The extracytoplasmic function (ECF) σ factors are fundamental for bacterial adaptation to distinct environments and for survival under different stress conditions. The emerging pathogen Arcobacter butzleri possesses seven putative pairs of σ/anti-σ factors belonging to the ECF family. Here, we report the identification of the genes regulated by five out of the seven A. butzleri ECF σ factors. Three of the ECF σ factors play an apparent role in transport, energy generation and the maintenance of redox balance. Several genes like the nap, sox and tct genes are regulated by more than one ECF σ factor, indicating that the A. butzleri ECF σ factors form a network of overlapping regulons. In contrast to other eubacteria, these A. butzleri ECF regulons appear to primarily regulate responses to changing environments in order to meet metabolic needs instead of an obvious role in stress adaptation.
Citation: Martinez-Malaxetxebarria I, Muts R, van Dijk L, Parker CT, Miller WG, Huynh S, et al. (2012) Regulation of Energy Metabolism by the Extracytoplasmic Function (ECF) σ Factors of Arcobacter butzleri. PLoS ONE 7(9): e44796. https://doi.org/10.1371/journal.pone.0044796
Editor: Roy Martin Roop II, East Carolina University School of Medicine, United States of America
Received: January 19, 2012; Accepted: August 14, 2012; Published: September 18, 2012
Copyright: © This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported in part by the Basque Government (IT-528-10) through a Predoctoral Fellowship of the Basque Government for the Training of Researches (BF106.85); by a parallel incentive within the Predoctoral Fellowship of the Basque Government for short stays in different Research Centers (EC-2009-1-4); and by a European Molecular Biology Organization (EMBO) Short Term Fellowship (ASTF29-2010) to IMM. This work was also supported by a fellowship of Nederlandse Organisatie voor Wetenschappelijk Onderzoek (NWO-Vidi) grant 917.66.330 to MMSMW and by funds from US Department of Agriculture Current Research Information System (USDA-CRIS) project 5325-42000-047-00D. No additional external funding received for this study. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Arcobacter spp. are Gram-negative, small, motile and spiral-shaped bacteria belonging to the Campylobacteraceae family. Arcobacter is currently comprised of fifteen species , . Within this genus, A. butzleri, A. cryaerophilus and A. skirrowii are associated with animal and human diseases, such as reproductive disorders, mastitis and diarrhoea in animals –, and enteritis and occasionally bacteraemia in humans –. Arcobacter spp. have been classified in 2002 as emerging pathogens by the ICMSF (International Commission on Microbiological Specifications for Foods) .The main reservoirs for Arcobacter spp. are water environments, especially sewage and coastal waters –.
In 2007 the complete genome of the human clinical isolate A. butzleri RM4018 was sequenced . The bacterium appears to have a large number of signal transduction systems, indicating that this organism is able to respond to many different environmental signals. Apart from having one of the highest densities of two component systems per megabase, A. butzleri RM4018, unlike Campylobacter spp. or Helicobacter spp., is also predicted to contain seven σ/anti-σ factor pairs belonging to the ECF family (Extracytoplasmic function) of sigma factors. The seven A. butzleri RM4018 ECF σ factor pairs are genetically unlinked but for each pair, the σ factor gene is positioned adjacent to and in the same orientation as the putative cognate anti-σ factor gene. The amino acid identity between any two of the seven ECF σ factors varies between 30 and 49%, suggesting that each ECF pair plays a different role in the biology of strain RM4018 and responds perhaps to a different suite of external signals.
