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The Staphylococcus aureus RNome and Its Commitment to Virulence

  • Brice Felden mail,

    brice.felden@univ-rennes1.fr

    Affiliation: Université de Rennes, Inserm U835, UPRES EA2311, Biochimie Pharmaceutique, Rennes, France

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  • François Vandenesch,

    Affiliation: Inserm U851, Université de Lyon, Centre National de Référence des Staphylocoques, Lyon, France

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  • Philippe Bouloc,

    Affiliation: Laboratoire Signalisation et Réseaux de Régulations Bactériens, Institut de Génétique et Microbiologie, CNRS, UMR 8621, IFR115, Centre Scientifique d'Orsay, Université Paris Sud 11, Orsay, France

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  • Pascale Romby

    Affiliation: Architecture et Réactivité de l'ARN, Université de Strasbourg, CNRS, IBMC, Strasbourg, France

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  • Published: March 10, 2011
  • DOI: 10.1371/journal.ppat.1002006

Abstract

Staphylococcus aureus is a major human pathogen causing a wide spectrum of nosocomial and community-associated infections with high morbidity and mortality. S. aureus generates a large number of virulence factors whose timing and expression levels are precisely tuned by regulatory proteins and RNAs. The aptitude of bacteria to use RNAs to rapidly modify gene expression, including virulence factors in response to stress or environmental changes, and to survive in a host is an evolving concept. Here, we focus on the recently inventoried S. aureus regulatory RNAs, with emphasis on those with identified functions, two of which are directly involved in pathogenicity.

Introduction

Staphylococcus aureus belongs to the normal human flora. About one in three healthy individuals are colonized asymptomatically with S. aureus in the nostrils without any associated disease. However, S. aureus is also a leading cause of hospital- and community-acquired infections worldwide [1]. This potent Gram-positive pathogen can grow in any part of the human body, and also propagates in other animals. The severity and locations of infections vary widely, from minor skin infections to deep-seated infections such as endocarditis, bone and joint infections, or severe pneumonia. Concern about S. aureus infections is heightened because of the emergence and spread of hypervirulent, drug-resistant, and community-acquired strains [2]. The pathogenesis of S. aureus is intricate and relies on an arsenal of virulence-associated factors including toxins, adhesins, enzymes, and immune-modulators [3]. These proteins are delivered in a coordinated manner by sophisticated regulatory networks. To this end, multiple trans-acting modulators, including regulatory proteins, secondary metabolites, small peptides, and RNAs, are brought into play [4], [5].

The universality of small, usually non-coding, RNAs (sRNAs) playing a role in gene regulation in bacteria is now well established [6], [7]. The number of sRNA identified in bacteria has considerably increased this past decade [8]. Most of them exert regulatory functions by interacting with proteins and by pairing with mRNAs. Besides these trans-acting sRNAs, a variety of large mRNA leaders sense environmental cues or intracellular concentrations of small metabolites to adopt structures that prevent/activate their extended transcription or translation. Examples of sRNA-dependent regulations are given in Figure 1. Recent studies on various bacteria indicated that pervasive transcription generates massive antisense transcription [9][11]. All these sRNAs are members of regulatory circuits involved in metabolism, stress adaptation, and virulence. Although still a recent field, the study of sRNAs has already extended our knowledge of regulatory circuits in bacteria, in relation to pathogenesis. In S. aureus, the multifunctional regulatory RNA, called RNAIII, is a paradigm for RNA-mediated regulation of virulence genes [12], [13]. It is the effector of the accessory gene regulator (agr) system [4], which controls the switch between the expression of surface proteins and excreted toxins. Within the last few years, several reports highlighted the importance and diversity of staphylococcal sRNAs [14][18]. This review focuses on S. aureus regulatory RNAs including RNAIII, newly discovered island-encoded sRNAs, cis-encoded antisense RNAs (asRNA), and cis-acting regulatory regions of mRNAs. For all these RNAs, their structural diversity and phylogenetic distribution is documented and discussed, with emphasis on those for which their targets were identified and regulatory mechanisms elucidated. Some of these sRNAs have been demonstrated as tractable targets for compounds inhibiting S. aureus pathogenesis.

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Figure 1. General mechanisms given for several S. aureus regulatory RNAs.

(A) S-adenosyl methionine (SAM) riboswitch regulates several operons encoding enzymes and transporter proteins. SAM binds to an aptamer domain and stabilizes the formation of a terminator hairpin (the alternate pairings are in red) to arrest transcription [75]. (B) Schematic representation of a T-Box involved in the regulation of aminoacyl-tRNA synthetases (aaRS). Non aminoacylated tRNA binds to the leader region at two different sites: the anticodon sequence of the tRNA base paired with a codon-like triplet present in the “specifier loop”, and the ACCA end of the tRNA binds to a complementary sequence located in the T-Box motif [82]. This interaction stabilizes an anti-terminator structure allowing transcription of the downstream genes. *The aminoacyl-tRNA synthetases regulated by this mechanism are the ValRS, MetRS, IleRS, PheRS, GlyRS, SerRS, HisRS, and the AspRS. (C) The SprD pathogenicity island RNA (in red) binds to the ribosome binding site (The SD is green) of sbi mRNA to repress translation initiation [37]. (D) The RsaOX (in red) (or Teg14as) cis-acting asRNA [17], [18] is complementary to the coding sequence of tnp mRNA and is predicted to induce rapid degradation of tnp mRNA. Both the asRNA and the mRNA target site are highly folded, suggesting that the pairing is initiated by a loop–loop interaction.

doi:10.1371/journal.ppat.1002006.g001

Diversity of sRNAs Expressed from the S. aureus Genome

The complex structure of RNAIII, the first sRNA reported in S. aureus, and the intriguing pleiotropic phenotypes associated with its inactivation, led to the proposal and subsequent demonstration that RNAIII was a regulatory RNA [12] (cf. below). In 2001, with the exception of tmRNA, the sRNAs were ignored from the analysis of the first staphylococcal genome sequences [19]. As sRNAs initially emerged as major regulators for bacterial physiology in Escherichia coli, several laboratories engaged in a quest to identify sRNAs in various S. aureus strains. In 2005, Pichon and Felden demonstrated for the first time the existence of sRNAs produced by horizontally acquired genomic islands by identifying seven sRNAs encoded on pathogenicity islands (PIs) in S. aureus [14]. Recently, several publications on this bacterium have contributed to an impressive catalog of putative and experimentally validated sRNAs that place S. aureus as a new model organism for sRNA studies. Approaches for identifications were based on dedicated computing software [14], [15], [20], Affymetrix microarrays [21], [22], conventional cloning/sequencing of small sized cDNAs [16], and 454 [17] and Illumina [18] high throughput sequencing (HTS). The sRNA genes are located randomly in the core genome and mobile accessory elements, and some of them are present in multiple copies. Besides the housekeeping RNAs (such as 4.5S, RNase P, and tmRNA), 6S RNA, and cis-acting regulatory sequences, conservation of most sRNAs is restricted to the genus Staphylococcus, and among them, about 50% are found so far only within the S. aureus species. Approximately 100 trans-encoded sRNAs, 100 cis-encoded asRNAs, and more than 30 cis-acting regulatory regions of mRNAs (e.g., riboswitch, T-Box, protein-binding motif) were discovered to be encoded on the S. aureus chromosome, and nine sRNAs on the pN315 plasmid. The expression of more than 90 of these was confirmed by alternative methods such as northern blots, RNA extremity mapping, or RT-qPCR (Table S1). The HTS study performed by Beaume et al. [18] confirmed almost all sRNAs from other studies [14], [15], [17], [20], with the exception of 12 sRNAs that were reported solely by Abu-Qatouseh et al. [16]. This singularity might reflect the distance between the unsequenced clinical isolates and the S. aureus strains in which sRNAs are mainly studied. This observation may suggest that the sRNA profile is a signature of a given strain; if in the case of N315 we are approaching a full inventory, it is not the case for the other S. aureus strains.

Numerous cis-Encoded Antisense RNAs (asRNAs)

These RNAs pair with an extended perfect match to RNAs expressed from their complementary gene strand (Figure 1D). The first one identified in S. aureus was shown to control the rolling-circle replication of plasmid pT181 by transcriptional attenuation [23]; the striking discovery of the recent studies is the large proportion of asRNAs among the inventoried sRNAs [14], [16][18]. Many asRNAs are expressed from PIs and mobile elements (plasmids or transposons). Transposable genetic elements are important motors of genetic variability but can also compromise genome integrity. Hence, transposition would expectedly be tightly regulated. The control of transposase synthesis occurs through different mechanisms, one being by asRNAs [24]. Among them, RsaOX is complementary to the coding sequence of SA0062 mRNA encoding a transposase [17] (Figure 1D). Another interesting case is the control of the IS1181 transposase, which has its gene repeated eight times in the S. aureus N315 genome. Two small RNAs, Teg17/RsaOW and Teg24as complementary to the 5′ and 3′ IS1181 UTRs, respectively, were detected. The expression of Teg17/RsaOW is constitutive during growth [17], and is strongly enhanced in response to pH and temperature changes [18]. Interestingly, these asRNAs (Figures 1D and 2) show predicted structural similarity to the E. coli “RNA-OUT” asRNA, which regulates tnp translation of the IS10 insertion element, suggesting that these asRNAs have been tuned for fast binding to mRNAs [25][27]. Some of these asRNAs are surprisingly long; for example, one of them, which is complementary to SA0620 encoding a secretory antigen, SsaA-like, exceeds 1 kb [18]. AsRNAs may participate in the differential expression of genes belonging to the same operon; this could be the case for two asRNAs that are complementary to capF and capM mRNA regions of the large cap operon mRNA encoding enzyme for capsular polysaccharide synthesis [16], [18]. Several overlapping 3′UTRs of convergent mRNAs were also detected in staphylococci, in which the 3′UTR of one mRNA overlaps the mRNA on the opposite strand, and convergent genes share the same terminator hairpin. Since they pair between each other with extended perfect matches, these 3′UTRs could be categorized as asRNAs. sRNAs that likely issue from the processing of extended 3′ UTRs were also found. How these overlapping and processed UTRs affect gene expression is unknown [18].

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Figure 2. Secondary structures of selected S. aureus sRNAs.

The secondary structures of RsaA and RsaE [15] and of SprD [37] were experimentally determined. The secondary structure of the antisense RNA RsaOX (or Teg14as) is proposed based on computer predictions [17], [18]. The genomic locations and flanking genes of the sRNAs are indicated. The known regulatory domains of the sRNA, which bind to mRNA targets, are in red. The black circled nucleotides are accessible C-rich motifs that are proposed to be crucial for the initial binding with mRNA [15].

doi:10.1371/journal.ppat.1002006.g002

A Global sRNA Expression Variation Associated with a Phenotype

Small colony variant (SCV) isolates exhibit particular properties such as host intracellular persistence and the ability to cause antibiotic-refractory, latent, or recurrent infections [28]. Several asRNAs and sRNAs showed differential expression in the SCV compared to a wild type strain [16]. In addition, SCVs does not express RNAIII [16], [29]. SCVs also repressed an asRNA that presumably regulates expression of PhoB, an alkaline phosphatase involved in inorganic ion transport [16]. These variations of regulatory RNA expression may correlate with electron transport deficiencies associated with SCVs [28]. Hence, perturbation of genetic regulatory circuits and their associated effects on virulence may be a consequence of and/or contribute to the SCV phenotype.

RNome-Related S. aureus Specificities

S. aureus has a small genome (2.8 M bp) with a low GC composition (32.8%); these features affect its RNome and it is likely that the features of sRNA as learned from studies in enteric bacteria will differ in S. aureus. Specifically, in E. coli and many other bacteria, RNase E is implicated in the sRNA-dependent mRNA turnover, and the RNA chaperone Hfq is required for the activity of most trans-encoded sRNAs and, as shown recently, for a cis-encoded asRNA [27]. However, S. aureus do not have an RNase E, but instead possesses RNases J1, J2, and Y functional homologs [30]. In Bacillus subtilis, a complex resembling the E. coli degradosome, including the three RNases J1/J2/Y, glycolytic enzymes (enolase, phosphofructokinase PfkA) and the RNA helicase CshA were recently reported [31][33]. Homologs of all these enzymes are present in the staphylococcal strains, but whether these enzymes form a “degradosome” remains to be addressed [30]. Concerning Hfq, this protein is not expressed in several tested S. aureus strains [34], [35], and the deletion of its corresponding gene was thought to have no effect on bacterial physiology [36]. However, a recent report indicates that in strains where Hfq is detected, the deletion of its coding gene could result in decreased toxicity and virulence of S. aureus, leading to the conclusion that Hfq is a global regulator that controls pathogenicity [35]. In these strains, analyzing more precisely the regulatory functions of Hfq as well as its involvement on the characterized sRNA-dependent regulations would be required. The commitment of Hfq is not straightforward since several strains in which Hfq is not detected produce toxins and are virulent. Moreover, Hfq is not required for the reported cases of sRNA-induced translational repression [13], [15], [34], [37]; in several of these examples, the sRNAs efficiently bind to the mRNA targets and form extended pairings that are specifically cleaved by the double-strand-specific RNase III [13], [38], [39]. The dispensability of Hfq in several S. aureus strains could be due, as compared to E. coli, to the presence of longer “sRNA–mRNA” hybrids that compensate for low GC content of the pairings [40].

General strategies for the use of RNA-dependent regulation by bacteria vary according to species as the result of environmental and evolutionary constraints. For instance, in B. subtilis and S. aureus, the autocatalytic site-specific cleavage in the 5′ UTR of glmS mRNA, encoding glucosamine 6 phosphate synthase, is stimulated by the binding of glucosamine-6-phosphate; in E. coli and Salmonella the glmS gene is regulated by two sRNAs [41][43]. Mechanistic and functional analyses performed on several S. aureus sRNAs revealed its RNome specificity by pointing out its differential roles in the regulation of mobile elements, metabolism, stress adaptation, and virulence.

