Bacteroides are Gram-negative, obligate anaerobic, non-motile, non-spore forming rods, and among the most abundant bacterial genera in the human intestine1. Bacteroides thetaiotaomicron has emerged as a model representative of the gut microbiota, due to its widespread distribution among human populations and the relative ease of studying these bacteria under laboratory conditions1. The extensive metabolic potential encoded in the B. thetaiotaomicron genome, including 88 defined polysaccharide utilization loci (PULs)2,3, forms the prerequisite for gut colonization. However, persistence within this notoriously dynamic niche requires coordinated control of gene expression in response to fluctuating nutrient levels.

Bacteroidetes lack the classical housekeeping sigma factor (σ70) encoded by the proteobacterial rpoD gene, and consequently, the classical –10 and –35 boxes recognized by σ70 are absent from their promoters. Rather, members of this phylum contain an unusual, RpoD-like primary transcription factor, σABfr, as well as an arsenal of alternative, extra-cytoplasmic function (ECF) sigma factors4,5. The consensus recognition sequence of σABfr was deduced by manual inspection of 23 promoter sequences in B. fragilis as ‘TAnnTTTG’ at the –7 region and a ‘TTTG’ motif at around the –33 region6,7. Inspection of global RNA-seq data recently confirmed the –7 consensus in another Bacteroidetes member, Flavobacterium johnsoniae, whereas the –33 motif could not be identified8. While in B. fragilis the sequence motif recognized by the oxidative stress-related alternative ECF sigma-factor EcfO was recently identified9, no such motif is currently known for any of the B. thetaiotaomicron alternative ECFs. Besides sigma factors, SusR-like regulators10 and hybrid two-component signal transduction systems11,12, wherein sensor kinase and response regulator are fused into a single polypeptide, contribute further to the adaptation of Bacteroides gene expression upon sensing of defined environmental cues, and DNA recognition motifs have been predicted for some of these regulators based on comparative genomics13,14.

Knowledge of post-transcriptional control mechanisms is sparse in B. thetaiotaomicron. Lacking classical Shine-Dalgarno (SD) sequences, messenger RNAs (mRNAs) of Bacteroidetes were recently shown to be enriched for adenine residues at position –3, –6, and –11 to –15 relative to the translational start codon, with adenine overrepresentation at these positions positively correlating with translation efficiency8. In Proteobacteria, small regulatory RNAs (sRNAs) can regulate target mRNAs through imperfect base-pairing interactions that typically occlude the SD sequence and/or the start codon, thus interfering with translation initiation15. As of now, only two sRNAs are known in Bacteroides spp. RteR is a trans-encoded sRNA of 90 nt that promotes discoordinate expression of the tra operon, required to assemble the mating apparatus for the transfer of the conjugative transposon, CTnDot16,17. DonS is a representative of a family of 78–128 nt-long cis-antisense RNAs divergently encoded to—and negatively impacting expression of—susC homologs of PUL systems involved in the binding and degradation of mucosa-derived glycans18. Lastly, a mRNA leader sequence was recently shown to tie B. thetaiotaomicron colonization to the presence of dietary sugars—and the authors speculated an sRNA could be involved in this process19. Together, these examples imply that RNA-mediated control mechanisms may be commonly employed by B. thetaiotaomicron to couple expression of metabolic genes to nutrient availability. However, the mode-of-action for all of these regulators is currently unknown, and RNA biology in B. thetaiotaomicron has not yet been investigated in a systematic manner. Particularly, given the lack of SD sequences in Bacteroidetes mRNAs, it is an open question if and how trans-encoded sRNAs could post-transcriptionally regulate target transcripts in this phylum.

Here, we performed differential RNA sequencing (dRNA-seq)20,21 of B. thetaiotaomicron grown in rich medium in three defined growth phases. This led to the annotation of a total of 4507 transcription start sites (TSSs) and untranslated regions (UTRs), as well as the identification of promoter motifs, RNA processing sites, and operon structures. To provide easy access to our transcriptome data, we have developed the intuitive Open-Access online database ‘Theta-Base’. We report the identification of 269 noncoding RNA candidates from all major classes including cis- and trans-encoded, 5′- and 3′-derived, and intra-operonic sRNAs as well as riboswitches, RNA thermometers, and putative type-I toxin–antitoxin (TA) systems. We selected one of the newly identified intergenic sRNAs (GibS), determined its secondary structure, and—as the first example of a trans-encoded Bacteroidetes noncoding RNA—identified its target mRNAs in a genome-wide screen. Biochemical and genetic experiments revealed that GibS utilizes a highly conserved, single-stranded seed sequence in its 5′ portion to mediate base-pairing with the translation initiation regions of two metabolic target mRNAs (BT_0771, BT_3893), resulting in repression of the respective transcripts. Altogether, the presented data imply that B. thetaiotaomicron employs riboregulatory mechanisms for adapting its gene expression to changing environmental conditions and should foster future studies to explore RNA biology in bacterial members of the human microbiota.


TSSs of B. thetaiotaomicron VPI-5482 grown in rich medium

By selectively enriching triphosphates at the 5′ end of primary transcripts, dRNA-seq identifies TSSs in a genome-wide manner, resulting in high-resolution transcriptome maps20,21. To globally identify TSSs in B. thetaiotaomicron, we transferred the dRNA-seq protocol to total RNA samples extracted from the type strain B. thetaiotaomicron VPI-5482 in three defined growth phases in TYG (tryptone-yeast extract glucose) medium—at the transition from lag to exponential phase, in mid-exponential and stationary phase—and analyzed the resulting data using the ANNOgesic bioinformatic tool set22 (Fig. 1a). This approach reliably mapped TSSs in the B. thetaiotaomicron genome, as illustrated for the roc (regulator of colonization) mRNA for which dRNA-seq identified the exact TSS as previously mapped using primer-extension19.

Fig. 1: High-resolution view at the B. thetaiotaomicron transcriptome.
figure 1

a Experimental workflow of the dRNA-seq approach and close-up view on the transcription start site (TSS; indicated by a bent arrow) of the regulator of colonization (roc) gene. Bacteria (AWS-001) from three different growth phases in TYG medium—early exponential (EEP), mid-exponential (MEP), and stationary phase (stat)—were analyzed. TEX, terminator exonuclease. Growth data refer to the mean +/− standard deviation from three biological replicates. For the read coverage plots, one representative replicate out of three is depicted. b Definition of categories for TSS annotation (upper) and overlap among TSS categories (lower). CDS, coding sequence. Note that pTSS and sTSS are mutually exclusive (thus no overlap in the Venn diagram). c Length distribution of transcripts (left) and 5′ UTRs (right). Long operons are labeled by name. d Motif searches upstream of B. thetaiotaomicron TSSs reveal the canonical σABfr promoter (upper) and a second, near-palindromic motif (‘PM2’; lower). Percentage values below the respective motif denote the frequency of that sequence upstream of the respective TSS category as defined in b. Source data to this figure are provided in the Source Data file.

In the B. thetaiotaomicron core genome and plasmid, we identified a total of 4507 TSSs that were classified into five categories based on their genomic location relative to annotated CDSs (Fig. 1b). Primary TSSs (pTSSs; 40% of all TSSs) were defined as the TSS with the highest coverage and secondary TSSs (sTSSs; 8%) as all remaining TSSs within a 300 nt window upstream of a given CDS. Internal TSSs (iTSSs; 21%) and antisense TSSs (aTSSs; 24%) arise from within a given CDS (or in case of an aTSS, within a 100 nt window flanking the CDS), in either sense or antisense orientation, respectively. The remaining 5% of predicted TSSs, not associated with any CDS, were classified as orphan (oTSSs) and might reflect an incomplete annotation of open reading frames or be indicative of intergenic sRNA genes (see below). Of the predicted TSSs, 1951 were detected in all growth phases with the total number of TSSs detected per condition ranging between 2265 and 3606 (Supplementary Data 1). The majority of TSSs were detected in stationary phase (~34% expressed exclusively under this condition; Supplementary Data 1). Functional analysis of genes with stationary phase-specific pTSSs using the PANTHER Classification System23 revealed enrichment of gene ontology (GO)-terms including DNA recombination, DNA integration, and integral membrane components (Supplementary Data 1).

Antisense transcription is widespread in bacteria, with between 5 and 75% of CDSs exhibiting antisense transcription depending on bacterial species, experimental condition, and RNA-seq protocol24. While functions for a number of specific antisense transcripts have been described25, their relevance as a general functional class remains unclear. Manual inspection of the predicted aTSSs in B. thetaiotaomicron revealed ~22% of them to serve as pTSS for CDSs further downstream (i.e., exceeding the set window of 300 nt; Fig. 1b), whereas the majority (73%) of identified aTSSs gave rise to relatively short, weakly expressed transcripts, suggesting some aTSSs may arise from spurious transcription initiation rather than being associated with a functional transcript26. For future analyses of specific antisense transcripts in B. thetaiotaomicron we advise readers to consider the here-reported aTSSs and consult the provided database (which will be described below). Manual inspection of predicted iTSSs revealed several examples of transcriptionally inter-connected genes/operons with related functions, e.g., the TSS for BT_3336, involved in the biosynthesis of lipid A, is located within the upstream oprM gene for an efflux pump involved in multidrug resistance, highlighting the link between cell envelope modifications and antibiotic stress.

Sequence alignment of all identified TSSs revealed the purine bases adenine and guanine as the preferred initiating nucleotides (45% or 41% of cases, respectively). As purine triphosphates serve as major energy storage molecules in cells, purine base overrepresentation in initiator nucleotides may help couple transcriptional activity to metabolic state, as observed previously in aerobic bacteria27,28,29.

Global assessment of transcript features

By combining TranstermHP30 and RNAfold31, ANNOgesic predicts intrinsic transcription terminators, which—together with the experimentally mapped TSSs—enables the deduction of transcript boundaries. B. thetaiotaomicron expressed transcripts in a range from 20 nt to ~18 kb (Fig. 1c, left). The longest transcripts correspond to ribosomal operons (BT_2700BT_2731 and BT_2733BT_2742), cell surface and iron transport operons (BT_1950BT_1958), and metabolic gene clusters (BT_1099BT_1108).

5′ UTRs were inferred from the identified TSSs and annotated CDSs, revealing average and median lengths of 52 and 32 nt, respectively (Fig. 1c, right). Most mRNAs harbored a 5′ UTR of 23 nt; ~10 nt shorter than the assumed optimal length for translation initiation in Proteobacteria20,32. In line with leaderless mRNAs being considered rare in Gram-negative species33, our dRNA-seq screen identified only ~3.7% Bacteroides 5′ UTRs shorter than 10 nt, e.g. of mRNAs for several transposases (BT_0280, BT_1996), two-component sensor kinases (BT_3967, BT_2166), and transporters (BT_0161, BT_0158). In contrast, 13.5% of mRNAs had unusually long (>100 nt) 5′ UTRs that might serve as targeting platforms for sRNAs or RNA-binding proteins (RBPs), or contain cis-regulatory RNA elements. Indeed, as inferred from homology to known RNA elements from other bacteria, ~2% of the long 5′ UTRs were predicted to harbor a putative riboswitch (Supplementary Data 2). Manual inspection revealed yet other long 5′ UTRs to actually contain short open reading frames (sORFs; Supplementary Data 3) reminiscent of leader peptides mediating transcription attenuation34. For instance, the 5′ UTR associated with the mRNA for the hypothetical protein BT_4401 (462 nt in length) contains several putative sORFs (sORF_378 to −381), whose existence needs to be validated in the future.

Small proteins have long gone unnoticed, due to difficulties in annotation and detection, but recently this class of molecules has gained attention as biological functions for several representatives could be demonstrated35,36. In total, ANNOgesic predicted 409 sORF candidates in B. thetaiotaomicron over growth in TYG medium (Supplementary Data 3). However, only seven of those are supported by a recent ribosome profiling study37 (Supplementary Fig. 1a). To some extent, this divergence can be explained by the Ribo-seq study considering only conserved sORFs, thus deliberately accepting false-negatives for the sake of enriching true-positives. sORF candidates called exclusively in our screen might thus be strain-specifically encoded, condition-specifically expressed (growth for maximally 10 h in TYG in the present study vs. 72 h growth in brain infusion medium in ref. 37), or false-positives. Inspection of the Ribo-seq-exclusive sORFs revealed 18 of the 21 remaining candidates to possess few to no aligned RNA-seq reads in our experimental conditions, explaining their neglection in the present screen. The other three sORF candidates (NC_004663.1_3066620_3066739_−1, NC_004663.1_951512_951613_−1 and NC_004663.1_4594728_4594793_1 in ref. 37) were relatively highly expressed in our RNA-seq data, but located within annotated CDSs for larger proteins and, consequently, were not called as sORFs by ANNOgesic.

B. thetaiotaomicron promoter architectures

A search for promoters upstream (–50 to +1) of the cognate TSS using the MEME38 and GLAM239 toolkits identified two conserved motifs (Fig. 1d). Motif 1, consisting of two sequence elements centered at the –7 and –33 nt positions separated by an AT-rich spacer of variable length, strongly resembles the canonical σABfr promoter of B. fragilis6. In B. thetaiotaomicron, this promoter was found upstream of 81% of pTSSs as well as 60% of sTSSs and oTSSs (Fig. 1d).

The second motif comprised sequence elements centered at the –10 and –30 positions relative to the TSS and was generally associated with more lowly expressed genes (Supplementary Fig. 1b). As is exemplified for BT_4614 (Supplementary Fig. 1c), we noticed certain cases where transcription of genes driven by promoter motif 2 (PM2) initiated from a different TSS in stationary phase compared to earlier growth stages. More generally, functional annotation of all 75 PM2-containing coding genes in our study revealed an enrichment of the oxidative stress response (Supplementary Fig. 1d) and differential expression analysis an upregulation of oxidative stress-related genes in the stationary growth phase (Supplementary Fig. 1e).

Theta-Base: an interactive online browser to interrogate the Bacteroides transcriptome

B. thetaiotaomicron is emerging as a model anaerobic bacterium; however, the community currently lacks an online repository for transcriptomic features and gene expression profiles. Inspired by online community data visualization platforms40 such as the SalCom41 and AcinetoCom29 databases compiled by the Hinton group for the bacterial pathogens Salmonella enterica and Acinetobacter baumannii, we generated Theta-Base as an intuitive online tool to easily interrogate the here-presented transcriptomic data. Theta-Base enables search queries for any annotated B. thetaiotaomicron coding gene as well as the here-identified noncoding genes (see below) and visualizes their expression profiles over growth in TYG in a simple heatmap format (Fig. 2a) that can be exported to the interactive graphing environment Plotly42. Moreover, a linkout to JBrowse43 allows the transcriptomic data to be viewed in the context of the B. thetaiotaomicron chromosome or plasmid (Fig. 2b), and additionally features the annotations of transcriptomic parts including TSSs and Rho-independent terminators. We hope this database will be routinely consulted by researchers of the Bacteroides community to retrieve information about transcript borders (relevant for cloning purposes or the design of PCR primers) or relative expression levels, and plan to further complement the current dataset with transcriptome profiles derived from B. thetaiotaomicron grown under various experimental conditions in the future. Theta-Base can freely be interrogated at

Fig. 2: Theta-Base allows easy access to B. thetaiotaomicron transcriptomic features.
figure 2

a Heatmap representation of absolute (reads per kilobase of transcript per million mapped reads [rpkm]; left) or relative (rpkm divided by row average; right) transcript levels illustrates the anti-correlation in expression of GibS (a.k.a. BTnc035) and its repressed targets (BT_0771, BT_3893; as identified in Fig. 5) over growth in TYG. For visualization, query genes (coding and noncoding) may either be entered individually in the upper left box or selected from pre-defined gene sets. Biological replicates can be displayed individually or (as in the given example) the average expression over each three replicates may be shown. ‘EEP’ refers to early, ‘MEP’ to mid-exponential, and ‘stat’ to stationary phase. The heatmap can be exported as a graphic file in the upper right corner. At the lower left corner is a link to the genome browser (b). b JBrowse view on the read coverages over the GibS-encoding locus within the B. thetaiotaomicron genome. Tracks for display can be selected on the left (i.e., annotated coding and noncoding genes and transcript features [transcription start sites, terminators] as well as different experimental conditions and replicates). At the top, gene names or genome coordinates may be entered; zoom-in and -out functions exist. Inset: By clicking on any of the annotated features, primary sequences can be retrieved in FASTA format.

The noncoding RNA landscape of B. thetaiotaomicron

Our dRNA-seq analysis uncovered a wealth of noncoding RNAs in B. thetaiotaomicron scattered throughout the genome (Fig. 3a). This included abundant housekeeping transcripts such as the RNA component of RNase P (M1 RNA) and transfer-messenger RNA (tmRNA). We also detected the Bacteroides 6S RNA and obtained evidence for the existence of product RNAs (pRNAs) (Supplementary Fig. 2a), which were previously predicted in the Bacteroidetes phylum44, but remained to be validated. In fact, we detected two classes of pRNAs in B. thetaiotaomicron (denoted pRNA and pRNA* in Supplementary Fig. 2a), reminiscent of previous observations in the ε-proteobacterium Helicobacter pylori20.

