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1.
Food Microbiol ; 53(Pt A): 51-9, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26611169

RESUMO

Few studies have extensively investigated probiotic functions associated with biofilms. Here, we show that strains of Lactobacillus plantarum and Lactobacillus fermentum are able to grow as biofilm on abiotic surfaces, but the biomass density differs between strains. We performed microtiter plate biofilm assays under growth conditions mimicking to the gastrointestinal environment. Osmolarity and low concentrations of bile significantly enhanced Lactobacillus spatial organization. Two L. plantarum strains were able to form biofilms under high concentrations of bile and mucus. We used the agar well-diffusion method to show that supernatants from all Lactobacillus except the NA4 isolate produced food pathogen inhibitory molecules in biofilm. Moreover, TNF-α production by LPS-activated human monocytoid cells was suppressed by supernatants from Lactobacillus cultivated as biofilms but not by planktonic culture supernatants. However, only L. fermentum NA4 showed anti-inflammatory effects in zebrafish embryos fed with probiotic bacteria, as assessed by cytokine transcript level (TNF-α, IL-1ß and IL-10). We conclude that the biofilm mode of life is associated with beneficial probiotic properties of lactobacilli, in a strain dependent manner. Those results suggest that characterization of isolate phenotype in the biofilm state could be additional valuable information for the selection of probiotic strains.


Assuntos
Antibiose , Biofilmes/crescimento & desenvolvimento , Lactobacillus plantarum/crescimento & desenvolvimento , Lactobacillus plantarum/fisiologia , Limosilactobacillus fermentum/crescimento & desenvolvimento , Limosilactobacillus fermentum/fisiologia , Probióticos , Animais , Bile/microbiologia , Meios de Cultura/química , Escherichia coli/fisiologia , Humanos , Imunidade Inata , Imunomodulação , Interleucina-10/biossíntese , Limosilactobacillus fermentum/imunologia , Lactobacillus plantarum/imunologia , Monócitos/imunologia , Muco/microbiologia , Salmonella enterica/fisiologia , Fator de Necrose Tumoral alfa/biossíntese , Peixe-Zebra
2.
Cell Microbiol ; 16(12): 1836-53, 2014 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-25052472

RESUMO

The predominant form of life for microorganisms in their natural habitats is the biofilm mode of growth. The adherence and colonization of probiotic bacteria are considered as essential factors for their immunoregulatory function in the host. Here, we show that Lactobacillus casei ATCC334 adheres to and colonizes the gut of zebrafish larvae. The abundance of pro-inflammatory cytokines and the recruitment of macrophages were low when inflammation was induced in probiotic-fed animals, suggesting that these bacteria have anti-inflammatory properties. We treated human macrophage-differentiated monocytic THP-1 cells with supernatants of L. casei ATCC334 grown in either biofilm or planktonic cultures. TNF-α production was suppressed and the NF-κB pathway was inhibited only in the presence of supernatants from biofilms. We identified GroEL as the biofilm supernatant compound responsible, at least partially, for this anti-inflammatory effect. Gradual immunodepletion of GroEL demonstrated that the abundance of GroEL and TNF-α were inversely correlated. We confirmed that biofilm development in other Lactobacillus species affects the immune response. The biofilms supernatants of these species also contained large amounts of GroEL. Thus, our results demonstrate that the biofilm enhances the immunomodulatory effects of Lactobacillus sp. and that secreted GroEL is involved in this beneficial effect.


Assuntos
Aderência Bacteriana , Biofilmes/crescimento & desenvolvimento , Lacticaseibacillus casei/imunologia , Lacticaseibacillus casei/fisiologia , Peixe-Zebra/imunologia , Peixe-Zebra/microbiologia , Animais , Anti-Inflamatórios/metabolismo , Linhagem Celular , Chaperonina 60/metabolismo , Trato Gastrointestinal/microbiologia , Humanos , Tolerância Imunológica , Lacticaseibacillus casei/metabolismo , Larva/microbiologia , Macrófagos/imunologia , Fator de Necrose Tumoral alfa/metabolismo
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