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  1. Book ; Online ; Thesis: Der Einfluss des multifunktionalen extrazellulären Adhäsionsproteins (Eap) von Staphylococcus aureus auf die Morphologie und Funktion von eukaryotischen Zellen

    Eisenbeis, Janina [Verfasser] / Bischoff, Markus [Akademischer Betreuer]

    2019  

    Author's details Janina Eisenbeis ; Betreuer: Markus Bischoff
    Keywords Medizin, Gesundheit ; Medicine, Health
    Subject code sg610
    Language German
    Publisher Saarländische Universitäts- und Landesbibliothek
    Publishing place Saarbrücken
    Document type Book ; Online ; Thesis
    Database Digital theses on the web

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  2. Article ; Online: Epidemiological trends and susceptibility patterns of bloodstream infections caused by Enterococcus spp. in six German university hospitals: a prospectively evaluated multicentre cohort study from 2016 to 2020 of the R-Net study group.

    Hornuss, Daniel / Göpel, Siri / Walker, Sarah V / Tobys, David / Häcker, Georg / Seifert, Harald / Higgins, Paul G / Xanthopoulou, Kyriaki / Gladstone, Beryl Primrose / Cattaneo, Chiara / Mischnik, Alexander / Rohde, Anna M / Imirzalioglu, Can / Trauth, Janina / Fritzenwanker, Moritz / Falgenhauer, Jane / Gastmeier, Petra / Behnke, Michael / Kramme, Evelyn /
    Käding, Nadja / Rupp, Jan / Peter, Silke / Schmauder, Kristina / Eisenbeis, Simone / Kern, Winfried V / Tacconelli, Evelina / Rieg, Siegbert

    Infection

    2024  

    Abstract: Purpose: To analyse recent epidemiological trends of bloodstream infections (BSI) caused by Enterococcus spp. In adult patients admitted to tertiary care centres in Germany.: Methods: Epidemiological data from the multicentre R-NET study was analysed. ...

    Abstract Purpose: To analyse recent epidemiological trends of bloodstream infections (BSI) caused by Enterococcus spp. In adult patients admitted to tertiary care centres in Germany.
    Methods: Epidemiological data from the multicentre R-NET study was analysed. Patients presenting with E. faecium or E. faecalis in blood cultures in six German tertiary care university hospitals between October 2016 and June 2020 were prospectively evaluated. In vancomycin-resistant enterococci (VRE), the presence of vanA/vanB was confirmed via molecular methods.
    Results: In the 4-year study period, 3001 patients with BSI due to Enterococcus spp. were identified. E. faecium was detected in 1830 patients (61%) and E. faecalis in 1229 patients (41%). Most BSI occurred in (sub-) specialties of internal medicine. The pooled incidence density of enterococcal BSI increased significantly (4.0-4.5 cases per 10,000 patient days), which was primarily driven by VRE BSI (0.5 to 1.0 cases per 10,000 patient days). In 2020, the proportion of VRE BSI was > 12% in all study sites (range, 12.8-32.2%). Molecular detection of resistance in 363 VRE isolates showed a predominance of the vanB gene (77.1%).
    Conclusion: This large multicentre study highlights an increase of BSI due to E. faecium, which was primarily driven by VRE. The high rates of hospital- and ICU-acquired VRE BSI point towards an important role of prior antibiotic exposure and invasive procedures as risk factors. Due to limited treatment options and high mortality rates of VRE BSI, the increasing incidence of VRE BSI is of major concern.
    Language English
    Publishing date 2024-04-30
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 185104-4
    ISSN 1439-0973 ; 0300-8126 ; 0173-2129
    ISSN (online) 1439-0973
    ISSN 0300-8126 ; 0173-2129
    DOI 10.1007/s15010-024-02249-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Human infections caused by Staphylococcus argenteus in Germany: genetic characterisation and clinical implications of novel species designation.

