Influence of the incubation conditions on culture media to optimize primary isolation of Mycobacterium bovis

Detalhes bibliográficos
Autor(a) principal: Ikuta, Cássia Yumi
Data de Publicação: 2016
Outros Autores: Morato, Flávia, Souza, Gisele Oliveira de, Heinemann, Marcos Bryan, Amaku, Marcos, Ferreira Neto, José Soares
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Semina. Ciências Agrárias (Online)
DOI: 10.5433/1679-0359.2016v37n5Supl2p3693
Texto Completo: https://ojs.uel.br/revistas/uel/index.php/semagrarias/article/view/27316
Resumo: The isolation of Mycobacterium bovis is critical to a surveillance system for bovine tuberculosis based on detection of lesions in abattoirs. Thus, four solid culture media and three incubation conditions were investigated to elucidate which combination overcomes the others by assessing growth, time to the first appearance of colonies and their number. Ninety-seven samples of granulomatous lesions were submitted to the decontamination procedure by 1-hexadecylpyridinium chloride at 0.75% w/v, and inoculated on two egg-based media, Stonebrink’s (ST) and Löwenstein-Jensen’s with sodium pyruvate (LJp), and two agar-based media, tuberculosis blood agar (B83) and Middlebrook 7H11 medium (7H11). Each medium was incubated at 37°C for 90 days in three incubation conditions: in air, in air containing 10% carbon dioxide (CO2), and in air in slopes closed with burned hydrophobic cotton and subsequently plugged with a cork to create a microaerophilic atmosphere. The colonies appeared faster and in higher number when incubated in air containing 10% CO2 (p < 0.01), independent of media. B83 showed a faster growth and detected more isolates at 30 days of incubation, when compared to ST (0.0178), LJp (p < 0.0001) and 7H11 (p < 0.0001), though there was no difference between B83, ST and LJp at 60 and 90 days of incubation. 7H11 presented the lowest number of isolates (p < 0.0001) and a longer period for the appearance of the first colony (p < 0.001). According to our findings, the concomitant use of ST and B83 media incubated in air containing 10% CO2 increases the isolation of M. bovis in a shorter period of time, which improves bovine tuberculosis diagnosis.
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spelling Influence of the incubation conditions on culture media to optimize primary isolation of Mycobacterium bovisInfluência das condições de incubação nos meios de cultura para otimizar o primo isolamento de Mycobacterium bovisPrimary isolationBovine tuberculosisMycobacterium bovisCulture mediaIncubation conditions.Primo isolamentoTuberculose bovinaMycobacterium bovisMeios de culturaCondições de incubação.The isolation of Mycobacterium bovis is critical to a surveillance system for bovine tuberculosis based on detection of lesions in abattoirs. Thus, four solid culture media and three incubation conditions were investigated to elucidate which combination overcomes the others by assessing growth, time to the first appearance of colonies and their number. Ninety-seven samples of granulomatous lesions were submitted to the decontamination procedure by 1-hexadecylpyridinium chloride at 0.75% w/v, and inoculated on two egg-based media, Stonebrink’s (ST) and Löwenstein-Jensen’s with sodium pyruvate (LJp), and two agar-based media, tuberculosis blood agar (B83) and Middlebrook 7H11 medium (7H11). Each medium was incubated at 37°C for 90 days in three incubation conditions: in air, in air containing 10% carbon dioxide (CO2), and in air in slopes closed with burned hydrophobic cotton and subsequently plugged with a cork to create a microaerophilic atmosphere. The colonies appeared faster and in higher number when incubated in air containing 10% CO2 (p < 0.01), independent of media. B83 showed a faster growth and detected more isolates at 30 days of incubation, when compared to ST (0.0178), LJp (p < 0.0001) and 7H11 (p < 0.0001), though there was no difference between B83, ST and LJp at 60 and 90 days of incubation. 7H11 presented the lowest number of isolates (p < 0.0001) and a longer period for the appearance of the first colony (p < 0.001). According to our findings, the concomitant use of ST and B83 media incubated in air containing 10% CO2 increases the isolation of M. bovis in a shorter period of time, which improves bovine tuberculosis diagnosis.O isolamento do Mycobacterium bovis é fundamental para um sistema de vigilância para tuberculose bovina baseado na detecção de lesões em abatedouro. Assim, quatro meios de cultura sólidos e três condições de incubação foram investigados para elucidar qual combinação supera as outras através da avaliação de crescimento, tempo para o aparecimento da primeira colônia e número de colônias. Noventa e sete amostras de lesões granulomatosas foram submetidas ao processo de descontaminação por cloreto de 1-hexadecilpiridínio a 0,75%, e inoculadas em dois meios a base de ovo, Stonebrink (ST) e Löwenstein-Jensen com piruvato de sódio (LJp), e dois meios a base de ágar, ágar sangue tuberculose (B83) e Middlebrook 7H11 (7H11). Cada meio foi incubado a 37°C por 90 dias, em três condições de incubação: em atmosfera normal, em atmosfera com acréscimo de 10% de dióxido de carbono (CO2), e em atmosfera normal em tubos fechados com algodão hidrófobo queimado e subsequentemente fechado com rolha para criar uma atmosfera microaerófila. As colônias apareceram mais rapidamente e em maior número quando incubadas em atmosfera com 10% de CO2 (p < 0,01), independente dos meios. As micobactérias cresceram em maior abundância e mais rapidamente no meio B83 aos 30 dias de incubação, comparado a ST (0,0178), LJp (p < 0,0001) e 7H11 (p < 0,0001), apesar de não ter havido diferença entre B83, ST e LJp aos 60 e 90 dias de incubação. 7H11 exibiu o número mais baixo de isolados (p < 0,0001) e um período mais longo para o aparecimento da primeira colônia (p < 0,001). De acordo com nossos resultados, o uso concomitante dos meios ST e B83, incubados em atmosfera com acréscimo de 10% de CO2, aumenta a proporção de isolados e o número de UFC de M. bovis, além de abreviar o tempo para aparecimento das primeiras colônias, melhorando o diagnóstico direto de tuberculose.UEL2016-11-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://ojs.uel.br/revistas/uel/index.php/semagrarias/article/view/2731610.5433/1679-0359.2016v37n5Supl2p3693Semina: Ciências Agrárias; Vol. 37 No. 5Supl2 (2016); 3693-3700Semina: Ciências Agrárias; v. 37 n. 5Supl2 (2016); 3693-37001679-03591676-546Xreponame:Semina. Ciências Agrárias (Online)instname:Universidade Estadual de Londrina (UEL)instacron:UELenghttps://ojs.uel.br/revistas/uel/index.php/semagrarias/article/view/27316/19935Copyright (c) 2016 Semina: Ciências Agráriashttp://creativecommons.org/licenses/by-nc/4.0info:eu-repo/semantics/openAccessIkuta, Cássia YumiMorato, FláviaSouza, Gisele Oliveira deHeinemann, Marcos BryanAmaku, MarcosFerreira Neto, José Soares2022-11-29T16:56:49Zoai:ojs.pkp.sfu.ca:article/27316Revistahttp://www.uel.br/revistas/uel/index.php/semagrariasPUBhttps://ojs.uel.br/revistas/uel/index.php/semagrarias/oaisemina.agrarias@uel.br1679-03591676-546Xopendoar:2022-11-29T16:56:49Semina. Ciências Agrárias (Online) - Universidade Estadual de Londrina (UEL)false
dc.title.none.fl_str_mv Influence of the incubation conditions on culture media to optimize primary isolation of Mycobacterium bovis
Influência das condições de incubação nos meios de cultura para otimizar o primo isolamento de Mycobacterium bovis
title Influence of the incubation conditions on culture media to optimize primary isolation of Mycobacterium bovis
spellingShingle Influence of the incubation conditions on culture media to optimize primary isolation of Mycobacterium bovis
Influence of the incubation conditions on culture media to optimize primary isolation of Mycobacterium bovis
Ikuta, Cássia Yumi
Primary isolation
Bovine tuberculosis
Mycobacterium bovis
Culture media
Incubation conditions.
Primo isolamento
Tuberculose bovina
Mycobacterium bovis
Meios de cultura
Condições de incubação.
Ikuta, Cássia Yumi
Primary isolation
Bovine tuberculosis
Mycobacterium bovis
Culture media
Incubation conditions.
Primo isolamento
Tuberculose bovina
Mycobacterium bovis
Meios de cultura
Condições de incubação.
