16 Sep 2009:
Tuberculous latency and reactivation play a significant role in the pathogenesis of tuberculosis, yet the mechanisms that regulate these processes remain unclear. The Mycobacterium tuberculosis universal stress protein (USP) homolog, rv2623, is among the most highly induced genes when the tubercle bacillus is subjected to hypoxia and nitrosative stress, conditions thought to promote latency. Induction of rv2623 also occurs when M. tuberculosis encounters conditions associated with growth arrest, such as the intracellular milieu of macrophages and in the lungs of mice with chronic tuberculosis. Therefore, we tested the hypothesis that Rv2623 regulates tuberculosis latency. We observed that an Rv2623-deficient mutant fails to establish chronic tuberculous infection in guinea pigs and mice, exhibiting a hypervirulence phenotype associated with increased bacterial burden and mortality. Consistent with this in vivo growth-regulatory role, constitutive overexpression of rv2623 attenuates mycobacterial growth in vitro. Biochemical analysis of purified Rv2623 suggested that this mycobacterial USP binds ATP, and the 2.9-Å-resolution crystal structure revealed that Rv2623 engages ATP in a novel nucleotide-binding pocket. Structure-guided mutagenesis yielded Rv2623 mutants with reduced ATP-binding capacity. Analysis of mycobacteria overexpressing these mutants revealed that the in vitro growth-inhibitory property of Rv2623 correlates with its ability to bind ATP. Together, the results indicate that i) M. tuberculosis Rv2623 regulates mycobacterial growth in vitro and in vivo, and ii) Rv2623 is required for the entry of the tubercle bacillus into the chronic phase of infection in the host; in addition, iii) Rv2623 binds ATP; and iv) the growth-regulatory attribute of this USP is dependent on its ATP-binding activity. We propose that Rv2623 may function as an ATP-dependent signaling intermediate in a pathway that promotes persistent infection.
Mycobacterium tuberculosis poses serious threats to public health worldwide. The ability of this pathogen to establish in the host a clinically silent, persistent latent infection that can subsequently reactivate to cause diseases constitutes a major challenge in controlling tuberculosis. Our study showed that an M. tuberculosis mutant that is deficient in a universal stress protein (USP) designated Rv2623 fails to establish a chronic persistent infection in animal hosts. The mutant strain exhibits a hypervirulent phenotype as assessed by increased bacillary growth, pathology, and mortality in infected animals relative to the parental strain. Consistent with this in vivo growth-regulating attribute, we demonstrated that Rv2623, when expressed in mycobacteria at levels higher than that of the wild-type strain, retards bacterial growth in vitro. Using biochemical and biophysical analyses, including the Rv2623 crystal structure, we showed that this USP binds to ATP within a novel ATP-binding pocket. Through targeted mutagenesis studies, we further determined that the ability of Rv2623 to regulate bacillary growth is dependent on its ATP-binding capacity. Our data strongly suggest Rv2623 as a critical component that regulates the entry of M. tuberculosis into a chronic persistent growth phase, and therefore provide valuable insight into tuberculous dormancy and uncover new opportunities for the development of novel anti-tuberculous therapies.
Citation: Drumm JE, Mi K, Bilder P, Sun M, Lim J, Bielefeldt-Ohmann H, et al. (2009) Mycobacterium tuberculosis Universal Stress Protein Rv2623 Regulates Bacillary Growth by ATP-Binding: Requirement for Establishing Chronic Persistent Infection. PLoS Pathog 5(5): e1000460. doi:10.1371/journal.ppat.1000460
Editor: Lalita Ramakrishnan, University of Washington, United States of America
Received: June 18, 2008; Accepted: April 30, 2009; Published: May 29, 2009
Copyright: © 2009 Drumm et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work is supported by the Albert Einstein College of Medicine Center for AIDS Research (P30AI051519) as well as by the following NIH grants: T32 AI07501, AI07289, R01HL071241, P30AI051519, R01GM54469. Guinea pig infection studies were performed at Colorado State University, supported by the NIH TB Vaccine Testing and Research Materials contract HHSN266200400091c. Financial support for the crystallographic data collection comes principally from the Offices of Biological and Environmental Research and of Basic Energy Sciences of the US Department of Energy and from the National Center for Research Resources of the National Institutes of Health. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Mycobacterium tuberculosis, one of the most successful human pathogens, infects one-third of the world's population, causing nearly two million deaths per year . Epidemiological data estimate that, in the immunocompetent host, only ~10% of M. tuberculosis infection progress to active pulmonary disease. The remaining 90% of the infected individuals are asymptomatic, and are generally believed to harbor latent bacilli that can reactivate to cause tuberculous diseases, sometimes decades after the initial infection. Recrudescence of latent bacilli contributes significantly to the incidence of adult tuberculosis , yet the physiological state of latent bacilli and the signals that promote dormancy in the host remain incompletely defined. Understanding the dynamic interaction between host and pathogen during the establishment of persistent M. tuberculosis infection will guide the design of novel treatment for the latently infected population.
An intracellular pathogen, M. tuberculosis must possess a finely tuned signaling network to sense and transduce complex environmental signals, ensuring survival of the bacilli within host cells. Nitric oxide (NO) produced by infected macrophages and relative hypoxia are signals likely to be encountered within tuberculous lesions that are believed, based on in vitro studies, to promote latency by prompting the M. tuberculosis dormancy response. Exposure to these stimuli results in the induction of ~50 M. tuberculosis genes, designated the dormancy regulon, via the two-component regulatory system DosR-DosS (see Table S1 for accession numbers) ,,. Among this set of genes is rv2623, one of eight M. tuberculosis genes annotated as containing the universal stress protein (USP) domain ,. Members of this ancient and conserved family of proteins are found in all forms of life and can be induced by a variety of environmental stresses ,. However, the roles of USP proteins in microbial pathogenesis are incompletely understood.
Interestingly, rv2623 is one of the most strongly induced transcripts of the dormancy regulon ,,. Increased expression of rv2623 was also observed following phagocytosis by macrophages  and in the lungs of chronically infected mice , supporting a functional role during persistent M. tuberculosis infection. The present study reveals that: i) deletion of rv2623 confers hypervirulence on the tubercle bacillus in animal models, suggesting that expression of Rv2623 may be conducive to the establishment of persistence in vivo; ii) overexpression of Rv2623 results in growth retardation of recipient strains in vitro, further supporting a growth-regulatory role; iii) Rv2623 binds ATP; and finally, through mutagenesis study guided by crystallographic analysis of Rv2623 (the first such study for a tandem-domain USP), we show that iv) the growth-regulating attribute of this M. tuberculosis USP is linked to its ATP-binding capacity.
Mycobacterium tuberculosis Rv2623 regulates growth in vitro
An rv2623-deletion mutant of the virulent M. tuberculosis Erdman strain was generated by specialized transduction . The rv2623-specific allelic exchange construct was delivered via recombinant mycobacteriophage phAE159 and transformants were analyzed by Southern blot, confirming replacement of rv2623 with the hyg gene, which confers hygromycin resistance (Figure 1A). Aliquots of a single knockout clone, designated as Δrv2623, were stored at −70°C. Deletion of rv2623 is not likely to affect transcription of neighboring genes, given the sequence-confirmed precise excision of the rv2623 coding region and the gene organization at the rv2623 locus (the downstream rv2624c is transcribed in the direction opposite to that of rv2623) (Figure 1B).
(A) Genomic organization of the rv2623 gene locus. Genes appear as large arrows in their native orientation. Small arrows represent forward and reverse primers used for long range PCR. Sizes of the rv2623 deletion and hyg-insertion are indicated. The location of the radiolabeled probe (black bar) as well as relevant Sph1 sites (S) is indicated as they pertain to the Southern blot. (B) An autoradiograph of the Southern blot shows radiolabeled Sph1 fragments from the wild type (lane 1) and Δrv2623 strain (lane 2). The sizes indicated represent those expected for wild type and the deletion mutant.
Deletion of specific USPs in E. coli results in growth defects in vitro ,,. For example, an E. coli strain deficient for UspA exhibits reduced survival in stationary phase culture . However, the in vitro growth kinetics of Δrv2623 M. tuberculosis in OADC-supplemented Middlebrook 7H9 or minimal Sauton's medium is comparable to that of wildtype Erdman up to 14 days post-inoculation (Figure 2A). We reasoned that a potential growth-regulating attribute of Rv2623 might be masked by functional redundancy among the M. tuberculosis USP homologs. Indeed, partial functional overlap has been demonstrated among the E. coli USPs ,. We therefore examined the effect of overexpression of this USP in the rapidly growing M. smegmatis strain mc2155 . As seen in Figure 2B, constitutive overexpression of M. tuberculosis rv2623 using the multi-copy plasmid pMV261 resulted in growth deficiency of the recipient strain both on solid medium (Middlebrook 7H10 agar) and in the liquid medium-based BD BACTEC 9000MB system. These results strongly suggest that M. tuberculosis Rv2623 regulates mycobacterial growth in vitro.
(A) Growth curves of cultures inoculated (106 CFU/ml) into 7H9+10% OADC+0.05% Tween 80 (top) and in minimal Sauton's media (bottom); Erdman (closed boxes, solid line) and Δrv2623 (open boxes, dashed line) cultures. Error bars represent the standard error of the means; each curve is a combination of at least three independent experiments. (B) Overexpression of Rv2623 in M. smegmatis. The top panel represents serial dilutions (1:10) of the empty vector pMV261-containing negative control strain and Rv2623-overexpressing strain harboring pMV261::rv2623. Diluted stationary phase M. smegmatis culture was spotted (5 µl) onto solid 7H10 media supplemented with 10% OADC and kanamycin (40 µg/mL). Photographs were taken after three days incubation at 37°C. Growth of corresponding strains in liquid medium was assessed based on the time to detection determined using a BD BACTEC 9000MB system (bottom). The various strains were inoculated at 104 CFU/ml in triplicates. Data shown are representative of several independent experiments. ***p<0.001.
Rv2623 regulates mycobacterial growth in vivo
Although USP family proteins are expressed by many bacterial pathogens ,, to date, there has only been one in vivo study, which showed that a Salmonella USP promotes virulence in mice . The observation that Rv2623 modulates mycobacterial growth in vitro prompted us to examine the effect of this USP on the in vivo kinetics of M. tuberculosis infection. Low dose aerosol infection of outbred Hartley guinea pigs with ~30 CFU revealed a clear growth advantage of the Δrv2623 mutant strain relative to wildtype. As early as 20 days post-infection, the number of M. tuberculosis bacilli present in the lungs of Δrv2623-infected guinea pigs was ~10-fold higher (p<0.05) than those infected with wildtype Erdman, and continued to rise, attaining a 15-fold (p<0.001) difference by 60 days post-infection (Figure 3A). Guinea pigs are able to control the growth of Erdman bacilli following the onset of adaptive immunity at ~3 weeks post-infection, as evident by the relatively stable pulmonary bacterial burden beyond the 3 week time point, yet levels of Δrv2623 bacilli continued to increase at a reduced but steady rate resulting in a rapidly progressing infection. Moreover, Δrv2623-infected guinea pigs were moribund at 60 days post-infection, while those challenged with wildtype Erdman remained relatively healthy, providing further evidence that the mutant strain is hypervirulent in this model. Finally, complementation with a single integrated copy of rv2623 expressed from a constitutive mycobacterial promoter (Δrv2623 attB::Phsp60Rv2623) abrogated the growth advantage of the deletion mutant (Figure 3A). Also consistent with the fulminate disease progression displayed by Δrv2623-infected guinea pigs are the more severe pathological changes observed as early as 20 days post-infection in the lungs of these animals, as assessed by histopathological studies, including the semi-quantitative Total Lung Score analysis (Figure 3B and Protocol S1). Overall, the progression of pulmonic lesions was accelerated in Δrv2623-infected animals compared to those infected with wildtype Erdman, accompanied by more extensive necrosis and widespread fibrosis. This increase in lung pathology was also largely reversed in animals infected with the complemented Δrv2623 attB::Phsp60Rv2623 strain (Figure 3B and C). Results of the complementation experiments were further validated using a complemented strain Δrv2623 attB::Prv2623Rv2623, whose expression of the wildtype universal stress protein is driven by the native rv2623 promoter  (Figure 3D and E).
Outbred Hartley guinea pigs given an aerosol challenge of ~30 CFU were assessed for pulmonic bacterial burden (A,D) and the severity of lung pathology (B,E). Closed box, open box, and triangle represent guinea pigs infected with Erdman, in (A,B,D,E), Δrv2623, in (A,B,D,E), and Δrv2623 attB::Phsp60 Rv2623, in (A,B), or Δrv2623 attB::Prv2623 Rv2623, in (D,E). Comparing the wildtype Erdman and the Δrv2623 strains: *p<0.05; **p<0.01; ***p<0.001. Comparing the Δrv2623 and the Δrv2623::complemented strains (Δrv2623 attB::Phsp60 Rv2623 or Δrv2623 attB::Prv2623 Rv2623): +++p<0.001; +p<0.05. (C) Hematoxylin & Eosin-stained lung sections (40 days post infection) from guinea pigs infected with Erdman (top), Δrv2623 (middle), and Δrv2623 attB::Phsp60 Rv2623 (bottom) M. tuberculosis. Error bars represent the standard error of the mean.
In contrast to the result of the guinea pig study, we observed no difference in the kinetics of infection between C57BL/6 mice infected with wildtype M. tuberculosis, Δrv2623, or the attB::Phsp60 Rv2623 complemented strain in a low dose aerogenic model , as assessed by lung bacterial burden (Figure 4A). However, the mouse is a relatively resistant host to M. tuberculosis, particularly in strains such as C57BL/6 ,. In fact, evidence exists that M. tuberculosis triggers an immune response in mice that is in excess of that required for controlling the infection ,. Thus, the hypervirulence phenotype of Δrv2623 observed in the susceptible guinea pig model could have been masked in the C57BL/6 mice. Consequently, we examined the virulence of Δrv2623 in the relatively susceptible C3H/HeJ mouse strain . Indeed, the Δrv2623 mutant was markedly more virulent relative to wildtype Erdman M. tuberculosis following aerogenic infection, as assessed by the mean survival time of C3H/HeJ mice infected with these strains (62 and 25.5 days post infection for Erdman- and Δrv2623-infected mice, respectively, p = 0.0014; Figure 4B). In agreement with the survival data, quantification of tissue bacterial burden revealed a growth advantage for the Rv2623-deficient mutant relative to wildtype M. tuberculosis Erdman (Figure 4C). Manifestation of this hypervirulence phenotype is apparent as early as 3 weeks post-infection, with the lung bacterial burden of mice infected with Δrv2623 M. tuberculosis ~100 fold higher than that in the wildtype-infected animals. As in the guinea pig studies, results of complementation experiments involving the reintroduction of a single copy of wildtype rv2623 into Δrv2623 M.tuberculosis reverses the hypervirulence (Figure 4C) exhibited in the C3H/HeJ model, thus indicating that the observed growth phenotype of the tubercle bacillus deficient for the universal stress protein is rv2623-specific. Finally, survival of Δrv2623-infected mice was also significantly reduced in another susceptible mouse strain, C3HeB/FeJ (Figure S1). Together, the animal studies provide strong evidence that Rv2623 regulates the growth of M. tuberculosis in vivo: in the absence of Rv2623, the tubercle bacillus fails to establish a chronic persistent infection, exhibiting a hypervirulent phenotype.
(A) C57BL/6 mice infected with various strains of M. tuberculosis via the aerosol route with a low dose (~100 CFU) were assessed for lung bacteria burden. Wild type Erdman (closed box, solid line); Δrv2623 (open box, dashed line) and the complemented strain Δrv2623 Phsp60::Rv2623 (triangle, dashed line). (B) Survival curve of C3H/HeJ mice infected via aerosol with 750–1000 CFU. Erdman and Δrv2623-infected mice are represented by solid and dashed lines, respectively. (C) Kinetics of infection, established via aerolization (inoculum: ~1,000 CFU) of wildtype Erdman (dark), Δrv2623 (dark grey), and the complemented strain Δrv2623 Phsp60::Rv2623 (light grey), as assessed by lung bacterial burden. **p<0.01; ***p<0.001.
Effects of environmental stress on growth of M. tuberculosis Δrv2623 in vitro
Although the functions of universal stress proteins have yet to be completely defined, there is evidence that many USPs play differential roles in protecting microbes against various environmental stresses . Therefore, the hypervirulence of Δrv2623 in guinea pigs and susceptible mice is intriguing; if Rv2623 provides M. tuberculosis protection against stress, it might be expected that the Rv2623-deficient mutant would be attenuated in vivo. The growth kinetics and survival of the Δrv2623 strain was examined under various stress conditions, including those likely to be present during M. tuberculosis infection. These included oxidative stress (superoxide anion, O2−), DNA damage (UV irradiation, mitomycin C), heat shock (53°C), and acidic culture (pH 4.0). The use of streptonigrin, an antibiotic whose toxicity correlates with levels of free iron, was based on the observation that the intracellular environment of macrophages can induce a iron-scavenging response in mycobacteria , perhaps as a means of maintaining adequate levels of this important growth factor, and that an E. coli USP was shown to regulate iron uptake . The results showed that the mutant strain was no more susceptible to growth inhibition than was wild type Erdman under all of the stress conditions tested (Figure S2). These results support the notion that it is unlikely that M. tuberculosis Rv2623 is essential for resistance to stresses encountered in the host, which is consistent with the observed in vivo hypervirulence phenotype of Δrv2623.
M. tuberculosis Rv2623 is a nucleotide-binding protein
We began a biochemical characterization of Rv2623 in order to gain insight into the relationship between the molecular structure/function of this USP and it's growth-regulatory properties. M. tuberculosis Rv2623 was expressed in E. coli and purified to homogeneity for biochemical studies. SDS-PAGE analysis of affinity-purified His6-Rv2623 revealed a single band that approximates the predicted molecular mass of ~31.6 kDa, which was identified by immunoblotting as Rv2623 (Figure S3). Gel filtration analysis of native His6-Rv2623 revealed that the purified protein exists primarily as a single species with an apparent molecular mass of 61±1 kDa; suggesting that Rv2623 is a dimer under native conditions (Figure S3), an observation that was later confirmed using nano electrospray ionization (nano ESI) mass spectrometry (data not shown).
The nucleotide-binding capacity of a subset of USPs was discovered following the observation that MJ0577, a single-domain USP from Methanococcus jannaschii, co-purifies and co-crystallizes with ATP . On the basis of structures of ATP-binding and non-ATP-binding USPs, a G-2X-G-9X-G(S/T) motif was suggested to be essential for the binding of ATP . The presence of this motif in each of the two tandem USP domains of Rv2623  raised the possibility that this protein possesses ATP binding activity. An HPLC-based examination of supernatants from boiled samples of His6-Rv2623 demonstrated that His6-Rv2623 co-purifies with both ATP and ADP (Figure 5). Analysis of E. coli-expressed Rv2623 using nano ESI mass spectrometry also demonstrated that an ATP-saturated form of dimeric Rv2623 (composed of 2 bound ATP molecules per monomer) constitutes at least half of the purified sample (data not shown). Measurement of the binding stoichiometry, which comprised HPLC-based quantification of adenine nucleotides from the boiled supernatant and spectral analysis of heat denatured Rv2623 following reconstitution in 6 M guanidine-HCl, yields 1.4±0.2 nucleotide equivalents/monomer with an overall content of 86±4% ATP (14±4% ADP). Thus, Rv2623 binds endogenous adenine nucleotides in E. coli, and the association is sufficiently tight that nearly 75% of the nucleotide binding sites are occupied upon purification. Indeed, nucleotide did not completely dissociate from the protein following an extensive, two-week dialysis with multiple changes against nucleotide-free buffer (approximately 0.3 nucleotide equivalents per monomer remain). It is conceivable that the presence of ADP is the consequence of an Rv2623-associated ATP activity and this putative ATPase function is currently under investigation.
High Performance Liquid Chromatography (HPLC) analysis of endogenously bound nucleotides from purified His6-Rv2623. Nucleotides species were identified based on their specific retention times on the Mono Q HR 5/5 column, represented by peaks in absorbance at 260 nm, which correspond to that of nucleotide standards (not shown). Bound nucleotides were extracted by boiling, and separated and quantified from a standard curve that relates absorbance peak area to the known amount of ATP injected onto the column (inset).
The crystal structure of M. tuberculosis Rv2623: Dimer assembly and ATP-binding capacity
To examine the biochemical mechanisms responsible for Rv2623 function, we determined the crystal structure of wild-type Rv2623 at a resolution of 2.9 Å. The structure reveals a compact, 2-fold symmetric dimer. Each monomer is composed of tandem USP domains [residues 6–154 (domain 1), 155–294 (domain2)] that share 26% sequence identity and significant structural homology (residues 6–154 and 155–294 comprise domains 1 and 2, respectively; interdomain rms = 2.04 Å for 140 equivalent Cα's). Individual domains, which consist of a twisted, five-stranded, parallel β sheet flanked by four α helices, unite through an antiparallel, cross-strand (β5–β10) interaction that produces a central dyad axis between β5/β10 and a continuous, ten-stranded, mixed β sheet in the complete monomer. Each domain possesses a pair of conserved βαβ motifs (domain 1: β1-L1-α1- β2, β4-L2-α4-β5; domain 2: β6-L3-α5-β7, β9-L4-α8-β10) that encompass four loops (designated L1–L4) responsible for ATP recognition (Figure 6A and C). A “U-shaped” ATP molecule that lies within a cleft near the monomer surface is stabilized by 1) a cluster of hydrophobic residues (I14, V41, H42, V116/132/261/277/281, L136, A175) that forge the adenine/ribose-binding scaffold, 2) a pair of conserved L1/L3 aspartates (D15-L1/D167-L3), and 3) small phosphoryl/ribosyl-binding residues within the G-2X-G-9X-G (S/T) motifs that comprise L2/L4 (G120/265/267/268 and S131/276) (Figures 6A,C and 7A). Dimerization of Rv2623 occurs along a 2-fold axis orthogonal to the intramonomer dyad and juxtaposes ATP binding pockets from opposing monomers (Figure 6B).
(A,B) A ribbon representation of the Rv2623 monomer (A) and dimer (B) with bound ATP (sticks) and Mg2+ (chocolate spheres). The three, mutually perpendicular pseudo-two-fold axes of the dimer are represented by lines with double arrows (along x, y) and a central ellipse (along z). The atoms of the bound ATP are colored cyan (carbon), red (oxygen), blue (nitrogen), and orange (phosphorus) in (A) and (B). (C) A structure-based sequence alignment of Rv2623, the N631 subfamily consensus, Methanococcus jannaschii protein 0577 (MJ0577), and domains 1 and 2 of Rv2623. Invariant residues in the alignment (>85% conserved in N631) are shaded in bold red and similarities are boxed in blue but left unshaded. Regions with consensus ATP binding motifs comprising L1/L2 (domain 1) and L3/L4 (domain 2) are colored dark violet and smudge, respectively. The positions of the mutated amino acids (D15, G117) are indicated in green. The structure-based sequence alignment was produced using ESPript and the structural representations were produced using PyMOL.
(A) A ribbon and stick representation of the mutation sites within the ATP binding pocket of domain 1. Mg2+ is shown as a green sphere; dotted lines indicate hydrogen-bonding contacts; atoms that constitute ATP are colored cyan (carbon), red (oxygen), blue (nitrogen), and orange (phosphorus). (B) The ATP-binding capacity of mutant Rv2623 was compared to that of wild type protein following nucleotide extraction and HPLC. Data presented are derived from analysis of three independent protein preparations. ATP binding capacity is expressed as: [(the amount of ATP bound in mutant)/(the amount of ATP bound by wild type Rv2623) * 100]. (C) Thermal denaturation curves of two individual protein preparations of Rv2623WT (WT-1, WT-2) as compared to Rv2623G117A (G117A) and Rv2623D15E (D15E). The data is expressed as the negative first-derivative of the fluorescence intensity as a function of temperature.
Phylogenomic analysis places Rv2623 in a Uniprot/TrEMBL family (Q5YVE7) of 370 tandem-domain USPs, and a 113-member subfamily (N631) that consists almost exclusively of actinobacterial representatives (Text S1). Structure-based sequence alignments of both Rv2623 domains with the N631 consensus suggest that domain 2, which exhibits significantly higher conservation than domain 1 across global and ATP-binding subfamily consensus sequences, represents the ancestral domain among ATP-binding USPs with tandem-type architectures. Interestingly, the domain fold and interdomain organization observed for Rv2623 is broadly conserved: these features are shared among single domain USP structures, both monomeric and dimeric, that are presently represented within the PDB. As this manuscript was under preparation, a second, lower resolution (3.2 Å) crystal form of Rv2623 (PDB ID 2JAX) was released for public access. This structure is nearly identical to the present model as demonstrated by superposition over the ATP ligands and the monomeric and dimeric forms (rmsds are 0.57 and 0.81 for 258 and 517 matched CA's, respectively). The differences localize primarily to flexible loop regions (residues 44–58, 150–159) that, while disordered in 2JAX, are partially stabilized in the present structure by local crystal contacts.
To gain insight into the ATP-binding mode(s) exhibited by Rv2623, the structural features of the ATP-binding pocket of domains 1/2 were compared to the monomer fold of the representative ATP-binding USP, MJ0577 (PDBID 1MJH) . Overlay of these structures reveals very considerable similarity for the residues that form the binding pockets and the associated ATP molecules, for which the triphosphoryl moieties assume virtually indistinguishable conformations. Relatively subtle structural and phylogenetic differences that exist between the ATP-binding pockets might nevertheless confer divergent binding and/or regulatory properties to the tandem domains.
Generation and analysis of ATP-binding–deficient Rv2623 mutants
To explore the relationship between the putative ATP-dependent biochemical function of Rv2623 and the growth-regulating attribute of Rv2623, we engineered mutations within the L1 (D15E) and β4 (G117A) conserved residues that were predicted, on the basis of the crystal structure, to disrupt ATP recognition (Figure 7A). In silico replacement of the β4 G117 side chain hydrogen with a methyl group suggested that any residue larger than glycine at this position is likely to perturb both of the conserved loop regions in contact with the nucleotide. Similarly, extension of the D15 side chain to glutamate was also predicted to interfere with the ATP-binding conformation (Figure 7A). HPLC analysis of nucleotides extracted from Rv2623D15E and Rv2623G117A revealed that the mutant proteins are indeed deficient in ATP-binding, exhibiting ~34% (p<0.001) and ~29% (p = 0.0018) of the amount of ATP bound by wild-type Rv2623, respectively (Figure 7B). Likewise, following an overnight incubation with [α-33P] ATP at 4°C, the amount of protein-bound radioactivity, which represented a very small fraction of the total ATP binding sites, was significantly less for the mutant proteins than wild-type Rv2623 (data not shown). Importantly, thermal denaturation profiles of wild-type Rv2623, Rv2623D15E and Rv2623G117A demonstrated virtually identical Tm values, implying that the native Rv2623 fold was not destabilized by these mutations (Figure 7C). It is therefore likely that the D15E and G117A mutations produced local structural changes in the ATP binding loops that contributed directly to the reduced levels of bound ATP in comparing to wild-type Rv2623.
The growth-regulating property of M. tuberculosis Rv2623 is dependent on its ability to bind ATP
We next sought to probe the relationship between the nucleotide-binding capacity and growth regulation by this mycobacterial USP. Both the D15E and G117A mutant proteins were overexpressed in M. smegmatis mc2155 at levels equivalent to that of wild-type Rv2623 (Figure S4). Results of these studies demonstrated that while overexpression of wildtype Rv2623 retards the growth of the recipient strain relative to cells transformed with vector alone, growth of the strains overexpressing ATP-binding-deficient mutant Rv2623 are only minimally affected by overexpression as assessed by spotting serial dilutions of the cultures of the appropriate strains onto solid Middlebrook 7H10 agar (data not shown) as well as by monitoring the time to detection using the BD BACTEC 9000MB system (Figure 8A). The distinct effects exhibited by the wild type and the G117A and D15E mutants defective in ATP binding suggests a direct correlation between growth attenuation and ATP binding (Figure 7B). To examine whether the effects of overexpression of Rv2623 on M. smegmatis are operative in virulent M. tuberculosis, the growth kinetics of the Erdman strain overexpressing wildtype Rv2623, as well as the Rv2623G117A and the Rv2623D15E mutant proteins, were evaluated in vitro using the BACTEC 9000MB system (Figure 8B). As in the M. smegmatis studies, the results show that overexpression of Rv2623 in M. tuberculosis results in marked retardation of growth. Furthermore, this growth attenuation is not observed in M. tuberculosis strains overexpressing the G117A or the D15E mutant Rv2623 (Figure 8B). Taken together, these data strongly suggest that the ability of Rv2623 to regulate growth of M. smegmatis and M. tuberculosis is dependent on an ATP-dependent process.
Growth of M. smegmatis (A) or M. tuberculosis (B) overexpressing wild type or mutant Rv2623 inoculated at 104, 105 CFU/ml into a BD BACTEC 9000MB system; the time to detection of triplicate cultures is indicated. While overexpression of wildtype Rv2623 attenuates mycobacterial growth, overexpression of either ATP-binding-deficient Rv2623 mutant (Rv2623G117A or Rv2623D15E) significantly shifts the time to detection back towards that of the pMV261 vector control strain. ***p<0.001.
Despite the significance of M. tuberculosis latency in pathogenesis, the mechanisms by which the tubercle bacillus establishes and maintains the latent state remain incompletely defined. Identification of M. tuberculosis genes that are induced by hypoxia and nitric oxide (NO) in vitro provides a framework for understanding the physiology of dormant bacilli ,,. These genes, referred to as the dormancy regulon, are transcriptionally regulated by the mycobacterial two-component system DosR-DosS under hypoxic conditions . Indeed, it has been shown that both the cognate sensor histidine kinase DosS (a member of the dormancy regulon) as well as an “orphan” kinase, DosT, functioning as redox and hypoxia sensors, respectively; can regulate DosR activity, and that O2, NO, and CO can modulate the activity of these two kinases via interaction with a haem prosthetic group ,,,,. The biological significance of the dormancy regulon has been underscored by in vitro studies of dosR mutants of BCG and M. tuberculosis, which demonstrated the requirement of this transcription factor for survival under hypoxic conditions ,. Further, upregulation of the expression of certain dormancy regulon genes have been implicated in tuberculosis transmission as well as the virulence of the epidemiologically important W-Beijing lineage of M. tuberculosis ,.
There are eight genes in the M. tuberculosis genome annotated to encode USP family proteins . We studied the M. tuberculosis USP rv2623 because it is one of the most highly induced genes in the dormancy regulon when bacilli are subjected to hypoxia and nitrosative stress ,,,,. More important, rv2623 was also shown to be up-regulated when the tubercle bacillus is internalized by human and mouse macrophages , as well as in the lungs of mice with persistent M. tuberculosis infection . These latter observations suggest that the induction of rv2623 may have biological relevance. The precise mechanisms by which Rv2623 expression is regulated remain to be defined. Recent transcriptional analysis of Rv2623, while confirming the essentiality of the two 18 bp palindromic DosR-binding motifs that are present in the promoter region of this gene  for induction of Rv2623 under low oxygen conditions, also demonstrated the presence of additional regulatory elements within the rv2623 5′-untranslated region . These results suggest that the regulation of Rv2623 is likely complex.
The M. tuberculosis dormancy response features a dramatic decrease in metabolic activity, resulting in a rapid decrease in bacterial replication . Therefore, it is possible that deficiency in certain members of the dormancy regulon could result in inability of the tubercle bacillus to enter a latent state in the infected host, leading to unrestrained growth and thus, hypervirulence. Indeed, specific members of the M. tuberculosis dormancy regulon whose insufficiency results in a hypervirulence phenotype have been reported ,. In certain experimental tuberculosis animal models, DosR deficiency has been associated with a hypervirulence phenotype . However, DosR deficiency has also been reported to have no effect on M. tuberculosis virulence or to lead to an attenuated phenotype ,. The discrepancies regarding M. tuberculosis virulence in these DosR studies are unclear, but could be due to differences in experimental systems employed. Insufficiency of the chaperone-like α-crystallin encoded by M. tuberculosis hspX (acr) has also been shown to be associated with hypervirulence in a BALB/c mouse model of tuberculosis .
In the present study, an rv2623 knockout mutant of virulent M. tuberculosis Erdman fails to establish a chronic persistent infection, displaying a hypervirulent phenotype in susceptible hosts, as assessed by lung bacterial burden, histopathology, and mortality. Results of the complementation studies indicate that the phenotype is Rv2623-specific. This growth-regulating phenomenon is echoed by the observation that ectopic overexpression of Rv2623 results in attenuation of mycobacterial growth. Together, these data strongly suggest that the M. tuberculosis USP Rv2623 has the ability to regulate growth in vitro and in vivo, and is required for the establishment of a persistent infection. Intriguingly, ectopic overexpression of HspX by the same means employed by our study also resulted in an attenuated growth phenotype compared with LacZ-overexpressing controls , suggesting that these two tightly co-regulated “stress” proteins might have similar growth-regulatory roles during dormancy.
Bioinformatic and experimental evidence suggest that nucleotide-binding capacity represents a discriminating biochemical feature that facilitates USP protein classification. Putative functional differences between USPs are implied by their assignment to two subclasses: one whose members do not bind ATP and another whose constituents bind and hydrolyze adenine nucleotide substrates ,,,,. A structural comparison between the prototypic members of the two subclasses, the non-ATP-binding UspA homolog (H. influenzae, PDB ID 1JMV) and the ATP-binding USP, MJ0577 (M. jannaschii, PDB ID 1MJH) revealed that while both proteins exhibit a similar fold, conserved glycine residues within the ATP-binding loop of the latter are substituted with bulky amino acids that preclude ATP recognition in the former ,. The unique nucleotide-binding pocket of this protein family is structurally distinct from those commonly encountered in ATP-binding proteins ,,. Specific roles for USP family proteins are just beginning to be characterized, and early functional classifications have been informed by ATP-binding capacity . While the non-ATP-binding UspA homologs appear to play diverse roles in promoting survival under a variety of environmental insults ,,,, the function(s) of ATP-binding type USPs remain unclear . Based on in silico analyses, Florczyk et al. classified Rv2623 as belonging to a novel class of ATPases , although formal evidence for ATP binding by this protein has not been reported.
This study has provided substantial biochemical and structural evidence that M. tuberculosis Rv2623 is a bona fide nucleotide-binding USP: i) E. coli-expressed His6-Rv2623 co-purifies with tightly bound ATP and ADP; ii) analysis of the 2.9 Å -resolution Rv2623 crystal structure, the first molecular model of a tandem-type USP, reveals four ATP-bound nucleotide-binding pockets; and iii) point mutations (D15E, G117A) within the conserved L1 (D15E) and β4 (G117A) regions of the structure, which were predicted to disrupt nucleotide-binding, yielded mutant proteins with attenuated ATP-binding capacity. Furthermore, given that the attenuated growth phenotype caused by overexpression of Rv2623 could be abrogated by mutations that interfere with the binding of this protein to its nucleotide substrate, it is likely that the mycobacterial growth-regulatory faculty of Rv2623 is mediated by an ATP-dependent function.
In summary, the results of the present study have revealed that the M. tuberculosis USP Rv2623 has the ability to regulate mycobacterial growth, as evident by the in vivo hypervirulence phenotype of Δrv2623, which fails to establish a persistent infection in susceptible hosts, as well as the growth attenuation observed in mycobacteria overexpressing this USP. Thus, M. tuberculosis Rv2623 may serve the function of promoting mycobacterial transition into latency. The latent state allows persistence in infected individuals of tubercle bacilli that can reactivate to cause active disease and to disseminate when the immune status of the host is compromised. As a result, Rv2623 may contribute significantly to the propagation of the tubercle bacillus in the human host and the difficulties in eradicating tuberculosis. Mechanistically, results of the mutagenesis studies have shown that Rv2623 regulates growth through ATP-dependent function. Clearly, much remains to be learned regarding how the ATP-dependent function of Rv2623 contributes to growth regulation. It has been proposed that a nucleotide-binding USP from M. jannaschii, MJ0577, whose ability to hydrolyze ATP is dependent on interaction with factor(s) present in the cell extract of this hyperthermophile , functions as a molecular switch much like the Ras protein family, whose GTP hydrolysis ability is modulated by interaction with a number of regulatory proteins ,,. The fact that E. coli-expressed Rv2623 co-purifies with ADP as well as ATP suggests the possibility that this mycobacterial USP, like MJ0577, is capable of ATP hydrolysis. It is therefore conceivable that M. tuberculosis Rv2623, as a component of the yet-to-be defined dormancy signaling pathway(s), functions as a molecular switch by virtue of its ATP-binding and putative ATP-hydrolyzing properties, to mediate the establishment of tuberculous latency. Experiments designed to investigate the potential ATP-hydrolyzing activity of Rv2623 are currently underway. Recent identification of the DosR-dependent dormancy regulon ,,; the DosR-independent enduring hypoxic response, which involves over 200 mycobacterial genes, including those known to regulate bacteriostasis ; and the demonstration that M. tuberculosis redox and hypoxia sensors can interact with multiple ligands that differentially modulate the activity of these important kinases ,,,,, predict a complex regulatory network for tuberculous latency. Elucidation of how ATP-binding and, potentially, the hydrolysis of ATP by Rv2623 regulate M. tuberculosis dormancy-signaling pathways will likely illuminate the mechanisms by which the tubercle bacillus establishes persistence.
Materials and Methods
Bacterial strains and culture conditions
Liquid cultures of M. tuberculosis and M. smegmatis strains were grown in Middlebrook 7H9 medium (Becton Dickinson, Sparks, MD) supplemented with 0.2% glycerol (Sigma, St. Louis, MO), 0.05% Tween 80 (Sigma, St. Louis, MO), and 10% oleic acid-albumin-dextrose-catalase (OADC) enrichment media (Becton Dickinson, Sparks, MD). For the determination of the number of colony forming units (CFU) and examination of growth on solid media, Middlebrook 7H10 agar medium (Becton Dickinson) supplemented with 0.5% glycerol and 10% OADC was used. The Δrv2623 mutant strain was maintained in media supplemented with 50 µg/ml hygromycin B (Roche) and cultures of complemented, Rv2623-overexpressing strains contained kanamycin (40 µg/ml). Growth was also examined in minimal Sauton's medium (4 g asparagine, 2 g sodium citrate, 0.5 g K2HPO4·3H2O, 0.5 g MgSO4·7H2O, 0.05 g ferric ammonium citrate, 60 g glycerol in 1 L of H2O supplemented with 0.05% Tween80 and antibiotics as required). For some experiments, growth was monitored by the BD BACTEC 9000 system (Becton Dicinson). Stationary phase M. tuberculosis or M. smegmatis cultures were inoculated in triplicates (105 or 104 CFU) into vials of liquid medium containing a sensor compound that fluoresces upon depletion of oxygen as a result of bacterial growth. The time to detection reflects the rate of bacterial growth.
Generation of Δrv2623 mutant strain, complemented and overexpression strains
Replacement of genomic rv2623 was performed by allelic exchange using a specialized transducing phage delivery system as previously described . Transformants were analyzed by PCR and Southern blot to confirm replacement of rv2623 with a hygromycin cassette, yielding Δrv2623. A complemented strain was generated as described previously  by transformation of Δrv2623 with a plasmid vector that integrates at the attB site and bears the rv2623 coding sequence under transcriptional control of the constitutive hps60 promoter or the endogenous rv2623 promoter , yielding Δrv2623 attB::Phsp60 Rv2623 and Δrv2623 attB::Prv2623 Rv2623; respectively. The M.tuberculosis hsp60 promoter fusion was also used to overexpress Rv2623 via subcloning of this region into pMV261, a non-integrating variant of pMV361 to yield pMV261::rv2623, which is self-replicating at 3–5 copies/cell  (Text S1).
Response of Δrv2623 mutant to stress
Log phase cultures (OD600 = 0.8–1.0) of Erdman and Δrv2623 were diluted 1:10 into Sauton's media containing various stress-inducing chemical agents (phenazine methosulfate, streptonigrin and mitomycin C) at the indicated concentrations or for acid stress into 7H9+10% OADC+0.05% Tween 80 (pH = 4.0) and grown at 37°C for several days. Growth was monitored by OD600. Survival of these strains following heat shock was compared after a shift of log phase cultures from 37°C to 53°C and determining the number of CFU/ml at various time points thereafter. For irradiation with UV light, cells were plated onto solid 7H10 agar supplemented with 0.05% Tween80 and exposed to increasing amounts of UV energy (UV Stratalinker 1800, Stratagene). Surviving cells were enumerated and the data are expressed as percent survival as compared to unexposed controls. In addition, cells were treated with the indicated concentrations of mitomycin C for a period of 1 hour followed by determination of surviving CFU/ml. See Figure S2 for details.
Outbred Hartley guinea pigs (~500 g body weight) (Charles River Laboratories, North Wilmington, MA) were given a low dose of M. tuberculosis using a Madison chamber aerosol generation device calibrated to deliver ~30 CFU . Guinea pigs were sacrificed (n = 5) at 20, 40, and 60 days post infection for histological analysis and determination of organ bacterial burden. Histological analysis of infected tissues was performed by scoring individual tissue sections based on criteria described in Protocol S1.
For the murine tuberculosis model, six-to-eight-week-old mice (Jackson Laboratories, Bar Harbor, Maine) were infected with M. tuberculosis via aerosol (In-Tox Products, Albuquerque, NM) as previously described  with ~100 CFU (C57BL/6) or 750–1000 CFU (C3H/HeJ, C3HeB/FeJ). For CFU determination, mice were sacrificed (n = 3) at the times indicated and portions of the lung, liver and spleen were homogenized in PBS+0.05% Tween 80, diluted, and plated onto solid 7H10 media.
Cloning, expression and purification of Rv2623
The coding sequence of rv2623 was PCR-amplified from M. tuberculosis Erdman genomic DNA and subcloned into the expression vector pQE80L (Qiagen, Inc.), which encodes an N-terminal His6-tag, producing the plasmid pQE-rv2623 (Text S1). Expression was carried out following isopropyl beta-D-thiogalactoside (IPTG) induction of BL21 E. coli transformed with pQE-rv2623. His6-Rv2623 was then affinity-purified to homogeneity from BL21 cell lysates using Ni-NTA agarose (Qiagen, Inc.) according to the manufacturer's instructions. For crystallization, purified Rv2623 was concentrated to 12 mg/ml using a 10 kDa Molecular Weight Cut Off (MWCO) centrifugal filter (Amicon), and frozen at −80°C.
Gel filtration chromatography
A Superdex 200 10/300 GL column (GE Healthcare Life Sciences) was equilibrated with Rv2623 dialysis buffer (Text S1) and calibrated using the following molecular mass standards: aldolase (158 kDa), bovine serum albumin (67 kDa), ovalbumin (43 kDa), chymotrypsinogen A (25 kDa) as described in the Amersham Pharmacia technical notes (GE Healthcare Life Sciences). The flow rate was set to 0.15 ml/min and elution of the protein was monitored at 280 nm.
High performance liquid chromatography (HPLC)
Nucleotides were extracted from purified Rv2623 by boiling. Samples were then loaded onto an analytical, anion-exchange HPLC column (AX300, Eprogen Inc. or Mono Q HR 5/5, GE Healthcare). Samples were eluted isocratically using NaH2PO4, pH 5.5 (AX300) or using a ammonium phosphate pH 7.0 (0.02–1.0 M) step gradient (Mono Q) (Text S1). Nucleotides were identified on the basis of retention time relative to nucleotide standards, and quantified by peak area.
Stoichiometry of nucleotide binding
Following Ni affinity chromatography, His6-Rv2623 samples for stoichiometry measurements (500 µl, 8–120 µM protein) were attained by subjecting the Ni-purified fractions to rapid desalting over a HiPrep Desalting 26/10 column (GE Healthcare) equilibrated with 50 mM NaCl, 2 mM MgCl2, 10% glycerol, 20 mM HEPES pH 8.0 and/or an additional purification using a MonoQ 10/100 GL column (GE Healthcare) equilibrated with the desalting buffer and eluted with a linear salt gradient ranging from 50 mM to 250 mM NaCl. Amicon centrifugal filtration concentrators (MWCO = 30 kDa) were employed for final concentration steps prior to analysis. Bound nucleotide was then released by boiling and quantified by HPLC (under the Mono Q HR 5/5 conditions) according to the methodology described above and Text S1. The heat-precipitated protein was subsequently reconstituted in 6 M guanidine HCl and its concentration was determined by spectrophotometric measurement of the protein peak at 280 nM and a molar extinction coefficient for Rv2623 at 280 nm (54,640/Mcm). This extinction coefficient was determined using a 6 M GuHCl-reconstituted (nucleotide-free) sample of Rv2623 that had been subject to quantitative amino acid analysis at the Yale Keck Facility. The nucleotide binding stoichiometry was calculated as the molar ratio of the released nucleotide to protein.
Site-directed mutagenesis of Rv2623
Single amino acid substitutions were incorporated into the rv2623 coding region contained in appropriate expression vectors by mismatched PCR priming (Text S1). Individual PCR reactions were performed using either pMV261::rv2623 or pQE-rv2623 plasmid templates for mycobacterial overexpression and protein purification, respectively. Then the pMV261:: rv2623 mutants expression vector DNA was used to transformed into M.smegamatis mc2155 and the DNA of pQE-rv2623 mutants was transformed into E.coli BL21(DE3). Thermal denaturation curves were determined for purified wild type and mutant Rv2623 using an IQ5 Real Time PCR Detection System (Bio-Rad) following incubation with SYPRO Orange protein gel stain (Invitrogen) (Text S1).
Crystallization and data collection
ATP and MgCl2 were added to final concentrations of 0.8 mM and 1.8 mM, respectively, in the protein sample prior to crystallization by sitting-drop vapor-diffusion at 4°C (Text S1). Diffraction data were collected at the National Synchrotron Light Source beamline X29A on an ADSC Q315 detector through the Macromolecular Crystallography Research Resource (PXRR) mail-in crystallography program. Data processing and scaling was performed with the HKL2000 suite.
Structure determination and refinement
The structure of M. tuberculosis Rv2623, which contains two USP domains in tandem, and whose first domain shares 25% sequence identity with the USP M. tuberculosis Rv1636, was solved using the molecular replacement method and a CHAINSAW-generated search model consisting of the Rv1636 dimer (PDB ID 1TQ8 chains A, B), using a 2.9 Å, C2221 dataset (a = 173, b = 241.5, c = 241.7). A starting polyalanine model (R/Rfree = .56/.57) of four dimers was subject to four refinement cycles, each consisting of multi-domain rigid-body refinement in Molrep, a single cycle of restrained MLF refinement in Refmac5 (to obtain input FOMs for DM), 20 cycles of phase extension in DM (as above), and manual rebuilding of the polyalanine backbone in Coot. As R-factors converged (R/Rfree = .40/.42), ~80% of the side chains were positioned and the Rv2623 dimers were further rebuilt and refined (R/Rfree = .31/.33) in CNS using high NCS restraint weights (400 kcal/mol) with rigid-body, energy minimization, grouped isotropic B factor, and simulated annealing refinement protocols. ATP and Mg2+ were built within composite omit density (calculated in CNS) during the final rebuilding/refinement cycles conducted with relaxed NCS restraints in Arp-waters and Refmac5, yielding final R/Rfree = 24.5/26.5. SigmaA-weighted difference maps calculated with the refined model reveal weak, fragmented density for a pseudotranslated copy of the Rv2623 dimer whose corresponding NCS translational vector (uvw = .500, .012, .494) appears in the native patterson at 7.7% of the origin peak height. Data collection and refinement statistics are summarized in Protocol S1. The coordinates of M. tuberculosis Rv2623 have been submitted to the protein databank (PBDID 3CIS).
Survival curve of C3HeB/FeJ mice infected with wildtype of Δrv2623M. tuberculosis Erdman. C3HeB/FeJ mice were infected via aerosol with a high dose 750–1000 CFU of either Erdman or Δrv2623M. tuberculosis (n = 6). The median survival times for Erdman- and Δrv2623-infected mice are 56 and 27 days post infection, respectively (p = 0.0037). Statistical significance was determined using GraphPad Prism version 4.0c for Mac, GraphPad Software, San Diego California, USA, www.graphpad.com; ** indicates p<0.01.
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Characterization of the response of Δrv2623 to environmental stress. Optical density(OD600) was used to monitor the growth of Erdman (solid line) and Δrv2623 (dashed line) cultures in the presence of (A) superoxide anion (O2−) following 1:10 dilution of log-phase culture into fresh Sauton's media containing 10 µM (triangles) or 20 µM (circles) phenazine methosulfate (PMS) or (B) the Fe3+-dependent quinone antibiotic streptonigrin at concentrations of 0.01 µM (triangles) or 0.1 µM (circles). For (A,B): Untreated control cultures are represented by square symbols. (C) Sensitivity to ultraviolet irradiation was examined by exposing cells on solid media to the indicated energies and determining the number of surviving bacilli. Data are expressed as a percent survival relative to unexposed control plates for each strain. (D) The number of surviving CFU/ml was determined following treatment of log phase culture with increasing amounts of mitomycin C for 1 hour at 37°C. (E) Similarly, the number of surviving bacilli was determined following incubation at 53°C for the indicated times. (F) Log phase cultures were diluted 1:10 into media at pH 7.0 or pH 4.0 and grown for several days and the number of surviving CFU/ml was monitored. Error bars represent the standard error of the means; each is a combination of at least two independent experiments performed in triplicate.
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Purification and gel filtration profile of His6-Rv2623. (A) Expression and purification of His6-Rv2623. Lane 1: Uninduced pQE-rv2623E.coli cell lysate carrying expression construct pQE-rv2623; Lane 2: Induced pQE-rv2623E.coli cell lysate; Lane 3 and Lane 4: Purified His6-Rv2623: 0.3 mg and 3 mg, respectively; Lane 5: Western blot probed with anti-RGS-His antibody. Arrow indicates His6-Rv2623 (32 kDa). (B) Gel filtration profile of purified His6-Rv2623 eluted from a Superdex 200 10/300 GL column. Molecular weight (61 kDa) was determined based on the specific retention time corresponding to the His6-Rv2623 peak compared to molecular weight standards. The predicted molecular weight of Rv2623 is 32 kDa and purified protein is representative of a dimer of Rv2623.
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Relative expression level of wildtype(WT) and mutant Rv2623 in M. smegmatis. Strains of M. smegmatis that carried pMV261::rv2623WT, pMV261::rv2623G117A, and pMV261::rv2623D15E overexpression plasmids were grown to late log phase in 7H9 media supplemented with kanamycin (40 µg/ml). The OD600 of the cultures was measured and used to estimate the number of CFU/ml (conversion factor: OD600 1 = 3×108 CFU/ml). An equivalent number of cells for each strain were boiled for 5 minutes in denaturing sample loading buffer and separated by SDS-PAGE. (A) Western blotting techniques were used to detect Rv2623 in the total protein extract from these strains using monoclonal anti-Rv2623. (B) The immunoblot was scanned and analyzed with ImageQuant densitometry software (Molecular Dynamics). As different amounts of cells were boiled in different experiments, the relative intensity of the bands is expressed as a percent of the signal corresponding to Rv2623WT overexpression so that multiple experiments could be combined. The error bars represent the standard deviation and the percent of wild type Rv2623 expression is indicated above the bars. The data indicates that mutant Rv2623 overexpressed at similar levels compared to WT Rv2623.
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Semiquantitative scoring system for immunopathology of guinea pig tissues; and Crystallography: Summary of data collection and refinement statistics.
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Gene list and accession numbers.
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Supporting materials and methods.
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Sandra Alvarez, Lee Kozakiewicz, Rachel Pinto, and Eleanor Russell are gratefully acknowledged for their contributions to this work. We thank Jordan Kriakov, Morad Hassani, and Hideaki Ohno for their contribution of essential biological reagents. We are grateful to Dr. Eddie Nieves for many helpful discussions regarding the nano-ESI analysis of Rv2623. We also thank Dr. Annie Heroux for collecting the crystallographic data following submission to the PXRR Mail-in Crystallography Program at Brookhaven National Laboratory. Crystallographic data for this study were measured at beamlines X25/X29 of the National Synchrotron Light Source.
Conceived and designed the experiments: JED KM PB MS AAI IMO SCA TSL JC. Performed the experiments: JED KM PB MS JL HBO RB MS AAI. Analyzed the data: JED KM PB MS JL HBO RB GZ JMT AAI IMO SCA TSL JC. Contributed reagents/materials/analysis tools: PB MS JL GZ JMT AAI IMO SCA TSL JC. Wrote the paper: JED KM PB SCA TSL JC.
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