An antibody-lectin sandwich assay for the determination of CA125 antigen in ovarian cancer patients

A two-step forward sandwich assay was developed for the determination of the ovarian tumour associated glycoconjugate antigen CA125 with anti-CA125 Monoclonal antibody B27.1 on the solid phase and¹²⁵I-labelled wheat germ lectin as tracer in the solution phase. This Mab-lectin heterosandwich assay was optimized and the clinical utility was evaluated in sera from healthy volunteers and ovarian cancer patients. A correlation was established between Mab-lectin assay and the dual monoclonal antibody sandwich assay, TRUQUANT®OV2 RIA, that uses the same MAb B27.1 on the solid phase and a second¹²⁵I-labelled B43.13 MAb in the solution phase. A potentially improved clinical utility is suggested for the Mab-lectin assay. The unique format seems to identify novel isoforms of CA125 with different carbohydrate side chains that would otherwise be undetectable in the MAb-MAb sandwich assay wherein the paratopes are likely directed to protein determinants.     

A novel Acinetobacter sp. for treating highly acidic rubber latex centrifugation effluent

Summary A novel Acinetobacter sp. BTJR-10 isolated from highly acidic (pH 2.5–4.5) rubber latex centrifugation effluent with high COD (22000 mg/L) and BOD (5000 mg/L). This strain could effect 39.5% COD reduction on free cell inoculation of effluent without incorporation of additional nutrients after 8 days. Calcium alginate immobilized cells showed 16.4% and 25% COD reduction after 6 hrs. without aeration and after 1 hr. with mild aeration under batch process respectively. Whereas 44.0% COD reduction could be achieved after 6 hrs. on continuous treatment in a packed bed reactor with mild aeration. Further, even after 3 cycles 37% COD reduction was recorded with continuous treatment.     

Behavioral responses of the small hive beetle,Aethina tumida,to odors of three meliponine bee species and honey bees,Apis mellifera scutellata

Recent studies have shown that honey bees, bumble bees, and some meliponine bee species of the genera Trigona, Meliponula, and Dactylurina are hosts of the small hive beetle (SHB) Aethina tumidaMurray (Coleoptera: Nitidulidae), a pest of honey bee colonies in various regions of the world. Olfaction has been implicated in SHB infestations of honey bee and bumble bee colonies. We used olfactometer bioassays to investigate responses of adult male and female SHBs to odors from intact colonies and separate hive components (pot honey, pot pollen, cerumen, and propolis) of three African meliponine bee species, Meliponula ferruginea (Lepeletier) (black morphospecies), M. ferruginea (reddish brown morphospecies), and Meliponula bocandei (Spinola) (Hymenoptera: Apidae). Although both sexes of the beetle strongly preferred intact colony, pot honey, and pot pollen odors, there was no evidence of attraction to propolis and cerumen odors from the three meliponine bee species. Both sexes of SHB also strongly preferred odors from honey bees, Apis mellifera L. (Hymenoptera: Apidae), over odors from the three meliponine bee species. Our results provide substantial evidence of the host potential of African meliponine bees for the SHB, and we discuss this complex association of the SHB with species within the Apidae family.     

Length–weight relationships for four mullets from the Chilika lagoon,East coast of India

Current study provides information on Length–weight relationship (LWR) of four fish species of family Mugilidae i.e., Planiliza macrolepis (Smith, 1846), Chelon parsia (Hamilton, 1822), Osteomugil cunnesius (Valenciennes, 1836) and Valamugil speigleri (Bleeker, 1858) from Chilika Lagoon, East coast of India. Samples were collected during monsoon (July 2016), winter (November 2016) and summer (April 2017) seasons from the fisher's boats inside the lagoon while fishing with screen barrier nets (mesh size 18‐38 mm) and gill nets (mesh size 34, 38, 46, 62 and 86 mm). The b values were determined from the data set in LWRs as 2.958 for P. macrolepis, 2.952 for O. cunnesius and 2.919 for C. parsia and 2.883 for V. peigleri. In all species, regression values were statistically significant (p < .05).     

Consortia of cyanobacteria/microalgae and bacteria in desert soils: an underexplored microbiota

Applied Microbiology and Biotechnology - Desert ecosystem is generally considered as a lifeless habitat with extreme environmental conditions although it is colonized by extremophilic...     

