Abstract

Mimivirus is one the largest DNA virus identified so far, infecting several Acanthamoeba species. Analysis of its genome revealed the presence of a nine-gene cluster containing genes potentially involved in glycan formation. All of these genes are co-expressed at late stages of infection, suggesting their role in the formation of the long fibers covering the viral surface. Among them, we identified the L136 gene as a pyridoxal phosphate-dependent sugar aminotransferase. This enzyme was shown to catalyze the formation of UDP-4-amino-4,6-dideoxy-D-glucose (UDP-viosamine) from UDP-4-keto-6-deoxy-D-glucose, a key compound involved also in the biosynthesis of L-rhamnose. This finding further supports the hypothesis that Mimivirus encodes a glycosylation system that is completely independent of the amoebal host. Viosamine, together with rhamnose, (N-acetyl)glucosamine, and glucose, was found as a major component of the viral glycans. Most of the sugars were associated with the fibers, confirming a capsular-like nature of the viral surface. Phylogenetic analysis clearly indicated that L136 was not a recent acquisition from bacteria through horizontal gene transfer, but it was acquired very early during evolution. Implications for the origin of the glycosylation machinery in giant DNA virus are also discussed.

Highlights

  • Mimivirus is highly glycosylated; nothing is known about its glycan composition and structure

  • Vio is found in several bacterial glycans, such as the LPS O-antigens of Shigella disenteriae type 7 and of the Shiga toxin-producing Escherichia coli O121 [16], the fiber-associated pentasaccharide of Bacillus anthracis exosporium [17], the O-polysaccharide of Francisella tularensis and of the emerging pathogen Photorabdus asymbyotica [18], the glycans of Pseudomonas syringae flagellin [19], and the capsular polysaccharides of several marine bacteria belonging to the genus Pseudoalteromonas and Shewanella (20 –21)

  • E. coli and Salmonella enterica WecE, which are involved in the synthesis of D-fucosamine found in the enterobacterial common antigen [37], were 25% identical with L136 over 354 and 227 amino acids, respectively

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Summary

Background

Mimivirus is highly glycosylated; nothing is known about its glycan composition and structure. We identified the L136 gene as a pyridoxal phosphate-dependent sugar aminotransferase This enzyme was shown to catalyze the formation of UDP-4-amino-4,6-dideoxyD-glucose (UDP-viosamine) from UDP-4-keto-6-deoxy-D-glucose, a key compound involved in the biosynthesis of L-rhamnose. This finding further supports the hypothesis that Mimivirus encodes a glycosylation system that is completely independent of the amoebal host. Mimivirus genome analysis revealed many genes potentially encoding proteins involved in glycan formation, including glycosyltransferases and sugar-modifying enzymes [2]. This strongly suggests that this virus encodes an independent glycosylation system. Putative enzymes involved in the synthesis of 3-deoxy-D-

The abbreviations used are
EXPERIMENTAL PROCEDURES
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