- Research article
- Open Access
Spontaneous phenotypic suppression of GacA-defective Vibrio fischeri is achieved via mutation of csrA and ihfA
© Foxall et al. 2015
- Received: 2 May 2015
- Accepted: 17 August 2015
- Published: 16 September 2015
Symbiosis defective GacA-mutant derivatives of Vibrio fischeri are growth impaired thereby creating a selective advantage for growth-enhanced spontaneous suppressors. Suppressors were isolated and characterized for effects of the mutations on gacA-mutant defects of growth, siderophore activity and luminescence. The mutations were identified by targeted and whole genome sequencing.
Most mutations that restored multiple phenotypes were non-null mutations that mapped to conserved domains in or altered expression of CsrA, a post-transcriptional regulator that mediates GacA effects in a number of bacterial species. These represent an array of unique mutations compared to those that have been described previously. Different substitutions at the same amino acid residue were identified allowing comparisons of effects such as at the R6 residue, which conferred relative differences in luminescence and siderophore levels. The screen revealed residues not previously identified as critical for function including a single native alanine. Most csrA mutations enhanced luminescence more than siderophore activity, which was especially evident for mutations predicted to reduce the amount of CsrA. Although CsrA mutations compensate for many known GacA mutant defects, not all CsrA suppressors restore symbiotic colonization. Phenotypes of a suppressor allele of ihfA that encodes one subunit of the integration host factor (IHF) heteroduplex indicated the protein represses siderophore and activates luminescence in a GacA-independent manner.
In addition to its established role in regulation of central metabolism, the CsrA regulator represses luminescence and siderophore as an intermediate of the GacA regulatory hierachy. Siderophore regulation was less sensitive to stoichiometry of CsrA consistent with higher affinity for the targets of this trait. The lack of CsrA null-mutant recovery implied these mutations do not enhance fitness of gacA mutants and alluded to this gene being conditionally essential. This study also suggests a role for IHF in the GacA-CsrB-CsrA regulatory cascade by potentially assisting with the binding of repressors of siderohphore and activators of luminescence. As many phosphorelay proteins reduce fitness when mutated, the documented instability used in this screen also highlights a potentially universal and underappreciated problem that, if not identified and strategically avoided, could introduce confounding variability during experimental study of these regulatory pathways.
- Siderophore Production
- Suppressor Mutation
- Integration Host Factor
- Siderophore Activity
- gacA Mutant
During host colonization, bacteria use complex regulatory hierarchies to orchestrate the adaptive changes that are necessary to bypass host defenses and secure nutrients. For many bacterial species, the GacA regulator directs the expression of multiple, disparate traits important for colonization, primarily by activating the transcription of several non-coding CsrB regulatory RNAs that sequester CsrA, a regulator that binds and influences translation or stability of target mRNAs [1–3]. Many defects conferred by mutations in GacA homologs are due to their inability to relieve CsrA repression of key transcripts involved in central metabolism, motility, and virulence [4–9]. For squid light organ symbiotic Vibrio fischeri, GacA is required for normal metabolism, motility, siderophore-mediated iron sequestration, and production of the key symbiosis factor luminescence, which provides protective counter-illumination camouflage for its squid host [10, 11]. The metabolic defects of GacS/GacA mutants in culture recently revealed accumulation of citrate as a potential signal for GacS in a cascade whereby GacA activates the expression of csrB1 and csrB2 to antagonize CsrA, and linked regulation of metabolisms to luminescence . In the absence of GacA, V. fischeri is impaired in the early initiation stages of host colonization, and is unable to achieve robust growth within light organs, thereby only rarely reaching large enough populations to induce low levels of luminescence via quorum sensing . Although the importance of GacA to squid symbiosis has been established and its relation to CsrA appears conserved and has already revealed important insights into the pathway , the extent of CsrA interaction with targets in the complex GacA regulatory hierarchy are not yet fully elucidated.
Even though characterization of global regulators like GacA provides an opportunity to simultaneously identify multiple phenotypes involved in colonization and elucidate the signal transduction cascades that direct the complex colonization process, their pleiotropy creates challenges for their study. Even though many defects in gacA mutants in culture, including altered luminescence, motility and siderophore production, are not detrimental under most laboratory conditions, gacA mutants’ associated growth defects reduce fitness [10, 13] which could provide strong selection for secondary mutations that allow escape from the defect, known as suppression. Depending on whether suppressor mutations dramatically change the appearance or behavior of mutants, they may go unnoticed and undetected without whole genome re-sequencing.
Suppression, when applied in a genetic screen, is a powerful tool for identifying interacting partner proteins, domains of importance in protein activity and specificity, and associated defects that provide biological insight . Here we characterize a high frequency suppression phenomena observed in gacA mutants of V. fischeri that allowed the characterization of effects of a broader distribution of csrA mutations than previously. Genetic analysis of the naturally occurring gacA suppressors indicates that the suppressor mutations reduced the amount or function of the CsrA post-transcriptional regulator, consistent with an epistatic relationship of CsrA below GacA in its regulatory hierarchy. The screen also implicates the integration host factor (IHF) heterodimer as a potential mediator of GacA-CsrA regulation. Our results suggest that null mutations in CsrA are not tolerated in V. fischeri even in the absence of its regulator, GacA.
