Skip to main content
Download PDF

Transcriptomic analysis of caecal tissue in inbred chicken lines that exhibit heritable differences in resistance to Campylobacter jejuni

BMC Genomics volume 22, Article number: 411 (2021) Cite this article

Abstract

Background

Campylobacter jejuni is the leading cause of bacterial gastroenteritis in humans and the handling or consumption of contaminated poultry meat is a key source of infection. Selective breeding of poultry that exhibit elevated resistance to Campylobacter is an attractive control strategy. Here we studied the global transcriptional response of inbred chicken lines that differ in resistance to C. jejuni colonisation at a key site of bacterial persistence.

Results

Three-week-old chickens of line 61 and N were inoculated orally with C. jejuni strain M1 and caecal contents and tonsils were sampled at 1 and 5 days post-infection. Caecal colonisation was significantly lower in line 61 compared to line N at 1 day post-infection, but not 5 days post-infection. RNA-Seq analysis of caecal tonsils of both lines revealed a limited response to C. jejuni infection compared to age-matched uninfected controls. In line N at days 1 and 5 post-infection, just 8 and 3 differentially expressed genes (DEGs) were detected (fold-change > 2 and false-discovery rate of < 0.05) relative to uninfected controls, respectively. In the relatively resistant line 61, a broader response to C. jejuni was observed, with 69 DEGs relating to immune regulation, cell signalling and metabolism at 1 day post-infection. However, by day 5 post-infection, no DEGs were detected. By far, the greatest number of DEGs were between uninfected birds of the two lines implying that differential resistance to C. jejuni is intrinsic. Of these genes, several Major Histocompatibility Complex class I-related genes (MHCIA1, MHCBL2 and MHCIY) and antimicrobial peptides (MUC2, AvBD10 and GZMA) were expressed to a greater extent in line N. Two genes within quantitative trait loci associated with C. jejuni colonisation were also more highly expressed in line N (ASIC4 and BZFP2). Quantitative reverse-transcriptase PCR analysis of a subset of transcripts confirmed the RNA-Seq results.

Conclusions

Our data indicate a limited transcriptional response in the caecal tonsils of inbred chickens to intestinal colonisation by Campylobacter but identify a large number of differentially transcribed genes between lines 61 and N that may underlie variation in heritable resistance to C. jejuni.

Peer Review reports

Background

Campylobacter is estimated to have caused 95 million cases of acute gastroenteritis in humans in 2010, with the loss of 21,000 lives and 2.1 million disability-adjusted life years [1]. In the United Kingdom alone, 63,946 laboratory-confirmed cases of human campylobacteriosis were recorded in 2017 [2] and a further 9.3 cases were predicted to be unreported for every one captured by national surveillance [3]. Such infections have been estimated to cost the UK economy approximately £50 million per annum through lost productivity and healthcare costs [4]. Campylobacter infections in humans often involve watery diarrhoea, abdominal cramps and nausea but generally resolve within a week [5]. However, infections can relapse and severe sequelae exist, including inflammatory neuropathies such as the Guillain-Barré syndrome [5].

Source attribution studies unequivocally implicate the handling or consumption of contaminated poultry meat as a key risk factor for human campylobacteriosis, with up to 80% of cases thought to be attributable to the avian reservoir [6, 7]. The caeca are a key site of persistence of Campylobacter in poultry, where numbers of C. jejuni can reach as high as 1010 colony forming units (CFU)/g of contents in the absence of overt pathology. Given such levels, contamination of carcasses with numbers of C. jejuni predicted to be adequate for human infection is challenging to prevent during the slaughter process [8]. A recent survey in the United Kingdom found that 54% of fresh retail chicken was contaminated with Campylobacter [9]. Birds generally become colonized with C. jejuni from their environment, and across Europe the prevalence of C. jejuni positive flocks ranges from 18 to 90%, with seasonal variation and the highest levels occurring in the summer months [10]. Control of Campylobacter in poultry primarily relies on stringent on-farm biosecurity measures and carcass treatments. No commercial vaccines exist and it is likely that a multifactorial approach will be required.

It has been estimated that a 2 log 10 reduction in the level of poultry carcass contamination by C. jejuni could lower the incidence of human cases due to this source by 12 to 30-fold [11]. However, more modest estimates suggest a 3 log10 reduction in caecal colonisation would reduce human cases by 58%, although with a high degree of uncertainty [12]. One option to achieve this is to improve the intrinsic resistance of chickens to Campylobacter colonisation. Differences exist in the levels of colonisation across and within commercial broiler lines [13, 14] and these have been associated with variation in the transcriptome of the caeca [14,15,16] and spleen [17]. Genome-wide association studies in a commercial broiler population have indicated that resistance to caecal C. jejuni colonisation is under moderate genetic control [14]. However, heritable differences in resistance have been associated with quantitative trait loci (QTL) [14, 18], and the transcription of genes related to immunity [14, 19].

White Leghorn-derived inbred chicken lines 61 and N have been reported to be relatively resistant and susceptible to colonisation by several C. jejuni strains, respectively [20, 21], with F1 progeny of a cross exhibiting intermediate phenotypes [20]. Genome-wide association studies using backcross [(61 x N) x N] and ninth generation advanced intercross (61 x N) populations have identified QTLs associated with resistance to caecal colonisation by C. jejuni in these lines [21]. In this study, two candidate genes were identified in the QTL regions, ASIC4, located on chromosome 7, and BZFP2 located on chromosome 16, indicating a potential association with the Major Histocompatibility Complex (MHC) locus also present on chromosome 16. Immune-related genes such as IL6, CXCLi2 and CCLi2 [22] and immune-related pathways including lymphocyte activation, cytokine signalling and Ig production [15, 17, 19] have also been proposed to contribute to the differential resistance of chicken lines. Irrespective of the association of genes or expression patterns with heritable resistance, a need exists to better understand how birds respond to C. jejuni during infection, where previous studies have suggested a pro-inflammatory response that is limited in magnitude and timing [23,24,25,26], but which may also differ between commercial broiler lines [27].

Line 61 and N chickens not only differ in resistance to Campylobacter, but to gut colonisation by Salmonella enterica serovar Typhimurium and genetic associations have been mapped using a backcross [28]. We recently demonstrated that limited differences exist between lines 61 and N in their caecal microbiota and reciprocal transplants of caecal microbiota did not alter their resistance to C. jejuni colonisation, suggesting a role for host factors [29]. Here, we used RNA-Seq to investigate the caecal transcriptome of line 61 and N chickens, both in uninfected birds to identify differences between the lines that may underlie differential resistance to pathogens and following experimental challenge with C. jejuni.

Results

Challenge of line 61 and line N birds with C. jejuni M1 confirms differential resistance early after inoculation

To examine the level of resistance and susceptibility of lines 61 and N to colonisation by C. jejuni M1, three-week-old birds from each line were challenged with 108 CFU of C. jejuni M1 and the resulting numbers of C. jejuni in the caecal content determined at 1 and 5 days post-infection (dpi). At 1 dpi, line 61 birds exhibited a significantly (P < 0.01) lower level of C. jejuni colonisation in the caeca compared to line N by approximately 3 log10 CFU/g (Fig. 1). At 5 dpi, no significant difference in caecal colonisation by C. jejuni was observed between the two lines. These results indicate that line 61 is relatively resistant to C. jejuni M1 during early colonisation, as reported for other strains [20, 21, 29].

Fig. 1
figure 1

C. jejuni M1 colonisation in line 61 and line N birds. Birds were orally inoculated at 3 weeks of age with 108 CFU of C. jejuni M1 and the number of C. jejuni M1 per gram of caecal content determined at 1 and 5 dpi. Shown are the log10 CFU of C. jejuni per gram of caecal content from individual birds. N = 3 for each line at each time point. Crosshairs represent the mean count for each group. Significant differences were determined by Anova where * indicates significance at P < 0.01

Full size image

Transcriptional responses to infection in chicken lines differing in C. jejuni resistance

To explore transcriptomic differences underlying the relative resistance of line 61 and susceptibility of line N to C. jejuni M1 colonisation, RNA-Seq analysis was performed on caecal tonsil tissue from both infected and age-matched uninfected control birds of both lines. Birds were inoculated with C. jejuni at 3 weeks-of-age for parity with earlier reports on differential resistance to C. jejuni at this age [20, 21]. Differentially expressed genes (DEGs) were identified between experimental groups as follows: (1) line N infected vs control birds at 1 dpi, (2) line N infected vs control birds at 5 dpi, (3) line 61 infected vs control birds at 1 dpi, (4) line 61 infected vs control birds at 5 dpi and (5) line N vs line 61 control birds from both 1 and 5 dpi due to the high similarity between control samples across both time points, identified by sample clustering analysis. Gene Ontology (GO) analysis using GSEABase [30] and Ingenuity Pathway Analysis (IPA) [31] were used to identify enriched gene sets and their roles in biological systems.

