Next Article in Journal
Role of Hydrogen Sulfide in NRF2- and Sirtuin-Dependent Maintenance of Cellular Redox Balance
Next Article in Special Issue
Molecular Mechanisms of the Methionine Sulfoxide Reductase System from Neisseria meningitidis
Previous Article in Journal
Involvement of Neutrophil Dynamics and Function in Exercise-Induced Muscle Damage and Delayed-Onset Muscle Soreness: Effect of Hydrogen Bath
Previous Article in Special Issue
Methionine Sulfoxide Reductases of Archaea
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Antioxidants
Volume 7
Issue 10
10.3390/antiox7100128
antioxidants-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

The Role of Methionine Sulfoxide Reductases in Oxidative Stress Tolerance and Virulence of Staphylococcus aureus and Other Bacteria

by
Vineet K. Singh
1,*,
Kuldeep Singh
2 and
Kyle Baum
1
1
Department of Microbiology and Immunology, A.T. Still University of Health Sciences, Kirksville, MO 63501, USA
2
Mayo Clinic, Rochester, MN 53905, USA
*
Author to whom correspondence should be addressed.
Antioxidants 2018, 7(10), 128; https://doi.org/10.3390/antiox7100128
Submission received: 31 August 2018 / Revised: 19 September 2018 / Accepted: 26 September 2018 / Published: 28 September 2018
(This article belongs to the Special Issue Methionine Sulfoxide Reductases and Oxidative Damage)
Versions Notes

Abstract

:
Methionine sulfoxide reductases (MSRA1 and MSRB) are proteins overproduced in Staphylococcus aureus during exposure with cell wall-active antibiotics. Later studies identified the presence of two additional MSRA proteins (MSRA2 and MSRA3) in S. aureus. These MSR proteins have been characterized in many other bacteria as well. This review provides the current knowledge about the conditions and regulatory network that mimic the expression of these MSR encoding genes and their role in defense from oxidative stress and virulence.

1. Methionine Sulfoxide Reductases

The presence of reactive oxygen species (ROS) is potentially damaging to all cellular macromolecules. Oxidizing agents, such as hydrogen peroxide (H2O2), superoxides, and hydroxyl radicals, oxidize the sulfur atom of methionine residues, resulting in methionine sulfoxide (MetO) that typically leads to loss of protein function [1,2]. In 1981, an enzyme capable of reducing protein-bound methionine sulfoxide was identified [3,4]. These oxidized MetO residues are reduced back to methionine by methionine sulfoxide reductase (MSR) enzymes that restore normal protein functions [5,6]. Oxidation of methionine results in two stereoisomeric forms of MetO (R-MetO and S-MetO), which are reduced by two different MSR enzymes (MSRA and MSRB). MSRA is specific to S-MetO, and MSRB is specific to R-MetO [7,8,9,10]. The MetO/Met, MSRA/B-mediated oxidation and reduction of methionine residues are thus an important antioxidant mechanism [11], and methionine is no longer needed just for protein initiation [12].

2. MSRA and MSRB Enzymes in Staphylococcus aureus and Other Bacteria

In the S. aureus chromosome, there are three MSRA genes (MSRA1, MSRA2 and MSRA3) and one MSRB gene. These four MSR genes are expressed from three different promoters. The MSRA1 and MSRB genes are co-expressed as part of a polycistronic message, and the MSRA2 and MSRA3 genes are expressed independently from their respective promoters [13]. In bacteria, most species contain at least one copy of each of the MSRA and MSRB genes. However, similar to S. aureus, multiple copies of MSR encoding genes have been identified in many bacteria. Vibrio cholera contains two MSRA and three MSRB genes distributed in its two chromosomes. Rhizobium meliloti contains three MSRA and three MSRB genes with one copy of each found on a plasmid [14,15]. In addition, there is no set pattern in terms of the genetic organization of MSR genes across species. In some bacterial species, e.g., Escherichia coli, Mycobacterium tuberculosis, Bordetella pertussis, Pseudomonas aeruginosa, Salmonella Typhimurium, and S. aureus, MSRA and MSRB genes are two separate entities. In other bacterial species, e.g., Bacillus subtilis and S. aureus, the MSRA and MSRB genes are found adjacent to each other and are co-transcribed. Interestingly, in some other species, e.g., Neisseria gonorrhoeae, Neisseria meningitidis, and Helicobacter pylori, the MSRA and MSRB genes are fused and translated as separate domains within a single larger polypeptide [7,16].

3. Methionine and MSR Enzymes as Part of an Antioxidant System

While all amino acid residues can be oxidized, their sensitivity to oxidation is variable [17]. Methionine has a much higher propensity for oxidation than other amino acids. It is present in high concentrations on the surface of certain proteins [17] and can be oxidized without affecting the functionality of proteins. In the case of E. coli glutamine synthase, eight of the 16 methionine residues distant to the catalytic site could be oxidized without affecting activity [17]. Similar results were also seen in another E. coli protein, GroEL [18]. This protein remained fully functional even when all of its 23 methionine residues were oxidized after exposure to 15 mM H2O2 for three hours. It was only when an even higher H2O2 concentration was used, causing the oxidation of cysteines and tyrosines, that the GroEL chaperonin activity was eventually reduced [18]. The scavenging ability of methionines was further exemplified when about 40% of methionine residues in E. coli cells were substituted with norleucine, a carbon analog of methionine in which sulfur is replaced with a methylene group. These norleucine-substituted bacterial cells were more susceptible to killing by hypochlorite and peroxide [19]. Several proteins from the human gastric pathogen H. pylori were shown to interact with MSR enzymes. Many of these proteins (e.g., GroEL, catalase, and recombinase) are significantly more methionine rich than other bacterial proteins and, in all likelihood, are oxidized under oxidative stress and salvaged by the activity of MSR enzymes [20]. Thus, MSR proteins not only repair oxidative damage to methionine residues through the oxidation/reduction cycle but also serve as scavengers of ROS and protect cells from more widespread oxidative damage [11,17].

