Gene target selection for loop-mediated isothermal amplification for rapid discrimination of Treponema pallidum subspecies.

We show proof of concept for gene targets (polA, tprL, and TP_0619) that can be used in loop-mediated isothermal amplification (LAMP) assays to rapidly differentiate infection with any of the three Treponema pallidum subspecies (pallidum (TPA), pertenue (TPE), and endemicum (TEN)) and which are know...

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Main Authors: Sascha Knauf, Simone Lüert, David Šmajs, Michal Strouhal, Idrissa S Chuma, Sieghard Frischmann, Mohammed Bakheit
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-04-01
Series:PLoS Neglected Tropical Diseases
Online Access:http://europepmc.org/articles/PMC5978989?pdf=render
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spelling doaj-0bfdaa85b1974bdabed5dc11a98e8ef22020-11-25T02:27:09ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352018-04-01124e000639610.1371/journal.pntd.0006396Gene target selection for loop-mediated isothermal amplification for rapid discrimination of Treponema pallidum subspecies.Sascha KnaufSimone LüertDavid ŠmajsMichal StrouhalIdrissa S ChumaSieghard FrischmannMohammed BakheitWe show proof of concept for gene targets (polA, tprL, and TP_0619) that can be used in loop-mediated isothermal amplification (LAMP) assays to rapidly differentiate infection with any of the three Treponema pallidum subspecies (pallidum (TPA), pertenue (TPE), and endemicum (TEN)) and which are known to infect humans and nonhuman primates (NHPs). Four TPA, six human, and two NHP TPE strains, as well as two human TEN strains were used to establish and validate the LAMP assays. All three LAMP assays were highly specific for the target DNA. Amplification was rapid (5-15 min) and within a range of 10E+6 to 10E+2 of target DNA molecules. Performance in NHP clinical samples was similar to the one seen in human TPE strains. The newly designed LAMP assays provide proof of concept for a diagnostic tool that enhances yaws clinical diagnosis. It is highly specific for the target DNA and does not require expensive laboratory equipment. Test results can potentially be interpreted with the naked eye, which makes it suitable for the use in remote clinical settings.http://europepmc.org/articles/PMC5978989?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Sascha Knauf
Simone Lüert
David Šmajs
Michal Strouhal
Idrissa S Chuma
Sieghard Frischmann
Mohammed Bakheit
spellingShingle Sascha Knauf
Simone Lüert
David Šmajs
Michal Strouhal
Idrissa S Chuma
Sieghard Frischmann
Mohammed Bakheit
Gene target selection for loop-mediated isothermal amplification for rapid discrimination of Treponema pallidum subspecies.
PLoS Neglected Tropical Diseases
author_facet Sascha Knauf
Simone Lüert
David Šmajs
Michal Strouhal
Idrissa S Chuma
Sieghard Frischmann
Mohammed Bakheit
author_sort Sascha Knauf
title Gene target selection for loop-mediated isothermal amplification for rapid discrimination of Treponema pallidum subspecies.
title_short Gene target selection for loop-mediated isothermal amplification for rapid discrimination of Treponema pallidum subspecies.
title_full Gene target selection for loop-mediated isothermal amplification for rapid discrimination of Treponema pallidum subspecies.
title_fullStr Gene target selection for loop-mediated isothermal amplification for rapid discrimination of Treponema pallidum subspecies.
title_full_unstemmed Gene target selection for loop-mediated isothermal amplification for rapid discrimination of Treponema pallidum subspecies.
title_sort gene target selection for loop-mediated isothermal amplification for rapid discrimination of treponema pallidum subspecies.
publisher Public Library of Science (PLoS)
series PLoS Neglected Tropical Diseases
issn 1935-2727
1935-2735
publishDate 2018-04-01
description We show proof of concept for gene targets (polA, tprL, and TP_0619) that can be used in loop-mediated isothermal amplification (LAMP) assays to rapidly differentiate infection with any of the three Treponema pallidum subspecies (pallidum (TPA), pertenue (TPE), and endemicum (TEN)) and which are known to infect humans and nonhuman primates (NHPs). Four TPA, six human, and two NHP TPE strains, as well as two human TEN strains were used to establish and validate the LAMP assays. All three LAMP assays were highly specific for the target DNA. Amplification was rapid (5-15 min) and within a range of 10E+6 to 10E+2 of target DNA molecules. Performance in NHP clinical samples was similar to the one seen in human TPE strains. The newly designed LAMP assays provide proof of concept for a diagnostic tool that enhances yaws clinical diagnosis. It is highly specific for the target DNA and does not require expensive laboratory equipment. Test results can potentially be interpreted with the naked eye, which makes it suitable for the use in remote clinical settings.
url http://europepmc.org/articles/PMC5978989?pdf=render
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