- Research article
- Open Access
TasA-tasB, a new putative toxin-antitoxin (TA) system from Bacillus thuringiensis pGI1 plasmid is a widely distributed composite mazE-doc TA system
© Fico and Mahillon; licensee BioMed Central Ltd. 2006
- Received: 05 July 2006
- Accepted: 13 October 2006
- Published: 13 October 2006
Post-segregational killing systems are present in a large variety of microorganisms. When found on plasmids, they are described as addiction systems that act to maintain the plasmid during the partitioning of the cell. The plasmid to be maintained through the generations harbours a group of two genes, one coding for a stable toxin and the other coding for an unstable antitoxin that inhibits the effects of the toxin. If, during cell division, the plasmid is lost, the toxin and antitoxin proteins present in the cytosol cease to be newly expressed. The level of unstable antitoxin protein then rapidly decreases, leaving the toxin free to act on the cellular target, leading to cell death. Consequently, only cells harbouring the plasmid can survive.
The pGI1 plasmid of Bacillus thuringiensis H1.1 harbours a group of two genes, one showing similarities with the Doc toxin of the phd-doc toxin-antitoxin system, potentially coding for a toxin-antitoxin system. Attempts were made to clone this putative system in the Gram-negative host Escherichia coli. The putative antitoxin tasA was easily cloned in E. coli. However, although several combinations of DNA fragment were used in the cloning strategy, only clones containing a mutation in the toxin gene could be recovered, suggesting a toxic activity of TasB. An exhaustive search was carried out in order to index genes homologous to those of the putative tasA-tasB system among microorganisms. This study revealed the presence of this system in great number and in a large variety of microorganisms, either as tasA-tasB homologues or in association with toxins (or antitoxins) from other TA systems.
In this work, we showed that the pGI1 plasmid of B. thuringiensis H1.1 harbours genes resembling a toxin-antitoxin system, named tasA-tasB for t huringiensis a ddiction s ystem. This system appeared to be functional but unregulated in E. coli. Bioinformatics studies showed that the tasAB system is present on plasmids or chromosomes of a large variety of microorganisms. Moreover, the association between TasA antitoxin with toxins other than TasB (and vice versa) revealed the composite and modular nature of bacterial TA systems.
- Toxin Gene
- Conserve Domain Database
- Upstream Gene
- Putative Toxin
- Antitoxin Gene
Plasmids are extrachromosomal elements that carry mostly non-essential genes. However, they often confer advantages to their host, because of determinants such as antibiotic-resistance or virulence genes. When a mother-cell divides, plasmids have to be partitioned into the daughter-cells to keep for the progeny to retain this advantage. For high copy number plasmids, this process occurs by random distribution. However, when a plasmid is present in the cell at a low copy number, the cell has to develop active systems in order to avoid the production of plasmid-free progeny by loss of plasmid during partitioning. One strategy is to actively distribute the plasmid by a mechanism that relies on the presence of centromere-like functions [1, 2].
Another strategy is the mechanism called post-segregational killing system or toxin-antitoxin (TA) system. The plasmid to be maintained harbours a group of two genes, one coding for a stable toxin, and the other one expressing the antitoxin counterpart. This antitoxin is an unstable protein that is continuously degraded by a protease. When the plasmid is present in the cell, both toxin and antitoxin are expressed and the antitoxin acts on the toxin to prevent its toxic effects. If, during segregation, the plasmid is lost, toxin and antitoxin are no longer produced and the level of antitoxin rapidly decreases in the cell, leaving the toxin free to act on its target and leading to the death of the cell. Only cells harbouring the plasmid do survive.
