenotypic fitness. Genes whose knockout alleles are synthetically
lethal with one or more AMR mutation are potential candidates as drug targets. This study
has demonstrated a new therapeutic method to combat AMR mutations by utilizing the
concept of synthetic lethal interactions. | en_US |
dc.language.iso | en | en_US |
dc.publisher | faculty of Basic Medical Science - Libyan International Medical University | en_US |
dc.rights | Attribution 3.0 United States | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/us/ | * |
dc.title | Investigating the effects of genetic background on the fitness of quinolone resistant mutations in Escherichia coli | en_US |
dc.type | Other | en_US |