Line N transcriptional responses

Despite the high levels of caecal C. jejuni M1 colonisation observed in susceptible line N, only 8 and 3 DEGs were identified between infected and control birds at 1 and 5 dpi respectively (Table 1). At 1 dpi, all 8 DEGs were upregulated in infected compared to control birds whereas at 5 dpi, 2 DEGs were upregulated and 1 downregulated. DEGs relating to immune function included Interleukin 1 Receptor Like 1 (IL1RL1) and the C-C motif chemokine 7 (CCL7), which were both upregulated in infected compared to control line N birds at 1 and 5 dpi, respectively. Other DEGs detected in line N were involved in cell growth and survival such as Sestrin 2 (SESN2) and GTPase, IMAP Family Member 8 (GIMAP8), which were both upregulated in infected birds. Overall, RNA-Seq analysis revealed that C. jejuni colonisation in line N birds produced very limited changes in gene expression.

Table 1 DEGs between control and infected susceptible line N birds at 1 and 5 dpi
Full size table

Due to the limited number of DEGs identified between control and infected line N birds, functional annotation analysis was performed on all 8 DEGs combined from both time points. GO term enrichment analysis did not identify any enriched gene sets in the caecal tonsils of line N birds following C. jejuni colonisation probably due to the limited number of DEGs. IPA identified molecular functions associated with the DEGs between infected and uninfected line N birds, with pathways involved in cell death and survival, cell to cell signalling and interaction and cellular function and maintenance being the most significant (Additional File 1: Fig. S1A). IPA also identified a significant network of genes involved in inflammatory responses (Additional File 1: Fig. S1B), indicating that C. jejuni may elicit a limited inflammatory response in susceptible line N.

Line 61 transcriptional responses

At 1 dpi, 69 DEGs were identified between infected and control line 61 birds. Of these, 38 were upregulated and 31 were downregulated in C. jejuni-infected birds compared to controls (Additional file 2: Table S1). Genes involved in the activity of macrophages (including MIP1a and MPEG1), natural killer (NK) cells and CD8α+ T lymphocytes (including EOMES, PRF1, CCL1, CD8α chain-like 3 (ENSGALG00000032967), CD8α-like (ENSGALG00000044720)) were amongst those with the highest increase in expression in infected compared to control birds, indicating that early C. jejuni colonisation may stimulate inflammatory and/or antimicrobial responses in which these cell populations play a role.

Genes with the greatest reduction in expression following C. jejuni colonisation in line 61 included members of the solute carrier family (SLC4A9, SLC26A4, SLC51B), G protein coupled receptor 6 member A (GPRC6A), TBC1 Domain Family Member 24 (TBC1D24), H6 Family Homeobox 2 (HMX2) and fibroblast growth factors (FGF19 and FGFBP1). At 5 dpi, no DEGs were identified between infected and uninfected line 61 birds, despite the high levels of C. jejuni colonisation observed. None of the identified DEGs were shared between the two lines.

GO enrichment analysis of DEGs between infected and control line 61 birds at 1 dpi identified 10 associated GO terms, seven of which were upregulated in infected birds. Immune-related GO terms associated with DEGs identified included ‘Negative regulation of IL-17 Production’, ‘Chemokine Activity’ and ‘Interleukin 1 production’, all of which were upregulated in response to C. jejuni colonisation (Additional File 3: Table S2). Of the three GO terms downregulated in response to C. jejuni colonisation, all were involved in nucleotide transport and processing.

By IPA 18 canonical pathways associated with DEGs were identified, of which 11 were immune-related (Fig. 2A). Some of the most significant of these included ‘Communication between Innate and Adaptive Immune Cells’, ‘Phagosome Maturation’, ‘Granulocyte Adhesion and Diapedesis’, ‘Agranulocyte Adhesion and Diapedesis’, ‘TREM1 signaling’ and ‘Crosstalk between Dendritic Cells (DC) and Natural Killer Cells’. Other canonical pathways linked to resistance in line 61 at 1 dpi included the FXR/RXR Activation and Iron Homeostasis signalling pathways. A number of molecular functions were identified as being significant to resistance in line 61 birds following C. jejuni colonisation, the most significant including pathways concerning ‘Molecular Transport’, ‘Lipid Metabolism’ and ‘Small Molecule Biochemistry’ (Fig. 2B). Of the physiological functions found to be significantly related to C. jejuni resistance in line 61, the most significant were related to immune function and included ‘Hematological System Development and Function’, ‘Immune Cell Trafficking’, ‘Cell-Mediated Immune Responses’, ‘Lymphoid System Development and Function’ and ‘Hematopoesis’ (Fig. 2C). IPA network analysis identified two significant networks of genes, involved in the antimicrobial response and cellular movement (Additional File 4: Fig. S2A) and lipid metabolism and transport (Additional File 4: Fig. S2B).

Fig. 2
figure 2

IPA of DEGs in the caecal tonsils of control and C. jejuni M1 colonised line 61 birds at 1 dpi. Shown are the significant canonical pathways (A), molecular functions (B) and physiological functions (C) associated with DEGs. N = 3 for both groups

Full size image

Comparative analysis of responses between lines after C. jejuni infection

To compare differences in pathway activation in response to C. jejuni colonisation between the two lines, an IPA comparison was performed between activated pathways in infected birds of each line at 1 dpi (Fig. 3). A number of immune-related pathways were found to be active in line 61 birds at 1 dpi, but not in line N birds, including pathways involved in macrophage activity such as ‘Phagosome Maturation’, ‘MIF-mediated Glucocorticoid’, ‘MIF Regulation of Innate Immune Responses’, and the ‘Inflammasome Pathway’. In contrast, pathways linked to Th2 (‘IL-10 Signalling’, the ‘Th2 pathway’) and IL-6 responses (‘STAT3 Pathway’ and ‘IL-6 Signalling’) were activated in line N but not line 61 at 1 dpi with C. jejuni. With few DEG identified in line N, the same genes may underlie the pathways related to these responses. Pathways mainly involved in regulating bile and cholesterol in the liver, but which are also relevant to intestinal inflammation, were also activated to different extents in the caecal tonsils of the two lines at 1 dpi. These included the ‘FXR/RXR Activation’, ‘Hepatic Cholestasis’ and the ‘Iron Homeostasis Signalling’ pathways which were more active in line 61 and the ‘LXR/RXR activation’, ‘VDR/RXR activation’ and ‘PPAR signalling’ pathways which were more active in line N. These results indicate inherent differences in the regulation of immune pathways during the early stages of C. jejuni infection, which may have implications for C. jejuni colonisation of the caeca. Significant molecular functions were also associated with the DEGs between infected birds of the two lines, including those involved in lipid and amino acid metabolic pathways (Additional File 5: Fig. S3A). We also identified a significant network of genes, mainly expressed to a higher degree in line N, relating to endocrine pathways (Additional File 5: Fig. S3B).

Fig. 3
figure 3

IPA comparison analysis of DEGs identified between line 61 and N C. jejuni M1 colonised birds at 1 dpi. Shown are significant canonical pathways identified from a comparison of DEGs between 3 infected compared to 3 control birds of each line. The degree of difference in expression is denoted by the depth of colour, with a darker colour indicating a greater degree of expression

Full size image

Transcriptome comparison of uninfected line 61 and line N birds

Gene expression

To investigate inherent differences between chicken lines 61 and N, caecal tonsil transcriptomes were compared between control birds from each line. In total, 948 DEGs were identified between control birds of the two lines, pooled from both time points, of which 528 were more highly expressed in line N compared to line 61 (Additional File 6: Table S3). Genes with the highest level of expression in line N compared to line 61 included Histone Cluster 1 H4 Family Member D (HIST1H4D), Ornithine Carbamoyltransferase (OTC), Choline O-Acetyltransferase (CHAT2), CD8 alpha chain-like (ENSGALG00000045876) and GTPase, IMAP Family Member 5-like (GIMAP5L). Several genes of the major histocompatibility complex I (MHCI) were also expressed to a greater extent in line N, including MHCIA1, MHCBL2 and MHCIY. Mucin 2 (MUC2), β-defensin 10 (AvBD10) and granzyme A (GZMA) were also expressed at a significantly higher level in susceptible line N. Interestingly, two genes identified in the QTL regions associated with C. jejuni colonisation in these lines were expressed at higher levels in line N. Acid Sensing Ion Channel Subunit Family Member 4 (ASIC4) was present in the QTL region on Chromosome 7 whereas ENSGALG00000028367, a zinc finger protein, was in the QTL identified on Chromosome 16 [21].

