Mycoplasma hyopneumoniae (Mhp) exists in every country where pigs are raised and is the main pathogen leading to respiratory disease in the swine industry (Maes et al., 2008; Stark, Nicolet & Frey, 1998). The pathogen resides in the respiratory tract, and its secretions can be found in infected pigs for a long time (Maes et al., 1996). The main clinical symptoms of infected pigs are dry cough, as well as dramatically reduced porcine growth and feed conversion rates, which cause great losses to the pig industry (Maes et al., 1996; Sarradell et al., 2003).
Production practices on some Chinese pig farms revealed that Chinese local breeds are more sensitive to Mhp than imported breeds such as Duroc and Landrace. The Meishan and Erhualian, which are characterized by high fecundity, show extremely high susceptibility to Mhp infection (Fang et al., 2015; Maingi et al., 2014). This suggests that genetic components contribute to breed susceptibility or resistance to Mhp infection. Recently, it was reported that quantitative trait loci (QTLs) are associated with respiratory disease lesions, and five QTL were detected in Landrace pigs (Okamura et al., 2012). In Chinese Erhualian pigs, QTLs affecting respiratory disease were identified by a genome-wide association study; CXCL6, CXCL8, KIT, and CTBP2 were highlighted as candidates that might associated with resistance or susceptibility to swine enzootic pneumonia-like respiratory disease (Huang et al., 2016). However, the genetic basis for the immune response to Mhp infection among different pig breeds remains largely unknown.
Jiangquhai is a Chinese pig breed distributed in the central Jiangsu Province. Similar to the Meishan and Erhualian breeds, Jiangquhai pigs exhibit sensitivity to Mhp infection (Maingi et al., 2014). Vaccines and antibiotics are used to control the occurrence of mycoplasma pneumonia of swine (MPS); however, these methods are not sufficient. It is therefore necessary to study the molecular mechanism of pathogenesis. This knowledge can be applied to carry out disease resistance breeding. In this study, we investigated the immune response of Jiangquhai and Duroc pigs to artificial Mhp infection using an RNA-sequencing (RNA-seq) approach. The goals were to identify genetic components that contribute to Mhp susceptibility or resistance and lay a foundation for genetic breeding that improve pig health.
Materials & Methods
Experimental design and sample collection
Twenty healthy 50-day-old Jiangquhai pigs were selected from the Jiangquhai Pig Breed Conservation Farm (Taizhou, China), and twenty healthy 50-day-old Duroc pigs were selected from the Xingtai Agriculture and Animal Husbandry Technology Development Company (Yangzhou, China). All pigs were free of all major porcine diseases and confirmed to be negative for Mhp, PRRSV, pseudorabies virus, and classical swine fever virus infection by PCR or reverse-transcription (RT)-PCR. Jiangquhai and Duroc pigs were randomly assigned to the control or infected group during the experiment and raised separately in isolation. Ten Jiangquhai and ten Duroc pigs were inoculated with 5 mL viral suspension of a virulent strain of Mhp (106 colour changing units [CCU]) (Xiong et al., 2014), which was provided by the Veterinary Medicine Institute of Jiangsu Academy of Agricultural Sciences (Nanjing, China). The remaining ten Jiangquhai and ten Duroc pigs were treated with an equivalent volume of aseptic physiological saline, which served as a negative control group. Four groups (i.e., Jiangquhai infection, Jiangquhai control, Duroc infection, Duroc control) were raised in isolation rooms to prevent cross-infection. Approval for the study was provided by the ethics committee of Yangzhou University (SYXK(Su) IACUC 2016-0131).
On day 28, all pigs were euthanized by stunning, and lung tissues were collected and stored at −70 °C. At this time, pulmonary MPS lesions were confirmed and assessed with the scoring system (Steinmann, Blaha & Meemken, 2014; Lee et al., 2011). From the beginning to the end (day 28) of the study, all experimental pigs were weighed prior to feeding in the morning to compare weight gain between groups. To assess the immune response, blood samples were collected on days 0 and 28 via jugular venipuncture into normal serum tubes without anticoagulant. The serum was separated by centrifugation (1,600× g for 10 min at 4 °C), divided into aliquots, and stored at −20 °C until analysis. Mhp-specific antibody in peripheral blood was detected.
