- Open Access
Time-resolved dual RNA-seq reveals extensive rewiring of lung epithelial and pneumococcal transcriptomes during early infection
© The Author(s). 2016
- Received: 19 July 2016
- Accepted: 1 September 2016
- Published: 27 September 2016
Streptococcus pneumoniae, the pneumococcus, is the main etiological agent of pneumonia. Pneumococcal infection is initiated by bacterial adherence to lung epithelial cells. The exact transcriptional changes occurring in both host and microbe during infection are unknown. Here, we developed a time-resolved infection model of human lung alveolar epithelial cells by S. pneumoniae and assess the resulting transcriptome changes in both organisms simultaneously by using dual RNA-seq.
Functional analysis of the time-resolved dual RNA-seq data identifies several features of pneumococcal infection. For instance, we show that the glutathione-dependent reactive oxygen detoxification pathway in epithelial cells is activated by reactive oxygen species produced by S. pneumoniae. Addition of the antioxidant resveratrol during infection abates this response. At the same time, pneumococci activate the competence regulon during co-incubation with lung epithelial cells. By comparing transcriptional changes between wild-type encapsulated and mutant unencapsulated pneumococci, we demonstrate that adherent pneumococci, but not free-floating bacteria, repress innate immune responses in epithelial cells including expression of the chemokine IL-8 and the production of antimicrobial peptides. We also show that pneumococci activate several sugar transporters in response to adherence to epithelial cells and demonstrate that this activation depends on host-derived mucins.
We provide a dual-transcriptomics overview of early pneumococcal infection in a time-resolved manner, providing new insights into host-microbe interactions. To allow easy access to the data by the community, a web-based platform was developed (http://dualrnaseq.molgenrug.nl). Further database exploration may expand our understanding of epithelial–pneumococcal interaction, leading to novel antimicrobial strategies.
- Streptococcus pneumoniae
- Dual RNA-seq
- Host-microbe interaction
- Lung epithelial cells
- Systems biology
Lower respiratory tract infections (LRTIs), or pneumonia, claim more lives than any other communicable disease worldwide; the main etiologic agent behind this infection is the Gram-positive opportunistic pathogen Streptococcus pneumoniae (pneumococcus) . Normally part of the human nasopharyngeal microflora, S. pneumoniae can invade the lower airways where it provokes host inflammatory and immune responses . At the earliest stage of infection, pneumococcus adheres to epithelial cells and interacts intimately with the epithelium . Meanwhile, host and microbe cross-communicate and simultaneously affect each other in a disruptive manner [2, 4]. This interspecies interaction activates numerous processes in epithelial and pneumococcal cells [5, 6]. To obtain comprehensive and meaningful biological knowledge of the infection processes involved in pathogenesis, simultaneous monitoring of the transcriptome changes in both species is required .
Lung epithelial cells perform vital roles during infection. First, the cells form a physical barrier to the external environment. On top of these cells, a thick layer of epithelium-derived mucus offers extra protection that traps and removes pathogens . Mucins, the main component of mucus, are large glycoprotein polymers rich in sialic acids and other aminosaccharides . Additionally, epithelial cells kill pathogens directly by producing antimicrobial peptides, e.g., defensins and cathelicidins . Moreover, epithelial cells regulate innate immune responses by secreting a wide array of pro-inflammatory cytokines that recruit neutrophils and activate macrophages . Finally, epithelial cells activate adaptive immune cells, including dendritic cells and T cells, via chemokine expression .
Pneumococcal adherence to epithelial cells is the first necessary step to pathogenesis . In order to adhere, pneumococcus must quickly shed the thick exopolysaccharide capsule, which protects against phagocytes [14, 15]. The shedding exposes surface adhesion factors and desensitizes the bacterium from antimicrobial peptides [16, 17]. Subsequently, S. pneumoniae must acquire nutrients to support growth and, at the same time, evade host immune responses . Pneumococcal factors may be involved in multiple processes; e.g., PsaA, a surface-exposed protein, acts concurrently as adhesion factor and manganese transporter . The scarce manganese  helps in neutralizing reactive oxygen species (ROS) and in bacterial fitness .
Interspecies interaction during infection is a complex process which necessitates rapid and massive adaptation for epithelial and pneumococcal survival. During the adaptation, transcriptional changes are a focal point, in both the host  and pathogen . RNA-sequencing (RNA-seq) delivers genome-wide quantitative snapshots of the transcriptome . In a thought experiment, Vogel and co-workers argued that simultaneous profiling of host and pathogen transcriptomics by dual RNA-seq might provide valuable insights for infection biology . Recent dual RNA-seq studies were successful in elucidating the host–pathogen regulatory network in Candida albicans , the role of small RNAs (sRNAs) in the intracellular pathogen Salmonella typhimurium , cross-talk in the Gram-negative LRTI pathogen Haemophilus influenzae , and transcription profiles in the protozoan Leishmania major  during infection.
