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Enabling metagenomic surveillance for bacterial tick-borne pathogens using nanopore sequencing with adaptive sampling

Evan J. Kipp, Laramie L. Lindsey, Benedict S. Khoo, View ORCID ProfileChristopher Faulk, Jonathan D. Oliver, Peter A. Larsen
doi: https://doi.org/10.1101/2021.08.17.456696
Evan J. Kipp
1Department of Veterinary and Biomedical Sciences - College of Veterinary Medicine, University of Minnesota—Twin Cities, St. Paul, Minnesota, United States; (E.J.K.); (L.L.L.); (P.A.L.)
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  • For correspondence: kipp0046@umn.edu linds758@umn.edu plarsen@umn.edu
Laramie L. Lindsey
1Department of Veterinary and Biomedical Sciences - College of Veterinary Medicine, University of Minnesota—Twin Cities, St. Paul, Minnesota, United States; (E.J.K.); (L.L.L.); (P.A.L.)
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  • For correspondence: kipp0046@umn.edu linds758@umn.edu plarsen@umn.edu
Benedict S. Khoo
2Division of Environmental Health Sciences - School of Public Health, University of Minnesota—Twin Cities, Minneapolis, Minnesota, United States; (B.K.); (J.D.O.)
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  • For correspondence: khoo0011@umn.edu joliver@umn.edu
Christopher Faulk
3Department of Animal Science - College of Food, Agricultural and Natural Resource Sciences, University of Minnesota—Twin Cities, St. Paul, Minnesota, United States; (C.F.)
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  • For correspondence: cfaulk@umn.edu
Jonathan D. Oliver
2Division of Environmental Health Sciences - School of Public Health, University of Minnesota—Twin Cities, Minneapolis, Minnesota, United States; (B.K.); (J.D.O.)
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  • For correspondence: khoo0011@umn.edu joliver@umn.edu
Peter A. Larsen
1Department of Veterinary and Biomedical Sciences - College of Veterinary Medicine, University of Minnesota—Twin Cities, St. Paul, Minnesota, United States; (E.J.K.); (L.L.L.); (P.A.L.)
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  • For correspondence: plarsen@umn.edu kipp0046@umn.edu linds758@umn.edu plarsen@umn.edu
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Abstract

Technological and computational advancements in the fields of genomics and bioinformatics are providing exciting new opportunities for pathogen discovery and surveillance. In particular, single-molecule nucleotide sequence data originating from Oxford Nanopore Technologies (ONT) sequencing platforms can be bioinformatically leveraged, in real-time, for enhanced biosurveillance of a vast array of zoonoses. The recently released nanopore adaptive sampling (NAS) pipeline facilitates immediate mapping of individual nucleotide molecules (i.e., DNA, cDNA, and RNA) to a given reference as each molecule is sequenced. User-defined thresholds then allow for the retention or rejection of specific molecules, informed by the real-time reference mapping results, as they are physically passing through a given sequencing nanopore. Here, we show how NAS can be used to selectively sequence entire genomes of bacterial tick-borne pathogens circulating in wild populations of the blacklegged tick vector, Ixodes scapularis. The NAS method provided a two-fold increase in targeted pathogen sequences, successfully enriching for Borrelia (Borreliella) burgdorferi s.s.; Borrelia (Borrelia) miyamotoi; Anaplasma phagocytophilum; and Ehrlichia muris eauclairensis genomic DNA within our I. scapularis samples. Our results indicate that NAS has strong potential for real-time sequence-based pathogen surveillance.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • ↵† shared senior author

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted August 17, 2021.
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Enabling metagenomic surveillance for bacterial tick-borne pathogens using nanopore sequencing with adaptive sampling
Evan J. Kipp, Laramie L. Lindsey, Benedict S. Khoo, Christopher Faulk, Jonathan D. Oliver, Peter A. Larsen
bioRxiv 2021.08.17.456696; doi: https://doi.org/10.1101/2021.08.17.456696
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Enabling metagenomic surveillance for bacterial tick-borne pathogens using nanopore sequencing with adaptive sampling
Evan J. Kipp, Laramie L. Lindsey, Benedict S. Khoo, Christopher Faulk, Jonathan D. Oliver, Peter A. Larsen
bioRxiv 2021.08.17.456696; doi: https://doi.org/10.1101/2021.08.17.456696

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