Microbes from apiarian sources: Bacillus spp. in frass of the greater wax moth

Frass from the greater wax moth, Galleria mellonella, obtained from feral colonies of honey bees, Apis mellifera; from managed honey bee colonies; and from a laboratory culture of the wax moth was sampled for aerobic Gram-positive spore-forming rods. One hundred eighty-five strains belonging to the genus Bacillus were isolated, and most were identified. One hundred and three of the isolates were from frass from the wax moth culture, 61 were from frass from managed honey bee colonies, and 21 were from frass from feral honey bee colonies. The species most frequently isolated varied with the source. Fifty-eight isolates from frass from managed honey bee colonies were B. cereus which was isolated from this source only, but B. sphaericus was the most frequent isolate from frass from the wax moth culture. Bacillus megaterium and organisms belonging to the B. alvei-B. thiaminolyticus spectrum were the most frequent isolates from frass from feral honey bee colonies. Most strains isolated produced caprylate esterase-lipase, leucine aminopeptidase, and phosphoamidase. The numbers of isolates, the species, and the enzymatic activity of the strains varied with the source of the frass. In fact, the complete microbial complement varied with the source. These results are discussed in relation to possible roles of Bacillus spp. in the nutrition of the wax moth as well as the microbial ecology of the honey bee colony.     

Major trends of evolution in palms

From the diversity found among palms the following evolutionary trends are suggested:habit: from sympodial to monopodial;size: from moderate toward large and also toward small;stem: from unbranched to dichotomously branched, from little to much sclerenchyma, from short to elongate internodes;leaf: from an undivided eophyll to a palmate, costapalmate, pinnately ribbed or pinnate blade; from undivided and plicate to divided along the adaxial rib (“induplicate”) or along the abaxial rib (“reduplicate”); from pinnate to bipinnate or to pinnae onceor twicedivided longitudinally; from sheath split opposite the petiole to sheath tubular; from marcescent to deciduous; from central vascular bundles of the petiole with a single phloem strand to two phloem strands;inflorescence units: from moderately branched to spicate or less frequently to more diffusely branched, from one unit per leaf axil to more than one per axil, from among the leaves to below them or to above them in a compound terminal inflorescence, from pleonanthic to hapaxanthic;prophyll: from completely to incompletely encircling the peduncle, from incompletely to completely sheathing in bud;bracts: from conspicuous to small or absent at maturity, first peduncular bract from tubular and open at the apex to completely enclosing the inflorescence in bud, and then from ungrooved to deeply plicate;flower arrangement: from solitary, pedicellate, bracteolate flowers to a sympodial cincinnus of 2 or 3 or more, or to a short monopodial axis of 2–4 or more;bracteoles: from sheathing and prophyllate to completely closed or to incompletely developed or absent;flowers: from bisexual to unisexual, then associated with polygamy or monoecism to dioecism;perianth: from trimery to dimery or tetramery to decamery or to reduced and monochlamydeous;sepals: from distinct and imbricate to connate or separated;petals: from distinct and imbricate to valvate, or strongly imbricate, or connate; from small and ovate to large and variously shaped, or to small;stamens: from 6 to 3 or to more than 6 (to 950+);filaments: from relatively slender and distinct to broad and thick, and often connate or adnate to the perianth or both;staminodes: from stamenlike with abortive anthers only, to short teeth, or to a cupule at the base of the ovary, or to absent;pollen: from monosulcate to trichotomosulcate to dicolpate to monocolpate, diporate, or triporate;gynoecium: from apocarpous to syncarpous, from thin walls to thick, variously specialized walls;carpels or locules: from 3 to 2-1 or to 4–10;ovules: from moderate to small or to large, from anatropous to hemianatropous to campylotropous to orthotropous;pistillode: from only slightly modified from the gynoecium to vestigial or lacking or rarely to prominent;fruit: from fleshy to dry and fibrous;endocarp: from little differentiated or thin, to thick and hard, and sometimes with a pore or operculum over the embryo;seed: from moderate to small or to very large, from entire to dissected, bilobed, or perforate;endosperm: from homogeneous to invaginated or ruminate;germination: from remotetubular or -ligular to adjacent-ligular;chromosome complement: fromn = 18 ton = 17, 16, 15, 14, 13.     

