- Research article
- Open Access
Alternative sigma factor σH activates competence gene expression in Lactobacillus sakei
© Schmid et al; licensee BioMed Central Ltd. 2012
- Received: 8 June 2011
- Accepted: 12 March 2012
- Published: 12 March 2012
Alternative sigma factors trigger various adaptive responses. Lactobacillus sakei, a non-sporulating meat-borne bacterium, carries an alternative sigma factor seemingly orthologous to σH of Bacillus subtilis, best known for its contribution to the initiation of a large starvation response ultimately leading to sporulation. As the role of σH-like factors has been little studied in non-sporulating bacteria, we investigated the function of σH in L. sakei.
Transcription of sigH coding for σH was hardly affected by entry into stationary phase in our laboratory conditions. Twenty-five genes potentially regulated by σH in L. sakei 23 K were revealed by genome-wide transcriptomic profiling of sigH overexpression and/or quantitative PCR analysis. More than half of them are involved in the synthesis of a DNA uptake machinery linked to genetic competence, and in DNA metabolism; however, σH overproduction did not allow detectable genetic transformation. σH was found to be conserved in the L. sakei species.
Our results are indicative of the existence of a genetic competence state activated by σH in L. sakei, and sustain the hypothesis that σH-like factors in non sporulating Firmicutes share this common function with the well-known ComX of naturally transformable streptococci.
- Sigma Factor
- Competence Gene
- lacZ Reporter Gene
- Alternative Sigma Factor
Sigma factors are subunits of the RNA polymerase complex responsible for specific recognition and melting of promoter DNA, which enable the polymerase to initiate transcription. All eubacteria of known genome sequence code for at least one sigma factor, called primary, housekeeping or vegetative, and most encode additional sigma factors. For example, Streptomyces coelicolor or Sorangium cellulosum carry as many as 60 to 80 predicted sigma factors [1, 2]. These so-called alternative sigma factors may be induced or activated by specific environmental signals, and consequently redirect transcription by competitively associating with the core RNA polymerase. Alternative sigma factors have been shown to mediate various cellular responses linked to stress conditions, growth transitions or morphological changes and development .
Sigma factors are classified into two structurally and evolutionarily distinct superfamilies , σ70 and σ54. Most eubacterial sigma factors belong to the σ70 superfamily, which is further divided into four phylogenetic groups on the basis of protein structure and physiological function [1, 4]. Group 1 comprises the housekeeping sigma factors. Group 2 is close to group 1 but accommodates non essential sigma factors, including the master regulator of general stress response in stationary phase, RpoS, as was well characterized in Escherichia coli. Sigma factors in group 3 are phylogenetically diverse, and regulate major cellular functions such as sporulation, motility, heat-shock or general stress response. Group 4, known as the extracytoplasmic function (ECF) subfamily, has been distinguished more recently. It comprises highly diverged sigma factors mainly involved in responses to extracytoplasmic stimuli, which may affect the correct folding of envelope proteins. These factors typically contain only domains refgrped to as 2 and 4, involved in core polymerase binding and promoter DNA recognition and melting , with a spacer domain of less than 50 residues . However, due to the high divergence across sigma factors, their classification in the previously identified phylogenetic groups may need to be revised, and new cellular functions controlled by sigma factors may be discovered .
Our research concerns a putative σH factor in the lactic acid bacterium Lactobacillus sakei. The closest characterized homolog is the σH of Bacillus subtilis (σBsuH), encoded by sigH (formerly spo0H), which is best-known for its role in initiating sporulation, an ultimate differentiation response to starvation. σBsuH directs transcription of genes involved in polar septum formation and provokes induction of several regulator genes that in turn affect expression of signaling pathways or turn on pathways for endospore engulfment (e.g. via the σF sigma factor) [5, 6]. σBsuH is also associated with genetic competence, which enables the uptake of exogenous DNA and its assimilation as new genetic information, leading to natural genetic transformation. This transient state occurs in about 10% of the cells as part of the same nutrient depletion response as sporulation. σBsuH increases expression of one of the two peptide pheromones needed for optimal activation of the master regulator of the competence pathway ComK [7, 8]. While σBsuH is essential for initiating sporulation, its absence reduces, but does not abolish transformation (efficiency is decreased by ~16-fold) . The whole decision-making pathway leading to sporulation or competence is an elaborate signal transduction network relying on multiple partners [7, 10]. In addition, σBsuH reportedly affects expression of about 10% of the genome and was proposed to be involved in the growth transition to stationary phase .
