Literature DB >> 2917796

Binding of cholera toxin to pig intestinal mucosa glycosphingolipids: relationship with the ABO blood group system.

F R Bennun1, G A Roth, C G Monferran, F A Cumar.   

Abstract

A search for compounds from intestinal mucosa of pigs carrying and not carrying blood group A-active substances (A+ and A- pigs, respectively) capable of binding cholera toxin (CT) was performed. Glycolipid extracts from a pool of pig intestinal mucosa resolved in thin-layer chromatography (TLC) revealed the presence of six to eight compounds capable of binding 125I-CT, two of them running as the ganglioside standards GM1 and GD1b. When intestinal mucosa glycolipids from single pigs were assayed by TLC for CT-binding capacity, two different patterns of labeling were observed. The main difference was at the level of compounds running below GD1b. The A+ pigs but not the A- pigs showed CT binding at this level. The major CT-binding compound detected only in A+ pigs was purified and some properties were determined. After TLC developed with different solvent systems, the purified compound bound CT and also immunoreacted with anti-A and anti-AB antisera but not with anti-B antiserum. The compound was also able to inhibit the hemagglutination of human A erythrocytes caused by anti-A antiserum, but inhibition was not observed with the B-anti-B or O (H)-Ulex europaeus lectin systems. A partial chemical characterization indicated that the active compound is a neutral glycosphingolipid containing glucose, fucose, galactose, and hexosamine. The existence of a blood group-active substance(s) able to interact with CT may help to explain the relationship between ABO blood groups and the diarrheal disease caused by infection with Vibrio cholerae.

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Year:  1989        PMID: 2917796      PMCID: PMC313207          DOI: 10.1128/iai.57.3.969-974.1989

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  35 in total

1.  Identification of a novel hepraglycosylceramide with two fucose residues and a terminal hexosamine.

Authors:  E L Smith; J M Mckibbin; M E Breimer; K A Karlsson; I Pascher; B E Samuelson
Journal:  Biochim Biophys Acta       Date:  1975-07-22

2.  Branched blood group A-active fucolipids of hog gastric mucosa.

Authors:  B L Slomiany; A Slomiany
Journal:  Biochim Biophys Acta       Date:  1977-03-25

3.  Deactivation of cholera toxin by a sialidase-resistant monosialosylganglioside.

Authors:  C A King; W E Van Heyningen
Journal:  J Infect Dis       Date:  1973-06       Impact factor: 5.226

4.  Skeletal association of the cholera toxin receptor in rat erythrocytes.

Authors:  N Sahyoun; T Shatila; H LeVine; P Cuatrecasas
Journal:  Biochem Biophys Res Commun       Date:  1981-10-30       Impact factor: 3.575

Review 5.  Actions of cholera toxin and the prevention and treatment of cholera.

Authors:  J Holmgren
Journal:  Nature       Date:  1981-07-30       Impact factor: 49.962

6.  Protein A isolated from Staphylococcus aureus after digestion with lysostaphin.

Authors:  J Sjöquist; B Meloun; H Hjelm
Journal:  Eur J Biochem       Date:  1972-09-25

7.  A new ganglioside showing choleragenoid-binding activity in mouse spleen.

Authors:  K Nakamura; M Suzuki; F Inagaki; T Yamakawa; A Suzuki
Journal:  J Biochem       Date:  1987-04       Impact factor: 3.387

8.  Tryptophan fluorescence properties of cholera toxin upon interacting with ganglioside GD1b.

Authors:  M G Mestrallet; F R Bennun; B Maggio; F A Cumar
Journal:  J Neurosci Res       Date:  1984       Impact factor: 4.164

9.  Phytosphingosine is a characteristic component of the glycolipids in the vertebrate intestine.

Authors:  K Nishimura
Journal:  Comp Biochem Physiol B       Date:  1987

10.  Disialogangliosides in bovine adrenal medulla.

Authors:  T Ariga; M Sekine; R K Yu; T Miyatake
Journal:  J Biol Chem       Date:  1982-03-10       Impact factor: 5.157

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  8 in total

Review 1.  Blood Groups in Infection and Host Susceptibility.

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2.  Inhibition of cholera toxin binding to membrane receptors by pig gastric mucin-derived glycopeptides: differential effect depending on the ABO blood group antigenic determinants.

Authors:  C G Monferran; G A Roth; F A Cumar
Journal:  Infect Immun       Date:  1990-12       Impact factor: 3.441

3.  Blood group A and D negativity are associated with symptomatic West Nile virus infection.

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4.  Interaction of cholera toxin and Escherichia coli heat-labile enterotoxin with glycoconjugates from rabbit intestinal brush border membranes: relationship with ABH blood group determinants.

Authors:  L E Balanzino; J L Barra; E M Galván; G A Roth; C G Monferran
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Review 5.  Swine and cattle enterotoxigenic Escherichia coli-mediated diarrhea. Development of therapies based on inhibition of bacteria-host interactions.

Authors:  M Mouricout
Journal:  Eur J Epidemiol       Date:  1991-11       Impact factor: 8.082

6.  Intestinal organoid-based 2D monolayers mimic physiological and pathophysiological properties of the pig intestine.

Authors:  Pascal Hoffmann; Nadine Schnepel; Marion Langeheine; Katrin Künnemann; Guntram A Grassl; Ralph Brehm; Bettina Seeger; Gemma Mazzuoli-Weber; Gerhard Breves
Journal:  PLoS One       Date:  2021-08-23       Impact factor: 3.240

7.  Escherichia coli heat-labile enterotoxin preferentially interacts with blood group A-active glycolipids from pig intestinal mucosa and A- and B-active glycolipids from human red cells compared to H-active glycolipids.

Authors:  J L Barra; C G Monferran; L E Balanzino; F A Cumar
Journal:  Mol Cell Biochem       Date:  1992-09-22       Impact factor: 3.396

8.  Differential interaction of Escherichia coli heat-labile toxin and cholera toxin with pig intestinal brush border glycoproteins depending on their ABH and related blood group antigenic determinants.

Authors:  L E Balanzino; J L Barra; C G Monferran; F A Cumar
Journal:  Infect Immun       Date:  1994-04       Impact factor: 3.441

  8 in total

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