ORIGINAL RESEARCH article
Avian Pathogenic Escherichia coli (APEC) Strain-Dependent Immunomodulation of Respiratory Granulocytes and Mononuclear Phagocytes in CSF1R-Reporter Transgenic Chickens
- 1Division of Infection and Immunity, The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh, United Kingdom
- 2Department of Animal Science, Iowa State University, Ames, IA, United States
- 3Infectiologie Santé Publique, Institut National de la Recherche Agronomique, Université de Tours, Nouzilly, France
Avian pathogenic Escherichia coli (APEC) cause severe respiratory and systemic disease in chickens, commonly termed colibacillosis. Early immune responses after initial infection are highly important for the outcome of the infection. In this study, the early interactions between GFP-expressing APEC strains of serotypes O1:K1:H7 and O2:K1:H5 and phagocytic cells in the lung of CSF1R-reporter transgenic chickens were investigated. CSF1R-reporter transgenic chickens express fluorescent protein under the control of elements of the CSF1R promoter and enhancer, such that cells of the myeloid lineage can be visualized in situ and sorted. Chickens were separately inoculated with APEC strains expressing GFP and culled 6 h post-infection. Flow cytometric analysis was performed to phenotype and sort the cells that harbored bacteria in the lung, and the response of the sorted cells was defined by transcriptomic analysis. Both APEC strains were mainly detected in CSF1R-transgeneneg (CSF1R-tgneg) and CSF1R-tglow MHC IIneg MRC1L-Bneg cells and low numbers of APEC were detected in CSF1R-tghigh MHC IIpos MRC1L-Bpos cells. Transcriptomic and flow cytometric analysis identified the APECpos CSF1R-tgneg and CSF1R-tglow cells as heterophils and the APECpos CSF1R-tghigh cells as macrophages and dendritic cells. Both APEC strains induced strong inflammatory responses, however in both CSF1R-tgneg/low and CSF1R-tghigh cells, many immune related pathways were repressed to a greater extent or less activated in birds inoculated with APEC O2-GFP compared to APEC O1-GFP inoculated birds. Comparison of the immune pathways revealed the aryl hydrocarbon receptor (AhR) pathway, IL17 and STAT3 signaling, heterophil recruitment pathways and the acute phase response, are modulated particularly post-APEC O2-GFP inoculation. In contrast to in vivo data, APEC O2-GFP was more invasive in CSF1R-tghigh cells in vitro than APEC O1-GFP and had higher survival rates for up to 6 h post-infection. Our data indicate significant differences in the responses induced by APEC strains of prevalent serotypes, with important implications for the design and interpretation of future studies. Moreover, we show that bacterial invasion and survival in phagocyte populations in vitro is not predictive of events in the chicken lung.
APEC are the etiologic agent of colibacillosis in chickens, a complex of severe respiratory and systemic infections that constitute an important threat to all sectors of the poultry industry. Colibacillosis causes losses due to early mortality, condemnation of carcasses and reduced productivity (1). APEC constitute a large group of diverse serotypes, with the O1, O2, and O78 serogroups amongst the most prevalent globally (2).
The mechanisms underlying mucosal colonization and systemic translocation by APEC are ill-defined. Physical barriers, such as mucociliary clearance and host defense peptides may limit APEC from establishing an infection in the respiratory tract (3, 4) and the early innate immune responses, including the response by heterophils and macrophages, are thought to be important in the control of colibacillosis (5–9). In a recent study we showed that very early responses were instrumental to the fate of the birds, as chickens of a relatively susceptible inbred line succumbed to intra-air sac APEC O1:K1:H7 infection within 14 h post-inoculation whereas birds of a relatively resistant line survived (10).
Previous observational studies with strains of APEC of serogroups O1, O2, and O78 showed that APEC caused localized inflammation in the lung, often the site of onset of colibacillosis, with heterophil and macrophage recruitment to the site of inflammation within 6–12 h post-infection (5, 8), although the phenotype of the lung cells associated with APEC was never unambiguously characterized. Resistance to phagocytosis has been suggested to be an important mechanism in the development of colibacillosis. The ability of blood-derived macrophages to phagocytose and kill APEC varied between APEC strains with more virulent strains hypothesized to be able to resist the bactericidal activity of macrophages to a greater extent than less virulent strains (5, 6) or non-pathogenic avian E. coli (6). Several APEC virulence factors, including surface polysaccharides and fimbriae, and the K1 capsule in particular (6), were shown to contribute toward evasion of phagocytosis in birds (11). However, the role of lung phagocytes in APEC clearance and their immune response to APEC in the lung has not been previously studied.
