Safety and intestinal microbiota modulation by the exopolysaccharide-producing strains Bifidobacterium animalis IPLA R1 and Bifidobacterium longum IPLA E44 orally administered to W...

Autores
Salazar, Nuria; Binetti, Ana Griselda; Gueimonde, Miguel; Alonso, Ana; Garrido, Pablo; González del Rey, Carmen; González, Celestino; Ruas-Madiedo, Patricia; de los Reyes-Gavilán, Clara G.
Año de publicación
2011
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Bifidobacterium animalis subsp. lactis IPLA R1 and Bifidobacterium longum IPLA E44 strains were tested in vivo for their safety and ability to modulate the intestinal microbiota. Chemically simulated gastrointestinal digestion showed a considerably lower survival of E44 than R1 strain, the first microorganism being also more sensitive to the refrigerated storage in 10%-skimmed milk at 4ºC. Male Wistar rats 12 weeks-old were distributed into three groups, eight rats each. Two groups were daily administered 108 to 109 cfu of the corresponding strain suspended in 10%-skimmed milk during 24 days whereas rats in the placebo group received skimmed milk without microorganisms added. The microbiota and short chain fatty acids (SCFA) were monitored daily in faeces during treatment and in caecum-content at the end of the assay. Quantitative real-time PCR (qPCR) showed that faecal and caecal Bifidobacterium levels were higher in bifidobacteria-fed than in the placebo rats at the end of the intervention whereas total anaerobic-plate counts did not show significant differences. Quantification of B. animalis and B. longum by q-PCR evidenced that, independently on the microorganism administered, treatment with bifidobacteria resulted in higher levels of B. animalis in the caecum. PCR-DGGE analysis of microbial populations revealed a higher diversity of bands in caecum-content of rats fed B. animalis IPLA R1 than in the placebo and rats fed B. longum IPLA E44. Remarkably, although no variations in the proportion of acetate, propionate and butyrate were found, at the end of the assay total SCFA concentration in faeces of rats fed bifidobacteria were significantly higher and those in caecum-content significantly lower than that of the placebo group, suggesting a displacement of the SCFA production to parts in the intestine more distal that caecum in rats receiving bifidobacteria. Harmful glycosidic activities were absent or at low levels in the strains R1 and E44. Both strains were sensitive to most antibiotics although, similarly to some other bifidobacteria strains, they displayed a moderate resistance against tetracycline which in the case of R1correlated with the presence of tet (W) gene. The general parameters indicating well-being status as well as translocation to different organs and histological examination of the gut tissues revealed no changes induced by the administration of bifidobacteria. Therefore, the oral administration of B. animalis IPLA R1 and B. longum E44 can be considered safe, these microorganisms having the ability to modulate the intestinal microbiota of rats by influencing SCFA and the bifidobacterial population levels.
Fil: Salazar, Nuria. Instituto de Productos Lácteos de Asturias; España
Fil: Binetti, Ana Griselda. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Lactología Industrial. Universidad Nacional del Litoral. Facultad de Ingeniería Química. Instituto de Lactología Industrial; Argentina
Fil: Gueimonde, Miguel. Instituto de Productos Lácteos de Asturias; España
Fil: Alonso, Ana. Universidad de Oviedo; España
Fil: Garrido, Pablo. Universidad de Oviedo; España
Fil: González del Rey, Carmen. Agustin Hospital; España
Fil: González, Celestino. Universidad de Oviedo; España
Fil: Ruas-Madiedo, Patricia. Instituto de Productos Lácteos de Asturias; España
Fil: de los Reyes-Gavilán, Clara G.. Instituto de Productos Lácteos de Asturias; España
Materia
probiotic
bifidobacteria
exopolysacharide
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/103205

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network_name_str CONICET Digital (CONICET)