4. Environmental Impact on MSR Expression

In S. aureus, MSRA1 and MSRB proteins were first identified as proteins overproduced in response to the presence of cell wall-active antibiotics [21]. Later, the expression of MSRA1 and MSRB genes were determined to be induced at the transcriptional level and specifically in response to cell wall-active antibiotics [22,23]. Using a promoter-lacZ fusion, it was shown that none of the S. aureus MSR genes were induced under conditions of oxidative stress [24]. Cell wall-active antibiotics only induced the expression of the MSRA1/MSRB locus and had no effect on the expression of MSRA2 or MSRA3 genes [24]. A high salt concentration caused some induction of MSRA3 but not of the other S. aureus MSR genes [24]. The expression of MSRA2 and MSRA3 genes was very low, and both were expressed higher during the early exponential phase of bacterial growth [24]. The expression of the MSRA1/MSRB locus occurs at a much higher level than the expression of MSRA2 and MSRA3 and is most expressed during the late log and stationary phases of growth [24]. Surprisingly, cell wall-active antibiotics induce the expression of MSRA1 and MSRB genes in S. aureus, but these MSR enzymes appear to play no direct role in defense from these antibiotics [13]. It is speculated that cell wall-active antibiotics destabilize the cell wall and allow the oxidants easy access to cellular macromolecules. MSRA1 and MSRB might be needed at higher concentrations during exposure of S. aureus to the cell wall inhibitors.
When the role of SigmaB (stress responsive sigma factor) was investigated, it enhanced, but was not required for, the expression of the S. aureus MSRA1/MSRB locus [25,26]. In addition, induction of the MSRA1/MSRB locus by cell wall-active antibiotics was inhibited by glycerol monolaurate that interfered with signal transduction pathways. This result led to the speculation that an unidentified signal transduction pathway might be involved in the induced expression of MSRA1/MSRB in the presence of cell wall-active antibiotics [26]. More recently, a higher level of expression of MSRA2 gene was observed in S. aureus after sunlight exposure in both oxic and anoxic conditions. Thus, it has been speculated that MSRA probably defends the bacteria from oxygen-dependent and oxygen-independent photostresses [27].
Expression of MSR genes in other pathogenic species has also been investigated. Similar to S. aureus MSRA1/MSRB, in H. pylori [20], E. coli [28], and B. subtilis [29] the late log and stationary phase cultures of these bacteria had the highest MSR activity. In addition to MSRA1/MSRB induction by cell wall-active antibiotics, piplartine, a biologically active alkaloid from peppers [30], showed enhanced MSR expression in the pathogenic parasite, Trypanosoma cruzi [31].
There is no doubt that MSRs protect cells from oxidative stress, but there are only a handful of species where oxidative stress conditions have been shown to induce the expression of MSR genes. In Streptococcus gordonii, H2O2 induced expression of the MSRA gene [32]. Oxidative stress conditions induced the expression of MSRA in the xenobiotics-degrading bacterium Ochrobactrum anthropic [33]. The expression of MSRA gene in plant bacterium Xanthomonas campestris pv. phaseoli was highly induced by exposure to oxidants and N-ethylmaleimide [34]. In P. aeruginosa, H2O2, paraquat, or sodium hypochlorite had no effect on MSRA1 expression, but expression of MSRB was induced by sodium hypochlorite [35]. Oxidative stress conditions caused transcriptional upregulation of MSR in H. pylori [36]. In addition to oxidative stress, a slight upshift in pH (from 6.2 to 7.3) also led to increased expression of MSRA in S. gordonii [37]. Finally, the B. subtilis MSRA/MSRB operon was induced by paraquat but not by H2O2 [38].

5. Cellular Control of MSR Expression

In S. aureus and B. subtilis, the expression of MSRA and MSRB genes appears to be under the control of SigmaA [26,38]. In B. subtilis, a transcriptional regulator, Spx, has a positive impact on the expression of MSRA/MSRB genes [38]. Further, paraquat induces expression of MSRA/MSRB in B. subtilis, and this phenomenon is seen even in Spx-deficient cells, suggesting that some unidentified factors also play a role [38]. YjbH acts as a post-transcriptional negative regulator of global oxidative/thiol stress in B. subtilis [39], binding and stabilizing Spx [40]; thus, YjbH may be indirectly involved in the regulation of MSRA/MSRB expression in this bacterium. Spx is believed to be required for the upregulation of MSRA1/MSRB in S. aureus as well [41]. In E. coli, although iron has no influence on the expression of MSRA, an iron-responsive small RNA RyhB downregulates the expression of MSRB and also interferes with the translation of MSRB transcripts [42]. The csrA gene of Enterococcus faecalis encodes a protein with homology to MSRA and is upregulated in the presence of cadmium, mercury, lead, copper and manganese; this outcome can be used as a biosensor for monitoring heavy metals in the environment [43]. In N. meningitidis, MSRA is part of the SigmaE regulon [44], and in the rhizobacterium Azospirillum brasilense expression of MSRA is controlled by heat-shock sigma factor RpoH2 [45]. In S. gordonii, an amylase-binding protein A (AbpA) positively upregulates the expression of peptide MSR [46].