We aimed to study the first line of cellular defense against APEC in the respiratory tract, a key porte d'entrée for pathogenic E. coli in poultry. We identified and phenotyped APEC-infected lung cells at 6 h post-infection (hpi) with fluorescent bacterial strains using flow cytometry and performed transcriptomic analysis on the sorted APEC-harboring cells in the lung. Owing to the large diversity of APEC strains, we inoculated chickens with sequenced strains representing two globally prevalent serotypes (O1:K1:H7 or O2:K1:H5) of the sequence-type (ST) 95 lineage, enabling us to directly compare for the first time the cellular immune response at 6 hpi in the chicken lung to these strains.
Materials and Methods
CSF1R-mApple transgenic chickens (12) were provided by the National Avian Research Facility (NARF), Edinburgh, UK. All birds were hatched in a conventional animal unit and transferred to the experimental room immediately post-hatch and reared under specified pathogen-free (SPF) conditions with ad libitum access to feed and water. Frozen lung cells from non-transgenic Hy-Line birds (Hy-Line Brown) were used as controls for flow cytometry and cell sorting.
The genome sequenced strain named APEC O1 of serotype O1:K1:H7 and ST95 was kindly provided by Professor Lisa Nolan, Iowa State University, USA [(13); GenBank NC_008563]. The strain naturally exhibits gentamicin resistance and was transformed with plasmid pFVP25.1, which constitutively expresses green fluorescent protein (GFP) (14) enabling APEC-infected cells to be detected by virtue of their fluorescence (APEC O1-GFP). The genome sequenced APEC O2 strain of serotype O2:K1:H5 and ST95 (named BEN2908; GCA_902705295 (https://www.ebi.ac.uk/ena/data/view/GCA_902705295) available at European Nucleotide Archive) was also transformed with pFVP25.1, generating strain APEC O2-GFP (15, 16). APEC strains were cultured overnight to stationary phase in Lysogeny Broth (LB, Luria formulation, Sigma Aldrich, UK) containing 100 μg/ml ampicillin (Sigma Aldrich, UK) to maintain pFVP25.1, with shaking at 180 rpm at 37°C. The inocula were prepared by collection of bacteria from fresh cultures by centrifugation and resuspension in sterile, apyrogenic phosphate-buffered saline (PBS) and the inoculation dose confirmed by retrospective plating of serial dilutions onto MacConkey agar (MCA) plates.
Six-week old CSF1R-reporter transgenic chickens were inoculated with 1 × 109 colony-forming units (CFU) of APEC O1-GFP or APEC O2-GFP in 100 μl PBS or 100 μl PBS as control, administered into the right caudal thoracic air sac, and culled 6 hpi. Clinical signs and colibacillosis lesions were recorded as previously described (10) with cumulative scores based on lesions in the lungs, air sacs, liver and pericardium. Viable bacteria in the cranial right and left lung, blood, spleen, and liver were enumerated as described below. Right and left lung tissue was collected independently to prepare gradient purified lung leukocytes and an aliquot used to phenotype APECpos cells by flow cytometry in parallel to the cell sorting to obtain APECpos cells for transcriptomic analysis. Two birds per day were inoculated due to the time and resources required for downstream processing. A total of 22 birds from three hatches were used for the APEC O1-GFP studies (APEC O1-GFP, n = 13; PBS controls, n = 9). A total of 24 birds from two hatches were used for the APEC O2-GFP studies (APEC O2-GFP, n = 12; PBS controls, n = 12).
Bacteriological Analysis of Tissues
Viable bacteria in tissues were enumerated as previously described (10), with minor changes. APEC O1-GFP samples were plated onto MCA plates containing 10 μg/ml gentamicin (ThermoFisher, UK). APEC O2-GFP samples were plated onto antibiotic-free MCA plates. To account for potential unrelated bacterial contaminants and for potential loss of pFVP25.1 within 6 hpi in birds, all right lung samples from birds inoculated with both APEC strains were additionally plated onto antibiotic-free LB agar plates and their fluorescence confirmed under UV light. All obtained colonies were GFP positive (not shown).
