Literature DB >> 9003237

Emergence of multiple xylitol-resistant (fructose PTS-) mutants from human isolates of mutans streptococci during growth on dietary sugars in the presence of xylitol.

L Trahan1, G Bourgeau, R Breton.   

Abstract

The growth inhibition of mutans streptococci is one of the proposed mechanisms of action of xylitol, a caries-preventive natural carbohydrate sweetener. Xylitol is taken up and accumulated as non-metabolizable, toxic xylitol phosphate via a constitutive fructose PTS, and selects, during in vitro growth at the expense of glucose, for natural xylitol-resistant mutants that lack constitutive fructose PTS activity. Since long-term xylitol consumption leads to the emergence of xylitol-resistant mutans populations in humans in an oral environment containing sugars of dietary origin, we wanted to test the hypothesis that xylitol-resistant cells could be selected from mutans streptococci strains during in vitro growth on fructose, sucrose, or lactose. Three laboratory strains and three fresh mutans streptococcal isolates were repeatedly transferred in trypticase-yeast extract medium supplemented with glucose, fructose, sucrose, or lactose in the presence and absence of xylitol. Depending on the growth sugar, the presence of xylitol resulted in the selection of xylitol-resistant populations for several of the six strains tested, but not necessarily in the presence of all four sugars. All six strains rapidly became xylitol-resistant when grown on glucose in the presence of xylitol. All three fresh isolates became xylitol-resistant after 9 to 16 transfers in the presence of fructose or sucrose plus xylitol, while none of the laboratory strains became xylitol-resistant after 16 transfers in the presence of these sugars. The growth rates of 12 xylitol-resistant mutants in the presence of eight sugars suggested the existence of various types of xylitol-resistant mutants. The data partially explain the occurrence of xylitol-resistant mutans populations in long-term xylitol consumers and suggest a mechanism consistent with a selection process. Since various preliminary results suggest that xylitol-resistant natural mutants may be less virulent and less cariogenic than their parent strains, this selection process may alter, for the better, the mutans streptococci population of the plaque and play a role in the caries-preventive action of xylitol.

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Year:  1996        PMID: 9003237     DOI: 10.1177/00220345960750111201

Source DB:  PubMed          Journal:  J Dent Res        ISSN: 0022-0345            Impact factor:   6.116


  5 in total

1.  Effect of chewing gums containing xylitol or probiotic bacteria on salivary mutans streptococci and lactobacilli.

Authors:  E Caglar; S C Kavaloglu; O O Kuscu; N Sandalli; P L Holgerson; S Twetman
Journal:  Clin Oral Investig       Date:  2007-06-16       Impact factor: 3.573

2.  Synergistic effect of xylitol and ursolic acid combination on oral biofilms.

Authors:  Yunyun Zou; Yoon Lee; Jinyoung Huh; Jeong-Won Park
Journal:  Restor Dent Endod       Date:  2014-08-27

3.  Mutans streptococci genetic strains in children with severe early childhood caries: follow-up study at one-year post-dental rehabilitation therapy.

Authors:  Elizabeth A Palmer; Alex Vo; Shelby B Hiles; Patricia Peirano; Samyia Chaudhry; Amy Trevor; Iraj Kasimi; Jill Pollard; Christopher Kyles; Michael Leo; Beth Wilmot; John Engle; John Peterson; Tom Maier; Curtis A Machida
Journal:  J Oral Microbiol       Date:  2012-12-14       Impact factor: 5.474

4.  D‑Tagatose inhibits the growth and biofilm formation of Streptococcus mutans.

Authors:  Khaleque Hasibul; Haruyuki Nakayama-Imaohji; Masahito Hashimoto; Hisashi Yamasaki; Takaaki Ogawa; Junpei Waki; Ayano Tada; Saori Yoneda; Masaaki Tokuda; Minoru Miyake; Tomomi Kuwahara
Journal:  Mol Med Rep       Date:  2017-11-08       Impact factor: 2.952

5.  The Impact of Maltitol-Sweetened Chewing Gum on the Dental Plaque Biofilm Microbiota Composition.

Authors:  Bart J F Keijser; Tim J van den Broek; Dagmar E Slot; Lodewic van Twillert; Jolanda Kool; Clémentine Thabuis; Michel Ossendrijver; Fridus A van der Weijden; Roy C Montijn
Journal:  Front Microbiol       Date:  2018-03-06       Impact factor: 5.640

  5 in total

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