Detection of circulating parasite-derived microRNAs in filarial infections.

Filarial nematodes cause chronic and profoundly debilitating diseases in both humans and animals. Applications of novel technology are providing unprecedented opportunities to improve diagnosis and our understanding of the molecular basis for host-parasite interactions. As a first step, we investiga...

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Main Authors: Lucienne Tritten, Erica Burkman, Andrew Moorhead, Mohammed Satti, James Geary, Charles Mackenzie, Timothy Geary
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-07-01
Series:PLoS Neglected Tropical Diseases
Online Access:http://europepmc.org/articles/PMC4102413?pdf=render
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spelling doaj-2e9d172c8811416e9a76967b8a159f632020-11-24T23:57:12ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352014-07-0187e297110.1371/journal.pntd.0002971Detection of circulating parasite-derived microRNAs in filarial infections.Lucienne TrittenErica BurkmanAndrew MoorheadMohammed SattiJames GearyCharles MackenzieTimothy GearyFilarial nematodes cause chronic and profoundly debilitating diseases in both humans and animals. Applications of novel technology are providing unprecedented opportunities to improve diagnosis and our understanding of the molecular basis for host-parasite interactions. As a first step, we investigated the presence of circulating miRNAs released by filarial nematodes into the host bloodstream. miRNA deep-sequencing combined with bioinformatics revealed over 200 mature miRNA sequences of potential nematode origin in Dirofilaria immitis-infected dog plasma in two independent analyses, and 21 in Onchocerca volvulus-infected human serum. Total RNA obtained from D. immitis-infected dog plasma was subjected to stem-loop RT-qPCR assays targeting two detected miRNA candidates, miR-71 and miR-34. Additionally, Brugia pahangi-infected dog samples were included in the analysis, as these miRNAs were previously detected in extracts prepared from this species. The presence of miR-71 and miR-34 discriminated infected samples (both species) from uninfected samples, in which no specific miRNA amplification occurred. However, absolute miRNA copy numbers were not significantly correlated with microfilaraemia for either parasite. This may be due to the imprecision of mf counts to estimate infection intensity or to miRNA contributions from the unknown number of adult worms present. Nonetheless, parasite-derived circulating miRNAs are found in plasma or serum even for those species that do not live in the bloodstream.http://europepmc.org/articles/PMC4102413?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Lucienne Tritten
Erica Burkman
Andrew Moorhead
Mohammed Satti
James Geary
Charles Mackenzie
Timothy Geary
spellingShingle Lucienne Tritten
Erica Burkman
Andrew Moorhead
Mohammed Satti
James Geary
Charles Mackenzie
Timothy Geary
Detection of circulating parasite-derived microRNAs in filarial infections.
PLoS Neglected Tropical Diseases
author_facet Lucienne Tritten
Erica Burkman
Andrew Moorhead
Mohammed Satti
James Geary
Charles Mackenzie
Timothy Geary
author_sort Lucienne Tritten
title Detection of circulating parasite-derived microRNAs in filarial infections.
title_short Detection of circulating parasite-derived microRNAs in filarial infections.
title_full Detection of circulating parasite-derived microRNAs in filarial infections.
title_fullStr Detection of circulating parasite-derived microRNAs in filarial infections.
title_full_unstemmed Detection of circulating parasite-derived microRNAs in filarial infections.
title_sort detection of circulating parasite-derived micrornas in filarial infections.
publisher Public Library of Science (PLoS)
series PLoS Neglected Tropical Diseases
issn 1935-2727
1935-2735
publishDate 2014-07-01
description Filarial nematodes cause chronic and profoundly debilitating diseases in both humans and animals. Applications of novel technology are providing unprecedented opportunities to improve diagnosis and our understanding of the molecular basis for host-parasite interactions. As a first step, we investigated the presence of circulating miRNAs released by filarial nematodes into the host bloodstream. miRNA deep-sequencing combined with bioinformatics revealed over 200 mature miRNA sequences of potential nematode origin in Dirofilaria immitis-infected dog plasma in two independent analyses, and 21 in Onchocerca volvulus-infected human serum. Total RNA obtained from D. immitis-infected dog plasma was subjected to stem-loop RT-qPCR assays targeting two detected miRNA candidates, miR-71 and miR-34. Additionally, Brugia pahangi-infected dog samples were included in the analysis, as these miRNAs were previously detected in extracts prepared from this species. The presence of miR-71 and miR-34 discriminated infected samples (both species) from uninfected samples, in which no specific miRNA amplification occurred. However, absolute miRNA copy numbers were not significantly correlated with microfilaraemia for either parasite. This may be due to the imprecision of mf counts to estimate infection intensity or to miRNA contributions from the unknown number of adult worms present. Nonetheless, parasite-derived circulating miRNAs are found in plasma or serum even for those species that do not live in the bloodstream.
url http://europepmc.org/articles/PMC4102413?pdf=render
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