    Alhussein, Farah / Fürstenberg, Judith / Gaupp, Rosmarie / Eisenbeis, Janina / Last, Katharina / Becker, Sören L / Papan, Cihan

    European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology

    2020  Volume 39, Issue 12, Page(s) 2461–2465

    Abstract: We report a series of Staphylococcus argenteus infections from Saarland, Germany. Travel histories were unremarkable for extra-European sojourns, indicating an autochthonous transmission mode. Multilocus sequence typing revealed that all isolates were ... ...

    Abstract We report a series of Staphylococcus argenteus infections from Saarland, Germany. Travel histories were unremarkable for extra-European sojourns, indicating an autochthonous transmission mode. Multilocus sequence typing revealed that all isolates were members of the clonal complex CC2250. In only one case, guideline-adherent treatment with an isoxazolyl penicillin was prescribed. Our report illustrates the perils of novel species designations, which may lead to misconceptions and suboptimal treatment choices among clinicians.
    MeSH term(s) Aged, 80 and over ; Female ; Germany ; Humans ; Male ; Microbial Sensitivity Tests ; Middle Aged ; Multilocus Sequence Typing ; Serogroup ; Staphylococcal Infections/diagnosis ; Staphylococcal Infections/microbiology ; Staphylococcus/genetics ; Staphylococcus/isolation & purification
    Language English
    Publishing date 2020-06-23
    Publishing country Germany
    Document type Case Reports ; Journal Article
    ZDB-ID 603155-9
    ISSN 1435-4373 ; 0934-9723 ; 0722-2211
    ISSN (online) 1435-4373
    ISSN 0934-9723 ; 0722-2211
    DOI 10.1007/s10096-020-03950-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Association of ward-level antibiotic consumption with healthcare-associated Clostridioides difficile infections: an ecological study in five German university hospitals, 2017-2019.

    Rohde, Anna M / Mischnik, Alexander / Behnke, Michael / Dinkelacker, Ariane / Eisenbeis, Simone / Falgenhauer, Jane / Gastmeier, Petra / Häcker, Georg / Herold, Susanne / Imirzalioglu, Can / Käding, Nadja / Kramme, Evelyn / Peter, Silke / Piepenbrock, Ellen / Rupp, Jan / Schneider, Christian / Schwab, Frank / Seifert, Harald / Steib-Bauert, Michaela /
    Tacconelli, Evelina / Trauth, Janina / Vehreschild, Maria J G T / Walker, Sarah V / Kern, Winfried V / Jazmati, Nathalie

    The Journal of antimicrobial chemotherapy

    2023  Volume 78, Issue 9, Page(s) 2274–2282

    Abstract: Objectives: To analyse the influence of antibiotic consumption on healthcare-associated healthcare onset (HAHO) Clostridioides difficile infection (CDI) in a German university hospital setting.: Methods: Monthly ward-level antibiotic consumption ... ...

