Open Access

Chloramphenicol acetyltransferase as a selection marker for chlamydial transformation

BMC Research Notes20136:377

Received: 8 July 2013

Accepted: 11 September 2013

Published: 23 September 2013



Chlamydia is a common bacterial pathogen responsible for many diseases. Methods for transforming this important organism using a β-lactamase as a selection marker have been developed very recently. However, the National Institutes of Health Guidelines for Research Involving Recombinant DNA Molecules do not permit transformation experiments with β-lactamase gene-containing vectors for certain human chlamydial pathogens. Therefore, a different selection marker is urgently needed for transformation of those chlamydiae.


After transformation of plasmid-free Chlamydia trachomatis with pGFP:SW2, which carries a β-lactamase and a chloramphenicol acetyltransferase gene fused to a green fluorescence protein gene, transformants were obtained by selection with either ampicillin or chloramphenicol. Stable chloramphenicol-resistant, but ampicillin-sensitive, transformants were obtained using a pGFP:SW2 derivative without the β-lactamase. All transformants expressed green fluorescence protein and had glycogen synthesis activity restored.


Chloramphenicol resistance may be used as a selection marker for genetic experiments in Chlamydia. This eliminates the requirement for the use of β-lactamase, of which dissemination to some C. trachomatis serovars may jeopardize clinical treatment of chlamydial infections in pregnant women. Chloramphenicol acetyltransferase may also serve as a useful secondary selection marker for genetic analyses in β-lactamase-transformed chlamydial strains.


Chlamydia Chlamydia trachomatis Chloramphenicol Chloramphenicol acetyltransferase Sexually transmitted infections Transformation Transformation selection marker


Chlamydia is a bacterium that replicates only inside a eukaryotic host cell, and is a causative agent for a number of human diseases [1, 2]. Acquired by sexual transmission, replication of Chlamydia trachomatis at the lower genital tract causes cervicitis [1]. Subsequently, chlamydiae ascend to the upper genital tract, causing inflammation leading to tissue disruption and scarring in the uterus and oviducts. Inflammation in the uterus during pregnancy may lead to abortion and premature birth, whereas chlamydial oviductal pathology constitutes the number one cause of female infertility, and ectopic pregnancy [1]. Furthermore, an infant of an infected mother may acquire the pathogen while passing the birth canal, and develop respiratory infection [1]. C. pneumonia is a common pathogen of community-acquired respiratory infection, and a co-factor for arteriosclerosis and late-onset Alzheimer disease [35]. At the present time, no vaccine effective against human chlamydial diseases or other preventive means are available [6, 7].

Chlamydia has a unique developmental cycle, which consists of two alternating cellular forms: the infectious but non-dividing elementary body (EB) and the dividing but non-infectious reticulate body (RB). Developmental events including conversion of EB to RB, replication of RBs, and RB to EB reorganization take place inside a cytoplasm vacuole designated inclusion. For a long period of time, study of Chlamydia has been severely hampered by a lack of a convenient genetic system. Fortunately, a method for transforming C. trachomatis with shuttle vectors using CaCl2 has been developed very recently by Wang et al. [8], and has been adopted by others [9, 10]. Furthermore, Gérard et al. have transformed C. pneumoniae using dendrimers as a delivery tool [11]. Both these methods were established with plasmids carrying a β-lactamase, which degrades penicillin family antibiotics, and thus relieves their inhibitory effects of these drugs on the cytokinesis of RBs [8, 9]. Since amoxicillin, a penicillin family member, is recommended for treatment of chlamydial cervicitis in pregnant women, transformation experiments using β-lactamase marker for sexually transmitted, non-LGV chlamydial pathogens (i.e., C. trachomatis serovar D to K), are not permitted by the National Institutes of Health Guidelines for Research Involving Recombinant DNA Molecules. Therefore, there is an urgent need to identify selection markers for recombination studies in those chlamydial serovars. In addition, there is also a need to identify secondary selection markers for chlamydiae which may already carry an established resistant marker such as a β-lactamase for different reasons in future studies. Here, we report the identification of a chloramphenicol acetyltransferase (CAT) gene as a useful selection marker.


