The gut microbiota contributes to host health and fitness, and imbalances in its composition are associated with pathology. However, what shapes microbiota composition is not clear, in particular the role of genetic factors. Previous work in Caenorhabditis elegans defined a characteristic worm gut microbiota significantly influenced by host genetics. The current work explores the role of central regulators of host immunity and stress resistance, employing qPCR and CFU counts to measure abundance of core microbiota taxa in mutants raised on synthetic communities of previously-isolated worm gut commensals. This revealed a bloom, specifically of Enterobacter species, in immune-compromised TGFβ/BMP mutants. Imaging of fluorescently labeled Enterobacter showed that TGFβ/BMP-exerted control operated primarily in the anterior gut and depended on multi-tissue contributions. Enterobacter commensals are common in the worm gut, contributing to infection resistance. However, disruption of TGFβ/BMP signaling turned a normally beneficial Enterobacter commensal to pathogenic. These results demonstrate specificity in gene-microbe interactions underlying gut microbial homeostasis and highlight the pathogenic potential of their disruption.
All animals harbor complex communities made of diverse microbes, and those of the gut are the most extensive ones. Gut microbes are often referred to as commensals—that is, causing no harm and having no benefit—and in any given condition some may indeed be just so, but overall, gut microbiotas are beneficial, contributing to features as diverse as development, metabolism, immunity, fecundity, and even behavior1,2,3,4,5. Furthermore, abnormal microbiota composition (or dysbiosis) is associated with pathology, and in some cases (i.e., obesity and potentially aging) has been shown to play causal roles6,7.
In determining the factors that shape microbiota composition, work in vertebrates has been instrumental in revealing a significant impact of diet7,8. Environmental factors, such as geography, or life style, were also shown to contribute9,10,11. Less is known about the role of genetic factors, which was suggested to have a relatively modest effect size on the microbiota12. Nevertheless, one might expect that advantages provided by beneficial microbes to a host over its peers should promote selection of genes and gene variants that enable colonization by such microbes, resulting in host-specific microbiotas shaped to varying degrees by genetic factors. Consistent with this, species-specific gut microbiotas have been identified in various organisms, including apes, bees, termites, and Caenorhabditis elegans13,14,15,16. In a few instances, composition of these microbiotas was shown to be associated with host evolution. For example, in bees, the appearance of specific core gut bacterial lineages coincides with the emergence of eusocial bees from solitary ancestors14, and the composition and functional impact of microbiotas was found to track phylogenetic relatedness between species of several clades, including deer mice, Drosophila, mosquitoes, and wasps17. Our own analysis of nematode microbiotas identified a significant contribution of host genetics to microbiota composition18. However, the specific genes behind such contributions are mostly unknown. Results from human studies demonstrated that host metabolism and immunity can shape the human gut microbiota. Human twin studies identified the lactase gene locus as associated with the abundance of Bifidobacterium19, and innate immune genes, such as C-type lectins, have been shown to contribute to shaping human gut microbiota function and composition20. Whereas human studies rely on associations between natural genetic variation and microbiome composition, studies using model organisms, such as mice, can directly test the effect of a specific host function. In one such study, mice lacking CARD9, an adaptor protein required for innate immune responses, were found to harbor an altered microbiota, compromised in the production of aryl hydrocarbon receptor ligands, which led to increased susceptibility to colitis21. However, for the most part, distinguishing gene effects from inter-individual variation in vertebrate models is not trivial, hindering the ability to identify influences of host factors on microbiota composition.
An alternative is offered by invertebrate models such as Drosophila melanogaster and C. elegans. Studies in Drosophila have identified mechanisms enabling immune tolerance of gut microbes, and determining the abundance of gut commensals22,23. C. elegans offers the additional advantage of working with self-fertilizing genetically homogeneous populations, averaging-out inter-individual variation to discern gene effects. C. elegans has been used extensively for studying molecular mechanisms of innate immunity24,25, but decades of growth on monoxenic cultures, typically of an Escherichia coli strain unable to colonize healthy worms, has left a gap in the understanding of its biology and its interactions with benign microbes. This is now changing. Studies of C. elegans interactions with different food bacteria provide insights into metabolic regulation and aging26,27,28,29, and recent work defined a characteristic C. elegans gut microbiota, and showed that its composition was conserved across different strains and geographical locations13,30,31. Moreover, this composition bore functional significance for worms, with positive impact mainly on development and on immunity, provided typically by Pseudomonadaceae and Enterobacteriaceae bacteria, including host-specific contributions (reviewed in32).
Taking advantage of the availability of C. elegans mutants, we examined the contribution of host genes to shaping the C. elegans gut microbiota. RNAseq identified genes involved in digestion and in innate immunity as those upregulated during interactions with complex microbiotas. Analysis of mutants for genes central to these processes, using synthetic communities composed of previously isolated worm gut commensals, and providing a defined environment, identified a role for Transforming Growth Factor (TGF)β/Bone Morphogenetic Protein (BMP) signaling in controlling bacterial abundance of Enterobacter commensals and in determining their contributions to the host.
Genes modulated during interactions with complex microbiotas
RNAseq analysis was performed to identify C. elegans genes and processes involved in host–microbiota interactions, comparing gene expression in worms grown on complex environmental microbiotas to that in worms grown on E. coli. Two comparisons were performed: one in composted soil microcosms (autoclaved compost reconstituted either with the microbiota from an unautoclaved batch of the same soil, or with a saturated E. coli culture); the second on plates, seeded either with E. coli or with synthetic microbiotas prepared with equal portions of 30 C. elegans gut isolates representing the main core microbiota families (SC1, see Methods). Analyses were performed in age-matched adult worms from synchronized populations; three independent populations were analyzed per group. Measurements were obtained for 28,555 unique RNA transcripts (measured in at least one sample), representing 18,873 genes (see Data availability).
In worms raised on the synthetic community, 127 genes were significantly upregulated and 163 genes were significantly downregulated compared with worms raised on E. coli (false-discovery-rate-corrected q-value < 0.05, likelihood ratio test, Supplementary Data file 1). Enrichment was found among the upregulated genes for immune genes, as well as for hydrolases (peptidases in particular) (Fig. 1a, Supplementary Data file 2). This is in spite of lack of any indication that SC1 included pathogens that compromised worm survival (Supplementary Fig. 1a), suggesting that elevated immune activity underlies normal host–microbiota interactions. Among the downregulated genes, only broad gene ontology (GO) terms, such as catabolic processes, were enriched.
