Abstract
The bacteriovorous nematode Caenorhabditis elegans has been used to investigate many aspects of animal biology, including interactions with pathogenic bacteria. However, studies examining C. elegans interactions with bacteria isolated from environments in which it is found naturally are relatively scarce. C. elegans is frequently associated with cultivation of the edible mushroom Agaricus bisporus, and has been reported to increase the severity of bacterial blotch of mushrooms, a disease caused by bacteria from the Pseudomonas fluorescens complex. We observed that pseudomonads isolated from mushroom farms showed differential resistance to nematode predation. Under nutrient poor conditions, in which most pseudomonads were consumed, the mushroom pathogenic isolate P. fluorescens NZI7 was able to repel C. elegans without causing nematode death. A draft genome sequence of NZI7 showed it to be related to the biocontrol strain P. protegens Pf-5. To identify the genetic basis of nematode repellence in NZI7, we developed a grid-based screen for mutants that lacked the ability to repel C. elegans. The mutants isolated in this screen included strains with insertions in the global regulator GacS and in a previously undescribed GacS-regulated gene cluster, ‘EDB’ (‘edible’). Our results suggest that the product of the EDB cluster is a poorly diffusible or cell-associated factor that acts together with other features of NZI7 to provide a novel mechanism to deter nematode grazing. As nematodes interact with NZI7 colonies before being repelled, the EDB factor may enable NZI7 to come into contact with and be disseminated by C. elegans without being subject to intensive predation.
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Introduction
Laboratory studies of bacteria–nematode interactions, most notably studies using clinical isolates of Pseudomonas aeruginosa, have shown that many environmental and human pathogenic bacteria possess mechanisms to inhibit bacteriovores such as Caenorhabditis elegans (Tan et al., 1999, O’Quinn et al., 2001; Sifri et al., 2005; Powell and Ausubel, 2008; Troemel et al., 2008; Bjornlund et al., 2009; Pedersen et al., 2009; Tampakakis et al., 2009; Zaborin et al., 2009; Irazoqui et al., 2010; Niu et al., 2010; Rae et al., 2010). Examples of such mechanisms include poisoning by cyanide production (Gallagher and Manoil, 2001), pore formation by Bacillus thuringiensis Cry toxins (Marroquin et al., 2000) and biofilm formation across the nematode pharynx by Yersinia pestis (Darby et al., 2002). Aversive olfactory responses to bacteria have also been described (Zhang et al., 2005; Shtonda and Avery, 2006; Pradel et al., 2007; Ha et al., 2010). However, studies examining the interaction of C. elegans with bacteria it encounters in the environments in which it is commonly found are relatively scarce (Félix and Braendle, 2010; Freyth et al., 2010).
The model strain C. elegans strain N2 was originally isolated from a mushroom farm (Hansen et al., 1959; Grewal and Richardson, 1991; Chen et al., 2006). C. elegans has also been isolated from compost, snails, rotting fruit and wild decaying mushrooms (Hodgkin and Doniach, 1997; Barriere and Felix, 2005; Caswell-Chen et al., 2005; Barriere and Felix, 2007). On mushroom farms C. elegans is known to colonise the fruiting bodies (sporophores) of Agaricus bisporus, where bacteria belonging to the genus Pseudomonas commonly occur (Grewal and Richardson, 1991; Grewal, 1991a). Synergistic interactions between C. elegans and mushroom pathogenic pseudomonads have been reported to increase the severity of blotch disease of cultivated mushrooms (Grewal, 1991a, 1991b). Furthermore, fluorescent pseudomonads both antagonistic and beneficial to mushroom growth have been isolated directly from C. elegans (Grewal, 1991a; Grewal and Hand, 1992). Thus, in a mushroom farm environment, C. elegans may be likely to interact more frequently with pseudomonads than with bacteria that are commonly used as food sources in laboratory studies, such as Escherichia coli (Zarkower et al., 1984; Atkey et al., 1992; Grewal and Hand, 1992; Tsukamoto et al., 2002; Viji et al., 2003; Curran et al., 2005). We have found that many pseudomonads isolated from mushrooms possess mechanisms for inhibiting nematode growth or deterring nematode feeding. Our investigation of the mushroom pathogenic pseudomonad Pseudomonas fluorescens NZI7, described here, has uncovered a novel and highly effective mechanism that deters nematode feeding, even in nutrient limited conditions where production of nematicidal factors is insufficient to confer protection.
