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2311 results.
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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Derivatives and Coordination Polymer Modifications of Giese salt
Derivate und Koordinationspolymermodifikationen des Giese-Salzes
Project Investigators: Dr. S. A. Bräuninger; Prof. H. Seifert
Duration: Beginning 2024 until Beginning 2027
Project Details:
As part of chemical synthesis and subsequent modern spectroscopic studies, targeted modifications of ammonium iron hexacyanoferrate are being investigated.
Cooperation Partners:

Dr. Damian A. Motz, Leibniz Universität Hannover

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Antibacterial effect of silver-modified implant materials
Antibakterielle Wirkung von silber-modifizierten Implantatwerkstoffen
Project Investigators: Jessica Meißner
Duration: 2024 until 2027
Funding: Deutsche Forschungsgemeinschaft (DFG) , 322.642 EUR
Project Details:
The proposed research project aims to develop iron-based materials with an antibacterial effect as innovative implant materials to prevent implant infections. Infections counteract the benefits of the implants and are associated with considerable patients burdens and follow-up costs. They are connected with biofilm growth on the implant surface, which protects the causative germs from the immune system and therapies. Even with high medical standards, an infection cannot be completely avoided. Thus, among others, the increasing spread of multi-resistant germs endangers progress in medical technology. Most of the currently used inert implant materials have been developed without considering the problem of infection. Therefore, various approaches to modify implants are increasingly being addressed, e.g. by releasing anti-bacterially effective silver ions. The scope of the proposed research project is to create near-surface phases of a degradable silver alloy within an inert iron-based implant material for an adapted release of silver to prevent infection. Low doses are sufficient as the ions are released directly at the target site thus, bypassing the shielding effect of the biofilm. The complete insolubility of iron and silver in each other enables the setting of these silver phases but makes processing challenging. Powder metallurgical processes, such as laser powder bed fusion (LPBF), enable the processing of powder mixtures of the individual material components. Thus, LPBF is applied to set adapted phases of a degradable, functional silver alloy at the surface of iron-based, inert material 316L, resulting in a targeted release of silver ions. Due to particle release from the alloy, biocompatibility studies are examined with different cell types like primary osteoblasts and cell lines (fibroblasts and endothelial cells) to study inflammation parameters and anomalies of cell metabolism. Furthermore, co-incubation experiments with bacteria and cells are planned to study the antibacterial effect in various infection scenarios.
Results:

https://gepris.dfg.de/gepris/projekt/538437364?language=en

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Antibiotic alternatives for bovine mastitis
Alternative Behandlungsmöglichkeiten bei der Mastitistherapie des Rindes
Project Investigators: Jessica Meißner
Duration: October 2024 until September 2027
Funding: Associations, 54.000 EUR
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Role of the ecoimmunology of *Culex pipiens* biotype molestus in the West Nile virus transmission cycle (Rumo)
Rolle der Ökoimmunolgie von Culex pipiens Biotyp molestus im West-Nil-Virus Übertragungszyklus (Rumo)
Project Investigators: Mareike Heinig-Hartberger; Stefanie Becker
Duration: Novemer 2024 until June 2027
Funding: Bundesministerium für Bildung und Forschung (BMBF), 179.695 EUR
Project Details:
The study of animal immune systems in their natural environment is gaining increasing importance. In addition to naturally occurring factors influencing the immune system, the growing environmental stressors to which animals are exposed highlight the significance of the research field of ecoimmunology. This is particularly true for mosquitoes, the most important vectors of various pathogens, whose development, immune system, and vector competence are strongly influenced by environmental conditions. A key environmental factor is exposure to pollutants, which have become increasingly prevalent due to their widespread use.

This project focuses on analyzing mosquito breeding sites, assessing their contamination with various pollutants, and investigating the interaction between pollutant exposure and mosquito vector competence. In the first work package, field samples are collected and analyzed, and the most common pollutants are tested in laboratory experiments for their effects on mosquito larvae. Dose-response experiments are conducted to determine sublethal doses of these substances for use in subsequent experiments. In the second work package, behavioral assays are performed to assess oviposition preferences of female mosquitoes in pollutant-contaminated water samples. Larvae are reared in the test waters defined in Work Package 1 to investigate the impact of pollutant exposure on their development. Additionally, transcriptome analyses are carried out to explore changes in gene expression in larvae resulting from pollutant exposure.