Here, we exploited the dual RNA-seq approach to simultaneously monitor the transcriptome cross-talk between lung alveolar epithelial cells and pneumococci during early infection. Due to the transient and highly dynamic nature of the transcriptome , we monitored the transcriptional changes in a time-resolved manner. Moreover, since pneumococcal adherence to epithelial cells determines the outcome of early infection, we compared a mostly adherent unencapsulated mutant and mostly non-adherent wild-type encapsulated S. pneumoniae strain to allow specific transcriptional interrogation on adherence. Additionally, we confirmed our dual RNA-seq gene expression data by quantitative real-time PCR (qRT-PCR) and quantitative fluorescence microscopy to visualize pneumococcal proteins and thereby confirm several novel biological observations identified in the dataset. Finally, we developed a user-friendly online database (http://dualrnaseq.molgenrug.nl), giving access to our detailed time-resolved dual transcriptome data to the pneumococcal, microbiology, immunology, and pulmonology research communities.
Model of early pneumococcal infection of epithelial cells
To analyze the time-resolved dual RNA-seq dataset, a combination of freely available bioinformatics tools was used (Fig. 1f). First, raw reads were trimmed  and aligned  to a chimeric genome containing the concatenated genome of Homo sapiens (Ensembl, release 84) and S. pneumoniae (Ensembl, release 31, bacteria 13 collection ). One-step mapping was chosen to minimize rates of false negatives. Reads were then separately counted  and classified as either epithelial or pneumococcal. Following differential gene expression analysis, three groups of genes were removed (see “Dual RNA-seq generates high-quality datasets with clusters of epithelial and pneumococcal co-expressed genes” below) and unbiased automatic clustering  and functional enrichment were performed [36, 37].
Dual RNA-seq generates high-quality datasets with clusters of epithelial and pneumococcal co-expressed genes
To simplify further analyses, we excluded three gene fractions (Fig. 2b). First, we removed unexpressed genes, i.e., those without any counts in all libraries (13,925 (23 %) epithelial genes and none of the pneumococcal genes). The relatively large fraction of unexpressed epithelial genes might be due to the relatively low sequence coverage (average coverage of 1.8). Nevertheless, it is in accordance with recent studies on the human epithelial transcriptome [39, 40]. Second, we excluded genes that were differentially expressed (p < 0.05, adjusted p value by DESeq2) at 0 mpi between unencapsulated (∆cps2E) and encapsulated (wild-type) libraries. While 17 epithelial genes were removed, 409 (20 %) pneumococcal genes were already differentially expressed at 0 mpi. Although a polar effect due to cps2E disruption can explain differential expression of genes in the 17-kb-long cps operon, it remains unknown why other genes were differentially expressed. We speculate that constructing the thick exopolysaccharide capsule requires specific transcriptional fine-tuning of numerous genes outside the cps locus. Finally, we removed genes with no significant difference (p > 0.05) and genes with fold changes (FC) less than 2 in all comparisons (Additional file 1: Figure S2). In total, the epithelial working libraries contained 4337 (7 % of total) genes and the pneumococcal working libraries 860 (41 % of total) genes.
To compare gene expression, we normalized expression values using DESeq2  and centered and clustered the values . Note that differential gene analysis was performed before excluding any of the gene fractions (Fig. 1f). The centered normalized values were visualized as heat maps, divided into two panels, one for each bacterial strain. Strikingly, heat maps showed obvious clusters of co-expressed genes and clear gene expression differences between adhering (∆cps2E) and less-adhering (wild type) bacteria (Fig. 2c, d). Specifically, the left panel of Fig. 2c shows the epithelial transcriptional response when exposed to encapsulated S. pneumoniae at different time points (30, 60, 120 and 240 mpi) while the right panel displays the response when in contact with the unencapsulated strain. Vice versa, co-expressed clusters of pneumococcal genes are differentially expressed when the bacteria were in contact with human epithelial cells (Fig. 2d).