6. Defense from Oxidants

There are numerous reports that provide evidence that lack of MSR activity and, as a result, increased methionine oxidation can lead to severe growth defects and even cell death. Most studies suggest that the MSRA enzyme is critical for defense of bacterial cells from oxidative stress and that MSRB plays little-to-no role under these stresses. In E. coli, the catalytic activity of MSRA enzyme was 1000-fold higher than that of MSRB in reducing free methionine sulfoxide [8]. However, in S. aureus, MSRB was shown to have 28-fold higher activity than MSRA [22]. Nonetheless, lack of MSRB had no effect on the oxidative stress tolerance of this bacterium, and MSRA1 appeared to be more significant for defending against these conditions [13]. In addition, individual deletions of MSRA2 or MSRA3 genes resulted in no change in oxidative stress resistance of S. aureus when compared with the wild-type bacterium [13]. However, the sensitivity to oxidative stress was confounded when S. aureus lacked all three MSRA proteins [13]. Incubation with hypochlorous acid (HOCl) led to the oxidation of a significant fraction of methionine residues in S. aureus and E. coli. When the percentage of oxidized methionine residues increased from exposure to 150 µM HOCl, the cellular MetO content increased from 6% (untreated cells) to 22%, resulting in a 55% decrease in viability [47]. Exposure to 200 µM HOCl oxidized 40% of the cellular methionine residues and resulted in an almost complete loss of bacterial viability [47].
The significance of MSR enzymes is also apparent from the growth impairment and survival of MSR mutants in E. coli [48] and S. gordonii [32,37] after H2O2 treatment. In Xanthomonas campestris pv. phaseoli, MSRA mutant cells in stationary growth phase are 10–100-fold more sensitive to H2O2, tert-butyl hydroperoxide, menadione, and N-ethylmaleimide [34]. In the microaerophilic pathogen Campylobacter jejuni, the double MSRA-MSRB mutant showed a growth defect under in vitro microaerobic conditions, but the individual MSRA or MSRB mutants did not [49]. However, during conditions of oxidative and nitrosative stress, the double MSRA-MSRB mutant was markedly more sensitive, and the individual MSRA and MSRB mutants also showed increased sensitivity [49]. In M. tuberculosis, lack of MSRA or MSRB showed no change in resistance to oxidants, but a double mutant was vulnerable to reactive oxygen and reactive nitrogen intermediates [50]. An MSR mutant of H. pylori with no detectable MSR activity showed severe growth defects and survival in the presence of oxidants. A derivative strain of H. pylori that still produced MSRA but not MSRB activity remained sensitive to oxidants [36]. Inactivation of the MSRA gene of S. gordonii led to increased bacterial sensitivity to H2O2 [37]. In P. aeruginosa, mutations in MSRA and MSRB increased sensitivity to oxidative stress, and an MSRA-MSRB double mutant showed an additive effect in terms of oxidant sensitivity [35]. E. faecalis hasone MSRA and one MSRB encoding genes in different parts of the chromosome. The individual MSRA and MSRB mutants of this bacterium were sensitive to H2O2, and as in P. aeruginosa, mutational effects were additive in the double MSRA-MSRB mutant [51].
Oxidation of methionine residues of acid-soluble spore proteins, (SASP), in MSRA-deficient cells of B. subtilis reduces their ability to bind DNA, which is significant for the long-term survival of spores [52]. MSRA-deficient S. Typhimurium showed normal growth in broth but was sensitive to HOCl [53]. Lack of MSRAB2 in Streptococcus pneumoniae enhanced its killing by H2O2 [54]. While the MSRA mutants of Mycobacterium smegmatis were sensitive to the presence of oxidants, the MSRB mutants showed no such defect. Thus, as in S. aureus, MSRA and not MSRB may be the important MSR in M. smegmatis [55]. Even among fungal species, such as Aspergillus nidulans, the MSRs are important for defense against oxidants [56]. However, sometimes the protective role of MSR enzymes from oxidative stress is not as evident. In the case of the oral pathogen Aggregatibacter actinomycetemcomitans, no difference in growth was apparent between the wild-type and MSR mutant strains when exposed to H2O2 or paraquat.

7. Methionine Sulfoxide Reductases and Virulence

Many studies have provided evidence about the role of MSR proteins in the virulence of bacterial pathogens. Based on analysis of nucleotide sequences and the presence of synonymous vs. non-synonymous single nucleotide polymorphism, the role of MSRA enzyme has been postulated in the transition of the bacterium Staphylococcus epidermidis from commensalism to pathogenicity [57]. In S. aureus, recent findings suggest that MSRA1 plays a role in virulence, but other MSRs (MSRA2, MSRA3, and MSRB) play almost no such role. Strains of S. aureus deficient in MSRA1 showed reduced hemolysis and were less adherent to human lung epithelial cells [13]. These MSRA1-deficient cells also showed a decrease in survival in mouse tissue when compared with wild-type S. aureus [13]. Further, reduced MSRA activity in many bacteria impacted survival inside phagocytic cells [47,53,58,59].
MSRA was shown to be required for the full virulence of the plant pathogen Erwinia chrysanthemi [60]. The presence of MetO in the gut increased the viability of Drosophila infected with V. cholera [61]. MetO in enterocytes probably competes with protein-bound MetO, titrating away the host MSRs that favors the Drosophila and this in turn reduces the virulence of V. cholera [61]. In S. Typhimurium, MSRA but not MSRB has an important role in oxidative stress protection and virulence [62]. Deletion of MSRA in S. Typhimurium led to very little colonization of poultry [63]. Further, in S. Typhimurium, MSRB has only a weak activity against peptidyl R-MetO, but MSRA shows activity against both free and peptidyl S-MetO [62]. In this bacterium, an additional gene, MSRC, is present that codes for a protein that reduces only free R-MetO and has been shown to be essential for survival in the presence of H2O2 inside macrophages and in mice [62].
In E. faecalis, individual MSRA and MSRB mutants were also sensitive to activated macrophages and were attenuated in the Galleria mellonella insect infection assay [51]. In another study, MSRB was shown to have a role in the virulence of E. faecalis [51]. Mutations in MSRA and MSRB genes in P. aeruginosa decreased virulence in a Drosophila melanogaster infection model, and a double MSRA-MSRB mutant showed an additive effect for reduction in virulence [35]. An MSRA mutant of M. smegmatis had more reduced survival inside mice macrophages than the wild-type strain [64]. However, an MSRB mutant of M. smegmatis showed only a moderate reduction in survival inside the macrophages. This supports again that MSRA, not MSRB, is the important MSR in M. smegmatis [55]. MSR-deficient H. pylori showed severe reduction in the colonization of mouse stomach [36], and loss of MSRAB2 in S. pneumoniae dramatically reduced virulence and enhanced its uptake by macrophages [54].
Factors contributing to decreased virulence may arise from reduced colonization efficiency of MSR-deficient bacteria. Further, lack of MSR enzymes may compromise the integrity of the bacterial surface proteins responsible for adherence to eukaryotic cells [15,16,54,65]. MSRA in Mycoplasma genitalium was shown to affect adherence to sheep erythrocytes, and in the absence of this enzyme, the bacterium could not grow in hamsters [65]. Lack of MSRA also reduced cytotoxicity of M. genitalium to cervical epithelial cells and monocytic cells [66]. In terms of cellular localization, the S. gordonii MSRA was detectable in the cell wall fraction and probably played a role in repair of proteins, such as SspAB adhesins [32]. The MSRA mutant of S. gordonii was significantly impaired in fibronectin binding, which is significant for initial colonization of human tissues [67].
The MSRA and MSRB genes in Francisella tularensis are located in different regions of the chromosome. Surprisingly, MSRB not MSRA appears to be a key determinant of virulence in F. tularensis. Lack of MSRB reduces growth and resistance to oxidants and macrophages, but lack of MSRA produces no such effect. However, the lack of MSRA reduces the in vivo number of F. tularensis in mouse tissues, but the effect is much more pronounced in the absence of MSRB [68]. In an in vivo competition experiment, the MSRB mutants of Lactobacillus reuteri showed an ecological fitness and were recovered in smaller numbers than their wild-type counterparts in the gut of 50% of the inoculated mice [69]. Even in the parasite Leishmania major, a mutation in the MSRA gene increased sensitivity to H2O2 and decreased infectivity in macrophages [70]. However, these mutants induced normal lesions in BALB/c mice, suggesting a limited or no role in virulence [70].
Some reports, however, have questioned the role of MSR proteins in bacterial virulence. MSRA was initially thought to play a role in adherence of N. gonorrhoeae to eukaryotic cells [16]. In N. gonorrhoeae, two forms of MSRA/B are produced: one has a signal peptide that gets localized to the outer membrane and the other lacks the signal peptide but remains in the cytoplasm. Even though MSRA/B conferred protection from oxidative damage, lack of MSRA/B had no effect on bacterial adherence to conjunctival cells [71]. In addition, the MSRA mutant of N. gonorrhoeae showed no reduction in sensitivity to in vitro killing by polymorphonuclear cells from BALB/c mice, and there was reduced recovery of these mutants when compared with wild-type bacteria from BALB/c infected mice after only eight days of infection [72]. A mutation in the MSRA gene of the oral pathogen A. actinomycetemcomitans abolished MSR activity, but the mutant showed no reduction in resistance to oxidative stress or adherence to epithelial cells, suggesting the MSRA system has no role for virulence in this bacterium [73]. Similar to the no change in oxidative stress tolerance in MSRA mutants of A. actinomycetemcomitans, these mutants exhibited unaltered survival inside the macrophages and adherence to the epithelial cells. These findings also suggest that MSRA may not be a virulence contributor in this pathogen [73].

