DNA barcoding green microalgae isolated from neotropical inland waters.

Detalhes bibliográficos
Autor(a) principal: HADI, S. I. I. A
Data de Publicação: 2016
Outros Autores: SANTANA, H., BRUNALE, P. P. M., GOMES, T. G., OLIVEIRA, M. D. de, MATTHIENSEN, A., OLIVEIRA, M. E. C., SILVA, F. C. P., BRASIL, B. dos S. A. F.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
Texto Completo: http://www.alice.cnptia.embrapa.br/alice/handle/doc/1046770
http://dx.doi.org/10.1371/journal.pone.0149284
Resumo: This study evaluated the feasibility of using the Ribulose Bisphosphate Carboxylase Large subunit gene (rbcL) and the Internal Transcribed Spacers 1 and 2 of the nuclear rDNA (nuITS1 and nuITS2) markers for identifying a very diverse, albeit poorly known group, of green microalgae from neotropical inland waters. Fifty-one freshwater green microalgae strains isolated from Brazil, the largest biodiversity reservoir in the neotropics, were submitted to DNA barcoding. Currently available universal primers for ITS1-5.8S-ITS2 region amplification were sufficient to successfully amplify and sequence 47 (92%) of the samples. On the other hand, new sets of primers had to be designed for rbcL, which allowed 96% of the samples to be sequenced. Thirty-five percent of the strains could be unambiguously identified to the species level based either on nuITS1 or nuITS2 sequences? using barcode gap calculations. nuITS2 Compensatory Base Change (CBC) and ITS1-5.8S-ITS2 region phylogenetic analysis, together with morphological inspection, confirmed the identification accuracy. In contrast, only 6% of the strains could be assigned to the correct species based solely on rbcL sequences. In conclusion, the data presented here indicates that either nuITS1 or nuITS2 are useful markers for DNA barcoding of freshwater green microalgae, with advantage for nuITS2 due to the larger availability of analytical tools and reference barcodes deposited at databases for this marker.
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spelling DNA barcoding green microalgae isolated from neotropical inland waters.MicroalgasAnálise molecularSequenciamento genéticoIdentificação morfológicaThis study evaluated the feasibility of using the Ribulose Bisphosphate Carboxylase Large subunit gene (rbcL) and the Internal Transcribed Spacers 1 and 2 of the nuclear rDNA (nuITS1 and nuITS2) markers for identifying a very diverse, albeit poorly known group, of green microalgae from neotropical inland waters. Fifty-one freshwater green microalgae strains isolated from Brazil, the largest biodiversity reservoir in the neotropics, were submitted to DNA barcoding. Currently available universal primers for ITS1-5.8S-ITS2 region amplification were sufficient to successfully amplify and sequence 47 (92%) of the samples. On the other hand, new sets of primers had to be designed for rbcL, which allowed 96% of the samples to be sequenced. Thirty-five percent of the strains could be unambiguously identified to the species level based either on nuITS1 or nuITS2 sequences? using barcode gap calculations. nuITS2 Compensatory Base Change (CBC) and ITS1-5.8S-ITS2 region phylogenetic analysis, together with morphological inspection, confirmed the identification accuracy. In contrast, only 6% of the strains could be assigned to the correct species based solely on rbcL sequences. In conclusion, the data presented here indicates that either nuITS1 or nuITS2 are useful markers for DNA barcoding of freshwater green microalgae, with advantage for nuITS2 due to the larger availability of analytical tools and reference barcodes deposited at databases for this marker.SÁMED, I. I. A. HADI, UFT; HUGO SANTANA, UFBA; PATRÍCIA P. M. BRUNALE, UnB; TAÍSA G. GOMES, UFT; MARCIA DIVINA DE OLIVEIRA, CPAP; ALEXANDRE MATTHIENSEN, CNPSA; MARCOS ENE CHAVES OLIVEIRA, CPATU; FLÁVIA C. P. SILVA; BRUNO DOS SANTOS ALVES FIGUEIREDO B, CNPAE.HADI, S. I. I. ASANTANA, H.BRUNALE, P. P. M.GOMES, T. G.OLIVEIRA, M. D. deMATTHIENSEN, A.OLIVEIRA, M. E. C.SILVA, F. C. P.BRASIL, B. dos S. A. F.2018-05-11T00:41:13Z2018-05-11T00:41:13Z2016-06-1020162018-05-11T00:41:13Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlePlos One, v. 11, n. 2, Feb. 2016.http://www.alice.cnptia.embrapa.br/alice/handle/doc/1046770http://dx.doi.org/10.1371/journal.pone.0149284enginfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)instname:Empresa Brasileira de Pesquisa Agropecuária (Embrapa)instacron:EMBRAPA2018-05-11T00:41:20Zoai:www.alice.cnptia.embrapa.br:doc/1046770Repositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestopendoar:21542018-05-11T00:41:20falseRepositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestcg-riaa@embrapa.bropendoar:21542018-05-11T00:41:20Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa)false
dc.title.none.fl_str_mv DNA barcoding green microalgae isolated from neotropical inland waters.
title DNA barcoding green microalgae isolated from neotropical inland waters.
spellingShingle DNA barcoding green microalgae isolated from neotropical inland waters.