RNA-seq library preparation and sequencing
Total RNA was extracted from lung tissue of three infected and three control pigs of each breed (three pigs selected randomly from each group) using TRIzol reagent (Invitrogen, South San Francisco, CA, USA) following the manufacturer’s protocol. RNA integrity was evaluated using the Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA). Samples with an RNA Integrity Number (RIN) >7 were subjected to subsequent analysis. The libraries were constructed using the TruSeq Stranded mRNA LTSample Prep kit (Illumina, San Diego, CA, USA) according to the manufacturer’s instructions. Then, these libraries were sequenced on the Illumina Hiseq 2500 platform (Shanghai OE Biotech Co., Ltd, Shanghai, China), and 125-bp paired-end reads were generated.
Quality control and mapping
Raw data (raw reads) were processed using the NGS QC Toolkit (Ravi, Mukesh & Liu, 2012). Low-quality reads and those containing poly-N were removed to ensure high-quality mapping. Then the clean reads were mapped using the Sus scrofa genome 11.1 as a reference with bowtie2 (Langmead & Salzberg, 2012) or Tophat software packages (http://tophat.cbcb.umd.edu/) (Kim et al., 2013).
RNA-seq data analysis
The FPKM (Fragments Per Kilobase of transcript per Million fragments mapped) value of each gene was calculated using cufflinks (Cole et al., 2012), and the read counts of each gene were obtained by HTSeq-Count (Anders, Pyl & Huber, 2015). Differentially expressed genes (DEGs) were identified using the DESeq estimateSizeFactors and nbinomTest functions, corrected p-value of 0.05 and log2 (Fold change) (log2 FC) of 1 were set as the threshold for significantly differential expression. Hierarchical clustering analysis of DEGs was performed to inspect sample relations. The DEGs were annotated by GO functional enrichment and KEGG pathway analysis using the Database for Annotation, Visualization and Integrated Discovery (DAVID).
RNA was extracted from lung tissue of six infected and six control pigs of each breed using the TRIzol reagent following the manufacturer’s protocol. First-strand cDNA synthesis was performed using 5 µg of RNA and the Superscript II cDNA amplification system (Invitrogen, South San Francisco, CA, USA) according to the manufacturer’s protocol. Quantitative PCR was performed using an ABI 7500 real-time PCR system (Applied Biosystems, Foster City, CA, USA) and Power SYBR Green PCR Master Mix (Invitrogen, South San Francisco, CA, USA). The gene for glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was included as an endogenous control, and the specific primers used in the RT-qPCR assays are listed in Table S1. Relative expression of target genes was determined by the comparative cycle threshold (CT) method (Livak & Schmittgen, 2001) and the ΔCT value was calculated by subtracting the target CT of each sample from its GAPDH CT value.
Weight gain and antibody level data are presented as mean ± standard error (SE). Comparison of variables was performed using one-way analysis of variance with SPSS13.0 software (SPSS Inc., Chicago, IL, USA).
Effect of Mhp infection on weight gain, antibody production, and lung lesions in Jiangquhai and Duroc pigs
The average daily weight gain (ADG) of the Jiangquhai infected pigs was highly significantly lower than the Jiangquhai control pigs (p < 0.01), while the ADG of Duroc infected pigs was not significantly different from Duroc control pigs (p > 0.05) (Table 1). These results demonstrate that Mhp infection had a greater impact on the growth rate of Jiangquhai pigs compared to Duroc pigs.
|Groups||N||Average body weight (kg)||ADG (g/d)||Antibody levels (s/p)|
|Jiangquhai infection||10||8.54 ± 0.77||12.26 ± 0.51||132.86 ± 14.56A||0.05 ± 0.03||0.85 ± 0.20A|
|Jiangquhai control||10||8.46 ± 0.50||15.29 ± 0.76||244.11 ± 21.10B||0.05 ± 0.04||0.08 ± 0.07|
|Duroc infection||10||10.64 ± 0.83||18.41 ± 0.49||277.50 ± 25.81||0.02 ± 0.01||0.48 ± 0.19B|
|Duroc control||10||10.53 ± 0.72||18.81 ± 0.58||295.89 ± 18.86||0.02 ± 0.01||0.04 ± 0.01|
Different letters in the same column indicate significant differences of mean values (A and B) (p < 0.01).