The position of σBsuH in the tree of σ70-type sigma factors is unclear. It exhibits structural characteristics similar to ECF sigma factors (group 4), yet phylogenetic analyses placed it between groups 3 and 4 [2, 4, 11]. Unexpectedly, database and phylogenetic analyses revealed that σH-like gene products are largely distributed in various members of the Firmicutes, sporulating or not [11, 12]. Interestingly, σH-like factors appear to be more divergent across non-sporulating bacteria than in sporulating bacteria . At the same time, structural elements similar to the conserved Gram-positive DNA uptake machinery appeared to be encoded in the genome in members of the Firmicutes not known for being naturally transformable, suggesting that this capacity may be more widespread than previously expected [12–14]. Two factors, classified in a single large σH-family of sigma factors by Morikawa et al. , are directly involved in transcription of competence genes in non-sporulating bacteria: the well-known ComX of naturally transformable streptococci , and the product of the so-called sigH gene of Staphylococcus aureus, a species which has not yet been shown to be transformable . These observations suggested the link between σH-like factors and genetic competence in non sporulating Firmicutes .
L. sakei belongs to the microbiota that develops on meats under storage, especially during vacuum packing. It is largely used as a starter for the manufacture of fermented sausages in Western Europe and its potential use in meat product biopreservation is currently under study [16–18]. Survival of L. sakei ranges from one day in aerated chemically defined liquid medium, to a few months in dry sausages, although little is known about the factors determining its stability. The existence in L. sakei of sigHLsa, an apparent sigHBsu ortholog, led us to identify the gene set regulated by σLsaH, and to determine whether and how this regulator is implicated in competence and stationary phase survival. A strain allowing experimental sigHLsa induction was constructed, and used in a genome-wide microarray study. Genes activated by sigHLsa overexpression appeared mainly involved in genetic competence, although we could not obtain evidence for natural transformation. This study provides further suggestive evidence that the conserved role of the σH-like sigma factors in non-sporulating Firmicutes is to activate competence gene expression.
Identification of sigH in the genome of L. sakeiand other lactobacilli
Nevertheless, the locus comprising σH-like gene may have experienced genetic rearrangements across the different genera and also among species of the same genus (Figure 1). Moreover, the σH-like gene location seems to be variable in members of the Firmicutes, especially in the Lactobacillales (Figure 1). A putative σH-like gene is not found at the same location in Lactobacillus salivarius as in L. sakei (locus cysS-nusG). Likewise, the location of the unique gene for the ComX factor differs in the naturally competent Streptococcus thermophilus LMD9 from those of each of the identical comX copies in S. pneumoniae R6, in which both copies are adjacent to a tRNA gene and ribosomal operons.
Conservation of sigH genes in the L. sakeispecies
L. lactis subspecies lactis and cremoris exhibit two comX allelic types whose nucleotide divergence is at most 27.5% . In contrast, sigH divergence (4.5% maximum divergence) was incongruent with the previously reported genotypic classification of L. sakei strains , and its two proposed subspecies (Figure 3). This discrepancy may be explained either by a particular evolutionary history of that gene in L. sakei or by the possibility that the classification based on the flexible gene pool does not reflect the phylogenetic relationships between strains which remain to be established.
High nucleotide divergence between species, contrasted with generally higher conservation within species, was also observed for sigH loci in the genus Staphylococcus . The reason for such high inter-species polymorphism is unknown. However, rapid evolution after species divergence rather than lateral gene transfer may be responsible, as the phylogeny of sigH genes was reported to be concordant with species phylogeny in staphylococci .
As reported in this paper, functional studies were further conducted on RV2002, a derivative of L. sakei strain 23 K, for which genome data is available, and in which the endogenous β-galactosidase encoding gene is inactivated, thus enabling the use of a lacZ reporter gene .
Temporal transcription of sigH
Overexpression of σH
Relative expression ratio$ of sigH and comEA with or without overexpression of sigH
control of the inducer effect in wt strain
presence of the additional copy of sigH
cumulative effect of induced additional copy
comEA transcription was not increased at the onset of stationary phase in the WT nor in the induced sigH(hy)* strain, suggesting that the competence genes are not naturally induced under laboratory conditions. Activation of comEA tended to diminish after a four hour-induction despite high levels of sigHLsa transcripts, possibly indicative of another regulatory loop on comEA or post-transcriptional regulation of sigHLsa. This transcription pattern was similar for comGA exhibiting a 280-fold increase in transcript amounts one hour after sigHLsa induction in sigH(hy)* followed by a 3-fold decrease between one and four hours. These results show that in L. sakei, conditions of σLsaH overexpression lead to activation of comEA and comGA. Nevertheless, other factors likely modulate com gene expression, as suggested from the drop of expression late in growth.
