A revision of the family Zoogonidae Odhner, 1902 (Platyhelminthes: Digenea): Subfamily Lepidophyllinae and comments on some aspects of biology

Summary A detailed revision of the zoogonid subfamily Lepidophyllinae is presented, using morphological characters discussed in an earlier paper. Twelve genera and 50 species are treated in detail with keys and cladograms to genera and species. The genera and species covered are: Lepidophyllum steenstrupi, L. appyi, L. armatum, L. brachycladium, L. cameroni, L. pleuronectini, L. pyriforme, L. schantaricum, Urinatrema hispidum, U. hirudinacea, Panopula cavernossa, P. bridgeri, P. spinosa, Limnoderetrema minutum (Manter, 1954) [formerly Deretrema] n.g. (in freshwater fishes; genital pore at oral sucker or pharynx level), n. comb., Brachyenteron peristedioni, B. acropomatis, B. campbelli, B. doederleiniae, B. magnibursatum, B. parexocoeti, B. pycnorganum, Steganodermatoides kergeleni, S. agassizi, S. allocytti, S. maceri, Neosteganoderma glandulosum, N. infundibulum, Proctophantastes abyssorum, P. gillissi, Deretrema (Deretrema) fusillus, D. (D.) cholaeum, D. (D.) pacificum, D. (Spinoderetrema) plotosi, D. (S.) acutum, D. (S.) fellis, D. (S.) ovale, D.(S.) sebastodis, D. (Luxitrema) philippinensis, D. plagiorchis, Pseudochetosoma salmonicola, Overstreetia sodwanaensis, Steganoderma (Steganoderma) formosum, S. (S.) atherinae, S. (Lecithostaphylus) retroflexum, S. (L.) depauperati (Yamaguti, 1970) n. comb., S. (L.) hemirhamphi, S. (L.) nitens, S. (L.) parexocoeti, S. macrophallos, S. oviformis. Most zoogonids were found to exhibit some level of predilection for a particular piscine host group, but little general information on the zoogeography of the group was discovered. Ultrastructural evidence is presented suggesting that the membranous egg-capsule of the zoogonines shows vestiges of the three layers of a normal tanned egg-shell.     

The effect of 3-methylindole on the rates of phospholipid and neutral lipid synthesis in cultured fibroblasts

The present study was designed to test the hypothesis that a pneumotoxin, 3-methylindole, alters the basic metabolic pathways involved in phospholipid and neutral lipid synthesis in cultured fibroblasts. Rat skin fibroblasts were obtained from day-old pups. Confluent monolayers were preincubated for up to 24 h with a range of concentrations (0-0.76 mM) of 3-methylindole. Following these treatments, the cell lipids were labelled by incubation for 6 h with [14C]glycerol. The lipids were extracted, separated by thin layer chromatography, and the radioactivity in each fraction was determined. 3-Methylindole had no effect on the total incorporation of [14C]glycerol into lipids, but significantly altered the distribution among lipid fractions. Incubation with 3-methylindole caused a decrease in the incorporation of [14C]glycerol into phosphatidylcholine, while radioactivity accumulated in the neutral lipid fraction. The other lipid fractions responded variably. Similarily, Flow 2000 human diploid lung fibroblasts were incubated for 24 h with 3-methylindole followed by treatment with [14C]glycerol, resulting in a 74% decrease in the incorporation of [14C]glycerol into phosphatidylcholine and a 50% increase in its accumulation in neutral lipid. The results indicate that 3-methylindole inhibits the synthesis of phosphatidylcholine from diacylglycerol precursors on the endoplasmic reticulum in cultured fibroblasts. This is an important observation as it shows that 3-methylindole affects the synthesis of phospholipids required for membrane turnover in cells that are not specialized for the production of phospholipids for surfactant.     

Anti-thrombin activities of heparin. Effect of saccharide chain length on thrombin inhibition by heparin cofactor II and by antithrombin.