Pathogenicity Island–Encoded RNAs

Mobile genetic elements have essential roles in genome evolution. In facultative pathogens such as S. aureus, they mediate acquisition of antibiotic resistance genes, including the highly problematic methicillin resistance via the staphylococcal chromosome mec cassette (SCCmec), and have conferred a wide range of adaptive processes for survival in their hosts. Among these elements, which include phages, genomic islands, transposons, and plasmids, the horizontally acquired PIs are the repository of many toxins, adherence and invasion factors, superantigens, and secretion systems [44], [45]. In addition to the protein-coding genes, several SaPIs including phage-related chromosomal islands encode and express several sRNAs [14], [16][18] (Table 1). Some sRNAs are present in multiple copies scattered around the S. aureus genome (up to eight genomic copies; repeated events of horizontal transfer as well as gene duplications may account for the presence of multiple copies), and additional copies are on plasmids [14]. The location of sRNAs on SaPIs suggests that these sRNAs would play important roles during S. aureus infections.

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Table 1. RNAs expressed from N315 S. aureus PIs.

doi:10.1371/journal.ppat.1002006.t001

Although the sRNAs expressed from SaPIs are expected to regulate expression of genes located on the cognate PI, they could also establish functional links between the PIs and the core genome. An example is provided by the SprD RNA, expressed from PIφ (Table 1), which represses translation initiation of the sbi mRNA encoding an immune-evasion molecule located at a core genomic locus distant from SprD [37]. A central hairpin from SprD pairs to the sbi mRNA ribosome binding sites and prevents translation initiation (Figures 1C and 2). Interestingly, SprD contributes significantly to causing disease in a mouse infection model, although this effect is not only linked to the down-regulation of Sbi production. Moreover, overproducing SprD in vivo is toxic for the cells and reduces bacterial growth (S. Chabelskaya, N. Sayed, and B. Felden, unpublished data), possibly suggesting that SprD targets essential function(s). Since SprD has a significant impact on virulence, it implies possible strategies in controlling staphylococcal infections by modulating SprD expression levels. Additional sRNAs expressed from the PIs might also be involved in S. aureus pathogenicity, either directly or via intricate regulatory networks including transcriptional regulatory factors.

Among the currently characterized asRNAs expressed in S. aureus, four are located in PIs and six in the SCCmec mobile genetic element, all ranging in sizes from 54 to 400 nucleotides [18]. Most of them have perfect base complementarities with regions of mRNAs encoding hypothetical protein genes, and are likely to act as regulators. Two of these sRNAs, Teg152 and SprF, are fully complementary to SprA1 and SprG sRNAs, respectively (Table 1): the “SprA1/Teg152” and “SprG/SprF” RNA pairs are predicted to form type I “toxin-antitoxin” modules in which SprA and SprG would encode hydrophobic small peptides [46]. These modules are found in multiple copies in several S. aureus strains, and several copies are expressed (A. Jousselin, M. L. Pinel, and B. Felden, unpublished data). The independent transcriptional activation of the copies allows the production of accurate sRNA levels for precise functions. SprA1 is a multifunctional RNA with putative antisense properties since its 3-end can pair with the 3′-UTRs of three mRNA targets [14]. Interestingly, SCCmec carries determinants other than antibiotic resistance genes, which confer selective advantages to methicillin-resistant S. aureus (MRSA) in the host. An sRNA carrying a small ORF was recently identified within the SCCmec. This ORF encodes a peptide that has pro-inflammatory and cytolytic characteristics typical of phenol-soluble modulins (PSM). The PSM-mec peptide had significant impact on immune evasion and disease, thus revealing a role of methicillin resistance clusters in staphylococcal pathogenesis [47]. The expression of the PSM-sRNA (Teg4) was strongly enhanced in response to oxidative stress [18].

A Multifunctional RNA Couples Quorum Sensing to Virulence

RNAIII is the effector of the agr system, which functions as a sensor of population density. The complex cascade of events orchestrated by agr has been extensively studied (see [4], [12] for review). Briefly, it comprises a density-sensing cassette (agrD and agrB) and a two-component sensory transduction system (agrA and agrC) in which autoinducing peptide (AIP), the agrD gene product, is continuously released in the extracellular environment. Upon reaching a critical concentration, AIP activates the two-component agrA-agrC system, which triggers transcription of RNAIII, of its own operon, and of genes encoding metabolic factors and PSM peptides [12], [48]. In this cascade, expression of RNAIII is maximal in the late logarithmic and stationary phase of growth. RNAIII has the unique property of acting both as an mRNA that encodes the 26-aa delta hemolysin (PSM) peptide, and as a critical regulator that represses early virulence factors and activates post-exponentially expressed exotoxins (Figure 3). Further genetic, transcriptomic, and proteomic studies revealed that agr belongs to a rich and complex network of regulatory genes in which agr is both a target and an effector of regulation (reviewed in [4]). As an effector, RNAIII governs not only the expression of key virulence factors including cell wall–associated proteins and exotoxins, but also numerous two-component systems and global regulators (arl, sae, srr, rot) and an impressive list of other processes impacting biofilm formation, peptidoglycan and amino acid metabolism, and transport pathways [49][51]. These effects are quantitatively but not qualitatively variable depending on the staphylococcal strain. For instance, the effect of agr inactivation was more marked on the transcriptome of NCTC 8325 derivatives as compared to the UAMS-1 strain [50]. The question as to whether these effects result from direct or indirect mechanisms has been only solved for a limited number of genes and benefited from the experimental determination of RNAIII structure [52]. RNAIII, a highly stable molecule (half-life >45 min) [38] is characterized by 14 stem-loop structures and two long helices formed by long-range base pairings that close off independent structural domains [52]. Specific domains of RNAIII control the expression of different targets (Figure 3). The 5′ end of RNAIII positively regulates hla translation (encoding alpha hemolysin) by competing directly with an intramolecular RNA secondary structure that sequesters the hla ribosomal binding site (RBS) ([53], [54]; Figure 3A). The RNAIII hairpin H13 and terminator hairpin H14 of the 3′ domain, and hairpin H7 of the central domain, act separately or coordinately to repress the synthesis of early expressed virulence factors (i.e., coagulase, protein A, and the repressor of toxins, Rot) at the post-transcriptional level by a conserved mechanism with slight variations (Figure 3C). The common theme is that RNAIII functions as an asRNA that anneals to target mRNAs, and the formed complexes result in the repression of translation initiation and in rapid mRNA degradation triggered by RNase III. Structures of the complexes depend on the target mRNA, and may comprise i) an extended duplex between RNAIII and the RBS of mRNAs (e.g., spa, the peptidoglycan hydrolase LytM, and SA1000 encoding a fibrinogen-binding protein), or ii) an imperfect duplex that sequesters the RBS completed by a loop–loop interaction in the coding region (for coa encoding coagulase), or two loop–loop interactions, one involving the 5′UTR and the other the RBS (for rot mRNA) ([13], [39]; Figure 3). In these three cases, a single loop–loop interaction is not sufficient for efficient repression, thus limiting the capacity of RNAIII to act as a repressor to the mRNA targets that not only possess a Shine and Dalgarno (SD) sequence complementary to H7, H13, or H14 of RNAIII, but that also display an additional region of interaction or the capacity to form an extended duplex. As discussed above, the RNA-binding protein Hfq, which is an important RNA chaperone in several species [55], is not involved in the RNAIII-dependent regulatory processes, although Hfq binds to RNAIII in vitro [38].

