Is pearl colour produced from Pinctada margaritifera predictable through shell phenotypes and rearing environments selections?

The black‐lipped pearl oyster, Pinctada margaritifera, is the most important farmed mollusc species in French Polynesia. Donor oyster selection among wild P. margaritifera individuals, chosen according to their inner shell colour, makes it possible to obtain the broadest range of cultured pearl colours of any species. This study demonstrates the relative influence of using black [B] or red [R] outer shell phenotypes, combined with green [G] or yellow [Y] inner shell phenotypes, on pearl darkness level, colour categories and lustre. A large scale grafting experiment was designed and carried out over five grow‐out locations, covering three archipelagos: Tuamotus, Society and Gambier. Results revealed that the [B + G] phenotypes may be used as donors to produce dark green pearl, which suit the demands of the Asian market; whereas, phenotypes incorporating [R] and/or [Y] phenotypes may be used to obtain multicolour pearls of medium/light darkness, which suit the demands of the European market. From an environmental point of view, the 1) [B] phenotype showed no significant variation for light and other pearl colour production, and 2) [Y] phenotype produced both the same rate of pearl darkness level and green colour pearls whatever the grow‐out location. A classification tree model was built to predict, according to shell phenotype and culture location, the colour and darkness level of harvested pearls. Lustre was shown to be more influenced by the environment than by phenotype. These results should be taken into account in pearl farm production management and in selective breeding programmes.     

Le développement de l' activité des estérases carboxyliques et de la phosphatase alcaline dans l' oesophage,le réseau,le rumen et le f euillet du boeuf1

The development of carboxylic esterases and alkaline phosphatase activity in the bovine forestomachs and esophagus The reticulum, the rumen, the omasum and the esophagus of 8 adult cattle, 6 veal calves, one four-day-old calf and 4 fetuses were examined for esterase and alkaline phosphatase activity. The localization and the intensity of these enzymes in the proventricular compartments are age-related. In the fetuses and the four-day-old calf the esterases are found only in the deeper epithelial cell layers, whereas in the veal calves and in the adults the horny and the transitional cell layer become strongly positive. Alkaline phosphatase is not present in the epithelium of the fetuses. A reaction band of this enzyme occurs at the level of the stratum transitionale in the four-day-old calf. In the adults the upper cells of the stratum spinosum and all the cells of the strata transitionale and corneum are positive. The enzyme activity in the esophagus is very slightly agerelated. The esterases are only found in the deeper epithelial layers, and alkaline phosphatase does not appear in the epithelium. The activity and the localization of these enzymes may be related to the keratinization and especially in the proventricular compartments of the adult, also to the absorption.     

A study of the ultrastructure and staining characteristics of the 'dental star' of equine incisors

The objective of this study was to examine the diameter, extent, orientation and contents of dentinal tubules in order to validate the hypothesis of pigment penetration into the dental star of equine incisival occlusal surfaces. The time of appearance and the configuration of the dental star on the incisival occlusal surface are macroscopically visible features that, along with other more reliable parameters, are used for the determination of horses' age. Although dental stars are an integral part of the equine incisor occlusive surface, the exact nature and microstructure of the dental star are poorly documented. Therefore, equine incisor dentine was examined macroscopically and by scanning electron microscopy to elucidate numerical density, diameter and 3-dimensional organisation of the dentinal tubules in the dental star. The dental star is surrounded by primary dentine and consists of a central core of tertiary dentine, an intermediate ring of pale secondary dentine and a peripheral rim of darker, yellowish-brown secondary dentine. The central core of tertiary dentine contains relatively few dentinal tubules (<8000/mm2) that have small diameters (mean +/- s.d. 1.67 +/- 034 microm) and are arranged in an irregular pattern. The surrounding pale ring of secondary dentine comprises manifestly more and wider tubules that lie almost parallel to the occlusal surface. The dark peripheral rim of the dental star contains high numbers of tubules (28,000-58,000/mm2) that have wide luminal diameters (mean +/- s.d. 3.09 +/- 0.31 microm) and open perpendicular to the occlusal surface. In contrast, the primary dentine surrounding the dental star is made up by a lower number of dentinal tubules (<25,000/mm2). The tubules of primary dentine, which are initially mean +/- s.d. 5.15 +/- 0.80 microm wide, are narrowed by circumferential deposits of peritubular dentine and are obliquely exposed at the occlusal surface. From these observations, it was concluded that the regional differences in numerical density, diameter and spatial orientation of the dentinal tubules may influence the penetration of food pigments into the equine occlusal surface and result in the particular staining of the dental star.     