On day 28, the level of Mhp-specific antibody (reported as the sample mean/positive control mean (s/p) value) in the peripheral blood of Jiangquhai infected pigs reached at 0.85 ± 0.20, which was significantly higher than that of Duroc infected pigs (0.48 ± 0.19) (p < 0.01) (Table 1). Mhp-specific antibody was not detected in control pigs.
Our analysis of lung tissue on day 28 revealed that Jiangquhai infected pigs had more serious Mhp lung lesions (Fig. 1), a greater difference in Mhp lung lesion scores from Jiangquhai infected pigs compared to Duroc infected pigs (p < 0.01) (Fig. 2).
Preliminary analysis and summary of RNA-Seq data quality
We performed RNA-seq to analyze the transcriptional profile of lung tissue from the four experimental groups. We found that 87.54–96.47% of clean reads were mapped to the reference genome (Sus scrofa 11.1), and 80.19–93.33% were uniquely mapped (Table S2). The sample to sample distance heat map showed a good degree of similarity between all three replicates (Fig. S1), indicating that there were no significant differences in gene expression among the biological replicates. These results showed that the RNA-seq data were reliable and met the conditions for differential expression analysis.
DEGs analysis and RT-qPCR validation
We analyzed the DEG profiles of lung tissues from Mhp-infected Jiangquhai and Duroc pigs by comparing infected and control animals of the same breed. Genes with relative expression levels that showed log2 FC > 1 (p < 0.05) were considered up-regulated, and those with log2 FC <−1 (p < 0.05) were considered down-regulated. Of the 2,250 DEGs detected in Jiangquhai pigs, 966 genes were up-regulated and 1,284 down-regulated. Of the 3,526 DEGs detected in Duroc pigs, 1,326 and 2,200 were up- and down-regulated, respectively (Fig. 3). Jiangquhai and Duroc pigs shared 1,669 DEGs in response to Mhp infection, with 632 up-regulated genes and 1,037 down-regulated genes. Further analysis showed that Duroc pigs had 694 uniquely up-regulated DEGs, which was two times higher than the number in Jiangquhai pigs (334 DEGs) (Fig. 3).
To verify the RNA-seq results, eight genes were randomly selected for RT-qPCR analysis. Expression FCs determined by RT-qPCR analysis was compared against the profiles predicted by RNA-seq. The RT-qPCR results verified the changes in expression levels of the eight genes (Fig. 4), indicating that the RNA-seq data were reliable.
Terms and pathways associated with immunobiology were enriched in both breeds
To determine the biological function of DEGs after Mhp infection in lung tissue, the common 1,669 DEGs were submitted to DAVID for GO analysis, which revealed enrichment of 281 GO terms (p < 0.05). The top 10 significant enrichments are shown in Fig. 5, among which cell adhesion, inflammatory response and immune response were the most significantly regulated by Mhp infection. Pathway analysis based on the KEGG database revealed the top 20 significant signaling pathways of the two breeds (Fig. 6). Many immune-related pathways were enriched, including the cytokine-cytokine receptor interaction (IL18, IL1R1), PI3K-Akt signaling pathway (TLR2, ITGA1, ITGB7, PIK3R5), and chemokine signaling pathway (CXCL8, CXCL13).
