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Detection of Echinococcus multilocularis in repurposed environmental DNA samples from river water

Environmental DNA (eDNA) is an increasingly popular tool in biological and ecological studies. As a biproduct of its increasing use, large number of eDNA samples are being collected and stored, that potentially contain information of many non-target species. One potential use for these eDNA samples...

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Autores principales: Mori, Kensuke, Imamura, Akio, Hirayama, Itsuki, Minamoto, Toshifumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10276553/
https://www.ncbi.nlm.nih.gov/pubmed/37334136
http://dx.doi.org/10.7717/peerj.15431
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author Mori, Kensuke
Imamura, Akio
Hirayama, Itsuki
Minamoto, Toshifumi
author_facet Mori, Kensuke
Imamura, Akio
Hirayama, Itsuki
Minamoto, Toshifumi
author_sort Mori, Kensuke
collection PubMed
description Environmental DNA (eDNA) is an increasingly popular tool in biological and ecological studies. As a biproduct of its increasing use, large number of eDNA samples are being collected and stored, that potentially contain information of many non-target species. One potential use for these eDNA samples is a surveillance and early detection of pathogens and parasites that are otherwise difficult to detect. Echinococcus multilocularis is such a parasite with serious zoonotic concern, and whose range has been expanding. If eDNA samples from various studies can be repurposed in detecting the parasite, it can significantly reduce the costs and efforts in surveillance and early detection of the parasite. We designed and tested a new set of primer-probe for detecting E. multilocularis mitochondrial DNA in environmental medium. Using this primer-probe set, we conducted real-time PCR on repurposed eDNA samples collected from three streams flowing through an area of Japan endemic to the parasite. We detected the DNA of E. multilocularis in one of the 128 samples (0.78%). The discovery suggests that while detecting E. multilocularis using eDNA samples is possible, the rate of detection appear to be very low. However, given the naturally low prevalence of the parasite among wild hosts in endemic areas, the repurposed eDNAs may still be a valid option for surveillance in newly introduced areas with the reduced cost and efforts. Further work is needed to assess and improve the effectiveness of using eDNA for detection of E. multilocularis.
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spelling pubmed-102765532023-06-18 Detection of Echinococcus multilocularis in repurposed environmental DNA samples from river water Mori, Kensuke Imamura, Akio Hirayama, Itsuki Minamoto, Toshifumi PeerJ Genetics Environmental DNA (eDNA) is an increasingly popular tool in biological and ecological studies. As a biproduct of its increasing use, large number of eDNA samples are being collected and stored, that potentially contain information of many non-target species. One potential use for these eDNA samples is a surveillance and early detection of pathogens and parasites that are otherwise difficult to detect. Echinococcus multilocularis is such a parasite with serious zoonotic concern, and whose range has been expanding. If eDNA samples from various studies can be repurposed in detecting the parasite, it can significantly reduce the costs and efforts in surveillance and early detection of the parasite. We designed and tested a new set of primer-probe for detecting E. multilocularis mitochondrial DNA in environmental medium. Using this primer-probe set, we conducted real-time PCR on repurposed eDNA samples collected from three streams flowing through an area of Japan endemic to the parasite. We detected the DNA of E. multilocularis in one of the 128 samples (0.78%). The discovery suggests that while detecting E. multilocularis using eDNA samples is possible, the rate of detection appear to be very low. However, given the naturally low prevalence of the parasite among wild hosts in endemic areas, the repurposed eDNAs may still be a valid option for surveillance in newly introduced areas with the reduced cost and efforts. Further work is needed to assess and improve the effectiveness of using eDNA for detection of E. multilocularis. PeerJ Inc. 2023-06-14 /pmc/articles/PMC10276553/ /pubmed/37334136 http://dx.doi.org/10.7717/peerj.15431 Text en ©2023 Mori et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Genetics
Mori, Kensuke
Imamura, Akio
Hirayama, Itsuki
Minamoto, Toshifumi
Detection of Echinococcus multilocularis in repurposed environmental DNA samples from river water
title Detection of Echinococcus multilocularis in repurposed environmental DNA samples from river water
title_full Detection of Echinococcus multilocularis in repurposed environmental DNA samples from river water
title_fullStr Detection of Echinococcus multilocularis in repurposed environmental DNA samples from river water
title_full_unstemmed Detection of Echinococcus multilocularis in repurposed environmental DNA samples from river water
title_short Detection of Echinococcus multilocularis in repurposed environmental DNA samples from river water
title_sort detection of echinococcus multilocularis in repurposed environmental dna samples from river water
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10276553/
https://www.ncbi.nlm.nih.gov/pubmed/37334136
http://dx.doi.org/10.7717/peerj.15431
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