Preparation of Lung Leukocytes for RNAseq
After collecting cranial lung tissue to enumerate viable bacteria, the right and left lungs were collected separately in 5 ml PBS with 100 μl heparin (5,000 units/ml, Wockhardt, UK) and 50 μl RNAse inhibitor (0.4 units/μl RNAsin Plus, Promega, UK). Maintaining the tissue in collection buffer with RNAse inhibitor (0.4 units/μl), tissues were cut into small pieces and enzymatically digested with an equal mix of DNAse I and collagenase A (1 and 3 mg/ml, respectively, Sigma Aldrich, UK) in supplement-free RPMI 1640 media (Sigma Aldrich, UK) for 30 min at 37°C and 5% CO2. The digested lung tissue was passed through a 70 μm cell strainer on ice. Samples were washed once with cold PBS (350 x g, 5 min, 4°C) and lung leukocytes obtained by gradient purification with Histopaque 1.077 (Sigma Aldrich, UK) for 20 min at 400 x g at room temperature (RT). The interface and layer above were collected and the samples washed twice with cold PBS. The cell numbers and viability were determined by Trypan Blue staining (Corning, UK) and the cells re-suspended in cell sorting buffer (PBS with 0.5% bovine serum albumin, BSA; Sigma Aldrich, UK) with RNAse inhibitor.
Flow Cytometry and Cell Sorting
Flow cytometry was performed with a BD LSRFortessa™ (BD Biosciences, UK) flow cytometer in parallel to the cell sorts as previously described (10). All gate settings were based on fluorescence minus one (FMO) and isotype-matched controls using previously isolated and frozen lung cells from non-transgenic Hy-Line and CSF1R-reporter transgenic chickens. The following gating strategy was applied: single cells, live cells, CSF1R-tgneg, CSF1R-tglow, or CSF1R-tghigh cells, and results are expressed as percentage thereof by using FlowJo® 10.4 (FlowJo, US). The following antibodies were used: mouse anti-chicken CD45 (clone UM16-6), mouse anti-chicken CD3 (clone CT-3), mouse anti-chicken chB6 (Bu-1; clone AV20), and mouse anti-chicken MRC1L-B (KUL01) all purchased from Bio-Rad, UK; mouse anti-chicken MHC II (clone 2G11, Abcam, UK); mouse anti-chicken putative CD11 (clone 8F2) and mouse anti-chicken K1 (both kind gifts from Dr. S. Härtle, LMU, Germany); mouse anti-chicken GRL1 and mouse anti-chicken GRL2 (Developmental Studies Hybridoma Bank, University of Iowa, US); and goat anti-mouse IgG1:Alexa Fluor®647 (AF647), goat anti-mouse IgG2a:AF647, and goat anti-mouse IgG3:AF647 all from ThermoFisher, UK. All samples were stained with SYTOXTM Blue (ThermoFisher, UK) for live cell gating.
APECpos lung cells were sorted with a BD FACS ARIA IIIu (BD Biosciences, UK) cell sorter. Three cell populations were sorted from the APEC-inoculated birds, with all gate settings based on single, live cells gated similar as for the flow cytometry performed in parallel. The CSF1R-tglow and CSF1R-tgneg cell populations that harbored APEC could not be distinguished from each other with sufficient accuracy and were therefore sorted as one population (CSF1R-tgneg/low). From the APEC-inoculated birds the APECpos CSF1R-tghigh, APECneg CSF1R-tghigh, and APECpos CSF1R-tgneg/low cells were sorted. From the PBS control birds, the CSF1R-tghigh cells were collected. All cell populations were collected in cold cell sorting buffer with RNAse inhibitor and processed immediately post-sort. For RNA isolation, the samples were centrifuged for 10 min at 400 x g and 4°C, cell pellets lysed in RLT lysis buffer with β-mercaptoethanol (QIAGEN, UK) and stored at −80°C.
Pilot RNA extractions showed that a minimum of 4 x 104 cells were required from the APECpos CSF1R-tghigh cell populations and 1.5 × 105 cells from the APECpos CSF1R-tgneg/low cell populations to obtain sufficient total RNA for cDNA generation. To achieve these cell numbers the left and right lung samples of the same bird were pooled (Supplementary Table 1). Additionally, combining samples from two birds where required did not alter the final analysis as described below. A minimum of 4 and maximum of 6 samples per sorted cell population were submitted for RNAseq (Supplementary Tables 1, 2).
RNA from sorted cells was extracted using the RNeasy micro kit (QIAGEN, UK) and concentrated using the SpeedVac RC1022 (ThermoFisher, UK). RNA quantity and quality (RNA integrity index > 7.5) was assessed by high sensitivity Agilent RNA ScreenTape assay with the TapeStation 2200. cDNA was amplified with the Ovation RNAseq System v2 kit (NuGen, UK) using 7 ng total RNA with all APEC O1-GFP and 3.5 ng total RNA with all APEC O2-GFP samples. TruSeq DNA Nano gel free libraries (350 bp insert, Illumina, UK) were prepared and sequenced on the NovaSeq S4 (Illumina, UK), yielding at least 68 M total 75 bp paired-end reads per sample. All procedures were performed according to manufacturer's instructions.
Obtained reads were trimmed using Trimmomatic [version 0.36, (17)] to remove adaptor sequences of the TruSeq DNA Nano kit and for quality. Reads after trimming were required to have a minimum length of 50 bases. The RNAseq reads were mapped to the reference genomes using STAR aligner software package [version 2.5.1b, (18)]. Reads were initially annotated to the respective APEC genome, and subsequently to the Gallus gallus (Gallus_gallus-5.0) Ensembl reference genome (annotation version 84). Raw counts for each annotated gene were obtained using the feature counts software [version 1.5.2, (19)].
Differential gene expression analysis was performed within the Bioconductor edgeR package [version 3.16.5, (20)]. Statistical assessment of differential expression was carried out with the likelihood-ratio test. Contrasts specified were pairs of sorted cell populations within APEC O1-GFP or APEC O2-GFP (APECpos CSF1R-tghigh, APECpos CSF1R-tgneg/low, APECneg CSF1R-tghigh, PBS CSF1R-tghigh). Differentially expressed genes were defined as those with a false-discovery rate (FDR) < 0.05 and log2 fold-change (FC) > 2. Heatmaps were constructed in R using the pheatmap package (v. 1.0.10; https://CRAN.R-project.org/package=pheatmap). Over-representation of gene ontology (GO) terms was investigated using the PANTHER Over-representation Test [released 20171205; (21)] using Fisher's Exact with FDR multiple test correction. Chicken gene symbols were converted to the orthologous human symbols and analyzed using the human PANTHER database. Network analysis for both sample-sample network and gene-gene network was performed in BioLayout 3D (22) which performs a Pearson correlation matrix calculated for each pair of samples or genes, using a modified Fruchterman-Rheingold algorithm. Clustering was performed on these networks using the Markov clustering algorithm (MCL) with an inflation value of 1.8. For graphical purposes, clusters in the gene-gene network graph were required to have a minimum of 30 nodes, and clusters showing even expression across treatment groups or associated with gender were removed. The Ingenuity Pathway Analysis (IPA) program (QIAGEN, UK) was used to identify cellular canonical pathways and physiological functions (P ≤ 0.05 and Q ≤ 0.05).
Combining samples from two birds where required did not alter the final analysis, as evidenced by processing of individual and pooled samples from four APEC O1-GFP inoculated samples with sufficient RNA yield (Bird 8, 9, 10, and 19). Transcriptomic analysis of these samples was performed identically to the other study samples and as described above with the result of zero significantly differentially expressed genes (DEGs) between groups with either individual or pooled samples.
