The role of inner staminodes in the floral display of some relicMagnoliales

The inner staminodes (between stamens and carpels) in some relicMagnoliales (Austrobaileyaceae, Degeneriaceae, Eupomatiaceae, andHimantandraceae) are not just reduced stamens; they are very elaborate organs. InEupomatiaceae, Himantandraceae, and probablyDegeneriaceae they have their own secretory structures which do not occur on the stamens. These play an important role in floral biology. They contribute to the floral coloration pattern; they effect herkogamy by their position and by movements; they provide shelter and food tissue and food secretions (?) for pollinating beetles; they secrete odouriferous oils, mucilage (probably for pollen adherence) and water or nectar (?). For theHimantandraceae a new secretory region on the base of the inner staminode is described. These complicated inner staminodes are extreme specializations of primitive floral types. They have no counterparts in more advanced subclasses of the angiosperms.     

Generation of biologically contained, readily transformable, and genetically manageable mutants of the biotechnologically important Bacillus pumilus

Bacillus pumilus mutants were generated by targeted deletion of a set of genes eventually facilitating genetic handling and assuring biological containment. The well-defined and stable mutants do not form functional endospores due to the deletion of yqfD, an essential sporulation gene; they are affected in DNA repair, as ΔuvrBA rendered them UV hypersensitive and, thus, biologically contained; they are deficient for the uracil phosphoribosyl-transferase (Δupp), allowing for 5-fluorouracil-based counterselection facilitating rapid allelic exchanges; and they are readily transformable due to the deletion of the restrictase encoding locus (ΔhsdR) of a type I restriction modification system. Vegetative growth as well as extracellular enzyme production and secretion are in no case affected. The combination of such gene deletions allows for development of B. pumilus strains suited for industrial use and further improvements.     

Occurrence of fungi in combs of fungus-growing termites (Isoptera: Termitidae, Macrotermitinae)

Fungus-growing termites cultivate their mutualistic basidiomycete Termitomyces species on a substrate called a fungal comb. Here, the Suicide Polymerase Endonuclease Restriction (SuPER) method was adapted for the first time to a fungal study to determine the entire fungal community of fungal combs and to test whether fungi other than the symbiotic cultivar interact with termite hosts. Our molecular analyses show that although active combs are dominated by Termitomyces fungi isolated with direct Polymerase Endonuclease Restriction - Denaturing Gradient Gel Electrophoresis (PCR-DGGE), they can also harbor some filamentous fungi and yeasts only revealed by SuPER PCR-DGGE. This is the first molecular evidence of the presence of non-Termitomyces species in active combs. However, because there is no evidence for a species-specific relationship between these fungi and termites, they are mere transient guests with no specialization in the symbiosis. It is however surprising to notice that termite-associated Xylaria strains were not isolated from active combs even though they are frequently retrieved when nests are abandoned by termites. This finding highlights the implication of fungus-growing termites in the regulation of fungi occurring within the combs and also suggests that they might not have any particular evolutionary-based association with Xylaria species.     

The surface of Bacillus anthracis

Bacillus anthracis is a Gram positive organism possessing a complex parietal structure. An S-layer, a bi-dimensional crystalline layer, and a peptidic capsule surround the thick peptidoglycan of bacilli harvested during infection. A review of the current literature indicates that elements from each of these three structures, as well as membrane components, have been studied. So-called cell-wall secondary polymers, be they attached to the cell-wall or to the membrane play important functions, either per se or because they permit the anchoring of proteins. Some surface proteins, whichever compartment they are attached to, play, as had been hypothesized, key roles in virulence. Others, of yet unknown function, are nevertheless expressed in vivo. This review will focus on well-studied polymers or proteins and indicate, when appropriate, the mechanisms by which they are targeted to their respective locations.     