Of the DEGs identified between line 61 and N birds, 420 genes were expressed at higher levels in line 61 compared to line N. Of these, those with the greatest fold-change in expression included Class I histocompatibility antigen, F10 alpha chain-like (LOC107050538), Forkhead Box M1 (FOXM1), adenylate cyclase 5 (ADCY5), Deleted In Malignant Brain Tumors 1 (DMTB1), BPI Fold Containing Family B Member 3 (BPIFB3). Several other genes more highly expressed in line 61 included the macrophage marker CD163-like protein (DMBT1L), glutathione peroxidase 2 (GPX2; involved in protection against oxidative stress), and trefoil factor 2 (TFF2; involved in stabilisation of the mucosal layer and healing of the epithelial layer).

Functional analysis

GO enrichment analysis performed on DEGs between the control birds of each line identified 10 associated GO terms, five of which were enriched in each line and some of which had immune function (Additional File 7: Table S4). Immune-related GO terms enriched in line 61 compared to line N included the ‘Detection of Molecules of Bacterial Origin’, ‘Negative Regulation of IL-1β Production’ and ‘Negative Regulation of Hematopoietic Progenitor Cell Differentiation’ whereas GO terms enriched in line N compared to line 61 included ‘Negative Regulation of Viral Release from Host Cell’ and ‘Negative Regulation of Leukocyte Chemotaxis’, indicating that these chicken lines may be in different states of immune readiness prior to their interactions with pathogens.

IPA further identified inherent differences in the level of activity of canonical pathways between the two lines (Fig. 4A). Blood coagulation pathways were more activated in line N, and included the ‘Coagulation System’ and ‘Intrinsic Prothrombin Pathway’. The ‘eNOS signalling’ pathway was also more activated in line N. Pathways more active in resistant line 61 included ‘Estrogen Biosynthesis’ and ‘Nicotine Degradation II and III’. IPA also identified significant differences in molecular functions, with the most significant being ‘Cell-to-Cell Signalling and Interaction’, ‘Molecular Transport’ and ‘Protein Synthesis’ (Fig. 4B).

Fig. 4
figure 4

IPA of DEGs identified between control birds of line 61 and N. Shown are significant canonical pathways (A) and molecular functions (B) associated with DEGs between control birds. In (A), red bars indicate canonical pathways upregulated in line N and blue bars indicate pathways upregulated in line 61. N = 6 for each line (3 control birds pooled from each time point)

Full size image

Significant networks of genes associated with cell-to-cell signalling (Additional File 8: Fig. S4A), gastrointestinal pathways (Additional File 8: Fig. S4B) and amino acid (Additional File 8: Fig. S4C) and lipid metabolism (Additional File 8: Fig. S4D) were identified with higher activity in line N compared to line 61, highlighting that these two lines may be in different metabolic states prior to C. jejuni challenge and susceptibility to C. jejuni in line N may be due in part to distinct metabolism. Furthermore, some genes potentially acting as upstream regulators of DEGs were found to be significantly upregulated in line N, including the B-cell receptor (BCR) (Additional File 9: Fig. S5A), microRNA mir155 (Additional File 9: Fig. S5B) and the nuclear factor of activated T-cells (NFAT) (Additional File 9: Fig. S5C).

Gene cluster analysis

Graphia software [32] analysis revealed the most prominent clustering was by bird line, suggesting that basal gene expression differences between lines 61 and N may explain intrinsic resistance as opposed to differences in their response to C. jejuni infection. Two components containing the majority of DEGs were identified. These were Component 1 comprising of 2822 genes expressed to a greater extent in line N and Component 2 comprising of 2285 genes expressed to a greater extent in line 61 (Fig. 5A and B respectively). Mean histogram plots of all genes present within these two components indicated that genes were generally expressed at higher levels in one line compared to the other indicating major differences in the regulation of groups of genes are key to the resistance and susceptible phenotypes in these lines (Fig. 5C and D).

Fig. 5
figure 5

Graphia clustering of RNA-Seq data across all samples. Each node (circle) in the graph represents a gene, and each edge (line) a correlation exceeding a threshold (rho ≥ 0.93). MCL cluster granularity was set to 1.5. The most prominent clustering is by bird line with two main components being identified: component 1 - genes expressed at higher levels in line N (A) and component 2 - genes expressed at higher levels in line 61 (B). Colours indicate clusters of genes which have a similar expression pattern. (C) and (D) show the number of genes from each cluster in individual birds, identified by matching colours in corresponding components

Full size image

Validation of DEGs by qRT-PCR

RNA-Seq data was validated by qRT-PCR analysis of a subset of genes. These were chosen for validation based on their possible biological significance during C. jejuni colonisation and the degree to which they were DE. Genes were mainly selected from the pairwise comparison between control birds of each line, owing to the high number of DEGs identified in this group. Correlation of the qRT-PCR results with the RNA-Seq results produced a correlation co-efficient of R2 = 0.86 (p < 0.001) therefore the qRT-PCR results are comparable to the RNA-Seq data (Fig. 6).

Fig. 6
figure 6

qRT-PCR validation of DEGs identified by RNA-Seq. Shown is the correlation of the log2 fold change in mRNA transcripts as determined by RNA-Seq (y-axis) with the log2 fold change of mRNA transcripts as determined by qRT-PCR (x-axis). DEGs that were validated are given in Additional file 11: Table 6. The line of best fit is represented in blue with the R2 value denoted on the graph

Full size image

Discussion

With the handling or consumption of contaminated chicken accounting for a high proportion of human campylobacteriosis [6, 7], a pressing need exists to reduce the prevalence of C. jejuni in commercial broiler flocks. White Leghorn inbred lines 61 and N have an established difference in heritable resistance to C. jejuni colonisation, with genetic variation associated with C. jejuni resistance identified by genome-wide association studies using backcross and advanced 61 x N intercross populations [21]. Furthermore, key QTL associated with resistance to C. jejuni are shared between these inbred lines and commercial broilers [14] indicating that findings in inbred chickens can be highly relevant to C. jejuni control in commercial flocks. Using RNA-Seq, we evaluated transcriptomic differences in the caecal tonsils of these inbred lines, both inherently and following C. jejuni colonisation, to investigate the basis of their differential resistance to C. jejuni and potentially obtain biomarkers that could be selected in commercial populations.

We showed that compared to line N, line 61 was relatively resistant to early C. jejuni M1 colonisation in the caeca at 1 dpi, however by 5 dpi both lines were similarly susceptible to colonisation. Previously, Boyd et al reported resistance to cloacal and caecal colonisation was apparent in line 61 compared to line N from 4 to 20 dpi [20], a discrepancy with this study likely due, in part, to the different C. jejuni strains used by Boyd (C. jejuni 14 N and 81–176) and in this report (C. jejuni M1). Chintoan-Uta et al recently reported line N birds to be colonised by C. jejuni 11168H at c. 104 CFU/g caecal contents 9 dpi at 3 weeks-of-age whereas the challenge strain was absent at the limit of detection by direct plating at this time in line 61 birds [29]. M1 rapidly colonises the chicken caeca from doses as low as 100 CFU [33, 34] and both the rate of colonisation and caecal burden have proven greater than for other C. jejuni strains tested in the same model, including 11168H (Stevens et al, unpublished data). For many C. jejuni strains, there is a minimum infective dose which can cause high levels of colonisation in the chicken caeca [35,36,37]. It is plausible that both chicken lines may have been overwhelmed by the dose of C. jejuni M1 administered, now known to be considerably higher than the minimum dose required for reliable colonisation (102 CFU, [33]).