Making raw data publicly available has been common practice in recent years, as we have done for this project (Gene Expression Omnibus (GEO) accession number GSE79595). Unfortunately, publicly available datasets are not directly explorable for the extraction of biological insights for the majority of researchers. Therefore, we built an easily accessible online platform which hosts the complete dual RNA-seq database (http://dualrnaseq.molgenrug.nl). To access and visualize the data, users can simply select the gene of interest (or multiple genes of interests) and examine their expression during early infection (Additional file 1: Figure S3). Expression data can be downloaded and opened in common spreadsheet software, e.g., Microsoft Excel®. To visualize expression, users can choose from three normalization methods: DESeq2 normalization , TPM (transcript per million , and log2-transformed TPM values.
Validation of dual RNA-seq by qRT-PCR and pneumococcal protein fusions
Since transcript levels do not necessarily correspond with protein expression [44, 45], we quantified four pneumococcal protein levels whose genes showed upregulation during adherence to epithelial cells. We fused a fast-folding variant of the green fluorescent protein (GFP) to the carboxyl termini of SPD_0475, SPD_0963, SPD_1711, and SPD_1716 at their own locus while preserving all upstream regulatory elements (Fig. 3b). We transformed these constructs into an unencapsulated strain constitutively expressing a red fluorescent protein (RFP) fused to a housekeeping gene (hlpA_hlpA-rfp) . SPD_0475 encodes a 204 amino acid CAAX amino terminal protease with unknown function, SPD_0963 encodes a 45 amino acid hypothetical protein, SPD_1711 (132 amino acids) was described as a single-stranded DNA binding protein and may assist in competence , and SPD_1716 is a 63 amino acid ortholog of cell wall or choline - binding protein in other Streptococcaceae.
We imaged adherent S. pneumoniae with fluorescence microscopy during the indicated time points (Fig. 3c). Since (i) RFP serves as an accurate proxy for cell number and viability , (ii) hlpA does not change during early infection (p > 0.05, FC < 2), and (iii) the ratio between GFP and RFP indicates relative expression of the protein of interest (red circle and line, Fig. 3d), we were able to quantify the proteins of interest. Gene expression values from the dual RNA-seq data (blue circles and line, Fig. 3d) show a degree of correlation with protein level in three out of the four cases, suggesting that pneumococcal transcriptional changes reflect, to some extent, changes in protein level .
Pneumococcal ROS induce expression of glutathione-mediated detoxification genes in epithelial cells
Glutathione, a tripeptide of glutamic acid, cysteine, and glycine, is produced and secreted by epithelial cells . This vital molecule is biosynthesized through amino acid polymerization and, in the presence of ROS (e.g., hydrogen peroxide, lipid superoxide, or oxygen radicals), it readily donates an electron or hydrogen atom to quench them. The process is assisted by ligands and glutathione peroxidase (GPX2). Oxidized glutathione can be recycled by glutathione reductase (GSR) dependent on NADPH (Fig. 4b). Alternatively, glutathione conjugates and neutralizes ROS . Expression of eight glutathione-associated genes showed a sustained significant increase in epithelial cells exposed to the encapsulated strain (p < 0.05, 60 versus 30 mpi; Fig. 4c).
To validate the abovementioned finding, we repeated the experiment, isolated total RNA, and performed qRT-PCR on four genes: GPX2, involved in detoxification, and GSR, IDH1, and PGD, involved in glutathione recycling. As expected, we observed significant upregulation of these genes between 30 and 60 mpi (Fig. 4d). Interestingly, Rai et al. showed that pneumococcal supernatant is sufficient to instigate DNA breaks caused by oxidative damage in A549 lung cells . To test whether the glutathione-dependent reactive oxygen detoxification pathway could be upregulated by S. pneumoniae supernatant, we incubated epithelial cells with filtered pneumococcal supernatants. As shown in Fig. 4d, the genes were indeed activated. To establish that pneumococci-derived ROS was behind the response, we added the antioxidant resveratrol (100 μM) to the epithelial–pneumococcal model and did not observe activation (Fig. 4d). Together, these results partly explain the findings of Rai et al.  and reveal that lung epithelial cells try to counter the ROS produced by S. pneumoniae by upregulating glutathione biosynthesis.
Pneumococcal transcriptional adaptation in response to epithelial cells
We clustered pneumococcal genes of the working library based on centered normalized gene expression in response to co-incubation with epithelial cells . Clusters of genes were then categorized based on their reported functions [36, 50–52].
Another gene cluster showed repression of gene expression at 30 mpi followed by increased expression at later time points. Seventeen genes encoding transporters are members of this cluster  (Fig. 5c). Various substrates have been reported to be transported by the transporters, including iron (SPD_0917/8), amino acids (brnQ), sugars (SPD_0740/1), and ions (SPD_1436). Song et al.  reported repression of SPD_0740, which encodes a sugar transporter, at the same time point (30 mpi). In our data, however, significant repression (p < 0.05) at 30 mpi occurred only in the unencapsulated and not the wild-type strain.