Phagocytosis and Killing Assays
Phagocytosis and killing assays were performed as previously described (10). In short, lung cells from 6- to 8-week-old CSF1R-reporter transgenic birds were isolated using gradient purification and the freshly isolated cells in suspension were inoculated with APEC O1-GFP or APEC O2-GFP in stationary phase at a multiplicity of infection (MOI) of 10 for 30 min at 41°C, after which extracellular bacteria were killed by addition of 500 μg/ml ceftazidime hydrate (Sigma Aldrich, UK) for 30 min. Then, the cells were collected (0 h, phagocytosis and invasion) or incubated for a further 2, 4, or 6 h to enumerate viable bacteria. The same sample was analyzed by flow cytometry to phenotype the APECpos cells. To determine whether the bacteria actively invaded or were phagocytosed the same experimental settings were used, using live and heat-killed bacteria and cells were collected at 0 hpi. The bacteria were killed by incubation at 56°C for 24 h in a water bath. GFP expression was checked for each experiment prior to inoculation and was not affected by heat treatment. Two independent phagocytosis and killing assays were performed (7 birds in total). Phagocytosis of live and killed bacteria was compared in two studies (4 birds in total).
Primary lung CSF1R-tghigh mononuclear phagocytes were obtained from 6- to 8-week-old CSF1R-reporter transgenic birds by virtue of their adherence to plastic during culture as previously described (23). Cells were seeded at 7 x 106 cells on Nunc Lab-Tek 4-well chamber slides (ThermoFisher, UK). After 24 h culture, cells were washed twice with PBS followed by inoculation with APEC O1-GFP or APEC O2-GFP with an MOI of 10 for 30 min at 41°C, 5% CO2. Extracellular bacteria were killed by 500 μg/ml ceftazidime hydrate treatment for 30 min. Cells were washed twice with cold PBS and fixed with 4% paraformaldehyde for 20 min on ice. Cells were stained with mouse anti-chicken MRC1L-B (clone KUL01, Bio-Rad, UK) and mouse anti-chicken MHC II (clone 2G11, Southern Biotech, UK) followed by goat anti-mouse IgG1:AF647 and counterstained with 4',6-diamidino-2-phenylindole (DAPI). All antibodies were diluted in PBS supplemented with 1% BSA and 0.5% Triton X-100 (Sigma Aldrich, UK) and incubated on ice for 1 h. For cell images and 3D rendering, Z-stacks were obtained using an inverted laser-scanning microscope (LSM) 710 (Zeiss, UK), 40X or 63X Nikon oil lenses and images were captured using ZEN 2012 software (black edition, Carl Zeiss, UK) and analyzed using ZEN 2012 (Blue edition, Zeiss, UK) or Imaris software (version 9.3, Bitplane, Switzerland).
All data were not normally distributed and were therefore analyzed by Mann Whitney tests for the APEC comparison throughout the study, using GraphPad Prism 7.00 (GraphPad, US). The probability level for significance was taken as P ≤ 0.05. Statistical tests performed for the transcriptomic analysis are outlined in the relevant methods section.
APEC O1-GFP and APEC O2-GFP Cause Systemic Infection Within 6 h Post-inoculation
All CSF1R-reporter transgenic birds inoculated with either strain of APEC were examined for clinical signs and macroscopic lesions. Clinical signs were limited to hunched posture at 6 hpi and no differences were seen between the APEC O1-GFP and APEC O2-GFP inoculated birds (not shown). In contrast, the macroscopic lesion scores were significantly lower in the APEC O2-GFP inoculated birds compared to the birds inoculated with APEC O1-GFP (Figure 1A; P = 0.0028). Inoculation with APEC O1-GFP or APEC O2-GFP resulted in rapid systemic dissemination and bacterial loads typically in excess of 104 CFU per ml or gram were detected in blood, spleen and liver. The bacterial loads in the right lung, spleen and blood did not significantly differ between the strains. However, in the left lung, opposite the inoculation site, and liver, the bacterial loads were significantly higher after APEC O2-GFP inoculation compared to inoculation with APEC O1-GFP (Figure 1B; P = 0.0398 and 0.0411, respectively).
Figure 1. Colibacillosis lesion scores and bacterial colonization of tissues post-APEC inoculation. (A) Colibacillosis lesion scores of APEC-inoculated birds and (B) bacterial loads in right and left lung, liver, spleen and blood of APEC-inoculated birds. O1 is APEC O1-GFP, O2 is APEC O2-GFP, tissues as indicated on graphs. n = 13 APEC O1-GFP, n = 12 APEC O2-GFP. The mean with standard error of the mean (SEM) is shown. *P < 0.05, **P < 0.01.
