Project description:Green algae associated microbial communities from Chlorella culture in LANL, New Mexico, United States - Vampirovibrio chlorellavorus metagenome
Project description:Enriched cells of Vampirovibrio chlorellavorus culture contaminated with Chlorella, University of Arizona, USA - Vampirovibrio chlorellavorus Vc_AZ 8_2 metagenome
Project description:Enriched cells of Vampirovibrio chlorellavorus culture contaminated with Chlorella, University of Arizona, USA - Vampirovibrio chlorellavorus Vc_AZ 1_2 metagenome
Project description:Enriched cells of Vampirovibrio chlorellavorus culture contaminated with Chlorella, University of Arizona, USA - Vampirovibrio chlorellavorus Vc_AZ 7_2 metagenome
Project description:Enriched cells of Vampirovibrio chlorellavorus culture contaminated with Chlorella, University of Arizona, USA - Vampirovibrio chlorellavorus Vc_AZ 3_1 metagenome
Project description:Metatranscriptome of green algae associated microbial communities from Chlorella culture in University of Arizona, USA - V. chlorellavorus infection vv_d4_1
Project description:Metatranscriptome of green algae associated microbial communities from Chlorella culture in University of Arizona, USA - V. chlorellavorus infection vv_d4_2
Project description:Micro algae's are used as alternative protein source in human and animal diets. Besides micro algae contain substantial amounts of proteins they also contain a high concentration of, often unique, biological and chemical substances with potential to induce beneficial and health promoting effects in humans and animals. This study was set up to evaluate the potential of these substances to improve (intestinal) health. The effect of extracts prepared from 3 monocultures of micro algae's (Chlorella vulgaris [C], Haematococcus pluvialis [H], and Spirulina platensis [S]) and a mixed culture of micro algae's (AM; a mixture of Scenedesmus sp. and Chlorella sp. ) was studied in the presence and absence of the enterotoxigenic bacterium Escherichia coli k99 strain (ETEC, [E]) as an in vitro challenge. The E.coli-k99 strain with adhesion factor F41 (41/32) was isolated from a mastitis-infected udder. Gene expression was measured in cultured intestinal porcine epithelium cells (IPECJ2 cell line) after 2 and 6 hours incubation with C, H, and S extracts, and after 6 hours with the AM extract, using “whole genome” porcine microarrays. Gene expression profiles were analysed using functional bioinformatics programs to provide insight in the biological processes induced by micro algae extracts.
