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The human genome, as with the genome of most organisms, is comprised of various types of mobile genetic element derived repeats. Mobile genetic elements that mobilize by an RNA intermediate, include both autonomous and non-autonomous retrotransposons, and mobilize by a “copy and paste” mechanism that relies of the presence of a functional reverse transcriptase activity. The extent to which these different types of elements are actively mobilizing varies among organisms, as revealed with the advent of Next Generation DNA sequencing (NGS).To understand the normal and aberrant mechanisms that impact the mobility of these elements requires a more extensive understanding of how these elements interact with molecular pathways of the cell, including DNA repair, recombination and chromatin. In addition, epigenetic based-mechanisms can also influence the mobility of these elements, likely by transcriptional activation or repression in certain cell types. Studies regarding how mobile genetic elements interface and evolve with these pathways will rely on genomic studies from various model organisms. In addition, the mechanistic details of how these elements are regulated will continue to be elucidated with the use of genetic, biochemical, molecular, cellular, and bioinformatic approaches. Remarkably, the current understanding regarding the biology of these elements in the human genome, suggests these elements may impact developmental biology, including cellular differentiation, neuronal development, and immune function. Thus, aberrant changes in these molecular pathways may also impact disease, including neuronal degeneration, autoimmunity, and cancer.
transposon --- genome stability --- model organisms --- reverse transcriptase --- Mobile DNA --- RNA-dependent DNA polymerase --- cellular differentiation --- retrotransposon --- DNA repair --- transposon --- genome stability --- model organisms --- reverse transcriptase --- Mobile DNA --- RNA-dependent DNA polymerase --- cellular differentiation --- retrotransposon --- DNA repair
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The human genome, as with the genome of most organisms, is comprised of various types of mobile genetic element derived repeats. Mobile genetic elements that mobilize by an RNA intermediate, include both autonomous and non-autonomous retrotransposons, and mobilize by a “copy and paste” mechanism that relies of the presence of a functional reverse transcriptase activity. The extent to which these different types of elements are actively mobilizing varies among organisms, as revealed with the advent of Next Generation DNA sequencing (NGS).To understand the normal and aberrant mechanisms that impact the mobility of these elements requires a more extensive understanding of how these elements interact with molecular pathways of the cell, including DNA repair, recombination and chromatin. In addition, epigenetic based-mechanisms can also influence the mobility of these elements, likely by transcriptional activation or repression in certain cell types. Studies regarding how mobile genetic elements interface and evolve with these pathways will rely on genomic studies from various model organisms. In addition, the mechanistic details of how these elements are regulated will continue to be elucidated with the use of genetic, biochemical, molecular, cellular, and bioinformatic approaches. Remarkably, the current understanding regarding the biology of these elements in the human genome, suggests these elements may impact developmental biology, including cellular differentiation, neuronal development, and immune function. Thus, aberrant changes in these molecular pathways may also impact disease, including neuronal degeneration, autoimmunity, and cancer.
transposon --- genome stability --- model organisms --- reverse transcriptase --- Mobile DNA --- RNA-dependent DNA polymerase --- cellular differentiation --- retrotransposon --- DNA repair
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The human genome, as with the genome of most organisms, is comprised of various types of mobile genetic element derived repeats. Mobile genetic elements that mobilize by an RNA intermediate, include both autonomous and non-autonomous retrotransposons, and mobilize by a “copy and paste” mechanism that relies of the presence of a functional reverse transcriptase activity. The extent to which these different types of elements are actively mobilizing varies among organisms, as revealed with the advent of Next Generation DNA sequencing (NGS).To understand the normal and aberrant mechanisms that impact the mobility of these elements requires a more extensive understanding of how these elements interact with molecular pathways of the cell, including DNA repair, recombination and chromatin. In addition, epigenetic based-mechanisms can also influence the mobility of these elements, likely by transcriptional activation or repression in certain cell types. Studies regarding how mobile genetic elements interface and evolve with these pathways will rely on genomic studies from various model organisms. In addition, the mechanistic details of how these elements are regulated will continue to be elucidated with the use of genetic, biochemical, molecular, cellular, and bioinformatic approaches. Remarkably, the current understanding regarding the biology of these elements in the human genome, suggests these elements may impact developmental biology, including cellular differentiation, neuronal development, and immune function. Thus, aberrant changes in these molecular pathways may also impact disease, including neuronal degeneration, autoimmunity, and cancer.
