dc.contributor.author |
Mustafa Zeeshan |
|
dc.date.accessioned |
2021-01-01T06:12:57Z |
|
dc.date.available |
2021-01-01T06:12:57Z |
|
dc.date.issued |
2018 |
|
dc.identifier.uri |
http://10.250.8.41:8080/xmlui/handle/123456789/20294 |
|
dc.description.abstract |
Multi-drug resistance has grown to be a major global health issue in recent years hindering the
use of bactericidal drugs in effective treatment of infections. Carbapenem is considered the
effective remedy drug against antibiotic-resistant Pseudomonas aeruginosa which is at the top
of the list for a range of life-threatening infections. Rapid emergence of Carbapenem resistance
in recent years in P.aeruginosa and its high propensity of resistance genes integration across
multiple bacterial species is posing aserious threat that needs to be addressed immediately.
Different Carbapenem resistant genes has detected successfully in multi-drug resistant strains
of A. bumanii and K. pneumoniae. Here we evaluate aquirred carbapenem resistance genes
emergence in P. aeruginosa by Multiplex PCR. Our target genes were blaKPC, blaNDM,
blaVIM, blaSIM, blaSPM, blaIMP, blaOXA, and blaAIM. We anticipate that bacteria acquired
antibiotic resistance genes in stress condition to overcome or efflux antibiotics. Bacterial
resistome analysis enable us to limit the application of unnecessary use of range of antibiotics
and move towards its vaccine development or effective therapies. In result we found blaNDM
presence 6% and blaVIM presence 30%. Later in genome analysis we used resfinder 2.0 and
found OXA 10 and OXA 50 as well but amazing thing in CARD most antibiotic resistance
present because of point mutation. We also highlighted the virulence part of bacteria in DNA
Plotter by which we can design a vaccine for future preventive treatment. P. aeruginosa isn’t
simple as we used Island Viewer to check its ability to acquire the necessary genes by various
ways like conjugation and phages. Our strain have no plasmid checked by PlasmidFinder 1.3
which clears the thing acquired gene comes through phages because we found some phage
sequences in the sequence Phaster 3.0. We did its core and pan phylogeny through BPGA. P.
aeruginosa evolved within Asian region and acquired genes to neighborhood. It is current real
threat to the public health we should work on it. |
en_US |
dc.description.sponsorship |
Dr. Saadia Andleeb |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Atta Ur Rahman School of Applied Biosciences (ASAB), NUST |
en_US |
dc.subject |
CLINICAL ISOLATES, PHENOTYPIC AND GENOTYPIC ANALYSIS |
en_US |
dc.title |
PHENOTYPIC AND GENOTYPIC ANALYSIS OF CARBAPENEM RESISTANT PSEUDOMONAS AERUGINOSA CLINICAL ISOLATES |
en_US |
dc.type |
Thesis |
en_US |