Age-related morphometry of equine incisors

In the present study the age-related morphological characteristics of 948 equine incisors were investigated. After extraction, total incisival length and root length were measured at the vestibular side of the teeth. Equine incisors reach their maximal length 2-3 years after eruption. Notwithstanding severe occlusal wear, this maximal length is maintained during most of the horses' life due to prolonged root formation. Root formation, at the rate of 2.5 mm per year, starts at the age of 5-6 years and continues until the age of 17. As the root of the incisor develops, its apical foramen narrows and changes position. In young horses the apical foramen is situated at the apex of the tooth, whereas in older individuals it is located at the mesial, distal, or lingual side of the tooth at a distance of 5-15 mm from the dental apex. In horses aged over 20 years apical foramina are still present. Radiographic imaging is a good method with which to obtain reliable information concerning the total incisival length and the size and position of the apical foramen.     

Flukicidal action of closantel against immature and mature Fasciola hepatica in experimentally infected rats and sheep

The relative importance of peak level- and residual level-related flukicidal activity of closantel against immature and mature Fasciola hepatica was evaluated in a comparative efficacy trial using two animal species with a different plasma elimination pattern, that is, the rat and the sheep with an elimination half-life of less than one week and of two to three weeks, respectively. The rats were dosed orally with closantel at 20 mg kg-1 at two, four, six, eight and 10 weeks; the sheep at 10 mg kg-1 at eight, 10 and 12 weeks after artificial infection. Necropsy was performed either one week after treatment or 12 weeks after infection. Efficacy rates and the length of the recovered flukes were evaluated. It was demonstrated that the flukicidal effect of closantel is directly related to its peak plasma levels and less to its residual plasma concentrations. In the rat, a high efficacy (P less than 0.001) could be demonstrated against immature stages of four weeks or older. The two-week immature stages were less markedly affected. No significant differences in efficacy and size of the flukes were noted between the animals autopsied one week after treatment and those autopsied 12 weeks after infection. In the sheep, the efficacy against six-week and eight-week-old immature stages varied between 70.3 and 76.8 per cent and between 92.8 and 96.5 per cent, respectively. As in the rats, no marked differences in efficacy were noted between the animals autopsied one week after treatment and those autopsied 12 weeks after infection.(ABSTRACT TRUNCATED AT 250 WORDS)     

Molecular basis for the antimycotic and antibacterial activity of N-substituted imidazoles and triazoles: The inhibition of isoprenoid biosynthesis

The antimycotic N-substituted imidazoles and triazoles, such as imazalil, ketoconazole and itraconazole, interfere selectively at low concentrations (≥0.01nm) with the 14α-demethylase system (which is dependent on cytochrome P-450) of fungal cells, for example, Candida albicans and Penicillium italicum. This results in a decreased availability of ergosterol and the accumulation of 14α-methyl-sterols such as lanosterol. Cholesterol synthesis in a subcellular fraction of rat liver, in intact fibroblasts, and in vivo in rat liver, was much less sensitive, for example, to ketoconazole. The imidazole derivatives imazalil, miconazole, ketoconazole and parconazole, and the triazole derivatives propiconazole, terconazole and itraconazole affect the cytochrome P-450 species of microsomal fractions from Saccharomyces cerevisiae and rat liver. Cytochrome P-450 of rat-liver microsomes was much less sensitive to these azole derivatives, in parallel with the lower sensitivity of cholesterol synthesis. Using unilamellar vesicles composed of phosphatidylcholine, phosphatidyl-ethanolamine and diphosphatidylcholine, multilamellar vesicles of dipalmitoylphos-phatidylcholine, and intact S. cerevisiae, it was shown that the substitution of ergosterol by lanosterol leads to functional changes in the membranes. It is speculated that the selective interaction of the azole derivatives with the yeast microsomal cytochrome P-450 leads to the accumulation of 14a-methyl-sterols and results in changes in the permeability of the membranes and leakages. The observed inhibition of growth may have its origin in these changes. Miconazole, ketoconazole and deacylated ketoconazole (R-39519) also affect the growth of Staphylococcus aureus, miconazole being 12.5 and 14 times, respectively, more active than R-39519 and ketoconazole. The greater antibacterial activity of miconazole coincides with its greater inhibition of the biosynthesis of C-55 isoprenoid alcohol and vitamin K. The phosphorylated derivative of C-55 isoprenoid alcohol has functional importance in the biosynthesis of bacterial cell wall and membrane polymers, and the menaquinone vitamin K plays a role in the electron transport of Gram-positive bacteria. The reduced synthesis of these vital compounds may contribute to the antibacterial activity of miconazole.     

