Limosilactobacillus reuteri, REUTERI, 2020
publication ID |
https://doi.org/10.1099/ijsem.0.004107 |
DOI |
https://doi.org/10.5281/zenodo.4728764 |
persistent identifier |
https://treatment.plazi.org/id/03A8D903-D23C-0272-FC95-FD975424351B |
treatment provided by |
Valdenar (2021-04-29 20:05:09, last updated by Guilherme 2025-02-06 14:43:30) |
scientific name |
Limosilactobacillus reuteri |
status |
comb. nov. |
DESCRIPTIONOF LIMOSILACTOBACILLUS REUTERI COMB. NOV.
Limosilactobacillus reuteri (reu ′ te.ri. N.L. gen. n. reuteri , of Reuter; named for G. Reuter, a German bacteriologist).
Basonym: Lactobacillus reuteri Kandler et al. 1982 , 266 VL
Prior to 1980, strains of the species were classified as L. fermentum Biotype II [ 268]. The species has been studied as model species to determine host-adaptation of intestinal lactobacilli, and co-adaptation of Limosilactobacillus and Lactobacillus species (e.g. L. taiwanensis ) that coexist in biofilms in intestinal ecosystems and preferentially different substrates [ 55, 56, 269]. L. reuteri is divided in host-adapted lineages that are equivalent to the taxonomic rank of subspecies [ 269, 270] and differ in their ability to form biofilms in the mouse forestomach [ 271]. Few strains of L. reuteri produce the antimicrobial compound reutericyclin with a polyketide synthase, which is a unique ability among lactobacilli [ 272]. The genome size of the type strain is 1.94 Mbp. The mol% G+C content of DNA is 38.6.
Isolated as dominant members of the intestinal microbiota of rodents, birds, swine, and in other intestinal ecosystems; also occurs in cereal fermentations, particularly type II sourdoughs [ 58]. Food isolates are of intestinal origin [ 273].
Thetype strain of the species is F 275 T = ATCC 23272 T =DSM 20016 T = JCM 1112 T =LMG 9213 T = LMG 13557 T.
Genome sequence accession number: AZDD00000000.
16S rRNA gene accession number: AP007281 View Materials .
269. Duar RM, Frese SA, Lin XB, Fernando SC, Burkey TE et al. Experimental evaluation of host adaptation of Lactobacillus reuteri to different vertebrate species. Appl Environ Microbiol 2017; 83: e 00132 - 17.
270. Frese SA, Benson AK, Tannock GW, Loach DM, Kim J et al. The evolution of host specialization in the vertebrate gut symbiont Lactobacillus reuteri. PLoS Genet 2011; 7: e 1001314.
271. Frese SA, MacKenzie DA, Peterson DA, Schmaltz R, Fangman T et al. Molecular characterization of host-specific biofilm formation in a vertebrate gut symbiont. PLoS Genet 2013; 9: e 1004057.
58. Ganzle MG. Fermented Foods. In: Doyle MP, Diez Gonzalez F, Hill C (editors). Food Microbiol. Fundam. Front, 5 th ed. ASM Press; 2019. pp. 855 - 900.
268. Kandler O, Stetter K-O, Kohl R. Lactobacillus reuteri sp. nov., a new species of heterofermentative lactobacilli. Zentralbl Bakteriol Hyg Abt IOrig C 1980; 1: 264 - 269.
272. Lin XB, Lohans CT, Duar R, Zheng J, Vederas JC et al. Genetic determinants of reutericyclin biosynthesis in Lactobacillus reuteri. Appl Environ Microbiol 2015; 81: 2032 - 2041.
55. Lin XB, Wang T, Stothard P, Corander J, Wang J et al. The evolution of ecological facilitation within mixed-species biofilms in the mouse gastrointestinal tract. ISME J 2018; 12: 2770 - 2784.
56. Tannock GW, Wilson CM, Loach D, Cook GM, Eason J et al. Resource partitioning in relation to cohabitation of Lactobacillus species in the mouse forestomach. ISME J 2012; 6: 927 - 938.
273. Zheng J, Zhao X, Lin XB, Ganzle M. Comparative genomics Lactobacillus reuteri from sourdough reveals adaptation of an intestinal symbiont to food fermentations. Sci Rep 2015; 5: 18234.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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