Reference values for selected ophthalmic diagnostic tests of the capuchin monkey (Cebus apella)

Purpose To perform selected ophthalmic diagnostic tests in healthy capuchin monkeys (Cebus apella) with the aim of establishing normal physiological reference values for this species. Methods A total of 15 healthy, capuchin monkeys were used to test most of the parameters in this investigation. Five of the 15 monkeys were used for the evaluation of normal conjunctival flora. Ages varied from 6 to 20 years of age. Selected diagnostic ocular tests were performed including Schirmer tear test (STT), tonometry using an applanation tonometer (Tonopen^®), central corneal thickness (CCT) using an ultrasonic pachymeter (Sonomed, Micropach^®, Model 200P+) and culture of the normal conjunctival bacterial flora. Results and discussion Results for selected ocular diagnostic tests investigated here for the capuchin monkey eye were as follows: IOP: 18.4 ± 3.8 mmHg; STT: 14.9 ± 5.1 mm/min; CCT: 0.46 ± 0.03 mm. No statistically significant differences between ages or genders were found for any of the results. Streptococcus sp. and Corynebacterium sp. were isolated from healthy conjunctival and eyelid margins, suggesting they are normal constituents of the conjunctival flora of the capuchin monkey. The data obtained in this investigation will help veterinary ophthalmologists and laboratory animal medicine specialists to more accurately diagnose ocular diseases in the capuchin monkey. These ophthalmic reference values will be particularly useful to diagnose discrete or unusual pathological changes of the capuchin monkey eye.     

Resistant accessions of wild Psidium spp. to Meloidogyne enterolobii and histological characterization of resistance

Meloidogyne enterolobii has been reported in some states of Brazil and other countries causing severe damage on commercial guava (Psidium guajava). The use of resistant varieties is the most effective way to manage nematode parasitism. This study screened 51 accessions of Psidium spp. selected from the Psidium Germplasm Collection (Embrapa) to look for resistance against M. enterolobii. Six months after inoculation, nematode reproduction factor (RF) was used to assess resistance. The following species were resistant to M. enterolobii: P. cattleianum (yellow guava), P. friedrichsthalianum (Costa Rican guava), Acca sellowiana (feijoa) and P. rufum (purple guava). All 43 wild accessions of P. guajava were susceptible, as well as three accessions of P. guineense (Brazilian guava), one of P. acutangulum (pear guava) and the susceptible control P. guajava cv. Paluma. When used as rootstocks under greenhouse conditions, P. cattleianum and P. friedrichsthalianum were compatible with cv. Paluma; however, in greenhouse and field conditions only 50% of both scions survived. No apparent hypersensitive response (HR) was seen in the resistant guava P. cattleianum and P. friedrichsthalianum. Juveniles were able to develop normal feeding sites similar to those in susceptible roots 6–13 days after inoculation (dai). From 27 to 32 dai, giant cell deterioration was observed and nematodes showed arrested development. The majority of nematodes failed to reach maturity and did not begin laying eggs in resistant roots. These results suggested that the induction of resistance is relatively late in this pathosystem.     

Canopy leaf area and leaf mass in the upper stratum of Urochloa hybrid ‘Mavuno’ grass subjected to nitrogen fertilisation

Nitrogen (N) inputs are recognised to maximise herbage mass (HM) in tropical perennial grasses, whereas less is clear on their impact on HM distribution and the effects on leaf mass (LM) and leaf area index (LAI) in the upper stratum. This 2 year study, carried out in Pirassununga, Brazil, assessed the HM distribution in the upper (>20 cm) and lower (<20 cm) strata in Urochloa hybrid ‘Mavuno’ grass maintained under similar pre- and post-cutting canopy heights with contrasting N fertilisation rates applied after each cutting (no-nitrogen, 15, 30, and 45 kg N ha⁻¹). The relevance of specific leaf area (SLA), leaf N concentration (NLeaf), tiller weight (TW) and population density to the LM and LAI of the upper stratum were also examined. Mavuno grass expressed a stable HM < 20 cm (59%–71% during Year I and 66%–80% for Year II), and apparent N fertilisation impacts on HM > 20 cm were verified at specific regrowth cycles during Year II. Mavuno grass pastures expressed plasticity for adjustments on leaf, tiller and population attributes, which were modulated by both climatic conditions and N fertilisation. Under favourable growth conditions during Year I, fertilised pastures were able to sustain higher NLeaf and SLA but associated with lower TW, resulting in maximisation of LAI but not in LM in the upper stratum. During Year II, fertilised pastures expressed higher NLeaf, SLA, number of basal tillers, despite the lowest TW, which resulted in higher LAI and LM in the upper stratum compared with non-fertilised pastures. Our results highlighted that adjustments on leaf and population attributes within the canopy were driven to maximise the upper stratum LAI, being positively affected by N fertilisation.     

