Climate change effects on trematodiases,with emphasis on zoonotic fascioliasis and schistosomiasis

The capacity of climatic conditions to modulate the extent and intensity of parasitism is well known since long ago. Concerning helminths, among the numerous environmental modifications giving rise to changes in infections, climate variables appear as those showing a greater influence, so that climate change may be expected to have an important impact on the diseases they cause. However, the confirmation of the impact of climate change on helminthiases has been reached very recently. Only shortly before, helminthiases were still noted as infectious diseases scarcely affected by climate change, when compared to diseases caused by microorganisms in general (viruses, bacteriae, protozoans). The aim of the present paper is to review the impact of climate change on helminthiases transmitted by snails, invertebrates which are pronouncedly affected by meteorological factors, by focusing on trematodiases. First, the knowledge on the effects of climate change on trematodiases in general is reviewed, including aspects such as influence of temperature on cercarial output, cercarial production variability in trematode species, influences of magnitude of cercarial production and snail host size, cercarial quality, duration of cercarial production increase and host mortality, influence of latitude, and global-warming-induced impact of trematodes. Secondly, important zoonotic diseases such as fascioliasis, schistosomiasis and cercarial dermatitis are analysed from the point of view of their relationships with meteorological factors. Emphasis is given to data which indicate that climate change influences the characteristics of these trematodiases in concrete areas where these diseases are emerging in recent years. The present review shows that trematodes, similarly as other helminths presenting larval stages living freely in the environment and/or larval stages parasitic in invertebrates easily affected by climate change as arthropods and molluscs as intermediate hosts, may be largely more susceptible to climate change impact than those helminths in whose life cycle such phases are absent or reduced to a minimum. Although helminths also appear to be affected by climate change, their main difference with microparasites lies on the usually longer life cycles of helminths, with longer generation times, slower population growth rates and longer time period needed for the response in the definitive host to become evident. Consequently, after a pronounced climate change in a local area, modifications in helminth populations need more time to be obvious or detectable than modifications in microparasite populations. Similarly, the relation of changes in a helminthiasis with climatic factor changes, as extreme events elapsed relatively long time ago, may be overlooked if not concretely searched for. All indicates that this phenomenon has been the reason for previous analyses to conclude that helminthiases do not constitute priority targets in climate change impact studies.     

Oxidative Stability of Spray-Dried Microencapsulated Fish Oils with Different Wall Materials

Multilayer microencapsulation of fish oil was evaluated by using fish gelatin (treated with or without microbial transglutaminase [MTGase]), chitosan, and maltodextrin for its ability to control lipid oxidation. This study showed that a mixture containing gelatin and maltodextrin obtained the highest percentage of core release. The oxidative stability of the formulated mixtures and the bulk oils was investigated during a period of 60 days. The peroxide value (PV) was assessed as a parameter for primary oxidation products, and p-anisidine (p-AV) and thiobarbituric acid reactive sub-stances (TBARS) was used to analyze secondary oxidation compounds. Observation of oxidation products showed that combinations of gelatin and maltodextrin made by adding MTGase and a mixture of gelatin and chitosan were able to increase the oxidative stability, and increases in PV and p-AV and TBARS were found for all oils.     

Use of haloperidol and azaperone for stress control in roe deer (Capreolus capreolus) captured by means of drive-nets

The physical capture of wild ungulates is performed for different purposes when anaesthesia in field conditions is not possible or advisable. The use of tranquilizers may contribute to improved welfare of captured animals. We studied the effect of haloperidol and azaperone on the stress response of roe deer (Capreolus capreolus) through the study of physiological, haematological and serum biochemical parameters. Thirty one roe deer were drive-net captured and randomly injected with haloperidol (0.30 ± 0.04 mg/kg IM; n = 13), azaperone (0.43 ± 0.07 mg/kg IM; n = 11) or saline (0.5 mL IM; n = 7), and restrained for 3 h. The interindividual variability of heart rate was lower in the treated deer, suggesting a calming effect, and erythrocyte and biochemical parameters indicated vasodilation, splenic sequestration, hemodilution, improvement of renal perfusion and a protective effect on muscle. These results support the suitability of using either azaperone or haloperidol in capture operations of roe deer, in order to reduce stress and prevent its adverse effects.     