title_short Influence of the incubation conditions on culture media to optimize primary isolation of Mycobacterium bovis
title_full Influence of the incubation conditions on culture media to optimize primary isolation of Mycobacterium bovis
title_fullStr Influence of the incubation conditions on culture media to optimize primary isolation of Mycobacterium bovis
Influence of the incubation conditions on culture media to optimize primary isolation of Mycobacterium bovis
title_full_unstemmed Influence of the incubation conditions on culture media to optimize primary isolation of Mycobacterium bovis
Influence of the incubation conditions on culture media to optimize primary isolation of Mycobacterium bovis
title_sort Influence of the incubation conditions on culture media to optimize primary isolation of Mycobacterium bovis
author Ikuta, Cássia Yumi
author_facet Ikuta, Cássia Yumi
Ikuta, Cássia Yumi
Morato, Flávia
Souza, Gisele Oliveira de
Heinemann, Marcos Bryan
Amaku, Marcos
Ferreira Neto, José Soares
Morato, Flávia
Souza, Gisele Oliveira de
Heinemann, Marcos Bryan
Amaku, Marcos
Ferreira Neto, José Soares
author_role author
author2 Morato, Flávia
Souza, Gisele Oliveira de
Heinemann, Marcos Bryan
Amaku, Marcos
Ferreira Neto, José Soares
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Ikuta, Cássia Yumi
Morato, Flávia
Souza, Gisele Oliveira de
Heinemann, Marcos Bryan
Amaku, Marcos
Ferreira Neto, José Soares
dc.subject.por.fl_str_mv Primary isolation
Bovine tuberculosis
Mycobacterium bovis
Culture media
Incubation conditions.
Primo isolamento
Tuberculose bovina
Mycobacterium bovis
Meios de cultura
Condições de incubação.
topic Primary isolation
Bovine tuberculosis
Mycobacterium bovis
Culture media
Incubation conditions.
Primo isolamento
Tuberculose bovina
Mycobacterium bovis
Meios de cultura
Condições de incubação.
description The isolation of Mycobacterium bovis is critical to a surveillance system for bovine tuberculosis based on detection of lesions in abattoirs. Thus, four solid culture media and three incubation conditions were investigated to elucidate which combination overcomes the others by assessing growth, time to the first appearance of colonies and their number. Ninety-seven samples of granulomatous lesions were submitted to the decontamination procedure by 1-hexadecylpyridinium chloride at 0.75% w/v, and inoculated on two egg-based media, Stonebrink’s (ST) and Löwenstein-Jensen’s with sodium pyruvate (LJp), and two agar-based media, tuberculosis blood agar (B83) and Middlebrook 7H11 medium (7H11). Each medium was incubated at 37°C for 90 days in three incubation conditions: in air, in air containing 10% carbon dioxide (CO2), and in air in slopes closed with burned hydrophobic cotton and subsequently plugged with a cork to create a microaerophilic atmosphere. The colonies appeared faster and in higher number when incubated in air containing 10% CO2 (p < 0.01), independent of media. B83 showed a faster growth and detected more isolates at 30 days of incubation, when compared to ST (0.0178), LJp (p < 0.0001) and 7H11 (p < 0.0001), though there was no difference between B83, ST and LJp at 60 and 90 days of incubation. 7H11 presented the lowest number of isolates (p < 0.0001) and a longer period for the appearance of the first colony (p < 0.001). According to our findings, the concomitant use of ST and B83 media incubated in air containing 10% CO2 increases the isolation of M. bovis in a shorter period of time, which improves bovine tuberculosis diagnosis.
publishDate 2016
dc.date.none.fl_str_mv 2016-11-09
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://ojs.uel.br/revistas/uel/index.php/semagrarias/article/view/27316
10.5433/1679-0359.2016v37n5Supl2p3693
url https://ojs.uel.br/revistas/uel/index.php/semagrarias/article/view/27316
identifier_str_mv 10.5433/1679-0359.2016v37n5Supl2p3693
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://ojs.uel.br/revistas/uel/index.php/semagrarias/article/view/27316/19935
dc.rights.driver.fl_str_mv Copyright (c) 2016 Semina: Ciências Agrárias
http://creativecommons.org/licenses/by-nc/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2016 Semina: Ciências Agrárias
http://creativecommons.org/licenses/by-nc/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv UEL
publisher.none.fl_str_mv UEL
dc.source.none.fl_str_mv Semina: Ciências Agrárias; Vol. 37 No. 5Supl2 (2016); 3693-3700
Semina: Ciências Agrárias; v. 37 n. 5Supl2 (2016); 3693-3700
1679-0359
1676-546X
reponame:Semina. Ciências Agrárias (Online)
instname:Universidade Estadual de Londrina (UEL)
instacron:UEL
instname_str Universidade Estadual de Londrina (UEL)
instacron_str UEL
institution UEL
reponame_str Semina. Ciências Agrárias (Online)
collection Semina. Ciências Agrárias (Online)
repository.name.fl_str_mv Semina. Ciências Agrárias (Online) - Universidade Estadual de Londrina (UEL)
repository.mail.fl_str_mv semina.agrarias@uel.br
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dc.identifier.doi.none.fl_str_mv 10.5433/1679-0359.2016v37n5Supl2p3693