Illuminating the Prevalence of Trypanosoma brucei s.l. in Glossina Using LAMP as a Tool for Xenomonitoring.

<h4>Background</h4>As the reality of eliminating human African trypanosomiasis (HAT) by 2020 draws closer, the need to detect and identify the remaining areas of transmission increases. Here, we have explored the feasibility of using commercially available LAMP kits, designed to detect t...

Full description

Saved in:
Bibliographic Details
Main Authors: Lucas J Cunningham, Jessica K Lingley, Lee R Haines, Joseph M Ndung'u, Stephen J Torr, Emily R Adams
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-02-01
Series:PLoS Neglected Tropical Diseases
Online Access:https://journals.plos.org/plosntds/article/file?id=10.1371/journal.pntd.0004441&type=printable
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849331822096285696
author Lucas J Cunningham
Jessica K Lingley
Lee R Haines
Joseph M Ndung'u
Stephen J Torr
Emily R Adams
author_facet Lucas J Cunningham
Jessica K Lingley
Lee R Haines
Joseph M Ndung'u
Stephen J Torr
Emily R Adams
author_sort Lucas J Cunningham
collection DOAJ
description <h4>Background</h4>As the reality of eliminating human African trypanosomiasis (HAT) by 2020 draws closer, the need to detect and identify the remaining areas of transmission increases. Here, we have explored the feasibility of using commercially available LAMP kits, designed to detect the Trypanozoon group of trypanosomes, as a xenomonitoring tool to screen tsetse flies for trypanosomes to be used in future epidemiological surveys.<h4>Methods and findings</h4>The DNA extraction method was simplified and worked with the LAMP kits to detect a single positive fly when pooled with 19 negative flies, and the absolute lowest limit of detection that the kits were able to work at was the equivalent of 0.1 trypanosome per ml. The DNA from Trypanosoma brucei brucei could be detected six days after the fly had taken a blood meal containing dead trypanosomes, and when confronted with a range of non-target species, from both laboratory-reared flies and wild-caught flies, the kits showed no evidence of cross-reacting.<h4>Conclusion</h4>We have shown that it is possible to use a simplified DNA extraction method in conjunction with the pooling of tsetse flies to decrease the time it would take to screen large numbers of flies for the presence of Trypanozoon trypanosomes. The use of commercially-available LAMP kits provides a reliable and highly sensitive tool for xenomonitoring and identifying potential sleeping sickness transmission sites.
format Article
id doaj-art-5c785cf48dde4e979bda91e671eb7fe9
institution Kabale University
issn 1935-2727
1935-2735
language English
publishDate 2016-02-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Neglected Tropical Diseases
spelling doaj-art-5c785cf48dde4e979bda91e671eb7fe92025-08-20T03:46:24ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352016-02-01102e000444110.1371/journal.pntd.0004441Illuminating the Prevalence of Trypanosoma brucei s.l. in Glossina Using LAMP as a Tool for Xenomonitoring.Lucas J CunninghamJessica K LingleyLee R HainesJoseph M Ndung'uStephen J TorrEmily R Adams<h4>Background</h4>As the reality of eliminating human African trypanosomiasis (HAT) by 2020 draws closer, the need to detect and identify the remaining areas of transmission increases. Here, we have explored the feasibility of using commercially available LAMP kits, designed to detect the Trypanozoon group of trypanosomes, as a xenomonitoring tool to screen tsetse flies for trypanosomes to be used in future epidemiological surveys.<h4>Methods and findings</h4>The DNA extraction method was simplified and worked with the LAMP kits to detect a single positive fly when pooled with 19 negative flies, and the absolute lowest limit of detection that the kits were able to work at was the equivalent of 0.1 trypanosome per ml. The DNA from Trypanosoma brucei brucei could be detected six days after the fly had taken a blood meal containing dead trypanosomes, and when confronted with a range of non-target species, from both laboratory-reared flies and wild-caught flies, the kits showed no evidence of cross-reacting.<h4>Conclusion</h4>We have shown that it is possible to use a simplified DNA extraction method in conjunction with the pooling of tsetse flies to decrease the time it would take to screen large numbers of flies for the presence of Trypanozoon trypanosomes. The use of commercially-available LAMP kits provides a reliable and highly sensitive tool for xenomonitoring and identifying potential sleeping sickness transmission sites.https://journals.plos.org/plosntds/article/file?id=10.1371/journal.pntd.0004441&type=printable
spellingShingle Lucas J Cunningham
Jessica K Lingley
Lee R Haines
Joseph M Ndung'u
Stephen J Torr
Emily R Adams
Illuminating the Prevalence of Trypanosoma brucei s.l. in Glossina Using LAMP as a Tool for Xenomonitoring.
PLoS Neglected Tropical Diseases
title Illuminating the Prevalence of Trypanosoma brucei s.l. in Glossina Using LAMP as a Tool for Xenomonitoring.
title_full Illuminating the Prevalence of Trypanosoma brucei s.l. in Glossina Using LAMP as a Tool for Xenomonitoring.
title_fullStr Illuminating the Prevalence of Trypanosoma brucei s.l. in Glossina Using LAMP as a Tool for Xenomonitoring.
title_full_unstemmed Illuminating the Prevalence of Trypanosoma brucei s.l. in Glossina Using LAMP as a Tool for Xenomonitoring.
title_short Illuminating the Prevalence of Trypanosoma brucei s.l. in Glossina Using LAMP as a Tool for Xenomonitoring.
title_sort illuminating the prevalence of trypanosoma brucei s l in glossina using lamp as a tool for xenomonitoring
url https://journals.plos.org/plosntds/article/file?id=10.1371/journal.pntd.0004441&type=printable
work_keys_str_mv AT lucasjcunningham illuminatingtheprevalenceoftrypanosomabruceislinglossinausinglampasatoolforxenomonitoring
AT jessicaklingley illuminatingtheprevalenceoftrypanosomabruceislinglossinausinglampasatoolforxenomonitoring
AT leerhaines illuminatingtheprevalenceoftrypanosomabruceislinglossinausinglampasatoolforxenomonitoring
AT josephmndungu illuminatingtheprevalenceoftrypanosomabruceislinglossinausinglampasatoolforxenomonitoring
AT stephenjtorr illuminatingtheprevalenceoftrypanosomabruceislinglossinausinglampasatoolforxenomonitoring
AT emilyradams illuminatingtheprevalenceoftrypanosomabruceislinglossinausinglampasatoolforxenomonitoring