Comparative study of Mycobacterium bovis primary isolation methods

Detalhes bibliográficos
Autor(a) principal: Issa,Marina de Azevedo
Data de Publicação: 2017
Outros Autores: Soares Filho,Paulo Martins, Fonseca Júnior,Antônio Augusto, Hodon,Mikael Arrais, Santos,Lílian Cristian dos, Reis,Jenner Karlisson Pimenta dos, Cerqueira Leite,Rômulo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Microbiology
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822017000100139
Resumo: Abstract For the definitive diagnosis of bovine tuberculosis, isolation of the etiologic agent is required. However, there is no consensus on the best methodology for isolation of Mycobacterium bovis in Brazil. This study evaluated the most used decontaminants and culture media in the country, in order to identify the best combination for the Brazilian samples. Three decontaminants - 2% sodium hydroxide (w/v), 0.75% hexadecylpiridinium chloride (w/v) and 5% sulphuric acid (v/v) and four culture media - 7H11 Middlebrook with additives and OADC supplement “A” (7H11 A), the same media with another supplement trademark (7H11 B), tuberculosis blood agar (B83) and Stonebrink's medium were compared. Regarding the isolation, there were no significant differences between the decontaminants and media combinations, except 7H11A combined to any decontaminant. However, the mean colonies score was significantly greater when the samples were decontaminated with 5% sulphuric acid and inoculated in 7H11 B or SB, without significant difference between them, although colonies appeared earlier on 7H11B than on SB. The trademark of OADC supplement influenced the isolation rate and the number of isolated colonies in Middlebrook 7H11. An incubation time of four weeks was required to detect all positive samples in 7H11 B after decontamination with 5% sulphuric acid but there was an increase in the number of colonies until the sixth week of incubation. Overall, the best strategy for the primary isolation of M. bovis from Brazilian samples was the decontamination with 5% sulphuric acid (final concentration) and inoculation in Middlebrook 7H11 medium formulated with OADC supplement “B”.
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spelling Comparative study of Mycobacterium bovis primary isolation methodsMycobacterium bovisDiagnosisMiddlebrook 7H11IsolationSulphuric acidAbstract For the definitive diagnosis of bovine tuberculosis, isolation of the etiologic agent is required. However, there is no consensus on the best methodology for isolation of Mycobacterium bovis in Brazil. This study evaluated the most used decontaminants and culture media in the country, in order to identify the best combination for the Brazilian samples. Three decontaminants - 2% sodium hydroxide (w/v), 0.75% hexadecylpiridinium chloride (w/v) and 5% sulphuric acid (v/v) and four culture media - 7H11 Middlebrook with additives and OADC supplement “A” (7H11 A), the same media with another supplement trademark (7H11 B), tuberculosis blood agar (B83) and Stonebrink's medium were compared. Regarding the isolation, there were no significant differences between the decontaminants and media combinations, except 7H11A combined to any decontaminant. However, the mean colonies score was significantly greater when the samples were decontaminated with 5% sulphuric acid and inoculated in 7H11 B or SB, without significant difference between them, although colonies appeared earlier on 7H11B than on SB. The trademark of OADC supplement influenced the isolation rate and the number of isolated colonies in Middlebrook 7H11. An incubation time of four weeks was required to detect all positive samples in 7H11 B after decontamination with 5% sulphuric acid but there was an increase in the number of colonies until the sixth week of incubation. Overall, the best strategy for the primary isolation of M. bovis from Brazilian samples was the decontamination with 5% sulphuric acid (final concentration) and inoculation in Middlebrook 7H11 medium formulated with OADC supplement “B”.Sociedade Brasileira de Microbiologia2017-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822017000100139Brazilian Journal of Microbiology v.48 n.1 2017reponame:Brazilian Journal of Microbiologyinstname:Sociedade Brasileira de Microbiologia (SBM)instacron:SBM10.1016/j.bjm.2016.07.026info:eu-repo/semantics/openAccessIssa,Marina de AzevedoSoares Filho,Paulo MartinsFonseca Júnior,Antônio AugustoHodon,Mikael ArraisSantos,Lílian Cristian dosReis,Jenner Karlisson Pimenta dosCerqueira Leite,Rômuloeng2017-01-24T00:00:00Zoai:scielo:S1517-83822017000100139Revistahttps://www.scielo.br/j/bjm/ONGhttps://old.scielo.br/oai/scielo-oai.phpbjm@sbmicrobiologia.org.br||mbmartin@usp.br1678-44051517-8382opendoar:2017-01-24T00:00Brazilian Journal of Microbiology - Sociedade Brasileira de Microbiologia (SBM)false
