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156 results.
Future-oriented Fattening Pig Farming - ZERN Initial Project
Zukunftsorientierte Mastschweinehaltung - ZERN-Initialprojekt
Project Investigators: Kemper, Nicole; Kunzmann, Peter; Plötz, Madeleine; Visscher, Christian; Nicolaisen, Thies
Duration: April 2023 until July 2029
Funding: Nds. Ministerium für Wissenschaft und Kultur über Georg-August-Universität Göttingen, 1.811.726 EUR
Project Details:
This initial project within the ZERN research and transfer network is dealing with the future-oriented keeping and use of fattening pigs. There are deficits in current fattening pig husbandry, particularly in the areas of animal welfare, emissions and nutrient efficiency. This project has therefore set the objective of scientifically evaluating relevant aspects of sustainable pork production synergistically and gaining new, practice-relevant knowledge.
Cooperation Partners:

Georg-August-Universität Göttingen

Deutsches Institut für Lebensmitteltechnik (DIL)

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Development and validation of a loop-mediated isothermal amplification (LAMP) assay to investigate the transmission potential of Toxoplasma gondii through various high-risk foods
Entwicklung und Validierung eines Loop-mediated isothermal amplification (LAMP)-Assays zur Untersuchung des Übertragungspotenzials von Toxoplasma gondii durch verschiedene Risikolebensmittel
Project Investigators: PD Dr. Amir Abdulmawjood; Dr. Antonia Kreitlow; Dr. Lisa Siekmann; Prof. Dr. Christina Strube; Prof. Dr. Madeleine Plötz
Duration: May 2025 until April 2027
Funding: Fritz-Ahrberg-Stiftung, 100.000 EUR
Project Details:
The protozoan parasite Toxoplasma gondii is the causative agent of toxoplasmosis, a zoonosis that can be transmitted to humans by infected cats or through the consumption of contaminated foodstuffs or inadequately heated meat from infected intermediate hosts. Primary infections during the early stages of pregnancy are of particular concern due to the absence of maternal immunity, which allows the pathogen to cause severe foetal damage and abortions. There is currently no comprehensive and systematic monitoring of the pathogen in the food chain in Germany. Moreover, the accessibility of the pertinent testing methodologies is constrained. The project therefore aims to develop a rapid, field-proven detection method based on the loop-mediated isothermal amplification (LAMP) technique and to corroborate its validity for pertinent food matrices. Thereafter, the method will be employed to appraise the impact of diverse manufacturing techniques employed on sample products on the pathogen load, and to extrapolate recommendations for industrial manufacturing processes.
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HePro2 - Development of a physical process for the extraction, preparation and characterization of brewer's yeast proteins
HePro2 - Entwicklung eines physikalischen Prozesses für die Gewinnung, Aufbereitung und Charakterisierung von Bierhefeproteinen
Project Investigators: Prof. Dr. Kemal Aganovic
Duration: April 2024 until 2027
Funding: BMEL, 318.427 EUR
Project Details:
The project is carried out on DIL e.V., Quakenbrück.
The aim of this project is to develop and evaluate a concept for the extraction and processing of proteins from brewer's yeast in the highest possible native and functional form on a pilot scale. The proteins and other valuable substances of the yeast are mostly located within the cells and are therefore not easily accessible for conventional extraction or precipitation. Therefore, cell disruption is necessary, in order to increase access to the proteins. Residues from the brewing process also adhere to the yeast. These include gluten and bitter substances from the hops. Therefore, in the first step the aim is to develop a process for removing the bitter substances and gluten as far as technically possible (AP 1). The yeast cells are then physically disrupted so that the proteins dissolved in the cell plasma can escape. For this purpose, two mechanical methods are used in this research project: (1) electroporation using pulsed electric fields (PEF, WP 3), and (2) ultra-high-pressure homogenization (UHPH, WP 2). After the cell disruption, the cell wall components are separated from the protein-rich suspension/solution using the principle of separation by density or centrifugal forces in a plate separator. The proteins obtained will then be processed and stabilized and examined for their sensory, techno-functional and nutritional properties (WP 4), as well as their suitability to produce selected exemplary food products (WP 5). Once the process has been established for brewer's yeast, it will be validated with yeasts from other sources (WP 6). Finally, a life cycle assessment (LCA, WP 7) will be carried out using the data obtained during the proejct to compare the environmental impact of the proteins obtained to protein of soy and milk. During the LCA, the entire process will be included, i.e. the energy requirements of the new technologies will also be taken into account and compared with the production process of soy and milk proteins. In cooperation with the industrial partners, the feasibility and economic viability of the entire process will be evaluated (AP 8).
Cooperation Partners:

Elea Technology GmbH, Leiber GmbH

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Effects of a transient increase or decrease in temperature during in ovo development on epigenetic, transcriptomic and metabolic features of day-old broilers and laying chicks
Auswirkungen einer vorübergehenden Temperaturerhöhung oder -senkung während der in-ovo-Entwicklung auf epigenetische, transkriptomische und metabolische Merkmale von Eintagsküken und Legeküken
Project Investigators: Prof. Dr. Carsten Krischek
Duration: September 2024 until February 2027
Funding: Deutsche Forschungsgemeinschaft (DFG) , 287.753 EUR
Project Details:
Prenatal (in ovo) events have an impact on postnatal life. Prenatal "treatments"" may have a positive influence on adaptation to postnatal conditions. The targeted modulation of conditions during in ovo development could be a means for improving productive adaptability relating to growth and thermotolerance. The in ovo development of birds is a valuable model for studying environmental influences on early development and their long-term consequences. This is especially pertinent for myogenesis, where the response mechanisms to environmental influences on cell proliferation and differentiation can be studied. As chicken embryos have no active temperature regulation, a change in incubation temperature directly affects their body temperature. This leads to changes in the kinetics of biochemical processes and, in particular, the kinetics of relevant metabolic enzymes, which are likely associated with activity-dependent muscle and body growth. Our previous study demonstrated the respective effects on energy metabolism of low and high incubation temperatures between ED 7-10 and ED 10-13 immediately after treatment and in adulthood in broilers and identified changes in gene expression underlying the phenotypic responses. We intend to follow up on and answer the questions arising from this earlier study by analysing the effects of increased and decreased incubation temperatures within a specific treatment period (ED 10-13) on various metabolic, biochemical, and histological traits as well as on gene expression and epigenetic changes in day-old broiler and layer chicks. We will consider the one-day-of-age stage as representing the cumulative effect of the in ovo developmental processes. The aim is to uncover functional relationships along the genotype-phenotype map from the genome to the metabolome, via the epigenome and transcriptome, in response to changes in incubation temperature."
Cooperation Partners:

PD Dr. Siriluck Wimmers und Prof. Dr. Klaus Wimmers, Forschungsinstitut für Nutztierbiologie, Dummerstorf

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Investigation of food hygiene aspects of plant-based sausage and meat substitutes in comparison to traditional sausage and meat products
Untersuchung lebensmittehygienischer Aspekte von pflanzenbasierten Wurst- und Fleischersatzprodukten im Vergleich zu konventionellen Wurst- und Fleischwaren
Project Investigators: PD Dr. Nadja Jeßberger ; Dr. Theresa Büthe; Dr. Johanna Vahle; Prof. Dr. Madeleine Plötz
Duration: Novemer 2024 until June 2027
Funding: Fritz-Ahrberg-Stiftung, 70.000 EUR
Project Details:
Consumer behaviour in our society is changing, with vegetarian and vegan diets becoming increasingly popular. This has led to a significant increase in the production of vegetarian and vegan sausage and meat substitutes in Germany. Various products made from plant-based protein sources are now available. With intensified production, however, the importance of food hygiene is also increasing. In terms of consumer health, vegetarian and vegan substitute are required to be of impeccable microbiological quality. Currently, there are no explicit legal specifications for assessing the microbiological parameters of these products. There has also been little scientific research into this topic to date. Only a few studies focus on the microbiological quality of vegan minced meat or other selected vegetarian and vegan meat substitutes. So far, few studies have focused on microbiological growth during the shelf life of these products. A direct comparison with conventional sausage and meat products has not been made.
The initial aim of this project is to obtain an overview of the microbiological composition of commercially available vegetarian and vegan sausage and meat substitutes. In addition, data on the persistence and proliferation of pathogenic germs in these products over the entire shelf life is to be collected. In this way, a foundation can be established for microbiological guidance, warning and critical values as well as for the assessment of the health risk of these products. In particular, differences and similarities in comparison to conventional sausage and meat products will be analysed. Are the plant-based substitutes generally more or less contaminated with germs than conventional products? Which (pathogenic) germs are to be expected in the substitutes? How do survival, persistence and growth rates of selected pathogenic germs in the substitutes compare to conventional sausage and meat products? These key food hygiene aspects will be addressed in this project.
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Closing the loop with sustainable recycling of lignocellulose rich organic (by-)products for insect development and pet food production
Kreislaufschließung durch nachhaltiges Recycling von lignozellulosereichen organischen (Neben-)Produkten für die Insektenproduktion und die Herstellung von Heimtierfuttermitteln
Project Investigators: Prof. Dr. C. Visscher; Dr. C. Schwennen; Prof. Dr. M. Plötz; Dr. J. B. Lingens
Duration: January 2024 until December 2027
Funding: Volkswagenstiftung, 657.600 EUR
Project Details:
Eine potentiell flächendeckende Wiedervernässung der Moore zwecks Revitalisierung und CO2-Speicherung führt über die extensive Nutzung zum Anfall ligninreicher Primärbiomasse, die nicht effizient für die klassische Tierhaltung nutzbar ist. Diese Biomasse kann bisher maximal energetischen Zwecken dienen, was aber in Zukunft im Sinne einer ehrgeizigen Energiewende und Kreislaufwirtschaft nicht mehr zielführend ist. Im Rahmen diese Projektes soll die Lignozellulosestruktur der organischen Rohstoffe technisch durch Vorbehandlungen aufgebrochen werden und die dann insgesamt besser verdauliche Biomasse anschließend für eine dezentrale Insektenproduktion genutzt werden. Modellhaft sollen Standard-Insektenlarven (schwarze Soldatenfliege) und Spezialitäten (Mehlwurm, Grillen etc.) aufgezogen werden. So sollen skalierbar hochwertige Rohstoffe für die Heimtierernährung oder perspektivisch neuartige Lebensmittel produziert werden.
Cooperation Partners:

Deutsches Institut für Lebensmitteltechnik e.V., Quakenbrück

Dr. Kashif ur Rehman

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Chronic Pain in a dish - In vitro modeling of neuron-mediated chronic pain in the skin for Pharmacology and Toxicology
Chronic Pain in a dish - In vitro-Modellierung Neuronen-vermittelter chronischer Schmerzen in der Haut für Pharmakologie und Toxikologie
Project Investigators: Prof. Bettina Seeger, Ph.D.
Duration: April 2024 until October 2026
Funding: Stiftung zur Förderung der Erforschung von Ersatz- und Ergänzungsmethoden zur Einschränkung von Tierversuchen, 125.000 EUR
Project Details:
Chronic pain represents a significant health problem affecting approximately 20 to 50% of the world's population. Therapeutic methods are largely developed in behavioral tests with induced pain in rodents. This approach does not allow for pain treatment, leading to severe distress for the animals. Nevertheless, therapeutics developed in animals are not always effective in humans. Therefore, two in vitro models using human cells will be developed to quantify neuron-mediated chronic pain with the highest possible predictive power. For this purpose, stem cell-derived sensory neurons will be used (1.) to develop a luciferase-based exocytosis assay to easily quantify the increased release of neuropeptides (Substance P and Calcitonin Gene-Related Peptide) involved in the chronic pain response. Additionally, (2.) an innervated skin model will be developed to quantify neurite outgrowth and the expression of regulated genes associated with chronic pain receptors and ion channels involved in signal transduction in vitro. The proof-of-concept for the use of these models in pharmacology and toxicology will be provided by inhibiting induced neuropeptide release, induced neurite outgrowth, and induced gene expression with therapeutically effective substances or by triggering them through the addition of exogenous substances. This approach allows for the modeling of molecular pathways of chronic pain development in vitro, directly in human cells, to avoid unnecessary animal experiments and to develop effective and safe therapeutics for humans. Following the project, the skin model will be adapted to model atopic dermatitis using induced pluripotent stem cells and primary cells from patients, aiming to bring specific in vitro disease models into application for the development of new therapies in cooperation with industrial partners. Furthermore, the project should serve as a foundation for further cross-disciplinary in vitro modeling, such as the simulation of chronic joint pain.
Cooperation Partners:

Prof. Dr. Annemarie Lang, Ph.D., University of Michigan

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Isolation and characterization of salmonella-specific phages in bearded dragons
Isolation und Charakterisierung von salmonellenspezifischen Phagen bei Bartagamen
Project Investigators: Pees, Michael; Kittler, Sophie; Küper, Kim; Peh, Elisa; Plötz, Madeleine
Duration: June 2024 until June 2026
Project Details:
Salmonella-specific phages are isolated and characterized from bearded dragons. Their spectrum of activity is determined, and their in vitro and in vivo effectiveness is examined.
Cooperation Partners:

Robert-Koch-Institut RKI Wernigerode

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PARC Partnership for the Assessment of Risks from Chemicals WP 5.2.1.e PeriMyelinTox -Development of a human stem cell-based assay on myelin toxicity influencing peripheral sensory and motor functions
PARC Partnership for the Assessment of Risks from Chemicals WP 5.2.1.e PeriMyelinTox - Entwicklung eines auf menschlichen Stammzellen basierenden Tests zur Myelin-Toxizität, die die peripheren sensorischen und motorischen Funktionen beeinflusst
Project Investigators: Prof. Bettina Seeger, Ph.D.; Dr. Lisa Haiber
Duration: August 2023 until July 2026
Funding: cofinanziert durch die Europäische Kommission, 107.187 EUR
Project Details:
This project aims to address a critical gap in neurotoxicity assessment by developing a novel in vitro methodology specifically targeting myelin toxicity?a decisive factor influencing peripheral sensory and motor functions. Building upon established modes-of-action (MoA) in adult neurotoxicity, the study utilizes human induced pluripotent stem cells to differentiate into mature motor and sensory neurons, along with Schwann cells. Distinguishing itself from existing in vitro methods, the project focuses on myelin toxicity, an unexplored MoA not yet incorporated into existing approaches, thereby influencing neurotoxicity assessment.
Acknowledging the regulatory imperative for swifter and more human-relevant neurotoxicity evaluations, the project aims to deliver an effective myelin toxicity assessment method. The methodology involves co-cultivating sensory or motor neurons with Schwann cells in both 3D spheres and 2D configurations. The plan encompasses characterizing cell types and scrutinizing myelin formation through immunocytochemical stainings and RT-qPCR after 4-8 weeks in culture. A pivotal aspect of the study is the exploration of optimal conditions for high-throughput testing.
Milestones include achieving the expression of neuron and Schwann cell markers, determining the optimal 2D or 3D setup for automated high-throughput myelin quantification, and scientifically validating the test method. The ultimate objective is to furnish a robust tool for assessing myelin toxicity, utilizing a compound training set.
In conclusion, this project pioneers an approach to address the gap in myelin toxicity testing within in vitro neurotoxicity assessment. By leveraging human induced pluripotent stem cells and advanced co-culture techniques, the study aims to make a substantial contribution to the development of a more comprehensive and effective neurotoxicity evaluation testing battery for regulatory use.
Results:

https://www.eu-parc.eu/

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Response of human intestinal cells and structures to Bacillus cereus enterotoxins
Antwortverhalten humaner Intestinalzellen und Strukturen auf Bacillus cereus-Enterotoxine
Project Investigators: PD Dr. Nadja Jeßberger
Duration: October 2023 until September 2026
Funding: Drittmittelprojekt, gefördert durch die Deutsche Forschungsgemeinschaft (DFG)., 269.600 EUR
Project Details:
Bacillus cereus is a common soil bacterium responsible for two types of foodborne gastrointestinal diseases. The emetic variant leads to food poisoning and manifests in nausea and vomiting, while infections with enteropathogenic strains cause diarrhoea and abdominal pain. These symptoms are caused by various toxins, including the cyclic dodecadepsipeptide cereulide and the protein-based enterotoxins haemolysin BL (Hbl), non-haemolytic enterotoxin (Nhe) and cytotoxin K (CytK).
The principle of action of the pore-forming three-component toxin Hbl was investigated in detail in a previous project. The complex formation of the three protein components in solution, the binding order to the target cells, the optimum concentration ratio for fastest pore formation and maximum cytotoxicity, as well as the effect of a fourth protein component were determined. While the preliminary work focused on the toxin itself, this project investigates the effects of pore formation on the host.
This project provides answers to the cellular response of the primary target of B. cereus enterotoxins, namely human cells of the gastrointestinal tract. Firstly, relevant toxin concentrations and exposure times for the survival of intestinal cells or the onset of apoptosis will be determined. In addition, the onset of possible repair mechanisms within the target cells is investigated. These initial data already provide a model for the onset of diarrhoea caused by enteropathogenic B. cereus. Following these studies, the interaction of B. cereus and its enterotoxins with more complex structures, namely human intestinal organoids, is investigated. The use of organoid culture systems enables more elaborate studies on host-microorganism interactions. Various aspects are investigated, including gene expression, ion transport and the activation of signalling pathways within the target cells and structures.
Important new insights into the physiological processes that lead to enterotoxin-induced diarrhoea are expected.
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