The interactions of two proteinase inhibitors, heparin cofactor II and antithrombin, with thrombin are potentiated by heparin. Using two methods, we have studied the potentiating effects of a series of heparin (poly)saccharides with high affinity for antithrombin and mean Mr ranging from approx. 1700 to 18,800. First, catalytic amounts of heparin (poly)saccharide were added to purified systems containing thrombin and either heparin cofactor II or antithrombin. Residual thrombin activity was determined with a chromogenic substrate. It was found that only the higher-Mr polysaccharides (Mr greater than 8000) efficiently catalysed thrombin inhibition by heparin cofactor II, there being a progressive catalytic effect with increasing Mr of the polysaccharide. Weak accelerating effects were noted with low-Mr saccharides (Mr less than 8000). This contrasted with the well-characterized interaction of heparin with antithrombin and thrombin, where heparin oligosaccharides of Mr less than 5400 had absolutely no ability to accelerate the reaction, while (poly)saccharides of Mr exceeding 5400 showed rapidly increasing catalytic activity with increasing Mr. Secondly, these and other heparin preparations were added in a wide concentration range to plasma with which 125I-labelled thrombin was then incubated for 30 s. Inhibited thrombin was determined from the distribution of labelled thrombin amongst inhibitor-thrombin complexes, predominantly antithrombin-thrombin and heparin cofactor II-thrombin complexes. In this situation, where the inhibitors competed for thrombin and for the (poly)saccharides, it was found that, provided the latter were of high affinity for antithrombin and exceeded a Mr of 5400, thrombin inhibition in plasma was mediated largely through antithrombin. Polysaccharides of Mr exceeding 8000 that were of low affinity for antithrombin accelerated thrombin inhibition in plasma through their interaction with heparin cofactor II. High concentrations of saccharides of Mr 1700-5400 exhibited a size-dependent acceleration of thrombin inhibition, not through their interaction with antithrombin, but through their interaction with heparin cofactor II.     

The Opecoelidae (Digenea) of sparid fishes of the western Mediterranean. III. Macvicaria Gibson & Bray, 1982

Macvicaria obovata (Molin) n. comb. is redescribed from Sparus aurata off the Mediterranean coast of France and a neotype is designated. Specimens from Oblada melanura off Israel may belong to the same species. It is mainly characterized by the uterine extension between the ovary and the anterior testis and the lack of a vitelline confluence in the forebody. M. maillardi n. sp. is also described from Sparus aurata off the southern coast of France. Its uterus does not pass between ovary and testes and the vitelline fields are confluent in the forebody. M. crassigula (Linton) n. comb. is redescribed from Diplodus annularis, D. sargus, D. vulgaris, Pagellus erythrinus and Sparus pagrus off Corsica, Calamus bajonado off Bermuda, Spicara smaris, D. annularis off Yugoslavia, D. sargus off Israel, and D. cervinus, Sparodon durbanensis and Cheilodactylus fasciatus in the SW Indian Ocean. It is similar to M. maillardi, but differs in being smaller, having a greater sucker ratio and a larger pharynx. It may well be a species-complex. M. dubia (Stossich) n. comb. is redescribed from Oblada melanura off Corsica and Yugoslavia. It is similar to M. maillardi and M. crassigula, but has a more anteriorly situated genital pore.     

The Lepocreadiidae (Digenea) of fishes from the north-east Atlantic: review of the genus Neolepidapedon Manter, 1954, with a description of N. smithi n. sp.

A new species, Neolepidapedon smithi, is described from the fish Mora moro in the north-eastern Atlantic Ocean and is distinguished from other members of the genus. It differs from its congeners in the extension of the vitellarium into the forebody and/or the body shape. The genus Neolepidapedon is reviewed and a key to species given. The genus has previously contained up to 20 species, but is here restricted to eight species, which possess a very thick male duct wall within the cirrus-sac, a narrow internal seminal vesicle, an excretory vesicle restricted to the hindbody and no eye-spots. The remaining nominal species with a relatively thin-walled internal male duct, a globular internal seminal vesicle, an excretory system which reaches into the forebody and eye-spots are considered to belong to a separate group which is related to Opechona. Some of these species were included by Yamaguti (1971) in his new subgenus Neolepidapedon (Neolepidapedoides), which is raised to full generic status. Eight new combinations are made: Neolepidapedoides belizensis (Fischthal, 1977), N. dollfusi (Durio & Manter, 1968), N. equilatum (Siddiqi & Cable, 1960), N. hypoplectri (Nahhas & Cable, 1964), N. israelense (Fischthal, 1980), N. macrum (Overstreet, 1969), N. medialunae (Montgomery, 1957) and N. mycteropercae (Siddiqi & Cable, 1960).     

Elevation of lung glutathione by oral supplementation of L-2-oxothiazolidine-4-carboxylate protects against oxygen toxicity in protein-energy malnourished rats.