ECF σ factors have been identified in both Gram-negative and Gram-positive bacteria and they are fundamental for bacterial adaptation to different environments and for survival under different stress conditions , . Their role in cellular physiology is highly variable and includes adaptation to membrane-affecting compounds, extreme temperatures and pH, light, high pressure, carbon, nitrogen and iron starvation, oxidative and osmotic stress, and the regulation of virulence in pathogenic organisms , . Despite their diverse effects, ECF σ factors share common features. In most cases ECF σ factors are co-transcribed with their cognate anti-σ factor. The anti-σ factor, which often spans the inner membrane, sequesters and inactivates the cognate σ factor at the inner face of the cytoplasmic membrane. Upon a specific external stimulus, the ECF anti-σ factor is inactivated by protein degradation and the σ factor is released from the membrane, where it associates with RNA polymerase and mediates transcriptional activation of its target genes . The ECF anti-σ factor can also be released from the ECF σ factor by a phosphorylated response regulator NepR, this partner-switching mechanism has recently be discovered in alphaproteobacteria . Some ECF σ/anti-σ factors form together with an outer membrane TonB-dependent receptor, a trans-envelope signal transduction pathway . These TonB-dependent receptors are involved in the uptake of specific molecules but also they sense and transmit, via the anti-σ factor, extracellular signals, which lead to the activation of a specific ECF σ factor.
In the present study, we investigated the role of the A. butzleri RM4018 ECF σ factors. We developed the genetic tools to manipulate A. butzleri and determined the regulons of most ECF σ factors using a combination of microarray-based transcriptome analysis and functional assays.
Materials and Methods
Bacterial Strains, Plasmids and Growth Conditions
Bacterial strains and plasmids used in this work are listed in Table 1. A. butzleri strains were routinely grown at 30°C in Brain Heart Infusion (BHI) broth (Oxoid) or on Mueller Hinton (MH) agar (Oxoid) supplemented with 5% sheep blood (Biotrading). E. coli strains were routinely grown at 37°C in Luria-Bertani (LB) broth or on LB agar plates (Biotrading) supplemented with ampicillin (100 µg/ml) or kanamycin (50 µg/ml) when needed.
Construction of A. Butzleri ECF σ Factor and ECF Anti-σ Factor Mutants
The genes encoding the seven ECF σ factors and their cognate anti-σ factors were amplified using the primer pairs AB0986F/AB0987R, AB1044F/AB1044R, AB1437F2/AB1437R2, AB1460F/AB1460R, AB1576F/1576R, AB2151F/AB2151R and AB2300F/2300R (Table 2), the proofreading enzyme Pfu (Promega) and A. butzleri RM4018 chromosomal DNA as template. The PCR products were tailed with a 5′-A nucleotide using Taq polymerase (Invitrogen) and ligated into the pGEM-T Easy vector (Promega) to obtain pGEMab0983–0984, pGEMab1040–1041, pGEMab1429–1430, pGEMab1452–1453, pGEMab1567–1568, pGEMab2164–2165 and pGEMab2315–2316 (Table 1). Inverse PCR was performed on the σ/anti-σ plasmids to delete a large part of both the σ and anti-σ factor (σ/anti-σ knock-out plasmids) or of only the anti-σ factor encoding genes (anti-σ knock-out plasmids). Unique BamHI restriction sites were introduced at the same time. The plasmid pGEMΔab1429–1430 was obtained by digesting plasmid pGEMΔab1429 with BamHI and BclI. The knockout constructs were created by digestion of the inverse PCR products with BamHI and ligation to a 1.4-kb BamHI fragment containing a kanamycin resistance gene (aph(3′)-III) from pMW2 .
The ECF σ factor genes were inactivated by marker exchange mutagenesis. First, the knock-out plasmids were introduced into A. butzleri RM4018 by electrotransformation. To obtain electrocompetent A. butzleri RM4018, a 5 ml overnight culture was diluted 20 times in 100 ml fresh BHI medium and incubated at 30°C on a shaking platform (150 rpm). Bacteria were harvested by centrifugation (4,500×g, 1 h, 4°C) when the optical density at 550 nm had reached values between 0.2 and 0.6. The bacteria were washed twice in 5 ml of ice-cold sucrose-glycerol solution (15% glycerol; 272 mM sucrose in water), resuspended in 0.5 ml ice-cold sucrose-glycerol solution and aliquoted into 50 µl solutions containing approximately 3−5×109 CFU. One µg of each plasmid was added to 50 µl (approximately 3−5×109 CFU) of competent A. butzleri RM4018 and incubated for 3 min on ice. The cells were transferred to a 0.2 cm electroporation cuvette (Bio-Rad) and electroporated using a Bio-Rad Gene Pulser set at 2.25 kV, 400 Ω and 25 µF. Bacteria were recovered in 1 ml of BHI broth for 10 min at room temperature, transferred to 2 ml of pre-warmed BHI and incubated for 3 hours at 30°C on a shaking platform (150 rpm). Mutants were selected by growing the cells for two to five days at 30°C aerobically on kanamycin-containing MH plates. Homologous recombination resulting in double-crossover events was verified by PCR.