Such systems are known to be present in a wide range of prokaryotes . Although the targets of the toxins may differ and sequence homologies may be quite low, these systems tend to be very similar in structure and regulation . One of these systems, phd-doc, has been described in bacteriophage P1 as an addiction operon . This temperate bacteriophage is stably maintained as a plasmid prophage in the Gram-negative bacterium Escherichia coli. The bacteriophage harbours a group of two genes, one coding for a toxin, doc (d eath o n c uring), and an upstream gene coding for its antitoxin, phd (p revent h ost d eath) . In host cells possessing the P1 genome, stable Doc toxin and unstable Phd antitoxin are continuously expressed . Phd antitoxin interacts with the Doc toxin, preventing it from carrying out its molecular action on the target, which is unknown. It has been suggested that a trimeric complex P2D is formed, sterically or structurally altering the Doc toxin activity on the target by buffering free Doc molecules within the cell . Moreover, Phd is also known to repress both its own transcription and that of the Doc molecule by binding to an operator DNA site that overlaps the addiction promoter . It has also been suggested that the Phd antitoxin might exert its action by activating another protein that neutralizes the Doc toxin . The Phd antitoxin is continuously degraded in the host cell by the ClpXP protease system , composed of the ClpP protease and the regulatory ClpX ATPase subunits [9–11]. Phd-doc is thus an active system that ensures stable inheritance of the P1 genome in the host cell population by killing any segregants that are free of the P1 genome.
The actual function of TA systems had to be re-examined, however, when chromosomal TA systems were discovered. A first hypothesis proposes that chromosomal TA systems contribute to programmed cell death (PCD) that occurs in response to various stress signals [12–15]. Indeed, experiments carried out on the mazEF system have shown that high levels of ppGpp, the signal molecule of nutritional stress, repress the mazEF promoter. This repression leads to the drop of MazE antitoxin levels and subsequently to the death of the cell . By the same mechanism, antibiotics inhibiting transcription, such as rifampicin, or translation, such as chloramphenicol and spectinomycin, have been shown to induce PCD via the activation of the mazEF system . A second hypothesis suggests that, rather than activating programmed cell death, chromosomal TA systems may induce a reversible bacteriostatic state to protect the cell in response to stressful conditions . Indeed, it was shown that the induction of the antitoxin MazE after exposition to overproduction of the toxin MazF restored the viability of the cell, suggesting that the toxin MazF is bacteriostatic rather than bacteriocide.
Bacillus thuringiensis H1.1 is a member of the Bacillus cereus group of Gram-positive bacteria. This bacterium occurs naturally in soil and on plants and is considered to be harmless to human. During sporulation, it produces δ-endotoxins that are toxic to insects. B. thuringiensis strain H1.1 contains at least four large plasmids (> 30 kb) and three small plasmids: pGI1, pGI2, pGI3 . The complete sequences of pGI2, pGI3 and pGI1 plasmids have been determined [18–20]. Based on the analysis of the 8254 bp pGI1 plasmid, five ORFs larger than 100 aa in size have been identified : a rep gene encoding the Rep protein, which is responsible for the autonomous replication of the plasmid, a mob gene that enables mobilization of the plasmid, and ORF5, which is a putative transcriptional regulator. Another ORF, downstream of the mob gene, encodes a 133-residue protein and shows a high degree of similarity to the Doc toxin of the P1 bacteriophage. The last ORF (95 aa) located upstream of the putative toxin gene could potentially code for the antitoxin counterpart.
TasB of pGI1 from B. thuringiensis H1.1 is toxic in E. coli
Oligonucleotide primers. Oligonucleotide primers used in PCR assays to clone different segments of the toxin-antitoxin system from pGI1.
Region amplified (Accession number : AY138809)a
Length (bp) of amplified region
Since it was found to be impossible to clone the tasB toxin gene alone in E. coli, a PCR fragment (AP) spanning the full sequence of both genes from the start codon of the antitoxin tasA to the stop codon of the toxin tasB was inserted into pCR4-TOPO and transformed into E. coli. However, as for tasB alone (P fragment), all the recombinant clones contained mutations in the tasB toxin gene.
An alternative was to clone the tasAB cluster with its own promoter region into E. coli. Two constructions were tested: pAP, containing a region of 232 bp upstream of the start codon of antitoxin tasA, and p2AP, containing an upstream region of 311 bp. Once again, only recombinants possessing a mutation in the toxin gene tasB could be recovered on selective plates.
