Evaluating methods for purifying cyanobacterial cultures by qPCR and high-throughput Illumina sequencing
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.mimet.2016.07.023 http://hdl.handle.net/11449/165322 |
Resumo: | Cyanobacteria are commonly found in association with other microorganisms, which constitutes a great challenge during the isolation of cyanobacterial strains. Although several methods have been published for obtaining axenic cyanobacterial cultures, their efficiency is usually evaluated by observing the growth of non-cyanobacteria in culture media. In order to verify whether uncultured bacteria should be a concern during cyanobacterial isolation, this work aimed to detect by molecular methods sequences from cyanobacteria and other bacteria present before and after a technique for obtaining axenic cultures from plating and exposure of Fischerella sp. CENA161 akinetes to the Extran detergent and sodium hypochlorite. Solutions containing 0.5, 1, and 2% sodium hypochlorite were able to remove contaminant bacterial CFUs from the culture. However, qPCR pointed that the quantity of sequences amplified with universal bacteria primers was higher than the number of cyanobacteria-specific sequences before and after treatments. The presence of uncultured bacteria in post-hypochlorite cultures was confirmed by high-throughput Illumina sequencing. These results suggest that culturing may overlook the presence of uncultured bacteria associated to cyanobacterial strains and is not sufficient for monitoring the success of cyanobacterial isolation by itself. Molecular methods such as qPCR could be employed as an additional measure for evaluating axenity in cyanobacterial strains. (C) 2016 Elsevier B.V. All rights reserved. |
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Evaluating methods for purifying cyanobacterial cultures by qPCR and high-throughput Illumina sequencingAkinetesAxenic culturesFischerellaMetagenomicsSymbiosisCyanobacteria are commonly found in association with other microorganisms, which constitutes a great challenge during the isolation of cyanobacterial strains. Although several methods have been published for obtaining axenic cyanobacterial cultures, their efficiency is usually evaluated by observing the growth of non-cyanobacteria in culture media. In order to verify whether uncultured bacteria should be a concern during cyanobacterial isolation, this work aimed to detect by molecular methods sequences from cyanobacteria and other bacteria present before and after a technique for obtaining axenic cultures from plating and exposure of Fischerella sp. CENA161 akinetes to the Extran detergent and sodium hypochlorite. Solutions containing 0.5, 1, and 2% sodium hypochlorite were able to remove contaminant bacterial CFUs from the culture. However, qPCR pointed that the quantity of sequences amplified with universal bacteria primers was higher than the number of cyanobacteria-specific sequences before and after treatments. The presence of uncultured bacteria in post-hypochlorite cultures was confirmed by high-throughput Illumina sequencing. These results suggest that culturing may overlook the presence of uncultured bacteria associated to cyanobacterial strains and is not sufficient for monitoring the success of cyanobacterial isolation by itself. Molecular methods such as qPCR could be employed as an additional measure for evaluating axenity in cyanobacterial strains. (C) 2016 Elsevier B.V. All rights reserved.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Univ Sao Paulo, Ctr Nucl Energy Agr, Sao Paulo, BrazilUniv Estadual Paulista, Fac Ciencias Agr & Vet, Sao Paulo, BrazilUniv Estadual Paulista, Fac Ciencias Agr & Vet, Sao Paulo, BrazilFAPESP: FAPESP 2013/09192-0FAPESP: 2013/20142-4FAPESP: 2011/08092-6FAPESP: 2010/18732-0CNPq: 310244/2015-3Elsevier B.V.Universidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Heck, KarinaMachineski, Gabriela SilvaAlvarenga, Danillo OliveiraMarcal Vieira Vaz, Marcelo GomesVarani, Alessandro de Mello [UNESP]Fiore, Marli Fatima2018-11-27T21:34:10Z2018-11-27T21:34:10Z2016-10-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article55-60application/pdfhttp://dx.doi.org/10.1016/j.mimet.2016.07.023Journal Of Microbiological Methods. Amsterdam: Elsevier Science Bv, v. 129, p. 55-60, 2016.0167-7012http://hdl.handle.net/11449/16532210.1016/j.mimet.2016.07.023WOS:000383941500009WOS000383941500009.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal Of Microbiological Methods0,696info:eu-repo/semantics/openAccess2024-06-07T15:31:11Zoai:repositorio.unesp.br:11449/165322Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T13:58:08.775177Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Evaluating methods for purifying cyanobacterial cultures by qPCR and high-throughput Illumina sequencing |