Neurodegenerative diseases: model organisms,pathology and autophagy

A proteostasis view of neurodegeneration (ND) identifies protein aggregation as a leading causative reason for damage seen at the cellular and organ levels. While investigative therapies that aim at dissolving aggregates have failed, and the promises of silencing expression of ND associated pathogenic proteins or the deployment of engineered induced pluripotent stem cells (iPSCs) are still in the horizon, emerging literature suggests degrading aggregates through autophagy-related mechanisms hold the current potential for a possible cure. Macroautophagy (hereafter autophagy) is an intracellular degradative pathway where superfluous or unwanted cellular cargoes (such as peroxisomes, mitochondria, ribosomes, intracellular bacteria and misfolded protein aggregates) are wrapped in double membrane vesicles called autophagosomes that eventually fuses with lysosomes for their degradation. The selective branch of autophagy that deals with identification, capture and degradation of protein aggregates is called aggrephagy. Here, we cover the workings of aggrephagy detailing its selectivity towards aggregates. The diverse cellular adaptors that bridge the aggregates with the core autophagy machinery in terms of autophagosome formation are discussed. In ND, essential protein quality control mechanisms fail as the constituent components also find themselves trapped in the aggregates. Thus, although cellular aggrephagy has the potential to be upregulated, its dysfunction further aggravates the pathogenesis. This phenomenon when combined with the fact that neurons can neither dilute out the aggregates by cell division nor the dead neurons can be replaced due to low neurogenesis, makes a compelling case for aggrephagy pathway as a potential therapeutic option.     

Chemoprophylactic studies with ivermectin against subperiodic Brugia malayi infection in the leaf monkey, Presbytis cristata

Four Presbytis cristata were treated with oral ivermectin at the same time as the subcutaneous inoculation of 100 infective larvae monthly for three months. Two animals given 0.2 mg/kg monthly and two others given 0.3 mg/kg monthly as well as three control animals became patent for microfilaraemia. However, only 1% of the infective dose was recovered as adult worms from animals in the higher drug dosage group compared to 8.2% and 6.2% in the lower dosage and control groups respectively.     

Amino acid residues distinct from the determinant region can profoundly affect activation of T cell clones by related antigens

Hen egg-white lysozyme (HEL)-specific T cell clones derived from the C57BL/6 strain were found to be about 100-fold more sensitive to the closely related ring-necked pheasant lysozyme (REL) in a dose-dependent proliferation assay. This apparent heteroclicity of REL was independent of the fine specificity of the clones. However, when stimulations by corresponding cyanogen bromide-cleaved peptides (L2H and L2R) known to contain the determinants recognized by all of the clones were compared, the preference for REL was lost. Conversely, an HEL-specific, I-Ad-restricted clone that did not respond to REL responded equally well to L2H and to L2R. Because the HEL/REL reactivity differences involved only the T cells and antigen-presenting cells (APC), and were correlated with differential sensitivity to the lysosomotropic drug chloroquine, it appears that the reactivity differences relate to the manner in which lysozymes are processed by the APC. Thus, conclusions about T cell "clonal specificity," usually attributed to differences in recognition of the determinant regions, may in some cases reflect differential antigen handling that depends on sites on the molecule distant from the determinant.     

Expression of catfish amino acid taste receptors inXenopus oocytes

We demonstrate that poly (A⁺)RNA isolated from catfish barbels directs the expression of functional amino acid taste receptors in theXenopus oocyte. The activity of these receptors is monitored in ovo by the two electrode voltage clamp technique. Specific conductance changes recorded in response to amino acid stimulation are analogous to those recorded electrophysiologically from intact catfish barbels. These responses exhibit specificity, reproducibility, rapid onset and termination, and desensitization to repetitive stimulation. A functional assay system that encompasses the full complement of transduction events from the ligand-receptor interaction to subsequent conductance changes is necessary to identify molecular components responsible for these events. Our results demonstrate that theXenopus oocyte can be used to characterize and identify clones coding for amino acid taste receptors analogous to its use in studying receptor molecules for other neuroactive compounds.Special issue is dedicated to Dr. Sidney Udenfriend.