Specific terms and pathways in Jiangquhai and Duroc pigs
Jiangquhai and Duroc pigs also had different responses to Mhp infection. The specific DEGs of Jiangquhai (581 DEGs) and Duroc pigs (1,857 DEGs) were separately submitted to DAVID for GO analysis. The results revealed 100 GO enrichments in Jiangquhai pigs and 314 GO enrichments in Duroc pigs. Table S3 shows the top 10 significant enrichments in Jiangquhai pigs, including cell adhesion, leukocyte migration and extracellular matrix disassembly. Table S4 lists the top 10 significant enrichments in Duroc pigs, including cilium assembly, cilium-dependent cell motility and interleukin-7-mediated signaling pathway.
KEGG pathway analysis revealed 38 specific signaling pathways in Jiangquhai pigs (Table S5) and 54 specific signaling pathways in Duroc pigs (Table S6). Further analysis found that Duroc pigs had more immune-related pathways (18 immune-related pathways), including chemokine signaling pathway, NOD-like receptor signaling pathway, antigen processing and presentation, toll-like receptor signaling pathway, 253 DEGs were enriched in those 18 pathways (Table 2). Jiangquhai pigs only identified 8 immune-related pathways, including leukocyte transendothelial migration, hematopoietic cell lineage, cell adhesion molecules, 99 DEGs were enriched in those 8 pathways (Table 2).
|Duroc pigs||Cytosolic DNA-sensing pathway||Immune system||IFNB1, NFKBIA, CXCL10, IRF7, ZBP1, CCL5, CCL4, DDX58, IL6, RIPK3, POLR3D, NFKBIB|
|Intestinal immune network for IgA production||Immune system||CCR9, CXCL12, ICOS, SLA-DRB1, CD28, LOC106504372, IL10, IL6, AICDA, IL15RA|
|Complement and coagulation cascades||Immune system||C1QA, C1S, F7, BDKRB1, F2, THBD, VSIG4, C1QB, C1QC, VWF, SERPINE1, C7, CPB2, C1R|
|Chemokine signaling pathway||Immune system||CCR5, CCR1, XCR1, CXCR6, CCR9, CXCL2, NFKBIA, CXCL10, CXCL12, CCL5, AKT3, CCL4, PTK2B, ADCY4, GRK5, JAK3, CXCR3, NFKBIB, LOC110255211, GNG3, PARD3, CXCR2, HCK, ADCY1, PLCB2|
|NOD-like receptor signaling pathway||Immune system||NFKBIA, CCL5, PSTPIP1, TNFAIP3, IL6, MAPK10, TRIP6, NFKBIB, BIRC3, MAPK11|
|RIG-I-like receptor signaling pathway||Immune system||IFNB1, NFKBIA, CXCL10, IRF7, ISG15, DHX58, DDX58, TKFC, MAPK10, NFKBIB, TANK, MAPK11|
|Antigen processing and presentation||Immune system||TAP1, SLA-DRB1, CALR, PDIA3, LOC106504372, CD8B, HSP70.2, IFNG, PSME2, KLRD1, LOC100523789|
|Toll-like receptor signaling pathway||Immune system||IFNB1, NFKBIA, CXCL10, IRF7, CD14, LY96, CCL5, IFNAR2, AKT3, CCL4, IL6, MAPK10, MAP3K8, MAP2K6, MAPK11|
|T cell receptor signaling pathway||Immune system||NFKBIA, ICOS, PDCD1, AKT3, CD28, CD8B, IFNG, IL10, CTLA4, NFKBIB, MAP3K8, CARD11, MAPK11, PAK6, NFKBIE|
|TNF signaling pathway||Signal transduction||CXCL2, NFKBIA, CXCL10, CREB3L4, CCL5, AKT3, TNFAIP3, FAS, PTGS2, IL6, LTA, RIPK3, MAPK10, MAP3K8, MAP2K6, BIRC3, TRAF1, MAPK11|
|Jak-STAT signaling pathway||Signal transduction||IFNB1, IL7R, SOCS1, IFNAR2, IL27RA, AKT3, IL2RA, CSF3, IFNG, IL10, IL2RG, IL6, JAK3, OSMR, IL15RA, IL20RB, LOC100736818, PIM1, CDKN1A, IL2RB, TSLP, IL22, PTPN2|
|cAMP signaling pathway||Signal transduction||NFKBIA, TNNI3, CREB3L4, GABBR1, SSTR1, PLD1, AKT3, HTR1B, AMH, ADCY4, MAPK10, GRIA4, GRIA3, PDE4D, SUCNR1, LOC110255845, GRIN3A, PPP1R1B, HCAR2, GRIA1, ADCY1, GLI3, PDE3B, GRIN2A, GRIN2B, CACNA1C, GIPR, CNGB1|
