Successional Sequences of Microbial Colonization on Three Species of Rhodophycean Macroalgae

The successional sequences of microbial colonization of Centrocerasclavulatum, Bryocladia cuspidata, and Gelidium crinale wereobserved by SEM. Colonization was initiated by filamentous andsmaller rod or coccoid bacteria, and these microbes were replacedby diatom populations in a successional pattern on Centrocerasand Bryocladia. Gelidium was colonized primarily by bacteria.The spatial fouling patterns on each host plant could be correlatedwith plant shape. Differences in epiphyte attachment morphologiescould be correlated in some species with the host plant or withthe position of the epiphyte on the host plant. Diatoms, epiphytes, fouling, microbial colonization, periphyton     

Phytosterols and Other Lipids as Survival Factors for Tetrahymena at 0–5 C

SYNOPSIS. Tetrahymena pyriformis syngen 1, mating type II, (optimal growth temperature ∼ 37 C) ordinarily dies out in 5-14 days at 0-5 C. Dying cells were lumpy, suggesting membrane damage. By supplying crude soy lecithin, survival at 0-5 C was prolonged (after growth in peptone-yeast-dextrin) to at least 22 weeks. Crude soy sterols or sitosterol or stigmasterol, and antioxidant, e.g., Ionox 330 or ascorbylpalmitate, permitted survival of cells in suspension or in growth media for at least 16-22 weeks. These sterols are known to protect against triparanol toxicity, which suggested that triparanol, which blocks cholesterol synthesis in higher animals, might enhance cold-induced injury. Triparanol was more toxic at 0–5 than at 28 C for cell suspensions and cells in growth medium; this toxicity was annulled by crude soy lecithin or β-sitosterol, the only phytosterol tested. The synthetic medium intended as a control on the crude media became toxic at 0–5 C. Protection against cold damage is discussed as a means of elucidating the role of sterols—especially phytosterols—and other lipids in maintaining the integrity of the ciliate cell membrane.     

Physical and Serologic Properties of an Antigen Prepared from Erythrocytes of Horses with Acute Babesiosis*

SYNOPSIS. By means of precipitation with protamine sulfate, a soluble antigen (PS) was obtained from erythrocytes of horses with acute babesiosis due to Babesia caballi and B. equi. This antigen reacted in gel diffusion tests with sera from horses recovered from acute babesiosis. The PS antigen was found to be muco-protein, susceptible to destruction by trypsin and taka-diastase. Analysis of the antigen by paper electrophoresis revealed 2 components which were not present in similar preparations made from erythrocytes of Babesia-free horses. When the PS antigen was heated in boiling water for 30 minutes, a serologically inactive precipitate was formed; however, the supernate remained serologically active and was termed boiled PS (BPS) antigen. This antigen was polysaccharide in nature; its serologic activity was destroyed by taka-diastase. In gel diffusion tests with sera of recovered horses, the PS antigen formed 2 lines of precipitation which coalesced in a single line formed between these sera and the BPS antigen. Both PS and BPS antigens reacted with sera of horses recovered from acute babesiosis in the gel-diffusion test, but not with sera of dogs and rats recovered from acute infection with Babesia canis and Babesia rodhaini, respectively. The serologic specificity of these antigens suggests that they might have application in the serodiagnosis of inapparent Babesia infections of equine animals.     

Efficiency of Selenite Cystine and TT Enrichment Broths for the Detection of Salmonella

Comparisons of selenite cystine (SC) and TT enrichment broths for detecting salmonellas were made with pure culture suspensions, with samples of naturally or artificially contaminated foods and with poultry feed. Selenite cystine recovered higher numbers of salmonellas from pure cultures and ground beef, while TT broth recovered higher numbers from pork sausage and poultry feed. Differences in the recovery of salmonellas from other food products appeared to be insignificant. The use of both SC and TT is thus recommended for maximal recovery of these organisms.     

Reticulo-Endothelial Activity in Haemamoeba (=Plasmodium) gallinacea Infections

SYNOPSIS. The effect of H. gallinacea infection on the phagocytic activity of the reticulo-endothelial system in chicks has been investigated. Changes occurring in the pattern of R.E. activity show that there is initial stimulation of phagocytosis within 24 hr and that this increases up to the 4th and 5th days after which time parasites appear in the blood. Thereafter there is a rapid drop in R.E. activity with a proportional increase in parasitaemia following which death ensues. The importance of the protective value of the reticulo-endothelial system is indicated and it is suggested that a toxin produced by the parasites or by their break-down products is the likely cause of phagocytic depression.     

Growth of Tetrahymena in Carbohydate-Free High-Glutamate Media

SYNOPSIS. In chemically defined media, pH 6.4–6.8, supplementation with glycerol permitted growth equal to that with a carbohydrate supplement. In a pH 5.4 medium described in detail, containing L-glutamic acid 0.25%, supplementation with L-serine (essential for this strain), especially when further supplemented with proline, likewise permitted growth nearly equal to that with carbohydrate. These results are discussed in relation to the question of which components of peptone act as substrates and the resemblances of the Tetrahymena pattern of substrate utilization to that of metazoa.     

Diapause in a Glasgow strain of the flour moth, Ephestia kuehniella

ABSTRACT. The incidence of diapause in Ephestia kuehniella Zeller from an unhealed granary in Scotland was influenced by both photoperiod and temperature. At 25°C, nearly 50% of larvae entered diapause when reared in continuous darkness (DD) and up to 30% did so in short photoperiods. Little diapause was detected around LD 14:10 but a second, smaller peak of about 20% occurred at LD 16:8 and LD 18:6, falling away again to nearly zero in continuous light. More larvae entered diapause when reared continuously at 15 or 20°C than at 25 and 30°C. However, when larvae reared from hatch at 25°C in LD 16:8 were transferred after 1 week to 15°C in LD 9:15, almost twice as many entered diapause as did those reared at 15°C throughout. The sensitive phase for diapause induction occurred near the start of the final instar. The mean duration of diapause was between 2 and 3 months in most photoperiods at 20 and 25°C, and was shorter at 15°C. However, in DD at 25°C, it lasted about 7 months. Termination of diapause was hastened in larvae reared at 25°C in DD by transferring them to LD 14:10, and also by chilling them at 7.5°C for 6 weeks before returning to 25°C in DD. In an unhealed store in southern England, viable adults emerged from May to July and originated from larvae which terminated diapause relatively late. It would appear from the results of transferring larvae back to the laboratory at various times during the winter that some phases of diapause development were completed quite early after exposure to low temperatures, although no further development took place in the store until temperatures rose again in April.