Cell shape analysis of random tessellations based on Minkowski tensors

To which degree are shape indices of individual cells of a tessellation characteristic for the stochastic process that generates them? Within the context of stochastic geometry and the physics of disordered materials, this corresponds to the question of relationships between different stochastic models. In the context of image analysis of synthetic and biological materials, this question is central to the problem of inferring information about formation processes from spatial measurements of resulting random structures. We address this question by a theory-based simulation study of shape indices derived from Minkowski tensors for a variety of tessellation models. We focus on the relationship between two indices: an isoperimetric ratio of the empirical averages of cell volume and area and the cell elongation quantified by eigenvalue ratios of interfacial Minkowski tensors. Simulation data for these quantities, as well as for distributions thereof and for correlations of cell shape and volume, are presented for Voronoi mosaics of the Poisson point process, determinantal and permanental point processes, and Gibbs hard-core and random sequential absorption processes as well as for Laguerre tessellations of polydisperse spheres and STIT- and Poisson hyperplane tessellations. These data are complemented by mechanically stable crystalline sphere and disordered ellipsoid packings and area-minimising foam models. We find that shape indices of individual cells are not sufficient to unambiguously identify the generating process even amongst this limited set of processes. However, we identify significant differences of the shape indices between many of these tessellation models. Given a realization of a tessellation, these shape indices can narrow the choice of possible generating processes, providing a powerful tool which can be further strengthened by density-resolved volume-shape correlations.Comment: Chapter of the forthcoming book "Tensor Valuations and their Applications in Stochastic Geometry and Imaging" in Lecture Notes in Mathematics edited by Markus Kiderlen and Eva B. Vedel Jense

Mammalian cell entry genes in Streptomyces may provide clues to the evolution of bacterial virulence

Understanding the evolution of virulence is key to appreciating the role specific loci play in pathogenicity. Streptomyces species are generally non-pathogenic soil saprophytes, yet within their genome we can find homologues of virulence loci. One example of this is the mammalian cell entry (mce) locus, which has been characterised in Mycobacterium tuberculosis. To investigate the role in Streptomyces we deleted the mce locus and studied its impact on cell survival, morphology and interaction with other soil organisms. Disruption of the mce cluster resulted in virulence towards amoebae (Acanthamoeba polyphaga) and reduced colonization of plant (Arabidopsis) models, indicating these genes may play an important role in Streptomyces survival in the environment. Our data suggest that loss of mce in Streptomyces spp. may have profound effects on survival in a competitive soil environment, and provides insight in to the evolution and selection of these genes as virulence factors in related pathogenic organisms

Novel Two-Component Systems Implied in Antibiotic Production in Streptomyces coelicolor

The abundance of two-component systems (TCSs) in Streptomyces coelicolor A3(2) genome indicates their importance in the physiology of this soil bacteria. Currently, several TCSs have been related to antibiotic regulation, and the purpose in this study was the characterization of five TCSs, selected by sequence homology with the well-known absA1A2 system, that could also be associated with this important process. Null mutants of the five TCSs were obtained and two mutants (ΔSCO1744/1745 and ΔSCO4596/4597/4598) showed significant differences in both antibiotic production and morphological differentiation, and have been renamed as abr (antibiotic regulator). No detectable changes in antibiotic production were found in the mutants in the systems that include the ORFs SCO3638/3639, SCO3640/3641 and SCO2165/2166 in any of the culture conditions assayed. The system SCO1744/1745 (AbrA1/A2) was involved in negative regulation of antibiotic production, and acted also as a negative regulator of the morphological differentiation. By contrast, the system SCO4596/4597/4598 (AbrC1/C2/C3), composed of two histidine kinases and one response regulator, had positive effects on both morphological development and antibiotic production. Microarray analyses of the ΔabrC1/C2/C3 and wild-type transcriptomes revealed downregulation of actII-ORF4 and cdaR genes, the actinorhodin and calcium-dependent antibiotic pathway-specific regulators respectively. These results demonstrated the involvement of these new two-component systems in antibiotic production and morphological differentiation by different approaches. One is a pleiotropic negative regulator: abrA1/A2. The other one is a positive regulator composed of three elements, two histidine kinases and one response regulator: abrC1/C2/C3