Phenotypic Characterization of the Host Cells Harboring APEC
To determine the phenotype of the cells harboring APEC O1-GFP or APEC O2-GFP, the lung cells were analyzed by flow cytometry 6 hpi. Flow cytometric phenotyping of APEC O1-GFP or APEC O2-GFP positive cells revealed similar results. Both strains were detected in CD45pos leukocytes (Supplementary Figure 1). The CSF1R-transgene population could be divided into CSF1R-tglow and CSF1R-tghigh populations (Figure 2A). The CSF1R-tglow and CSF1R-tghigh cell populations significantly increased relative to control birds at 6 hpi, with no significant difference observed between the APEC strains (Figures 2A,B). Phenotypic characterization indicated that the bacteria were primarily found in CSF1R-tglow and CSF1R-tgneg cells, with no significant difference between the APEC strains (Figures 2C,D). These APECpos CSF1R-tglow and CSF1R-tgneg cells expressed CD45, CD11, GRL1, and GRL2 but not T or B cell markers, CD3 and chB6, and lacked MHC II expression or markers expressed on monocytes, macrophages and thrombocytes, such as MRC1L-B, and K1. In contrast, APECpos CSF1R-tghigh cells expressed CD45, CD11, GRL1, GRL2, MRC1L-B, and MHC II, were K1−/low and lacked surface expression of CD3 and chB6 (Supplementary Figures 1A–F).
Figure 2. Flow cytometric analysis of single, live lung cells from APEC inoculated birds. Gradient purified lung cells were isolated and subjected to flow cytometric analysis to detect APECpos cells. (A) Representative plots showing the increase of CSF1R-tghigh and CSF1R-tglow cell numbers within 6 hpi, (B) quantification of the increase of CSF1R-tghigh and CSF1R-tglow cell numbers amongst all birds, (C) representative plots showing the APECpos cells in CSF1-tgneg, CSF1R-tglow, and CSF1R-tghigh cells of a representative APEC O1-GFP and APEC O2-GFP inoculated bird and (D) quantification of the APECpos cells in CSF1R-tgneg, CSF1R-tglow, and CSF1R-tghigh cells amongst all birds. O1 is APEC O1-GFP, O2 is APEC O2-GFP. n = 9 APEC O1-GFP, n = 7 APEC O2-GFP. The mean with SEM is shown. *P < 0.05, **P < 0.01, ****P < 0.0001.
For transcriptomic analysis the APECpos and APECneg cells were collected based on their CSF1R-transgene expression. The CSF1R-tglow and CSF1R-tgneg cell populations that harbored APEC were sorted as one population as they could not be distinguished from each other with sufficient accuracy and named CSF1R-tgneg/low. The other populations were sorted based on their APECpos CSF1R-tghigh and APECneg CSF1R-tghigh phenotype, in addition to CSF1R-tghigh cells from PBS-inoculated control birds. To establish the nature of the APECpos cells, transcriptomic analysis was performed. Using previously published data on key macrophage and heterophil gene markers in the chicken [20 markers for each population (24)] we compared the expression of these genes between the APECpos CSF1R-tgneg/low and APECpos CSF1R-tghigh cells for both APEC O1-GFP and APEC O2-GFP inoculated birds. The APECpos CSF1R-tghigh cells had high expression of macrophage related genes and low expression of heterophil related genes and vice versa for the APECpos CSF1R-tgneg/low cells (Figure 3A). Heatmaps were generated and included DC related genes which further revealed that the CSF1R-tghigh cells from PBS-inoculated control birds contained both macrophages and dendritic cells, whilst the CSF1R-tghigh cells post-APEC O1-GFP or APEC O2-GFP inoculation were enriched for macrophage related genes, with higher expression levels of macrophage genes (LGALS1, GDA, CKB, CTSB, LRPAP1, LRP1, HADHB, UQCRC1) and lower expression levels of most DC related genes (KIT, CD83, CIITA, CADM1, FLT3, XCR1, CCR7, FAM46C, CCR6) (Figure 3B).
