Ellipsomyxa gobii (Myxozoa: Ceratomyxidae) in the common goby Pomatoschistus microps (Teleostei: Gobiidae) uses Nereis spp. (Annelida: Polychaeta) as invertebrate hosts

Nereis diversicolor O.F. Müller and N. succinea Frey et Leuckart (Polychaeta, Nereidae) living in brackish shallow areas in Denmark are naturally infected with tetractinomyxon actinospores. Infected Nereis spp. were experimentally fed to various potential fish hosts, and the actinosporean stages developed into myxosporean stages of Ellipsomyxa gobii K?ie, 2003 (Ceratomyxidae) in the gallbladder of the common goby Pomatoschistus microps (Kr?yer) (Gobiidae). The European eel Anguilla anguilla (L.), three-spined stickleback Gasterosteus aculeatus L., small sand eel Ammodytes tobianus L., flounder Platichthys flesus (L.), European plaice Pleuronectes platessa L. and common sole Solea solea (L.) did not become experimentally infected. In Danish shallow brackish areas P. microps is naturally infected with E. gobii, in some areas with a prevalence >90%. We compared small subunit ribosomal DNA sequences of the actinosporean with E. gobii from P. microps. Sequences were identical, which further verifies that both forms belong to the same organism. This is the first myxozoan two-host life cycle in the marine environment.     

Internal Transcribed Spacer Sequence-Based Phylogeny and Polymerase Chain Reaction-Restriction Fragment Length Polymorphism Differentiation of Tilletia walkeri and T. indica

ABSTRACT A polymerase chain reaction-restriction fragment length polymorphism assay to distinguish Tilleita walkeri, a rye grass bunt fungus that occurs in the southeastern United States and Oregon, from T. indica, the Karnal bunt fungus, is described. The internal transcribed spacer (ITS) region of the ribosomal DNA repeat unit was amplified and sequenced for isolates of T. indica, T. walkeri, T. horrida, and a number of other taxa in the genus Tilletia. A unique restriction digest site in the ITS1 region of T. walkeri was identified that distinguishes it from the other taxa in the genus. Phylogenetic analysis of the taxa based on ITS sequence data revealed a close relationship between T. indica and T. walkeri, but more distant relationships between these two species and other morphologically similar taxa.     

A combination of different polymerase chain reaction (PCR) assays for the presumptive identification of Yersinia pestis

A combination of four polymerase chain reaction (PCR) assays targeting the Yersinia pestis-specific plasmoidal genes of the fraction 1 capsular antigen and plasminogen activator/coagulase, the gene of the V antigen of the Yersinia virulence plasmid, and the chromosomal 16S rRNA gene was evaluated for the identification of Y. pestis isolates. All four assays were subjected to the same sample preparation technique, reagents and cycling conditions. Eighteen Y. pestis, 66 Y. pseudotuberculosis, 40 Y. enterocolitica strains, the type strains of the other Yersinia species, and 20 other pathogenic bacterial strains were investigated. By using the proposed combination of PCR assays all Y. pestis strains were identified correctly. The applicability of this combination of PCR assays was demonstrated by the detection of Y. pestis DNA in spiked tissues from Rattus norwegicus and fleas (Xenopsylla cheopis and Ctenocephalides spp.). As little as 60 genome equivalents were detected. This system is applicable for monitoring Y. pestis and its vectors in enzootic natural foci and in the diagnosis of plague in humans and animals.     

Occurrence of zearalenone, alpha- and beta-zearalenol in bile of breeding sows in relation to reproductive performance

