In vitro production of conidia of Alternaria solani
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | LOCUS Repositório Institucional da UFV |
Texto Completo: | http://dx.doi.org/10.1590/S1982-56762010000400001 https://locus.ufv.br//handle/123456789/27239 |
Resumo: | Sporulation of Alternaria solani can be scarce and is often reduced when the fungus is cultivated in vitro. A series of experiments were conducted to assess the effects of moisture, mycelial wounding, light quality and photoperiod, and culture media on conidial production. A procedure to induce sporulation based on mycelial wounding and dehydration was adapted and validated. Best results were obtained when fungal colonies were grown in V8 medium at 25ºC in the dark with agitation for seven days; the mycelium mass was ground, poured into potato dextrose agar (pH 6.5) in plates, and incubated at 25 ± 2ºC under near ultraviolet light and 12 h-photoperiod. The procedure was validated with 30 isolates of A. solani from different hosts, sampling locations, ages, and storage conditions. Conidial production, germination, and infectivity were quantified. Seventy-five percent of the isolates sporulated and the lowest germination rate was 68%. Inoculations of conidial suspension of all isolates resulted in lesions on tomato and potato plants. The effect of subculturing on A. solani sporulation was also assessed. After six subcultures, every seven days, there was no reduction in sporulation of colonies that were induced with the protocol. |
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In vitro production of conidia of Alternaria solaniEarly blightBiphasic techniqueSubcultureInfection frequencyPinta pretaTécnica bifásicaSubculturaFrequência de infecçãoSporulation of Alternaria solani can be scarce and is often reduced when the fungus is cultivated in vitro. A series of experiments were conducted to assess the effects of moisture, mycelial wounding, light quality and photoperiod, and culture media on conidial production. A procedure to induce sporulation based on mycelial wounding and dehydration was adapted and validated. Best results were obtained when fungal colonies were grown in V8 medium at 25ºC in the dark with agitation for seven days; the mycelium mass was ground, poured into potato dextrose agar (pH 6.5) in plates, and incubated at 25 ± 2ºC under near ultraviolet light and 12 h-photoperiod. The procedure was validated with 30 isolates of A. solani from different hosts, sampling locations, ages, and storage conditions. Conidial production, germination, and infectivity were quantified. Seventy-five percent of the isolates sporulated and the lowest germination rate was 68%. Inoculations of conidial suspension of all isolates resulted in lesions on tomato and potato plants. The effect of subculturing on A. solani sporulation was also assessed. After six subcultures, every seven days, there was no reduction in sporulation of colonies that were induced with the protocol.A esporulação de Alternaria solani in vitro pode ser escassa e tende a reduzir após sucessivas repicagens. Conduziram-se vários experimentos para avaliar o efeito da umidade, injúria da colônia, qualidade de luz e fotoperíodo, bem como do meio de cultura na produção de conídios. Adaptou-se a técnica bifásica para induzir esporulação, por meio de injúria de micélio e desidratação do meio de cultura. Obtiveram-se melhores resultados quando colônias cresceram em meio V8 a 25ºC, no escuro, sob agitação durante sete dias; a massa de micélio foi triturada e a suspensão depositada em meio BDA (pH 6,5) em placas de Petri, incubando-se a 25 ± 2ºC, sob luz negra com 12 h de fotoperíodo. Validou-se o protocolo para 30 isolados de A. solani distintos quanto ao hospedeiro, local de origem, idade e forma de armazenamento. Quantificaram-se a produção, germinação e infectividade de conídios. Dos 30 isolados, 75% esporularam e a germinação mínima de conídios foi de 68%. Todos os isolados foram patogênicos em seus respectivos hospedeiros. Avaliou-se, também, o efeito de repicagens sucessivas na esporulação. Todos os isolados produziram conídios após seis repicagens sucessivas.Tropical Plant Pathology2019-10-04T13:27:02Z2019-10-04T13:27:02Z2010-07info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlepdfapplication/pdf1983-2052http://dx.doi.org/10.1590/S1982-56762010000400001https://locus.ufv.br//handle/123456789/27239engv. 35, n. 04, p. 203- 212, jul./ ago. 2010Rodrigues, Tatiana T. M. S.Maffia, Luiz A.Dhingra, Onkar D.Mizubuti, Eduardo S. G.info:eu-repo/semantics/openAccessreponame:LOCUS Repositório Institucional da UFVinstname:Universidade Federal de Viçosa (UFV)instacron:UFV2024-07-12T08:27:03Zoai:locus.ufv.br:123456789/27239Repositório InstitucionalPUBhttps://www.locus.ufv.br/oai/requestfabiojreis@ufv.bropendoar:21452024-07-12T08:27:03LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV)false |
