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  1. Artikel ; Online: Correction: Subdomains of the

    Roberts, Jacquelyn R / Tran, Sirena C / Frick-Cheng, Arwen E / Bryant, Kaeli N / Okoye, Chiamaka D / McDonald, W Hayes / Cover, Timothy L / Ohi, Melanie D

    Life science alliance

    2024  Band 7, Heft 8

    Sprache Englisch
    Erscheinungsdatum 2024-05-13
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Published Erratum
    ISSN 2575-1077
    ISSN (online) 2575-1077
    DOI 10.26508/lsa.202402801
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Subdomains of the

    Roberts, Jacquelyn R / Tran, Sirena C / Frick-Cheng, Arwen E / Bryant, Kaeli N / Okoye, Chiamaka D / McDonald, W Hayes / Cover, Timothy L / Ohi, Melanie D

    Life science alliance

    2024  Band 7, Heft 6

    Abstract: ... ...

    Abstract The
    Mesh-Begriff(e) Helicobacter pylori ; Type IV Secretion Systems/chemistry ; Periplasm
    Chemische Substanzen Type IV Secretion Systems
    Sprache Englisch
    Erscheinungsdatum 2024-04-17
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ISSN 2575-1077
    ISSN (online) 2575-1077
    DOI 10.26508/lsa.202302560
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Identification of an Essential LolD-Like Protein in Helicobacter pylori.

    McClain, Mark S / Bryant, Kaeli N / McDonald, W Hayes / Algood, Holly M Scott / Cover, Timothy L

    Journal of bacteriology

    2023  Band 205, Heft 4, Seite(n) e0005223

    Abstract: The localization of lipoprotein (Lol) system is used by Gram-negative bacteria to export lipoproteins to the outer membrane. Lol proteins and models of how Lol transfers lipoproteins from the inner to the outer membrane have been extensively ... ...

    Abstract The localization of lipoprotein (Lol) system is used by Gram-negative bacteria to export lipoproteins to the outer membrane. Lol proteins and models of how Lol transfers lipoproteins from the inner to the outer membrane have been extensively characterized in the model organism Escherichia coli, but in numerous bacterial species, lipoprotein synthesis and export pathways deviate from the E. coli paradigm. For example, in the human gastric bacterium Helicobacter pylori, a homolog of the E. coli outer membrane component LolB is not found, E. coli LolC and LolE correspond to a single inner membrane component (LolF), and a homolog of the E. coli cytoplasmic ATPase LolD has not been identified. In the present study, we sought to identify a LolD-like protein in H. pylori. We used affinity-purification mass spectrometry to identify interaction partners of the H. pylori ATP-binding cassette (ABC) family permease LolF and identified the ABC family ATP-binding protein HP0179 as its interaction partner. We engineered H. pylori to conditionally express HP0179 and showed that HP0179 and its conserved ATP binding and ATP hydrolysis motifs are essential for H. pylori growth. We then performed affinity purification-mass spectrometry using HP0179 as the bait and identified LolF as its interaction partner. These results indicate that H. pylori HP0179 is a LolD-like protein and provide a more complete understanding of lipoprotein localization processes in H. pylori, a bacterium in which the Lol system deviates from the E. coli paradigm.
    Mesh-Begriff(e) Humans ; Escherichia coli/metabolism ; Helicobacter pylori/genetics ; Helicobacter pylori/metabolism ; Escherichia coli Proteins/metabolism ; Protein Transport ; Lipoproteins/genetics ; Lipoproteins/metabolism ; Gram-Negative Bacteria/metabolism ; Adenosine Triphosphate/metabolism ; Bacterial Outer Membrane Proteins/metabolism
    Chemische Substanzen Escherichia coli Proteins ; Lipoproteins ; Adenosine Triphosphate (8L70Q75FXE) ; Bacterial Outer Membrane Proteins
    Sprache Englisch
    Erscheinungsdatum 2023-03-27
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, U.S. Gov't, Non-P.H.S. ; Research Support, N.I.H., Extramural
    ZDB-ID 2968-3
    ISSN 1098-5530 ; 0021-9193
    ISSN (online) 1098-5530
    ISSN 0021-9193
    DOI 10.1128/jb.00052-23
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Remodeling of the gastric environment in

    Shuman, Jennifer H B / Lin, Aung Soe / Westland, Mandy D / Bryant, Kaeli N / Piazuelo, M Blanca / Reyzer, Michelle L / Judd, Audra M / McDonald, W Hayes / McClain, Mark S / Schey, Kevin L / Algood, Holly M S / Cover, Timothy L

    mSystems

    2023  Band 9, Heft 1, Seite(n) e0109823

    Abstract: Helicobacter ... ...

