- Research article
- Open Access
Differential regulation of two closely related integrative and conjugative elements from Streptococcus thermophilus
© Carraro et al; licensee BioMed Central Ltd. 2011
Received: 24 June 2011
Accepted: 24 October 2011
Published: 24 October 2011
Two closely related ICEs, ICESt1 and ICESt3, have been identified in the lactic acid bacterium Streptococcus thermophilus. While their conjugation and recombination modules are almost identical (95% nucleotide identity) and their regulation modules related, previous work has demonstrated that transconjugants carrying ICESt3 were generated at rate exceeding by a 1000 factor that of ICESt1.
The functional regulation of ICESt1 and ICESt3 transcription, excision and replication were investigated under different conditions (exponential growth or stationary phase, DNA damage by exposition to mitomycin C). Analysis revealed an identical transcriptional organization of their recombination and conjugation modules (long unique transcript) whereas the transcriptional organization of their regulation modules were found to be different (two operons in ICESt1 but only one in ICESt3) and to depend on the conditions (promoter specific of stationary phase in ICESt3). For both elements, stationary phase and DNA damage lead to the rise of transcript levels of the conjugation-recombination and regulation modules. Whatever the growth culture conditions, excision of ICESt1 was found to be lower than that of ICESt3, which is consistent with weaker transfer frequencies. Furthermore, for both elements, excision increases in stationary phase (8.9-fold for ICESt1 and 1.31-fold for ICESt3) and is strongly enhanced by DNA damage (38-fold for ICESt1 and 18-fold for ICESt3). Although ICEs are generally not described as replicative elements, the copy number of ICESt3 exhibited a sharp increase (9.6-fold) after mitomycin C exposure of its harboring strain CNRZ385. This result was not observed when ICESt3 was introduced in a strain deriving ICESt1 host strain CNRZ368, deleted for this element. This finding suggests an impact of the host cell on ICE behavior.
All together, these results suggest a novel mechanism of regulation shared by ICESt1, ICESt3 and closely related ICEs, which we identified by analysis of recently sequenced genomes of firmicutes. This is the first report of a partial shutdown of the activity of an ICE executed by a strain belonging to its primary host species. The sharp increase of ICESt3 copy number suggests an induction of replication; such conditional intracellular replication may be common among ICEs.
Acquisition of genomic islands (GIs) plays a key role in bacterial evolution [1, 2]. In silico analyses revealed that numerous GIs probably belong to Integrative and Conjugative Elements (ICEs) or are ICE-deriving elements [3, 4]. ICEs, including conjugative transposons, were defined as autonomous mobile elements that encode the functions needed for their excision, conjugative transfer and integration .
Cis-acting sequences and genes involved in a same biological process (for example conjugation) are generally grouped in a module, such as oriT and genes encoding relaxosome and conjugation pore. The recombination, conjugation and regulation modules are frequently grouped to form the core region of the ICEs. Although ICEs replicate during their conjugative transfer, it was originally assumed that they are incapable of autonomous intracellular replication and that their maintenance during cell growth and division only relies on their integration in the chromosome. Besides one or few core regions, they also harbor highly variable regions that encode functions potentially useful for the bacterial host . Comparison of the organization of related ICEs, such as Tn916 and its close relatives, revealed that they evolve by deletion, acquisition and/or exchange of modules. The conjugation, tetracycline resistance and regulation modules of Tn916 and Tn5397 are closely related whereas their recombination modules are unrelated . Likewise, the Tn1549 recombination module is closely related to the one of Tn916, but their conjugation and resistance modules are unrelated .
The closely related ICEs of the lactic acid bacterium Streptococcus thermophilus, ICESt1 and ICESt3, are integrated within the 3' end of the fda gene encoding a putative fructose 1, 6-diphosphate aldolase [8, 9]. They carry recombination and conjugation modules that are almost identical (95% nucleotide identity), related regulation modules (three homologous genes showing about 85% identity; to two or three unrelated genes) and various modules that could be advantageous for their hosts (including phage resistance). Their conjugation modules are very distantly related to modules of a large group of ICEs found in firmicutes, including Tn916 and ICEBs1 . As the conjugative transfer of ICESt1 occurs at a frequency one thousand times lower than that of ICESt3, their divergent regulation modules might be involved in these very different transfer activities .
