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      Structure and genetics of Escherichia coli O antigens

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          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.

          Abstract

          This review summarizes the diversity of E. coli O antigen structures and gene clusters, and gives a systematic analysis of the genetic basis for structural diversity.

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          OrthoMCL: identification of ortholog groups for eukaryotic genomes.

          The identification of orthologous groups is useful for genome annotation, studies on gene/protein evolution, comparative genomics, and the identification of taxonomically restricted sequences. Methods successfully exploited for prokaryotic genome analysis have proved difficult to apply to eukaryotes, however, as larger genomes may contain multiple paralogous genes, and sequence information is often incomplete. OrthoMCL provides a scalable method for constructing orthologous groups across multiple eukaryotic taxa, using a Markov Cluster algorithm to group (putative) orthologs and paralogs. This method performs similarly to the INPARANOID algorithm when applied to two genomes, but can be extended to cluster orthologs from multiple species. OrthoMCL clusters are coherent with groups identified by EGO, but improved recognition of "recent" paralogs permits overlapping EGO groups representing the same gene to be merged. Comparison with previously assigned EC annotations suggests a high degree of reliability, implying utility for automated eukaryotic genome annotation. OrthoMCL has been applied to the proteome data set from seven publicly available genomes (human, fly, worm, yeast, Arabidopsis, the malaria parasite Plasmodium falciparum, and Escherichia coli). A Web interface allows queries based on individual genes or user-defined phylogenetic patterns (http://www.cbil.upenn.edu/gene-family). Analysis of clusters incorporating P. falciparum genes identifies numerous enzymes that were incompletely annotated in first-pass annotation of the parasite genome.
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            Dynamics and Stabilization of the Human Gut Microbiome during the First Year of Life.

            The gut microbiota is central to human health, but its establishment in early life has not been quantitatively and functionally examined. Applying metagenomic analysis on fecal samples from a large cohort of Swedish infants and their mothers, we characterized the gut microbiome during the first year of life and assessed the impact of mode of delivery and feeding on its establishment. In contrast to vaginally delivered infants, the gut microbiota of infants delivered by C-section showed significantly less resemblance to their mothers. Nutrition had a major impact on early microbiota composition and function, with cessation of breast-feeding, rather than introduction of solid food, being required for maturation into an adult-like microbiota. Microbiota composition and ecological network had distinctive features at each sampled stage, in accordance with functional maturation of the microbiome. Our findings establish a framework for understanding the interplay between the gut microbiome and the human body in early life.
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              Pathogenic Escherichia coli.

              Few microorganisms are as versatile as Escherichia coli. An important member of the normal intestinal microflora of humans and other mammals, E. coli has also been widely exploited as a cloning host in recombinant DNA technology. But E. coli is more than just a laboratory workhorse or harmless intestinal inhabitant; it can also be a highly versatile, and frequently deadly, pathogen. Several different E. coli strains cause diverse intestinal and extraintestinal diseases by means of virulence factors that affect a wide range of cellular processes.
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                Author and article information

