Increase in the population of duodenal immunoglobulin A plasmocytes in axenic mice associated with different living or dead bacterial strains of intestinal origin - PubMed (original) (raw)
Increase in the population of duodenal immunoglobulin A plasmocytes in axenic mice associated with different living or dead bacterial strains of intestinal origin
M C Moreau et al. Infect Immun. 1978 Aug.
Abstract
Various bacterial strains were tested for their ability to stimulate immunoglobulin A (IgA) plasmocytes to populate the duodenal lamina propria in axenic mice. The mice were associated with the strains for at least 4 weeks. The strains inhabiting the conventional mouse intestine and belonging to the genera Lactobacillus, Streptococcus, Eubacterium, Actinobacillus, Micrococcus, Corynebacterium, and Clostridium (including the extremely oxygen-sensitive ones) are only slightly or nonimmunogenic, whereas the strains belonging to the genera Bacteroides and Escherichia have an immunogenic effect. The same result was obtained with Bacteroides and Escherichia strains isolated from the digestive tract of other animal species. The kinetics of appearance of intestinal IgA plasmocytes are similar in axenic mice monoassociated with a stimulatory strain and in conventional mice. The association of two or more strains with axenic mice leads either to the same or a greater number of duodenal IgA plasmocytes as that obtained with the most stimulatory strain monoassociated with axenic mice. The maximum stimulation recorded in all of these trials represents about two-thirds of that observed in conventional mice and was obtained in the duodenum of gnotoxenic mice harboring four bacterial strains isolated from the conventional mouse microflora. The orally administered killed cells of two immunogenic strains, E. coli and Bacteroides sp., are as immunogenic as the living cells, provided that their concentration in the digestive tract is sufficient.
Similar articles
- [Interest in gnotoxenic systems for the study of host-microbial flora of the digestive tract].
Ducluzeau R, Raibaud P. Ducluzeau R, et al. Reprod Nutr Dev (1980). 1980;20(5B):1667-78. Reprod Nutr Dev (1980). 1980. PMID: 6296940 French. - Intestinal microflora: elimination of germfree characteristics by components of the normal microbial flora.
Pesti L. Pesti L. Comp Immunol Microbiol Infect Dis. 1979;1(3):141-52. doi: 10.1016/0147-9571(79)90040-7. Comp Immunol Microbiol Infect Dis. 1979. PMID: 117972 Review. No abstract available. - B-1 cells and the intestinal microflora.
Bos NA, Cebra JJ, Kroese FG. Bos NA, et al. Curr Top Microbiol Immunol. 2000;252:211-20. doi: 10.1007/978-3-642-57284-5_22. Curr Top Microbiol Immunol. 2000. PMID: 11125478 Review. No abstract available.
Cited by
- Host-microbial interactions and regulation of intestinal epithelial barrier function: From physiology to pathology.
Yu LC, Wang JT, Wei SC, Ni YH. Yu LC, et al. World J Gastrointest Pathophysiol. 2012 Feb 15;3(1):27-43. doi: 10.4291/wjgp.v3.i1.27. World J Gastrointest Pathophysiol. 2012. PMID: 22368784 Free PMC article. - Considering the Microbiome in Stress-Related and Neurodevelopmental Trajectories to Schizophrenia.
Hoffman KW, Lee JJ, Corcoran CM, Kimhy D, Kranz TM, Malaspina D. Hoffman KW, et al. Front Psychiatry. 2020 Jul 3;11:629. doi: 10.3389/fpsyt.2020.00629. eCollection 2020. Front Psychiatry. 2020. PMID: 32719625 Free PMC article. Review. - Class-switch recombination to IgA in the Peyer's patches requires natural thymus-derived Tregs and appears to be antigen independent.
Gribonika I, Eliasson DG, Chandode RK, Schön K, Strömberg A, Bemark M, Lycke NY. Gribonika I, et al. Mucosal Immunol. 2019 Nov;12(6):1268-1279. doi: 10.1038/s41385-019-0202-0. Epub 2019 Sep 9. Mucosal Immunol. 2019. PMID: 31501516 - Human IgA binds a diverse array of commensal bacteria.
Sterlin D, Fadlallah J, Adams O, Fieschi C, Parizot C, Dorgham K, Rajkumar A, Autaa G, El-Kafsi H, Charuel JL, Juste C, Jönsson F, Candela T, Wardemann H, Aubry A, Capito C, Brisson H, Tresallet C, Cummings RD, Larsen M, Yssel H, von Gunten S, Gorochov G. Sterlin D, et al. J Exp Med. 2020 Mar 2;217(3):e20181635. doi: 10.1084/jem.20181635. J Exp Med. 2020. PMID: 31891367 Free PMC article. - Roles of Secretory Immunoglobulin A in Host-Microbiota Interactions in the Gut Ecosystem.
León ED, Francino MP. León ED, et al. Front Microbiol. 2022 Jun 2;13:880484. doi: 10.3389/fmicb.2022.880484. eCollection 2022. Front Microbiol. 2022. PMID: 35722300 Free PMC article. Review.
References
- Jpn J Microbiol. 1973 May;17(3):181-7 - PubMed
- Ann Immunol (Paris). 1973 May;124(2):253-72 - PubMed
- J Infect Dis. 1974 Oct;130(4):419-40 - PubMed
- Infect Immun. 1972 Oct;6(4):525-32 - PubMed
- Ann Microbiol (Paris). 1973 Jan;124(1):83-109 - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous