Systematic re‐appraisal of the gall‐usurping wasp genus Synophrus Hartig, 1843 (Hymenoptera: Cynipidae: Synergini)

Several unanswered questions remain regarding the taxonomy and phylogeny of inquiline gallwasps (Cynipidae: Synergini), obligate inhabitants of plant galls induced primarily by other gallwasps (Cynipidae: Cynipini and Diplolepidini). Here we use morphological and molecular data to revise the inquiline genus Synophrus, members of which are notable for extensively modifying the structure of galls induced by oak gallwasp hosts on oaks in the section Cerris of Quercus subgenus Quercus in the Western Palaearctic. Previous taxonomic treatments have recognized three Western Palaearctic species of Synophrus: S. pilulae, S. politus and S. olivieri. Our results support the establishment of four additional Western Palaearctic species: Synophrus hungaricus sp.n. , S. libani sp.n. , S. syriacus sp.n. and S. hispanicus sp.n. We describe and diagnose these new taxa, analyse their phylogenetic relationships, and show that Synophrus inquilines are able to impose their own gall phenotypes on those of their hosts. We provide an updated key to Synophrus.     

Ca2+-induced conformational transitions of phosphorylated peptides

CD spectroscopic studies on protected peptides containing lysine and serine, or phosphoserine, and on serine-containing fragments of the neurofilament protein midsized subunit, both in the unphosphorylated and phosphorylated form, are reported. The introduction of the phosphoryl group was not found to have a significant spectral effect in aqueous solution. In trifluoroethanol (TFE), spectral shifts toward unordered (type U) spectra or the appearance of distorted spectra likely reflect the adoption of aperiodic polypeptide conformations due to salt bridge(s) between negatively charged phosphoserine and positive lysine side-chain groups. A turn-stabilizing effect of phosphorylation was also observed. CD-monitored titration experiments in TFE revealed a high conformational sensitivity of phosphopeptides toward Ca²⁺ ions. The appearance of the unordered spectra or spectral shifts were the sign of a bulk disordering effect of Ca²⁺ ions. Spectra with specific spectroscopic features reflect the formation of Ca²⁺complexes and the adoption of ordered unique backbone conformations. When ordered structures were obtained on addition of Ca²⁺ ions, the observed CD curves showed a resemblance to the spectrum of β-pleated sheets. This may originate from chain extension and the formation of β-pleated sheet segments fixed by Ca²⁺ bridges between PO₃H groups of adjacent peptide chains. The data clearly show that the effect of the Ca²⁺ ions is highly specific: the sequence, chain length, presence and distribution of charged side-chain groups, degree and site of phosphorylation, and environmental factors appear to be determining in the process of chain extension or β-sheet formation. © 1993 John Wiley & Sons, Inc.     

The TNF Receptors p55 and p75 Mediate Chemotaxis of PMN Induced by TNFalpha and a TNFalpha 36-62 Peptide

The present study was performed to examine whether residues 36-62 of TNFalpha contain the chemotactic domain of TNFalpha, and whether the p55 and p75 TNF receptors are involved in TNFalpha induced chemotaxis. The chemotactic effect of TNFalpha on PMN was inhibited by the mAbs Hrt-7b and Utr-1, against the p55 and p75 TNF receptors, respectively. Both receptors may therefore be required for mediating the chemotactic effect of TNFcz. The synthetic TNFalpha 36-62, similar to TNFalpha, had chemotactic effects on both PMN and monocytes. The chemotactic activity of the TNFalpha 36-62 peptide on PMN, was inhibited by Htr-7b, Utr-1 and soluble p55 receptor, which shows that the peptide possessed the ability to induce chemotaxis through the TNF receptors. In contrast to TNFalpha, the peptide did not show a cytotoxic activity against WEHI 164 flbrosarcoma cells. It is suggested that different domains of the TNFalpha molecule induce distinct biological effects.     

A 'polarisation sun-dial' dictates the optimal time of day for dispersal by flying aquatic insects

1. Daily changes in the flight activity of aquatic insects have been investigated in only a few water beetles and bugs. The diel flight periodicity of aquatic insects and the environmental factors governing it are poorly understood. 2. We found that primary aquatic insects belonging to 99 taxa (78 Coleoptera, 21 Heteroptera) fly predominantly in mid‐morning, and/or around noon and/or at nightfall. There appears to be at least four different types of diurnal flight activity rhythm in aquatic insects, characterised by peak(s): (i) in mid‐morning; (ii) in the evening; (iii) both in mid‐morning and the evening; (iv) around noon and again in the evening. These activity maxima are quite general and cannot be explained exclusively by daily fluctuations of air temperature, humidity, wind speed and risks of predation, which are all somewhat stochastic. 3. We found experimental evidence that the proportion (%) P(θ) of reflecting surfaces detectable polarotactically as ‘water’ is always maximal at the lowest (dawn and dusk) and highest (noon) angles of solar elevation (θ) for dark reflectors while P(θ) is maximal at dawn and dusk (low solar elevations) for bright reflectors under clear or partly cloudy skies. 4. From the temporal coincidence between peaks in the diel flight activity of primary aquatic insects and the polarotactic detectability P(θ) of water surfaces we conclude that the optimal times of day for aquatic insects to disperse are the periods of low and high solar elevations θ. The θ‐dependent reflection–polarisation patterns, combined with an appropriate air temperature, clearly explain why polarotactic aquatic insects disperse to new habitats in mid‐morning, and/or around noon and/or at dusk. We call this phenomenon the ‘polarisation sun‐dial’ of dispersing aquatic insects.     

Killing of Escherichia coli by mononuclear phagocytes and neutrophils stimulated in vitro with beta-1,3-D-polyglucose derivatives.

Human monocytes, human peritoneal macrophages, mouse peritoneal macrophages and human peripheral neutrophils pretreated with beta-1,3-D-polyglucose derivatives showed pronounced bactericidal capacity to Escherichia coli compared to control cells. The increased bactericidal capacity was detectable in mononuclear phagocytes over a wide range of concentrations of bacteria. Granulocytes, however, showed bactericidal capacity only at low concentrations of bacteria. The pretreated mononuclear phagocytes released significant amounts of IL-1 and PGE2. However, there was no significant release of tumor necrosis factor (TNF). By incubating unstimulated cells with purified IL-1 and TNF, the bactericidal activity of neutrophils and mononuclear phagocytes was enhanced. Our data indicate that the inability of neutrophils stimulated with beta-1,3-D-polyglucose derivatives to kill large numbers of bacteria could be overcome by a combined treatment with purified IL-1 or TNF in addition to beta-1,3-D-polyglucose derivatives. By incubating unstimulated cells with medium from beta-1,3-D-polyglucose-treated human peritoneal macrophages, the bactericidal activity of the cells was enhanced to the same extent as cells pretreated with purified TNF and IL-1. Cells incubated with IL-1-depleted medium from beta-1,3-D-polyglucose-treated human peritoneal macrophages, showed reduced bactericidal activity compared to cells incubated with undepleted medium. These studies demonstrate that beta-1,3-D-polyglucose-treated mononuclear phagocytes and neutrophils show enhanced bactericidal activity. The enhanced activity is partly caused by stimulation of the cells with IL-1 released from mononuclear phagocytes and partly by other unknown effects of beta-1,3-D-polyglucose derivatives on both mononuclear phagocytes and neutrophils.