Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/23978
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dc.contributor.authorPaton, A.-
dc.contributor.authorMorona, R.-
dc.contributor.authorPaton, J.-
dc.date.issued2006-
dc.identifier.citationNature Reviews Microbiology, 2006; 4(3):193-200-
dc.identifier.issn1740-1526-
dc.identifier.issn1740-1534-
dc.identifier.urihttp://hdl.handle.net/2440/23978-
dc.description© 2007 Nature Publishing Group-
dc.description.abstractMany microbial pathogens, including those responsible for major enteric infections, exploit oligosaccharides that are displayed on the surface of host cells as receptors for toxins and adhesins. Blocking crucial ligand–receptor interactions is therefore a promising therapeutic strategy. One approach is to express molecular mimics of host receptors on the surface of harmless recombinant bacteria that can survive in the gut. These ‘designer probiotics’ bind bacterial toxins in the gut lumen with very high avidity, thereby preventing disease. This article discusses recent progress with this strategy.-
dc.description.statementofresponsibilityAdrienne W. Paton, Renato Morona and James C. Paton-
dc.language.isoen-
dc.publisherNature Publishing Group-
dc.source.urihttp://dx.doi.org/10.1038/nrmicro1349-
dc.subjectAnimals-
dc.subjectBacteria-
dc.subjectGastroenteritis-
dc.subjectOligosaccharides-
dc.subjectAdhesins, Bacterial-
dc.subjectReceptors, Cell Surface-
dc.subjectBacterial Toxins-
dc.subjectSpecies Specificity-
dc.subjectMolecular Mimicry-
dc.subjectDrug Design-
dc.subjectProbiotics-
dc.titleDesigner probiotics for prevention of enteric infections-
dc.typeJournal article-
dc.identifier.doi10.1038/nrmicro1349-
pubs.publication-statusPublished-
dc.identifier.orcidMorona, R. [0000-0001-7009-7440]-
dc.identifier.orcidPaton, J. [0000-0001-9807-5278]-
Appears in Collections:Aurora harvest 6
Molecular and Biomedical Science publications

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