Literature DB >> 15007099

Diversity of microbial sialic acid metabolism.

Eric R Vimr1, Kathryn A Kalivoda, Eric L Deszo, Susan M Steenbergen.   

Abstract

Sialic acids are structurally unique nine-carbon keto sugars occupying the interface between the host and commensal or pathogenic microorganisms. An important function of host sialic acid is to regulate innate immunity, and microbes have evolved various strategies for subverting this process by decorating their surfaces with sialylated oligosaccharides that mimic those of the host. These subversive strategies include a de novo synthetic pathway and at least two truncated pathways that depend on scavenging host-derived intermediates. A fourth strategy involves modification of sialidases so that instead of transferring sialic acid to water (hydrolysis), a second active site is created for binding alternative acceptors. Sialic acids also are excellent sources of carbon, nitrogen, energy, and precursors of cell wall biosynthesis. The catabolic strategies for exploiting host sialic acids as nutritional sources are as diverse as the biosynthetic mechanisms, including examples of horizontal gene transfer and multiple transport systems. Finally, as compounds coating the surfaces of virtually every vertebrate cell, sialic acids provide information about the host environment that, at least in Escherichia coli, is interpreted by the global regulator encoded by nanR. In addition to regulating the catabolism of sialic acids through the nan operon, NanR controls at least two other operons of unknown function and appears to participate in the regulation of type 1 fimbrial phase variation. Sialic acid is, therefore, a host molecule to be copied (molecular mimicry), eaten (nutrition), and interpreted (cell signaling) by diverse metabolic machinery in all major groups of mammalian pathogens and commensals.

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Year:  2004        PMID: 15007099      PMCID: PMC362108          DOI: 10.1128/MMBR.68.1.132-153.2004

Source DB:  PubMed          Journal:  Microbiol Mol Biol Rev        ISSN: 1092-2172            Impact factor:   11.056


  154 in total

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7.  In vivo enzymatic removal of alpha 2-->6-linked sialic acid from the glomerular filtration barrier results in podocyte charge alteration and glomerular injury.

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Authors:  Sammia El-Labany; Baljinder K Sohanpal; Maryam Lahooti; Robert Akerman; Ian C Blomfield
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Authors:  Andrew G Watts; Iben Damager; Maria L Amaya; Alejandro Buschiazzo; Pedro Alzari; Alberto C Frasch; Stephen G Withers
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  228 in total

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2.  Sialylation of lipooligosaccharides is dispensable for the virulence of Haemophilus ducreyi in humans.

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Journal:  Infect Immun       Date:  2011-12-05       Impact factor: 3.441

Review 3.  Multifarious roles of sialic acids in immunity.

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4.  Cloning and characterization of a viral α2-3-sialyltransferase (vST3Gal-I) for the synthesis of sialyl Lewisx.

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Journal:  Microb Ecol       Date:  2017-07-18       Impact factor: 4.552

6.  Function and expression of an N-acetylneuraminic acid-inducible outer membrane channel in Escherichia coli.

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7.  Identification of Streptomyces coelicolor M145 genomic region involved in biosynthesis of teichulosonic acid-cell wall glycopolymer.

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8.  Cloning, expression, purification, crystallization and preliminary X-ray diffraction analysis of N-acetylmannosamine-6-phosphate 2-epimerase from methicillin-resistant Staphylococcus aureus.

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9.  Cloning, expression, purification, crystallization and preliminary X-ray diffraction analysis of N-acetylmannosamine kinase from methicillin-resistant Staphylococcus aureus.

Authors:  Rachel A North; Simona Seizova; Anja Stampfli; Sarah A Kessans; Hironori Suzuki; Michael D W Griffin; Marc Kvansakul; Renwick C J Dobson
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10.  Metabolism of sialic acid by Bifidobacterium breve UCC2003.

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