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  1. Article ; Online: Aerosolized delivery of ESKAPE pathogens for murine pneumonia models.

    Rox, Katharina / Medina, Eva

    Scientific reports

    2024  Volume 14, Issue 1, Page(s) 2558

    Abstract: Murine pneumonia models for ESKAPE pathogens serve to evaluate novel antibacterials or to investigate immunological responses. The majority of published models uses intranasal or to a limited extent the intratracheal instillation to challenge animals. In ...

    Abstract Murine pneumonia models for ESKAPE pathogens serve to evaluate novel antibacterials or to investigate immunological responses. The majority of published models uses intranasal or to a limited extent the intratracheal instillation to challenge animals. In this study, we propose the aerosol delivery of pathogens using a nebulizer. Aerosol delivery typically results in homogeneous distribution of the inoculum in the lungs because of lower particle size. This is of particular importance when compounds are assessed for their pharmacokinetic and pharmacodynamic (PK/PD) relationships as it allows to conduct several analysis with the same sample material. Moreover, aerosol delivery has the advantage that it mimics the 'natural route' of respiratory infection. In this short and concise study, we show that aerosol delivery of pathogens resulted in a sustained bacterial burden in the neutropenic lung infection model for five pathogens tested, whereas it gave a similar result in immunocompetent mice for three out of five pathogens. Moreover, a substantial bacterial burden in the lungs was already achieved 2 h post inhalation. Hence, this study constitutes a viable alternative for intranasal administration and a refinement of murine pneumonia models for PK/PD assessments of novel antibacterial compounds allowing to study multiple readouts with the same sample material.
    MeSH term(s) Animals ; Mice ; Respiratory Aerosols and Droplets ; Administration, Inhalation ; Lung ; Pneumonia/drug therapy ; Anti-Bacterial Agents/therapeutic use ; Anti-Bacterial Agents/pharmacokinetics
    Chemical Substances Anti-Bacterial Agents
    Language English
    Publishing date 2024-01-31
    Publishing country England
    Document type Journal Article
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-024-52958-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Myeloid-derived suppressor cells impair CD4+ T cell responses during chronic Staphylococcus aureus infection via lactate metabolism.

    Goldmann, Oliver / Medina, Eva

    Cellular and molecular life sciences : CMLS

    2023  Volume 80, Issue 8, Page(s) 221

    Abstract: Staphylococcus aureus is an important cause of chronic infections resulting from the failure of the host to eliminate the pathogen. Effective S. aureus clearance requires CD4+ T cell-mediated immunity. We previously showed that myeloid-derived suppressor ...

    Abstract Staphylococcus aureus is an important cause of chronic infections resulting from the failure of the host to eliminate the pathogen. Effective S. aureus clearance requires CD4+ T cell-mediated immunity. We previously showed that myeloid-derived suppressor cells (MDSC) expand during staphylococcal infections and support infection chronicity by inhibiting CD4+ T cell responses. The aim of this study was to elucidate the mechanisms underlying the suppressive effect exerted by MDSC on CD4+ T cells during chronic S. aureus infection. It is well known that activated CD4+ T cells undergo metabolic reprogramming from oxidative metabolism to aerobic glycolysis to meet their increased bioenergetic requirements. In this process, pyruvate is largely transformed into lactate by lactate dehydrogenase with the concomitant regeneration of NAD+, which is necessary for continued glycolysis. The by-product lactate needs to be excreted to maintain the glycolytic flux. Using SCENITH (single-cell energetic metabolism by profiling translation inhibition), we demonstrated here that MDSC inhibit CD4+ T cell responses by interfering with their metabolic activity. MDSC are highly glycolytic and excrete large amount of lactate in the local environment that alters the transmembrane concentration gradient and prevent removal of lactate by activated CD4+ T. Accumulation of endogenous lactate impedes the regeneration of NAD+, inhibit NAD-dependent glycolytic enzymes and stop glycolysis. Together, the results of this study have uncovered a role for metabolism on MDSC suppression of CD4+ T cell responses. Thus, reestablishment of their metabolic activity may represent a mean to improve the functionality of CD4+ T cells during chronic S. aureus infection.
    MeSH term(s) Humans ; CD4-Positive T-Lymphocytes/metabolism ; Myeloid-Derived Suppressor Cells ; Staphylococcus aureus/metabolism ; NAD/metabolism ; Staphylococcal Infections/metabolism ; Lactates/metabolism
    Chemical Substances NAD (0U46U6E8UK) ; Lactates
    Language English
    Publishing date 2023-07-22
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 1358415-7
    ISSN 1420-9071 ; 1420-682X
    ISSN (online) 1420-9071
    ISSN 1420-682X
    DOI 10.1007/s00018-023-04875-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Mechanisms underlying immunosuppression by regulatory cells.