Comparison of cell wall components between Fragaria × ananassa and Fragaria chiloensis grown in Chile

Summary

Fruit firmness and cell wall composition were compared among five cultivars of F. × ananassa (‘Chandler’, ‘Seascape’, ‘Tudla’, ‘Hokowase’ and ‘Reiko’) and two land races of F. chiloensis (‘94BAU-1A’ and ‘97PUR-1A’) grown in central Chile. Fruits of F. chiloensis were smaller than those of F. × ananassa. Firmness of epidermal tissue did not differ significantly between F. × ananassa and F. chiloensis. Firmness of cortical tissue, however, was significantly lower in F. chiloensis than in F.× ananassa and as a result, difference in the firmness between epidermal and cortical tissues was significantly greater in F. chiloensis than in F. × ananassa. Calcium concentration was low in ‘Reiko’ and ‘Hokowase’ while high in the other varieties of F. × ananassa. F. chiloensis showed intermediate values between these two groups. Higher levels of total uronic acid and neutral sugars in cell wall fractions of F. chiloensis as compared with F. × ananassa were mainly due to its high concentration in the water soluble fraction. Total uronic acid in cell wall fraction was significantly higher in F. chiloensis than in F. × ananassa, mainly due to significantly higher concentrations in the water-soluble fraction. Non-cellulosic neutral sugars, especially arabinose in the water, CDTA, and Na₂CO₃-soluble fractions were significantly higher in F. chiloensis than in F. × ananassa. On the other hand, galactose in the CDTA-, Na₂CO₃-, and KOH-soluble fractions was significantly lower in F. chiloensis than in F. × ananassa. Moreover, cellulose concentration of F. chiloensis was also significantly lower than that of F. × ananassa. Results obtained from cell wall analysis suggest that softer cortex in F. chiloensis might be due to either lower cellulose content, higher solubilization rate of pectic substances, and/or compositional differences in the branching of neutral sugars.     

Follicular wave dynamics and Growth factors gene expression in Braford heifers

The objectives of the present study were (experiment 1) to characterized development and dynamics of the dominant follicles (DF) and the corpus luteum (CL) to determine patterns of two (W2) and three (W3) follicular waves in beef heifers, and (experiment 2) to determine gene expression of growth factors gene expression in follicular cells of W2 and W3 heifer. Twenty-eight Braford heifers were used. Dominant follicular and CL were monitored daily by ultrasonography to identify the development W2 and W3 in heifers. Pre-ovulatory DF were aspirated on day 19 in W2 and on day 22 in W3 heifers. In W2 and W3, follicular cells (FC) of gene expression of growth differentiation factor 9, bone morphogenetic protein 15 (BMP15), fibroblast growth factor basic, transforming growth factor beta receptor 1, bone morphogenetic protein receptor type IB and fibroblast growth factor receptor 2 were evaluated. The regression of the DF of the first follicular wave and the emergency of the DF of the second follicular wave began later in the heifers W2 than in W3 (p = .02 and p < .01). The regression of the CL began earlier in the W2 than in W3 group (p < .01). Gene expression of growth factors and receptors was similar between groups. However, higher relative levels of BMP15 was observed in W2 group (p = .07). Results propose that wave patterns were regulated by the development time of the DF in the first wave and the life of the CL. Furthermore, higher levels of BMP15 could produce shorter life of CL. The present work suggest that ultrasonography associated with molecular assays could be used as an easy and effective tool to characterize follicular wave patterns.     

Changes in soluble and cell wall-bound hydroxycinnamic and hydroxybenzoic acids in sugarcane cultivars inoculated with <Emphasis Type="Italic">Sporisorium scitamineum</Emphasis> sporidia

The accumulation of soluble and cell wall-bound phenolics in the sugarcane stems of young plants from highly resistant cv. My 5514 and susceptible cv. B 42231, inoculated or not inoculated with smut sporidia, was studied. The ratio of inoculated to uninoculated plants of some cell wall-bound phenolics, such as ferulic, caffeic, and syringic acids increased for the resistant cv. My 5514, whereas it was maintained more or less constantly for the susceptible cv. B 42231. The highest increase of this ratio in the resistant cv. My 5514 corresponded to both caffeic and syringic acids. This could result in a better capacity to cv. My 5514 for an increase in the frequency of bridges between lignin fragments through ester-ether linkages for reinforcing the cell wall and major resistance to the disease. This reinforcement of the cell wall could provide an effective barrier to pathogen entry and spread. Soluble sub-fractions of all phenolics detected showed non-stable patterns. Caffeic acid, that regulates phenylalanine ammonia-lyase activity in sugarcane, showed a significant decrease in its titre at 24 h in the resistant cultivar, principally in the free soluble fraction, whilst the susceptible cultivar enhanced it. We hypothesise that the pathway of hydroxybenzoic acids is only activated once the level of p-coumaric acid justifies the accumulation of hydroxycinnamic acids required for reinforcing the cell wall after inoculation.