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.
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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)