Invasive parasites in multiple invasive hosts: the arrival of a new host revives a stalled prior parasite invasion

The success of a biological invasion can depend upon other invasions; and in some cases, an earlier invader may fail to spread until facilitated by a second invader. Our study documents a case whereby an invasive parasite has remained patchily distributed for decades due to the fragmented nature of available hosts; but the recent arrival of a broadly distributed alternative invasive host species provides an opportunity for the parasite to expand its range considerably. At least 20 years ago, endoparasitic pentastomids (Raillietiella frenata) were brought with their native host, the invasive Asian house gecko Hemidactylus frenatus, to the port city of Darwin in tropical Australia. These geckos rarely disperse away from human habitation, restricting the transmission of their parasites to urban environments – and thus, their pentastomids have remained patchily distributed and have only been recorded in scant localities, primarily surrounding Darwin. The recent range expansion of the invasive cane toad Rhinella marina into the Darwin area has provided an alternative host for this pentastomid. Our results show that the cane toad is a competent host for Ra. frenata– toads shed fully embryonated pentastomid eggs in their faeces – and that pentastomids are now common in cane toads near Darwin. Likely reflecting the tendency for the parasite's traditional definitive host (the Asian house gecko) and only known intermediate host (the cockroach) to reside around buildings, we found the prevalence of this parasite follows an urban distribution. Because cane toads are widely distributed through urban and rural habitat and can shed viable pentastomid eggs, the toad invasion is likely to facilitate the parasite's spread across the tropics, into areas (and additional susceptible hosts) that were previously inaccessible to it.     

Chloride cell apical surface changes in gill epithelia of the armoured catfish Hypostomus plecostomus during exposure to distilled water

Armoured catfish Hypostomus plecostomus were exposed to distilled water for 15 days. High chloride cell proliferation occurred on the filament and lamellar gill epithelia. The apical surface of the chloride cells (66% of cells in both epithelia) showed significant reduction in the aquatic environment which was characterized by the development of a sponge-like organization. The chloride cell response suggests that these features could create a microenvironment which may favour either the reduction of ion loss or ion uptake in a environment characterized by an absence of ions.     

Chloride channel in vanadocytes of a vanadium-rich ascidian Ascidia sydneiensis samea

Ascidians, so-called sea squirts, can accumulate high levels of vanadium in the vacuoles of signet ring cells, which are one type of ascidian blood cell and are also called vanadocytes. In addition to containing high concentrations of vanadium in the +3 oxidation state, the proton concentrations in vanadocyte vacuoles are extremely high. In order to elucidate the entire mechanism of the accumulation and reduction of vanadium by ascidian vanadocytes, it is necessary to clarify the participation of anions, which might be involved as counter ions in the active accumulation of both vanadium and protons. We examined the chloride channel, since chloride ions are necessary for the acidification of intracellular vesicles and coexist with H(+)-ATPase. We cloned a cDNA encoding a chloride channel from blood cells of a vanadium-rich ascidian, Ascidia sydneiensis samea. It encoded a 787-amino-acid protein, which showed striking similarity to mammalian ClC3/4/5-type chloride channels. Using a whole-mount in situ hybridization method that we developed for ascidian blood cells, the chloride channel was revealed to be transcribed in vanadocytes, suggesting its participation in the process of vanadium accumulation.     

The Role of Chloride Channels and Chloride Ions in Regulation of Steroidogenesis in the Gonads of Amphibians,Birds, and Mammals

The paper represents the first review of data on the involvement of chloride channels (their inhibitors and media, in which chloride ions are substituted for anions that poorly penetrate in the cell) in the regulation of basal and gonadotropin-stimulated steroidogenesis in the gonads of amphibians, birds, and mammals. Possible causes are considered for different reactions of the gonad steroidogenic cells in representatives of different vertebrate classes to a decreased medium concentration of chloride and the involvement of chloride channels and/or chloride ions in the regulation of steroidogenesis is discussed.     

