Comparisons of commercial organic and chemical fertilizer solutions on growth and composition of lettuce

The objective of this experiment was to assess the effects of organic or chemical nutrient solutions on the growth and composition of lettuce (Lactuca sativa L.) in greenhouse production. Hoagland and Arnon nutrient solution, an organic hydroponics solution, and no fertilization were factored with lettuce cultivars of different phenotypes, iceberg, romaine, loose head, and loose leaf. Lettuce growth was higher with Hoagland and Arnon solution than with the organic fertilizer or with no fertilization. The organic fertilizer increased growth above no fertilizer applied. Hoagland and Arnon solution gave the highest concentration of nitrogen, potassium, magnesium, and iron in the lettuce whereas lettuce grown with the organic fertilizer had the highest phosphorus. Plant nutrient accumulation differed slightly among the cultivars. Hoagland and Arnon solution produced high nitrate in leaves. Nitrate concentrations with organic or no fertilization were low. Loose head or loose leaf cultivars had higher nitrate than romaine or iceberg.     

Biomass and nutrient concentration of lettuce grown with organic fertilizers

The responses of lettuce (Lactuca sativa L. ‘Arroyo’) to organic nitrogen (N) fertilizers were investigated in a greenhouse. Fertilizers were blood meal (BLO), feather meal (FM), cottonseed meal, alfalfa meal, sewage sludge, compost, cow manure, a chemical fertilizer, and a treatment without fertilizer. Amounts of N from fertilizers were 100, 200, 400, or 800?mg per pot. Lettuce yield was higher for plants receiving fertilizers than with no fertilizer and increased with increased N applications, but high applications of BLO or FM suppressed yields. Nitrogen and nitrate increased in leaves as N supply increased with all fertilizers. Small changes in leaf nutrient contents other than N occurred among or with increased application of the various fertilizers. The soil carbon dioxide release and ammonia volatilization were high from fertilizers with high N concentrations. Organic fertilizers with high N increased lettuce growth at lower applications than those with low N content.     

Determination of antibiotic resistance pattern and virulence genes in Escherichia coli isolated from bovine with subclinical mastitis in southwest of Iran

The aims of the present study were to investigate the prevalence of some virulence genes and also determine the antimicrobial resistance pattern of E. coli isolated from bovine with subclinical mastitis. The milk of 502 cows was collected from 8 dairy herds in the southwest of Iran. Conventional biochemical tests were used for identification of E. coli at the species level. Antimicrobial susceptibility patterns of E. coli isolates were determined by disc agar diffusion method and polymerase chain reaction (PCR) was used for detection of seven virulence genes including f17A, afaE-8, afaD-8, eaeA, cnf1, cnf2, and iucD. Seventy (13.94%) isolates of E. coli were identified in 502 milk samples. The highest rate of resistance was observed against tetracycline (18.6%), while none of the isolates were resistant to streptomycin. Eight (11.5%) out of 70 E. coli isolates carried at least one of the virulence genes. The afaD-8 was the most prevalent gene detected in 5 (7.1%) isolates. The afaE-8, iucD, and eaeA were detected in 3, 3, and 2 isolates respectively. Low prevalence of virulence factors may be indicating that most of the E. coli isolates originated from the commensal flora of cows and enter to the udders via environment contamination with feces.

     

Designing an in‐house ELISA to detect antibody against viral haemorrhagic septicaemia virus using recombinant N protein in Iranian farmed rainbow trout (Oncorhynchus mykiss)

Viral haemorrhagic septicaemia (VHS) is one of the most important viral diseases in rainbow trout that has caused great losses to Iranian rainbow trout aquaculture industry in the last 3 years. Therefore, rapid and reliable diagnosis of VHS virus infections is of great importance. An enzyme linked immunosorbent assay (ELISA) method was performed to study serum antibodies against viral haemorrhagic septicaemia virus (VHSV) using recombinant fragments of their N protein. For this purpose, the virus was first isolated from an infected farm. A part of the nucleocapsid (1–505 bp) gene was amplified by RT‐PCR using specific primers. The amplified fragment was ligated to pMALc2x vector and transferred to DH5α strain of Escherichia coli. Then, recombinant plasmids were tested for protein expression in E. coli Rosetta strain. SDS‐PAGE analysis indicated the production of a recombinant protein with an expected molecular weight of 61 KDa. Analysis of trout serum samples from seven previously infected farms and two VHS free farms showed that the designed ELISA method was effective in diagnosing the infected fish. The results revealed that the developed serological assay using designed ELISA based on recombinant protein (N) has the potential to be used in monitoring studies and to determine the prevalence of VHS in rainbow trout farms. The present data allow evaluating the levels of nonneutralizing antibodies without crude virus preparations.     