Tissue culture and molecular biology reagents

Dulbecco’s modified Eagle’s medium (DMEM) with high glucose (4.5 g/L) and 110 mg/L sodium pyruvate, fetal bovine serum (FBS), Dulbecco’s phosphate-buffered saline (PBS), trypsin-EDTA solution for cell culture, Trizma base, cycloheximide, CaCl2, ampicillin, chloramphenicol and Lugol solution were purchased from Sigma Aldrich. Gentamycin and transformation-competent Escherichia coli stbl2 cells were purchased from Invitrogen. Pfu Ultra DNA polymerase was purchased from Agilent. Bam H1 and the Q5 Site-Directed Mutagenesis Kit were purchased from New England Biolabs.


pGFP::SW2 is a shuttle vector containing an E. coli replication origin, a β-lactamase gene, a chloramphenicol acetyltransferase gene fused to DNA coding for a red-shifted green fluorescence protein (GFP), and nearly the complete sequence of a C. trachomatis plasmid designated SW2 (Figure 1, top) [8]. pGFP-CAT::SW2 (Figure 1, bottom) was derived by deletion of the β-lactamase gene from pGFP::SW2. Briefly, the 7169 bp SW2 DNA was removed from the plasmid by first amplifying the non-chlamydial DNA sequence using the Pfu Ultra DNA polymerase and a pair of mutually complementary primers, GFP-5’c (5’TAGATTAATGTCGACTCTAGAGGATCCGGGTACCGAGCTCGAA3’) and GFP-3’c (5’TTCGAGCTCGGTACCCGGATCCTCTAGAGTCGACATTAATCTA3’), which target the termini of the non-chlamydial DNA fragments, and then circularization of the fragment in E. coli. Likewise, the Bam H1 site within the GFP coding sequence of the resulting 4,370 bp plasmid, designated pBETA-GFP-CAT, was inactivated using the mutually complementary primers GFP-Del-BamH1-5’c (5’AAGCCGATATGGTGGATTCCCGGGTACCAATGA3’) and GFP-Del-BamH1-3’c (5’TCATTGGTACCCGGGAATCCACCATATCGGCTT3’). The 861 bp β-lactamase open reading frame was removed from the plasmid using the Q5 Site Directed Mutagenesis Kit to yield the plasmid pGFP-CAT. Primers for Q5-mediated mutagenesis were Del-amp1 (5’CTGTCAGACCAAGTTTAC3’) and Del-amp2 (5’ACTCTTCCTTTTTCAATATTATTG3’). Finally, the 7168 bp SW2 fragment was inserted to the Bam H1 site of the pGFP-CAT to yield pGFP-CAT:SW2 (Figure 1). Chloramphenicol was used to select E. coli transformed with pGFP-CAT and pGFP-CAT:SW2 (Figure 1). Sequence authenticity of the SW2 portion of pGFP-CAT::SW2 was confirmed through paid service provided by Macrogen USA.
Figure 1

Schematic presentation of pGFP::SW2 (top) [[8]] and its derivative pGFP-CAT::SW2 (bottom). Sequence originated from the C. trachomatis SW2 plasmid is shown in red, and non-chlamydial sequences in black. Compared to pGFP::SW2, the β-lactamase gene has been removed and a Bam H1 cutting site located upstream of the GFP-CAT fusion gene has been inactivated in pGFP-CAT::SW2. All other features, including the C. trachomatis plasmid replication origin (pSW2 ori) and coding sequences (CDS) 1-8, E. coli pUC replication origin (pUC ori), the GFP-CAT fusion gene and the Neisseria meningitidis promoter (nmP) that drives the expression of GFP-CAT, remain unchanged in pGFP-CAT::SW2. See Methods for construction details.

Plasmid DNA preparation

E. coli stbl2 cells were used to grow plasmids. Plasmid DNA was purified using Qiagen Midi DNA purification columns, precipitated by ethanol and redissolved in 10 mM Tris-HCl (pH 8.5). DNA concentration of final preparations was 2.5 μg/μl or above.

Cells and culture conditions

HeLa and McCoy cells were purchased from American Type Culture Collections (ATCC, Manassas, VA), and maintained as adherent cultures in 5% CO2 incubators with 100% humidity using DMEM containing 10% FBS [8].