|NF-kappa B signaling pathway||Signal transduction||NFKBIA, CXCL12, CD14, LY96, BCL2A1, TNFAIP3, CCL4, DDX58, PTGS2, LTA, BIRC3, TRAF1, NFKB2, CARD11|
|MAPK signaling pathway||Signal transduction||CD14, NTF3, DDIT3, PLA2G4B, RPS6KA1, AKT3, HSP70.2, FAS, EGF, FGF14, NTRK1, FGFR4, MAPK10, DUSP4, PRKCG, GADD45B, MAP3K8, MAP2K6, PTPN7, CACNA2D2, CACNA2D3, FGF12, NFKB2, CACNA1H, DUSP2, MAPK8IP2, MAPK11, CACNA1C, CACNA1I, MAP4K1, CACNA1E|
|FoxO signaling pathway||Signal transduction||CCNB2, IL7R, PCK2, CCNB1, AKT3, EGF, IL10, IL6, MAPK10, PRKAG2, GADD45B, CCNB3, CDKN1A, IRS2, PLK1, MAPK11|
|Cytokine-cytokine receptor interaction||Signaling molecules and interaction||CCR5, CCR1, XCR1, CXCR6, CCR9, CXCL2, IFNB1, CXCL10, CXCL12, CCL5, IL7R, IFNAR2, TNFRSF9, CD27, CCL4, IL2RA, FAS, CSF3, IFNG, EGF, IL10, IL2RG, AMH, IL6, LTA, OSMR, CXCR3, IL15RA, IL20RB, LOC100736818, IL18RAP, IL25, IL2RB, CXCR2, TSLP, IL22|
|Cell adhesion molecules (CAMs)||Signaling molecules and interaction||ICOS, SELL, SLA-DRB1, OCLN, PDCD1, VCAN, CLDN1, CD28, LOC106504372, CD8B, CTLA4, MPZ, L1CAM, TIGIT, NLGN3, LOC100525346, ITGA8, NCAM2, NEGR1|
|Neuroactive ligand–receptor interaction||Signaling molecules and interaction||P2RY2, BDKRB1, F2, GABBR1, GZMA, CRHR2, SSTR1, P2RY6, TRH, TSPO, HRH4, OPRL1, HTR1B, PTH1R, TAAR1, LTB4R2, THRB, PTGDR, GRIA4, GRIA3, P2RX3, PTGIR, GRIK1, GABRB2, CNR1, LRRC74B, PARD3, GRIN3A, P2RX1, GRM2, GABRR3, GRIK2, GRIA1, GRIN2A, GRIN2B, GIPR|
|Jiangquhai pigs||Complement and coagulation cascades||Immune system||C5, MBL1, C6, PLAU, F5, SERPINA5, ITGAM, KNG1, SERPINF2|
|Leukocyte transendothelial migration||Immune system||CLDN23, CLDN18, CLDN5, PECAM1, ITGAM, TXK, ESAM, GNAI1, PLCG2|
|Natural killer cell mediated cytotoxicity||Immune system||NCR1, IFNAR1, KLRK1, CD244, LOC100739080, SHC3, LOC100523789, PLCG2|
|Hematopoietic cell lineage||Immune system||CD4, GP1BB, CD34, CD19, ITGAM, CD7|
|Hippo signaling pathway||Signal transduction||PARD6B, BMP2, WNT10B, WNT16, GDF7, WNT11, TCF7L1, GDF6, WTIP, FZD1|
|cAMP signaling pathway||Signal transduction||FXYD2, FOS, PDE4A, DRD2, GNAI1, LOC100738425, LOC110255845, LOC110255846, CACNA1F, PDE4C|
|Notch signaling pathway||Signal transduction||HES1, DTX2, RBPJL|
|Cell adhesion molecules (CAMs)||Signaling molecules and interaction||NECTIN1, CD4, CLDN23, CLDN18, CLDN5, PECAM1, CD34, ITGAM, VTCN1, ESAM, CDH4, CNTNAP2|
Analysis of important DEGs related to immune responses
In this study, we mainly focused on the important DEGs related to immune responses. Based on gene clustering and specific KEGG pathways (Table 2), some DEGs that we identified were well-known components of the innate immune response, such as chemokines, interleukins, interferon response factors and complement components. Forty-five important specific DEGs related to innate immune responses had been identified in Duroc pigs (Fig. 7B), and only 20 important specific DEGs had been identified in Jiangquhai pigs (Fig. 7A). Furthermore, some immune-related genes were down-regulated in Jiangquhai pigs, such as adhesion molecules (PECAM1, CD34, CD7, CDH4), WNT molecules (WNT11, WNT16). As for Duroc pigs, more immune-related genes were up-regulated, including chemokines (CCL4, CCL5, CCR1, CCR5, CXCL2, CXCL10, CXCL12, CXCR6), interferon response factors (IFNAR2, IFNG), and interleukins (IL6, IL10, IL15RA, IL2RA, IL18RAP, IL2RB, IL2RG, IL27RA, IL7R). Among these immune-related genes, CXCL10, CCL4, IL6 and IFNG were the most differently expressed genes.