The activity of almost all prophages and at least some ICEs is controlled by a central repressor that can belong to two unrelated families, either cI or ImmR (also known as cI-like, although they are not homologous to cI repressor). Both types of repressor carry a HTH XRE domain that allows their binding to promoter sequences upstream from their target genes. Transfer of the element requires the inactivation of the corresponding regulator, as shown during the RecA-dependent SOS response [11–13] of many cI-encoding prophages and two ICEs, SXT from Vibrio cholerae  and ICEBs1 from Bacillus subtilis , which encode respectively a cI and an ImmR repressor. Derepression of the ICE is due to the cleavage of the transcriptional regulator catalyzed by either the cI autopeptidase function  or a metalloprotease encoded by a gene adjacent to the gene encoding ImmR [12, 16]. Previous studies showed that various stimuli can activate ICEs, such as antibiotic treatment, cell density, stationary phase, DNA damage or presence of chlorocatechol [5, 11, 15].
Within the regulation module of ICESt1 and ICESt3, genes encoding homologs of cI (named arp1) and ImmR (arp2) and its associated protease (orfQ) were identified. ICESt1 and ICESt3 are the only two characterized elements which encode both cI and ImmR repressors, suggesting a novel and complex regulatory mechanism.
In order to explain the differences of transfer frequency previously observed for ICESt1 and ICESt3 of S. thermophilus, a transcriptional mapping of these elements was undertaken. Furthermore their excision/replication rates were investigated in different conditions (growth medium, exponential growth, stationary phase, after exposure to DNA damaging agent). Finally the influence of the host background was also explored. These experiments revealed that the two ICEs harbor closely related core regions, differ in their transcriptional organization and regulation. They provide further evidence of ICE replication. Our results also pointed out an impact of host cell on the ICE behavior.
Transcriptional organization and promoter analyses of the ICESt1 and ICESt3core region
To determine which genes were co-transcribed, RT-PCR amplification of core region was performed by grouping ORFs two by two or three by three. For ICESt1, amplifications of orfR/arp1/orfQ and orfP/arp2, respectively, were positive while that of the orfQ/orfP junction was negative (see additional file 1: S1B). These data comfort the hypothesis of a two-operon organization for ICESt1 (see additional file 1: S1A) with a functional rho-independent transcription terminator located between the two operons. By contrast, for ICESt3, all the RT-PCR amplifications of the regulation module were positive (see additional file 1: S1D) indicating a co-transcription of all the regulation genes (see additional file 1: S1C). The free energy of the transcriptional terminator detected between orf385B and orfQ genes in ICESt3 (Figure 1) was calculated with the mFold software . It is different from the one for ICESt1 (ΔG = -4.3 kcal.mol-1 for ICESt3 and ΔG = -8.2 kcal.mol-1 for ICESt1). This difference could explain why all genes of the regulation module of ICESt3 can be co-transcribed while two independent transcriptional units were found in ICESt1.
We then examined the activity of the promoter located upstream from the orfQ gene by Rapid Amplification of cDNA ends (5' RACE). For both elements, the start point (A nucleotide) was located seven nucleotides downstream from a -10 box separated by 17 nt from a -35 box, which overlapped the rho-independent transcription terminator (Figure 1A). This result is consistent with the S. thermophilus promoter consensus sequence (TTGACA - 17 nt - TATAAT) . Therefore, both ICEs possess a functional PorfQ promoter. However, it was previously showed that ICESt3 differs from ICESt1 by a -1 frameshift in the 5' end of its orfQ gene (orfQ1) . A second RBS, that could enable the translation from an initiation codon located downstream, was identified in silico (Figure 1A). All together, these data suggest that the orfQ2 gene of ICESt3 is truncated of 54 nucleotides at its 5' end compared to the orfQ gene of ICESt1.
For both elements, the functionality of the predicted arp2 promoter Parp2 was established with a (A) start site located seven nucleotides downstream from a -10 box (TACAAT) (Figure 1B). For both ICEs, transcriptional analyses showed that all the promoters (Pcr, PorfQ and Parp2), which are active during the stationary phase, are also active during exponential the growth phase (data not shown). However, an additional promoter was identified in ICESt3 upstream from the Parp2 promoter during stationary phase. Amplicons were obtained using arp2.f/r3 and arp2.f/r4 primers (Figure 2C). 5'RACE experiments revealed a start site located within a (A)6 stretch in this region (between the r4 and r5 primers, Figure 2C). Therefore, an alternative transcript originating from a distal arp2 promoter in ICESt3 (called "Parp2s") is expressed during the stationary phase (Figure 1C). This promoter does not match the classical promoter consensus as its -35 (TTATCA) and -10 (TGTAAT) boxes are separated by only 15 nucleotides (Figure 1C). The functionality of this promoter was highlighted only during stationary phase (Figure 2C) and only in ICESt3 (data not shown), although its sequence is strictly identical in ICESt1 (Figure 1C). Sequence analyses failed to detect any ORF in the 389 nucleotides between the Parp2s and Parp2 promoters.
Taken together, these data demonstrate that ICESt1 and ICESt3 do not share the same transcriptional organization of their regulation module: ICESt1 is organized as two operons, while in ICESt3 the whole module can be co-transcribed. Furthermore, ICESt3 possesses an additional distal promoter upstream the module, which is activated during stationary phase.
Growth phase and MMC exposure modulate the transcription of the ICESt1 and ICESt3core genes
Previous analyses showed a derepression of conjugative transfer of ICESt3 but not of ICESt1 after exposure to mitomycin C (MMC) . In order to explain this difference, we quantified by real-time RT-PCR, three regions (orfM/orfL junction, orfD/orfC junction and integrase gene) of the conjugation-recombination transcript of ICESt1 and ICESt3.
For both elements, quantitative RT-PCR was also performed on three loci of the regulation module (Figure 3). In ICESt1, the amount of arp2-orfP transcripts was similar whatever the conditions considered, while the amount of arp1 transcripts increased 10-fold after MMC treatment (Figure 3A). Regardless of conditions, no amplification was detected at the junction between the two operons (orfQ/orfP junction), which corroborates the lack of cotranscription of these genes. For ICESt3, the level of arp1 and orf385A/arp2 transcripts increased after MMC treatment (40-fold) and in stationary phase (about 10-fold) (Figure 3B). Co-transcription of the two operons was quantified by considering the orfQ/orf385B junction. During exponential growth phase and MMC exposure, co-transcription represented 20 and 38% of transcripts respectively, indicating that the terminator and the promoter PorfQ were active. However, in stationary phase, the amount of this junction was similar to that of the two operons, probably reflecting an activity of the Parp2s promoter.
After MMC exposure during stationary phase, transcript quantities were found to be similar to the ones observed in stationary phase without MMC. Therefore, MMC has an impact on DNA metabolism (lower level of DNA) during stationary phase but does not affect levels or organization of transcripts (data not shown).
Growth phase and mitomycin C affect ICESt1 and ICESt3excision
The excision percentage of ICESt3 was found seven-fold higher than the one of ICESt1 in exponential growth phase (Figure 4B), consistent with the higher level of ICESt3 conjugation-recombination transcript (described above), and its higher transfer frequency . For both ICEs, excision frequency was higher in stationary phase compared to exponential growth phase (Figure 4B). For these experiments, cells were grown in LM17 rich medium, in which transfer has been demonstrated . A similar excision rate of ICESt3 was measured in another rich medium (HJGL medium) that do not support the transfer of the two ICEs (data not shown). Therefore, the lack of ICESt3 transfer in this medium can not be due to a low excision level.
Transcriptional analyses have shown an increase of core transcript level for ICESt3 and ICESt1 after MMC treatment during exponential growth. This DNA damaging agent leads to an increase of excision percentage up to 90% for ICESt3, but only 4.3% for ICESt1 (Figure 4C). However, the increase is higher for ICESt1 (38-fold) compare to ICESt3 (18-fold). Therefore, under all tested conditions, ICESt3 is more active in excision than ICESt1.
DNA damage induces replication of ICESt3
Quantitative PCR was performed to measure the amounts of excised and integrated ICEs at different growth phases and after MMC treatment. According to the previously proposed ICE model (Figure 4A) attI and attB were expected to have the same copy number after ICE excision. This was found for both ICEs whatever the tested conditions, except for ICESt3 DNA extracted from strain CNRZ385 exposed to MMC (with a attI/attB value of 9.95 ± 1.42). To confirm this data, the orfM/orfL junction localized in the conjugation module was quantified and normalized to levels of different chromosomal loci: fda, dnaA and xerS (data not shown). The same result was obtained with an amount of M/L reaching about nine-fold the one of fda (9.60 ± 1.04). As fda is adjacent to integrated ICESt3 and replicates prior to the ICE during host chromosome replication, ICESt3 could be able to replicate autonomously under this condition. Different loci along ICEs (from J/I to M/L) were quantified at similar levels (data not shown) and thus did not allow us to propose a replicative mechanism (theta v/s rolling-circle).