Global transcriptome profiling of the σHoverexpression strain suggests the existence of a genetic competence state
To identify the genes of L. sakei regulated by σLsaH, the experimental system described above was used in a full-genome comparative transcriptome analysis of sigH(hy)* and sigH(wt)* after one hour induction with 30 μM CuSO4. Quantification and statistical analysis of the microarray data (see Methods for parameters) led to relatively few differentially expressed candidate genes. The overexpressed sigH gene in sigH(hy)* was 11 ± 3 times induced compared to the WT strain in this microarray experiment; qPCR-based quantification of the same RNA samples showed a 149 ± 42-fold greater expression relative to the WT strain, confirming the successful overexpression of sigHLsa. Differences in fold ratios between microarray-profiling and qPCR analysis are not unusual but were high in our experiment; they might reflect a less efficient detection on microarray or an overestimation by qPCR especially when genes are weakly expressed in one of the conditions, which seemed to be the case for the com genes.
Genome-wide transcriptome profiling of SigHLsa overexpression in L.sakei 23 K
Functional category and CDS
common variance model
Pvalue (FDR) varmixt model
DNA uptake machinery §
1.5 ± 0.4
286 ± 88
DNA uptake machinery
2.2 ± 0.2
DNA uptake machinery
1.9 ± 0.2
DNA uptake machinery
2.5 ± 0.3
261 ± 115
DNA uptake machinery
3 ± 2
DNA uptake machinery
3.7 ± 0.5
DNA uptake machinery
2.8 ± 0.3
DNA uptake machinery
7 ± 2
421 ± 104
DNA uptake machinery
2.0 ± 0.3
DNA uptake machinery
1.9 ± 0.2
DNA uptake machinery
3.2 ± 0.2
608 ± 199
DNA metabolism: replication, repair, recombination, RM
Single-stranded DNA binding protein
1.4 ± 0.1
1.2 ± 0.3
Putative DNA methyltransferase (apparently stand-alone)
1.6 ± 0.4
Putative DNA methyltransferase (apparently stand-alone)
1.9 ± 0.4
1.8 ± 0.3
Purines, pyrimidines, nucleosides and nucleotides
Inosine-uridine preferring nucleoside hydrolase
1.7 ± 0.4
1.9 ± 0.4
1.5 ± 0.4
Putative transcriptional regulator, MerR family
2.5 ± 0.5
Hypothetical protein, conserved in some lactobacilli
2.5 ± 0.5
Hypothetical integral membrane protein
0.61 ± 0.01
Hypothetical protein with putative NAD-binding domain, NmrA structural superfamily
1.6 ± 0.4
Hypothetical protein, peptidase S66 superfamily
0.6 ± 0.1
Hypothetical protein with putative NAD-binding domain, NmrA structural superfamily
1.6 ± 0.2
Hypothetical protein, conserved in bacteria
2.1 ± 0.5
DNA recombinase A
2.7 ± 0.7
DNA protecting protein, involved in DNA transformation
2163 ± 1242
Two genes coding for hypothetical proteins, LSA0409 and LSA0779, were down-regulated in the sigHLsa overexpression strain. As sigma factors are usually positive regulators, we consider it likely that down-regulation of these genes is an indirect effect of sigHLsa overexpression, e.g., this effect could correspond to σH-mediated activation of an unidentified repressor. The sole transcriptional regulator (LSA0421) listed as σH-activated in Table 2 is probably not responsible for this effect, since MerR-type regulators reportedly act as activators . No clue for the function of LSA0421 could be drawn from the genetic context or multiple alignments with other MerR-type proteins from E. coli and B. subtilis.
