Lymphocyte emperipolesis into autologous monocytes in leukocyte cultures exposed to mitogenic lectins

Virchows Archiv B Cell Pathology - Lymphocyte-monocyte synergistic interaction in cooperative response to mitogens and antigens is well established. This paper describes a less known —...     

ULTRASTRUCTURAL ASPECTS OF SEXUAL REPRODUCTION IN THE RED TIDE DINOFLAGELLATE GONYAULAX TAMARENSIS1

The marine dinoflagellate Gonyaulax tamarensis Lebour is best known for its propensity to form blooms known as red tides in coastal waters worldwide. This paper examines the sexual cycle of this organism using light and electron microscopy. Sexual reproduction begins with contact between thecate gametes which subsequently shed their thecae to fuse along their pellicular layers. Nuclear fusion occurs well after cytoplasmic fusion and is characterized by several distinctive features: a highly vesiculate nucleoplasm without microtubules; nucleoli and V-shaped chromosomes abut the nuclear envelope distal to the region of nuclear contact; and each chromosome possesses a longitudinal line, the central chromosomal axis. Fusion results in a planozygote with numerous cytoplasmic storage products and a slightly thickened layer beneath the pellicle. Subsequent loss of thecal plates and a thickening of the sub-pellicular layer results in a non-motile hypnozygote. A newly-formed hypnozygote possesses numerous minute papillae along its outer surface, formed by the up-folding of the accumulating wall layer. Maturation of the hypnozygote wall results in a smooth three-layered wall, the outermost layer of which is the pellicular layer. Hypnozygote germination produces a large quadriflagellate plan-omeiocyte with a single nucleus and thecal plates identical to vegetative cells. Two subsequent divisions, presumably meiotic, result in Jour cells morphologically identical to vegetative cells.     

ROLE OF GOLGI APPARATUS IN MUCILAGE PRODUCTION AND CYST FORMATION IN EUGLENA GRACILIS (EUGLENOPHYCEAE)1

Dark grown cells of Euglena gracilis Klebs (strain Z Pringsheim) encyst when placed in minus nitrogen media for 48–72 h in the dark. The number of cisternae per dictyosome decreases from 10–20 to 6–12 during encystment. Cisternae dilate and fill with mucilage within 12–18 h after induction. The material is secreted into the reservoir and deposited onto the cell surface. The encysting cells rotate as they develop resulting in the deposition of a thick mucilaginous layer over the cell surface. The secretion product has been identified as polysaccharide with the periodic acid-silver methenamine reaction. Mucilage has not been observed in the endoplasmic reticulum adjacent to the pellicle. The product present in the dictyosornes and on the cell surface react identically to the silver reagent.     

Phylogenetic Reappraisal of the Genus Monomorphina (Euglenophyceae) Based on Molecular and Morphological Data

A morphological and molecular examination of the genus Monomorphina was conducted on 46 strains isolated mainly from Korea. The strains were divided into two types based on morphological data: Monomorphina aenigmatica and M. pyrum ‐ like species. Phylogenetic analysis based on a combined data set of nuclear SSU and LSU and plastid SSU and LSU rDNA showed that the strains could be divided into eight clades: Clade A of M. aenigmatica, Clade B of the isolates (M. pyropsis) from Michigan, USA, Clade C of M. pseudopyrum, Clade D of the isolates (M. pyroria) from Bremen, Germany, Clade E of M. soropyrum, Clade F of M. pyriformis, Clade G of M. parapyrum, and Clade H of M. pyrum. Six of these clades came from strains that would be considered M. pyrum sensu Kosmala et Zakry?, one of which could be recognized as a traditional species (M. pyrum) and five were designated as new species; each species had unique molecular signatures at nr SSU rDNA helix 17 and 17′ and spacer E23_14′‐E23_15. The species of Monomorphina had a wide range of genetic diversity with interspecies sequence similarity of 85.6%–97.1% and intraspecies similarity of 96.4%–99.9%. Our results suggested that genetic diversity found in the M. pyrum complex justifies the recognition of a minimum of eight species within this genus, based on specific molecular signatures and gene divergence of the nr SSU rDNA sequences.     

Cryptic Speciation in the Genus Cryptoglena (Euglenaceae) Revealed by Nuclear and Plastid SSU and LSU rRNA Gene

The photosynthetic euglenoid genus Cryptoglena is differentiated from other euglenoid genera by having a longitudinal sulcus, one chloroplast, two large trough‐shaped paramylon plates positioned between the chloroplast and pellicle, and lack of metaboly. The genus contains only two species. To understand genetic diversity and taxonomy of Cryptoglena species, we analyzed molecular and morphological data from 25 strains. A combined data set of nuclear SSU and LSU and plastid SSU and LSU rRNA genes was analyzed using Bayesian, maximum likelihood, maximum parsimony, and distance (neighbor joining) methods. Although morphological data of all strains showed no significant species‐specific pattern, molecular data segregated the taxa into five clades, two of which represented previously known species: C. skujae and C. pigra, and three of which were designated as the new species, C. soropigra, C. similis, and C. longisulca. Each species had unique molecular signatures that could be found in the plastid SSU rRNA Helix P23_1 and LSU rRNA H2 domain. The genetic similarity of intraspecies based on nr SSU rDNA ranged from 97.8% to 100% and interspecies ranged from 95.3% to 98.9%. Therefore, we propose three new species based on specific molecular signatures and gene divergence of the nr SSU rDNA sequences.     

