Proteomic Differences between Tellurite-Sensitive and Tellurite–Resistant E.coli

PLOS ONE, Dec 2019

Tellurite containing compounds are in use for industrial processes and increasing delivery into the environment generates specific pollution that may well result in contamination and subsequent potential adverse effects on public health. It was the aim of the current study to reveal mechanism of toxicity in tellurite-sensitive and tellurite-resistant E. coli at the protein level. In this work an approach using gel-based mass spectrometrical analysis to identify a differential protein profile related to tellurite toxicity was used and the mechanism of ter operon-mediated tellurite resistance was addressed. E. coli BL21 was genetically manipulated for tellurite-resistance by the introduction of the resistance-conferring ter genes on the pLK18 plasmid. Potassium tellurite was added to cultures in order to obtain a final 3.9 micromolar concentration. Proteins from tellurite-sensitive and tellurite-resistant E. coli were run on 2-D gel electrophoresis, spots of interest were picked, in-gel digested and subsequently analysed by nano-LC-MS/MS (ion trap). In addition, Western blotting and measurement of enzymatic activity were performed to verify the expression of certain candidate proteins. Following exposure to tellurite, in contrast to tellurite-resistant bacteria, sensitive cells exhibited increased levels of antioxidant enzymes superoxide dismutases, catalase and oxidoreductase YqhD. Cysteine desulfurase, known to be related to tellurite toxicity as well as proteins involved in protein folding: GroEL, DnaK and EF-Tu were upregulated in sensitive cells. In resistant bacteria, several isoforms of four essential Ter proteins were observed and following tellurite treatment the abovementioned protein levels did not show any significant proteome changes as compared to the sensitive control. The absence of general defense mechanisms against tellurite toxicity in resistant bacteria thus provides further evidence that the four proteins of the ter operon function by a specific mode of action in the mechanism of tellurite resistance probably involving protein cascades from antioxidant and protein folding pathways.

