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Article

Plasmid Identification and Plasmid-Mediated Antimicrobial Gene Detection in Norwegian Isolates

by
Abdolrahman Khezri
1,
Ekaterina Avershina
1,2 and
Rafi Ahmad
1,3,4,*
1
Department of Biotechnology, Inland Norway University of Applied Sciences, 2318 Hamar, Norway
2
Laboratory or Postgenomic Technologies, Izmerov Research Institute of Occupational Health, 105275 Moscow, Russia
3
Division of Medical Services-Clinical Microbiology, Inland Hospital, 2609 Lillehammer, Norway
4
Institute of Clinical Medicine, Faculty of Health Sciences, UiT—The Arctic University of Norway, Hansine Hansens veg 18, 9019 Tromsø, Norway
*
Author to whom correspondence should be addressed.
Microorganisms 2021, 9(1), 52; https://doi.org/10.3390/microorganisms9010052
Submission received: 23 November 2020 / Revised: 22 December 2020 / Accepted: 23 December 2020 / Published: 27 December 2020
(This article belongs to the Special Issue Bacterial Genomes and Evolution by Horizontal Gene Transfer (HGT))

Abstract

Norway is known for being one of the countries with the lowest levels of antimicrobial resistance (AMR). AMR, through acquired genes located on transposons or conjugative plasmids, is the horizontal transmission of genes required for a given bacteria to withstand antibiotics. In this work, bioinformatic analysis of whole-genome sequences and hybrid assembled data from Escherichia coli, and Klebsiella pneumoniae isolates from Norwegian patients was performed. For detection of putative plasmids in isolates, the plasmid assembly mode in SPAdes was used, followed by annotation of resulting contigs using PlasmidFinder and two curated plasmid databases (Brooks and PLSDB). Furthermore, ResFinder and Comprehensive Antibiotic Resistance Database (CARD) were used for the identification of antibiotic resistance genes (ARGs). The IncFIB plasmid was detected as the most prevalent plasmid in both E. coli, and K. pneumoniae isolates. Furthermore, ARGs such as aph(3″)-Ib, aph(6)-Id, sul1, sul2, tet(D), and qnrS1 were identified as the most abundant plasmid-mediated ARGs in Norwegian E. coli and K. pneumoniae isolates, respectively. Using hybrid assembly, we were able to locate plasmids and predict ARGs more confidently. In conclusion, plasmid identification and ARG detection using whole-genome sequencing data are heavily dependent on the database of choice; therefore, it is best to use several tools and/or hybrid assembly for obtaining reliable identification results.
Keywords: Escherichia coli; Klebsiella pneumoniae; antimicrobial resistance; plasmid; plasmid-mediated genes; horizontal gene transfer Escherichia coli; Klebsiella pneumoniae; antimicrobial resistance; plasmid; plasmid-mediated genes; horizontal gene transfer

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MDPI and ACS Style

Khezri, A.; Avershina, E.; Ahmad, R. Plasmid Identification and Plasmid-Mediated Antimicrobial Gene Detection in Norwegian Isolates. Microorganisms 2021, 9, 52. https://doi.org/10.3390/microorganisms9010052

AMA Style

Khezri A, Avershina E, Ahmad R. Plasmid Identification and Plasmid-Mediated Antimicrobial Gene Detection in Norwegian Isolates. Microorganisms. 2021; 9(1):52. https://doi.org/10.3390/microorganisms9010052

Chicago/Turabian Style

Khezri, Abdolrahman, Ekaterina Avershina, and Rafi Ahmad. 2021. "Plasmid Identification and Plasmid-Mediated Antimicrobial Gene Detection in Norwegian Isolates" Microorganisms 9, no. 1: 52. https://doi.org/10.3390/microorganisms9010052

APA Style

Khezri, A., Avershina, E., & Ahmad, R. (2021). Plasmid Identification and Plasmid-Mediated Antimicrobial Gene Detection in Norwegian Isolates. Microorganisms, 9(1), 52. https://doi.org/10.3390/microorganisms9010052

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