Overall, the qPCR analysis validates our statistical analysis of the microarray data based on the common variance model associated with the correction of Bonferroni (Table 2). Indeed, although calculated expression ratios were very similar for comFA and ssb (around 1.5), the former, which had an associated P value < 0.05 with the Bonferroni correction, was confirmed as overexpressed in the qPCR analysis, whereas the latter (which passed the other applied statistical test) was found to be almost unaffected by σH in the qPCR analysis (Table 2). Therefore, we expect that all genes with a better score than comFA in the microarray anlaysis (i.e. P value Bonferroni ≤ 1.54 E-02) are good candidates for belonging to the σLsaH regulon. Altogether, results of this study thus identify 25 genes as belonging to the σLsaH regulon. Some genes (e.g., dprA), while truly activated by σLsaH, may not be detected in this microarray experiment, indicating the need for further studies to define the full regulon.
Transcriptional reprogramming caused by sigHLsa overexpression is consistent with the existence of a competent state in L. sakei, supported by the observed up-regulation of com genes involved in pseudopilus morphogenesis and DNA translocation as well as of dprA (which shares 47% aa identity with the S. pneumoniae dprA gene product). ssb and recA appear little or not activated one hour after sigHLsa induced overexpression, whereas their level of induction during the competence state in S. pneumoniae and B. subtilis reportedly varies from 5 to over ten-fold [32, 35]. These genes might be transiently regulated (in a narrower window than com operons and dprA), regulated by other factors, or their up-regulation may not be required in L. sakei. Indeed both genes participate in the bacterial vegetative life cycle and are expected to be transcribed at a significant basal level when cells are not in the competence state . Interestingly, L. sakei possesses a unique ssb gene (ssbA-type), whereas B. subtilis and S. pneumoniae have paralog genes [36, 37]. The need for a transformation-dedicated SSB protein has been discussed . Although known natural transformation is frequently associated with multiple ssb in Firmicutes , an additional competence-induced SSB may be a facilitator rather than an essential contributor to the transformation process, since transformation frequency is only reduced by two- to ten-fold when ssbB is inactivated in S. pneumoniae or in B. subtilis .
Is L. sakeicapable of natural genetic transformation?
As the σH-activated transcriptome of L. sakei was indicative of a competence state, we looked for genetic transformation in this species. The first strategy involved the overproducer strain sigH(hy)*. As the strain harbors a resident plasmid conferring erythromycin resistance, a compatible plasmid conferring chloramphenicol resistance (pVI1056) was used for transformation tests. After cultivation under inducing conditions (i.e., addition of 30 μM CuSO4), the strain was mixed with 100 ng of pVI1056 and plated on selective medium. Experiments were performed under various conditions: i) glucose concentration at 1% or 0.1%, ii) growth in microaerobiosis or aeration, and induction at early, middle or late exponential phase iii) addition of MgCl2 (80 mM) during contact between cells and DNA, after middle phase induction in microaerobiosis or aeration; in addition, chromosomal L. sakei DNA (1 μg) was also used as exogenous DNA. None of the tested conditions resulted in DNA transformation.
Development of natural transformation may be strain-dependent [30, 38, 39]. We therefore used a second strategy (independent of sigH overexpression) to test different L. sakei isolates for competence, using a protocol where DNA and strains are deposited on solid medium. In addition to 23 K, four strains (64 K, 332 F, 160 K and LTH675) were chosen based on their different genotypes and genome sizes, and known capacities to be transformed by electroporation [20, 58]; Chaillou and Anba, personal communication]. Two replicative plasmids and chromosomal L. sakei DNA were used. In spite of varying media (MRS or MCD) and incubation temperatures (4°C, 30°C or 37°C), no colonies were recovered on selective medium.
Among the Lactobacillales, natural genetic transformation has been reported for many species of the genus Streptococcus  and has been suspected for one Lactobacillus . In recent years, natural transformation has been demonstrated in several Gram-positive or Gram-negative species, previously unsuspected to develop genetic competence [42, 43]. Overproduction of the activator protein has proven to be an efficient way to trigger genetic transformation in various bacteria, e.g., TfoX in Vibrio cholerae  or ComK in Bacillus species [14, 44]. However, artificially raising transcription of the ComX master regulator gene initially failed to induce efficient genetic transformation for S. thermophilus strain LMD-9 , which was very recently shown to be efficiently naturally transformable . In the present and previous studies, a failure to achieve a competent state in bacteria (either spontaneously or triggered by artificial overexpression of a master activator) may be due to the use of inappropriate growth conditions, which might not allow the detection by the cells of a needed specific triggering factor [38, 42] or the full activation of multiple converging regulatory pathways . As such, in the case of L. lactis , S. pyogenes , S. aureus , or L. sakei (this paper), only the activation of several competence genes, but not genetic transformation, could be obtained after ectopic expression of the activating sigma factor. Our results suggest that some of the genes induced in other naturally competent Firmicutes are not activated by the sole sigHLsa overexpression in L. sakei. In the case of S. pyogenes, the identification of a novel pheromone in related species of Streptococcus might pave the way for deciphering a natural genetic transformation system in this bacterium . Whether competence gene activation by ComX/σH is linked to the capacity of being transformable in these species, and under which conditions, remains to be determined.