    Abstract Objectives: To analyse the influence of antibiotic consumption on healthcare-associated healthcare onset (HAHO) Clostridioides difficile infection (CDI) in a German university hospital setting.
    Methods: Monthly ward-level antibiotic consumption measured in DDD/100 patient days (pd) and CDI surveillance data from five university hospitals in the period 2017 through 2019 were analysed. Uni- and multivariable analyses were performed with generalized estimating equation models.
    Results: A total of 225 wards with 7347 surveillance months and 4 036 602 pd participated. With 1184 HAHO-CDI cases, there was a median incidence density of 0.17/1000 pd (IQR 0.03-0.43) across all specialties, with substantial differences among specialties. Haematology-oncology wards showed the highest median incidence density (0.67/1000 pd, IQR 0.44-1.01), followed by medical ICUs (0.45/1000 pd, IQR 0.27-0.73) and medical general wards (0.32/1000 pd, IQR 0.18-0.53). Multivariable analysis revealed carbapenem (mostly meropenem) consumption to be the only antibiotic class associated with increased HAHO-CDI incidence density. Each carbapenem DDD/100 pd administered increased the HAHO-CDI incidence density by 1.3% [incidence rate ratio (IRR) 1.013; 95% CI 1.006-1.019]. Specialty-specific analyses showed this influence only to be valid for haematological-oncological wards. Overall, factors like ward specialty (e.g. haematology-oncology ward IRR 2.961, 95% CI 2.203-3.980) or other CDI cases on ward had a stronger influence on HAHO-CDI incidence density (e.g. community-associated CDI or unknown association case in same month IRR 1.476, 95% CI 1.242-1.755) than antibiotic consumption.
    Conclusions: In the German university hospital setting, monthly ward-level carbapenem consumption seems to increase the HAHO-CDI incidence density predominantly on haematological-oncological wards. Furthermore, other patient-specific factors seem to be equally important to control HAHO-CDI.
    MeSH term(s) Humans ; Anti-Bacterial Agents/therapeutic use ; Hospitals, University ; Clostridioides difficile ; Cross Infection/drug therapy ; Cross Infection/epidemiology ; Carbapenems ; Clostridium Infections/drug therapy ; Clostridium Infections/epidemiology ; Incidence ; Retrospective Studies
    Chemical Substances Anti-Bacterial Agents ; Carbapenems ; canertinib dihydrochloride (ICJ93X8X90)
    Language English
    Publishing date 2023-08-01
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 191709-2
    ISSN 1460-2091 ; 0305-7453
    ISSN (online) 1460-2091
    ISSN 0305-7453
    DOI 10.1093/jac/dkad232
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Bioinspired Liposomes for Oral Delivery of Colistin to Combat Intracellular Infections by Salmonella enterica.

    Menina, Sara / Eisenbeis, Janina / Kamal, Mohamed Ashraf M / Koch, Marcus / Bischoff, Markus / Gordon, Sarah / Loretz, Brigitta / Lehr, Claus-Michael

    Advanced healthcare materials

    2019  Volume 8, Issue 17, Page(s) e1900564

    Abstract: Bacterial invasion into eukaryotic cells and the establishment of intracellular infection has proven to be an effective means of resisting antibiotic action, as anti-infective agents commonly exhibit a poor permeability across the host cell membrane. ... ...

    Abstract Bacterial invasion into eukaryotic cells and the establishment of intracellular infection has proven to be an effective means of resisting antibiotic action, as anti-infective agents commonly exhibit a poor permeability across the host cell membrane. Encapsulation of anti-infectives into nanoscaled delivery systems, such as liposomes, is shown to result in an enhancement of intracellular delivery. The aim of the current work is, therefore, to formulate colistin, a poorly permeable anti-infective, into liposomes suitable for oral delivery, and to functionalize these carriers with a bacteria-derived invasive moiety to enhance their intracellular delivery. Different combinations of phospholipids and cholesterol are explored to optimize liposomal drug encapsulation and stability in biorelevant media. These liposomes are then surface-functionalized with extracellular adherence protein (Eap), derived from Staphylococcus aureus. Treatment of HEp-2 and Caco-2 cells infected with Salmonella enterica using colistin-containing, Eap-functionalized liposomes resulted in a significant reduction of intracellular bacteria, in comparison to treatment with nonfunctionalized liposomes as well as colistin alone. This indicates that such bio-invasive carriers are able to facilitate intracellular delivery of colistin, as necessary for intracellular anti-infective activity. The developed Eap-functionalized liposomes, therefore, present a promising strategy for improving the therapy of intracellular infections.
    MeSH term(s) Administration, Oral ; Bacterial Proteins ; Biomimetics ; Caco-2 Cells ; Colistin/administration & dosage ; Colistin/pharmacology ; Colistin/therapeutic use ; Epithelial Cells/microbiology ; Humans ; Intracellular Space/microbiology ; Liposomes ; Microbial Viability/drug effects ; RNA-Binding Proteins ; Salmonella Infections/drug therapy ; Salmonella Infections/microbiology ; Salmonella enterica/drug effects ; Salmonella enterica/physiology
    Chemical Substances Bacterial Proteins ; Eap-N protein, Staphylococcus aureus ; Liposomes ; RNA-Binding Proteins ; Colistin (Z67X93HJG1)
    Language English
    Publishing date 2019-07-22
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2649576-4
    ISSN 2192-2659 ; 2192-2640
    ISSN (online) 2192-2659
    ISSN 2192-2640
    DOI 10.1002/adhm.201900564
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Increasing numbers and complexity of Staphylococcus aureus bloodstream infection-14 years of prospective evaluation at a German tertiary care centre with multi-centre validation of findings.

