DOE PAGES title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Impact of primer dimers and self-amplifying hairpins on reverse transcription loop-mediated isothermal amplification detection of viral RNA

Abstract

Loop-mediated isothermal amplification (LAMP), coupled with reverse transcription (RT), has become a popular technique for detection of viral RNA due to several desirable characteristics for use in point-of-care or low-resource settings. The large number of primers in LAMP (six per target) leads to an increased likelihood of primer-dimer interactions, and the inner primers in particular are prone to formation of stable hairpin structures due to their length (typically 40-45 bases). Although primer-dimers and hairpin structures are known features to avoid in nucleic acid amplification techniques, there is little quantitative information in literature regarding the impact of these structures on LAMP or RT-LAMP assays. In this study, we examine the impact of primer-dimers and hairpins on previously-published primer sets for dengue virus and yellow fever virus. We demonstrate that minor changes to the primers to eliminate amplifiable primer dimers and hairpins improves the performance of the assays when monitored in real time with intercalating dyes, and when monitoring a fluorescent endpoint using the QUASR technique. We also discuss the thermodynamic implications of these minor changes on the overall stability of amplifiable secondary structures, and we present a single thermodynamic parameter to predict the probability of non-specific amplification associated with LAMP primers.

Authors:
 [1];  [1];  [1];  [2];  [2]
  1. Sandia National Lab. (SNL-CA), Livermore, CA (United States)
  2. Univ. of Texas Medical Branch, Galveston, TX (United States)
Publication Date:
Research Org.:
Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)
Sponsoring Org.:
National Institutes of Health (NIH); USDOE
OSTI Identifier:
1429722
Report Number(s):
SAND-2017-13686J
Journal ID: ISSN 0003-2654; ANALAO; 659610
Grant/Contract Number:  
AC04-94AL85000
Resource Type:
Accepted Manuscript
Journal Name:
Analyst
Additional Journal Information:
Journal Volume: 143; Journal Issue: 8; Journal ID: ISSN 0003-2654
Publisher:
Royal Society of Chemistry
Country of Publication:
United States
Language:
English
Subject:
59 BASIC BIOLOGICAL SCIENCES

Citation Formats

Meagher, Robert J., Priye, Aashish, Light, Yooli K., Huang, Cheng, and Wang, Eryu. Impact of primer dimers and self-amplifying hairpins on reverse transcription loop-mediated isothermal amplification detection of viral RNA. United States: N. p., 2018. Web. doi:10.1039/c7an01897e.
Meagher, Robert J., Priye, Aashish, Light, Yooli K., Huang, Cheng, & Wang, Eryu. Impact of primer dimers and self-amplifying hairpins on reverse transcription loop-mediated isothermal amplification detection of viral RNA. United States. https://doi.org/10.1039/c7an01897e
Meagher, Robert J., Priye, Aashish, Light, Yooli K., Huang, Cheng, and Wang, Eryu. Tue . "Impact of primer dimers and self-amplifying hairpins on reverse transcription loop-mediated isothermal amplification detection of viral RNA". United States. https://doi.org/10.1039/c7an01897e. https://www.osti.gov/servlets/purl/1429722.
@article{osti_1429722,
title = {Impact of primer dimers and self-amplifying hairpins on reverse transcription loop-mediated isothermal amplification detection of viral RNA},
author = {Meagher, Robert J. and Priye, Aashish and Light, Yooli K. and Huang, Cheng and Wang, Eryu},
abstractNote = {Loop-mediated isothermal amplification (LAMP), coupled with reverse transcription (RT), has become a popular technique for detection of viral RNA due to several desirable characteristics for use in point-of-care or low-resource settings. The large number of primers in LAMP (six per target) leads to an increased likelihood of primer-dimer interactions, and the inner primers in particular are prone to formation of stable hairpin structures due to their length (typically 40-45 bases). Although primer-dimers and hairpin structures are known features to avoid in nucleic acid amplification techniques, there is little quantitative information in literature regarding the impact of these structures on LAMP or RT-LAMP assays. In this study, we examine the impact of primer-dimers and hairpins on previously-published primer sets for dengue virus and yellow fever virus. We demonstrate that minor changes to the primers to eliminate amplifiable primer dimers and hairpins improves the performance of the assays when monitored in real time with intercalating dyes, and when monitoring a fluorescent endpoint using the QUASR technique. We also discuss the thermodynamic implications of these minor changes on the overall stability of amplifiable secondary structures, and we present a single thermodynamic parameter to predict the probability of non-specific amplification associated with LAMP primers.},
doi = {10.1039/c7an01897e},
journal = {Analyst},
number = 8,
volume = 143,
place = {United States},
year = {Tue Mar 27 00:00:00 EDT 2018},
month = {Tue Mar 27 00:00:00 EDT 2018}
}

