A comparative analysis of multi-biomarker responses to environmental stress: Evaluating differences in landfill leachate and pathogenic oomycete effects between wild and captive Salmo trutta.

Phenotypic plasticity is one of the major means by which organisms can manage with environmental factor changes. Captivity-related stress and artificial rearing settings have been shown to dramatically alter fish response plasticity in terms of physiology, behavior, and health, potentially reducing overall fitness and fish survival. Understanding the variations in plasticity between captive-bred (kept in a homogenous environment) and wild fish populations in response to varied environmental pressures is becoming increasingly important, particularly in risk assessment research. In this study, we investigated whether captive-bred trout (Salmo trutta) are more susceptible to stress stimuli than their wild counterparts. In both wild and captive-bred trout, we investigated a battery of biomarkers that depicts the effects at various levels of biological organization in response to landfill leachate as a chemical pollutant, and after exposure to pathogenic oomycetes Saprolegnia parasitica. According to the findings, wild trout were more susceptible to chemical stimuli based on cytogenetic damage and catalase activity changes, whereas captive-bred trout were more sensitive to biological stress as evidenced by changes in overall fish activity and increasing cytogenetic damage in gills erythrocytes. Our findings emphasize the significance of exercising caution when conducting risk assessments of environmental pollutants using captive-bred animals, especially when seeking to extrapolate hazards and better understand the consequences of environmental contamination on wild fish populations. Additional comparative studies are required to investigate the impact of environmental stressors on multi-biomarker responses in both wild and captive fish populations in order to uncover changes in the plasticity of various traits that can result in adaptation or maladaptation to environmental stimuli within these fish populations, affecting data comparability and transferability to wildlife.

Response patterns of biomarkers in omnivorous and carnivorous fish species exposed to multicomponent metal (Cd, Cr, Cu, Ni, Pb and Zn) mixture. Part III.

Toxicity to fish of multicomponent metal mixtures at maximum-permissible-concentrations (MPC: Cd-0.005, Cr-0.01, Cu-0.01, Ni-0.01, Pb-0.005 and Zn-0.1 mg/L) set for EU inland waters was evaluated using the whole-mixture approach. An extended follow-up study on the biological effects of multicomponent metal mixtures on three ecologically different fish species, i.e. Perca fluviatilis, Rutilus rutilus, and Salmo salar is reported. The aim of this study was to assess response patterns of biomarkers (erythrocytic nuclear abnormalities (ENAs), metal accumulation and metallothioneins) in tissues of fish species after 14-day treatment with multicomponent metal mixtures at MPC and metal mixtures with one of its components at reduced MPC (↓). After treatments with Cu↓ and Cr↓, the lowest amount of Ni was found in all tissues (except the liver) of all fish species tested. After Zn↓ and Pb↓ treatments, the amount of Ni in muscle of all the tested fish species significantly decreased. The highest amounts of Cr in gills and Pb in muscle were detected in all fish species after treatments with Ni↓ and Cd↓ mixtures, respectively. R. rutilus accumulated significantly larger amounts of metals than P. fluviatilis and S. salar. The data obtained show that tissues of the omnivorous R. rutilus exposed to metal mixtures accumulated higher amounts of Cr, Cu, Ni and Zn, while tissues of carnivorous S. salar and P. fluviatilis higher amounts of Cd and Pb. The analysis of ENAs revealed concentration-dependent responses, indicating Cu↓ and Cr↓ treatments as causes of higher geno- and cytotoxicity levels.

Toxicological Potential of Cadmium Impact on Rainbow Trout (Oncorhynchus mykiss) in Early Development.

Cadmium (Cd) is a toxic element widely distributed in the aquatic environment and producing a wide variety of harmful effects. In this study, the acute toxicity (96 h LC50) of Cd to rainbow trout Oncorhynchus mykiss embryos and larvae was determined. The obtained results showed that hatched larvae were the most sensitive to Cd exposure. After 4 days of exposure, embryos were found to have accumulated greater concentrations of Cd than larvae. Exposure to Cd at sublethal concentrations produced deleterious, exposure duration-related effects on biological parameters (mortality, heart rate and gill ventilation frequency) of larvae. Cd induced a significant elevation of all the studied geno- and cytotoxicity endpoints in larval erythroblasts.

Responses of biomarkers in Atlantic salmon (Salmo salar) following exposure to environmentally relevant concentrations of complex metal mixture (Zn, Cu, Ni, Cr, Pb, Cd). Part II.

