Evaluating methods for purifying cyanobacterial cultures by qPCR and high-throughput Illumina sequencing

Detalhes bibliográficos
Autor(a) principal: Heck, Karina
Data de Publicação: 2016
Outros Autores: Machineski, Gabriela Silva, Alvarenga, Danillo Oliveira, Marcal Vieira Vaz, Marcelo Gomes, Varani, Alessandro de Mello [UNESP], Fiore, Marli Fatima
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.
id UNSP_bd00822ed4b56aa74167bbecce77b961
oai_identifier_str oai:repositorio.unesp.br:11449/165322
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling 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