    Mathé, Philipp / Göpel, Siri / Hornuss, Daniel / Tobys, David / Käding, Nadja / Eisenbeis, Simone / Kohlmorgen, Britta / Trauth, Janina / Gölz, Hanna / Walker, Sarah V / Mischnik, Alexander / Peter, Silke / Hölzl, Florian / Rohde, Anna M / Behnke, Michael / Fritzenwanker, Moritz / Häcker, Georg / Steffens, Benedict / Vehreschild, Maria /
    Kramme, Evelyn / Falgenhauer, Jane / Peyerl-Hoffmann, Gabriele / Seifert, Harald / Rupp, Jan / Gastmeier, Petra / Imirzalioglu, Can / Tacconelli, Evelina / Kern, Winfried / Rieg, Siegbert

    Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases

    2023  Volume 29, Issue 9, Page(s) 1197.e9–1197.e15

    Abstract: Objectives: Staphylococcus aureus bloodstream infection (SAB) is a common and severe infection. This study aims to describe temporal trends in numbers, epidemiological characteristics, clinical manifestations, and outcomes of SAB.: Methods: We ... ...

    Abstract Objectives: Staphylococcus aureus bloodstream infection (SAB) is a common and severe infection. This study aims to describe temporal trends in numbers, epidemiological characteristics, clinical manifestations, and outcomes of SAB.
    Methods: We performed a post-hoc analysis of three prospective SAB cohorts at the University Medical Centre Freiburg between 2006 and 2019. We validated our findings in a large German multi-centre cohort of five tertiary care centres (R-Net consortium, 2017-2019). Time-dependent trends were estimated using Poisson or beta regression models.
    Results: We included 1797 patients in the mono-centric and 2336 patients in the multi-centric analysis. Overall, we observed an increasing number of SAB cases over 14 years (6.4%/year and 1000 patient days, 95% CI: 5.1% to 7.7%), paralleled by an increase in the proportion of community-acquired SAB (4.9%/year [95% CI: 2.1% to 7.8%]) and a decrease in the rate of methicillin-resistant-SAB (-8.5%/year [95% CI: -11.2% to -5.6%]). All of these findings were confirmed in the multi-centre validation cohort (6.2% cases per 1000 patient cases/year [95% CI: -0.6% to 12.6%], community-acquired-SAB 8.7% [95% CI: -1.2% to 19.6%], methicillin-resistant S. aureus-SAB -18.6% [95% CI: -30.6 to -5.8%]). Moreover, we found an increasing proportion of patients with multiple risk factors for complicated/difficult-to-treat SAB (8.5%/year, 95% CI: 3.6% to 13.5%, p < 0.001), alongside an overall higher level of comorbidities (Charlson comorbidity score 0.23 points/year, 95% CI: 0.09 to 0.37, p 0.005). At the same time, the rate of deep-seated foci such as osteomyelitis or deep-seated abscesses significantly increased (6.7%, 95% CI: 3.9% to 9.6%, p < 0.001). A reduction of in-hospital mortality by 0.6% per year (95% CI: 0.08% to 1%) was observed in the subgroup of patients with infectious diseases consultations.
    Discussion: We found an increasing number of SAB combined with a significant increase in comorbidities and complicating factors in tertiary care centres. The resulting challenges in securing adequate SAB management in the face of high patient turnover will become an important task for physicians.
    MeSH term(s) Humans ; Methicillin-Resistant Staphylococcus aureus ; Staphylococcus aureus ; Tertiary Care Centers ; Bacteremia/microbiology ; Staphylococcal Infections/microbiology ; Community-Acquired Infections/microbiology ; Anti-Bacterial Agents/therapeutic use
    Chemical Substances Anti-Bacterial Agents
    Language English
    Publishing date 2023-06-03
    Publishing country England
    Document type Journal Article
    ZDB-ID 1328418-6
    ISSN 1469-0691 ; 1470-9465 ; 1198-743X
    ISSN (online) 1469-0691
    ISSN 1470-9465 ; 1198-743X
    DOI 10.1016/j.cmi.2023.05.031
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Development and validation of BLOOMY prediction scores for 14-day and 6-month mortality in hospitalised adults with bloodstream infections: a multicentre, prospective, cohort study.