Morphological and molecular identification of hymenolepidid cestodes in children and synanthropic rodents from rural Mexico

Hymenolepidid cestodes of synanthropic rodents represent a risk for public health. In order to describe the occurrence of hymenolepidids in children and the role of rodents as a potential source of infection, we conducted a morphological and molecular survey on cestodes in two rural villages from Yucatan, Mexico. One hundred and thirty-five stool samples from children (64 from Paraíso and 71 from Xkalakdzonot), 233 Mus musculus (159 from Paraíso and 74 from Xkalakdzonot) and 125 Rattus rattus (7 from Paraíso and 118 from Xkalakdzonot) were analyzed for the presence of cestodes. Three hymenolepidid species were identified morphologically: Hymenolepis nana in 7.8% of children from Paraíso, Hymenolepis microstoma in 4.4% of M. musculus from Paraíso and Hymenolepis diminuta in 15.3% of R. rattus from Xkalakdzonot. The molecular characterization and phylogenetic analysis based on mitochondrial cytochrome c subunit 1 (CO1) gene and ribosomal internal transcribed spacer 1 (ITS1) region, confirmed the identity of the three cestodes isolated from Yucatan. Phylogeny of the CO1 gene identified intraspecific genetic differences within H. nana ranging from 0 to 5%, in H. microstoma from 0 to 0.4%, and in H. diminuta ranged from 0 to 6.5% which suggests, the presence of complex species within H. nana and H. diminuta infecting humans and rodents, as reported by other authors. Based on the morphological and molecular results, and the epidemiological evidence, infections with H. nana suggest a non-zoonotic transmission; however, the presence of H. microstoma and H. diminuta in synanthropic rodents serve as a possible source for human infection.     

LYCOSPORA FROM CARBONIFEROUS LEPIDOSTROBUS COMPRESSIONS

Spores were extracted from Carboniferous Lepidostrobus compressions in order to associate in situ microspores with dispersed species of Lycospora. Two hundred twenty-six cones were examined, of which 61 contained spores. Fertile cones came from the Westphalian D of England, Namurian B through Westphalian D of the Appalachian and Illinois basins, and the Westphalian D of the Western Interior. Cones were separated into species based on microspore and cone morphology. Lycospora trigonoreticulata was produced by Lepidostrobus princeps from Westphalian C-D rocks from Missouri, the Illinois Basin, and the Appalachian Basin. Lycospora rotunda was produced by Lepidostrobus sp. A from Westphalian A rocks of Alabama. Two cone species produced Lycospora torquifer: Lepidostrobus praelongus from the Westphalian D of Pennsylvania and Lepidostrobus variabilis from the Westphalian A and C of the Illinois and Appalachian basins. Lycospora punctata was produced by Lepidostrobus cf. squarrosus from the Westphalian D of England, the Appalachian Basin, and Illinois Basin. Lycospora noctuina was produced by Lepidostrobus haslingdenensis from the Namurian B/C of Illinois. Microspore species are differentiated primarily on the basis of size, cingulum structure and width, and ornamentation. Cone species differ in width and distal lamina size, shape, and attitude. Lycospora species isolated from clastic species of Lepidostrobus differ completely from those of coal-swamp species, confirming that lycopod trees from clastic environments represent biologically different species from those centered in coal swamps.     

