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Journal of Bacteriology, March 2009, p. 1979-1981, Vol. 191, No. 6
0021-9193/09/$08.00+0     doi:10.1128/JB.01549-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

The Rcs Two-Component System Regulates Expression of Lysozyme Inhibitors and Is Induced by Exposure to Lysozyme

Lien Callewaert, Kristof G. A. Vanoirbeek, Ine Lurquin, Chris W. Michiels, and Abram Aertsen^*

Laboratory of Food Microbiology and Leuven Food Science and Nutrition Research Center (LFoRCe), Katholieke Universiteit Leuven, Kasteelpark Arenberg 22, B-3001 Leuven, Belgium

Received 31 October 2008/ Accepted 5 January 2009

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The Escherichia coli Rcs regulon is triggered by antibiotic-mediated peptidoglycan stress and encodes two lysozyme inhibitors, Ivy and MliC. We report activation of this pathway by lysozyme and increased lysozyme sensitivity when Rcs induction is genetically blocked. This lysozyme sensitivity could be alleviated by complementation with Ivy and MliC.

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In gram-negative bacteria, the cell envelope represents an important functional compartment that extends from the cytoplasmic membrane to the outer membrane and supports a number of essential processes, such as solute transport, protein translocation, and respiratory energy generation (15). In addition, the cell envelope accommodates the bacterial peptidoglycan layer, a distinct and structurally vital element of the cell. Most recently, Laubacher and Ades (10) have demonstrated that the Rcs phosphorelay system of Escherichia coli, originally described as regulator of capsule synthesis, is activated by β-lactam antibiotics that inhibit penicillin-binding proteins and consequently interfere with peptidoglycan synthesis. Moreover, mutational activation of the Rcs pathway provided significant protection against these antibiotics, indicating that members of this regulon can prevent or repair the peptidoglycan damage caused by β-lactam antibiotics (10).

Interestingly, ivy and ydhA, two genes encoding specific lysozyme inhibitors, were found to reside under this Rcs regulon (8, 10). Ivy (inhibitor of vertebrate lysozyme, formerly known as YkfE) was discovered in 2001 as the first bacterial lysozyme inhibitor (1, 14), while the inhibitory activity of YdhA was only recently revealed by our research group (3). Although Ivy and YdhA are both able to inhibit c-type lysozymes, such as human lysozyme and hen egg white lysozyme (HEWL), they are structurally unrelated (1, 16). Interestingly, YdhA belongs to a group of proteins with a common conserved COG3895 domain that are widely spread among the Proteobacteria (3, 16). Unlike Ivy, which resides in the periplasm, YdhA is a lipoprotein and was therefore renamed MliC (membrane-bound lysozyme inhibitor of c-type lysozyme) (3).

Given the elementary observation that the two currently known lysozyme inhibitors of E. coli are both part of the Rcs regulon that can in turn be induced by antibiotic-mediated peptidoglycan stress, we wondered whether Rcs induction could also result from exposure to lysozyme itself. To test this, we introduced a tolA knockout from MG1655 tolA (3) into strain DH300 that is equipped with a genomic rprA-lacZ fusion able to report Rcs activation (12), in order to increase outer membrane permeability for HEWL (Table 1 lists all strains). A stationary-phase culture of the resulting strain, designated LC100, was diluted 1/100 in 4 ml fresh LB medium with different final concentrations of HEWL (0, 5, 10, 25, and 50 µg/ml), and after 2.5 h of further growth at 37°C, β-galactosidase activity was measured (13). Interestingly, rprA-lacZ was significantly induced at HEWL concentrations of >10 µg/ml, up to 4.4-fold at 50 µg/ml (Fig. 1A). This induction could be completely abolished upon the additional introduction of a knockout of rcsB (strain LC102), the response regulator required to activate gene expression in the Rcs pathway. Moreover, knocking out rcsF (strain LC101), the outer membrane lipoprotein sensor that triggers the Rcs pathway upon antibiotic-mediated peptidoglycan stress (10), also resulted in a loss of lysozyme induction. As a comparison, rprA-lacZ induction in DH300 treated with amdinocillin (Sigma-Aldrich, Bornem, Belgium), as previously described (10), resulted in a 16-fold increase in β-galactosidase activity (Fig. 1B). Please note that the difference in basal β-galactosidase levels between LC100 and DH300 (Fig. 1A and B) is probably due to the tolA mutation in LC100, which is known to result in a higher basal expression of the Rcs pathway (5). These data clearly demonstrate that the Rcs phosphorelay can indeed be activated by exposure to lysozyme and that this induction is mediated by the outer membrane sensor rcsF. This also implies that the Rcs pathway responds to different types of peptidoglycan stress, as β-lactam antibiotics block the formation of peptide side-chain cross-links by binding irreversibly to the transpeptidases, while lysozyme hydrolyzes the heteropolysaccharide backbone.

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TABLE 1. Bacterial strains and plasmids used in the study

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FIG. 1. Induction of the Rcs pathway in LC100 (tolA::Kn Rcs+) with different HEWL concentrations (0 to 50 µg/ml) (A) and in DH300 (Rcs+) with (+) or without (–) amdinocillin treatment (B). Rcs induction is measured as β-galactosidase activity originating from a genomic rprA-lacZ reporter fusion and expressed in Miller units (13). Error bars indicate standard deviations of results from three replicate experiments. The corresponding RcsB– strain (LC102) and the RcsF– strain (LC101) showed rprA-lacZ inductions of <10 Miller units when subjected to lysozyme treatments and are therefore not shown.