In order to avoid the killing effect of the TasB toxin, an E. coli strain expressing the TasA antitoxin was constructed as follows: the pGI1 tasA antitoxin gene was inserted into the positive-selection vector pCR4-TOPO and electroporated in E. coli TOP10, leading to the construct pGIF02 (see Material and Methods). The tasA antitoxin gene was then inserted into the pCYB10 vector downstream of the IPTG-inducible promoter ptac and electroporated into E. coli TOP10. Sequencing confirmed the absence of any mutation in the antitoxin gene. The newly constructed vector was named pGIF03. The A, P, AP, pAP and p2AP fragments inserted into vector pCR4-TOPO (see Fig. 1 and Table 2) were then electroporated into the E. coli TG1/pGIF03 strain, in the presence of 1 mM of IPTG to induce expression of the antitoxin. Once more, no recombinants harbouring the wild-type tasB toxin gene were obtained from the P-, AP-, pAP- and p2AP-containing constructions.
These cloning experiments strongly indicated a toxic effect of TasB when cloned into E. coli. This supports the proposal that the pGI1 plasmid of B. thuringiensis H1.1 encodes a new putative toxin-antitoxin system. However, this system appeared to be functional but unregulated in E. coli. Indeed, the addition of a plasmid containing the tasA gene failed to inhibit the lethal activity of TasB in E. coli. This may be explained by an inappropriate expression of the antitoxin in the Gram-negative background. TA systems are regulated at transcriptional level by the antitoxin and/or the antitoxin-toxin complex, and this antitoxin is continuously degraded by a specific protease present in the cytosol of the bacterium. It has been shown that the toxin/antitoxin stoichiometry influences the binding of the complex to the promoter-operator region . When cloned into E. coli, the tasA-tasB system might be misregulated by a change in the TasA/TasB ratio, as a consequence of its dependence on a different system of proteases than in the host B. thuringiensis. Experiments are currently underway to determine the TasA level in this bacterium.
Homologues of the tasA-tasB genes of pGI1 reveal the existence of combinatory TA systems in a large variety of microorganisms
Homologues of tasA-tasB from pGI1 are found in a large variety of microorganisms
In 55 cases, the ORF found upstream of the TasB homologue displayed significant similarity to the TasA antitoxin of pGI1. These loci were found in a large variety of microorganism including 14 firmicutes, 26 proteobacteria, 6 chlorobi, 4 cyanobacteria, 2 chlamydiae, 1 acidobacterium, 1 bacteroidete and even 1 planctomycete (see Additional file 2). In this group, all putative antitoxin proteins had about the same size as TasA. Almost all members in this group displayed a gene organization found in many TA systems in which the stop codon of the antitoxin overlaps the start codon of the toxin. This was however not the case for those found in Bacillus clausii, Geobacillus kaustophilus, Lactobacillus acidophilus, Lactobacillus gasseri, Nitrosomonas europaea, Rhodospirillum rubrum, Rhodopseudomonas palustris BisB5 and HaA2, Salinibacter rubber, Xhanthomonas oryzae KACC10331 and MAFF 311018, Xhanthomonas campestris vesicatoria and Gloeobacter violaceus (see Additional file 2). In this group, all the TasB homologues were found on the chromosome of the bacteria, except for Glucunobacter oxydans 621H in which the corresponding locus is found on the plasmid pGOX2 (see Additional file 2).
These 55 loci displaying similarities with both TasA and TasB were grouped into a family named the TasAB family (Fig. 4 and Additional file 2). To our knowledge, the tasAB system is the first described in this novel family.
TasB homologues can be associated with putative antitoxins unrelated to TasA
In addition to the loci described above, the bioinformatic analysis provided 62 more TasB homologues (E value < 1) that were associated with upstream genes unrelated to the putative antitoxin TasA. These loci were also found in a large variety of microorganisms including 35 proteobacteria, 10 actinobacteria, 8 firmicutes, 4 archaea, 2 cyanobacterium, 1 chloroflexi, 1 chlamydiae and 1 phage (P1). All are chromosomal loci, except for one that was found in the pCC7120epsilon plasmid of Nostoc sp. PCC 7120 and one found on the pKLH205 plasmid of Acinetobacter sp. ED-4525. The upstream ORFs were compared to the Conserved Domain Database (CDD)  and classified according to their similarities with other published sequences or with other upstream genes found in this analysis (see Additional file 3). By this classification, 10 groups of composite TA loci were obtained (Fig. 4).