Previous reports state that the primary effect of Mhp infection on pigs is reduced growth performance (Maes et al., 2008; Pointon, Byrt & Heap, 1985). However, the degree to which Mhp effect differs between Chinese local breeds and imported breeds (such as Duroc and Landrace), and the effect on Chinese local breeds is much more serious (Fang et al., 2015). Our results were consistent with previous reports, Jiangquhai pigs infected with Mhp exhibited poorer growth performance than Duroc pigs. Some studies have reported that Mhp infection causing a humoral immune response in pigs (Blanchard et al., 1992). Moreover, the level of antigen-specific antibody is an important indicator of MPS lesion formation in animals, and increased antigen-specific antibody production may exacerbate MPS lung lesion severity (Borjigin et al., 2016; Davis et al., 1985; Katayama et al., 2011). Our results also showed Mhp-infected Jiangquhai pigs exhibited higher blood levels of Mhp antibody and more serious Mhp lung lesions. These results confirm that Jiangquhai pigs are more susceptible to Mhp infection, and Duroc pigs possess greater resistance. In addition, it was reported that the age and weight of pigs do not affect the susceptibility to Mhp infection (Piffer & Ross, 1984). Therefore, it is theoretically possible that genetic components contribute to Mhp resistance/susceptibility differs among breeds.
To gain insight into how the transcriptome profiles of different pig breeds vary in response to Mhp infection, we performed RNA-seq to analyze the transcriptional profiles of lung tissue from two breeds. We identified 2,250 and 3,526 DEGs in lung tissue from Jiangquhai pigs and Duroc pigs, respectively. Duroc pigs had 694 unique up-regulated DEGs, whereas Jiangquhai pigs only had 334. Taken together, these results indicate that the molecular interactions and signaling pathways following Mhp infection may be more complex in Duroc pigs.
Our analysis revealed 1,669 DEGs shared between Jiangquhai and Duroc pigs in response to Mhp infection. These common DEGs also showed significant enrichment of many immune-relevant terms and pathways. Among these, many up-regulated immune-relevant genes were observed in both breeds that could play a role in resistance to Mhp infection. One TLR family member, TLR2, has a fundamental role in pathogen recognition, signal transmission and activation of innate immunity, and stimulation of inflammatory cytokine production (Yoshihiro et al., 2003). IL18 and IL1R1 are pro-inflammatory mediators involved in many cytokine-induced immune and inflammatory responses (Dale & Nicklin, 1999). PI3Ks (PIK3R5) are important enzymes involved in various signal transduction pathways, and play important roles in regulating cell growth, survival, death and chemotaxis (Margaria et al., 2019). Chemokines such as CXCL8 and CXCL13 can recruit immune cells to the site of infection (Strieter et al., 1999; Sun et al., 2006). Moreover, ITGA1 and ITGB7, which help recruit immune cells such as T, B, and natural killer (NK) cells, were up-regulated following Mhp infection (Campbell & Humphries, 2011; Cheli et al., 2007; Lim, Leung & Krissansen, 1998). These immune-related DEGs help clarify the immune response in pigs following Mhp infection.