    Goldmann, Oliver / Nwofor, Obiageli Vivian / Chen, Qian / Medina, Eva

    Frontiers in immunology

    2024  Volume 15, Page(s) 1328193

    Abstract: Regulatory cells, such as regulatory T cells (Tregs), regulatory B cells (Bregs), and myeloid-derived suppressor cells (MDSCs), play a crucial role in preserving immune tolerance and controlling immune responses during infections to prevent excessive ... ...

    Abstract Regulatory cells, such as regulatory T cells (Tregs), regulatory B cells (Bregs), and myeloid-derived suppressor cells (MDSCs), play a crucial role in preserving immune tolerance and controlling immune responses during infections to prevent excessive immune activation. However, pathogens have developed strategies to hijack these regulatory cells to decrease the overall effectiveness of the immune response and persist within the host. Consequently, therapeutic targeting of these immunosuppressive mechanisms during infection can reinvigorate the immune response and improve the infection outcome. The suppressive mechanisms of regulatory cells are not only numerous but also redundant, reflecting the complexity of the regulatory network in modulating the immune responses. The context of the immune response, such as the type of pathogen or tissue involved, further influences the regulatory mechanisms involved. Examples of these immunosuppressive mechanisms include the production of inhibitory cytokines such as interleukin 10 (IL-10) and transforming growth factor beta (TGF-β) that inhibit the production of pro-inflammatory cytokines and dampen the activation and proliferation of effector T cells. In addition, regulatory cells utilize inhibitory receptors like cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) and programmed cell death protein 1 (PD-1) to engage with their respective effector cells, thereby suppressing their function. An alternative approach involves the modulation of metabolic reprogramming in effector immune cells to limit their activation and proliferation. In this review, we provide an overview of the major mechanisms mediating the immunosuppressive effect of the different regulatory cell subsets in the context of infection.
    MeSH term(s) T-Lymphocytes, Regulatory ; Immune Tolerance ; Cytokines ; Transforming Growth Factor beta ; Immunosuppression Therapy
    Chemical Substances Cytokines ; Transforming Growth Factor beta
    Language English
    Publishing date 2024-02-06
    Publishing country Switzerland
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2024.1328193
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: The emerging potential of microbiome transplantation on human health interventions

    Junca, Howard / Pieper, Dietmar H. / Medina, Eva

    Computational and Structural Biotechnology Journal. 2022, v. 20

    2022  

    Abstract: The human microbiome has been the subject of intense research over the past few decades, in particular as a promising area for new clinical interventions. The microbiota colonizing the different body surfaces are of benefit for multiple physiological and ...

    Abstract The human microbiome has been the subject of intense research over the past few decades, in particular as a promising area for new clinical interventions. The microbiota colonizing the different body surfaces are of benefit for multiple physiological and metabolic processes of the human host and increasing evidence suggests an association between disturbances in the composition and functionality of the microbiota and several pathological conditions. This has provided a rationale for beneficial modulation of the microbiome. One approach being explored for modulating the microbiota in diseased individuals is transferring microbiota or microbiota constituents from healthy donors via microbiome transplantation. The great success of fecal microbiome transplantation for the treatment of Clostridioides difficile infections has encouraged the application of this procedure for the treatment of other diseases such as vaginal disorders via transplantation of vaginal microbiota, or of skin pathologies via the transplantation of skin microbiota. Microbiome modulation could even become a novel strategy for improving the efficacy of cancer therapies. This review discusses the principle, advantages and limitations of microbiome transplantation as well as different clinical contexts where microbiome transplantation has been applied.
    Keywords Clostridium difficile ; biotechnology ; human health ; humans ; microbiome ; microorganisms
    Language English
    Size p. 615-627.
    Publishing place Elsevier B.V.
    Document type Article
    ZDB-ID 2694435-2
    ISSN 2001-0370
    ISSN 2001-0370
    DOI 10.1016/j.csbj.2022.01.009
    Database NAL-Catalogue (AGRICOLA)

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  5. Article: Promoting Health Education through Mobile Apps: A Quantitative Analysis of American Hospitals.

