On the verge of colistin resistance. (c2019)
Colistin has often become the last option to treat infections by carbapenemase producing Klebsiella pneumoniae (CPKP). The PhoPQ two-component system (TCS), insertional inactivation of mgrB gene, and crrAB TCS have recently gained attention as mediators of colistin resistance and lipid A remodeling....
Saved in:
| Main Author: | |
|---|---|
| Format: | masterThesis |
| Published: |
2019
|
| Subjects: | |
| Online Access: | http://hdl.handle.net/10725/11582 https://doi.org/10.26756/th.2019.148 http://libraries.lau.edu.lb/research/laur/terms-of-use/thesis.php |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Summary: | Colistin has often become the last option to treat infections by carbapenemase producing Klebsiella pneumoniae (CPKP). The PhoPQ two-component system (TCS), insertional inactivation of mgrB gene, and crrAB TCS have recently gained attention as mediators of colistin resistance and lipid A remodeling. Through whole-genome sequencing and lipidomic approaches, genetic alterations and lipid A modifications responsible for colistin resistance can be detected with high precision. Three colistin resistant, seven heteroresistant and one susceptible isolate were studied to explore the underlying mechanisms of colistin resistance. Colistin broth microdilution antimicrobial susceptibility testing was performed, coupled with Etest phenotypic testing. The nucleotide sequence of genes encoding for two-component regulatory systems such as phoP, phoQ, pmrA, pmrB, crrA, and crrB were screened in silico. Plasmid encoded mcr-1 gene was screened through in silico PCR. The mgrB gene was screened through PCR and was manually sequenced through sanger sequencing. Core genome single nucleotide polymorphisms (cg-SNP) were analyzed to determine the phylogenetic evolution among the isolates. Lipid A extraction procedure was optimized for Lipopolysaccharide hydrolysis from both Escherichia coli and K. pneumoniae using acetic acid extraction procedure. For the purpose of lipid A detection and profiling, MALDI-TOF MS was operated in the negative reflectron mode and served as a golden standard for lipid A analysis. None of the plasmid encoded colistin resistance genes were detected. PCR amplification of mgrB revealed insertional inactivation Δ in three of the studied isolates (designated as KP5, KP6, and KP16) showing MICs ≥ 64 mg/L. ISKpn14 was associated with KP5 and KP6, while IS903 was detected in KP16. Wild-type mgrB gene in the remaining seven isolates might suggest the involvement of other mechanisms underlying their heteroresistance to colistin. All 11 isolates were negative for the crrA and crrB genes. Lipid A major mass ion was observed at (m/z 1840) in all KP isolates. KP5 had an altered lipid A moiety corresponding to 4-amino-4-deoxy-L-arabinose (L-Ara4N) modification (1892 m/z). This is the first study detecting lipid A modifications in colistin resistant K. penumoniae in Lebanon and the first reporting colistin heteroresistant subpopulations. |
|---|