Materials and methods
Bacteria and nematode cultivation
Pseudomonas and E. coli strains were cultured on Luria–Bertani medium (Sambrook and Russell, 2001) at 28C and 37 °C, respectively, for 24 h before use. Strains used are listed in Supplementary Table S1. Wild-type C. elegans Bristol N2 and Caenorhabditis briggsae nematodes were maintained at either 15, 20 or 22 °C on nematode growth medium (NGM) (Brenner, 1974) inoculated with E. coli OP50 and synchronous cultures were produced according to the protocols available on NematodeBook (Girard et al., 2007). Antibiotics were used at the following concentrations: kanamycin 50 μg ml−1, tetracycline 20 μg ml−1, chloramphenicol 25 μg ml−1. Nematode rapid killing assays were performed on brain heart infusion (BHI) agar (Oxoid, Hampshire, UK).
Quantitative nematode feeding and choice assays
Quantitative nematode feeding and choice assays were performed by washing overnight bacterial cultures twice in dH2O and resuspending bacteria at an OD600 of 0.1. Fifty microlitres of this suspension were spotted onto the centre of a 45-mm diameter NGM plate and incubated for 24 h at 28 °C. Ten synchronous L2/L3 nematodes were transferred to each plate and plates were incubated at 20 °C. Lawns were photographed daily and the area occupied by the lawn determined using the magnetic lasso function in Adobe Photoshop (Adobe Systems Incorporated, San Jose, CA, USA). Mixed bacterial populations were tested similarly, except that overnight cultures were mixed in different ratios before aliquoting onto NGM.
Choice assays were set up by spotting 25 μl of an overnight culture of the strains to be tested equidistant from a central point on an NGM plate and incubating the plates for 2 days at 28 °C. Nematode preference was assessed by placing ∼20 L3/L4 nematodes into the centre of each plate and scoring for presence of nematodes and the extent to which each colony was consumed over 3 days at 22 °C. Chemotaxis assays were performed similarly except larger numbers of nematodes were used per plate (∼200) and the number of nematodes at the bacterial colonies counted 6 h after transfer. The chemotaxis index was calculated as (number on spot 2—number on spot 1)/total number of nematodes at both spots.
Biochemical complementation of edible mutants was tested by supplementing NGM plates with 1 mM thiamine or 1 mM anthranilic acid. Plates streaked with mutants of interest were incubated for 24 h at 28 °C and then between 15 and 20 L3/L4 nematodes were transferred to the centre of the lawns. Plates were incubated at 20 °C and observed daily for 5 days.
Screen for loss of nematode repellence
The construction and phenotypic analysis of an ordered library of 9696 insertional mutants of NZI7 using mini-Tn5::gfp::lux is described in Supplementary Methods. Oligonucleotides used are listed in Supplementary Table S2. To identify mutants that showed reduced ability to repel nematodes, mutants were replicated using a 48-point colony replicator onto NGM plates. Two colonies of E. coli OP50 were inoculated at opposite sides of the mutant grid to serve as a food source while nematodes explored the plate. Plates were incubated for 2 days at 28 °C to allow colonies to grow. After incubation, ∼20 L4/adult nematodes were placed adjacent to the E. coli colonies. Plates were incubated for 3 days at 20 °C and observed daily. The mutant library was screened twice using this protocol. Mutants identified in the initial screen were validated in two replicate ‘dummy grids’, in which 46 of the positions contained wild-type NZI7, and as individual lawns. Individual edibility assays were performed by streaking the test strain across an NGM or BHI plate, allowing the strain to grow for 24 h and then placing ∼20 synchronous L2/L3 nematodes in the centre of the bacterial lawn.