Proteomic Differences between Tellurite-Sensitive and Tellurite–Resistant E.coli

Lubec G (2013) Proteomic Differences between Tellurite-Sensitive and Tellurite-Resistant E.coli. PLoS ONE 8(11): e78010. doi:10.1371/journal.pone.0078010 Proteomic Differences between Tellurite-Sensitive and Tellurite-Resistant E.coli Jana Aradska 0 Roman Smida k 0 Lenka Turkovic ova 0 Ja n Turn a 0 Gert Lubec 0 Mario Sobero n, Instituto de Biotecnologa, Universidad Nacional Auto noma de Mexico, Mexico 0 1 Department of Molecular Biology, Faculty of Natural Science, Comenius University , Bratislava , Slovakia , 2 Department of Pediatrics, Medical University of Vienna , Vienna , Austria Tellurite containing compounds are in use for industrial processes and increasing delivery into the environment generates specific pollution that may well result in contamination and subsequent potential adverse effects on public health. It was the aim of the current study to reveal mechanism of toxicity in tellurite-sensitive and tellurite-resistant E. coli at the protein level. In this work an approach using gel-based mass spectrometrical analysis to identify a differential protein profile related to tellurite toxicity was used and the mechanism of ter operon-mediated tellurite resistance was addressed. E. coli BL21 was genetically manipulated for tellurite-resistance by the introduction of the resistance-conferring ter genes on the pLK18 plasmid. Potassium tellurite was added to cultures in order to obtain a final 3.9 micromolar concentration. Proteins from tellurite-sensitive and tellurite-resistant E. coli were run on 2-D gel electrophoresis, spots of interest were picked, in-gel digested and subsequently analysed by nano-LC-MS/MS (ion trap). In addition, Western blotting and measurement of enzymatic activity were performed to verify the expression of certain candidate proteins. Following exposure to tellurite, in contrast to tellurite-resistant bacteria, sensitive cells exhibited increased levels of antioxidant enzymes superoxide dismutases, catalase and oxidoreductase YqhD. Cysteine desulfurase, known to be related to tellurite toxicity as well as proteins involved in protein folding: GroEL, DnaK and EF-Tu were upregulated in sensitive cells. In resistant bacteria, several isoforms of four essential Ter proteins were observed and following tellurite treatment the abovementioned protein levels did not show any significant proteome changes as compared to the sensitive control. The absence of general defense mechanisms against tellurite toxicity in resistant bacteria thus provides further evidence that the four proteins of the ter operon function by a specific mode of action in the mechanism of tellurite resistance probably involving protein cascades from antioxidant and protein folding pathways. - Tellurium (Te) is a trace element belonging to the same chemical group as selenium, sulphur and oxygen. Toxic ions are mustered mostly from industrial activities and represent a potential danger to human health. Tellurite oxyanions are highly toxic for most forms of life even at micromolar levels [1], even though the ultimate molecular mechanism underlying tellurite toxicity is not fully understood. Several different mechanisms have been proposed to account for the toxicity of tellurite. Part of it results from ROS generation as by-product of tellurite reduction [2], [3], [4], [5], either by specific superoxide dismutation by SOD or by accidental transfer of electrons to O2 during auto-oxidation of respiratory dehydrogenases [6]. Tellurite oxidizes cellular thiols as glutathione [7] or causes specific damage to [Fe-S] clusters present in essential enzymes [8] and may replace sulphur and/or selenium in critical metabolites or enzymes thus abating essential functions [9]. Moreover, tellurite causes lipid peroxidation with subsequent generation of toxic breakdown products like short-chain (C3C9) aldehydes [10]. Taken together, the toxicity of tellurite results from an ability to act as a strong oxidizing agent over a variety of cell components. Most pathways that are activated in the cell after tellurite exposure tend to mitigate these effects. Natural resistance to toxic compounds results from high adaptability of cellular systems to environmental changes. To cope with chemical stress, microorganisms use various defense mechanisms involving complementary action of distinct pathways. These include the evolution of specific mechanisms targeted against a particular dangerous agent along with the recruitment of well-established general defense [11], [12]. In the current study sensitive cells E. coli BL21(pACYC184) and cells carrying a tellurite resistance gene determinant from the E. coli KL53, one of the five genetic determinants of tellurite resistance found in gram-negative bacteria, were used. Bacteria bearing the Ter operon can grow at significantly higher concentrations of tellurite (MIC,4 mM) in comparison to the wild type form (MIC,4 mM). This operon was also detected within the pathogenicity island in the genome of foodborne pathogens such as E. coli O157:H7 [13]. Homologous genes have also been found in Shigella flexneri, Yersinia pestis [1], Klebsiella pneumoniae [14], Vibrio cholerae, Proteus mirabilis [15], Deinococcus radiodurans [13], etc. The corresponding DNA fragment conferring the resistance is comprised of four essential ORFs that were named terB, terC, terD and terE. The functional properties of the four gene products and therefore the mechanism of resistance mediated by ter operon remains elusive. Several studies have proposed a role for ter genes in resistance to bacteriophages, colicins, oxidative stress which was also shown to be important for E. coli pathogens to overcome the host immune system [13], [16], [17]. Furthermore, Anantharaman et al. [18] recently employed a systemic approach to predict the involvement of the ter gene at different levels of highly complex bacterial defense systems involving sensing, signalling pathways or DNA repair. Taken together, data reported so far are anecdotal and warrant a systematic approach for the determination of probably involved pathways and cascades involved in tellurite sensitivity: It was the aim of the study to provide insight into proteomic differences between E.coli sensitive or resistant to tellurite by a gel-based proteomic approach using mass spectrometry. Herein the comparative analysis of the total cell lysate proteomes from sensitive cells E. coli BL21(pACYC184) and resistant cells E. coli BL21(pLK18) against tellurite is reported and the identification of proteins from several networks involved in the molecular stress response were revealed. Determination of the sub-lethal concentration of potassium tellurite The minimum inhibitory concentration (MIC) of potassium tellurite was determined for the sensitive strain E. coli BL21(pACYC184) as 4.5 mM. After 10 min incubation in telluritesupplemented LB medium <50 percent of cells survived at 0.5 mM and ,1 percent of cells survived at 3.9 mM K2TeO3. A concen (...truncated)


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Jana Aradská, Roman Šmidák, Lenka Turkovičová, Ján Turňa, Gert Lubec. Proteomic Differences between Tellurite-Sensitive and Tellurite–Resistant E.coli, PLOS ONE, 2013, 11, DOI: 10.1371/journal.pone.0078010