Phenotypic suppression of gacA mutants occurs through the selective growth advantage conferred by spontaneous csrA mutations
Distribution of spontaneous csrA mutations suggested reduced activity rather than null CsrA mutations enhanced gacA mutant fitness
Several informative patterns of acquired mutations in csrA became apparent from the distribution and types of spontaneous mutations. Independently-derived identical mutations were recovered at nucleotide position 14, 17 and 44 and all possible substitutions were recovered at position 16, suggesting the screen was near saturation for mutations in csrA that provide a fitness benefit (Table 1). The only frame-shift mutations, all generated by single nucleotide deletions, mapped within the sequence encoding the last 10 amino acids which are absent in some naturally occurring CsrA homologs (e.g., RsmA from Pseudomonas putida ), and each of these were predicted to extend rather than truncate the CsrA protein. No other missense or non-sense mutations that altered or truncated the CsrA protein in these 10 amino acids were recovered, suggesting their loss would not impair CsrA function and thus were not predicted to compensate for the gacA mutants’ inability to relieve CsrA repression (Table 1). However, two point mutations that caused truncations of 12 and 14 amino acids were recovered (Table 1). Interestingly, all insertions/duplications maintained the original reading frame. Since frame-shift mutations along with nonsense mutations have a high potential to eliminate protein function (except in the C-terminus, as described) the most plausible explanation for their absence is that null csrA mutations did not improve gacA mutant fitness. The remaining mutations in the csrA ORF were missense point mutations (Table 1).
Spontaneous csrA mutations typically enhanced luminescence to a greater extent than siderophore
In GacA− derivatives, mutations in csrA simultaneously restored growth on the simple sugars, restored growth yield in rich medium, restored siderophore production and often greatly enhanced luminescence (Figs. 2 and 3) . The lack of relative differences for growth yield and utilization of simple sugars contrasts with the highly variable degree of luminescence and siderophore enhancement observed in different suppressors. Furthermore, the relative improvement in luminescence and siderophore activity often did not correlate with each other (Figs. 2 and 3), which has also been reported for different CsrA-regulated traits in E. coli . Siderophore activity was on average restored to wild-type levels with a range of 0.2 to 10-fold the wild-type level, and was greater in only 36 % of suppressors. Luminescence much more often surpassed wild-type levels, on average 6-fold, with a minimum of 0.1 and a maximum of 32-fold. Whereas 95 % of the csrA mutations fully restored luminescence, only 60 % restored siderophore activity to wild-type levels. The general trend of greater relative increase in luminescence than for siderophore activity with CsrA-impairment may allude to a higher binding affinity of CsrA to regulatory target(s) that govern siderophore: a siderophore defect remained in many suppressors despite mutations that presumably impaired CsrA function. However, other regulatory changes in gacA mutants may act synergistically with reduced csrA repression in the complex regulation of luminescence. Interestingly, half of the suppressors with 20-fold or more increased luminescence over wild-type harbored mutations that we predict resulted in decreased levels of wild-type CsrA suggesting CsrA binding of mRNA substrate(s) for this trait was especially sensitive to stoichiometry and would agree with a lower affinity (Figs. 2 and 3) although other explanations are possible and this hypothesis may be tested once targets are identified. One mutation that enhanced luminescence more than 24-fold (A36S), did not map to any conserved domain. A valine substitution at this same position that arose in the presence of the ihfAS2 allele did not enhance luminescence and suggested it only modestly impaired CsrA function, although the ihfAS2 allele could influence this phenotype separately from CsrA.
The colony opacity-enhancing ihfA mutation increased siderophore and attenuated luminescence of isolates that harbored csrA mutant alleles
The primary ihfAS2 suppressor mutation in strain VCW2E2 had no restorative effect on luminescence, and only slightly increased siderophore production and growth (Fig. 2), but analysis of gacA csrA suppressor mutants either harboring or lacking the ihfAS2 mutation (triple and double mutants respectively) revealed a striking pattern. Most ihfAS2 mutants surpassed wild type for siderophore activity and all three mutants with a greater increase in siderophore than luminescence levels harbored the ihfAS2 allele. In support of this conclusion, a suppressor harboring an ihfAS2 mutation and a csrA allele with a predicted R6L substitution (VCW9D2) produced more than twice as much siderophore as a suppressor with the same csrA allele without the ihfAS2 mutation (VCW9H6). Three triple mutants also surpassed wild type for growth yield (Figs. 2 and 3). Luminescence was attenuated in triple mutants compared to double mutants with the same csrA alleles (i.e., VCW6C6 and VCW9E2).
As a part of the heterodimeric integration host factor (IHF) protein, IhfA is a global regulator that bends DNA and facilitates recognition and binding of regulatory proteins thereby influences diverse functions . Because the GacA ortholog of Legionella pneumophila represses IHF , reduced function of IHF does provide a simple explanation for suppression if that hierarchy were conserved in V. fischeri and some gacA mutant defects were due to overproduction of IHF and enhanced regulatory protein binding. If this hypothesis is true, few defects (e.g., colony translucence) of gacA mutants resulted from a lack of ihfA repression alone. Alternatively, the spontaneous ihfAS2 mutation may only modestly alter IHF function, which would be expected for an important global regulator.
