Phylogenetic distribution and membrane topology of the LytR-CpsA-Psr protein family
© Hübscher et al; licensee BioMed Central Ltd. 2008
Received: 25 September 2008
Accepted: 19 December 2008
Published: 19 December 2008
The bacterial cell wall is the target of many antibiotics and cell envelope constituents are critical to host-pathogen interactions. To combat resistance development and virulence, a detailed knowledge of the individual factors involved is essential. Members of the LytR-CpsA-Psr family of cell envelope-associated attenuators are relevant for β-lactam resistance, biofilm formation, and stress tolerance, and they are suggested to play a role in cell wall maintenance. However, their precise function is still unknown. This study addresses the occurrence as well as sequence-based characteristics of the LytR-CpsA-Psr proteins.
A comprehensive list of LytR-CpsA-Psr proteins was established, and their phylogenetic distribution and clustering into subgroups was determined. LytR-CpsA-Psr proteins were present in all Gram-positive organisms, except for the cell wall-deficient Mollicutes and one strain of the Clostridiales. In contrast, the majority of Gram-negatives did not contain LytR-CpsA-Psr family members. Despite high sequence divergence, the LytR-CpsA-Psr domains of different subclusters shared a highly similar, predicted mixed a/β-structure, and conserved charged residues. PhoA fusion experiments, using MsrR of Staphylococcus aureus, confirmed membrane topology predictions and extracellular location of its LytR-CpsA-Psr domain.
The LytR-CpsA-Psr domain is unique to bacteria. The presence of diverse subgroups within the LytR-CpsA-Psr family might indicate functional differences, and could explain variations in phenotypes of respective mutants reported. The identified conserved structural elements and amino acids are likely to be important for the function of the domain and will help to guide future studies of the LytR-CpsA-Psr proteins.
The cell envelope forms a protective shield around bacteria and is also the site of primary host-pathogen interactions. Its composition and surface characteristics are therefore important in pathogenesis, and may, in view of increasing resistance against all commonly used cell wall-directed antibiotics, present novel potential antibacterial targets.
The LytR-CpsA-Psr family of cell envelope-associated transcriptional attenuators has been brought into focus of scientific interest upon the discovery that members of this family influence various virulence factors as well as antibiotic resistance of important human pathogens and, interestingly, seem to play a role in bacterial cell envelope maintenance [1–5]. Therefore, this protein family represents a promising target to gain more insight into virulence and antibiotic resistance development.
The LytR-CpsA-Psr family members are putative transmembrane proteins carrying a so-called LytR-CpsA-Psr domain, which is predicted to be extracellular. LytR was first described in Bacillus subtilis, where it acts as an attenuator of the expression of both itself and the divergently transcribed lytABC operon, which encodes a putative lipoprotein (LytA), an N-acetylmuramoyl-L-alanine amidase (LytC) and its modifier LytB . CpsA is suggested to play a role in transcription activation of the capsular polysaccharide synthesis operon of Streptococcus agalactiae . Psr was initially proposed to be a repressor of penicillin-binding protein 5 (PBP5) synthesis in Enterococcus hirae , however, Sapunaric et al. could neither confirm an effect on PBP5 synthesis nor autolysis nor β-lactam resistance . In contrast, the LytR homolog BrpA affects autolytic activity of Streptococcus mutans  and positively influences biofilm formation ability as well as acidic and oxidative stress tolerance . Furthermore, BrpA inactivation alters phagocytosis by human polymorphonuclear leukocytes and the outcome of bacteremia in a rat model . In Staphylococcus aureus, the LytR-CpsA-Psr member MsrR contributes to β-lactam resistance . MsrR of S. aureus as well as Psr of Enterococcus faecalis were both shown to increase virulence in the model host Caenorhabditis elegans [9, 10]. Furthermore, expression of SA0908, another member of the LytR-CpsA-Psr family in S. aureus, is increased during infection in a murine renal abscess model .
The function of the LytR-CpsA-Psr domain, however, is still unknown and so far information about these proteins is based on phenotypic characterizations. A more comprehensive knowledge about the occurrence of LytR-CpsA-Psr proteins and analyses of their sequence will provide a basis for experimental determination of interactions or structure/function relationships.
In the present study, we investigated the phylogenetic distribution of the LytR-CpsA-Psr proteins and analyzed secondary structure predictions. In addition, the staphylococcal LytR-CpsA-Psr protein MsrR was used as a model to confirm membrane topology.
Results and discussion
Sequence collection of LytR-CpsA-Psr proteins
A comprehensive sequence collection was obtained by searching the InterPro database  for LytR-CpsA-Psr members (InterPro entry IPR004474) and using PSI-BLAST  to identify further homologous sequences as described in the Methods section. Sequences representing fragments of the LytR-CpsA-Psr domain were excluded from the studies. The revised dataset comprised 1'079 sequences.
Occurrence of the LytR-CpsA-Psr domain
The LytR-CpsA-Psr domain is restricted to the kingdom of bacteria with two exceptions occurring in the moss Physcomitrella patens subsp. patens (Bryophyta, Moss Superclass V) and the freshwater amoeba Paulinella chromatophora. Physcomitrella is widely used as a model organism in plant genetics as it undergoes integrative homologous recombination with a high efficiency , while Paulinella contains photosynthetic inclusions (chromatophores) affiliated with the cyanobacteria Prochlorococcus and Synechococcus spp. . BLAST analysis of the LytR-CpsA-Psr sequences found in Paulinella and Physcomitrella revealed high similarities to those found in Synechococcus sp. WH5701 and Paenibacillus sp. JDR-2, respectively (data not shown). It is therefore conceivable that the LytR-CpsA-Psr proteins found in Physcomitrella and Paulinella are of bacterial origin.
Analysis of the genomes available at the National Center for Biotechnology Information (NCBI)  revealed that all of the completely sequenced Firmicutes contain at least one member of the LytR-CpsA-Psr family, except for Clostridium kluyveri strain DSM 555 and the whole order of Mollicutes. In the phylum of Actinobacteria, LytR-CpsA-Psr proteins were found in every completely sequenced genome and the same was true for Deinococcus-Thermus, Spirochaetes, and Thermotogae. In contrast, only two strains of the Bacteroidetes, i.e. Pedobacter sp. BAL39 (Sphingobacteriales) and Bacteroides capillosus ATCC 29799 (Bacteroidales) harbor LytR-CpsA-Psr proteins, but none of the completely sequenced strains. Among the Chloroflexi, the Dehalococcoides do not possess LytR-CpsA-Psr members, whereas they were found in the orders Chloroflexales and Herpetosiphonales. Most of the Cyanobacteria genomes contain LytR-CpsA-Psr members, but only two out of twelve Prochlorococcus marinus genomes.
Characteristics of LytR-CpsA-Psr carriers
The organisms having LytR-CpsA-Psr proteins represent the immense diversity of bacteria with regard to morphology, ultrastructure, motility, metabolic characteristics, and habitat preferences. LytR-CpsA-Psr family members were found in pathogens of human, animals, or plants as well as in non-pathogenic organisms, in generalists and specialists such as hyperthermophilic bacteria. This heterogeneity raises the question: Is there a common trait to the LytR-CpsA-Psr carriers? One of the most striking observations was that the LytR-CpsA-Psr proteins are absent in the large Gram-negative phylum of Proteobacteria and many other Gram-negative groups, while all of the Gram-positive bacteria contain at least one copy. Given the proposed role of the LytR-CpsA-Psr proteins in cell envelope maintenance and the lack of the respective domain in the cell wall-deficient order Mollicutes, this finding might indicate a correlation with the Gram-positive cell wall in particular. However, the list of LytR-CpsA-Psr carriers also comprised Spirochaetes and numerous organisms classified as Gram-negatives, such as members of the Cyanobacteria, Thermus, Thermotogae, Bacteroidetes, and Chloroflexi.
Nevertheless, many of the Gram-negative LytR-CpsA-Psr carriers show features of a typical Gram-positive cell wall, such as a thick, multilayered peptidoglycan, a high cross-linking extent, or polysaccharides cross-linked to the peptidoglycan. Intermediate types between a typical Gram-negative and Gram-positive cell wall are for example observed in various Cyanobacteria , Chloroflexus aurantiacus , and Deinococcus radiodurans . In conclusion, however, a common feature related to peptidoglycan composition or amount was not apparent.
Loss and gain of LytR-CpsA-Psr proteins in the course of evolution
The LytR-CpsA-Psr proteins described so far are not essential, and viable knock out mutants were obtained in S. aureus, S. mutans, and E. hirae [1, 4, 7]. These particular organisms, however, contain more than one member of the LytR-CpsA-Psr family. It would be interesting to know if the inactivation of all LytR-CpsA-Psr proteins affects viability. On the other hand, our sequence collection showed that this protein family was lost in certain organisms in the course of evolution. As mentioned above, only two Prochlorococcus strains carry LytR-CpsA-Psr members. The respective strains, MIT9303 and MIT9313, are distinct from other Prochlorococcus isolates in that the size and GC content of their genomes are more similar to those of the genus Synechococcus . The differences in genome size reflect gene gain and loss during the evolution of Prochlorococcus, which lost the LytR-CpsA-Psr proteins after divergence from the MIT9303/MIT9313 clade. Interestingly, besides the LytR-CpsA-Psr members, numerous genes that are present in MIT9303/MIT9313 and most Synechococcus, but absent in the other completely sequenced Prochlorococcus, are involved in cell envelope biogenesis . Apart from Prochlorococcus, C. kluyveri is likely to be another example for the loss of LytR-CpsA-Psr proteins. C. kluyveri differs from other members of the genus Clostridium by unique metabolic features and its genome shows only very low syntheny on protein level to other Clostridia .
The occurrence of the LytR-CpsA-Psr family in the Thermotogae, which are considered an evolutionary early branch of bacteria , might indicate that this family already appeared in a common procaryotic ancestor and was lost by some lineages during the process of diversification, e.g. in the Proteobacteria. From this point of view, the incidence in P. pacifica SIR-1 could be the result of lateral gene transfer. However, the GC content of the LytR-CpsA-Psr protein encoding gene and the GC content of P. pacifica SIR-1 do not differ and a more thorough investigation would be required to address this question. Yet, lateral gene transfer plays a significant role in evolution , and it is possible that LytR-CpsA-Psr proteins were (re-) acquired in the time course of procaryotic diversification.
Our sequence collection revealed that from one, e.g. in C. tetani, to eleven, e.g. in Streptomyces coelicolor, any number of LytR-CpsA-Psr members could be found in a single species. In order to investigate if there existed sub-families and a particular distribution, we performed a cluster analysis based on pair-wise sequence similarities resulting from a BLAST all against all search using CLANS  with a P-value cut off of 10-35.
A step-wise increase in the P-value cut off caused the clusters A1, Ch, F1, F2, and M to merge in a supercluster (data not shown), suggesting a close relationship of the enclosed sequences. Decreasing the P-value cut off resulted in disconnection of the clusters into subclusters mainly following phylogenetic affiliations (data not shown). To verify whether unequal family sizes or redundant sequences distorted cluster analysis, CLANS was subsequently applied to a reduced dataset of 576 sequences with a maximum similarity of 90%. The use of this reduced dataset had no significant effect on the outcome of the clustering (data not shown) and the following discussion is based on the results obtained using the unfiltered list of LytR-CpsA-Psr proteins.
Cluster M – taxonomically mixed central cluster
Cluster M was the only one containing proteins of organisms belonging to various phyla, i.e. Firmicutes, Actinobacteria, Bacteroidetes, Deinococcus-Thermus, and Cyanobacteria, and might represent those sequences that have diverged the least from a presumed ancestral LytR-CpsA-Psr protein. A clearly separated subcluster (Ma) contained exclusively sequences of Prochlorococcus and Synechococcus species as well as of the amoeba Paulinella.
Cluster A1 – common Actinobacteria sequences
Most LytR-CpsA-Psr proteins of the high GC Gram-positive organisms grouped in cluster A1. A1-type sequences were identified in each member of the Actinobacteria and therefore represent the sequences characteristic for this phylum. The proteins of this cluster were predominantly predicted to have a single transmembrane segment with an extracellular LytR-CpsA-Psr domain, a trait attributed to the majority of LytR-CpsA-Psr proteins.
Within cluster A1, three separated subclusters were distinguished. Subcluster A1a enclosed solely sequences of different Mycobacterium species, whereas A1b and A1c both covered sequences of various Actinobacteria.
Cluster A1 also harboured FrnA [UniProt:O68907], which contains an SBP_bac5 domain (bacterial extracellular solute-binding protein family 5 domain; PFAM:PF00496). The family 5 solute-binding proteins comprise peptide-binding proteins, such as the oligopeptide transporter subunit OppA of Gram-negative bacteria. FrnA was exclusively found in Streptomyces roseofulvus, and is encoded by the first gene of a 25 kb-region, containing genes involved in biosynthesis of the polyketide antibiotic frenolicin . In Saccharopolyspora erythraea, two A1-type proteins, SACE_6482 and SACE_6483, are encoded adjacent to aveBII (SACE_6480), a dTDP-glucose 4,6-dehydratase involved in the biosynthesis of a polyketide sugar unit precursor and hence of the macrolide antibiotic erythromycin A . However, any involvement of LytR-CpsA-Psr proteins in biosynthesis of secondary metabolites by organisms of the order Actinomycetales remains open.
Cluster A2 – Actinobacteria proteins with multiple transmembrane segments
A few LytR-CpsA-Psr family members of the Actinobacteria clustered in A2. In contrast to the A1-type proteins and the LytR-CpsA-Psr family members in general, those proteins found in A2 were calculated to cross the membrane two to four times. In accordance with predictions for LytR-CpsA-Psr members with one transmembrane helix and independently of the number of predicted transmembrane helices, the LytR-CpsA-Psr domains of A2-type proteins were mainly suggested to be extracellular by the various programs used. A2-type proteins were only present in some organisms of the Propionibacterineae, Streptosporangineae, and Micrococcineae.
Cluster A3 – Streptomyces-specific proteins
This cluster contained four sequences, which are rich in glycine and the polar amino acid glutamine predominantly located within a stretched, uncharged segment close to the N-terminus. The A3-type proteins also differ from other LytR-CpsA-Psr members by their exceptional length ranging from 559 to 617 aa and were only found in Streptomyces.
Cluster F1 – Psr/MsrR-like proteins of Firmicutes
Apart from those sequences comprised in cluster M, the Firmicutes sequences divided into three main clusters F1–F3 and two peripheric clusters F4 and F5. Cluster F1 contained proteins of the orders Bacillales and Lactobacillales (subcluster F1a) as well as of Clostridiales and the two non-Firmicutes Pedobacter sp. (phylum Bacteroidetes) and Fervidobacterium nodosum (phylum Thermotogae) (subcluster F1b).
F1-type proteins included Psr of enterococci, which is suggested to be an activator of its own transcription, especially in the presence of ampicillin . In the food-borne pathogen Listeria monocytogenes, transcription of psr is increased in response to growth at 10°C . Cluster F1 also included MsrR of Staphylococcus aureus, which is involved in β-lactam resistance . msrR belongs to the cell wall stress stimulon, a set of genes collectively induced upon exposure to antibiotics damaging the cell wall [29, 30].
Cluster F2 – LytR/BrpA-like proteins of Firmicutes
Cluster F2 mainly contained sequences of the orders Bacillales and Lactobacillales and included LytR of B. subtilis and BrpA of S. mutans. BrpA has an impact on autolysis, biofilm formation, stress tolerance, and virulence [1, 5], and LytR acts as an attenuator of the lytABC operon encoding the major autolytic amidase of B. subtilis . LytR belongs to the σX regulon, which controls genes participating in cell envelope metabolism and modulation [31, 32]. YwtF, a further F2-type protein in B. subtilis, is a member of the σM regulon. The σM regulon plays a role in response to cell envelope stress, and in contrast to lytR, ywtF gene expression is upregulated by bacitracin and vancomycin [33–35]. A similar situation as in B. subtilis was observed for transcription of lytR and ywtF in B. licheniformis . The two F2-type LytR-CpsA-Psr members of S. aureus, SA0908 and SA2103 in strain N315, both belong to the cell wall stress stimulon as does msrR of cluster F1 [30, 37, 38].
In Bacillus thuringiensis subsp. thuringiensis strain 407-1, the F2-type LytR-CpsA-Psr protein EcfY is thought to be encoded in an operon with sigW (similar to extracytoplasmic function σ factor) and ecfX (putative anti-σ factor). sigW and ecfX contribute to β-exotoxin production, and ecfY was proposed to be involved in negative control of sigW expression .
In cluster F2, a LytR-CpsA-Psr protein with a type 2 phosphatidic acid phosphatase superfamily domain (PAP2, PFAM:PF01569) was contained, which is encoded by E. faecalis EF_3245. Certain PAP2 family members have undecaprenyl pyrophosphate phosphatase activity, and thus may play a role in peptidoglycan biosynthesis by providing the lipid carrier undecaprenyl phosphate [40, 41]. Moreover, the LytR-CpsA-Psr protein of the eukaryote Physcomitrella also clustered in F2.
The staphylococcal protein LytR (SA0251 in strain N315), the response regulator of the two-component system LytSR , does not belong to the LytR-CpsA-Psr protein family despite its name.
Cluster F3 – CpsA-like Firmicutes proteins with multiple transmembrane segments
The third Firmicutes cluster was formed by the CpsA-like proteins, which are predominantly found in the genus Streptococcus. In streptococci, cpsA (also cpsX, epsA, wzg) is the first gene of the capsular biosynthesis locus, and CpsA is assumed to be a transcriptional regulator of capsule production in S. agalactiae . In S. pneumoniae, however, although encapsulation is reduced in a cpsA mutant, no evidence for an effect of CpsA on transcription of the cps operon was found . Yet, the mutant exhibited reduced tyrosine phosphorylation of CpsD, which is thought to be required for production of elevated amounts of capsule .
All F3-type proteins were predicted to have three transmembrane helices with an intracellular N-terminus. Additionally, CpsA and related proteins of streptococci possess a DNA polymerase processivity factor domain (DNA-PPF, PFAM:PF02916), a subdomain of the replisome sliding clamp unit. However, the subunits of the sliding clamp ring are composed of two homologous subdomains, the DNA-PPF domain and a gp45-slide C subdomain (PFAM:PF09116) , which is absent in CpsA. Moreover, in CpsA the DNA-PPF domain was predicted to span the third putative membrane segment with the major portion of the domain located extracellularly. These findings imply that the DNA-PPF domain found in CpsA proteins fulfils a different function. The extracellular portion of the CpsA DNA-PPF domain overlaps with a structural periplasmic binding protein-like II domain (SCOP superfamily 53850) as identified using SCOP (Structural Classification Of Proteins) . This superfamily includes various binding proteins such as phosphate-binding proteins, glutamine-binding proteins, or ferric-binding proteins. Interestingly, SCOP superfamily 53850 also covers the family 5 solute-binding proteins discussed with respect to the A1-type LytR-CpsA-Psr protein FrnA.
A number of proteins of the Clostridiales also clustered in F3. Although these proteins did not produce a significant hit to the DNA-PPF domain in a PFAM search, they were of similar length as CpsA (456–559 amino acids), and four of them [UniProt:A5KKW2, A8RE01, A8R906, and B1C5F5) were also predicted to carry a periplasmic binding protein-like II domain.
Clusters F4 and F5 – small 'peripheric' Firmicutes subclusters
Cluster F4 only contained sequences of Lactococcus lactis and Streptococcus thermophilus, whereas F5 only contained sequences of certain Clostridiales. The F4- and F5-type sequences showed the same transmembrane organization, and family domain architecture as those of the Firmicutes main clusters F1 and F2.
Clusters Ch, Cy, D, S and T – other taxonomy-specific clusters
The sequences of the Chloroflexi grouped in one single cluster (Ch) closely related to M, and all LytR-CpsA-Psr members of Thermotoga and one of the two members found in F. nodosum assembled in the Thermotogae cluster T. Cluster D comprised those Deinococcus-Thermus sequences not included in cluster M. Cluster Cy enclosed a set of Synechococcus and Prochlorococcus sequences, and finally the LytR-CpsA-Psr members of the Spirochaetes Borrelia were grouped in cluster S. The sequences of the other Spirochaetes, i.e. Leptospira and Treponema, were not included in any cluster.
All sequences enclosed in these clusters showed for the LytR-CpsA-Psr proteins a characteristic organization with a short cytoplasmic domain, one transmembrane segment, and a putative extracellular domain carrying the LytR-CpsA-Psr element.
The accumulation of multiple LytR-CpsA-Psr proteins most probably often happened through duplication from an ancestral species- or group-specific sequence, leading to as many as 11 members in S. coelicolor. Ten of the S. coelicolor LytR-CpsA-Psr proteins clustered in A1, while the eleventh [UniProt:Q9RDK8] clustered in A3. In contrast to Q9RDK8, all genes of the ten A1-type proteins lie within the central core region of the S. coelicolor genome, and seven of the LytR-CpsA-Psr genes are consecutively encoded. The core region of S. coelicolor comprises genes likely to be essential, such as genes involved in cell division, DNA replication, transcription, translation, and amino acid biosynthesis .
Gene duplication might also have happened in an ancestor of the Deinococcus-Thermus group, which is likely to have carried two members of the LytR-CpsA-Psr family: one of the M cluster-type and a more differentiated, phylum-specific one. Both of these LytR-CpsA-Psr proteins have been retained in all of the fully sequenced organisms of this taxon.
An identical distribution of LytR-CpsA-Psr proteins was found in the genus Staphylococcus and Listeria, which share one member in the MsrR/Psr-like cluster F1 and two members in the LytR/BrpA-like cluster F2. Only Staphylococcus haemolyticus encodes a fourth LytR-CpsA-Psr protein, CapM, which clusters in F2 and is the last gene of a putative capsular polysaccharide biosynthesis locus capA-capM. capA-capG show ≥ 76% amino acid identity to the cap5A-cap5G genes of S. aureus, while capH-capM are unique to S. haemolyticus and might be of exogenous origin . The three LytR-CpsA-Psr proteins common to staphylococci and listeria most likely were present in an evolutionary older organism before their phylogenetic separation, however, the cluster analysis leaves the phylogeny of the LytR-CpsA-Psr proteins in general open, and a hypothesis that cluster M represents the most original group remains speculative.
In order to infer evolutionary relatedness of the LytR-CpsA-Psr proteins represented by the 30 strains selected, phylogenetic trees were constructed. However, the LytR-CpsA-Psr proteins show only low amino acid identity and the domain characterizing this family is only about 150 amino acids in length (average value of the respective 93 sequences), rendering construction of phylogenetic trees problematic. Reliable bootstrap support was only obtained close to the terminal nodes, though the results of the cluster analyses were supported (Additional file 3), reflecting taxonomic relationships as shown in the 16S rRNA gene tree in Figure 3.
Secondary structure prediction
A subset of twelve sequences representing the LytR-CpsA-Psr proteins of clusters M, A1, F1, F2, F3, Ch, and T was subjected to secondary structure prediction. The sequences analyzed included the three eponymous proteins LytR, CpsA, and Psr, as well as other family members that have been described in literature, i.e. BrpA, MsrR, and SA0908. The sequences varied in length from 293 to 485 amino acids and they showed very different contents of charged amino acids and theoretical isoelectric points (pI) ranging from 5.17 to 9.66 (Additional file 4). All sequences contained one consensus transmembrane region predicted by all of the four servers used, except for CpsA, which was predicted to have three transmembrane helices. The majority of the membrane topology predictions suggested an intracellular N-terminus, implicating an extracellular location of the LytR-CpsA-Psr domain.
The amino acid identities of the extended LytR-CpsA-Psr domains ranged from 21 to 44% (Additional file 5) and were hence only little above those of the full length proteins. Interestingly, the few fully conserved residues included nine charged amino acids: aspartic acid, arginine, and lysine. Charged residues are often involved in the active site of proteins, where they interact with charged ligands or bind substrates. Moreover, they may play a role in formation of protein-protein complexes and are important for folding, stability, and solubilization of proteins . It is therefore very likely that at least some of the conserved residues are indispensable for the function of the LytR-CpsA-Psr domain in these proteins.
High sequence divergence was observed with regard to some of the peripheric clusters, e.g. the Spirochaetes cluster S. Although the secondary structure predictions mainly agreed with those of the other LytR-CpsA-Psr members, there was a very weak conservation of amino acids (data not shown), possibly indicating a different function.
Confirmation of membrane topology
The predicted membrane topology of the LytR-CpsA-Psr proteins was verified by PhoA fusions using the staphylococcal protein MsrR as a representative of the protein family. The amino acid sequence of MsrR is identical in twelve of the 14 sequenced S. aureus strains available on the NCBI website  and there is only one amino acid difference in strains Mu50 and Mu3, which both have lysine at position 146 instead of glutamic acid (Additional files 5 and 6). For the following analyses, the sequence represented by S. aureus strain N315 was employed (see also Additional file 4).
PhoA fusions and activity assay
These findings confirmed the predicted arrangement of the LytR-CpsA-Psr protein MsrR in the membrane: The short N-terminal tail is located inside of the cell and is followed by one transmembrane helix and an extracellular domain carrying the LytR-CpsA-Psr domain. Most members of the LytR-CpsA-Psr protein family show very similar predicted architectures as MsrR.
Members of the LytR-CpsA-Psr family are known to influence clinically important attributes of various pathogens [2, 4, 5]. The LytR-CpsA-Psr domain was found to be restricted to the kingdom of bacteria. Being present in hyperthermophilic organisms of evolutionary early branches, the LytR-CpsA-Psr proteins appear to constitute an ancient protein family. All Gram-positive organisms were found to possess LytR-CpsA-Psr proteins, except for the Mollicutes that seem to have lost this protein family in the course of diversification. In contrast, the LytR-CpsA-Psr domain was only observed in a minority of the Gram-negatives, and it is conceivable that the LytR-CpsA-Psr proteins were lost in Proteobacteria and Chlamydiae as well as in most of the Bacteroidetes during evolution. LytR-CpsA-Psr proteins are shared by the most diverse procaryotic phyla, including the thermophiles of the first bacterial branches, and the genes encoding LytR-CpsA-Psr proteins often belong to the core genome. Although these proteins do not appear to be essential, they presumably confer a selective advantage to their carriers, as becomes apparent in vitro when mutant cells are challenged with antibiotic, acidic, or oxidative stress [4, 5].
The finding that various members of this protein family are part of the cell wall stress stimulon in different organisms [30, 33–38] might further suggest a role in ensuring cell envelope integrity. Nevertheless, the specific functions of the LytR-CpsA-Psr proteins are probably more diverse than originally anticipated, as indicated by the results of the cluster analysis, explaining discrepancies in phenotypes of knock out mutants [1–4, 7].
Our analyses of the occurrence and distribution of the LytR-CpsA-Psr proteins as well as the determination of putative structural elements and conserved amino acids of the family-specific domain will provide a guideline for the design of future experiments to elucidate structure-function relationships.
As of August 20, 2008, accession numbers of LytR-CpsA-Psr protein family members included in the InterPro database (InterPro entry IPR004474), a consortium of the member databases PROSITE, Pfam, Prints, ProDom, SMART, and TIGRFAMs , were obtained. Homologues sequences not present in InterPro were identified by PSI-BLAST  against the NCBI non-redundant protein sequence database (nr) using MsrR of S. aureus strain N315 [UniProt:Q99Q02] as a query and an E-value threshold of 10-4. Amino acid sequences were retrieved from UniProt  or from NCBI .
To identify closely related sequences within the LytR-CpsA-Psr members, CLANS (CLuster ANalyis of Sequences) was used . For two-dimensional visualization of pairwise sequence similarities, based on P-values of high-scoring segment pairs (HSPs) resulting from a BLAST all against all search, the P-value cut off was set to 10-35 and the attraction (attract) and repulsion (repuls) exponents were set to 2. Network-based clustering was applied to assist designation of clusters.
Sequence compositions and theoretical pI were analyzed using ProtParam . Transmembrane regions were predicted using TMHMM , the "DAS"-Transmembrane Prediction server , TMpred , and HMMTOP . Secondary structures were predicted using SsPro , PSIPRED , and Jpred .
Amino acid sequence alignments
Phylogenetic trees were constructed using programs of the PHYLIP 3.67 package . For construction of a species tree, aligned 16S rRNA genes were downloaded from the ribosomal RNA database RDP-II . Misaligned characters were manually edited using SeaView version 2.2 . The C- and N-termini were trimmed and gap-only sites were deleted from the alignment. A distance matrix, computed with DNADIST using the F84 model of nucleotide substitution, was used for construction of a distance tree with FITCH (Fitch-Margoliash criterion) allowing global rearrangements and randomizing the input order of the sequences 10 times. For construction of protein sequence trees, bootstrap resampling was performed using SEQBOOT. Consensus distance trees were generated using PROTDIST with the Jones-Taylor-Thornton substitution matrix, NEIGHBOR, and CONSENSE. Phylogenetic trees were drawn with Dendroscope version 1.2.4 .
Bacterial strains and culture conditions
Strains and plasmids
Strain or plasmid
Relevant genotype or phenotypea)
Reference or source
Clinical isolate (ATCC 25904)
supE 44 ΔlacU 169(φ 80 lacZ ΔM15) hsdR 17 recA 1 endA 1 gyrA 96 thi-1 rel A1
Δ(ara-leu)7679 ΔlacX 74 ΔphoA 20 galE galK thi rpsE rpoB argE(am) recA 1
E. coli plasmid containing an arabinose inducible promoter 5' of a signal sequence-less phoA reporter gene, Amr
PhoA fusion constructs
PCR products covering different lengths of msrR of S. aureus strain Newman were generated using the forward primer 5'-GCGCCTCGAG ATGGATAAAGAAACTAATGA-3' and the following reverse primers: 5'-GCGCGGTACC TCTTCATCTAAAAAGTCTTT-3' (full length), 5'-GCGCGGTACC GTTCTAAAATTAACCATTTC-3' (Deletion of 80 aa from the C-terminus, Δ80), 5'-GCGCGGTACC TCAGGCATTAATTCATCAA-3 (Δ147), 5'-GCGCGGTACC CCATCATTTTTTACTGGTCC-3' (Δ246), and 5'-GCGCGGTACC AATTTCCTAATTTTCTTCTT-3' (Δ295). Recognition sites of restriction endonucleases are underlined. The amplicons were digested using XhoI and KpnI and inserted into pHA-1 downstream of the araB arabinose-inducible promoter and upstream of the phoA gene lacking both the 5' segment coding for the signal sequence and the first five residues of the mature protein. The resulting plasmids were transferred into the phoA- E. coli strain CC118.
Expression of PhoA fusion proteins and PhoA activity assay
Overnight cultures of E. coli strain CC118 harboring the msrR-phoA fusion constructs of interest were diluted 1:100 in LB broth containing 100 μg/ml ampicillin and grown to an optical density at 600 nm of 0.5. Bacterial cultures were then divided into halves: in one half, protein expression was induced with 0.2% arabinose, while the other half was left untreated. After growth for an additional hour, 1 ml of induced and non-induced cells, respectively, were harvested for determination of PhoA activity by a p-nitrophenyl phosphate (p NPP) (Sigma-Aldrich) cleavage assay . In addition, 200 μl of each cell suspension were collected for verification of PhoA fusion protein expression by Western blot using an α-PhoA antibody conjugated to horseradish peroxidase (HRP) (Abcam Ltd., UK).
Western blot analysis
Whole cells were heated for 5 min at 65°C in 5× SDS loading buffer supplemented with 0.05% N-lauroylsarcosyl and subjected to SDS-12%-PAGE. Separated proteins were transferred onto nitrocellulose membranes (Hybond-ECL; Amersham Biosciences), and for detection of PhoA, a HRP-conjugated α-PhoA antibody (Abcam) diluted 1:100'000 and the SuperSignal West Pico Chemiluminescent detection kit (Pierce) were used.
We are grateful to D. Sjöstrand and T. Urbig (Department of Biochemistry and Biophysics, Stockholm University, Sweden) for providing plasmid pHA-1.
This study was supported by European Commission grant LSHM-CT-2003-503335 (SBF03.0098), and Swiss National Science Foundation grants 31-117707 and PMPDB-114323 to BBB and PSM, respectively.
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