Many more genes were affected in worms raised in composted soil microcosms: 1269 genes were significantly upregulated and 1815 downregulated, compared with worms grown on E. coli-supplemented soil (Supplementary Data file 1). The larger number of differentially expressed genes in soil-grown worms compared with those raised on SC1 indicates that C. elegans does not respond to complex microbiotas in a stereotypical way and suggests that the extent of changes in gene expression may depend on microbial diversity. Among both upregulated and downregulated genes, we found enrichment for genes associated with developmental programs, and to a lesser degree (and specific for downregulated genes) with reproduction (Supplementary Data file 2). In agreement with this, gravid worms harvested from normal soil microcosms held fewer eggs in their uterus compared with those raised on E. coli, either on plates or in soil (one row of eggs versus two). Using SC1 plates, we followed worm development and reproduction more closely. Worms raised on SC1 started laying eggs 1–2 h earlier than worms raised on E. coli, but laid in total 25% fewer eggs (Supplementary Fig. 1b). This correlated with the identified expression trends, and suggested that exposure to a diverse microbiota modulated host development resulting in a trade-off between development and fecundity. Another prominent trend emerging in microcosm-raised worms was enrichment for upregulated genes involved in response to external stimuli, many of which were immune genes (p = 5E–15, Bonferroni corrected, Supplementary Data file 2). This corroborated the trends observed in worms raised on SC1.
The overlap between genes significantly upregulated on microcosm microbiotas or on SC1 included 25 genes (Table 1). The great majority of these (21/25) are reported to be expressed in the intestine (Wormbase [http://www.wormbase.org]). These included C-type lectins, saposins, peptidases, as well as enzymes involved in sphingomyelin metabolism, and were significantly enriched for genes associated with defense and immune responses (p = 6E–5, Bonferroni corrected) and for genes encoding hydrolytic enzymes (p = 4E–5), including several lysosomal enzymes (p = 2E–6), pointing to immune functions as a common denominator among host factors that interact with the microbiota. Expression patterns for several of the genes were confirmed by quantitative (q)RT-PCR, see Supplementary Fig. 2.
Among the genes upregulated by the exposure to diverse microbiotas were genes previously described to respond to environmental bacteria, specifically to a Comamonas isolate33 (11/25 genes, Supplementary Table 1). Although this is not surprising considering that SC1 included a Comamonas isolate, upregulation of these genes in worms raised in compost microcosms suggests similar interactions in natural-like environments, which is in agreement with previous reports of Comamonas species being part of the C. elegans gut microbiota13,31. Further in agreement with enrichment for immune genes, a significant overlap was observed between the microbiota-upregulated 25 genes and targets of central immune regulators, including the p38 pathway34, the DAF-16/FOXO transcription factor35, and TGFβ/ΒΜP signaling36 (Fig. 1a, Table 1 and Supplementary Table 1). However, how these regulators contributed to responses to, and interactions with complex microbiotas was not immediately obvious, as their targets appeared also among downregulated genes. An exception to this broad overlap was the specific enrichment of p38 targets among genes upregulated on SC1, potentially associated with the presence of a Pseudomonas mendocina isolate previously shown to prime p38-dependent immune responses37.
TGFβ/BMP signaling is involved in shaping the gut microbiota
Since immunity emerged as a common denominator in worm responses to complex microbiotas, and immune regulators as potential players in shaping these responses, we tested the significance of disrupting such regulators for the composition of the worm gut microbiota. Mutants examined included pmk-1(km25) and tir-1(qd4), disrupted for the p38 MAPK ortholog and its SARM adaptor, respectively38; dbl-1(nk3) mutants, lacking the TGFβ/BMP-like ligand DBL-139; daf-16(mu86) mutants, disrupted for a FOXO transcription factor central for stress resistance, immunity, and longevity, along with mutants for one of its targets, the ctl-2 catalase35; and tol-1(nr2033) mutants, disrupted for the sole toll receptor homolog in C. elegans40. As a control, we examined tnt-3(ok1011) mutants, which are defective in grinding ingested bacteria, allowing more intact bacteria into the intestine41. Beyond factors that operate in the intestinal niche, we examined mutants for osm-6 and ttx-3, which are involved in feeding behavior, which might also affect microbiota structure42. All worm strains were raised on plates with the SC1 synthetic community, and their gut microbiota size (total bacterial load) and composition were evaluated in the first day of adulthood, using qPCR with eubacterial and taxa-specific primers, calibrated to known quantities of a full-length amplicon of the 16S ribosomal RNA gene (rDNA) from the respective taxa (see Methods). Measured taxa included Enterobacteriaceae and Pseudomonadaceae, which are the most abundant families in the C. elegans gut, as well as the less common Bacillaceae, which are nevertheless part of the worm core gut microbiota13.
The tnt-3 control strain showed a significantly greater gut bacterial load than wild-type animals (Fig. 1b). This was expected, as it is impaired in the grinding of bacteria. In contrast, most tested mutants showed only small or insignificant changes in their total bacterial load. The exception was dbl-1 mutants, which demonstrated a threefold increase. This was associated with increases in the abundance of Enterobacteriaceae, and more variably, of Pseudomonadaceae (Figs. 1c, d). The abundance of Bacillaceae family members in wild-type or mutant animals was variable to the extent that no clear differences could be discerned (Fig. 1e).
Although total bacterial load in tnt-3 mutants was much larger than in wild-type animals, microbiota composition, represented by the relative abundance of measured taxa, did not significantly change, indicating proportional increases in different microbiota members (Fig. 1f). A similar trend in taxa relative abundance was observed in feeding behavior mutants, suggesting that at least in the context of the plate microbiota, food preference was not a significant factor shaping the gut microbiota. In contrast, mutants for stress and immunity regulators, which had the same total bacterial load as wild-type animals (excluding dbl-1 mutants), showed significantly altered composition: pmk-1, tir-1, and daf-16 mutants showed relative expansion in taxa (one or more) for which we did not have specific primers, i.e., Comamonas, Aeromonas, or others (bundled as “other”), on the expense of the taxa that in wild-type animals are the dominant ones, Enterobacteriaceae and Pseudomonas (Fig. 1f). dbl-1 mutants, on the other hand, harboring an expanded gut microbiota, showed a significant increase in the relative abundance of Enterobacteriaceae. Both the increase in total bacterial load in dbl-1 mutants, and the particular expansion of Enterobacteriaceae were confirmed with colony- forming unit (CFU) counts, evaluating the number of live bacteria in the intestine of wild-type and dbl-1 animals (Fig. 1g).