HADI, S. I. I. A
Microalgas
Análise molecular
Sequenciamento genético
Identificação morfológica
title_short DNA barcoding green microalgae isolated from neotropical inland waters.
title_full DNA barcoding green microalgae isolated from neotropical inland waters.
title_fullStr DNA barcoding green microalgae isolated from neotropical inland waters.
title_full_unstemmed DNA barcoding green microalgae isolated from neotropical inland waters.
title_sort DNA barcoding green microalgae isolated from neotropical inland waters.
author HADI, S. I. I. A
author_facet HADI, S. I. I. A
SANTANA, H.
BRUNALE, P. P. M.
GOMES, T. G.
OLIVEIRA, M. D. de
MATTHIENSEN, A.
OLIVEIRA, M. E. C.
SILVA, F. C. P.
BRASIL, B. dos S. A. F.
author_role author
author2 SANTANA, H.
BRUNALE, P. P. M.
GOMES, T. G.
OLIVEIRA, M. D. de
MATTHIENSEN, A.
OLIVEIRA, M. E. C.
SILVA, F. C. P.
BRASIL, B. dos S. A. F.
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv SÁMED, I. I. A. HADI, UFT; HUGO SANTANA, UFBA; PATRÍCIA P. M. BRUNALE, UnB; TAÍSA G. GOMES, UFT; MARCIA DIVINA DE OLIVEIRA, CPAP; ALEXANDRE MATTHIENSEN, CNPSA; MARCOS ENE CHAVES OLIVEIRA, CPATU; FLÁVIA C. P. SILVA; BRUNO DOS SANTOS ALVES FIGUEIREDO B, CNPAE.
dc.contributor.author.fl_str_mv HADI, S. I. I. A
SANTANA, H.
BRUNALE, P. P. M.
GOMES, T. G.
OLIVEIRA, M. D. de
MATTHIENSEN, A.
OLIVEIRA, M. E. C.
SILVA, F. C. P.
BRASIL, B. dos S. A. F.
dc.subject.por.fl_str_mv Microalgas
Análise molecular
Sequenciamento genético
Identificação morfológica
topic Microalgas
Análise molecular
Sequenciamento genético
Identificação morfológica
description This study evaluated the feasibility of using the Ribulose Bisphosphate Carboxylase Large subunit gene (rbcL) and the Internal Transcribed Spacers 1 and 2 of the nuclear rDNA (nuITS1 and nuITS2) markers for identifying a very diverse, albeit poorly known group, of green microalgae from neotropical inland waters. Fifty-one freshwater green microalgae strains isolated from Brazil, the largest biodiversity reservoir in the neotropics, were submitted to DNA barcoding. Currently available universal primers for ITS1-5.8S-ITS2 region amplification were sufficient to successfully amplify and sequence 47 (92%) of the samples. On the other hand, new sets of primers had to be designed for rbcL, which allowed 96% of the samples to be sequenced. Thirty-five percent of the strains could be unambiguously identified to the species level based either on nuITS1 or nuITS2 sequences? using barcode gap calculations. nuITS2 Compensatory Base Change (CBC) and ITS1-5.8S-ITS2 region phylogenetic analysis, together with morphological inspection, confirmed the identification accuracy. In contrast, only 6% of the strains could be assigned to the correct species based solely on rbcL sequences. In conclusion, the data presented here indicates that either nuITS1 or nuITS2 are useful markers for DNA barcoding of freshwater green microalgae, with advantage for nuITS2 due to the larger availability of analytical tools and reference barcodes deposited at databases for this marker.
publishDate 2016
dc.date.none.fl_str_mv 2016-06-10
2016
2018-05-11T00:41:13Z
2018-05-11T00:41:13Z
2018-05-11T00:41:13Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv Plos One, v. 11, n. 2, Feb. 2016.
http://www.alice.cnptia.embrapa.br/alice/handle/doc/1046770
http://dx.doi.org/10.1371/journal.pone.0149284
identifier_str_mv Plos One, v. 11, n. 2, Feb. 2016.
url http://www.alice.cnptia.embrapa.br/alice/handle/doc/1046770
http://dx.doi.org/10.1371/journal.pone.0149284
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv reponame:Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
instname:Empresa Brasileira de Pesquisa Agropecuária (Embrapa)
instacron:EMBRAPA
instname_str Empresa Brasileira de Pesquisa Agropecuária (Embrapa)
instacron_str EMBRAPA
institution EMBRAPA
reponame_str Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
collection Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
repository.name.fl_str_mv Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa)
repository.mail.fl_str_mv cg-riaa@embrapa.br
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