The distribution of intratubular dentine in equine incisors: a scanning electron microscopic study

The distribution of intratubular (peritubular) dentine was studied by scanning electron microscopy in 12 equine incisor teeth. High levels of intratubular dentine were found in the peripheral regions of the dentine. In these areas, a marked asymmetry occurred, as intratubular dentine was predominantly deposited onto the side of the dentinal tubular walls nearest to the dentino-enamel junction. The quantity and asymmetry of intratubular dentine were reduced towards the centre of the tooth. The significance of these variations in the amount and distribution of intratubular dentine between the different dentinal regions is discussed.     

Cell-specific Distribution of Oestrogen Receptor-alpha in the Bovine Ovary

In this study, the expression of estrogen receptor alpha (ERα) in the bovine ovary is described. ERα was visualized by immunohistochemistry on paraffin sections of ovaries obtained from 11 non‐pregnant and 2 pregnant animals. In general, ERα was not observed in cells of primordial, primary and secondary follicles, whereas weak expression was noticed in cells of healthy and arteric tertiary follicles. In corpora lutea cells the expression of ERα was obvious. Intermediate to high ERα expression was present in thecal cells and in cells of the superficial and deep stroma, tunica albuginea and surface epithelium. Furthermore, the expression of ERα in stroma and tunica albuginea cells was in general, highest in cows with the lowest plasma progesterone levels, and lowest in cows with the highest plasma progesterone levels. Remarkably, the ERα expression in pregnant cows was in general, lower than in non‐pregnant cows with similar plasma progesterone levels. The relatively high expression of ERα in thecal and stromal cells in comparison with that in follicle cells suggests an indirect effect of estrogen on the follicular development. However, the exact function of ERα in the bovine ovary together with the cycle‐dependent variations in ERα expression remain to be elucidated.     

Trichoderma sp. endochitinase and β-1,3-glucanase impede Rhizoctonia solani growth independently,and their combined use does not enhance impediment

Rhizoctonia solani causing rice sheath blight is responsible for significant crop yield losses. Trichoderma spp., biological control agents, have been reported to antagonize R. solani through coordinated action of several cell wall-degrading enzymes including endochitinase and β-1,3-glucanase. In this study two antifungal genes, encoding endochitinase and β-1,3-glucanase, isolated from Trichoderma sp. antagonistic to R. solani, were cloned individually in His-tagged expression vectors and mobilized in Escherichia coli for protein expression. The purified proteins assayed in vitro with R. solani impeded pathogen growth independently by causing hyphal distortions revealed through scanning electron microscopy. The combined use of endochitinase and β-1,3-glucanase did not enhance the inhibition. The distortions caused by endochitinase were due to catalytic activity of Glu172 and Asp241 residues on glycosidic linkages in chitin polymers, whereas Glu628, Tyr631, and Asp569 in β-1,3-glucanase targeted glucan polymers. The distinctions of this study from earlier reports are (a) chitin polymers in the R. solani cell wall are exposed and not embedded within the β-glucan matrix; (b) chitin and β-1,3-glucan are vital polymers in the R. solani cell wall, rather than chitin as the only main polymer; and (c) hyphal tips of R. solani remain unaffected after an antifungal assay with endochitinase and β-1,3-glucanase, instead of exhibiting distortion.