BMP/DBL-1 signaling specifically affects Enterobacter abundance
Focusing on the prominent effects of dbl-1 disruption, we examined whether microbiota expansion in dbl-1 mutants was a general trend in these mutants, or unique to the particular composition of SC1. To this end, we raised wild-type worms and dbl-1 mutants on a different synthetic community (SC2), in which approximately two-thirds of SC1 strains were replaced with distinct isolates, while keeping the same genera represented (Supplementary Table 2). Both on SC1 and on SC2, dbl-1 mutants showed a significantly greater bacterial load compared with wild-type worms ( p < 0.001, Fig. 2a), as well as a threefold more Enterobacteriaceae (Fig. 2b). Furthermore, when grown in composted soil microcosms, providing natural-like microbial diversity, dbl-1 mutants showed only a modest increase in total bacterial load, but a significant twofold increase in the abundance of Enterobacteriaceae (Fig. 2c–f). Together, these observations support the notion that gut microbiota expansion in dbl-1 mutants, and in particular an increase in the abundance of Enterobacteriaceae, represented a general feature of these mutants.
To determine whether any specificity could be discerned in the effects of dbl-1 disruption on the gut microbiota, we created modified versions of SC1 with reduced diversity. The first modified community configuration, SC1R, excluded all Pseudomonas isolates, as well as most of the Enterobacteriaceae (Supplementary Table 2). While dbl-1 mutants raised on SC1 have an expanded microbiota compared with wild-type animals, those raised on SC1R did not show this expansion (Fig. 3a), indicating that disruption of dbl-1 had somewhat restricted effects, allowing a bloom of Pseudomonas and/or Enterobacteriaceae, but not of other members of the community. In contrast, tnt-3 mutants raised on SC1R demonstrated an expanded microbiota similar to when raised on SC1, supporting the indiscriminate effects of defective grinding on microbiota expansion. A subtler modification of SC1, SC1R*, which excluded only Enterobacteriaceae species (not all), also abolished the increase in microbiota size in dbl-1 mutants, further indicating specificity toward certain Enterobacteriaceae species. Finally, eliminating only Enterobacter isolates from the synthetic community (SC1R**), leaving-in several other Enterobacteriaceae species (e.g., Escherichia sp., Buttiauxella sp.), was sufficient to abolish microbiota expansion in dbl-1 mutants, pointing at Enterobacter isolates as those affected by dbl-1 disruption. Supporting this, re-examination of the microbiota in dbl-1 mutants raised on SC1, using primers specific for the Enterobacter hsp60 gene, revealed an increase in the Enterobacter load in dbl-1 mutants that could account for the entire increase in bacterial load observed in these animals (Fig. 3b, as compared with Fig. 3a).
The observed increase in Enterobacter abundance in dbl-1 mutants could be due to direct effects of host TGFβ/BMP signaling on Enterobacter colonization and/or proliferation, or caused indirectly by changes in microbial interactions affecting the balance between Enterobacter and its competitors. To examine which of the two alternatives is more likely, we raised worms on a tdTomato-expressing derivative of one of the SC1 isolates, a previously characterized Enterobacter cloacae commensal of C. elegans, CEN2ent1 (shortened here to CEent1)18. Fluorescent microscopy of adult dbl-1 and wild-type animals demonstrated a significant increase in the abundance of these bacteria in dbl-1 mutants compared with wild-type animals (Fig. 3c). As no other bacteria are present to affect CEent1 abundance, these results indicate that dbl-1 disruption directly affected Enterobacter abundance.
Enterobacter bloom is not due to mutants’ impaired development
TGFβ/BMP signaling involves ligand binding and activation of heterodimer receptors, downstream SMAD transcriptional regulators (Sma and Mothers against decapentaplegic homologs), and co-activators43. In C. elegans, this pathway contributes to immunity, but more visibly to development, and all known mutants have small body size. Whereas the smaller dbl-1 mutants showed a greater bacterial load than wild-type animals, we nevertheless wished to ascertain that this bloom was not caused (perhaps indirectly) by altered development. Disruption of the TGFβ type I receptor gene, sma-6, or the R-SMAD (Receptor-regulated SMAD) gene, sma-3, both led to an Enterobacteriaceae expansion, either slightly smaller than in dbl-1 mutants (sma-6) or larger (sma-3) (Fig. 4a–c). In contrast, mutants for the sma-9 co-activator, which are as small as dbl-1 mutants44, showed no bacterial expansion whatsoever (Fig. 4a, b). Fluorescent imaging, using the tdTomato-expressing CEent1 to follow Enterobacter colonization, corroborated these results (Fig. 4d, e), further diminishing the likelihood that Enterobacter bloom in TGFβ/BMP mutants was due to altered development in mutants. This in turn leaves impaired immunity as the more likely cause for the Enterobacter bloom. In line with this, while sma-6, sma-3, and dbl-1 are central immune regulators, sma-9 was reported to be redundant for immune gene induction45.
TGFβ/BMP-exerted control acts primarily in the anterior gut
To examine the opposite case of dbl-1 disruption, we employed a strain overexpressing dbl-1 from an integrated genomic fragment (dbl-1 o/e)39. As observed in animals raised to adulthood on tdTomato-CEent1, Enterobacter load in dbl-1 o/e animals was overall comparable to that in wild-type animals (Fig. 5a, b). However, the distribution of bacteria in the gut was very different: although wild-type animals showed prominent accumulation of Enterobacter in the anterior gut, this was mostly missing in dbl-1 o/e animals (Fig. 5a, b). This suggested that TGFβ/BMP signaling exerted its control over Enterobacter colonization/proliferation mainly in the anterior gut.
DBL-1 is expressed primarily in neurons, but its receptors and downstream mediators are expressed in the epidermis, pharynx and in the intestine43. To gain insight into where TGFβ/BMP signaling might function to delimit Enterobacter accumulation, we took advantage of sma-3(wk30) mutants, which are heavily colonized with Enterobacter, and a panel of transgenic strains employing tissue-specific promoters to rescue sma-3 expression in different tissues46. Expression of sma-3 from its endogenous promoter effectively restored accumulation of tdTomato-CEent1 to wild-type levels (Fig. 5c). Expression of sma-3 from the epidermal dpy-7 promoter also delimited Enterobacter accumulation, although not quite to wild-type levels, and expression from the pharyngeal myo-2 promoter showed Enterobacter accumulation to levels intermediate between those of wild-type and those in sma-3 animals. In contrast, worms with intestinal sma-3 expression (relying on the vha-6 promoter) showed Enterobacter accumulation that was not significantly different from that seen in sma-3 mutants. Similar trends were observed in measurements performed on the anterior gut or on its posterior parts (Supplementary Fig. 3). These results suggest multi-tissue contributions of TGFβ/BMP signaling to controlling intestinal Enterobacter, with the epidermis providing the more dominant input, whereas local TGFβ/BMP signaling in the intestine appearing to be mostly redundant.
