Multilabel hybridization probes for sequence-specific detection of sepsis-related drug resistance genes in plasmids

Emerging antimicrobial drug resistance is increasing the complexity involved in treating critical conditions such as bacterial induced sepsis. Methods for diagnosing specific drug resistance tend to be rapid or sensitive, but not both. Detection methods like sequence-specific single-molecule analysi...

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Main Authors: Robert L. Hanson, Elaine Lazalde, Radim Knob, David H. Harris, Yesman Akuoko, Jacob B. Nielsen, Adam T. Woolley
Format: Article
Language:English
Published: Elsevier 2021-08-01
Series:Talanta Open
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2666831921000047
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spelling doaj-f8854e44d012440aa279f60cc27bbca52021-06-25T04:50:59ZengElsevierTalanta Open2666-83192021-08-013100034Multilabel hybridization probes for sequence-specific detection of sepsis-related drug resistance genes in plasmidsRobert L. Hanson0Elaine Lazalde1Radim Knob2David H. Harris3Yesman Akuoko4Jacob B. Nielsen5Adam T. Woolley6Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT 84602, USADepartment of Chemistry and Biochemistry, Brigham Young University, Provo, UT 84602, USADepartment of Chemistry and Biochemistry, Brigham Young University, Provo, UT 84602, USADepartment of Chemistry and Biochemistry, Brigham Young University, Provo, UT 84602, USADepartment of Chemistry and Biochemistry, Brigham Young University, Provo, UT 84602, USADepartment of Chemistry and Biochemistry, Brigham Young University, Provo, UT 84602, USACorresponding author.; Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT 84602, USAEmerging antimicrobial drug resistance is increasing the complexity involved in treating critical conditions such as bacterial induced sepsis. Methods for diagnosing specific drug resistance tend to be rapid or sensitive, but not both. Detection methods like sequence-specific single-molecule analysis could address this concern if they could be adapted to work on smaller targets similar to those produced in traditional clinical situations. In this work we demonstrate that a 120 bp double stranded polynucleotide with an overhanging single stranded 25 bp probe sequence can be created by immobilizing DNA with a biotin/streptavidin magnetic bead system, labeling with SYBR Gold, and rinsing the excess away while the probe retains multiple fluorophores. These probes with multiple fluorophores can then be used to label a bacterial plasmid target in a sequence-specific manner. These probes enabled the detection of 1 pM plasmid samples containing a portion of an antibiotic resistance gene sequence. This system shows the possibility of improving capture and fluorescence labeling of small nucleic acid fragments, generating lower limits of detection for clinically relevant samples while maintaining rapid processing times.http://www.sciencedirect.com/science/article/pii/S2666831921000047DNA hybridizationSequence-specific hybridizationMultilabel fluorescenceDrug resistancePlasmid detection
collection DOAJ
language English
format Article
sources DOAJ
author Robert L. Hanson
Elaine Lazalde
Radim Knob
David H. Harris
Yesman Akuoko
Jacob B. Nielsen
Adam T. Woolley
spellingShingle Robert L. Hanson
Elaine Lazalde
Radim Knob
David H. Harris
Yesman Akuoko
Jacob B. Nielsen
Adam T. Woolley
Multilabel hybridization probes for sequence-specific detection of sepsis-related drug resistance genes in plasmids
Talanta Open
DNA hybridization
Sequence-specific hybridization
Multilabel fluorescence
Drug resistance
Plasmid detection
author_facet Robert L. Hanson
Elaine Lazalde
Radim Knob
David H. Harris
Yesman Akuoko
Jacob B. Nielsen
Adam T. Woolley
author_sort Robert L. Hanson
title Multilabel hybridization probes for sequence-specific detection of sepsis-related drug resistance genes in plasmids
title_short Multilabel hybridization probes for sequence-specific detection of sepsis-related drug resistance genes in plasmids
title_full Multilabel hybridization probes for sequence-specific detection of sepsis-related drug resistance genes in plasmids
title_fullStr Multilabel hybridization probes for sequence-specific detection of sepsis-related drug resistance genes in plasmids
title_full_unstemmed Multilabel hybridization probes for sequence-specific detection of sepsis-related drug resistance genes in plasmids
title_sort multilabel hybridization probes for sequence-specific detection of sepsis-related drug resistance genes in plasmids
publisher Elsevier
series Talanta Open
issn 2666-8319
publishDate 2021-08-01
description Emerging antimicrobial drug resistance is increasing the complexity involved in treating critical conditions such as bacterial induced sepsis. Methods for diagnosing specific drug resistance tend to be rapid or sensitive, but not both. Detection methods like sequence-specific single-molecule analysis could address this concern if they could be adapted to work on smaller targets similar to those produced in traditional clinical situations. In this work we demonstrate that a 120 bp double stranded polynucleotide with an overhanging single stranded 25 bp probe sequence can be created by immobilizing DNA with a biotin/streptavidin magnetic bead system, labeling with SYBR Gold, and rinsing the excess away while the probe retains multiple fluorophores. These probes with multiple fluorophores can then be used to label a bacterial plasmid target in a sequence-specific manner. These probes enabled the detection of 1 pM plasmid samples containing a portion of an antibiotic resistance gene sequence. This system shows the possibility of improving capture and fluorescence labeling of small nucleic acid fragments, generating lower limits of detection for clinically relevant samples while maintaining rapid processing times.
topic DNA hybridization
Sequence-specific hybridization
Multilabel fluorescence
Drug resistance
Plasmid detection
url http://www.sciencedirect.com/science/article/pii/S2666831921000047
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