Contributions to the Life Cycle of Peneroplis planatus (Fichtel and Moll) Montfort

Direct observations of schizonts and agamonts releasing megalospheres clarified the asexual phase of the life cycle of Peneroplis planatus and made it most probable that this species has a paratrimorphic life cycle. Specimens with maximum lengths between 837 and 3,503 μm released about 500 to 1,500 megalospheric juveniles, which possessed two chambers (proloculi and flexostyles) prior to emergence from the parental shell. The presence of gamonts was not shown and was only implied by the occurrence of the agamonts. Since agamonts and schizonts have been found from December to May and since asexual reproduction occurs in spring in Elat, sexual reproduction probably occurs at another time of year (June to December). More detailed studies of this species need to be conducted throughout the year to improve our knowledge of the life cycle of this species.     

Allogromia laticollaris: A Foraminiferan with an Unusual Apogamic Metagenic Life Cycle*

SYNOPSIS. The life cycles of 3 strains of Allogromia laticollaris, a monothalamous foraminiferan, have been studied. Each of the strains had a different, nonclassical, and basically apogamic, life cycle. The Cold Spring Harbor (CSH) strain regularly alternated between 2 agamontic forms: agamont I (uninucleate and diploid) and agamont II (multinucleate and diploid). The complete life cycle took 26 days. Sexual reproduction was rare (0.01%) and autogamous. Small numbers of organisms also underwent budding, binary fission, and cytotomy. The life cycles of the Towd Point (TPA) and Sippewissett (SIP) strains were comparatively abbreviated. Agamont II dominated their typical life cycles, which were completed in 16-18 days. The life cycle of SIP was basically a continuous cycling of the agamont II phase. Approximately 75% of the schizozoites of the TPA strain developed into agamont II. The other 25% alternated between agamont II and agamont I phase. In the CSH strain schizozoites with ～ 8 (range 5-15) nuclei characterized newly formed agamonts II. More nuclei (～ 25) were found in the other 2 strains. The nuclei in young agamonts II underwent rapid morphologic changes leading to a “mushroom-like” chromosome appearance and extensive RNA synthesis. Nucleolar material accumulated at the nuclear periphery and eventually was discharged to the cytoplasm. Karyokinesis took place without the breakdown of the nuclear membrane. The single nucleus of young agamont I forms was proportionally quite large. The S₁ phase occurred quite early (2-5 days) in this part of the life cycle. RNA in the CSH strain formed a compact, subcortical, coarsely granular ring, while in the TPA it was cortical and differentiated into finely granular matrix with randomly distributed coarse granules. During the G₂ phase the nucleus became further enlarged and eventually amoeba-form. Intermediate stages in nuclear breakdown were not found.     

A revision of the genus Homoeogenus Waterhouse with notes on the immature stages of H.laurae sp.n. (Coleoptera: Psephenidae: Eubriinae)

Abstract. The genus Homoeogenus Waterhouse is revised. H.punctatum Waterhouse is redescribed, and two new species, H.chinensis sp.n. (Szechuan) and H.laurae sp.n. (Taiwan), are described. The morphology of the immature stages and the ecology of H.laurae are described. A key to the Oriental genera of Eubriinae is included.     

Evaluation of Virulence Test Procedures for Yersinia enterocolitica Recovered from Foods

Recently a heat stable toxin (ST) and the vw factors of the plague bacteria were identified in Yersinia enterocolitica recovered from human infections. The vw factors were reported to be associated with a plasmid of 42-46 M Daltons in size and were essential for the expression of virulence. With this knowledge virulence tests were developed which allowed us to assess the virulence potential of food-borne Y. enterocolitica regardless of biotypes or serotypes. The tests evaluated were: (1) rapid presumptive test for the virulence plasmid; (2) gel electrophoretic confirmation of the virulence plasmid; (3) Laird's qualitative oral feeding test with thirst stressed mice; (4) quantitative LD₅₀ determination by i.p. injection of the mouse lethal ( i.e. serotype 0:8) strains in saline; (5) quantitative LD₅₀ determination of mouse non-lethal ( i.e. serotype 0:3) strains by i.p. injection of these strains suspended in 1 ml of 10% iron dextran saline solution for virulence enhancement. These tests were evaluated with the serotypes 0:3 and 0:8 strains associated with human infections with and without the virulence plasmid with reproducible results. Then the virulence tests procedures were applied to 79 food isolates. The virulence plasmid was detected only in the Nilehn biotype 2, 3 and 4 strains, but it was absent in Nilehn biotype 1 or the atypical strains that ferment rhamnose. The virulence of food and clinical isolates of Y. enterocolitica can be assayed fairly accurately with the above tests.