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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2018-04-01
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Series: | PLoS Neglected Tropical Diseases |
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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 |
work_keys_str_mv |
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