8. Conclusions

The MSR enzymes have gained significance as key determinants of protection of bacterial species from oxidative stress and of contributors of virulence. While most literature suggests that the MSRA protein is key to these functions, little is known about the precise function of MSRB. These enzymes are overproduced in response to cell wall-active antibiotics and are considered to be important members of cell wall stress stimulon in an important bacterium, S. aureus. More studies are needed to understand why many bacteria need so many genes that encode these enzymes, how they are regulated, why S. aureus turns on the expression of these genes under cell wall-active antibiotic stress, and what their precise function is in bacterial physiology and virulence.

Funding

This research was supported in part by a Warner/Fermaturo grant and A.T. Still University Board of Trustees Research Funds, by grant 1R15AI090680-01 from the National Institutes of Health to VKS, and grants from the Kirksville College of Osteopathic Medicine Biomedical Sciences Graduate Program to KRB and KS.

Acknowledgments

Authors acknowledge Deborah Goggin, the scientific writer at A.T. Still University, for critical reading of this manuscript.

Conflicts of Interest

These authors declare no conflict of interest.

References

  1. Achilli, C.; Ciana, A.; Minetti, G. The discovery of methionine sulfoxide reductase enzymes: An historical account and future perspectives. Biofactors 2015, 41, 135–152. [Google Scholar] [CrossRef] [PubMed]
  2. Vogt, W. Oxidation of methionyl residues in proteins: Tools, targets, and reversal. Free Radic. Biol. Med. 1995, 18, 93–105. [Google Scholar] [CrossRef]
  3. Abrams, W.R.; Weinbaum, G.; Weissbach, L.; Weissbach, H.; Brot, B. Enzymatic reduction of oxidized alpha-1-proteinase inhibitor restores biological activity. Proc. Natl. Acad. Sci. USA 1981, 78, 7483–7486. [Google Scholar] [CrossRef] [PubMed]
  4. Brot, N.; Weissbach, L.; Werth, J.; Weissbach, H. Enzymatic reduction of protein-bound methionine sulfoxide. Proc. Natl. Acad. Sci. USA 1981, 78, 2155–2158. [Google Scholar] [CrossRef] [PubMed]
  5. Brot, N.; Weissbach, H. Peptide methionine sulfoxide reductase: Biochemistry and physiological role. Biopolymers 2000, 55, 288–296. [Google Scholar] [CrossRef]
  6. Moskovitz, J.; Berlett, B.S.; Poston, M.J.; Stadtman, E.R. The yeast peptide-methionine sulfoxide reductase functions as an antioxidant in vivo. Proc. Natl. Acad. Sci. USA 1997, 94, 9585–9589. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Delaye, L.; Becerra, A.; Orgel, L.; Lazcano, A. Molecular evolution of peptide methionine sulfoxide reductases (MSRA and MSRB): On the early development of a mechanism that protects against oxidative damage. J. Mol. Evol. 2007, 64, 15–32. [Google Scholar] [CrossRef] [PubMed]
  8. Grimaud, R.; Ezraty, B.; Mitchell, J.K.; Lafitte, D.; Briand, C.; Derrick, P.J.; Barras, F. Repair of oxidized proteins. Identification of a new methionine sulfoxide reductase. J. Biol. Chem. 2001, 276, 48915–48920. [Google Scholar] [PubMed]
  9. Minetti, G.; Balduini, C.; Brovelli, A. Reduction of DABS-L-methionine-dl-sulfoxide by protein methionine sulfoxide reductase from polymorphonuclear leukocytes: Stereospecificity towards the l-sulfoxide. Ital. J. Biochem. 1994, 43, 273–283. [Google Scholar] [PubMed]
  10. Moskovitz, J.; Singh, V.K.; Requena, J.; Wilkinson, B.J.; Jayaswal, R.K.; Stadtman, E.R. Purification and characterization of methionine sulfoxide reductases from mouse and Staphylococcus aureus and their substrate stereospecificity. Biochem. Biophys. Res. Commun. 2002, 290, 62–65. [Google Scholar] [CrossRef] [PubMed]
  11. Stadtman, E.R.; Moskovitz, J.; Berlett, B.S.; Levine, R.L. Cyclic oxidation and reduction of protein methionine residues is an important antioxidant mechanism. Mol. Cell Biochem. 2002, 234, 3–9. [Google Scholar] [CrossRef] [PubMed]
  12. Lim, J.M.; Kim, G.; Levine, R.L. Methionine in proteins: It’s Not Just for Protein Initiation Anymore. Neurochem. Res. 2018, 1, 1–11. [Google Scholar] [CrossRef] [PubMed]
  13. Singh, V.K.; Vaish, M.; Johansson, T.R.; Baum, K.R.; Ring, R.P.; Singh, S.; Shukla, K.; Moskovitz, J. Significance of four methionine sulfoxide reductases in Staphylococcus aureus. PLoS ONE 2015, 10, e0117594. [Google Scholar] [CrossRef] [PubMed]
  14. Ezraty, B.; Aussel, L.; Barras, F. Methionine sulfoxide reductases in prokaryotes. Biochim. Biophys. Acta 2005, 1703, 221–229. [Google Scholar] [CrossRef] [PubMed]
  15. Sasindran, S.J.; Saikolappan, S.; Dhandayuthapani, S. Methionine sulfoxide reductases and virulence of bacterial pathogens. Future Microbiol. 2007, 2, 619–630. [Google Scholar] [CrossRef] [PubMed]
  16. Wizemann, T.M.; Moskovitz, J.; Pearce, B.J.; Cundell, D.; Arvidson, C.G.; So, M.; Weissbach, H.; Brot, N.; Masure, H.R. Peptide methionine sulfoxide reductase contributes to the maintenance of adhesins in three major pathogens. Proc. Natl. Acad. Sci. USA 1996, 93, 7985–7990. [Google Scholar] [CrossRef] [PubMed]
  17. Levine, R.L.; Berlett, B.S.; Moskovitz, M.J.; Mosoni, L.; Stadtman, E.R. Methionine residues may protect proteins from critical oxidative damage. Mech. Ageing Dev. 1999, 107, 323–332. [Google Scholar] [CrossRef]