Journal Article:
Free Publicly Available Full Text
Publisher's Version of Record

Citation Metrics:
Cited by: 60 works
Citation information provided by
Web of Science

Figures / Tables:

Table 1 Table 1: Comparison of performance for YFV primers for replicate reactions at two-fold dilutions near the expected limit of detection (700 copies = 1 PFU).

Save / Share:

Works referenced in this record:

A smartphone-based diagnostic platform for rapid detection of Zika, chikungunya, and dengue viruses
journal, March 2017

  • Priye, Aashish; Bird, Sara W.; Light, Yooli K.
  • Scientific Reports, Vol. 7, Issue 1
  • DOI: 10.1038/srep44778

Detection of Loop-Mediated Isothermal Amplification Reaction by Turbidity Derived from Magnesium Pyrophosphate Formation
journal, November 2001

  • Mori, Yasuyoshi; Nagamine, Kentaro; Tomita, Norihiro
  • Biochemical and Biophysical Research Communications, Vol. 289, Issue 1
  • DOI: 10.1006/bbrc.2001.5921

Analysis of genotype diversity and evolution of Dengue virus serotype 2 using complete genomes
journal, January 2016

  • Waman, Vaishali P.; Kolekar, Pandurang; Ramtirthkar, Mukund R.
  • PeerJ, Vol. 4
  • DOI: 10.7717/peerj.2326

Colorimetric detection of loop-mediated isothermal amplification reaction by using hydroxy naphthol blue
journal, March 2009

  • Goto, Motoki; Honda, Eiichi; Ogura, Atsuo
  • BioTechniques, Vol. 46, Issue 3
  • DOI: 10.2144/000113072

Nearest-Neighbor Thermodynamics and NMR of DNA Sequences with Internal A·A, C·C, G·G, and T·T Mismatches
journal, March 1999

  • Peyret, Nicolas; Seneviratne, P. Ananda; Allawi, Hatim T.
  • Biochemistry, Vol. 38, Issue 12
  • DOI: 10.1021/bi9825091

A real-time reverse transcription loop-mediated isothermal amplification assay for the rapid detection of yellow fever virus
journal, October 2013


Clustal W and Clustal X version 2.0
journal, September 2007


Loop-mediated isothermal amplification of DNA
journal, June 2000


Detection of Japanese yam mosaic virus by RT-LAMP
journal, January 2003


Comparison of fluorescent intercalating dyes for quantitative loop-mediated isothermal amplification (qLAMP)
journal, July 2016

  • Oscorbin, Igor P.; Belousova, Ekaterina A.; Zakabunin, Aleksandr I.
  • BioTechniques, Vol. 61, Issue 1
  • DOI: 10.2144/000114432

Robustness of a loop-mediated isothermal amplification reaction for diagnostic applications
journal, June 2011


Loop-Mediated Isothermal Amplification Technology: Towards Point of Care Diagnostics
journal, June 2012


Loop-mediated isothermal amplification (LAMP) of gene sequences and simple visual detection of products
journal, April 2008

  • Tomita, Norihiro; Mori, Yasuyoshi; Kanda, Hidetoshi
  • Nature Protocols, Vol. 3, Issue 5
  • DOI: 10.1038/nprot.2008.57

Establishment of an accurate and fast detection method using molecular beacons in loop-mediated isothermal amplification assay
journal, January 2017

  • Liu, Wei; Huang, Simo; Liu, Ningwei
  • Scientific Reports, Vol. 7, Issue 1
  • DOI: 10.1038/srep40125

Detection of Acute HIV-1 Infection by RT-LAMP
journal, May 2015


Sequence-specific detection method for reverse transcription, loop-mediated isothermal amplification of HIV-1
journal, June 2009

  • Curtis, Kelly A.; Rudolph, Donna L.; Owen, S. Michele
  • Journal of Medical Virology, Vol. 81, Issue 6
  • DOI: 10.1002/jmv.21490