transposon --- genome stability --- model organisms --- reverse transcriptase --- Mobile DNA --- RNA-dependent DNA polymerase --- cellular differentiation --- retrotransposon --- DNA repair
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DNA Transposable Elements. --- Elements, Insertion Sequence --- Sequence Elements, Insertion --- DNA Insertion Elements --- DNA Transposons --- IS Elements --- Insertion Sequence Elements --- Tn Elements --- Transposable Elements --- DNA Insertion Element --- DNA Transposable Element --- DNA Transposon --- Element, DNA Insertion --- Element, DNA Transposable --- Element, IS --- Element, Insertion Sequence --- Element, Tn --- Element, Transposable --- Elements, DNA Insertion --- Elements, DNA Transposable --- Elements, IS --- Elements, Tn --- Elements, Transposable --- IS Element --- Insertion Element, DNA --- Insertion Elements, DNA --- Insertion Sequence Element --- Sequence Element, Insertion --- Tn Element --- Transposable Element --- Transposable Element, DNA --- Transposable Elements, DNA --- Transposon, DNA --- Transposons, DNA --- Mutagenesis, Insertional --- Retroelements --- DNA Transposable Elements --- Conferences - Meetings --- Microbial genetics --- Congresses --- Translocation (Genetics)
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PLASMIDS --- CELLS --- Genetic engineering --- Cells. --- Genetic Engineering. --- Plasmids. --- 577.21 --- biologie --- drosophila --- eukaryoten --- gisten --- moleculaire biologie --- plasmiden --- transposon --- vectoren biologie --- Episome --- Plasmid --- Episomes --- DNA Transposable Elements --- Engineering, Genetic --- Intervention, Genetic --- Genetic Intervention --- Genetic Interventions --- Interventions, Genetic --- Biotechnology --- Cloning, Molecular --- DNA, Recombinant --- Industrial Microbiology --- Artificial Gene Fusion --- Organisms, Genetically Modified --- Animals, Genetically Modified --- Plants, Genetically Modified --- Cell --- Cell Biology --- Virophages --- Plasmids --- Eukaryotic cells --- Plasmides --- Cellules eucaryotes --- Génie génétique --- Cells --- Genetic Engineering
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Carbapenem-resistant Enterobacterales (CRE) are a common cause of infections in both community and healthcare settings and have become an increasing threat to public health worldwide. The focus of this Special Issue includes aspects concerning plasmid-mediated antimicrobial resistance along with other carbapenem resistance mechanisms. Understanding the prevalence and routes of transmission of CRE is important in developing specific interventions for healthcare facilities, as well as the general impact of CRE circulation on the environment. Attention has also been focused on carbapenemase testing in order to provide advanced phenotypic and molecular assays for the identification of CRE, as a valid tool for active global surveillance, and from this perspective, the study of resistance mechanisms can provide significant support for the development of new and appropriate antimicrobial molecules. For all of these reasons, the phenomenon of carbapenem resistance deserves more attention, for the sake of public health.
Research & information: general --- Biology, life sciences --- Microbiology (non-medical) --- carbapenem resistance --- carbapenemase --- whole genome sequencing --- long reads, plasmid --- Klebsiella pneumoniae --- extensively drug-resistant --- molecular typing --- carbapenemases --- Enterobacteriales --- human --- animal --- food --- environment --- carbapenemase-producing Enterobacterales --- KPC --- carbapenem --- multidrug resistance --- nosocomial --- Enterobacteriaceae --- ESBL --- resistance genes --- cattle --- blaOXA-48 --- ERIC-PCR --- plasmid profile analysis --- biofilm formation --- PCR-based replicon typing --- antibiotic-resistance --- sequence types --- multilocus sequence typing --- plasmids --- antimicrobial resistance --- carbapenem inactivation method --- carbapenem-resistant Enterobacterales --- real-time multiplex PCR --- whole-genome sequencing --- carbapenem-resistance --- Qatar --- CRE --- OXA-48 --- carbapenems resistance --- Gram-negative bacteria --- infection --- colonization --- COVID-19 --- K. pneumoniae --- porins --- ceftazidime/avibactam --- ESKAPE --- healthcare-associated infections --- antimicrobial peptides --- Temporin L --- Klebsiella michiganensis --- Citrobacter farmeri --- KPC-2 --- plasmid --- transposon --- carbapenem-resistant Enterobacteriaceae (CRE) --- outbreak --- infection control --- pulsed-field gel electrophoresis (PFGE) --- multilocus sequence typing (MLST) --- IMP-6 --- porin --- efflux pump --- nosocomial infections --- NDM-1 --- Fourier transform infrared spectroscopy --- Eazyplex® SuperBug CRE assay --- extended-spectrum beta-lactamases --- gram-negative rods --- LAMP method --- NDM --- VIM --- molecular epidemiology --- PFGE --- Carbapenemase producing Enterobacterales --- IncX-3 --- one health --- water --- colistin susceptibility testing --- broth microdilution --- colistin broth disc elution --- Vitek 2 compact --- rapid polymyxin NP test --- Etest --- ChromID colistin R agar --- micronaut MIC-strip colistin --- population analysis profiling --- Enterobacterales --- neonates --- plasmid-typing --- sequence type --- wastewater --- virulence --- carbapenem resistance --- carbapenemase --- whole genome sequencing --- long reads, plasmid --- Klebsiella pneumoniae --- extensively drug-resistant --- molecular typing --- carbapenemases --- Enterobacteriales --- human --- animal --- food --- environment --- carbapenemase-producing Enterobacterales --- KPC --- carbapenem --- multidrug resistance --- nosocomial --- Enterobacteriaceae --- ESBL --- resistance genes --- cattle --- blaOXA-48 --- ERIC-PCR --- plasmid profile analysis --- biofilm formation --- PCR-based replicon typing --- antibiotic-resistance --- sequence types --- multilocus sequence typing --- plasmids --- antimicrobial resistance --- carbapenem inactivation method --- carbapenem-resistant Enterobacterales --- real-time multiplex PCR --- whole-genome sequencing --- carbapenem-resistance --- Qatar --- CRE --- OXA-48 --- carbapenems resistance --- Gram-negative bacteria --- infection --- colonization --- COVID-19 --- K. pneumoniae --- porins --- ceftazidime/avibactam --- ESKAPE --- healthcare-associated infections --- antimicrobial peptides --- Temporin L --- Klebsiella michiganensis --- Citrobacter farmeri --- KPC-2 --- plasmid --- transposon --- carbapenem-resistant Enterobacteriaceae (CRE) --- outbreak --- infection control --- pulsed-field gel electrophoresis (PFGE) --- multilocus sequence typing (MLST) --- IMP-6 --- porin --- efflux pump --- nosocomial infections --- NDM-1 --- Fourier transform infrared spectroscopy --- Eazyplex® SuperBug CRE assay --- extended-spectrum beta-lactamases --- gram-negative rods --- LAMP method --- NDM --- VIM --- molecular epidemiology --- PFGE --- Carbapenemase producing Enterobacterales --- IncX-3 --- one health --- water --- colistin susceptibility testing --- broth microdilution --- colistin broth disc elution --- Vitek 2 compact --- rapid polymyxin NP test --- Etest --- ChromID colistin R agar --- micronaut MIC-strip colistin --- population analysis profiling --- Enterobacterales --- neonates --- plasmid-typing --- sequence type --- wastewater --- virulence
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Carbapenem-resistant Enterobacterales (CRE) are a common cause of infections in both community and healthcare settings and have become an increasing threat to public health worldwide. The focus of this Special Issue includes aspects concerning plasmid-mediated antimicrobial resistance along with other carbapenem resistance mechanisms. Understanding the prevalence and routes of transmission of CRE is important in developing specific interventions for healthcare facilities, as well as the general impact of CRE circulation on the environment. Attention has also been focused on carbapenemase testing in order to provide advanced phenotypic and molecular assays for the identification of CRE, as a valid tool for active global surveillance, and from this perspective, the study of resistance mechanisms can provide significant support for the development of new and appropriate antimicrobial molecules. For all of these reasons, the phenomenon of carbapenem resistance deserves more attention, for the sake of public health.