Preparation of EBs for transformation

EBs for transformation experiments were prepared as previously described [8] with minor modification. Five T150 flasks of 95% confluent HeLa cells were inoculated with an EB stock of the plasmid-free C. trachomatis 2566R (L2R) [12] at a multiplicity of ~5 inclusion-forming units (IFU) per cell, and cultured with medium containing 20 μg/ml gentamycin and 1 μg/ml cycloheximide. 46 h after inoculation, the infected monolayers in each flask were briefly rinsed with 5 ml PBS, and 3 ml of trypsin-EDTA. When cells appeared to have rounded up under an inverted microscope, they were collected into 8 ml DMEM-FBS. Cells from all 5 flasks were pooled, and subjected to centrifugation at 500 g for 10 min. Following the removal of the supernatant, cells were resuspended in 1 ml SPG buffer [13] and disrupted by three cycles of 5-s on/5-s off sonication using a Sonic Ultrasonic Processor (Model number: GEX 130) equipped with a 3-mm diameter stepped microtip. The energy intensity level of the sonicator was set at 40% [14]. The cell lysate was centrifuged at 750g for 10 min. Aliquots of the supernatant, which contained EBs, were made and stored at -80°C. The titer of this batch of EB stock was determined to be 2 × 109 IFU/ml.

Transformation and selection of transformants

Transformation was carried out as previously described [8] with modifications. 7.5 μl of the above frozen L2R EB stock was combined with 10 μg plasmid DNA in 3.5 μl volume and 189 μl 50 mM CaCl2 buffer (prepared with 10 mM Tris, pH 7.4) in a 1.5 ml tube, which was let stand at room temperature for 40-45 min. McCoy cells of a 20 h culture at 80% confluence in a 145-mm diameter plate were trypsinized, collected into 14 ml antibiotic-free DMEM-FBS, and centrifuged at 500 g for 5 min. Following the removal of the supernatant, the cell pellet was rinsed gently with 10 ml of PBS, resuspended with 14 ml PBS, and centrifuged again. The pellet was resuspended in 220 μl CaCl2 buffer. 200 μl of the cell suspension was then added into the plasmid-EB-CaCl2 mix. The final transformation mix was incubated at room temperature for 20 min, during which the tube was shaken from time to time to prevent settling of the cells. At the end of the 20 min incubation period, the cells were diluted with 20 ml DMEM-FBS, and plated onto four T25 flasks (5 ml/flask) and were cultured at 37°C under 5% CO2 and 100% humidity.

Selection of transformants was initiated 10 h after the initial plating of the transformation. Ampicillin and chloramphenicol were added to the cultures to yield a final concentration of 2 μg/ml and 0.1 μg/ml, respectively. This initial passage was defined as passage 1. 46 h later, cells in the T25 flasks were harvested and disrupted by sonication. The entirety of the P1 culture was passed onto a new T25 flask of McCoy cells at 80-90% confluence. The P2 flasks were cultured with DMEM-FBS containing 1 μg/ml cycloheximide plus 5 μg/ml ampicillin or 0.2 μg/ml chloramphenicol. Passage and selection were repeated every 48 h for two additional passages through passage 4. 90% harvest of passage 4 was frozen and the remaining was expanded with medium containing 5 μg/ml ampicillin or 0.5 μg/ml chloramphenicol.

Glycogen stain

To stain glycogen in chlamydial inclusions, the culture medium was replaced with Lugol solution, which contains iodine, at 40 h after inoculation.

Imaging acquisition and processing

All phase contrast and GFP images were obtained at 40 h post inoculation from live cultures in PBS supplemented with 1.3 mM CaCl2, 1.0 mM MgCl2 and 1.0 g/L (w/v) glucose using an Olympus IX-51 microscope and an Olympus monochrome CCD camera. Images processing (coloring and color overlay) were accomplished by using the Picture Frame software [15, 16].

Results and discussion

pGFP::SW2, the shuttle vector constructed by Wang et al, contained a β-lactamase gene as a selection marker. It also carries a CAT gene that is fused to the GFP gene [8]. We found that E. coli transformed with the pGFP::SW2 plasmid was able to grow in medium containing chloramphenicol (final concentration: 170 μg/ml), suggesting that the CAT gene may also be used as a selection marker for chlamydial transformation experiments. As cautioned by Wang et al., an adverse effect of chloramphenicol on host mitochondria, as demonstrated by Li et al. [17] may affect the utility of this antibiotic for chlamydial transformation [8]. In Li et al.’s report, the minimal toxic concentration of chloramphenicol was 10 μg/ml, which caused a mild 20% reduction of ATP production. We have determined that the apparent lowest chloramphenicol concentration that completely inhibited inclusion formation in the plasmid-free C. trachomatis L2 strain designated L2R was only 0.05 μg/ml (data not shown), which was far below the concentrations toxic to host cells. Therefore, we reasoned that this antibiotic could be used to select CAT-expressing transformants without significantly stressing host cells.