TGFβ/BMP disruption turns an Enterobacter commensal to pathogenic
CEent1 was previously shown to be beneficial for C. elegans, accelerating development compared with worms raised on the standard E. coli food, and enhancing resistance to the pathogen Enterococcus faecalis18 (Fig. 6a). A 4-h exposure of worms to the commensal late in development (at the L4 stage) was sufficient to increase resistance to subsequent infection (Supplementary Table 3). However, dbl-1 mutants developing on CEent1 (or exposed to it late in development) no longer showed enhanced pathogen resistance and instead were significantly more susceptible (Fig. 6b and Supplementary Table 3). sma-3 mutants showed an even greater susceptibility (Fig. 6c, d). Furthermore, sma-3 mutants raised on tdTomato-CEent1 and shifted late in development to pathogen were still colonized 24 h after the shift (9 out of 24 examined) (Fig. 6f), and even 48 h after the shift, at which point colonization was further observed in three out of five cadavers. In contrast, wild-type animals showed no CEent1 colonization persisting after the shift. These results indicate that impaired TGFβ/BMP signaling results in a more persistent Enterobacter colonization, turning the normally beneficial commensal to pathogenic. Interestingly, dbl-1 overexpressing worms, which were more resistant to E. faecalis to begin with, showed no significant increase in their resistance when initially exposed to CEent1 instead of E. coli (Fig. 6e).
With the microbiome linked to many aspects of host health, understanding the interactions between host and its microbes is imperative for the development of therapeutic strategies aiming to alter the microbiota. An important aspect of this is understanding how host genes determine abundance and function of gut commensals. This understanding has been slow to emerge, to some extent due to inter-individual variation in microbiota composition in vertebrate models, which masks gene effects. Here, we demonstrate the utility of C. elegans as a model organism facilitating the identification and characterization of such gene effects, including the distinction between effects on microbiota size (total microbial load) and microbiota composition. Using this model, and screening candidate regulators, we identified a role for TGFβ/BMP immune signaling in controlling the abundance of members of the genus Enterobacter, common inhabitants of the worm gut, which affect host development and immunity. TGFβ/BMP-exerted control was focused on restricting Enterobacter accumulation in the anterior gut, but full effects depended on contributions from several tissues. Disruption of TGFβ/BMP signaling resulted in an Enterobacter bloom, and turned an otherwise useful commensal to pathogenic. Gut dysbiosis is typically considered a condition that enables invasion and proliferation of environmental opportunistic pathogens. Our results demonstrate that given impairment in host immunity and ensuing dysbiosis, pathogenicity can emerge directly from otherwise beneficial members of the gut community.
Current understanding of how host genes and processes shape microbiota composition highlights the importance of mucosal structure and immunity. Genes identified as affecting abundance of gut bacteria include antimicrobial peptides, pattern recognition receptors, cytokines, and genes affecting IgA antibody production47,48,49, as well as enzymes glycosylating barrier mucins, which provide sugars harvested by gut bacteria50,51. Our RNAseq analysis indicated a similar trend in C. elegans, as worms interacting with a diverse microbiota had elevated expression of genes, mostly intestinal, which are associated with host immunity. Some of these genes encode hydrolytic enzymes, which may serve immune functions, but could also be relevant for releasing nutrients from susceptible ingested bacteria for the benefit of resistant gut commensals. Mutant analysis supported the importance of host immunity in shaping the gut microbiota. Since many of the identified overexpressed genes are members of multi-gene families, implying potential functional redundancy, we focused instead on central upstream immune regulators. The contribution of immune regulators to microbiota composition was conspicuous, and in the case of dbl-1 mutants was recapitulated with different synthetic communities, as well as (with regards to the main feature of Enterobacteriaceae expansion) in worms raised in a natural-like compost microcosm. In contrast, disruption of daf-16, which encodes a general stress resistance regulator and contributes also to immunity, had no effect on microbiota composition52. Feeding behavior may also be thought to affect microbiota composition. However, disruption of osm-6 and ttx-3, did not show any effect. This cannot completely rule out involvement of food sensing and feeding behavior in determining microbiota composition, as the synthetic microbiota used is solely made of gut isolates (i.e., commensals) and is thoroughly mixed; under more natural conditions regulators of feeding behavior may contribute by identifying pockets of desirable bacteria in a non-homogeneous environment. Nevertheless, the finding that impaired grinding in tnt-3 mutants affected microbiota size but not composition supports an important role for post-feeding mechanisms, likely those defining the intestinal niche, in shaping microbiota composition.
TGFβ/BMP signaling regulates diverse processes in C. elegans, including growth, male tail development, and immunity43. Our results point at its roles in immune regulation as those affecting gut bacterial load. To date, not much is known about how TGFβ/BMP signaling regulates intestinal immunity53,54. Our results indicate that in controlling commensal colonization it relied on multi-tissue contributions, primarily from the epidermis, but also from the pharynx. Contributions of TGFβ/BMP signaling in the intestinal niche itself were marginal at best (although it seemed to affect Enterobacter accumulation in the posterior gut more than it did in the anterior, see Supplementary Fig. 3). This suggests that TGFβ/BMP signaling may affect the Enterobacter niche indirectly, potentially involving an additional signaling pathway that targets the gut. This mode of regulation may also apply to TGFβ/BMP involvement in resistance to intestinal pathogens. At the same time, results from experiments with dbl-1 o/e worms suggest that the Enterobacter niche in question is the anterior gut, as overexpression of the ligand and the presumed over-activation of the pathway prevented Enterobacter accumulation particularly in that region. It is further possible that colonization of this region is essential for the protective effects of Enterobacter, explaining the inability of CEent1 to enhance infection resistance in dbl-1 o/e animals.
The role of immunity in shaping the gut microbiota may be thought to be nonspecific, especially if considering the reliance of C. elegans solely on innate immunity (as all invertebrates). If so, disruption of any immune pathway will cause a relatively indiscriminate proliferation of gut commensals. However, this was not the case, as bacterial proliferation was selective and specific to the disrupted pathway: disruption of TGFβ/BMP signaling led to blooming only of Enterobacter species, not affecting other members of the microbiota, including other isolates of the Enterobacteriaceae family; and disruption of p38 signaling did not affect the abundance of major examined taxa (Pseudomonadaceae and Enterobacteriaceae), and only caused an increase in relative abundance of other taxa, yet to be defined. It might be speculated that such specificity depends on the profile of immune effectors regulated by each of the pathways, and differential susceptibility of different gut microbes to components of these profiles.
