ZUR AUSLÖSUNG DER EIABLAGE BEI DER APHIDOPHAGEN GALLMÜCKE APHIDOLETES APHIDIMYZA (DIPTERA: CECIDOMYIIDAE)

Die Eiablage von Aphidoletes aphidimyza (Rond.) konnte im Experiment durch Honigtau oder durch tote Blattläuse (Myzus persicae, Aphis fabae und Acyrthosiphon pisum), jedoch wesentlich stärker durch beide zusammen ausgelöst werden. Siphonensekret von Acyrthosiphon pisum wurde ebenfalls belegt. Dagegen gelang es nicht, die Gallmücken durch klebrige Substanzen, deren Konsistenz der des Honigtaus ähnlich ist, zur Eiablage zu bringen. Während Exuvien der Erbsenblattlaus für sich allein fast keine Wirkung zeigten, lösten sie in Kombination mit Honigtau die Eiablage ebenso stark aus wie die toten Blattläuse mit Honigtau. Dagegen waren kleine Steinchen in Blattlaus-Größe anstelle der Exuvien unwirksam. Auch Duftstoffe von Blattläusen und Honigtau führten nicht zur Eiablage. Von den Bestandteilen des Honigtaus waren bestimmte Kohlehydrate und Aminosäuren schwach, andere, vor allem Fruktose und Arginin, besser wirksam; reproduzierbar war die Wirkung nur in Kombination mit getöteten Blattläusen.     

Salinity reduction of the end-Triassic sea from the Alpine region into northwestern Europe

A palaeoecological analysis of the Penarth Group (='Rhaetic') of southern England and Wales is undertaken in terms of a species-richness comparison with the Zlambach and Kössen Beds of the Austrian Alps. The three groups studied, bivalves, foraminifers and ostracodes, comprise the most important invertebrate faunas occurring in the deposits cited. All show significant diversity from the Alps into northwest Europe. Coupled with the disappearance of stenohaline elements including ammonites, and taking into account other facies information, the evidence suggests a transgression of a shallow epicontinental sea in northwest Europe at the end of the Triassic. The salinity of this sea (˜25–30%□) was appreciably below that of the Tethyan ocean.     

Crown Gall on Castor Bean Leaves: II. FORMATION OF SECONDARY TUMOURS

Secondary tumours were formed on the cotyledonary leaf petiole,the hypocotyl, and first true leaf of castor bean seedlingsafter inoculating the blades of the cotyledonary leaves withAgrobacterium tumefaciens. Depending on the strain of bacteriaemployed, 0 to 80 per cent of the plants developed secondarytumours. The ability of different strains to initiate secondarytumours was not obviously correlated with their relative effectivenessin initiating primary tumours. Though all produced primary tumours,five out of ten auxotrophic strains failed to yield secondarytumours, whereas only one out of 14 prototrophic strains failedto do so. Both the number of plants developing secondary tumoursand the frequency with which these tumours occurred on differentparts of the plant were positively correlated with the concentrationof the primary inoculum. Tumours also developed on the cotyledonaryleaf petiole and on the hypocotyl after vacuum infiltrationof A. tumefaciens into the blade of cotyledonary leaves. Inmost instances (9 out of 11 plants) no tumours were formed onthe blade of the infiltrated leaf. Thus, tumour formation equivalentto secondary tumours can occur in the absence of a primary tumouror an overt primary wound. Excision of inoculated leaves showedthat the stimulus for secondary tumour formation moves fromthe blade to the hypocotyl within 24 h. Attempts to demonstratethe presence of a sub-cellular tumour-initiating agent in homogenatesof inoculated leaves were unsuccessful. A. tumefaciens, however,was found in the petiole of the cotyledonary leaf and in thehypocotyl within 24 h of inoculation. The migrating agent responsiblefor secondary tumour formation in castor beans is concludedto be intact bacteria.     

Intracellular phosphorylation of benzyladenosine is related to apoptosis induction in tobacco BY-2 cells

Treatment of tobacco BY‐2 cells with micromolar concentration of benzyladenosine ([9R]BA) resulted in the loss of cell viability in a time‐ and concentration‐dependent manner. Cell death induced by [9R]BA exhibited typical apoptotic hallmarks including cell shrinkage, chromatin condensation and degradation of nuclear DNA to characteristic high molecular weight (HMW) as well as nucleosomal size fragments. Externally added [9R]BA was very rapidly and almost quantitatively phosphorylated within BY‐2 cells. Accumulation of [9R]BA‐monophosphate was accompanied by massive production of endogenous reactive oxygen species (ROS), intracellular ATP depletion, and these events were followed by the loss of cell viability. Inhibition of intracellular phosphorylation of [9R]BA by adenosin kinase inhibitor, 5′‐amino‐5′‐deoxyadenosine (AdAs), diminished ROS production, ATP depletion, and consequently prevented cells from death. Selective inhibition of ROS production without restoring ATP production, however, did not provide any protection to cells. In contrast, even enhanced phosphorylation of [9R]BA caused by adenosine that simultaneously revived ATP synthesis reduced the number of dying cells. This is the first evidence of a direct relationship between intracellular phosphorylation of [9R]BA and apoptosis induction in BY‐2 cells. ATP depletion but not ROS production is the key secondary event that determines the cellular decision between life and death.     

Vibrio cholerae laboratory infection of the adult house fly Musca domestica

The present study was designed to test the hypothesis that house flies may be capable of specifically harbouring ingested Vibrio cholerae in their digestive tracts. Flies were continuously fed green fluorescent protein (GFP)‐labelled, non‐O1/non‐O139 environmental strains of V. cholerae. Bacterial burdens were quantitatively measured using plate counts and localization was directly observed using confocal microscopy. Vibrio cholerae were present in the fly alimentary canal after just 4 h, and reached a plateau of ～10⁷ colony‐forming units (CFU)/fly after 5 days in those flies most tolerant of the pathogen. However, individual flies were resistant to the pathogen: one or more flies were found to carry < 180 V. cholerae CFU at each time‐point examined. In flies carrying V. cholerae, the pathogen was predominantly localized to the midgut rather than the rectal space or crop. The proportion of house flies carrying V. cholerae in the midgut was dose‐dependent: the continuous ingestion of a concentrated, freshly prepared dose of V. cholerae increased the likelihood that fluorescent cells would be observed. However, V. cholerae may be a transient inhabitant of the house fly. This work represents the first demonstration that V. cholerae can inhabit the house fly midgut, and provides a platform for future studies of host, pathogen and environmental mediators of the successful colonization of this disease vector.     

Role of 4-hydroxy-<Emphasis Type="Italic">trans</Emphasis>-2-nonenal in cell functions

The role of lipid peroxidation product 4-hydroxy-trans-2-nonenal (4-HNE) in functional activity of cells under normal and different pathological conditions is discussed. Different pathways of 4-HNE metabolism in tissues are analyzed, with particular focus on the role the glutathione system in this process. 4-HNE is implicated in regulation of cell growth, proliferation, differentiation, and apoptosis. 4-HNE and metabolic products of other antioxidants (carotenoids) resemble each other in chemical nature of the product and influence general pathways of signal transduction. Manifestation of 4-HNE toxicity under oxidative stress conditions is regarded as a link to many diseases whose pathogenesis is connected with modifications of proteins and nucleic acids.