Congenital deformity of the paw in a captive tiger: case report

Background

Although Morbillivirus and Toxoplasma gondii have emerged as important pathogens for several cetaceans populations over the last 20 years, they have never been identified together in a Mysticete. In particular, morbilliviral infection has been never described in the Mediterranean fin whale population.

Case presentation

On January 2011 an adult male of fin whale (Balaenoptera physalus) stranded along the Tyrrhenian coastline of Italy. During necropsy, tissue samples from heart, skeletal muscle, mesenteric lymph nodes, liver, spleen, lung, and kidney were collected and subsequently analyzed for Morbillivirus and Toxoplasma gondii by microscopic and molecular methods. Following the detailed necropsy carried out on this whale, molecular analysis revealed, for the first time, the simultaneous presence of a Dolphin Morbillivirus (DMV) and T. gondii infection coexisting with each other, along with high organochlorine pollutant concentrations, with special reference to DDT.

Conclusion

This report, besides confirming the possibility for Mysticetes to be infected with DMV, highlights the risk of toxoplasmosis in sea water for mammals, already immunodepressed by concurrent factors as infections and environmental contaminants.     

On the reality of local and ecological races in lymnaeid snails (Mollusca,Gastropoda, Lymnaeidae)

The reality of ecological and local races was investigated in two widespread Palearctic species of lymnaeid snails (Lymnaea stagnalis and Radix auricularia). Several methods of statistical analysis were used, including two-way ANOVA, cluster analysis, and discriminant analysis for six plastic shell characters. It was shown that none of the methods used could convincingly demonstrate that ecological and local races were present in the studied species. Even in cases when statistically significant differences among the populations in the morphology of shells were revealed, these differences were very small and did not correspond to the meaning that was put into the concept of “race” by malacologists in the past. Perhaps, the formation of such races in pond snails is possible only in case of populations being formed in suboptimal conditions, for example, in thermal springs or at large depths. This being the case, the distinguishing of races requires using other shell characters, both quantitative and qualitative ones.     

Are there general rules governing parasite diversity? Small mammalian hosts and gamasid mite assemblages

Parasite biodiversity varies on several scales, and in particular among different host species. Previous attempts at finding relationships between host features and the diversity of the parasite assemblages they harbour have yielded inconsistent results, suggesting strongly that any patterns might be taxon-specific. Here, we examined the potential of three host characteristics (host body mass, basal metabolic rate, and area of the geographical range) as determinants of parasite diversity in one group of ectoparasites, gamasid mites (superfamily Dermanyssoidea), using data from 63 species of small mammalian hosts. Our analyses used three measures of parasite diversity (species richness, the Shannon diversity index, and average taxonomic distinctness), and controlled for sampling effort and phylogenetic influences. Although several significant relationships were observed, they depended entirely on which diversity measure was used, or on which host taxon was investigated (insectivores vs. rodents and lagomorphs). In addition, the present results on patterns of mite diversity were not consistent with those of an earlier study involving roughly the same host taxa and the same biogeographical area, but a different group of ectoparasites, i.e. fleas. Thus, there appears to be no universal determinant of parasite diversity, and associations between host features and parasite diversity probably evolve independently in different host–parasite systems.     

Bayesian DNA copy number analysis

Background  

Some diseases, like tumors, can be related to chromosomal aberrations, leading to changes of DNA copy number. The copy number of an aberrant genome can be represented as a piecewise constant function, since it can exhibit regions of deletions or gains. Instead, in a healthy cell the copy number is two because we inherit one copy of each chromosome from each our parents.     