  18. Melkani, G.C.; Kestetter, J.; Sielaff, R.; Zardeneta, G.; Mendoza, J.A. Protection of GroEL by its methionine residues against oxidation by hydrogen peroxide. Biochem. Biophys. Res. Commun. 2006, 347, 534–539. [Google Scholar] [CrossRef] [PubMed]
  19. Luo, S.; Levine, R.L. Methionine in proteins defends against oxidative stress. FASEB J. 2009, 23, 464–472. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  20. Alamuri, P.; Maier, R.J. Methionine sulfoxide reductase in Helicobacter pylori: Interaction with methionine-rich proteins and stress-induced expression. J. Bacteriol. 2006, 188, 5839–5850. [Google Scholar] [CrossRef] [PubMed]
  21. Singh, V.K.; Jayaswal, R.K.; Wilkinson, B.J. Cell wall-active antibiotic induced proteins of Staphylococcus aureus identified using a proteomic approach. FEMS Microbiol. Lett. 2001, 199, 79–84. [Google Scholar] [CrossRef]
  22. Singh, V.K.; Moskovitz, J.; Wilkinson, B.J.; Jayaswal, R.K. Molecular characterization of a chromosomal locus in Staphylococcus aureus that contributes to oxidative defence and is highly induced by the cell-wall-active antibiotic oxacillin. Microbiology 2001, 147, 3037–3045. [Google Scholar] [CrossRef] [PubMed]
  23. Utaida, S.; Dunman, P.M.; Macapagal, D.; Murphy, E.; Projan, S.J.; Singh, V.K.; Jayaswal, R.K.; Wilkinson, B.J. Genome-wide transcriptional profiling of the response of Staphylococcus aureus to cell-wall-active antibiotics reveals a cell-wall-stress stimulon. Microbiology 2003, 149, 2719–2732. [Google Scholar] [CrossRef] [PubMed]
  24. Singh, K.; Singh, V.K. Expression of four methionine sulfoxide reductases in Staphylococcus aureus. Int. J. Microbiol. 2012, 2012, 719594. [Google Scholar] [CrossRef] [PubMed]
  25. Baum, K.R.; Ahmad, Z.; Singh, V.K. Regulation of expression of oxacillin-inducible methionine sulfoxide reductases in Staphylococcus aureus. Int. J. Microbiol. 2015, 2015, 617925. [Google Scholar] [CrossRef] [PubMed]
  26. Pechous, R.; Ledala, N.; Wilkinson, B.J.; Jayaswal, R.K. Regulation of the expression of cell wall stress stimulon member gene msrA1 in methicillin-susceptible or -resistant Staphylococcus aureus. Antimicrob. Agents Chemother. 2004, 48, 3057–3063. [Google Scholar] [CrossRef] [PubMed]
  27. McClary, J.S.; Sassoubre, L.M.; Boehm, A.B. Staphylococcus aureus strain newman photoinactivation and cellular response to sunlight exposure. Appl. Environ. Microbiol. 2017, 83, e01052. [Google Scholar] [CrossRef] [PubMed]
  28. Moskovitz, J.; Rahman, M.A.; Rahman, J.; Yancey, S.O.; Kushner, S.R.; Brot, N.; Weissbach, H. Escherichia coli peptide methionine sulfoxide reductase gene: Regulation of expression and role in protecting against oxidative damage. J. Bacteriol. 1995, 177, 502–507. [Google Scholar] [CrossRef] [PubMed]
  29. Madeira, J.-P.; Alpha-Bazin, B.M.; Armengaud, J.; Duport, C. Methionine residues in exoproteins and their recycling by methionine sulfoxide reductase ab serve as an antioxidant strategy in Bacillus cereus. Front. Microbiol. 2017, 8, 1342. [Google Scholar] [CrossRef] [PubMed]
  30. Bezerra, D.P.; Pessoa, C.; de Moraes, M.O.; Saker-Neto, N.; Silveira, E.R.; Costa-Lotufo, L.V. Overview of the therapeutic potential of piplartine (piperlongumine). Eur. J. Pharm. Sci. 2013, 48, 453–463. [Google Scholar] [CrossRef] [PubMed]
  31. Vieira, G.A.L.; da Silva, M.T.A.; Regasini, L.O.; Cotinguiba, F.; Laure, H.J.; Rosa, J.C.; Furlan, M.; Cicarelli, R.M.B. Trypanosoma cruzi: Analysis of two different strains after piplartine treatment. Braz. J. Infect. Dis. 2018, 22, 208–218. [Google Scholar] [CrossRef] [PubMed]
  32. Lei, Y.; Zhang, Y.; Guenther, B.D.; Kreth, J.; Herzberg, M.C. Mechanism of adhesion maintenance by methionine sulphoxide reductase in Streptococcus gordonii. Mol. Microbiol. 2011, 80, 726–738. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Tamburro, A.; Robuffo, L.; Heipieper, H.J.; Allocati, N.; Rotilio, D.; Di, C.I.; Favaloro, B. Expression of glutathione S-transferase and peptide methionine sulphoxide reductase in Ochrobactrum anthropi is correlated to the production of reactive oxygen species caused by aromatic substrates. FEMS Microbiol. Lett. 2004, 241, 151–156. [Google Scholar] [CrossRef] [PubMed]
  34. Vattanaviboon, P.; Seeanukun, C.; Whangsuk, W.; Utamapongchai, S.; Mongkolsuk, S. Important role for methionine sulfoxide reductase in the oxidative stress response of Xanthomonas campestris pv. phaseoli. J. Bacteriol. 2005, 187, 5831–5836. [Google Scholar] [CrossRef] [PubMed]
  35. Romsang, A.; Atichartpongkul, S.; Trinachartvanit, W.; Vattanaviboon, P.; Mongkolsuk, S. Gene expression and physiological role of Pseudomonas aeruginosa methionine sulfoxide reductases during oxidative stress. J. Bacteriol. 2013, 195, 3299–3308. [Google Scholar] [CrossRef] [PubMed]
  36. Alamuri, P.; Maier, R.J. Methionine sulphoxide reductase is an important antioxidant enzyme in the gastric pathogen Helicobacter pylori. Mol. Microbiol. 2004, 53, 1397–1406. [Google Scholar] [CrossRef] [PubMed]
  37. Vriesema, A.J.; Dankert, J.; Zaat, S.A. A shift from oral to blood pH is a stimulus for adaptive gene expression of Streptococcus gordonii CH1 and induces protection against oxidative stress and enhanced bacterial growth by expression of msrA. Infect. Immun. 2000, 68, 1061–1068. [Google Scholar] [CrossRef] [PubMed]