In the first group (group 1), which was composed of 5 loci, one of the TasB homologues was a confirmed toxin from the known phd-doc TA locus of enterobacterial phage P1 . All the systems included in this group harboured an upstream ORF similar (identity > 39%) to the Phd antitoxin of the phd-doc system. This group was thus composed of loci displaying similarities to both the TasB/Doc toxins and the Phd antitoxin. The 5 members of this group were all similar in size and organization (translation coupling). The second group (group 2) was composed of five TA loci (identity > 44%) that were all found in γ-proteobacteria. All antitoxins of this group were very similar in size except for the one found in Ps. aeruginosa, which was smaller than the others. It is also interesting to note that in the putative toxin gene of the Ps. aeruginosa TA locus, two frameshifts give rise to a hybrid protein. Group 3 of composite TA systems included small antitoxins (identity > 66%). However, in two cases, Vibrio cholerae O1 eltor N16961 and in V. cholerae V52, the putative antitoxin seemed to be fused at its amino-terminal part with a putative acetyl-transferase (not shown). In the next 6 groups (groups 4 to 9), all upstream proteins were similar to each other within a group (identity > 38%), but shared no similarities with other known proteins. The last group (group 10) was composed of 2 members (100% identical) from the same organism delta proteobacterium MLMS-1. They were larger than tasA and contained a domain similar to that of ParB, which has been proposed to be a nuclease involved in plasmid stability .
In addition to these 10 groups, a number of orphan upstream genes were found (see Additional file 2). These genes were predicted to code for proteins displaying no similarity to TasA or to other known genes. It is possible that new groups of antitoxins could be discovered.
Furthermore, nine TasB homologues, all originating from the proteobacteria phylum, were found to be significantly larger than the others (see Additional file 2). While the carboxy-termini of the corresponding proteins were similar to the pGI1 TasB toxin, their amino-termini displayed similarity with the COG3943 domain. This domain is defined in the Conserved Domain Database as related to a virulence protein because of its similarities to RhuM. This protein, located in the SPI-3 pathogenicity island of S. enterica , is predicted to be a virulence protein because mutants carrying a knocked out copy exhibit diminished ability to invade epithelial cell and/or to induce polymorphonuclear leukocyte migration in a tissue culture model of mammalian enteropathogenesis . In this group, no upstream antitoxin seemed to be associated with these putative toxins.
Finally, 10 TasB homologues were defined as "solitary toxin" , since they had the same size as TasB but were apparently not associated with an antitoxin partner (not shown). These solitary toxins were found in a broad range of microorganisms including 4 proteobacteria, 2 actinobacteria, 2 archaea, 1 fusobacterium and even 1 fungus. The latter was found in Aspergillus fumigatus. This gene has been annotated as a putative member of the Doc family ([GenBank:EAL85381], Nierman et al., unpublished), but the exact function of the protein has not been demonstrated. If this homologue were proved to be functional, this would be the first TA locus identified in a fungal species.
Similar cases of solitary genes have already been reported in the study of homologues of the YdcE toxin (MazF family) from the ycDE operon of Bacillus subtilis , in a study describing a number of TA loci from the vapBC family (vapC is a toxin containing a PIN domain)  and in an exhaustive study of TA homologues . This suggests that if those solitary toxins were found to be functional, other mechanisms of regulations specific to each species would have to exist.
TasA homologues can be associated with either TasB homologues or with other toxin families
As in the case of the TasB toxin, the TasA antitoxin of pGI1 was compared to potential downstream ORFs for their similarities and putative functions. Homologues of the TasA antitoxin found in this study were separated into three classes: those with a TasB-like downstream gene as described above (Fig. 2 and Fig. 4), the second including TasA homologues with a toxin-like downstream gene (Fig. 4), and TasA homologues not associated with a putative toxin.