Anion transport in red blood cells and arginine-specific reagents. Interaction between the substrate-binding site and the binding site of arginine-specific reagents

Phenylglyoxal is found to be a potent inhibitor of sulfate equilibrium exchange across the red blood cell membrane at both pH 7.4 and 8.0. The inactivation exhibits pseudo-first-order kinetics with a reaction order close to one at both pH 7.4 and 8. The rate constant of inactivation at 37 degrees C was found to be 0.12 min-1 at pH 7.4 and 0.19 min-1 at pH 8.0. Saturation kinetics are observed if the pseudo-first order rate constant of inhibition is measured as a function of phenylglyoxal concentration. Sulfate ions as well as chloride ions markedly decrease the rate of inactivation by phenylglyoxal at pH 7.4, suggesting that the modification occurs at or near to the binding site for chloride and sulfate. The decrease of the rate of inactivation produced at pH 8.0 by chloride ions is much higher than that produced by sulfate ions. Kinetic analysis of the protection experiments showed that the loaded transport site is unable to react with phenylglyoxal. From the data it is concluded that the modified amino acid(s) residues, presumably arginine, is (are) important for the binding of the substrate anion.     

Catabolite inactivation of phosphoenolpyruvate carboxykinase in spheroplasts from Saccharomyces Cerevisiae

Catabolite inactivation of phosphoenolpyruvate carboxykinase was studied in yeast spheroplasts using 0.9 M mannitol or 0.6 M potassium chloride as the osmotic support. In the presence of potassium chloride the rate of catabolite inactivation was nearly the same as that occurring in intact yeast cells under different conditions of incubation. However, in the presence of mannitol, catabolite inactivation in spheroplasts was prevented. The mannitol inhibition of catabolite inactivation was released by addition of ammonium or phosphate ions. At a concentration of 0.3 M ammonium or 0.06 M phosphate ions, the maximum rate of catabolite inactivation in spheroplasts suspended in mannitol was achieved and was comparable with that observed in spheroplasts incubated in 0.6 M potassium chloride as the osmotic stabilizer. Sodium sulfate (0.04 and 0.4 M) or potassium chloride (0.06 and 0.6 M) did not release the mannitol inhibition of catabolite inactivation in spheroplasts. In intact yeast cells, 0.9 M mannitol, 0.08 M ammonium or 0.1 M phosphate ions did not influence the rate of catabolite inactivation. The nature of the effects of mannitol, ammonium and phosphate ions on catabolite inactivation in yeast spheroplasts is disscussed.     

Spectral and kinetic evidence for reaction of superoxide with compound I of myeloperoxidase

Superoxide and myeloperoxidase (MPO) are essential for the oxidative killing of bacteria by neutrophils. Previously, we developed a kinetic model to demonstrate that within the confines of neutrophil phagosomes, superoxide should react exclusively with MPO and be converted to hypochlorous acid. The model consists of all known reactions and rate constants for reactions of superoxide, hydrogen peroxide, and chloride ions with MPO, except for the reaction of superoxide with compound I, which could only be estimated. Compound I is a transitory redox intermediate of MPO that is responsible for oxidizing chloride ions to hypochlorous acid. To tackle the challenge of observing the reaction between two transient species, we combined stopped-flow spectrophotometry with pulse radiolysis. Using this technique, we directly observed the reduction of compound I by superoxide. The rate constant for the reaction was determined to be 5.6±0.3×10(6)M(-1)s(-1). This value establishes superoxide as one of the best substrates for compound I. Based on this value, the rate constant for reduction of compound II by superoxide was determined to be 1.2±0.1×10(6)M(-1)s(-1). Within phagosomes, the reduction of compound I by superoxide will compete with the oxidation of chloride ions so that the relative concentrations of these two substrates will affect the yield of hypochlorous acid. Characterization of this reaction confirms that superoxide is a physiological substrate for MPO and that their interactions are central to an important host defense mechanism.     

Catabolite inactivation of phosphoenolpyruvate carboxykinase in spheroplasts from Saccharomyces cerevisiae.