Figure 5d depicts a cluster of genes with a late activation profile starting at 60 mpi, continuing to 120 mpi and plateauing at 240 mpi. The profile is shared by 45 genes belonging to the competence regulon . While Orihuela et al.  reported that only three competence genes (ccs4, dprA, and cinA) were activated in their study, we observed massive gene activation involving most of the competence genes in our model. Furthermore, we fused gfp to one of the competence genes, SPD_1711 (ssbB), under its own promoter and followed its expression using fluorescence microscopy. As shown in Fig. 3c, d, the protein level increased over time during early infection starting at 80 mpi, in line with increased gene expression occurring at 60 mpi.
Interestingly, a cluster containing genes of unknown function showed a varied profile, including early activation at 30 mpi, repression at 30 mpi, and later sustained activation starting at 60 mpi (Fig. 5e). Specifically, two genes (SPD_1426 and SPD_2043) were activated under our experimental conditions and were previously reported as being activated during infection using S. pneumoniae strain TIGR4 (SP1601 and SP2216, respectively) . A complete list of genes and fold changes is available as Additional file 2: Table S1.
Adherent S. pneumoniae repress the epithelial innate immune response
CXCL8 (IL8), encoding interleukin-8, was one of the repressed immunity genes. CXCL8 is a potent chemoattractant for neutrophil and other granulocytes. Interestingly, at 60 mpi, ∆cps2E-exposed epithelial cells expressed 2.8 ± 1.2 less CXCL8 than epithelial cells exposed to wild-type S. pneumoniae (Fig. 6c). This difference was validated by qRT-PCR (Fig. 6d). Further, we asked whether CXCL8 repression is an active process or merely mediated by physical adherence. To assess this, we co-incubated heat-inactivated ∆cps2E and heat-inactivated wild-type pneumococci with epithelial cells. Note that heat inactivation preserves pneumococcal epitope and protein structures . CXCL8 was still significantly repressed by dead ∆cps2E but not by dead wild-type pneumococci (Fig. 6d), suggesting that CXCL8 repression is independent of viability but dependent on the presence of the capsule or on the accessibility of surface-exposed (protein) factors in the absence of capsule. Intriguingly, Graham and Paton  showed that epithelial interleukin-8 production and release was suppressed by pneumococcal surface protein CbpA and incubation with ∆cbpA leads to higher CXCL8 expression. We speculate that the absence of the capsule in ∆cps2E increases accessibility of pneumococcal surface-exposed factors, including CbpA, to epithelial receptors, leading to repression of CXCL8.
DEFB1, encoding β-defensin-1, is an important epithelial-derived, constitutively expressed antimicrobial peptide . In our model, however, DEFB1 was not expressed constitutively but repressed 3.0 ± 1.2 times (p < 0.05, 60 mpi) in ∆cps2E-exposed epithelial cells compared with wild type-exposed cells (Fig. 6c, validated in Fig. 6d). Additionally, while heat-inactivated wild type pneumococci stimulated comparable levels of DEFB1 compared to viable wild-type bacteria, non-viable ∆cps2E repressed DEFB1 expression even more (p < 0.05) than viable ∆cps2E (Fig. 6d). We conclude that DEFB1 expression is affected by adherence, accessibility of pneumococcal surface proteins, and pneumococcal viability by an as of yet unknown mechanism. In summary, we show that adherent pneumococci modulate epithelial expression of innate immunity genes, including CXCL8 and DEFB1, mediated by pneumococcal surface factors.
Adherent S. pneumoniae activate sugar importers
At 60 mpi, 12 carbohydrate transporters were differentially expressed (p < 0.05, FC > 2) between ∆cps2E and encapsulated pneumococci exposed to epithelial cells. In the presence of high glucose (2 g/L), ∆cps2E expressed 1.5-fold less manLM, encoding glucose transporters, than encapsulated S. pneumoniae (Fig. 7d). Moreover, eight importers were activated in the adherent strain compared to the mostly free-floating encapsulated strain. The eight non-glucose transporter-genes and their substrates are SPD_0089 (disaccharides: galactose, mannose, N-acetylmannosamine), celC (disaccharides: cellobiose, gentiobiose), SPD_0232/33/34 (disaccharides: cellobiose), SPD_0295 (disaccharides: lactose and lactulose), rafE (oligosaccharides: raffinose, stachyose, melliobiose) and malD (polysaccharides: maltotitriol, maltodextrine, glycogen) (Fig. 7d). At the same time, four genes were repressed in unencapsulated S. pneumoniae exposed to human epithelial cells, glpF (glycerol) and SPD_0740/41/42 (ribonucleosides). We selected three transporter genes, malD (polysaccharides), rafE (oligosaccharides), and SPD_0234 (disaccharides), and validated the abovementioned observations by qRT-PCR (Fig. 7e).
