Serum alpha1-acid glycoprotein (AGP) concentration in non-symptomatic cats with feline coronavirus (FCoV) infection

Previous studies have demonstrated that the concentration of alpha1-acid glycoprotein (AGP) transiently increases in asymptomatic cats infected with feline coronavirus (FCoV). In order to establish whether these fluctuations depend on the FCoV status, the serum concentration of AGP and anti-FCoV antibody titres and/or faecal shedding of FCoVs in clinically healthy cats from catteries with different levels of prevalence of FCoV infection were monitored over time. Serum AGP concentrations fluctuated over time in clinically healthy cats from the cattery with the highest prevalence of feline infectious peritonitis (FIP) and significantly increased just before an outbreak of FIP. Further studies are required to clarify whether the observed increase of AGP concentration is a consequence of the increased viral burden or a protective response against mutated viral strains. Nevertheless, the results of the present study suggest that AGP might be useful in monitoring FCoV-host interactions in FCoV-endemic catteries.     

Fungal endophyte diversity in Paspalum and effects on plant growth

In natural ecosystems, plants appear to be in symbiosis with diverse fungal endophytes which can have impacts on plant communities. Paspalum is one of the most important grass genera in South American grasslands. The aim of this work was to determine the presence of fungal endophytes in two Paspalum species and evaluate their effects on plant growth. Sixty plant samples were collected for Paspalum notatum in a rangeland in northeastern Argentina, and the same number for Paspalum dilatatum in central Argentina. A triple-sterilization process was carried out by submerging small pieces of leaves and stems for the isolation of fungi from the collected plants. In order to identify endophytes, morphological characters and fungal sequences corresponding to the ITS (Internal Transcribed Spacer) region were analysed. A total of eight genera were identified: Acremonium, Alternaria, Aspergillus, Bipolaris, Cladosporium, Fusarium, Penicillium and Trichoderma. A greenhouse trial was conducted to determine the effects of fungal endophytes on growth. Trichoderma significantly increased relative chlorophyll content in P. notatum and Acremonium endophytes increased tiller number, and above- and below-ground biomass in P. dilatatum. The diversity of fungal endophytes that was present in P. notatum and P. dilatatum was described. In conclusion, some aspects of growth of these Paspalum species seem to be positively affected by Trichoderma and Acremonium.     

Morphological and physiological behaviour of sweet cherry ‘somaclone’ HS plants in field

We reported earlier that somaclonal variant HS (HS), regenerated from Prunus avium `Hedelfinger’ (H) leaf explants, showed reduced apical dominance both in vitro and in vivo. In this report we found that the somaclone HS, showed reduced vegetative vigour as determined by trunk circumference and tree height nevertheless natural architecture of the tree was preserved. HS canopy was less crowded as to compare to H and leaves were shorter with a shorter petiole, they were better spaced out as indicated by internodes length. HS had a significantly thinner cuticle and wax layer compared to H leaves surface. Histological analysis of leaves also showed that HS had thicker mesophyll and palisade the latter composed of more than one layer which, together with increased stomatal density, are distinguishing signs of extensive exposure of leaves to sun. Chlorophyll a and chlorophyll b content did not differ between H and HS, β-carotene content was slightly lower in HS leaves. However no significant differences were found between the two genotypes in terms of net photosynthesis, intercellular CO₂ concentration, leaf transpiration and water use efficiency. HS flowered 1-year later than H and number of flowers was reduced. Fruit size, shape, skin colour change during the ripening process and the main parameters of fruit quality as assessed in the wild type and the somaclone were basically the same.     