Effect of sigH on L. sakeisurvival
This study gives further insight into the function of σH-family sigma factors from Firmicutes, whether they belong to sporulating or non-sporulating bacteria. Two main models emerge: ComX of non-sporulating streptoccoci is the master activator of the genetic competence pathway, participating directly in the transcription of late com genes . σH of B. subtilis activates a complex response leading to spore formation as an ultimate outcome and to the development of genetic competence during a transition period. Unlike ComX, σBsuH does not directly activate genes encoding the DNA uptake machinery, but participates as an intermediate in the upstream signaling pathway controlling the master regulator of competence ComK [5, 48]. sigH genes from the non-sporulating L. sakei and S. aureus species are organized similarly to the sigH locus of the sporulating bacterium B. subtilis. However, unlike B. subtilis, they act like streptococcal ComX by activating late com genes [; this paper]. We speculate that this function may be conserved in the order Lactobacillales, irrespective of the exact location of the so-called ComX or σH encoding gene. The regulon of σLsaH as deduced by assessing the effects of σLsaH overexpression was rather small. It should be mentioned that the genome size of the model strain used was 136 kb less than the average size within the species  and that our strategy mainly identified genes that were strongly affected by σLsa,H independently of possible other, undetermined, environmental signals. A large number of reported regulatory effects of σBsuH are actually mediated in conjunction with other transcriptional regulators, especially Spo0A and AbrB . L. sakei and more generally Lactobacillales do apparently not possess orthologs of these regulatory proteins, neither do they possess a ComK homologue. Deciphering all the functions of the conserved σH sigma factor in other groups of Firmicutes, sporulating or not, and equipped with different combinations of these known global regulators will probably help to clarify σH evolution in this group of bacteria.
Media and growth conditions
L. sakei was grown at 30°C in MRS medium  or in the chemically defined medium MCD , both containing 1% glucose. A two-step preculture was used to assure reproducibility of experiments. First, 5 ml MRS was inoculated with one freshly isolated colony and incubated for about 8 h without agitation. After centrifugation, cells were resuspended in MCD at an OD600 of 1 and 10 to 20 μl of the suspension was used to inoculate 40 ml of fresh MCD. This second preculture was incubated without agitation for about 15 h so as to collect the cells in exponential growth phase. This preculture was then concentrated to an OD600 of 10 in fresh MCD, and used to inoculate the test culture to give an initial OD600 of 0.1 to 0.15. Unless otherwise indicated, growth conditions under microaerobiosis were used. Different aeration conditions were obtained by varying the agitation parameter and volume of cultures. Typically microaerobiosis corresponded to non-agitated cultures in closed centrifugation tubes, aerobiosis to 140 rpm of 1/10th full ehrlenmeyer flasks, and anaerobiosis to N2-saturated cultures in sealed bottles . Growth was followed by OD600 measured in a Secomah spectrophotometer. As 30 μM CuSO4 may be added to the culture, we monitored its global effect on L. sakei growth. In static or anaerobic growth conditions, 30 μM CuSO4 had no effect on growth. In aeration conditions, 30 μM CuSO4 had a slight effect on growth (2-10% lower OD600 at the end of growth), and slightly extended viability.
Meat juice was obtained from beef meat homogenized with half volume of sterile water in a Stomacher for 2 cycles of 3 min each. The supernatant obtained after centrifugation (10,000g for 15 min) was filter sterilized and stocked at -20°C (M.-C. Champomier Vergès, unpublished). Escherichia coli (DH5αF' or TGI) was cultured aerobically in LB at 37°C. Selective pressure for plasmids was maintained in E. coli with ampicillin 100 mg.l-1, and in L. sakei, with erythromycin 5 mg.l-1.
Standard procedures were used for DNA manipulation. Classical PCR reactions were performed with Taq polymerase (Fermentas) or Pfu polymerase (Promega) for cloning purpose, and run in MJ research PTC-200 thermocycler. Extraction of plasmids and chromosomal DNA as well as electroporation of L. sakei and L. casei BL23 was carried out as described . Primers are listed in additional file 4.
