Intracellular monitoring of target protein production in Staphylococcus aureus by peptide tag-induced reporter fluorescence.
Bottom Line: An intracellular approach for monitoring protein production in Staphylococcus aureus is described. mCherry, fused to the dodecapeptide Tip, was capable of inducing tetracycline repressor (TetR).Time- and concentration-dependent production of mCherry could be correlated to TetR-controlled GFPmut2 activity.This approach can potentially be extended to native S. aureus proteins.
Affiliation: Lehrbereich Mikrobielle Genetik, Waldhäuser Str. 70/8, Eberhard Karls Universität Tübingen, Germany.Show MeSH
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Mentions: To set‐up strains capable of responding to Tip, a tetR(B) expression cassette was inserted into the chromosomal lip locus of S. aureus SA113 (wt) and its derivative RAB171 (harbouring a TetR‐controlled Pxyl/tet‐gfpmut2 fusion). To this end, tetR(BD) was exchanged against tetR(B) in a pRAB2‐derived vector, which was subsequently integrated as described (Stary et al., 2010). Oligonucleotides, plasmids and bacterial strains are listed in Tables 1 and 2; further details are available on request. Epifluorescence microscopy (DM 5500 B microscope and DFC 360 FX camera, Leica) confirmed that cells of the RAB171‐derived strain RAB201B (Pxyl/tet‐gfpmut2, tetR(B)), but not those of RAB200B (tetR(B)), devoid of a TetR controlled reporter gene, exhibited bright green fluorescence when cultured with a final concentration of 0.4 µM ATc (data not shown). Thus, TetR(B) (henceforth referred to as TetR for convenience) can functionally regulate gene expression in this genomic architecture, as shown for TetR(BD) before (Stary et al., 2010). Subsequent excision of the aphAIII resistance markers of RAB200B and RAB201B by Cre recombinase (Leibig et al., 2008) yielded kanamycin‐sensitive strainsRAB210B and RAB211B respectively (Fig. 1A). As a prototype carrier for Tip, the monomeric protein mCherry was chosen (Shaner et al., 2004), which is an established red fluorescent reporter in S. aureus (Malone et al., 2009; Pereira et al., 2010). Intracellular detection and quantification does not require substrates or co‐factors and its structural properties, including solvent exposed N‐ and C‐termini (Shu et al., 2006), make it very suitable for protein fusions. In analogy to comparable fluorescent protein encoding genes, successfully adapted to the codon usage of S. aureus (Sastalla et al., 2009; Paprotka et al., 2010), a new mcherry allele termed gp‐mcherry (Gram‐positive adapted mCherry) was designed (DNA 2.0, Menlo Park, CA, USA). Furnished with the ribosomal binding site of sod (Franke et al., 2007), it was cloned into the xylose inducible vector pKX15. Cloning of further synthetic DNA fragments (Entelechon, Regensburg) into the obtained vector pRAB32‐gp gave rise to plasmids pRAB32‐ntgp and pRAB32‐ctgp, encoding mCherry N‐ or C‐terminally linked to Tip respectively (Fig. 1B). RAB210B and RAB211B cells carrying either one of the three pRAB32 plasmids (Fig. 1A) were cultivated in rich basic medium (BM) (Bera et al., 2005) without glucose and analysed for xylose‐dependent red fluorescence using three different methods. In all strains induced by adding xylose to a final concentration of 0.5% (w/v), cells glowed strongly red, indicating high levels of functional mCherry irrespective of any Tip‐appendix. In contrast, weak but clearly discernible green fluorescence was observed only in induced RAB211B (pRAB32‐ntgp) cells, as depicted in Fig. 2A. The same reporter strains were subjected to flow cytometry (FACSCalibur, BD) and accordingly, a shift towards red fluorescence by about one order of magnitude was observed in all populations of induced cultures. Again, gfpmut2 expression appeared to be solely triggered in the strain disposing of N‐terminally Tip‐tagged mCherry (Fig. 2B). In order to quantify red and green fluorescence, cells