The associated phenotypes of the ihfAS2 allele are consistent with a role for IHF in co-activation of the lux luminescence operon, and co-repression of the iuc siderophore biosynthetic operon through its ability to enhance the binding of regulatory proteins related to these traits. Because there is an established precedent for IHF mediating activation of csrB gene homologs in other species [27, 28], the reduced luminescence of csrA mutant strain harboring the ihfAS2 allele suggests IHF could promote csrB1 and csrB2 gene expression and positive regulation of lux independently of GacA activation of these genes. However, other mechanisms for IHF activation of lux are possible. In Vibrio vulnificus IHF works in partnership with the LitR ortholog (SmcR) to activate virulence-associated vvpE [26, 29] suggesting IHF activation of luminescence in V. fischeri could occur through the promotion of binding of the quorum sensing regulator LitR thereby enhancing expression of LuxR and in turn the lux operon. The effect of ihfAS2 on siderophore activity was consistent with several studies that report transcripts related to iron acquisition are increased by IhfA mutations [26, 30, 31]. The ferric uptake regulator, Fur, and ArcA are the most likely candidates for the co-repression of siderophore with IHF, as other studies report IHF enhancement of aerobic Fur repression, and in the absence of Fur enhancement of anaerobic repression by ArcA [32, 33]. Additional studies to determine whether these or other mechanisms are at play in IHF activation and repression are warranted.
Newly identified patterns of altered function from comparison of the effects of spontaneous csrA mutations with those achieved by alanine scan in CsrA of Escherichia coli
A previously applied alanine-scanning mutagenesis that was performed with the E. coli csrA gene, used to examine the relative contribution each amino acid residue to CsrA protein function , provides an invaluable comparator to our spontaneous suppression screen. Our complementary screen differs in that all potential amino acid substitutions are possible, even the single native alanine residue that was not altered in the alanine scan. In our screen, an A36S substitution caused a 20-fold increase in luminescence and restored siderophore activity indicating the highly conserved A36, positioned into the hydrophobic core of the CsrA homodimer, could be critical to protein folding and 3- dimensional stability [20, 23]. Even the conservative substitution of this alanine with the non-polar and fairly compact valine (VCW2G2) altered CsrA function (Fig. 2). Also, only mutations that improve growth would likely improve fitness. Thus, mutations that map to non-conserved regions that do not contribute to critical protein folding, dimerization, or RNA binding were not recovered, as described previously with the lack of C-terminal truncations. Finally, the screen also dictates that mutations that further impair fitness of the double gacA csrA mutant would not be recovered. For example, if the CsrA protein was essential, then none of the spontaneous mutations should eliminate CsrA function. The lack of mutations in highly conserved residues of functional domains, especially for the two guanidine residues of the GxxG HA motif, the absence of frame-shift mutations (except in the last 10 non-essential amino acids), and the detection of a csrA transcript in the promoter-deletion mutant with one of most dramatic suppressor phenotypes implies no mutant recovered harbors a null allele and supports our interpretation that CsrA may be essential under the conditions of this screen in V. fischeri. Until recently, CsrA was not thought to be essential in most bacterial species ; however, among the many published csrA mutants, several have insertions near the C-terminus of the protein [35, 36], and such mutations could alter rather than eliminate activity. One report now suggests that CsrA is conditionally essential in E. coli .
The suppressor screen recovered 8 mutants with mutations that effected the two predicted regions essential to CsrA function, that were confirmed by the alanine scan . Seven were substitutions in amino acids in conserved region 1 that is essential to CsrA function (L2, I3, L4, T5, R6, R7), and a single predicted amino acid insertion in the less conserved region 2 (V40, S41, V42, H43, R44, E45, E46, I47)  (Fig. 2). Two possible explanations for the relatively low recovery of suppressor mutations mapping to region 2 are that there are more neutral amino acid substitutions in this more variable region whereas any non-neutral mutations may generate null alleles. Another explanation is that amino acid substitutions in region 2 are well tolerated, and few impair CsrA function enough to confer suppression. Targeted mutagenesis may elucidate whether one of these possibilities is true, although this would be best accomplished through heterologous expression in E. coli, given the difficulties in generating a csrA null mutation in V. fischeri and the impaired growth that multi-copy csrA confers of the wild-type ES114 .
Suppressors with CsrA mutations in R6 had dramatic phenotypes, implying it is especially critical to CsrA function and is in agreement with the alanine mutagenesis screen in E.coli . The CsrA R6A mutation in E.coli positively affects expression of all transcripts measured, including highly enhanced glgCA and pgaA expression, and modest increase of flhDC expression . To reduce the confounding phenotypes already described, our focus was only on suppressor mutants lacking the ihfAS2 primary mutation, leaving three different suppressors available for comparison at this site. The R6C substitution enhanced levels of both siderophore and luminescence (~10-fold wild type). Whereas R6L, which is likely a more neutral substitution as both amino acids contain charged side chains, had a similar effect on luminescence, but only restored siderophore activity to wild-type levels; thus, this substitution conferred less impairment on CsrA regulation of siderophore activity. The R6S substitution also resulted in wild-type luminescence implying repression of luminescence was not substantially impaired by this mutation, but siderophore activity increased to 3-fold over wild-type, indicating a greater dysfunction of siderophore repression. That different amino acid substitutions at the same position could influence relative regulation of two different traits, likely through different target transcripts, would not have been revealed by an alanine scan and the basis of these differences warrants further investigation.
In E.coli, alanine substitutions in some regions of CsrA had differential influence on certain transcripts, rather than generally affecting function . Substitutions in residues 18–23, and 31–38 differentially affected biofilm formation, and 11–14 and 22 differentially affected glycogen accumulation and motility . Focusing on only mutants lacking the ihfAS2 mutation, there were five suppressors with CsrA mutations in the biofilm-specific residues and one with a mutation in the glycogen/motility specific residues identified in the E. coli CsrA. All six of these mutations resulted in moderate to severe dysfunction of luminescence regulation (wild type levels to 10-fold higher than wild type). Among the phenotype-dependent residues identified, two mutations falling in the biofilm-specific residues, 31–38, were among the nine suppressors with fully restored or increased siderophore activity. Thus, the previously identified biofilm-specific residues appear to contribute substantially to siderophore regulation in V.fischeri. Mutations that we propose decreased levels of wild-type CsrA (Fig. 3) and all C-terminal alterations (Fig. 2), had only moderate effects on siderophore activity suggesting these did not interfere as much with siderophore regulation as they did with luminescence regulation.