Geographical patterns of abundance: testing expectations of the ‘abundance optimum’ model in two taxa of ectoparasitic arthropods

Aim The ‘abundance optimum’ hypothesis predicts that species abundance peaks in the locality with the most favourable conditions and decreases with an increase of distance from that locality. We tested this prediction for 9 fleas and 13 gamasid mite species. Location We used published data on fleas and gamasid mites that are parasitic on small mammals throughout the Palaearctic. Methods For each ectoparasite, we computed the correlation between the relative abundance on its principal host species in a region and the distance from that region to the region of maximum abundance. Then, the correlation coefficients were used in a meta‐analysis. We also made a cross‐species comparison between relative abundances in localities (a) closest to and (b) furthest from the locality of maximum abundance. Results Although the relationship between the relative abundance in a region and the distance from that region to the region of maximum abundance was negative in 19 out of 22 ectoparasites, it was only statistically significant in three of them. However, a meta‐analysis of coefficients of correlations across all species revealed a significant negative effect of the distance from the region of maximum abundance on relative abundance in a particular region. A cross‐species comparison between relative abundances in the localities closest to and furthest from the locality of maximum abundance demonstrated that the former were significantly higher than the latter. Main conclusions A lack of strict host specificity in the ectoparasites studied, and the absence of any strong spatial correlations among the environmental variables affecting ectoparasite reproduction and abundance, may provide an explanation for the spatial independence in abundance values of most species. However, a preference for a particular host even in host‐opportunistic parasites combined with species‐specific environmental preferences could be the reason behind the weak, but significant, negative abundance–distance relationship across species. The contradiction between results obtained when separate species were considered and when the overall pattern was analysed across species suggests that there exists a general underlying spatial pattern that can often be masked by other factors.     

Optimization of mycophenolic acid production in solid state fermentation using response surface methodology

Mycophenolic acid (MPA) can be produced in solid state fermentation. An isolate of Penicillium brevi-compactum ATCC 16024 grown on moist wheat bran produced a titre of 425 mg per kg of wheat bran. Central composite rotatable design and response surface methodology were employed to derive a statistical model for media optimization towards production of mycophenolic acid. Five levels with a five factorial design were adopted. The correlation coefficient was 0.82, ensuring a satisfactory adjustment of the model to the experimental values. This statistical design was very effective in improving the titre of mycophenolic acid up to 3286 mg per kg of wheat bran. Received 24 July 1998/ Accepted in revised form 4 December 1998     

Biogeography of parasite abundance: latitudinal gradient and distance decay of similarity in the abundance of fleas and mites,parasitic on small mammals in the Palearctic,at three spatial scales

We tested whether biogeographic patterns characteristic for biological communities can also apply to populations and investigated geographic patterns of variation in abundance of ectoparasites (fleas and mites) collected from bodies of their small mammalian hosts (rodents and shrews) in the Palearctic at continental, regional and local scales. We asked whether (i) there is a relationship between latitude and abundance and (ii) similarity in abundance follows a distance decay pattern or it is better explained by variation in extrinsic biotic and abiotic factors. We analysed the effect of latitude on mean intraspecific abundance using general linear models including proportional abundance of its principal host as an additional predictor variable. Then, we examined the relative effect of geographic distance, biotic and abiotic dissimilarities among regions, subregions or localities on the intraspecific dissimilarity in abundance among regions, subregions or localities using Generalized Dissimilarity Modelling. We found no relationship between latitude and intraspecific flea or mite abundance. In both taxa, environmental dissimilarity explained the largest part of the deviance of spatial variation in abundance, whereas the effect of the dissimilarity in the principal host abundance was of secondary importance and the effect of geographic distance was minor. These patterns were generally consistent across the three spatial scales, although environmental variation and dissimilarity in principal host abundance were equally important at the local scale in fleas but not in mites. We conclude that biogeographic patterns related to latitude and geographic distance do not apply to spatial variation of ectoparasite abundance. Instead, the geographic distribution of abundance in arthropod ectoparasites depends on their responses, mainly to the off-host environment and to a lesser extent the abundance of their principal hosts.     

Sexual size dimorphism and sex ratio in arthropod ectoparasites: contrasting patterns at different hierarchical scales

