Rana Pipiens: Health and Disease--How Little We Know

The potential impact of frog diseases on basic research is discussedin practical terms.     

A Freeze-Fracture Electron Microscope Study of Trichomonas vaginalis Donné and Tritrichomonas foetus (Riedmüller)1

Two strains of Trichomonas vaginalis, JH162A, with low pathogenicity, and Balt 44, with high pathogenicity, as well as one highly pathogenic strain, KV-1, of Tritrichomonas foetus were studied by freeze-fracture electron microscopy. The protoplasmic faces (PFs) of the cell membranes of all three strains of both species had similar numbers of intramembranous particles (IMPs); however, the particles in the external faces (EFs) of these membranes were least abundant in Trichomonas vaginalis strain Balt 44 and most numerous in those of strain JH162A of this species. In Tritrichomonas foetus strain KV-1 the number of IMPs in the EF was close to but somewhat lower than that in the mild strain of the human urogenital trichomonad. In both species, the anterior, but not the recurrent, flagella had rosette-like formations, consisting of ～9 to 12 IMPs on both the PFs and EFs. The numbers and distribution of the rosettes appeared to vary among different flagella and in different areas of individual flagella of a single organism belonging to either species. The freeze-fracture electron micrographs provided a more complete understanding of the fine structure of undulating membranes of Trichomonadinae, as represented by Trichomonas vaginalis, and of Tritrichomonadinae (the Tritrichomonas augusta-type), as exemplified by Tritrichomonas foetus, than was gained from previous transmission and scanning electron microscope studies. Typically three longitudinal rows of IMPs on the PF of the recurrent flagellum of Trichomonas vaginalis were noted in the area of attachment of this flagellum to the undulating membrane. The functional aspects of the various structures and differences between certain organelles revealed in the two trichomonad species by the freeze-fracture method are discussed.     

Ultrastrukturen Und Cytochemie Der Pellikula Und Des Apikalkomplexes Der Kineten Von Babesia Bigemina Und Babesia Ovis In Hämolymphe Und Ovar Von Zecken*,†

SYNOPSIS The term kinete is used in this paper for the cigar-shaped, motile development stages (“vermicule”) of Babesia occurring intra- and extracellularly in hemolymph and ovary (including oocytes) of vectors, hard ticks (Ixodoidea). The structure of, and cyto-chemical activities of hydrolases (acid phosphatase, nonspecific esterase) in the pellicle and the apical complex were studied at the fine-structural level in kinetes of Babesia bigemina Smith & Kilborne, in hemolymph of female Boophilus microplus Canestrini. The cytochemistry of acid hydrolases was studied also in kinetes of Babesia ovis (Babes) Starcovici, in hemolymph and ovary of Rhipi-cephultis bursa Canestrini & Fanzago. The pellicle of the B. bigemina kinetes is composed of 3 membranes (pellicular complex): an outer membrane, ?8 nm thick (the plasmalemma) and 2 inner ones, each ?6 nm thick, lying closely together. The outer membrane appears to be covered by a structureless coat, 3 nm thick. The space between the inner double membrane and the plasmalemma is 7.5 nm. The whole pellicular complex is 30 nm in diameter. The 2 inner pellicular membranes appear to be derived from the endoplasmic reticulum (ER) for the following reasons: (a) a layer of hydrolase-active material is enclosed by these membranes; (b) in the spheroid parasite stages which transform from kinetes inside hemocytes, the inner double membrane is apparently replaced by an ER cisterna; (c) the thickness of each of the inner pellicular membranes is approximately the same as that of the ER membrane. There are circular openings in the pellicular double membrane with average diameters of 100 nm; despite some similarity to micropores, they have a specific structure. The term Intrapellikularfenster (IPF) (intrapellicular windows) or pseudomicropores is proposed for these pellicular differentiations. The margin of an FPF is formed by the 2 inner membranes folding into each other; cytoplasmic, electron-dense material is accumulated alongside this edge. Unlike that of micropores, the plasmalemma of the IPF is not invaginated. The IPF appears as a single, dark ring in tangential sections. At times, rhoptry-like bodies are associated with the openings. The function of the IPF is not known. An intrapellicular opening similar to the IPF, although wider, is present at the apex of the parasite. Its margin coincides with the inner edge of the apical ring. Typical subpellicular microtubuli were not observed in the Babesia kinetes. The apical complex of the B. bigemina kinetes consists of an Apikalschirm (apical umbrella), a crown of microtubuli beneath it, and rhoptries: micronemes are also present in large numbers. The Apikalschirm is located beneath the pellicle of the apical pole of the parasite. It is a wheel-like structure composed of spokes radiating from a wide, hub-like central ring (apical ring). It should be stressed that the apical ring is not identical with the polar ring described as an integral part of the pellicular complex in other Apicomplexa. Beneath each “rib” of the Apikalschirm there is one microtubule (subcostal microtubule). In kinetes of B. ovis the “ribs” are less well developed. In addition, the Apikalschirm is more pointed in kinetes of this species in tick oocytes and ova. The rhoptries of the kinetes are spindle-shaped and largely located directly beneath the Apikalschirm. They are arranged radially, each row being associated with a “rib”. A conoid was not observed. Occasionally, low hydrolytic activity could be detected in micronemes. The rhoptries and the Apikalschirm were always negative for phosphatase and esterase activity. With regard to the number and arrangement of its membranes and to its hydrolase activity, the pellicle of the kinetes of Babesia closely resembles the pellicular complex of the Coccidia. It differs from the latter by the presence of the IFF and by the lack of micropores and of true subpellicular microtubules. In the complexity of their pellicle and in some details of the organization of their apical complex (lack of a conoid; umbrella-like structure), the kinetes of Babesia resemble the ookinetes of the Haemosporidia.     