The objectives of this study were to investigate whether oral supplementation of L-2-oxothiazolidine-4-carboxylate (OTC) is effective for increasing tissue glutathione (GSH) concentrations in rats fed a diet very low (0.5%) in protein-a model of wasting malnutrition-and to determine the efficacy of OTC for protection against pulmonary oxygen toxicity. Weanling rats, fed a 0.5 or 15% protein diet for 2 wk, were given an oral supplement of OTC, and tissue GSH concentrations were measured over a 24 h period. OTC supplementation to rats fed 0.5% protein significantly increased GSH concentrations in liver and lung, but not in kidney and blood, when compared with the 0.5% protein unsupplemented group. The liver GSH concentration in the 0.5% protein OTC-supplemented group was higher than the 15% control group. Daily supplementation of OTC protected rats from pulmonary oxygen toxicity during 4 days of 85% oxygen exposure as determined by lung-to-body weight ratios and in vivo proton magnetic resonance imaging. Although hyperoxia exposure increased lung GSH concentrations in all groups, OTC supplementation was effective for increasing lung GSH concentration in rats fed the 0.5% protein diet. This study demonstrated that oral administration of OTC to wasting malnourished rats is an effective procedure to increase GSH concentration rapidly in target organs such as lung, and that daily supplementation of a low dose of OTC has a sustained effect to protect against pulmonary oxygen toxicity during 4 days of hyperoxia exposure.     

Preferential expression of neo-CRP epitopes on the surface of human peripheral blood lymphocytes

Antibodies specific for C-reactive protein (CRP) have been reported to react with certain human peripheral blood lymphocytes (PBL); however, the nature of the antigen has not been clearly defined. In the present study we identified the CRP antigenicity on PBL as a CRP neoepitope not seen on the native-CRP molecule. Neo-CRP epitopes are expressed when the native pentameric form of CRP is dissociated into free subunits. Commercial anti-CRP antisera were found to possess a significant proportion of specificities (up to 16% of the total reactivity) directed against neo-CRP antigenicity. Since similar reagents had been used in previous studies on the reactivity of anti-CRP antisera with PBL, we set out to determine if either native- or neo-CRP epitopes were preferentially expressed on PBL. We prepared antisera monospecific for native-CRP and neo-CRP, respectively, and characterized these reactivities in both direct and indirect enzyme immunoassays. When analyzed by flow cytometry, anti-neo-CRP but not anti-native-CRP antiserum was found to react with normal PBL. F(ab')2 fragments of affinity-purified anti-neo-CRP had identical activity, and the reactivity against CRP was absorbed by reagents expressing neo-CRP but not native-CRP epitopes. Flow cytometric analyses of monocyte-depleted PBL from 25 normal donors detected a mean of 23.8 +/- 5.8% anti-neo-CRP-positive cells, a higher proportion of PBL expressing the CRP antigen than previously reported. Our findings indicate that a molecule identical to, or cross-reactive with, a neo-antigenic form of CRP is present on the surface of a significant proportion of normal human PBL.     

Macvicaria taksengi n. sp. (Digenea: Opecoelidae) in marine teleosts from Pinang,Malaysia

Summary A new species, Macvicaria taksengi (Opecoelidae: Plagioporinae), is described from the fishes Otolithes ruber and Sillago sihama from Pinang, Malaysia. It differs from most other members of the genus in the position of the ovary relative to the testes and the anterior position of the genital pore. A brief discussion on the Indo-West Pacific forms of the genus Macvicaria and related genera includes references to several new combinations: M. [Lebouria] isaitschikowi (Layman, 1930), M. [Plagioporus] sillagonis (Yamaguti, 1938), M. [Plagioporus] chrysophrys (Nagaty & Abdel Aal, 1969) and M. [Plagioporus (Plagioporus)] longisaccus (Fischthal & Kuntz, 1964).     

Leishmania mexicana mexicana: attachment and uptake of promastigotes to and by macrophages in vitro

Promastigotes of Leishmania mexicana mexicana attach to mouse macrophages in vitro in the absence of serum by a wheat germ agglutinin-like ligand on the surface of the promastigote that binds to the N-acetyl glucosamine moiety of a receptor on the surface of the macrophage. The binding is temperature dependent, and the macrophage receptor is trypsin, cytochalasin B, and is assisted or inhibited as for attachment. Treatment of promastigotes with proteolytic enzymes uncovers a receptor for a serum component that binds strongly to a mouse macrophage receptor in vitro. The strain of mice donating the macrophages had little effect upon attachment and uptake except that A strain mouse macrophages attached fewer promastigotes in 10 min than those of outbred mice, but took up as many promastigotes over 90 min as those of outbred mice. Low responder Biozzi mouse macrophages took up more promastigotes than high responder Biozzi mouse macrophages. Normal unheated human, rabbit, and guinea pig sera lysed promastigotes and so inhibited their attachment to macrophages in vitro. Unheated immune serum showed an enhanced inhibition of attachment. Heated normal serum allowed attachment and uptake, while promastigotes treated with heated immune serum showed enhanced attachment to and uptake by macrophages. Treatment of macrophages in vitro with immune serum enhanced their ability to attach promastigotes and to engulf them. Repeated 90-min exposures of a population of promastigotes to uptake by mouse macrophages in vitro did not deplete the population of any sub-population more likely to be taken by macrophages.(ABSTRACT TRUNCATED AT 250 WORDS)