Results
P. fluorescens NZI7 repels feeding by C. elegans
We tested a collection of 60 Pseudomonas isolates, including 32 strains isolated from mushroom farms, to determine whether they showed differential interactions with C. elegans. Considerable heterogeneity in nematode–bacteria interactions was observed; some strains showed high resistance to nematode grazing, while others supported higher rates of nematode growth and reproduction than E. coli OP50, which is commonly used as a food source for C. elegans (Table 1). One strain, the mushroom pathogen P. fluorescens NZI7 (Godfrey et al., 2001b; henceforth referred to as NZI7), was of particular interest, as it exhibited a distinctive and highly effective mechanism for repelling C. elegans without killing when grown on NGM. The same phenomenon was observed with the related species C. briggsae (data not shown). Nematodes initially explored NZI7 lawns but became averse to further interaction, preferentially occupying bacteria-free parts of the agar surface and showing a severe impairment in growth. When the assay was repeated using nutrient rich BHI media, nematodes died after a few hours exposure to NZI7. We quantitatively analysed nematode feeding by monitoring the area of the bacterial lawn and nematode size. Both NZI7 and the biocontrol strain P. protegens Pf-5 (formerly P. fluorescens Pf-5 (Ramette et al., 2011), and henceforth referred to as Pf-5), were highly resistant to nematode grazing (Figure 1). Pf-5 produces an arsenal of molecules with anti-eukaryote activity that could target C. elegans (Loper and Gross, 2007), and caused nematode death on both BHI and NGM.
Chemotaxis mutants of C. elegans are able to feed on NZI7 without exhibiting deleterious effects
In binary choice assays in which nematodes were able to choose between colonies of E. coli OP50 or NZI7, wild-type nematodes were strongly repelled by NZI7 (chemotaxis index −0.91±0.09, N=6). In contrast, C. elegans chemotaxis mutants tax-2 and tax-4 (reviewed by Bargmann (2006)) showed substantially reduced repulsion (chemotaxis indices −0.38±0.18, N=5 and −0.44±0.15, N=7, respectively). Complete loss of repulsion would result in a chemotaxis index of 0, so the residual repulsion suggests that avoidance of NZI7 has both chemotactic and non-chemotactic elements. Recent work by Chang et al. (2011) has demonstrated that pathogen avoidance by C. elegans can be affected by the lateral outer labial mechanosensory head neurons. tax mutants feeding on NZI7 grew well and showed no evidence of deleterious effects or pharyngeal dysfunction, allowing us to conclude that NZI7 is not intrinsically pathogenic to C. elegans and that the failure of wild-type nematodes to feed on it was due only to aversion and did not involve additional physical effects such as the pharyngeal blockage observed for C. elegans feeding on Y. pestis (Darby et al., 2002). The resistance of NZI7 to nematodes was stable with no evidence of either nematode lethality or later nematode acclimation.
The P. fluorescens NZI7 genome is similar to that of the biocontrol strain P. protegens Pf-5
NZI7 causes brown blotch disease on mushrooms, which was attributed to production of a lipodepsipeptide similar to tolaasin (Godfrey et al., 2001a). However, although NZI7 produces a diffusible molecule that behaves like tolaasin in the white line bioassay it is more closely related to Pf-5 than to the tolaasin-producing type strain P. tolaasii NCPPB 2192 (Supplementary Figure S1). To identify candidate genes involved in NZI7–nematode interactions we generated a draft NZI7 genome (see Supplementary Methods). De novo assembly of 165 948 reads (∼8 × coverage) generated 1034 contigs with a sum of contig lengths of 6 814 598 nt. The genome of NZI7 showed a high degree of similarity to that of Pf-5, consistent with their close phylogenetic relationship (Supplementary Figure S2).
