Cydia pomonella granulovirus (CpGV, Baculoviridae) is one of the most important agents for the control of codling moth (CM, Cydia pomonella, L.) in both biological and integrated pest management. The rapid emergence of resistance against CpGV-M, which was observed in about 40 European CM field populations from 2003 on, could be traced back to a single, dominant, sex-linked gene. Since then, resistance management has been based on mixtures of new CpGV isolates (CpGV-I12, -S), which are able to overcome this resistance. Recently, resistance even to these novel isolates was observed in CM field populations. This resistance does not follow the described dominant, sex-linked inheritance trait. At the same time, another isolate CpGV-V15 was identified showing high virulence against these resistant populations. To elucidate this novel resistance mechanism and to identify the resistance gene(s) involved, we propose a comprehensive analysis of this resistance on the cellular and genomic level of codling moth. Because of the lack of previous knowledge of the molecular mechanisms of virus resistance in insects, several different and complementary approaches will be pursued. This study will not only give an in-depth insight into the genetic possibilities for development of baculovirus resistance in CM field populations and how the virus overcomes it, but can also serve as an important model for other baculovirus-host interaction systems.
Outbreaks of foodborne illness linked to consumptions of fresh, or partially processed, agricultural products are a growing concern in industrialized and developing countries. The incidence of human pathogens on fresh fruits and vegetables is often related to the use of recycled wastewaster in surface irrigation as well as high amounts of animal manure in agricultural management practice. Thereby the soil inhabiting fauna plays an important role in the transport and dissemination of microorganisms. The focus of the proposed project is on nematodes, well known vectors for bacteria and viruses in soil. The major goals are to: (1) survey human pathogens in soil and on/in free-living and plant parasitic nematodes in agriculture field sites irrigated with recycled wastewater or fertilized with fresh animal manure in Israel and the Palestinian Authority, (2) assess the function of nematodes as vectors in transmitting bacteria from microbial hot spots to plants, and (3) localize bacteria on and/or within the nematode and identify bacterial factors required for survival in the nematode host. Understanding the mechanisms involved in dissemination of human pathogens by nematodes will enhance the ability to develop practical means to minimize contamination of fresh produce and increase safety in food production.
Cherry leaf roll virus (CLRV) is a plant pathogen of economic and ecologic importance. It is globally distributed in a wide range of forest, fruit, and ornamental trees and shrubs. In several areas of cherry and walnut production CLRV causes severe losses in yield and quality. With current reference to the rapid dissemination and strong symptom expression in Finnish birches and the Germany-wide distribution of CLRV in birches and elderberry, we continuously investigate and gradually reveal CLRV transmission pathways as by pollen, seeds or water. However, modes and interactions responsible for the wide intergeneric host transmission as well as for the exceptional CLRV epidemic in Fennoscandia still remain unknown. In this project systematic studies shall investigate biological vectors as a causal agent to finally derive control mechanisms and strategies to avoid new epidemics in different hosts and geographic regions. Detailed monitoring of the invertebrate fauna of birch stands/forests and elderberry plantations in Germany and Finland shall reveal potential vectors to subsequently study them in detail by approved virus detection methods and transmission experiments. Molecular analyses of the CLRV coat protein shall prove its role as a viral determinant for a virus/vector interaction. Consequently, this project essentially will contribute important answers on the CLRV epidemiology, and this will be a key element within the first network of research on plant viral pathogens in forest trees.
