Abstract:
Since the first rise of extended spectrum beta lactamases (ESBL), ESBLproducing
organisms have posed a remarkable threat to hospitalized patients due to their
activity against cephalosporins, restricting available treatment option. This rapid
emergence of ESBLs has been confronted by limited data regarding both phenotypic
and genotypic profiles. This lack of information requires more exploration. The aim of
this study was, in the first place, to investigate the effect of garlic (A ilium sativum)
ethanolic plant extract against ESBL- producing Escherichia co/i and its effect in
combination with cefotaxime, and secondly, to characterize the genotypic properties of
ESBL-producing E. co/i and correlate it with the efficacy of the combinations of
cefotaxime and garlic. The methods used included the agar-well diffusion method to
determine the inhibition zone with the double disk synergy test, the microdilution
method to determine minimum inhibitory concentration (MIC), the checkerboard
technique to quantitatively determine the ameliorative effect, and the polymerase chain
reaction method to detect genotypically ESBL genes. The results showed that 30 tg
cefotaxime had inhibition zones ranging between 7 and 22mm against ESBL-producing
E. co/i indicating that all isolates as resistant to cefotaxime. Using the checkerboard
method, all the combinations of ethanolic garlic extract and CTX showed indifference
except for some combinations that demonstrated an antagonistic activity with FIC>4.
PCR analyses showed that the most common ESBL gene belonged to the CTX-M
group. All isolates of E. co/i, except isolate 2, contain this allele according to the
following proportions: 36.36% harbored CTX-M gene only, 36.36% harbored CTX-M
and OXA genes, and 9.09% harbored CTX-M and TEM. TEM was found in 18.18% of
the isolates. No correlation between the phenotype and the genotype of the bacteria was
Fill found. A highly resistant isolate of ESBL-producing E. coil (isolate 2) to garlic
ethanolic extract was discovered. Further research is needed in order to understand the
mechanism of this resistance.
Description:
M.S. -- Faculty of Natural and Applied Sciences, Notre Dame University, Louaize, 2018; "A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in Biology"; Includes bibliographical references (leaves 33-46).