Although zearalenone-induced reproductive disorders and the clinical appearance of hyperestrogenism were reproduced and documented quite often the role of zearalenone-contaminated fodder as a cause for fertility problems in sow breeding is still discussed controversial. Therefore the correlation of zearalenone and zearalenone-derivatives in bile (n = 794) and feed (n = 158) with fertility problems of unknown origin was investigated in this study. For the analysis of zearalenone and its derivatives in bile a HPLC/EIA combination was used. On the one hand, this procedure guaranteed the quantitatively reproducible detection, on the other hand, the investigation expenditure could be kept small with regard to a later effort in the routine diagnostics. The detection limits for zearalenone, alpha- and beta-zearalenol in bile were at 1.0 ng/ml, 1.0 ng/ml, and 3.0 ng/ml, respectively. Results were confirmed by GC-MS. Zearalenone and zearalenone-derivatives were detected in almost every bile analysed. The contamination rate was 96.2%. In opposition to recent investigations beta-zearalenol was perceived as a relevant metabolite in swine. The contamination rate of feeding stuffs was 25.9%. Incubation of samples with beta-glucosidase did not elevate the detected amounts of zearalenone. As the measurable concentrations in bile and fodder were only slightly correlated the analysis of bile represents a reasonable alternative for fodder investigation. However, a correlation between the occurrence of zearalenone, alpha- and beta-zearalenol in bile of sows and non-infectious reproductive disorders could not be established at the loading level found. These results are in line with those statements obtained in feeding experiments regarding the risk evaluation of zearalenone in sow reproduction.     

Detection of the genome of bovine viral diarrhea virus (BVDV) using the polymerase chain reaction after reverse transcription (RT-PCR): comparison of methods for the isolation of ribonucleic acid (RNA) from clinical samples

The RT-PCR is an in vitro technique that is increasingly being used for diagnosis of viral animal pathogens. Due to its high sensitivity it is considered as an alternative to current standard methods for detecting BVDV especially in pooled samples, e.g. from bulk tank milk. A prerequisite for the performance of RT-PCR is an efficient and simple method for sample preparation. The aim of this work was to compare the efficiency of three commercially available kits for RNA extraction, and their suitability for sample preparation for the detection of the BVDV genome by RT-PCR in blood, milk and tissue samples. The kits were based on different methods for extraction of RNA and differed in costs, labour and time consumption. The most sensitive RT-PCRs (exception: heparinised blood) were obtained when sample preparation was performed by acidic guanidinium-isothiocyanate-phenol-chloroform extraction with the Trizol (Gibco) reagent. Using a kit based on the binding of RNA to silica membrane in a spin column, positive results in RT-PCR were obtained from all samples, but with lower sensitivity. The advantage of the column-based kits is that they are less time-consuming, easier to handle and suitable for automatisation of sample preparation. A kit using salt precipitation of the desoxribose nucleic acid (DNA) and proteins was unsuitable for the isolation of viral RNA from the samples.     

Victor Hofmeister (1829-1994), Königl. Dresden Veterinary School--contributions to digestive physiology and animal nutrition

Victor Hofmeister (1829-1894), a chemist, was active between 1862-1894 at the Tier?rztliche Hochschule Dresden. His common work with Haubner, Siedamgrotzky and especially Ellenberger supplied basis information on digestibility of feestuffs (sheep, horses) about various clinical-chemical or toxicological questions, but particularly about the digestive physiology in horses, pigs, dogs and ruminants. The main results of the research group in Dresden outlast the last 100 years and represent valuable aspects for present knowledge in this field.     

Effects on Soft Wheat (Triticum aestivum L.) Quality of Increased Puroindoline Dosage

Wheat (Triticum aestivum L.) grain hardness affects many end‐product quality traits and is controlled primarily by the Hardness (Ha) locus that contains the Puroindoline a and b genes (Pina and Pinb, respectively). All soft hexaploid wheats carry the same Pin alleles, and hard wheats carry a mutation in Pina or Pinb. Here we test the heritability and milling and flour quality effects of increased Pin dosage in soft wheat. Previous experiments have suggested that grain softness can be enhanced by increasing Ha locus dosage through chromosome substitutions. Segregation data from a cross of cultivar Chinese Spring substitution lines with six doses of the Ha locus to the locally adapted soft wheat cultivar Vanna indicate that the substituted B genome Ha locus was not transmitted and that the A genome Ha locus was transmitted normally. Genotypes with the added Pins on the A genome produced seeds that were 7.4 hardness units softer. These softer double Ha genotypes were lower in flour yields, but produced flour with lower ash content, reduced starch damage, and smaller mean particle size. Soft wheats with increased Ha dosage may be useful in improving soft wheat quality through its effects on particle size and starch damage.     

