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Ten genotypes of sugar beet plant either monogerm or multigerm seeds were screened under greenhouse conditions for both susceptibility and biochemical reaction to root-knot nematode (RKN) Meloidogyne incognita. All the tested genotypes were susceptible to nematode infection according to the number of root galls and gall indices. All infected genotypes exhibited significant reduction in chlorophyll a, b and carotenoids compared to non-infected ones. The total indole acetic acid and total phenolic compounds contents (mean of both shoot and root) increased significantly in most infected genotypes compared to non-infected genotypes except Disk-01-99 and Monte Rosa as well as LP16 and LP15 genotypes, respectively. Also, total polyamine contents (putrescine, spermidine and spermine) showed significant increases in response to infection with nematodes in all genotypes. The same trend was observed in lipid peroxidation expressed with malondialdehyde content in all tested genotypes. Activities of polyphenol oxidase, peroxidase, superoxide dismutase and catalase enzymes were also induced in most infected genotypes compared with non-infected genotypes. Generally, infection with RKNs induced the appearance of new protein bands at molecular masses 303, 288, 42 and 37 KDa in all infected genotypes. The differentiation in the appearance and/or disappearance of protein bands according to susceptibility to infection reflects the variation between genotypes in defense against infection.
The efficacy of applying biocontrol agents, chemical fungicide and nematicide as protective treatments against the soilborne parasites, Fusarium spp. (Fusaria) and citrus nematode Tylenchulus semipenetrans Cobb was evaluated. The experiment took place under field conditions in a citrus orchard cultivated with 16-year-old sweet orange (Citrus sinensis L.) osbech cv. Valencia trees grafted on sour orange (C. aurantium L.) rootstock during the growing season November 2006/ October 2007. This orchard is located at Bader district, Behera governorate, Egypt. The populations of soil fauna and flora under trees canopy were examined just before treatment, and 1, 3, 6, 9 and 12 months after the treatment application. A visual inspection for the appearance of symptoms related to Fusarium or nematode infection on treated and untreated citrus trees was carried out periodically every two weeks throughout the experimental period. The populations of Fusarium spp. were gradually decreased throughout the experimental period. However, the antagonistic bacterial isolates showed drastic effect for reducing the Fusaria population from 38.5% before treatments to a range of 1.2–4.0% after one month of such a bacterial application followed by the Kocide (fungicide) treatment which recorded 6.6%. Meanwhile, Fusaria populations of 18.4 and 16.3% were recorded as Fusaria population in treatments of the nematicide Carbofuran and entompathogenic nematode, respectively. Also, the population density of T. semipenetrans juveniles drastically decreased soon after all the treatment applications. Then after the nematode population build up during the growing season followed a natural distribution decline shape starting from the third month of application up to the ninth month, then it decreased. The citrus nematode increased steadily in the untreated check till September 2007 then its population level decreased. Treatments of Bacillus subtilis – B (20 ml) and Pseudomonas fluorescens (20 ml) gave the highest citrus yield followed by B. subtilis A (10 ml); B. subtilis B (10 ml) and Kocide (fungicide). Moreover, citrus trees treated with B. subtilis A (10 ml); P. fluorescens (10 ml) and Carbofuran (nematicide) had a higher yield production than trees treated with entomopathogenic nematodes Heterorhabditis egyptii (Abd-Elgawad and Ameen 2005). Yet, visual monitoring for disease incidence throughout the citrus orchard during the whole period of the study revealed no disease symptoms of any fusaria or nematode infection in treated trees. Untreated trees had a 1.9 and 3.1% fusaria and nematode infection, respectively. The importance of the present work, therefore, is based on the proposed bioagents as protective applications that are able to inhibit the citrus pathogens and prevent them from causing citrus damage.
Two Schistosoma mansoni cDNA clones 30S and 1H were identified by immuno- screening of sporocyst 2gt11 library and by random sequencing of clones from 2Zap libraries, respectively. Clone 30S was one of 30 clones identified by an antibody raised against tegument of 3-h schistosomules. The clone was found to encode an 81 amino-acid protein fragment. It was expressed in Escherichia coli as a fusion protein of calculated molecular mass of about 35 kDa with C-terminus of Schistosoma japonicum glutathione-S-transferase (Sj26; about 26 kDa). The recombinant fusion protein was specifically recognized by serum of rabbits immunized with irradiated cercariae. Clone 1H is one of 76 expressed sequence tags derived from an adult worm library. It encodes the complete sequence of a tegumental membrane protein, Sm13. The 104 amino-acid open reading frame encodes a protein with a calculated molecular mass of about 11.9 kDa. Clone 1H was expressed in E. coli as an insoluble fusion pro­tein with Sj26 of about 40 kDa. In Western blots, the fusion protein was recognized by serum from rabbits vaccinated with irradiated cercariae but not by preimmune rabbit sera. The cloning, characterization and expression of those proteins are therefore po­tentially usefull for vaccine development.
Expressed sequence tags (ESTs) are partial cDNA sequences read from both ends of random expressed gene fragments used for discovering new genes. DNA libraries from four different developmental stages of Schistosoma mansoni used in this study generated 141 ESTs representing about 2.5% of S. mansoni sequences in dbEST. Se­quencing was done by the dideoxy chain termination method. The sequences were submitted to GenBank for homology searching in nonredundant databases using Ba­sic Local Alignment Search Tool for DNA (BLASTN) alignment and for protein (BLASTX) alignment at the National Center for Biotechnology Information (NCBI). Among submitted ESTs, 29 were derived from λgt11 sporocyst library, 70 from λZap adult worm library, 31 from λZap cercarial library, and 11 from λZap female B worm library. Homology search revealed that eight (5.6%) ESTs shared homology to previ­ously identified S. mansoni genes in dbEST, 15 (10.6%) are homologous to known genes in other organisms, 116 (81.7%) showed no significant sequence homology in the databases, and the remaining sequences (2.1%) showed low homologies to rRNA or mitochondrial DNA sequences. Thus, among the 141 ESTs studied, 116 sequences are derived from noval, uncharactarized S. mansoni genes. Those 116 ESTs are im­portant for identification of coding regions in the sequences, helping in mapping of schistosome genome, and identifying genes of immunological and pharmacological significance.
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