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  1. Article ; Online: Co- and polymicrobial infections in the gut mucosa: The host-microbiota-pathogen perspective.

    Frisan, Teresa

    Cellular microbiology

    2020  Volume 23, Issue 2, Page(s) e13279

    Abstract: Infections in humans occur in the context of complex niches where the pathogen interacts with both the host microenvironment and immune response, and the symbiotic microbial community. The polymicrobial nature of many human infections adds a further ... ...

    Abstract Infections in humans occur in the context of complex niches where the pathogen interacts with both the host microenvironment and immune response, and the symbiotic microbial community. The polymicrobial nature of many human infections adds a further layer of complexity. The effect of co- or polymicrobial infections can result in enhanced severity due to pathogens cooperative interaction or reduced morbidity because one of the pathogens affects the fitness of the other(s). In this review, the concept of co-infections and polymicrobial interactions in the context of the intestinal mucosa is discussed, focusing on the interplay between the host, the microbiota and the pathogenic organisms. Specifically, we will examine examples of pathogen-cooperative versus -antagonistic behaviour during co- and polymicrobial infections. We discuss: the infection-induced modulation of the host microenvironment and immune responses; the direct modulation of the microorganism's fitness; the potentiation of inflammatory/carcinogenic conditions by polymicrobial biofilms; and the promotion of co-infections by microbial-induced DNA damage. Open questions in this very exciting field are also highlighted.
    MeSH term(s) Animals ; Biofilms ; Coinfection ; Dysbiosis ; Gastrointestinal Microbiome ; Host-Pathogen Interactions ; Humans ; Immunity ; Intestinal Mucosa/immunology ; Microbial Interactions ; Symbiosis
    Language English
    Publishing date 2020-10-22
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 1468320-9
    ISSN 1462-5822 ; 1462-5814
    ISSN (online) 1462-5822
    ISSN 1462-5814
    DOI 10.1111/cmi.13279
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Book ; Online: Faculty Opinions recommendation of Substantial undocumented infection facilitates the rapid dissemination of novel coronavirus (SARS-CoV2).

    Frisan, Teresa

    Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature

    2020  

    Keywords covid19
    Publisher Faculty Opinions Ltd
    Publishing country uk
    Document type Book ; Online
    DOI 10.3410/f.737557783.793572927
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article: Bacterial genotoxins: The long journey to the nucleus of mammalian cells.

    Frisan, Teresa

    Biochimica et biophysica acta

    2016  Volume 1858, Issue 3, Page(s) 567–575

    Abstract: Bacterial protein genotoxins target the DNA of eukaryotic cells, causing DNA single and double strand breaks. The final outcome of the intoxication is induction of DNA damage responses and activation of DNA repair pathways. When the damage is beyond ... ...

    Abstract Bacterial protein genotoxins target the DNA of eukaryotic cells, causing DNA single and double strand breaks. The final outcome of the intoxication is induction of DNA damage responses and activation of DNA repair pathways. When the damage is beyond repair, the target cell either undergoes apoptosis or enters a permanent quiescent stage, known as cellular senescence. In certain instances, intoxicated cells can survive and proliferate. This event leads to accumulation of genomic instability and acquisition of malignant traits, underlining the carcinogenic potential of these toxins. The toxicity is dependent on the toxins' internalization and trafficking from the extracellular environment to the nucleus, and requires a complex interaction with several cellular membrane compartments: the plasma membrane, the endosomes, the trans Golgi network and the endoplasmic reticulum, and finally the nucleus. This review will discuss the current knowledge of the bacterial genotoxins internalization pathways and will highlight the issues that still remain unanswered. This article is part of a Special Issue entitled: Pore-Forming Toxins edited by Mauro Dalla Serra and Franco Gambale.
    MeSH term(s) Animals ; Bacteria/metabolism ; Bacteria/pathogenicity ; Bacterial Infections/metabolism ; Bacterial Proteins/metabolism ; Bacterial Toxins/metabolism ; Cell Membrane/metabolism ; Cell Nucleus/metabolism ; Cellular Senescence ; DNA Damage ; Endoplasmic Reticulum/metabolism ; Endosomes/metabolism ; Golgi Apparatus/metabolism ; Humans ; Mutagens/metabolism ; Protein Transport
    Chemical Substances Bacterial Proteins ; Bacterial Toxins ; Mutagens
    Language English
    Publishing date 2016-03
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 60-7
    ISSN 1879-2596 ; 1879-260X ; 1872-8006 ; 1879-2642 ; 1879-2618 ; 1879-2650 ; 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    ISSN (online) 1879-2596 ; 1879-260X ; 1872-8006 ; 1879-2642 ; 1879-2618 ; 1879-2650
    ISSN 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    DOI 10.1016/j.bbamem.2015.08.016
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Bacterial Genotoxin-Induced DNA Damage and Modulation of the Host Immune Microenvironment.