Our data indicate that adherent unencapsulated bacteria detect non-glucose sugars in their immediate vicinity. Epithelial mucus may provide non-glucose carbohydrates [60, 61] and simultaneously limit the interaction of epithelial cells with encapsulated wild-type bacteria . We then removed epithelial-associated mucus by washing the surface with warm PBS and observed that the genes were no longer activated (FC < 2; Fig. 7e). Next, we incubated pneumococcal strains with type III porcine mucin (5 g/L), mimicking complex carbohydrates in the medium. Interestingly, the importers were not differentially expressed between strains (FC < 2), indicating similar access to non-glucose sugars (Fig. 7e). We conclude that following adherence to epithelial cells, S. pneumoniae bacteria sense host-derived non-glucose carbohydrates and, in turn, activate expression of genes encoding transporters to import the now-available sugars.
Early infection is a complex and disruptive encounter between host and pathogen. In both species, a multitude of transcriptionally mediated cellular processes are fine-tuned, being activated, maintained, and repressed to ensure survival. The recently described dual RNA-seq approach allows simultaneous host–pathogen monitoring during their interaction [25–28]. In this study, we exploited the approach by applying dual RNA-seq to a model of pneumococcal infection of human lung alveolar epithelial cells. We have generated a detailed time-resolved dataset of epithelial–pneumococcal transcriptomes up to 4 h after infection. Moreover, we have validated the rich dataset by qRT-PCR and quantitative fluorescence microscopy. Furthermore, we have shown that adherence-specific transcriptional responses in host and pathogen can be identified by comparing the transcriptomes of lung epithelial cells in the presence of either encapsulated or unencapsulated pneumococci. Since adherence is the first step towards pathogenesis, adherence-specific regulated genes might provide interesting novel drug and/or vaccination targets that have not yet been picked up by conventional screens aimed at targeting essential and/or surface exposed proteins.
Our early infection model recapitulated three major in vivo characteristics of pneumococcal infection: pneumococcal adhesion, bacterial multiplication, and epithelial responses to the pneumococcus. Our model recapitulated these infection characteristics: (i) adherence for both encapsulated and unencapsulated pneumococci (Fig. 1); (ii) pneumococcal viability and growth during early infection, e.g., generation of ROS, activation of competence, and expression of carbohydrate importers (Figs. 4, 5 and 7); and (iii) host response to pneumococcal presence, e.g., glutathione-associated detoxification and innate immune responses (Figs. 4 and 6). Furthermore, as shown by upregulation of carbohydrate transporters (Fig. 7), pneumococci sense the presence of the epithelium and subsequently adapt their transcriptome.
Remarkably, we observed that all pneumococcal genes are expressed at one point or another during the infection process (Fig. 2). While this observation might partly stem from the high sequencing depth undertaken here (494 to 1588× for the pneumococcal genome, average coverage 1120×) the genome-wide bacterial gene expression confirms recent reports on bacteria adapting to multiple conditions [63, 64]. We speculate that interspecies interaction necessitates massive pneumococcal transcriptional adaptation. Moreover, we have observed activation of detoxification genes (GPX2 and GSR) in epithelial cells, protecting these cells against pneumococci-derived ROS (Fig. 4). Indeed, S. pneumoniae has been reported to secrete high levels of peroxides as a by-product of its pyruvate metabolism  and has recently been shown to cause DNA damage-dependent apoptosis in alveolar lung epithelial cells . Future work should also examine whether small non-coding RNAs play a role in pneumococcal early infection as they do in Salmonella , something beyond the scope of the current study. The hybrid column-based RNA isolation method we developed here to simultaneously recover high quality eukaryotic and prokaryotic total mRNA does not, unfortunately, allow the effective inclusion of small RNA species. In addition, the D39 genome is poorly annotated for snRNAs, further hindering differential sRNA analysis in our model. Future work may benefit from column-independent RNA isolation methods coupled with sufficient sequencing depth and transcriptome assembly to identify pneumococcal sRNAs important for infection.