The aim of this research was to assess interactions between metals at low exposure concentrations (Maximum-Permissible-Concentrations accepted for the inland waters in EU) and to assess possible influence of background exposure (10-times reduced concentration of a single metal) on toxicological significance of selected biomarkers in Salmo salar after treatment with metal mixture (Zn - 0.1, Cu - 0.01, Ni - 0.01, Cr - 0.01, Pb - 0.005 and Cd - 0.005 mg/L). The tissue-specific bioaccumulation, genotoxicity and cytotoxicity responses (erythrocytic nuclear abnormalities assay) in peripheral blood, kidneys, gills and liver erythrocytes of fish to metal mixtures were assessed after 14 days treatment. Treatment with primary mixture (MIX) or two variants of this mixture (Cr↓ (10 times reduced Cr6+ concentration) and Cu↓ (10 times reduced Cu2+ concentration)) induced the strongest responses in genotoxicity and cytotoxicity endpoints. Exposure to these mixtures highly affected Zn, Cu and Cd bioaccumulation in liver tissue. The highest amount of Ni accumulated was measured after Cd↓ treatment in all tissues. Treatments with reduced concentration of non-essential metal resulted in an increased accumulation of Pb, Ni, or Cd; treatments with reduced concentration of essential metal resulted in a reduced accumulation of certain metals (especially Cd and Pb) in tissues compared between treatments. Glucose content in blood and behavioural endpoints were evaluated after short-term exposure to metal mixtures (MIX, Cr↓, Cu↓). Significant increase in blood glucose concentration was measured after all treatments. These metal mixtures elicit significant behavioural alterations in fish. Consequently, this research revealed a significant influence of background exposure considering mixture toxicity.

Identification and characterization of type II toxin-antitoxin systems in the opportunistic pathogen Acinetobacter baumannii.

Acinetobacter baumannii is an opportunistic pathogen that causes nosocomial infections. Due to the ability to persist in the clinical environment and rapidly acquire antibiotic resistance, multidrug-resistant A. baumannii clones have spread in medical units in many countries in the last decade. The molecular basis of the emergence and spread of the successful multidrug-resistant A. baumannii clones is not understood. Bacterial toxin-antitoxin (TA) systems are abundant genetic loci harbored in low-copy-number plasmids and chromosomes and have been proposed to fulfill numerous functions, from plasmid stabilization to regulation of growth and death under stress conditions. In this study, we have performed a thorough bioinformatic search for type II TA systems in genomes of A. baumannii strains and estimated at least 15 possible TA gene pairs, 5 of which have been shown to be functional TA systems. Three of them were orthologs of bacterial and archaeal RelB/RelE, HicA/HicB, and HigB/HigA systems, and others were the unique SplT/SplA and CheT/CheA TA modules. The toxins of all five TA systems, when expressed in Escherichia coli, inhibited translation, causing RNA degradation. The HigB/HigA and SplT/SplA TA pairs of plasmid origin were highly prevalent in clinical multidrug-resistant A. baumannii isolates from Lithuanian hospitals belonging to the international clonal lineages known as European clone I (ECI) and ECII.

mTHPC-mediated photodynamic treatment of Lewis lung carcinoma in vitro and in vivo.

BACKGROUND AND OBJECTIVE: The ongoing search for the enhancement of efficacy of photodynamic therapy stimulates the interest in molecular mechanisms of the response to the treatment. Looking for the cell line suitable for investigation of cellular response both in vivo and in vitro, we evaluated phototoxicity of m-tetrakis-(3-hydroxyphenyl)-chlorin (mTHPC) on viability of Lewis lung carcinoma (LLC1) cells in vitro, growth of murine transplantable tumor, and mice survival. MATERIAL AND METHODS: LLC1 cell culture and male C57BL/6 mice bearing Lewis lung carcinoma were used for the experiments. Photodynamic treatment was mediated by m-tetrakis-(3-hydroxyphenyl)-chlorin as a photosensitizer. Light emitting diode array was used for illumination. The effect of the photodynamic treatment was evaluated by comparison of viability of control and treated cells, growth of tumors, and survival of the control and treated mice. RESULTS: In vitro, a cytotoxic dose inducing a reduction in viability of LLC1 cells by 50% was achieved at 60 mJ/cm(2) and approximately 400 ng/mL of the photosensitizer, or 30 mJ/cm(2) and 600 ng/mL of mTHPC. Both the concentration of the photosensitizer and duration of light exposure were significant determinants of cytotoxic effect. In vivo, an injection of 0.25 mg/kg of mTHPC to mice bearing Lewis lung tumor and illumination at 120 J/cm(2) taking place after 24 h significantly inhibited tumor growth and prolonged mice survival. However, the tumors regained their growth potential after 9 days. CONCLUSIONS: Photodynamic treatment mediated by m-tetrakis-(3-hydroxyphenyl)-chlorin had a significant effect on LLC1 cells in vitro and growth of Lewis lung carcinoma in vivo.

Escherichia coli dinJ-yafQ genes act as a toxin-antitoxin module.

Bacterial toxin-antitoxin (TA) systems are operons that code for a stable toxic protein and a labile antitoxin. TA modules are widespread on the chromosomes of free-living Bacteria and Archaea, where they presumably act as stress response elements. The chromosome of Escherichia coli K-12 encodes four known TA pairs, as well as the dinJ-yafQ operon, which is hypothesized to be a TA module based on operon organization similar to known TA genes. Induction of YafQ inhibited cell growth, but its toxicity was counteracted by coexpression of dinJ cloned on a separate plasmid. YafQ(His)(6) and DinJ proteins coeluted in Ni(2+)-affinity and gel filtration chromatography, implying the formation of a specific and stable YafQ-DinJ protein complex with an estimated molecular mass of c. 37.3 kDa. Induction of YafQ reduced protein synthesis up to 40% as judged by incorporation of [(35)S]-methionine, but did not influence the rates of DNA and RNA synthesis. Structure modelling of E. coli YafQ revealed its structural relationship with bacterial toxins of known structure suggesting that it might act as a sequence-specific mRNA endoribonuclease.