Clear Media for the Recovery of Pasteurella tularensis

Peptic digests of blood and hemoglobin were investigated as substitutes for the blood used in the preparation of glucose-cysteine-blood agar plating medium for the recovery of the virulent Schu strain of Pasteurella tularensis. Digest media so prepared were found to be satisfactory for the quantitative recovery of freshly grown cells but not for cells stored longer than several days. The addition of appropriate quantities of human plasma, bovine sera, or soluble starch rendered the digest media appropriate for use with stored cultures. The peptic digest-plasma (PDP) and peptic digest-starch (PDS) media were evaluated and found satisfactory for the quantitative recovery of P. tularensis Schu from freshly prepared and stored cultures, and from aerosols produced therefrom. With cultures stored longer than 6 weeks, the starch modification (PDS) was not as satisfactory as, and the plasma variation (PDP) was better than, glucose-cysteine-blood agar (GCBA) for the recovery of the organisms. PDP was superior to either GCBA or PDS medium for the recovery of the weakly virulent Jap 4 and Niieg-blue strains of P. tularensis.     

A COMPARISON OF THE CHANGES IN FINE STRUCTURE OF L CELLS DURING SINGLE CYCLES OF VIRAL MULTIPLICATION, FOLLOWING THEIR INFECTION WITH THE VIRUSES OF MENGO AND ENCEPHALOMYOCARDITIS

The virus of encephalomyocarditis (EMC), examined by the negative-contrast method, is indistinguishable from the serologically related Mengovirus. The particles are 270 to 280 A in diameter. The surface of EMC is composed of an undetermined number of subunits. Frequent sampling of infected cells was carried out throughout one-step cycles of viral multiplication to observe cytopathic changes occurring in L cells infected by these two related RNA viruses. EMC and Mengovirus, which multiply at equal rates, in most respects elicit similar alterations in cell fine structure. Rearrangement and changes in nuclear material accompanied by formation of small vesicles in the centrosphere region commence at 4 to 6 hours after infection. Thereafter a progressive degeneration of the nucleus and vesiculation of the cytoplasm are observed up to 18 to 20 hours. Increased numbers of small dense granules, indistinguishable from ribonucleoprotein particles, appear in the cytoplasm between 8 and 14 hours after infection. L cells infected with Mengovirus become permeable to Erythrocin more slowly than those infected with EMC. Only in the case of Mengovirus infection are large aggregates of dense material first observed in the cytoplasm at 8 hours, followed by the appearance of crystals probably composed of Mengovirus particles, at 12 hours. Differences in the rates of cell permeability after infection with EMC and Mengovirus are discussed in relation to formation of virus crystals and plaque-type mutants.     

THALASSIOMYCETES II. NEW GENERA AND SPECIES OF DEUTEROMYCETES

Meyers , Samuel P. (U. Miami, Coral Gables, Fla.) and Royall T. Moore . Thalassiomycetes II. New genera and species of Deuteromycetes. Amer. Jour. Bot. 47(5) : 345-349. Illus. 1960.–On the basis of taxonomic studies, 3 new monotypic thalassic genera are erected. These are: Cirrenalia, type C. macrocephala (=Helicoma macrocephala Kohlmeyer) ; Cremasteria, type C. cymatilis; Culcitalna, type C. achraspora . Also described is a new species of Humicola, H. alopallonella, which constitutes the first report of this genus from the marine environment.     

Aspects of the life cycle of marine nematodes

Summary 1. Life cycles of approximately one month are recorded for laboratory maintained cultures of chromadorid, monhysterid and oncholaimid nematodes.2. Amphimictic and parthenogenetic reproduction occurs in the species investigated. Reproduction inMonhystera parelegantula is by parthenogenesis.3. The chromadoridChromadorina epidemos and the oncholaimidViscosia macramphida are able to reproduce by either amphimixis or parthenogenesis.4.Acanthonchus cobbi, Chromadora macrolaimoides andEuchromadora gaulica are amphimitically reproducing species.

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Aspekte des Lebenszyklus mariner Nematoden

Kurzfassung Bei einigen marinen Nematoden, die in Biscayne Bay (Florida) gesammelt und im Labor gezüchtet worden sind, vollzieht sich der gesamte Lebenszyklus ungefähr innerhalb eines Monats. BeiAcanthonchus cobbi, Chromadora macrolaimoides undEuchromadora gaulica ist zweigeschlechtliche Fortpflanzung festgestellt worden.Monohystera parelegantula vermehrt sich parthenogenetisch. Ein möglicherweise durch Umwelteinflüsse bedingter Wechsel von bisexueller und parthenogenetischer Fortpflanzung tritt beiChromadora epidemos undViscosia macramphida auf.