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1.
Int J Occup Med Environ Health ; 31(3): 307-315, 2018 Jan 15.
Article in English | MEDLINE | ID: mdl-29072711

ABSTRACT

OBJECTIVES: Data on high frequency of hepatitis A virus (HAV) antibodies for wastewater treatment staff is contradictory. Literature lacks data on the seroprevalence of antibodies to HAV (anti-HAV) among workers in wastewater treatment plants (WWTPs) in Bulgaria. The aim of this study is to establish a specific humoral immune response to hepatitis A virus - anti-HAV total antibodies among staff in WWTPs. MATERIAL AND METHODS: A complex study of health and working conditions included 110 subjects working in 3 WWTPs in Bulgaria (74% of all workers in the 3 studied WWTPs and 20% of all employees in Bulgaria registered in 2014 under the wastewater collection, discharge and treatment code of economic activity). Workers had been differentiated in 3 groups on the basis of their occupational work: operators, support staff and other workers exposed to biological agents. Venous blood from all 110 subjects was tested once for carriers of HAV antibodies. RESULTS: Anti-HAV total antibodies were found for 52.7% of workers in WWTPs. There is a positive association between activity performed in WWTPs (operators, maintenance personnel and others exposed) and a positive one for the presence of anti-HAV (Chi2 = 6.882, df = 2, p = 0.032). Odds ratio (OR) for hepatitis A increases 2.9 times in the group of operators vs. others exposed to biological agents in WWTPs (OR = 2.914, 95% confidence interval (CI): 1.149-7.393, Fisher's p = 0.039). Odds ratio for hepatitis A increases 4.3 times in the group of support staff from WWTPs vs. others exposed to biological agents in WWTP (OR = 4.295, 95% CI: 1.075-17.167, Fisher's p = 0.049). CONCLUSIONS: Higher frequency of anti-HAV antibodies among operators and maintenance personnel at WWTPs has been established as compared to other workers exposed to biological agents in WWTPs. There is a positive association between increasing age of the workers and the presence of anti-HAV. Int J Occup Med Environ Health 2018;31(3):307-315.


Subject(s)
Hepatitis A Antibodies/blood , Hepatitis A , Seroepidemiologic Studies , Waste Disposal, Fluid , Adult , Age Factors , Bulgaria/epidemiology , Female , Humans , Male , Middle Aged , Occupational Exposure/statistics & numerical data , Prevalence , Wastewater
2.
J Neurochem ; 120(2): 248-58, 2012 Jan.
Article in English | MEDLINE | ID: mdl-22066784

ABSTRACT

The synaptic vesicle cycle encompasses the pre-synaptic events that drive neurotransmission. Influx of calcium leads to the fusion of synaptic vesicles with the plasma membrane and the release of neurotransmitter, closely followed by endocytosis. Vacated release sites are repopulated with vesicles which are then primed for release. When activity is intense, reserve vesicles may be mobilized to counteract an eventual decline in transmission. Recently, interplay between endocytosis and repopulation of the readily releasable pool of vesicles has been identified. In this study, we show that exo-endocytosis is necessary to enable detachment of synapsin from reserve pool vesicles during synaptic activity. We report that blockage of exocytosis in cultured mouse hippocampal neurons, either by tetanus toxin or by the deletion of munc13, inhibits the activity-dependent redistribution of synapsin from the pre-synaptic terminal into the axon. Likewise, perturbation of endocytosis with dynasore or by a dynamin dominant-negative mutant fully prevents synapsin redistribution. Such inhibition of synapsin redistribution occurred despite the efficient phosphorylation of synapsin at its protein kinase A/CaMKI site, indicating that disengagement of synapsin from the vesicles requires exocytosis and endocytosis in addition to phosphorylation. Our results therefore reveal hitherto unidentified feedback within the synaptic vesicle cycle involving the synapsin-managed reserve pool.


Subject(s)
Endocytosis/physiology , Exocytosis/physiology , Neurons/cytology , Neurons/metabolism , Synapsins/metabolism , Synaptic Vesicles/metabolism , Animals , Animals, Newborn , Cells, Cultured , Chelating Agents/pharmacology , Egtazic Acid/analogs & derivatives , Egtazic Acid/pharmacology , Endocytosis/drug effects , Enzyme Inhibitors/pharmacology , Excitatory Amino Acid Antagonists/pharmacology , Exocytosis/drug effects , Female , Green Fluorescent Proteins/genetics , Hippocampus/cytology , Hydrazones/pharmacology , Intracellular Signaling Peptides and Proteins/deficiency , Male , Membrane Potentials/drug effects , Membrane Potentials/genetics , Mice , Mice, Inbred C57BL , Mice, Knockout , Nerve Tissue Proteins/deficiency , Neurons/drug effects , Neurotoxins/pharmacology , Patch-Clamp Techniques , Phosphorylation , Statistics, Nonparametric , Synapses/drug effects , Synapses/genetics , Synaptic Vesicles/drug effects , Tetanus Toxin/pharmacology , Transfection/methods
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