Mandibular glands in the endoparasitic larva of Uropsylla tasmanica Rothschild (Siphonaptera : Pygiopsyllidae)

An histological study of flea larvae was carried out in order to compare free-living, larvae with the unique endoparasitic larva of Uropsylla tasmanica Rothschild (Siphonaptera : Pygiopsyllidae), a species confined to dasyurid hosts in Tasmania and Victoria, Australia. The free-living species examined were Ctenocephalides felis Bouché (Siphonaptera : Pulicidae) and Odontopsyllus quirosi Gil Collado (Siphonaptera : Leptopsyllidae). Mandibular glands are present in 1st and 3rd instar U. tasmanica, but are absent from 2nd and 3rd instar O. quirosi and all larval instars of C. felis. Such glands in flea larvae have not beeb described previously and they appear to be unique to the endoparasitic U. tasmanica larva. Their presence during the 3rd instar as well as in the 1st instar suggests that although it is possible they play a role in the initial penetration of host skin by the newly hatched larva, they are active in secretion also during the time when the larvae are feeding on host tissue within the dermis.     

Characterization of the unusual basic proteins of cricket spermatid nuclei on the basis of their molecular weights and amino acid compositions

Typical somatic cell type histones are lost from the nucleus during late spermiogenesis in the house cricket; they are replaced by unusual basic proteins specific to the spermatid. We wish to characterize these proteins because they appear to determine the unusual chromatin structures of the spermatid. Molecular weights of the unusual basic proteins were estimated by chromatographing them on Bio-Gel A 0.5 M agarose columns eluted with 6 M guanidine hydrochloride. Two proteins named TH1 and TH2 have molecular weights in the range spanned by the somatic histones. The molecular weight of TH1 is 17 500 and that of TH2 is 15 500. Three additional spermatid proteins were also analyzed by molecular weight determination. They are called here protamines A, B and C, and they have molecular weights in the range typical of protamines. That of A is 6200, of B is 5500 and of C is 3800. They span the range from the large protamines typical of mammalian sperm to the small protamines of salmonid fish. The molecular weights of the TH proteins were also examined by electrophoresis on SDS-polyacrylamide gels. Amino acid compositions determined for TH1 and TH2 show that both are basic proteins rich in arginine relative to lysine. Their compositions are histone-like, but they appear to be distinct histone types rather than variant forms of the somatic histones.     

Nanos functions to maintain the fate of the small micromere lineage in the sea urchin embryo

The translational regulator nanos is required for the survival and maintenance of primordial germ cells during embryogenesis. Three nanos homologs are present in the genome of the sea urchin Strongylocentrotus purpuratus, all of which are expressed with different timing in the small micromere lineage. This lineage is set-aside during embryogenesis and contributes to constructing the adult rudiment. Small micromeres lacking Sp-nanos1 and Sp-nanos2 undergo an extra division and are not incorporated into the coelomic pouches. Further, these cells do not accumulate Vasa protein even though they retain vasa mRNA. Larvae that develop from Sp-nanos1 and 2 knockdown embryos initially appear normal, but do not develop adult rudiments; although they are capable of eating, over time they fail to grow and eventually die. We conclude that the acquisition and maintenance of multipotency in the small micromere lineage requires nanos, which may function in part by repressing the cell cycle and regulating other multipotency factors such as vasa. This work, in combination with other recent results in Ilyanassa and Platynereis dumerilii, suggests the presence of a conserved molecular program underlying both primordial germ cell and multipotent cell specification and maintenance.     

Genetic Factors Affecting Recovery of Nonpoint Mutations in the Region of a Gene Coding for Ornithine Transcarbamylase: Involvement of Both the F Factor in Its Chromosomal State and the recA Gene