TGFβ signaling is highly conserved, regulating development and immunity also in vertebrates55. Whereas TGFβ/BMP signaling was shown to be associated with immune responses both in Drosophila and in vertebrates56,57, it is the role of TGFβ signaling in vertebrate T-cell differentiation and mucosal homeostasis that is better known58. Of particular relevance is the role of TGFβ signaling in production of IgA antibodies, which delimit microbiota proliferation in the gut59. Early results showed that TGFβ1 deficiency correlated with ulcerative colitis-associated colon cancer, and studies in mice suggested that colitis and cancer might depend on gut microbes60. More recently, it has been shown that deficiency in TGFβ signaling in intestinal dendritic cells led to changes in epithelial structure, Enterobacteriaceae-driven dysbiosis, and colitis61. Together, these reports describe a central role for TGFβ signaling in controlling gut microbial proliferation. Our results in C. elegans suggest that this role is conserved, even without specialized immune cells or antibodies, and further suggest particular importance, with ancient origins, for TGFβ signaling in controlling gut commensals of the Enterobacteriaceae family.
C. elegans strains and maintenance
Strains used in this study included N2 wild-type worms, the mutant strains pmk-1(km25), tir-1(qd4), tol-1(nr2033), dbl-1(nk3), sma-3(e491), sma-6(wk7), sma-9(wk55), daf-16(mu86), ctl-2(ok1137), osm-6(p811), ttx-3(ot22), and tnt-3(ok1011), and the dbl-1 overexpressing strain BW1940 (which harbors several copies of the genomic dbl-1 locus), all acquired from the Caenorhabditis Genetic Center. In addition, strains with tissue-specific expression, gratefully received from Meng Wang’s lab, included sma-3(wk30);him-5(e1490);qcEx24[sma-3p::GFP::sma-3 + rol-6], sma-3(wk30); him-5(e1490);qcEx52[myo-2p::GFP::sma-3 + rol-6], sma-3(wk30);him-5(e1490);qcEx53[vha-6p::GFP::sma-3 + rol-6], and sma-3(wk30);him-5(e1490);qcEx5[dpy-7p::GFP::sma-3 + rol-6]. sma-3(wk30);him-5(e1490) were obtained by picking non-rollers, who lost the extrachromosomal transgene. All strains were cultured on nematode growth media (NGM) at 25 °C.
Worm growth in soil and harvesting
Fresh local soil was supplemented with chopped over-ripe apples. The soil produce mixture was allowed to decompose for 2 weeks in the lab, cleared of garden variety worms by autoclaving, and re-inoculated with a microbial extract from the original batch of unautoclaved soil 24 h prior to addition of worms (extracts were the supernatants (1800 rpm) from soil resuspended and vortexed in M9 salt solution)13. Initially germ-free L1 larvae, obtained by bleaching of gravid worms to release eggs, and hatching them on NGM plates without food, were transferred to soil and grown at 25 °C for 3 days. One batch of prepared soil was split into separate 20 mL glass beakers (5 g per vial), and independent worm populations were raised in each (four replicates per genotype). Approximately 100–200 gravid worms were harvested from each population using a Baermann funnel lined with two layers of tissue paper, washed extensively (6 × ), and surface sterilized on plates containing 100 μg/ml gentamicin prior to DNA extraction, using the MO BIO PowerSoil DNA isolation kit (#12888)13.
Synthetic community and worm growth
Bacteria were previously isolated from worms grown in soil, and identified by 16S sequencing or multi-locus sequencing13,18,37. Enterobacteriaceae isolates were cultured on an Enterobacteriaceae-selective medium (Violet Red Bile Glucose, VRBG), whereas all others were cultured on Lysogeny Broth (LB) agar plates. A total of 30 isolates were selected for the synthetic community, representing most core taxa of the previously characterized C. elegans gut microbiota taxa13 (Supplementary Table 2). Several configurations of this community were used, including SC1 and SC2, which include the same genera, but differ in the specific strains used; SC1R resembles SC1, but lacks Enterobacteriaceae and Pseudomonas isolates; SC1R* lacks most of the Enterobacteriaceae isolates; and SC1R** contains all the SC1 isolates, except for the Enterobacter isolates. For each microbiota, isolates were grown in 1 mL of LB broth at 37 °C overnight with shaking. Saturated cultures were combined in equal proportions, concentrated 10 × , and seeded onto NGM plates approximately 30 min before the addition of eggs, obtained from bleaching gravid worms.
For each worm strain, 2–3 independent populations of worms, synchronized at L1, were grown on the synthetic microbiotas at 25 °C for 3 days. Adult worms were washed, surface sterilized, and used for DNA extraction, as described for worms raised on soil.
For each plate, 30 washed worms were transferred to a lysis buffer of a constant volume (per 30 worms: 6 μl of 10X PCR buffer (Invitrogen #11304011), 3.6 μl of Proteinase K (Fisher Scientific #EO0491), and 50.4 μl of PCR-grade water), and were lysed at 60 °C for 1 h, followed by a 15-min incubation at 95 °C to inactivate the proteinase K. Samples were stored at –20 °C until use. To rule out measurement biases introduced by DNA extraction method, DNA was extracted from synthetic communities mixed in different ratios either using the proteinase K protocol, or the MO BIO PowerSoil DNA isolation kit (#12888). Comparisons (demonstrating similar measurements of microbiota composition) are shown in Supplementary Fig. 4.
RNAseq library preparation and analysis
Synchronized worm populations, initiated with eggs obtained from bleached gravid worms, were grown on either NGM plates seeded with E. coli, NGM plates seeded with the synthetic community, in autoclaved soil supplemented with E. coli, or in composted soil, as described above (three independent populations per condition). RNA was extracted from gravid worms using a modified CTAB protocol with Aluminum Ammonium Sulfate and PEG precipitation62, followed by purification with the Qiagen AllPrep kit (#80204) to separate RNA from DNA. Sequencing libraries were prepared from total RNA using the Illumina TruSeq RNA Library Kit v2 (RS-122-2001), which synthesizes complementary DNA (cDNA) from mRNA fragments using random primers, and provides 24 indexed adapters for multiplex sequencing. Paired-end sequencing was performed on Illumina HiSeq4000, generating 100 base-pair reads, from which adapter sequences, as well as low-quality reads, were removed prior to analysis, providing 30,270,407 reads/sample on average. Both forward and reverse sequences were used for analysis, employing Kallisto to identify and quantify transcripts, and Sleuth to identify differentially expressed genes, using a false discovery rate-corrected p-value (q-value) cutoff of 0.05, as previously described63.
GoTermFinder was used to identify enrichment among identified genes for representatives of annotated processes or functions. Enrichment for gene targets of various regulators was calculated using the hypergeometric test.
RNA extraction and qRT-PCR
RNA was extracted from 100 to 200 worms per group using Trizol (Invitrogen). Genomic DNA contamination was removed with Turbo DNase (QIAGEN), cDNA was synthesized using iScriptTM (Bio-Rad), and quantitative real-time PCR was carried out using Bio-Rad’s SsoAdvanced Universal SYBR Green Supermix, and on a StepOnePlus system (Applied Bio). Ct values were normalized to the respective actin values for each sample, and are presented as fold change over wild-type worm expression value. See Supplementary Table 4 for primer sequences.