To identify regions of nucleotide sequence similarity between Pf-5 and NZI7, we used BLASTN searches with an e-value threshold of 10−6 between the Pf-5 genome (Paulsen et al., 2005) and NZI7 genome sequence data (both the de novo assembly and the raw sequence reads). The genome of Pf-5 contained 972 predicted genes that showed no detectable nucleotide sequence similarity with NZI7 (Supplementary Table S3) including genes involved in the production of rhizoxin, the Mcf/Fit toxin, pyoluteorin, orfamide and pyrrolnitrin, allowing us to discount these as being responsible for the repellence and lethality of NZI7 to nematodes when grown on NGM and BHI, respectively. The NZI7 genome does contain genes predicted to be involved in synthesis of cyanide, 2,4-diacetylphloroglucinol and the extracellular protease AprA, all of which have been implicated in inhibition of C. elegans, or of plant parasitic nematodes such as Meloidogyne incognita (Gallagher and Manoil, 2001; Siddiqui et al., 2005; Meyer et al., 2009; Neidig et al., 2011). However, one recent study has shown that purified 2,4-diacetylphloroglucinol promotes egg hatch in C. elegans J1, and has no effect on the viability of juvenile or adult nematodes (Meyer et al., 2009).
The majority of the 602 genes detected in NZI7 and not Pf-5 (Supplementary Table S4) are not obviously associated with nematode repellence or toxicity. However, the NZI7 genome is predicted to encode a number of cell surface-associated genes that are not present in Pf-5, including genes associated with exopolysaccharide synthesis, type IV pilus and fimbrial assembly and type II, IV, V and VI secretion. Cell surface structures have been shown to influence bacterial interactions with nematodes (for example, Essex-Lopresti et al., 2005; Maier et al., 2010). Thus, it is possible that NZI7-specific factors contribute to repellence.
Identification of ‘edible’ mutants of P. fluorescens NZI7
To identify the genetic basis of nematode repellence in NZI7 we constructed an ordered library of 9696 insertional mutants using a mini-Tn5 transposon that contains a promoterless gfp::lux reporter cartridge (Fones et al., 2010). We developed a grid-based assay to identify mutants that were unable to repel C. elegans (Figure 2), which was validated by confirming that nematodes were able to locate ‘edible’ pseudomonads, such as P. fluorescens SBW25, placed in random positions in a grid of wild-type NZI7 colonies (data not shown). The library was also used to identify mutants with alterations in other traits that might affect mushroom pathogenesis or nematode predation: lipase, chitinase and lecithinase activity, cyanide production, haemolysis and production of the tolaasin-like toxin (TOL) (Supplementary Table S5). Transposon insertion points were determined by two step semi-degenerate PCR (Jacobs et al., 2003).
A total of 84 NZI7 transposon mutants (0.87% of the total, summarised in Table 2) were identified and validated as ‘edible’. Of these 84 mutants, 45 displayed a wild-type phenotype in screens for cyanide, exoenzyme and toxin production (Supplementary Table S5). Sequencing led to the determination of insertion points for 75 mutants. Overlay of transposon hits onto corresponding ORF positions in the draft NZI7 genome, mapped onto the complete genome of Pf-5, showed that none of these mutants were unique to NZI7 (Supplementary Figure S2). However, 11 ‘edible’ mutants that had wild-type phenotypes in the other screens performed were associated with a single gene cluster of unknown function, present in both NZI7 and Pf-5 (Figure 3), which is henceforth referred to as the EDB (edible) gene cluster. The region of the NZI7 genome containing the complete EDB cluster (ORFs 1–12) and flanking ORFs (equivalent to PFL_5539 to PFL_5553 in Pf-5) was sub-cloned into the cosmid pLAFR6 (Huynh et al., 1989) to create pLAF4EDB and transformed into NZI7 EDB mutants. The presence of pLAF4EDB restored the ability of EDB cluster mutants to repel C. elegans, confirming the role of the EDB cluster in nematode repellence (Figure 4).