Using array-based technology, Bootsma et al.  were the first to interrogate genome-wide transcriptional responses of human epithelial cells to S. pneumoniae. They reported that epithelial immunity and apoptosis genes are activated at 2 h post-infection. Here, we confirmed their observations and find that subsets of immunity and apoptotic genes displayed complex expression profiles in response to pneumococci, including repression followed by an immediate rebound, and activation followed by deactivation (Additional file 1: Figure S5 and Additional file 2: Table S6). In response to co-incubation with epithelial cells, pneumococcus adapts its transcription and adherence factors, transporters, and competence, among others, are activated (Fig. 5). Transcriptional activation of transporters has been reported in previous array-based studies of pneumococci infecting epithelial cells [6, 55, 56]. Nevertheless, by exploiting time-resolved simultaneous monitoring of host and pathogen, the dynamics underlying differential gene expression can be observed in greater detail. It should be noted that comparing specific results between two infection studies can be problematic. Aside from different technologies to monitor gene expression (qRT-PCR versus RNA-seq versus microarrays), numerous details, such as multiplicities of infection, history of epithelial cells, pre-treatment of the host and pathogen, infection medium, and pathogen strains can add layers to the complexity. In this regard, it is satisfying to note that many of the here-observed transcriptional responses have also been documented previously using different experimental set-ups.
The model used here could be expanded further by incorporating relevant LRTI agents. For example, alveolar macrophages and epithelial cells together form the epithelium lining the lower respiratory tract. The cells reciprocally influence cellular phenotypes and behaviors , highly relevant to infection. Moreover, pneumococcal co-infection and secondary infection with, for instance, influenza virus or H. influenzae are not unheard of [67–69]. Incorporation of other agents into the model and exploiting dual (or triple and quadruple) RNA-seq approaches may provide novel insights into respiratory infection.
Besides its relevance in communicable diseases, gained insights into pneumococcal infection are also applicable to understanding several non-communicable respiratory diseases. Asthma, the most common chronic respiratory disease, is a major risk factor for pneumococcal infection . Additionally, chronic obstructive pulmonary disease (COPD)  and cigarette smoking  have been reported to increase the risk of pneumococcal LRTI. Here, we report the first study to show simultaneous transcriptomic changes of the pathogen S. pneumoniae and human lung alveolar epithelial cells during early infection, which might aid in identifying new biomarkers and drug targets to combat infection.
Though transcriptome rewiring is a focal point during interspecies interaction [22, 23], non-transcriptional regulation plays an important part during early infection. Capsule shedding, a hallmark of pneumococcal infection, is regulated by autolysin-A (LytA). LytA is activated when the bacterium encounters alveolar cathelicidin , which is independent of transcriptional regulation. Heterogeneity of cellular responses is another confounding factor . Recently, dual RNA-seq combined with cell sorting was used to identify heterogeneous activity of Salmonella virulence factors that, in turn, drives a heterogeneous interferon response in macrophages . This highlights the relevance of noise in gene expression and cell-to-cell variability in host–pathogen interactions. Furthermore, whole organism infection models offer a more systemic perspective. For instance, the dual RNA-seq approach has been used to monitor infection of wheat by bacteria  and mosquitoes by filaria . Whole organism dual RNA-seq is not without its challenges, including averaging (host) effects to gene expression across all cell types.
We have shown that a time-resolved dual RNA-seq approach can identify novel cellular processes during pneumococcal early infection. Furthermore, we have made the time-resolved dual transcriptomics dataset available to the broader research community (http://dualrnaseq.molgenrug.nl). We invite pneumococcal researchers to use the database to formulate research questions in the development of preventive and curative strategies against pneumococcal infection. Finally, we invite researchers from the fields of microbiology, immunology, and pulmonology to access the dataset and use it to develop their own hypotheses.
Culture of the epithelial cell line and S. pneumoniae D39 and pneumococcal transformation
Human type II lung epithelial cell line A549 (ATCC® CCL-185) and S. pneumoniae D39 were routinely cultured without antibiotics. Strain construction is described in detail in Additional file 1: Supplemental methods. Oligonucleotides are listed in Additional file 2: Table S2 and strains in Additional file 2: Table S3.
Confluent monolayers of A549 were co-incubated with S. pneumoniae D39 at a MOI of 10 in 1 % fetal bovine serum in RPMI1640 medium without phenol red. Prior to infection, epithelial monolayers were kept for 10 more days after confluence. To optimize cell-to-cell contact, centrifugation was employed (2000 × g, 5 min, 4 °C). Adherence assays were performed by enumeration of plated colony-forming units in blood agar. More details are given in Additional file 1: Supplemental methods.