ICESt3excision and replication depend on the host strain
A family of streptococcal ICEs shares related regulation and conjugation modules
All these putative elements harbor closely related regulation modules that would be transcribed divergently from the conjugation and recombination modules. All these modules possess a similar organization and encode putative cI repressors, ImmR repressors and metalloproteases related to the ones of ICESt1/3 (64-90% protein sequence identity) and one to four unrelated proteins (Figure 6). Sequence comparison of the intergenic core regions of the closely related streptococci ICEs revealed similar regulatory signals at the same positions as in ICESt1/3 with high sequence conservation (see additional file 2: S2B, S2C and S2D), suggesting a similar regulation.
More distantly related conjugation modules (35-70% identity for at least seven proteins with similar organization) are found not only in previously described elements - RD2 from S. pyogenes  and four elements integrated in a tRNALys gene from four S. agalactiae strains  - but also in novel putative ICEs that we found in various Streptococci including S. agalactiae ATCC13813 (incompletely sequenced), S. dysgalactiae ATCC12394 (two elements), S. downei F0415, Streptococcus sp. 2_1_36FAA and S. gallolyticus UCN34. Only the elements found in S. dysgalactiae encode a putative cI repressor, ImmR repressor and metalloprotease.
This study of ICESt1 and ICESt3, showed that their respective transcriptional organization and their mobility behaviors differ. As previously proposed from sequence analyses, all genes included in the conjugation and recombination modules of the two elements were found to be transcriptionally linked and controlled by a single promoter. This organization allows a coordinated regulation of genes involved in conjugation and recombination, which are functionally associated during ICE transfer.
For ICESt1 and ICESt3 regulation module, the cI-like encoding gene and one to two genes located downstream are expressed from the convergent promoter Parp2 or from a distal conditional promoter Parp2s. The genes encoding metalloprotease (orfQ) and cI homologs belong to a different operon expressed from another promoter PorfQ. These two operons are separated by a rho-independent transcription terminator. The ICESt1 regulation module includes two independent transcriptional units. By contrast, co-transcription of all the ORFs belonging to the regulation module was observed for ICESt3. This is probably enabled by a weaker transcriptional terminator and perhaps a higher transcription level and the activation of the stationary phase promoter Parp2s. These differences probably induce ICESt3 and ICESt1 differential regulations.
The mechanisms of ICE regulation based on cI or ImmR repressors, previously described for SXT and ICEBs1, are characterized by a decrease of transcript level of the cI or immR gene and an activation of the conjugation-recombination module transcription . By contrast, in ICESt3 from S. thermophilus, a transcriptional derepression was observed for the two operons of the regulation module, whereas in ICESt1, only the transcript level of the operon containing arp1 was affected. Under all tested conditions, ICESt3 is more transcriptionally active than ICESt1. The partial derepression of transcription of the regulation module may explain the lower activation of ICESt1 (conjugation-recombination transcript level, excision, replication) compared to ICESt3. So far, ICESt1 and ICESt3 were the only known elements (ICEs and prophages) encoding homologs of both cI and ImmR repressors. The gene encoding a putative metalloprotease is generally cotranscribed and located immediately downstream from the gene encoding the ImmR repressor [12, 16]. However, in ICESt1 and ICESt3, the metalloprotease gene (orfQ) is adjacent to the cI gene (arp1) but not to the cI-like gene (arp2), suggesting that the regulation involving both cI and cI-like regulators fundamentally differs from those identified in ICEs and related elements encoding only one regulator. Genomic analyses revealed, in various streptococci, ICEs that harbor conjugation module related to the ICESt1/3 ones These elements carry a regulation module related to the ICESt1/3 ones, suggesting that they could share a similar regulation.
