The chlamydial functional homolog of KsgA confers kasugamycin sensitivity to Chlamydia trachomatisand impacts bacterial fitness
© Binet and Maurelli; licensee BioMed Central Ltd. 2009
Received: 30 June 2009
Accepted: 31 December 2009
Published: 31 December 2009
rRNA adenine dimethyltransferases, represented by the Escherichia coli KsgA protein, are highly conserved phylogenetically and are generally not essential for growth. They are responsible for the post-transcriptional transfer of two methyl groups to two universally conserved adenosines located near the 3'end of the small subunit rRNA and participate in ribosome maturation. All sequenced genomes of Chlamydia reveal a ksgA homolog in each species, including C. trachomatis. Yet absence of a S-adenosyl-methionine synthetase in Chlamydia, the conserved enzyme involved in the synthesis of the methyl donor S-adenosyl-L-methionine, raises a doubt concerning the activity of the KsgA homolog in these organisms.
Lack of the dimethylated adenosines following ksgA inactivation confers resistance to kasugamycin (KSM) in E. coli. Expression of the C. trachomatis L2 KsgA ortholog restored KSM sensitivity to the E. coli ksgA mutant, suggesting that the chlamydial KsgA homolog has specific rRNA dimethylase activity. C. trachomatis growth was sensitive to KSM and we were able to isolate a KSM resistant mutant of C. trachomatis containing a frameshift mutation in ksgA, which led to the formation of a shorter protein with no activity. Growth of the C. trachomatis ksgA mutant was negatively affected in cell culture highlighting the importance of the methylase in the development of these obligate intracellular and as yet genetically intractable pathogens.
The presence of a functional rRNA dimethylase enzyme belonging to the KsgA family in Chlamydia presents an excellent chemotherapeutic target with real potential. It also confirms the existence of S-adenosyl-methionine - dependent methylation reactions in Chlamydia raising the question of how these organisms acquire this cofactor.
Ribosomes are complex macromolecular machines that are found in abundance in all cells that are actively making proteins. Two-thirds of the ribosome is composed of RNA molecules (rRNA) that share a high degree of conservation in primary sequence as well as in secondary and tertiary structural elements across kingdoms . Numerous nucleotide modifications, mainly but not exclusively via methylation, are found on rRNAs but the functional importance of these post-transcriptional modifications remains unclear . For example, the two adenosine residues in the loop of helix 45 near the 3'end of the small subunit rRNA (positions 1518 and 1519 of the 16S rRNA in the Escherichia coli numbering system) are universally conserved, and are dimethylated by a specific enzyme belonging to the rRNA adenine dimethylase family, which is represented by the E. coli KsgA protein . While these enzymes are present in all three kingdoms of life including mitochondria and chloroplasts , a few KsgA orthologs adopted additional roles within the cell, serving for example as a transcription factor in mitochondria  or an essential ribosome biogenesis factor in yeast . However, dimethylation is generally not essential for growth at optimal temperature.
The order Chlamydiales forms a deep lineage of obligate intracellular bacteria, infecting free-living amoebae, various invertebrates and all the vertebrates, and includes four families: Chlamydiaceae, Parachlamydiaceae, Waddliaceae, and Simkaniaceae . The Chlamydiaceae are well known agents of multiple diseases in animals and in humans, with two species, C. trachomatis and C. pneumoniae, being pathogenic for humans. C. trachomatis is recognized as the most prevalent cause of bacterial sexually transmitted infections worldwide and, in underdeveloped nations, is also responsible for trachoma a potentially blinding disease. C. pneumoniae is a significant agent of respiratory disease in adolescents and adults and also is associated with cardiovascular diseases. The other chlamydial species are less relevant to human medicine, although severe zoonotic diseases in humans are caused by C. psittaci, C. abortus and C. felis. Species of Parachlamydiaceae, Waddliaceae, and Simkaniaceae are also suspected to be involved in human infections .
In addition to being obligate intracellular Gram-negative bacteria, all chlamydiales share a unique biphasic developmental cycle. The environmentally stable, metabolically inert and infectious elementary bodies (EBs) enter susceptible host cells and convert into the replicating and metabolically active but noninfectious reticulate bodies (RBs) inside cytoplasmic vacuoles (also called inclusions) before converting back into EBs from 18 to 48 hours post-infection depending on the species, and exiting the host cell to repeat the cycle . While effective antibiotic therapies are available to treat chlamydial infections, it is becoming clear that the low number of rRNA operons in these bacteria presents an actual risk for emergence of resistance against the current preferred therapies of tetracycline or azithromycin [10, 11]. Then, similar to other bacteria, targets for the development of new antimicrobials need to be identified.
The evolution of Chlamydia as an obligate intracellular pathogen has been associated with loss of genes encoding functions that became redundant within the host during the adaptation to parasitic/symbiotic lifestyles, similarly to mycoplasmas, phytoplasmas, α- and γ-proteobacteria . Sequencing data available for eleven Chlamydia species reveal the presence of a KsgA dimethyltransferase homolog, yet they all lack the S-adenosyl-methionine synthetase that is required for synthesis of S-adenosyl-methionine, the donor of methyl groups in all methylation reactions. This raises the question of whether the ksgA homolog encodes a functional methylase in these organisms. The lack of tools for genetically manipulating Chlamydia has been a major barrier to the analysis of their putative virulence genes  and characterization of chlamydial genes has mainly relied on expression in a heterologous host system such as E. coli. In this study, we show that the chlamydial KsgA protein is able to functionally replace the orthologous enzyme in E. coli, indicating that they share the same activity, i.e. specific methylation of the small subunit ribosomal RNA. KsgA activity conferred sensitivity to the antibiotic kasugamycin (KSM) in Chlamydia, similarily to E. coli, and we were able to isolate low level KSMR mutants in C. trachomatis which contain a frameshift mutation in ksgA. These mutant bacteria were severely impaired for growth, highlighting the critical role KsgA plays in Chlamydia biology.
Results and discussion
1-Characterization of the chlamydial KsgA orthologs and their phylogenetic relationship with other family members
A gene encoding a protein highly similar to the dimethyltransferase KsgA is present in the genomes of all sequenced Chlamydia. Using degenerate primers, we were amplified a 5 kb-genomic region of C. psittaci 6BC carrying the ksgA-like gene. ksgA is the second gene of a predicted bicistronic operon in Chlamydia , downstream of a gene, named ct355 in C. trachomatis serovar D, with no homology outside the chlamydiae lineage. CT355 ORF shows 59 to 100% homology amongst the Chlamydiacee and 26% with the protochlamydial pc0396 ORF which precedes the protochlamydial ksgA gene.
Genomic transcriptional profiling of C. trachomatis serovar D showed that both ksgA and ct355 genes are transcribed by 8 hours post-infection when the bacteria are in the metabolically active stage of development . Surprisingly, while most ksgA orthologs use the AUG canonical translation initiation codon, an alternative ksgA start codon is predicted amongst the Chlamydiaceae, either GUG in C. trachomatis, C. muridarum and C. pneumoniae or UUG in C. psittaci 6BC, C. felis, C. caviae and C. abortus. While use of an alternative start codon usually results in low expression in E. coli, its impact on efficiency of translation in Chlamydia is not known. Nevertheless like E. coli, most chlamydial genes rely on AUG as a start codon .