Growth curves were generated by diluting pre-cultures grown overnight in BHI to a starting optical density (OD550) of 0.05 in 30 ml of BHI. The 30 ml cultures were grown in conical flask under aerobic conditions, 150 rpm at 30°C. Bacterial growth and cell density were monitored by measuring the absorbance at 550 nm at different time intervals. The exponential growth rate was calculated from four separated growth experiments. Several stress conditions which limited the growth of the wildtype Arcobacter strain were tested. To measure the influence of extreme temperatures, the starting cultures were incubated at 4°C or 60°C for 15 min prior to their incubation at 30°C. To study the effect of the pH on the growth of the strains, the pH of the BHI was adjusted to pH 5 or 9. Osmotic stress was tested by adding 0.35 M NaCl to the BHI. In additional experiments, other stress-inducing chemicals were added to the BHI to concentrations which limited the growth of the wildtype Arcobacter strain. These chemicals included: ethanol (5%); SDS (1%); the iron chelator 2,2-dipyridyl (300 µM); the oxidative stress-inducing chemicals H2O2 (0.04%) and diamide (2 mM); or antimicrobial compounds such as penicillin G and polymyxin B (25 µg/ml). Motility assays were performed by stabbing the strains with a pipette tip into semisolid medium (thioglycolate medium containing 0.4% agar, Difco), followed by incubations under aerobic conditions at 30°C or 37°C for 48 hours.
Overnight grown cultures of A. butzleri were diluted to an OD550 of 0.1 in BHI and incubated at 30°C on a shaking platform set at 150 rpm. RNA was isolated from 5 ml of mid-logarithmic phase cultures (OD550 of approximately 0.5), using the RNA-Bee™ kit (Tel-Test, Inc) following the manufactureŕs specifications.
Microarray Hybridization and Analysis
For expression profiling, an indirect comparison of gene expression levels was performed , . In this microarray experimental design, each labeled cDNA was combined with labeled genomic DNA from A. butzleri RM4018. Mixtures were hybridized to a previously designed and manufactured A. butzleri DNA array . Labeling of RNA and DNA, hybridization procedure and microarray data analysis were performed as previously described . Details of the microarray have been deposited in the NCBI GEO repository (http://www.ncbi.nlm.nih.gov/geo/) under platform accession number GPL14948. The microarray data set has been deposited in the NCBI Gene Expression Omnibus (GEO) repository (http://www.ncbi.nlm.nih.gov/geo/) under accession number GSE34089.
Primers used in this assay were designed using the Primer Express software (Applied Biosystems) and are listed in Table 2. Prior to amplification, RNA samples were treated with RNase-free DNase I (Invitrogen). RT-PCR was performed on 0.2 µg of DNase I treated RNA with 1 µM of primers and the SYBR® Green I kit (Eurogentec) using a LightCycler® 480 Real-Time PCR System (Roche). The PCR parameters were 30 min at 48°C; 10 min at 95°C, 40 cycles of 95°C for 15 s and 60°C for 1 min and a final dissociation step of 95°C for 15 s, 60°C for 20 s and 95°C for 15 s. To compensate for the variance in the amount of mRNA in the reactions, the calculated threshold cycle (Ct) for each gene amplification was normalized to the Ct values for the gyrA gene. Fold changes were calculated according to the ΔΔCt method . Each sample was examined in four replicates and was repeated with at least two independent preparations of RNA. Standard deviations were calculated and displayed as error bars.