Taxonomy of monogeneans of deep sea fishes in southeastern Australia

The following monogeneans from deepwater fish in southeastern Australia are described, based on a survey of 1,563 fish (66 or 67 species, 35 families, 15 orders): Reimericotyle ceratoscopeli from Myctophum phengodes, M. hygomi, Hygophum hygomi and Ceratoscopelus warmingii; Diclidophora tubiformis n. sp. from Coryphaenoides serrulatus and C. subserrulatus; Diclidophora sp. from Lepidorhynchus denticulatus; Polycliphora nezumiae from Coryphaenoides serrulatus; Paracyclocotyla sp. from Lepidion microcephalus; juvenile Paracyclocotyla sp. from Hoplostethus atlanticus; Polyipnicola hygophi from Hygophum hygomi, Notoscopelus resplendens, Electrona risso and Myctophum phengodes; Diclidophoropsis sp. from Nezumia sp.; Eurysorchis manteri from Hyperoglyphe sp.; Heteraxinoides sp. from Synagrops japonicus; Megalocotyle helicoleni from Helicolenis papillosus. The following species are recorded but not described: Allocotylophora polyprionum (Diclidophoroidea), four unidentified species of the Diclidophoroidea from Diastobranchus capensis, both Hoplostethus atlanticus and H. intermedius, Chlorophthalmus sp. and Synagrops japonicus, respectively, one species of the Capsaloidea from Enoplosus armatus, one species of the Capsalidae from Lepidotrigla argus, one species of the Dactylogyrinae from Atypichthys strigatus, and one species of the Ancyrocephalinae from Chlorophthalmus nigripinnis.     

New genera,species and records of rhinebothriidean cestodes (Platyhelminthes) parasitic in Australian stingrays (Elasmobranchii: Batoidea)

Collections of rhinebothriidean cestodes (Platyhelminthes) from Australian batoid elasmobranchs revealed the presence of a number of new genera and species. Ruptobothrium louiseuzeti n. g., n sp. is described from the reticulate whipray, Himantura australis Last, Naylor & Manjaji-Matsumoto, from off the Northern Territory and Mixobothrium queenslandense n. g., n sp. is described from the green sawfish, Pristis zijsron Bleeker, from off north-eastern Queensland. Two new species of Rhabdotobothrium Euzet, 1953 are described: Rhabdotobothrium meridionale n. sp. from the southern eagle ray Myliobatis tenuicaudatus Hector from off South Australia and Rhabdotobothrium anoxypristidis n. sp. from the narrow sawfish, Anoxypristis cuspidatus (Latham) from off north Western Australia. A new species of Scalithrium Healy & Reyda, 2016, Scalithrium australiense n. sp., is described from the reticulate whipray, Himantura australis Last, Naylor & Manjaji-Matsumoto, from off northern Western Australia. Scalithrium smitii (Shinde, Deshmukh & Jadhav, 1981) n. comb. is reported from Australian waters for the first time in the black spotted stingray Maculabatis toshi (Whitley) from off northern Western Australia. New host and geographical records are provided for Stillabothrium jeanfortiae Forti, Aprill & Reyda, 2016 from the brown whipray Maculobatis toshi (Whitley) and the black-spotted whipray, Maculabatis cf. astra (Last, Manjaji-Matsumoto & Pogonoski) from Moreton Bay in southern Queensland.

     

Lepocreadiidae (Digenea) from the batfish of the genus Platax Cuvier (Teleostei: Ephippidae) from the southern Great Barrier Reef,Queensland, Australia

The following species are described from Platax spp.: Neomultitestis aspidogastriformis n. sp., from P. teira, off Heron Island, Queensland, which can be distinguished from its congeners by the transversely elongate ventral sucker divided into three loculi and probably by testis number; Multitestis magnacetabulum Mamaev, 1970, from P. teira, off Heron Island, Queensland; Diploproctodaeum rutellum (Mamaev, 1970), from P. teira, off Heron Island, Queensland; Diploproctodaeum tsubameuo n. sp., from P. batavianus, from the Swain Reefs, off Queensland, which differs from its congeners in its overlapping, posteriorly attenuated testes and 38-55 ovarian lobes; and Diplocreadium sp., from P. batavianus, from the Swain Reefs, off Queensland.     

