Expression of Surface Coat Glycoconjugates by Bacteria-Fed Tetrahymena1

ABSTRACT. We have shown that bacteria-fed Tetrahymena express at their surface and excrete into the medium a glycoconjugate absent in axenically grown cells. A preliminary analysis of the purified molecule is given. Immunolabeling of blotted surface extracts and fixed cells shows that bacteria-fed Tetrahymena build up a surface coat whose material originates totally or in part in the mucocysts. The glycoconjugate is located externally on the coat and mediates cell immobilization and immunolabeling by the serum. The results also indicate that axenic cells are probably devoid of surface coat.     

Mesure d'une activité métabolique in vivo. Cas du catabolisme purique chez le Pharbitis nil

In vivo measurement of a metabolic activity. — Purine catabolism in Pharbitis nil cotyledons. To study the influence of light and darkness on the level of purine degradation, an in vivo method of measuring this catabolic pathway has been developed. Cotyledon discs of Pharbitis nil were incubated in an aqueous solution of hypoxanthine-8-¹⁴C. This purine base was first oxidized by a NAD⁺ dependent xanthine dehydrogenase. The metabolic flow was expressed either by the quantity of products (xanthine + uric acid + allantoin + allantoic acid) or by the rate of hypoxanthine degradation in the discs. This easy, reproducible and very sensitive technique of measurement has been investigated with respect to several variables including tissue quantity, length of incubation time, hypoxanthine and NAD⁺ concentrations, and pH. The quantity of products varied proportionally with the tissue quantity but the catabolic rate was not linked to this. The best conditions of measurement were to incubate discs for at least 60 min in distilled water containing only hypoxanthine-8-¹⁴C at low concentrations (below 0.25 mM). The values obtained represent the actual in vivo level of the studied metabolic pathway. The NAD⁺ concentration within the tissue does not seem to be a limiting factor for hypoxanthine degradation, the hypoxanthine concentration itself appears to be the only limiting factor in endogenous purine catabolism.     

Generalist dung attraction response in a New Zealand dung beetle that evolved with an absence of mammalian herbivores

1. Dung beetles (Scarabaeidae: Scarabaeinae) are integral parts of many ecosystems because of their role in decomposition of dung; particularly mammal dung, which forms the diet of both larvae and adults. 2. New Zealand dung beetles are unusual as they are flightless and evolved on islands with a highly depauperate mammal fauna and thus without the usual dung resource used by dung beetles elsewhere. The diet of New Zealand dung beetles is unknown. 3. We hypothesised (1) that the endemic dung beetle Saphobius edwardsi would be attracted to a broad range of food types, and (2) that S. edwardsi would be able to survive and reproduce on a range of dung types and puriri (Vitex lucens) humus. 4. Laboratory choice tests identified that S. edwardsi was attracted to a range of mammal, bird, invertebrate, and reptile dung types, but not to non‐dung food sources. Five‐month no‐choice tests found that beetle survival rates were lower for beetles fed with humus compared with those fed on mammal, bird, or invertebrate dung. None of the beetles reproduced. 5. This study suggests S. edwardsi have a strong preference for dung, and are likely to be broad dung generalists in their feeding behaviour.     

Two Distinct Varieties of Giardia in a Mixed Infection from a Single Human Patient

ABSTRACT. Twenty-five in vitro cultures of Giardia duodenalis derived from a Brisbane patient were established to assess the genetic heterogeneity of a population. Each of the established lines carried a predominance of one of two distinct varieties of Giardia . The two varieties were heterogeneous by four unambiguous criteria that were representative of the whole genome. These included restriction enzyme polymorphisms, hybridization with the cloned rDNA repeat and with a gene encoding a cysteine-rich surface protein, electrophoretic karyotyping and DNA fingerprinting. Differences between parasites derived from this patient were greater than have been seen between all other established G. duodenalis in vitro cultures from both human and animals. The culture were heavily selected such that a single Giardia line carried a predominance of one genotype and was not representative of the entire original population.