Taxonomy of Senecio multilobatus and its allies

A revision is presented for ten closely related species of western North America. The assemblage approximates the sectionsBolanderiani Greenman andLobati Rydb. Two new infraspecific combinations are made:Senecio bolanderi Gray var.harfordii (Greenman) T. M. Barkley, andS. eurycephalus Torr. & Gray ex Gray var.Iewisrosei (J. T. Howell) T. M. Barkley.     

A taximetric study of infraspecific variation in autogamous Limnanthes floccosa (Limnanthaceae)

Limnanthes floccosa Howell is a variable autogamous species of recent origin. The phenetic relationships of a large number of populations ofL. floccosa were studied using taximetric techniques. Five subspecies are recognized inL. floccosa on the basis of the taximetric results.Limnanthes floccosa ssp.californica andL. floccosa ssp.grandiflora are described as new, andL. floccosa ssp.pumila andL. floccosa ssp.bellingeriana are proposed as new combinations. Aspects of autogamy responsible for the highly discrete pattern of variation inL. floccosa are discussed.     

Effect of herbivory by Teleonemia scrupulosa on the performance of Longitarsus bethae on their shared host,Lantana camara

Herbivory by insects may change the characteristics of nutrients and secondary plant chemicals of the foliage, thereby altering the acceptability and suitability of the plant for oviposition, feeding and development for subsequent herbivores. In the current study, the effect of herbivory by the sap-sucking lace bug, Teleonemia scrupulosa Stäl (Heteroptera: Tingidae), on the suitability of Lantana camara L. (Verbenaceae) for the root-feeding flea beetle, Longitarsus bethae Savini & Escalona (Chrysomelidae: Alticinae), was investigated under laboratory conditions. Preference of adult L. bethae was not influenced by the intensity of feeding damage caused by T. scrupulosa adults. However, high densities of T. scrupulosa nymphs and their feeding damage caused L. bethae adults to emigrate and colonize less infested or uninfested plants. Oviposition by L. bethae was significantly reduced at high densities of T. scrupulosa nymphs. While low infestation of T. scrupulosa had no effect the survival of L. bethae, moderate and high infestations caused significant reduction in percentage survival of L. bethae. The number of T. scrupulosa nymphs was negatively correlated with the percentage survival of L. bethae. Neither the duration of development nor the body size of L. bethae was influenced by the intensity of T. scrupulosa infestation. Overall, undamaged or slightly damaged plants that allowed better survival of L. bethae were often chosen as oviposition sites in preference to those that were highly infested, and on which survival was poor. Although the present study indicates the likelihood of inter-specific competition between L. bethae larvae and T. scrupulosa, this is likely to be mitigated by female flea beetles choosing to oviposit on less infested or uninfested plants in the field.     

In vitro culture and somatic embryogenesis of four Trifolium species

Callus cultures were induced from hypocotyl sections of Trifolium incarnatum L., T. vesiculosum Savi., T. ambiguum Bieb., and T. repens L. Callus production was the greatest for T. incarnatum and T. ambiguum on Phillips and Collins L2 medium with 0.06 mg/l picloram and 0.1 mg/l 6-benzylaminopurine and for T. vesiculosum and T. repens on Gamborg B5 medium with 1.25 mg/l 2,4-dichlorophenoxyacetic acid (2.4-D), 0.5 mg/l naphthaleneacetic acid (NAA), and 0.5 mg/l 6-furfurylaminopurine (kinetin). Proembryos or somatic embryos were formed in all four species though germination and subsequent plantlet formation only occured in t. incarnatum and T. vesiculosum. Mature plants were obtained via somatic embryogenesis for T. incarnatum. The regenerated plants were fertile and had the normal diploid number of chromosomes (2n = 14).     