No suppressors were recovered with CsrA mutations in any of the positions where alanine substitution in E.coli affected CsrA levels as would happen if they decreased the stability of the transcript or protein triggering more rapid turnover . Alanine substitutions at positions 18, 20, 34, 52, and 55 lowers CsrA levels, however the mutants have wild-type levels of activity . Our results implied that if substitutions of residues other than alanine at these positions also reduce production, they do not impair function enough to confer suppression. Approximately 16 positions in CsrA cause a decrease in its production when substituted with alanine and also decreased activity . Three suppressors in position 5, 11 and 15 were recovered indicating non-alanine substitutions at these same sites similarly impaired activity.
A csrA suppressor mutation restored squid colonization ability, but only modestly enhanced luminescence in situ compared to in vitro
The CsrA homologs have been described in many bacterial species where they affect behaviors essential for host association, as now inferred in V. fischeri as an intermediary of GacA regulation of multiple symbiosis-related traits [9, 12, 17, 39]. Particularly focused in vitro analysis of the CsrA protein in a few target species such as E. coli has provided insight into structure-function of this post-transcriptional regulator . This study complements those in that the nature of the selective screen allowed the evaluation of effects of a wider array of accessible mutations that alter function and expression. We expect several mutations identified in this screen will provide targets of interest for further analysis in other species where full null alleles can be generated, which has not yet been possible in V. fischeri. Although those other systems facilitate such analysis, there are still limitations for extending the in vitro analysis in model organisms such as E. coli to biologically relevant models for animal infection where these regulatory cascades play a role. For V. fischeri, the traits under control of the GacA-CsrA cascade facilitated the colonization process of an accessible host, and revealed subtle differences (e.g., luminescence) in the host compared to in vitro analysis. Expanded analysis will likely identify new regulatory partners and mediators of the cascade, such as IHF identified in this screen. Upon identification of the regulatory targets of CsrA that controlled siderophore activity and luminescence, both of which are established as important in this symbiotic model, the potential differences in affinity for targets may be elucidated both in vitro and in vivo. Thus, this study sets the stage for further analysis of the regulatory hierarchy and regulation in a natural host context that cannot be fully extrapolated from in vitro results alone but at the same time, builds upon the wealth of knowledge gained from its study in model laboratory systems.
Bacterial strains and growth conditions
Two previously described gacA mutants generated in the squid symbiotic strain ES114, VCW2A1 and VCW2F5 , were used for isolation of suppressors (Table 1). Eschericia coli strains for cloning and plasmid propagation included DH5α, and Top10 (for pCR2.1TOPO) (Invitrogen). V. fischeri was grown in SWT , LBS , or minimal media derived from CAS solid agar  at 28 °C. Media were occasionally supplemented with kanamycin (Km) at 50 μg/ml or chloramphenicol (Ch) at 25 μg/ml for E. coli or 2.5 μg/ml for V. fischeri to hold selection on the presence of resistance cassettes.
Oligonucleotide primers used for amplification in PCR
Sequence (5′ - 3′)
CsrA SOE A
CsrA SOE B
CsrA SOE C
CsrA SOE D
After consideration that null mutations harbored by these constructs may be lethal, we attempted to introduce a transposon in the extreme C-terminus of csrA at nucleotide 148 as confirmed by sequencing using the EZ::TN™ < Kan-2 > Insertion Kit following the manufacturers protocols (Epicentre) generating plasmid (pJCM24). The transposon was inserted at five amino acids downstream of the mutation generated in E. coli . Conjugation and isolation of single crossover derivatives was done, and confirmed by PCR using primers RsmAF3 and RsmAR7 with Kan-2 FP-1 (Table 3). Following second crossover events and loss of the previously integrated mutagenic plasmid, PCR screening with primers RsmAF3 and RsmAR7 with Kan fp-1 (Table 3) of 5000 Kmr Chs derivatives revealed no csrA::TnKm mutants were ever generated.
Isolation and identification of spontaneous suppressors
Spontaneous GacA suppressor mutants harboring unknown mutations were isolated from late log and stationary phase cultures of either the ΔgacA mutant or gacA::TnKm that were subsequently plated onto LBS or CAS agar and allowed to incubate for approximately 72 h. Large, opaque colonies on LBS or CAS, or siderophore producing colonies with orange halos on CAS agar were isolation streaked onto LBS agar, individual colonies grown in LBS to md-log phase, and immediately stored in 15 % glycerol at −80 °C. For all derivatives restored in one or more phenotype, DNA was extracted  and the csrA gene was amplified using Expand HiFi polymerase (Roche) using csrA-specific forward (RmsAF8) and reverse (RmsAR9) primers (Table 3) and the PCR product directly sequenced by the Hubbard Center for Genome Studies at the University of New Hampshire. The sequenced csrA genes from these gacA sup mutant suppressors were compared to that of csrA from the published genome of V. fischeri  in order to identify the location of the mutation. Probable siblings were identified by determining if two mutants that harbored an identical mutation were isolated from the same overnight seed culture used to select for suppression; only one such mutant was identified, and removed from further characterization. For the two suppressors that did not harbor mutations in the csrA gene, the csrB1 and csrB2 genes were amplified with gene specific primers: RsmB1F and RsmB1R for csrB1, and RsmB2F and RsmB2R for csrB2 (Table 3).