Fig. 3: The noncoding transcriptome of B. thetaiotaomicron.
figure 3

a DNAPlotter maps111 denote the genomic position of the identified noncoding genes within the chromosome or plasmid, respectively. Position of coding sequences (CDS), polysaccharide utilization loci (PUL), and capsular polysaccharide synthesis loci (CPS) were retrieved from NCBI and published literature5. Positions of transcription start sites (TSS) and noncoding RNAs (ncRNA) were identified in the present study. b Overview table on the numbers of predicted and experimentally validated (probed/detected on northern blot) ncRNA candidates of the different classes. c GC content of different transcript classes. The center lines refer to the medians, the lower and upper borders of the boxes refer to the 25% and 75%, respectively, and whiskers indicate the minimal/maximal GC contents of CDSs (n = 4816), tRNAs (n = 71), rRNAs (n = 15), 5′ UTRs (n = 1373), cis-antisense RNAs (n = 78), and all putative or the high-confidence intergenic sRNAs (n = 124; 49). The dashed line represents the average GC content of the genome. d Northern blot validation of predicted ncRNA candidates. Left: sRNA locus orientation. Right: Total RNA was extracted from wild-type B. thetaiotaomicron (AWS-001) grown in TYG to early exponential (EEP), mid-exponential (MEP) or stationary phase (stat) and used for Northern blotting (representative images from each two biological replicates are shown). Apparent sizes in nucleotides are given to the right of the blot. 5S rRNA served as loading control. Source data to this figure are provided in the Source Data file.

Noncoding RNA candidates were identified and classified on the basis of homology to described representatives of cis-regulatory elements into riboswitches and RNA thermometers (Rfam database45) or based on their genomic location into cis-antisense, intergenic, 5′- or 3′-derived and intra-operonic sRNAs (Fig. 3b; Supplementary Fig. 2b–i; Supplementary Data 2). ANNOgesic rediscovered three putative thiamine pyrophosphate (TPP) riboswitches46,47 in the 5′ UTRs of BT_0653 (encoding the thiamine biosynthesis protein ThiS), BT_2390 (for an outer membrane thiamine transporter), and BT_2396 (for a protein involved in nicotinamide mononucleotide transport). Further, B. thetaiotaomicron expressed 78 cis-antisense and 124 intergenic sRNAs, respectively, during growth in rich medium; the latter number was reduced to 49 when requiring the presence of a Rho-independent terminator structure at the 3′ end as an additional selection criterion (along with a cognate TSS and a minimum read coverage; see Methods for details). We refer to this subset of 49 candidates as “high-confidence” intergenic sRNAs. Conservational analysis revealed 22 of these sRNAs to be conserved within two or more genera within the Bacteroidetes phylum, while the remaining 27 are strain-specific (Supplementary Fig. 3a). Analysis of the nucleobase composition of cis-antisense and intergenic sRNAs revealed GC contents of 38% or 35%, respectively, which is lower than that of CDSs, transfer RNAs (tRNAs) and ribosomal RNAs (rRNAs), in line with observations previously made in Escherichia coli48 (Fig. 3c). Selected cis-antisense RNA representatives were predicted to fold into extensive secondary structures, whereas several intergenic sRNAs exhibited extended unfolded regions (Supplementary Fig. 3b). Promoter analysis revealed the canonical σABfr promoter to be associated with 52% or 76%, and the non-canonical PM2 with 24% or 13% of cis-antisense or intergenic sRNA candidates, respectively (Supplementary Data 2).

CRISPR (clustered regularly interspaced short palindromic repeats) systems protect their host against bacteriophage infections and are encoded by ~45% of sequenced bacterial genomes, including that of B. fragilis49. In contrast, no CRISPR array nor any Cas (CRISPR-associated) proteins have been annotated in B. thetaiotaomicron. In agreement with this, the CRISPR Recognition Tool50, which is included in the ANNOgesic pipeline, failed to identify any CRISPR-RNAs in our dataset.

Experimental validation of B. thetaiotaomicron sRNAs

To validate the predicted sRNAs, we performed Northern blot assays for 31 randomly selected RNA candidates from diverse classes (Fig. 3d). DonS, the prototypical PUL-associated antisense RNA18, was not expressed when B. thetaiotaomicron grew in TYG medium and consequently, not identified in our screen. However, our transcriptomic approach readily detected ten further cis-antisense RNAs with a DonS-like genomic orientation, and we validated the expression of five of them (BTnc009, −055, −077, −249, and −123) by Northern blot (Fig. 3d). Of note, we observed anti-correlation in the expression of some of these antisense RNAs and their cognate susC homologs in our RNA-seq data (highlighted in red in Supplementary Fig. 4a), arguing that B. thetaiotaomicron cis-antisense RNAs may repress their corresponding PUL system in the presence of a prioritized carbon source, similarly to DonS in B. fragilis. Another seven pairs of cis-encoded antisense RNAs had a genomic architecture reminiscent of type-I TA systems, with each one of the divergently encoded genes harboring a candidate sORF. These putative TA systems showed a similar expression pattern with the presumed toxin mRNAs expressed at constant—albeit low—levels and the putative antitoxin RNA specifically induced in stationary phase (Supplementary Fig. 4b).

To assess the reliability of intergenic sRNA predictions, we independently tested the existence of selected candidates by Northern blot. This way, we validated nine of eleven tested candidates, from which eight (including BTnc035 [renamed to GibS: see below], BTnc201, and BTnc231; Fig. 3d; Supplementary Fig. 2d–f) possess both a TSS and an intrinsic terminator—features characteristic of canonical intergenic sRNAs. Thus—while not a hard selection criterion in the default ANNOgesic pipeline—the presence of a 3′ terminator may enhance our confidence in sRNA predictions and we therefore prioritized these high-confidence intergenic sRNAs in the following.

We also uncovered several putative sRNAs originating from the 5′ or 3′ UTR of mRNAs of which we validated one representative candidate each (BTnc259, BTnc028; Supplementary Fig. 2g, h) by Northern blot (Fig. 3d). Finally, ANNOgesic classified sRNAs into a fifth group termed inter-CDS-derived (more appropriately, intra-operonic) sRNAs. These are similar to 5′ UTR-derived sRNAs, however, they may originate at either a TSS or a processing site and can end at a Rho-independent terminator or a processing site. We identified six members belonging to this class, and experimentally validated BTnc069 (Fig. 3d; Supplementary Fig. 2i).

GibS—an intergenic sRNA conserved within Bacteroides spp

To successfully colonize and persist in the human gut, B. thetaiotaomicron relies in large part on its ability to rapidly adapt to the ever-changing conditions associated with this dynamic environment. Given that sRNAs in other organisms are known to regulate gene expression in response to specific environmental cues15,51, we wondered whether B. thetaiotaomicron would also harness its sRNA repertoire to adapt to environmental changes. Of the 49 high-confidence intergenic sRNAs identified, we focused on GibS (GlcNAc-induced Bacteroides sRNA; renamed from BTnc035 for reasons below)—a sRNA encoded in between a putative para-aminobenzoate synthase cluster (BT_076368) and a glycogen biosynthesis operon (BT_076971) (Fig. 4a). GibS was highly expressed during growth in TYG media, especially upon entry into the stationary growth phase (Fig. 3d). Moreover, its primary sequence and the non-canonical PM2 (–10 and –30 box; Fig. 1d) are well conserved within the Bacteroides genus (Fig. 4b, upper; Supplementary Fig. 3a); features indicative of a functional transcript.

Fig. 4: Conservation, secondary structure, and expression profile of GibS sRNA.
figure 4

a Shown is the overview of the gibS locus in seven indicated Bacteroides species. b Upper: Sequence alignment of the gibS gene and flanking regions in the same Bacteroides species as in a. The sequence at the bottom refers to the consensus and the brackets below indicate the determined intra-molecular base-pairings (see c and d). Red and blue colors indicate perfectly conserved and less-conserved ribonucleobases, respectively. The numbers denote the position relative to the 5′ end of GibS (+1 position; validated in Supplementary Fig. 5). Lower: Read coverage plot over the gibS locus (stationary phase, ‘–TEX’ sample). At the position of the presumed intrinsic terminator (indicated above the alignment) read coverage drops, likely due to strong hairpins being less efficiently converted into cDNA. c Secondary structure prediction of B. thetaiotaomicron GibS was performed using the webserver for aligning structural RNAs52 and reflects the consensus structure of 14 different prediction programs, considering both, minimal free energy and covariation. The colors of the ribobases reflect their conservation within Bacteroides and numbering is as in b. R1 and R2 seed regions as identified in Fig. 5e are labeled. d In vitro structure probing of 5′ end-labeled GibS confirms the in silico prediction (representative image from two independent replicate experiments is depicted). T1 and OH ladders refer to partial digestion under denaturing conditions with nuclease T1 (lane 1; cleaves unpaired G residues, indicated to the left), or alkali (lane 2; cleaves at all positions), respectively, and ‘control′ (lane 3) refers to untreated GibS. Lanes 4–6 reveal cleavages induced by lead (II) acetate (cleaves single-stranded nucleotides), RNase T1, or RNase III (cleaves double-stranded regions), respectively, under native conditions. e Northern blot-based expression profiling of GibS in wild-type B. thetaiotaomicron (AWS-001) grown to stationary phase in either TYG medium or in minimal medium (MM) in presence of glucose (Glc), fructose (Fru), galactose (Gal), mannose (Man), N-acetylglucosamine (GlcNAc), xylose (Xyl) or maltose (Mal), respectively, as the sole carbon source (representative image from two biological replicates). 5S rRNA was the loading control. Source data are provided in the Source Data file.