  38. You, C.; Sekowska, A.; Francetic, O.; Martin-Verstraete, L.; Wang, Y.; Danchin, A. Spx mediates oxidative stress regulation of the methionine sulfoxide reductases operon in Bacillus subtilis. BMC Microbiol. 2008, 8, 128. [Google Scholar] [CrossRef] [PubMed]
  39. Larsson, J.T.; Rogstam, A.; von Wachenfeldt, C. YjbH is a novel negative effector of the disulphide stress regulator, Spx, in Bacillus subtilis. Mol. Microbiol. 2007, 66, 669–684. [Google Scholar] [CrossRef] [PubMed]
  40. Kommineni, S.; Garg, S.K.; Chan, C.M.; Zuber, P. YjbH-enhanced proteolysis of Spx by ClpXP in Bacillus subtilis is inhibited by the small protein YirB (YuzO). J. Bacteriol. 2011, 193, 2133–2140. [Google Scholar] [CrossRef] [PubMed]
  41. Renzoni, A.; Andrey, D.O.; Jousselin, A.; Barras, C.; Monod, A.; Vaudaux, P.; Lew, D.; Kelley, W.L. Whole genome sequencing and complete genetic analysis reveals novel pathways to glycopeptide resistance in Staphylococcus aureus. PLoS ONE 2011, 6, e21577. [Google Scholar] [CrossRef] [PubMed]
  42. Bos, J.; Duverger, Y.; Thouvenot, B.; Chiaruttini, C.; Branlant, C.; Springer, M.; Charpentier, B.; Barras, F. The sRNA RyhB regulates the synthesis of the Escherichia coli methionine sulfoxide reductase MSRB but not MSRA. PLoS ONE 2013, 8, e63647. [Google Scholar] [CrossRef] [PubMed]
  43. Laplace, J.M.; Hartke, A.; Giard, J.C.; Auffray, Y. Cloning, characterization and expression of an Enterococcus faecalis gene responsive to heavy metals. Appl. Microbiol. Biotechnol. 2000, 53, 685–689. [Google Scholar] [CrossRef] [PubMed]
  44. Hopman, C.T.; Speijer, D.; van der Ende, A.; Pannekoek, Y. Identification of a novel anti-sigmaE factor in Neisseria meningitidis. BMC Microbiol. 2010, 10, 164. [Google Scholar] [CrossRef] [PubMed]
  45. Kumar, S.; Rai, A.K.; Mishra, M.N.; Shukla, M.; Singh, P.K.; Tripathi, A.K. RpoH2 sigma factor controls the photooxidative stress response in a non-photosynthetic rhizobacterium, Azospirillum brasilense Sp7. Microbiology 2012, 158, 2891–2902. [Google Scholar] [CrossRef] [PubMed]
  46. Haase, E.M.; Feng, X.; Pan, J.; Miecznikowski, J.C.; Scannapieco, F.A. Dynamics of the Streptococcus gordonii transcriptome in response to medium, salivary alpha-amylase, and starch. Appl. Environ. Microbiol. 2015, 81, 5363–5374. [Google Scholar] [CrossRef] [PubMed]
  47. Rosen, H.; Klebanoff, S.J.; Wang, Y.; Brot, N.; Heinecke, J.W.; Fu, X. Methionine oxidation contributes to bacterial killing by the myeloperoxidase system of neutrophils. Proc. Natl. Acad. Sci. USA 2009, 106, 18686–18691. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  48. St John, G.; Brot, N.; Ruan, J.; Erdjument-Bromage, H.; Tempst, P.; Weissbach, H.; Nathan, C. Peptide methionine sulfoxide reductase from Escherichia coli and Mycobacterium tuberculosis protects bacteria against oxidative damage from reactive nitrogen intermediates. Proc. Natl. Acad. Sci. USA 2001, 98, 9901–9906. [Google Scholar] [CrossRef] [PubMed]
  49. Atack, J.M.; Kelly, D.J. Contribution of the stereospecific methionine sulphoxide reductases MSRA and MSRB to oxidative and nitrosative stress resistance in the food-borne pathogen Campylobacter jejuni. Microbiology 2008, 154, 2219–2230. [Google Scholar] [CrossRef] [PubMed]
  50. Lee, W.L.; Gold, B.; Darby, C.; Brot, N.; Jiang, X.; De Carvalho, L.P.S.; Wellner, D.; John, G.S.; Jacobs, W.R., Jr.; Nathan, C. Mycobacterium tuberculosis expresses methionine sulphoxide reductases A and B that protect from killing by nitrite and hypochlorite. Mol. Microbiol. 2009, 71, 583–593. [Google Scholar] [CrossRef] [PubMed]
  51. Zhao, C.; Hartke, A.; Sorda, M.L.; Posteraro, B.; Laplace, J.-M.; Auffray, Y.; Sanguinetti, M. Role of methionine sulfoxide reductases A and B of Enterococcus faecalis in oxidative stress and virulence. Infect Immun. 2010, 78, 3889–3897. [Google Scholar] [CrossRef] [PubMed]
  52. Hayes, C.S.; Illades-Aguiar, B.; Casillas-Martinez, L.; Setlow, P. In vitro and in vivo oxidation of methionine residues in small, acid-soluble spore proteins from Bacillus species. J. Bacteriol. 1998, 180, 2694–2700. [Google Scholar] [PubMed]
  53. Trivedi, R.N.; Agarwal, P.; Kumawat, M.; Pesingi, P.K.; Gupta, V.K.; Goswami, T.K.; Mahawar, M. Methionine sulfoxide reductase A (MSRA) contributes to Salmonella Typhimurium survival against oxidative attack of neutrophils. Immunobiology 2015, 220, 1322–1327. [Google Scholar] [CrossRef] [PubMed]
  54. Saleh, M.; Bartual, S.G.; Abdullah, M.R.; Jensch, I.; Asmat, T.M.; Petruschka, L.; Pribyl, T.; Gellert, M.; Lillig, C.H.; Antelmann, H.; et al. Molecular architecture of Streptococcus pneumoniae surface thioredoxin-fold lipoproteins crucial for extracellular oxidative stress resistance and maintenance of virulence. EMBO Mol. Med. 2013, 5, 1852–1870. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Dhandayuthapani, S.; Jagannath, C.; Nino, C.; Saikolappan, S.; Sasindran, S.J. Methionine sulfoxide reductase B (MSRB) of Mycobacterium smegmatis plays a limited role in resisting oxidative stress. Tuberculosis 2009, 89, S26–S32. [Google Scholar] [CrossRef]
