The existence of a pleomorphic development cycle is demonstrated in epitheliocystis organisms obtained from fish of the following families: Sparidae, Sparus aurata L.; Mugilidae, Liza ramada (Risso), Liza aurata (Risso) and Mugil cephalus L.; Cichlidae, Tilapia mossambica (Peters) and Tilapia aurea x nilotica; and Serranidae, Dicentrarchus labrax L. Ultrastructure of the successive developmental stages, primary long cells, intermediate long cells and small cells are described as well as the division process between stages. An additional stage, the round cell, was found in infected chloride cells. The affinities between epitheliocystis organisms and known chlamydial organisms of vertebrates and invertebrates are discussed.
85 Vibrio phages, 84 of them tailed and 1 filamentous, were surveyed. The tailed phages belonged to six basic morphotypes and to the Myoviridae, Siphoviridae, or Podoviridae families. 63 phages were classified into 18 species. The filamentous phage is a member of the Inovirus genus of the Inoviridae family. Vibrio phages are very heterogenous and include some morphologically interesting viruses. Several Vibrio phages closely resemble phages of other gram-negative bacteria, possibly indicating phylogenetic relationships between their hosts.
A method has been developed to separate the cell envelope of encapsulated (type b) Haemophilus influenzae into its outer and inner membrane components with procedures that avoided two problems encountered in fractionation of this envelope: (i) the tendency of the outer and inner membranes to hybridize and (ii) the tendency of the apparently fragile inner membrane to fragment into difficulty sedimentable units. Log phase cells, whose lipids were radioactively labeled, were lysed by passage throdgh a French press. The lysate was applied to a discontinuous sucrose gradient, and envelope-rich material was collected by centrifugation onto a cushion of dense sucrose under carefully controlled conditions. This material was then further fractionated by isopycnic centrifugation in a sucrose gradient to yield four membrane fractions which were partially characterized. On the basis of their radioactivity, buoyant density, ultrastructure, polypeptide composition, and content of phospholipid, protein, lipopolysaccharide, and succinic dehydrogenase, these fractions were identified as follows: fraction 1, outer membrane vesicles with very little inner membrane contamination (<4%); fraction 2, outer membrane vesicles containing entrapped inner membrane; fraction 3, a protein-rich fraction of inner membrane; fraction 4, a protein-poor fraction of inner membrane. Fractions 3 and 4 contained about 25% outer membrane contamination.
Virus was isolated from the brain and pancreatic tissues of Atlantic menhaden with 'spinning' disease. The hiological, physical and chemical properties ofthe isolate were similar to those of infectious pancreatic necrosis virus. Inoculation of the virus into healthy menhaden resulted in the characteristic signs and mortality associated with the natural disease.
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