The nitrate reductase activity was determined by measuring the production of nitrite from nitrate as previously described . Briefly, strains were grown overnight (16 h) under aerobic conditions in BHI broth containing 20 mM of sodium nitrate. Nitrite accumulation in the supernatant was detected by mixing 50 µl of the culture supernatants with 850 µl of 1% (w/v) sulphanilamide dissolved in 1 M of HCl and 100 µl of 0.02% (w/v) naphthylethylenediamine solution. After 15 minutes the formation of p-sulfobenzene-azo α-naphthylamine was measured at 540 nm. The amount of nitrite present in 50 µl culture supernatant was estimated using a nitrite standard curve. The nitrite production was adjusted to the total bacterial proteins present in the culture as estimated by using the BCA protein assay kit. To determine the nitrate concentration in Arcobacter culture supernatants the supernatants were 10 times diluted in BHI. The diluted culture supernatants were incubated with sulphanilamide and naphthylethylenediamine as described for the nitrite detection. Next a trace amount of zinc dust was added to the mixture. The zinc dust reduces nitrate to nitrite and a red color develops due to the formation of p-sulfobenzene-azo α-naphthylamine. After 2 minutes the zinc has settled on the bottom and 900 µl of the supernatant was transferred to a new tube and the absorbance of the red color was measured at 540 nm. The amount of nitrate present in 50 µl culture supernatant was estimated using a nitrate standard curve which was also treated with zinc dust. Reactions were measured four times and repeated with two independent cultures.
Sox Enzyme Activity Assay
Overnight cultures in BHI were washed once with Arcobacter Minimal 1 (AM1) medium (4.2 mM Na2HPO4, 2.4 mM KH2PO4, 9 mM NaCL, 19 mM NH4Cl 1×M9 salts, 1 mM of MgCl2, 0.2% of sodium pyruvate, 0.02% of FeNH4citrate; adjusted to pH 7.5) amended with 20 mM of sodium sulfite, and 10 µg of phenol red per milliliter. The bacteria were subsequently diluted in sodium sulfite-, phenol red-amended AM1 medium to an OD550 of 0.05 and allowed to grow in completely filled capped 5 cm glass vials. The strains which were able to oxidize sulfur caused a drop in the pH that was visible as a color change from red to yellow. After 6 hour of growth at 30°C, absorbance at 564 nm was measured and the results obtained for the wild-type strain were set at 100%.
Citrate Uptake Assay
The ability of the strains to utilize citrate was determined using Simmons citrate agar (Oxoid). Strains grown overnight on MH agar supplemented with 5% sheep blood were streaked onto Simmons Citrate Agar supplemented with 0.01% sodium pyruvate. Cells were incubated at 30°C under aerobic conditions for 48 hours. The strains which were able to use the citrate as carbon source increased the pH of medium, resulting in a color change of the medium from green to blue.
Mutagenesis of the ECF σ Factor and Anti-σ Factor Encoding Genes
For each ECF σ/anti-σ pair, mutational inactivation of the anti-σ factor results in constitutive induction of the σ response, while mutational inactivation of the σ factor results in the down-regulation of ECF-dependent transcription , . This allowed us to study the function of the ECFs in A. butzleri strain RM4018 without knowing the specific signal(s) that activate them. In order to address the role of the seven ECF σ factors in A. butzleri RM4018, we inactivated either both the σ and the anti-σ factor, or the anti-σ factor alone. Since no suitable Arcobacter antibiotic resistance cassettes were available and the previously-used chloramphenicol cassette of Campylobacter coli could not be used since A. butzleri RM4018 is resistant to chloramphenicol, we replaced a large part of the ECF coding regions with a kanamycin resistance gene (aph(3′)-III) of C. coli . After modifying the Arcobacter mutagenesis protocol described by Ho et al. , we were able to replace the ECF σ/anti-σfactor genes AB0986/0987 (σ1, Aσ1), AB1044/1045 (σ2, Aσ2), AB1460/1461 (σ4, Aσ4), AB1576/1577 (Aσ5, σ5) and AB2300/2301 (Aσ7, σ7) with the Kmr cassette. We also obtained single mutants in the anti-σ factor genes Aσ1, Aσ2, Aσ4, Aσ5 and Aσ7. All mutants contained the Kmr cassette in the same orientation as the ECF genes. As no suitable Arcobacter shuttle plasmids exist and no other antibiotic cassettes could be used, we were unable to perform complementation studies.