Chloroplast Genome Evolution in the Euglenaceae

Over the last few years multiple studies have been published outlining chloroplast genomes that represent many of the photosynthetic euglenid genera. However, these genomes were scattered throughout the euglenophyceaean phylogenetic tree, and focused on comparisons with Euglena gracilis. Here, we present a study exclusively on taxa within the Euglenaceae. Six new chloroplast genomes were characterized, those of Cryptoglena skujai, E. gracilis var. bacillaris, Euglena viridis, Euglenaria anabaena, Monomorphina parapyrum, and Trachelomonas volvocina, and added to six previously published chloroplast genomes to determine if trends existed within the family. With this study: at least one genome has now been characterized for each genus, the genomes of different strains from two taxa were characterized to explore intraspecific variability, and a second taxon has been characterized for the genus Monomorphina to examine intrageneric variability. Overall results showed a large amount of variability among the genomes, though a few trends could be identified both within Euglenaceae and within Euglenophyta. In addition, the intraspecific analysis indicated that the similarity of a genome sequence between strains was taxon dependent, and the intrageneric analysis indicated that the majority of the evolutionary changes within the Euglenaceae occurred intergenerically.     

RECONSTRUCTION OF THE FEEDING APPARATUS IN PLOEOTIA COSTATA (EUGLENOPHYTA) AND ITS RELATIONSHIP TO OTHER EUGLENOID FEEDING APPARATUSES

The ultrastructure of the feeding apparatus in Ploeotia costata Farmer and Triemer was determined and compared to other euglenoid feeding apparatuses. The feeding apparatus opened subapically onto the ventral surface and extended nearly the entire length of the cell. It consisted of four parts at the anterior surface: a comb, cytostome/pocket, vanes, and supporting rods. The comb was a multilayered structure of three horizontal microtubular rows encased in cement and formed the dorsal lip of the apparatus. The cytostome/pocket was located between the comb and the supporting rods, tapered into the cell as the cytopharynx and was surrounded by five vanes. The electron-opaque vanes extended the entire length of the feeding apparatus and were lined with microtubules for most of their length. Finally, two cement supporting rods that were joined by a crosspiece at the anterior end formed the ventral lip. The rods separated briefly before merging with the vanes. As the merged rods and vanes descended into the cell, they gradually narrowed and terminated. Comparisons of the feeding apparatus with Ploeotia vitrea, Diplonema ambulator, Lentomonas applanatum, and other euglenoids have led to the conclusion that the Type II feeding apparatus is found only in Ploeotia species.     

ULTRASTRUCTURE OF THE DINOFLAGELLATE PERIDINIUM CINCTUM F. OVOPLANUM. I. VEGETATIVE CELL ULTRASTRUCTURE

Vegetative cells of Peridinium cinctum f. ovoplanum have a dense cytoplasm containing those organelles characteristic of eukaryotic cells. Thecal plates have a fibrillar substructure with numerous 200-nm pores. Chloroplasts are radially arranged and contain a simple internal pyrenoid. An eyespot is associated with the chloroplast. The large, centrally located nucleus contains over 100 chromosomes dispersed in a granular nucleoplasm. Chromosomal bands with a periodicity of 86 nm are present perpendicular to the long axis of the chromosome. Numerous chromosomes are attached to the nuclear envelope. Peridinium cinctum vegetative cell morphology is compared to other dinoflagellates examined.     

Evolutionary History of the Enzymes Involved in the Calvin–Benson Cycle in Euglenids

Euglenids are an ancient lineage that may have existed as early as 2 billion years ago. A mere 65 years ago, Melvin Calvin and Andrew A. Benson performed experiments on Euglena gracilis and elucidated the series of reactions by which carbon was fixed and reduced during photosynthesis. However, the evolutionary history of this pathway (Calvin–Benson cycle) in euglenids was more complex than Calvin and Benson could have imagined. The chloroplast present today in euglenophytes arose from a secondary endosymbiosis between a phagotrophic euglenid and a prasinophyte green alga. A long period of evolutionary time existed before this secondary endosymbiotic event took place, which allowed for other endosymbiotic events or gene transfers to occur prior to the establishment of the green chloroplast. This research revealed the evolutionary history of the major enzymes of the Calvin–Benson cycle throughout the euglenid lineage and showed that the majority of genes for Calvin–Benson cycle enzymes shared an ancestry with red algae and/or chromophytes suggesting they may have been transferred to the nucleus prior to the acquisition of the green chloroplast.