title |
Evaluating methods for purifying cyanobacterial cultures by qPCR and high-throughput Illumina sequencing |
spellingShingle |
Evaluating methods for purifying cyanobacterial cultures by qPCR and high-throughput Illumina sequencing Heck, Karina Akinetes Axenic cultures Fischerella Metagenomics Symbiosis |
title_short |
Evaluating methods for purifying cyanobacterial cultures by qPCR and high-throughput Illumina sequencing |
title_full |
Evaluating methods for purifying cyanobacterial cultures by qPCR and high-throughput Illumina sequencing |
title_fullStr |
Evaluating methods for purifying cyanobacterial cultures by qPCR and high-throughput Illumina sequencing |
title_full_unstemmed |
Evaluating methods for purifying cyanobacterial cultures by qPCR and high-throughput Illumina sequencing |
title_sort |
Evaluating methods for purifying cyanobacterial cultures by qPCR and high-throughput Illumina sequencing |
author |
Heck, Karina |
author_facet |
Heck, Karina Machineski, Gabriela Silva Alvarenga, Danillo Oliveira Marcal Vieira Vaz, Marcelo Gomes Varani, Alessandro de Mello [UNESP] Fiore, Marli Fatima |
author_role |
author |
author2 |
Machineski, Gabriela Silva Alvarenga, Danillo Oliveira Marcal Vieira Vaz, Marcelo Gomes Varani, Alessandro de Mello [UNESP] Fiore, Marli Fatima |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade de São Paulo (USP) Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Heck, Karina Machineski, Gabriela Silva Alvarenga, Danillo Oliveira Marcal Vieira Vaz, Marcelo Gomes Varani, Alessandro de Mello [UNESP] Fiore, Marli Fatima |
dc.subject.por.fl_str_mv |
Akinetes Axenic cultures Fischerella Metagenomics Symbiosis |
topic |
Akinetes Axenic cultures Fischerella Metagenomics Symbiosis |
description |
Cyanobacteria are commonly found in association with other microorganisms, which constitutes a great challenge during the isolation of cyanobacterial strains. Although several methods have been published for obtaining axenic cyanobacterial cultures, their efficiency is usually evaluated by observing the growth of non-cyanobacteria in culture media. In order to verify whether uncultured bacteria should be a concern during cyanobacterial isolation, this work aimed to detect by molecular methods sequences from cyanobacteria and other bacteria present before and after a technique for obtaining axenic cultures from plating and exposure of Fischerella sp. CENA161 akinetes to the Extran detergent and sodium hypochlorite. Solutions containing 0.5, 1, and 2% sodium hypochlorite were able to remove contaminant bacterial CFUs from the culture. However, qPCR pointed that the quantity of sequences amplified with universal bacteria primers was higher than the number of cyanobacteria-specific sequences before and after treatments. The presence of uncultured bacteria in post-hypochlorite cultures was confirmed by high-throughput Illumina sequencing. These results suggest that culturing may overlook the presence of uncultured bacteria associated to cyanobacterial strains and is not sufficient for monitoring the success of cyanobacterial isolation by itself. Molecular methods such as qPCR could be employed as an additional measure for evaluating axenity in cyanobacterial strains. (C) 2016 Elsevier B.V. All rights reserved. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-10-01 2018-11-27T21:34:10Z 2018-11-27T21:34:10Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.mimet.2016.07.023 Journal Of Microbiological Methods. Amsterdam: Elsevier Science Bv, v. 129, p. 55-60, 2016. 0167-7012 http://hdl.handle.net/11449/165322 10.1016/j.mimet.2016.07.023 WOS:000383941500009 WOS000383941500009.pdf |
url |
http://dx.doi.org/10.1016/j.mimet.2016.07.023 http://hdl.handle.net/11449/165322 |
identifier_str_mv |
Journal Of Microbiological Methods. Amsterdam: Elsevier Science Bv, v. 129, p. 55-60, 2016. 0167-7012 10.1016/j.mimet.2016.07.023 WOS:000383941500009 WOS000383941500009.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal Of Microbiological Methods 0,696 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
55-60 application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier B.V. |
publisher.none.fl_str_mv |
Elsevier B.V. |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808128297534488576 |