Homologues of TasA associated with proteins unrelated to TasB were found in 15 archaea, 6 proteobacteria, 4 firmicutes and 1 spirochaete (see Additional file 2). Downstream proteins of TasA homologues were grouped according to their similarities (see Additional file 3); four groups of composite TA loci were obtained (see Additional file 2). The first group (group 11) was composed of 6 TA loci (identity > 27%) very similar in size, originating from phylogenetically distant species, and all sharing similarities with the mazF toxin of the confirmed TA locus mazEF. This high similarity between TasB and the Doc toxin (28% identity ; E-value = 2e-19 in the CDD), combined with the similarity between TasA and the MazE antitoxin (23% ; E-value = 2e-3 in the CDD), indicated that the tasA-tasB toxin-antitoxin system from pGI1 is thus a composite mazE-doc-like system. In the second group (group 12), 12 TA loci were found (identity > 27%). The putative toxins downstream of the TasA-like genes were all similar in size, except for the one originating from Pyrococcus horikoshii, smaller than the others and than the TasB toxin from pGI1. All the putative toxins found in this group belonged to the conserved domain COG1848. Proteins of this group are predicted nucleic acid-binding proteins, containing a PIN domain. The PIN (PilT N-terminus) domain was first annotated on the basis of sequence similarity to the N-terminal domain of the pilT protein from Myxococcus xanthus . Proteins containing such a domain can be found in the genome of a large variety of prokaryotes and eukaryotes. By analogy with eukaryotic PIN proteins, which are ribonucleases , prokaryotic PIN proteins have been predicted to be toxic components of chromosomally encoded TA operons . The vapBC locus of Leptospirra interrogans has been described as a toxin-antitoxin system in which the VapC toxin contains a PIN domain .
Both loci of the next group (group 13) harboured a conserved domain COG5573. This group is related to the COG1848 group and also contains a PIN domain. The last group (group 14) contained 3 loci of which the downstream proteins belonged to the pfam01850 group, also harbouring a PIN domain. These 3 groups were thus considered to be functionally related as they all contained a PIN domain. In addition to these groups, three orphan cases of composite TA loci were found in which the associated toxin showed no similarity with other toxins (see Additional file 2).
In addition to those found above, a number of TasA homologues were found for which no gene could be identified immediately downstream of their genomic location (not shown). These genes were often longer than the antitoxin of pGI1. Only the N-part of the protein displayed a high degree of homology with the antitoxin. These homologues have been annotated as transcriptional regulator of the AbrB- and SpoVT-family. Comparison with the CDD (Conserved Domain Database, NCBI) showed that they all harboured a SpoVT/AbrB-like domain . The product of the AbrB gene is an ambiactive repressor and activator of the transcription of genes expressed during the transition state between vegetative growth and the onset of stationary phase and sporulation . AbrB is thought to interact directly with the transcription initiation regions of genes under its control . The product of the B. subtilis gene spoVT is another member of this family and is also a transcriptional regulator .
It has been shown that antitoxins contain motifs common to different classes of DNA-binding proteins and can therefore be classified according to their structural homologies: MetJ/Arc superfamily and related ribbon-helix-helix fold proteins, Phd/YefM and AbrB/MazE superfamilies . Multiple alignments of the TasA homologues showed a highly conserved amino-terminal domain (Fig. 2). This was consistent with other studies that have used mutational analyses to show that antitoxins bind to DNA through their N-terminal domain .
In this work, we showed that the pGI1 plasmid of B. thuringiensis H1.1 encodes a new toxin-antitoxin system, called tasA-tasB for t huringiensis a ddiction s ystem. This system appeared to be functional in E. coli, and a single mutation in the tasB gene was sufficient to inhibit the lethal activity of the toxin in E. coli. However, the addition of a plasmid containing the tasA gene failed to restore the viability of the cells, probably due to an inappropriate expression in the Gram-negative background.