    Tacconelli, Evelina / Göpel, Siri / Gladstone, Beryl P / Eisenbeis, Simone / Hölzl, Florian / Buhl, Michael / Górska, Anna / Cattaneo, Chiara / Mischnik, Alexander / Rieg, Siegbert / Rohde, Anna M / Kohlmorgen, Britta / Falgenhauer, Jane / Trauth, Janina / Käding, Nadja / Kramme, Evelyn / Biehl, Lena M / Walker, Sarah V / Peter, Silke /
    Gastmeier, Petra / Chakraborty, Trinad / Vehreschild, Maria Jgt / Seifert, Harald / Rupp, Jan / Kern, Winfried V

    The Lancet. Infectious diseases

    2022  Volume 22, Issue 5, Page(s) 731–741

    Abstract: Background: The burden of bloodstream infections remains high worldwide and cannot be confined to short-term in-hospital mortality. We aimed to develop scores to predict short-term and long-term mortality in patients with bloodstream infections.: ... ...

    Abstract Background: The burden of bloodstream infections remains high worldwide and cannot be confined to short-term in-hospital mortality. We aimed to develop scores to predict short-term and long-term mortality in patients with bloodstream infections.
    Methods: The Bloodstream Infection due to Multidrug-resistant Organisms: Multicenter Study on Risk Factors and Clinical Outcomes (BLOOMY) study is a prospective, multicentre cohort study at six German tertiary care university hospitals to develop and validate two scores assessing 14-day and 6-month mortality in patients with bloodstream infections. We excluded patients younger than 18 years or who were admitted to an ophthalmology or psychiatry ward. Microbiological, clinical, laboratory, treatment, and survival data were prospectively collected on day 0 and day 3 and then from day 7 onwards, weekly. Participants were followed up for 6 months. All patients in the derivation cohort who were alive on day 3 were included in the analysis. Predictive scores were developed using logistic regression and Cox proportional hazards models with a machine-learning approach. Validation was completed using the C statistic and predictive accuracy was assessed using sensitivity, specificity, and predictive values.
    Findings: Between Feb 1, 2017, and Jan 31, 2019, 2568 (61·5%) of 4179 eligible patients were recruited into the derivation cohort. The in-hospital mortality rate was 23·75% (95% CI 22·15-25·44; 610 of 2568 patients) and the 6-month mortality rate was 41·55% (39·54-43·59; 949 of 2284). The model predictors for 14-day mortality (C statistic 0·873, 95% CI 0·849-0·896) and 6-month mortality (0·807, 0·784-0·831) included age, body-mass index, platelet and leukocyte counts, C-reactive protein concentrations, malignancy (ie, comorbidity), in-hospital acquisition, and pathogen. Additional predictors were, for 14-day mortality, mental status, hypotension, and the need for mechanical ventilation on day 3 and, for 6-month mortality, focus of infection, in-hospital complications, and glomerular filtration rate at the end of treatment. The scores were validated in a cohort of 1023 patients with bloodstream infections, recruited between Oct 9, 2019, and Dec 31, 2020. The BLOOMY 14-day score showed a sensitivity of 61·32% (95% CI 51·81-70·04), a specificity of 86·36% (83·80-88·58), a positive predictive value (PPV) of 37·57% (30·70-44·99), and a negative predictive value (NPV) of 94·35% (92·42-95·80). The BLOOMY 6-month score showed a sensitivity of 69·93% (61·97-76·84), a specificity of 66·44% (61·86-70·73), a PPV of 40·82% (34·85-47·07), and a NPV of 86·97% (82·91-90·18).
    Interpretation: The BLOOMY scores showed good discrimination and predictive values and could support the development of protocols to manage bloodstream infections and also help to estimate the short-term and long-term burdens of bloodstream infections.
    Funding: DZIF German Center for Infection Research.
    Translation: For the German translation of the abstract see Supplementary Materials section.
    MeSH term(s) Adult ; Cohort Studies ; Humans ; Predictive Value of Tests ; Proportional Hazards Models ; Prospective Studies ; Sepsis
    Language English
    Publishing date 2022-01-19
    Publishing country United States
    Document type Journal Article ; Multicenter Study ; Research Support, Non-U.S. Gov't
    ZDB-ID 2061641-7
    ISSN 1474-4457 ; 1473-3099
    ISSN (online) 1474-4457
    ISSN 1473-3099
    DOI 10.1016/S1473-3099(21)00587-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: The

