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Rapid identification of intact bacterial resistance plasmids via optical mapping of single DNA molecules

Lena Nyberg (Institutionen för biologi och bioteknik, Kemisk biologi) ; S. Quaderi ; Gustav Emilsson (Institutionen för fysik (Chalmers)) ; N. Karami ; E. Lagerstedt ; Vilhelm Müller (Institutionen för biologi och bioteknik) ; C. Noble ; S. Hammarberg ; A. N. Nilsson ; F. Sjoberg ; Joachim Fritzsche (Institutionen för fysik, Kemisk fysik (Chalmers)) ; E. Kristiansson ; L. Sandegren ; T. Ambjornsson ; Fredrik Westerlund (Institutionen för biologi och bioteknik, Kemisk biologi)
Scientific Reports (2045-2322). Vol. 6 (2016),
[Artikel, refereegranskad vetenskaplig]

The rapid spread of antibiotic resistance - currently one of the greatest threats to human health according to WHO - is to a large extent enabled by plasmid-mediated horizontal transfer of resistance genes. Rapid identification and characterization of plasmids is thus important both for individual clinical outcomes and for epidemiological monitoring of antibiotic resistance. Toward this aim, we have developed an optical DNA mapping procedure where individual intact plasmids are elongated within nanofluidic channels and visualized through fluorescence microscopy, yielding barcodes that reflect the underlying sequence. The assay rapidly identifies plasmids through statistical comparisons with barcodes based on publicly available sequence repositories and also enables detection of structural variations. Since the assay yields holistic sequence information for individual intact plasmids, it is an ideal complement to next generation sequencing efforts which involve reassembly of sequence reads from fragmented DNA molecules. The assay should be applicable in microbiology labs around the world in applications ranging from fundamental plasmid biology to clinical epidemiology and diagnostics.

Denna post skapades 2016-08-26. Senast ändrad 2016-10-05.
CPL Pubid: 240821


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