A unique novel reptilian paramyxovirus, four atadenovirus types and a reovirus identified in a concurrent infection of a corn snake (Pantherophis guttatus) collection in Germany

In 2009, 26 clinical samples (organs and oral/cloacal swabs) from a total of 24 corn snakes (Pantherophis guttatus) from a single owner were sent to our laboratory to be tested for the presence of viruses. Paramyxoviruses (PMV), adenoviruses (AdV) and reoviruses were detected by RT-PCR, PCR and virus isolation methods. Three snakes were infected with all three viruses at the same time, while two other snakes had a double infection (PMV and reo, AdV and reo) and nine other snakes had a single infection with any of the three viruses. No viruses were detected in 10 animals. All isolated reoviruses were identical to one another and to the reptilian orthoreovirus isolate 55-02 in the partial RNA dependent RNA polymerase (RDRP) gene sequence. AdV partial polymerase sequences represented four different types, one of which was first described here: most similar to SnAdV-1, while the other three were identical to known types: SnAV-1, -2 and -3. However, the detected single PMV differed distinctly from described reptile PMV and was a new type. According to partial L gene, HN gene and U gene sequences it may be the first described representative of a third squamatid PMV cluster: "group C" within the proposed reptilian PMV genus "Ferlavirus". Nucleotide identity values for the L gene of the new PMV compared to group A viruses range between 76.5 and 80.3%, and between 80.5 and 81.2% compared to group B viruses. For the HN gene, these values were similar: 78.2-80% (A) and 79.9-80.5% (B) and somewhat lower for the U gene: 72.7-75.4% (A) and 69.7-70% (B). No reports on the prevalence of concurrent viral infection in captive snake populations have been published so far. The possibility of concurrent infection with several different viruses and subsequent consequences for animal health should be kept in mind when testing reptile samples for viruses.     

Extended-spectrum beta-lactamases-producing gram-negative bacteria in companion animals: action is clearly warranted!

Extended-spectrum beta-lactamases (ESBL)-producing Gram-negative bacteria pose a serious threat to Public Health in human medicine as well as increasingly in the veterinary context worldwide. Several studies reported the transmission of zoonotic multidrug resistant bacteria between food-producing animals and humans, whilst the contribution of companion animals to this scenario is rather unknown. Within the last decades a change in the social role of companion animals has taken place, resulting in a very close contact between owners and their pets. As a consequence, humans may obtain antimicrobial resistant bacteria or the corresponding resistance genes not only from food-producing animals but also via close contact to their pets.This may give rise to bacterial infections with limited therapeutic options and an increased risk of treatment failure. As beta-lactams constitute one of the most important groups of antimicrobial agents in veterinary medicine, retaliatory actions in small animal and equine practices are urgently needed. This review addresses the increasing burden of extended-spectrum beta-lactam resistance among Enterobacteriaceae isolated from companion animals. It should emphasize the urgent need for the implementation of antibiotic stewardship as well as surveillance and monitoring programs of multi resistant bacteria in particular in view of new putative infection cycles between humans and their pets.     

Gene expression and hormonal regulation of adiponectin and its receptors in bovine mammary gland and mammary epithelial cells

Although the functions of adiponectin, a differentiated adipocyte‐derived hormone, in regulating glucose and fatty acid metabolism are regulated by two subtypes of adiponectin receptors (AdipoRs; AdipoR1 and AdipoR2), those in ruminants remain unclear. Therefore we examined the messenger RNA (mRNA) expression levels of adiponectin and its receptors in various bovine tissues and mammary glands among different lactation stages, and the effects of lactogenic hormones (insulin, dexamethasone and prolactin) and growth hormone (GH) on mRNA expression of the AdipoRs in cultured bovine mammary epithelial cells (BMEC). AdipoRs mRNAs were widely expressed in various bovine tissues, but adiponectin mRNA expression was significantly higher in adipose tissue than in other tissues. In the mammary gland, although adiponectin mRNA expression was significantly decreased at lactation, AdipoR1 mRNA expression was significantly higher at peak lactation than at the dry‐off stage. In BMEC, lactogenic hormones and GH upregulated AdipoR2 mRNA expression but did not change that of AdipoR1. In conclusion, adiponectin and its receptor mRNA were expressed in various bovine tissues and the adiponectin mRNA level was decreased during lactation. These results suggest that adiponectin and its receptors ware changed in mammary glands by lactation and that AdipoRs mRNA expression was regulated by different pathways in BMEC.     

Optimization, in-house validation, and application of a liquid chromatography-tandem mass spectrometry (LC-MS/MS)-based method for the quantification of selected polyphenolic compounds in leaves of grapevine (Vitis vinifera L.)

Polyphenols in grapevine can be constitutive or induced, depending upon cultivar, plant organ, and environmental influences. The aim of the presented work was to develop and optimize a liquid chromatography-tandem mass spectrometry (LC-MS/MS) method to study the pattern and amount of selected polyphenols in leaves of Vitis vinifera L. The method is simple and does not require any sample cleanup. It covers representative metabolites of the structure classes cinnamic acids, flavonoids, and stilbenes and enables the simultaneous separation and quantification of 13 polyphenols within 9 min at concentration levels between 0.1 and 3 μg/g. We present the method performance characteristics and its application to the quantification of polyphenols in grapevine leaves of the cultivars Riesling and Pinot noir. A total of 7 of 13 target polyphenols were detected at concentrations above the limits of quantification. Interestingly, instead of the expected trans-resveratrol, the investigated leaf samples of both cultivars contained cis-resveratrol-3-O-glucoside. The measurements also showed that Riesling leaves tended to contain higher concentrations of the selected polyphenols than Pinot noir. In view of its intended future use, the developed method has been shown to be a powerful and fast tool to study polyphenols in grapevine leaves subjected to environmental stress conditions.     