dc.title.none.fl_str_mv |
In vitro production of conidia of Alternaria solani |
title |
In vitro production of conidia of Alternaria solani |
spellingShingle |
In vitro production of conidia of Alternaria solani Rodrigues, Tatiana T. M. S. Early blight Biphasic technique Subculture Infection frequency Pinta preta Técnica bifásica Subcultura Frequência de infecção |
title_short |
In vitro production of conidia of Alternaria solani |
title_full |
In vitro production of conidia of Alternaria solani |
title_fullStr |
In vitro production of conidia of Alternaria solani |
title_full_unstemmed |
In vitro production of conidia of Alternaria solani |
title_sort |
In vitro production of conidia of Alternaria solani |
author |
Rodrigues, Tatiana T. M. S. |
author_facet |
Rodrigues, Tatiana T. M. S. Maffia, Luiz A. Dhingra, Onkar D. Mizubuti, Eduardo S. G. |
author_role |
author |
author2 |
Maffia, Luiz A. Dhingra, Onkar D. Mizubuti, Eduardo S. G. |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Rodrigues, Tatiana T. M. S. Maffia, Luiz A. Dhingra, Onkar D. Mizubuti, Eduardo S. G. |
dc.subject.por.fl_str_mv |
Early blight Biphasic technique Subculture Infection frequency Pinta preta Técnica bifásica Subcultura Frequência de infecção |
topic |
Early blight Biphasic technique Subculture Infection frequency Pinta preta Técnica bifásica Subcultura Frequência de infecção |
description |
Sporulation of Alternaria solani can be scarce and is often reduced when the fungus is cultivated in vitro. A series of experiments were conducted to assess the effects of moisture, mycelial wounding, light quality and photoperiod, and culture media on conidial production. A procedure to induce sporulation based on mycelial wounding and dehydration was adapted and validated. Best results were obtained when fungal colonies were grown in V8 medium at 25ºC in the dark with agitation for seven days; the mycelium mass was ground, poured into potato dextrose agar (pH 6.5) in plates, and incubated at 25 ± 2ºC under near ultraviolet light and 12 h-photoperiod. The procedure was validated with 30 isolates of A. solani from different hosts, sampling locations, ages, and storage conditions. Conidial production, germination, and infectivity were quantified. Seventy-five percent of the isolates sporulated and the lowest germination rate was 68%. Inoculations of conidial suspension of all isolates resulted in lesions on tomato and potato plants. The effect of subculturing on A. solani sporulation was also assessed. After six subcultures, every seven days, there was no reduction in sporulation of colonies that were induced with the protocol. |
publishDate |
2010 |
dc.date.none.fl_str_mv |
2010-07 2019-10-04T13:27:02Z 2019-10-04T13:27:02Z |
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 |
1983-2052 http://dx.doi.org/10.1590/S1982-56762010000400001 https://locus.ufv.br//handle/123456789/27239 |
identifier_str_mv |
1983-2052 |
url |
http://dx.doi.org/10.1590/S1982-56762010000400001 https://locus.ufv.br//handle/123456789/27239 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
v. 35, n. 04, p. 203- 212, jul./ ago. 2010 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
pdf application/pdf |
dc.publisher.none.fl_str_mv |
Tropical Plant Pathology |
publisher.none.fl_str_mv |
Tropical Plant Pathology |
dc.source.none.fl_str_mv |
reponame:LOCUS Repositório Institucional da UFV instname:Universidade Federal de Viçosa (UFV) instacron:UFV |
instname_str |
Universidade Federal de Viçosa (UFV) |
instacron_str |
UFV |
institution |
UFV |
reponame_str |
LOCUS Repositório Institucional da UFV |
collection |
LOCUS Repositório Institucional da UFV |
repository.name.fl_str_mv |
LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV) |
repository.mail.fl_str_mv |
fabiojreis@ufv.br |
_version_ |
1822610720113557504 |