                Contributors
                Journal
                FEMS Microbiol Rev
                FEMS Microbiol Rev
                femsre
                FEMS Microbiology Reviews
                Oxford University Press
                0168-6445
                1574-6976
                28 November 2019
                November 2020
                28 November 2019
                : 44
                : 6
                : 655-683
                Affiliations
                TEDA Institute of Biological Sciences and Biotechnology , Nankai University, 23 Hongda Street, TEDA, Tianjing 300457, China
                The Key Laboratory of Molecular Microbiology and Technology, Ministry of Education , 23 Hongda Street, TEDA, Tianjin 300457, China
                Tianjin Key Laboratory of Microbial Functional Genomics , 23 Hongda Street, TEDA, Tianjin 300457, China
                Department of Organic Chemistry, Arrhenius Laboratory, Svante Arrhenius väg 16C, Stockholm University , S-106 91 Stockholm, Sweden
                N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences , Leninsky Prospect, 47, Moscow, Russia
                TEDA Institute of Biological Sciences and Biotechnology , Nankai University, 23 Hongda Street, TEDA, Tianjing 300457, China
                The Key Laboratory of Molecular Microbiology and Technology, Ministry of Education , 23 Hongda Street, TEDA, Tianjin 300457, China
                Tianjin Key Laboratory of Microbial Functional Genomics , 23 Hongda Street, TEDA, Tianjin 300457, China
                TEDA Institute of Biological Sciences and Biotechnology , Nankai University, 23 Hongda Street, TEDA, Tianjing 300457, China
                The Key Laboratory of Molecular Microbiology and Technology, Ministry of Education , 23 Hongda Street, TEDA, Tianjin 300457, China
                Tianjin Key Laboratory of Microbial Functional Genomics , 23 Hongda Street, TEDA, Tianjin 300457, China
                TEDA Institute of Biological Sciences and Biotechnology , Nankai University, 23 Hongda Street, TEDA, Tianjing 300457, China
                The Key Laboratory of Molecular Microbiology and Technology, Ministry of Education , 23 Hongda Street, TEDA, Tianjin 300457, China
                Tianjin Key Laboratory of Microbial Functional Genomics , 23 Hongda Street, TEDA, Tianjin 300457, China
                School of Molecular and Microbial Bioscience, University of Sydney , 2 Butilin Ave, Darlington NSW 2008, Sydney, Australia
                N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences , Leninsky Prospect, 47, Moscow, Russia
                TEDA Institute of Biological Sciences and Biotechnology , Nankai University, 23 Hongda Street, TEDA, Tianjing 300457, China
                The Key Laboratory of Molecular Microbiology and Technology, Ministry of Education , 23 Hongda Street, TEDA, Tianjin 300457, China
                Tianjin Key Laboratory of Microbial Functional Genomics , 23 Hongda Street, TEDA, Tianjin 300457, China
                Department of Organic Chemistry, Arrhenius Laboratory, Svante Arrhenius väg 16C, Stockholm University , S-106 91 Stockholm, Sweden
                Author notes
                Corresponding author: TEDA Institute of Biological Sciences and Biotechnology, Nankai University, 23 Hongda Street, TEDA, Tianjin 300457, China. Tel: +86 22 66229588; E-mail: wanglei@ 123456nankai.edu.cn
                Corresponding author: Department of Organic Chemistry, Arrhenius Laboratory, Svante Arrhenius väg 16C, Stockholm University, S-106 91 Stockholm, Sweden. Tel: +46 721 464748; E-mail: goran.widmalm@ 123456su.se

                Current address: Department of Immunology, School of Basic Medical Sciences, Tianjin Medical University, 22 Qixiangtai Road, Heping District, Tianjin 300070, China.

                These authors contributed equally to this work.

                Article
                fuz028
                10.1093/femsre/fuz028
                7685785
                31778182
                28915189-9ce1-4cef-8437-538b6eee7564
                © The Author(s) 2019. Published by Oxford University Press on behalf of FEMS.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@ 123456oup.com

                History
                : 18 December 2018
                : 22 November 2019
                Page count
                Pages: 29
                Funding
                Funded by: National Natural Science Foundation of China, DOI 10.13039/501100001809;
                Award ID: 31530083
                Award ID: 31820103002
                Funded by: Russian Science Foundation, DOI 10.13039/501100006769;
                Award ID: 14-14-01042
                Funded by: Swedish Research Council, DOI 10.13039/501100004359;
                Award ID: 2017–03703
                Categories
                Review Article
                AcademicSubjects/SCI01150

                Microbiology & Virology
                escherichia coli,o antigen,gene cluster,serogroup,diversity,structure
                Microbiology & Virology
                escherichia coli, o antigen, gene cluster, serogroup, diversity, structure

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