Aloe vera long-term saline irrigation increases contents of hydrogen peroxide,lipid peroxidation and phenolic compounds

Salt stress is more and more becoming a serious problem in the world especially if we consider its damaging effect on the plant growth and yield. The cultivation of medicinal plants, such as Aloe vera, might be an alternative for the saline water use and salt-affected soils occupation. Aloe vera, commonly known as aloe, is one of the primary medicinal plants with multipurpose applications going from pharmaceutical to cosmetic aspects with a promising economic return. Aloe plants were cultivated and irrigated, for 14 months, with drinking water (C0) and with two levels of salt (C1 and C2). Changes in growth, hydrogen peroxide (H₂O₂), lipid peroxidation and phenolic compounds were examined in leaves at harvest. Depressive effects of salt irrigation on the plant growth parameters and a perturbation in inorganic ion contents were found especially with a high level of salt in the irrigation water. The intracellular oxidative stress was evaluated with the H₂O₂ production. Our results showed that the H₂O₂ content increased with the accumulation of the toxic ion (Na) in the leaf tissues. In addition, lipid peroxidation, measured by the malondialdehyde (MDA) level, increased as well with salt augmentation in the irrigation water. In response to salt stress, Aloe leaves showed a significant increase in the levels of phenolic compounds too. These results suggest that Aloe can be planted in soils affected by salinity and irrigated with salt water at least at a moderate concentration used in the present study.     

Radical scavenging activity of black cumin (Nigella sativa L.), coriander (Coriandrum sativum L.), and niger (Guizotia abyssinica Cass.) crude seed oils and oil fractions

Crude vegetable oils are usually oxidatively more stable than the corresponding refined oils. Tocopherols, phospholipids (PL), phytosterols, and phenols are the most important natural antioxidants in crude oils. Processing of vegetable oils, moreover, could induce the formation of antioxidants. Black cumin (Nigella sativa L.), coriander (Coriandrum sativum L.), and niger (Guizotia abyssinica Cass.) crude seed oils were extracted with n-hexane and the oils were further fractionated into neutral lipids (NL), glycolipids (GL), and PL. Crude oils and their fractions were investigated for their radical scavenging activity (RSA) toward the stable galvinoxyl radical by electron spin resonance (ESR) spectrometry and toward 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical by spectrophotometric method. Coriander seed oil and its fractions exhibited the strongest RSA compared to black cumin and niger seed oils. The data correlated well with the total content of polyunsaturated fatty acids, unsaponifiables, and PL, as well as the initial peroxide values of crude oils. In overall ranking, RSA of oil fractions showed similar patterns wherein the PL exhibited greater activity to scavenge both free radicals followed by GL and NL, respectively. The positive relationship observed between the RSA of crude oils and their color intensity suggests the Maillard reaction products may have contributed to the RSA of seed oils and their polar fractions. The results demonstrate the importance of minor components in crude seed oils on their oxidative stability, which will reflect on their food value and shelf life. As part of the effort to assess the potential of these seed oils, the information is also of importance in processing and utilizing the crude oils and their byproducts.     

Folic acid and flaxseed oil supplements in Ossimi ewes: effect on body weight changes,progesterone profile,blood chemistry,and litter traits

Tropical Animal Health and Production - The aim was to explore the impact of periconceptional folic acid or flaxseed oil (FXO) supplementation on fertility, progesterone profile, and blood...     

Biochemical indices (RNA/DNA ratio and protein content) in studying the nutritional status of Ruditapes decussatus (Linnaeus 1758) juveniles

In this work, we investigated the nutritional status of Ruditapes decussatus juveniles under different rearing conditions, using biochemical indices (RNA/DNA ratio and protein content) and the linear instantaneous growth rate (IGR). Two experiments were conducted to study the effect of starvation, addition of substrate (sand) as rearing support and diet composition on somatic growth and biochemical indices. Results show that biochemical indices of fed juveniles were significantly (P<0.05) higher. Highest RNA/DNA values and protein content were recorded in fed juveniles reared with substrate (P<0.05); conversely, lowest values were recorded in starved ones reared without substrate. In the second experiment, the highest RNA/DNA ratio was recorded in juveniles fed with control algal mixture composed of species commonly used in bivalve nurseries [Isochrysis galbana (clone T-Iso), Chaetoceros calcitrans and Tetraselmis suecica] and lowest in those fed with algal species isolated from Tunisian coasts. This confirms the usefulness of the RNA/DNA ratio and protein content in the clam's nutritional status evaluation. This assay is useful to provide information about the nutritional status and health of the clam in field conditions.     

Diversity of root-knot nematodes in Moroccan olive nurseries and orchards: does <Emphasis Type="Italic">Meloidogyne javanica</Emphasis> disperse according to invasion processes?

Background

Root-knot nematodes (RKN) are major pest of olive tree (Olea europaea ssp. europaea), especially in nurseries and high-density orchards. Soil samples were collected from main olive growing areas of Morocco, to characterize Meloidogyne species and to discuss the contribution of biotic and abiotic factors in their spatial distribution.