Comparison of the specific DEGs between Jiangquhai and Duroc pigs revealed some important DEGs related to immune responses were specifically altered in Jiangquhai or Duroc pigs, and these important DEGs enriched in immune-related pathways play an important role in the underlying host mechanism to defend against Mhp infection.
Adhesion molecules are important signal transmitters of the immune system, they function as signal transduction, transported signals from outside to inside of cell (Kumar et al., 2016; Korytina et al., 2019), In this study, many adhesion molecules were specifically down-regulated in Jiangquhai pigs, including PECAM1, CD34, CD7 and CDH4. These adhesion molecules were significantly enriched in Cell adhesion molecules (CAMs) and Hematopoietic cell lineage pathway, have the function in pathogen recognition, signal transmission and regulating cell movement (Chasiotis et al., 2012; Samanta & Almo, 2015; Xiao et al., 2010). However, these adhesion molecules were down-regulated may reduce host’s capacity for antigen presentation and processing. In addition, two WNT molecules (WNT11, WNT16) enriched in Hippo signaling pathway were identified in Jiangquhai pigs. WNT genes exert immune modulatory functions during pathogens infection (Brandenburg & Reiling, 2016), and could regulate the expression of immune response genes during challenge by pathogens, such as interferon genes, Toll-like receptors and MHC genes (Garcia-Rodriguez et al., 2017). WNT11 and WNT16 were down-regulated, which may induce the inhibition of its downstream signaling, including cell growth, survival and cell-cycle progression. Therefore, thus results may interfere with Jiangquhai pigs to establish an effective immune response against Mhp infection.
Chemokines constitute a large family of chemotactic molecules that are fundamentally involved in the inflammatory response by attracting immune cells to sites of inflammation, and promote the immune response and wound healing (Le et al., 2004; Zlotnik & Yoshie, 2012). Many chemokines are expressed in immune tissues and cells in pigs infected with Mhp (Li et al., 2014; Zhang et al., 2011). In this study, many specific up-regulated chemokines (CCL4, CCL5, CCR1, CCR5, CXCL2, CXCL10, CXCL12 and CXCR6) were identified in Duroc pigs, these chemokines were mainly enriched in cytokine-cytokine receptor interaction and chemokine signaling pathway. The two pathways are involved in specific functional tasks that recruit immune cells to induce inflammatory and adaptive immune responses (Carvalho et al., 2012; Hu et al., 2016). Therefore, these up-regulated chemokines could recruit more immune cells for pathogen defense, and Duroc pigs exhibited a larger chemotactic immune cell capacity. Among these chemokines, CXCL10 and CCL4 were most highly expressed. CXCL10 is an important regulator of pulmonary diseases (Gao et al., 2018; Tighe et al., 2011), and has the function of chemotactic monocytes/macrophages, T cells, and NK cells and promotion of T-cell adhesion to endothelial cells (Angiolillo et al., 1995; Dufour et al., 2002). CCL4 is an important chemoattractant for natural killer cells, monocytes and a variety of other immune cells, regulates immune response to pathogen infection (Bystry et al., 2001; Zhao et al., 2007). Therefore, CXCL10 and CCL4 maybe important chemokines involved in chemokine signaling pathway, and regulate the process of immune response to Mhp infection.