Identification of the ihfAS2 mutation
Genomic DNA was extracted from ES114, and VCW2E2 late log cultures grown in LBS using the Wizard Genomic DNA Purification Kit and supplied manufacturer protocol (Promega, WI, USA). The DNA quality was assessed visually by electrophoresis. Sequencing libraries were generated from 1 μg of genomic DNA as determined using the Qubit 2.0 fluorimeter (LifeTech, CA, US). DNA was sheared on the Covaris M220 Ultasonicator to a mean size of 500 bp. Libraries were generated using the TruSeq Kit and targeted size selection of 500 bp was completed using the optional gel-extraction method in the TruSeq protocol (Illumina). Genomes were sequenced by a high output mode run 101 bp paired-end reads using an Illumina HiSeq 2500 at the Hubbard Center for Genome Studies at the University of New Hampshire. The Illumina reads were aligned to the published reference ES114 strain (PRJNA58163, assembly GCA_000011805.1) using Breseq pipeline . The predicted mutations (Additional file 1) were cross-referenced with ~60 ES114 (VCW1C6) derivatives also re-sequenced using Illumina HiSeq 2500 101 bp paired-end reads, which revealed differences from the published ES114 reference genome (Additional file 1). Each identified mutant allele was compared to orthologous loci in various Vibrio species using BLAST  and the nucleotide nr database, which indicated in each instance that the genomic variation in VCW1C6 represented wild-type and likely ancestral, not mutant alleles suggesting they represent errors from the original ES114 genome assembly. For all remaining variant loci identified in VCW2E2 not present in ES114 (VCW1C6) oligonucleotide primers were designed flanking the mutation (Additional file 1) and Phusion High-Fidelity DNA Polymerase (Life Technologies) used to amplify regions by PCR in both VCW2E2 and its parental strain VCW2A1 using an initial denaturation of 1 min at 94 °C, followed by 30 cycles of denaturation of 1 min 94 °C, annealing at described temperature (Table 3) for 1 min, followed by elongation for 1 min at 68 °C. The amplicons were sequenced by the Sanger method  using both forward and reverse primers at the Hubbard Center for Genome Studies at the University of New Hampshire. The sequencing reads were aligned with ES114 (BioProject PRJNA58163, assembly GCA_000011805.1) using SeqMan Pro (DNASTAR, Inc. Madison, WI) which allowed confirmation that the single nucleotide polymorphism C > G at base pair position 178 in ihfA as the suppressor mutation in VCW2E2 (BioProject PRJNA283549). All other sequences in VCW2E2 were identical to the reference, and were not considered as potential suppressor mutations.
Semi-quantitative assessment of csrA transcripts
For one suppressor whose promoter was presumably deleted, and which exhibited a strong suppressor phenotype, we determined whether the csrA transcript was indeed produced by semi-quantitative PCR using the rpoB transcript as a housekeeping control gene. Primers amplifying rpoB (QRpoBF1 and QRpoBR2) and csrA (QCsrAF1, and QCsrAR2) were designed to produce amplicons ~100 bp in length (Table 3). Total RNA was extracted from two biological replicates of late-log cultures of ES114, VCW2A1 (gacA::TnKm), and VCW9A1 (gacA::TnKmsup(ihfAS2 csrAE)) grown in SWT. Cells were pelleted and suspended in half the volume of RNA protect (Ambion) and held overnight at 4 °C. RNA was extracted using the UltraClean Microbial RNA Isolation Kit (MoBio Laboratories) followed by DNase treatment with the RTS-DNase kit (MoBio Laboratories). Absence of contaminating DNA was confirmed by end-point PCR using 1 μl of template. The RNA quantity and purity was determined spectrophotometrically using a NanoDrop 2000, and the quality and integrity of RNA assessed by agarose gel electrophoresis. cDNA was synthesized from 500 ng of total RNA using the qScript™ Flex cDNA Synthesis Kit (Quanta Biosciences, MD, US) using 0.5 μM each gene-specific reverse primer and 5 % final volume qScript Reverse Transcriptase at 42 °C for 1 h following the manufacturers protocols. The resulting cDNA was diluted 1/5 with nuclease free water, and immediately used for assays. Assays were performed on 1 μl of cDNA template, in triplicate in 10 μl reactions using using AccuStart PCR Supermix (Quanta Biosciences, MD, US) in separate reactions for csrA and rpoB cycled at the same time for 30 cycles with a 1 min denaturation at of 94 °C, a 1 min annealing at 57 °C, and a 30 s elongation at of 72 °C. Two replicate RT reactions for each biological replicate RNA were performed. The production of amplicons was assessed at 10, 15, 20, 25, and 30 cycles by electrophoresis of 5 μl of PCR reaction and the presence of amplicons of the correct size visualized after separation with 1.2 % agarose gel electrophoresis in 1x TAE and 1x Gel Red (Phenix Research). Amplicons for rpoB were produced from all strains by 20–25 cycles, and from csrA between 20 and 30 cycles.