Additionally, our study revealed a new family of TA loci, the TasAB family which is presently composed of at least 56 members, found in a large variety of microorganisms. TA systems have been extensively described and their toxins have been classified into superfamilies, according to their structural homologies: the MazF/Kid/CcdB, the RelE/ParE, the Doc and the PIN superfamilies . In the TasAB family, exhaustive protein sequence searches showed that the TasB toxin of the tasAB system from pGI1 is similar to Doc of the phd-doc system. Interestingly, TasA was not similar to the antitoxin Phd, but presented similarities with the MazE antitoxin from the mazEF TA system. The tasAB system and members of its family can thus be viewed as hybrid systems between the phd-doc and the mazEF systems. Moreover, other associations between toxins and antitoxins from different families can be found, as illustrated in our extensive protein search which showed that TasA and TasB homologues can be found in association with partners from other TA systems.
The present study confirmed that more than multiple TA systems can be found in the same bacterium. In the Sulfolobus solfataricus genome for exemple, 22 TA loci, all from the vapBC family (vapC is a member of the PIN domain family) have been found . Interestingly, microarray experiments have revealed the implication of these TA loci in the heat shock response, which involves the modulation of their expression under stress conditions . Since TA system could be stress-response elements, it has been suggested that free-living organisms, which grow slowly and are exposed to many environmental changes in comparison to host-associated organism, would benefit from having many TA loci .
There seems to be a common organization within the TA systems, featuring two genes, one coding for a toxin and the other coding for a DNA-binding protein that functions as an antitoxin and a transcription factor. Because composite associations of different toxins and antitoxins were found, it has been suggested that TA systems do not descend from a common ancestor but have been assembled from different proteins which can be displaced by functional equivalents, while the operon architecture itself is preserved . Consistently with this idea, ORF of unknown function associated with a TasB homologue could potentially represent members of new antitoxin families.
Bacterial strains, plasmids and growth conditions
Strains and plasmids. Strains and plasmids used in this study, including their origin, reference and main characteristics
Strains or plasmids
Construction, source or reference
B. thuringiensis H1.1
Isolated from Ephestia kühniella, Canada
IEBC (International Entomopathogenic Bacillus Center, Pasteur Institute, Paris, France)
E. coli TOP10
E. coli TG1
Resident plasmid from B. thuringiensis H1.1
Mahillon and Seurinck, 1988
Positive-selection cloning vector, AmpR, KanR
Cloning vector, AmpR, IPTG-inducible ptac promoter
New England Biolabs Inc.
pCYB1 deleted of intein gene
J. Mahillon and F. Bilocq unpubl. results
Cloning vector, CmR, arabinose-inducible promoter pBAD
Guzman et al., 1995
PCR fragment containing antitoxin gene of pGI1 cloned into pCR4-TOPO
Nde I-Sal I pGIF02 fragment containing the antitoxin gene A cloned into pCYB1O
PCR fragment containing the toxin gene P cloned into pCR4-TOPO, 4 clones obtained M1 → M4
PCR fragment containing the antitoxin-toxin locus AP cloned into pCR4-TOPO, 4 clones obtained M1 → M4
PCR fragment containing the antitoxin-toxin locus pAP cloned into pCR4-TOPO
PCR fragment containing the antitoxin-toxin locus p2AP cloned into pCR4-TOPO, 15 clones obtained M1 → M15
The primary cloning of the toxin and antitoxin genes was performed using the kanamycin-resistance, positive-selection plasmid vector pCR4-TOPO (InVitrogen), and electroporated into E. coli TOP10 strain. The antitoxin gene was subsequently cloned in the ampicillin-resistance plasmid pCYB10 and the toxin gene in the chloramphenicol-resistance plasmid pBAD33 (see PCR and cloning strategies). Newly constructed plasmids were electroporated in E. coli TG1 strains. The antibiotics were used at the following concentrations: 50 μg/ml kanamycin (Kan), 100 μg/ml ampicillin (Amp), and 15 μg/ml chloramphenicol (Cm).