2-Complementation of a ksgA mutant of E. coli by the chlamydial ksgAhomologs
Bacterial strains used in this study and MICs for KSM
Source or reference
KSM MIC (μg ml-1)
F-ϕ80Δ(lacZY-argF)U169 deoR recA1 endA1 phoA hsdR17 supE44 λ - thi-1 gyrA96 relA1 Δ(lacZ)M15
Δ(araD-araB)567 ΔlacZ4787 (::rrnB-3) λ - rph-1 Δ(rhaD-rhaB)568 hsdR514
F- araD139 Δ(argF-lac)U169 rpsL150 relA1 deoC1 rbsR fthD5301 fruA25 λ-
MC4100 Δ ksgA::cat
ATM809 transformed with pRAK297 [Plac::E. coli ksgA in pGEMT]
ATM809 transformed with pRAK325 [Plac:: C. psittaci 6BC UUG-ksgA in pGEMT]
ATM809 att:: E.coli ksgA
ATM809 att:: C.trachomatis GUG-ksgA
ATM809 att:: C.trachomatis AUG-ksgA
ATM809 att:: C.trachomatis AUG-ksgAE9
C. psittaci 6BC
Spontaneous KsmR variant of C. psittaci 6BC with A794G mutation in the 16S rRNA gene
C. trachomatis L2
biovar lymphogranuloma venereum L2/434/Bu
C. trachomatis L2 ksgAE9
3-Inhibition of C. trachomatis L2 and C. psittaci6BC growth by KSM and selection of resistant mutants
Although KSM has been used clinically in the treatment of Pseudomonas aeruginosa infections , this aminoglycoside antibiotic is only currently used in agricultural protection of rice crops against the fungus Pyricularia oryzae. Genetic, biochemical, and structural analyses have provided insights into KSM binding and inhibition [38–42]. The drug binds to the 30S ribosomal subunits within the path of the messenger RNA (mRNA), overlapping both the peptidyl-tRNA (P) and exit (E) sites. This affects the binding of the initiator tRNA onto canonical mRNAs and the subsequent joining of the large 50S subunits to form the translationally active 70S ribosomes. KSM is held in place by interactions with universally conserved residues A794 and G926 on the 16S rRNA and although the antibiotic does not appear to interact directly with the two adenosines at positions 1518 and 1519, lack of methylation in A1519 decreases KSM binding to rRNA. [39, 40]. The conservation of these nucleotides in Chlamydia predicts that these obligate intracellular bacteria should be sensitive to KSM, provided that both the cell and the inclusion membrane are permeable to the drug.
In our laboratory, sensitivity of Chlamydia spp. to antibiotics is measured in the plaque assay and the MIC is defined as the concentration of drug that inhibits the development of 105 plaque-forming units (PFU). The number of input bacteria corresponds to a multiplicity of infection (MOI) of 0.01 in a confluent monolayer of L2 mouse fibroblasts in 60 mm dishes [10, 11, 13]. Due to low intracellular penetration, aminoglycosides are considered poorly active or not active against obligate intracellular bacteria and indeed C. psittaci 6BC and C. trachomatis L2 MIC for KSM were high, i.e. 1100 and 800 μg ml-1, respectively (Table 1). Although such elevated MICs would classify the organisms as KSM resistant from a clinical stand point, we hypothesized that alterations in the drug binding site, in the KsgA methylase or in the rRNA methylation site would allow Chlamydia to grow in the presence of even higher concentrations of KSM, as reported for other bacteria [28, 38, 43, 44].
When monolayers were infected with 106 to 107 PFU in the presence of KSM at 2000, 3000 or 5000 μg ml-1, resistant plaques appeared at a frequency of 2.20 ± 0.64 × 10-5 for C. psittaci 6BC while no plaques were seen for C. trachomatis under the same conditions (frequency <5.3 × 10-8). We have previously observed this difference in behavior between the two chlamydial strains for acquisition of resistance towards other ribosome targeting antibiotics [10, 11]. Because expression of resistance requires that more than 50% of the ribosome population be of the resistant phenotype, C. trachomatis with two rRNA operons is at a disadvantage compared to C. psittaci 6BC which harbors only one rRNA operon. KSM started to affect C. trachomatis L2 growth at 100 μg ml-1, but a concentration of 200 μg ml-1 was completely inhibitory when cells were infected with a few hundred PFUs. Therefore we reasoned that serial passage in subinhibitory concentrations of antibiotic would allow the enrichment of putative low level KSMR bacteria, as previously seen for azithromycin . Three independent cultures of C. trachomatis L2 were passaged up to 14 times in KSM ranging from 100 to 800 μg ml-1. Three individual clones were then selected and purified in the plaque assay using 300 μg KSM ml-1.
4-Molecular and phenotypic characterizations of KSM resistance mutations in C. psittaci 6BC and C. trachomatisL2
Sixteen independent spontaneous KSMR plaques were isolated for C. psittaci 6BC, expanded twice in the presence of 2000 μg KSM ml-1 and further analyzed. DNA sequence analysis showed that none carried a mutation in ksgA. However, sequencing of the unique 16S rRNA gene revealed an A to G mutation at position 794 which is known as one of the binding sites for KSM [39, 40]. Similarly, three C. trachomatis L2 isolates that arose in the presence of 300 μg KSM ml-1 were further expanded in the presence of the drug and analyzed. None carried a mutation in the drug binding sites as expected from the presence of two rRNA operons in the strain . None carried a mutation in rpsI encoding the 30S ribosomal subunit S9 protein that is a target for KSM resistance . Sequencing of the ksgAL2 DNA region revealed the insertion of a tg nucleotide doublet in the last third of the gene. This doublet base-pair insertion, likely the result of a replication slippage , creates an early in-frame stop codon in the ksgA coding sequence, resulting in the expression of a KsgA variant of 213 residues instead of 277 (Figure 2).
Stability of the acquired phenotype was then tested on one representative mutant of both classes (Table 1) by growth in the absence of selective pressure (i.e. no KSM). Plaques formed by the C. psittaci 6BC BCK1 and the C. trachomatis L2 ksgAE9 variants grown for a minimum of 14 days in the absence of selection displayed the same number of infectious particles when titered in the presence or absence of 2000 and 200 μg KSM ml-1, respectively, indicating that the resistance phenotype was stable (data not shown). Growth of C. psittaci BCK1 was not affected by 5 mg KSM ml-1, the highest concentration of KSM that was not toxic to the mouse fibroblast cells. On the other hand, plaques formed by C. trachomatis ksgAE9 were already smaller in the presence of 200 μg ml-1 KSM, while 3 mg ml-1 of the drug inhibited at least 105 ksgAE9 PFUs (i.e. MIC) (Table 1). The moderate level (i.e. less than 4-fold) of KSM resistance conferred by mutations in ksgA likely precluded C. psittaci 6BC ksgA mutants from being selected directly in the plaque assay [10, 11].
High level KSM resistance associated with mutations in the drug binding sites has only been observed previously in engineered strains of E. coli  and B. subtillis  in which each of the seven or ten rRNA operons, respectively, were inactivated, and the strains expressed only one rRNA operon encoded on a plasmid. Although both studies still reported that ksgA mutations are the main mechanism of resistance to KSM, mutations in the drug-binding site at position A794 and G926 of the 16S rRNA conferred four to eight times more resistance to KSM than KsgA inactivation or alteration of the adenosine targeted by the methylase at position 1519 of the 16S rRNA. In this study, all KSMR mutations selected in C. psittaci 6BC mapped to the drug-binding site at position A794G. Our inability to isolate KSMR plaques for C. psittaci 6BC with mutations in the 16S rRNA gene at position 926 or 1519 suggests that either they do not confer KSM resistance levels high enough to be selected in the plaque assay or they impose a significant burden on bacterial fitness. Such species-specific bias for drug resistance mutations has been reported for other ribosome-targeting antibiotics including tetracycline, linezolid and macrolides .