Catabolite inactivation of phosphoenolpyruvate carboxykinase was studied in yeast spheroplasts using 0.9 M mannitol or 0.6 M potassium chloride as the osmotic support. In the presence of potassium chloride the rate of catabolite inactivation was nearly the same as that occurring in intact yeast cells under different conditions of incubation. However, in the presence of mannitol, catabolite inactivation in spheroplasts was prevented. The mannitol inhibition of catabolite inactivation was released by addition of ammonium or phosphate ions. At a concentration of 0.3 M ammonium or 0.06 M phosphate ions, the maximum rate of catabolite inactivation in spheroplasts suspended in mannitol was achieved and was comparable with that observed in spheroplasts incubated in 0.6 M potassium chloride as the osmotic stabilizer. Sodium sulfate (0.04 and 0.4 M) or potassium chloride (0.06 and 0.6 M) did not release the mannitol inhibition of catabolite inactivation in spheroplasts. In intact yeast cells, 0.9 M mannitol, 0.08 M ammonium or 0.1 M phosphate ions did not influence the rate of catabolite inactivation. The nature of the effect of mannitol, ammonium and phosphate ions on catabolite inactivation in yeast spheroplasts is discussed.     

Prevalence and intensity of pentastomid infection in two species of snakes from northeastern Brazil.

This study aimed to evaluate the infection rates of snakes by pentastomids in the semi-arid region of Brazil. Fifteen snakes (four Micrurus ibiboboca (Merrem, 1820) and eleven Philodryas nattereri Steindachner, 1870) were collected between January and April of 2005, in the municipality of Crato (07 degrees 14' S and 39 degrees 24' W), State of Ceará, Brazil. Laboratorial analysis of the respiratory tracts of the sampled snakes indicated differences in host infection rates: four individuals of P. nattereri (36.4%) were infected by Cephalobaena tetrapoda Heymons, 1922 (mean infection intensity 1.5 +/- 0.28, 1-2) and three specimens (27.3%) by Raillietiella furcocerca (Diesing, 1863) (2.3 +/- 1.32, 1-5). Only one individual of M. ibiboboca (25%) was infected by a non-identified species of Raillietiella sp. These are the first data on pentastomid infection in snakes in Northeastern Brazil and both snake species comprise new host records for the pentastomids. The results also indicate that the generalist parasites C. tetrapoda and R. furcocerca share their definitive hosts.     

POTASSIUM EFFECTS ON ION TRANSPORT IN BRAIN SLICES

—(1) Fluxes of sodium, potassium, chloride and glutamate ions were studied in brain slices by aid of radio-isotopes. Desaturation curves showed the efflux to occur from at least two compartments with widely different kinetics. (2) The slowly exchanging component comprises from about 10 (sodium, potassium, chloride) to about 30 (glutamate) per cent of the radioactivity in the tissue. An energy-requiring uptake of potassium and extrusion of sodium seems to occur in this compartment, which probably includes the nerve cells. (3) A rather slow efflux of especially potassium ions from the rapidly exchanging fraction indicates that this component may not be purely extracellular, but also seems to include cells, which possibly are neuroglial. The hypothesis of a cellular origin is supported by the demonstration of an increase in the rate constant of the potassium efflux evoked in the presence of oxygen by high concentrations of potassium. (4) Evidence is presented that the increase in the rate constant of the potassium efflux is due to a potassium-induced stimulation of active transport. No coupling seems to occur between the stimulated potassium transport and movements of sodium, but potassium ions may be accompanied by glutamate ions.     

The possible role of the frontal and sub-parietal gland systems of the pentastomid Reighardia sternae (Diesing, 1864) in the evasion of the host immune response.