Analysis of a Reverse Transcription Loop-mediated Isothermal Amplification (RT-LAMP) for yellow fever diagnostic
journal, December 2015


Visual detection of isothermal nucleic acid amplification using pH-sensitive dyes
journal, February 2015

  • Tanner, Nathan A.; Zhang, Yinhua; Evans, Thomas C.
  • BioTechniques, Vol. 58, Issue 2
  • DOI: 10.2144/000114253

A unified view of polymer, dumbbell, and oligonucleotide DNA nearest-neighbor thermodynamics
journal, February 1998

  • SantaLucia, J.
  • Proceedings of the National Academy of Sciences, Vol. 95, Issue 4
  • DOI: 10.1073/pnas.95.4.1460

Universal Single-Probe RT-PCR Assay for Diagnosis of Dengue Virus Infections
journal, December 2014


MUSCLE: multiple sequence alignment with high accuracy and high throughput
journal, March 2004

  • Edgar, R. C.
  • Nucleic Acids Research, Vol. 32, Issue 5, p. 1792-1797
  • DOI: 10.1093/nar/gkh340

Yellow fever virus: Genetic and phenotypic diversity and implications for detection, prevention and therapy
journal, March 2015


Robust Strand Exchange Reactions for the Sequence-Specific, Real-Time Detection of Nucleic Acid Amplicons
journal, March 2015

  • Jiang, Yu Sherry; Bhadra, Sanchita; Li, Bingling
  • Analytical Chemistry, Vol. 87, Issue 6
  • DOI: 10.1021/ac504387c

The effect of main urine inhibitors on the activity of different DNA polymerases in loop-mediated isothermal amplification
journal, January 2017

  • Jevtuševskaja, Jekaterina; Krõlov, Katrin; Tulp, Indrek
  • Expert Review of Molecular Diagnostics, Vol. 17, Issue 4
  • DOI: 10.1080/14737159.2017.1283218

Colorimetric Detection of Dengue by Single Tube Reverse-Transcription-Loop-Mediated Isothermal Amplification
journal, September 2015


Development of a TaqMan Array Card for Acute-Febrile-Illness Outbreak Investigation and Surveillance of Emerging Pathogens, Including Ebola Virus
journal, October 2015

  • Liu, Jie; Ochieng, Caroline; Wiersma, Steve
  • Journal of Clinical Microbiology, Vol. 54, Issue 1
  • DOI: 10.1128/JCM.02257-15

Simultaneous multiple target detection in real-time loop-mediated isothermal amplification
journal, August 2012

  • Tanner, Nathan A.; Zhang, Yinhua; Evans, Thomas C.
  • BioTechniques, Vol. 53, Issue 2
  • DOI: 10.2144/0000113902

Complete Genome Sequence of Clostridium botulinum CJ0611A1, a Type A(B) Isolate Associated with an International Outbreak of Botulism from Commercial Carrot Juice
journal, January 2021

  • Harris, Richard; Dussault, Forest; Flint, Annika
  • Microbiology Resource Announcements, Vol. 10, Issue 1
  • DOI: 10.1128/mra.01111-20

Works referencing / citing this record:

Rapid sex determination of a wild passerine species using loop‐mediated isothermal amplification (LAMP)
journal, April 2019

  • Koch, Hanna R.; Blohm‐Sievers, Elke; Liedvogel, Miriam
  • Ecology and Evolution, Vol. 9, Issue 10
  • DOI: 10.1002/ece3.5168

A CRISPR–Cas9-triggered strand displacement amplification method for ultrasensitive DNA detection
journal, November 2018


Field diagnosis and genotyping of chikungunya virus using a dried reverse transcription loop-mediated isothermal amplification (LAMP) assay and MinION sequencing
journal, June 2019

  • Hayashida, Kyoko; Orba, Yasuko; Sequeira, Patricia C.
  • PLOS Neglected Tropical Diseases, Vol. 13, Issue 6
  • DOI: 10.1371/journal.pntd.0007480

Rapid sex determination of a wild passerine species using loop‐mediated isothermal amplification (LAMP)
journal, April 2019

  • Koch, Hanna R.; Blohm‐Sievers, Elke; Liedvogel, Miriam
  • Ecology and Evolution, Vol. 9, Issue 10
  • DOI: 10.1002/ece3.5168