Hybridization but No Evidence for Backcrossing and Introgression in a Sympatric Population of Great Reed Warblers and Clamorous Reed Warblers

Hybridization is observed frequently in birds, but often it is not known whether the hybrids are fertile and if backcrossing occurs. The breeding ranges of the great reed warbler (Acrocephalus arundinaceus) and the clamorous reed warbler (A. stentoreus) overlap in southern Kazakhstan and a previous study has documented hybridization in a sympatric population. In the present study, we first present a large set of novel microsatellite loci isolated and characterised in great reed warblers. Secondly, we evaluate whether hybridization in the sympatric breeding population has been followed by backcrossing and introgression

Introgression and rapid species turnover in sympatric damselflies

<p>Abstract</p> <p>Background</p> <p>Studying contemporary hybridization increases our understanding of introgression, adaptation and, ultimately, speciation. The sister species <it>Ischnura elegans </it>and <it>I. graellsii </it>(Odonata: Coenagrionidae) are ecologically, morphologically and genetically similar and hybridize. Recently, <it>I. elegans </it>has colonized northern Spain, creating a broad sympatric region with <it>I. graellsii</it>. Here, we review the distribution of both species in Iberia and evaluate the degree of introgression of <it>I. graellsii </it>into <it>I. elegans </it>using six microsatellite markers (442 individuals from 26 populations) and five mitochondrial genes in sympatric and allopatric localities. Furthermore, we quantify the effect of hybridization on the frequencies of the genetically controlled colour polymorphism in females of both species.</p> <p>Results</p> <p>In a principal component analysis of the microsatellite data, the first two principal components summarised almost half (41%) of the total genetic variation. The first axis revealed a clear separation of <it>I. graellsii </it>and <it>I</it>. <it>elegans </it>populations, while the second axis separated <it>I. elegans </it>populations. Admixture analyses showed extensive hybridization and introgression in <it>I. elegans </it>populations, consistent with <it>I. elegans </it>backcrosses and occasional F₁-hybrids, suggesting hybridization is on-going. More specifically, approximately 58% of the 166 Spanish <it>I. elegans </it>individuals were assigned to the <it>I. elegans </it>backcross category, whereas not a single of those individuals was assigned to the backcross with <it>I. graellsii</it>. The mitochondrial genes held little genetic variation, and the most common haplotype was shared by the two species.</p> <p>Conclusions</p> <p>The results suggest rapid species turnover in sympatric regions in favour of <it>I. elegans</it>, corroborating previous findings that <it>I. graellsii </it>suffers a mating disadvantage in sympatry with <it>I. elegans</it>. Examination of morph frequency dynamics indicates that hybridization is likely to have important implications for the maintenance of multiple female morphs, in particular during the initial period of hybridization.</p

A rare leucine codon in adpA is implicated in the morphological defect of bldA mutants of Streptomyces coelicolor

Streptomycetes are mycelial bacteria that produce sporulating aerial hyphae on solid media. Bald (bld) mutants fail to form aerial mycelium under at least some conditions. bldA encodes the only tRNA species able to read the leucine codon UUA efficiently, implying the involvement of a TTA-containing gene in initiating aerial growth. One candidate for such a gene was bldH, because the bldH109 mutant of Streptomyces coelicolor resembles bldA mutants in some aspects. In the work reported here, adpAc, an S. coelicolor gene similar to the Streptomyces griseus A factor-regulated adpAg, was found to complement the bldH109 mutant partially at both single and multiple copies. The sequence of adpAc from the bldH109 mutant revealed a frameshift. A constructed in frame deletion of adpAc conferred a bald colony phenotype, and the mutant behaved like bldA mutants and bldH109 in its pattern of extracellular signal exchange. Both adpAc and adpAg contain a TTA codon. A TTA-free version of adpAc was engineered by replacing the TTA leucine codon with a cognate TTG leucine codon. The adpA(TTA→TTG) gene could partially restore aerial mycelium formation to a bldA mutant when it was followed in cis by the gene ornA, as in the natural chromosomal arrangement. This indicated that the UUA codon in adpAc mRNA is the principal target through which bldA influences morphological differentiation. It also implied that translational arrest at the UUA codon in adpAc mRNA caused a polar effect on the downstream ornA, and that the poor translation of both genes contributes extensively to the deficiency of aerial mycelium formation in bldA mutants. Unlike the situation in S. griseus, adpAc transcription does not depend on the host’s γ-butyrolactone signalling system, at least in liquid cultures. In addition, sigma factor BldN, which is the homologue of an S. griseus sigma factor AdsA that is absent from adpAg mutants of S. griseus, was present in the constructed adpAc null mutant of S. coelicolor