The frontal and sub-parietal glands of the pentastomid Reighardia sternae elaborate lamellate secretion which is poured on to the cuticle. The entire surface of the cuticle, including the mouth, hook pits and reproductive apertures, is coated with secretion. Electron microscope studies indicate that the glands are continuously active, which implies a turnover of surface membranes. The postulated function of these membranes is to protect certain vital areas of the host--parasite interface, notably the pores of ion-transporting cells, from the host immune response. The available evidence suggests that pentastomids do evoke a strong immune response but since most are long-lived they must circumvent it. We believe the surface membrane system to be instrumental in this. Studies on another pentastomid, Porocephalus crotali in rats have shown that an immune response stimulated by a primary infection will kill subsequent infections and that the surface membranes are strongly immunogenic. Obvious parallels between this situation and that of schistosome infections in mammals are discussed. An alternative explantation of concomitant immunity is proposed.     

Changes in chloride cell distribution during early larval stages of Clupea harengus

A non-uniform distribution of cutaneous chloride cells was found in the early, pre-feeding larval stages of herring Clupea harengus . Chloride cells on the head, yolk-sac and trunk regions were unevenly distributed, whereas more densely packed chloride cells were observed in the pericardial and prebranchial regions. The pattern of chloride cell distribution changed during development and two distinct changes are described. The density of choride cells on the ventral trunk increased substantially during the period of yolk absorption, presumably due to contraction of the yolk sac and selective retention of yolk-sac chloride cells. Also during this period the cells on the lateral body wall increased in number and became distributed in segmental bands overlying the myosepta. Most chloride cells were found in association with the haemocoel or primordial blood vessels. Superficial segmental blood vessels were not found in the early larva, but the segmental bands of chloride cells overlay nerve tracts in the myosepta which were tentatively identified as the focal innervation of myotomes. It is concluded that both the circulatory system and the peripheral nervous system may play a role in determining chloride cell distribution in early larvae.     

Amphibians as definitive hosts for pentastomids: Raillietiella bufonis n.sp. from Bufo lemur in Puerto Rico and a reassessment of Raillietiella indica Gedoelst, 1921

Summary A new species of a cephalobaenid pentastomid infecting the lungs of a toad, Bufo lemur, from Puerto Rico is described. The single infection comprises all stages from infective larvae to mature males and females and therefore we consider the toad to be a definitive host. We reassess the evidence concerning Raillietiella indica Gedoelst, 1921, another raillietiellid from the lungs of an Indian toad, B. melanostictus which, hitherto, has been considered by most authors an immature stage from an intermediate host. It now appears that the type specimen was probably a gravid female and that R. indica is a valid species which also matures in a toad. Thus amphibians are established as a new class of definitive hosts for pentastomids. ac]19820218     

The ultrastructure of chloride cells in the gills of the teleostOreochromis mossambicus during exposure to acidified water

Summary Branchial chloride cells, which actively take up ions in the gills of freshwater fish, were studied in tilapia (Oreochromis mossambicus) exposed to sublethally acidified freshwater. Structural damage of cells, resulting in cell death by necrosis, only occurred transiently, when the reduction of water pH was acute rather than gradual. The most prominent effects of water acidification were the rapid increase in the number of chloride cells and the changes in frequency of the different stages of the chloride cell cycle. In the opercular inner epithelium, a twofold increase in cells occurred 48 h after gradual acidification. Cell density stabilized after 4 weeks at a level 5 times that of control fish. Four transitory stages were distinguished in the chloride cell cycle: accessory or replacement cells, immature, mature, and degenerating (apoptotic) cells. In control fish, mature chloride cells dominated (over 50%) with immature and apoptotic cells totalling about 40%. After 4 weeks in acid water, only 13% of the cells were mature. Immature and apoptotic cells dominated, each representing about 40% of the total number of chloride cells. Mature cells apparently age rapidly under these conditions. Thus, chloride cells turn over quickly in acid water, with a minor increase in ion transport capacity of the gills. This conclusion is supported by the observation that opercular and branchial Na⁺/K⁺ ATPase activities in treated fish are only 40%–50% higher than in controls.     