Effects of the N-terminal and C-terminal domains of <Emphasis Type="Italic">Meiothermus ruber</Emphasis> CBS-01 trehalose synthase on thermostability and activity

Numerous trehalose synthases (TreS) from thermophilic microorganisms have extra C-terminal domains. To determine the function of the N- and C-terminal domains of TreS from the thermophilic bacterium Meiothermus ruber CBS-01, the two domains were expressed. From the findings, the N-terminal domain from M. ruber was not active when compared with that from Thermus thermophilus, which had been studied previously. The circular dichroism spectrum showed that the secondary structure of N-terminal domain from M. ruber underwent a greater change than that of C terminus. In addition, the N-terminal domain from T. thermophilus and C terminus from M. ruber were fused. The fusion protein TSTtMr was more efficient and thermostable than the TreS from M. ruber. The N-terminal domain from M. ruber and C terminus from T. thermophilus were fused. The optimum temperature and thermostability of fusion protein TSMrTt were similar to the TreS from M. ruber. It was presumed that aside from the C-terminal domain, the N-terminal domain of TreS from thermophilic bacteria could influence thermostability. For the TreS from M. ruber, the mutant protein R392F led to a complete loss in activity, and R392A showed a sharp decrease in activity.     

Chronic Nicotine Administration Differentially Affects Neurotransmitter Release from Rat Striatal Slices

Abstract: The objective of these experiments was to determine whether the chronic administration of nicotine, at a dose regimen that increases the density of nicotine binding sites, alters the nicotine-induced release of [³H]dopamine ([³H]DA), [³H]norepinephrine ([³H]NE), [³H]serotonin ([³H]5-HT), or [³H]acetylcholine ([³H]ACh) from rat striatal slices. For these experiments, rats received subcutaneous injections of either saline or nicotine bitartrate [1.76 mg (3.6 µmol)/kg, dissolved in saline] twice daily for 10 days, and neurotransmitter release was measured following preloading of the tissues with [³H]DA, [³H]NE, [³H]5-HT, or [³H]choline. Chronic nicotine administration did not affect the accumulation of tritium by striatal slices, the basal release of radioactivity, or the 25 mM KCl-evoked release of neurotransmitter. Superfusion of striatal slices with 1, 10, and 100 µM nicotine increased [³H]DA release in a concentration-dependent manner, and release from slices from nicotine-injected animals was significantly (p < 0.05) greater than release from saline-injected controls; release from the former increased to 132, 191, and 172% of release from the controls following superfusion with 1, 10, and 100 µM nicotine, respectively. Similarly, [³H]5-HT release increased in a concentration-related manner following superfusion with nicotine, and release from slices from nicotine-injected rats was significantly (p < 0.05) greater than that from controls. [³H]5-HT release from slices from nicotine-injected rats evoked by superfusion with 1 and 10 µM nicotine increased to 453 and 217%, respectively, of release from slices from saline-injected animals. The nicotine-induced release of [³H]NE from striatal slices was also concentration dependent but was unaffected by chronic nicotine administration. [³H]ACh release from striatal slices could not be detected when samples were superfused with nicotine but was measurable when tissues were incubated with nicotine. The release of [³H]ACh from slices from nicotine-injected rats was significantly (p < 0.05) less than release from controls and decreased to 36, 83, and 77% of control values following incubation with 1, 10, or 100 µM nicotine, respectively. This decreased [³H]ACh release could not be attributed to methodological differences because slices from nicotine-injected rats incubated with nicotine exhibited an increased [³H]DA release, similar to results from superfusion studies. In addition, it is unlikely that the decreased release of [³H]ACh from striatal slices from nicotine-injected rats was secondary to increased DA release because [³H]ACh release from slices from hippocampus, which is not tonically inhibited by DA, also decreased significantly (p < 0.05) in response to nicotine; hippocampal slices from nicotine-injected rats incubated with 1 and 10 µM nicotine decreased to 42 and 70%, respectively, of release from slices from saline-injected animals. Results indicate that the chronic administration of nicotine increases the ability of nicotine to induce the release of [³H]DA and [³H]5-HT and decreases the ability of nicotine to evoke the release of [³H]ACh but does not alter the nicotine-induced release of [³H]NE from brain slices.     