dc.title.none.fl_str_mv Comparative study of Mycobacterium bovis primary isolation methods
title Comparative study of Mycobacterium bovis primary isolation methods
spellingShingle Comparative study of Mycobacterium bovis primary isolation methods
Issa,Marina de Azevedo
Mycobacterium bovis
Diagnosis
Middlebrook 7H11
Isolation
Sulphuric acid
title_short Comparative study of Mycobacterium bovis primary isolation methods
title_full Comparative study of Mycobacterium bovis primary isolation methods
title_fullStr Comparative study of Mycobacterium bovis primary isolation methods
title_full_unstemmed Comparative study of Mycobacterium bovis primary isolation methods
title_sort Comparative study of Mycobacterium bovis primary isolation methods
author Issa,Marina de Azevedo
author_facet Issa,Marina de Azevedo
Soares Filho,Paulo Martins
Fonseca Júnior,Antônio Augusto
Hodon,Mikael Arrais
Santos,Lílian Cristian dos
Reis,Jenner Karlisson Pimenta dos
Cerqueira Leite,Rômulo
author_role author
author2 Soares Filho,Paulo Martins
Fonseca Júnior,Antônio Augusto
Hodon,Mikael Arrais
Santos,Lílian Cristian dos
Reis,Jenner Karlisson Pimenta dos
Cerqueira Leite,Rômulo
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Issa,Marina de Azevedo
Soares Filho,Paulo Martins
Fonseca Júnior,Antônio Augusto
Hodon,Mikael Arrais
Santos,Lílian Cristian dos
Reis,Jenner Karlisson Pimenta dos
Cerqueira Leite,Rômulo
dc.subject.por.fl_str_mv Mycobacterium bovis
Diagnosis
Middlebrook 7H11
Isolation
Sulphuric acid
topic Mycobacterium bovis
Diagnosis
Middlebrook 7H11
Isolation
Sulphuric acid
description Abstract For the definitive diagnosis of bovine tuberculosis, isolation of the etiologic agent is required. However, there is no consensus on the best methodology for isolation of Mycobacterium bovis in Brazil. This study evaluated the most used decontaminants and culture media in the country, in order to identify the best combination for the Brazilian samples. Three decontaminants - 2% sodium hydroxide (w/v), 0.75% hexadecylpiridinium chloride (w/v) and 5% sulphuric acid (v/v) and four culture media - 7H11 Middlebrook with additives and OADC supplement “A” (7H11 A), the same media with another supplement trademark (7H11 B), tuberculosis blood agar (B83) and Stonebrink's medium were compared. Regarding the isolation, there were no significant differences between the decontaminants and media combinations, except 7H11A combined to any decontaminant. However, the mean colonies score was significantly greater when the samples were decontaminated with 5% sulphuric acid and inoculated in 7H11 B or SB, without significant difference between them, although colonies appeared earlier on 7H11B than on SB. The trademark of OADC supplement influenced the isolation rate and the number of isolated colonies in Middlebrook 7H11. An incubation time of four weeks was required to detect all positive samples in 7H11 B after decontamination with 5% sulphuric acid but there was an increase in the number of colonies until the sixth week of incubation. Overall, the best strategy for the primary isolation of M. bovis from Brazilian samples was the decontamination with 5% sulphuric acid (final concentration) and inoculation in Middlebrook 7H11 medium formulated with OADC supplement “B”.
publishDate 2017
dc.date.none.fl_str_mv 2017-03-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822017000100139
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822017000100139
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1016/j.bjm.2016.07.026
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Microbiologia
publisher.none.fl_str_mv Sociedade Brasileira de Microbiologia
dc.source.none.fl_str_mv Brazilian Journal of Microbiology v.48 n.1 2017
reponame:Brazilian Journal of Microbiology
instname:Sociedade Brasileira de Microbiologia (SBM)
instacron:SBM
instname_str Sociedade Brasileira de Microbiologia (SBM)
instacron_str SBM
institution SBM
reponame_str Brazilian Journal of Microbiology
collection Brazilian Journal of Microbiology
repository.name.fl_str_mv Brazilian Journal of Microbiology - Sociedade Brasileira de Microbiologia (SBM)
repository.mail.fl_str_mv bjm@sbmicrobiologia.org.br||mbmartin@usp.br
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