Role of AQP2 during apoptosis in cortical collecting duct cells

Background information. A major hallmark of apoptosis is cell shrinkage, termed apoptotic volume decrease, due to the cellular outflow of potassium and chloride ions, followed by osmotically obliged water. In many cells, the ionic pathways triggered during the apoptotic volume decrease may be similar to that observed during a regulatory volume decrease response under hypotonic conditions. However, the pathways involved in water loss during apoptosis have been largely ignored. It was recently reported that in some systems this water movement is mediated via specific water channels (aquaporins). Nevertheless, it is important to identify whether this is a ubiquitous aspect of apoptosis as well as to define the mechanisms involved. The aim of the present work was to investigate the role of aquaporin‐2 during apoptosis in renal‐collecting duct cells. We evaluated the putative relationship between aquaporin‐2 expression and the activation of the ionic pathways involved in the regulatory volume response. Results. Apoptosis was induced by incubating cells with a hypertonic solution or with cycloheximide in two cortical collecting duct cell lines: one not expressing aquaporins and the other stably transfected with aquaporin‐2. Typical features of apoptosis were evaluated with different approaches and the water permeability was measured by fluorescence videomicroscopy. Our results show that the rate of apoptosis is significantly increased in aquaporin‐2 cells and it is linked to the rapid activation of volume‐regulatory potassium and chloride channels. Furthermore, the water permeability of cells expressing aquaporin‐2 was strongly reduced during the apoptotic process and it occurs before DNA degradation. Conclusions. These results let us propose that under apoptotic stimulation aquaporin‐2 would act as a sensor leading to a co‐ordinated activation of specific ionic channels for potassium and chloride efflux, resulting in both more rapid cell shrinkage and more rapid achievement of adequate levels of ions necessary to activate the enzymatic apoptotic cascade.     

Halide fluxes in epithelial cells measured with an automated cell plate reader

A method is introduced to measure chloride permeability in cultured epithelial cells using 6-methoxy-N-(3-sulfopropyl)quinolinium (SPQ) and 6-methoxy-N-ethylquinolinium iodide quinolinium (MEQ) as fluorescent chloride-sensitive probes. The method involves growing cells in multiwell plates, incubating cells with SPQ or MEQ, and then exchanging intracellular or extracellular halide ions with nitrate. The resulting time course of SPQ or MEQ fluorescence is followed by repetitive readings with a multiwell fluorescence plate reader. Exchange times are extracted by fitting the time course with a single exponential function of time. The method was validated by measuring the effect of chloride channel activators and blockers in A6 and MDCK cells. The baseline iodide/nitrate exchange time was 200-300 s. Isoproterenol (a modulator of cAMP-activated chloride channels) increased the exchange rate by a factor of 1.4+/-0.1; A23187 (a modulator of calcium-activated chloride channels) increased the rate by 3.4+/-0.4; bradykinin (also a modulator of calcium-activated chloride channels) increased the rate by 2.0+/-0.4; forskolin (a direct stimulator of adenylate cyclase) increased the rate by 2.7+/-0.3. Diphenylamine-2-carboxylate (a chloride channel blocker) decreased the rate by 0.12+/-0.03. These results indicate that our method is a valid indicator of halide-nitrate exchange in cultured epithelial cells.     

Comparative studies of the development and differentiation of chloride cells in tilapine fish with different reproductive styles

Using light and electron microscopy and fluorescent probes, we followed the ontogenesis of selected organs in embryos of several species of tilapia (Cichlidae, Pisces) with emphasis on chloride cell differentiation in species with two different reproductive styles: we compared the substrate-brooder Tilapia zillii and the mouth-brooders Oreochromis niloticus, O. aureus, Sarotherodon galilaeus, and Tristramella sacra. In all species a transitory blood network system nurtured by the vena caudalis inferiores supplied the yolk sac and preanal finfold during the advanced stages of embryonic and initial stages of larval development. During these stages chloride cells occurred on the yolk sac, as a part of the abdominal epithelium. The cells and their associated blood plexus remained active here until the gill-lamellae, operculum, and mouth became functional. The chloride cells of their epithelium and blood system then took over, concomitant with a gradual degradation of the transitory blood system on the yolk sac. Ontogenesis of these systems (transitory and permanent) progressed at a higher rate in substrate-brooders than in mouth-brooders and was correlated with the earlier functioning of the gill-operculum system. Thus, at a constant temperature of 26 degrees C, the more exposed T. zillii progeny completed metamorphosis at 7-8 days after fertilization, calculated around 5,000 +/- 80 h/temp, whereas juveniles of more protected mouth-brooders attained a similar stage only 15 +/- 1 days after fertilization and around 9,000 +/- 200 h/temp. This earlier development of chloride cells and other pivotal organs in environmentally exposed progeny of substrate-brooders, as compared to the protected progeny of mouth-brooders, shows that their ontogeny was selected for the optimal survival style under specific etho-ecological conditions.     