Studies on R-phycoerythrins from two Antarctic marine red algae and a mesophilic red alga

R-phycoerythrin was purified from two benthic red algae, Iridaea cordata and Phyllophora antarctica, obtained growing at ?2°C under thick sea ice off the coast of Antarctica. For the I. cordata protein, the molecular mass was 245,000 Da, and its secondary structure was 60% α helix, 17% β sheet, 16% turn, and 7% other. The light-harvesting faculties of the I. cordata protein resembled those of R-phycoerythrins from mesophilic red algae and were distinctive from the novel R-phycoerythrin from P. antarctica. Deconvolution of the visible absorption spectrum of R-phycoerythrin from I. cordata indicated a minimum of five component bands having maxima at 568, 558, 534, 496, and 481?nm. R-phycoerythrins from the mesophilic Porphyra tenera and psychrophilic Phyllophora antarctica had the same five bands. The protein from Phyllophora antarctica obtained its unique spectrum from a more intense component at 482?nm, and a less intense band at 533?nm. This change was probably produced by a replacement of phycoerythrobilin by phycourobilin. A temperature study of the circular dichroism CD was obtained for R-phycoerythrin from I. cordata from 4 to 80°C. Laser time-resolved fluorescence studies on R-phycoerythrin showed bilin to bilin energy transfer with a 60.2-ps lifetime, which should occur by the Förster resonance. The similarities in spectra between the proteins from I. cordata and Porphyra tenera and the different spectrum for the protein from Phyllophora antarctica show that only particular antarctic habitats require unique R-phycoerythrins.     

Yangtse River sediments and erosion rates from source to sink traced with cosmogenic Be: Sediments from major rivers

Estimates of regional erosion and sediment mixing from different sources in the Yangtse River system are presented, based on sand samples collected from major tributaries and the trunk stream, at 23 sites between western Sichuan and the Yangtse Delta. Mixing is estimated from concentrations of Mg, Ca, Sr, Ti, Mn and Fe, which are substantially higher in sand from major tributaries in the western Yangtse River catchment than from tributaries in the eastern catchment. Intermediate concentrations occur in sand from the Yangtse Delta, both for modern samples from the surface and for early Holocene samples from drill holes. Mixing ratios indicate that 35 ± 5% of sand in the delta came from eastern sources. A similar result was obtained using cosmogenic ¹⁰Be in quartz grains as a tracer of mixing. Regional erosion rate estimated from ¹⁰Be in sand grains from high mountain catchments of the western Yangtse River are mostly similar to rates based on sediment gauging but are sometimes higher, and range to over 700 m Ma^− 1, while ¹⁰Be measured at upper Yangtse River tributaries on the northeast Tibetan plateau gave rates of 20-30 m Ma^− 1. For the eastern catchments, ¹⁰Be measurements from quartz sand and sediment gauging both gave rates of 30-70 m Ma^− 1. Eroding at this rate, the eastern catchments could not supply more than 20% of the sediment in the delta, in contrast with 35% estimated from geochemical fingerprints. The relative input from eastern sources may have been higher in Late Pleistocene times, under a different climatic regime, and reworking of Pleistocene deposits may still be in progress.     

Isolation and Partial Characterization of Bacteriophages of the Phytopathogen Pseudomonas syringae

Bacteriophages isolated from culture supernatants of Pseudomonas syringae pv. syringae and from sewage were identified. The DNA from each phage was isolated and digested with the restriction endonuclease EcoRI. Eight isolates were determined to be different, with two phage isolates from sewage having restriction patterns identical to two phages from culture supernatants. The sizes of the phage DNA ranged from 24 to49 kilobases for isolates from sewage and from 39 to 52.5 kilobases for the isolates from culture supernatants. Buoyant densities of phage particles in CsCl varied from 1.498 to 1.507 g/cm³ for isolates from sewage and from 1.506 to 1.516 g/cm³ for isolates from culture supernatants. Electron microscopy revealed four morphological types. Based on plaque-forming ability of culture supernatants, 31 out of 47 strains of P. syringae are probably lysogenic.     