Diversity of sigH in L. sakei
L. sakei strains (18, 21, 23 K, 64, 112, 160 K, 300, 332, JG3, MF2091, MF2092, ATCC15521, CIP105422, SF771, LTH677, LTH2070) were from our collection or different sources as described . PCR amplification of the sigH locus was carried out with two pairs of primers (AML31/AML32 and AML50/AML58). Sequence of the 561 nt fragment corresponding to entire CDS and the 77 nucleotides of the upstream intergenic region was performed on PCR-amplified genomic DNA using each of the four primers. Pairwise distances were calculated by MEGA 4  using a Kimura 2-parameter substitution model.
Construction of sigH mutant and sigHexpression strains
SigH production and sigH mutant strains were constructed from RV2002, a derivative of L. sakei 23 K that had undergone a deletion of the lacLM gene encoding β-galactosidase . Their construction used plasmids pRV610 and pRV613  which contain two replication origins, one functional in E. coli (pBluescript) and one for Gram-positive bacteria (pRV500).
The L. sakei σH overproducer strain sigH(hy)* was obtained by introducing plasmid pRV619 into RV2002. pRV619 was constructed from pRV613 which bears the PatkY copper-inducible promoter cassette of L. sakei fused to the E. coli lacZ reporter gene . lacZ was replaced by sigHLsa in pRV619 as follows. The sigHLsa coding region was PCR-amplified from L. sakei strain 23 K chromosomal DNA with primers AML31 and AML32 and the BamHI/XbaI fragment was cloned into pRV613 digested by the same enzymes, using Lactobacillus casei BL23 as a host, since neither L. sakei nor E. coli were successful for direct cloning. The extracted plasmid was then successfully introduced into E. coli from which we could obtain the needed high-quality plasmid preparation (Qiagen Plasmid Kits) to electroporate L. sakei RV2002.
The L. sakei sigH null mutant (RV7003 designated sigH(nul) in the text) was obtained via a double cross-over homologous recombination with the pRV622 integrative plasmid. To inactivate the sigH gene we deleted its putative promoter and the first 34 codons while introducing an in-frame stop codon at the endpoint of the deletion (see additional file 2: Genotypes of L. sakei strains affected in sigH). The upstream and downstream fragments were generated by PCR using respectively AML51/AML52 and AML53/AML54 primer pairs, thereby introducing an EcoRI site in sigH. Each amplicon was digested with EcoRI, followed by DNA ligation and digestion with PstI and XhoI. The resulting 1.1 kb fragment was then reamplified by the distal primers AML51 and AML54 and cloned by blunt-end ligation after treatment with T4 polymerase, into the pRV610 cloning vector  cut by SmaI. As above, L. casei BL23 was used as a host for cloning, giving plasmid pRV621. This plasmid was then successfully introduced into E. coli and an intra-molecular deletion of the Gram + replication cassette was generated between unique restriction sites EcoRV and KpnI repaired by T4 polymerase, giving pRV622 which replicates in E. coli. Gene replacement in L. sakei was carried out as described , with two successive single crossovers, the first one leading to chromosomal integration of the plasmid (maintained by erythromycin selection), and the second one allowing plasmid excision, monitored by loss of erythromycin resistance. The mutant chromosomal structure was checked by PCR. Correct sequence of the inserts was checked for pRV619 and pRV622.
Induction of PatkYpromoter utilization and monitoring using β-galactosidase activity
The copper-inducible PatkY promoter was used as described  for sigH overexpression. For this purpose, CuSO4 was added to a final concentration of 30 μM when cultures reached an OD600 of about 0.4. Induction of the PatkY promoter was controlled with the sigH(wt)* strain, harboring a PatkY-directed lacZ reporter gene. Sampling was done one hour after induction and β-galactosidase activity was measured according to  using ONPG (o-nitrophenyl-β-D-galactopyranoside) as a substrate. Activities expressed as Miller units relative to OD600 of the culture  were observed to be between 10 and 25 after induction, whereas the non induced standard was around 0.5.
Extraction of total RNA
L. sakei strains were cultivated at 30°C in MCD under microaerobiosis following the standardized procedure described in the upper section, in the presence of erythromycin for plasmid-containing strains. Cultures of L. sakei were distributed in as many centrifugation tubes as scheduled collecting points and were incubated at 30°C without agitation. Cell pellets were collected by brief centrifugation at the time indicated, freezed in liquid nitrogen and preserved at -80°C. Total RNA was extracted with TRIzol reagent (Invitrogen) as previously described . Integrity of RNA was checked by Bioanalyzer 2100 (Agilent). RIN values were above 9.