    Martin, Océane C B / Frisan, Teresa

    Toxins

    2020  Volume 12, Issue 2

    Abstract: ...

    Abstract :
    MeSH term(s) Animals ; Bacterial Toxins/toxicity ; DNA Damage ; Humans ; Immunologic Factors/toxicity ; Mutagens/toxicity
    Chemical Substances Bacterial Toxins ; Immunologic Factors ; Mutagens
    Language English
    Publishing date 2020-01-21
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2518395-3
    ISSN 2072-6651 ; 2072-6651
    ISSN (online) 2072-6651
    ISSN 2072-6651
    DOI 10.3390/toxins12020063
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Bacterial Toxins Are a Never-Ending Source of Surprises: From Natural Born Killers to Negotiators.

    Lopez Chiloeches, Maria / Bergonzini, Anna / Frisan, Teresa

    Toxins

    2021  Volume 13, Issue 6

    Abstract: The idea that bacterial toxins are not only killers but also execute more sophisticated roles during bacteria-host interactions by acting as negotiators has been highlighted in the past decades. Depending on the toxin, its cellular target and mode of ... ...

    Abstract The idea that bacterial toxins are not only killers but also execute more sophisticated roles during bacteria-host interactions by acting as negotiators has been highlighted in the past decades. Depending on the toxin, its cellular target and mode of action, the final regulatory outcome can be different. In this review, we have focused on two families of bacterial toxins: genotoxins and pore-forming toxins, which have different modes of action but share the ability to modulate the host's immune responses, independently of their capacity to directly kill immune cells. We have addressed their immuno-suppressive effects with the perspective that these may help bacteria to avoid clearance by the host's immune response and, concomitantly, limit detrimental immunopathology. These are optimal conditions for the establishment of a persistent infection, eventually promoting asymptomatic carriers. This immunomodulatory effect can be achieved with different strategies such as suppression of pro-inflammatory cytokines, re-polarization of the immune response from a pro-inflammatory to a tolerogenic state, and bacterial fitness modulation to favour tissue colonization while preventing bacteraemia. An imbalance in each of those effects can lead to disease due to either uncontrolled bacterial proliferation/invasion, immunopathology, or both.
    MeSH term(s) Animals ; Bacterial Proteins ; Bacterial Toxins ; Humans ; Immunologic Factors ; Mutagens
    Chemical Substances Bacterial Proteins ; Bacterial Toxins ; Immunologic Factors ; Mutagens
    Language English
    Publishing date 2021-06-17
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2518395-3
    ISSN 2072-6651 ; 2072-6651
    ISSN (online) 2072-6651
    ISSN 2072-6651
    DOI 10.3390/toxins13060426
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Senescence and Host-Pathogen Interactions.

    Humphreys, Daniel / ElGhazaly, Mohamed / Frisan, Teresa

    Cells

    2020  Volume 9, Issue 7

    Abstract: Damage to our genomes triggers cellular senescence characterised by stable cell cycle arrest and a pro-inflammatory secretome that prevents the unrestricted growth of cells with pathological potential. In this way, senescence can be considered a powerful ...

    Abstract Damage to our genomes triggers cellular senescence characterised by stable cell cycle arrest and a pro-inflammatory secretome that prevents the unrestricted growth of cells with pathological potential. In this way, senescence can be considered a powerful innate defence against cancer and viral infection. However, damage accumulated during ageing increases the number of senescent cells and this contributes to the chronic inflammation and deregulation of the immune function, which increases susceptibility to infectious disease in ageing organisms. Bacterial and viral pathogens are masters of exploiting weak points to establish infection and cause devastating diseases. This review considers the emerging importance of senescence in the host-pathogen interaction: we discuss the pathogen exploitation of ageing cells and senescence as a novel hijack target of bacterial pathogens that deploys senescence-inducing toxins to promote infection. The persistent induction of senescence by pathogens, mediated directly through virulence determinants or indirectly through inflammation and chronic infection, also contributes to age-related pathologies such as cancer. This review highlights the dichotomous role of senescence in infection: an innate defence that is exploited by pathogens to cause disease.
    MeSH term(s) Animals ; Bacteria/metabolism ; Cellular Microenvironment ; Cellular Senescence ; Host-Pathogen Interactions ; Humans ; Infections/pathology ; Models, Biological
    Keywords covid19
    Language English
    Publishing date 2020-07-21
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2661518-6
    ISSN 2073-4409 ; 2073-4409
    ISSN (online) 2073-4409
    ISSN 2073-4409
    DOI 10.3390/cells9071747
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Characterization of macrophage infiltration and polarization by double fluorescence immunostaining in mouse colonic mucosa.

