A member of the tryptophan-rich protein family is required for efficient sequestration of Plasmodium berghei schizonts

Protein export and host membrane remodeling are crucial for multiple Plasmodium species to establish a niche in infected hosts. To better understand the contribution of these processes to successful parasite infection in vivo, we sought to find and characterize protein components of the intraerythrocytic Plasmodium berghei-induced membrane structures (IBIS) that form in the cytoplasm of infected erythrocytes. We identified proteins that immunoprecipitate with IBIS1, a signature member of the IBIS in P. berghei-infected erythrocytes. In parallel, we also report our data describing proteins that co-precipitate with the PTEX (Plasmodium translocon of exported proteins) component EXP2. To validate our findings, we examined the location of three candidate IBIS1-interactors that are conserved across multiple Plasmodium species, and we found they localized to IBIS in infected red blood cells and two further colocalized with IBIS1 in the liver-stage parasitophorous vacuole membrane. Successful gene deletion revealed that these two tryptophan-rich domain-containing proteins, termed here IPIS2 and IPIS3 (for intraerythrocytic Plasmodium-induced membrane structures), are required for efficient blood-stage growth. Erythrocytes infected with IPIS2-deficient schizonts in particular fail to bind CD36 as efficiently as wild-type P. berghei-infected cells and therefore fail to effectively sequester out of the circulating blood. Our findings support the idea that intra-erythrocytic membrane compartments are required across species for alterations of the host erythrocyte that facilitate interactions of infected cells with host tissues

Metagenomics-Based Proficiency Test of Smoked Salmon Spiked with a Mock Community

peer reviewedAn inter-laboratory proficiency test was organized to assess the ability of participants to perform shotgun metagenomic sequencing of cold smoked salmon, experimentally spiked with a mock community composed of six bacteria, one parasite, one yeast, one DNA, and two RNA viruses. Each participant applied its in-house wet-lab workflow(s) to obtain the metagenomic dataset(s), which were then collected and analyzed using MG-RAST. A total of 27 datasets were analyzed. Sample pre-processing, DNA extraction protocol, library preparation kit, and sequencing platform, influenced the abundance of specific microorganisms of the mock community. Our results highlight that despite differences in wet-lab protocols, the reads corresponding to the mock community members spiked in the cold smoked salmon, were both detected and quantified in terms of relative abundance, in the metagenomic datasets, proving the suitability of shotgun metagenomic sequencing as a genomic tool to detect microorganisms belonging to different domains in the same food matrix. The implementation of standardized wet-lab protocols would highly facilitate the comparability of shotgun metagenomic sequencing dataset across laboratories and sectors. Moreover, there is a need for clearly defining a sequencing reads threshold, to consider pathogens as detected or undetected in a food sample

Kopplung von elektrochemischen Methoden mit oberflächenverstärkter Ramanstreuung

Die Bedeutung der Spektroelektrochemie nimmt in der modernen chemischen Forschung immer mehr zu. Die Anwendungsbereiche reichen hierbei von der Sensorik bis hin zur Energiekonversion. In dieser Arbeit wurde eine Methode entwickelt, die es ermöglicht, sowohl ergänzend als auch parallel, elektrochemische und spektroskopische Untersuchungen durchzuführen. Besonderes Augenmerk lag dabei auf der Kopplung von elektrochemischen Methoden mit der oberflächenverstärkten Ramanstreuung (SERS). Dazu wurde eine Oberfläche entwickelt, die sowohl den elektrochemischen als auch den spektroskopischen Anforderungen entspricht. Anhand von zwei Anwendungsbeispielen, zum einen die Detektion von interkalierter DNA mittels elektrochemischer Impedanzspektroskopie (EIS) und zum anderen bei der Detektion von lokalen Veränderungen auf einer Oberfläche mit Hilfe der elektrochemischen Rastermikroskopie (SECM), wurden die Vorteile einer Kopplung deutlich gemacht

The Plasmodium berghei translocon of exported proteins reveals spatiotemporal dynamics of tubular extensions.

Contains fulltext : 154127.pdf (publisher's version ) (Open Access

Cytotoxic dinuclear titanium-salan complexes : structural and biological characterization

Controlled hydrolysis of donor-substituted titanium-salan complexes led to the formation of well-defined dinuclear complexes. Structure determination by means of X-ray and NMR-studies revealed the presence of a single My-oxo bridge and one labile alkoxide ligand per titanium center. Concomitant cytotoxicity assays of the isolated dinuclear complexes showed cytotoxicities in the low micro-molar region, surpassing in this respect even their monomeric ancestors, thus making them possible highly active metabolites of titanium-salan anti-cancer drugs

Absence of PEXEL-Dependent Protein Export in Plasmodium Liver Stages Cannot Be Restored by Gain of the HSP101 Protein Translocon ATPase

Host cell remodeling is critical for successful Plasmodium replication inside erythrocytes and achieved by targeted export of parasite-encoded proteins. In contrast, during liver infection the malarial parasite appears to avoid protein export, perhaps to limit exposure of parasite antigens by infected liver cells. HSP101, the force-generating ATPase of the protein translocon of exported proteins (PTEX) is the only component that is switched off during early liver infection. Here, we generated transgenic Plasmodium berghei parasite lines that restore liver stage expression of HSP101. HSP101 expression in infected hepatocytes was achieved by swapping the endogenous promoter with the ptex150 promoter and by inserting an additional copy under the control of the elongation one alpha (ef1α) promoter. Both promoters drive constitutive and, hence, also pre-erythrocytic expression. Transgenic parasites were able to complete the life cycle, but failed to export PEXEL-proteins in early liver stages. Our results suggest that PTEX-dependent early liver stage export cannot be restored by addition of HSP101, indicative of alternative export complexes or other functions of the PTEX core complex during liver infection.Peer Reviewe

Electrolyte Extraction—Sub and Supercritical CO2

This chapter reports on experiments aimed at investigating the capability of pressurized carbon dioxide to extract the electrolyte from commercial available LIBs on a laboratory scale. Two different phase conditions of carbon dioxide (subcritical and supercritical) and two different extraction (static and dynamic) have been considered and analyzed for their strengths and weaknesses. Furthermore, the addition of co-solvents is examined with regard to their contribution to higher recovery rates. After reporting the optimized extraction method, the extracted electrolyte was analyzed by gas and ionic chromatography methods for potential de-composition products and their relative amount