Quantifying bacterial load (microbiota size) and microbe abundance
Quantitative PCR (qPCR) was used to estimate taxa abundance by quantifying their respective DNA (in pg). Eubacterial 16S rDNA was quantified using the conserved primers 806f and 895r (Supplementary Table 4), and taxa-specific primers were used to quantify Enterobacteriaceae 16S (Ent_MB_F and R), Pseudomonadaceae 16S (Pse435F, Pse686R), and Bacilli 16S (BacilliF, BacilliR) in DNA extracts from worm samples obtained either using standard proteinase K based lysis, or PowerSoil, as described above. In addition, taxa-specific primers targeting the Hsp60 gene were used to quantify Enterobacter cloacae (Ent-Hsp60f, Ent-Hsp60r). Cycling parameters: 95 °C for 5 min; 45 cycles of 95 °C for 15 s, 60 °C for 30 s, 72 °C for 15 s [30 s for Bacilli]; 72 °C for 5 min. Specificity of each primer pair used was confirmed by PCR on each individual member of the synthetic communities, further ensuring no amplification of C. elegans mitochondrial DNA, which can be amplified with some 16S primers. All measurements were performed in duplicate with 1 μl of DNA extract as template, prepared from 30 worms in 60 μl of lysis buffer (for worms grown on synthetic microbiotas) or from 100 worms in 30 μl (DNA extraction from worms grown on soil), to enable comparison of values between worm populations. DNA quantities were estimated using standard curves created for each taxa from qPCR measurements of 10-fold serial dilutions of an appropriate full-length 16S bacterial rDNA in known concentrations, ranging from 25 ng to 0.2 pg/μl (amplified using the same primers as described above); E. coli 16S was used for calibrating both eubacterial and Enterobacteriaceae measurements, Pseudomonas mendocina 16S for Pseuomonadaceae measurements, Bacillus subtilis 16S for Bacilli measurements, and a 500-bp region of the Hsp60 gene from Enterobacter cloacae for Enterobacter Hsp60 measurements. Relative abundance was estimated by dividing the quantity of DNA from each bacterial group by the quantity measured with the universal primers. The ability to estimate relative abundance of bacterial families in a gut community was validated by measuring abundance of members of the different families in plated synthetic communities prepared with different ratios of members of these families. Measured relative abundances reflected the expected mix ratios and were unaffected by the method used for DNA extraction (Supplementary Fig. 4).
Following harvesting and washing, worms were ground (10 worms in 250 μl of M9), releasing live bacteria, which were serially diluted. Aliquots were plated onto either LB or VRBG plates, which were incubated at 37 °C overnight before counting.
Fluorescently tagged Enterobacter cloacae
A plasmid that constitutively expresses tdTomato from the Enterobacter cysB promotor (fragment 132a)64, with kanamycin resistance as a selection marker, was constructed at the UC Berkeley MacroLab. The plasmid was introduced into a C. elegans commensal, CEN2ent1, which is naturally ampicillin resistant18, using a triparental mating approach65. Briefly, the tdTomato plasmid was transformed into competent DH5ɑ E. coli cells using a standard heat shock protocol. CEN2ent1, DH5ɑ-tdTomato, and the DH5ɑ E. coli helper strain, which harbors the pRK2073 F conjugative plasmid with streptomycin resistance, were separately streaked out onto LB plates with either ampicillin, kanamycin, or streptomycin, respectively, and incubated at 37 °C overnight. Cells were scraped off from each plate, mixed together on a new LB plate, and incubated overnight at 37 °C. Colonies were streaked onto a new LB plate with ampicillin and kanamycin to select for CEN2ent1-tdTomato cells. The isolate was confirmed to not have the conjugative plasmid by testing for streptomycin sensitivity and was confirmed to be CEN2ent1 by sequencing of the full-length 16S gene.
CEN2ent1-tdTomato was grown overnight in LB broth with 100 μg/ml kanamycin. Cells were concentrated 10× and seeded onto NGM with 100 μg/ml kanamycin before eggs, obtained by bleaching, were added. After 3 days at 25 °C, worms were washed off the plates, and washed three times more with M9 buffer to remove external bacteria. Fluorescent images were captured using a Leica MZ16F equipped with a QImaging MicroPublisher 5.0 camera. Worm colonization was scored based on degree of colonization: “high colonization”, for colonization throughout the intestine; “moderate colonization”, for colonization in no more than half the length of the intestine; “light colonization”, for faint colonization, or “no colonization”. Alternatively, colonization was quantified using ImageJ, by drawing a line selecting the gut area for each worm and quantifying background-subtracted average intensity in this area. When relevant, signal intensity in the anterior and posterior parts of the intestine were quantified separately.
Worms were exposed to CEent1 (or to control E. coli OP50) from the egg stage till larval L4 stage, or shifted to such plates as L4 larvae, for a 4-h exposure. Subsequently, worms were transferred to plates (Brain Heart Infusion agar, 20 µg/mL gentamicin) pre-plated with the pathogen Enterococcus faecalis strain V58366. Dead worms were counted to assess infection resistance. All experiments were carried out at 25 °C.
Comparisons of worm fecundity, qRT-PCR measurements, and CFU counts were evaluated using two-sided Student’s t-test. qPCR measurements of microbiota size/total bacterial load and taxa-specific bacterial abundance were evaluated using a one-way analysis of variance (ANOVA) for repeated measures, to account for within-experiment replication (lme function from the nlme R package), with host genotype as a fixed effect, and within-experiment replication as a random effect67. Differences in worm colonization by CEent1::GFP were evaluated using ANOVA (aov function in R) followed by Tukey’s Honest Significant Difference (HSD) post hoc test when all comparisons were relevant, or linear model when one condition could serve as a reference for comparisons. Kaplan–Meier analysis was used to evaluate survival experiments, followed by a two-sided log-rank test, or a two-sided Wilcoxon test, which assigns greater weight to early time points, representing the bulk of the population.
Further information on experimental design is available in the Nature Research Reporting Summary linked to this article.
All relevant data are available from the corresponding author. RNAseq raw data are available at: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE97934.
McKenney, P. T. & Pamer, E. G. From hype to hope: the gut microbiota in enteric infectious disease. Cell 163, 1326–1332 (2015).
Nicholson, J. K. et al. Host-gut microbiota metabolic interactions. Sci. (80-.) 336, 1262–1267 (2012).
Sampson, T. R. & Mazmanian, S. K. Control of brain development, function, and behavior by the microbiome. Cell. Host. Microbe 17, 565–576 (2015).