Mhp stimulates host immune response by inducing macrophages to release pro-inflammatory cytokines, such as IL-2, IL-6, IL-8, IL10 and IL-1β (Fourour et al., 2019; Lorenzo et al., 2006). These pro-inflammatory cytokines are important players in innate and adaptive immunity, and affect immune balance by suppressing cell-mediated immunity (Zhang et al., 2018). In this study, we also identified some specific up-regulated interleukins (IL6, IL10, IL15R A, IL2RA, IL18RAP, IL2RB, IL2RG, IL27RA and IL7R) in Duroc pigs. These interleukin cytokines can modulate a broad spectrum of immune response processes, such as NOD-like receptor signaling pathway, toll-like receptor signaling pathway, TNF signaling pathway and Jak-STAT signaling pathway. Thus, activation of interleukin cytokines in Duroc pigs may induce additional immune cytokine production and immune cell recruitment for pathogen defense. In addition, interferon response factors have the function of activate macrophages, protect host cells to resist pathogen infection (Rodriguez et al., 2007). Two interferon response factors (IFNAR2, IFNG) were highly expressed in Duroc pigs, which may further activated macrophages and enhanced the ability to resistance Mhp infection. Moreover, IL6 and IFNG were most highly expressed among these cytokines. IL-6 is a primary cytokine, which could activate macrophages to secrete inflammatory cytokines and chemokines (Yan et al., 2012), and responsible for Mhp clearance in lungs (Wu et al., 2008). IFNG had been detected in the lungs of pathogen-infected pigs and be postulated to be a necessary component for host control of pathogen (Zhang et al., 2011). Therefore, IL6 and IFNG were also important cytokines involved in the regulation of immune response to Mhp infection.
Apoptosis is a mechanism of programmed cell death and is essential for the regulation of immune responses (Rantong & Gunawardena, 2015). Our results further revealed that the apoptosis-related gene (FAS) was specifically activated in Duroc pigs. The FAS gene has been reported to play a central role in the physiological regulation of programmed cell death and has been implicated in the pathogenesis of various diseases of the immune system (Strasser, Jost & Nagata, 2009). Previous studies have shown that the FAS gene involved in the regulation of inflammatory response in pulmonary (Liu et al., 2017). Therefore, the FAS gene activation can induce apoptosis and regulate the immune response in response to the Mhp infection. In addition, in the Duroc-specific DEGs involved in GO enrichments (cilium assembly, cilium-dependent cell motility), we found intraflagellar transport (IFT) genes, which can modulate primary cilia formation and function (Pedersen & Rosenbaum, 2008), such as IFT172 and IFT81. Primary cilia are found on the cell surface of almost every cell type, which play an important role in signaling and development (Singla & Reiter, 2006) and influence immune cell migration (Finetti, Onnis & Baldari, 2015). Therefore, intraflagellar transport genes may play an important role in the immune response to Mhp infection. Further elucidating the function remains to be a near future goal.
This is the first study to describe the transcriptional profiles of lung tissue from different pig breeds following Mhp infection. RNA-seq analysis identified 966 up-regulated and 1,284 down-regulated genes in Jiangquhai pigs compared to 1,326 up-regulated and 2,200 down-regulated genes in Duroc pigs. Both breeds shared some KEGG pathways, including cytokine-cytokine receptor interaction, PI3K-Akt signaling pathway, and chemokine signaling pathway. All of these may play important roles in Mhp infection resistance. In Duroc pigs, 1857 specific DEGs were identified, KEGG pathway analysis revealed 18 immune-related pathways. I Jiangquhai pigs, 581 specific DEGs were identified and eight immune-related pathways were identified. Compared to Jiangquhai pigs, chemokines, interferon response factors, interleukins, complement components, apoptosis-related molecule and other immune-related molecules were specifically activated in Duroc pigs, and they may help host enhance immune response and reduce Mhp susceptibility. The results of our analysis reveal an important role of genetics in the immune response to Mhp infection, and this should be investigated further to improve pig health during breeding.
Sample clustering based on RNA-seq profiles
Variance-stabilizing transformed count data was used for all samples. The heat map shows a greyscale false colour representation of the Euclidean distance matrix, and the dendrogram represents a hierarchical clustering.