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17 results for “Limosilactobacillus reuteri”
Limosilactobacillus reuteri IDCC 3701 - Cell Free Supernatant
<p>This is the raw-data regarding the CFS of the probiotic <em>Limosilactobacillus reuteri</em> IDCC 3701. </p>
Fig. 2. A in Limosilactobacillus balticus sp. nov., Limosilactobacillus agrestis sp. nov., Limosilactobacillus albertensis sp. nov., Limosilactobacillus rudii sp. nov. and Limosilactobacillus fastidiosus sp. nov., five novel Limosilactobacillus species isolated from the vertebrate gastrointestinal tract, and proposal of six subspecies of Limosilactobacillus reuteri adapted to the gastrointestinal tract of specific vertebrate hosts
Fig. 2. A maximum-likelihood phylogenetic tree reconstructed using core genes (n=100) identified from whole-genome sequences, showing the evolutionary relationships among five novel Limosilactobacillus species, six L. reuteri subspecies and other recognized species in the genus Limosilactobacillus. GenBank or JGI accession numbers of these genomes are provided in parentheses. The tree was inferred based on the GTR+G model with 1000 bootstrap replicates and only bootstrap values above 60% are shown. Strains of five novel Limosilactobacillus species are labelled by different colours; labels of six L. reuteri subspecies are colour representing vertebrate host origin: green for rodents, red for pigs, blue for humans and orange for poultry. The tree was drawn with iTOL [54].
Fig. 1. A maximum-likelihood phylogenetic tree reconstructed using 16S in Limosilactobacillus balticus sp. nov., Limosilactobacillus agrestis sp. nov., Limosilactobacillus albertensis sp. nov., Limosilactobacillus rudii sp. nov. and Limosilactobacillus fastidiosus sp. nov., five novel Limosilactobacillus species isolated from the vertebrate gastrointestinal tract, and proposal of six subspecies of Limosilactobacillus reuteri adapted to the gastrointestinal tract of specific vertebrate hosts
Fig. 1. A maximum-likelihood phylogenetic tree reconstructed using 16S rRNA gene sequences. GenBank or JGI accession numbers of these genomes are provided in parentheses. The tree was inferred based on the GTR+G model with 1000 bootstrap replicates and only bootstrap values above 60% are shown. Strains of five novel Limosilactobacillus species are labelled by different colours; labels of six L. reuteri subspecies are colour representing vertebrate host origin: green for rodents, red for pigs, blue for humans and orange for poultry. The tree was drawn with iTOL [54].
Fig. 3. A in Limosilactobacillus balticus sp. nov., Limosilactobacillus agrestis sp. nov., Limosilactobacillus albertensis sp. nov., Limosilactobacillus rudii sp. nov. and Limosilactobacillus fastidiosus sp. nov., five novel Limosilactobacillus species isolated from the vertebrate gastrointestinal tract, and proposal of six subspecies of Limosilactobacillus reuteri adapted to the gastrointestinal tract of specific vertebrate hosts
Fig. 3. A maximum-likelihood phylogenetic tree reconstructed using core genes (n=100) identified from whole-genome sequences, showing the evolutionary relationships among six L. reuteri subspecies. The tree was reconstructed using 33 L. reuteri genomes available in public databases (n=6 for L. reuteri subsp. kinnaridis, n=2 for L. reuteri subsp. porcinus, n=5 for L. reuteri subsp. murium, n=10 for L. reuteri subsp. reuteri, n=5 for L. reuteri subsp. suis and n=5 for L. reuteri subsp. rodentium) and L. balticus BG-AF3-AT was used as an outgroup. Further information on the involved genome sequences is listed in Table S1. The tree was inferred based on the GTR+G model with 1000 bootstrap replicates and only bootstrap values above 60% are shown. The tree was drawn with iTOL [54].