spelling Safety and intestinal microbiota modulation by the exopolysaccharide-producing strains Bifidobacterium animalis IPLA R1 and Bifidobacterium longum IPLA E44 orally administered to Wistar ratsSalazar, NuriaBinetti, Ana GriseldaGueimonde, MiguelAlonso, AnaGarrido, PabloGonzález del Rey, CarmenGonzález, CelestinoRuas-Madiedo, Patriciade los Reyes-Gavilán, Clara G.probioticbifidobacteriaexopolysacharidehttps://purl.org/becyt/ford/2.11https://purl.org/becyt/ford/2Bifidobacterium animalis subsp. lactis IPLA R1 and Bifidobacterium longum IPLA E44 strains were tested in vivo for their safety and ability to modulate the intestinal microbiota. Chemically simulated gastrointestinal digestion showed a considerably lower survival of E44 than R1 strain, the first microorganism being also more sensitive to the refrigerated storage in 10%-skimmed milk at 4ºC. Male Wistar rats 12 weeks-old were distributed into three groups, eight rats each. Two groups were daily administered 108 to 109 cfu of the corresponding strain suspended in 10%-skimmed milk during 24 days whereas rats in the placebo group received skimmed milk without microorganisms added. The microbiota and short chain fatty acids (SCFA) were monitored daily in faeces during treatment and in caecum-content at the end of the assay. Quantitative real-time PCR (qPCR) showed that faecal and caecal Bifidobacterium levels were higher in bifidobacteria-fed than in the placebo rats at the end of the intervention whereas total anaerobic-plate counts did not show significant differences. Quantification of B. animalis and B. longum by q-PCR evidenced that, independently on the microorganism administered, treatment with bifidobacteria resulted in higher levels of B. animalis in the caecum. PCR-DGGE analysis of microbial populations revealed a higher diversity of bands in caecum-content of rats fed B. animalis IPLA R1 than in the placebo and rats fed B. longum IPLA E44. Remarkably, although no variations in the proportion of acetate, propionate and butyrate were found, at the end of the assay total SCFA concentration in faeces of rats fed bifidobacteria were significantly higher and those in caecum-content significantly lower than that of the placebo group, suggesting a displacement of the SCFA production to parts in the intestine more distal that caecum in rats receiving bifidobacteria. Harmful glycosidic activities were absent or at low levels in the strains R1 and E44. Both strains were sensitive to most antibiotics although, similarly to some other bifidobacteria strains, they displayed a moderate resistance against tetracycline which in the case of R1correlated with the presence of tet (W) gene. The general parameters indicating well-being status as well as translocation to different organs and histological examination of the gut tissues revealed no changes induced by the administration of bifidobacteria. Therefore, the oral administration of B. animalis IPLA R1 and B. longum E44 can be considered safe, these microorganisms having the ability to modulate the intestinal microbiota of rats by influencing SCFA and the bifidobacterial population levels.Fil: Salazar, Nuria. Instituto de Productos Lácteos de Asturias; EspañaFil: Binetti, Ana Griselda. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Lactología Industrial. Universidad Nacional del Litoral. Facultad de Ingeniería Química. Instituto de Lactología Industrial; ArgentinaFil: Gueimonde, Miguel. Instituto de Productos Lácteos de Asturias; EspañaFil: Alonso, Ana. Universidad de Oviedo; EspañaFil: Garrido, Pablo. Universidad de Oviedo; EspañaFil: González del Rey, Carmen. Agustin Hospital; EspañaFil: González, Celestino. Universidad de Oviedo; EspañaFil: Ruas-Madiedo, Patricia. Instituto de Productos Lácteos de Asturias; EspañaFil: de los Reyes-Gavilán, Clara G.. Instituto de Productos Lácteos de Asturias; EspañaElsevier Science2011-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/103205Salazar, Nuria; Binetti, Ana Griselda; Gueimonde, Miguel; Alonso, Ana; Garrido, Pablo; et al.; Safety and intestinal microbiota modulation by the exopolysaccharide-producing strains Bifidobacterium animalis IPLA R1 and Bifidobacterium longum IPLA E44 orally administered to Wistar rats; Elsevier Science; International Journal of Food Microbiology; 144; 3; 1-2011; 342-3510168-1605CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.ijfoodmicro.2010.10.016info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:02:57Zoai:ri.conicet.gov.ar:11336/103205instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:02:58.035CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Safety and intestinal microbiota modulation by the exopolysaccharide-producing strains Bifidobacterium animalis IPLA R1 and Bifidobacterium longum IPLA E44 orally administered to Wistar rats
title Safety and intestinal microbiota modulation by the exopolysaccharide-producing strains Bifidobacterium animalis IPLA R1 and Bifidobacterium longum IPLA E44 orally administered to Wistar rats
spellingShingle Safety and intestinal microbiota modulation by the exopolysaccharide-producing strains Bifidobacterium animalis IPLA R1 and Bifidobacterium longum IPLA E44 orally administered to Wistar rats