Interactions between Pseudomonas syringae pv. tabaci and Two Rhizosphere Hosts, Medicago sativa and Avena sativa

The interactions between Pseudomonas syringae pv. tabaci and either nodulating alfalfa (Medicago sativa) or oat (Avena sativa) seedlings were examined to further our understanding of this rhizosphere association. P. syringae pv. tabaci produces and releases a toxin, tabtoxinine-β-lactam (TβL), that inactivates glutamine synthetase (GS). Sinorhizobium meliloti grew well in the presence of TβL in culture and on alfalfa roots. The alfalfa symbiont, S. meliloti, and its bacteroids contained TβL-sensitive glutamine synthetases and TβL detoxifying-β-lactamase. The GS of alfalfa leaves is also sensitive to TβL, but GS activity was unaffected in infested plants. Toxin production was apparently suppressed in the alfalfa and nitrate-fed oat rhizospheres since these plants survived and retained significant amounts of leaf GS activity. The water-soluble extracts of these rhizospheres inhibited TPL production in culture and the inhibition was correlated with the amount of reduced nitrogen present. Furthermore, representative mixtures of pure ammonium and amino acids inhibited TβL production in culture in a concentration dependent manner. Thus, a bi-directional interaction occurs between the nitrogen metabolism of alfalfa and oat and TβL production by P. syringae pv. tabaci.     

Identification of Ribosomal Protein L1-Binding Sites in <Emphasis Type="Italic">Thermus thermophilus</Emphasis> and <Emphasis Type="Italic">Thermotoga maritima</Emphasis> mRNAs

The conserved two-domain ribosomal protein (r-protein) L1 is a structural part of the L1 stalk of the large ribosomal subunit and regulates the translation of the operon that comprises its own gene. The regulatory properties of the bacterial r-protein L1 have only been studied in detail for Escherichia coli; however, there were no such studies for other bacteria, in particular, Thermus thermophilus and Thermotoga maritima, which are more evolutionarily ancient. It is known that domain I of the r-protein L1 might have regulatory properties of the whole protein. The aim of this study was to identify regulatory sites on the mRNA of T. thermophilus and T. maritima that interact with r-proteins L1, as well as with their domains I from the same organisms. An analysis of the mRNA of the L11 operon T. thermophilus showed the presence of one potential binding site of the L1 r-protein, two such regions were found also in the mRNA sequence of the L11 operon of T. maritima. The dissociation constants for the L1 proteins from T. thermophilus and T. maritima and their domains I with mRNA fragments from the same organisms that contain the supposed L1-binding sites were determined by surface plasmon resonance. It has been shown that the ribosomal proteins L1 as their domains I bind specific fragments of mRNA from the same organisms that may suggest regulatory activity of the L1 protein in the T. thermophilus and T. maritima and conservatism of the principles of L1-RNA interactions.     

Inflammasome-Mediated Inhibition of Listeria monocytogenes-Stimulated Immunity Is Independent of Myelomonocytic Function

Activation of the Nlrc4 inflammasome results in the secretion of IL-1β and IL-18 through caspase-1 and induction of pyroptosis. L. monocytogenes engineered to activate Nlrc4 by expression of Legionella pneumophilia flagellin (L. monocytogenes L.p.FlaA) are less immunogenic for CD8⁺ T cell responses than wt L. monocytogenes. It is also known that IL-1β orchestrates recruitment of myelomonocytic cells (MMC), which have been shown to interfere with T cell-dendritic cells (DC) interactions in splenic white pulp (WP), limiting T cell priming and protective immunity. We have further analyzed the role of MMCs in the immunogenicity of L. monocytogenes L.p.FlaA. We confirmed that MMCs infiltrate the WP between 24–48 hours in response to wt L. monocytogenes infection and that depletion of MMCs enhances CD8⁺ T cell priming and protective memory. L. monocytogenes L.p.FlaA elicited accelerated recruitment of MMCs into the WP. While MMCs contribute to control of L. monocytogenes L.p.FlaA, MMC depletion did not increase immunogenicity of L.p.FlaA expressing strains. There was a significant decrease in L. monocytogenes L.p.FlaA in CD8α⁺ DCs independent of MMCs. These findings suggest that limiting inflammasome activation is important for bacterial accumulation in CD8α⁺ DCs, which are known to be critical for T cell response to L. monocytogenes.     