  56. Soriani, F.M.; Kress, M.R.; de Gouvêa, P.F.; Malavazi, I.; Savoldi, M.; Gallmetzer, A.; Strauss, J.; Goldman, M.H.S.; Goldman, G.H. Functional characterization of the Aspergillus nidulans methionine sulfoxide reductases (MSRA and MSRB). Fungal Genet. Biol. 2009, 46, 410–417. [Google Scholar] [CrossRef] [PubMed]
  57. Wei, W.; Cao, Z.; Zhu, Y.-L.; Wang, X.; Ding, G.; Xu, H.; Jia, P.; Qu, D.; Danchin, A.; Li, Y. Conserved genes in a path from commensalism to pathogenicity: Comparative phylogenetic profiles of Staphylococcus epidermidis RP62A and ATCC12228. BMC Genomics 2006, 7, 112. [Google Scholar] [CrossRef] [PubMed]
  58. Mahawar, M.; Tran, V.; Sharp, J.S.; Maier, R.J. Synergistic roles of Helicobacter pylori methionine sulfoxide reductase and GroEL in repairing oxidant-damaged catalase. J. Biol. Chem. 2011, 286, 19159–19169. [Google Scholar] [CrossRef] [PubMed]
  59. Pang, Y.Y.; Schwartz, J.; Bloomberg, S.; Boyd, J.M.; ·Horswill, A.R.; Nauseef, W.M. Methionine sulfoxide reductases protect against oxidative stress in Staphylococcus aureus encountering exogenous oxidants and human neutrophils. J. Innate Immun. 2014, 6, 353–364. [Google Scholar] [CrossRef] [PubMed]
  60. Hassouni, M.E.; Chambost, J.P.; Expert, D.; Gijsegem, F.V.; Barras, F. The minimal gene set member MSRA, encoding peptide methionine sulfoxide reductase, is a virulence determinant of the plant pathogen Erwinia chrysanthemi. Proc. Natl. Acad. Sci. USA 1999, 96, 887–892. [Google Scholar] [CrossRef] [PubMed]
  61. Vanhove, A.S.; Hang, S.; Vijayakumar, V.; Wong, A.C.; Asara, J.M.; Watnick, P.I. Vibrio cholerae ensures function of host proteins required for virulence through consumption of luminal methionine sulfoxide. PLoS Pathog. 2017, 13, e1006428. [Google Scholar] [CrossRef] [PubMed]
  62. Denkel, L.A.; Horst, S.A.; Rouf, S.F.; Kitowski, V.; Böhm, O.M.; Rhen, M.; Jäger, T.; Bange, F.-C. Methionine sulfoxide reductases are essential for virulence of Salmonella typhimurium. PLoS ONE 2011, 6, e26974. [Google Scholar] [CrossRef] [PubMed]
  63. Sarkhel, R.; Rajan, P.; Gupta, A.K.; Kumawat, M.; Agarwal, P.; Shome, A.; Puii, L.; Mahawar, M. Methionine sulfoxide reductase A of Salmonella Typhimurium interacts with several proteins and abets in its colonization in the chicken. Biochim. Biophys. Acta 2017, 1861, 3238–3245. [Google Scholar] [CrossRef] [PubMed]
  64. Douglas, T.; Daniel, D.S.; Parida, B.K.; Jagannath, C.; Dhandayuthapani, S. Methionine sulfoxide reductase A (MSRA) deficiency affects the survival of Mycobacterium smegmatis within macrophages. J. Bacteriol. 2004, 186, 3590–3598. [Google Scholar] [CrossRef] [PubMed]
  65. Dhandayuthapani, S.; Blaylock, M.W.; Bebear, C.M.; Rasmussen, W.G.; Baseman, J.B. Peptide methionine sulfoxide reductase (MSRA) is a virulence determinant in Mycoplasma genitalium. J. Bacteriol. 2001, 183, 5645–5650. [Google Scholar] [CrossRef] [PubMed]
  66. Das, K.; la Garza, G.D.; Maffi, S.; Saikolappan, S.; Dhandayuthapani, S. Methionine sulfoxide reductase A (MSRA) deficient Mycoplasma genitalium shows decreased interactions with host cells. PLoS ONE 2012, 7, e36247. [Google Scholar] [CrossRef] [PubMed]
  67. Giomarelli, B.; Visai, L.; Hijazi, K.; Rindi, S.; Ponzio, M.; Iannelli, F.; Speziale, P.; Pozzi, G. Binding of Streptococcus gordonii to extracellular matrix proteins. FEMS Microbiol. Lett. 2006, 265, 172–177. [Google Scholar] [CrossRef] [PubMed]
  68. Saha, S.S.; Hashino, M.; Suzuki, J.; Uda, A.; Watanabe, K.; Shimizu, T.; Watarai, M. Contribution of methionine sulfoxide reductase B (MSRB) to Francisella tularensis infection in mice. FEMS Microbiol. Lett. 2017, 364, fnw260. [Google Scholar] [CrossRef] [PubMed]
  69. Walter, J.; Chagnaud, P.; Tannock, G.W.; Loach, D.M.; Bello, F.D.; Jenkinson, H.F.; Hammes, W.P.; Hertel, C. A high-molecular-mass surface protein (Lsp) and methionine sulfoxide reductase B (MSRB) contribute to the ecological performance of Lactobacillus reuteri in the murine gut. Appl. Environ. Microbiol. 2005, 71, 979–986. [Google Scholar] [CrossRef] [PubMed]
  70. Sansom, F.M.; Tang, L.; Ralton, J.E.; Saunders, E.C.; Naderer, T.; McConville, M.J. Leishmania major methionine sulfoxide reductase A is required for resistance to oxidative stress and efficient replication in macrophages. PLoS ONE 2013, 8, e56064. [Google Scholar] [CrossRef] [PubMed]
  71. Skaar, E.P.; Tobiason, D.M.; Quick, J.; Judd, R.C.; Weissbach, H.; Etienne, F.; Brot, N.; Seifert, H.S. The outer membrane localization of the Neisseria gonorrhoeae MSRA/B is involved in survival against reactive oxygen species. Proc. Natl. Acad. Sci. USA 2002, 99, 10108–10113. [Google Scholar] [CrossRef] [PubMed]
  72. Wu, H.; Soler-Garcia, A.A.; Jerse, A.E. A strain-specific catalase mutation and mutation of the metal-binding transporter gene mntC attenuate Neisseria gonorrhoeae in vivo but not by increasing susceptibility to oxidative killing by phagocytes. Infect. Immun. 2009, 77, 1091–1102. [Google Scholar] [CrossRef] [PubMed]
  73. Mintz, K.P.; Moskovitz, J.; Wu, H.; Fives-Taylor, P.M. Peptide methionine sulfoxide reductase (MSRA) is not a major virulence determinant for the oral pathogen Actinobacillus actinomycetemcomitans. Microbiology 2002, 148, 3695–3703. [Google Scholar] [CrossRef] [PubMed]