Susceptible line N displayed a very limited caecal transcriptional response to C. jejuni colonisation compared to resistant line 61 where a wider, albeit brief, response at 1 dpi was observed. Although functional annotation analysis identified significant pathways related to immune function in both lines, the difference in magnitude between the responses of the two lines may partly explain the relative resistance and susceptibility displayed at 1 dpi. DEGs related to macrophage, NK cell and CD8α+ T cell activity were upregulated in resistant line 61 at 1 dpi, with functional annotation analysis identifying pathways involved in communication between the innate and adaptive arms of immunity, phagosome maturation and crosstalk between NK cells and DC as involved. It follows that the lower level of colonisation in line 61 at 1 dpi may, in part, be attributable to this innate response whereas at 5 dpi, this response is absent and coincides with line 61 caecal colonisation levels matching those of line N. It is possible that NK cells are involved in the initial response to C. jejuni observed in line 61 as the NK complex is located in close proximity to the chicken MHC B complex, which influences the responsiveness of chicken NK cells [38], and several DE MHCI genes were identified between lines N and 61, including MHCIA1, MHCBL2 and MHCIY.

Innate inflammatory responses have been linked to reduced C. jejuni colonisation elsewhere. Although not detected in our study, Psifidi et al found CXCLi1 and CXCLi2 (proinflammatory chemokines involved in heterophil chemotaxis) expression was reduced in the caecal tonsils of both line 61 and N following C. jejuni infection [21], but more so in line N, further implying innate responses may be involved in controlling C. jejuni colonisation at this site. Moreover, broilers selected for an inflammatory phenotype (high levels of IL-6, CXCLi2 and CCLi2) are less likely to become colonised by C. jejuni compared to those selected for lower inflammatory phenotype [22], indicating that an inherent proinflammatory status reduces the ability of C. jejuni to colonise the chicken caeca. However, in contrast, Humphrey et al found that levels of CXCLi1 and CXCLi2 expression were not related to differences in caecal C. jejuni load [27].

Iron homeostasis signalling pathways were upregulated in resistant line 61 at 1 dpi. Iron is essential for bacterial replication and mutants with defects in iron acquisition are frequently attenuated [39], therefore differences in iron availability in the gastrointestinal tract between chicken lines may factor in their relative resistance and merits further investigation. Additionally, higher activity related to MIF-mediated glucocorticoid, the MIF innate immune response and inflammasome pathways occurred during initial C. jejuni colonisation in line 61, indicating that MIF and the inflammasome may be mediators in the initial inflammatory response in line 61.

Major transcriptional differences were apparent between control birds of both lines, and were far greater than those observed in response to C. jejuni infection. Our study is not the first to identify such a degree of inherent transcriptional variation between White Leghorn inbred lines. For example, gene expression in the spleen and thymus differs by several hundred genes between lines 61 and 72, which are relatively resistant and susceptible to Marek’s Disease Virus respectively [40]. Significant networks of genes associated with amino acid and lipid metabolism were upregulated in line N control birds, consistent with other studies linking higher inherent metabolic states with susceptibility to C. jejuni. Li et al (2010) found amino acid, lipid and glucose metabolic pathways to be upregulated in a C. jejuni-susceptible line compared to a resistant line following colonisation, with amino acid processes also upregulated in control birds of the susceptible line [15]. Additionally, Li et al (2011) found increased expression of genes involved in fatty acid and protein metabolic processes between C. jejuni-colonised compared to non-colonised birds of the same line [16]. Our data identified differences in transcription of genes associated with metabolic activity between the lines coinciding with differential colonisation levels at 1 dpi. For example, higher activation in the farnesoid x receptor (FXR)/retinoid x receptor activation was present in line 61 but liver x receptor (LXR)/RXR, vitamin D receptor (VDR)/RXR and peroxisome proliferator-activated receptor (PPARα)/RXR activation was higher in line N. FXR, LXR and PPAR-α are mainly associated with lipid metabolism and in the regulation of triglyceride levels in mammals [41,42,43]. However, between them, FXR, LXR and PPAR-α also have various roles in regulating intestinal inflammation and immunity including effects on macrophage inflammatory activity, reducing the presence of reactive oxygen species (ROS) and maintaining the intestinal barrier [44,45,46,47,48,49], and are considered potential therapeutic targets in the case of mammalian IBD [45, 50, 51]. Expression of FXR, LXR and PPAR-α in these chicken lines may therefore modulate intestinal inflammatory responses, influencing C. jejuni colonisation. Furthermore, their roles in triglyceride metabolism may also influence colonisation as triglyceride-rich lipoprotein can bind LPS, reducing LPS toxicity during bacterial infection and reducing macrophage activation [52]. Vitamin D and its receptor are important in maintaining the mucosal barrier of the intestine [53] and modulate proinflammatory cytokine production [54]. Abiotic IL10−/− mice treated with artificial vitamin D suffered less diarrhoea and had lower levels of intestinal IL-6, IFN-γ and CCL2 during campylobacteriosis than mice that did not receive vitamin D [55], therefore the contribution of vitamin D and the vitamin D receptor to C. jejuni susceptibility in line N chickens warrants further study. Upstream gene regulators involved in several immune-related networks were associated with the DEGs identified between control birds of both lines (BCR, NFAT and miR-155). Previously, increased caecal miR-155, a regulator of inflammatory processes in mammals [56], was observed following C. jejuni colonisation in chickens [57]. These differences in inflammatory states prior to C. jejuni inoculation likely influence the speed and resulting level of colonisation in different chicken lines.

Lines 61 is also relatively resistant to S. Typhimurium colonisation compared to line N [28, 58]. QTLs associated with resistance to both S. Typhimurium and C. jejuni have been identified on chromosome 14 [21, 59] and chromosome 16 [21, 60, 61] implying that similar mechanisms of genetic control may confer resistance to both C. jejuni and Salmonella. Furthermore, greater inflammatory responses to Salmonella have been observed in resistant chicken lines compared to susceptible birds [62] highlighting the importance of innate responses in resistance to enteric bacterial pathogens.

As C. jejuni mainly resides in the chicken intestinal lumen, it is plausible that differences at the mucosal surface or extracellular milieu may account for resistance. Genes encoding MUC2 and AvBD10 were expressed to a higher level in line N compared to line 61 control birds. Previously, it has been shown that chicken mucus inhibits C. jejuni invasion of both chicken and human primary intestinal cells compared with human mucus [63]. It is therefore possible that inherent differences in the composition of chicken mucus between lines accounts for the differences in the colonisation levels observed. GZMA was also more highly expressed in line N, corresponding to a microarray study where GZMA expression was higher in the caeca of C. jejuni-colonised compared to non-colonised birds, indicating GZMA is linked with elevated C. jejuni levels in the caeca [16]. Recent studies have identified mostly limited differences in the microbial communities present in the caeca of lines 61 and N at the age they were inoculated herein, but the extent to which these differences drive distinct patterns of gene expression in the gut, or vice versa, is unknown [29].

Other studies have examined the impact of gene expression and host genetics on C. jejuni colonisation of the caeca [14, 16, 17, 19, 20, 23, 24]. However, these varied in the strain of C. jejuni used, bird line and challenge age of the birds (between 2 and 4 weeks-of-age), and sampling intervals (from 6 h to 14 dpi) resulting in variation of the level of colonisation observed and challenges in extrapolating from one study to the next. Despite these differences, a similar narrative can be seen throughout these studies whereby a moderate number of significant DEGs was identified upon Campylobacter challenge, but often at a low fold-change indicating that even high levels of C. jejuni colonisation does not elicit a dramatic response in the chicken [16, 17, 21, 64]. We elected to study the transcriptome of caecal tonsils as a gut-associated lymphoid tissue at a key site of Campylobacter persistence, and to permit direct comparison with RNA-Seq data from resistant or susceptible broilers from a recent genome-wide association study [14] and earlier qRT-PCR data on candidate resistance-associated genes in lines 61 and N [21]. The former study detected differentially transcribed genes in caecal tonsils within quantitative-trait loci associated with resistance to caecal colonisation, indicating that it is a relevant anatomical location to sample. However, we cannot preclude the possibility that the responses observed may not be typical of the wider caecal mucosa, or tissue at other key sites of Campylobacter persistence in poultry.