Northern blotting indicated a ~145 nt-long RNA species to be the major GibS transcript form (Fig. 3d), in line with a potential terminator structure after which the read coverage in the RNA-seq experiment drops (Fig. 4b, lower). Primer-extension analysis confirmed the TSS of GibS as mapped by dRNA-seq (Supplementary Fig. 5). In silico RNA alignment and folding of GibS homologs using WAR (webserver for aligning structural RNAs52), which provides a consensus alignment and structure based on a range of methods that consider both minimal free energy and residue co-variation, indicated GibS to adopt a relatively unfolded conformation (Fig. 4c). Indeed, chemical and enzymatic in vitro probing largely confirmed this prediction, with the highly conserved 5′ sequence being mainly single-stranded (positions 1-38), the middle region forming two consecutive meta-stable hairpins, followed by another linear region and the Rho-independent terminator (Fig. 4d). Apart from the extended single-stranded 5′ region, this is reminiscent of the structure of well-characterized proteobacterial trans-acting sRNAs53.

Within its gut niche, B. thetaiotaomicron uses simple sugars as signals to control the expression of metabolic modules12,54. Given their ability to mediate rapid responses to metabolic stimuli55, sRNAs might be involved in the adaptation of Bacteroides gene expression to nutrient availability. To test if GibS exhibits a monosaccharide-specific expression pattern, we profiled its steady-state levels in B. thetaiotaomicron grown to stationary phase in minimal medium with defined simple sugars as the sole carbon source (Fig. 4e). While GibS expression showed considerable variation across the panel of carbon sources, growth in the presence of N-acetyl-D-glucosamine (GlcNAc) resulted in the strongest induction (~1.6 fold higher GibS levels in stationary phase in GlcNAc than in TYG). Thus, GibS is a conserved, largely unstructured sRNA in B. thetaiotaomicron that is induced in the presence of select monosaccharides.

Identification of GibS targets

Toward characterizing the role of GibS in B. thetaiotaomicron physiology, we constructed a sRNA deletion mutant (∆gibS) by removing the gibS sequence from the chromosome. In addition, a trans-complementation strain (gibS+) was generated for which the gibS gene under control of a modified P1TDP promoter56 (designated P1TD) was re-inserted at an unrelated position into the ∆gibS chromosome. The promoter modification involved removal of the proximal tetO2 operator to ensure transcription of the sRNA from its native TSS, albeit with the cost of leaky expression (see Methods). However, upon addition of anhydrotetracycline (aTC; 200 ng mL−1), the resulting strain expressed GibS to wild-type levels (Supplementary Fig. 6). Interfering with GibS expression in bacteria grown in defined minimal medium in presence of GlcNAc as the sole carbon source resulted in subtle growth variations (Supplementary Fig. 7a). In contrast, strains grew nearly identically in the presence of glucose (Supplementary Fig. 7a).

Next, we employed a genome-wide comparative transcriptomic approach to search for GibS-dependent expression changes. To this end, wild-type B. thetaiotaomicron, ∆gibS, and gibS+ strains were grown to stationary phase in TYG—i.e., a growth phase when endogenous GibS is highly expressed (Fig. 3d)—and their total RNA was extracted, depleted for rRNA, and sequenced. In the absence of GibS, four genes were repressed and five genes induced as compared to their wild-type expression levels (Fig. 5a). Notably, with the exceptions of BT_0294 and BT_0823, expression of all these genes reverted to wild-type levels in the trans-complementation strain (Fig. 5a), indicating a sRNA-specific effect. BT_187172, i.e. the two genes seemingly activated by GibS (and thus, repressed in strain ∆gibS), comprise a dicistron encoding an α-galactosidase and a β-glucosidase, respectively, and are predicted to be part of the putative PUL22 involved in arabinan degradation (Supplementary Fig. 7b)57. The genes seemingly repressed by GibS (de-repressed in ∆gibS) included BT_1655 (encoding a hypothetical protein within the CPS5 locus; Supplementary Fig. 7c) and BT_3893 (the second gene within a dicistron and encoding a hypothetical protein; Supplementary Fig. 7e). BT_3892—the first gene in this operon and encoding a branched-chain amino acid aminotransferase—was unaffected by gibS status. Finally, the glycogen synthesis BT_076971 operon, which is encoded adjacent to gibS itself (Fig. 4a), was de-repressed in the ∆gibS mutant (Supplementary Fig. 7d). We rule out polar effects of sRNA deletion, as BT_076971 expression reverted to wild-type levels when GibS was re-introduced in trans in the ∆gibS background (strain gibS + in Fig. 5a). Altered expression levels of all target candidates except BT_1655 and BT_0769 were independently validated by quantitative real-time PCR (qRT-PCR) (Fig. 5b).

Fig. 5: GibS regulates the expression of target genes likely via direct base-pairing.
figure 5

a Comparative transcriptomics of isogenic wild-type B. thetaiotaomicron (WT; AWS-003), a gibS deletion mutant (∆gibS; AWS-028), and complementation strain (gibS+; AWS-035). Upper: Northern blot showing stationary phase expression of GibS in the three strains. Heatmap below: RNA-seq data for putative targets under the same condition (i.e., fold change >2 or <0.5 at an FDR < 0.05 between WT and ∆gibS; mean of two biological replicates). Gray labeled genes were not considered further, as their expression pattern was not predictive of a GibS-specific effect. b qRT-PCR-based validation of the identified target candidates. 16S rRNA was used as a reference transcript. Bars denote the mean from three biological replicates each in technical duplicates (represented as single dots). Significant differences compared to wild-type expression levels were assessed using two-way ANOVA (Sidak’s multiple comparisons test; p values for significant [p < 0.05] comparisons are given). c Locus representation of target genes (upper) and their predicted interactions with GibS (lower). Red/blue nucleotides: start codon/Kozak-like sequences; gray shading: coding region; R1, R2: seed regions interacting with BT_3893 (see e); ‘mut’: mutated nucleotides of BT_3893 (for d). Minimal free energy values are to the right. Coordinates are relative to the TSS. d EMSAs support the predicted sRNA targeting site within BT_3893. T7-transcribed and 5′ end-labeled GibS was incubated with increasing concentrations of a ~150 nt-long 5′ segment of either wild-type (WT; black) or mutated variant of BT_3893 (‘mut’; red; see c). Kd values represent the means of two independent replicate experiments. A representative gel from the WT is shown at the top and an image for binding to the mutated variant is given in Supplementary Fig. 8b (white and black arrowheads refer to free and bound GibS, respectively). e In-line probing of 0.2 pmol 32P-labeled GibS in the absence (lane 4) or presence of either 20 nM (lane 5) or 200 nM BT_3893 mRNA leader (lane 6). Untreated RNA (lane 1; ‘control’), partially RNase T1- (lane 2; ‘T1’) or alkali-digested (lane 3; ‘OH’) GibS served as ladders. R1 and R2 denote GibS seed regions protected from cleavage in the presence of the target. Two independent replicate experiments were performed of which a representative image is depicted. f Working model for the role of GibS in B. thetaiotaomicron. Source data are provided as a Source Data file.