Effects of impermeant medium ions on the composition of rabbit renal cortical slices

When incubated in isosmotic oxygenated medium in which chloride was completely replaced by gluconate, rabbit renal cortical slices lost chloride with sodium, potassium and water before reaching a new steady-state composition after 15-30 min. When corrected for extracellular space, there was an electroneutral loss of alkali metal cations (Na + K) with chloride, accompanied by isosmotic loss of water from the cells. The losses of chloride and water were independent of medium pH over the range of 6.4-8.2, and were the same with potassium rather than sodium as the dominant medium cation. Incubation in isosmotic sodium chloride medium restored tissue composition of slices transferred from gluconate medium. This recovery was not dependent specifically upon medium chloride, for slice water content also recovered when nitrate rather than chloride was substituted for medium gluconate. With sodium completely replaced by n-methyl d-glucamine (nmdG+), cells in slices lost far more sodium and potassium than chloride before reaching a new steady-state composition after some 30 min. However, the loss of water was as predicted from the total losses of measured inorganic ions. With sodium and chloride completely replaced by nmdG+ and gluconate, there was a greater loss of water than found with unilateral substitutions. Again, the combined loss of diffusible inorganic cations exceeded the loss of chloride but the water loss was that expected for isosmotic loss accompanying the measured losses of ions. These results reveal that both gluconate and nmdG+ behave as impermeant ions in this tissue preparation. It is suggested that, in the absence of medium sodium, sodium-hydrogen exchange is inhibited. Retained hydrogen ions are buffered on charged cellular non-diffusible solutes and the associated hydroxyl (or bicarbonate) ions are lost from the cells accompanied by the inorganic univalent cations lost in excess of chloride in nmdG+ medium.     

Trypanosoma cruzi: interaction with vertebrate cells in vitro. 2. Quantitative analysis of the penetration phase

A technique is described for quantifying the in vitro penetration of vertebrate cells by trypomastigotes of Trypanosoma cruzi. It was found that the parasites are distributed among host cells in a manner described by the negative binomial distribution. The rate at which trypomastigotes penetrate bovine embryonic skeletal muscle cells (BESM) decreased exponentially in time in this system. The rate of the exponential decrease was dependent upon the concentration of parasites, being faster for more concentrated suspensions of trypomastigotes. A significantly lower penetration rate of canine kidney and HeLa cells was found when compared to bovine embryonic skeletal muscle cells. Within a single population of BESM cells, the smaller cells were penetrated more rapidly than the larger ones per unit cell area.     

铜离子胁迫下玉米根边缘细胞数量及存活率

采用悬空培养及离体培养的方式,观察玉米的根边缘细胞在铜离子胁迫下发生的形态、数量及存活率变化情况,结果表明,在玉米根长为32mm的时候,边缘细胞的数量达到最大,为4125个,但其存活率此时最低。玉米的根边缘细胞随着铜离子浓度增加,边缘细胞的数量发生变化。当处理浓度为50umol·L-1时,边缘细胞的死细胞数量达到758个（存活率为24．80％）,随后铜离子处理浓度增加到100umol·L-1时,存活率降低了17．54％。玉米根边缘细胞的数量随着铜离子浓度的增加呈现出逐渐减少的趋势,而存活率逐渐降低,说明在重金属铜离子胁迫下,根边缘细胞的释放起到对根际区域的保护作用。