Susceptibility of gut indigenous lactic acid bacteria in BALB/c mice to oral administered Lactobacillus plantarum.
Administration, Oral
Animals
Antibiosis
Bacteroides
/ genetics
Cecum
/ microbiology
Clostridiales
/ genetics
Feces
/ microbiology
Gastrointestinal Microbiome
Inflammatory Bowel Diseases
Intestines
/ microbiology
Lactobacillales
/ genetics
Lactobacillus
/ genetics
Lactobacillus plantarum
/ genetics
Limosilactobacillus reuteri
/ genetics
Male
Mice, Inbred BALB C
Probiotics
RNA, Ribosomal, 16S
Salmonella Infections
Species Specificity
BALB/c mouse
Lactobacillus plantarum
gut microbiota
indigenous lactic acid bacteria
Journal
International journal of food sciences and nutrition
ISSN: 1465-3478
Titre abrégé: Int J Food Sci Nutr
Pays: England
ID NLM: 9432922
Informations de publication
Date de publication:
Feb 2019
Feb 2019
Historique:
pubmed:
18
5
2018
medline:
6
4
2019
entrez:
18
5
2018
Statut:
ppublish
Résumé
Cells of Lactobacillus plantarum strains AN1 and Tennozu-SU2 exert anti-inflammatory responses in ICR mouse models of inflammatory bowel disease and protective effects against S. Typhimurium infection in BALB/c mice, respectively. To clarify the existence of L. plantarum-susceptible gut indigenous bacteria, AN1 and Tennozu-SU2 cells were administered to BALB/c mice via drinking water. Gene amplicon sequencing of 16S rRNA of caecal content revealed that the AN1 and Tennozu-SU2 cells affected the abundance of caecal indigenous lactobacilli, but the effect on the dominant Clostridiales and Bacteroidales was not clear. With Blood and Liver (BL) agar containing 5% v/v horse blood, six typical colonies from faecal samples were detected as the principal lactobacilli. Among them, two typical colonies were isolated and identified to be AN1 and Tennozu-SU2. Two and one typical colonies detected in all mice were identified to be L. reuteri and L. murinus, respectively. The other one was identified and estimated to be indigenous L. plantarum detected in the Tennozu-SU2 group.
Identifiants
pubmed: 29768968
doi: 10.1080/09637486.2018.1471590
doi:
Substances chimiques
RNA, Ribosomal, 16S
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
53-62Commentaires et corrections
Type : ErratumIn