Microstructural characterisation of open foams using 3d images

Open cell foams are a promising and versatile class of porous materials. Open metal foams serve as crash absorbers and catalysts, metal and ceramic foams are used for filtering, and open polymer foams are hidden in every-day-life items like mattresses or chairs. Due to their high porosity, classical 2d quantitative analysis can give only very limited information about the microstructure of open foams. On the other hand, micro computed tomography (&#956;CT) yields high quality 3d images of open foams. Thus 3d imaging is the method of choice for open cell foams. In this report we summarise a variety of methods for the analysis of the resulting volume images of open foam structures developed or refined and applied at the Fraunhofer ITWM over a course of nearly ten years: The model based determination of mean characteristics like the mean cell volume or the mean strut thickness demanding only a simple binarisation as well as the image analytic cell reconstruction yielding empirical distributions of cell characteristics

Histochemical and contractile properties following neonatal denervation in the fast-twitch extensor digitorum longus muscle of the mouse

Mature fast-twitch skeletal muscle depends on innervation for complete differentiation and maintenance of its fast-twitch histochemical and contractile properties. The motorneuron plays a dominant role in the development of many of these characteristics, and therefore developing muscle is even more dependent on its innervation. This study was done to look at some of the changes in histochemical and contractile properties brought about by denervation, and to examine the effects of neonatal denervation on the pattern of development of these properties in the extensor digitorum longus muscle (EDL) of the C57/BL6 mouse, at 7, 14 and 21 days of age. At 1 day of age, a unilateral sciatic neurectomy was performed. Silver and acetylcholinesterase staining was used to confirm that reinnervation does not occur by this method. Extrafusal fiber types were examined histochemically for oxidative enzyme and myosin ATPase activities (pH 4.2 and 9.4). Isometric contractile properties, including time-to-peak twitch tension, time from peak twitch tension to one-half peak twitch tension, twitch tension, tetanus tension, post-tetanic twitch potentiation, maximum velocity of unloaded shortening and resistance to fatigue were measured, in vitro, at 20°C. Denervated and control muscles were examined at 7, 14 and 21 days of age, and normal muscles were also examined at 1 day of age. At 1 day of age, all fibers stained for myosin ATPase following alkaline and acid preincubation, and all fibers were uniformly oxidative, according to NADH staining, typical of immature fibers. Over the next 21 days, normal muscles showed an increase in twitch and tetanus tension, post-tetanic twitch potentiation and velocity of unloaded shortening, with a reduction in time-to-peak twitch tension, time to one-half relaxation and in resistance to fatigue. Histochemically, the extrafusal fibers differentiated into mature fast fibers with H6% of fibers being type IIA (anaerobic in the mouse), 40% type IIB (aerobic), with the remainder being type I. In the denervated muscle there was a significant prolongation of time-to-peak twitch tension and half-relaxation compared with controls. In addition, post-tetanic twitch potentiation was absent, the maximum velocity of unloaded shortening remained low, and there was marked resistance to fatigue, at all ages studied. All denervated muscles showed significant atrophy. Histochemically, there was evidence of some continued maturation at 7 days of age, but by 14 days only two fiber groups could be distinguished. Of these, 70% were atypical fibers exhibiting dual staining for myosin ATPase and were oxidative, as seen in immature fibers. The second group stained as type IIA but, unlike the control muscles, they were oxidative. The denervated muscles returned toward slow properties of immature muscles, but the changes in the physiological properties preceeded changes in fiber type. These results suggest that removal of neural influence neonatally to extensor digitorum longus results in loss of control over the differentiation into fast-twitch muscle. In addition, there is an immediate and significant slowing of the contractile properties and although denervated muscle continues to mimick the pattern of development of normal muscle, it becomes stalled at 14 days of age, preventing further maturation. Further studies are suggested that may identify the factors contributing to the changes seen in this study.Medicine, Faculty ofGraduat