Comparison of the various mutants with the parent strain RM4018 revealed neither differences in bacterial shape or colony formation on sheep blood plates nor in growth rate in BHI medium as statistically estimated by Anova F = 1,777 (P>0.05) (Figure 1A and B). A common role of ECF σ factors is to protect bacteria against external stress . Exposure of the A. butzleri mutant strains to extreme temperatures (e.g., 4°C or 60°C), pH 5 or 9, or sub-inhibitory concentrations of stress-inducing chemicals (e.g., ethanol, SDS, metal ion chelators EDTA or 2,2-dipyridyl, the oxidative stress-inducing chemicals H2O2 and diamide, or the antimicrobial compounds penicillin G and polymyxin B) did not yield significant growth or morphology differences (data not shown). Similarly, the motility of the mutants on semisolid medium was unchanged compared to the wild-type. These results indicated that the functions of the Arcobacter ECF σ factors might be different from those in other bacterial species.
(A) Growth curves of the wild-type strain RM4018, the ECF anti-σ mutants and the ECF σ/anti-σ double mutants. Strains were grown in BHI at 30°C under aerobic conditions. Data correspond to one representative of four independent experiments. (B) Exponential growth rates (hr−1) with standard deviations of four growth curves including one shown in (A).
Identification of ECFσ Factor-regulated Genes
To identify the genes regulated by the RM4018 ECF σ factors, RNA was isolated from wild-type and mutant strains grown to mid logarithmic phase and subjected to microarray-based transcriptome analysis. To obtain maximal ECF σ factor-dependent transcript differences, transcripts of each σ/Aσ mutant and its cognate Aσ mutant were compared. Genes showing more than a fourfold change in transcript levels were considered as ECF σ-dependent. Based on this criterion, the ECF σ factors σ1, σ2, σ4, σ5 and σ7 were found to regulate 3, 65, 14, 42 and 72 genes, respectively (Tables S1 to S5). None of the ECF σ factors appeared to regulate its own transcription. Interestingly, more than thirty genes were regulated by two or more ECF σ factors (Table 3). In agreement with the phenotypic characterization, the identified ECF σ-dependent genes indicate that the ECF σ factors of A. butzleri regulate other genes than ECF σ factors in other bacterial species.
Genes Regulated by AB0986 (ECF σ1)
The transcriptome analysis revealed that σ1 activates the transcription of AB0988, encoding a putative TonB-dependent receptor protein, and down-regulates the transcription of AB1593 and AB0033, that encode a putative sodium: alanine symporter and a L-lactate permease, respectively (Table S1).
Genes Regulated by AB1044 (ECF σ2)
Based on the microarray data, ECF σ2 activates the transcription of 35 genes and caused a down-regulation of the expression of 30 genes (Table S2). All annotated gene products represent putative proteins. The sodium: solute symporter AB0504 is the most strongly up-regulated gene product. Apart from this, ECF σ2 is predicted to control the transcription of the genetic loci: AB0345-AB0346, encoding a Nrf-type nitrite reductase; AB0353 to AB0359, coding for a Nap- type nitrate reductase and a C4-dicarboxylate transport system; AB0376–0377, encoding an aldehyde dehydrogenase and an uncharacterized protein; AB0494–AB0495, encoding an acetate kinase and a phosphate acetyltransferase; AB0563 to AB0570, encoding the Sox multi-enzyme complex; and AB1442–1443, encoding a Ni/Fe-hydrogenase. A putative operon (AB0102–0106) coding for the tricarboxylic transport proteins TctABC and a large locus (AB1664 to AB1682) coding for phage related proteins were among the genes that are down-regulated by ECF σ2.