    Medina Aguerrebere, Pablo / Medina, Eva / Gonzalez Pacanowski, Toni

    Healthcare (Basel, Switzerland)

    2022  Volume 10, Issue 11

    Abstract: Using mobile apps as a corporate communication tool helps hospitals to improve their health education initiatives. This paper aims to analyze how these organizations can use mobile apps to implement health education initiatives addressed to patients. To ... ...

    Abstract Using mobile apps as a corporate communication tool helps hospitals to improve their health education initiatives. This paper aims to analyze how these organizations can use mobile apps to implement health education initiatives addressed to patients. To achieve this, we conducted a literature review (health education, mobile apps, role of doctors and patients), and we resorted to using 38 quantitative indicators to evaluate how the 100 best hospitals in the United States manage mobile apps for implementing health education initiatives addressed to patients. Our results prove that 95% of hospitals displayed general mobile apps for patients, but just some of these organizations proposed mobile apps for patients suffering from non-communicable diseases, including: heart diseases (9.47%), cancer (7.37%), chronic respiratory diseases (3.26%), and diabetes (3.16%). We concluded that hospitals should create a department specializing in designing mobile apps that are adapted to patients' medical and social needs, and that are also consistent with public health priorities.
    Language English
    Publishing date 2022-11-08
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2721009-1
    ISSN 2227-9032
    ISSN 2227-9032
    DOI 10.3390/healthcare10112231
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: The emerging potential of microbiome transplantation on human health interventions.

    Junca, Howard / Pieper, Dietmar H / Medina, Eva

    Computational and structural biotechnology journal

    2022  Volume 20, Page(s) 615–627

    Abstract: The human microbiome has been the subject of intense research over the past few decades, in particular as a promising area for new clinical interventions. The microbiota colonizing the different body surfaces are of benefit for multiple physiological and ...

    Abstract The human microbiome has been the subject of intense research over the past few decades, in particular as a promising area for new clinical interventions. The microbiota colonizing the different body surfaces are of benefit for multiple physiological and metabolic processes of the human host and increasing evidence suggests an association between disturbances in the composition and functionality of the microbiota and several pathological conditions. This has provided a rationale for beneficial modulation of the microbiome. One approach being explored for modulating the microbiota in diseased individuals is transferring microbiota or microbiota constituents from healthy donors via microbiome transplantation. The great success of fecal microbiome transplantation for the treatment of
    Language English
    Publishing date 2022-01-19
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 2694435-2
    ISSN 2001-0370
    ISSN 2001-0370
    DOI 10.1016/j.csbj.2022.01.009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Book: Identifizierung genetischer und immunologischer Wirtsfaktoren bei der Resistenz/Empfindlichkeit gegenüber Staphylococcus aureus-Infektionen im Mausmodell

    Medina, Eva

    Schlussbericht zum Forschungsvorhaben ; (Förderzeitraum 01.08.2010 bis 31.07.2013) : [TP 7]

    2014  

    Title variant Schlussbericht zum Forschungsvorhaben 01KI1009B ; Staphylococcus-aureus-Infektionen Teilprojekt
    Institution Helmholtz-Zentrum für Infektionsforschung
    Author's details Helmholtz-Zentrum für Infektionsforschung GmbH. Projektleitung: Eva Medina
    Language German
    Size 21 Bl., Ill., graph. Darst.
    Publishing place Braunschweig
    Document type Book
    Note Förderkennzeichen BMBF 01KI1009B. - Verbund-Nr. 01058134 ; Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden
    Database Library catalogue of the German National Library of Science and Technology (TIB), Hannover

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  8. Book ; Online: Identifizierung genetischer und immunologischer Wirtsfaktoren bei der Resistenz/Empfindlichkeit gegenüber Staphylococcus aureus-Infektionen im Mausmodell

    Medina, Eva

    Schlussbericht zum Forschungsvorhaben ; (Förderzeitraum 01.08.2010 bis 31.07.2013) : [TP 7]