Several of the ‘edible’ mutants identified in the screen were found have insertions in genes previously shown to be important in P. aeruginosa pathogenesis towards C. elegans: the global virulence regulator gacS; dsbA, required for correct folding of periplasmic disulphide-bonded proteins; the phosphoenolpyruvate-protein phosphotransferase gene ptsP; purine biosynthesis genes; the two-component sensor histidine kinase cbrA, and a haemagglutinin repeat protein with weak similarity to PA0041 (Tan et al., 1999; Gallagher and Manoil, 2001; Tan, 2002; Yorgey et al., 2001). An edible mutant containing an insertion close to the 3′ end of algU, and immediately upstream of the algU regulatory proteins mucA and mucB, was observed to have a mucoid phenotype, which has been reported to result in loss of pathogen avoidance in P. aeruginosa interactions with C. elegans (Reddy et al., 2011). Edible mutants with insertions in genes with predicted roles in aromatic amino acid metabolism (anthranilate and chorismate synthase genes) and thiamine biosynthesis could be chemically complemented by addition of 1 mM anthranilate or thiamine to the growth medium, respectively (Supplementary Figure S3).
C. elegans has been shown to avoid Serratia marcescens Db10 producing the lipodepsipeptide serrawettin W2 (Pradel et al., 2007). However, NZI7 mutants disrupted in the biosynthesis of TOL retained the ability to repel C. elegans. TOL mutants were, however, unable to cause disease symptoms on mushroom sporophore tissue (Supplementary Figure S4), confirming the importance of this toxin for mushroom pathogenesis. In contrast, mutation of the EDB cluster did not alter disease symptoms on mushroom tissue.
Delineation and bioinformatic analysis of the EDB gene cluster
The EDB gene cluster is highly conserved in both NZI7 and Pf-5 (Figure 3, Supplementary Table S6). EDB-like gene clusters were also detected in the genomes of several other pseudomonads: P. fluorescens WH6 (Kimbrel et al., 2010), Pseudomonas brassicacearum NFM421 (Ortet et al., 2011), P. brassicacearum Q8r1-96 (Loper et al., 2012), and the insect pathogen Pseudomonas entomophila L48 (Vodovar et al., 2006b). We have also identified EDB-like gene clusters in the draft genomes of other mushroom pathogenic pseudomonads, including P. fluorescens NZ007, P. tolaasii NCPPB2192, P. tolaasii PMS117S and P. gingeri NCPPB3146 (Supplementary Figure S5). The genomic context of the EDB cluster is not conserved in all of these strains, but four additional ORFs found downstream of the NZI7 EDB cluster genes, corresponding to Pfl_5548-Pfl_5551 in Pf-5, are adjacent to the EDB-like genes in all but two of these strains (Supplementary Figure S5). Two of these ORFs, ORF 10 (Pfl_5549) and ORF 11 (Pfl_5550), display some similarity to ORF 7 (Pfl_5546) and ORF 8 (Pfl_5547), respectively. We were unable to detect features characteristic of genomic islands associated with the EDB region. However, a partial transposase-like sequence is located adjacent to the EDB-like gene cluster in P. fluorescens WH6.
To test whether these four downstream ORFs were involved in nematode repellence, we constructed deletion mutants lacking ORF 1, ORFs 9–12 and the complete cluster (ORFs 1–12). Mutants lacking ORF1 or the complete cluster displayed a similar loss of repellence to the transposon mutants identified in the initial screen. However, mutants lacking ORFs 9–12 retained the ability to repel nematode predation (data not shown). Thus, only ORFs 1–8 are required for nematode repellence.