Evaluation of Leptospirillum ferrooxidans for Leaching

The importance of Leptospirillum ferrooxidans for leach processes has been evaluated by studying the lithotrophic flora of three mine biotopes and a heap leaching operation, by percolation experiments with inoculated, sterilized ore, and by morphological, physiological, and genetic investigations of pure and mixed cultures of L. ferrooxidans, Thiobacillus ferrooxidans, and Thiobacillus thiooxidans. In biotopes of 20°C or above, Leptospirillum-like bacteria are as abundant as T. ferrooxidans. Leptospirilli represent at least one-half of the ferrous-iron-oxidizing population. Percolation experiments confirmed this result. Leptospirilli were as numerous as T. ferrooxidans. At reduced temperatures, the generation times of leptospirilli increase more so than those of T. ferrooxidans. At 14°C, Leptospirillum grows slowly and T. ferrooxidans dominates the population. Physiological investigations indicate that L. ferrooxidans is a strict chemolithoautotroph, metabolizing only ferrous iron and pyrite. Even an addition of 0.05% (wt/vol) yeast extract inhibited its growth. The maximum ferrous-iron-oxidizing activity of L. ferrooxidans amounts to about 40% of the activity of T. ferrooxidans. After growth on sulfidic ore, both species exhibit reduced iron-oxidizing activities, L. ferrooxidans exhibiting one-third and T. ferrooxidans exhibiting one-seventh of their maximum activities. Surprisingly, the absolute values are similar. For indirect leaching, L. ferrooxidans is as important as T. ferrooxidans. This was confirmed by the results of percolation experiments. L. ferrooxidans together with T. thiooxidans mobilized metals at least as well as T. ferrooxidans did. The best results were obtained with a mixed culture of all three species.     

Specific features of photorespiration in photosynthetically active organs of C3 plants

Photorespiration of photosynthetically active organs of C₃ plants (leaf, ear, stem, and leaf sheath) and C₄ plants (leaf, tassel, stem, leaf sheath, ear husk) grown under greenhouse and field conditions was studied. Photorespiration was measured using a PTM-48A high-technology monitor of photosynthesis (Bioinstruments S.R.L., Moldova). It is shown that photorespiration (CO₂ ejection after light turning off — apparent photorespiration) in C₃ plants is characteristic only for their leaves. In other photosynthesizing organs, photorespiration was absent, like in the photosynthesizing organs of C₄ plants. The absence of such after-light CO₂ outburst was observed for 31 genotypes: 18 cereal species belonging to four species (Triticum aestivum L., T. durum Desf., Secale cereale L., and Triticale); 6 grain legumes belonging to 2 species (Pisum sativum L. and Glycine max L.); 7 species of wild and rarely cultivated genotypes (T. boeoticum Boiss., T. dicoccoides Koern., T. dicoccum Schuebl., T. spelta L., T. compactum Host., T. monococcum L., and T. sphaerococcum Persiv.), and 2 genotypes of C₄ plants (Zea mays L. and Sorgum vulgaris L.). In all tested photosynthetically active genotypes, except of the C₃ plant leaves, apparent photorespiration was absent, but rather active glycolate cycle operated. The activity of this cycle was determined from the activity of the key enzyme of this cycle — glycolate oxidase. It was supposed that C₃ plants have two mechanisms of CO₂ assimilation: the first one — the mechanism of C₃ type localized in the leaves and the second one localized in other photosynthesizing organs, similar or with some elements of C₄ mechanism of CO₂ assimilation, limiting after-light CO₂ ejection during the metabolism of glycolate.     

The type species of the Ordovician agnostid trilobiteGeragnostus Howell, 1935

The type of the widespread Ordovician agnostid trilobiteGeragnostus, G. sidenbladhi (Linnarsson, 1869) from the upper Tremadocian Ceratopyge Limestone of Sweden, is redescribed and a lectotype is selected.Geragnostus Howell, 1935 bears a strong similarity toArthrorhachis Hawle & Corda, 1847. Obviously the two genera are closely allied, andGeragnostus may eventually be regarded as a junior subjective synonym ofArthrorhachis. It is suggested, however, that the distinction betweenGeragnostus andArthrorhachis might be upheld if the latter genus is taken to include metagnostids in which the posterior lobe (M3) of the pygidial rhachis is distinctly shorter than the length (sag.) of the anterior and middle lobes combined (M1 + M2).     

