Genetic variability of Bipolaris sorokiniana isolates using URP-PCR

Detalhes bibliográficos
Autor(a) principal: Mann, Michele Bertoni
Data de Publicação: 2014
Outros Autores: Spadari, Cristina de Castro, Feltrin, Thaisa, Frazzon, Ana Paula Guedes, Germani, Jose Carlos, Van der Sand, Sueli Terezinha
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/99269
Resumo: Spot blotch disease, caused by Bipolaris sorokiniana, is one of the major diseases of wheat and is responsible for large losses of wheat crops worldwide. We used polymerase chain reaction (PCR) with universal rice primers (URP) for molecular characterization of 60 monosporic B. sorokiniana isolates from Brazil and other countries, and evaluated the diversity of the samples. PCR amplification generated 232 different DNA fragments ranging in size from 100 to 2018 bp. The primers URP-4R, URP-2R, and URP-1F generated greater numbers of amplified fragments (36, 30, and 25, respectively) from the single-spore isolates, and some diversity was observed among the isolates generated using these primers. The primers URP-2F, URP-6R, URP-17R, URP-30F, and URP-38F produced a pattern of monomorphic fragments and 73% of the isolates showed an average of 44 different DNA-amplified fragments. Primer URP-2F generated a 578-bp fragment that was common to 83.7% of the isolates; primer URP-6R generated a 548-bp fragment and primer URP-38F generated a 650- bp product that was common to 89.1% and 80% of the isolates, respectively. The URP-PCR primers provided important information about the genetic profiles of the monosporic cultures, which showed intraspecific variability among the monoconidial isolates and among the monosporic cultures that originated from the same polysporic strain. Our results indicate that URP’s are sensitive and give reproducible results for assaying the genetic variability of B. sorokiniana.
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spelling Mann, Michele BertoniSpadari, Cristina de CastroFeltrin, ThaisaFrazzon, Ana Paula GuedesGermani, Jose CarlosVan der Sand, Sueli Terezinha2014-08-08T02:07:05Z20141982-5676http://hdl.handle.net/10183/99269000919818Spot blotch disease, caused by Bipolaris sorokiniana, is one of the major diseases of wheat and is responsible for large losses of wheat crops worldwide. We used polymerase chain reaction (PCR) with universal rice primers (URP) for molecular characterization of 60 monosporic B. sorokiniana isolates from Brazil and other countries, and evaluated the diversity of the samples. PCR amplification generated 232 different DNA fragments ranging in size from 100 to 2018 bp. The primers URP-4R, URP-2R, and URP-1F generated greater numbers of amplified fragments (36, 30, and 25, respectively) from the single-spore isolates, and some diversity was observed among the isolates generated using these primers. The primers URP-2F, URP-6R, URP-17R, URP-30F, and URP-38F produced a pattern of monomorphic fragments and 73% of the isolates showed an average of 44 different DNA-amplified fragments. Primer URP-2F generated a 578-bp fragment that was common to 83.7% of the isolates; primer URP-6R generated a 548-bp fragment and primer URP-38F generated a 650- bp product that was common to 89.1% and 80% of the isolates, respectively. The URP-PCR primers provided important information about the genetic profiles of the monosporic cultures, which showed intraspecific variability among the monoconidial isolates and among the monosporic cultures that originated from the same polysporic strain. Our results indicate that URP’s are sensitive and give reproducible results for assaying the genetic variability of B. sorokiniana.application/pdfengTropical Plant Pathology, Brasília. Vol. 39, no. 21 (Mar./Apr. 2014), p. 163-171FungosBipolaris sorokinianaReação em cadeia da polimeraseTrigoTriticum aestivunSpot blotch diseaseWheatGenetic variability of Bipolaris sorokiniana isolates using URP-PCRinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL000919818.pdf000919818.pdfTexto