5-KsgA is critical for optimal growth of Chlamydia
Serial passages in sub-inhibitory concentrations of KSM allowed the purification of a C. trachomatis variant synthesizing a shortened rRNA adenine dimethyltransferase enzyme in which the eight structural and catalytic methyltransferase motifs were maintained, but harboring 20 unrelated amino acids because of the frameshift at codon 203 (Figure 2). Overexpression of the truncated chlamydial protein in ATM809, the E. coli ksgA mutant, was strongly inhibitory for cell growth, as observed earlier with the wild-type KsgAL2 protein. On the other hand expression from a copy of ksgAE9, the frameshift mutant, integrated in the bacterial chromosome, i.e. in ATM815, had no consequence on bacterial growth in the absence or in the presence of KSM (Figure 3), with a MIC of 2000 μg.ml-1 (Table 1). This shows that the chlamydial KsgA C-terminal tail is essential for activity in this heterologous system. Crystal structure analyses revealed that the N-terminal and the C-terminal portions of E. coli and Thermus thermophilus KsgA orthologs form two domains and the presence of several positively charged residues in the C-terminal domain predicted its involvement in binding to rRNA [31, 49]. Recent evidence has shown that both domains interact with 16S rRNA in 30S ribosomal subunits . More specifically the C-terminal domain of KsgA competes with the C-terminal domain of initiation factor IF3 for binding with the central domain of 16S rRNA. Accordingly, KsgA would prevent ribosomes that are undergoing methylation from entering the translational cycle . As a result one might expect immature ribosomes to enter translation in cells that lack KsgA thus bearing a physiological cost.
Screening for KSM resistance in C. trachomatis allowed us to select for ksgA mutations in these as yet genetically intractable pathogens . Interestingly, plaques formed by the C. trachomatis L2 ksgAE9 variant in the absence of antibiotic were smaller than the wild-type strain (p < 0.0001 by t-test) with sizes of 0.27 mm ± 0.11 and 0.45 mm ± 0.13, respectively. This result shows that alteration in KsgA affects the fitness of C. trachomatis in vitro, similarly to Mycobacterium tuberculosis . It is worth noting that although inactivation of ksgA has a minimal effect on growth of E. coli or B. subtilis at 37°C, recent studies have shown that the mutants are outcompeted by the wild-type strains at 37°C . Similarly, while growth of a Y. pseudotuberculosis ksgA mutant is not severely affected under normal laboratory conditions, the mutant strain is attenuated in the mouse model indicating that dimethylation is essential for optimal fitness of the pathogen in vivo . Although, the lack of a small animal model for C. trachomatis L2 precludes us from testing the consequences of KsgA inactivation on the pathogenicity of the strain, it is tempting to assume that the impairment of C. trachomatis L2 growth in vitro seen for our ksgA mutant would be reflected by an attenuation in virulence in vivo.
When high throughput screening of compounds predicted to bind to Bacillus subtillis RNA methyltransferase ErmC identified new compounds that were inhibitory to the growth of C. pneumoniae in vitro, Alvesalo et al. proposed that these small compounds were targeting the bacterial KsgA homolog . Considering that ribosome biogenesis factors are emerging as potential therapeutic targets to combat pathogens , the present work provides evidence that Chlamydia possess a functional rRNA dimethylase enzyme that is important for optimal growth of these obligate intracellular organisms. The demonstration of two methyltransferases in Chlamydia ( and this study) raises the question of how these obligate intracellular bacteria obtain S-adenosyl-methionine to carry out these modifications. Our laboratory is currently investigating this aspect of Chlamydia biology.
Bacterial strains and antibiotics
The bacterial strains used in this study are listed in Table 1. Escherichia coli strain DH5α was used for cloning purposes. E. coli strains were grown in Luria-Bertani (LB) broth with aeration or on LB agar. Ampicillin (Sigma) was used at 100 μg ml-1 to maintain plasmids in E. coli and at 25 μg ml-1 to select for the ATM809 derivatives harboring a single copy of the pGEMT-insert integrated in the chromosome (Table 1). KSM (Biomol) was used at the concentrations indicated.
Propagation of Chlamydiaand tissue culture cells
C. trachomatis serovar L2/LGV/434/Bu and C. psittaci serovar 6BC were grown in mouse fibroblast L2 cells as previously described .