    Abstract Helicobacter pylori
    Mesh-Begriff(e) Animals ; Humans ; Gastritis, Atrophic/chemically induced ; Helicobacter pylori ; Stomach Neoplasms/pathology ; Gerbillinae ; Gastric Mucosa/pathology ; Gastritis/pathology ; Atrophy/pathology ; Helicobacter Infections/complications ; Precancerous Conditions/pathology ; Carcinogenesis/pathology
    Sprache Englisch
    Erscheinungsdatum 2023-12-07
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ISSN 2379-5077
    ISSN (online) 2379-5077
    DOI 10.1128/msystems.01098-23
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel ; Online: An infection-induced oxidation site regulates legumain processing and tumor growth.

    Kovalyova, Yekaterina / Bak, Daniel W / Gordon, Elizabeth M / Fung, Connie / Shuman, Jennifer H B / Cover, Timothy L / Amieva, Manuel R / Weerapana, Eranthie / Hatzios, Stavroula K

    Nature chemical biology

    2022  Band 18, Heft 7, Seite(n) 698–705

    Abstract: Oxidative stress is a defining feature of most cancers, including those that stem from carcinogenic infections. Reactive oxygen species can drive tumor formation, yet the molecular oxidation events that contribute to tumorigenesis are largely unknown. ... ...

    Abstract Oxidative stress is a defining feature of most cancers, including those that stem from carcinogenic infections. Reactive oxygen species can drive tumor formation, yet the molecular oxidation events that contribute to tumorigenesis are largely unknown. Here we show that inactivation of a single, redox-sensitive cysteine in the host protease legumain, which is oxidized during infection with the gastric cancer-causing bacterium Helicobacter pylori, accelerates tumor growth. By using chemical proteomics to map cysteine reactivity in human gastric cells, we determined that H. pylori infection induces oxidation of legumain at Cys219. Legumain oxidation dysregulates intracellular legumain processing and decreases the activity of the enzyme in H. pylori-infected cells. We further show that the site-specific loss of Cys219 reactivity increases tumor growth and mortality in a xenograft model. Our findings establish a link between an infection-induced oxidation site and tumorigenesis while underscoring the importance of cysteine reactivity in tumor growth.
    Mesh-Begriff(e) Cell Transformation, Neoplastic/metabolism ; Cysteine/metabolism ; Cysteine Endopeptidases/metabolism ; Helicobacter Infections ; Helicobacter pylori ; Humans ; Oxidation-Reduction ; Stomach Neoplasms/metabolism ; Stomach Neoplasms/microbiology ; Stomach Neoplasms/pathology
    Chemische Substanzen Cysteine Endopeptidases (EC 3.4.22.-) ; asparaginylendopeptidase (EC 3.4.22.34) ; Cysteine (K848JZ4886)
    Sprache Englisch
    Erscheinungsdatum 2022-03-24
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2202962-X
    ISSN 1552-4469 ; 1552-4450
    ISSN (online) 1552-4469
    ISSN 1552-4450
    DOI 10.1038/s41589-022-00992-x
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: Computational methods for corpus callosum segmentation on MRI: A systematic literature review.

    Cover, G S / Herrera, W G / Bento, M P / Appenzeller, S / Rittner, L

    Computer methods and programs in biomedicine

    2018  Band 154, Seite(n) 25–35

    Abstract: Background and objective: The corpus callosum (CC) is the largest white matter structure in the brain and has a significant role in central nervous system diseases. Its volume correlates with the severity and/or extent of neurodegenerative disease. Even ...