Chemical Composition and Insecticidal Activity of Artemisia scoparia Essential Oil against Three Coleopteran Stored-Product Insects

Chemical composition of the essential oil from Artemisia scoparia Waldst et Kit, and its fumigant and repellent activity were investigated against three stored product insects, Callosobruchus maculatus (Fab.), Sitophilus oryzae (L.), and Tribolium castaneum (Herbst). Dry ground leaves were subjected to hydrodistillation using a modified clevenger-type apparatus and the chemical composition of the volatile oil was studied by GC-MS. Nineteen components (99.51% of the total composition) were identified. β-Pinene (19.01%), capillin (17.45%), limonene (15.11%), myrcene (10.95) were found to be the major constituents of the oil. The mortality of 1-7 day old adults of the insect pests increased with concentration from 37 to 926 μL per L air and with exposure time from 3 to 24 h. A concentration of 37 μL per L air and exposure time of 24 h was sufficient to obtain 100% kill of the insects. Callosobruchus maculatus was more susceptible than S. oryzae and T. castaneum. A second more detailed bioassay gave estimates for the LC₅₀ of C. maculatus as 1.46 μL per L air, S. oryzae 1.87 μL per L air and T. castaneum 2.05 μL per L air. Also, the essential oil was significantly more repellent to T. castaneum and S. oryzae than C. maculatus. However, half-life time of the oil for C. maculatus was longer than S. oryzae and T. castaneum. These results show the efficacy of A. scoparia oil for use in organic food protection.     

Exosomes Secreted by Toxoplasma gondii-Infected L6 Cells: Their Effects on Host Cell Proliferation and Cell Cycle Changes

Toxoplasma gondii infection induces alteration of the host cell cycle and cell proliferation. These changes are not only seen in directly invaded host cells but also in neighboring cells. We tried to identify whether this alteration can be mediated by exosomes secreted by T. gondii-infected host cells. L6 cells, a rat myoblast cell line, and RH strain of T. gondii were selected for this study. L6 cells were infected with or without T. gondii to isolate exosomes. The cellular growth patterns were identified by cell counting with trypan blue under confocal microscopy, and cell cycle changes were investigated by flow cytometry. L6 cells infected with T. gondii showed decreased proliferation compared to uninfected L6 cells and revealed a tendency to stay at S or G2/M cell phase. The treatment of exosomes isolated from T. gondii-infected cells showed attenuation of cell proliferation and slight enhancement of S phase in L6 cells. The cell cycle alteration was not as obvious as reduction of the cell proliferation by the exosome treatment. These changes were transient and disappeared at 48 hr after the exosome treatment. Microarray analysis and web-based tools indicated that various exosomal miRNAs were crucial for the regulation of target genes related to cell proliferation. Collectively, our study demonstrated that the exosomes originating from T. gondii could change the host cell proliferation and alter the host cell cycle.     

Interactions between the phloem-feeding speciesTomicus piniperda (Col.: Scolytidae) andAcanthocinus aedilis (Col.: Cerambycidae), and the predatorThanasimus formicarius (Col.: Cleridae) with special reference to brood production

Interactions betweenTomicus piniperda (L.) (Col.: Scolytidae),Acanthocinus aedilis (L.) (Col.: Cerambycidae) andThanasimus formicarius (L.) (Col.: Cleridae) were investigated in caged pine bolts. The treatments wereT. piniperda alone,A. aedilis alone,T. piniperda together withA. aedilis, T. piniperda together withT. formicarius and all three species together. T. piniperda offspring production per m² was reduced by 92% when reared withT. formicarius, by 78% when reared withA. aedilis, and by 94% when all three species were reared together, compared withT. piniperda reared alone.A. aedilis had a negative influence on the offspring production ofT. formicarius and vice versa. When both species were present in the same bolt (together withT. piniperda) offspring production was reduced by 74% forA. aedilis and by 42% forT. formicarius compared with their respective production values when each species was present alone with the bark beetle. The new generation ofT. formicarius emerged as larvae from June to August while most of theA. aedilis offspring emerged as adults from September to October, leaving only a few larvae in the bolts to hibernate.A. aedilis only reproduced in a small part of one of the bolts without bark beetles.     

Sensitivity of Iron-Oxidizing Bacteria, Thiobacillus ferrooxidans and Leptospirillum ferrooxidans, to Bisulfite Ion