The majority of the 12 ORFs in the EDB cluster show only weak sequence similarity to genes with known or predicted functions (Table 2, Supplementary Table S6). However, the presence of a 3-dehydroquinate synthase domain in the first ORF, a UbiA prenyltransferase family domain in the second ORF, and the similarity of additional ORFs to enzymes involved in modification of carbohydrate substrates, suggests that this cluster encodes enzymes that contribute to the synthesis of a novel compound. Functional predictions for EDB cluster proteins, based on structure prediction using I-TASSER (Roy et al., 2010), also suggest that they are involved in the synthesis or modification of a carbohydrate-containing compound (Supplementary Table S6).
Bioinformatic analyses using PSORTdb V2.0 (http://www.psort.org/psortb/ (Rey et al., 2005)) and Phobius (http://phobius.sbc.su.se/ (Käll et al., 2004)) indicated that the putative 3-dehydroquinate synthase-like and UbiA prenyltransferase-like proteins are likely to be membrane associated while the remaining proteins are predicted to be cytoplasmic. The domain architecture of the first ORF is atypical for 3-dehydroquinate synthase proteins as it contains a domain similar to the SNARE-associated (SNARE_assoc) superfamily domain at the N-terminus. This suggests that some of the proteins encoded in the EDB cluster are associated with the membrane or cell surface. We speculate that the compound(s) synthesised by these proteins may also remain membrane or cell surface associated, which is consistent with the observation that nematodes can discriminate between colonies grown in close proximity in the grid screen.
GacS regulates expression of the EDB gene cluster
gacS mutant lawns showed the greatest reduction in their ability to repel C. elegans (Figures 4 and 5). GacS positively regulates the expression of numerous secreted factors (Rahme et al., 1995; Blumer et al., 1999; Vodovar et al., 2006a; Lapouge et al., 2008) and as expected, gacS mutants lacked the ability to produce cyanide, exoenzymes and TOL. However, transposon mutants of NZI7 that lacked the ability to produce these individual traits, and a deletion mutant lacking the 2,4-diacetylphloroglucinol biosynthetic cluster, retained the ability to repel nematodes (Supplementary Table S5, data not shown). This suggested that GacS regulates expression of the EDB cluster along with other unidentified factors that affect NZI7–nematode interactions.
The promoterless lux reporter cassette in the mini-Tn5 transposon provides a tool for examining gene expression when the transposon is oriented to place this cassette under the control of an endogenous promoter. We tested whether GacS regulated the expression of the EDB cluster by deleting gacS in two such mutants (79G1 and 54G10), in which the transposon is inserted into ORF 1 (PFL_5540) and ORF 8 (PFL_5547), respectively. Luminescence was strongly reduced in double ΔgacS/EDB mutants relative to the EDB reporter mutants (Figure 6a). We observed a similar reduction in luminescence when gacS was deleted in the TOL mutant 5E3 (Figure 6b, Supplementary Table S5). Luminescence in ΔgacS/EDB reporter mutants could be restored to wild-type levels by complementation with gacS (Figure 6d).
RT-PCR experiments indicated that EDB cluster mRNA was absent in NZI7 gacS mutants (Figure 6c) raising the possibility that GacS may regulate EDB at a transcriptional level rather than at the post-transcriptional level described for several other GacS-regulated genes (Whistler et al., 1998; Heeb et al., 2005; Kay et al., 2005). However, we cannot exclude the possibility that the lack of EDB mRNA reflects RNA instability rather than transcriptional regulation (Lapouge et al., 2008). Interestingly, global transcriptional analysis of Gac-regulated genes in Pf-5 did not identify PFL_5540-PFL_5551 as components of its Gac regulon (Hassan et al., 2010), suggesting that the regulation of this locus may differ between the two strains.
Environmental regulation of EDB expression
We used the lux reporter fusions within the EDB cluster to monitor the impact of environmental conditions on EDB gene expression. EDB expression was enhanced by mildly acidic pH, rich media, moderate-high iron availability and an optimal carbon-nitrogen balance (Supplementary Figure S6A–D). EDB expression increased in late log and early stationary phase but was repressed in stationary phase by carbon sources such as glucose and mannose (Supplementary Figure S6E). Expression was not significantly altered by introduction of the complementing clone pLAF4EDB into reporter strains, indicating that it is not autoregulatory (Supplementary Figure S6F). As EDB mutants continue to produce TOL, cyanide and exoenzymes (Supplementary Table S5) the product of the EDB cluster does not seem to affect the expression of other GacS-regulated factors.
