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Current D-Mannose
Research Effect of D-mannose and D-glucose on Escherichia coli bacteriuria in rats. Urol Res 1983;11(2):97-102 Michaels EK, Chmiel JS, Plotkin BJ, Schaeffer AJ. The effect of D-mannose and D-glucose on bacteriuria due to Escherichia coli with mannose-sensitive adhesins was investigated in adult male Sprague-Dawley rats undergoing diuresis. Inocula of 10(5), 10(7), or 10(8) bacteria in 0.1 ml of normal saline or 2.5% or 10% D-mannose or D-glucose were injected intravesically and urine was cultured 1, 3, 5, 7 and 9 days later. The levels of bacteriuria on days 1 and 5 were significantly lower in rats inoculated with 10(5) E coli and 10% D-mannose than in controls (p less than 0.05 and 0.01 respectively) and the percentages of rats with less than 100 bacteria/ml were higher on days 1 and 3 (p = 0.05 and 0.02 respectively). Bacteriuria was significantly lower in rats inoculated with 10(7) bacteria and 10% D-mannose than in controls on days 5 and 7 (p less than 0.01 for each day) and the percentage of rats with less than 100 bacteria/ml was higher on day 7 (p = 0.01). D-glucose reduced bacteriuria significantly only with a concentration of 10% after instillation of 10(5) E. coli (p less than 0.05, day 1). The results indicate that D-mannose and D-glucose can significantly reduce bacteriuria within 1 day and that their efficacy is dependent upon the concentration of both saccharide and bacteria. PMID: 6346629 [PubMed - indexed for MEDLINE] Safe as mother's milk: carbohydrates as future anti-adhesion drugs for bacterial diseases. Department of Biological Chemistry, The Weizmann Institute of Science, Rehovot, Israel. bfsharon@weizmann.weizmann.ac.il Sharon N, Ofek I. The majority of infectious diseases are initiated by adhesion of pathogenic organisms to the tissues of the host. In many cases, this adhesion is mediated by lectins present on the surface of the infectious organism that bind to complementary carbohydrates on the surface of the host tissues. Lectin-deficient mutants often lack ability to initiate infection. Soluble carbohydrates recognized by the bacterial lectins block the adhesion of the bacteria to animal cells in vitro. Moreover, they have also been shown to protect against experimental infection by lectin-carrying bacteria in different organs of mammals such as mice, rabbits, calves and monkeys. [truncated to 100 words] Zafriri D, Ofek I, Adar R, Pocino M, Sharon N Department of Human Microbiology, Sackler Faculty of Medicine, Tel Aviv University, Israel. Inhibition of bacterial adherence
to bladder cells has been assumed to account for the beneficial
action ascribed to cranberry juice and cranberry juice
cocktail in the prevention of urinary tract infections
(A. E. Sobota, J. Urol. 131:1013-1016, 1984). We have
examined the effect of the cocktail and juice on the adherence
of Escherichia coli expressing surface lectins of defined
sugar specificity to yeasts, tissue culture cells, erythrocytes,
and mouse peritoneal macrophages. Cranberry juice cocktail
inhibited the adherence of urinary isolates expressing
type 1 fimbriae (mannose specific) and P fimbriae [specific
for alpha-D-Gal(1----4)-beta-D-Gal] but had no effect
on a diarrheal isolate expressing a CFA/I adhesin. The
cocktail also inhibited yeast agglutination by purified
type 1 fimbriae. The inhibitory activity for type 1 fimbriated
E. coli was dialyzable and could be ascribed to the fructose
present in the cocktail; this sugar was about 1/10 as
active as methyl alpha-D-mannoside in inhibiting the adherence
of type 1 fimbriated bacteria. The inhibitory activity
for the P fimbriated bacteria was nondialyzable and was
detected only after preincubation of the bacteria with
the cocktail. Cranberry juice, orange juice, and pineapple
juice also inhibited adherence of type 1 fimbriated E.
coli, most likely because of their fructose content. However,
the two latter juices did not inhibit the P fimbriated
bacteria. We conclude that cranberry juice contains at
least two inhibitors of lectin-mediated adherence of uropathogens
to eucaryotic cells. Further studies are required to establish
whether these inhibitors play a role in vivo. Effect of D-mannose and D-glucose on Escherichia coli bacteriuria in rats, Urol Res 11(2):97-102, 1983. Mannose-sensitive adherence of Escherichia coli to epithelial cells from women with recurrent urinary tract infections, J Urol 131(5):906-910, May 1984. Mannose-sensitive hemagglutination in the absence of piliation in Escherichia coli, Mol Microb 4(8):1311-1318, August 1990. Mannose Sensitive Adherence of Escherichia coli to Epithelial Cells. Eighty-First Annual Meeting of the American Society for Microbiology. Dallas, Texas. March 2-4, 1981. Effect of D-Mannose on Escherichia coli Adherence to Human Vaginal Epithelial Cells and Hemagglutination. American Urological Association. Seventy-Sixth Annual Meeting. Boston, Massachusetts. May 11, 1981 Prevention of Escherichia coli Bacteriuria in Rats by D-Mannose. American Urological Association. Boston, Massachusetts. May 11, 1981. Regulation of Mannose-Sensitive Hemagglutination in Clinical Isolates of Escherichia coli. In Kass EH, Svanborg-Eden C, eds: Host-Parasite Interactions in Urinary Tract Infections 115-121, Chicago, Illinois, 1989. The University of Chicago Press. Contribution of Escherichia coli Type l Pili to Ascending
Urinary Tract Colonization in Mice. eds: Host-Parasite Interactions in
Urinary Tract Infections 341-347, Chicago, Illinois, 1989. The University
of Chicago Press.
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