A GWAS on an advanced intercross of line 61 and N previously identified 6 SNPs on chromosomes 4, 14 and 16 associated with resistance to C. jejuni colonisation [21]. We identified two genes located within the QTL regions associated with C. jejuni colonisation in these lines, ASIC4 (Acid Sensing Ion Channel Subunit Family Member 4) and ENSGALG00000028367, both of which were inherently expressed to a greater extent in line N. ASIC4 is broadly expressed in the mammalian nervous system but its role in birds is unknown. In mammals, ASICs are known for their role in neuroinflammation [65] and promote exocytosis and maturation in bone marrow-derived macrophages stimulated by extracellular acidosis [66]. ENSGALG00000028367, or BZFP2, is a zinc finger-like protein which likely binds nucleic acids, proteins and other small molecules [67], and bares similarity to the CKR1-like gene and is present in a region of the MHC-B locus [68].

To conclude, RNA-Seq analysis demonstrated an initial inflammatory response to C. jejuni infection of a greater magnitude in resistant line 61 compared to line N, which may be associated with caecal colonisation. This response was short lived and absent at later intervals when differential resistance was not detected. By far, the most striking differences in gene expression were detected between uninfected control birds of the two lines. The identification of candidate genes involved in early innate responses and metabolic pathways provides a foundation for future studies on avian heritable resistance to Campylobacter.

Methods

Animals

Two inbred White Leghorn chicken lines were used in this study. Lines 61 and N, reported to be relatively resistant and susceptible to C. jejuni colonisation respectively, originate from the USDA ARS Avian Disease and Oncology Laboratory (formerly the Regional Poultry Laboratory) in East Lansing, MI, USA [12]. Flocks of both lines were maintained under specified pathogen-free (SPF) conditions at the National Avian Research Facility (NARF) at the Roslin Institute, UK.

Bacterial culture, experimental design and sample collection

C. jejuni strain M1 [69] was used to inoculate animals in this study. C. jejuni M1 was cultured on modified charcoal-cephoperazone-microaerophillic agar (mCCDA; Oxoid) or in Mueller-Hinton (MH) broth (Oxoid) at 37 °C with 5% O2, 5% CO2 and 90% N2 in a microaerophilic cabinet. Liquid cultures in broth were with shaking at 400 rpm under the same atmospheric conditions.

Twelve birds each of White Leghorn lines 61 and N were obtained on the day of hatch and housed under SPF conditions with access to feed and water ad libitum. For each line there were 6 control and 6 infected birds. At 3 weeks-of-age, birds of the infected groups were challenged by oral gavage with 108 C. jejuni M1 in 0.1 ml of MH broth and birds of the control groups given an equivalent volume of MH broth only. At 1 and 5 dpi, 3 chickens of each group were culled by cervical dislocation and death confirmed by permanent cessation of blood circulation. At post mortem examination, caeca were collected for the enumeration of C. jejuni by plating 100 μl of triplicate 10-fold serial dilutions of caecal contents in phosphate-buffered saline (PBS) to mCCDA plates. Caecal tonsils were collected promptly into RNAlater® (Life Technologies) and stored at − 80 °C until processing.

RNA-Seq library preparation, sequencing and data analysis

RNA was extracted from both caecal tonsils using the Qiagen RNeasy mini kit according to the manufacturer’s instructions. RNA preparations were assessed for quantity and quality using a Qubit™ Fluorimeter (Invitrogen) and an Agilent 2200 TapeStation (Agilent Technologies) respectively. The resulting RNA integrity number (RIN) values for all RNA samples was greater than 9 therefore all 24 samples (n = 3 per group) were subsequently submitted to the Edinburgh Genomics sequencing facility (Edinburgh, UK) for RNA-Seq. The TruSeq stranded mRNA-Seq Library Prep kit (Illumina) was used to generate mRNA libraries free from ribosomal RNA and the resulting transcriptomes sequenced using the Illumina HiSeq 4000 system to generate 75 bp paired end reads at a depth of 50 million reads per sample.

The quality of the raw sequence reads was assessed using FASTQC (v0.11.5) [70]. Cutadapt (v1.14) [71] was used to trim adapter sequences, remove bases with a Phred score of less than 30 and ensure resulting sequences were at least 50 bp in length. Trimmed reads were then mapped to the Gallus gallus reference genome (GalGal5, Ensembl release 89) using the STAR aligner software package (v2.5.1b) [72] with a minimum alignment of 52.5 million input reads for each sample (Additional File 10: Table S5). In all samples, over 90% of reads were uniquely mapped with fewer than 10% either unmapped or mapped to multiple loci. The number of reads aligning to genomic features were determined using FeatureCounts (v1.5.3) [73] using default parameters. Analysis of DEGs was performed in R using EdgeR package with DEGs exhibiting a fold change (FC) > 2 and a false discovery rate (FDR) < 0.05 considered significant.

Gene ontology term enrichment analysis was performed in R using the GSEABase package (downloaded from the Gene Set Enrichment Analysis (GSEA) website, https://software.broadinstitute.org/gsea/index.jsp, file: C5.all.v6.0.symbols). Significant gene ontology was determined using the mRoast function of the Limma package in R for each pairwise comparison. Ingenuity Pathway Analysis (IPA) was performed on significant DEGs using IPA software (Qiagen Bioinformatics, www.qiagenbioinformatics.com/products/ingenuity-pathway-analysis) to classify their associated biological functions, canonical pathways and biological networks. Network analysis was performed using the normalised raw counts in Graphia Pro [32] with a Pearson correlation threshold of r = 0.93. The number of nodes (genes) in the analysis was 6066 linked by 181.1 k edges. Markov Clustering (MCL) was performed with a granularity of 1.5 on these networks to identify components containing genes of similar expression patterns. Components of less than 10 nodes were removed from the analysis. Gene lists derived from Graphia were submitted to the functional annotation tool DAVID [74] to further investigate the roles of genes identified in the components, with Gallus gallus selected as the background for these lists.

cDNA preparation and quantitative reverse-transcriptase polymerase chain reaction (qRT-PCR)

Genes related to immune function that were observed to be DE by RNA-Seq were validated by qRT-PCR. The Verso cDNA Synthesis kit (Thermo Scientific) was used to prepare cDNA from 1 μg of total RNA according to the manufacturer’s instructions. Quantitative PCR reactions were performed using the Forget-Me-Not™ qPCR Master Mix (Biotium) in 20 μL volumes containing 1 X Forget-Me- Not™ qPCR Master Mix, 0.5 μM each of the forward and reverse primers, 50 nM of ROX reference dye and 2 μL of cDNA at a 1:10 dilution in template buffer. Gene-specific primers were purchased from Sigma and are detailed in Additional File 11: Table S6. The amplification and detection of specific DNA was achieved using the AB 7500 FAST Real-Time PCR System (Applied Biosystems) to the following program: 95 °C for 2 min followed by 40 cycles of 95 °C for 5 s then 60 °C for 30 s. To confirm the presence of a single PCR product, melting curves were generated by 1 cycle of 60 °C for 1 min, increasing to 95 °C in 1% increments every 15 s. Samples were run in triplicate and each qPCR experiment contained 3 no-template controls and a 5-fold dilution series in duplicate of pooled caecal tonsil-derived cDNA from several birds from which standard curves were generated. The relative expression of genes were calculated as described by Pfaffl [75] and normalised to the geometric mean of three reference genes; r28S, TBP and GAPDH. A Spearman’s correlation was calculated between the log2 fold-change of the RNA-Seq results to the log2 fold-change detected by qPCR in R.

Availability of data and materials

Sequencing data have been submitted to the European Nucleotide Archive (https://www.ebi.ac.uk/ena) under accession number PRJEB24399.

Abbreviations

cDNA:

Complementary DNA

DC:

Dendritic cell

DE:

Differentially expressed

DEGs:

Differentially expressed genes

dpi:

Days post-infection

FC:

Fold change

FDR:

False discovery rate

GO:

Gene ontology

IPA:

Ingenuity Pathway Analysis

mCCDA:

Modified charcoal-cefoperazone-deoxycholate agar

NK:

Natural killer

qRT-PCR:

Quantitative reverse-transcriptase polymerase chain reaction

SPF:

Specified pathogen-free

References

  1. Havelaar AH, Kirk MD, Torgerson PR, Gibb HJ, Hald T, Lake RJ, et al. World Health Organization global estimates and regional comparisons of the burden of foodborne disease in 2010. PLoS Med. 2015;12(12):e1001923.