All phenotypic analyses were conducted as outlined previously . Briefly, luminescence and growth was determined from cultures grown at 28 °C with shaking (200 RPM) in SWT. Luminescence and density (OD600) were measured from 1 ml of culture using a luminometer (Turner Designs) and a spectrophotometer (Eppendorf). LPS was observed as difference in colony opacity on LBS plates. Growth on simple sugars was assessed as cell density in minimal medium supplemented with 32.6 mM glycerol or with 32.6 mM glycerol and 0.5 % casamino acids as a control. Growth yield OD600 was measured from cultures grown in SWT overnight (18 h) at 28 °C. The experiments contained 3 replicates and were repeated at least 2 times. Data shown is from a representative experiment and error is expresses as SE. Siderophore production was measured using a modified liquid chrome azurol S (CAS) liquid assay . Briefly, Cultures were grown in minimal medium based on that used for CAS agar plates , and grown for eight hours with shaking. The density (OD600) was measured and cells removed by pelleting. Equal volumes of the culture supernatant and a CAS assay solution were mixed along with 1 % of shuttle solution (0.2 M 5-Sulfosalicylic acid). After 20 min the absorbance at 630 nm of these mixtures was measured using a plate reader (Tecan). Siderophore is reported percent siderophore units (compared to the blank control) per OD600.
Squid colonization was performed exactly as outlined previously [10, 15]. Luminescence was determined with a luminometer (Turner Designs) and colonization by homogenization and plating of squid first frozen at −80 °C at 12, 24 and 48 h after hatching [10, 15]. Luminescence of strains in light organs is reported relative to the average lum/CFU of ES114 colonized squid.
Availability of supporting data
The data sets supporting the results of this article are included within the article and its additional files. The draft genome sequencing project of V. fischeri VCW2E2 is has been deposited with NCBI Genomes under the BioProject PRJNA283549.
Invertebrate animal studies to assess the mutualistic bacterial colonization of juvenile squid conducted herein are not regulated in the United States therefore the Institutional Animal Care and Use Committee has no authority for review of such protocols. In lieu of these not falling under the jurisdiction of regulation in the United States, the authors hereby state that these studies were conducted with sincere effort towards the ethical use, care, and treatment of these animals, the number of individuals was minimized and these efforts are consistent with the Basal Declaration (http://www.basel-declaration.org/basel-declaration/) and the International Council for Laboratory Animal Science (ICLAS) ethics guidelines.
We thank Victoria Seetaram, Victoria Sicard, Tucker Noyes, Summer Morrill, and Jennifer Mahoney for their assistance with mutant isolation, and E.V. Stabb for insightful conversations and reviewing the manuscript. This work was funded in part by a US Army Academy of Applied Sciences Research and Engagement Apprenticeship Program; National Science Foundation IOS 0843633, IOS 1258099, and DBI 1229361 MRI; NHAES Animal Health NH00497-A (accession 0208415) and Hatch NH00479 (accession 0205144); and National Institutes of Health 5R03A1076831-02. This is Scientific Contribution Number 2624 for the New Hampshire Agricultural Experiment Station.
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- Romeo T. Global regulation by the small RNA-binding protein CsrA and the non-coding RNA molecule CsrB. Mol Microbiol. 1998;29(6):1321–30.View ArticlePubMedGoogle Scholar
- Liu MY, Gui G, Wei B, Preston 3rd JF, Oakford L, Yuksel U, et al. The RNA molecule CsrB binds to the global regulatory protein CsrA and antagonizes its activity in Escherichia coli. J Biol Chem. 1997;272(28):17502–10.View ArticlePubMedGoogle Scholar
- Bachman MA, Swanson MS. The LetE protein enhances expression of multiple LetA/LetS-dependent transmission traits by Legionella pneumophila. Infect Immun. 2004;72(6):3284–93.PubMed CentralView ArticlePubMedGoogle Scholar
- Blumer C, Heeb S, Pessi G, Haas D. Global GacA-steered control of cyanide and exoprotease production in Pseudomonas fluorescens involves specific ribosome binding sites. Proc Natl Acad Sci U S A. 1999;96(24):14073–8.PubMed CentralView ArticlePubMedGoogle Scholar
- Chancey ST, Wood DW, Pierson 3rd LS. Two-component transcriptional regulation of N-acyl-homoserine lactone production in Pseudomonas aureofaciens. Appl Environ Microbiol. 1999;65(6):2294–2299.Google Scholar
- Cui Y, Chatterjee A, Chatterjee AK. Effects of the two-component system comprising GacA and GacS of Erwinia carotovora subsp. carotovora on the production of global regulatory rsmB RNA, extracellular enzymes, and harpinEcc. Mol Plant Microbe Interact. 2001;14(4):516–26.View ArticlePubMedGoogle Scholar
- Parkins MD, Ceri H, Storey DG. Pseudomonas aeruginosa GacA, a factor in multihost virulence, is also essential for biofilm formation. Mol Microbiol. 2001;40(5):1215–26.View ArticlePubMedGoogle Scholar