Sison-Mangus, M. P., Mushegian, A. A. & Ebert, D. Water fleas require microbiota for survival, growth and reproduction. ISME. J. 9, 59–67 (2015).
Sommer, F. & Backhed, F. The gut microbiota--masters of host development and physiology. Nat. Rev. Microbiol. 11, 227–238 (2013).
Thevaranjan, N. et al. Age-associated microbial dysbiosis promotes intestinal permeability, systemic inflammation, and macrophage dysfunction. Cell. Host. Microbe 21, 455–466.e4 (2017).
Turnbaugh, P. J., Backhed, F., Fulton, L. & Gordon, J. I. Diet-induced obesity is linked to marked but reversible alterations in the mouse distal gut microbiome. Cell. Host. Microbe 3, 213–223 (2008).
David, L. A. et al. Diet rapidly and reproducibly alters the human gut microbiome. Nature 505, 559–563 (2014).
Rothschild, D. et al. Environmental factors dominate over host genetics in shaping human gut microbiota composition. bioRxiv https://doi.org/10.1101/150540 (2017).
Lax, S. et al. Longitudinal analysis of microbial interaction between humans and the indoor environment. Sci. (80-.) 345, 1048–1052 (2014).
Yatsunenko, T. et al. Human gut microbiome viewed across age and geography. Nature 486, 222–227 (2012).
Kurilshikov, A., Wijmenga, C., Fu, J. & Zhernakova, A. Host genetics and gut microbiome: challenges and perspectives. Trends Immunol. https://doi.org/10.1016/j.it.2017.06.003(2017).
Berg, M. et al. Assembly of the Caenorhabditis elegans gut microbiota from diverse soil microbial environments. Isme. J. 10, 1998–2009 (2016).
Kwong, W. K. et al. Dynamic microbiome evolution in social bees. Sci. Adv. 3, e1600513 (2017).
Moeller, A. H. et al. Cospeciation of gut microbiota with hominids. Sci. (80-.) 353, 380–382 (2016).
Otani, S. et al. Identifying the core microbial community in the gut of fungus-growing termites. Mol. Ecol. 23, 4631–4644 (2014).
Brooks, A. W., Kohl, K. D., Brucker, R. M., van Opstal, E. J. & Bordenstein, S. R. Phylosymbiosis: relationships and functional effects of microbial communities across host evolutionary history. PLoS Biol. https://doi.org/10.1371/journal.pbio.2000225 (2016).
Berg, M., Zhou, X. Y. & Shapira, M. Host-specific functional significance of Caenorhabditis gut commensals. Front. Microbiol. 7, 1622 (2016).
Goodrich, J. K. et al. Genetic determinants of the gut microbiome in UK twins. Cell. Host. Microbe 19, 731–743 (2016).
Bonder, M. J. et al. The effect of host genetics on the gut microbiome. Nat. Genet. 48, 1407–1412 (2016).
Lamas, B. et al. CARD9 impacts colitis by altering gut microbiota metabolism of tryptophan into aryl hydrocarbon receptor ligands. Nat. Med. 22, 598–605 (2016).
Chaston, J. M., Dobson, A. J., Newell, P. D. & Douglas, A. E. Host genetic control of the microbiota mediates the Drosophila nutritional phenotype. Appl. Environ. Microbiol. 82, 671–679 (2016).
Dantoft, W. et al. The Oct1 homolog Nubbin is a repressor of NF-κB-dependent immune gene expression that increases the tolerance to gut microbiota. BMC Biol. 11, 99 (2013).
Ewbank, J. J. & Pujol, N. Local and long-range activation of innate immunity by infection and damage in C. elegans . Curr. Opin. Immunol. 38, 1–7 (2016).
Cohen, L. B. & Troemel, E. R. Microbial pathogenesis and host defense in the nematode C. elegans. Curr. Opin. Microbiol. 23, 94–101 (2015).
Gusarov, I. et al. Bacterial nitric oxide extends the lifespan of C. elegans. Cell 152, 818–830 (2013).
Han, B. et al. Microbial genetic composition tunes host longevity. Cell 169, 1249–1262.e13 (2017).
Sonowal, R. et al. Indoles from commensal bacteria extend healthspan. Proc. Natl. Acad. Sci. USA 2017, 06464 (2017).
Yilmaz, L. S. & Walhout, A. J. Worms, bacteria, and micronutrients: an elegant model of our diet. Trends Genet. 30, 496–503 (2014).
Dirksen, P. et al. The native microbiome of the nematode Caenorhabditis elegans: gateway to a new host-microbiome model. BMC Biol. 14, 1–16 (2016).
Zhang, F. et al. Caenorhabditis elegans as a model for microbiome research. Front. Microbiol. 8, 485 (2017).
Shapira, M. Host–microbiota interactions in Caenorhabditis elegans and their significance. Curr. Opin. Microbiol. 38, 142–147 (2017).
MacNeil, L. T., Watson, E., Arda, H. E., Zhu, L. J. & Walhout, A. J. Diet-induced developmental acceleration independent of TOR and insulin in C. elegans. Cell 153, 240–252 (2013).
Troemel, E. R. et al. p38 MAPK regulates expression of immune response genes and contributes to longevity in C. elegans . PLoS Genet. 2, e183 (2006).
Murphy, C. T. et al. Genes that act downstream of DAF-16 to influence the lifespan of Caenorhabditis elegans. Nature 424, 277–283 (2003).
Roberts, A. F., Gumienny, T. L., Gleason, R. J., Wang, H. & Padgett, R. W. Regulation of genes affecting body size and innate immunity by the DBL-1/BMP-like pathway in Caenorhabditis elegans. Bmc. Dev. Biol. 10, 61 (2010).
Montalvo-Katz, S., Huang, H., Appel, M. D., Berg, M. & Shapira, M. Association with soil bacteria enhances p38-dependent infection resistance in Caenorhabditis elegans. Infect. Immun. 81, 514–520 (2013).
Liberati, N. T. et al. Requirement for a conserved Toll/interleukin-1 resistance domain protein in the Caenorhabditis elegans immune response. Proc. Natl. Acad. Sci. USA 101, 6593–6598 (2004).
Suzuki, Y. et al. A BMP homolog acts as a dose-dependent regulator of body size and male tail patterning in Caenorhabditis elegans. Development 126, 241–250 (1999).
Tenor, J. L. & Aballay, A. A conserved Toll-like receptor is required for Caenorhabditis elegans innate immunity. EMBO Rep. 9, 103–109 (2008).
Kim, D. H. et al. A conserved p38 MAP kinase pathway in Caenorhabditis elegans innate immunity. Science (80-.) 297, 623–626 (2002).
