Assessment of Genetic Diversity in Guava (Psidium guajava) Germplasm Using Microsatellites

Although the varietal diversity is fairly rich in guava, most varieties lack one or more desirable characters. Hence, attempts were made for improving specific traits, viz., attractive pink pulp colour, soft seeds, medium fruit size, high TSS and high ascorbic acid. Genetic diversity analysis is a prerequisite for identifying potential parents in breeding programs and germplasm conservation. Molecular characterization helps discriminate closely-related genotypes, as, this technique is unaffected by environment, rendering it more reliable. In this study, 48 polymorphic SSRs screened from a total of 115 SSR markers were used for analyzing marker segregation in 72 guava accessions. Statistical analysis was done using IDENTITY1.0 and CERVUS 3.0 software. Cluster analysis was done with DARwin 5.0 software, using Wards Minimum Variance method, and weighted group neighbour joining method, to check reliability of grouping among clusters. The trend in grouping was found to be similar in both methods. Dendrograms generated showed that the hybrids clustered with their parents; exotic collections fell into two different sub-groups based on productivity; the wild species formed one group; and Navalar cultivars from Dharwad clustered together, reflecting similar origin

Characterization of protective epitopes in a highly conserved Plasmodium falciparum antigenic protein containing repeats of acidic and basic residues

The delineation of putatively protective and immunogenic epitopes in vaccine candidate proteins constitutes a major research effort towards the development of an effective malaria vaccine. By virtue of its role in the formation of the immune clusters of merozoites, its location on the surface of merozoites, and its highly conserved nature both at the nucleotide sequence level and the amino acid sequence level, the antigen which contains repeats of acidic and basic residues (ABRA) of the human malaria parasite Plasmodium falciparum represents such an antigen. Based upon the predicted amino acid sequence of ABRA, we synthesized eight peptides, with six of these (AB-1 to AB-6) ranging from 12 to 18 residues covering the most hydrophilic regions of the protein, and two more peptides (AB-7 and AB-8) representing its repetitive sequences. We found that all eight constructs bound an appreciable amount of antibody in sera from a large proportion of P. falciparum malaria patients; two of these peptides (AB-1 and AB-3) also elicited a strong proliferation response in peripheral blood mononuclear cells from all 11 human subjects recovering from malaria. When used as carrier-free immunogens, six peptides induced a strong, boostable, immunoglobulin G-type antibody response in rabbits, indicating the presence of both B-cell determinants and T-helper-cell epitopes in these six constructs. These antibodies specifically cross-reacted with the parasite protein(s) in an immunoblot and in an immunofluorescence assay. In another immunoblot, rabbit antipeptide sera also recognized recombinant fragments of ABRA expressed in bacteria. More significantly, rabbit antibodies against two constructs (AB-1 and AB-5) inhibited the merozoite reinvasion of human erythrocytes in vitro up to ∼90%. These results favor further studies so as to determine possible inclusion of these two constructs in a multicomponent subunit vaccine against asexual blood stages of P. falciparum

Characterization of protective epitopes in a highly conserved Plasmodium falciparum antigenic protein containing repeats of acidic and basic residues

