Gastrointestinal digestion of food-use silver nanoparticles in the dynamic SIMulator of the GastroIntestinal tract (simgi®). Impact on human gut microbiota

2019 ◽  
Vol 132 ◽  
pp. 110657 ◽  
Author(s):  
Carolina Cueva ◽  
Irene Gil-Sánchez ◽  
Alba Tamargo ◽  
Beatriz Miralles ◽  
Julian Crespo ◽  
...  
2019 ◽  
Vol 55 (61) ◽  
pp. 8935-8938 ◽  
Author(s):  
Nizar Akermi ◽  
Hela Mkaouar ◽  
Aicha Kriaa ◽  
Amin Jablaoui ◽  
Souha Soussou ◽  
...  

Eubacterium saburreum serpin from human gut microbiota inhibits the pancreatic elastase associated with pancreatitis, inhibition is strongly increased by para-sulphonato-calix[8]arene silver nanoparticles.


2019 ◽  
Vol 172 (2) ◽  
pp. 411-416 ◽  
Author(s):  
Richard T Agans ◽  
Alex Gordon ◽  
Saber Hussain ◽  
Oleg Paliy

Abstract Due to continued technological development, people increasingly come in contact with engineered nanomaterials (ENMs) that are now used in foods and many industrial applications. Many ENMs have historically been shown to possess antimicrobial properties, which has sparked concern for how dietary nanomaterials impact gastrointestinal health via microbial dysbiosis. We employed an in vitro Human Gut Simulator system to examine interactions of dietary nano titanium dioxide (TiO2) with human gut microbiota. Electron microscopy indicated a close association of TiO2 particles with bacterial cells. Addition of TiO2 to microbial communities led to a modest reduction in community density but had no impact on community diversity and evenness. In contrast, administration of known antimicrobial silver nanoparticles (NPs) in a control experiment resulted in a drastic reduction of population density. In both cases, communities recovered once the addition of nanomaterials was ceased. Constrained ordination analysis of community profiles revealed that simulated colonic region was the primary determinant of microbiota composition. Accordingly, predicted community functional capacity and measured production of short-chain fatty acids were not changed significantly upon microbiota exposure to TiO2. We conclude that tested TiO2 NPs have limited direct effect on human gut microbiota.


2018 ◽  
Vol 269 ◽  
pp. 618-627 ◽  
Author(s):  
Vemana Gowd ◽  
Tao Bao ◽  
Liling Wang ◽  
Ying Huang ◽  
Shenghuizi Chen ◽  
...  

LWT ◽  
2021 ◽  
Vol 141 ◽  
pp. 110921
Author(s):  
Teresa Requena ◽  
Ya Song ◽  
Carmen Peláez ◽  
M. Carmen Martínez-Cuesta

2018 ◽  
Vol 68 ◽  
pp. 41-52 ◽  
Author(s):  
Irene Gil-Sánchez ◽  
Carolina Cueva ◽  
Marisa Sanz-Buenhombre ◽  
Alberto Guadarrama ◽  
M. Victoria Moreno-Arribas ◽  
...  

2019 ◽  
Vol 651 ◽  
pp. 1489-1494 ◽  
Author(s):  
Naiyi Yin ◽  
Rui Gao ◽  
Brett Knowles ◽  
Jiasheng Wang ◽  
Pengfei Wang ◽  
...  

Planta Medica ◽  
2016 ◽  
Vol 81 (S 01) ◽  
pp. S1-S381
Author(s):  
EM Pferschy-Wenzig ◽  
K Koskinen ◽  
C Moissl-Eichinger ◽  
R Bauer

2017 ◽  
Author(s):  
EM Pferschy-Wenzig ◽  
A Roßmann ◽  
K Koskinen ◽  
H Abdel-Aziz ◽  
C Moissl-Eichinger ◽  
...  

2020 ◽  
Author(s):  
Y Liu ◽  
AL Heath ◽  
B Galland ◽  
N Rehrer ◽  
L Drummond ◽  
...  

© 2020 American Society for Microbiology. Dietary fiber provides growth substrates for bacterial species that belong to the colonic microbiota of humans. The microbiota degrades and ferments substrates, producing characteristic short-chain fatty acid profiles. Dietary fiber contains plant cell wall-associated polysaccharides (hemicelluloses and pectins) that are chemically diverse in composition and structure. Thus, depending on plant sources, dietary fiber daily presents the microbiota with mixtures of plant polysaccharides of various types and complexity. We studied the extent and preferential order in which mixtures of plant polysaccharides (arabinoxylan, xyloglucan, β-glucan, and pectin) were utilized by a coculture of five bacterial species (Bacteroides ovatus, Bifidobacterium longum subspecies longum, Megasphaera elsdenii, Ruminococcus gnavus, and Veillonella parvula). These species are members of the human gut microbiota and have the biochemical capacity, collectively, to degrade and ferment the polysaccharides and produce short-chain fatty acids (SCFAs). B. ovatus utilized glycans in the order β-glucan, pectin, xyloglucan, and arabinoxylan, whereas B. longum subsp. longum utilization was in the order arabinoxylan, arabinan, pectin, and β-glucan. Propionate, as a proportion of total SCFAs, was augmented when polysaccharide mixtures contained galactan, resulting in greater succinate production by B. ovatus and conversion of succinate to propionate by V. parvula. Overall, we derived a synthetic ecological community that carries out SCFA production by the common pathways used by bacterial species for this purpose. Systems like this might be used to predict changes to the emergent properties of the gut ecosystem when diet is altered, with the aim of beneficially affecting human physiology. This study addresses the question as to how bacterial species, characteristic of the human gut microbiota, collectively utilize mixtures of plant polysaccharides such as are found in dietary fiber. Five bacterial species with the capacity to degrade polymers and/or produce acidic fermentation products detectable in human feces were used in the experiments. The bacteria showed preferential use of certain polysaccharides over others for growth, and this influenced their fermentation output qualitatively. These kinds of studies are essential in developing concepts of how the gut microbial community shares habitat resources, directly and indirectly, when presented with mixtures of polysaccharides that are found in human diets. The concepts are required in planning dietary interventions that might correct imbalances in the functioning of the human microbiota so as to support measures to reduce metabolic conditions such as obesity.


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