    Article  PubMed  PubMed Central  Google Scholar 

  2. PHE. Anon. In: Zoonoses report UK. UK: Public Health England; 2017.

    Google Scholar 

  3. Tam CC, Rodrigues LC, Viviani L, Dodds JP, Evans MR, Hunter PR, et al. Longitudinal study of infectious intestinal disease in the UK (IID2 study): incidence in the community and presenting to general practice. Gut. 2012;61(1):69–77.

    Article  PubMed  Google Scholar 

  4. Tam CC, O'Brien SJ. Economic cost of Campylobacter, norovirus and rotavirus disease in the United Kingdom. PLoS One. 2016;11(2):e0138526.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  5. Janssen R, Krogfelt KA, Cawthraw SA, van Pelt W, Wagenaar JA, Owen RJ. Host-pathogen interactions in Campylobacter infections: the host perspective. Clin Microbiol Rev. 2008;21(3):505–18.

    Article  PubMed  PubMed Central  Google Scholar 

  6. EFSA Panel on Biological Hazards (BIOHAZ). Scientific Opinion on Campylobacter in broiler meat production: control options and performance objectives and/or targets at different stages of the food chain. EFSA J. 2011;9(4):2105.

  7. Skarp CPA, Hänninen ML, Rautelin HIK. Campylobacteriosis: the role of poultry meat. Clin Microbiol Infect. 2016;22(2):103–9.

    Article  CAS  PubMed  Google Scholar 

  8. Wagenaar JA, French NP, Havelaar AH. Preventing Campylobacter at the source: why is it so difficult? Clin Infect Dis. 2013;57(11):1600–6.

    Article  PubMed  Google Scholar 

  9. Jorgenson F, Charlett, A., Arnold, E., Swift, C., Elviss, N.C.: A microbiological survey of Campylobacter contamination in fresh whole UK-produced chilled chickens at retail sale. In. Edited by England PH; 2018.

  10. Newell DG, Fearnley C. Sources of Campylobacter colonization in broiler chickens. Appl Environ Microbiol. 2003;69(8):4343–51. https://doi.org/10.1128/AEM.69.8.4343-4351.2003.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Rosenquist H, Nielsen NL, Sommer HM, Nørrung B, Christensen BB. Quantitative risk assessment of human campylobacteriosis associated with thermophilic Campylobacter species in chickens. Int J Food Microbiol. 2003;83(1):87–103. https://doi.org/10.1016/S0168-1605(02)00317-3.

    Article  PubMed  Google Scholar 

  12. EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis K, Allende A, Alvarez-Ordóñez A, Bolton D, Bover-Cid S, et al. Update and review of control options for Campylobacter in broilers at primary production. EFSA J. 2020;18(4):e06090.

  13. Li X, Swaggerty C, Kogut M, Chiang H-I, Wang Y, He H, et al. The paternal effect of Campylobacter jejuni colonization in ceca in broilers. Poult Sci. 2008;87:1742–7.

    Article  CAS  PubMed  Google Scholar 

  14. Psifidi A, Kranis A, Rothwell LM, Bremner A, Russell K, Robledo D, et al. Quantitative trait loci and transcriptome signatures associated with avian heritable resistance to Campylobacter. Sci Rep. 2020;11:1623.

    Article  CAS  Google Scholar 

  15. Li X, Swaggerty CL, Kogut MH, Chiang HI, Wang Y, Genovese KJ, et al. Gene expression profiling of the local cecal response of genetic chicken lines that differ in their susceptibility to Campylobacter jejuni colonization. PLoS One. 2010;5(7):e11827.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  16. Li XY, Swaggerty CL, Kogut MH, Chiang HI, Wang Y, Genovese KJ, et al. Caecal transcriptome analysis of colonized and non-colonized chickens within two genetic lines that differ in caecal colonization by Campylobacter jejuni. Anim Genet. 2011;42(5):491–500.

    Article  PubMed  CAS  Google Scholar 

  17. Li X, Swaggerty C, Kogut M, Chiang H-I, Wang Y, He H, et al. Systemic response to Campylobacter jejuni infection by profiling gene transcription in the spleens of two genetic lines of chickens. Immunogenetics. 2011;64:59–69.

    Article  PubMed  Google Scholar 

  18. Connell S, Meade KG, Allan B, Lloyd AT, Downing T, O'Farrelly C, et al. Genome-wide association analysis of avian resistance to Campylobacter jejuni colonization identifies risk locus spanning the CDH13 gene. G3 (Bethesda). 2013;3(5):881–90.

    Article  Google Scholar 

  19. Connell S, Meade KG, Allan B, Lloyd AT, Kenny E, Cormican P, et al. Avian resistance to Campylobacter jejuni colonization is associated with an intestinal immunogene expression signature identified by mRNA sequencing. PLoS One. 2012;7(8):e40409.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Boyd Y, Herbert EG, Marston KL, Jones MA, Barrow PA. Host genes affect intestinal colonisation of newly hatched chickens by Campylobacter jejuni. Immunogenetics. 2005;57(3–4):248–53.

    Article  PubMed  Google Scholar 

  21. Psifidi A, Fife M, Howell J, Matika O, van Diemen PM, Kuo R, et al. The genomic architecture of resistance to Campylobacter jejuni intestinal colonisation in chickens. BMC Genomics. 2016;17:293.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Swaggerty CL, Pevzner IY, He H, Genovese KJ, Kogut MH. Selection for pro-inflammatory mediators produces chickens more resistant to Campylobacter jejuni. Poult Sci. 2017;96(6):1623–7.

    Article  CAS  PubMed  Google Scholar 

  23. Shaughnessy RG, Meade KG, Cahalane S, Allan B, Reiman C, Callanan JJ, et al. Innate immune gene expression differentiates the early avian intestinal response between Salmonella and Campylobacter. Vet Immunol Immunopathol. 2009;132(2–4):191–8.

    Article  CAS  PubMed  Google Scholar 

  24. Shaughnessy RG, Meade KG, McGivney BA, Allan B, O'Farrelly C. Global gene expression analysis of chicken caecal response to Campylobacter jejuni. Vet Immunol Immunopathol. 2011;142(1–2):64–71.

    Article  CAS  PubMed  Google Scholar 

  25. Smith CK, Abuoun M, Cawthraw SA, Humphrey TJ, Rothwell L, Kaiser P, et al. Campylobacter colonization of the chicken induces a proinflammatory response in mucosal tissues. FEMS Immunol Med Microbiol. 2008;54(1):114–21.

    Article  CAS  PubMed  Google Scholar 

  26. Reid WD, Close AJ, Humphrey S, Chaloner G, Lacharme-Lora L, Rothwell L, et al. Cytokine responses in birds challenged with the human food-borne pathogen Campylobacter jejuni implies a Th17 response. R Soc Open Sci. 2016;3(3):150541.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  27. Humphrey S, Chaloner G, Kemmett K, Davidson N, Williams N, Kipar A, et al. Campylobacter jejuni is not merely a commensal in commercial broiler chickens and affects bird welfare. mBio. 2014;5(4):e01364–14.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  28. Fife MS, Howell JS, Salmon N, Hocking PM, van Diemen PM, Jones MA, et al. Genome-wide SNP analysis identifies major QTL for Salmonella colonization in the chicken. Anim Genet. 2011;42(2):134–40.

    Article  CAS  PubMed  Google Scholar 

  29. Chintoan-Uta C, Wisedchanwet T, Glendinning L, Bremner A, Psifidi A, Vervelde L, et al. Role of cecal microbiota in the differential resistance of inbred chicken lines to colonization by Campylobacter jejuni. Appl Environ Microbiol. 2020;86(7):e02607–19.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Subramanian A, Tamayo P, Mootha VK, Mukherjee S, Ebert BL, Gillette MA, et al. Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles. Proc Natl Acad Sci. 2005;102(43):15545–50.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Krämer A, Green J, Pollard J Jr, Tugendreich S. Causal analysis approaches in ingenuity pathway analysis. Bioinformatics. 2014;30(4):523–30.

    Article  PubMed  CAS  Google Scholar 

  32. Livigni A, O'Hara L, Polak ME, Angus T, Wright DW, Smith LB, et al. A graphical and computational modeling platform for biological pathways. Nat Protoc. 2018;13(4):705–22.

