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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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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
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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
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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

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.
Keywords	Eap ; Staphylococcus aureus ; bacterial invasion ; bacteriomimetic nanocarriers ; extracellular adherence proteins ; simulated intestinal fluids
Subject code	610
Language	English
Publishing date	2019-07-22
Publisher	Wiley-VCH
Publishing country	de
Document type	Article ; Online
Database	BASE - Bielefeld Academic Search Engine (life sciences selection)

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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

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.
Keywords	Eap ; Staphylococcus aureus ; bacterial invasion ; bacteriomimetic nanocarriers ; extracellular adherence proteins ; simulated intestinal fluids
Subject code	610
Language	English
Publishing date	2019-07-22
Publisher	Wiley-VCH
Publishing country	de
Document type	Article ; Online
Database	BASE - Bielefeld Academic Search Engine (life sciences selection)

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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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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
Database	MEDical Literature Analysis and Retrieval System OnLINE

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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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Article ; Online: Simple Questionnaires to Improve Pooling Strategies for SARS-CoV-2 Laboratory Testing.

Annals of global health

2020 Volume 86, Issue 1, Page(s) 148

Abstract: Background: Liberal PCR testing for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is key to contain the coronavirus disease 2019 (COVID-19) pandemic. Combined multi-sample testing in pools instead of single tests might enhance laboratory ... ...

Abstract	Background: Liberal PCR testing for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is key to contain the coronavirus disease 2019 (COVID-19) pandemic. Combined multi-sample testing in pools instead of single tests might enhance laboratory capacity and reduce costs, especially in low- and middle-income countries. Objective: The purpose of our study was to assess the value of a simple questionnaire to guide and further improve pooling strategies for SARS-CoV-2 laboratory testing. Methods: Pharyngeal swabs for SARS-CoV-2 testing were obtained from healthcare and police staff, hospital inpatients, and nursing home residents in the southwestern part of Germany. We designed a simple questionnaire, which included questions pertaining to a suggestive clinical symptomatology, recent travel history, and contact with confirmed cases to stratify an individual's pre-test probability of having contracted COVID-19. The questionnaire was adapted repeatedly in face of the unfolding pandemic in response to the evolving epidemiology and observed clinical symptomatology. Based on the response patterns, samples were either tested individually or in multi-sample pools. We compared the pool positivity rate and the number of total PCR tests required to obtain individual results between this questionnaire-based pooling strategy and randomly assembled pools. Findings: Between March 11 and July 5, 2020, we processed 25,978 samples using random pooling (n = 6,012; 23.1%) or questionnaire-based pooling (n = 19,966; 76.9%). The overall prevalence of SARS-CoV-2 was 0.9% (n = 238). Pool positivity (14.6% vs. 1.2%) and individual SARS-CoV-2 prevalence (3.4% vs. 0.1%) were higher in the random pooling group than in the questionnaire group. The average number of PCR tests needed to obtain the individual result for one participant was 0.27 tests in the random pooling group, as compared to 0.09 in the questionnaire-based pooling group, leading to a laboratory capacity increase of 73% and 91%, respectively, as compared to single PCR testing. Conclusions: Strategies that combine pool testing with a questionnaire-based risk stratification can increase laboratory testing capacities for COVID-19 and might be important tools, particularly in resource-constrained settings.
MeSH term(s)	COVID-19/diagnosis ; COVID-19/epidemiology ; COVID-19 Testing/methods ; COVID-19 Testing/statistics & numerical data ; Clinical Laboratory Services/statistics & numerical data ; Clinical Laboratory Services/supply & distribution ; Germany/epidemiology ; Humans ; Pharynx/virology ; Prevalence ; Random Allocation ; Reverse Transcriptase Polymerase Chain Reaction ; Risk Factors ; SARS-CoV-2/isolation & purification ; Surveys and Questionnaires
Language	English
Publishing date	2020-11-18
Publishing country	United States
Document type	Journal Article
ZDB-ID	2821756-1
ISSN	2214-9996 ; 2214-9996
ISSN (online)	2214-9996
ISSN	2214-9996
DOI	10.5334/aogh.3126
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: The extracellular adherence protein (Eap) of Staphylococcus aureus acts as a proliferation and migration repressing factor that alters the cell morphology of keratinocytes.

Eisenbeis, Janina / Peisker, Henrik / Backes, Christian S / Bur, Stephanie / Hölters, Sebastian / Thewes, Nicolas / Greiner, Markus / Junker, Christian / Schwarz, Eva C / Hoth, Markus / Junker, Kerstin / Preissner, Klaus T / Jacobs, Karin / Herrmann, Mathias / Bischoff, Markus

International journal of medical microbiology : IJMM

2017 Volume 307, Issue 2, Page(s) 116–125

Abstract: Staphyloccocus aureus is a major human pathogen and a common cause for superficial and deep seated wound infections. The pathogen is equipped with a large arsenal of virulence factors, which facilitate attachment to various eukaryotic cell structures and ...

Abstract	Staphyloccocus aureus is a major human pathogen and a common cause for superficial and deep seated wound infections. The pathogen is equipped with a large arsenal of virulence factors, which facilitate attachment to various eukaryotic cell structures and modulate the host immune response. One of these factors is the extracellular adherence protein Eap, a member of the "secretable expanded repertoire adhesive molecules" (SERAM) protein family that possesses adhesive and immune modulatory properties. The secreted protein was previously shown to impair wound healing by interfering with host defense and neovascularization. However, its impact on keratinocyte proliferation and migration, two major steps in the re-epithelialization process of wounds, is not known. Here, we report that Eap affects the proliferation and migration capacities of keratinocytes by altering their morphology and adhesive properties. In particular, treatment of non-confluent HaCaT cell cultures with Eap resulted in cell morphology changes as well as a significant reduction in cell proliferation and migration. Eap-treated HaCaT cells changed their appearance from an oblong via a trapezoid to an astral-like shape, accompanied by decreases in cell volume and cell stiffness, and exhibited significantly increased cell adhesion. Eap had a similar influence on endothelial and cancer cells, indicative for a general effect of Eap on eukaryotic cell morphology and functions. Specifically, Eap was found to interfere with growth factor-stimulated activation of the mitogen-activated protein kinase (MAPK) pathway that is known to be responsible for cell shape modulation, induction of proliferation and migration of epithelial cells. Western blot analyses revealed that Eap blocked the phosphorylation of extracellular signal-regulated kinase 1 and 2 (Erk1/2) in keratinocyte growth factor (KGF)-stimulated HaCaT cells. Together, these data add another antagonistic mechanism of Eap in wound healing, whereby the bacterial protein interferes with keratinocyte migration and proliferation.
MeSH term(s)	Bacterial Proteins/metabolism ; Cell Adhesion/drug effects ; Cell Line ; Cell Movement/drug effects ; Cell Proliferation/drug effects ; Endothelial Cells/drug effects ; Epithelial Cells/drug effects ; Humans ; Keratinocytes/cytology ; Keratinocytes/drug effects ; Keratinocytes/physiology ; RNA-Binding Proteins/metabolism ; Signal Transduction/drug effects ; Staphylococcus aureus/pathogenicity ; Wound Healing/drug effects
Chemical Substances	Bacterial Proteins ; Eap-N protein, Staphylococcus aureus ; RNA-Binding Proteins
Language	English
Publishing date	2017-02
Publishing country	Germany
Document type	Journal Article
ZDB-ID	2006518-8
ISSN	1618-0607 ; 1438-4221
ISSN (online)	1618-0607
ISSN	1438-4221
DOI	10.1016/j.ijmm.2017.01.002
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