When grown on iron-salt medium supplemented with the bisulfite ion, Leptospirillum ferrooxidans was much more sensitive to the ion than was Thiobacillus ferrooxidans. The causes of the sensitivity of L. ferrooxidans to the bisulfite ion were studied. The bisulfite ion completely inhibited the iron-oxidizing activities of L. ferrooxidans and T. ferrooxidans at 0.02 and 0.2 mM, respectively. A trapping reagent for the bisulfite ion, formaldehyde, completely reversed the inhibition. The treatment of intact cells with 1.0 mM bisulfite ion for 1 h and washing the bisulfite ion from the cells had no harmful effects on the iron-oxidizing activity of T. ferrooxidans. However, the treatment of L. ferrooxidans with 0.1 mM bisulfite ion for 1 h completely destroyed the iron-oxidizing activity. T. ferrooxidans had sulfite:ferric ion oxidoreductase activity. In contrast, a quite low level of sulfite:ferric ion oxidoreductase activity was found in L. ferrooxidans, suggesting that it is much more difficult for L. ferrooxidans to oxidize the bisulfite ion to the less harmful sulfate than it is for T. ferrooxidans. These results suggest that the sensitivity of L. ferrooxidans to the bisulfite ion is due to a lack of an active sulfite:ferric ion oxidoreductase and the sensitivity of its iron oxidase to bisulfite ion.     

Cytotaxonomic study ofTragopogon L. in czechoslovakia

Karyotypes ofTragopogon orientalis L. subsp.orientalis, T orientalis L. subsp.leiocarpos (Sauter)Trnka,T. pratensis L.,T. minor Miller,T. dubius Scop. subsp.dubius andT. dubius Scop. subsp.major (Jacq.)Vollmann were studied. The occurrence in Slovakia ofT. pratensis was karyologically proved.     

Taxonomical studies on Oriental Platygastridae (Hymenoptera: Platygastroidea)

14 species new to science are described, viz. Amblyaspis joenssoni, Euxestonotus sabahensis, Leptacis cheyi (all from Malaysia), L. jani (from Laos), L. maliauensis (from Malaysia), L. ongkudoni (from Malaysia), L. pederseni (from Laos), L. reticulaticeps (from Malaysia), L. solodovnikovi, L. vilhelmseni (both from Laos), Sacespalus viklundi (from Malaysia), Synopeas laosianum (from Laos), S. opaciceps and S. waidii (both from Malaysia). The following species described in Leptacis by Ushakumari, R., Narendran, T.C., 2007. A taxonomic revision of Leptacis Foerster (Hymenoptera: Platygasteridae) of India. Rec. Zool. Surv. India 107, 7–32 are transferred to Synopeas: L. aeros, L. alus, L. asiaticus, L. benazeer, L. diversus, L. manii, L. mustus, L. nuperus and L. scaposus. Synopeas saltaense is a nom. nov. for S. intermedius Buhl, 2005 preoccupied by S. intermedius (Ushakumari, R., 2004. Diversity of Platygaster Latreille (Hymenoptera: Platygastridae) of Kerala. In Rajmohana, K., Narendran, T.C., Perspectives on biosystematics and biodiversity: Prof. T. C. Narendran commemoration volume. Systematic Entomology Research Scholars Association, University of Calicut, Kozhikode, India, pp. 573–591). New locality records for 20 already known Oriental platygastrid species are given.     

Intraspecific Epitopic Variation in a Carbohydrate Antigen Exposed on the Surface of Trichostrongylus colubriformis Infective L3 Larvae

The carbohydrate larval antigen, CarLA, is present on the exposed surface of all strongylid nematode infective L3 larvae tested, and antibodies against CarLA can promote rapid immune rejection of incoming Trichostrongylus colubriformis larvae in sheep. A library of ovine recombinant single chain Fv (scFv) antibody fragments, displayed on phage, was prepared from B cell mRNA of field-immune sheep. Phage displaying scFvs that bind to the surface of living exsheathed T. colubriformis L3 larvae were identified, and the majority of worm-binding scFvs recognized CarLA. Characterization of greater than 500 worm surface binding phage resulted in the identification of nine different anti-CarLA scFvs that recognized three distinct T. colubriformis CarLA epitopes based on blocking and additive ELISA. All anti-CarLA scFvs were specific to the T. colubriformis species of nematode. Each of the three scFv epitope classes displayed identical Western blot recognition patterns and recognized the exposed surface of living T. colubriformis exsheathed L3 larvae. Surprisingly, each of the anti-CarLA scFvs was able to bind to only a subset of worms. Double-labelling indirect immunofluorescence revealed that the three classes of anti-CarLA scFvs recognize distinct, non-overlapping, T. colubriformis sub-populations. These results demonstrate that individual T. colubriformis L3 larvae display only one of at least three distinct antigenic forms of CarLA on their surface at any given time, and suggest that antigenic variation within CarLA is likely a mechanism of immune evasion in strongylid nematodes.