Fig. 4 in Limosilactobacillus balticus sp. nov., Limosilactobacillus agrestis sp. nov., Limosilactobacillus albertensis sp. nov., Limosilactobacillus rudii sp. nov. and Limosilactobacillus fastidiosus sp. nov., five novel Limosilactobacillus species isolated from the vertebrate gastrointestinal tract, and proposal of six subspecies of Limosilactobacillus reuteri adapted to the gastrointestinal tract of specific vertebrate hosts
Fig. 4. Pairwise average nucleotide identity values (ANI; %) of genome sequences belonging to the same or different L. reuteri subspecies. ANI values within the same subspecies and between different subspecies were calculated for 33 L. reuteri genomes available in public databases (n=6 for L. reuteri subsp. kinnaridis, n=2 for L. reuteri subsp. porcinus, n=5 for L. reuteri subsp. murium, n=10 for L. reuteri subsp. reuteri, n=5 for L. reuteri subsp. suis and n=5 for L. reuteri subsp. rodentium). Further information on the involved genome sequences is listed in Table S1.
Clinical Effects of Limosilactobacillus Reuteri Probiotics as an Adjunct to the Treatment of Periodontitis
ClinicalTrials.gov study NCT05734274. IPD Sharing: NO. Countries: 1. Publications: 6.
Rewilding the Human Gut: Reintroduction of the Species Limosilactobacillus Reuteri
ClinicalTrials.gov study NCT03501082. IPD Sharing: YES. Countries: 1. Publications: 8.
Dataset for: Enhanced tameness by Limosilactobacillus reuteri from gut microbiota of selectively bred mice
<p>This dataset comprises a non-redundant set of 374 metagenome-assembled genomes (MAGs), generated from the shotgun metagenomic data of faecal samples from 80 mice. Among these, 27 MAGs have been identified as novel within the mice gut microbiome. Additionally, the code utilized for the generation of these MAGs has been included with the dataset for reference and reproducibility. All raw shotgun metagenomic sequencing datasets generated in this study are available in the NCBI under BioProject PRJDB15857 (https://www.ncbi.nlm.nih.gov/bioproject/?term=PRJDB15857), with BioSample accession numbers from SAMD00614304 to SAMD00614383 and SRA accession numbers from DRR480456 to DRR480535. </p>
Effect of Limosilactobacillus Reuteri DSM 17648 in Healthy Adults Reporting Upper Gastrointestinal Discomfort
ClinicalTrials.gov study NCT07163637. IPD Sharing: NO. Countries: 1. Publications: 0.
Limosilactobacillus Reuteri as an Adjuvant in the Treatment of Peri-implant Mucositis
ClinicalTrials.gov study NCT05758103. IPD Sharing: YES. Countries: 1. Publications: 0.
Investigating the Impact of Humiome B2 (Colon Delivered Riboflavin) and Riboflavin-overproducer Probiotic Strain Limosilactobacillus Reuteri AMBV339 on Intestinal and Vaginal Microbiome and Health of
ClinicalTrials.gov study NCT06425081. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Effect of Probiotic Limosilactobacillus Reuteri (L. Reuteri) on Crying and Fussing Time in Infants With Colic
ClinicalTrials.gov study NCT06462651. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Lactobacillus Acidophilus and Limosilactobacillus Reuteri for Acute Diarrhea in Children
ClinicalTrials.gov study NCT07342088. IPD Sharing: NO. Countries: 1. Publications: 0.
Effect of Probiotic Limosilactobacillus Reuteri (L. Reuteri) on Crying Time in Infants With Colic
ClinicalTrials.gov study NCT05512234. IPD Sharing: Not stated. Countries: 2. Publications: 0.
Evaluating the Effect of Probiotic Limosilactobacillus Reuteri (L. Reuteri) on Crying and Fussing Time in Infants With Colic
ClinicalTrials.gov study NCT07190859. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Preventive Effect of a Dietary Supplement With Two Probiotic Limosilactobacillus Reuteri Strains on Excessive Crying and Colic in Healthy Newborns.
ClinicalTrials.gov study NCT07347743. IPD Sharing: Not stated. Countries: 1. Publications: 0.
RNA-seq analysis on the liver of darkness rats treated with Limosilactobacillus reuteri
GEO Series GSE169501. Rattus norvegicus. 24 samples. Type: Expression profiling by high throughput sequencing.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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