Total DNA from B. thuringiensis H1.1 was prepared using standard protocol and stored at -20°C. Plasmid DNA preparations were obtained using the High Pure Plasmid Kit (Roche).
PCR and cloning strategies
Cloning fragments of the toxin-antitoxin system from pGI1 of B. thuringiensis H1.1 in pCR4-TOPO
Table 2 shows the oligonucleotide primers (purchased from Sigma-Genosys) used in the PCR method for cloning different gene fragments of the toxin-antitoxin system from pGI1 of B. thuringiensis H1.1. One pair of primer amplified the toxin gene only (P), while another pair amplified a region from the start of the antitoxin gene to the stop of the toxin gene (AP). A third pair flanked the toxin and antitoxin genes with an upstream region thought to contain the promoter region (pAP). Finally, the last pair of primers amplified an additional 78 bp region upstream of the antitoxin gene (p2AP) (Fig. 1B). One μl of total DNA (50-fold dilution) of B. thuringiensis H1.1 was used for the amplification of the gene fragments in a 50 μl mixture containing 1 μl of DyNAzyme I DNA polymerase (FINNZYME), 5 μl of the 10 × standard buffer, 0,5 μl dNTP (20 mM) and 5 μl primers (10 μM). The reaction was performed in a Perkin Elmer GeneAmp PCR System 9600 thermal cycler using the following program: initial denaturation at 96°C for 10 min, 30 cycles of denaturation at 92°C for 1 min, annealing for 1 min at 50°C and extension at 72°C for 1 min 30 sec. An additional extension step for 10 min at 72°C ends the amplification program.
The PCR products were ligated into the plasmid vector pCR4-TOPO using the protocol described in the TOPO TA cloning Kit for sequencing (InVitrogen) and transformed by electroporation into E. coli TOP10. Inserts from the KanR recombinants were sequenced by Genome Express (France) using the M13 universal primers.
Cloning of the antitoxin gene in pCYB10
The pCR4-TOPO plasmid containing the A fragment (Fig. 1B), obtained as described above, was sequenced to assess the absence of any mutation, and called pGIF02. Both pGIF02 (KanR, AmpR) and pCYB10 plasmids (AmpR) were restricted by Nde I and Sal I enzymes. After extraction on gel using Quantum Prep Freeze'N Squeeze DNA Gel Extraction Spin Column (Biorad), the restricted fragments were ligated using 2 units of T4 DNA ligase (Fermentas, T4 DNA ligase Rapid ligation kit). The newly constructed plasmid, pGIF03 obtained in E. coli TG1 was sequenced by Genome Express (France).
Search for TasA and TasB homologues
The amino acid sequence of the putative TasB toxin was compared using standard BLASTP http://0-www.ncbi.nlm.nih.gov.brum.beds.ac.uk/BLAST. The cut-off E- value used in this analysis was 1. The genomic regions carrying potential toxin homologues were analyzed individually using DS Gene 1.5 (Accelrys), in order to find any upstream ORF. The same method was applied to the TasA antitoxin of pGI1 from B. thuringiensis H1.1, to find potential downstream partners. All the loci found in this computational study are listed in the Additional file 1.
Classification of putative toxins and antitoxin partners
Each immediate upstream ORF of TasB homologue, and downstream ORF of TasA homologue were translated in silico, using DS Gene 1.5, and compared to the Conserved Domain Database  in order to search for similarity with other known antitoxins/toxins from TA systems or with other known proteins. Identity percentages were calculated within a group by using NCBI/BLAST/align2sequences.
We are grateful to F. Bilocq and V. Op de Beek for initiating this project. We would like to thank L. Van Melderen for time devoted to the critical reading of this manuscript. We are also grateful to G. Van der Auwera for her help for the figure and time devoted to the proofreading of the manuscript, and to O. Minet for his technical help. This work was supported by the Region Wallonne (Convention n°991/4383), the FRIA (Fonds pour la Formation à la Recherche dans l'Industrie et dans l'Agriculture) (grant to S. Fico) and the Université catholique de Louvain.
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