- Chatterjee A, Cui Y, Yang H, Collmer A, Alfano JR, Chatterjee AK. GacA, the response regulator of a two-component system, acts as a master regulator in Pseudomonas syringae pv. tomato DC3000 by controlling regulatory RNA, transcriptional activators, and alternate sigma factors. Mol Plant Microbe Interact. 2003;16(12):1106–17.View ArticlePubMedGoogle Scholar
- Vakulskas CA, Potts AH, Babitzke P, Ahmer BM, Romeo T. Regulation of Bacterial Virulence by Csr (Rsm) Systems. Microbiol Mol Biol Rev. 2015;79(2):193–224.View ArticlePubMedGoogle Scholar
- Whistler CA, Ruby EG. GacA regulates symbiotic colonization traits of Vibrio fischeri and facilitates a beneficial association with an animal host. J Bacteriol. 2003;185(24):7202–12.PubMed CentralView ArticlePubMedGoogle Scholar
- Nyholm SV, McFall-Ngai MJ. The winnowing: establishing the squid-vibrio symbiosis. Nat Rev Microbiol. 2004;2(8):632–42.View ArticlePubMedGoogle Scholar
- Septer AN, Bose JL, Lipzen A, Martin J, Whistler C, Stabb EV. Bright luminescence of Vibrio fischeri aconitase mutants reveals a connection between citrate and the Gac/Csr regulatory system. Mol Microbiol. 2015;95(2):283–96.View ArticlePubMedGoogle Scholar
- Duffy BK, Defago G. Controlling instability in gacS-gacA regulatory genes during inoculant production of Pseudomonas fluorescens biocontrol strains. Appl Environ Microbiol. 2000;66(8):3142–50.PubMed CentralView ArticlePubMedGoogle Scholar
- Prelich G. Suppression mechanisms: themes from variations. Trends Genet. 1999;15(7):261–6.View ArticlePubMedGoogle Scholar
- Whistler CA, Koropatnick TA, Pollack A, McFall-Ngai MJ, Ruby EG. The GacA global regulator of Vibrio fischeri is required for normal host tissue responses that limit subsequent bacterial colonization. Cell Microbiol. 2007;9(3):766–78.View ArticlePubMedGoogle Scholar
- Kulkarni PR, Cui X, Williams JW, Stevens AM, Kulkarni RV. Prediction of CsrA-regulating small RNAs in bacteria and their experimental verification in Vibrio fischeri. Nucleic Acids Res. 2006;34(11):3361–9.PubMed CentralView ArticlePubMedGoogle Scholar
- Ballok AE. GacA regulation of luminescence in the symbiotic bacterium Vibrio fischeri, Theses (M.S.). University of New Hampshire: Genetics Program; 2007.Google Scholar
- Edwards AN, Patterson-Fortin LM, Vakulskas CA, Mercante JW, Potrykus K, Vinella D, et al. Circuitry linking the Csr and stringent response global regulatory systems. Mol Microbiol. 2011;80(6):1561–80.PubMed CentralView ArticlePubMedGoogle Scholar
- Rife C, Schwarzenbacher R, McMullan D, Abdubek P, Ambing E, Axelrod H, et al. Crystal structure of the global regulatory protein CsrA from Pseudomonas putida at 2.05 A resolution reveals a new fold. Proteins. 2005;61(2):449–53.View ArticlePubMedGoogle Scholar
- Mercante J, Suzuki K, Cheng X, Babitzke P, Romeo T. Comprehensive alanine-scanning mutagenesis of Escherichia coli CsrA defines two subdomains of critical functional importance. J Biol Chem. 2006;281(42):31832–42.View ArticlePubMedGoogle Scholar
- Schubert M, Lapouge K, Duss O, Oberstrass FC, Jelesarov I, Haas D, et al. Molecular basis of messenger RNA recognition by the specific bacterial repressing clamp RsmA/CsrA. Nat Struct Mol Biol. 2007;14(9):807–13.View ArticlePubMedGoogle Scholar
- Sacerdot C, Fayat G, Dessen P, Springer M, Plumbridge JA, Grunberg-Manago M, et al. Sequence of a 1.26-kb DNA fragment containing the structural gene for E.coli initiation factor IF3: presence of an AUU initiator codon. EMBO J. 1982;1(3):311–5.PubMed CentralPubMedGoogle Scholar
- Gutierrez P, Li Y, Osborne MJ, Pomerantseva E, Liu Q, Gehring K. Solution structure of the carbon storage regulator protein CsrA from Escherichia coli. J Bacteriol. 2005;187(10):3496–501.PubMed CentralView ArticlePubMedGoogle Scholar
- Mercante J, Edwards AN, Dubey AK, Babitzke P, Romeo T. Molecular geometry of CsrA (RsmA) binding to RNA and its implications for regulated expression. J Mol Biol. 2009;392(2):511–28.PubMed CentralView ArticlePubMedGoogle Scholar
- Browning DF, Cole JA, Busby SJ. Suppression of FNR-dependent transcription activation at the Escherichia coli nir promoter by Fis, IHF and H-NS: modulation of transcription initiation by a complex nucleo-protein assembly. Mol Microbiol. 2000;37(5):1258–69.View ArticlePubMedGoogle Scholar
- Pitre CA, Tanner JR, Patel P, Brassinga AK. Regulatory control of temporally expressed integration host factor (IHF) in Legionella pneumophila. Microbiology. 2013;159(Pt 3):475–92.View ArticlePubMedGoogle Scholar
- Humair B, Wackwitz B, Haas D. GacA-controlled activation of promoters for small RNA genes in Pseudomonas fluorescens. Appl Environ Microbiol. 2010;76(5):1497–506.PubMed CentralView ArticlePubMedGoogle Scholar
- Martinez LC, Martinez-Flores I, Salgado H, Fernandez-Mora M, Medina-Rivera A, Puente JL, et al. In silico identification and experimental characterization of regulatory elements controlling the expression of the Salmonella csrB and csrC genes. J Bacteriol. 2014;196(2):325–36.PubMed CentralView ArticlePubMedGoogle Scholar