Nucleic acid manipulation and sequence data analysis
Total genomic DNA was prepared from C. trachomatis L2 or C. psittaci 6BC infected cells with DNeasy Tissue Kits (Qiagen). To identify the ksgA genomic region in C. psittaci 6BC, a 5.6 kb product was amplified by PCR using degenerate primers designed from highly conserved genes surrounding the ksgA chromosomal region in the Chlamydiaceae (i.e. UpK-F1 [5'-CGACCACTCTGCCACTCTTCC-3'] and DWK-R1 [5'-CCYGTRATYTTWGCKATAGATCGTCGAGG-3']). The PCR product was cloned into pGEMT (Promega) and sequenced by the Biomedical Instrumentation Center at USUHS. Nucleotide sequences and predicted protein sequences were analyzed and aligned using Clone Manager 8 (Scientific & Educational Software, Durham, NC), focusing mainly on ksgA and its upstream gene, i.e. CT354 and CT355 respectively (C. trachomatis serovar D designation, GenBank accession number NC000117). Protein homolog searches used the bioinformatic tools provided by the National Center for Biotechnology Information (NCBI) and by the Berkeley Phylogenomics group http://phylogenomics.berkeley.edu/tools.php.
KsgA phylogenetic analysis was performed on the Phylogeny.fr platform  and comprised the following steps. Sequences were aligned with MUSCLE (v3.7) configured for highest accuracy (MUSCLE with default settings). After alignment, ambiguous regions (i.e. containing gaps and/or poorly aligned) were removed with Gblocks (v0.91b) using the following parameters: -minimum length of a block after gap cleaning: 10; -no gap positions were allowed in the final alignment; -all segments with contiguous non conserved positions bigger than 8 were rejected; -minimum number of sequences for a flank position: 85%. The phylogenetic tree was reconstructed using the maximum likelihood method implemented in the PhyML program (v3.0 aLRT). The WAG substitution model was selected assuming an estimated proportion of invariant sites (of 0.055) and 4 gamma-distributed rate categories to account for rate heterogeneity across sites. The gamma shape parameter was estimated directly from the data (gamma=1.612). Reliability for internal branch was assessed using the aLRT test (SH-Like). Graphical representation and edition of the phylogenetic tree were performed with TreeDyn (v198.3).
Construction of the E. coliK12 ΔksgA mutant, ATM809
An E. coli ksgA-mutant was generated first in strain BW25113 (Table 1) using the λ Red recombinase method described by Datensko and Wanner . The pKD4 template plasmid (chloramphenicol resistance) was used with the primers KD5 [5'-CACCCAATGAATAATCGAGTCCACCAGGGCCACTTAGCCCGTAAACGCtgtgtaggctggagctgcttc-3'] and KD6 [5'-CGAATTGATCATCGTTAACTCTCCTGCAAAGGCGCGTTCTCCGCCAcatatgaatatcctccttagttcc-3']. The PCR product that contains 46 bp of DNA homologous to the E. coli chromosomal regions flanking ksgA, shown underlined in the above primers, was used to electroporate BW25113 containing the λ Red recombinase expression plasmid pKD46. Expression of the λ Red system allowed for recombination of the PCR product into the bacterial chromosome and replacement of the chromosomal ksgA copy by the chloramphenicol resistance gene. This mutation was confirmed using PCR analysis of genomic DNA using the primers ksgA-F3 [5'-ACCCAATGAATAATCGAGTCCACC-3'] and ksgA-R2 [5'-TGATCATCGTTAACTCTCCTGCAAAG-3']. Next, a P1L4 lysate was grown on the ΔksgA::cat strain and used to transduce MC4100 to chloramphenicol resistance, creating ATM809 (Table 1). Deletion of ksgA in ATM809 was confirmed by PCR analysis (see above) and resulted in increased resistance to KSM (Table 1).