    Eisenbeis, Janina / Saffarzadeh, Mona / Peisker, Henrik / Jung, Philipp / Thewes, Nicolas / Preissner, Klaus T / Herrmann, Mathias / Molle, Virginie / Geisbrecht, Brian V / Jacobs, Karin / Bischoff, Markus

    Frontiers in cellular and infection microbiology

    2018  Volume 8, Page(s) 235

    Abstract: The extracellular adherence protein (Eap) ... ...

    Abstract The extracellular adherence protein (Eap) of
    MeSH term(s) Bacterial Proteins/metabolism ; Cells, Cultured ; DNA-Binding Proteins/metabolism ; Extracellular Traps/metabolism ; Host-Pathogen Interactions ; Humans ; Microscopy, Atomic Force ; Neutrophils/immunology ; Neutrophils/microbiology ; RNA-Binding Proteins/metabolism ; Staphylococcus aureus/immunology ; Staphylococcus aureus/physiology
    Chemical Substances Bacterial Proteins ; DNA-Binding Proteins ; Eap-N protein, Staphylococcus aureus ; RNA-Binding Proteins
    Language English
    Publishing date 2018-07-09
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2619676-1
    ISSN 2235-2988 ; 2235-2988
    ISSN (online) 2235-2988
    ISSN 2235-2988
    DOI 10.3389/fcimb.2018.00235
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Bacterial MgrB peptide activates chemoreceptor Fpr3 in mouse accessory olfactory system and drives avoidance behaviour.

    Bufe, Bernd / Teuchert, Yannick / Schmid, Andreas / Pyrski, Martina / Pérez-Gómez, Anabel / Eisenbeis, Janina / Timm, Thomas / Ishii, Tomohiro / Lochnit, Günter / Bischoff, Markus / Mombaerts, Peter / Leinders-Zufall, Trese / Zufall, Frank

    Nature communications

    2019  Volume 10, Issue 1, Page(s) 4889

    Abstract: Innate immune chemoreceptors of the formyl peptide receptor (Fpr) family are expressed by vomeronasal sensory neurons (VSNs) in the accessory olfactory system. Their biological function and coding mechanisms remain unknown. We show that mouse Fpr3 (Fpr- ... ...