We transformed L2R with pGFP::SW2, and selected one half of the transformed cells with ampicillin, and the other half with chloramphenicol. The antibiotics (2 μg/ml ampicillin or 0.1 μg/ml chloramphenicol) were added to the cultures at 10 h after transformation. Starting at passage 2, their concentrations were increased to 5 and 0.2 μg/ml, respectively, and they were added at the time of inoculation. The splitting ratio between passages remained 1:1 from passage 1 though passage 4. Even though the MIC of chloramphenicol, which was determined at low multiplicity of infection (~0.1 inclusion-forming units per cell), was 0.05 μg/ml, some of the untransformed chlamydiae were expected to form inclusions in the presence of 0.1 - 0.2 μg/ml the antibiotic, because we used a high EB to cell ratio for transformation, and efficacy of chlamydial growth inhibition by antibiotics is influenced by the multiplicity of infection [18]. With the above described selection protocol, in cultures selected with ampicillin, under a phase-contrast microscope, nearly 100% cells were found to contain an inclusion with aberrant RBs at the initial passage. The aberrant RB-containing inclusions were still present in a small proportion of cells at passage 2, but were mostly replaced by apparently normal inclusions at passage 3. Normal inclusions were found in about 20% cells, and abnormal inclusions were rarely observed at passage 4. At passage 5, which resulted from inoculation with 10% harvest from passage 4, inclusions were found in 80% cells; apparently, none of these inclusions contained aberrant RBs.

Since chloramphenicol does not cause chlamydiae to form aberrant RBs, we judged resistance to the antibiotic by the inclusion size. Inclusions of smaller-than-normal sizes were detected in almost all cells at passage 1. Some, but very small-sized, inclusions were found at passage 2, and most of those inclusions were replaced with normal-sized inclusions by passage 3. Normal-sized inclusions were found in more than 20% cells at passage 4. At passage 5, derived after inoculation with 10% passage 4 harvest, and an increase in chloramphenicol concentration (from 0.2 μg/ml to 0.5 μg/ml), normal-sized inclusions were found in nearly 100% cells 0000000.

In addition to apparent resistance to the selection agents, we used GFP expression and restoration of glycogen synthesis as additional markers for successful transformation [8, 9, 19]. EBs harvested from passage 5 were used to infect McCoy cells at a 1:100 dilution rate (cell number equivalence) for experiments determining GFP expression and glycogen synthesis (Figure 2). As expected, neither wild-type plasmid-replete C. trachomatis L2 (434/bu) (Figure 2A) nor untransformed plasmid-free L2R (Figure 2B) expressed GFP. Consistent with established findings that glycogen synthesis in C. trachomatis requires its plasmid [8, 9, 19, 20], iodine stain showed that glycogen was accumulated in the inclusions of wild-type L2 (Figure 2A) but not those of L2R (Figure 2B). In the presence of 5 μg/ml ampicillin, which inhibits RB division, non-transformed L2R (Figure 2C) formed inclusions containing giant RBs without producing glycogen; whereas chloramphenicol (final concentration: 0.5 μg/ml) completely inhibited the formation of visible inclusions in L2R infected-cells (Figure 2D). Consistent with data published by Wang et al. [8], pGFP::SW2-transformed L2R selected with ampicillin formed GFP-positive inclusions with glycogen (Figure 2E). pGFP::SW2-transformed L2R selected with chloramphenicol also formed GFP-positive inclusions containing glycogen (Figure 2F). As expected, ampicillin-selected transformants were able to form normal-sized, GFP-positive, glycogen-containing inclusions in the presence of chloramphenicol (Figure 2G); likewise, chloramphenicol-selected transformants were completely resistant to ampicillin, expressed GFP and produced glycogen (Figure 2H). These results suggest that the CAT gene in the pGFP::SW2 plasmid is functional in chlamydiae, and chloramphenicol-resistance can be used as a selection marker for chlamydial transformation.
Figure 2

Inclusion, GFP expression and glycogen synthesis of pGFP::SW2 transformants of C . trachomatis L2. Untransformed plasmid-replete strain 434/bu (A), untranformed plasmid-free strain L2R (B-D), and transformed L2R selected with either ampicillin (E, G) or chloramphenicol (F, H) were cultured either with medium containing an indicated antibiotic or with antibiotic-free medium. Images of inclusions in unstained and iodine-stained cultures were acquired with phase contrast microscopy or fluorescence microscopy 48 h post-inoculation. In all panels, phase contrast and GFP images are superimposable.