Nutritional Status of Mediterranean Trees Growing in a Contaminated and Remediated Area

Soil contamination may contribute to forest decline, by altering nutrient cycling and acquisition by plants. This may hamper the establishment of a woody plant cover in contaminated areas, thus limiting the success of a restoration program. We studied the nutritional status of planted saplings of Holm oak (Quercus ilex subsp. ballota (Desf.) Samp.), white poplar (Populus alba L.), and wild olive tree (Olea europaea var. sylvestris Brot.) in the Guadiamar Green Corridor (SW Spain) and compared it with established adult trees. Soils in this area were affected by a mine-spill in 1998 and a subsequent restoration program. The spill resulted in soil acidification, due to pyrite oxidation, and deposited high concentrations of some trace elements. In some sites, we detected a phosphorus deficiency in the leaves of Q. ilex and O. europaea saplings, as indicated by a high N:P ratio (>16). For O. europaea, soil contamination explained 40% of the variability in leaf P and was negatively related to chlorophyll content. Soil pH was a significant factor predicting the variability of several nutrients, including Mg, P, and S. The uptake of Mg and S by P. alba was greater in acidic soils. The monitoring of soil pH is recommended since long-term effects of soil acidification may negatively affect the nutritional status of the trees.     

Comparison of different direct diagnostic methods to identify Babesia bovis and Babesia bigemina in animals vaccinated with live attenuated parasites

Blood smear examination, flow cytometry, duplex Polymerase Chain Reaction (PCR), and duplex nested PCR (nPCR) were evaluated for detection of Babesia bigemina and Babesia bovis infections in cattle vaccinated with live attenuated strains. Two groups of four cattle were immunized with either B. bigemina (Bi) or B. bovis (Bo). On day 23 post inoculation (PI), Bi cattle were vaccinated with B. bovis (BiBo) and Bo cattle were vaccinated with B. bigemina (BoBi). Babesia bigemina was first detected by blood smear examination 7.5+/-3.5 days PI in the Bi group and 32.2+/-1.7 days PI in the BoBi group. The first occurrence of B. bovis in blood smears was 8.0 days PI in the Bo group and 36.0+/-2.6 days PI in the BiBo group. Flow cytometry detected parasitized erythrocytes on day 1.7+/-1.5 and 2.2+/-1.5 PI in the Bi and Bo groups, respectively, but did not discriminate between the two Babesia spp. Duplex PCR detected B. bigemina on day 4.0+/-0.8 and 26.0+/-0.8 PI in the Bi and BoBi groups, respectively, and B. bovis on day 4.0 and 25.3+/-0.5 PI in the Bo and BiBo groups, respectively. The duplex nPCR detected B. bigemina on 3.0+/-0.8 and 25.0+/-0.0 days PI in the Bi and BoBi groups, respectively, and 4.7+/-1.7 and 27.7+/-6.2 days PI in the Bo and BiBo groups, respectively. Duplex nPCR outperformed the other tests in terms of specificity and sensitivity, indicating that it is the most useful method for identifying Babesia spp. in cattle following vaccination.     

Validation of a fecal glucocorticoid metabolite assay for collared peccaries (Pecari tajacu)

The possibility of assessing endogenous adrenal activity in the collared peccary (Pecari tajacu) was tested by using an adrenocorticotropic hormone (ACTH) challenge in a fecal glucocorticoid metabolite (FGM) assay. Feces were collected from 12 captive adult male peccaries beginning 48 hr prior to challenge; six of these animals received the challenge as an ACTH injection and the other six were injected with saline solution. Feces collection ended 120 hr after injections. As a control, feces were collected for eight consecutive days from another six adult male peccaries that remained in their original mixed-sex herds in semiconfined paddocks. All feces samples were freeze-dried, extracted by an ethanol vortex method, and assayed for glucocorticoids by means of an enzyme immunoassay. FGM concentrations were compared between the treatments by a repeated measures analysis of variance (ANOVA) followed by a post hoc Tukey test. The assay is reliable but, instead of the usual proportion of 1:50 in ethanol (fecal mass:solvent), 1:10 is recommended for best extraction of FGM. Baseline FGM concentrations were similar among the ACTH, saline, and control treatments (29.7 +/- 11.2 ng/g(-1) dry feces) during the 48 hr before the challenge. The ACTH group reached an FGM excretion peak at 24 hr post-treatment, followed by a decline, while in the control and saline groups FGM levels remained relatively constant. Therefore, the fecal glucocorticoid metabolite assay reflects endogenous adrenal activity in the collared peccary and is a powerful tool for noninvasive stress monitoring in peccaries.