We subsequently wondered whether an Rcs-compromised mutant would display a higher sensitivity to lysozyme due to its inability to induce lysozyme inhibitor production. In fact, during optimization of the previous experiment, we had already noticed that the RcsB^– and RcsF^– strains (LC102 and LC101) both showed a slight concentration-dependent growth retardation compared to the growth of the Rcs⁺ strain (LC100) in the presence of HEWL (data not shown). To further investigate this effect of the Rcs pathway on growth inhibition by HEWL, and especially the role of lysozyme inhibitors in this phenotype, the rates of growth of strains LC100, LC101, and LC102 carrying a plasmid that enables arabinose-induced expression of either Ivy (pAA410) (Table 1) or MliC (pAA530) (Table 1) were compared in the presence of 25 µg/ml HEWL (Fig. 2).

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FIG. 2. Growth curves (OD600) in the presence of 25 µg/ml HEWL of LC100 (tolA::Kn Rcs+) (squares), LC102 (tolA RcsB–) (triangles), and LC101 (tolA::Kn RcsF–) (circles) harboring plasmid pAA410 driving arabinose-inducible expression of Ivy (A and C) or plasmid pAA530 driving arabinose inducible-expression of MliC (B and D). Stationary-phase cultures were diluted (1/100) in fresh medium with HEWL in either the absence (open symbols) or presence (filled symbols) of 0.02% arabinose, and growth was measured as increase in OD600 (Multiscan RC; Thermo Scientific, Zellik, Belgium) at 37°C for 6 h. Error bars indicate standard deviations of results from three replicate experiments.

In the absence of arabinose induction, the RcsF^– and RcsB^– strains were clearly inhibited by lysozyme compared to their Rcs⁺ counterparts. While Rcs mutation did not appear to affect the lag phase, the exponential-growth rates (change in optical density at 600 nm [OD₆₀₀]/h) of LC101(pAA410) and LC101(pAA530) were about 42% lower than those of LC100(pAA410) and LC100(pAA530) in the presence of lysozyme. Similarly, the growth rates of LC102(pAA410) and LC102(pAA530) were 53% lower than those of LC100(pAA410) and LC100(pAA530) in the presence of lysozyme. The Rcs⁺ strains were not affected by the lysozyme dosage used in this experiment, since their growth rates were the same in LB without lysozyme (data not shown). A more detailed inspection of the growth curves indicated a two-step exponential-growth phase of the RcsB^– and RcsF^– strains in the presence of lysozyme, with a downward bend at an OD₆₀₀ of about 0.15. This behavior was reproducible, but the reason is not clear. In the absence of the tolA mutation, neither the rcsB nor rcsF mutation resulted in lysozyme sensitivity in MG1655 (data not shown), indicating that these mutations did not themselves increase outer membrane permeability for lysozyme.

Interestingly, the growth of LC102(pAA410) and LC101(pAA410) was largely rescued upon arabinose induction of Ivy expression (Fig. 2A and C). For LC102(pAA530) and LC101(pAA530), only a partial restoration of growth could be achieved by arabinose-induced MliC expression (Fig. 2B and D). Control experiments showed that the growth of neither strain was affected by the addition of arabinose in the absence of lysozyme. Furthermore, with a plasmid identical to pAA410 and pAA530 but with the gfp gene, encoding green fluorescent protein, replacing Ivy or MliC (pAA100) (Table 1), the growth of LC100, LC101, and LC102 was only marginally affected by arabinose addition (data not shown). Thus, our results show that the lysozyme sensitivity caused by impairing the induction of the Rcs pathway can be overcome specifically by enhanced expression of lysozyme inhibitors, in particular, Ivy.

In conclusion, we demonstrated that the Rcs phosphorelay system responds to exogenous lysozyme challenge and confers enhanced lysozyme resistance in E. coli via induction of lysozyme inhibitors. These findings extend the role of the Rcs phosphorelay as a peptidoglycan stress response pathway in several Enterobacteriaceae. With the exception of the plant pathogen Erwinia carotovora, a functional Rcs pathway seems to be present only in Enterobacteriaceae species that colonize the gut of an animal host either as pathogens or as commensals (7, 9). Furthermore, Rcs mutants of Salmonella enterica serovar Typhimurium showed attenuated systemic infection of mice, and at least one Rcs-activated gene was implicated in this phenotype (7). For these reasons, the Rcs pathway has been suggested to be a specific host interaction pathway. The demonstration in the current work that the Rcs pathway is inducible by lysozyme and triggers lysozyme tolerance by induction of lysozyme inhibitors lends further support to this hypothesis.

 
L.C. was supported by a doctoral fellowship from the Flemish Institute for the Promotion of Scientific Technological Research (IWT), and A.A. by a postdoctoral fellowship from the Research Foundation-Flanders (FWO-Vlaanderen). This work was further supported by research grants from FWO-Vlaanderen (G.0308.05 and G.0363.08) and by the Research Fund K.U.Leuven (research project GOA/03/10).

 
* Corresponding author. Mailing address: Laboratory of Food Microbiology, Kasteelpark Arenberg 22, B-3001 Leuven, Belgium. Phone: 32-16-321752. Fax: 32-16-321960. E-mail: abram.aertsen{at}biw.kuleuven.be

Published ahead of print on 9 January 2009.

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Journal of Bacteriology, March 2009, p. 1979-1981, Vol. 191, No. 6
0021-9193/09/$08.00+0     doi:10.1128/JB.01549-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Callewaert, L. Articles by Aertsen, A. Search for Related Content PubMed PubMed Citation Articles by Callewaert, L. Articles by Aertsen, A.