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Structure and genetics of Escherichia coli O antigens.

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TLDR
Several pairs or groups of the E. coli antigens that have related structures show close relationships of the O antigen gene clusters within clades, thereby highlighting the genetic basis of the evolution of diversity.
Abstract
Escherichia coli includes clonal groups of both commensal and pathogenic strains, with some of the latter causing serious infectious diseases. O antigen variation is current standard in defining strains for taxonomy and epidemiology, providing the basis for many serotyping schemes for Gram-negative bacteria. This review covers the diversity in E. coli O antigen structures and gene clusters, and the genetic basis for the structural diversity. Of the 187 formally defined O antigens, six (O31, O47, O67, O72, O94 and O122) have since been removed and three (O34, O89 and O144) strains do not produce any O antigen. Therefore, structures are presented for 176 of the 181 E. coli O antigens, some of which include subgroups. Most (93%) of these O antigens are synthesized via the Wzx/Wzy pathway, 11 via the ABC transporter pathway, with O20, O57 and O60 still uncharacterized due to failure to find their O antigen gene clusters. Biosynthetic pathways are given for 38 of the 49 sugars found in E. coli O antigens, and several pairs or groups of the E. coli antigens that have related structures show close relationships of the O antigen gene clusters within clades, thereby highlighting the genetic basis of the evolution of diversity.

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Lipopolysaccharide O-antigens - bacterial glycans made to measure

TL;DR: The current understanding of the mechanisms involved in regulating O-PS chain-length distribution are reviewed and their impact on microbial cell biology is discussed.
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Systematic exploration of Escherichia coli phage-host interactions with the BASEL phage collection.

TL;DR: The BASEL (BActeriophage SElection for your Laboratory) collection as mentioned in this paper is a collection of 68 newly isolated phages infecting the model organism Escherichia coli.
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Physiological Functions of Bacterial "Multidrug" Efflux Pumps.

TL;DR: A broad survey of the proteins involved in multidrug efflux pumps can be found in this paper, together with detailed examples of their evolution, energetics, structures, chemical recognition, and molecular mechanisms, together with experimental strategies that enable rapid and economical progress in understanding their true physiological roles.
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Structure and Function of the Branched Receptor-Binding Complex of Bacteriophage CBA120

TL;DR: It is demonstrated that according to the specificity of its tailspikes TSP2, TSP3, and TSP4, CBA120 can infect E. coli O157, O77, and O78, respectively and that CBA 120 infects Salmonella enterica serovar Minnesota and this host range expansion is likely due to the function of TSP1.
Posted ContentDOI

Systematic exploration of Escherichia coli phage-host interactions with the BASEL phage collection

TL;DR: The BASEL collection as discussed by the authors is a collection of 66 newly isolated bacteriophages infecting the model organism Escherichia coli that is shared with the community as the BActeriophage SElection for your Laboratory.
References
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Journal ArticleDOI

OrthoMCL: identification of ortholog groups for eukaryotic genomes.

TL;DR: OrthoMCL provides a scalable method for constructing orthologous groups across multiple eukaryotic taxa, using a Markov Cluster algorithm to group (putative) orthologs and paralogs.
Journal ArticleDOI

Diarrheagenic Escherichia coli

TL;DR: The current level of understanding of the pathogenesis of the diarrheagenic E. coli strains is discussed and how their pathogenic schemes underlie the clinical manifestations, diagnostic approach, and epidemiologic investigation of these important pathogens are described.
Journal ArticleDOI

Pathogenic Escherichia coli

TL;DR: Few microorganisms are as versatile as Escherichia coli; it can also be a highly versatile, and frequently deadly, pathogen.
Journal ArticleDOI

Characterisation of the Escherichia coli strain associated with an outbreak of haemolytic uraemic syndrome in Germany, 2011: a microbiological study

TL;DR: Augmented adherence of the strain to intestinal epithelium might facilitate systemic absorption of Shiga toxin and could explain the high progression to haemolytic uraemic syndrome.
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