Share and Cite

MDPI and ACS Style

Singh, V.K.; Singh, K.; Baum, K. The Role of Methionine Sulfoxide Reductases in Oxidative Stress Tolerance and Virulence of Staphylococcus aureus and Other Bacteria. Antioxidants 2018, 7, 128. https://doi.org/10.3390/antiox7100128

AMA Style

Singh VK, Singh K, Baum K. The Role of Methionine Sulfoxide Reductases in Oxidative Stress Tolerance and Virulence of Staphylococcus aureus and Other Bacteria. Antioxidants. 2018; 7(10):128. https://doi.org/10.3390/antiox7100128

Chicago/Turabian Style

Singh, Vineet K., Kuldeep Singh, and Kyle Baum. 2018. "The Role of Methionine Sulfoxide Reductases in Oxidative Stress Tolerance and Virulence of Staphylococcus aureus and Other Bacteria" Antioxidants 7, no. 10: 128. https://doi.org/10.3390/antiox7100128

APA Style

Singh, V. K., Singh, K., & Baum, K. (2018). The Role of Methionine Sulfoxide Reductases in Oxidative Stress Tolerance and Virulence of Staphylococcus aureus and Other Bacteria. Antioxidants, 7(10), 128. https://doi.org/10.3390/antiox7100128

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop