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dc.contributor.authorDuarte, Sofia Alexandra Ferreirapor
dc.contributor.authorSimões, Luara Aparecidapor
dc.contributor.authorCosta, Filipe O.por
dc.date.accessioned2023-10-13T07:23:06Z-
dc.date.available2023-10-13T07:23:06Z-
dc.date.issued2023-12-15-
dc.identifier.citationDuarte, S., Simões, L., & Costa, F. O. (2023, June 14). Catch me if you can: current status and topical issues on the use of eDNA-based targeted detection of rare and endangered animal species. bioRxiv - the Preprint Server for Biology. Cold Spring Harbor Laboratory. http://doi.org/10.1101/2023.06.13.544783-
dc.identifier.urihttps://hdl.handle.net/1822/86848-
dc.descriptionbioRxiv - the Preprint Server for Biology-
dc.description.abstractAnimal detection through DNA present in environmental samples (eDNA) is a valuable tool for detecting rare species, that are difficult to observe and monitor. eDNA-based tools are underpinned by molecular evolutionary principles, which are key to devising tools to efficiently single out a targeted species from an environmental sample, using carefully chosen marker regions and customized primers. Here, we present a comprehensive review of the use of eDNA-based methods for the detection of targeted animal species, such as rare, endangered, or invasive species, through the analysis of 460 publications (2008-2022). Aquatic ecosystems have been the most surveyed, in particular, freshwaters (75%), and to a less extent marine (14%) and terrestrial systems (10%). Vertebrates, in particular, fish (38%), and endangered species, have been the most focused in these studies, and Cytb and COI are the most employed markers. Among invertebrates, assays have been mainly designed for Mollusca and Crustacea species (22%), in particular, to target invasive species, and COI has been the most employed marker. Targeted molecular approaches, in particular qPCR, have been the most adopted (73%), while eDNA metabarcoding has been rarely used to target single or few species (approx. 5%). However, less attention has been given in these studies to the effects of environmental factors on the amount of shed DNA, the differential amount of shed DNA among species, or the sensitivity of the markers developed, which may impact the design of the assays, particularly to warrant the required detection level and avoid false negatives and positives. The accuracy of the assays will also depend on the availability of genetic data from closely related species to assess both marker and primers’ specificity. In addition, eDNA-based assays developed for a particular species may have to be refined taking into account site-specific populations, as well as any intraspecific variation.eng
dc.description.sponsorshipThis work was funded by the project “River2Ocean – Socio-ecological and biotechnological solutions for the conservation and valorization of aquatic biodiversity in the Minho Region” (NORTE-01-0145-FEDER-000068), co-financed by the European Regional Development Fund (ERDF), through Programa Operacional Regional do Norte (NORTE 2020) and by the “Contrato-Programa” UIDB/04050/2020, funded by national funds through the Foundation for Science and Technology (FCT I.P). Financial support granted by the FCT to SD (CEECIND/00667/2017) and by the project ATLANTIDA (NORTE-01-0145-FEDER-000040), funded by Programa Operacional Regional do Norte (NORTE2020) to LS, is also acknowledged. We are also grateful to two reviewers for comments and suggestions that greatly improved the manuscript.por
dc.language.isoengpor
dc.publisherCold Spring Harbor Laboratory-
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F04050%2F2020/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/CEEC IND 2017/CEECIND%2F00667%2F2017%2FCP1458%2FCT0001/PTpor
dc.rightsopenAccesspor
dc.subjecteDNA-based toolspor
dc.subjectEndangered and invasive speciespor
dc.subjectEnvironmental factors effectspor
dc.subjectSpecies-specific assayspor
dc.titleCatch me if you can: current status and topical issues on the use of eDNA-based targeted detection of rare and endangered animal specieseng
dc.typepreprintpor
dc.peerreviewednopor
dc.relation.publisherversionhttps://www.biorxiv.org/content/10.1101/2023.06.13.544783v1por
dc.date.updated2023-10-12T17:35:39Z-
dc.identifier.doi10.1101/2023.06.13.544783por
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