Tilapia protein hydrolyzate improves growth performance,protein absorption and antioxidant status in Silver catfish (Rhamdia quelen)

This study evaluated the substitution of fish meal with tilapia protein hydrolyzate (TPH) in diets for Silver catfish (Rhamdia quelen) by verifying the effects on growth, body composition, blood and biochemical parameters, and biomarkers of oxidative stress. Five isoproteic and isoenergetic diets (37% crude protein, 3,800 kcal/kg) were produced with different substitution levels of TPH (0%, 5%, 10%, 15% and 20%) for fishmeal. The hydrolyzate was obtained by enzymatic hydrolysis from carcasses of Nile tilapia (Oreochromis niloticus), which were exposed to swine pepsin enzyme at 36°C for four hours. The experimental design was completely randomised with five treatments and four replications. The inclusion of 20% TPH in diets for silver catfish increased the growth of Silver catfish juveniles. At levels above 5%, there was an increase in body protein deposition and the efficiency of oxidative metabolism.     

Evaluation of growth and fatty acid profile of Nile tilapia (Oreochromis niloticus) fed with Schizochytrium sp.

The objective of this study was to evaluate growth, body chemical composition and lipid profile of Nile tilapia juvenile fed with Schizochytrium sp. Two hundred and forty Nile tilapia (Oreochromis niloticus) juvenile (1.33 ± 0.11 g) were distributed in 20 aquariums, at the density of 12 fish per aquarium. The juvenile were fed with five levels of Schizochytrium sp.: Control (0 g/kg of Schizochytrium sp. in feed); AS10 (10 g/kg of Schizochytrium sp. in feed); AS20 (20 g/kg of Schizochytrium sp. in feed); AS30 (30 g/kg of Schizochytrium sp. in feed) and AS40 (40 g/kg of Schizochytrium sp. in feed). The inclusion of Schizochytrium sp. increase the body weight, weight gain, final biomass and biomass gain of tilapia juvenile. The body crude protein of tilapia was increased after addition of microalgae. Juvenile lipid profile also was influenced when fed with 40 g of Schizochytrium sp. per kg and have it levels of omega‐3 and docosahexaenoic acid (DHA) increased, and omega 6:3 ratio decreased. Tilapia juvenile fed with Schizochytrium sp. per kg have better growth, omega‐3 and DHA levels rising in the body, being a considerable source of fatty acids for human nutrition. Levels above 20 g of Schizochytrium sp. per kg in the feed favour the increase of protein in Nile tilapia body.     

Are oestrogen receptors and protein tyrosine kinases involved in phytoestrogen-modulated steroid secretion by porcine adrenocortical cells?

The phytoestrogens genistein and daidzein had been found to affect the function of some tissues via oestrogen receptors (ER). In addition, genistein, but not daidzein, is considered to be a protein tyrosine kinase (PTK) inhibitor. Thus, the involvement of oestrogen receptors and PTK in phytoestrogen action on adrenocortical porcine steroidogenesis was examined in this study. The aims of the experiment were to test the effects of (i) ICI 182, 780 (ICI), an ER antagonist, on genistein- and daidzein-modulated cortisol and androstenedione (A4) secretion by adrenocortical cells isolated during the luteal and follicular phases of the porcine oestrous cycle; (ii) tyrphostin AG 957 (TAG), a nonsteroidal PTK inhibitor, on cortisol and A4 secretion by the cells and (iii) the phase of the porcine oestrous cycle on the mechanism of phytoestrogen action. Adrenals were harvested during the luteal (n = 5 animals) and follicular (n = 5 animals) phases of the oestrous cycle from locally slaughtered crossbred gilts. The isolated adrenocortical cells were incubated for 8 h (37 °C, 95% air, 5% CO2) with genistein (5 or 10 μM) or daidzein (5 or 10 μM) in the presence or absence of ICI (0.5 μM) or TAG (5 or 10 μM). Genistein and daidzein inhibited cortisol secretion and stimulated A4 secretion by porcine adrenocortical cells harvested during both the luteal and follicular phases of the oestrous cycle. The ER antagonist ICI did not eliminate phytoestrogen-induced changes in steroidogenesis. In contrast to genistein, TAG reduced the secretion of A4 and did not affect cortisol secretion. There was no observable effect due to the phase of the cycle. It is suggested that the mechanism of genistein and daidzein action in the adrenocortical cells of pigs is independent of ER and PTK. It is possible that PTK are involved in A4 secretion by porcine adrenocortical cells.