After MMC treatment, the transcript levels of the recombination module increases 16-fold for ICESt1 and 84-fold for ICESt3. The 10-fold increase in ICESt3 copy number, after MMC treatment, could contribute to this increase of transcript levels but is not sufficient to explain its range. MMC exposure could induce an overinitiation of DNA replication with an apparent increase in origin-proximal gene expression for a short distance (≈50 kb) , but ICESt1 and ICESt3 are out of this area on the chromosome. MMC thus stimulates ICE transfer [10, 15, 25], but also increases transcription of both ICESt3 and ICESt1.
As copy number of ICESt3 increases after MMC treatment, the quantification of the empty chromosomal integration site underestimates the level of extrachromosomal ICEs. It is worth noticing that the increase of excision after MMC exposure does not lead to an increase of ICESt1 transfer. Additionally, a similar excision level was obtained for ICESt3 in HJGL medium, although this medium does not support ICE transfer. It shows that, besides excision, additional factors affect transfer of these elements. Similarly, although prior excision is required to observe the conjugative transfer of Tn916, which is an ICE that harbors a conjugation module very distantly related to the one of ICESt1/3, the transfer frequency of this ICE is not correlated with excision .
Some preliminary results favor the hypothesis of multiple extrachromosomal copies of ICESt3 (data not shown). ICEs, as their name implies, are able to excise from their host chromosome. Then the circular extrachromosomal ICE transfers to recipient cell per conjugation and simultaneously replicates by rolling-circle mechanism. The site-specific recombination leads to integration in donor and recipient chromosomes. During division, ICE transmission to the daughter cells is thought to depend on the replication and partition of the host chromosome. However, it has been recently reported that at least some ICEs can replicate independently of their conjugative transfer. In particular, the amount of excised forms of ICEBs1 increases two- to five-fold under inducing conditions  ICEBs1 replication is initiated within oriT and is unidirectional . This replication is involved in the stability of ICEBs1 and required the relaxase encoded by the element. In silico analysis of the putative relaxases of ICESt1/3 and of ICEBs1 indicated that they are distantly related (27.4% amino acid identity for relaxase), suggesting that replication could have similar role for the two ICEs.
Furthermore, the ICE RD2 from S. pyogenes related to ICESt1/3  and the putative ICE pKLC102 from Pseudomonas aeruginosa  were reported to be simultaneously integrated and at extrachromosomal multiple copies while pP36 from Legionella pneumophila is present as a multiple extrachromosomal copies in some conditions . Whereas, in firmicutes, none of the known ICEs was found to encode a partitioning system; in proteobacteria, the ICEs belonging to pKLC102-ICEclc family encode a putative partition system [30, 31].
In its host strain CNRZ368, ICESt1 exhibits a stable copy number, even after a stimulation of its excision and core region transcription by MMC exposure. In this strain, ICESt3 excision percentage is reduced 3-fold in stationary phase and nine-fold after MMC treatment and ICESt3 copy number is not increased compared to the one observed in the strain CNRZ385. Additional factor(s) could explain these differences (excision percentage and copy number) of ICESt3 in different S. thermophilus strains. Some host factors are likely involved in key steps of the ICE behavior, like B. subtilis PolC, DnaN and PcrA for ICEBs1 replication  and IHF for SXT excision in V. cholerae . To our knowledge, our work is the first report of partial shutdown of ICE activity by a strain belonging to the primary host species.
Analysis of recently available sequences led us to identify a set of closely related putative ICEs among various streptococcal species. All of them exhibit closely related conjugation modules but highly variable recombination modules. This suggests that these elements can transfer between various streptococcal species and exchange modules between one another. However, these regulation modules all share arp2, orfQ and arp1 genes (Figure 6), suggesting a fundamental function of these 3 genes in governing transfer of this ICE family. Further investigations will be required to characterize these genes and of their functional interactions with host regulators.
In conclusion, the transcriptional organization of the conjugation and recombination modules of two closely related ICEs from S. thermophilus, ICESt1 and ICESt3, is identical, while that of their regulation module is somewhat different. Transcripts of core region and excision levels are higher for ICESt3, which is consistent with its higher transfer frequency. Despite these differences, the excision of both ICEs is stimulated by exposure to a DNA damaging agent and stationary phase. Data generated by the transcriptional study suggest a new mechanism of regulation of ICESt1/3. This behavior could be due to the atypical regulation module of these elements that encode homologues of both cI and ImmR repressors. Analyses of sequenced genomes revealed, among streptococci, a family of ICEs that encode cI and ImmR homologs and therefore could share similar regulation.