Mutants of E. coli K12 that overproduce ornithine transcarbamylase can be identified in Car^- strains because they permit utilization of citrulline as a carbamyl phosphate source, due to reversal of the normal OTCase reaction; they are called Cut mutants (citrulline utilizers). Hfr strains that carry the F factor adjacent to argF (one of two duplicate genes that code for ornithine transcarbamylase in E. coli K12) yield more Cut mutants than do F⁺ or F^- strains, or Hfr strains in which the F factor is not adjacent to argF. When Hfr strains in which the F factor is integrated adjacent to argF are made recA, they yield few Cut mutants. Many of the Cut mutants recovered from one of the Hfr strains used in the investigation (Hfr P4X) are unstable; the properties of these unstable mutations suggest that they carry aberrations in the region of the argF gene. Thus, the increased yields of Cut mutants probably result from aberrations that occur when the F factor is integrated adjacent to argF. The nature of these aberrations is not yet known. The unstable Cut mutants are to a large extent stabilized by recA; such stabilization is one of the properties of duplications. Other data indicate that the aberrations may be more complex than simple gene duplications; in particular properties of segregants and some recombinants derived from unstable Cut mutants are most easily interpreted by assuming that segregation from, and possibly formation of, the unstable mutants occurs in several stages.     

Species complexes in Hericium (Russulales, Agaricomycota) and a new species - Hericium rajchenbergii - from southern South America

Species of the genus Hericium are generally recognized by macro morphology of their basidiomes, while they are very similar in the microscope. As a result, species boundaries are not always clear, and many collections are subsumed under incorrect names. We report on a thorough phylogenetic analysis based on ITS sequences to clarify the application of the most common names in the genus. H. alpestre, H. americanum, and H. erinaceus cannot readily be distinguished by their ITS sequences alone, while they are kept separate by characters from substrate preferences, geographical distribution, and macro morphology. A neotype is selected for H. alpestre. A well supported clade includes H. coralloides together with other, unnamed taxa. One of these, H. rajchenbergii from Argentina, is here described as new to science.     

Evidence suggests that modified setae of the crab spiders Stephanopis spp. fasten debris from the background

Crab spiders (Thomisidae) are known by their ability to change their body colouration via change in epithelial pigments. However, the crab spider genus Stephanopis appears to match the colouration of the bark they are sitting on by having debris attached to its dorsal cuticle. The functional morphology, colouration, and evolution of this phenomenon were investigated in Stephanopis cf. scabra and S. cambridgei. Analysis under the microscope revealed that debris originated from the bark they were sitting on. Using scanning electron microscopy, three different types of setae likely related in the retention of debris were found in S. cf. scabra and one in S. cambridgei. These setae are branched and possess barbs, unlike the more filiform setae found in other crab spider species. In addition, the presence of debris improved the brightness background matching of spiders against the bark, but not hue and chroma matching. Ancestral character state reconstruction suggested that presence of debris evolved two to three times within Thomisidae. The evolution of both masking and colour change among crab spiders indicates that they are under a strong selection to avoid detection.     

Comparisons of the complete sequences of two collagen genes from Caenorhabditis elegans

Several collagen genes have been isolated from the nematode Caenorhabditis elegans. The complete nucleotide sequences of two of these genes, col-1 and col-2, have been determined. These collagen genes differ from vertebrate collagen genes in that they contain only one or two introns, their triple-helical regions are interrupted by nonhelical amino acid sequences and they are smaller. A high degree of nucleotide and amino acid homology exists between col-1 and col-2. In particular, the regions around cysteines and lysines are most highly conserved. The C. elegans genome contains 50 or more collagen genes, the majority of which probably encode cuticle collagens; col-1 and col-2 apparently are members of this large family of cuticle collagen genes.     

Phenylalanine Biosynthesis in Escherichia coli K-12: Mutants Derepressed for Chorismate Mutase P-Prephenate Dehydratase

Mutants were isolated which are derepressed for the synthesis of chorismate mutase P-prephenate dehydratase. No other enzymes involved in the synthesis of phenylalanine are derepressed in these strains. These mutants are able to grow in concentrations of o- and p-fluorophenylalanine that inhibit the growth of AB3259, the strain from which they were derived. They also excrete phenylalanine. Genetic analysis shows that the mutations causing this derepression are closely linked to the structural gene for this enzyme (cotransduction frequency of 95% or more with pheA). The gene in which they occur has been designated pheO since this gene has all of the properties predicted for an operator gene controlling the pheA structural gene. Finally, the pheO mutant alleles have been shown to be dominant in diploids.     

