Niche partitioning of the genetic lineages of the oak powdery mildew complex

Recent molecular studies have shown that four genetic lineages, probably cryptic species, cause oak powdery mildew in Europe. We tested the hypothesis of niche differentiation between the two most frequent species (Erysiphe alphitoides and Erysiphe quercicola), by determining their relative prevalences at various times during the growing season. E. quercicola was strictly associated with the flag-shoot symptom in a 2-yr sampling campaign of 35 natural oak seedling populations. Additional sampling during Aug.–Sep. in the same stands showed that E. alphitoides predominated in most (70 %) cases. Time-course monitoring of powdery mildew in two natural regenerating oak populations confirmed the inverse patterns of relative abundance for these two species in early and late season. The coexistence of these two closely related species may be due to the use of different strategies, resulting from a trade-off between overwintering (flag-shoots vs. chasmothecia) and late-season performance.     

Acidic pH-Induced Conformations and LAMP1 Binding of the Lassa Virus Glycoprotein Spike

Lassa virus is an enveloped, bi-segmented RNA virus and the most prevalent and fatal of all Old World arenaviruses. Virus entry into the host cell is mediated by a tripartite surface spike complex, which is composed of two viral glycoprotein subunits, GP1 and GP2, and the stable signal peptide. Of these, GP1 binds to cellular receptors and GP2 catalyzes fusion between the viral envelope and the host cell membrane during endocytosis. The molecular structure of the spike and conformational rearrangements induced by low pH, prior to fusion, remain poorly understood. Here, we analyzed the three-dimensional ultrastructure of Lassa virus using electron cryotomography. Sub-tomogram averaging yielded a structure of the glycoprotein spike at 14-Å resolution. The spikes are trimeric, cover the virion envelope, and connect to the underlying matrix. Structural changes to the spike, following acidification, support a viral entry mechanism dependent on binding to the lysosome-resident receptor LAMP1 and further dissociation of the membrane-distal GP1 subunits.     

Distribution of Bacillus megaterium QM B1551 plasmids among other B. megaterium strains and Bacillus species

Bacillus megaterium QM B1551 contains seven plasmids. Two are small rolling circle plasmids and five are theta-replicating plasmids with cross-hybridizing replicons that define a new family of very homologous yet compatible theta replicons. Previous sequencing of several of the plasmids has shown genes with high similarity to those on the genomes and plasmids of other Gram-positive bacteria. To test the possible distribution of these plasmids, nine other B. megaterium strains and 20 other Bacillus or related species were tested for the presence of similar replicons, and specific flanking DNA by both hybridization and PCR. The theta replicons were widespread among the B. megaterium strains, and two had one or more of the rolling circle plasmids, but none of the plasmid replicon regions were observed in the other Bacillus or related species. It appears from the data that even though some plasmids carry genes suggesting horizontal transfer, their replicons seem to be unique to B. megaterium, or rarely present in related species.     

Hematological and hemorheological Determinants of the Six-Minute Walk Test Performance in Children with Sickle Cell Anemia

The six-minute walk test is a well-established submaximal exercise reflecting the functional status and the clinical severity of sickle cell patients. The aim of the present cross-sectional study was to investigate the biological determinants of the six-minute walk test performance in children with sickle cell anemia. Hematological and hemorheological parameters, pulmonary function and the six-minute walk test performance were determined in 42 children with sickle cell anemia at steady state. The performance during the six-minute walk test was normalized for age, sex and height and expressed as percentage of the predicted six-minute walk distance. We showed that a high level of anemia, a low fetal hemoglobin expression and low red blood cell deformability were independent predictors of a low six-minute walk test performance. This study describes for the first time the impact of blood rheology in the six-minute walk test performance in children with sickle cell anemia.     

An acoustic telemetry study of seabream (Sparus aurata L.): first results on activity rhythm,effects of environmental variables and space utilization

The movements of seabream (Sparus aurata L) were recorded in two earthen ponds (250 m² and 400 m²) by tracking fish tagged with miniature acoustic transmitters. Five seabreams, 500 g in weight, were tracked for periods of four or five days. Fish positions were recorded continuously using an acoustic telemetry system. Each of the five tagged seabreams were tracked individually. Two fishes were released schooled with numerous other individuals, two others were released in isolation and one was grouped with three other individuals.The schooled seabreams were more active in general and, in the large school they were diurnal; isolated fishes however, were more active at night. Temperature influences significantly and progressively the fish activity. Activity decreases at night and increases during daylight. Oxygen saturation also influences swimming activity with a general positive relationship.The horizontal distribution of this species was not uniform. Its resting area was generally located around some particular landmarks such as inlet or outlet pipes in the ponds. No feverish feeding competition was observed between individuals of the same school. The feeding area was cleaned rapidly, in less than 10 minutes, without subsequent returns from the resting area to the feeding area.

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Résumé Les déplacements de la daurade (Sparus aurata L.) ont été enregistrés dans deux bassins en terre (250 m² et 400 m²) en suivant des poissons marqués avec des émetteurs acoustiques miniaturisés. Cinq daurades d'un poids individuel de 500 g furent suivies durant des périodes de 4 ou 5 jours. Les positions des poissons ont été enregistrées en continu avec un systéme de télémétrie acoustique. Chacun des cinq poissons marqués fut suivi individuellement. Deux poissons furent regroupés avec de nombreux autres individus, deux autres furent laissés seuls et le dernier fut mis avec trois autres individus.Les daurades groupées étaient en général plus actives et, en grand banc, étaient diurnes; les poissons isolés étaient toutefois plus actifs durant la nuit. La température influence significativement et progressivement l'activité des poissons. L'activité décroît durant la nuit et augmente pendant le jour. Le pourcentage de saturation en oxygéne agit aussi, de façon positive, sur l'activité de nage.La distribution horizontale de cette espéce n'est pas uniforme. Son aire de repos est généralement localisée dans quelques zones particuliéres comme les arrivées et les sorties d'eau. Aucune compétition alimentaire fébrile n'a été observée entre les individus d'un même banc. L'aire de nourrissage est rapidement nettoyée, en moins de 10 minutes, sans retours ultérieurs depuis la zone de repos jusqu' à la zone de nourrissage.

     

The RNA-binding protein Staufen1 impairs myogenic differentiation via a c-myc–dependent mechanism

Recent work has shown that Staufen1 plays key roles in skeletal muscle, yet little is known about its pattern of expression during embryonic and postnatal development. Here we first show that Staufen1 levels are abundant in mouse embryonic muscles and that its expression decreases thereafter, reaching low levels in mature muscles. A similar pattern of expression is seen as cultured myoblasts differentiate into myotubes. Muscle degeneration/regeneration experiments revealed that Staufen1 increases after cardiotoxin injection before returning to the low levels seen in mature muscles. We next prevented the decrease in Staufen1 during differentiation by generating stable C2C12 muscle cell lines overexpressing Staufen1. Cells overexpressing Staufen1 differentiated poorly, as evidenced by reductions in the differentiation and fusion indices and decreases in MyoD, myogenin, MEF2A, and MEF2C, independently of Staufen-mediated mRNA decay. However, levels of c-myc, a factor known to inhibit differentiation, were increased in C2C12 cells overexpressing Staufen1 through enhanced translation. By contrast, the knockdown of Staufen1 decreased c-myc levels in myoblasts. Collectively our results show that Staufen1 is highly expressed during early stages of differentiation/development and that it can impair differentiation by regulating c-myc, thereby highlighting the multifunctional role of Staufen1 in skeletal muscle cells.