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Article: Aflatoxicosis chemoprevention by probiotic Lactobacillius and lack of effect on the major histocompatibility complex

TitleAflatoxicosis chemoprevention by probiotic Lactobacillius and lack of effect on the major histocompatibility complex
Authors
KeywordsGene expression
Aflatoxin
Chemoprevention
Toxicology
Probiotics
Turkeys
Poultry
MHC
BG
Issue Date2014
PublisherWB Saunders Co Ltd. The Journal's web site is located at http://www.elsevier.com/locate/rvsc
Citation
Research in Veterinary Science, 2014, v. 97 n. 2, p. 274-281 How to Cite?
AbstractTurkeys are extremely sensitive to aflatoxin B1 (AFB1) which causes decreased growth, immunosuppression and liver necrosis. The purpose of this study was to determine whether probiotic Lactobacillus, shown to be protective in animal and clinical studies, would likewise confer protection in turkeys, which were treated for 11 days with either AFB1 (AFB; 1 ppm in diet), probiotic (PB; 1 × 1011 CFU/ml; oral, daily), probiotic + AFB1 (PBAFB), or PBS control (CNTL). The AFB1 induced drop in body and liver weights were restored to normal in CNTL and PBAFB groups. Hepatotoxicity markers were not significantly reduced by probiotic treatment. Major histocompatibility complex (MHC) genes BG1 and BG4, which are differentially expressed in liver and spleens, were not significantly affected by treatments. These data indicate modest protection, but the relatively high dietary AFB1 treatment, and the extreme sensitivity of this species may reveal limits of probiotic-based protection strategies.
Persistent Identifierhttp://hdl.handle.net/10722/201543
ISSN
2021 Impact Factor: 2.554
2020 SCImago Journal Rankings: 0.719
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorRawal, S-
dc.contributor.authorBauer, MM-
dc.contributor.authorMendoza, KM-
dc.contributor.authorEl-Nezami, H-
dc.contributor.authorHall, JR-
dc.contributor.authorKim, JE-
dc.contributor.authorStevens, JR-
dc.contributor.authorReed, KM-
dc.contributor.authorCoulombe, RA-
dc.date.accessioned2014-08-21T07:30:23Z-
dc.date.available2014-08-21T07:30:23Z-
dc.date.issued2014-
dc.identifier.citationResearch in Veterinary Science, 2014, v. 97 n. 2, p. 274-281-
dc.identifier.issn0034-5288-
dc.identifier.urihttp://hdl.handle.net/10722/201543-
dc.description.abstractTurkeys are extremely sensitive to aflatoxin B1 (AFB1) which causes decreased growth, immunosuppression and liver necrosis. The purpose of this study was to determine whether probiotic Lactobacillus, shown to be protective in animal and clinical studies, would likewise confer protection in turkeys, which were treated for 11 days with either AFB1 (AFB; 1 ppm in diet), probiotic (PB; 1 × 1011 CFU/ml; oral, daily), probiotic + AFB1 (PBAFB), or PBS control (CNTL). The AFB1 induced drop in body and liver weights were restored to normal in CNTL and PBAFB groups. Hepatotoxicity markers were not significantly reduced by probiotic treatment. Major histocompatibility complex (MHC) genes BG1 and BG4, which are differentially expressed in liver and spleens, were not significantly affected by treatments. These data indicate modest protection, but the relatively high dietary AFB1 treatment, and the extreme sensitivity of this species may reveal limits of probiotic-based protection strategies.-
dc.languageeng-
dc.publisherWB Saunders Co Ltd. The Journal's web site is located at http://www.elsevier.com/locate/rvsc-
dc.relation.ispartofResearch in Veterinary Science-
dc.subjectGene expression-
dc.subjectAflatoxin-
dc.subjectChemoprevention-
dc.subjectToxicology-
dc.subjectProbiotics-
dc.subjectTurkeys-
dc.subjectPoultry-
dc.subjectMHC-
dc.subjectBG-
dc.titleAflatoxicosis chemoprevention by probiotic Lactobacillius and lack of effect on the major histocompatibility complex-
dc.typeArticle-
dc.identifier.emailEl-Nezami, H: elnezami@hkucc.hku.hk-
dc.identifier.authorityEl-Nezami, H=rp00694-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.rvsc.2014.06.008-
dc.identifier.pmid24997556-
dc.identifier.scopuseid_2-s2.0-84925213623-
dc.identifier.hkuros232319-
dc.identifier.volume97-
dc.identifier.issue2-
dc.identifier.spage274-
dc.identifier.epage281-
dc.identifier.isiWOS:000345809300020-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl0034-5288-

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