In recent years science has taken an increased interest in mineralization processes in tropical soils in particular under minimal tillage operations. Plant litter quality and management strongly affect mineralization-nitrification processes in soil and hence the fate of nitrogen in ecosystems and the environment. Plant secondary metabolites like lignin and polyphenols are poorly degradable and interact with proteins (protein binding capacity) and hence protect them from microbial attack. Nitrification, a microbiological process, directly and indirectly influences the efficiency of recovery of N in the vegetation as well as the loss of N (through denitrification and leaching) causing environmental pollution to water bodies and contributes to global warming (e.g. the greenhouse gas N2O is emitted as a by-product of nitrification and denitrification). Nitrifiers comprise a relatively narrow species diversity (at least as known to date) and are generally thought to be sensitive to low soil pH and stress. Despite these properties nitrification occurs in acid tropical soils with high levels of aluminium and manganese. Thus the main objective of the project will be the identification of micro-organisms and mechanisms responsible for mineralization-nitrification processes in acid tropical soils and the influence of long-term litter input of different chemical qualities and minimal tillage options. The project will include the use of stable isotopes (15N, 13C), mass spectrometry, gas chromatography (CO2, N2O), biochemical methods (PLFA) and molecular biology (16s rRNA., PCR, DGGE)
Salinity reduces the productivity of cucumber (Cucumis sativus L.) through osmotic and ionic effects. For given atmospheric conditions we hypothesize the existence of an optimal canopy structure at which water use efficiency is maximal and salt accumulation per unit of dry matter production is minimal. This canopy structure optimum can be predicted by integrating physiological processes over the canopy using a functional-structural plant model (FSPM). This model needs to represent the influence of osmotic stress on plant morphology and stomatal conductance, the accumulation of toxic ions and their dynamics in the different compartments of the system, and their toxic effects in the leaf. Experiments will be conducted to parameterize an extended cucumber FSPM. In in-silico experiments with the FSPM we attempt to identify which canopy structure could lead to maximum long-term water use efficiency with minimum ionic stress. The results from in-silico experiments will be evaluated by comparing different canopy structures in greenhouses. Finally, the FSPM will be used to investigate to which extent the improvement of individual mechanisms of salt tolerance like reduced sensitivity of stomatal conductance or leaf expansion can contribute to whole-plant salt tolerance.
Fällt ein Regentropfen auf eine Wasseroberfläche oder platzt dort eine Gasblase, so wird in einem komplizierten strömungsmechanischen Prozess eine Vielzahl kleinster Tröpfchen produziert und in die Luft geschleudert. Diese Tröpfchen können ursprünglich im Wasser vorhandene Mikroplastikpartikel in die Luft übertragen. Da sowohl Regen als auch platzende Gasblasen in natürlichen und technischen Systemen wie Ozeanen, Pfützen oder Kläranlagen extrem häufige Ereignisse sind, liegt hier ein potenziell hochrelevanter Migrationspfad von Mikroplastik aus der Hydro- in die Atmosphäre vor. Dieser Prozess soll im vorliegenden Projekt durch eine Kombination aus Modell-Experimenten und Computersimulationen im Detail untersucht und verstanden werden.
Various species of pest insects cause substantial damage to agriculture every year, or transmit deadly diseases to animals and humans. A successful strategy to control pest insect populations is based on the Sterile Insect Technique (SIT), which uses the release of mass-reared, radiation sterilized male insects to cause infertile matings and thus reduce the pest population level. However, irradiation is not applicable to every insect species. Thus, new strategies based on genetic modifications of pest insects have been developed or are currently under investigation.The goal of the proposed research is to improve the development and ecological safety of genetically engineered (GE) insects created for enhanced biological control programs, including the SIT and new strategies based on conditional lethality. A major concern for GE insect release programs is transgene stability, and maintenance of their consistent expression. Transgene loss or intra-genomic movement could result in loss of strain attributes, and may ultimately lead to interspecies movement resulting in ecological risks. To address potential transgene instability, a new transposon vector that allows post-integration immobilization will be tested in the Mediterranean, Mexican and Oriental fruit fly tephritid pest species. In addition, the system will be established in the mosquito species Aedes and Anopheles - carriers of dengue and malaria.Random genomic insertion is also problematic for GE strain development due to genomic position effects that suppress transgene expression, and insertional mutations that negatively affect host fitness and viability. Diminished transgene expression could result in the unintended survival of conditional lethal individuals, or the inability to identify them. To target transgene vectors to defined genomic insertion sites having minimal negative effects on gene expression and host fitness, a recombinase-mediated cassette exchange (RMCE) strategy will be developed that. RMCE will also allow for stabilization of the target site, will be tested in tephritid and mosquito species, and will aid to the development of stabilized target-site strains for conditional lethal biocontrol. This will include a molecular and organismal evaluation of an RNAi-based lethality approach. Lethality based on an RNAi mechanism in the proposed insects would increase the species specificity and having multiple targets for lethality versus one target in existing systems. By seeking to improve transgene expressivity and stabilization of transposon-based vector systems, this proposal specifically addresses issues related to new GE insects by reducing their unintended spread after field release, and by limiting the possibilities for transgene introgression.