Furthermore, our results suggest that DNA damage induces not only the excision and transfer of ICESt3 but also its intracellular replication. This characteristic, which is not considered in the initial ICE model, may be shared by other ICEs. This study also revealed that ICESt3 has very different behaviors depending on its primary host species, suggesting a major role of host factor(s) in its excision and replication.
Strains and media
Strains and plasmid used in this study.
Strains or plasmids
Relevant phenotype or genotype
Wild-type strain carrying ICESt1
Wild-type strain carrying ICESt3
Wild-type strain cured from its ICESt1 resident element
X. Bellanger pers. com.
Wild-type strain carrying ICESt3 tagged with the cat gene inserted in the pseudogene Ψorf385J, Cmr
CNRZ368ΔICESt1 strain carrying ICESt3cat, Cmr
supE44 lacU169 (φ80 lacZ M15) hsdR17 endA1 gyrA96 thi-1 relA1
3, 4 kb, replication origin from pBR322, Ampr
Strain CNRZ368 ICESt3catconstruction
To test the ICESt3 behavior in different S. thermophilus strain background, a filter mating was done as described previously  using the donor strain CNRZ385, carrying ICESt3 tagged with the cat gene conferring the chloramphenicol resistance  and the recipient strain CNRZ368ΔICESt1, spontaneous rifampicin and streptomycin-resistant mutant (X. Bellanger unpublished data). Triple-resistant clones were isolated and mapped for cse gene polymorphism  to confirm that they are transconjugants harboring CNRZ368 ICESt3cat. Three independent CNRZ368 ICESt3cat clones, which have similar growth parameters, mitomycin C (MMC) minimal inhibitory concentration (MIC) and dnaA/xerS rates (exponential growth phase with and without MMC treatment and stationary phase) than strains CNRZ368 and CNRZ368 cured of ICESt1 were used for each experiments.
S. thermophilus strains were grown at 42°C in 30 mL of LM17 medium to an optical density at 600 nm of about 0.7. Measures of OD600 nm were performed with the Genesys 20 spectrophotometer (Thermo scientific, Illkirch, France). Cells were diluted until OD600 nm = 0.05 into 50 mL of preheated medium (42°C) and harvested at early (OD600 nm = 0.2), mid exponential growth phase (OD600 nm = 0.6) or stationary phase (after 1.5 hours at OD600 nm = 1.5) with or without MMC exposure during 2.5 hours at the half of the minimal inhibitory concentration (MIC/2 = 0.1 μg/mL, for all the S. thermophilus strains used in this study) for genomic DNA or RNA extractions. Cultures were centrifuged at 13, 000 g during 15 min at 42°C and cell pellets were stored at -80°C.
DNA quantity along the MMC exposure was investigated by colorimetric DNA dosage . Genomic DNA of S. thermophilus was extracted as described previously . Plasmid DNA isolation was performed using Genelute Plasmid Miniprep Kit (Sigma-Aldrich, Lyon, France). DNA fragment recovery was performed using the High Pure PCR Product purification kit (Roche, Neuilly-sur-Seine, France). DNA cloning, ligation and restriction enzyme digestion were all carried out according to standard procedures  or according to specific recommendations of the supplier (New England Biolabs, Evry, France). PCR primers were designed with the PrimerQuest software http://www.idtdna.com/scitools/applications/primerquest/ and synthesized by Eurogentec (Angers, France) at 100 μM. PCR and high fidelity PCR were carried out according to the instructions of the ThermoPol PCR kit (New England Biolabs, Evry, France) and of the Triple Master PCR System (Eppendorf, Le Pecq, France), respectively. Sequencing reactions on RACE PCR amplifications were performed by Cogenics (Beckman Coulter genomics, Villepinte, France).