Genes Regulated by AB1460 (ECF σ4)
According to the transcriptomics data, σ4 activates 11 genes and caused a down-regulation of the expression of 3 genes (Table S3). The main up-regulated gene product is the putative TonB-dependent receptor protein (AB1462) encoded by the same locus encoding the σ4/anti-σ4 factors. Among the other genes up-regulated by ECF σ4 are: napHGA (AB0354 to AB0356), aceEF (AB1480–1481), frdA (AB0297), nrfA (AB0345) and fdhA1 (AB1507) encoding, respectively, a part of a Nap-type nitrate reductase, two pyruvate dehydrogenase components, a fumarate reductase subunit, a cytochrome c552 nitrate reductase and a formate dehydrogenase subunit. A methyl-accepting chemotaxis protein (AB0602) is the most strongly down-regulated gene product.
Genes Regulated by AB1577 (ECF σ5)
Identification of ECF σ5-dependent genes by transcriptomics analysis revealed 16 up-regulated and 26 down-regulated genes (Table S4). The closely-linked TonB-dependent receptor gene AB1573, was the most strongly up-regulated. The putative TctABC transport proteins AB0102–AB0104, the carbonic anhydrase AB0107, the putative ammonia monooxygenase AB0108, and the ubiquinolcytochrome c oxidoreductase encoded by the petAB (AB2054–AB2055) genes are among the gene products up-regulated by σ5. The genes fur2 and cspA, and the genetic locus AB1062–1066, which includes NADPH quinonereductase, NADPH:flavodoxinoxidoreductase, and NADPH nitroreductase, were found to be repressed.
Genes Regulated by AB2301 (ECF σ7)
The transcriptome analysis revealed that σ7 activates 37 genes and represses another 35 (Table S5). Almost all annotated genes repressed by σ7 were activated by σ2. The genes encoding the putative TctABC transport proteins (AB0103–0105) are the most up-regulated genes by σ7, while the sox operon and AB0494–AB0495, encoding an acetate kinase and a phosphate acetyltransferase are the most down-regulated. Although it does not affect the transcription of its linked TonB-dependent receptor gene (AB2299), σ7 activated two other TonB-dependent receptor genes AB0705 and AB1870.
The A. butzleri ECF σ Factors Regulate Parts of the Electron Transport Chain
Unlike the tonB genes which also appear to be regulated by ECF sigma factors in other bacterial species, we found that a large number of genes regulated by A. butzleri ECF σ factors are involved in the electron transport chain. To verify that the ECF σ factors indeed influence the electron transport chain, we first performed real-time RT-PCR on the ECF-dependent tonB, nap, sox and tct genes. We could confirm that the tonB genes AB0988, AB1462 and AB1573 are indeed up-regulated by ECF σ1, σ4 and σ5 respectively (Figure 2a, c and d). ECF σ2 activates the nap and sox genes (Figure 2b) of which the latter are repressed by σ7 (Figure 2e). The real-time RT-PCR results also confirmed that the tct genes are down-regulated by ECF σ2 and up-regulated by σ5 and σ7 (Figure 2b, d and e).
(A) σ1, (B) σ2, (C) σ4, (D) σ5, and (E) σ7 regulon. Transcripts of each σ/Aσ mutant were compared to the cognate Aσ mutant. Fold change relative to the transcription levels was calculated using the arithmetic formula 2−ΔΔCt. Data represent the mean values and standard deviation of four independent experiments with two independent RNA preparations.