The aims of this study were to determine whether sexual size dimorphism in fleas and gamasid mites (i) conforms to Rensch’s rule (allometry of sexual size dimorphism) and (ii) covaries with sex ratio in infrapopulations (conspecific parasites harboured by an individual host), xenopopulations (conspecific parasites harboured by a population of a given host species in a locality) and suprapopulations (conspecific parasites harboured by an entire host community in a locality). Rensch’s rule in sexual size dimorphism was tested across 150 flea and 55 mite species, whereas covariation between sexual size dimorphism and sex ratio was studied using data on ectoparasites collected from small mammalian hosts in Slovakia and western Siberia. For fleas, we controlled for the confounding effect of phylogeny. The slope of the linear regression of female size on male size was significantly smaller than 1 in fleas, but did not differ from 1 in mites. The proportion of males in flea infrapopulations significantly increased with an increase in the female-to-male body size ratio. The same was true for obligatory haematophagous mites. No relationship between sex ratio and sexual size dimorphism was found for xenopopulations of either taxon or for mite suprapopulations. However, when controlling for the confounding effect of phylogeny, a significant negative correlation between sex ratio and sexual size dimorphism was revealed for flea suprapopulations. We conclude that (i) some macroecological patterns differ between ectoparasite taxa exploiting the same hosts (allometry in sexual size dimorphism), whereas other patterns are similar (sexual size dimorphism-sex ratio relationship in infrapopulations), and (ii) some patterns are scale-dependent and may demonstrate the opposite trends in parasite populations at different hierarchical levels.     

Ladislavella tumrokensis: The first molecular evidence of a Nearctic clade of lymnaeid snails inhabiting Eurasia

In this study, we provide the first molecular evidence for a possible connection between freshwater mollusc faunas across the Bering Strait via the Beringian Land Bridge using data inferred from gastropods of the family Lymnaeidae. The gastropods collected from geothermal springs in the Tumrok Mountains, West Kamchatka, Russia, share the nuclear internal transcribed spacer 2 (ITS2) and the cytochrome oxidase subunit I gene (COI) haplotypes, thus being as sister to those recorded for lymnaeid snails in the Stagnicola elodes group from Canada and the USA. Two lymnaeid species, Lymnaea (Orientogalba) tumrokensis Kruglov and Starobogatov, 1985 Kruglov, N. D., & Starobogatov, Y. I. (1985). Ob'yom podroda Galba i skhodnykh s nim podrodov roda Lymnaea [The volume of the subgenus Galba and of the other similar subgenera of the genus Lymnaea (Gastropoda, Pulmonata)]. Zoologicheskiy Zhurnal, 64, 24–35.[Web of Science ®] , [Google Scholar] and Lymnaea (Polyrhytis) kurenkovi Kruglov and Starobogatov, 1989 Kruglov, N. D., & Starobogatov, Y. I. (1989). Mollyuski podroda Polyrhytis roda Lymnaea fauny SSSR (Pulmonata, Lymnaeidae) [Molluscs of the subgenus Polyrhytis of the genus Lymnaea of the fauna of the USSR (Pulmonata, Lymnaeidae)]. Zoologicheskiy Zhurnal, 68, 14–20.[Web of Science ®] , [Google Scholar], were described from the Tumrok geothermal locality, but actually they are morphological variations of a single taxon of subspecies rank re-classified here as Ladislavella catascopium tumrokensis. This subspecies is the first discovered representative in the genus, which formed a dwarf race in a geothermal habitat. Our findings highlight the possible exchange between freshwater faunas in Beringia during the Pleistocene and an important role of geothermal ecosystems as possible cryptic refugia for freshwater hydrobionts.     

Emission analysis of RE3+ (RE = Sm,Dy):B2O3‐TeO2‐Li2O‐AlF3 glasses

This article reports on the optical properties of 0.5% mol of Sm³⁺, Dy³⁺ ion‐doped B₂O₃‐TeO₂‐Li₂O‐AlF₃ (LiAlFBT) glasses. The glass samples were characterized by optical absorption and emission spectra. Judd‐Ofelt theory was applied to analyze the optical absorption spectra and calculate the intensity parameters and radiative properties of the emission transitions. The emission spectra of Sm³⁺ and Dy³⁺:LiAlFBT glasses showed a bright reddish‐orange emission at 598 nm (⁴G_5/2 → ⁶H_7/2) and an intense yellow emission at 574 nm (⁴F_9/2 → ⁶H_13/2), respectively. Full width at half maximum (FWHM), stimulated emission cross section, gain bandwidth and optical gain values were also calculated to extend the applications of the Sm³⁺ and Dy³⁺:LiAlFBT glasses. Copyright © 2012 John Wiley & Sons, Ltd.