    Abstract Background and objective: The corpus callosum (CC) is the largest white matter structure in the brain and has a significant role in central nervous system diseases. Its volume correlates with the severity and/or extent of neurodegenerative disease. Even though the CC's role has been extensively studied over the last decades, and different algorithms and methods have been published regarding CC segmentation and parcellation, no reviews or surveys covering such developments have been reported so far. To bridge this gap, this paper presents a systematic literature review of computational methods focusing on CC segmentation and parcellation acquired on magnetic resonance imaging.
    Methods: IEEExplore, PubMed, EBSCO Host, and Scopus database were searched with the following search terms: ((Segmentation OR Parcellation) AND (Corpus Callosum) AND (DTI OR MRI OR Diffusion Tensor Imag* OR Diffusion Tractography OR Magnetic Resonance Imag*)), resulting in 802 publications. Two reviewers independently evaluated all articles and 36 studies were selected through the systematic literature review process.
    Results: This work reviewed four main segmentation methods groups: model-based, region-based, thresholding, and machine learning; 32 different validity metrics were reported. Even though model-based techniques are the most recurrently used for the segmentation task (13 articles), machine learning approaches achieved better outcomes of 95% when analyzing mean values for segmentation and classification metrics results. Moreover, CC segmentation is better established in T
    Conclusions: The analyzed computational methods used to perform CC segmentation on magnetic resonance imaging have not yet overcome all presented challenges owing to metrics variability and lack of traceable materials.
    Mesh-Begriff(e) Central Nervous System Diseases/diagnostic imaging ; Computer Simulation ; Corpus Callosum/diagnostic imaging ; Diffusion Tensor Imaging/methods ; Humans ; Image Processing, Computer-Assisted/methods ; Machine Learning ; Magnetic Resonance Imaging/methods ; Neurodegenerative Diseases/diagnostic imaging ; Reproducibility of Results
    Schlagwörter covid19
    Sprache Englisch
    Erscheinungsdatum 2018-02
    Erscheinungsland Ireland
    Dokumenttyp Journal Article ; Review
    ZDB-ID 632564-6
    ISSN 1872-7565 ; 0169-2607
    ISSN (online) 1872-7565
    ISSN 0169-2607
    DOI 10.1016/j.cmpb.2017.10.025
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  7. Artikel ; Online: Delineation of the pH-Responsive Regulon Controlled by the Helicobacter pylori ArsRS Two-Component System.

    Loh, John T / Shum, Miranda V / Jossart, Scott D R / Campbell, Anne M / Sawhney, Neha / McDonald, W Hayes / Scholz, Matthew B / McClain, Mark S / Forsyth, Mark H / Cover, Timothy L

    Infection and immunity

    2021  Band 89, Heft 4

    Abstract: Helicobacter ... ...

    Abstract Helicobacter pylori
    Mesh-Begriff(e) Computational Biology/methods ; Gene Expression Profiling ; Gene Expression Regulation, Bacterial ; Helicobacter pylori/physiology ; Humans ; Hydrogen-Ion Concentration ; Mutation ; Proteome ; Proteomics/methods ; Response Elements ; Trans-Activators/metabolism ; Transcription, Genetic
    Chemische Substanzen Proteome ; Trans-Activators
    Sprache Englisch
    Erscheinungsdatum 2021-03-17
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 218698-6
    ISSN 1098-5522 ; 0019-9567
    ISSN (online) 1098-5522
    ISSN 0019-9567
    DOI 10.1128/IAI.00597-20
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  8. Artikel: Summary of the Pharmacology of Sulfanilamide and Related Compounds.

    Cutting, W C / Cover, W L

    California and western medicine

    2008  Band 52, Heft 3, Seite(n) 110–113

    Sprache Englisch
    Erscheinungsdatum 2008-08-20
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2255398-8
    ISSN 2380-9922 ; 0093-4038
    ISSN (online) 2380-9922
    ISSN 0093-4038
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel ; Online: Effect of environmental salt concentration on the Helicobacter pylori exoproteome.

    Caston, Rhonda R / Loh, John T / Voss, Bradley J / McDonald, W Hayes / Scholz, Matthew B / McClain, Mark S / Cover, Timothy L

    Journal of proteomics

    2019  Band 202, Seite(n) 103374

    Abstract: Helicobacter pylori infection and a high salt diet are each risk factors for gastric cancer. In this study, we tested the hypothesis that environmental salt concentration influences the composition of the H. pylori exoproteome. H. pylori was cultured in ... ...