We next removed the β-lactamase gene from the pGFP::SW2 plasmid as described in the "Methods" section, and used the resulting pGFP-CAT::SW2 plasmid to transform L2R. Transformed chlamydiae were subjected to selection with chloramphenicol using the same regimen as described above. Chloramphenicol-resistant inclusions emerged in about 20% of the infected cells in the culture of passage 4. Fluorescence microscopy and iodine stain revealed GFP- and glycogen-positive inclusions in cells that were infected with EBs harvested from passage 5, and cultured in the presence of chloramphenicol (Figure 3, upper panel). However, as a result of a lack of β-lactamase in the pGFP-CAT::SW2 plasmid, the transformants were not able to form normal inclusions in the presence of ampicillin; instead, their inclusions were filled with aberrant RBs. While the irregular inclusions were still positive for GFP, they were largely free of glycogen (Figure 3, lower panel). After passage 5, the pGFP-CAT::SW2 transformants were cultured with 0.5 μg/ml chloramphenicol for additional four passages at a 1:100 splitting ratio for each passage. All inclusions at passage 9 had the same appearance as the inclusions of plasmid-replete chlamydiae and not that of the plasmid-free L2R, and all were found to express GFP (data not shown). These results prove that the CAT gene in the pGFP-CAT::SW2 plasmid, similar to the pGFP::SW2 plasmid, functions as a selection marker for C. trachomatis transformation.
Figure 3

Inclusion, GFP expression and glycogen synthesis in L2R transformed with pGFP-CAT::SW2. Cells infected with chloramphenicol-selected transformants were exposed to either chloramphenicol or ampicillin. Images of inclusions in unstained and iodine-stained cultures were acquired with phase contrast microscopy or fluorescence microscopy 48 h post-inoculation. Phase contrast and GFP images are superimposable.

It should be noted that Tam et al. has previously attempted to develop a transformation system with the CAT gene as a selective marker [21]. In that study, a shuttle vector containing a CAT gene was electroporated into EBs of C. trachomatis E (strain UW-5/CX) and L2 (strain 434/Bu). Although both CAT mRNA and enzyme activity were detectable in the initial cultures of transformed chlamydiae, the authors failed to obtain stable transformants after selection with chloramphenicol for 4 passages. It is important to note that both strains electroporated contain a native plasmid that shares the same replication origin with the recombinant plasmid used for transformation [21]. Since Wang et al. were able to obtain stable penicillin-resistant transformants only from L2R, a plasmid-free C. trachomatis L2 variant, but not the wild-type, plasmid-replete 434/Bu, under otherwise identical experimental settings [8], it is retrospectively not surprising that Tam et al. failed to derive stable chloramphenicol-resistant chlamydiae.


We have shown that for the plasmid-free C. trachomatis L2R, chloramphenicol can be used to select transformants when a shuttle vector that carries a CAT gene is used. Since Wang et al in Europe were able to select transformants of a clinical strain of serovar F with penicillin [19], CAT gene should be a highly useful and legally compatible selection marker for serovar F and other C. trachomatis serovars for which use of β-lactamase-carrying vectors are currently not permitted in the US. Furthermore, we envision that the CAT gene may also serve as a valuable secondary marker for conducting gene-targeting experiments and other genetic experiments such as in C. trachomatis lymphogranuloma strains that (will) have already been transformed with a β-lactamase-bearing plasmid.





Elementary body




Chloramphenicol acetyltransferase


Dulbecco’s modified Eagle’s medium


Ethylenediaminetetraacetic acid


Fetal bovine serum


Green fluorescence protein


Plasmid-free C. trachomatis L2 strain 2566R


Phosphate-buffered saline


Reticulate body.



We thank Dr. Ian Clarke (University of Southampton) for pGFP::SW2, and Dr. Guangming Zhong (University of Texas Health Sciences Center at San Antonio) for sharing transformation conditions in his lab. This study was funded by grants from the National Institutes of Health (AI071954) and New Jersey Health Foundation (PC7-13) to HF.

Authors’ Affiliations

Department of Pharmacology, Rutgers University Robert Wood Johnson Medical School
Rutgers University Graduate Program in Cell and Developmental Biology
Department of Pharmacology, Nantong University School of Medicine


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