Cloning of ksgAin plasmid pGEMT
Complementation plasmids were constructed by cloning PCR products generated from E. coli or chlamydial DNA lysates into pGEMT (Promega), under the control of the lactose promoter. Sequencing of all cloned genes was performed by the Biomedical Instrumentation Center at USUHS. E. coli K12 ksgA gene was amplified using primers ksgA-F3 and ksgA-R2, creating pRAK297. C. trachomatis L2 ksgA gene was amplified using primers DWK-R2 [5'-ACTCAAGATCTCTAATCATAATCCCA-3'] and ksgA-F [5'-AGGGTGGCACGGAGTTCTATAGAAC-3'] containing the genuine GUG start codon or ksgAF5 [5'-GGATGGCACGGAGTTCTATAGAAC-3'] where the GUG start codon has been replaced by the conventional AUG start codon, creating pRAK317 and pRAK316, respectively. pRAK363 was constructed similarly to pRAK316 except that the PCR product was amplified from C. trachomatis L2 ksgAE9 genomic DNA (Table 1). C. psittaci 6BC ksgA homolog was amplified using primers ksgA-F8 [5'-CGCTATGGCTTTGACTCATCG-3'] and ksgA-R6 [5'-CACTTAGGCGTGCAATGAGAG-3'] and cloned in pGEMT under the control of the lactose promoter, creating pRAK325. In this construct the putative KsgA6BC UUG start codon was ~ 60 bp downstream of the Ribosome Binding Site, and was consequently expected to be expressed at a low level in E. coli due to polar effect. Accordingly, unlike E. coli transformants harboring pRAK316, pRAK317 or pRAK363, we did not observe any growth defect in E. coli pRAK325 transformants after addition of IPTG (see below).
Insertion of the ksgA-pGEMT inserts into ATM809 chromosome
We predicted that expressing KsgAL2 at a physiological level will reduce the growth inhibition observed in E. coli when the gene was carried on high copy vectors. Therefore inserts from plasmids pRAK297, pRAK316, pRAK317 and pRAK363 were inserted at the att site in the chromosome of ATM809 using the λlnCh tool as described by Boyd et al. . Briefly, homology between the ksgA-pGEMT constructs (near-ori region and part of the bla gene) and sequences on the InCh bacteriophage allowed some phages to acquire both the ampicillin resistance gene (i.e. bla) and the vector ksgA insert by recombination. After subsequent infection of ATM809, the recombinant phage bla - ksgA region was transferred into the bacterial att site by site-specific recombination, creating lysogens. Finally recombination between the bacterial genome near att and the phage DNA that carry the same region resulted in deletion of the phage while leaving bla-ksgA in the bacterial genome, creating bacterial stable recombinants. Insertion sites were confirmed by PCR . Primers Puc-F and Puc-R  showed the presence of the ksgA insert in ATM810, ATM811, ATM812 and ATM815 (Table 1). Primers GalF [5'-CTTGCTGAGTACGTGAGTTC-3'] and IG-R [5'-ACGTTGGAGTCCACGTTCTT-3'] amplified a 1248 bp product in ATM810, ATM811 and ATM815 only, showing that these three strains were stable recombinants. On the other hand, we were unable to obtain "stable" recombinants from ATM812, as seen by PCR amplification of a 977 bp product using primers GalF and Att-R [5'-AAGCAGGCTTCAACGGATTC-3'], similarily to MC4100 and ATM809. Maintenance of the ksgA insert in ATM812 chromosome was followed throughout the study by PCR with Puc-F and Puc-R and by the constant presence of ampicillin for selection.
