Ultrastructural Study of Promastigotes of Leishmania from Reptiles*

SYNOPSIS. The ultrastructure of promastigotes of 4 reptilian isolates of Leishmania grown in culture, is described. One mammalian isolate of Leishmania is also examined for comparison. No differences in the basic ultrastructure of these strains are apparent; neither is there any significant digression from the organization described for other trypanosomatids. It appears, however, that the numbers of subpellicular microtubules are of potential use in taxonomy, and that differences in the spacing of these organelles exist between reptilian and mammalian forms. In addition, an attempt is made to clarify aspects of attachment of the flagellum to the subpellicular tubule network, and to the anterior face of the kinetoplast. Finally, the formation of multivesiculate bodies from the Golgi apparatus is described, together with some features of dividing forms.     

SOME STUDIES OF THE COLONY COUNT TECHNIQUE FOR SOIL BACTERIA

SUMMARY: A series of co-operative experiments was conducted to compare the bacterial colony counts of soil obtained by workers in different laboratories, using soil extract agar and other media for the determinations.
In the earlier experiments it was not possible to obtain a reasonable degree of reproducibility of results between laboratories even when the plating technique was carefully prescribed. By modification and more rigid standardization of the technique closer agreement was obtained in subsequent experiments. It is suggested that when co-operative investigations are contemplated the participating laboratories should check their technique by the examination of 'control' soils.
No evidence could be obtained to support the suggestion that higher colony counts are obtained by the use of soil extract media containing extract prepared from the same soil as the sample tested. The source appears to be immaterial so long as the soil for extract preparation is not of extreme type and has been well manured and cultivated.     

Phagocytosis in Dictyostelium: Nibbling, Eating and Cannibalism

ABSTRACT. Phagocytosis is a highly conserved biological process that serves numerous functions in a wide variety of organisms. Over the past few decades Dictyostelium has proven to be an excellent organism for investigations in cell biology and this is certainly no less the case for a study of phagocytosis. This review examines three distinct phagocytic activities which have been characterized in Dictyostelium. The first, "vegetative phagocytosis," represents the classical eukaryotic microbial uptake of food particles (bacteria). The second, a predatory form of phagocytosis, arises when one species such as Dictyostelium caveatum attacks another species of slime mold, engulfing small pieces of the target prey. This has been termed "cell nibbling." The third phagocytic process is "sexual cannibalistic phagocytosis." In this situation a zygote giant cell, having arisen from the fusion of gametic amoebae, attracts unfused nonzygotic amoebae of the same species and engulfs them as a food source. While cell nibbling has not been actively studied, vegetative and sexual cannibalistic phagocytosis have received varying amounts of attention leading to the idea that some of the elements (e.g., glycoprotein receptors and a G_αs subunit) involved in certain of these phagocytic events may be the same. On the other hand, some unique events (e.g., filopodial induction in prey by D. caveatum ) are also worthy of further investigation. Among other things, the presence of self-nonself recognition, the existence of opsonin-like substances and the presence of signal transduction elements (e.g., an A2-like receptor that negatively modulates sexual phagocytosis) once considered to be extant only in higher organisms suggest that much can be learned about phagocytosis in general by further studies in the classic, eukaryotic microbe Dictyostelium discoideum and related species.     

Production of benthic macroinvertebrate communities along a southern Appalachian river continuum