Dry‐Grind Processing of Corn with Endogenous Liquefaction Enzymes

An amylase corn has been developed that produces an α‐amylase enzyme that is activated in the presence of water at elevated temperatures (>70°C). Amylase corn in the dry‐grind process was evaluated and compared with the performance of exogenous amylases used in dry‐grind processing. Amylase corn (1–10% by weight) was added to dent corn (of the same genetic background as the amylase corn) as treatments and resulting samples were evaluated for dry‐grind ethanol fermentation using 150‐g and 3‐kg laboratory procedures. Ethanol concentrations during fermentation were compared with the control treatment (0% amylase corn addition or 100% dent corn) which was processed with a conventional amount of exogenous α‐amylase enzymes used in the dry‐grind corn process. The 1% amylase corn treatment (adding 1% amylase corn to dent corn) was sufficient to liquefy starch into dextrins. Following fermentation, ethanol concentrations from the 1% amylase corn treatment were similar to that of the control. Peak and breakdown viscosities of liquefied slurries for all amylase corn treatments were significantly higher than the control treatment. In contrast, final viscosities of liquefied slurries for all amylase corn treatments were lower than those of the control. Protein, fat, ash, and crude fiber contents of DDGS samples from the 3% amylase corn treatment and control were similar.     

Velvetbean (Mucuna pruriens) extracts: impact on Meloidogyne incognita survival and on Lycopersicon esculentum and Lactuca sativa germination and growth

Velvetbean (Mucuna spp.) is a summer annual that has been used as a cover crop to reduce erosion, fix nitrogen and suppress weeds and plant-parasitic nematodes. Crude aqueous extracts (1:15 dry weight plant/volume water) were made from velvetbean plant parts, and various concentrations of the extracts were evaluated in vitro for toxicities to different stages of Meloidogyne incognita (Kofoid and White) Chitwood and for suppression of hypocotyl and root growth and inhibition of germination of tomato (Lycopersicon esculentum L.) and lettuce (Lactuca sativa L.). Germination was only affected by the full-strength extract from leaf blades. Lettuce root growth was the most sensitive indicator of allelopathic activity of the plant part extracts. Lettuce and tomato root growth was more sensitive to the extract from main roots than to extracts of other plant parts, with lethal concentration (LC50) values of 1.2 and 1.1% respectively. Meloidogyne incognita egg hatch was less sensitive to extracts from velvetbean than the juvenile (J2) stage. There was no difference among LC50 values of the extracts from different plant parts against the egg stage. Based on LC50 values, the extract from fine roots was the least toxic to J2 (LC50 39.9%), and the extract from vines the most toxic (LC50 7.8%). The effects of the extracts were nematicidal because LC50 values did not change when the extracts were removed and replaced with water.     

Do intracoelomic telemetry transmitters alter the post‐release behaviour of migratory fish?

Electronic tags have become a common tool in fish research, enhancing our understanding of how fish interact with their environment and move among different habitats, for estimating mortality and recording internal physiological states. An often‐untested assumption of electronic tagging studies is that tagged fish are representative of untagged conspecifics and thus show ‘normal’ behaviour (e.g. movement rates, swimming activity, feeding). Here, we use a unique data set for potamadromous walleye (Sander vitreus) in Lake Huron and Lake Erie tributaries to assess whether the lack of appropriate controls in electronic tagging could seriously affect behavioural data. We used fish tagged in previous years and compared their migratory behaviour during the spawning season to fish tagged in a current year at the same location. The objective of the study was to determine whether intracoelomic acoustic tag implantation altered downstream movement of walleye after spawning. Fish tagged in a given season travelled slower downstream from two river spawning sites than fish tagged in previous years. Fish tagged one or two years earlier showed no differences between each other in downstream travel time, in contrast to fish tagged in a given year. Our results support notions that standard collection and intracoelomic tagging procedures can alter short‐term behaviour (i.e. days, weeks, months), and as such, researchers should use caution when interpreting data collected over such time periods. Further, whenever possible, researchers should also explicitly evaluate post‐tagging effects on behaviour as part of their experimental objectives.