Xylophagous entomofauna in branches of oaks (Quercus spp.) and its significance for oak health in the Karst region of Slovenia

Samples of dying branches from 121 trees of Quercus pubescens, Q. cerris, and Q. petraea were taken from 102 sites in Seslerio autumnalis-Quercetum petraeae and Ostryo-Quercetum pubescentis forests. After nine months’ rearing in eclectors, branches were cut to 20-cm sections, and signs of infestation as well as larvae and adult insects were noted. We analysed 395 sections of branches from Q. pubescens, 125 sections from Q. cerris, and 85 sections from Q. petraea. We found 44 adult insects: 45% were from the Cerambycidae family (Callimus angulatus ssp. angulatus, Poecilium alni, and Exocentrus adspersus), 18% were from the Scolytinae subfamily (Scolytus intricatus, Xyleborus dispar), 4% from the Buprestidae family (Coraebus florentinus), 4.5% from the Cleridae family (Tilloidea unifasciata), and 28.5% from other families. In addition, 145 larvae were found: 50% from the Cerambycidae family, 39% from the Buprestidae family, 4% from the Scolytinae subfamily, and 7% from other families. Significant difference in the abundance of adult insects and larvae with regard to the diameter of branch sections and the host species were found. 78% of dying branches showed signs of infestation. Species of the Buprestidae, Scolytinae, and Cerambycidae represent important factors in the decline in oak vitality in the lower Karst region of Slovenia.     

New species of rhigonematid and thelastomatid nematodes from indigenous New Zealand millipedes

Abstract

Seven new species of nematode are described from the hind-gut of several different millipedes indigenous to New Zealand: Heth hamatus n. sp. from Spirobollelus antipodarus and Icosidemus hochstetteri from Auckland, Erythrodemus echinopogon from Seddonville, and Eumasligonus sp. from Aickens, and Avenue Scenic Reserve; Thelastoma moko n. sp. from coastal specimens of Eumastigonus sp.; Thelastoma rigo n. sp. from montane specimens of Eumastigonus sp.; Dudekemia prolifica n. sp. from Spirobellelus antipodarus; Dudekemia alpinensis n. sp. from the montane Eumastigonus sp.; Dudekemia kaorinus n. sp. from Eumastigonus kaorinus from Hardys Creek; and Dudekemia hirsutus n. sp. from Erythrodemus echinopogon from Seddonville.

The family Rhigonematidae is reviewed.     

Lectins from latices of Euphorbia and Elaeophorbia species

Crude latex sera from 17 members of the genus Euphorbia and from Elaeophorbia drupifera (Euphorbiaceae) contained a wide range of agglutinating abilities. Homogeneous lectins were isolated from latices of Euphorbia coerulescens, E. hermentiana, E. lactea, E. lactea cristata, E. lathyris, E. trigona and Elaeophorbia drupifera. The M,s of the lectins ranged from 60 to 67 000, and the unit weights from 27 to 38 000. pI measurements showed that each latex contained from five to 13 isolectins. The amino acid compositions of the seven lectins were determined: those from E. hermentiana, E. lactea, E. lactea cristata, E. trigona and Elaeophorbia drupifera are related.     