Results

RKN were found in 159 soil samples out of 305 from nurseries (52.1% occurrence) and in 11 out of 49 soil samples from orchards (23.2% occurrence). Biochemical and molecular characterisation (PAGE esterase and SCAR) revealed the dominance of M. javanica both in nurseries and orchards with minor presence of M. incognita only in nurseries, and M. arenaria in only one nursery. RKN were distributed on aggregated basis. Frequent presence of M. javanica in orchards might have come from nurseries. In contrast, the detection of M. incognita in nurseries alone suggests that this species could not reproduce in orchards because of either the competition with other plant-parasitic nematodes or unfit local habitats. The impact of environmental variables (climate, habitat origin and physicochemical characteristics of the substrates) on the distribution of Meloidogyne species is also discussed.

Conclusion

Olive nurseries in Morocco are not able to guarantee the safety of rooted plants. As a result, olive production systems are exposed to strong RKN invasion risks. Consequently, the use of healthy substrates in nurseries may prevent plant-parasitic nematode induction in orchards.

     

The bleaching induced by the phenylpyridazinone herbicide Metflurazon in Chlorella is a metabolic and reversible process

The treatment of synchronized cells of the green alga Chlorella fusca under photoautotrophic conditions with metflurazon (SAN H 6706; 4-chloro-5-dimethylamino-2-(α,α,α-trifluoro-m-tolyl-3(2H)-pyridazinone)) induces a bleaching process and results in white-appearing cells. This process of bleaching was followed by quantitative analysis of cell growth and cell division, photosynthetic oxygen evolution, respiratory oxygen consumption, and of pigment pattern at 0, 6, 12, 18, 24, 48, and 72 hr after incubation with different concentrations of metflurazon. Increasing concentrations of metflurazon gradually affected cell growth of Chlorella measured as increase in cell diameter. Cell division was inhibited completely with 1, 10, and 100 μM metflurazon. Photosynthetic oxygen evolution and respiratory oxygen consumption were not inhibited by 1 μM metflurazon during the first 6 hr; after this time a gradually increased inhibition was observed. Both parameters were inhibited by 100 μM metflurazon immediately after herbicide addition. A detailed analysis of the pigment content during the bleaching process revealed that: (a) The bleaching of Chlorella cells by metflurazon is not a simple photochemical process like the photobleaching of boiled cells, but is directed by the active metabolism of Chlorella itself. (b) The bleaching process is characterized by two phases: an accumulation of pigments followed by their degradation. The accumulation phase extends to 6 hr after herbicide addition. (c) During the accumulation phase, chlorophyll is accumulated to 380 and 106% in cells treated with 1 and 100 μM metflurazon, respectively, compared to the initial pigment content. The breakdown of chlorophyll, however, during the degradation phase is 5 times faster in the 1 μM treatment than in the 100 μM treatment. This difference resulted in the faster appearance of white cells with the low metflurazon concentration. (d) During the accumulation phase in the 1 μM treatment, the biosynthesis of chlorophylls, xanthophylls, and carotenes is inhibited by 56, 74, and 78%, respectively, when compared to a nontreated control. When related to the initial amounts, chlorophylls, xanthophylls, and carotenes are accumulated to 380, 230, and 153%, respectively. However, the synthesis of violaxanthin is specifically inhibited, followed by α-carotene. During the degradation phase, violaxanthin and α-carotene again, are the most rapidly disappearing pigments. Continuous culturing of white Chlorella cells resulted in a regeneration to green cells after 96, 240, 384 hr for 1, 10, and 100 μM metflurazone, respectively. The bleaching of Chlorella by metflurazon is evidently dependent on a functioning metabolism and is itself a regulated disassembly of the photosynthetic apparatus, which is reversible and not lethal.     

Factor XI mutation in a Holstein cow with repeat breeding in Japan

Factor XI deficiency is an autosomal recessive coagulopathy in Holstein cattle. Affected cows have a tendency to show repeat breeding. Forty repeat breeding Holstein Friesian cows were selected and tested for the Factor XI mutation. Genomic DNA was isolated from the blood of the cows (n=40). Exon 12 of the Factor XI gene of the cows was amplified by PCR. One repeat breeding cow was heterozygous to the Factor XI mutation as indicated by the presence of two DNA fragments of 320 bp and 244 bp. The insertion of the 76 bp in the heterozygous cow was confirmed by DNA sequencing. The heterozygous cow was in her fourth lactation. She gave birth to male twins at the last calving. She was inseminated artificially four times after the last calving. Factor XI deficiency in cattle has been reported in different countries. However, no case was reported in Japan. This might be the first to report Factor XI mutation in Holstein cattle in Japan.     