harvested at different time‐points during exponential growth phase were analysed using a microplate reader (Infinite M200 Pro, Tecan). Activity profiles of mCherry and GFPmut2 expressed from the reporter strains were subsequently monitored in a time‐resolved and xylose‐dependent manner. As depicted in Fig. 3A, red fluorescence increased steadily over time in xylose‐induced cells, albeit somewhat less pronounced in case of C‐Tip mCherry. This might be due to improper folding or lower protein amounts, one or both of which might also be causative for the inefficiency of C‐Tip mCherry to induce GFPmut2 production. This also agrees with previous results, in which C‐terminally Tip‐tagged TrxA had proven to be a less effective inducer of TetR than N‐tip TrxA in E. coli (Klotzsche et al., 2005). The observed GFPmut2 activity was also consistent with observations from microscopy and flow cytometry, because only cells expressing N‐terminally tagged mCherry, fluoresced both red and green (Fig. 3B). To provide a control for full, rapid and direct induction of TetR, RAB211B was induced by 0.4 µM ATc. In comparison, green fluorescence due to Tip‐mediated induction in RAB211B (pRAB32‐ntgp) was delayed by ∼ 200 min. This might in part be attributed to 15 min maturation time for mCherry (Shaner et al., 2004), but most likely primarily reflects the time span between xylose induction and the production of sufficient amounts of N‐Tip mCherry to efficiently induce TetR. Induced RAB211B (pRAB32‐ntgp) cells reached ∼ 30% of the fluorescence intensity determined for RAB211B with ATc. Indeed, binding constants of Tip to TetR had been established to be about 2–3 orders of magnitude lower than for Tc effectors (Degenkolb et al., 1991; Klotzsche et al., 2005). As indicated by Figs 2 and 3A, the induced reporter strain appears to produce high amounts of mCherry when cultured with 0.5% xylose. According to a study by Zhang and colleagues (2000), a rough estimation indicates the presence of mCherry in a range of ∼ 104 proteins per cell in this state. Reducing the inducer concentrations for RAB211B (pRAB32‐ntgp) resulted in stepwise decreased red and green fluorescence (Fig. 4). Thus, the system appears to be capable of graded responses to different amounts of the Tip‐tagged target protein. Strains with enhanced sensitivity might be required to detect the presence of native S. aureus proteins that are only weakly or moderately produced. Increasing the inducer to TetR ratio is one promising way, since strains with less TetR, controlling the Pxyl/tet promoter upstream of gfpmut2, putatively respond better to lower levels of Tip‐tagged proteins (Klotzsche et al., 2005). To this end, S. aureus strains bearing autoregulated tetR, which generally ensures a balanced level of repressor molecules, might be exploited (Gründling and Schneewind, 2007), optionally combined with improved TetR/Tip pairs (Klotzsche et al., 2005; Klotzsche et al., 2007; Daam et al., 2008). Taken together, proof‐of‐concept for a functional Tip‐tagging architecture in S. aureus was achieved using mCherry as a carrier protein. Based upon our observations that N‐tip mCherry both glowed red and moonlighted as an inducer for TetR, it appears feasible to apply this approach to expression profiling of S. aureus encoded proteins. To this end, tip could be either fused to genes of interest on plasmids for chromosomal integration (Brückner, 1997; Arnaud et al., 2004; Bae and Schneewind, 2006), or it could be randomly attached to chromosomal genes via an integrative element in a transposon‐like fashion, as demonstrated for E. coli before (Schlicht et al., 2006). The Tip‐tagging technique might be particularly useful for in vivo grown S. aureus cells, e.g. in infection models, in which standard proteomic techniques might not be applicable.
Affiliation: Lehrbereich Mikrobielle Genetik, Waldhäuser Str. 70/8, Eberhard Karls Universität Tübingen, Germany.