The product(s) of the EDB gene cluster act with other factors to deter nematode feeding
The success of the grid screen in identifying edible mutants suggests that the factor(s) produced by the EDB locus are not active as a diffusible signal over distances >5 mm, as the phenotype of EDB mutants would be masked by surrounding colonies if this were the case. gacS mutants of P. protegens CHA0 have previously been shown to be protected by wild-type bacteria from C. elegans feeding when present at low frequency in mixed populations (Jousset et al., 2009). We observed that nematodes fed mixtures of NZI7 wild-type and EDB cluster mutants in different ratios grown on NGM would clear lawns where the initial ratio of EDB mutant: wild-type was 5:1 or greater. This suggests that nematodes make a decision based on an aggregate assessment or that there is a critical level at which the putative EDB product acts, below which it becomes ineffective.
We transformed several palatable P. fluorescens isolates with the cloned NZI7 EDB gene cluster (pLAF4EDB) and were able to confirm EDB expression in most of the transformed strains by RT-PCR (Supplementary Figure S7). However, none of the transformed strains showed enhanced resistance to C. elegans, either on NGM or on BHI medium on which EDB is more strongly expressed (Supplementary Figure S6B). E. coli transformed with pLAF4EDB also failed to recapitulate the repellent phenotype, although EDB expression was comparatively poor in this background (data not shown). It thus appears that the region of the NZI7 genome cloned into pLAF4EDB is insufficient to confer resistance to nematode predation. This suggests that NZI7 possesses additional genes that act together with the genes in this region to confer nematode resistance.
Cyanide is responsible for rapid nematode killing by NZI7
One factor that could act in conjunction with EDB to repel nematode predation is cyanide, which has been implicated in nematode repellence in P. protegens CHA0 (Neidig et al., 2011). NZI7 produces high levels of cyanide on BHI, causing rapid nematode killing by lethal paralysis, as previously reported for P. aeruginosa PAO1 (Gallagher and Manoil, 2001). However, NZI7 did not produce detectable levels of cyanide when grown on NGM, and a non-cyanogenic hcnB mutant was indistinguishable from the wild-type in nematode repellence assays. On BHI the hcnB mutant failed to kill nematodes but was highly repellent. An hcnB/EDB double mutant showed significantly less repellent activity than the hcnB mutant on BHI; some nematodes remained on the bacterial lawn and surrounding agar and grew to produce eggs within 3 days (Supplementary Figure S8). This confirmed that EDB contributes to nematode repellent activity on BHI and that cyanide is the primary nematicidal toxin produced by NZI7 on BHI. However, NZI7 gacS mutants supported a much larger nematode population than the hcnB/EDB mutant on BHI, which supports the hypothesis that additional gacS-regulated factors contribute to the inhibition of nematode growth. TOL does not appear to be one of these factors, as a triple hcnB/EDB/TOL mutant was indistinguishable from the hcnB/EDB double mutant on BHI and NGM (data not shown).
Discussion
The results presented in this study show that the mushroom pathogen P. fluorescens NZI7 is able to repel grazing by C. elegans, a naturally occurring bacteriovore in mushroom farms. The ability of NZI7 to repel C. elegans depends on the activity of a previously uncharacterised biosynthetic locus, the EDB cluster. Interestingly, EDB-dependent nematode repellence is effective even in low nutrient environments, where nematicidal factors such as cyanide are ineffective at limiting nematode predation. As the product of the EDB cluster seems to have no effect on its own expression, or on the expression of other GacS-regulated genes, it is logical to hypothesise that the product(s) of this cluster is sensed directly by C. elegans. However, heterologous expression of the EDB gene cluster in several palatable pseudomonads failed to recapitulate the phenotype seen in NZI7. Thus, while the EDB cluster is important for nematode repellence in NZI7, additional loci are necessary for NZI7 to effectively deter nematode predation. In our assays Pf-5 killed C. elegans, which may have masked any repellent activity present, so we do not yet know whether these loci are unique to NZI7 or also present in Pf-5.