Investigation on protective effect of recombinant protein (OmpTS) of Aeromonas hydrophila in Common carp (Cyprinus carpio)

The outer membrane protein of Aeromonas hydrophila is a potential candidate for vaccine development. In this study, after cloning and expression of ompTS, 270 common carp, weighing 44 ± 5.7 g divided into five groups, were injected intraperitoneally twice with 3‐week intervals. Groups included the following: PBS, PBS plus Freund's adjuvant, recombinant protein, recombinant protein plus Freund's adjuvant and 20 fish as negative control. Two weeks after the second injection, 30 fish of each group were challenged with a dose of 2 × LD₅₀ of Aeromonas hydrophila and RPS was measured. The antibody level was measured using ELISA test. The protection of recombinant protein in the immunized fish with and without adjuvant, respectively, was about 82.61% and 78.26% (the protection of recombinant protein electroeluted from an SDS–PAGE with and without adjuvant, respectively, was about 78.62% and 69.57%). The average of antibody level in recombinant protein with and without adjuvant was significantly higher than the PBS group (p < .05). The ability of recombinant ompTS to increase the antibody level and to protect the fish from challenge by A. hydrophila demonstrated that recombinant ompTS protein injection can be used to immunize common carp against A. hydrophila infection.     

Identification and characterization of bacterial strains associated with diseased oak trees in Northern Iran

Oak decline syndrome is characterized by periodic occurrences of decline and death of oaks over widespread areas. An outbreak of a new emerging disease on oak trees was reported in the Hyrcanian forest of Iran (Mazandaran and Golestan provinces) that showed stem bleeding and canker symptoms. Bacterial isolates were characterized through biochemical and physiological tests, protein electrophoresis, DNA fingerprinting (rep‐PCR, ERIC and BOX primers) and sequencing of 16S rRNA and MLSA (multilocus sequencing analysis) for housekeeping genes (gyrB, infB and atpD). A complex community of the genus Brenneria spp. (Brenneria goodwinii, Brenneria roseae subsp. roseae, Brenneria sp. and Brenneria nigrifluens) and a few isolates in the genus Gibbsiella were identified as major groups involved. Isolate differentiation was more accurate using concatenated partial gene sequences within the main groups. All bacterial isolates showed hypersensitivity reactions (HR) on Pelargonium leaves (Pelargonium × hortorum). Pathogenicity studies of different Brenneria and Gibbsiella strains revealed that they have potential to cause the disease in oak seedlings and devastating oak canker and stem bleeding symptoms in northern Iran. Due to the presence of several potentially pathogenic agent(s) associated with the oak decline, identification of the principal agent(s) is of major interest. To our knowledge, this is the first report of potentially pathogenic bacteria associated with oak bleeding and canker in Iran.     

NEW MOLYBDENUM-HYPERACCUMULATOR AMONG PLANT SPECIES GROWING ON MOLYBDENUM MINE- A BIOCHEMICAL STUDY ON TOLERANCE MECHANISM AGAINST METAL TOXICITY

The aim of this work was to determine metal accumulation by plants growing on three molybdenum-mine zones and their tolerance strategies. The plants from tailing, extracting and non-contaminated zones were sampled with their corresponding soils. The results show that molybdenum (Mo) and copper (Cu) were at toxic levels in soils and their levels varied in 44 collected species from 21 families. Ajuga chamaecistus and Cramb orientalis L. excluded Mo and Cu, respectively. Achilla tenuifollia as Mo-hyperaccumulator with total Mo (1979 mg kg^?1) and then Erodium ciconium with 1308 mg kg^?1 Mo and Conyza Canadensis with 618 mg kg^?1 Cu were moderate metal accumulators. They stored considerable levels of metals in their leaves vacuoles and elevated the levels of phytochelatins, cysteine and glutathione and induced antioxidant enzymes. In conclusion, this study indicated that some collected plants excluded metals. In metal-accumulators, antioxidant enzymes, phytochelatins and sequestration of excess metals were involved in their tolerance mechanism.     

Effects of PLGA nanofibrous scaffolds structure on nerve cell directional proliferation and morphology

Electrospinning has been recognized as an efficient technique for the fabrication of neural tissue engineering scaffolds. Many approaches have been developed on material optimization, electrospinning techniques, and physical properties of scaffolds to produce a suitable scaffold for tissue engineering aspects. In this study, structural properties of scaffolds were promoted by controlling the speed of fiber collection without any post-processing. PLGA scaffolds, in two significantly different solution concentrations, were fabricated by the electrospinning process to produce scaffolds with the optimum nerve cell growth in a desired direction. The minimum, intermediate and maximum rate of fiber collection (0.4, 2.4, 4.8 m/s) formed Random, Aligned and Drown-aligned fibers, with various porosities and hydrophilicities. The scaffolds were characterized by fiber diameter, porosity, water contact angle and morphology. Human nerve cells were cultured on fiber substrates for seven days to study the effects of different scaffold structures on cell morphology and proliferation, simultaneously. The results of MTT assay, the morphology of cells and scaffold characterization recommend that the best structure to promote cell direction, morphology and proliferation is accessible in an optimized hydrophilicity and porosity of scaffolds, which was obtained at the collector linear speed of 2.4 m/s.