Production of second generation triploid and tetraploid rainbow trout by mating tetraploid males and diploid females — Potential of tetraploid fish

Summary First generation tetraploids were produced by hydrostatic pressure treatment before the first cleavage and raised until the adult stage. Their survival and growth were severely depressed when compared to the diploid control: after two years, no ovulated females were found although males produced sperm at 1 and 2 years of age and were mated individually with diploid females. The progenies were consistently normal with high survival rates. They were found to be almost all triploids by karyology, which failed to detect a significant rate of aneuploidies. However, the fertilizing ability of tetraploid males was always low (0 to 97% of the control; average 40%). Several arguments presented here support the hypothesis that diploid spermatozoas, which are wider than haploid ones, would be frequently blocked during their penetration through the micropyle canal. Second generation tetraploids were produced after such matings by heat shocks, causing the retention of the second polar body. Their survival and growth were much more satisfactory than in the first generation, although still lower than in diploid and triploid controls issuing from diploid parents. Performances of second generation triploids were comparable to those of diploids, and slightly better than those of conventional triploids issuing from diploid parents. 94.5% of the second generation tetraploids were male.     

A collection of programs for nucleic acid and protein analysis, written in FORTRAN 77 for IBM-PC compatible microcomputers.

We have developed a collection of programs for manipulation and analysis of nucleotide and protein sequences. The package was written in Fortran 77 on a Sirius1/Victor microcomputer which can be easily implemented on a large variety of other computers. Some of the programs have already been adapted for use on a Vax 11. Our aim was to develop programs consisting of small, comprehensible and well documented units that have very fast execution times and are comfortably interactive. The package is therefore suitable for individual modifications, even with little understanding of computer languages.     

Fibronectin and laminin in the extracellular matrix and basement membrane of sea urchin embryos

Fibronectin and laminin have been found in the extracellular matrix and in the basement membrane of sea urchin embryos during early development. These glycoproteins are also found on the cell surfaces of the outer epithelial layer and on the secondary mesenchyme cells within the blastocoel. The similarity of functions of the extracellular matrix and basement membrane is discussed, as is the similarity of their molecular components. These observations suggest the possibility that fibronectin and laminin form a continuous matrix surrounding the cells which links the outer ECM (hyaline layer) to the inner ECM (basement membrane). Such a network could coordinate the various activities of the embryo during early morphogenesis.     

Identification and characterization of gp TFA-1, a guinea pig T cell surface antigen associated with T cell function

Monoclonal antibodies (Ab) were produced that specifically recognized guinea pig T cells. FACS analysis revealed that Ab 188 bound to the majority of peripheral T lymphocytes of strain 2 and strain 13 guinea pigs and to a minor population of thymocytes. It failed to react with the Ia-bearing guinea pig B cell leukemia line EN-L2C, with macrophages, bone marrow cells, erythrocytes, or thrombocytes. Treatment of T cells with Ab 188 and complement prevented T cell activation. Culturing primed T cells with antigen- or mitogen-pulsed syngeneic or with allogeneic macrophages in the continuous presence of Ab 188 produced a marked, dose-dependent inhibition of T cell proliferation. The antigen defined by Ab 188 was therefore designated guinea pig T lymphocyte function-associated antigen-1, gp TFA-1. The magnitude of inhibition by Ab 188 varied between 65 and 85% whereas three other antibodies to guinea pig T cells had no inhibitory effect on T cell proliferation. Time course experiments revealed that gp TFA-1 is critically involved in an early phase of T cell activation. Maximal inhibition was achieved only if the antibody was present from the beginning of the cell culture; the addition of antibody after 24 hr of culture no longer had an inhibitory effect. Ab 188 did not induce T cell mitogenesis. Two-dimensional analysis (one-dimensional, IEF; two-dimensional, SDS-PAGE) of immunoprecipitates obtained from NP40 lysates of [35S]methionine-labeled T cell blasts indicated that a molecule was specifically precipitated that consisted of two noncovalently associated polypeptide chains with apparent m.w. of 43,000 and 38,000. Both subunits displayed extensive charge heterogeneity focusing at an average isoelectric point of 5.0 and 6.5, respectively. The gp TFA-1 molecule exhibits striking similarities in its functional and structural properties to recently described clonotypically expressed T cell glycoproteins, which were shown to be involved in antigen recognition by T cells in the murine and human systems.     

Experience using two CT-guided stereotactic biopsy methods

15 patients had intracranial CT-guided stereotactic biopsies. Biopsies were performed either with a Riechert-Mundinger stereotactic frame modified for use in the CT or by using the CT scan to establish the relationship of the intracranial lesion to identifiable bony landmarks, and subsequently performing the biopsy in a standard stereotactic frame. Both systems provided safe and accurate methods for obtaining intracranial tissue.     