The delineation of putatively protective and immunogenic epitopes in vaccine candidate proteins constitutes a major research effort towards the development of an effective malaria vaccine. By virtue of its role in the formation of the immune clusters of merozoites, its location on the surface of merozoites, and its highly conserved nature both at the nucleotide sequence level and the amino acid sequence level, the antigen which contains repeats of acidic and basic residues (ABRA) of the human malaria parasite Plasmodium falciparum represents such an antigen. Based upon the predicted amino acid sequence of ABRA, we synthesized eight peptides, with six of these (AB-1 to AB-6) ranging from 12 to 18 residues covering the most hydrophilic regions of the protein, and two more peptides (AB-7 and AB-8) representing its repetitive sequences. We found that all eight constructs bound an appreciable amount of antibody in sera from a large proportion of P. falciparum malaria patients; two of these peptides (AB-1 and AB-3) also elicited a strong proliferation response in peripheral blood mononuclear cells from all 11 human subjects recovering from malaria. When used as carrier-free immunogens, six peptides induced a strong, boostable, immunoglobulin G-type antibody response in rabbits, indicating the presence of both B-cell determinants and T-helper-cell epitopes in these six constructs. These antibodies specifically cross-reacted with the parasite protein(s) in an immunoblot and in an immunofluorescence assay. In another immunoblot, rabbit antipeptide sera also recognized recombinant fragments of ABRA expressed in bacteria. More significantly, rabbit antibodies against two constructs (AB-1 and AB-5) inhibited the merozoite reinvasion of human erythrocytes in vitro up to ~90%. These results favor further studies so as to determine possible inclusion of these two constructs in a multicomponent subunit vaccine against asexual blood stages of P. falciparum

A Robust Data Hiding Scheme In Audio Signal Based On Double Density Dual Tree Discrete Wavelet Transform

ABSTRACT: The outline of this paper is that, we plot a twofold tree twofold thickness discrete wavelet transform (dwt), given the first channel bank.. The procured channels are then refined by nonlinear streamlining, such that they satisfy flawless changing commitments and the following sets of wavelets have the analyticity property. We show two instances of arrange that are through and through preferable over those got with a past method. We demonstrate the power of the shrouded watermark for added substance clamor, Mp3 squeezing, re-quantization, sifting, editing and testing. The correlation examination demonstrates that our system has preferred execution over watermarking plans reported as of late

Pyogenic granuloma: Reappraisal of etiopathogenesis and case report of large sized pyogenic granuloma

The Connective tissue disorder category encompasses variety of lesion & in that list pyogenic granuloma is most common. Though the term is a misnomer as there is no pyogenic organism involved in its pathogenesis but it’s just a reactive inflammatory lesion due to local trauma, hormonal influence & few drugs. Usually the pg are small in size not exceeding 2-3 cms but sometime it can grow to large extent as it is observe in our case. In such scenario proper diagnosis & differential diagnosis become mandatory as clinician may misdiagnose the lesions with some malignant lesion due its mammoth size. Our case report highlights the thorough evaluation of large pyogenic granuloma

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Developing Mapping Populations for Identifying Genomic Regions Controlling Resistance to Bark-Eating Caterpillar (<i>Indarbela tetraonis</i>) in Guava

<p>The bark-eating caterpillar (<i>Indarbela tetraonis</i> Moore) is one of the two species of insect pests known to infest guava (<i>Psidium guajava</i>). Severe infestation with this pest causes drying up of shoots, which ultimately results in substantial losses in fruit yield and quality. Genetic options are considered most eco-friendly and cost effective to mitigate such losses. DNA marker-assisted breeding of guava for improved resistance to bark-eating caterpillar is expected to increase the efficiency of developing resistant cultivars. As a prelude to this, an investigation was carried out to identify pairs of genotypes contrasting for responses to infestation by bark-eating caterpillar and for a large number of simple sequence repeat (SSR) markers, for use as putative parents to develop mapping populations for chromosomal localization of genomic regions controlling resistance to bark-eating caterpillar in guava. Dendrogram generated by 135 polymorphic SSR markers could separate five morphologically resistant and three morphologically highly susceptible genotypes into two different clusters, barring two exceptions (Bangalore Local and 7–12EC 147036). Four pairs of accessions, viz., Superior Sour Lucidum and Seedless, Portugal and Seedless, Lalit and Seedless, Spear Acid and Seedless, had contrasting response to bark-eating caterpillar and were polymorphic at 111, 103, 101, and 101, SSR loci, respectively. These contrasting pairs of accessions are suggested for use as parents to develop mapping populations to identify DNA markers linked to genomic regions controlling resistance to bark-eating caterpillar, which could help in implementing SSR marker-assisted breeding of guava for resistance to bark-eating caterpillar.</p