The observation that EDB mutants of NZI7 retain some ability to repel and inhibit nematodes relative to gacS mutants raises the possibility that the product of the EDB locus acts additively or synergistically with other factors to reach a threshold at which C. elegans decides to avoid grazing. We identified 40 distinct mutations, other than those within the EDB cluster, which reduced nematode repellence in NZI7. Although the majority of these mutations require further validation through complementation, it seems likely that many of the disrupted genes also contribute to the nematode repellent phenotype of this strain. Some may be involved in the synthesis of precursor molecules needed for the synthesis of the EDB product, while others could be involved in the synthesis of a second nematode repellent factor. We also identified an additional class of mutants, exemplified by a mutation affecting the algU/mucA operon, where the mucoid phenotype of mutant bacteria may compromise the ability of nematodes to respond to bacterial signals and of bacteria to repel nematode predation (Reddy et al., 2011). It should be noted that mutations affecting the production of additional nematode repellent factors may not have been detected in the grid screen if these factors are highly diffusible or individually contribute only a small fraction of the total NZI7 repellent activity.
C. elegans has been shown to respond to a wide range of chemoattractants and repellents (Ward, 1973; Dusenbery, 1975; Hilliard et al., 2004; Bargmann, 2006) and there is emerging evidence for the perception of bacterial metabolites by nematodes, notably quorum sensing molecules and serrawettin W2 (Beale et al., 2006; Pradel et al., 2007). Thus, the EDB locus may be involved in the synthesis of a molecule that identifies NZI7 as a strain to be avoided, even though the product of the EDB cluster itself is not directly toxic to nematodes. The ability to preferentially feed on non-deleterious bacteria would clearly be advantageous to nematodes in the natural environment, where bacterial populations are heterogeneous (Rodger et al., 2004; Zhang et al., 2005; Laws et al., 2006; Shtonda and Avery, 2006).
The grazing resistance of NZI7 is particularly intriguing when viewed in terms of the mushroom pathogenic lifestyle of this bacterium. We have observed that nematodes investigate bacterial colonies and then move away without consuming large quantities of bacteria rather than completely avoiding them. This physical contact between nematodes and NZI7 means that bacteria become transiently associated with the surface of the nematode, and in our assays NZI7 is clearly transported by the nematodes, visible as bacterial trails from visited colonies. The ability of NZI7 to be disseminated by nematodes, while avoiding nematode predation, could enhance both the survival and dispersal of this mushroom pathogen, contributing to the development of blotch disease.
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Acknowledgements
We would like to thank Scott Godfrey for providing the NZ strains used in this study. Joyce Loper for providing Pf-5 and for helpful discussions. Paul Rainey, Jeff Chang, Corné Pieterse, Pascale Frey-Klett, Gary Bending, Dawn Arnold, Mark Silby, Dennis Gross and Frederic Boccard for providing additional pseudomonads used. Helen Chapman for assistance with genomic DNA preparation. This work was supported by The Genome Analysis Centre Capacity and Capability Challenge Programme. PB was supported by funding from the Biotechnology and Biological Sciences Research Council (BBSRC). GP was supported by a Royal Society University Research Fellowship.
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Burlinson, P., Studholme, D., Cambray-Young, J. et al. Pseudomonas fluorescens NZI7 repels grazing by C. elegans, a natural predator. ISME J 7, 1126–1138 (2013). https://doi.org/10.1038/ismej.2013.9
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DOI: https://doi.org/10.1038/ismej.2013.9
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