Heterogeneity of Intermediate Filament Expression in Vascular Smooth Muscle: A Gradient in Desmin Positive Cells from the Rat Aortic Arch to the Level of the Arteria Iliaca Communis

The display of the two distinct intermediate filament proteins, desmin and vimentin, in rat vascular smooth muscle tissue was studied by immunofluorescence microscopy on frozen sections of aorta and other blood vessels. Vascular smooth muscle cells present in these vessels always appeared rich in vimentin. However, staining of sections covering six distinct but contiguous parts of the aorta showed that the number of desmin containing cells was low distal to the truncus brachiocephalicus, but increases until in distal parts of the aorta and in the arteria iliaca communis almost all cells appear positive for desmin. Thus blood vessels show heterogeneity of intermediate filament expression not only in cross-section but can also display heterogeneity along their length. Muscular arteries such as the renal artery and the arteria femoralis, as well as arterioles and veins including the vena jugularis and the vena cava also contain desmin. Thus it may be that low numbers of desmin-positive cells are typical of elastic arteries, while muscular arteries and other blood vessels are characterized by large numbers of desmin-positive cells. We discuss whether desmin-positive and desmin-negative vascular smooth muscle cells may perform different functions and raise the possibility that desmin expression may coincide with the turn on of a specially regulated contractility program.     

On the importance of g(0) for estimating bird population densities with standard distance-sampling: implications from a telemetry study and a literature review

Raw count data are often used to estimate bird population densities. However, such data do not consider detection probability. As an alternative, methods that model detection probability such as distance-sampling have been proposed. However, standard distance-sampling provides reliable estimates for absolute density only when the underlying assumptions are met. One of the most critical of these assumptions is that animals on a transect line or at an observation point have to be detected with certainty (the g (0) = 1 assumption). We radiotagged nine Orphean Warblers Sylvia hortensis and estimated their short-distance detection probability. Birds were radio-located in 264 cases in single bushes or trees. Their visual detection probability after a 5-min search was only 0.58 (sd = ±0.14, range = 0.38–0.80), although the observer knew the bird's location. Furthermore, we carried out a literature review to assess how the g (0) = 1 assumption is handled in practice. None of the 28 standard distance-sampling papers reviewed contained an estimation of g (0). In 57% of the papers, the g (0) = 1 assumption was not even mentioned. Nevertheless, none of the authors declared their estimates as being relative. Our empirical data show that the g (0) = 1 assumption would be severely violated for a foliage-gleaning bird species at a desert stopover site outside the breeding season. The literature review revealed that the testing of the g (0) = 1 assumption is largely ignored in practice. We strongly suggest that more attention should be paid to the testing of this key assumption, because results may not be reliable when it is violated. If it is not possible to test the g (0) = 1 assumption or g (0) is less than 1, alternative methods should be used. Another possibility is to estimate detection probability by the means of radiotagged individuals.     

Evolution of the limpet Patella candei d'Orbigny (Mollusca, Patellidae) in Atlantic archipelagos: human intervention and natural processes

The genetic and morphological structure of Patella candei in the Macaronesian Islands were studied by allozyme electrophoresis and multivariate analysis (canonical discriminant analysis), respectively. Sixteen enzymes, yielding 21 resolvable loci were analysed for all populations using the BIOSYS-1 program. A disjunct distribution of genetically similar populations from the Azores and Selvagens Islands ( P.c. gomesii – P.c. candei ) was found, which showed two diagnostic loci with P.c. ordinaria from Madeira. Patella c. crenata from the Canaries showed an intermediate composition of 92% P.c. ordinaria and 8% P.c. gomesii–P.c. candei . Hypotheses are presented to explain the evolution of the genetic and morphological structure of P.c. candei in the Macaronesian Islands, including the interaction of natural processes and human intervention. Patella c. candei is considered to represent the ancestral form. An extinction or near extinction event may have happened in Madeira after which P.c. ordinaria arose, carrying only a small part of the diversity of the original form, which evolved in isolation. The ancestral form, P.c. candei , was depleted by human extraction from high levels of the shore in the Azores and Canaries. Patella c. gomesii , from the Azores evolved by phyletic evolution, colonizing low levels of the shore, leaving only a relict population in the Selvagens Islands, that remained almost free of human exploitation. Patella c. crenata is a hybrid with a high degree of introgression to P.c. ordinaria , which is maintained by the forces of human extraction at high-tide levels and by intraspecific competition at low-tide levels.  © 2002 The Linnean Society of London, Biological Journal of the Linnean Society , 2002, 77 , 341−353.