    Article  CAS  PubMed  Google Scholar 

  33. Vohra P, Chintoan-Uta C, Terra VS, Bremner A, Cuccui J, Wren BW, et al. Evaluation of glycosylated FlpA and SodB as subunit vaccines against Campylobacter jejuni colonisation in chickens. Vaccines (Basel). 2020;8(3):520.

    Article  CAS  Google Scholar 

  34. Chaloner G, Wigley P, Humphrey S, Kemmett K, Lacharme-Lora L, Humphrey T, et al. Dynamics of dual infection with Campylobacter jejuni strains in chickens reveals distinct strain-to-strain variation in infection ecology. Appl Environ Microbiol. 2014;80(20):6366–72.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  35. Ringoir DD, Korolik V. Colonisation phenotype and colonisation potential differences in Campylobacter jejuni strains in chickens before and after passage in vivo. Vet Microbiol. 2003;92(3):225–35.

    Article  CAS  PubMed  Google Scholar 

  36. Young CR, Ziprin RL, Hume ME, Stanker LH. Dose response and organ invasion of day-of-hatch Leghorn chicks by different isolates of Campylobacter jejuni. Avian Dis. 1999;43(4):763–7.

    Article  CAS  PubMed  Google Scholar 

  37. Cawthraw SA, Wassenaar TM, Ayling R, Newell DG. Increased colonization potential of Campylobacter jejuni strain 81116 after passage through chickens and its implication on the rate of transmission within flocks. Epidemiol Infect. 1996;117(1):213–5.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. Kaufman J, Milne S, Göbel TWF, Walker BA, Jacob JP, Auffray C, et al. The chicken B locus is a minimal essential major histocompatibility complex. Nature. 1999;401(6756):923–5.

    Article  CAS  PubMed  Google Scholar 

  39. Palyada K, Threadgill D, Stintzi A. Iron acquisition and regulation in Campylobacter jejuni. J Bacteriol. 2004;186(14):4714–29.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Smith J, Sadeyen JR, Paton IR, Hocking PM, Salmon N, Fife M, et al. Systems analysis of immune responses in Marek's disease virus-infected chickens identifies a gene involved in susceptibility and highlights a possible novel pathogenicity mechanism. J Virol. 2011;85(21):11146–58.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  41. Patel MB, Oza NA, Anand IS, Deshpande SS, Patel CN. Liver x receptor: a novel therapeutic target. Indian J Pharm Sci. 2008;70(2):135–44.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Schultz JR, Tu H, Luk A, Repa JJ, Medina JC, Li L, et al. Role of LXRs in control of lipogenesis. Genes Dev. 2000;14(22):2831–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. van Raalte DH, Li M, Pritchard PH, Wasan KM. Peroxisome proliferator-activated receptor (PPAR)-alpha: a pharmacological target with a promising future. Pharm Res. 2004;21(9):1531–8.

    Article  PubMed  Google Scholar 

  44. A-Gonzalez N, Castrillo A. Liver X receptors as regulators of macrophage inflammatory and metabolic pathways. Biochim Biophys Acta. 2011;1812(8):982–94.

  45. Wildenberg ME, van den Brink GR. FXR activation inhibits inflammation and preserves the intestinal barrier in IBD. Gut. 2011;60(4):432–3.

    Article  PubMed  Google Scholar 

  46. Armstrong LE, Guo GL. Role of FXR in liver inflammation during nonalcoholic steatohepatitis. Curr Pharmacol Rep. 2017;3(2):92–100.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  47. Korbecki J, Bobiński R, Dutka M. Self-regulation of the inflammatory response by peroxisome proliferator-activated receptors. Inflamm Res. 2019;68(6):443–58.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  48. Zandbergen F, Plutzky J. PPARalpha in atherosclerosis and inflammation. Biochim Biophys Acta. 2007;1771(8):972–82.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  49. Le Menn G, Neels JG. Regulation of immune cell function by PPARs and the connection with metabolic and neurodegenerative diseases. Int J Mol Sci. 2018;19(6):1575.

    Article  PubMed Central  CAS  Google Scholar 

  50. Azuma YT, Nishiyama K, Matsuo Y, Kuwamura M, Morioka A, Nakajima H, et al. PPARα contributes to colonic protection in mice with DSS-induced colitis. Int Immunopharmacol. 2010;10(10):1261–7.

    Article  CAS  PubMed  Google Scholar 

  51. Klepsch V, Moschen AR, Tilg H, Baier G, Hermann-Kleiter N. Nuclear receptors regulate intestinal inflammation in the context of IBD. Front Immunol. 2019;10:1070.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  52. Barcia AM, Harris HW. Triglyceride-rich lipoproteins as agents of innate immunity. Clin Infect Dis. 2005;41(Suppl 7):S498–503.

    Article  CAS  PubMed  Google Scholar 

  53. Kong J, Zhang Z, Musch MW, Ning G, Sun J, Hart J, et al. Novel role of the vitamin D receptor in maintaining the integrity of the intestinal mucosal barrier. Am J Physiol Gastrointest Liver Physiol. 2008;294(1):G208–16.

    Article  CAS  PubMed  Google Scholar 

  54. Yin K, Agrawal DK. Vitamin D and inflammatory diseases. J Inflamm Res. 2014;7:69–87.

    CAS  PubMed  PubMed Central  Google Scholar 

  55. Mousavi S, Lobo de Sá FD, Schulzke JD, Bücker R, Bereswill S, Heimesaat MM. Vitamin D in acute Campylobacteriosis-results from an intervention study applying a clinical Campylobacter jejuni induced enterocolitis model. Front Immunol. 2019;10:2094.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  56. Mahesh G, Biswas R. MicroRNA-155: a master regulator of inflammation. J Interf Cytokine Res. 2019;39(6):321–30.

    Article  CAS  Google Scholar 

  57. Liu X, Liu L, Zhang M, Wang H, Yang N, Li X. Chicken cecal microRNAs in the response to Campylobacter jejuni inoculation by Solexa sequencing. Poult Sci. 2016;95(12):2819–23.

    Article  CAS  PubMed  Google Scholar 

  58. Barrow PA, Bumstead N, Marston K, Lovell MA, Wigley P. Faecal shedding and intestinal colonization of Salmonella enterica in in-bred chickens: the effect of host-genetic background. Epidemiol Infect. 2004;132(1):117–26.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  59. Calenge F, Vignal A, Demars J, Fève K, Menanteau P, Velge P, et al. New QTL for resistance to Salmonella carrier-state identified on fowl microchromosomes. Mol Gen Genomics. 2011;285(3):237–43.

    Article  CAS  Google Scholar 

  60. Calenge F, Lecerf F, Demars J, Feve K, Vignoles F, Pitel F, et al. QTL for resistance to Salmonella carrier state confirmed in both experimental and commercial chicken lines. Anim Genet. 2009;40(5):590–7.

    Article  CAS  PubMed  Google Scholar 

  61. Tilquin P, Barrow PA, Marly J, Pitel F, Plisson-Petit F, Velge P, et al. A genome scan for quantitative trait loci affecting the Salmonella carrier-state in the chicken. Genet Sel Evol. 2005;37(5):539–61.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  62. Swaggerty CL, Kogut MH, Ferro PJ, Rothwell L, Pevzner IY, Kaiser P. Differential cytokine mRNA expression in heterophils isolated from Salmonella-resistant and -susceptible chickens. Immunology. 2004;113(1):139–48.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  63. Byrne CM, Clyne M, Bourke B. Campylobacter jejuni adhere to and invade chicken intestinal epithelial cells in vitro. Microbiology. 2007;153(2):561–9.

    Article  CAS  PubMed  Google Scholar 

  64. Bailey RA, Kranis A, Psifidi A, Watson KA, Rothwell L, Hocking PM, et al. Colonization of a commercial broiler line by Campylobacter is under limited genetic control and does not significantly impair performance or intestinal health. Poult Sci. 2018.

  65. Ni L, Fang P, Hu Z-L, Zhou H-Y, Chen J-G, Wang F, et al. Identification and function of acid-sensing ion channels in RAW 264.7 macrophage cells. Current Medical Science. 2018;38(3):436–42.

    Article  CAS  PubMed  Google Scholar 

  66. Kong X, Tang X, Du W, Tong J, Yan Y, Zheng F, et al. Extracellular acidosis modulates the endocytosis and maturation of macrophages. Cell Immunol. 2013;281(1):44–50.