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Figure 3. The functional RNAIII structure and its mRNA targets.

(A) Schematic view of the RNAIII-mediated antisense activation mechanism. Hairpin loops H2 and H3 of RNAIII (red) bind to the hla mRNA (black) to activate translation initiation. The ribosomal 30S subunit is schematized. The SD sequence is green. (B) RNAIII secondary structure (adapted from [52]) and its genomic location within the agr locus (bottom). RNAIII encodes the delta-hemolysin (hld, in green). The 5′UTR activates alpha-hemolysin translation [54] and the 3′ domain represses the translation of virulence factors and of the transcriptional repressor of toxins (rot) [13], [34]. The conserved C-rich sequences detected in H7, H13, and H14 is indicated. (C) Schematic views of the RNAIII-mediated antisense translation initiation repression mechanisms. RNAIII structural domains H7, H13, and H14 (in red) are involved in interactions with target mRNAs (in black). The AUG codon and SD sequence are in green. The broken black arrows are the RNase III–induced cleavages.

doi:10.1371/journal.ppat.1002006.g003

With the exception of hla translational activation, all the direct effects of RNAIII lead to repression of mRNA targets. However, as Rot is a transcriptional regulatory protein, its repression by RNAIII results in the indirect transcriptional regulation of many genes, including activation of alpha-toxin and repression of protein A, both of which are also directly regulated by RNAIII [56]. These complex regulatory circuits involve several feed-forward loops (Figure 4) that regulate expression via RNAIII and Rot at both the transcriptional and post-transcriptional levels. For repression, these double controls prevent leakage at the transcriptional level, which could be particularly suitable for stable mRNAs like spa. Therefore, the involvement of RNAIII in such regulatory circuits not only guarantees tight regulation but also might ensure fast recovery after the external stimulus (quorum sensing) is over [57]. Hence, a number of genes—and the list will likely grow—are regulated by RNAIII at multiple levels (indirectly on promoter activity, directly on translation and mRNA degradation), suggesting that the amount and timing of production of certain virulence factors is precisely controlled during the course of infection. The in vivo requirement for such strict regulation of virulence protein expression is particularly plausible in the case of the protein A, which harbors multiple functions from anti-opsonic activity to the induction of tumor necrosis factor receptor 1 and B cell superantigenic properties [58], [59].

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Figure 4. Integrating the S. aureus sRNAs into gene regulation cascades.

The “agr-RNAIII” auto-activation circuit is indicated with the two feed-forward loops involving RNAIII. When reaching optimal density, the autoinducing peptide (AIP) activates the agr autocatalytic circuit, leading to RNAIII transcription. RNAIII represses the expression of rot, which activates spa transcription and represses that of hla. In the meantime, RNAIII also activates hla mRNA translation and represses spa mRNA translation. The plain and broken lines indicate the direct or indirect gene activations, respectively. The red lines indicate the down-regulations mediated by the various RNAs. The black question marks above the “see-sawing” triangles point to the unknown triggering factors. The transcriptional regulatory proteins are in blue. The complexity of this scheme will certainly increase as we learn more on the sRNA functions.

doi:10.1371/journal.ppat.1002006.g004

The importance of agr for S. aureus pathogenesis is the subject of an apparent paradox. In contrast with most other staphylococcal sRNAs, which have been found by bioinformatic approaches or deep sequencing, RNAIII was first identified in a transposon mutagenesis that revealed pleiotropic effects of a single-site insertion [60], [61]. Because of its impact on virulence factors, the agr system and its effector molecule RNAIII were thought to be of major importance for virulence. Indeed, the majorities of clinical isolates from acute infections have a functional agr system and produce RNAIII both in vitro and in vivo [62]. However, agr-defective mutant strains, which arose during infection, were isolated from patients [62]. Some of these strains have been associated with persistent bacteremia, notably in patients with intravascular devices and with reduced susceptibility to glycopeptides [63], [64]. Agr defects are also detected in colonizing isolates of patients, and a mixture of agr-positive and agr-defective S. aureus strains were described in healthy humans [65]. This supports the model of agr being important for full expression of virulence, notably during acute infection, whilst agr mutants would be positively selected in chronic infections and dormant states. However, the observation that RNAIII is also present in all staphylococcal species, including S. epidermidis, which is typically a nosocomial pathogen, highlights the fact that RNAIII is not solely a determinant of acute virulence but harbors various functions depending on the bacterial species background in which it evolved. Interestingly, the most conserved domain of RNAIII among staphylococcal species is the 3′ domain (H13 and H14), which is involved in the regulation of several S. aureus–specific virulence factors (see above). Its conservation in S. epidermidis, S. lugdunensis, and other species suggests that some of the target genes, such as those involved in peptidoglycan metabolism, require the presence of this regulatory domain [52], [66].

trans-Acting RNAs in Stress Response and Metabolism

Ongoing functional characterization of S. aureus sRNAs links them to various environmental and stress-related responses like pH and temperature variations, nutrient starvation, oxidative stress, and quorum sensing, all of which can be encountered during host infection [15][18], [21]. Such environmental stresses and growth conditions largely influence the toxin synthesis [67] and require several global transcriptional regulators, such as the alternative sigma B factor (σB). The σB regulon consists of numerous genes involved in metabolism, stress-related responses, membrane transport system, biofilm formation, antibiotic resistance, and virulence [68], [69]. Among these genes, several were repressed by σB via an indirect mechanism most probably involving a σB-induced regulatory protein or sRNA. Along those lines, recent studies showed that the expression of several sRNAs was induced by σB [15], [70]; among them, RsaA, which has a typical σB-promoter detected upstream of its corresponding gene [15]. RsaA, conserved among staphylococci, can potentially base pair with mRNAs repressed by σB like citM encoding an Mg-citrate transporter (Figure 2; [68]). Prediction of σB-promoter within intergenic regions of the S. aureus genome suggests the existence of additional σB-dependent sRNAs, which awaits experimental validation [15], [18]. Three σB-dependent sRNAs that are highly conserved in S. aureus have been recently described [71], and two of them are predicted to encode small highly basic peptides [18], [71].