Mapping and use of seed protein loci for marker-assisted selection of growth habit and photoperiod response in <Emphasis Type="Italic">Nuña</Emphasis> bean (<Emphasis Type="Italic">Phaseolus vulgaris</Emphasis> L.)

The individual segregations of 14 seed protein loci named, SpA to SpM and Pha (phaseolin), were analyzed in a RIL population developed from the cross Xana × Cornell 49242. These seed protein loci were included in a genetic map previously developed in the same population. Protein loci, SpA, SpB, SpE, SpI, SpJ, and Pha, are organized in two different clusters, both located in linkage group (LG) 7; SpF, SpG, SpK, SpL, and SpM, form a single cluster in LG 4; SpC, is located in LG 3; and SpD, in LG 1. A close linkage was identified between the SpD seed protein locus, and the fin gene, controlling determinate growth habit. The usefulness of the SpD locus as a marker for the indirect selection of determinate growth habit and photoperiod insensitivity was checked in a F₂ population derived from the cross G12587 (an indeterminate and photoperiod sensitive nuña bean) × Sanilac (determinate and photoperiod insensitive) and in a set of Mesoamerican and Andean genotypes. Results indicate that SpD protein locus was useful to detect individuals having determinate growth habit and photoperiod insensitivity in the cross G12587 × Salinac although some recombinants were found. However, the linkage between the SpD locus and the genes controlling growth habit and photoperiod sensitivity should be checked before using the SpD locus for the indirect selection of these traits in different backgrounds.     

The draft genome of Ciona intestinalis: insights into chordate and vertebrate origins

The first chordates appear in the fossil record at the time of the Cambrian explosion, nearly 550 million years ago. The modern ascidian tadpole represents a plausible approximation to these ancestral chordates. To illuminate the origins of chordate and vertebrates, we generated a draft of the protein-coding portion of the genome of the most studied ascidian, Ciona intestinalis. The Ciona genome contains approximately 16,000 protein-coding genes, similar to the number in other invertebrates, but only half that found in vertebrates. Vertebrate gene families are typically found in simplified form in Ciona, suggesting that ascidians contain the basic ancestral complement of genes involved in cell signaling and development. The ascidian genome has also acquired a number of lineage-specific innovations, including a group of genes engaged in cellulose metabolism that are related to those in bacteria and fungi.     

Fractionation of the platinum-group elements during mantle melting

Experiments in sulfide-silicate systems demonstrate that two sulfide phases are stable in the asthenospheric upper mantle: a crystalline osmium-iridium-ruthenium-enriched monosulfide and a rhodium-platinum-palladium-enriched sulfide melt. During silicate melt segregation, monosulfide stays in the solid residue, dominating the noble metal spectrum of residual mantle. The sulfide melt is entrained as immiscible droplets in the segregating silicate melt, defining the noble metal inventory of the basaltic component.     

Burrowing behaviour of unionid mussels in subtropical rivers: Implications for survey guidelines

1. Conservation efforts have increased in response to global mussel declines, and effective surveys are a crucial step in assessing and monitoring mussel populations and in determining their conservation status. The burrowing behaviour of mussels can affect their detectability, and a better understanding of these behaviours would help to improve survey design and guidelines.
2. The burrowing depth of mussels may differ between seasons, habitat conditions, species, and individuals, and little is known about the burrowing behaviour of mussels in subtropical rivers.
3. Burrowing depth variation was examined and compared at three sites in the San Marcos, Guadalupe, and San Antonio river drainages in central Texas. In addition, laboratory experiments were used to determine whether observed differences between field sites and seasons could be linked to differences in substrate type and water temperature and to examine differences between species.
4. Seasonal variation in burrowing depth was found at all field sites, and water temperature was a significant factor for explaining variation in burrowing depth, but there was no clear relationship between burrowing depth and temperature in shorter term laboratory experiments, where individual variation was high and burrowing behaviour seemed to be solely a function of time.
5. Mussels burrowed significantly deeper in finer substrate (sand vs. gravel) in both field and laboratory experiments. Few significant differences between species were found in the field, but no differences were found in the laboratory experiments.
6. The results suggest that surveys may need to follow different guidelines depending on local conditions, such as substrate and water temperature. Surveys will be less efficient and may fail to detect larger proportions of populations in colder water temperatures. In addition, a larger proportion of burrowed mussels can be expected at sites with finer substrate, such as sand. Under these conditions, visual searches will not suffice, as a large part of the population or specific species may be overlooked.

     

Biliary Cystadenoma in a Rabbit (Oryctolagus cuniculus)

Biliary tumors are rarely diagnosed in rabbits, and there are very few published case reports of this disease within this group of animals. This case involves an approximately 6-year-old spayed female pet rabbit that was referred for an abdominal mass noted on survey full-body radiographs obtained during an examination after presenting for acute onset anorexia. Otherwise, the patient had an unremarkable history, and physical examination abnormalities were limited to a slightly distended abdomen. Laboratory evaluation revealed an isolated elevation in gamma-glutamyl transpeptidase. Ultrasonography documented a 5.4-cm multicystic, intrahepatic mass with hyperechoic septations. The mass was surgically resected and described histopathologically as a proliferation of ectatic duct structures with a simple epithelial lining, supporting a diagnosis of biliary cystadenoma. The rabbit recovered without incident and was doing well 15 months postsurgery. The case is presented with a review of all reported cases and discussion of the potential origins of this unusual tumor in the rabbit. Surgery is recommended in rabbits that are diagnosed with a biliary tumor.