To test whether the observed GibS-dependent expression changes result from direct sRNA:mRNA base-pairing events, we searched for regions within the target candidates that showed partial complementarity to the GibS sequence. Among the differentially expressed genes identified above, the IntaRNA program58 predicted GibS to anneal within the CDS of BT_1871 and the region spanning the respective start codons of BT_0771 and BT_3893 (Fig. 5c). The correspondingly predicted seed region of GibS comprised its highly conserved and unstructured 5′ portion (Fig. 4c). To experimentally test these predictions, we performed electrophoretic mobility shift assays (EMSAs) using radiolabeled GibS and increasing concentrations of ~150 nt-long mRNA segments encompassing the assumed targeting sites. Binding of GibS to the 5′ region of both BT_3893 and BT_0771 occurred with high affinity (Kd = 16.01 and 18.06 nM) resulting in an upshift of the sRNA with increasing concentrations of each mRNA target segment (Fig. 5d; Supplementary Fig. 8a). This suggests BT_3893 and BT_0771 mRNAs to be direct targets of GibS. Indeed, in-line probing of radiolabeled GibS with or without in vitro-transcribed BT_3893 mRNA (Fig. 5e) validated the computationally predicted base-pairing events involving two adjacent regions in the 5′ portion of GibS (termed R1 and R2 in Fig. 5c), and mutating a hexameric sequence within the BT_3893 region targeted by R2 reduced its affinity to GibS (Fig. 5d; Supplementary Fig. 8b). In contrast, the in vitro interaction of GibS with BT_1871, for which binding was proposed to occur within the CDS, was of very low affinity (Supplementary Fig. 8c). This argues that in the bacterial cell, base-pairing between GibS and BT_1871 may depend on auxiliary factors, such as a RNA chaperone, or that activation of this gene by GibS (Fig. 5a, b) is indirect.


Only recently and thanks to technological breakthroughs that allow anaerobic culturing without the need for extensive lab equipment59 and the development of versatile protocols for genetic manipulation56,60,61,62, has it become possible for a wider group of researchers to functionally characterize anaerobic gut commensals. In this context, Bacteroides species—predominant members of the human microbiota—are gaining increasing attention by the scientific community63.

In the present work, we have compiled a high-resolution transcriptome map of the B. thetaiotaomicron type strain VPI-5482, which is freely accessible to the research community as an intuitive online database. Our screen identified ~4500 TSSs within the core genome and plasmid, and revealed high plasticity in the transcriptome structure of B. thetaiotaomicron. Inspection of the sequences upstream of the identified TSSs revealed the canonical σABfr promoter. Not only did our genome-wide motif search confirm the –7 box, but it also identified the –33 box that was initially inferred from manual inspection of a few dozen promoters6, but could not previously be verified globally within the Bacteroidetes phylum8. We assume that the variable spacing between the two boxes (Fig. 1d) might have hampered previous motif searches. In addition, our global promoter analysis revealed a second sequence motif enriched in front of oxygen tension-related genes, suggesting the motif could be recognized by a stationary phase-inducible alternative sigma factor to pre-adapt microbes against exposure to reactive oxygen species64. However, this motif differs substantially from the recognition sequence of the sigma factor EcfO, which protects B. fragilis against oxidative stress9 and deserves further investigation.

Comprehensive transcriptomic analyses are reliant on an accurate genome annotation. We intend to regularly update Theta-Base with the most recently reported genomic features. In addition, in the future, plasticity of the B. thetaiotaomicron transcriptome may be refined even further by similar RNA-seq studies under additional experimental settings, including growth on defined carbon sources or in face of specific stress conditions. For example, given that Bacteroides promoter inversions are commonly observed under stressful conditions such as antibiotics exposure or gut adaptation65, those data would be useful to explore the effects of invertible Bacteroides promoters on global gene expression.

In addition to bacterial transcriptional control networks, post-transcriptional regulation mediated by regulatory RNA molecules has been revealed as a second layer of adapting global gene expression to changing environmental and intrinsic cues. Particularly, trans-encoded sRNAs have been described in species across the bacterial phylogenetic tree15,53, where they regulate target mRNAs through imperfect base-pairing interactions mediated by short seed sequences and, in many Gram-negative species, dedicated RNA chaperones66. In the majority of the described cases, sRNA annealing to the SD sequence and/or start codon, interferes with translation initiation and induces target decay15. Conversely, certain sRNAs may promote translation of their target by unfolding inhibitory structures that otherwise block ribosome binding67,68. In addition, activating trans-encoded sRNAs in γ-proteobacteria may induce target gene expression by binding to nascent mRNA leaders and interfering with Rho-mediated premature transcription termination69,70. Besides targeting mRNAs, some sRNAs may bind to, and titrate, regulatory RBPs, thereby indirectly controlling the levels of the target mRNA set of the bound protein71. Conceptually related, an emerging class of sRNA sponges bind and titrate other sRNAs, creating complex post-transcriptional gene expression control networks72. In contrast, if and how trans-encoded sRNAs regulate target gene expression in Bacteroides has previously barely been addressed.

Overall, our study provides evidence for the existence of >200 noncoding RNAs from diverse classes in B. thetaiotaomicron. As an example, our screen experimentally validated the 6S RNA homologue of Bacteroides and provided evidence for the existence of pRNAs that rescue sequestered RNA polymerases, further highlighting 6S RNA-mediated regulation of transcriptional activity to be an ultra-conserved mechanism. Taking into account that dRNA-seq was performed in just three defined growth stages in a single (rich) medium, the reported numbers for cis-antisense (78) and intergenic sRNA candidates (124, of which we consider 49 as high-confidence) are probably conservative. In addition, the screen identified 21 UTR-derived sRNA candidates, suggesting that evolution of dual-function transcripts73 is not restricted to Proteobacteria. The full repertoire of B. thetaiotaomicron noncoding RNAs therefore appears consistent with the numbers reported in other bacteria20,29,74,75,76,77. However, we want to point out that antisense transcription might at least partially be due to the appearance of random promoters26, which is particularly likely in a genome with a low GC content. Consequently, not all identified cis-antisense RNA candidates might actually be functional.

Here, we began to mechanistically characterize the GibS sRNA. We selected GibS for several reasons: (i) its strong sequence conservation (especially in its 5′ portion) within the Bacteroides genus argues for functionality; (ii) the presence of PM2 upstream of its TSS renders it a representative for a larger set of transcripts; (iii) the generally high steady-state levels of this sRNA—particularly in stationary growth phase and in the presence of the simple sugar GlcNAc—enables robust detection and analysis; and (iv) gibS does not overlap with any other gene, which allowed for the straight-forward construction of a clean deletion mutant. In the course of our studies, we validated the TSS of GibS predicted by dRNA-seq and determined the secondary structure of the sRNA. Unlike many well-characterized trans-encoded sRNAs in Proteobacteria, GibS contains long single-stranded regions, particularly in its 5′ part. Expression profiling of wild-type B. thetaiotaomicron and a ∆gibS mutant identified potential target mRNAs of this sRNA and provided a possible explanation for the lack of structure at the 5′ end: GibS harbors an extended seed region, comprising the first 30-50 nt of its 5′ portion, that mediates base-pairing with the region around the target mRNA’s start codon (BT_0771, BT_3893) or, potentially, a region deep within the CDS of BT_1871.

What is the physiological role of this sRNA? We find GibS expression to peak when B. thetaiotaomicron is cultured in the presence of GlcNAc as the sole carbon source. This monosaccharide is a constituent of host-derived glycosaminoglycans such as chondroitin sulfate (CS), dermatan sulfate, and heparin/heparan sulfate (HS), with CS and HS being the priority nutrients for B. thetaiotaomicron78,79. The identified GibS targets are related to metabolic processes: The BT_1871-BT_1872 operon, which is activated by GibS, encodes a galactosidase and a periplasmic glucosidase, and BT_0770-BT_0771, that is repressed by GibS, encodes a glucan-branching enzyme. Together, this suggests a regulatory network, wherein sensing of a specific glycosaminoglycan-derived monosaccharide results in the induction of GibS, which in turn leads to post-transcriptional metabolic rearrangements in the bacterial cell (Fig. 5f). If true, this places GibS among the growing number of sRNAs involved in carbon catabolite repression in diverse bacterial organisms80. Dissecting the exact role of GibS, however, requires further work.

GibS targeting the translation initiation region of BT_0771 and BT_3893 mRNAs is reminiscent of the classical mechanism of sRNA-mediated target control, preventing ribosome loading and interfering with translation initiation, often accompanied by enhanced target mRNA decay15. We here provided the first example showing that, despite the lack of a SD sequence, Bacteroidetes mRNAs may still be repressed by sRNAs that anneal to their translation initiation region. Consequently, deleting gibS from the B. thetaiotaomicron genome resulted in an upregulation of both these mRNAs, and trans-complementation reverted their expression to wild-type levels. In contrast, sRNA targeting within the CDS is relatively rare, but could mask an endonucleolytic cleavage site, thereby stabilizing the target mRNA68. In line with such a mechanism, BT_1871 levels dropped in the absence of GibS as compared to both the wild-type and complementation strain. Alternatively, activation of BT_1871 mRNA in presence of GibS may occur indirectly.