DNA extraction from bovine mummified fetuses and detection of factor XI gene deficiency in the mummies

Genomic DNA extracted from bovine mummified tissue is valuable material for detection of some genes that may contribute to fetal abnormalities. In this study bovine genomic DNA was extracted from the hardened tissue samples of ten bovine mummified fetuses. The amount of genomic DNA extracted from 2 g of the mummified tissues by the phenol/chloroform-ethanol method was low (less than 4 microg/ml) for all samples. The extracted DNA was then amplified by the GenomiPhi DNA amplification system. After amplification, the amount of DNA was increased to more than 100 microg/ml for all samples. This amplification system was shown to be a good tool for amplifying the genomic DNA of the mummified fetuses. The amplified genomic DNA was used for testing the mummies for Factor XI gene deficiency, an autosomal recessive deficiency involved in the early stages of the intrinsic blood coagulation pathway. Exon 12 of the Factor XI gene of the mummies was amplified by PCR. Two of the ten mummified fetuses were heterozygous for the Factor XI gene as indicated by the presence of two amplified DNA fragments of 320 bp and 244 bp. Factor XI deficiency has already been described in Holstein cattle. However, no report is available for bovine fetus. In this study, DNA was extracted and amplified from the bovine mummified fetuses, and the samples were successfully tested for Factor XI gene deficiency in the mummies.     

Soil‐solution speciation by MINEQL+4.6 model and plant uptake of Cd and Zn by barley (Hordeum vulgare L.) after application of different phosphate fertilizers

A greenhouse experiment was conducted to investigate the immediate effect of application of mono‐ammonium phosphate (MAP), single superphosphate (SSP), and triple superphosphate (TSP) fertilizers containing varying concentrations of Cd on (1) chemical speciation of Cd and Zn in soil solution by chemical‐equilibrium calculations (MINEQL+4.6 model), (2) growth of barley plants, (3) concentrations of Cd, P, and Zn in soil solution and plant tissue, as well as total plant accumulation of Cd, P, and Zn, and (4) monitoring pH and element changes during incubation periods following phosphate application. Results show that, in general, the pH of soil solution increased during the first 40 d of incubation, then declined. Also, at the end of incubation period, pH of soil solution was affected by fertilization source and fertilization rate. The concentration of Cd in soil solution changed with time. Phosphate fertilization (p < 0.05) or fertilizer source (p < 0.05) showed consistent effects. Also, the application of phosphate fertilizers with three rates significantly increased Zn concentrations in soil solution during the first half (0–30 d) of incubation period and then decreased but still more than in the control. In general, application of different sources of phosphate at 100 g kg^–1 did not change the dominant forms of Cd in soil solution during all incubation time intervals. Speciation of Zn in the control after 30 d of incubation had changed, in comparison to 10 d of incubation, and the dominant forms were Zn²⁺, ZnOH⁺, ZnHCO₃, ZnCO₃(aq), and Zn(OH)₂(aq). Adding phosphate fertilizer significantly increased both shoot and root dry weight compared to control, indicating P was a growth‐limiting factor in the control plants. The Zn concentrations in shoot and root were lower in the TSP‐ and SSP‐fertilizers treatment than those in the MAP and fertilizer treatments at all rates of fertilization. Adding phosphate increased the Cd : Zn and P : Zn ratios in the shoot and root tissue, with the effect being greater with increasing fertilization rate. Phosphate fertilization greatly increased the total accumulation of Cd of barley compared with the control plants (p < 0.001), with the effect being greater with increasing fertilization rate. Source and rate of fertilizers, and their interactions had significant effect (p < 0.05) on Cd accumulation in the whole plant.     

Virulence traits of avian pathogenic (APEC) and fecal (AFEC) <Emphasis Type="Italic">E. coli</Emphasis> isolated from broiler chickens in Algeria

Avian pathogenic E. coli (APEC) is the etiologic agent of avian colibacillosis, the most common disease responsible for chicken morbidity in the world. Although multiple virulence-associated factors were identified, their prevalence in Algeria is still poorly known. In the present research, 92 avian pathogenic E. coli (APEC) isolates were recovered from broilers with clinical signs and lesions of colibacillosis. In addition, 32 E. coli isolates collected from feces of healthy birds (AFEC) were included for comparison. All isolates were investigated by PCR for the presence of a total of 11 virulence-associated genes described for avian pathogenic (iroN, ompT, hlyF, iss, iutA, and fimC) and diarrheagenic E. coli (eae, stx, elt/est, ipaH, and aggR). The sensitivity of 39 APEC isolates to 16 antibiotics was also determined using antimicrobial pretreated microplates. Here, we report that 98% of the examined isolates host at least one of the tested virulence factors. The most prevalent genes in APEC were iutA (90.6%), ompT (86.9%), and iss (85.8%); whereas, iutA (78.1%), fimC (78.1%), and iroN (68.7%) were the highest prevalent genes in AFEC. Our data showed that none of the AFEC isolates harbor any of the tested diarrheagenic genes. Moreover, only elt/est (5.4%), stx (2.1%), and ipaH (2.1%) genes were carried by APEC isolates. We further established that ceftazodime, ceftiofur, mequindox, amoxicillin/clavulanic acid, and meropenem were the most efficient antibiotics against the analyzed APEC isolates. Overall, our findings provide more insights about APEC and AFEC virulence potential in Algeria which could participate in the fight against colibacillosis.