To prove that the differences in nap, sox and tct transcripts result in phenotypic differences, we determined the nitrate reductase activity, the ability to oxidize sulfate, and the utilization of citrate in ECF mutants compared to the wild-type. As expected, none of the strains except A. butzleri Aσ2::Km produced nitrite from the supplied nitrate in the presence of oxygen (Figure 3a). The constitutive expression of σ2 in the case of Aσ2::Km mutant led to nitrite production regardless of the presence of oxygen, indicating that ECF σ2 up-regulates the Nap-type nitrate reductase. To investigate whether the altered transcription levels of the sox genes resulted in a change in Sox enzyme activity, all the strains were grown for 6 hours in AM1 medium supplemented with sulfite and the pH indicator phenol red. The mutants ΔAσ2 and Δσ7/Aσ7 further induced the change in medium pH observed during growth of the parental strain, indicating that these mutants have an increased ability to oxidize reduced sulfur compounds (Figure 3b). These results confirmed that ECF σ2 and σ7 regulate the Sox sulfur oxidation proteins in an opposite way. Finally, we investigated whether these strains are able to utilize citrate, which causes an increase in the pH and a color change of the medium when these bacteria are grown on Simmons agar. In agreement with microarray and real-time RT PCR results, all strains except the mutants ΔAσ2 and Δσ7/Aσ7 caused a color change of the media, indicating that the ΔAσ2 and Δσ7/Aσ7mutants could not metabolize citrate (Figure 3c).
(A) Nitrate reductase activity was determined under aerobic conditions. Nitrate and nitrite present in the culture supernatant was measured four times and experiments were repeated with two independent cultures. (B) Sox enzyme activity assays performed under anaerobic conditions. Standard errors based on four independent experiments are indicated. (C) Utilization of citrate tested on Simmons Citrate Agar. Strains which were able to utilize citrate as carbon source caused a change in pH of the Simmons agar which results in a color change of the medium from green to blue. The sign “−”means no bacteria inoculated.
Although Arcobacter has been classified as an emerging pathogen (ICMSF, 2002), knowledge on this organism is still limited. The genome sequence of A. butzleri strain RM4018  revealed that, unlike other characterized members of the epsilon proteobacteria, this strain possesses seven putative extracytoplasmic function (ECF) σ factors. These σ factors are often involved in the regulation of virulence or stress-related genes in other bacteria. In the present study, we developed genetic tools to manipulate A. butzleri and used these tools to investigate the function of the putative RM4018 ECF σ factors. A. butzleri is resistant to many different antibiotics , , ; therefore, it was difficult to find a suitable antibiotic cassette to inactivate the ECF σ factor-encoding genes. Only a kanamycin resistance gene from C. coli  appeared to be functional in strain RM4018. By electroporation we were able to generate 10 different mutants and were able to inactivate 5 of the 7 ECF σ factors and to identify the corresponding regulons. Despite repeated attempts, we were unable to mutate the ECF σ factors AB1430 (σ3) and AB2165 (σ6), which may indicate that these factors are essential for bacterial growth under the conditions employed.
ECF σ factors are involved in a wide range of environmental responses in many bacterial species . They are mainly divided into stress response ECF σ factors and iron-starvation ECF σ factors . Our results indicate that the ECF σ factors of the strain RM4018 are neither involved in iron-starvation nor in the stress response. Furthermore, we found no evidence of positive regulation of their own transcription, as often found for other ECF σ factors . Except for the tonB genes, the RM4018 ECF σ factors regulate completely different sets of genes. This seemingly atypical gene regulation in Arcobacter has also been noted for the regulation of the flagellar genes as Arcobacter lacks the σ factors FliA and RpoN, which in many bacterial species regulate flagellar biosynthesis . So, in contrast to other eubacteria, many conserved genes in A. butzleri appear to be regulated by a σ factor belonging to a different σ factor class; therefore, knowledge on transcription regulation of conserved genes described in other bacterial species cannot be simply extrapolated to A. butzleri.
