- Research article
- Open Access
Independent inactivation of arginine decarboxylase genes by nonsense and missense mutations led to pseudogene formation in Chlamydia trachomatisserovar L2 and D strains
© Giles et al; licensee BioMed Central Ltd. 2009
Received: 18 March 2009
Accepted: 16 July 2009
Published: 16 July 2009
Chlamydia have reduced genomes that reflect their obligately parasitic lifestyle. Despite their different tissue tropisms, chlamydial strains share a large number of common genes and have few recognized pseudogenes, indicating genomic stability. All of the Chlamydiaceae have homologs of the aaxABC gene cluster that encodes a functional arginine:agmatine exchange system in Chlamydia (Chlamydophila)pneumoniae. However, Chlamydia trachomatis serovar L2 strains have a nonsense mutation in their aaxB genes, and C. trachomatis serovar A and B strains have frameshift mutations in their aaxC homologs, suggesting that relaxed selection may have enabled the evolution of aax pseudogenes. Biochemical experiments were performed to determine whether the aaxABC genes from C. trachomatis strains were transcribed, and mutagenesis was used to identify nucleotide substitutions that prevent protein maturation and activity. Molecular evolution techniques were applied to determine the relaxation of selection and the scope of aax gene inactivation in the Chlamydiales.
The aaxABC genes were co-transcribed in C. trachomatis L2/434, during the mid-late stage of cellular infection. However, a stop codon in the aaxB gene from this strain prevented the heterologous production of an active pyruvoyl-dependent arginine decarboxylase. Replacing that ochre codon with its ancestral tryptophan codon rescued the activity of this self-cleaving enzyme. The aaxB gene from C. trachomatis D/UW-3 was heterologously expressed as a proenzyme that failed to cleave and form the catalytic pyruvoyl cofactor. This inactive protein could be rescued by replacing the arginine-115 codon with an ancestral glycine codon. The aaxC gene from the D/UW-3 strain encoded an active arginine:agmatine antiporter protein, while the L2/434 homolog was unexpectedly inactive. Yet the frequencies of nonsynonymous versus synonymous nucleotide substitutions show no signs of relaxed selection, consistent with the recent inactivation of these genes.
The ancestor of the Chlamydiaceae had a functional arginine:agmatine exchange system that is decaying through independent, parallel processes in the C. trachomatis lineage. Differences in arginine metabolism among Chlamydiaceae species may be partly associated with their tissue tropism, possibly due to the protection conferred by a functional arginine-agmatine exchange system against host nitric oxide production and innate immunity. The independent loss of AaxB activity in all sequenced C. trachomatis strains indicates continual gene inactivation and illustrates the difficulty of recognizing recent bacterial pseudogenes from sequence comparison, transcriptional profiling or the analysis of nucleotide substitution rates.
Members of the Chlamydiaceae family grow inside host cells, when infectious elementary bodies (EBs) differentiate into replicative reticulate bodies (RBs). Worldwide, Chlamydia trachomatis serovars A-C are responsible for millions of cases of conjunctivitis and trachoma . Genital infections by C. trachomatis serovars D-K cause the most commonly reported bacterial sexually transmitted disease . C. trachomatis lymphogranuloma venereum serovars L1-L3 are invasive strains that can disseminate to lymph nodes and cause chronic inflammation. Chlamydia (Chlamydophila)pneumoniae causes 10% of pneumonia cases each year, and most adults are seropositive for C. pneumoniae antigens . Despite differences in tissue tropism and virulence, these chlamydiae share a significant portion of their genomes, including about 711 coding DNA sequences (CDS) [4, 5].
The Chlamydiaceae diverged from a non-pathogenic ancestor about 700 mya . Intracellular bacterial pathogens such as Rickettsia and Chlamydia have undergone reductive evolution, as reduced purifying selection and a cascading loss of DNA repair genes led to gene inactivation and genome contraction . While rickettsial genomes have a high number of split genes, a high proportion of noncoding DNA, and a low G+C nucleotide composition (~30%) , chlamydial genomes have few recognized pseudogenes, high coding densities (~90%) and moderate G+C nucleotide compositions (~40%) . Despite the dramatic effects of gene loss, it has been difficult to determine the mode of reductive evolution from the snapshots provided by modern genome sequences. The chlamydial genomes are only half as large as the Parachlamydia sp. UWE25 genome, so both gene acquisition and gene loss have distinguished these lineages .
A comparison between genome sequences from C. trachomatis serovars A and D identified only 18 significant deletions in either strain, producing eight pseudogenes (interrupted open reading frames) in serovar A . Another comparison between genome sequences from L2 and serovar A/D strains of C. trachomatis identified 15 pseudogenes in L2 strains . Due to the relatively low number of chlamydial pseudogenes (< 2% of CDS) and the conservation of chlamydial genome size (1.0 to 1.2 Mbp), these bacteria are believed to have undergone reductive evolution, arriving at a stable genome structure. However, this model discounts gene transfer to the Chlamydiales, positive selection for antigenic proteins, and thousands of nonsynonymous amino acid substitutions that have occurred among the strains [9, 11–13]. Single nucleotide polymorphisms account for much of the diversity among C. trachomatis serovars . Deciphering the differences in their genetic content will provide important clues to understand tissue tropism and subsequent disease.
Most inactivated, or nonfunctionalized pseudogenes are recognized in genome sequences by the presence of nonsense mutations or indels that substantially truncate CDS compared with homologous sequences. However, these mutations occur less frequently than missense mutations, which can have either minimal or catastrophic effects on protein folding and function . Inactivating substitutions are particularly difficult to identify, since these genes can still be transcribed (and even translated): it is challenging to predict and prove their lack of activity . Even some genes with gross mutations can still be transcribed, leading to a broader definition of pseudogenes that may include many unrecognized elements . In this article, we describe the independent inactivation of two arginine decarboxylase orthologs from Chlamydia trachomatis strains, showing that gene loss continues in these pathogens, and illustrating the challenges of identifying recently nonfunctionalized genes.
We previously identified three genes from C. pneumoniae that comprise an arginine:agmatine exchange system (AAX). The aaxA gene encodes an outer-membrane porin protein that stimulates the activity of this system . The aaxB gene encodes an arginine decarboxylase proenzyme that self-cleaves at Ser53 to produce a small β-subunit and a larger α-subunit with a pyruvoyl cofactor that is essential for catalytic activity . Finally, the aaxC gene encodes a cytoplasmic-membrane arginine:agmatine antiporter . Together, these proteins catalyze the import of L-arginine, the decarboxylation of arginine to produce agmatine, and the export of agmatine from the cell. All chlamydial genome sequences contain orthologs of the aaxABC genes, which were apparently acquired by the chlamydial ancestor through horizontal gene transfer. Both the C. pneumoniae and C. trachomatis strains require exogenous arginine for growth, and their genomes lack arginine biosynthesis genes [19, 20]. Chlamydial genomes contain artJ and glnPQ genes encoding a putative ABC-type arginine transporter, which is controlled by the ArgR transcriptional regulator in some species . Therefore the AAX system is probably not used to acquire proteinogenic amino acids. Instead, this system could have several possible functions: it could raise the intracellular pH to resist acidification, produce agmatine – inhibiting host cell polyamine biosynthesis, or inhibit nitric oxide synthesis by host cells .
To determine whether the C. trachomatis L2/434 and D/UW-3 strains encode functional AaxB arginine decarboxylases, we cloned both aaxB genes in E. coli and determined heterologous expression using immunoblotting and activity assays. Neither gene produced a functional arginine decarboxylase in E. coli; however, site-directed mutagenesis experiments showed that AaxB from L2/434 could be rescued by an X128W replacement, and AaxB from D/UW-3 could be rescued by an R115G replacement. Multiple frameshift mutations in aaxC genes from C. trachomatis A/Har-13 and B/Jali are predicted to inactivate those genes . E. coli cells expressing AaxC demonstrated arginine uptake activity of the D/UW-3 AaxC, but not the L2/434 AaxC proteins. Therefore the AAX system appears to be undergoing inactivation in parallel among the C. trachomatis strains. Transcription of these nonfunctional genes suggests that bioinformatic analysis underestimates the number of inactive genes in organisms undergoing reductive evolution. Neither a comparison of d N /d S values nor amino acid substitution analysis was sufficiently sensitive or specific to detect recent gene inactivation by missense mutations.
Results and discussion
Expression of the aax genes in C. trachomatisL2/434
To determine the time course of aaxABC expression, cDNAs were prepared from RNA isolated 8, 24 or 46 h post-infection. As a control, cDNAs also were prepared from RNA isolated from a mock infection, containing only host cells. Amplification of an intragenic region of the constitutively expressed hsp60 gene confirmed the specificity and sensitivity of the analysis (Figure 2C). Amplification of intragenic regions of the aaxA, aaxB, or aaxC cDNAs showed significant levels of expression 24 and 46 h post-infection, but failed to detect expression during the early stage at 8 h (Figure 2D). Therefore, all three genes of the AAX system are preferentially transcribed at the mid- or late-stages of infection, when EBs begin to form. These results are consistent with expression profiles reported from microarray studies of global gene expression [23, 25]. Although the semi-quantitative transcript analysis shown in Figure 2D indicates that levels of aaxC expression are the same or lower than aaxA levels, we cannot rule out the possibility of multiple, unidentified promoters in this gene cluster.
Heterologous expression of AaxB from L2 and D strains
For comparison, the CT373 (aaxB) and CT374 (aaxC) genes from C. trachomatis D/UW-3 were expressed from the same vector, producing T7-tagged AaxB protein in cell lysates (Figure 3). However, this pyruvoyl-dependent arginine decarboxylase must be cleaved to produce active enzyme, and no epitope-tagged cleavage product was detected by immunoblotting. Presumably due to the lack of self-cleavage, no arginine decarboxylase activity was detected in these cell-free extracts either. In contrast, the C. pneumoniae AaxB protein was significantly activated in E. coli .
Restoration of AaxB activity by site-directed mutagenesis
Affinity-purified AaxB from D/UW-3 contained only proenzyme (Figure 4), yet this protein differs from the active X128W L2/434 protein in only two amino acid positions (Figure 1). The Val155Ile substitution is conservative, and probably reflects the ancestral state. However, a Gly115Arg substitution occurred after the divergence of the C. trachomatis L2 and A-D serovars. In the structure of the homologous arginine decarboxylase from Methanocaldococcus jannaschii , the corresponding Ile107 residue is found near the N-terminal end of β-strand 6 in the α-subunit. This strand forms the edge of one sheet in the αββα sandwich fold, and provides the Glu109 carboxylate group that facilitates cleavage in this protein family . The Gly115Arg replacement in C. trachomatis AaxB could alter the conformation of this β-strand, inhibiting cleavage. To test the significance of this substitution, site-directed mutagenesis was used to construct an Arg115Gly variant of the D/UW-3 protein. The affinity-purified protein was 61% cleaved, and it catalyzed L-arginine decarboxylation with a rate of 1.3 s-1 (Figure 4).
Arginine uptake activity of AaxC transporters
Evolution of aaxABC genes in the Chlamydiales
Most mutations predicted to convert protein-coding genes to pseudogenes are nonsense or frameshift mutations that prevent translation of full-length protein. However, the frequency of missense mutations may be much higher -these proteins can still be expressed, and they may fold correctly, yet they can be functionally impaired . Several strategies have been developed to identify detrimental missense mutations, using either protein structure models or comparative sequence analysis to predict the effects of amino acid substitutions . These models show great promise in predicting the effects of nonsynonymous single nucleotide polymorphisms in well-characterized human genes . When the predicted ancestral C. trachomatis AaxB sequence (Figure 1) was submitted to the Sorting Intolerant From Tolerant (SIFT) web server http://sift.jcvi.org/, the G115R replacement was "predicted to affect protein function" . However, when the C. pneumoniae AaxB sequence was submitted to the SIFT web server with a list of 22 observed replacements in the C. trachomatis sequence, all of the changes were predicted to be "tolerated." The G115R replacement alone also was predicted to be tolerated in the C. pneumoniae AaxB sequence. The PMUT server http://mmb2.pcb.ub.es:8080/PMut/ predicted 8 of the 22 replacements (including G115R) to be "pathological" for the C. pneumoniae sequence . Therefore these amino acid substitution prediction tools are neither sensitive nor specific enough to predict functional changes due to missense mutations in significantly diverged bacterial sequences.
For branches in the aaxA gene tree, d S values ranged from < 0.005 (among the C. trachomatis strains) to 66 (saturation, separating the Chlamydophila and Chlamydia lineages). d N /d S values range from 0.002 to more than 1, with the majority of lineages showing purifying selection (Figure 6). The highly diverged amino-terminal secretory signal sequence in C. trachomatis homologs accounted for most of the nonsynonymous substitutions. Otherwise, the d N /d S values for aaxA homologs are consistent with those of the major outer membrane protein (MOMP) porin. The d N /d S value was 0.114 for the C. trachomatis D/UW-3 and C. pneumoniae MOMP pair, and 0.144 for the C. trachomatis D/UW-3 and L2/434 MOMP sequences. From these data we infer that aaxA orthologs have been subjected to moderate purifying selection, punctuated by a dramatic change in the secretory signal region of the ancestral C. trachomatis and C. muridarum gene. Signal sequences can vary significantly among homologous proteins , so further experiments will be required to test whether these changes in the signal sequence alter protein localization or expression levels. A future site-based comparison of codon substitution rates could identify specific positions subject to relaxed selection, but will require many more aaxA sequences.
Despite the inactivating nonsense and missense mutations in C. trachomatis aaxB genes, the d S values for aaxB genes ranged from < 0.00005 in the C. trachomatis lineage to 14 separating the Chlamydia and Chlamydophila strains. There are correspondingly few nonsynonymous substitutions, so d N /d S values are uniformly low (Figure 6). The frequency of GC versus AT nucleotides was not substantially different at any codon position in the inactivated genes. As observed for several Rickettsial pseudogenes, gene inactivation does not always correspond to higher d N /d S values . The aaxC gene also shows no sign of relaxed selection, even in the C. trachomatis lineages with saturating synonymous substitution rates. Although homologs in C. trachomatis B/Jali and A/HAR-13 strains have 2 or 3 deletions, respectively, there are no other nucleotide substitutions compared to the D/UW-3 strain. Neutral evolution may be difficult to detect following such recent gene inactivation.
Parallel loss of AAX activity in C. trachomatisstrains correlates with modes of infection
While the AAX system from C. pneumoniae functions in E. coli, we have demonstrated that several homologous C. trachomatis genes have experienced inactivating mutations. The pathogenic Chlamydiales form two distinct phylogenetic groups: the Chlamydophila and Chlamydia genera . The latter includes C. trachomatis and Chlamydia muridarum, a strain that causes mouse pneumonitis. An alignment of AaxB sequences shows that the C. muridarum homolog contains none of the deleterious mutations found in C. trachomatis genes, so it should form an active arginine decarboxylase (Figure 1). Furthermore, a peptide from the AaxC transporter of this strain was identified bound to MHC class I molecules from infected murine dendritic cells . These data indicate the chlamydial ancestor had a functional AAX system, but independent mutations in the C. trachomatis homologs are progressively inactivating these genes. Recent demonstrations of gene transfer and recombination among chlamydiae temper the correlation between serotype and AAX functionality . Future sequences from clinical isolates and additional chlamydial species will help define the distribution and evolution of the AAX system.
In early stage acute respiratory infections, C. pneumoniae EBs infect granulocytes and alveolar macrophages, which both use arginine to produce nitric oxide [41–43]. Therefore the AAX system may be selected for its ability to reduce L-arginine levels and nitric oxide synthase activity during infection. C. pneumoniae, unlike C. trachomatis, can infect and replicate in neutrophil granulocytes . C. trachomatis strains rarely cause pneumonia, except in infants, who have immature alveolar macrophages . Instead, C. trachomatis strains primarily infect mucosal epithelial cells, which do not express the inducible nitric oxide synthase; however, disseminating C. trachomatis L2 cells can persist in unactivated macrophages . Consistent with this model, mice deficient in inducible nitric oxide synthase resolved genital C. trachomatis infections as well as normal mice .
A similar relationship between chlamydial strain-specific metabolism and tissue tropism has been described for tryptophan biosynthesis. When IFN-γ is produced by the host during infection, it causes the expression of indoleamine 2,3-dioxygenase (IDO), which degrades L-tryptophan. Genital tract isolates of C. trachomatis serovars B, D-K and L2 produce tryptophan synthase to make tryptophan from exogenous indole. In contrast, ocular C. trachomatis serovars A, Ba and C contain a deletion mutation in the trpA gene [48, 49]. Despite the inactivating deletion in trpA, both the trpAB genes are transcribed and translated in a serovar A strain . It has been proposed that ocular C. trachomatis strains do not encounter indole or IFN-γ induced IDO during infection .
The loss of arginine decarboxylase activity in the AaxB protein from L2/434 was predicted due to a nonsense mutation, but the inactivation of D/UW-3 AaxB was not obvious from the protein sequence. Nor could we predict that the L2/434 AaxC would be inactive, while the D/UW-3 AaxC would be active (the two protein sequences are 99% identical). Both aaxBC orthologs are transcribed. Therefore the AAX system has been inactivated via independent mechanisms in at least two lineages of C. trachomatis. Proteomic evidence suggests that the AaxA outer membrane protein is produced by L2/434 cells during infection, but this porin could have additional functions that are independent of AAX system. These results suggest a cautious interpretation of gene expression data for species undergoing reductive evolution. Neither sequence comparison nor transcriptional analysis is sufficient to detect all pseudogenes in these bacteria. Furthermore, recently inactivated genes may not show the hallmarks of relaxed selection, leading to over prediction of bacterial metabolic capabilities. Folded into the protein sequence databases, these inactive sequences may corrupt future genome annotations and protein-structure function analyses that rely on comparative sequence analysis.
Strains and DNA
List of microorganisms and plasmids
Strain or plasmid
Description and partial genotype
Reference or source
C. trachomatis L2/434
Lymphogranuloma venerum II serovar L2, strain 434
C. trachomatis D/UW-3
Trachoma serovar D, strain UW-3/Cx
Expression strain with T7 RNA polymerase gene
General cloning host
General cloning host
Expression vector with PBAD promoter
L2/434 CTL0627–0628 in pGEM-T
Cpn aaxBC in pBAD/HisA
L2/434 CTL0627–0628 in pBAD/HisA
L2/434 His10-CTL0627 in pET-19b
pDG479 with X128W substitution
D/UW-3 His6-CT373–374 in pBAD/HisA
D/UW-3 His10-CT373 in pET-19b
D/UW-3 His10-CT373 Arg115Gly in pET-19b
Primers used for cloning and sequencing
The CTL0627 and CTL0628 genes were amplified from pDFclone1 by PCR using primers 5CT373X and 3CT374H. The purified product was digested and ligated into the XbaI and HindIII restriction sites of vector pBAD/HisA to produce vector pDG479. Sequencing reactions using the primers pBAD-Fwd2, CTseq1 and pBAD-Rev confirmed that the cloned sequence was identical to that found in pDFclone1. The CTL0627 gene was amplified from pDFclone1 by PCR using primers 5CT373N and 3CT373B. The product was ligated into the NdeI and BamHI sites of vector pET-19b to produce vector pDG491. A QuikChange site-directed mutagenesis kit (Stratagene) was used with primers 5CT373X128W and 3CT373X128W to replace the ochre codon 128 of CTL0627 in pDG479 with a tryptophan codon, resulting in vector pDG543.
The CT373 (aaxB) gene from C. trachomatis D/UW-3 was amplified from genomic DNA using the 5CT373N and 3CT373B primers. The resulting product was cloned into pET-19b to produce vector pTG17, as described for CTL0627. The CT373 and CT374 (aaxC) genes were amplified using primers 5CT373X and 3CT374H and ligated into pBAD/HisA, as described above, to produce vector pDG558. DNA sequencing at the Institute for Cellular and Molecular Biology DNA Core Facility showed that the DNA cloned in these vectors was identical to the published sequence (GenBank accession NC_000117). Site directed mutagenesis was used with primers 5CT373R115G and 3CT373R115G and vector pTG17 to construct an Arg115Gly substitution in CT373, resulting in vector pTG20.
Analysis of gene expression
Primers used for operon RT-PCR
Forward primer sequence
Reverse primer sequence
CTL0625 to 626
CTL0626 to 627
CTL0627 to 628
CTL0628 to 629
Primers used for single gene RT-PCR
Forward primer sequence
Reverse primer sequence
Heterologous expression and protein purification
E. coli BL21(DE3) cells containing the indicated plasmids were grown in LB medium supplemented with 100 μg/ml ampicillin and induced with 1% α-D-lactose to express the following decahistidine-tagged proteins: His10-CTL0627 (pDG491), His10-CT373 (pTG17), and His10-CT373-R115G (pTG20). E. coli DEG0147 cells containing plasmids derived from pBAD/HisA and induced with 0.2% L-arabinose were used to express the following hexahistidine and T7 epitope-tagged proteins: His6-CTL0267–0268 (pDG479), His6-CTL0627-X128W (pDG543), and His6-CT373–374 (pDG558). The polyhistidine-tagged proteins were purified using Ni2+-affinity chromatography and analyzed by sodium dodecylsulfate-polyacrylamide gel electrophoresis (SDS-PAGE) as described previously .
Arginine uptake and decarboxylation assays
The transport of radiolabeled arginine was measured in whole cells collected by filtration, using a method that we reported previously . These assays contained 1 × 109 E. coli cells washed and suspended in E medium (pH 5) at 37°C for 20 min with 1 mM L-arginine and 2 μCi L-[2,3,4,5-3H]arginine. Arginine decarboxylase activity measurements using cell-free extracts or purified proteins were performed as described previously using 40 to 80 nCi L-[1-14C]arginine . 14CO2 was trapped and then measured by liquid scintillation counting.
Proteins were separated on a SDS-PAGE Tris-glycine gel, followed by electrotransfer to a PVDF membrane (Pall, Ann Arbor, MI). These blots were blocked with bovine serum albumin and then incubated for 1 h with a 1:5000 dilution of T7-Tag monoclonal antibody conjugated to horseradish peroxidase (Novagen, Madison, WI). An Image Station 4000 instrument (Carestream Health, New Haven, CT) was used to detect chemiluminescence produced during incubation with SuperSignal West Pico Substrate (Thermo Pierce, Rockford, IL).
Phylogenetic analysis and estimation of nucleotide substitution rates
Sequences used for phylogenetic analysis and substitution rate calculations
Chromosomal locus and GenBank RefSeq accession number
Chlamydia abortus S26/31
Chlamydia caviae GPIC1
Chlamydia muridarum Nigg
Chlamydia pneumoniae CWL0291
Chlamydia trachomatis A/HAR-13
Chlamydia trachomatis B/Jali
Chlamydia trachomatis D/UW-3
Chlamydia trachomatis L2/434
Chlamydia trachomatis L2b/UCH
This work was supported in part by Public Health Service grants 5R21AI064444 (to DEG), 5R01AI044033 (to Anthony T. Maurelli) and 1F32AI078655-01 (to DJF). We thank Garry Myers (University of Maryland School of Medicine) for providing access to the C. psittaci 6BC genome sequence prior to publication.
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