Research & information: general --- Biology, life sciences --- Microbiology (non-medical) --- carbapenem resistance --- carbapenemase --- whole genome sequencing --- long reads, plasmid --- Klebsiella pneumoniae --- extensively drug-resistant --- molecular typing --- carbapenemases --- Enterobacteriales --- human --- animal --- food --- environment --- carbapenemase-producing Enterobacterales --- KPC --- carbapenem --- multidrug resistance --- nosocomial --- Enterobacteriaceae --- ESBL --- resistance genes --- cattle --- blaOXA-48 --- ERIC-PCR --- plasmid profile analysis --- biofilm formation --- PCR-based replicon typing --- antibiotic-resistance --- sequence types --- multilocus sequence typing --- plasmids --- antimicrobial resistance --- carbapenem inactivation method --- carbapenem-resistant Enterobacterales --- real-time multiplex PCR --- whole-genome sequencing --- carbapenem-resistance --- Qatar --- CRE --- OXA-48 --- carbapenems resistance --- Gram-negative bacteria --- infection --- colonization --- COVID-19 --- K. pneumoniae --- porins --- ceftazidime/avibactam --- ESKAPE --- healthcare-associated infections --- antimicrobial peptides --- Temporin L --- Klebsiella michiganensis --- Citrobacter farmeri --- KPC-2 --- plasmid --- transposon --- carbapenem-resistant Enterobacteriaceae (CRE) --- outbreak --- infection control --- pulsed-field gel electrophoresis (PFGE) --- multilocus sequence typing (MLST) --- IMP-6 --- porin --- efflux pump --- nosocomial infections --- NDM-1 --- Fourier transform infrared spectroscopy --- Eazyplex® SuperBug CRE assay --- extended-spectrum beta-lactamases --- gram-negative rods --- LAMP method --- NDM --- VIM --- molecular epidemiology --- PFGE --- Carbapenemase producing Enterobacterales --- IncX-3 --- one health --- water --- colistin susceptibility testing --- broth microdilution --- colistin broth disc elution --- Vitek 2 compact --- rapid polymyxin NP test --- Etest --- ChromID colistin R agar --- micronaut MIC-strip colistin --- population analysis profiling --- Enterobacterales --- neonates --- plasmid-typing --- sequence type --- wastewater --- virulence
Choose an application
Carbapenem-resistant Enterobacterales (CRE) are a common cause of infections in both community and healthcare settings and have become an increasing threat to public health worldwide. The focus of this Special Issue includes aspects concerning plasmid-mediated antimicrobial resistance along with other carbapenem resistance mechanisms. Understanding the prevalence and routes of transmission of CRE is important in developing specific interventions for healthcare facilities, as well as the general impact of CRE circulation on the environment. Attention has also been focused on carbapenemase testing in order to provide advanced phenotypic and molecular assays for the identification of CRE, as a valid tool for active global surveillance, and from this perspective, the study of resistance mechanisms can provide significant support for the development of new and appropriate antimicrobial molecules. For all of these reasons, the phenomenon of carbapenem resistance deserves more attention, for the sake of public health.
carbapenem resistance --- carbapenemase --- whole genome sequencing --- long reads, plasmid --- Klebsiella pneumoniae --- extensively drug-resistant --- molecular typing --- carbapenemases --- Enterobacteriales --- human --- animal --- food --- environment --- carbapenemase-producing Enterobacterales --- KPC --- carbapenem --- multidrug resistance --- nosocomial --- Enterobacteriaceae --- ESBL --- resistance genes --- cattle --- blaOXA-48 --- ERIC-PCR --- plasmid profile analysis --- biofilm formation --- PCR-based replicon typing --- antibiotic-resistance --- sequence types --- multilocus sequence typing --- plasmids --- antimicrobial resistance --- carbapenem inactivation method --- carbapenem-resistant Enterobacterales --- real-time multiplex PCR --- whole-genome sequencing --- carbapenem-resistance --- Qatar --- CRE --- OXA-48 --- carbapenems resistance --- Gram-negative bacteria --- infection --- colonization --- COVID-19 --- K. pneumoniae --- porins --- ceftazidime/avibactam --- ESKAPE --- healthcare-associated infections --- antimicrobial peptides --- Temporin L --- Klebsiella michiganensis --- Citrobacter farmeri --- KPC-2 --- plasmid --- transposon --- carbapenem-resistant Enterobacteriaceae (CRE) --- outbreak --- infection control --- pulsed-field gel electrophoresis (PFGE) --- multilocus sequence typing (MLST) --- IMP-6 --- porin --- efflux pump --- nosocomial infections --- NDM-1 --- Fourier transform infrared spectroscopy --- Eazyplex® SuperBug CRE assay --- extended-spectrum beta-lactamases --- gram-negative rods --- LAMP method --- NDM --- VIM --- molecular epidemiology --- PFGE --- Carbapenemase producing Enterobacterales --- IncX-3 --- one health --- water --- colistin susceptibility testing --- broth microdilution --- colistin broth disc elution --- Vitek 2 compact --- rapid polymyxin NP test --- Etest --- ChromID colistin R agar --- micronaut MIC-strip colistin --- population analysis profiling --- Enterobacterales --- neonates --- plasmid-typing --- sequence type --- wastewater --- virulence
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