Reverse transcription PCR (RT-PCR)
Cell pellets were resuspended in 1 mL of Kirby mix (1% w/v of N-Lauroylsarcosine, 6% w/v p-aminosalicylic acid sodium salt, 0.1 M Tris HCl pH = 8, 6% v/v phenol pH = 8). Then total RNAs were extracted as described previously . The cDNAs were obtained by reverse transcription of 1 μg of DNase I-treated (Euromedex, Souffelweyersheim, France) total RNA with M-MLV reverse transcriptase (Invitrogen, Villebon sur Yvette, France) and random hexamer primers (Applied Biosystems, Villebon sur Yvette, France). PCR amplification of gyrA (40 cycles) was performed using gyrAR1 and gyrAR2 primers (see additional file 3: table S1) on retrotranscribed RNA and non retrotranscribed RNA, and used as positive and negative control, respectively. The quality of generated cDNA was controlled by amplifying a 1000-bp fragment by the J/I.f and G/H.r primers (see additional file 3: table S1). Transcriptional mapping was done using primers amplifying less than 1000-bp with a standard PCR program: 30 s at 95°C for denaturation, annealing 30 s at 50°C and extension 1 min at 72°C for 30 cycles. Primers are listed in the additional file 3, table S1 in part and available upon request for the rest.
Mapping of 5' extremity of RNA
5' ends of transcripts were mapped by Rapid Amplification of cDNA Ends using the 5'RACE PCR kit (Invitrogen, Villebon sur Yvette, France). PCR products were directly sequenced to determine the 5' ends. When they can not be precisely determined by direct sequencing, PCR products were subsequently cloned in pSL1180 (Table 1); 15 and 12 clones were sequenced for ICESt1 and ICESt3 respectively. Primers used are listed in the additional file 3 table S1.
Quantitative PCR (qPCR) was performed with 2 fg-200 ng DNA or cDNA, 5 μL qPCR Mastermix (Bio-rad, Marnes-la-Coquette, France) and 450 pM primers (see additional file 3: table S1) in 10 μL final volume. After activation of the hot start polymerase (30 s at 98°C), 40 cycles were performed: denaturation 10 s at 95°C and annealing/extension 45 s at 50°C for cDNA or denaturation 30 s at 95°C, annealing 30 s at 50°C and extension 1 min at 72°C for gDNA. The melting curve of the PCR product was analyzed with CFX manager software (Bio-rad, Marnes-la-Coquette, France) to verify PCR specificity. It was acquired each 0.5°C for 1 s by heating the PCR product from 60°C to 95°C. For each run, a standard dilution of the DNA fragment (preliminary obtained by PCR) was used to check the relative efficiency and quality of primers. A negative control (ultra-pure water obtained by the Direct8 Milli-Q system, Millipore, Molsheim, France) was included in all assays. Each reaction was performed at least in duplicate. Real-time PCR was carried out on a C1000 Thermocycler coupled by a CFX96 real-time PCR detection system (Bio-Rad, Marnes-la-Coquette, France). Strains depleted for their resident ICE, CNRZ368ΔICESt1 (X. Bellanger unpublished data) and CNRZ385ΔICESt3 , which have equal amount of attB and fda, were used as controls. cDNA quantities of studied genes were normalized to the amount of cDNA of the gyrA gene, whose transcription is considered as constitutive . Similar results were obtained when the ldh gene, encoding the lactate dehydrogenase, was used for normalization . Data are expressed as mean ± SD. Statistical analysis was performed with Student's E test. A p value < 0.05 was considered statistically different.
Protein and nucleic acid sequences from the recombination, regulation and conjugation modules of ICESt1 and ICESt3 were compared with sequences from Firmicutes on the NCBI server http://www.ncbi.nlm.nih.gov using BLASTP, BLASTN and/or tBLASTN. Identified sequences are from ICESpn8140 of S. pneumoniae [GenBank:FR671412] and from the partially or completely sequenced genomes of S. parasanguinis F0405 [GenBank:NZ_AEKM00000000] and ATCC15912 [GeneBank:NZ_ADVN00000000], S. australis ATCC700641 [GeneBank:NZ_AEQR00000000] S. infantis ATCC700779 [GeneBank:NZ_AEVD00000000], S. agalactiae ATCC13813 [GenBank:AEQQ01000089], S. dysgalactiae ATCC12394 [GenBank:CP002215], S. downei F0415 [GenBank:NZ_AEKN01000010], Streptococcus sp. 2_1_36FAA [GenBank:NZ_GG704942] and S. gallolyticus UCN34 [GenBank:NC_013798].
We thank S. Payot-Lacroix and J.B. Vincourt for critical reading of the manuscript. NC is supported by MNERT fellowship from the Ministère de l'Education et de la Recherche. The authors are grateful to X. Bellanger for CNRZ368ΔSt1 and M. Mourou for help with the CNRZ368 ICESt3cat.
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