Commonly, protein co-factors are involved in sRNA-mediated target control81. In Bacteroides, in absence of an obvious homologue of both Hfq and ProQ, sRNAs might either regulate targets in a protein-independent manner, or depend on an alternative, elusive RNA chaperone. The average GC content of the identified intergenic sRNAs was relatively low (~35%). Moreover, we identified several B. thetaiotaomicron sRNAs that appear rather unstructured (Supplementary Fig. 3b). Well-studied Hfq-dependent sRNAs in Proteobacteria typically contain seeds of ~6–10 nt in length82. The above features—AT richness and single-strandedness—might indicate that certain B. thetaiotaomicron sRNAs need more extended seeds for efficient target annealing, as is exemplified by GibS. Whether such extensive base-pairing events would be more or less likely to require assistance by RNA chaperones needs further investigation. While in the present case, GibS interactions with the 5′ region of BT_0771 and BT_3893 occurred at very high affinities even without a protein co-factor in vitro, long single-stranded seed regions may be inherently vulnerable to ribonucleases (homologs of RNase BN, –G, –HII, –III, –P, –R, and –Z are present in B. thetaiotaomicron according to Pfam83) and stability of the respective sRNAs in the bacterial cytosol could thus depend on RBP association.

Compared to species that have long served us as model organisms for prokaryotic RNA biology, there is currently no toolbox available to mechanistically decipher the functions of sRNAs in Bacteroides species. Here, we employed an aTC-triggered sRNA induction system, but leaky expression and limited dynamic range (Supplementary Fig. 6) prompted us to grow the respective strain (gibS+) for 2 h in presence of the inducer to reach high sRNA levels. Despite successfully complementing expression changes in the ∆gibS mutant, more tightly inducible sRNA pulse-expression systems might be harnessed in the future to facilitate discrimination between direct and indirect effects of sRNA overexpression84,85. For target validation, two-plasmid systems, consisting of an inducible sRNA expression vector and a constitutively expressed fluorescent reporter fusion with the respective target mRNA, are routinely used in Proteobacteria86,87. Despite the oxygen-dependent maturation of commonly used fluorescent proteins, similar reporters should also work in anaerobic bacteria because for sample preparation, cell suspensions are typically shifted to normoxic conditions that allow for fluorescence recovery88. Similarly, luciferase assays—albeit depending on molecular oxygen—have already been successfully employed in Bacteroides47,89 and β-galactosidase assays with lacZ-target fusions90 represent an oxygen-independent alternative.

Modern sequencing-based technologies have proven useful to gain global perspectives on bacterial sRNAs91 and their generic nature should allow sRNA systems biology approaches to be applied to currently understudied bacterial species. For example, pooled knockdown or knockout mutant libraries represent invaluable tools for global screens. Transposon-sequencing (Tn-seq) data exist for B. thetaiotaomicron92,93,94 and it will be intriguing to re-analyze them for phenotypes associated with a disruption of the here-identified noncoding RNA candidates. However, like any random mutagenesis approach, Tn-seq is inherently biased toward longer genes, typically resulting in an underrepresentation of sRNA mutants. In this context, targeted approaches such as CRISPR interference, whose applicability was already demonstrated for B. thetaiotaomicron89, appear as promising alternatives to simultaneously knock down hundreds of sRNAs and screen the resulting mutant pool under a variety of conditions. Obviously, implementing these technologies requires time and effort. The here-presented data, however, chart a rich world of Bacteroides RNA biology for us to explore.


Bacterial strains and genetics

Strains, plasmids, and oligonucleotides used in this study are listed in Supplementary Data 4. B. thetaiotaomicron type strain VPI-5482 is referred to as wild-type throughout the study. The gibS deletion mutant (ΔgibS) was generated as previously described95. Briefly, 1-kb sequences flanking the region to be deleted were amplified by PCR (using oligos AWO-053/−054, AWO-055/−56, AWO-314/−315, and AWO-316/−317) and assembled into the suicide vector pExchange-tdk by Gibson assembly (NEB) as per the manufacturer’s protocol. A 2-μL aliquot of this reaction was transformed into electro-competent E. coli S17-1 λpir. Transformants were conjugated with a tdk deletion mutant of B. thetaiotaomicrontdk) and conjugants counter-selected on 5-fluoro-2′-deoxyuridine (FUdR) plates. Single recombinants were selected on Brain Heart Infusion Supplemented (BHIS) agar containing 200 μg mL−1 gentamicin and 25 μg mL−1 erythromycin. Double recombinants, resulting in either scarless deletion mutants or wild-type revertants, were selected by growth on BHIS agar containing 200 μg mL−1 FUdR and an inability to grow on BHIS agar containing 25 μg mL−1 erythromycin. Successful deletions were subsequently confirmed by PCR (AWO-150/−151, AWO-111/−112, AWO-318/−319, AWO-340/−341, AWO-342/−343) and Sanger sequencing.

A gibS complementation strain (gibS+) was constructed using a variant of the pNBU2 vector system95 (Supplementary Data 4). The full gibS gene was integrated into the vector by Gibson assembly (AWO-156/−157) to ensure transcription from its native TSS. This resulted in a deletion of the proximal tetO2 (TP) operator downstream of the promoter P1TDP, while leaving the second operator (TD) intact56. This construct, expressing the GibS sRNA from its +1 nucleotide under control of the P1TD promoter, was conjugated into the Δtdk strain and selected on BHIS agar containing 25 μg mL−1 erythromycin. Successful insertion was confirmed by PCR (AWO-160/−161) and Sanger sequencing.

B. thetaiotaomicron culture conditions

Bacteroides strains were cultured in an anaerobic chamber (Coy Laboratory Products) in presence of an anoxic gas mix (85% N2, 10% CO2, 5% H2) at 37 °C. Routine cultivation involved the use of complex media; TYG (20 g L−1 tryptone, 10 g L−1 yeast extract, 0.5% glucose, 5 mg L−1 hemin, 1 g L−1 cysteine, 0.0008% CaCl2, 19.2 mg L−1 MgSO4.7H2O, 40 mg L−1 KH2PO4, 40 mg L−1 K2HPO4, 80 mg L−1 NaCl, 0.2% NaHCO3) and BHIS (52 g L−1 BHI agar powder, 1 g L−1 cysteine, 5 mg L−1 hemin, 0.2% NaHCO3). Carbohydrate growth assays were performed in minimal medium (1 g L−1 L-cysteine, 5 mg L−1 hemin, 20 mg L−1 L-methionine, 4.17 mg L−1 FeSO4, 0.2% NaHCO3, 0.9 g L−1 KH2PO4, 0.02 g L−1 MgCl2.6H2O, 0.026 g L−1 CaCl2.2H2O, 0.001 g L−1 CoCl2.6H2O, 0.01 g L−1 MnCl2.4H2O, 0.5 g L−1 NH4Cl, 0.25 g L−1 Na2SO4) supplemented with 0.5% of the indicated carbon sources96.

RNA extraction, TEX treatment, cDNA library preparation, and sequencing

For dRNA-seq (Figs. 13), wild-type B. thetaiotaomicron VPI-5482 (AWS-001) was grown overnight in 5 mL pre-reduced TYG medium followed by sub-culturing (1:100) into 50 mL fresh pre-reduced TYG. Total RNA was isolated by hot phenol extraction from culture aliquots of each three biological replicates at early exponential (4 h), mid-exponential (7 h), and stationary growth phase (10 h). Briefly, 4 OD equivalents of culture were harvested and 1.6 mL stop mix97 was added (95% vol vol−1 ethanol, 5% vol vol−1 water saturated phenol, pH >7.0). The bacterial cells were lysed by incubation with 600 μL lysozyme (0.5 mg mL−1) and 60 μL 10% SDS for 2 min at 64 °C, followed by the addition of 66 μL of 3 M NaOAc. Phenol extraction (750 μL; Roti-Aqua phenol) was performed at 64 °C for 6 min with the subsequent addition of 750 µL chloroform. RNA was precipitated from the aqueous phase with twice the volume of 30:1 (ethanol:3 M NaOAc, pH 6.5) mix and incubated at –80 °C overnight. After centrifugation, pellets were washed with 75% (vol vol−1) ethanol and re-suspended in 50 μL H2O. Contaminating genomic DNA was removed by treating 40 μg total RNA with 5 U of DNase I (Fermentas) and 0.5 μL Superase-In RNase Inhibitor (Ambion) in a 50 μL reaction. RNA quality was checked using a 2100 Bioanalyzer and the RNA 6000 Nano kit (Agilent Technologies). RNA integrity (RIN) values for all samples were between 9.2 and 9.6.