The third work package investigates the vector competence of mosquito larvae for West Nile virus (WNV) after exposure to different pollutants during development. Both WNV-infected larvae reared in pollutant-containing water are examined in the adult stage for their ability to transmit the virus to blood meals, and uninfected larvae are reared in the same test waters, then infected as adults to measure viral load in saliva and viral kinetics. The findings from these studies aim to enhance our understanding of the interactions between environmental pollution and vector competence.
Cooperation Partners:

RPTU Kaiserslautern-Landau, Institut für Umweltwissenschaften

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Glutaminyl cyclase as novel target for Parkinson's disease therapy - Genetic and pharmacologic proof-of-principle
Glutaminyl cyclase as novel target for Parkinson's disease therapy - Genetic and pharmacologic proof-of-principle
Project Investigators: Prof. Richter Assencio
Duration: April 2024 until March 2027
Funding: Else Kröner-Fresenius-Stiftung, 170.000 EUR
Project Details:
In this project we are testing a therapeutic drug candidate to reduce alpha-synuclein pathology in an animal model of Parkinson's disease.
Cooperation Partners:

Prof. Rossner, Paul Flechsig Institut für Hirnforschung, Universität Leipzig

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Monitoring of post-release success in rehabilitated wildlife
Die Evaluation des längerfristigen Auswilderungserfolges verschiedener rehabilitierten Wildtierarten
Project Investigators: Pees, Michael; Steiner, Natalie
Duration: October 2024 until September 2027
Project Details:
Wildlife populations in Germany and Europe are declining due to factors like habitat loss, intensive agriculture, and climate change. As more animals are rehabilitated, there is a lack of data on their survival after release. This project aims to monitor the survival and activity of species such as buzzards, sea eagles, and hedgehogs using telemetry and transponder systems to better understand the success and challenges of wildlife rehabilitation.
Cooperation Partners:

Wildtier und Artenschutz Station Sachsenhagen

Max-Planck-Institut für biologische Intelligenz

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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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Influence of Streptococcus suis SLY and DltA on the crosstalk between innate immune cells in different host compartments
Einfluss von Streptococcus suis SLY und DltA auf die Interaktion zwischen Zellen des angeborenen Immunsystems in verschiedenen Wirtskompartimenten
Project Investigators: Désirée Schaaf, PhD; PD Nicole de Buhr, PhD
Duration: April 2024 until March 2027
Funding: DFG, 482.000 EUR
Project Details:
Streptococcus suis is a frequent colonizer of the upper respiratory tract of pigs, but can also cause severe systemic diseases like meningitis and septicemia. However, pathogenesis of S. suis infection and the role of its virulence-associated factors, namely the pore-forming toxin suilysin (SLY) and the D-alanine-D-alanyl carrier ligase (DltA), is still not fully understood. So far, it is known that SLY damages different host cells by lytic pore formation and induces an inflammatory response leading to the release of cytokines, especially by monocytes/macrophages, and the recruitment of neutrophils. D-alanylation of lipoteichoic acids in the cell wall by DltA is known to increase resistance against antimicrobial peptides (AMPs) and phagocytosis of S. suis by neutrophils.
Our aim is to clarify the role of SLY and DltA in S. suis colonization of the porcine respiratory tract, systemic dissemination via the bloodstream, and invasion of the central nervous system. Thereby we will focus on their influence on innate immunity cells and the crosstalk between monocytes/macrophages and neutrophils. We hypothesize that the host compartments influence the expression of sly and dltA differentially and that vice versa SLY and DltA influence the host’s innate immune response by modulating the crosstalk between neutrophils and monocytes/macrophages contributing to the resistance of. S. suis towards immune defense mechanisms.
To investigate this, we will use complex in vitro cell culture systems that closely mimic the in vivo situation of the three main host compartments: a co-culture system of primary respiratory epithelial cells differentiated under air-liquid interface conditions and alveolar macrophages, porcine precision-cut lung slices, a reconstituted whole blood model, and the blood cerebrospinal fluid barrier model. Infection experiments will be performed with S. suis serotype 2 wild-type strain (wt), its isogenic mutants Δsly, ΔdltA, and ΔdltAΔsly as well as the respective complemented mutant strains.
We will start with the analysis of sly and dltA expression in the three compartments by quantitative real-time PCR and Western blotting, followed by the investigation of the neutrophil and the monocyte/macrophage response towards S. suis wt and sly- and dltA-deficient mutants. We will focus on the formation of neutrophil extracellular traps, reactive oxygen species production, phagocytic activity, and the release of certain cytokines and AMPs. Finally, we will investigate how secretions from monocytes/macrophages induced by S. suis infection influence neutrophils regarding their transmigration, inflammatory response, and phagocytic capacity, and vice versa.
The detailed investigation of the innate immune response towards S. suis infection in the three different compartments will help to better understand the switch of S. suis as a colonizer to an invasive pathogen, and how SLY and DltA are involved in this process.
Cooperation Partners:

Dr. Sophie Öhlmann (Institut für Bakteriologie und Mykologie, Veterinärmedizinische Fakultät, Universität Leipzig)

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