Whole-genome microarray analysis
The L. sakei microarray http://migale.jouy.inra.fr/sakei/?q=supplement comprises all the identified coding genes of strain 23 K represented by 70 nt long oligonucleotides synthesized by Operon Biotechnologies Inc. The manufacture of DNA chips as well as labelling, hybridization and image analysis were performed at the Biochips platform of Toulouse-Genopole http://biopuce.insa-toulouse.fr/Maquette/en/. Each oligonucleotide was spotted in triplicate on UltraGaps coated slides (Corning® Life Sciences). Total RNA (5 μg) was reverse transcribed and labeled with either Cy5 dCTP or Cy3 dCTP (Amersham Biosciences) using the ChipShot™ Direct Labeling System (Promega). Labelled cDNA (50 pmol of Cy3 and 50 pmol of Cy5) was included in a dye-switch hybridization protocol carried out in an automatic hybridization chamber (Discovery, Ventana Medical system). Images of scanned slides (GenePix 4000A Scanner-Axon Instruments) were analyzed, spots delimitated and hybridization signals were quantified and transformed into numerical values by GenePixPro v.3.01 software (Axon). Background noise was rather homogeneously distributed and only a few spots were saturated at 75%, mainly those corresponding to rRNA.
Statistical analysis of the data was conducted with the R Package Anapuce 2.1 by J. Aubert http://www.agroparistech.fr/mia/doku.php?id=productions:logiciels. Normalization rested on a global lowess regression followed by a block correction, after filtering out spots with a signal to noise ratio < 3 (including empty spots). Background was not subtracted. Differential analysis was performed on average values for the triplicate spots obtained by the MeanBySpot function. Three models of variance were applied: one variance by gene, a common variance for all the genes and clusters of genes with equal variance (varmixt). Two different multiple testing corrections were used to adjust raw P-values, Bonferroni correction (which is the most stringent) and False Discovery Rate of Benjamini and Hochberg, with a nominal type I error rate set to 0.05.
Microarray accession numbers
The microarray data have been deposited in the Array Express database http://www.ebi.ac.uk/arrayexpress/ under the accession numbers A-MEXP-2068 (array design) and E-MEXP-3238 (experiment).
Real-time qPCR for quantitation of steady-states transcripts
The mRNAs corresponding to the genes of interest were measured by qPCR using SYBR Green fluorescence, appropriate specific primers (see additional file 4: list of primers) and total first-strand cDNA as template. Contaminating DNA was first eliminated from RNA samples using TurboDNA-free from Ambion. Two series of reverse transcription and qPCR experiments were carried out in this study, for monitoring temporal expression and overexpression of sigH on the one hand and for validation of microarray data on the other hand. Total first strand cDNA was produced with random hexamer primers (Random Primer 6 5'd(N6)3', Biolabs) using either PowerScript Reverse Transcriptase (Clonetech) or PrimeScript Reverse Transcriptase (Takara). The quality of each template cDNA was checked using the Bioanalyzer 2100 (Agilent). qPCR was performed using specific primers (75-100 nM each) according to the recommended protocol for each SYBR Green mix used (SYBR Green MasterMix 2X from ABgene or MESA GREEN MasterMix from Eurogentec). Reactions were run on an ABI PRISM 7900 HT instrument (Applied Biosystems) or a Mastercycler Realplex 2 S instrument (Eppendorf) using 40 cycles of denaturation at 95°C for 15 s and extension at 60°C for 1 min. The cycles were preceded by DNA polymerase activation at 95°C and followed by a denaturation cycle to check the specificity of the PCR products. Mean Ct obtained for studied genes were between 16 and 28.5, with the exception of comC and dprA in WT strain at 31 and 32.9 respectively (in the same time 'No Template Controls' gave no signal after 34 cycles).
Primers were designed with Primer Express 2 (Applied Biosystems) or Primer 3 http://frodo.wi.mit.edu/primer3 and validated by determining slopes of standard curves for PCR efficiencies between 90% and 100%. In this context, we used the 2-ΔΔCt method to express results as fold change in the expression of each gene of interest relative to a calibrator sample and a reference gene used as an internal control for normalization of the results . The stability of transcription of the chosen reference gene ldh was checked by standard curves performed for all environmental conditions used in this study. Unless otherwise indicated, quantitation experiments were performed with three independent samples, each well being duplicated two or three times. Values are expressed as mean ± standard deviation.