Simultaneous total host–pathogen RNA isolation
On sterile, tissue culture-treated six-well plates (BD Falcon, The Netherlands), A549 was seeded until confluence and maintained (37 °C, 5 % (v/v) CO2) for another 10 days. Wild-type S. pneumoniae D39 and ∆cps2E were grown in C + Y medium to OD600nm ~0.2 and the medium was replaced with infection medium. As described, five time points were selected: 0, 30, 60, 120, and 240 mpi. Six technical replicates (individual wells) were pooled into one biological replicate. Two biological replicates were used for each time point, except for 240 mpi. To minimize transcriptional changes during sample handling, we did not separate the cellular mixture (epithelial cells, adherent pneumococci, and free-floating pneumococci). Rather, we simultaneously harvested the cells and isolated total RNA. To harvest the total RNA from host and pathogen at the same time, we treated the cellular mixture with a concentrated solution of ammonium sulfate to prevent any protein-dependent RNA degradation . Each milliliter of the ammonium sulfate solution (pH 5.2) contained 0.7 g (NH4)2SO4. The saturated solution also contained 20 mM EDTA and 25 mM sodium citrate. Three parts of saturated solution of ammonium sulfate was added directly to one part of medium. The suspension was vigorously pipetted to ensure the complete mixing of the ammonium sulfate solution and infection medium. Adherent host cells were scraped off (sterile, TPP, VWR, The Netherlands) and incubated further (room temperature, 5 min). The suspension was collected and centrifuged at full speed (20 min, 4 °C, 10,000 × g). The supernatant was removed and the cell pellet was snap-frozen with liquid nitrogen. The cell mixture contained host cells, adherent bacteria, and non-adherent bacteria; the last two fractions were of varying proportions depending on the duration of co-incubation and the absence/presence of capsule.
To disrupt cells, bead beating was used. In a 1.5 ml screw cap tube, a PCR tube full of sterile, RNase-free glass beads (100 μm) were added together with 50 μl 10 % SDS and 500 μl phenol-chloroform. In the meantime, the frozen cell pellet was resuspended in TE solution (10 mM Tris-HCl, 1 mM Na2DTA, pH 8.0) treated with DEPC (diethylpyrocarbonate). The cell suspension was added into the screw cap tube and bead beaten three times for 45 s each. Tubes were immediately placed on ice and centrifuged at full speed at 4 °C to separate the organic and aqueous phases. The aqueous phase was pipetted out and back-extraction was performed on the organic phase to optimize RNA yield. The subsequent part of the RNA isolation was performed based on the High Pure RNA Isolation Kit (Roche, The Netherlands). The aqueous phase from the phenol-chloroform extraction was mixed well with binding buffer and pipetted into the upper chamber of the column and centrifuged. DNase mix was then added onto the filter and incubated at room temperature for 30 min to digest total genomic DNA. Total RNA was eluted according to the manufacturer’s protocol. The quality of total RNA was assayed by Nanodrop and a 1 % bleach gel was employed to interrogate genomic DNA and host–pathogen rRNA bands (host, 28S, 5 kbp and 18S, 1.8 kbp; pathogen, 23S, 2.9 kbp and 16S, 1.5 kbp). Relative enrichment of pneumococcal reads in dual RNA-seq may stem from the total RNA isolation protocol. We developed the protocol from an existing protocol for pneumococcal RNA isolation. We expanded this protocol to accommodate RNA isolation from epithelial cells. We speculate that the first step involving organic–aqueous liquid–liquid separation may favor isolating more pneumococcal RNAs with different characteristics than epithelial RNAs. RNA liquid–liquid separation ultimately depended on pH and ion strength of the aqueous phase .
Library preparation, sequencing, data pipeline, and online database
Human and pneumococcal ribosomal RNAs were simultaneously depleted (“dual rRNA depletion”) by a 1:1 mixture of human/mouse/rat and Gram-positive bacteria capture probes (Ribo-Zero rRNA Removal Kits, Illumina, US). Stranded cDNA library preparation was performed with the TruSeq® Stranded Total RNA Sample Preparation Kit (Illumina, US) according to the manufacturer’s protocol. cDNA sequencing of the 18 samples was performed in three lanes (six samples per lane) of Illumina NextSeq 500 with a HighOutput Flowcell in 75 single end mode. Samples were de-multiplexed and analyzed further. The raw fastq data are accessible at http://0-www.ncbi.nlm.nih.gov.brum.beds.ac.uk/geo/ with accession number GSE79595.