The Search for Significance: A Few Peculiarities in the Distribution of P Values in Experimental Psychology Literature

In this project I investigate the use and possible misuse of p values in papers published in five (high-ranked) journals in experimental psychology. I use a data set of over 135’000 p values from more than five thousand papers. I inspect (1) the way in which the p values are reported and (2) their distribution. The main findings are following: first, it appears that some authors choose the mode of reporting their results in an arbitrary way. Moreover, they often end up doing it in such a way that makes their findings seem more statistically significant than they really are (which is well known to improve the chances for publication). Specifically, they frequently report p values “just above” significance thresholds directly, whereas other values are reported by means of inequalities (e.g. “p<.1”), they round the p values down more eagerly than up and appear to choose between the significance thresholds and between one- and two-sided tests only after seeing the data. Further, about 9.2% of reported p values are inconsistent with their underlying statistics (e.g. F or t) and it appears that there are “too many” “just significant” values. One interpretation of this is that researchers tend to choose the model or include/discard observations to bring the p value to the right side of the threshold.     

Streptococcus faecalis,Bacillus alvei, and sacbrood virus in European foulbrood of the honey bee

Contrary to reports from elsewhere, Streptococcus faecalis or Bacillus alvei did not cause European foulbrood in bee larvae also inoculated with sacbrood virus. The larvae died of sacbrood, by which time S. faecalis had mostly disappeared, although B. alvei multiplied saprophytically, as in European foulbrood, in some of the remains. Larvae that died of sacbrood already contained much sacbrood virus before they were sealed in their cells, when they appeared unaffected by the virus, but when they are most likely to die of European foulbrood, which is caused by Streptococcus pluton, often accompanied by secondary invaders, such as S. faecalis. Therefore, larvae killed by European foulbrood can be expected sometimes to contain much sacbrood virus, particularly as this virus is common.     

Morphological study on the immature stages of the Banana fruit caterpillar,Tiracola plagiata (Walker, 1857) and its close relative,Tiracola aureata Holloway, 1989 (Noctuidae: Noctuinae: Leucaniini) with their host plant information

Imature stages of the Banana fruit caterpillar, Tiracola plagiata (Walker, 1857) and its close relative, Tiracola aureata Holloway, 1989 are described and illustrated. We revealed the following four facts. 1: The sixth instar is estimated to be the last instar larvae in both species based on the width of head capsules. 2: Morphologically they are distinguishable in the third to sixth instar larvae, but not distinguishable in the eggs, first to second instar larvae and pupae by our study. 3: Both species are polyphagous. 4: Some of the formerly known host plant records of T. plagiata should be excluded because they are revealed to be the hostplants of T. aureata.     

Antennal sensilla on cave species of Australian Paratemnopteryx cockroaches (Blattaria : Blattellidae)

The external morphology and distribution of antennal sensilla of cave-dwelling Australian cockroaches, Paratemnopteryx stonei (Races B and C), P. howarthi and P. sp. nov. (Blattaria : Blattellidae), are described using scanning electron microscopy. Eight major types of sensilla were found. Long and medium-length sensilla chaetica are deeply grooved mechano and contact chemo-receptors with a terminal pore; the long type forms 5–11% and the medium-length 7–22% of all sensilla. Sensilla trichodea type 1 are very slender, non-porous, and form 43–60% of all sensilla. Sensilla trichodea type 2 are stouter, shorter and have wall pores; they form 5–14% of the sensilla. Sensilla basiconica type B are very short, non-porous, inflexible-socket receptors that are known to be hygro- and thermo-receptors; they comprise less than 0.6% of the sensilla. Sensilla basiconica type Gl are short, grooved and have a terminal pore; they form 5–11% of all sensilla. Type G2 are longer with indications of a terminal pore and form 7–10% of the sensilla. Sensilla basiconica type P are short with wall pores, and they form 3–9% of the sensilla. Total sensillar numbers ranged from 5700–8900 for P. stonei, depending on the race and sex, 6950–9950 for P. sp. nov. and 11,700-15,100 for the smaller and possibly more epigean-related P. howarthi. Females had 700–3150 fewer sensilla than males. Comparisons are made between Paratemnopteryx and common epigean cockroaches in relation to sensillar types and numbers.     

