Biochemistry and Metabolism of Giardia

Giardia lamblia, an aerotolerant anaerobe, respires in the presence of oxygen by a flavin, iron-sulfur protein-mediated electron transport system. Glucose appears to be the only sugar catabolized by the Embden-Meyerhof-Pamas and hexose monophosphate pathways, and energy is produced by substrate level phosphorylation. Substrates are incompletely oxidized to CO₂, ethanol and acetate by nonsedimentable enzymes. The lack of incorporation of inosine, hypoxanthine, xanthine, formate or glycine into nucleotides indicates an absence of de novo purine synthesis. Only adenine, adenosine, guanine and guanosine are salvaged, and no interconversion of these purines was detected. Salvage of these purines and their nucleosides is accomplished by adenine phosphoribosyltransferase, adenosine hydrolase, guanosine phosphonbosyltransferase and guanine hydrolase. The absence of de novo pyrimidine synthesis was confirmed by the lack of incorporation of bicarbonate, orotate and aspartate into nucleotides, and by the lack of detectable levels of the enzymes of de novo pyrimidine synthesis. Salvage appears to be accomplished by the action of uracil phosphoribosyltransferase, uridine hydrolase, uridine phosphotransferase, cytidine deaminase, cytidine hydrolase, cytosine phosphoribosyltransferase and thymidine phosphotransferase. Nucleotides of uracil may be converted to nucleotides of cytosine by cytidine triphosphate synthetase, but thymidylate synthetase and dihydrofolate reductase activities were not detected. Uptake of pyrmidine nucleosides, and perhaps pyrimidines, appears to be accomplished by carrier-mediated transport, and the common site for uptake of uridine and cytidine is distinct from the site for thymidine. Thymine does not appear to be incorporated into nucleotide pools. Giardia trophozoites appear to rely on preformed lipids rather than synthesizing them de novo. Major lipids include phosphatidylcholine, phosphatidylethanolamine, phosphatidylglycerol, sphingomyelin, sterol (probably cholesterol) and mono-, di- and triacylglycer-ides. The lipid composition of the cysts of G. lamblia isolated from gerbils and G. muris isolated from mice are similar to those obtained from the trophozoites of G. lamblia grown in vitro. The activities of several hydrolases of G. lamblia have been shown to be confined to a single lysosome-like particle population with an equilibrium density of approximately 1.15 in sucrose. Contrary to the trophozoites of Entamoeba and the trichomonads, Giardia trophozoites appear to lack most carbohydrate splitting hydrolases. Calmodulin has been reported in G. lamblia trophozoites, and it appears to have properties similar to the calmodulin isolated from other eucaryotic cells.     

Venom gland and reservoir morphology in the Doryctinae and related braconid wasps (Insecta, Hymenoptera, Braconidae)

Detailed venom reservoir and venom gland intima morphology has been investigated in reprsentatives of 84 genera and 10 subfamilies of Braconidae with particular reference to the Doryctinac, basal cyclostomes and related groups including the Opiinae, Alysiinae and Rogadinae sens. lat . Several new phylogenetically significant characters are described and illustrated. Extcnsivc secretory ductules on the primary venom duct is suggested as a synapomorphy for the subfamilies Braconinac, Doryctinae, Opiinae, Alysiinae and Gnamptodontinae. The presence of two separate venom gland insertions and their position beyond the spiral sculpture of the reservoir are suggested as synapomorphies for the subfamilies Doryctinae and Ypsistocerinac. An anterior, weakly sclerotized, probably glandular. expansion of the reservoir characterizes the Histeromerinae and Rhyssalinae and also the enigmatic genera Thoracoplites Fischer and Doryctomorpha Ashmead which are hcre transferred to the Rhyssalinae. Within the Doryctinac, venom reservoir morphology suggests three generic groups, one comprising the genera of the Odontohraconini and possibly also the genera Acanthodoryctes , Binareu and Monarea , all of which have an essentially undivided reservoir with extremely fine and uniform spiral sculpture. the second comprising the genera Doryctophasmus , Euscelinus, Gildoria, Halycea and Schlettereriella , which share horn-like processes at the base of the venom duct insertions, and a third including Acrophasmus. Dendro- soter, Heterospilus, Megaloproctus, Rutheia, Paraspathius, Schlettereriella. Spathius and Syngaster based on the presence of two markedly different densities of annulation of the reservoir. The degree to which external and other characters support these groups is discusscd.     