Salazar, Nuria
probiotic
bifidobacteria
exopolysacharide
title_short Safety and intestinal microbiota modulation by the exopolysaccharide-producing strains Bifidobacterium animalis IPLA R1 and Bifidobacterium longum IPLA E44 orally administered to Wistar rats
title_full Safety and intestinal microbiota modulation by the exopolysaccharide-producing strains Bifidobacterium animalis IPLA R1 and Bifidobacterium longum IPLA E44 orally administered to Wistar rats
title_fullStr Safety and intestinal microbiota modulation by the exopolysaccharide-producing strains Bifidobacterium animalis IPLA R1 and Bifidobacterium longum IPLA E44 orally administered to Wistar rats
title_full_unstemmed Safety and intestinal microbiota modulation by the exopolysaccharide-producing strains Bifidobacterium animalis IPLA R1 and Bifidobacterium longum IPLA E44 orally administered to Wistar rats
title_sort Safety and intestinal microbiota modulation by the exopolysaccharide-producing strains Bifidobacterium animalis IPLA R1 and Bifidobacterium longum IPLA E44 orally administered to Wistar rats
dc.creator.none.fl_str_mv Salazar, Nuria
Binetti, Ana Griselda
Gueimonde, Miguel
Alonso, Ana
Garrido, Pablo
González del Rey, Carmen
González, Celestino
Ruas-Madiedo, Patricia
de los Reyes-Gavilán, Clara G.
author Salazar, Nuria
author_facet Salazar, Nuria
Binetti, Ana Griselda
Gueimonde, Miguel
Alonso, Ana
Garrido, Pablo
González del Rey, Carmen
González, Celestino
Ruas-Madiedo, Patricia
de los Reyes-Gavilán, Clara G.
author_role author
author2 Binetti, Ana Griselda
Gueimonde, Miguel
Alonso, Ana
Garrido, Pablo
González del Rey, Carmen
González, Celestino
Ruas-Madiedo, Patricia
de los Reyes-Gavilán, Clara G.
author2_role author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv probiotic
bifidobacteria
exopolysacharide
topic probiotic
bifidobacteria
exopolysacharide
purl_subject.fl_str_mv https://purl.org/becyt/ford/2.11
https://purl.org/becyt/ford/2
dc.description.none.fl_txt_mv Bifidobacterium animalis subsp. lactis IPLA R1 and Bifidobacterium longum IPLA E44 strains were tested in vivo for their safety and ability to modulate the intestinal microbiota. Chemically simulated gastrointestinal digestion showed a considerably lower survival of E44 than R1 strain, the first microorganism being also more sensitive to the refrigerated storage in 10%-skimmed milk at 4ºC. Male Wistar rats 12 weeks-old were distributed into three groups, eight rats each. Two groups were daily administered 108 to 109 cfu of the corresponding strain suspended in 10%-skimmed milk during 24 days whereas rats in the placebo group received skimmed milk without microorganisms added. The microbiota and short chain fatty acids (SCFA) were monitored daily in faeces during treatment and in caecum-content at the end of the assay. Quantitative real-time PCR (qPCR) showed that faecal and caecal Bifidobacterium levels were higher in bifidobacteria-fed than in the placebo rats at the end of the intervention whereas total anaerobic-plate counts did not show significant differences. Quantification of B. animalis and B. longum by q-PCR evidenced that, independently on the microorganism administered, treatment with bifidobacteria resulted in higher levels of B. animalis in the caecum. PCR-DGGE analysis of microbial populations revealed a higher diversity of bands in caecum-content of rats fed B. animalis IPLA R1 than in the placebo and rats fed B. longum IPLA E44. Remarkably, although no variations in the proportion of acetate, propionate and butyrate were found, at the end of the assay total SCFA concentration in faeces of rats fed bifidobacteria were significantly higher and those in caecum-content significantly lower than that of the placebo group, suggesting a displacement of the SCFA production to parts in the intestine more distal that caecum in rats receiving bifidobacteria. Harmful glycosidic activities were absent or at low levels in the strains R1 and E44. Both strains were sensitive to most antibiotics although, similarly to some other bifidobacteria strains, they displayed a moderate resistance against tetracycline which in the case of R1correlated with the presence of tet (W) gene. The general parameters indicating well-being status as well as translocation to different organs and histological examination of the gut tissues revealed no changes induced by the administration of bifidobacteria. Therefore, the oral administration of B. animalis IPLA R1 and B. longum E44 can be considered safe, these microorganisms having the ability to modulate the intestinal microbiota of rats by influencing SCFA and the bifidobacterial population levels.