Prior to cDNA synthesis, total RNA was fragmented using ultrasound (4 pulses of 30 s at 4 °C) and treated with T4 polynucleotide kinase (NEB). Subsequently, half of each total RNA sample was treated with Terminator exonuclease (TEX) to enrich for primary transcripts, whereas the other half was left untreated. RNA samples were then poly(A)-tailed using poly(A) polymerase and 5′-PPP was removed with 5′ polyphosphatase (Epicentre). RNA adaptors were ligated and first-strand cDNA synthesis was carried out using oligo(dT) primers and M-MLV reverse transcriptase. The cDNA was PCR amplified to about 10-20 ng μL−1, purified using Agencourt AMPure XP kit (Beckman Coulter Genomics), and fractionated in a size range of 200–500 bp. Libraries were sequenced on an Illumina NextSeq platform (150 cycles) at the Core Unit SysMed of the University of Würzburg.

For conventional RNA-seq (Fig. 5a), B. thetaiotaomicrontdk (AWS-003), ∆gibS, (AWS-028), and gibS+ (AWS-035) strains (two biological replicates) were grown in TYG to stationary phase as described above, followed by the addition of aTC at a final concentration of 200 ng mL−1 (for maximal GibS expression with minimal growth attenuation; Supplementary Fig. 6a, b), and resumed growth therein for 2 h. Total RNA was extracted and RNA quality checked as above with RIN values between 7.7 and 9.5. Prior to library preparation, rRNA was depleted using the Pan-Prokaryote riboPOOLs kit (siTOOLs Biotech). In brief, 1 µg of total RNA was incubated for 10 min at 68 °C and 30 min at 37 °C with 100 pmol of rRNA-specific biotinylated DNA probes in 2.5 mM Tris-HCl pH 7.5, 0.25 mM EDTA, and 500 mM NaCl. DNA-rRNA hybrids were depleted from total RNA by two consecutive 15 min incubations with 0.45 mg streptavidin-coated magnetic Dynabeads MyOne C1 (ThermoFisher Scientific) in 2.5 mM Tris-HCl pH 7.5, 0.25 mM EDTA, and 1 M NaCl at 37 °C. The rRNA-depleted RNA samples were purified using the Zymo RNA Clean & Concentrator kit combined with DNase treatment on a solid support (Zymo Research).

cDNA libraries were prepared using the NEBNext Multiplex Small RNA Library Prep kit for Illumina (NEB) in accordance with the manufacturers’ instructions, except for the following modifications: RNA samples were fragmented with Mg2+ for 2.75 min at 94 °C using the NEBNext Magnesium RNA Fragmentation Module (NEB) followed by RNA purification with the Zymo RNA Clean & Concentrator kit. Fragmented RNA was dephosphorylated at the 3′ end, phosphorylated at the 5′ end, and decapped using 10 U T4-PNK +/− 40 nmol ATP and 5 U RppH, respectively (NEB). After each enzymatic treatment, RNA was purified with the Zymo RNA Clean & Concentrator kit. RNA fragments were ligated for cDNA synthesis to the 3′ SR and 5′ SR adapters pre-diluted 1:3 with nuclease-free water. PCR amplification to add Illumina adaptors and indices to the cDNA was performed for 14 cycles with 1:3 pre-diluted primers. Barcoded cDNA libraries were purified using magnetic MagSi-NGSPREP Plus beads (amsbio) at a 1.8:1 ratio of beads to sample volume. Libraries were quantified with the Qubit 3.0 Fluometer (ThermoFisher) and the library quality and size distribution was checked using a 2100 Bioanalyzer with the high sensitivity DNA kit (Agilent). Sequencing of ten pooled libraries spiked with 5% PhiX control library was performed in single-end mode on the NextSeq 500 platform (Illumina) with the Mid Output Kit v2.5 (75 cycles).

Read processing and mapping

Sequencing reads were quality filtered with the local run manager software from Illumina version 2.2.0. Generated reads were then trimmed for the NEBNext adapter sequence using Cutadapt version 2.5 with default parameters. In addition, Cutadapt was given the –nextseq-trim=20 switch to handle two-color sequencing chemistry and reads that were trimmed to length 0 were discarded.

For both sequencing protocols (dRNA-seq and conventional RNA-seq), reads were mapped to the B. thetaiotaomicron VPI-5482 reference genome (NC_004663.1) and plasmid (NC_004703.1) using the READemption pipeline98. Details of alignment statistics can be found in Supplementary Data 5. Aligned reads in wiggle format were visualized using both the Integrated Genome Browser99 and JBrowse43. Differential gene expression analysis was performed using DESeq2100 with log fold-change shrinkage using the DESeq2 betaprior method.

Identification of TSSs

We employed the ANNOgesic pipeline (version 0.7.33) that integrates a suite of tools to annotate bacterial genomes from both dRNA-seq and conventional RNA-seq data22. TSSs were identified using the ANNOgesic implementation of TSSpredator77 (usage: annogesic tss_ps) which compares the relative enrichment of reads between TEX-treated samples and their untreated counterparts. This resulted in characteristic enrichment peaks that were indicative of a 5′ triphosphate that protects against TEX digestion. Default settings were used with the addition of the gene validation option that relates identified TSSs to annotated genes (Supplementary Data 1). TSSs were categorized based on their enrichment and location relative to the start of the cognate coding gene. Primary TSSs were classified as having the highest coverage within 300 bp upstream of an ORF, while all other TSSs within this region were defined as secondary TSSs. Internal TSSs were identified as originating on the sense strand within a coding gene and antisense TSSs were located on the antisense strand overlapping with, or within a 100 bp flanking region, of a given sense gene. All remaining TSSs were classified as orphan TSSs. TSSs called by TSSpredator were manually curated based on read coverage plots to ensure accuracy of the assignments and the thus validated TSSs are incorporated in Theta-Base (

Search for promoter motifs

Conserved DNA sequences upstream of TSSs were identified by ANNOgesic (usage: annogesic promoter) integrating both, MEME for gapless motifs38 and GLAM2 for gapped motifs39. Default parameters were used with the addition of the flag –n set to 50 to increase sensitivity. Representative sequences containing consensus motifs were aligned using ClustalW (version 2.1)101 and logos generated with WebLogo (version 2.8)102.

Prediction of intrinsic terminators

ANNOgesic employs two heuristic algorithms for the prediction of Rho-independent terminators (usage: annogesic terminator). TransTermHP scans genome sequences for the presence of Rho-independent terminators30. To further substantiate these predictions and to detect the presence of Rho-independent terminators also in between convergent gene pairs, RNA-seq data were referenced to detect a significant decrease in coverage associated with the predicted terminators. All parameters were run at default values. The combined results of these predictions are available in Supplementary Data 6 and incorporated into Theta-Base (

sRNA identification

To detect putative sRNAs in B. thetaiotaomicron from our dataset, ANNOgesic (usage: srna) tested transcripts for several criteria. First, detected transcripts were compared with RNAs contained within the sRNA database (BSRD; and the non-redundant protein database (nr database; Homologs identified in the former were classified as putative sRNAs, while those contained in the latter were excluded from further analysis.

The remaining transcripts were further assessed and classified as intergenic sRNA candidates in case of the presence of a defined TSS, a stable secondary structure (folding energy change as calculated by RNAfold and normalized to sRNA length < –0.05), and a length ranging from 30 to 500 nt. Cis-antisense RNAs were identified in a similar manner except that in addition to the above criteria, they originated in antisense orientation to annotated genes. sRNAs sharing a TSS with a mRNA were classified as 5′ UTR-derived if they were associated with a sharp drop in coverage and/or a processing site in front of the cognate CDS. 3′ UTR-derived sRNAs required a TSS or processing site within the 3′ region of the cognate coding gene and either a processing site or shared terminator with the parental mRNA. Intra-operonic sRNAs required a TSS or processing site at the 5′ end as well as a coverage drop or processing site at their 3′ end.

To maximize detection of sRNAs while minimizing the number of false positives, we used a list of known or proposed cis-antisense RNAs from a previous study18 as a benchmark and lowered the minimum average coverage to 5. With this modification, ANNOgesic recovered five out of seven benchmark RNAs (Supplementary Data 2). The high success rate of experimental validation for the identified sRNA candidates from all categories (Fig. 3d) further supports the predictions.

sRNA conservation analysis

We constructed a custom genome database consisting of completed bacterial genomes from the ENA (, accessed 1/12/2017) belonging to class Bacteroidia according to the NCBI Taxonomy (Taxonomy ID: 200643). We then performed an iterative search for each candidate sRNA sequence using nhmmer 3.1b1103, similarly to as previously described104. In each round of iteration nhmmer was run with the flags --popen 0.4999 -E 0.001 --incE 0.001, hit sequences with an E value of 0.001 or less were additionally required to have near-full length alignments not missing more than 10% of sequence length at either end, and the resulting alignment was used as input for hmmbuild and fed into the next round of iteration. The alignments were then manually examined using the RALEE alignment editor105. The final homologous sequences identified for GibS were additionally subjected to realignment and structure prediction using the webserver for aligning structural RNAs (WAR) to improve prediction of secondary structure52.