    Abstract Helicobacter pylori infection and a high salt diet are each risk factors for gastric cancer. In this study, we tested the hypothesis that environmental salt concentration influences the composition of the H. pylori exoproteome. H. pylori was cultured in media containing varying concentrations of sodium chloride, and aliquots were fractionated and analyzed by liquid chromatography-tandem mass spectrometry (LC-MS/MS). We identified proteins that were selectively released into the extracellular space, and we identified selectively released proteins that were differentially abundant in culture supernatants, depending on the environmental salt concentration. We also used RNA-seq analysis to identify genes that were differentially expressed in response to environmental salt concentration. The salt-responsive proteins identified by proteomic analysis and salt-responsive genes identified by RNA-seq analysis were mostly non-concordant, but the secreted toxin VacA was salt-responsive in both analyses. Western blot analysis confirmed that VacA levels in the culture supernatant were increased in response to high salt conditions, and quantitative RT-qPCR experiments confirmed that vacA transcription was upregulated in response to high salt conditions. These results indicate that environmental salt concentration influences the composition of the H. pylori exoproteome, which could contribute to the increased risk of gastric cancer associated with a high salt diet. SIGNIFICANCE: Helicobacter pylori-induced alterations in the gastric mucosa have been attributed, at least in part, to the actions of secreted H. pylori proteins. In this study, we show that H. pylori growth in high salt concentrations leads to increased levels of a secreted VacA toxin. Salt-induced alterations in the composition of the H. pylori exoproteome is relevant to the increased risk of gastric cancer associated with consumption of a high salt diet.
    Mesh-Begriff(e) Bacterial Proteins/biosynthesis ; Dose-Response Relationship, Drug ; Gene Expression Regulation, Bacterial/drug effects ; Helicobacter pylori/metabolism ; Proteome/biosynthesis ; Proteomics ; Sodium Chloride, Dietary/pharmacology
    Chemische Substanzen Bacterial Proteins ; Proteome ; Sodium Chloride, Dietary
    Sprache Englisch
    Erscheinungsdatum 2019-05-04
    Erscheinungsland Netherlands
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2400835-7
    ISSN 1876-7737 ; 1874-3919
    ISSN (online) 1876-7737
    ISSN 1874-3919
    DOI 10.1016/j.jprot.2019.05.002
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel ; Online: Bacterial Energetic Requirements for Helicobacter pylori Cag Type IV Secretion System-Dependent Alterations in Gastric Epithelial Cells.

    Lin, Aung Soe / Dooyema, Samuel D R / Frick-Cheng, Arwen E / Harvey, M Lorena / Suarez, Giovanni / Loh, John T / McDonald, W Hayes / McClain, Mark S / Peek, Richard M / Cover, Timothy L

    Infection and immunity

    2020  Band 88, Heft 2

    Abstract: Helicobacter ... ...

    Abstract Helicobacter pylori
    Mesh-Begriff(e) Antigens, Bacterial/genetics ; Antigens, Bacterial/metabolism ; Bacterial Proteins/genetics ; Bacterial Proteins/metabolism ; Biological Transport ; DNA, Bacterial/metabolism ; Epithelial Cells/microbiology ; Helicobacter pylori/genetics ; Helicobacter pylori/metabolism ; Humans ; Interleukin-8/metabolism ; Lipopolysaccharides/metabolism ; NF-kappa B/metabolism ; Peptidoglycan/metabolism ; Toll-Like Receptor 9/metabolism ; Type IV Secretion Systems/genetics ; Type IV Secretion Systems/metabolism ; Virulence Factors/genetics ; Virulence Factors/metabolism
    Chemische Substanzen Antigens, Bacterial ; Bacterial Proteins ; DNA, Bacterial ; Interleukin-8 ; Lipopolysaccharides ; NF-kappa B ; Peptidoglycan ; Toll-Like Receptor 9 ; Type IV Secretion Systems ; Virulence Factors ; cagA protein, Helicobacter pylori
    Sprache Englisch
    Erscheinungsdatum 2020-01-22
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 218698-6
    ISSN 1098-5522 ; 0019-9567
    ISSN (online) 1098-5522
    ISSN 0019-9567
    DOI 10.1128/IAI.00790-19
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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