1. Annual production was estimated for macroinvertebrate communities of principle habitats along a first- to seventh-order river continuum in the southern Appalachian Mountains (U.S.A.). Annual production was relatively low in depositional habitats, pebble/gravel substrata, and on cobble devoid of plant biomass (mosses and hydrophytes). Production was greater in bedrock habitats and greatest on hydrophyte-covered cobble, with estimates reaching 364 g AFDM (ash-free dry mass)m^–2 yr^–1 in a sixth-order river reach. Annual production in depositional habitats was correlated to standing crops of benthic organic material (BOM) in low-order stream reaches but not in higher-order reaches, indicating differences in BOM availability with stream size. In cobble, pebble/gravel and bedrock habitats production was significantly correlated to standing crops of aquatic plants, which can stabilize substrata and enhance access of collector-filtering invertebrates to entrained food resources. 2. By accounting for proportional availability of habitats along the continuum, estimates of total production ranged from 5 to 154 g AFDM m^–2 yr^–1, and increased significantly with stream size. Annual production estimated for sixth- and seventh-order reaches of the continuum were amongst the highest reported thus far for lotic systems. Organization of the benthic community along the continuum, based on production estimates for individual functional feeding-groups, generally supported predictions of the River Continuum Concept (RCC): shredder contributions were greatest in low-order reaches and declined downstream; scraper percentages were greatest in the middle of the continuum; collector-filterer contributions increased with increasing stream size. Longitudinal trends for collector-gatherers and predators did not support RCC predictions; these groups appeared to be influenced by localized changes in habitat availability and occurrence of vertebrate predators along the continuum.     

Microsatellite DNA polymorphism confirms reproductive isolation and reveals differences in population genetic structure of cryptic pipistrelle bat species

Previous studies have indicated that the common European pipistrelle bat ( Pipistrellus pipistrellus ) comprises two cryptic species, P. pipistrellus and Pipistrellus pygmaeus , which differ in echolocation call frequency and mitochondrial DNA sequence. However, levels of divergence based on nuclear markers have not been examined, and hence the potential for male-mediated gene flow between the species cannot be discounted. Moreover, little is known about population structure and migration patterns in either species. Here, we describe the use of microsatellites to investigate nuclear DNA differentiation between, and the pattern of population genetic structure within, the two cryptic pipistrelle species. In total, 1300 individuals from 82 maternity colonies were sampled across the British Isles and Continental Europe. We show, using multivariate analyses, that colonies of the same species are generally genetically more similar to each other than to those from the other species regardless of geographical location. Our findings support the hypothesis that the species are reproductively isolated. Significant patterns of genetic isolation by distance were identified in both species, indicating that mating may occur before any long-distance autumnal migration. The presence of a sea channel does not confer higher levels of genetic differentiation among colonies over and above distance alone in either species. Differences in genetic population structure were identified between the species, with P. pipistrellus showing a wider range of levels of genetic differentiation among colonies and a stronger relationship between genetic and geographical distance than P. pygmaeus . Differences in dispersal, mating behaviour, colony size and/or postglacial colonization patterns could contribute to the differences observed.  © 2007 The Linnean Society of London, Biological Journal of the Linnean Society , 2007, 90 , 539–550.     

The effect of methanogen growth on mineral substrates: will Ni markers of methanogen‐based communities be detectable in the rock record?

Methanogens, thought to be present on early Earth, have a high requirement for Ni, suggesting that Ni utilization could be a potential biosignature for methanogens if enhanced Ni extraction from surrounding minerals accompanies methanogenic growth. To test the potential for such Ni extraction from minerals by methanogens, Ni release from Ni‐containing silicate glass was measured in Ni‐free growth medium in the presence of the methanogen Methanothermobacter thermoautotrophicus (average pH ∼7.0) and observed to be higher than an abiotic control (average pH ∼6.8). However, batch dissolution experiments and a siderophore assay indicate that cell exudates such as siderophores, low molecular weight organic acids, or lysates accompanying cell death are not responsible for the observed increase in Ni release rate. In addition, scanning electron microscopy (SEM) shows little to no evidence of direct microbe–mineral interactions such as biofilms or pitting. Instead, comparison with abiotic experiments suggests that changes in pH due to CO₂ uptake may be responsible for enhanced dissolution in the presence of metabolizing cells. These results document that methanogens may not preferentially extract Ni from surrounding minerals although they may indirectly affect mineral reaction rates that are pH sensitive. Thus identifiable Ni biosignatures may not exist in the rock record to document the presence of methanogens on early Earth or Mars.