dc.contributor.author |
Tokajian, Sima |
|
dc.contributor.author |
Eisen, Jonathan |
|
dc.contributor.author |
Jospin, Guillaume |
|
dc.contributor.author |
Coil, David |
|
dc.date.accessioned |
2016-04-05T09:48:39Z |
|
dc.date.available |
2016-04-05T09:48:39Z |
|
dc.date.copyright |
2015 |
|
dc.date.issued |
2016-04-05 |
|
dc.identifier.issn |
2235-2988 |
en_US |
dc.identifier.uri |
http://hdl.handle.net/10725/3487 |
|
dc.description.abstract |
Objective: The emergence of extended-spectrum β-lactamase (ESBL)-producing bacteria is now a critical concern. The ESBL-producing Klebsiella pneumoniae constitutes one of the most common multidrug-resistant (MDR) groups of gram-negative bacteria involved in nosocomial infections worldwide. In this study we report on the molecular characterization through whole genome sequencing of an ESBL-producing K. pneumoniae strain, LAU-KP1, isolated from a stool sample from a patient admitted for a gastrointestinal procedure/surgery at the Lebanese Amrican University Medical Center-Rizk Hospital (LAUMCRH) in Lebanon.
Methods: Illumina paired-end libraries were prepared and sequenced, which resulted in 4,220,969 high-quality reads. All sequence processing and assembly were performed using the A5 assembly pipeline.
Results: The initial assembly produced 86 contigs, for which no scaffolding was obtained. The final collection of contigs was submitted to GenBank. The final draft genome sequence consists of a combined 5,632,663 bases with 57% G+C content. Automated annotation was performed using the RAST annotation server. Sequencing analysis revealed that the isolate harbored different β-lactamase genes, including blaoxa−1, blaCTX−M−15, blaSHV−11, and blaTEM−1b. The isolate was also characterized by the concomitant presence of other resistance determinants most notably acc(6′)-lb-cr and qnrb1. The entire plasmid content was also investigated and revealed homology with four major plasmids pKPN-IT, pBS512_2, pRSF1010_SL1344, and pKPN3.
Conclusions: The potential role of K. pneumonia as a reservoir for ESBL genes and other resistance determinants is along with the presence of key factors that favor the spread of antimicrobial resistance a clear cause of concern and the problem that Carbapenem-non-susceptible ESBL isolates are posing in hospitals should be reconsidered through systematic exploration and molecular characterization. |
en_US |
dc.language.iso |
en |
en_US |
dc.title |
Whole genome sequencing of extended-spectrum β-lactamase producing Klebsiella pneumoniae isolated from a patient in Lebanon |
en_US |
dc.type |
Article |
en_US |
dc.description.version |
Published |
en_US |
dc.author |
Coil, David |
|
dc.author.school |
SAS |
en_US |
dc.author.idnumber |
199736770 |
en_US |
dc.author.idnumber |
200804713 |
|
dc.author.woa |
N/A |
en_US |
dc.author.department |
Natural Sciences |
en_US |
dc.description.embargo |
N/A |
en_US |
dc.relation.journal |
Frtontiers in Cellular and Infection Microbiology |
en_US |
dc.journal.volume |
5 |
en_US |
dc.article.pages |
1-7 |
|
dc.keywords |
ESBL |
en_US |
dc.keywords |
Klebsiella pneumoniae |
en_US |
dc.keywords |
Whole genome sequencing |
en_US |
dc.keywords |
CTX-M-15 |
en_US |
dc.keywords |
SHV-11 |
en_US |
dc.identifier.doi |
http://dx.doi.org/10.3389/fcimb.2015.00032 |
en_US |
dc.identifier.ctation |
Tokajian, S., Eisen, J. A., Jospin, G., Farra, A., & Coil, D. A. (2015). Whole genome sequencing of extended-spectrum β-lactamase producing Klebsiella pneumoniae isolated from a patient in Lebanon. Frontiers in cellular and infection microbiology, 5. |
en_US |
dc.author.email |
stokjian@lau.edu.lb |
|
dc.author.email |
anna.farra@lau.edu.lb |
|
dc.identifier.url |
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4389573/ |
|
dc.orcid.id |
https://orcid.org/0000-0002-3653-8940 |
|