    Chiloeches, María López / Bergonzini, Anna / Frisan, Teresa / Martin, Océane C B

    STAR protocols

    2021  Volume 2, Issue 4, Page(s) 100833

    Abstract: We recently characterized the association between DNA damage and ... ...

    Abstract We recently characterized the association between DNA damage and immunoresponse
    MeSH term(s) Animals ; Colon ; Fluorescent Antibody Technique ; Intestinal Mucosa ; Macrophages ; Mice ; Salmonella typhimurium
    Language English
    Publishing date 2021-09-15
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 2666-1667
    ISSN (online) 2666-1667
    DOI 10.1016/j.xpro.2021.100833
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Diagnostic Challenges during Inflammation and Cancer: Current Biomarkers and Future Perspectives in Navigating through the Minefield of Reactive versus Dysplastic and Cancerous Lesions in the Digestive System.

    Pateras, Ioannis S / Igea, Ana / Nikas, Ilias P / Leventakou, Danai / Koufopoulos, Nektarios I / Ieronimaki, Argyro Ioanna / Bergonzini, Anna / Ryu, Han Suk / Chatzigeorgiou, Antonios / Frisan, Teresa / Kittas, Christos / Panayiotides, Ioannis G

    International journal of molecular sciences

    2024  Volume 25, Issue 2

    Abstract: In the setting of pronounced inflammation, changes in the epithelium may overlap with neoplasia, often rendering it impossible to establish a diagnosis with certainty in daily clinical practice. Here, we discuss the underlying molecular mechanisms ... ...

    Abstract In the setting of pronounced inflammation, changes in the epithelium may overlap with neoplasia, often rendering it impossible to establish a diagnosis with certainty in daily clinical practice. Here, we discuss the underlying molecular mechanisms driving tissue response during persistent inflammatory signaling along with the potential association with cancer in the gastrointestinal tract, pancreas, extrahepatic bile ducts, and liver. We highlight the histopathological challenges encountered in the diagnosis of chronic inflammation in routine practice and pinpoint tissue-based biomarkers that could complement morphology to differentiate reactive from dysplastic or cancerous lesions. We refer to the advantages and limitations of existing biomarkers employing immunohistochemistry and point to promising new markers, including the generation of novel antibodies targeting mutant proteins, miRNAs, and array assays. Advancements in experimental models, including mouse and 3D models, have improved our understanding of tissue response. The integration of digital pathology along with artificial intelligence may also complement routine visual inspections. Navigating through tissue responses in various chronic inflammatory contexts will help us develop novel and reliable biomarkers that will improve diagnostic decisions and ultimately patient treatment.
    MeSH term(s) Humans ; Animals ; Mice ; Artificial Intelligence ; Neoplasms/diagnosis ; Inflammation ; Biomarkers ; Hyperplasia ; Digestive System
    Chemical Substances Biomarkers
    Language English
    Publishing date 2024-01-19
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms25021251
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Genotoxin-producing

    Lopez Chiloeches, Maria / Bergonzini, Anna / Martin, Océane C B / Bergstein, Nicole / Erttmann, Saskia F / Aung, Kyaw Min / Gekara, Nelson O / Avila Cariño, Javier F / Pateras, Ioannis S / Frisan, Teresa

    Frontiers in immunology

    2024  Volume 14, Page(s) 1270449

    Abstract: Introduction: Typhoid toxin-expressing : Methods: In situ: Result: The presence of the typhoid toxin protected from colonic bacteria-induced inflammation, despite nuclear localization of p53, enhanced co-expression of type-I interferons (: ... ...

    Abstract Introduction: Typhoid toxin-expressing
    Methods: In situ
    Result: The presence of the typhoid toxin protected from colonic bacteria-induced inflammation, despite nuclear localization of p53, enhanced co-expression of type-I interferons (
    Conclusions: Our work highlights the relevance of the tissue microenvironment in enabling the typhoid toxin to suppress the host inflammatory response
    MeSH term(s) Mice ; Animals ; Salmonella enterica/genetics ; Typhoid Fever ; Mutagens ; DNA Damage ; Inflammation ; DNA Repair
    Chemical Substances Mutagens
    Language English
    Publishing date 2024-01-11
    Publishing country Switzerland
    Document type Journal Article ; 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.2023.1270449
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Editorial: Why still study bacterial toxins in the third millennium?

    Frisan, Teresa / Sebo, Peter

    Pathogens and disease

    2016  Volume 74, Issue 3

    MeSH term(s) Animals ; Bacteria/pathogenicity ; Bacterial Toxins ; Humans ; Virulence Factors/metabolism
    Chemical Substances Bacterial Toxins ; Virulence Factors
    Language English
    Publishing date 2016-04
    Publishing country United States
    Document type Editorial
    ISSN 2049-632X
    ISSN (online) 2049-632X
    DOI 10.1093/femspd/ftw009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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