Verlässliche Vorhersagen von Wetter und Klimawandel erfordern ein gutes Verständnis der Eisbildung in troposphärischen Wolken. Von besonderer Bedeutung ist dabei die sogenannte heterogene Eisnukleation durch atmosphärische Aerosolpartikel. Das hier beantragte Projekt beinhaltet eine umfassende Untersuchung der heterogenen Eisnukleation in Zirruswolken und Mischphasenwolken, gemeinsam mit 8 weiteren Projekten der Forschergruppe INUIT. Eisbildung durch Kontaktgefrieren wird für einzelne Tröpfchen in einem elektrodynamischen Levitator (Paulfalle) untersucht. Experimente zum Einfluss von Aerosolen auf Immersionsgefrieren, Kontaktgefrieren und Depositionsnukleation werden in der AIDA-Wolkenkammer und einer neuen dynamischen Wolkenkammer durchgeführt, falls diese wie geplant bis Anfang 2016 zur Verfügung stehen wird. Hauptziele und Arbeitspakete des Projekts sind (a) Untersuchungen zum Immersionsgefrieren, Kontaktgefrieren und zur Depositionsnukleation von INUIT-2 Referenzaerosolen in enger Zusammenarbeit mit allen anderen lNUlT-2-Partnern, (b) AIDA-Wolkensimulationsexperimente mit redispergierten atmosphärischen Aerosolen die auf Filtern gesammelt wurden (in Zusammenarbeit mit RP8), (c) AIDA-Experimente mit porösen Partikeln zur Untersuchung des Einflusses von Kapillarkondensation und Prä-aktivierung auf Eisnukleationsprozesse, (d) EDB-Experimente zur Kontaktnukleation mit atmosphärisch relevanten und komplexen Aerosolen, (e) Untersuchungen zu den grundlegenden Mechanismen des Kontaktgefrierens, (f) die Entwicklung einer umfassenden und einheitlichen Parametrisierung heterogener Eisnukleation in enger Zusammenarbeit mit RP3 und RP5, (g) erste Experimente zur Kontaktnukleation in einer neuen Wolkenkammer unter Nutzung der Expertise aus langjährigen Experimenten zum Kontaktgefrieren und mit der Wolkensimulationskammer, (h) die Durchführung von zwei AIDA-Messkampagnen, eine nur für die INUIT-2- Partner und eine mit internationaler Beteiligung, bei denen Labormethoden und Feld Instrumente für die Messung von Aerosolen und eisbildenden Partikeln getestet und miteinander verglichen werden um hohe internationale Standards in der Eisnukleationsforschung zu entwickeln und zu erhalten. Die Aktivitäten an der AIDA-Wolkenkammer bieten auch eine gute Verknüpfung der Labor-, Feld und Modellieraktivitäten innerhalb der Forschergruppe INUIT und mit externen Partnern. In Ergänzung der laufenden INUIT-Arbeiten möchten wir in weiteren drei Jahren der Forschergruppe folgende neue Schwerpunkte setzen: die Eisnukleationseigenschaften von porösen Partikeln, Immersionsgefrieren und Depositionsnukleation von größenselektierten Partikeln mit Durchmessern bis zu einigen Mikrometern, die Quantifizierung von Kontaktgefrierraten von atmosphärisch relevanten komplexen Aerosolpartikeln, und erste Wolkenkammerexperimente zum Kontaktgefrieren. Außerdem werden wir die Erstellung und Pflege einer neuen Datenbank für Laborergebnisse zur heterogenen Eisnukleation unterstützen.
Verschiedene Modell-MP-Partikel sowie Modellpartikel für natürlich vorkommendes partikulares Material werden in Süßwasser und Boden inkubiert und daraus resultierende Oberflächenveränderungen werden biomolekular und physikalisch-chemisch charakterisiert. Daraufhin werden unterschiedliche Polyelektrolyt-Multilagen-beschichtete Modellpartikel hergestellt, welche in jeweils einer Eigenschaft (z.B. identische Mechanik oder Ladungsdichte) den inkubierten Partikeln gleichen. Durch einen Vergleich der verschiedenen Partikel wird daraufhin die Relevanz dieser Eigenschaft für die Adhäsion der Partikel an Zellen und die Internalisierung in Zellen quantitativ untersucht.
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