In A. butzleri RM4018, 5 out the 7 ECF σ/anti σ-factor pairs are flanked by genes encoding putative TonB-receptor proteins. In other species, the ECF σ/anti σ factors form, together with an outer membrane TonB-dependent receptor, a cell-surface signaling (CSS) system . Transcriptome analyses showed that σ1, σ4 and σ5 regulate the expression of the TonB-dependent receptors encoded by the same loci, suggesting the putative presence of three potential trans-envelope signal transduction systems in A. butzleri RM4018. Most of the described CSS systems are involved in iron signaling and transport . However, other functions have been described including for the Ralstonia solanacearum Prha-PrhIR system, which senses the presence of a plant cell-wall structure and initiates a regulatory cascade that induces the hypersensitive response and the transcription of pathogenicity genes . The role of the three putative CSS systems in A. butzleri RM4018 remains to be elucidated, as the growth of mutants in these systems are not affected by iron limitation.
Transcriptome analysis, as well as functional assays, showed that A. butzleri ECF σ factors also regulate a number of genes involved in the binding and transport of specific compounds, energy metabolism and sulfur oxidation. We showed that Arcobacter does not reduce nitrate under aerobic conditions (Figure 3A), although it does under anaerobic conditions (data not shown). The ECF σ2 is involved in this environmental adaptation as the Aσ2::Km mutant produces nitrite under aerobic conditions. This may indicate that oxygen stress has an effect on ECF σ2 activity. Several genes must be indirectly regulated by the ECF σ factors as they were up-regulated in the ECF σ mutants. Interestingly and also seen in Bacillus subtilis , a number of these genes are regulated by more than one ECF σ factor, which indicates that they may be needed under different growth conditions. For example, σ2 and σ7 regulate the dctPQM and sox genes in an opposite way. The DctPQM proteins form a tripartite ATP-independent periplasmic transporter, which catalyzes the uptake of C4-dicarboxylates like malate, fumarate and succinate in many aerobic bacteria . The Sox proteins which are not found in other members of the Campylobacteraceae are involved in the oxidation of reduced sulfur compounds in sulfur, photo- and chemo-lithotrophic bacteria . Similarly, we showed that σ5 and σ7 activate, while σ2 caused a down-regulation of the expression of the tctABC genes encoding a tricarboxylic transport system. Despite this, only σ7 and σ2 appeared to have a significant effect on citrate utilization. In many bacterial species a two-component signal transduction system activated by citrate is responsible for the activation of the tctABC genes . In A. butzleri, the putative TctABC system may also depend on the two-component system (AB0105–0106) located directly downstream of the putative tctABC genes. The expression of AB0105–0106 was not dramatically affected by σ5 and this may explain why citrate utilization was distinct between Δσ5/Aσ5 and Δσ7/Aσ7. All together, the genes regulated by the different A. butzleri ECF σ factors indicate that the ECF σ factors form a complex network of regulons that have a major role in regulating bacterial metabolism.
In conclusion, we have shown in this initial study that the ECF σ factors of A. butzleri control the transcription of a complex network of regulons that contain genes that are not commonly regulated by ECF σ factors family of proteins. These genes are mainly involved in the energy metabolism. In contrast to other eubacteria, many conserved genes in A. butzleri appear to be regulated by a σ factor belonging to a different σ factor class.
Genes identified by micro-array analyses which are more than fourfold up or down regulated by A. butzleri ECF sigma 1.
Genes identified by micro-array analyses which are more than fourfold up or down regulated by A. butzleri ECF sigma 2.
Genes identified by micro-array analyses which are more than fourfold up or down regulated by A. butzleri ECF sigma 4.
Genes identified by micro-array analyses which are more than fourfold up or down regulated by A. butzleri ECF sigma 5.
Conceived and designed the experiments: IMM CTP MMSMW. Performed the experiments: IMM RM SH LD lH. Analyzed the data: IMM CTP MMSMW. Contributed reagents/materials/analysis tools: CTP WGM AFA. Wrote the paper: IMM CTP JvP WG WGM MMSMW.
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