    2014  

    Title variant Schlussbericht zum Forschungsvorhaben 01KI1009B ; Staphylococcus-aureus-Infektionen Teilprojekt
    Institution Helmholtz-Zentrum für Infektionsforschung
    Author's details Helmholtz-Zentrum für Infektionsforschung GmbH. Projektleitung: Eva Medina
    Language German
    Size Online-Ressource (29 S., 11,2 MB), Ill., graph. Darst.
    Publisher Technische Informationsbibliothek u. Universitätsbibliothek
    Publishing place Hannover ; Braunschweig
    Document type Book ; Online
    Note Förderkennzeichen BMBF 01KI1009B. - Verbund-Nr. 01058134 ; Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden
    Database Library catalogue of the German National Library of Science and Technology (TIB), Hannover

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  9. Article ; Online: Effects of Different Mulching Materials on Soil Salinity of a Semi-Arid Drip-Irrigated Nectarine Orchard

    Zribi, Wided / Medina, Eva Teresa / Faci, José / Aragüès, Ramón

    Communications in Soil Science and Plant Analysis. 2023 Apr. 12, v. 54, no. 7 p.884-894

    2023  

    Abstract: The effectiveness of inorganic (plastic) and organic (geotextile and pine bark) mulching materials for soil salinity control as compared to the bare soil was assessed during three years in a semi-arid, drip-irrigated nectarine orchard. The soil solution ... ...

    Abstract The effectiveness of inorganic (plastic) and organic (geotextile and pine bark) mulching materials for soil salinity control as compared to the bare soil was assessed during three years in a semi-arid, drip-irrigated nectarine orchard. The soil solution electrical conductivity (ECss) was measured in 3174 samples regularly extracted with suction cups at two soil depths (20 and 40 cm) and three sampling positions (EM-emitter, EL-emitter line, and TR-tree row) during the 2010–2012 irrigation seasons. Considering all treatments, ECss increased (p < .05) with distance to emitters, both vertically (mean ECss = 4.7 dS m⁻¹ at 20 cm and 6.3 dS m⁻¹ at 40 cm soil depths) and horizontally (mean ECss (20 + 40 cm soil depth) = 2.9 dS m⁻¹ at EM, 4.4 dS m⁻¹ at EL, and 9.1 dS m⁻¹ at TR). The monthly changes in ECss were negatively correlated (p < .01) with the monthly field-wide leaching fraction estimates. Based on the 2010–2012 mean ECss values, the effectiveness for soil salinity control of the examined treatments was (p = .05): plastic (4.2 dS m⁻¹) = pine bark (4.6 dS m⁻¹) < bare soil (5.8 dS m⁻¹) = geotextile (5.9 dS m⁻¹). Overall, due to their lower soil water evaporation rates, the plastic and pine bark materials were best suited for soil salinity control under the prevailing climatic characteristics in the study area.
    Keywords bark ; electrical conductivity ; evaporation ; geotextiles ; microirrigation ; nectarines ; orchards ; plant analysis ; soil depth ; soil salinity ; soil solution ; soil water ; Geotextile ; pine bark ; plastic ; suction cup
    Language English
    Dates of publication 2023-0412
    Size p. 884-894.
    Publishing place Taylor & Francis
    Document type Article ; Online
    ZDB-ID 419718-5
    ISSN 1532-2416 ; 0010-3624
    ISSN (online) 1532-2416
    ISSN 0010-3624
    DOI 10.1080/00103624.2022.2137179
    Database NAL-Catalogue (AGRICOLA)

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  10. Book ; Online: Medizinische Infektionsgenomik: Metagenomics und Host-Pathogen Interactomics in diabetischen Fußinfektionen-Projektteil HZI

    Medina, Eva

    Schlussbericht zum Forschungsvorhaben ; (Förderzeitraum 01.12.2010 bis 30.11.2013)

    2013  

    Title variant Metagenomics and host-pathogen interactomics in diabetic foot infection
    Author's details Projektleitung: Eva Medina
    Language German
    Size Online-Ressource (PDF-Datei: 47 S., 16,3 MB), Ill., graph. Darst.
    Publisher Techn. Informationsbibl. und Univ.-Bibl ; Helmholtz-Zentrum für Infektionsforschung GmbH, Arbeitsgruppe Infektionsimmunologie
    Publishing place Hannover ; Braunschweig
    Document type Book ; Online
    Note Förderkennzeichen BMBF 0315830A. - Verbund-Nr. 01080360. - [Engl. Berichtsbl. u.d.T.: Metagenomics and host-pathogen interactomics in diabetic foot infection] ; Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden
    Database Library catalogue of the German National Library of Science and Technology (TIB), Hannover

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