completo (inglês)application/pdf2102548http://www.lume.ufrgs.br/bitstream/10183/99269/1/000919818.pdfd6a180952d87d47320f1fcf9e0ae289cMD51TEXT000919818.pdf.txt000919818.pdf.txtExtracted Texttext/plain29579http://www.lume.ufrgs.br/bitstream/10183/99269/2/000919818.pdf.txtb0dd40bb9c0672b1ce959bc269ab96e4MD52THUMBNAIL000919818.pdf.jpg000919818.pdf.jpgGenerated Thumbnailimage/jpeg2290http://www.lume.ufrgs.br/bitstream/10183/99269/3/000919818.pdf.jpg814a1b0a15ca8898f34beccd30a00813MD5310183/992692021-09-18 04:53:59.1808oai:www.lume.ufrgs.br:10183/99269Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-09-18T07:53:59Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Genetic variability of Bipolaris sorokiniana isolates using URP-PCR
title Genetic variability of Bipolaris sorokiniana isolates using URP-PCR
spellingShingle Genetic variability of Bipolaris sorokiniana isolates using URP-PCR
Mann, Michele Bertoni
Fungos
Bipolaris sorokiniana
Reação em cadeia da polimerase
Trigo
Triticum aestivun
Spot blotch disease
Wheat
title_short Genetic variability of Bipolaris sorokiniana isolates using URP-PCR
title_full Genetic variability of Bipolaris sorokiniana isolates using URP-PCR
title_fullStr Genetic variability of Bipolaris sorokiniana isolates using URP-PCR
title_full_unstemmed Genetic variability of Bipolaris sorokiniana isolates using URP-PCR
title_sort Genetic variability of Bipolaris sorokiniana isolates using URP-PCR
author Mann, Michele Bertoni
author_facet Mann, Michele Bertoni
Spadari, Cristina de Castro
Feltrin, Thaisa
Frazzon, Ana Paula Guedes
Germani, Jose Carlos
Van der Sand, Sueli Terezinha
author_role author
author2 Spadari, Cristina de Castro
Feltrin, Thaisa
Frazzon, Ana Paula Guedes
Germani, Jose Carlos
Van der Sand, Sueli Terezinha
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Mann, Michele Bertoni
Spadari, Cristina de Castro
Feltrin, Thaisa
Frazzon, Ana Paula Guedes
Germani, Jose Carlos
Van der Sand, Sueli Terezinha
dc.subject.por.fl_str_mv Fungos
Bipolaris sorokiniana
Reação em cadeia da polimerase
Trigo
topic Fungos
Bipolaris sorokiniana
Reação em cadeia da polimerase
Trigo
Triticum aestivun
Spot blotch disease
Wheat
dc.subject.eng.fl_str_mv Triticum aestivun
Spot blotch disease
Wheat
description Spot blotch disease, caused by Bipolaris sorokiniana, is one of the major diseases of wheat and is responsible for large losses of wheat crops worldwide. We used polymerase chain reaction (PCR) with universal rice primers (URP) for molecular characterization of 60 monosporic B. sorokiniana isolates from Brazil and other countries, and evaluated the diversity of the samples. PCR amplification generated 232 different DNA fragments ranging in size from 100 to 2018 bp. The primers URP-4R, URP-2R, and URP-1F generated greater numbers of amplified fragments (36, 30, and 25, respectively) from the single-spore isolates, and some diversity was observed among the isolates generated using these primers. The primers URP-2F, URP-6R, URP-17R, URP-30F, and URP-38F produced a pattern of monomorphic fragments and 73% of the isolates showed an average of 44 different DNA-amplified fragments. Primer URP-2F generated a 578-bp fragment that was common to 83.7% of the isolates; primer URP-6R generated a 548-bp fragment and primer URP-38F generated a 650- bp product that was common to 89.1% and 80% of the isolates, respectively. The URP-PCR primers provided important information about the genetic profiles of the monosporic cultures, which showed intraspecific variability among the monoconidial isolates and among the monosporic cultures that originated from the same polysporic strain. Our results indicate that URP’s are sensitive and give reproducible results for assaying the genetic variability of B. sorokiniana.
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dc.relation.ispartof.pt_BR.fl_str_mv Tropical Plant Pathology, Brasília. Vol. 39, no. 21 (Mar./Apr. 2014), p. 163-171
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