Shtonda, B. B. & Avery, L. Dietary choice behavior in Caenorhabditis elegans. J. Exp. Biol. 209, 89–102 (2006).
Gumienny, T. L. & Savage-Dunn, C. TGF-β signaling in C. elegans. WormBook https://doi.org/10.1895/wormbook.1.22.2 (2013).
Savage-Dunn, C. et al. Genetic screen for small body size mutants in C. elegans reveals many TGFbeta pathway components. Genesis 35, 239–247 (2003).
Zugasti, O. & Ewbank, J. J. Neuroimmune regulation of antimicrobial peptide expression by a noncanonical TGF-beta signaling pathway in Caenorhabditis elegans epidermis. Nat. Immunol. 10, 249–256 (2009).
Wang, J., Tokarz, R. & Savage-Dunn, C. The expression of TGFbeta signal transducers in the hypodermis regulates body size in C. elegans. Development 129, 4989–4998 (2002).
Biswas, A., Petnicki-Ocwieja, T. & Kobayashi, K. S. Nod2: a key regulator linking microbiota to intestinal mucosal immunity. J. Mol. Med. 90, 15–24 (2012).
Kumar, P. et al. Intestinal interleukin-17 receptor signaling mediates reciprocal control of the gut microbiota and autoimmune inflammation. Immunity 44, 659–671 (2016).
Suzuki, K. et al. Aberrant expansion of segmented filamentous bacteria in IgA-deficient gut. Proc. Natl. Acad. Sci. USA 101, 1981–1986 (2004).
Kashyap, P. C. et al. Genetically dictated change in host mucus carbohydrate landscape exerts a diet-dependent effect on the gut microbiota. Proc. Natl. Acad. Sci. USA 110, 17059–17064 (2013).
Sommer, F. et al. Altered mucus glycosylation in core 1 O-glycan-deficient mice affects microbiota composition and intestinal architecture. PLoS ONE https://doi.org/10.1371/journal.pone.0085254 (2014).
Garsin, D. A. et al. Long-lived C. elegans daf-2 mutants are resistant to bacterial pathogens. Sci. (80-.) 300, 1921 (2003).
Mallo, G. V. et al. Inducible antibacterial defense system in C. elegans . Curr. Biol. 12, 1209–1214 (2002).
Portal-Celhay, C., Bradley, E. R. & Blaser, M. J. Control of intestinal bacterial proliferation in regulation of lifespan in Caenorhabditis elegans . Bmc. Microbiol. 12, 49 (2012).
Massague, J., Blain, S. W. & Lo, R. S. TGFbeta signaling in growth control, cancer, and heritable disorders. Cell 103, 295–309 (2000).
Frandsen, J. L., Gunn, B., Muratoglu, S., Fossett, N. & Newfeld, S. J. Salmonella pathogenesis reveals that BMP signaling regulates blood cell homeostasis and immune responses in Drosophila. Proc. Natl. Acad. Sci. USA https://doi.org/10.1073/pnas.0808208105 (2008).
Martínez, V. G. et al. Autocrine activation of canonical BMP signaling regulates PD-L1 and PD-L2 expression in human dendritic cells. Eur. J. Immunol. https://doi.org/10.1002/eji.201343693 (2014).
Konkel, J. E. & Chen, W. J. Balancing acts: the role of TGF-β in the mucosal immune system. Trends Mol. Med. 17, 668–676 (2011).
Reboldi, A. et al. Mucosal immunology: IgA production requires B cell interaction with subepithelial dendritic cells in Peyer’s patches. Science (80-.). https://doi.org/10.1126/science.aaf4822 (2016).
Engle, S. J. et al. Elimination of colon cancer in germ-free transforming growth factor beta 1-deficient mice. Cancer Res. 62, 6362–6366 (2002).
Ihara, S. et al. TGF-β signaling in dendritic cells governs colonic homeostasis by controlling epithelial differentiation and the luminal microbiota. J. Immunol. 196, 4603–4613 (2016).
DeAngelis, K. M., Silver, W. L., Thompson, A. W. & Firestone, M. K. Microbial communities acclimate to recurring changes in soil redox potential status. Environ. Microbiol. 12, 3137–3149 (2010).
Pimentel, H., Bray, N. L., Puente, S., Melsted, P. & Pachter, L. Differential analysis of RNA-seq incorporating quantification uncertainty. Nat. Methods 14, 687–690 (2017).
Wang, Y. G. et al. Isolation of a strong promoter fragment from endophytic Enterobacter cloacae and verification of its promoter activity when its host strain colonizes banana plants. Appl. Microbiol. Biotechnol. 93, 1585–1599 (2012).
Wise, Aa, Liu, Z. & Binns, A. N. Three methods for the introduction of foreign DNA into Agrobacterium. Methods Mol. Biol. 343, 43–53 (2006).
Sifri, C. D. et al. Virulence effect of Enterococcus faecalis protease genes and the quorum-sensing locus fsr in Caenorhabditis elegans and mice. Infect. Immun. 70, 5647–5650 (2002).
Pinheiro, J., Bates, D., DebRoy, S. & Sarkar, D. nlme: Linear and Nonlinear Mixed Effects Models. R package version https://CRAN.R-project.org/package=nlme (2016).
We wish to thank Dr. Meng Wang and members of her lab in Baylor College of Medicine for tissue-specific BMP strains, and to Fauna Yarza for help with the triparental mating protocol. Completion of this work was made possible thanks to NIH grant R01OD024780. M.B. was supported by the National Science Foundation Graduate Research Fellowship Program (DGE 1106400).
The authors declare no competing interests.
Journal peer review information: Nature Communications thanks the anonymous reviewers for their contribution to the peer review of this work.
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Berg, M., Monnin, D., Cho, J. et al. TGFβ/BMP immune signaling affects abundance and function of C. elegans gut commensals. Nat Commun 10, 604 (2019). https://doi.org/10.1038/s41467-019-08379-8
TGF-βRII regulates glucose metabolism in oral cancer-associated fibroblasts via promoting PKM2 nuclear translocation
Cell Death Discovery (2022)
The TGF-β ligand DBL-1 is a key player in a multifaceted probiotic protection against MRSA in C. elegans
Scientific Reports (2021)
Rebuilding Microbiome for Mitigating Traumatic Brain Injury: Importance of Restructuring the Gut-Microbiome-Brain Axis
Molecular Neurobiology (2021)
Stenotrophomonas strain CPCC 101271, an intestinal lifespan-prolonging bacterium for Caenorhabditis elegans that assists in host resistance to “Bacillus nematocida” colonization
Archives of Microbiology (2021)
The functional repertoire contained within the native microbiota of the model nematode Caenorhabditis elegans
The ISME Journal (2020)