Abundance and Diversity of Psychrotolerant Cultivable Mycobiota in Winter of a Former Aluminous Shale Mine

This paper is a speleomycological report from a former aluminous shale mine in Janowiec, Poland. Fungi were identified morphologically and molecularly. Microclimatic conditions differed significantly between locations of the study. However, the external environment around the mine did not directly increase the community composition and concentration of fungi in the mine. The density of fungi isolated from the air outside the mine was 63.1 colony forming units (CFU) per 1 cm³ of air. Inside the mine, fungal density ranged from 287.5 to 655 CFU per 1 m³ from the air, 28.4 to 131.1 CFU per 1 cm² from the rock surfaces and 288.1 to 335.1 CFU per 1 cm³ from the water. Pearson correlation analysis showed that the levels of fungi isolated from the air were correlated positively with temperature, relative humidity and CO₂ concentration. The concentration of fungi isolated from the rock surfaces showed a positive correlation with air flow. Five species of filamentous fungi were isolated from the sampled external air, 10 species from the internal air, six species from the rock surface and 11 species from the water. The fungi most frequently isolated from the air and water of the mine belonged to Penicillium spp., whereas from the rock surface, Geomyces pannorum was most frequently isolated. Some of the fungi present in the mine can be psychrotolerant and pathogenic for humans and animals, and they can also cause degradation of rocks.     

Filamentous Fungi Associated with Bivalve Mollusks from Polluted Biotopes of Ussuriiskii Bay,Sea of Japan

We have studied for the first time the taxonomic composition of filamentous fungi associated with the bivalve mollusks Crenomytilus grayanus (Bunker, 1853) and Modiolus modiolus (Linnaeus, 1758), collected in polluted biotopes of Ussuriiskii Bay (Peter the Great Bay, Sea of Japan). One hundred fifty-five strains of higher fungi were isolated, and 35 species of filamentous fungi were identified. Out of these, 28 species were anamorphous fungi of the genera Aspergillus (12), Penicillium (10), Acremonium (1), Alternaria (1), Aureobasidium (1), and Cladosporium (3) (Deuteromycota), and 7 were species of the genera Chaetomium (6) and Myxotrichum (1) (Ascomycota). Twenty-four species of filamentous fungi were isolated from the internal organs of C. grayanus: 8 from the muscles, 8 from the hepatopancreas, 6 from the female gonads, 4 from the mantle, 3 from the kidneys and male gonads, and 1 from the gills. Twenty-one species of filamentous fungi were isolated from the internal organs of Modiolus modiolus: 10 from the muscles, 6 from the hepatopancreas, 5 from the female gonads, 3 from the kidneys, 3 from the mantle, and 1 from the gills. The bulk of the isolated species of the genera Aspergillus, Penicillium, Cladosporium, and Chaetomium were pathogenic and toxigenic fungi.     

ITS rDNA sequences of Pomphorhynchus laevis (Zoega in Müller, 1776) and P. lucyi Williams & Rogers, 1984 (Acanthocephala: Palaeacanthocephala)

The internal transcribed spacers (ITS-1 and ITS-2) of the ribosomal RNA gene of Pomphorhynchus laevis (Zoega in Müller, 1776) (Acanthocephala) isolated from various fish species across Central and Southern Europe were compared with those of P. lucyi Williams & Rogers, 1984 collected from the largemouth bass Micropterus salmonoides Boulenger from the USA. The nucleotide sequences of ITS regions of P. laevis from minnows Phoxinus phoxinus (L.) and chub Leuciscus cephalus (L.) from two distant localities in the Slovak Republic were found to be 100% identical. The ITS-1 and ITS-2 of P. laevis from chub from the Czech Republic and Italy were also mutually identical, but significantly different from Slovak worms (88.7% identity for ITS-1, 91.3% identity for ITS-2). A fifth sample collected from Barbus tyberinus Bonaparte from Italy was very similar to the sympatric Italian isolate from chub, possessing four nucleotide substitutions in ITS-1 (98.4% identity). The ITS rDNA sequences of P. lucyi differed significantly from those of P. laevis; the values of identity were 51.8–56.1% for ITS-1 and 63.1–65.3% for ITS-2, and were significantly higher than the range of P. laevis within-species variability. The results based on the ITS sequences confirmed the occurrence of strains in P. laevis from Continental Europe which are well defined by molecules but reveal only slight differences in their morphology.