Rapid plant identification using species- and group-specific primers targeting chloroplast DNA.

Plant identification is challenging when no morphologically assignable parts are available. There is a lack of broadly applicable methods for identifying plants in this situation, for example when roots grow in mixture and for decayed or semi-digested plant material. These difficulties have also imp...

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Autores principales: Corinna Wallinger, Anita Juen, Karin Staudacher, Nikolaus Schallhart, Evi Mitterrutzner, Eva-Maria Steiner, Bettina Thalinger, Michael Traugott
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Publicado: Public Library of Science (PLoS) 2012
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Acceso en línea:https://doaj.org/article/409895bcc02b4dda8696d2472424c05a
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spelling oai:doaj.org-article:409895bcc02b4dda8696d2472424c05a2021-11-18T07:30:23ZRapid plant identification using species- and group-specific primers targeting chloroplast DNA.1932-620310.1371/journal.pone.0029473https://doaj.org/article/409895bcc02b4dda8696d2472424c05a2012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22253728/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Plant identification is challenging when no morphologically assignable parts are available. There is a lack of broadly applicable methods for identifying plants in this situation, for example when roots grow in mixture and for decayed or semi-digested plant material. These difficulties have also impeded the progress made in ecological disciplines such as soil- and trophic ecology. Here, a PCR-based approach is presented which allows identifying a variety of plant taxa commonly occurring in Central European agricultural land. Based on the trnT-F cpDNA region, PCR assays were developed to identify two plant families (Poaceae and Apiaceae), the genera Trifolium and Plantago, and nine plant species: Achillea millefolium, Fagopyrum esculentum, Lolium perenne, Lupinus angustifolius, Phaseolus coccineus, Sinapis alba, Taraxacum officinale, Triticum aestivum, and Zea mays. These assays allowed identification of plants based on size-specific amplicons ranging from 116 bp to 381 bp. Their specificity and sensitivity was consistently high, enabling the detection of small amounts of plant DNA, for example, in decaying plant material and in the intestine or faeces of herbivores. To increase the efficacy of identifying plant species from large number of samples, specific primers were combined in multiplex PCRs, allowing screening for multiple species within a single reaction. The molecular assays outlined here will be applicable manifold, such as for root- and leaf litter identification, botanical trace evidence, and the analysis of herbivory.Corinna WallingerAnita JuenKarin StaudacherNikolaus SchallhartEvi MitterrutznerEva-Maria SteinerBettina ThalingerMichael TraugottPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 1, p e29473 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Corinna Wallinger
Anita Juen
Karin Staudacher
Nikolaus Schallhart
Evi Mitterrutzner
Eva-Maria Steiner
Bettina Thalinger
Michael Traugott
Rapid plant identification using species- and group-specific primers targeting chloroplast DNA.
description Plant identification is challenging when no morphologically assignable parts are available. There is a lack of broadly applicable methods for identifying plants in this situation, for example when roots grow in mixture and for decayed or semi-digested plant material. These difficulties have also impeded the progress made in ecological disciplines such as soil- and trophic ecology. Here, a PCR-based approach is presented which allows identifying a variety of plant taxa commonly occurring in Central European agricultural land. Based on the trnT-F cpDNA region, PCR assays were developed to identify two plant families (Poaceae and Apiaceae), the genera Trifolium and Plantago, and nine plant species: Achillea millefolium, Fagopyrum esculentum, Lolium perenne, Lupinus angustifolius, Phaseolus coccineus, Sinapis alba, Taraxacum officinale, Triticum aestivum, and Zea mays. These assays allowed identification of plants based on size-specific amplicons ranging from 116 bp to 381 bp. Their specificity and sensitivity was consistently high, enabling the detection of small amounts of plant DNA, for example, in decaying plant material and in the intestine or faeces of herbivores. To increase the efficacy of identifying plant species from large number of samples, specific primers were combined in multiplex PCRs, allowing screening for multiple species within a single reaction. The molecular assays outlined here will be applicable manifold, such as for root- and leaf litter identification, botanical trace evidence, and the analysis of herbivory.
format article
author Corinna Wallinger
Anita Juen
Karin Staudacher
Nikolaus Schallhart
Evi Mitterrutzner
Eva-Maria Steiner
Bettina Thalinger
Michael Traugott
author_facet Corinna Wallinger
Anita Juen
Karin Staudacher
Nikolaus Schallhart
Evi Mitterrutzner
Eva-Maria Steiner
Bettina Thalinger
Michael Traugott
author_sort Corinna Wallinger
title Rapid plant identification using species- and group-specific primers targeting chloroplast DNA.
title_short Rapid plant identification using species- and group-specific primers targeting chloroplast DNA.
title_full Rapid plant identification using species- and group-specific primers targeting chloroplast DNA.
title_fullStr Rapid plant identification using species- and group-specific primers targeting chloroplast DNA.
title_full_unstemmed Rapid plant identification using species- and group-specific primers targeting chloroplast DNA.
title_sort rapid plant identification using species- and group-specific primers targeting chloroplast dna.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/409895bcc02b4dda8696d2472424c05a
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