Most of the newly identified sRNAs are conserved among S. aureus clinical isolates or are expressed in various staphylococcal strains [14], [15], [17], [18]. One exception is the sRNA RsaE for which the sequence and structure have been found strictly conserved in the Staphylococcus, Macrococcus, and Bacillus genera, all of which share a common Gram-positive ancestor (Figure 2; [15]). The overproduction of RsaE causes a growth defect that is partially alleviated by the non-preferred carbon source, acetate, suggesting that RsaE accumulation alters essential metabolic functions [17]. Using comparative transcriptomic and proteomic analysis, RsaE was shown to co-regulate the synthesis of several metabolic pathways involved in amino acid and peptide transport (opp-3 operon), cofactor synthesis, folate-dependent one-carbon metabolism, lipid and carbohydrate metabolism, and the tricarboxylic acid (TCA) cycle [15], [17]. Like RNAIII, a conserved and unpaired C-rich motif within RsaE pairs with the SD sequence of several target mRNAs, including opp-3B/opp-3A (amino acid and peptide transporter), sucC (succinyl-CoA synthetase of the TCA cycle), and SA0873 (unknown function), all preventing ribosomal initiation complex formation (Figure 2; [15], [17]). Thus, RsaE would coordinate down-regulation of energy metabolism (via the TCA cycle) and purine biosynthesis when carbon sources become scarce, facilitating adaptation to the entry into stationary phase (Figure 4). The TCA cycle is integrally involved in the regulation of virulence factor synthesis, biofilm formation and antibiotic resistance (for a review, see [67]). Other sRNAs are probably involved in metabolic regulation (Figure 4). For instance, carbohydrate-dependent repression and oxygen availability correlate with altered expression of RNAIII [67]. Although no iron-dependent sRNA was so far identified in S. aureus as in Gram-negative bacteria [65], S. aureus sense the alteration of iron status via the ferric uptake regulator (Fur), initiating a regulatory program that modifies expression of a large number of virulence factors [72]. The ongoing functional analysis of the S. aureus sRNAs will provide a clearer picture of the links between sRNAs, metabolism, stress adaptation, and virulence programming.

RNAs as Antimicrobial Drug Targets

The continued evolution of anti-microbial resistance in hospitals and the emergence of community-associated MRSA strains are major threats to patient care. Current antibiotic drugs target a narrow spectrum of bacterial functions including peptidoglycan biogenesis, DNA replication, and protein synthesis. Therefore, there is a growing need for selecting new drugs that target other cellular pathways that should, in principle, result in a weaker selective pressure for the appearance of antibiotic resistance, and that can preserve the host endogenous microbiome. As alternative strategies that affect bacterial viability, anti-virulence strategies have been developed to target mechanisms leading to successful infections, such as virulence factors causing host damage and disease [73]. Among all the antibiotics currently used to treat clinical infections, more than half bind to the ribosomal RNAs [74]. Their success as antibacterial targets encourages the development of new antibacterial drugs based on regulatory structured sRNAs. Metabolite-sensing mRNAs, the so-called riboswitches, have been recently exploited as drug targets since they have evolved structured receptors to bind small metabolites with high selectivity and to control the expression of downstream essential genes [75].

Riboswitches are located in the 5′UTRs of some mRNAs and exhibit a structured receptor domain specifically recognized by a small compound. Metabolite binding induces a conformational change of the downstream mRNA that provokes either premature transcription, translation repression, or RNA degradation. In S. aureus, seven operons and 33 genes are under the control of riboswitches that respond to the intracellular concentration of S-adenosylmethionine (SAM) (Figure 1A), thiamine pyrophosphate (TPP), flavin mononucleotide (FMN), lysine, glycine, guanine, 7-aminomethyl-7-deazaguanine (preQ1), and glucosamine-6-phosphate (Glc-6P) [15], [17], [18], [20], [75]. Any agonistic molecule targeting one of these riboswitches would likely impact gene regulation even if cells are devoid of the natural metabolite. As a proof of principle, and based on the crystal structure of the guanine receptor binding domain [76], [77], several rationally designed guanine analogues that bind the purine riboswitch with affinities comparable to that of the natural ligand were shown to inhibit B. subtilis growth [78]. In S. aureus, the guanine riboswitch regulates expression of the operon, including xpt, pbuX, guaB, and guaA. Using the same strategy as Kim et al. [78], a novel pyrimidine derivative, 2,5,6-triaminopyrimidin-4-one (PC1), was designed to bind the purine-sensing riboswitch to repress the downstream genes [79]. For the first time, this work shows that PC1 has a selective bactericidal activity restricted to a sub-group of bacteria including S. aureus, which contains guaA under the control of the purine riboswitch. Although the GMP synthase GuaA is not essential for growth in rich media, the enzyme is nevertheless an important contributor to S. aureus survival during infection [79]. The administration of PC1 significantly reduced S. aureus infection in a murine model [79]. The narrow spectrum of bactericidal activity of PC1 also has the advantage of reducing the selective pressure for resistance. This work and the fact that S. aureus contains other types of riboswitches offer novel opportunities for the design of drugs that inhibit the function of structured regulatory RNAs. The increasing rate of S. aureus sRNA discovery, together with the intensified search for their mechanisms of action, should pave the way to exploit chemical strategies to interfere with sRNA functions and to fight against bacterial infections in a more specific way.

Concluding Remarks

This review provides a first hint at sRNA functions in S. aureus and shows that we are just beginning to fully appreciate their roles in gene regulation. The combined use of high throughput genomic methods and phenotypic analyses of S. aureus strains mutated for the sRNA genes, regulatory proteins, ribonucleases, and RNA-binding proteins will generate knowledge on how the regulatory RNAs and proteins are integrated into intertwined regulatory networks in stress adaptation and virulence (Figure 4). However, complications are expected due to the substantial genetic variability between S. aureus strains, which express a subset of regulatory RNAs, or unique RNAs, and are thus far from universal [14], [15].

Future research is also necessary to identify the signals that regulate sRNA transcription and the mechanisms by which sRNAs act on their targets. To date, most identified mechanisms have involved trans-acting sRNAs that bind to the RBS of mRNA targets, and only SprA was predicted to bind to the 3′UTRs. Binding to the coding sequence has not yet been observed. While scientific interest has been mainly focused on antisense regulation, regulatory RNAs are also expected to target proteins. For instance, direct interaction of S. aureus 6S RNA with the polymerase bound to σA and its implication in virulence needs to be analyzed. Multifunctional RNAs, like RNAIII, are most probably the rule rather than the exception, and this field is at present completely unexplored. We also need to consider other unexpected possibilities such as RNA-activating virulence factors, or bacterial sRNAs targeting host genes. Recent analysis of the MRSA operon also shows that many mRNAs have long UTRs, more frequently found at the 3′ ends [80]. These regions might have implications in regulation by promoting specific binding sites for trans-acting ligands or by their processing to generate sRNAs [18]. Mechanisms of RNA processing and turnover are not well studied in S. aureus and little is known about S. aureus RNA-binding proteins associated with sRNAs.

This review illustrates the great diversity in sizes, structures, and mechanisms of sRNAs, and shows that determinants required for regulation could sometimes be predicted from the RNA structure. For instance, several sRNAs and RNAIII carry a C-rich motif, located in hairpin loops or in accessible single strands, which is a specific recognition signature to target the mRNA RBS [13], [15]. Determination of the structures of regulatory complexes has paved the way to identify novel drugs that could interfere with RNA functions [79]. Also, the significant contribution of RNAIII and SprD to cause diseases in animal models of infection implies that these RNAs could be promising drug targets.

Another aspect, which might be important for virulence and host adaptation, would be to consider the cell differentiation within a population, as well as cell-to-cell communication. The expression of individual sRNAs might be variable within a population and these differences could confer the ability of a bacterial subpopulation to respond to stress or environmental changes. This is particularly true for biofilm formation. Furthermore, we have no idea how the host “microbiome” influences sRNA expression and their regulatory networks within S. aureus, and vice versa. Metagenomics and deep sequencing could address these questions and would contribute to an understanding of how commensal bacteria can cause diseases.

The recently identified S. aureus RNome (listed in Table S1) reveals additional layers of complexity to gene regulation mechanisms. sRNA-based regulation increases the number of possible regulatory sites and expectedly provides several advantages compared to protein-based regulation [81]. Since many sRNAs act at transcription termination or when translation starts, fast and efficient responses on protein levels can be achieved. Furthermore, it is also easier to control RNA turnover when compared to protein degradation. To date, the known S. aureus regulatory RNAs provide functional links between metabolism, quorum sensing, and virulence (Figure 4). As we learn more about sRNA functions, we expect to find more sRNAs involved in S. aureus pathogenesis as well as other connections between virulence and housekeeping networks.

Supporting Information

Table S1.

Compilation of 91 expressed RNAs forming the S. aureus RNome. It includes 18 cis-acting regulators including riboswitches (green), 7 cis-encoded sRNAs (purple) 47 trans-encoded RNAs (pink), 10 repeated sequences (yellow), and 9 potential 5′UTRs, 3′UTRs, or small CDSs. Both the gene and RNA names, their experimental confirmations, strand expression, genomic locations, predicted lengths, flanking and/or antisense genes, expression profiles, and conservations are indicated for each RNA with specific comments about their functions, when available.

doi:10.1371/journal.ppat.1002006.s001

(XLS)

Acknowledgments

We are thankful to all the members of our respective labs and collaborators for their scientific and intellectual input as well as for the stimulating discussions. We are thankful to Sandy Gruss for critical reading of the manuscript and helpful comments.

References

  1. 1. Deleo FR, Otto M, Kreiswirth BN, Chambers HF (2010) Community-associated meticillin-resistant Staphylococcus aureus. Lancet 375: 1557–1568.
  2. 2. Chambers HF, Deleo FR (2009) Waves of resistance: Staphylococcus aureus in the antibiotic era. Nat Rev Microbiol 7: 629–641.
  3. 3. Plata K, Rosato AE, Wegrzyn G (2009) Staphylococcus aureus as an infectious agent: overview of biochemistry and molecular genetics of its pathogenicity. Acta Biochim Pol 56: 597–612.
  4. 4. Novick RP, Geisinger E (2008) Quorum sensing in staphylococci. Annu Rev Genet 42: 541–564.
  5. 5. Wyatt MA, Wang W, Roux CM, Beasley FC, Heinrichs DE, et al. (2010) Staphylococcus aureus nonribosomal peptide secondary metabolites regulate virulence. Science 329: 294–296.
  6. 6. Vogel J (2009) A rough guide to the non-coding RNA world of Salmonella. Mol Microbiol 71: 1–11.
  7. 7. Waters LS, Storz G (2009) Regulatory RNAs in bacteria. Cell 136: 615–628.
  8. 8. Liu JM, Camilli A (2010) A broadening world of bacterial small RNAs. Curr Opin Microbiol 13: 18–23.
  9. 9. Toledo-Arana A, Dussurget O, Nikitas G, Sesto N, Guet-Revillet H, et al. (2009) The Listeria transcriptional landscape from saprophytism to virulence. Nature 459: 950–956.
  10. 10. Sharma CM, Hoffmann S, Darfeuille F, Reignier J, Findeiss S, et al. (2010) The primary transcriptome of the major human pathogen Helicobacter pylory. Nature 464: 250–255.
  11. 11. Dornenburg JE, Devita AM, Palumbo MJ, Wade JT (2010) Widespread antisense transcription in Escherichia coli. MBio 1: e00024–10.
  12. 12. Novick RP (2003) Autoinduction and signal transduction in the regulation of staphylococcal virulence. Mol Microbiol 48: 1429–1449.
  13. 13. Boisset S, Geissmann T, Huntzinger E, Fechter P, Bendridi N, et al. (2007) Staphylococcus aureus RNAIII coordinately represses the synthesis of virulence factors and the transcription regulator Rot by an antisense mechanism. Genes Dev 21: 1353–1366.
  14. 14. Pichon C, Felden B (2005) Small RNA genes expressed from Staphylococcus aureus genomic and pathogenicity islands with specific expression among pathogenic strains. Proc Natl Acad Sci U S A 102: 14249–14254.
  15. 15. Geissmann T, Chevalier C, Cros MJ, Boisset S, Fechter P, et al. (2009) A search for small noncoding RNAs in Staphylococcus aureus reveals a conserved sequence motif for regulation. Nucleic Acids Res 37: 7239–7257.
  16. 16. Abu-Qatouseh LF, Chinni SV, Seggewiss J, Proctor RA, Brosius J, et al. (2010) Identification of differentially expressed small non-protein-coding RNAs in Staphylococcus aureus displaying both the normal and the small-colony variant phenotype. J Mol Med 88: 565–575.
  17. 17. Bohn C, Rigoulay C, Chabelskaya S, Sharma CM, Marchais A, et al. (2010) Experimental discovery of small RNAs in Staphylococcus aureus reveals a riboregulator of central metabolism. Nucleic Acids Res 38: 6620–6636.
  18. 18. Beaume M, Hernandez D, Farinelli L, Deluen C, Linder P, et al. (2010) Cartography of methicillin-resistant S. aureus transcripts: detection, orientation and temporal expression during growth phase and stress conditions. PLoS ONE 5: e10725. doi:10.1371/journal.pone.0010725.
  19. 19. Kuroda M, Ohta T, Uchiyama I, Baba T, Yuzawa H, et al. (2001) Whole genome sequencing of meticillin-resistant Staphylococcus aureus. Lancet 357: 1225–1240.
  20. 20. Marchais A, Naville M, Bohn C, Bouloc P, Gautheret D (2009) Single-pass classification of all noncoding sequences in a bacterial genome using phylogenetic profiles. Genome Res 19: 1084–1092.
  21. 21. Anderson KL, Roberts C, Disz T, Vonstein V, Hwang K, et al. (2006) Characterization of the Staphylococcus aureus heat shock, cold shock, stringent, and SOS responses and their effects on log-phase mRNA turnover. J Bacteriol 188: 6739–6756.
  22. 22. Roberts C, Anderson KL, Murphy E, Projan SJ, Mounts W, et al. (2006) Characterizing the effect of the Staphylococcus aureus virulence factor regulator, SarA, on log-phase mRNA half-lives. J Bacteriol 188: 2593–2603.
  23. 23. Novick RP, Iordanescu S, Projan SJ, Kornblum J, Edelman I (1989) pT181 plasmid replication is regulated by a countertranscript-driven transcriptional attenuator. Cell 59: 395–404.
  24. 24. Nagy Z, Chandler M (2004) Regulation of transposition in bacteria. Res Microbiol 155: 387–398.
  25. 25. Wagner EG, Altuvia S, Romby P (2002) Antisense RNAs in bacteria and their genetic elements. Adv Genet 46: 361–398.
  26. 26. Case CC, Simons EL, Simons RW (1990) The IS10 transposase mRNA is destabilized during antisense RNA control. EMBO J 9: 1259–1266.
  27. 27. Ross JA, Wardle SJ, Haniford DB (2010) Tn10/IS10 transposition is downregulated at the level of transposase expression by the RNA-binding protein Hfq. Mol Microbiol 78: 607–621.
  28. 28. Proctor RA, von Eiff C, Kahl BC, Becker K, McNamara P, et al. (2006) Small colony variants: a pathogenic form of bacteria that facilitates persistent and recurrent infections. Nat Rev Microbiol 4: 295–305.
  29. 29. Kahl BC, Belling G, Becker P, Chatterjee I, Wardecki K, et al. (2005) Thymidine-dependent Staphylococcus aureus small-colony variants are associated with extensive alterations in regulator and virulence gene expression profiles. Infect Immun 73: 4119–4126.
  30. 30. Anderson KL, Dunman PM (2009) Messenger RNA turnover processes in Escherichia coli, Bacillus subtilis, and emerging studies in Staphylococcus aureus. Int J Microbiol 2009: 525491.
  31. 31. Commichau FM, Rothe FM, Herzberg C, Wagner E, Hellwig D, et al. (2009) Novel activities of glycolytic enzymes in Bacillus subtilis: interactions with essential proteins involved in mRNA processing. Mol Cell Proteomics 8: 1350–1360.
  32. 32. Lehnik-Habrink M, Pfortner H, Rempeters L, Pietack N, Herzberg C, et al. (2010) The RNA degradosome in Bacillus subtilis: identification of CshA as the major RNA helicase in the multiprotein complex. Mol Microbiol 77: 958–971.
  33. 33. Shahbabian K, Jamalli A, Zig L, Putzer H (2009) RNase Y, a novel endoribonuclease, initiates riboswitch turnover in Bacillus subtilis. EMBO J 28: 3523–3533.
  34. 34. Geisinger E, Adhikari RP, Jin R, Ross HF, Novick RP (2006) Inhibition of rot translation by RNAIII, a key feature of agr function. Mol Microbiol 61: 1038–1048.
  35. 35. Liu Y, Wu N, Dong J, Gao Y, Zhang X, et al. (2010) Hfq is a global regulator that controls the pathogenicity of Staphylococcus aureus. PLoS ONE 5: e13069. doi:10.1371/journal.pone.0013069.
  36. 36. Bohn C, Rigoulay C, Bouloc P (2007) No detectable effect of RNA-binding protein Hfq absence in Staphylococcus aureus. BMC Microbiol 7: 10.
  37. 37. Chabelskaya S, Gaillot O, Felden B (2010) A Staphylococcus aureus small RNA is required for bacterial virulence and regulates the expression of an immune-evasion molecule. PLoS Pathog 6: e1000927. doi:10.1371/journal.ppat.1000927.
  38. 38. Huntzinger E, Boisset S, Saveanu C, Benito Y, Geissmann T, et al. (2005) Staphylococcus aureus RNAIII and the endoribonuclease III coordinately regulate spa gene expression. EMBO J 24: 824–835.
  39. 39. Chevalier C, Boisset S, Romilly C, Masquida B, Fechter P, et al. (2010) Staphylococcus aureus RNAIII binds to two distant regions of coa mRNA to arrest translation and promote mRNA degradation. PLoS Pathog 6: e1000809. doi:10.1371/journal.ppat.1000809.
  40. 40. Jousselin A, Metzinger L, Felden B (2009) On the facultative requirement of the bacterial RNA chaperone, Hfq. Trends Microbiol 17: 399–405.
  41. 41. Winkler WC, Nahvi A, Roth A, Collins JA, Breaker RR (2004) Control of gene expression by a natural metabolite-responsive ribozyme. Nature 428: 281–286.
  42. 42. Kalamorz F, Reichenbach B, Marz W, Rak B, Gorke B (2007) Feedback control of glucosamine-6-phosphate synthase GlmS expression depends on the small RNA GlmZ and involves the novel protein YhbJ in Escherichia coli. Mol Microbiol 65: 1518–1533.
  43. 43. Urban JH, Vogel J (2008) Two seemingly homologous noncoding RNAs act hierarchically to activate glmS mRNA translation. PLoS Biol 6: e64. doi:10.1371/journal.pbio.0060064.
  44. 44. Novick RP, Christie GE, Penades JR (2010) The phage-related chromosomal islands of Gram-positive bacteria. Nat Rev Microbiol 8: 541–551.
  45. 45. Novick RP, Subedi A (2007) The SaPIs: mobile pathogenicity islands of Staphylococcus. Chem Immunol Allergy 93: 42–57.
  46. 46. Fozo EM, Makarova KS, Shabalina SA, Yutin N, Koonin EV, et al. (2010) Abundance of type I toxin-antitoxin systems in bacteria: searches for new candidates and discovery of novel families. Nucleic Acids Res 38: 3743–3759.
  47. 47. Queck SY, Khan BA, Wang R, Bach TH, Kretschmer D, et al. (2009) Mobile genetic element-encoded cytolysin connects virulence to methicillin resistance in MRSA. PLoS Pathog 5: e1000533. doi:10.1371/journal.ppat.1000533.
  48. 48. Queck SY, Jameson-Lee M, Villaruz AE, Bach TH, Khan BA, et al. (2008) RNAIII-independent target gene control by the agr quorum-sensing system: insight into the evolution of virulence regulation in Staphylococcus aureus. Mol Cell 32: 150–158.
  49. 49. Dunman PM, Murphy E, Haney S, Palacios D, Tucker-Kellogg G, et al. (2001) Transcription profiling-based identification of Staphylococcus aureus genes regulated by the agr and/or sarA loci. J Bacteriol 183: 7341–7353.
  50. 50. Cassat J, Dunman PM, Murphy E, Projan SJ, Beenken KE, et al. (2006) Transcriptional profiling of a Staphylococcus aureus clinical isolate and its isogenic agr and sarA mutants reveals global differences in comparison to the laboratory strain RN6390. Microbiology 152: 3075–3090.
  51. 51. Jones RC, Deck J, Edmondson RD, Hart ME (2008) Relative quantitative comparisons of the extracellular protein profiles of Staphylococcus aureus UAMS-1 and its sarA, agr, and sarA agr regulatory mutants using one-dimensional polyacrylamide gel electrophoresis and nanocapillary liquid chromatography coupled with tandem mass spectrometry. J Bacteriol 190: 5265–5278.
  52. 52. Benito Y, Kolb FA, Romby P, Lina G, Etienne J, et al. (2000) Probing the structure of RNAIII, the Staphylococcus aureus agr regulatory RNA, and identification of the RNA domain involved in repression of protein A expression. RNA 6: 668–679.
  53. 53. Novick RP, Ross HF, Projan SJ, Kornblum J, Kreiswirth B, et al. (1993) Synthesis of staphylococcal virulence factors is controlled by a regulatory RNA molecule. EMBO J 12: 3967–3975.
  54. 54. Morfeldt E, Taylor D, von Gabain A, Arvidson S (1995) Activation of alpha-toxin translation in Staphylococcus aureus by the trans-encoded antisense RNA, RNAIII. EMBO J 14: 4569–4577.
  55. 55. Chao Y, Vogel J (2010) The role of Hfq in bacterial pathogens. Curr Opin Microbiol 13: 24–33.
  56. 56. Said-Salim B, Dunman PM, McAleese FM, Macapagal D, Murphy E, et al. (2003) Global regulation of Staphylococcus aureus genes by Rot. J Bacteriol 185: 610–619.
  57. 57. Shimoni Y, Friedlander G, Hetzroni G, Niv G, Altuvia S, et al. (2007) Regulation of gene expression by small non-coding RNAs: a quantitative view. Mol Syst Biol 3: 138.
  58. 58. Gomez MI, Lee A, Reddy B, Muir A, Soong G, et al. (2004) Staphylococcus aureus protein A induces airway epithelial inflammatory responses by activating TNFR1. Nat Med 10: 842–848.
  59. 59. Goodyear CS, Silverman GJ (2004) Staphylococcal toxin induced preferential and prolonged in vivo deletion of innate-like B lymphocytes. Proc Natl Acad Sci U S A 101: 11392–11397.
  60. 60. Morfeldt E, Janzon L, Arvidson S, Lofdahl S (1988) Cloning of a chromosomal locus (exp) which regulates the expression of several exoprotein genes in Staphylococcus aureus. Mol Gen Genet 211: 435–440.
  61. 61. Recsei P, Kreiswirth B, O'Reilly M, Schlievert P, Gruss A, et al. (1986) Regulation of exoprotein gene expression in Staphylococcus aureus by agr. Mol Gen Genet 202: 58–61.
  62. 62. Traber KE, Lee E, Benson S, Corrigan R, Cantera M, et al. (2008) agr function in clinical Staphylococcus aureus isolates. Microbiology 154: 2265–2274.
  63. 63. Sakoulas G, Eliopoulos GM, Moellering RC Jr, Wennersten C, Venkataraman L, et al. (2002) Accessory gene regulator (agr) locus in geographically diverse Staphylococcus aureus isolates with reduced susceptibility to vancomycin. Antimicrob Agents Chemother 46: 1492–1502.
  64. 64. Fowler VG Jr, Sakoulas G, McIntyre LM, Meka VG, Arbeit RD, et al. (2004) Persistent bacteremia due to methicillin-resistant Staphylococcus aureus infection is associated with agr dysfunction and low-level in vitro resistance to thrombin-induced platelet microbicidal protein. J Infect Dis 190: 1140–1149.
  65. 65. Shopsin B, Drlica-Wagner A, Mathema B, Adhikari RP, Kreiswirth BN, et al. (2008) Prevalence of agr dysfunction among colonizing Staphylococcus aureus strains. J Infect Dis 198: 1171–1174.
  66. 66. Tegmark K, Morfeldt E, Arvidson S (1998) Regulation of agr-dependent virulence genes in Staphylococcus aureus by RNAIII from coagulase-negative staphylococci. J Bacteriol 180: 3181–3186.
  67. 67. Somerville GA, Proctor RA (2009) At the crossroads of bacterial metabolism and virulence factor synthesis in Staphylococci. Microbiol Mol Biol Rev 73: 233–248.
  68. 68. Bischoff M, Dunman P, Kormanec J, Macapagal D, Murphy E, et al. (2004) Microarray-based analysis of the Staphylococcus aureus sigmaB regulon. J Bacteriol 186: 4085–4099.
  69. 69. Ziebandt AK, Becher D, Ohlsen K, Hacker J, Hecker M, et al. (2004) The influence of agr and sigmaB in growth phase dependent regulation of virulence factors in Staphylococcus aureus. Proteomics 4: 3034–3047.
  70. 70. Christiansen JK, Nielsen JS, Ebersbach T, Valentin-Hansen P, Sogaard-Andersen L, et al. (2006) Identification of small Hfq-binding RNAs in Listeria monocytogenes. RNA 12: 1383–1396.
  71. 71. Nielsen JS, Christiansen MH, Bonde M, Gottschlak S, Frees D, et al. (2011) Searching for small σB-regulated genes in Staphylococcus aureus. Arch Microbiol 193: 23–34.
  72. 72. Torres VJ, Attia AS, Mason WJ, Hood MI, Corbin BD, et al. (2010) Staphylococcus aureus fur regulates the expression of virulence factors that contribute to the pathogenesis of pneumonia. Infect Immun 78: 1618–1628.
  73. 73. Lynch SV, Wiener-Kronish JP (2008) Novel strategies to combat bacterial virulence. Curr Opin Crit Care 14: 593–599.
  74. 74. Wilson DN (2009) The A-Z of bacterial translation inhibitors. Crit Rev Biochem Mol Biol 44: 393–433.
  75. 75. Blount KF, Breaker RR (2006) Riboswitches as antibacterial drug targets. Nat Biotechnol 24: 1558–1564.
  76. 76. Serganov A, Yuan YR, Pikovskaya O, Polonskaia A, Malinina L, et al. (2004) Structural basis for discriminative regulation of gene expression by adenine- and guanine-sensing mRNAs. Chem Biol 11: 1729–1741.
  77. 77. Batey RT, Gilbert SD, Montange RK (2004) Structure of a natural guanine-responsive riboswitch complexed with the metabolite hypoxanthine. Nature 432: 411–415.
  78. 78. Kim JN, Blount KF, Puskarz I, Lim J, Link KH, et al. (2009) Design and antimicrobial action of purine analogues that bind Guanine riboswitches. ACS Chem Biol 4: 915–927.
  79. 79. Mulhbacher J, Brouillette E, Allard M, Fortier LC, Malouin F, et al. (2010) Novel riboswitch ligand analogs as selective inhibitors of guanine-related metabolic pathways. PLoS Pathog 6: e1000865. doi:10.1371/journal.ppat.1000865.
  80. 80. ten Broeke-Smits NJ, Pronk TE, Jongerius I, Bruning O, Wittink FR, et al. (2010) Operon structure of Staphylococcus aureus. Nucleic Acids Res 38: 3263–3274.
  81. 81. Beisel CL, Storz G (2010) Base pairing small RNAs and their roles in global regulatory networks. FEMS Microbiol Rev 34: 866–882.
  82. 82. Gutierrez-Preciado A, Jensen RA, Yanofsky C, Merino E (2005) New insights into regulation of the tryptophan biosynthetic operon in Gram-positive bacteria. Trends Genet 21: 432–436.