Analysis of bacterial growth
The effect of KsgA on bacterial growth was first studied in E. coli recombinants. Cells were grown at 37°C overnight in LB without salt  supplemented with ampicillin. Saturated cultures were diluted 1/100 in fresh expression medium (i.e. LB without salt supplemented with 1 mM IPTG) and incubated at 37°C for 2 to 3 hours, then normalized to an OD600 nm equivalent of 0.5. Bacteria were serially diluted in sterile buffered saline gelatin [150 mM NaCl, 2 mM KH2PO4, 4 mM Na2HPO4, 0.01% gelatin]. For each dilution, aliquots of 2 μl were spotted onto two expression medium agar plates. One plate was left at 20°C for about 30 hrs and the second plate was incubated at 30°C for 12 hrs (Figure 4). 100 μl of a 10-5 dilution was plated on expression medium agar plates and incubated at 37°C for 12 hrs. The sizes of 15 random colonies were determined for each strain and averaged.
The effect of KsgA on C. trachomatis growth was determined by measuring and averaging the size of a minimum of 60 plaques formed by the two C. trachomatis L2 variants in the absence of selection, two weeks after simultaneous inoculation onto three 60-mm confluent monolayers of mouse fibroblast cells each.
KSM sensitivity assays
MIC was determined for E. coli in test tubes inoculated with about 105 bacteria collected from exponential phase cultures grown at 37°C in expression medium containing various concentrations of KSM. MIC was defined as the lowest concentration at which no growth was visible after 16 hrs incubation at 37°C (Table 1). Subsequently, cultures were also incubated in triplicate with agitation for 24 hrs in the presence of 50, 250, 500, 750 and 1000 μg ml-1 of KSM in expression medium. Growth was determined spectrophotometrically at 600 nm and normalized to the value obtained for ATM809 at the same concentration of KSM. KSM inhibition growth curves (Figure 3) were generated using the Prism 3.0 software (GraphPad Software, Inc, San Diego, CA).
Susceptibility of C. trachomatis and C. psittaci to KSM was examined in the plaque assay. MIC was defined as the drug concentration that inhibits the development of 105 chlamydial plaque-forming units (PFU) in a confluent L2 monolayer in a 60 mm dish . To test for spontaneous drug resistance, 60 mm dishes were infected with 107 to 108 PFU (MOI 1 to 10) and the drug was added two hrs p.i. at a concentration high enough to inhibit the cytotoxicity associated with this inoculum size. The frequency of spontaneous mutation to drug resistance was determined by dividing the number of PFU on selective medium by the number of PFU added to the monolayer (as measured by titration of PFU in the absence of antibiotic) . Three clonal C. trachomatis KSMr isolates, including L2 ksgAE9 (Table 1) were independently purified in the plaque assay in the presence of 300 μg/ml of KSM, following 7 to 13 successive passages in mouse cells in the presence of increasing concentrations of antibiotic (from 100 to 800 μg ml-1).
PCR and DNA sequencing of the KSM resistance targets in Chlamydia
PCR amplification and DNA sequencing were used to determine whether chlamydial resistance to KSM was due to a mutation in the 16S rRNA gene as described in  or in ksgA using the primers described above. Because ksgA is apparently the second gene of a bicistronic operon in C. trachomatis and C. psittaci, we also sequenced about 2 kb upsteam of ksgA. DNA sequences for each antibiotic resistant isolate were aligned using Clone Manager 8 and compared to the respective DNA sequence obtained from the wild-type parental strain. We also amplified C. trachomatis L2 rpsI region using primers rpsI-F1 [5'-GCTGAGAAAGTGCGTTTGACTG-3'] and rpsI-R1 [5'-GAAAGCAAGCACGGGACAAATC-3'] and sequenced the PCR fragment using primer rpsI-F2 [5'-ACATGATTGCGCGAAAGC-3']. No mutation was seen in the three KSM resistant isolates.
Nucleotide sequence accession number
C. psittaci 6BC ksgA sequence determined in the present study has been deposited in GenBank under accession number GQ284731.
This work was supported by grant AI44033 from the National Institute of Allergy and Infectious Diseases.
Rachel Binet acknowledges Nancy E. Adams for cell culture assistance and Derek Fisher and Aishwarya V. Ramaswamy for critical reading of the manuscript.
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