Figure 3. Transcriptome analysis of sorted lung cells from uninfected and APEC infected birds. (A) Network graph of macrophage (blue) and heterophil (yellow) marker expression with the corresponding graph of the average expression of the markers across all samples. This macrophage and heterophil related genes each formed single clusters that showed high expression in the CSF1R-tghigh and CSF1R-tgneg/low samples, respectively. (B) Heatmaps of normalized expression of macrophage, DC and heterophil related genes cross the sorted cells post-infection. Heatmap coloring is based on counts per million with red indicating high counts and blue indicating low counts. (C) Annotation of the obtained reads of APEC O1 or APEC O2 genome from the RNA-seq data from the sorted cells showing a significantly higher percentage of bacterial reads in the APECpos CSF1R-tgneg/low cells as compared to the APECpos CSF1R-tghigh cells, and no difference between the APEC strains. The mean with SEM is shown. *P < 0.05.
Although flow cytometric analysis detected the cells harboring APEC, the bacterial load could not be determined in the cell subpopulations by direct plating. The transcriptome data revealed that APECpos CSF1R-tgneg/low cells had a 10-fold higher percentage of the reads annotated to the APEC O1:K1:H7 or APEC O2:K1:H5 genome, as compared to the APECpos CSF1R-tghigh cells (Figure 3C).
Overview of Relationships in the Transcriptome Data
An unbiased sample-sample network was produced using BioLayout 3D. This indicated that the main division of samples is between the CSF1R-tgneg/low and CSF1R-tghigh cells (Figure 4A). In the CSF1R-tghigh cluster, a division between PBS-inoculated and APEC-inoculated birds was observed, and the APECneg CSF1R-tghigh samples from infected birds were positioned between the PBS-inoculated and APECpos CSF1R-tghigh samples. This suggests that the APECnegCSF1R-tghigh cells in infected birds had a bystander response and were activated without harboring bacteria (Figure 3B). The APEC O1-GFP and APEC O2-GFP infected cells for each cell type do not show a clear separation in the graph for either CSF1R-tghigh or CSF1R-tgneg/low groups (Figure 4A).
Figure 4. Network graphs of gene expression (normalized counts per million). (A) Sample-sample network graph. The graph is colored based on experimental groups and shows primary separation of samples based on CSF1R-transgene expression. (B) Gene-gene network graphs. The graph is colored by clusters determined by MCL clustering, with three separated clusters of genes (A–C) comprised of 12 separate clusters. The expression of each cluster is shown in the graphs labeled 1–12, with the experimental groups denoted by a key at the base of the figure and used under each graph.
To examine the main trends in the data, an unbiased gene-gene network graph with Markov clustering was constructed (Figure 4B). Three main groups of genes were observed, the largest group (B) showed elevation in the CSF1R-tghigh samples, the second largest (A) showed elevated expression in the CSF1R-tgneg/low, and the smallest group (C) showed elevated expression in only a few of CSF1R-tgneg/low. One cluster showed elevated expression in the CSF1R-tgneg/low samples (cluster 1, 930 genes), and this was enriched for immune signaling pathways (determined by GO overrepresentation test) including TLR, interleukin, apoptosis and PDGF signaling pathways (Supplementary Table 3). Key genes in cluster 1 included AMPs (AvBD3, DEF6), cytokines and cytokine receptors (including CCL4, CSF3R, CXCL12, CXCR1, FASLG, FAS, IFNAR1, IFNGR2, IL16, IL17C, IL1B, IL8, TNFRSF10B, TNFRSF21, TNFSF11), TLRs (TLR15, TLR4), JAK/STAT genes (JAK1, JAK3), ISGs (including IFITM10, IRF7, IRF2, IFI6, RSAD2) and immune cell receptors and markers (including CD247, CD55, CHIR-AB1, CTSD, LYZ). The cluster with elevated expression in the CSF1R-tghigh samples from uninfected birds (cluster 4, 251 genes) was a heterogeneous group of genes enriched only for genes associated with biological regulation (Supplementary Table 3). The cluster contained 17 DC-related genes including FLT3, BCL11A, CADM1, CIITA, CX3CR1, VCAM1, and XCR1. The cluster with elevated expression in the CSF1R-tghigh samples from infected birds independent of whether the cells were APECpos (cluster 9, 99 genes), was enriched for genes associated with MHC I antigen processing (including CALR, CYBB, AP2M1) and many proteasome genes, and protein metabolism/catabolism process genes. Finally, the cluster with elevated expression specifically in the APECpos CSF1R-tghigh samples (cluster 10, 161 genes) was enriched for pathways associated with regulation of response to stimulus, regulation of cell migration and adhesion, and metabolism. It also included a high proportion of cytokines, particularly those associated with immune regulation and anti-inflammatory effects (including CXCL13, CXCL13L2, CXCL8, IL10, IL13RA2, IL19, IL20RA, and IL4I1).