Biologie comparée des interactions entre les macrophages et Trypanosoma cruzi,Leishmania spp. et Toxoplasma gondii

Macrophages have a central role in the immune system by eliminating a lot of pathogens. Nevertheless, they are often infected by pathogenic microorganisms in particular parasitic protozoa. They thus play the role of host cell by harbouring the intracellular survival and multiplication of these pathogens. Various mechanisms (receptors/ligands interactions, enzymes…) are involved in recognition and adhesion steps. When suitably activated, they become effector cells and they can control infection at least partially through the production of reactive oxygen derivatives. But parasitic protozoa can escape these defence mechanisms. In addition, macrophages are also antigen presenting cells and they are inductor cells of the immune response. Once again, parasitic protozoa interfere with these functions and induce chronic infections. Biology of Trypanosoma cruzi, Leishmania spp. and Toxoplasma gondii will be briefly reviewed to illustrate these various aspects of cellular parasitism.     

Enterococcus infection biology: Lessons from invertebrate host models

The enterococci are commensals of the gastrointestinal tract of many metazoans, from insects to humans. While they normally do not cause disease in the intestine, they can become pathogenic when they infect sites outside of the gut. Recently, the enterococci have become important nosocomial pathogens, with the majority of human enterococcal infections caused by two species, Enterococcus faecalis and Enterococcus faecium. Studies using invertebrate infection models have revealed insights into the biology of enterococcal infections, as well as general principles underlying host innate immune defense. This review highlights recent findings on Enterococcus infection biology from two invertebrate infection models, the greater wax moth Galleria mellonella and the free-living bacteriovorous nematode Caenorhabditis elegans.     

DisAp-dependent striated fiber elongation is required to organize ciliary arrays

Cilia-organizing basal bodies (BBs) are microtubule scaffolds that are visibly asymmetrical because they have attached auxiliary structures, such as striated fibers. In multiciliated cells, BB orientation aligns to ensure coherent ciliary beating, but the mechanisms that maintain BB orientation are unclear. For the first time in Tetrahymena thermophila, we use comparative whole-genome sequencing to identify the mutation in the BB disorientation mutant disA-1. disA-1 abolishes the localization of the novel protein DisAp to T. thermophila striated fibers (kinetodesmal fibers; KFs), which is consistent with DisAp’s similarity to the striated fiber protein SF-assemblin. We demonstrate that DisAp is required for KFs to elongate and to resist BB disorientation in response to ciliary forces. Newly formed BBs move along KFs as they approach their cortical attachment sites. However, because they contain short KFs that are rotated, BBs in disA-1 cells display aberrant spacing and disorientation. Therefore, DisAp is a novel KF component that is essential for force-dependent KF elongation and BB orientation in multiciliary arrays.     

Major gene mutations associated with obesity and diabetes mellitus

Obesity and diabetes mellitus are associated with low or elevated serum leptin and insulin levels (U-like relation). Mutations in LEP and INS are linked to decreases in leptin and insulin while mutations in LEPR and INSR are linked to their increase. Homozygous LEP mutations are associated with the early onset of severe obesity and the diverse impairment of physiological functions. The recessive LEPR mutations are associated with similar pathology in homozygous state. Missense mutations of INS are dominant and induce the synthesis of chimeric proinsulin, which may interfere with the folding and processing of active insulin molecules. In the heterozygous state, they cause insulin deficiency and PND. Recessive INS mutations do not induce the synthesis of anomalous proinsulin, and they are only associated with PND in the homozygous state. Mutations of INSR induce insulin resistance, lipodystrophy, other pathologies, and suggest the important role of insulin in glucose level regulation and in the stimulation of fat accumulation.