Fil: Salazar, Nuria. Instituto de Productos Lácteos de Asturias; España
Fil: Binetti, Ana Griselda. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Lactología Industrial. Universidad Nacional del Litoral. Facultad de Ingeniería Química. Instituto de Lactología Industrial; Argentina
Fil: Gueimonde, Miguel. Instituto de Productos Lácteos de Asturias; España
Fil: Alonso, Ana. Universidad de Oviedo; España
Fil: Garrido, Pablo. Universidad de Oviedo; España
Fil: González del Rey, Carmen. Agustin Hospital; España
Fil: González, Celestino. Universidad de Oviedo; España
Fil: Ruas-Madiedo, Patricia. Instituto de Productos Lácteos de Asturias; España
Fil: de los Reyes-Gavilán, Clara G.. Instituto de Productos Lácteos de Asturias; España
description Bifidobacterium animalis subsp. lactis IPLA R1 and Bifidobacterium longum IPLA E44 strains were tested in vivo for their safety and ability to modulate the intestinal microbiota. Chemically simulated gastrointestinal digestion showed a considerably lower survival of E44 than R1 strain, the first microorganism being also more sensitive to the refrigerated storage in 10%-skimmed milk at 4ºC. Male Wistar rats 12 weeks-old were distributed into three groups, eight rats each. Two groups were daily administered 108 to 109 cfu of the corresponding strain suspended in 10%-skimmed milk during 24 days whereas rats in the placebo group received skimmed milk without microorganisms added. The microbiota and short chain fatty acids (SCFA) were monitored daily in faeces during treatment and in caecum-content at the end of the assay. Quantitative real-time PCR (qPCR) showed that faecal and caecal Bifidobacterium levels were higher in bifidobacteria-fed than in the placebo rats at the end of the intervention whereas total anaerobic-plate counts did not show significant differences. Quantification of B. animalis and B. longum by q-PCR evidenced that, independently on the microorganism administered, treatment with bifidobacteria resulted in higher levels of B. animalis in the caecum. PCR-DGGE analysis of microbial populations revealed a higher diversity of bands in caecum-content of rats fed B. animalis IPLA R1 than in the placebo and rats fed B. longum IPLA E44. Remarkably, although no variations in the proportion of acetate, propionate and butyrate were found, at the end of the assay total SCFA concentration in faeces of rats fed bifidobacteria were significantly higher and those in caecum-content significantly lower than that of the placebo group, suggesting a displacement of the SCFA production to parts in the intestine more distal that caecum in rats receiving bifidobacteria. Harmful glycosidic activities were absent or at low levels in the strains R1 and E44. Both strains were sensitive to most antibiotics although, similarly to some other bifidobacteria strains, they displayed a moderate resistance against tetracycline which in the case of R1correlated with the presence of tet (W) gene. The general parameters indicating well-being status as well as translocation to different organs and histological examination of the gut tissues revealed no changes induced by the administration of bifidobacteria. Therefore, the oral administration of B. animalis IPLA R1 and B. longum E44 can be considered safe, these microorganisms having the ability to modulate the intestinal microbiota of rats by influencing SCFA and the bifidobacterial population levels.
publishDate 2011
dc.date.none.fl_str_mv 2011-01
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/103205
Salazar, Nuria; Binetti, Ana Griselda; Gueimonde, Miguel; Alonso, Ana; Garrido, Pablo; et al.; Safety and intestinal microbiota modulation by the exopolysaccharide-producing strains Bifidobacterium animalis IPLA R1 and Bifidobacterium longum IPLA E44 orally administered to Wistar rats; Elsevier Science; International Journal of Food Microbiology; 144; 3; 1-2011; 342-351
0168-1605
CONICET Digital
CONICET
url http://hdl.handle.net/11336/103205
identifier_str_mv Salazar, Nuria; Binetti, Ana Griselda; Gueimonde, Miguel; Alonso, Ana; Garrido, Pablo; et al.; Safety and intestinal microbiota modulation by the exopolysaccharide-producing strains Bifidobacterium animalis IPLA R1 and Bifidobacterium longum IPLA E44 orally administered to Wistar rats; Elsevier Science; International Journal of Food Microbiology; 144; 3; 1-2011; 342-351
0168-1605
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ijfoodmicro.2010.10.016
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier Science
publisher.none.fl_str_mv Elsevier Science
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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