- Jeong HS, Kim SM, Lim MS, Kim KS, Choi SH. Direct interaction between quorum-sensing regulator SmcR and RNA polymerase is mediated by integration host factor to activate vvpE encoding elastase in Vibrio vulnificus. J Biol Chem. 2010;285(13):9357–66.PubMed CentralView ArticlePubMedGoogle Scholar
- Graf J, Ruby EG. Novel effects of a transposon insertion in the Vibrio fischeri glnD gene: defects in iron uptake and symbiotic persistence in addition to nitrogen utilization. Mol Microbiol. 2000;37(1):168–79.View ArticlePubMedGoogle Scholar
- Arfin SM, Long AD, Ito ET, Tolleri L, Riehle MM, Paegle ES, et al. Global gene expression profiling in Escherichia coli K12. The effects of integration host factor. J Biol Chem. 2000;275(38):29672–84.View ArticlePubMedGoogle Scholar
- Compan I, Touati D. Interaction of six global transcription regulators in expression of manganese superoxide dismutase in Escherichia coli K-12. J Bacteriol. 1993;175(6):1687–96.PubMed CentralPubMedGoogle Scholar
- Escolar L, de Lorenzo V, Perez-Martin J. Metalloregulation in vitro of the aerobactin promoter of Escherichia coli by the Fur (ferric uptake regulation) protein. Mol Microbiol. 1997;26(4):799–808.View ArticlePubMedGoogle Scholar
- Timmermans J, Van Melderen L. Conditional essentiality of the csrA gene in Escherichia coli. J Bacteriol. 2009;191(5):1722–4.PubMed CentralView ArticlePubMedGoogle Scholar
- Romeo T, Gong M, Liu MY, Brun-Zinkernagel AM. Identification and molecular characterization of csrA, a pleiotropic gene from Escherichia coli that affects glycogen biosynthesis, gluconeogenesis, cell size, and surface properties. J Bacteriol. 1993;175(15):4744–55.PubMed CentralPubMedGoogle Scholar
- Lenz DH, Miller MB, Zhu J, Kulkarni RV, Bassler BL. CsrA and three redundant small RNAs regulate quorum sensing in Vibrio cholerae. Mol Microbiol. 2005;58(4):1186–202.View ArticlePubMedGoogle Scholar
- Visick KL, Skoufos LM. Two-component sensor required for normal symbiotic colonization of Euprymna scolopes by Vibrio fischeri. J Bacteriol. 2001;183(3):835–42.PubMed CentralView ArticlePubMedGoogle Scholar
- Hussa EA. Identification and characterization of Vibrio fischeri response regulators, and discovery of new symbiotic determinants, Doctoral Dissertation. Illinois: Loyola University Chicago; 2008.Google Scholar
- Mukherjee A, Cui Y, Liu Y, Dumenyo CK, Chatterjee AK. Global regulation in Erwinia species by Erwinia carotovora rsmA, a homologue of Escherichia coli csrA: repression of secondary metabolites, pathogenicity and hypersensitive reaction. Microbiology. 1996;142(Pt 2):427–34.View ArticlePubMedGoogle Scholar
- Boettcher KJ, Ruby EG: Depressed light emission by symbiotic Vibrio fischeri of the sepiolid squid Euprymna scolopes. J Bacteriol 1990, 172(7):3701-3706.Google Scholar
- Graf J, Dunlap PV, Ruby EG: Effect of transposon-induced motility mutations on colonization of the host light organ by Vibrio fischeri. J Bacteriol 1994, 176(22):6986-6991.Google Scholar
- Graf J, Ruby EG: Host-derived amino acids support the proliferation of symbiotic bacteria. Proc Natl Acad Sci U S A 1998, 95(4):1818-1822.Google Scholar
- Stabb EV, Ruby EG: RP4-based plasmids for conjugation between Escherichia coli and members of the Vibrionaceae. Methods Enzymol 2002, 358:413-426.Google Scholar
- Horton RM, Cai ZL, Ho SN, Pease LR: Gene splicing by overlap extension: tailor-made genes using the polymerase chain reaction. Biotechniques 1990, 8(5):528-535.Google Scholar
- Murillo J, Keen NT: Two native plasmids of Pseudomonas syringae pathovar tomato strain PT23 share a large amount of repeated DNA, including replication sequences. Mol Microbiol 1994, 12(6):941-950.Google Scholar
- Ausubel FM, Brent R, Kingston RE, D.D. M, Seidman JG, Smith JA, Struhl K: Current Protocols in Molecular Biology. New York, New York: Wiley and Sons, Inc.; 1990.Google Scholar
- Ruby EG, Urbanowski M, Campbell J, Dunn A, Faini M, Gunsalus R, Lostroh P, Lupp C, McCann J, Millikan D et al: Complete genome sequence of Vibrio fischeri: a symbiotic bacterium with pathogenic congeners. Proc Natl Acad Sci U S A 2005, 102(8):3004-3009.Google Scholar
- Barrick JE, Yu DS, Yoon SH, Jeong H, Oh TK, Schneider D, Lenski RE, Kim JF: Genome evolution and adaptation in a long-term experiment with Escherichia coli. Nature 2009, 461(7268):1243-1247.Google Scholar
- Mount DW: Using the Basic Local Alignment Search Tool (BLAST). CSH Protoc 2007, 2007:pdb top17.Google Scholar
- Sanger F, Coulson AR: A rapid method for determining sequences in DNA by primed synthesis with DNA polymerase. J Mol Biol 1975, 94(3):441-448.Google Scholar
- Henderson DP, Payne SM: Vibrio cholerae iron transport systems: roles of heme and siderophore iron transport in virulence and identification of a gene associated with multiple iron transport systems. Infect Immun 1994, 62(11):5120-5125.Google Scholar
- Hilterbrand A, Saelens J, Putonti C: CBDB: the codon bias database. BMC Bioinformatics 2012, 13:62.Google Scholar