    Article  CAS  PubMed  Google Scholar 

  67. Miller MM, Taylor RL Jr. Brief review of the chicken major histocompatibility complex: the genes, their distribution on chromosome 16, and their contributions to disease resistance. Poult Sci. 2016;95(2):375–92.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  68. Shiina T, Briles WE, Goto RM, Hosomichi K, Yanagiya K, Shimizu S, et al. Extended gene map reveals tripartite motif, C-type lectin, and Ig superfamily type genes within a subregion of the chicken MHC-B affecting infectious disease. J Immunol. 2007;178(11):7162–72.

    Article  CAS  PubMed  Google Scholar 

  69. Friis C, Wassenaar TM, Javed MA, Snipen L, Lagesen K, Hallin PF, et al. Genomic characterization of Campylobacter jejuni strain M1. PLoS One. 2010;5(8):e12253.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  70. Andrews S: FastQC: a quality control tool for high throughput sequence data. Available online at: https://www.bioinformatics.babraham.ac.uk/projects/fastqc. 2010.

  71. Martin M. Cutadapt removes adapter sequences from high-throughput sequencing reads. J Comput Biol. 2011;17(1):3.

    Google Scholar 

  72. Dobin A, Davis CA, Schlesinger F, Drenkow J, Zaleski C, Jha S, et al. STAR: ultrafast universal RNA-seq aligner. Bioinformatics. 2013;29(1):15–21.

    Article  CAS  PubMed  Google Scholar 

  73. Liao Y, Smyth GK, Shi W. FeatureCounts: an efficient general purpose program for assigning sequence reads to genomic features. Bioinformatics. 2014;30(7):923–30.

    Article  CAS  PubMed  Google Scholar 

  74. Dennis G, Sherman BT, Hosack DA, Yang J, Gao W, Lane HC, et al. DAVID: database for annotation, visualization, and integrated discovery. Genome Biol. 2003;4(9):R60.

    Article  PubMed Central  Google Scholar 

  75. Pfaffl MW. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 2001;29(9):e45.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

We thank animal attendants at the Moredun Research Institute and technicians at Edinburgh Genomics for their assistance.

Funding

We gratefully acknowledge the support of the Scottish Government funding via the Rural & Environmental Science and Analytical Services programme of research for 2016–2021 and the Biotechnology & Biological Sciences Research Council (Institute Strategic Programme BBS/E/D/20002172 and Core Capability Grant in support of the National Avian Research Facility).

Author information

Authors and Affiliations

  1. The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Midlothian, EH25 9RG, UK

    Kay M. Russell, Jacqueline Smith, Abi Bremner, Cosmin Chintoan-Uta, Lonneke Vervelde & Mark P. Stevens

  2. The Royal Veterinary College, Hawkshead Lane, Hatfield, Hertfordshire, AL9 7TA, UK

    Androniki Psifidi

Authors
  1. Kay M. Russell
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Jacqueline Smith
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Abi Bremner
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Cosmin Chintoan-Uta
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Lonneke Vervelde
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Androniki Psifidi
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Mark P. Stevens
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

KMR: designed and carried out the study, performed transcriptomic analysis and co-wrote the manuscript. JS: assisted with downstream analysis and editing the manuscript. AB: qRT-PCR validation and co-wrote the manuscript. CCU: assisted with sample collection. LV and AP were co-investigators of one of the grants that funded the work, provided critical analysis of findings and edited the manuscript. MS: conceived the study, secured funding and edited the manuscript. All authors approved the final version of the manuscript.

Corresponding author

Correspondence to Mark P. Stevens.

Ethics declarations

Ethics approval

All procedures were conducted under Home Office project licence PCD70CB48 in full compliance with the requirements of the Animal (Scientific Procedures) Act 1986, with the approval of the Moredun Institute Animal Welfare and Ethical Review Board. Housing and husbandry complied with the Code of Practice for Housing and Care of Animals Bred, Supplied or Used for Scientific Purposes and were also overseen by the Moredun Institute Animal Welfare and Ethical Review Board. Animals were culled by a schedule one method authorized by the Animals (Scientific Procedures) Act 1986. This study was performed in compliance with the Animal Research: Reporting of In Vivo Experiments (ARRIVE) guidelines as defined by the National Centre for the Replacement, Refinement and Reduction of Animals in Research (NC3Rs).

Consent for publication

Not applicable.

Competing interests

The authors declare no conflicts of interest and no competing financial interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Figure S1.

IPA of DEGs in the caecal tonsils between control and C. jejuni M1 colonised line N birds at 1 dpi. Shown are significant molecular functions (A) associated with DEGs and a significant network of inflammatory responses involved during C. jejuni infection of line N at 1 dpi (B). In (B), genes or nodes coloured red are upregulated in C. jejuni colonised birds whereas those in green are downregulated. N = 3 for both groups.

Additional file 2: Table S1.

DEGs in the caecal tonsils between control and infected line 61 birds at 1 dpi. A fold change greater than 1 indicates genes that were upregulated in infected compared to control birds whereas a fold change less than 1 indicates genes which were downregulated in infected compared to control birds. N = 3 for both groups. FC: fold change, FDR: False Discovery Rate.

Additional file 3: Table S2.

Significant GO Terms associated with DEGs in the caecal tonsils between infected and control line 61 birds at 1 dpi. DEGs were identified between 3 infected and 3 control birds. FDR: False Discovery Rate.

Additional file 4: Figure S2.

IPA of DEGs in the caecal tonsils of control and C. jejuni M1 colonised line 61 birds at 1 dpi. Shown are a significant network of genes involved in the antimicrobial response and cellular movement (A) and of genes involved in lipid metabolism and transport (B). Genes or nodes coloured red are upregulated in colonised compared to control birds whereas those in green are downregulated.

Additional file 5: Figure S3.

IPA comparison of DEGs identified in the caecal tonsils between line 61 and N C. jejuni M1 colonised birds at 1 dpi. Shown are significant molecular functions (A) and a significant network of genes related to endocrine pathways (B) identified from the comparison of DEGs between 3 infected and 6 control birds of each line. In (B), genes or nodes coloured red are upregulated in colonised line N birds whereas those in green are upregulated in colonised line 61 birds.

Additional file 6: Table S3.

DEGs in the caecal tonsils between line N and line 61 control birds. Analysis compares the gene expression of all six control birds for each line. A fold change greater than 1 indicates genes more highly expressed in line N whereas a fold change less than 1 indicates genes more highly expressed in line 61. FC: fold change, FDR: False Discovery Rate.

Additional file 7: Table S4.

Significant GO Terms associated with DEGs in the caecal tonsils between line N and line 61 control birds. Upregulated GO terms are associated with genes with higher expression in line N and downregulated GO terms are associated with genes with higher expression in line 61. DEGs were identified between all six control birds of each line. FDR: False Discovery Rate.

Additional file 8: Figure S4.

IPA of DEGs in the caecal tonsils identified between control birds of line 61 and N. Shown are significant networks of genes relating to cell-to-cell signalling (A), gastrointestinal pathways (B), amino acid metabolism (C) and lipid metabolism (D). N = 6 for each line (3 control birds pooled from each time point) Genes or nodes coloured red are upregulated in colonised line N birds whereas those in green are upregulated in colonised line 61 birds.

Additional file 9: Figure. S5.

IPA of DEGs identified between control birds of line 61 and N. Shown are significant networks associated with predicted upstream regulators of DEGs: BCR (A), mir155 (B) and NFAT (C). Genes or nodes coloured red are upregulated in line N birds whereas those in green are upregulated in line 61 birds. N = 6 for each line (3 birds pooled from each time point)

Additional file 10: Table S5.

STAR Alignment statistics for RNA-Seq transcript reads. l6: line 61, ln: line N, i: infected, c: control, b: bird, dpi: days post-infection.

Additional file 11: Table S6.

Primer sequences for qRT-PCR

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

Reprints and Permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Russell, K.M., Smith, J., Bremner, A. et al. Transcriptomic analysis of caecal tissue in inbred chicken lines that exhibit heritable differences in resistance to Campylobacter jejuni. BMC Genomics 22, 411 (2021). https://doi.org/10.1186/s12864-021-07748-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12864-021-07748-2

Keywords

  • Campylobacter jejuni
  • Chicken
  • Resistance
  • Susceptibility
  • Transcriptome
  • Gene expression
  • Inbred
  • RNA-Seq

BMC Genomics

ISSN: 1471-2164

Contact us