Wirtskreis und Infektionscyclus eines neu isolierten Bdellovibrio bacteriovorus-Stammes

Zusammenfassung Der neu isolierte Stamm W von Bdellovibio bacteriovorus infiziert und lysiert Rhodospirillum rubrum F und alle anderen untersuchten Athiorhodaceae, nicht aber Pseudomonas aeruginosa und Spirillum serpens. Er befällt auch zahlreiche Enterobacteriaceae und von den grampositiven Bakterien Streptococcus faecalis und Lactobacillus plantarum.Nach dem Festheften an der Zellwand wird diese in 3–20 min durchdrungen. In 10–60 min ist Bdellovibrio vollständig in die Zelle eingedrungen und hat sich im Raum zwischen Zellwand und cytoplasmatischer Membran angesiedelt.In 3–5 Std wird der gesamte Zellinhalt bis auf die Membranen aufgelöst. In dieser Phase erfolgt die Vermehrung von Bdellovibrio. In den ghosts sind die Parasiten in lebhafter Bewegung. Die Geißel hat einen Gesamtdurchmesser von 29 m und eine Länge von etwa 3 . Sie ist von einer Geißelscheide umgeben, die in Verbindung zur Zellwand steht. Der Durchmesser der Geißel ohne Scheide beträgt etwa 18 m. Bdellovibrio kann oberhalb eines Sauerstoffpartialdruckes von 4–5 mm Hg infizieren und sich vermehren. Der Titer von Bdellovibrio nimmt bei Aufbewahrung in lysierten Kulturen in 36 Tagen von 10⁸ auf 10¹ pfu (plaque forming units) je ml ab. Bei Aufbewahrung in Nährkultur sinkt der Titer nur auf 10⁴ pfu/ml ab. Die Zahl der Plaques im Verhältnis zum Titer der Impfsuspension von Bdellovibrio schwankt in Abhängigkeit vom Wirtsstamm. Wenn man die Plaque-Bildungsrate bei R. rubrum gleich 1 setzt, beträgt sie bei Serratia marcescens 0,0001, bei Proteus vulgaris 10. Bd. bacteriovorus, Stamm W wächst nicht in synthetischer Nährlösung oder Lysaten. Ein geringes Wachstum ohne Zellteilung findet in Zellextrakten von R. rubrum statt. Der Stamm vermehrt sich jedoch in hitzeinaktiviertem R. rubrum. Die Plaque-Bildungsrate ist unter diesen Bedingungen aber sehr niedrig.In Lysaten treten encystierte Dauerformen von Bdellovibrio bacteriovorus auf.

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The host range and the infectious cycle of a new isolated, on gram-positive and gram-negative bacteria parasiting Bdellovibrio bacteriovorus strain

Summary Rhodospirillum rubrum and all other investigated Athiorhodaceae are infected and lysed by the new isolated strain W of Bdellovibrio bacteriovorus. This strain W parasites on numerous Enterobacteriaceae and the gram-positive bacteria Streptococcus faecalis and Lactobacillus plantarum, but not on Pseudomonas aeruginosa and Spirillum serpens.After attachment of Bdellovibrio to the host, the cell wall is penetrated in 3 to 20 min. In 10 to 60 min Bdellovibrio has completely entered the host cell. He remains in the space between cell wall and cytoplasmic membrane of the host.The host cell is completely lysed within 3 to 5 hours. During this phase the size and cell number of Bdellovibrio are increased and a new flagellum is likely to be formed. In the ghosts of the host cell a strong movement is observed. The single polar flagellum of Bdellovibrio has a diameter of 29 m. The flagellum consists of an inner core ( 18 m) and an outer sheath which is continued into the cell wall. Bdellovibrio is able to grow and to infect only under aerobic or semiaerobic conditions (oxygen partial pressure 4 to 5 mm Hg and more). The titer of Bdellovibrio is gradually decreased from 10⁸ to 10¹ plaque forming units (pfu) per ml, when kept in the lysate for 36 days. In a synthetic medium there is a diminution of 10⁴ pfu/ml only. The plating efficiency is dependent of the host strain. If the plating efficiency of Bdellovibrio with Rhodospirillum rubrum is 1.0, the rate varies from 0.0001 with Serratia marcescens to 10 with Proteus vulgaris. Bdellovibrio bacteriovorus strain W does not grow in a synthetic medium. However, it grows but does not multiply in cell free extracts of Rhodospirillum rubrum. The parasite is also able to infect and lyse heat inactivated R. rubrum. But the plating efficiency in this case is very low.It has been observed that in lysed cells of R. rubrum certain amount of Bdellovibrio is encysted. The morphology and fine structure of these cells is quite different from the normal virulent type.