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      Integrated mobile genetic elements in Thaumarchaeota

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          Summary

          To explore the diversity of mobile genetic elements (MGE) associated with archaea of the phylum Thaumarchaeota, we exploited the property of most MGE to integrate into the genomes of their hosts. Integrated MGE (iMGE) were identified in 20 thaumarchaeal genomes amounting to 2 Mbp of mobile thaumarchaeal DNA. These iMGE group into five major classes: (i) proviruses, (ii) casposons, (iii) insertion sequence‐like transposons, (iv) integrative‐conjugative elements and (v) cryptic integrated elements. The majority of the iMGE belong to the latter category and might represent novel families of viruses or plasmids. The identified proviruses are related to tailed viruses of the order Caudovirales and to tailless icosahedral viruses with the double jelly‐roll capsid proteins. The thaumarchaeal iMGE are all connected within a gene sharing network, highlighting pervasive gene exchange between MGE occupying the same ecological niche. The thaumarchaeal mobilome carries multiple auxiliary metabolic genes, including multicopper oxidases and ammonia monooxygenase subunit C (AmoC), and stress response genes, such as those for universal stress response proteins (UspA). Thus, iMGE might make important contributions to the fitness and adaptation of their hosts. We identified several iMGE carrying type I‐B CRISPR‐Cas systems and spacers matching other thaumarchaeal iMGE, suggesting antagonistic interactions between coexisting MGE and symbiotic relationships with the ir archaeal hosts.

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          Most cited references103

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          Mobile Genetic Elements Associated with Antimicrobial Resistance

          SUMMARY Strains of bacteria resistant to antibiotics, particularly those that are multiresistant, are an increasing major health care problem around the world. It is now abundantly clear that both Gram-negative and Gram-positive bacteria are able to meet the evolutionary challenge of combating antimicrobial chemotherapy, often by acquiring preexisting resistance determinants from the bacterial gene pool. This is achieved through the concerted activities of mobile genetic elements able to move within or between DNA molecules, which include insertion sequences, transposons, and gene cassettes/integrons, and those that are able to transfer between bacterial cells, such as plasmids and integrative conjugative elements. Together these elements play a central role in facilitating horizontal genetic exchange and therefore promote the acquisition and spread of resistance genes. This review aims to outline the characteristics of the major types of mobile genetic elements involved in acquisition and spread of antibiotic resistance in both Gram-negative and Gram-positive bacteria, focusing on the so-called ESKAPEE group of organisms ( Enterococcus faecium , Staphylococcus aureus , Klebsiella pneumoniae , Acinetobacter baumannii , Pseudomonas aeruginosa , Enterobacter spp., and Escherichia coli ), which have become the most problematic hospital pathogens.
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            Discovery and Functional Characterization of Diverse Class 2 CRISPR-Cas Systems.

            Microbial CRISPR-Cas systems are divided into Class 1, with multisubunit effector complexes, and Class 2, with single protein effectors. Currently, only two Class 2 effectors, Cas9 and Cpf1, are known. We describe here three distinct Class 2 CRISPR-Cas systems. The effectors of two of the identified systems, C2c1 and C2c3, contain RuvC-like endonuclease domains distantly related to Cpf1. The third system, C2c2, contains an effector with two predicted HEPN RNase domains. Whereas production of mature CRISPR RNA (crRNA) by C2c1 depends on tracrRNA, C2c2 crRNA maturation is tracrRNA independent. We found that C2c1 systems can mediate DNA interference in a 5'-PAM-dependent fashion analogous to Cpf1. However, unlike Cpf1, which is a single-RNA-guided nuclease, C2c1 depends on both crRNA and tracrRNA for DNA cleavage. Finally, comparative analysis indicates that Class 2 CRISPR-Cas systems evolved on multiple occasions through recombination of Class 1 adaptation modules with effector proteins acquired from distinct mobile elements.
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              Archaeal nitrification in the ocean.

              Marine Crenarchaeota are the most abundant single group of prokaryotes in the ocean, but their physiology and role in marine biogeochemical cycles are unknown. Recently, a member of this clade was isolated from a sea aquarium and shown to be capable of nitrification, tentatively suggesting that Crenarchaeota may play a role in the oceanic nitrogen cycle. We enriched a crenarchaeote from North Sea water and showed that its abundance, and not that of bacteria, correlates with ammonium oxidation to nitrite. A time series study in the North Sea revealed that the abundance of the gene encoding for the archaeal ammonia monooxygenase alfa subunit (amoA) is correlated with a decline in ammonium concentrations and with the abundance of Crenarchaeota. Remarkably, the archaeal amoA abundance was 1-2 orders of magnitude higher than those of bacterial nitrifiers, which are commonly thought to mediate the oxidation of ammonium to nitrite in marine environments. Analysis of Atlantic waters of the upper 1,000 m, where most of the ammonium regeneration and oxidation takes place, showed that crenarchaeotal amoA copy numbers are also 1-3 orders of magnitude higher than those of bacterial amoA. Our data thus suggest a major role for Archaea in oceanic nitrification.
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                Author and article information

                Contributors
                krupovic@pasteur.fr
                Journal
                Environ Microbiol
                Environ. Microbiol
                10.1111/(ISSN)1462-2920
                EMI
                Environmental Microbiology
                John Wiley & Sons, Inc. (Hoboken, USA )
                1462-2912
                1462-2920
                18 March 2019
                June 2019
                : 21
                : 6 , Special Issue on Environmental viruses and their role in shaping ecosystems ( doiID: 10.1111/emi.2019.21.issue-6 )
                : 2056-2078
                Affiliations
                [ 1 ] Institut Pasteur Unité Biologie Moléculaire du Gène chez les Extrêmophiles, 75015 Paris France
                [ 2 ] National Center for Biotechnology Information National Library of Medicine Bethesda MD 20894 USA
                [ 3 ] Center of Life Sciences Skolkovo Institute of Science and Technology Skolkovo Russia
                [ 4 ] Sorbonne Université Collège doctoral, 75005 Paris France
                [ 5 ] Institute for Integrative Biology of the Cell (I2BC) CEA, CNRS, Univ. Paris‐ Sud, Université Paris‐Saclay, Gif‐sur‐Yvette cedex Paris France
                Author notes
                [*] [* ]For correspondence. E‐mail krupovic@ 123456pasteur.fr ; Tel. +33 1 40 61 37 22; Fax +33 1 45 68 88 34.
                Author information
                https://orcid.org/0000-0001-5486-0098
                https://orcid.org/0000-0002-0812-9699
                Article
                EMI14564
                10.1111/1462-2920.14564
                6563490
                30773816
                52ca2534-222f-48e9-9889-9753d2f683c2
                © 2019 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 30 November 2018
                : 10 February 2019
                : 13 February 2019
                Page count
                Figures: 9, Tables: 1, Pages: 23, Words: 16989
                Funding
                Funded by: Agence Nationale de la Recherche
                Award ID: ANR‐17‐CE15‐0005‐01
                Funded by: H2020 European Research Council
                Award ID: UE 340440
                Funded by: Horizon 2020 Framework Programme
                Award ID: 685778
                Funded by: U.S. National Library of Medicine
                Award ID: intramural program
                Funded by: Campus France
                Award ID: RSF 14‐14‐00988
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                emi14564
                June 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.4 mode:remove_FC converted:13.06.2019

                Microbiology & Virology
                Microbiology & Virology

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