The quality of raw reads was checked by FastQC v0.11.5 (Babraham Bioinformatics, UK) . To improve the quality of reads and remove adapter sequences, we trimmed the reads in single end mode using these criteria: (i) adapter sequences removed based on TruSeq3-SE library; (ii) leading nucleotide with low quality removed; (iii) low quality trailing nucleotide removed; (iv) a five-nucleotide sliding window in which the average quality score must be above 20; and (v) with a minimum read length of 50 . The trimmed reads were again checked by FastQC. To align the reads, we generated a chimeric genome by concatenating the S. pneumoniae D39 genome (ENSEMBL, release 31, bacteria 13 collection, date of download 13 June 2016)  as an extra chromosome of Homo sapiens (ENSEMBL, release 84, date of download 13 June 2016) . The corresponding annotation files were downloaded from the aforementioned repositories. To ensure an undisrupted mapping of SPD_0001, a pneumococcal gene located at the very beginning of the pneumococcal genome sequence file, we copied the first 600 bp of the pneumococcal genome to the end of the genome and annotated this extra copy as SPD_0001a. Alignment of trimmed reads to the chimeric genome was performed by STAR, with the following options: (i) alignIntronMax 1 and (ii) sjdbOverhang 49 . The subsequently mapped reads were then counted  according to the chimeric annotation file in (i) multimapping mode (-M), in which fractional count was reported (--fraction), (ii) allowing for overlapping reads across features to accommodate bacterial operons (iii) in a stranded option.
Subsequently, we separately analyzed host and pathogen libraries in R-studio (R v3.3.1). We performed differential gene expression analysis on rounded raw count by DESeq2 . Epithelial and pneumococcal libraries were normalized by DESeq2: epithelial reads by regularized logarithm and pneumococcal reads by variance-stabilizing transformation. Aside from DESeq2-transformed counts, the rounded raw counts were transformed into TPM (transcripts per million) and log-transformed TPM . The three transformed counts are used to visualize gene expression level in our online database (http://dualrnaseq.molgenrug.nl).
Unexpressed genes were removed from the working libraries, i.e., genes with no reads in any of the libraries. Furthermore, we removed genes with significant differences between unencapsulated (∆cps2E) and encapsulated (wt) libraries at 0 mpi and genes with no significance (p > 0.05) and FC < 2 from the aforementioned contrasts (Additional file 1: Figure S3). Genes with significant fold changes (p > 0.05, FC > 2) are listed in Additional file 2: Table S4: Epithelial differential gene expression and Additional file 2: Table S5: Pneumococcal differential gene expression. NA notes FC < 2.
Soft clustering was used on normalized centered gene expression values with a fuzzifier value of 1.5 to obtain a better view of the dynamics of gene expression during infection . The number of clusters was approximated by a built-in function and further adjusted until a suitable number of clusters appeared, i.e., without any empty group. Enrichment of GO for host genes was analyzed by amiGO ver. 2.4 .
The database can be accessed at http://dualrnaseq.molgenrug.nl. The data are stored in a MySQL database containing both human and S. pneumoniae gene expression values. Gene expression graphs during early infection are generated by D3 (Data Driven Documents, https://d3js.org). Gene expression is presented in DESeq2-normalized values , TPM (transcripts per million)  or log-transformed TPM.
qRT-PCR and quantitative fluorescence microscopy
Infection studies were repeated, total RNA isolated, and qRT-PCR performed. For fluorescence microscopy, infection studies were performed in eight-well μ-slides (Ibidi, Germany). More details are provided in Additional file 1: Supplemental methods.
We thank W.J. Quax and R. Setroikromo (UMCG, Groningen) for the human cell line, V. Benes and B. Haase (GeneCore, EMBL, Heidelberg) for sequencing support, M. Kjos for fruitful discussions, A. de Jong for bioinformatics support, and S. El Aidy and L.E. Keller for comments on the manuscript.
Work in the Veening lab is supported by the EMBO Young Investigator Program, a VIDI grant (864.12.001) from the Netherlands Organization for Scientific Research, Earth and Life Sciences (NWO-ALW), and ERC Starting Grant 337399-PneumoCell.
Availability of data and materials
The datasets supporting the conclusions of this article are available in the GEO repository, accession number GSE79595, http://0-www.ncbi.nlm.nih.gov.brum.beds.ac.uk/geo/query/acc.cgi?acc=GSE79595.
The source code for the web platform of this article is available in Zenodo, http://0-dx.doi.org.brum.beds.ac.uk/10.5281/zenodo.61075. Licensed under Creative Commons Attribution-Non Commercial.
RA and JWV designed the research, analyzed the data, and wrote the article. RA performed research, JS analyzed the data, SH built the online database. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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