Viability and UV assays
Viable bacteria were counted by plating serial dilutions on MRS agar and incubating at 30°C for one to four days. For mixed cultures, classical enumeration on MRS supplemented with Xgal (5-bromo-4-chloro-3-indolyl-β-D-galactopyranoside, 0.04 g.l-1) distinguished sigH(hy)* (white) from sigH(wt)* (blue) as well as sigH(nul) (white) from 23 K lacLM + (blue). For other tests, sampling for stationary phase survival in MCD was done after 6-8 hour culturing which corresponds to growth arrest, then once or twice a day. In these cases, comparative enumeration was performed by depositing drops (5 μl) of serial decimal dilutions for each strain on an agar plate. UV resistance was examined by exposing bacteria freshly plated on MRS medium to 254 nm UV-light (VL-15 C, Apelex) with fluences of 40 to 120 J/m2 (by step of 20) measured by the radiometer VLX-3 W equipped with a 254 nm sensor (Vilber Lourmat, France). For that purpose, drops (5 μl) of serial dilutions of bacterial suspensions were rapidly plated after growth in MCD medium, one hour after addition of 30 μM CuSO4 or at the same time without addition of CuSO4.
Natural genetic transformation
Exogenous DNA used in this study comes from plasmid (pVI1056, pRV620, and pGKV259) and L. sakei chromosome (strain RV2000), and confers resistance to chloramphenicol (10 mg.l-1) to recipient bacterium. RV2000 is a derivative of L. sakei 23 K in which the cat194 gene interrupts ldh . pVI1056 (Van de Guchte in ) is a 7.5 kb pIP501-derived shuttle plasmid (theta-replicating), known to be replicative in L. sakei. pRV620 is a 5.6 kb shuttle plasmid derived from theta-replicating plasmid pRV500 of L. sakei . pGKV259 is a broad host range 5 kb rolling circle plasmid . Plasmids were purified from E. coli TG1 using Qiagen Plasmid preparation Kits, and checked by electrophoresis on agarose gel for the presence of multimers. 10 ng of plasmids pVI1056 and pRV620 were reportedly able to transform B. subtilis naturally competent cells . For transformation tests with L. sakei, sigH(hy)* overexpression strain was cultivated in MCD as described above. After 30 to 60 min induction with 30 μM CuSO4 (at usual OD600 of 0.4 and at OD600 of 0.2 and 0.9 when indicated), aliquots of 100 μl of cell suspension were mixed with 100 ng pVI1056 DNA in a microtube and incubated for one hour at 30°C. Suspensions were then plated on selective MRS medium and incubated for several days at 30°C. As sigH(hy)* strain already contained a plasmid, its transformability with incoming plasmid was verified by electroporation. Transformation tests on plates with other L. sakei strains were done as follows. 23 K, 64 K [plasmid-cured 64], 332 F [pRV500-cured 332], 160 K and LTH675 [20, 52, 58] were cultivated in liquid MRS and MCD medium until late exponential phase and plated on the same solid medium supplemented with 10 mg.l-1 chloramphenicol. Drops of pRV620 and pGKV259 (50 ng each), and RV2000 chromosome (500 ng) were deposited on the plates which were then incubated at the indicated temperatures.
ICE core facilities of INRA at Jouy-en-Josas (J.-C. Helbling, S. Makhzami, E. Rebours and P. Martin) and the Biochips platform of Toulouse-Genopole (V. Le Berre and collaborators) are acknowledged for their contribution to this work. F. Le Moel, J. Flor, and A. Le Nevé are acknowledged for participating in the study during their training period. We thank our colleagues of Micalis, from FLEC team (F. Baraige, S. Chaillou, M.-C. Champomier Vergès, M. Daty, A. Goubet and I. Lucquin) and other teams (C. Gautier, E. Guédon, I. Guillouard and M.-A. Petit) for providing material or advice in experiments; S. Chaillou and M. Zagorec for providing the L. sakei oligoset; C. Delorme and C. Neuvéglise for help with polymorphism analysis and phylogeny; M. Van de Guchte for help with English. Authors are grateful to J.-P. Claverys for helpful discussions on genetic competence, and indebted to A. Gruss for improvement of the manuscript. This work was supported by INRA funding.
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