Northern blotting and qRT-PCR analysis

The sequences of DNA oligonucleotides used for Northern blot and qRT-PCR are given in Supplementary Data 4. Northern blotting was performed as described previously106. Briefly, total RNA (2.5–10 μg) was run on a 6% (vol vol−1) polyacrylamide (PAA)-7 M urea gel and electro-blotted onto Hybond XL membranes (Amersham) at 50 V, 4 °C for 1 h. Blots were probed with 32P-labeled gene-specific oligonucleotides in Hybri-Quick buffer (Carl Roth AG) at 42 °C and exposed as required. Visualization was achieved using a phosphorimager (FLA‐3000 Series, Fuji) and images were quantified using ImageJ107.

For qRT-PCR assays, reverse transcription and PCR amplification were performed in the same reaction mix containing 1 µL of DNase I-treated RNA (adjusted in water to 10 ng µL−1), 5 µL master mix (No ROX SYBR MasterMix blue dTTP kit, Takyon), 0.1 µL of forward and reverse primer (10 µM each), and 0.08 µL reverse transcriptase (One-Step Kit converter, Takyon) per well in a 96-well format. Two technical replicates per each biological replicate were pipetted and plates analyzed on a CFX96 instrument (Biorad).

Primer-extension analysis

Primer-extensions were performed in 20 µL reactions containing 9 µL (10 µg) of DNase I-treated total RNA and 1 µL of 5′ end-labeled DNA oligonucleotide (AWO-348). After an initial denaturation step at 95 °C for 1 min followed by a 5-min incubation on ice, 10 µL of the elongation mix (4 µL 5x first-strand buffer, 0.5 mM dNTP mix, 0.5 µL RNase Inhibitor, and 5 mM DTT) were added to the sample and incubated for 5 min at 42 °C for annealing to occur. Thereafter, 1 µL of the reverse transcriptase (1:1 dilution; SuperScript III, Thermo Fischer Scientific) was added, followed by an incubation for 1 h at 50 °C. The reaction was terminated at 70 °C for 15 min, followed by the addition of 1 µL RNase H. For preparation of the sequencing ladder, oligonucleotides (AWO-347/−348) were used to PCR-amplify the region –50 nt to +87 nt relative to the TSS of GibS from genomic DNA. A sequencing reaction was set up using the labeled oligonucleotide and the DNA cycle sequencing kit (Jena Bioscience) according to the manufacturers’ instructions. Both, sample and sequencing ladder (10 µL each) were electrophoresed on a sequencing gel (10% [vol vol−1] PAA-7 M urea). The gel was dried, exposed, and visualized on a phosphorimager (FLA‐3000 Series, Fuji).

In vitro transcription and radiolabeling of RNA

Primer pairs carrying a T7 promoter and amplifying templates from genomic DNA are listed in Supplementary Data (AWO-241/−311, AWO-329/−313, AWO-331/−332, AWO-333/−334). Similarly, a hexanucleotide substitution (UAAUCU → AUUAGA) in the R2-targeted segment of BT_3893 (‘mut’) was generated by overlap extension PCR using primer pairs AWO-329/−369 and 359/−313. In vitro transcription was carried out using the MEGAscript T7 kit (Ambion) followed by DNase I digestion (1 U, 37 °C for 15 min). The in vitro-transcribed RNA product was extracted from a 6% (vol vol−1) PAA-7M urea gel by comparison to the LowRange RNA ladder (ThermoFisher Scientific) and subsequently eluted in RNA elution buffer (0.1 M NaOAc, 0.1% SDS, 10 mM EDTA) overnight in a thermoblock at 8 °C with shaking at 1400 rpm. The RNA was precipitated using ethanol:NaOAc (30:1) mix, washed with 75% ethanol, and re-suspended in 20 µL water (65 °C for 5 min).

For radioactive labeling, 50 pmol of the in vitro transcript were dephosphorylated using 25 U of calf intestine alkaline phosphatase (NEB) in a 50 µL reaction volume and incubated for 1 h at 37 °C. Following extraction with phenol:cholorform:isoamylalcohol (P:C:I, 25:24:1), the RNA was precipitated as described above. The dephosphorylated RNA (20 pmol) was 5′ end-labeled (20 µCi of 32P-γATP) using 1 U of polynucleotide kinase (NEB) for 1 h at 37 °C in a 20 µL reaction volume. The labeled RNA was purified on a G-50 column (GE Healthcare) and extracted from a PAA gel as above.

Structure and in-line probing

Structure probing was carried out in 10 μL reactions108. Briefly, 5′ end-labeled RNA (0.2 pmol) was denatured at 95 °C for 1 min and chilled on ice for 5 min. 1 μg of yeast RNA was added followed by the addition of 10x structure buffer (Ambion) and the reaction incubated at 37 °C for 10 min, prior to the addition of 2 μL of freshly prepared lead (II) acetate (25 mM; Fluka), 2 μL of RNase T1 (0.01 U μL−1; Ambion) or 2 μL of RNase III (New England Biolabs) and 1 mM DTT. The reactions were incubated for 45 s (lead [II] acetate), 3 min (RNase T1) or 10 min (RNase III), respectively, at 37 °C, stopped by adding 12 μL gel loading buffer II (Ambion), and stored on ice. The alkaline hydrolysis ladder was prepared by incubating 0.4 pmol labeled RNA with 9 μL 1x alkaline hydrolysis buffer (Ambion) and incubated at 95 °C for 5 min. The RNase T1 ladder was prepared by incubating 0.4 pmol labeled RNA in 8 μL of 1x sequencing buffer (Ambion) at 95 °C for 1 min followed by the addition of 1 μL RNase T1 (0.1 U µL−1) and incubation at 37 °C for 5 min. Both reactions were stopped by the addition of 12 μL loading buffer II and stored on ice. Immediately prior to loading, the samples were denatured at 95 °C for 3 min and resolved on an 8% (vol vol−1) PAA-7 M urea sequencing gel. The gel was visualized after appropriate exposure as described above.

In-line probing assays were performed by incubating 0.2 pmol labeled RNA for 40 h at room temperature in 1x in-line probing buffer (100 mM KCl, 20 mM MgCl2, 50 mM Tris-HCl, pH 8.3). RNase T1 and alkaline hydrolysis ladders were prepared as mentioned above. Reactions were stopped by the addition of 10 µL colorless loading dye (1.5 mM EDTA, pH 8, 10 M urea) on ice. Samples were run on a 10% (vol vol−1) PAA-7 M urea sequencing gel and visualized as described above.

Electrophoretic mobility shift assays

EMSAs were performed in 10 μL reactions as described109, containing 1x RNA structure buffer (SB; Ambion), 5′ end-labeled GibS RNA (4 nM final concentration), 1 μg yeast RNA (~4 μM final concentration), and putative target mRNA segments (~150 nt in length) at the following final concentrations: 0, 8, 16, 32, 64, 128, 256, 512, and 1024 nM. The reactions were incubated at 37 °C for 1 h following which 3 μL of 5x native loading dye (0.2% bromophenol blue, 0.5x TBE, 50% glycerol) were added. Electrophoresis of the samples was carried out on a native 6% (vol vol−1) PAA gel in 0.5x TBE buffer at 4 °C and 300 V, for 3 h. The gels were dried and visualized as above.


The Theta-Base website provides an interactive tool to interrogate the transcriptome structure and gene expression profile of B. thetaiotaomicron type strain VPI-5482 as determined in the course of this work. The user interface is implemented in Python using Dash by Plotly42. The Dash app uses the Flask web framework for the back end and is deployed with Gunicorn, a Python WSGI HTTP Server for UNIX. The experimental data are stored in an efficient SQLite database110. The app offers the possibility to create heatmaps of user- or pre-defined lists of coding or noncoding RNAs over the experimental conditions tested in this work (early exponential, mid-exponential, and stationary phase in TYG). The data can be exported to, and modified in, the interactive graphing library Plotly and the heatmaps can be saved. In addition, the website runs an instance of JBrowse43 to explore operon structures, the position of coding and noncoding loci, TSSs, and terminators in the B. thetaiotaomicron transcriptome.

Reporting summary

Further information on research design is available in the Nature Research Reporting Summary linked to this article.