    Abstract Innate immune chemoreceptors of the formyl peptide receptor (Fpr) family are expressed by vomeronasal sensory neurons (VSNs) in the accessory olfactory system. Their biological function and coding mechanisms remain unknown. We show that mouse Fpr3 (Fpr-rs1) recognizes the core peptide motif f-MKKFRW that is predominantly present in the signal sequence of the bacterial protein MgrB, a highly conserved regulator of virulence and antibiotic resistance in Enterobacteriaceae. MgrB peptide can be produced and secreted by bacteria, and is selectively recognized by a subset of VSNs. Exposure to the peptide also stimulates VSNs in freely behaving mice and drives innate avoidance. Our data shows that Fpr3 is required for neuronal detection and avoidance of peptides derived from a conserved master virulence regulator of enteric bacteria.
    MeSH term(s) Animals ; Avoidance Learning ; Bacterial Proteins/metabolism ; Enterobacteriaceae/immunology ; Escherichia coli Proteins/immunology ; Membrane Proteins/immunology ; Membrane Proteins/metabolism ; Mice ; Receptors, Formyl Peptide/agonists ; Receptors, Formyl Peptide/genetics ; Receptors, Formyl Peptide/metabolism ; Sensory Receptor Cells/immunology ; Vomeronasal Organ/cytology ; Vomeronasal Organ/metabolism
    Chemical Substances Bacterial Proteins ; Escherichia coli Proteins ; Fpr3 protein, mouse ; Membrane Proteins ; MgrB protein, E coli ; Receptors, Formyl Peptide
    Language English
    Publishing date 2019-10-25
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-019-12842-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: ClpC affects the intracellular survival capacity of Staphylococcus aureus in non-professional phagocytic cells.

    Gunaratnam, Gubesh / Tuchscherr, Lorena / Elhawy, Mohamed I / Bertram, Ralph / Eisenbeis, Janina / Spengler, Christian / Tschernig, Thomas / Löffler, Bettina / Somerville, Greg A / Jacobs, Karin / Herrmann, Mathias / Bischoff, Markus

    Scientific reports

    2019  Volume 9, Issue 1, Page(s) 16267

    Abstract: Invasion and persistence of bacteria within host cells requires that they adapt to life in an intracellular environment. This adaptation induces bacterial stress through events such as phagocytosis and enhanced nutrient-restriction. During stress, ... ...

    Abstract Invasion and persistence of bacteria within host cells requires that they adapt to life in an intracellular environment. This adaptation induces bacterial stress through events such as phagocytosis and enhanced nutrient-restriction. During stress, bacteria synthesize a family of proteins known as heat shock proteins (HSPs) to facilitate adaptation and survival. Previously, we determined the Staphylococcus aureus HSP ClpC temporally alters bacterial metabolism and persistence. This led us to hypothesize that ClpC might alter intracellular survival. Inactivation of clpC in S. aureus strain DSM20231 significantly enhanced long-term intracellular survival in human epithelial (HaCaT) and endothelial (EA.hy926) cell lines, without markedly affecting adhesion or invasion. This phenotype was similar across a genetically diverse collection of S. aureus isolates, and was influenced by the toxin/antitoxin encoding locus mazEF. Importantly, MazEF alters mRNA synthesis and/or stability of S. aureus virulence determinants, indicating ClpC may act through the mRNA modulatory activity of MazEF. Transcriptional analyses of total RNAs isolated from intracellular DSM20231 and isogenic clpC mutant cells identified alterations in transcription of α-toxin (hla), protein A (spa), and RNAIII, consistent with the hypothesis that ClpC negatively affects the intracellular survival of S. aureus in non-professional phagocytic cells, via modulation of MazEF and Agr.
    MeSH term(s) Bacterial Adhesion ; Bacterial Proteins/genetics ; Bacterial Proteins/metabolism ; Cytotoxicity, Immunologic ; Heat-Shock Proteins/genetics ; Heat-Shock Proteins/metabolism ; Host-Pathogen Interactions/genetics ; Host-Pathogen Interactions/immunology ; Humans ; Microbial Viability/immunology ; Mutation ; Phagocytes/immunology ; Phagocytes/metabolism ; Phagocytes/microbiology ; Staphylococcal Infections/genetics ; Staphylococcal Infections/immunology ; Staphylococcal Infections/microbiology ; Staphylococcus aureus/physiology ; Transcriptional Activation ; Virulence
    Chemical Substances Bacterial Proteins ; ClpC protein, Bacteria ; Heat-Shock Proteins
    Language English
    Publishing date 2019-11-07
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-019-52731-3
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