Clonal and Geographic Distribution of a Surface Antigen of Tritrichomonas foetus1

ABSTRACT. Geographically diverse strains and clones of Tritrichomonas foetus have been examined with respect to their expression of a major surface antigen of approximately 150,000 relative molecular weight (Mr), designated the 150 Ag. Radioiodination and ¹³S-methionine labeling of T. foetus followed by immunoprecipitation with monoclonal antibodies (MAbs), separation of polypeptides by SDS-PAGE, and autoradiography or fluorography confirmed the parasite origin of the 150 Ag. The results of flow cytometry analysis employing a panel of MAbs against live T. foetus parasites revealed that from 5 to 84% of individuals in a given population of T. foetus expressed a particular epitope of the 150 Ag. All strains and clones were positive for surface expression of epitopes of this antigen. These results show that the 150 Ag is widely distributed in populations of T. foetus, confirm the surface location of this antigen, and suggest its importance as a target for protective immune responses.     

Environmental context alters ecological trade‐offs controlling ant coexistence in a spatially heterogeneous region

1. Ecological trade‐offs in ant (Hymenoptera: Formicidae) assemblages and their implications for coexistence boast a rich history in entomology. Yet investigations of trade‐offs have largely been limited to homogeneous environments. We examined how environmental context modifies trade‐off expression in an ant assemblage spanning a heterogeneous region in central Florida, U.S.A. 2. We examined how trade‐off expression is altered among two contrasting habitat types: open shrub and forest. We tested for the presence of the dominance‐discovery trade‐off and two dominance‐thermal tolerance trade‐offs by estimating behavioral dominance, discovery ability, and thermal tolerance (foraging thermal limit, lethal temperature, and maximal abundance temperature) for a wide range of interacting ant species. 3. We found significantly linear dominance hierarchies in both shrub and forest habitats, showing dominant species out‐compete subordinates for food resources. In thermally stressful shrub habitats, subordinates exhibit higher thermal tolerances, take greater thermal risks, and reach maximum forager abundances at higher temperatures than do dominant species. This suggests temperature mediated trade‐offs control coexistence in shrub habitat. In thermally moderate forest habitat, we found limited evidence for trade‐offs between competitive dominance and resource discovery or between dominance and thermal traits, implying other processes control coexistence. These results demonstrate that trade‐offs controlling ant coexistence may be contingent on environmental context.     

Further data on Prokennalestes (Mammalia, Eutheria inc. sed.) from the Early Cretaceous of Mongolia

Four new incomplete lower jaws of Prokennalestes are described. bringing new data for establishing the primitive cutherian dental formula and its evolution in later placentals, as well as the possible relationships of the genus.     

Is bigger better? Water balance in the polymorphic desert harvester ant Messor pergandei

Abstract. Foraging activity of ants in xeric areas may be limited by desiccation stresses. To assess the extent of such stresses on a polymorphic ant species [Messor pergandei (Mayr), body mass range 1-12mg], we measured body water reserves, absolute rates of water loss, and cuticular permeability over the species' foraging temperature range (15–45C). Cuticular permeability of M. pergandei was typical of xeric arthropods (17μgcm^-2h^-1mmHg^-1). However, the effect of polymorphism on both absolute and relative rates of water loss was unexpected. Large workers lost water more slowly than small workers, even after adjusting for cuticular surface area. In addition, the body water reserves of large workers were larger, even after adjusting for body mass. Small workers of this ant species are therefore disproportionately prone to dehydration, yet, in spite of this, constitute a large and important component of the foraging force. To assess the practical relevance of desiccation to polymorphic ants, we developed a 'worst-case' model of desiccation-limited foraging parameters (time to complete loss of locomotor coordination in 5% of the foraging force). In this model, average actual foraging duration was substantially less than would be required to incapacitate the ants by dehydration. We discuss direct and indirect evidence suggesting that desiccation may, nevertheless, impose limitations on the foraging activity of ants.     

Effects of × Rays on Cell Lethality and Micronuclear Number in the Ciliate Spathidium spathula*

SYNOPSIS. Spathidium spathula irradiated with 0 to 55 kr of × rays showed one or more of the following kinds of behavior: (1) Death of an undivided cell (primary death); (2) death of a descendant of an irradiated cell (secondary death); (3) permanent injury including one or more of the following: low daily division rate, excessive macronuclear enlargement, total loss of micronuclei, cytostome replication, heavy pigmentation, and decreased motility; (4) temporary division retardation for 1 to 2 days followed by apparent complete recovery; and (5) no apparent injury. The first 3 kinds of behavior increased with increasing dosage from 15 to 25 to 55 kr. At 6 kr only the last 2 categories were observed. The LD₅₀ for 8 days was 46 kr for both primary and secondary death, or 60 kr for primary death alone. Micronuclear number varied greatly following irradiation in lines showing either permanent or temporary injury. Two different responses occurred: (1) The micronuclear number averaged about twice the normal number of 20 with a large range (0 to 360) 1 day after exposure. The number gradually decreased during the next 2 days; (2) some cells lost all micronuclei following irradiation, the incidence increasing with dose. At 55 kr complete loss of micronuclei occurred in 96% of the surviving lines.