Transcriptomic Response of APEC Harboring CSF1R-tghigh Cells
We examined pathway enrichment between the CSF1R-tghigh APEC O1-GFP and O2-GFP infected cells. In general, the response of APEC O1-GFPpos CSF1R-tghigh and APEC O2-GFPpos CSF1R-tghigh cells to infection was very similar, with mostly the same pathways activated or repressed compared to cells from uninfected controls (Figure 5). This included involvement of many inflammatory pathways including IL-8 and IL-6 signaling and the Th1 pathway, suggesting a robust immune response to infection by both APEC strains. However, there were numerous instances of pathways that were repressed to a greater extent during APEC O2-GFP infection relative to uninfected birds, when compared to APEC O1-GFP infection. For example, the “calcium-induced T Lymphocyte Apoptosis,” “Aryl Hydrocarbon Receptor (AhR) Signaling,” “STAT3 Pathway,” and “PCK theta signaling in T lymphocytes” pathways were repressed to a greater extent during APEC O2-GFP infection (Figure 5). Moreover, we found instances of pathways that were less activated in APEC O2-GFPpos cells relative to controls than observed during APEC O1-GFP infection, including “Neuregulin signaling and ErbB,” “NF-κB signaling,” and “HMGB1 and ILK signaling.” Neuregulins (NRGs) are a family of structurally related signaling proteins that bind to receptor tyrosine kinases of the ErbB family and mediate a myriad of cellular functions including survival, proliferation, and differentiation in both neuronal and non-neural cells including macrophages. HMGB1 is secreted by immune cells and activated macrophages and monocytes secrete HMGB1 as a cytokine mediator of inflammation.
Figure 5. Comparative pathway analysis of APEC O1-GFP vs. APEC O2-GFP infected CSF1R-tghigh cells based on the log fold-changes of genes differentially expressed compared to CSF1R-tghigh cells from PBS control samples. Coloring shows enrichment of pathways in APEC-bearing samples compared to PBS controls (blue = pathway suppressed, orange = pathway activated). A total of 1374 (O1) and 1405 (O2) genes were included in the analysis.
Strain-specific responses were analyzed by comparison of the genes that were differentially expressed in APEC O1-GFPpos CSF1R-tghigh and APEC O2-GFPpos CSF1R-tghigh cells. A hundred DEGs, of which 77 are annotated with gene symbols, were observed (Supplementary Table 4). This group of 77 genes had an over-representation of genes related to cell signaling and communication. The differences between the APEC O1-GFP and APEC O2-GFP infected CSF1R-tghigh cells were generally due to downregulation of gene expression in APEC O2-GFP samples, as seen when examining log fold-changes of infected samples to PBS controls (Figure 6). The genes showing the greatest difference between the two APEC strains were CYP1A1, which is a key component of AhR signaling, a chicken homolog of ZNF420 which regulates apoptosis, FKBP6 which has a role in immunoregulation, and two additional cytochrome P450 family members (CYP4B7, CYP26A1). Additional key genes that showed downregulation in APEC O2-GFP infected samples were CYP1A2, also part of the AhR signaling pathway, the complement component C4A and a protein involved in complement control (CSMD2), a gene key in apoptosis response (CASP7), and a homolog of SAMD9L, a gene involved in the regulating proliferation and maturation of blood cells. There were also two DC related genes that showed significant difference between O1 and O2 (FLT3 and CCR7); these were downregulated following both APEC O1-GFP and APEC O2-GFP infection, but to a greater extent in the APEC O2-GFP infected cells.
Figure 6. All annotated DEGs from the contrast of APEC O1-GFP vs. APEC O2-GFP infected CSF1R-tghigh cells. Coloring is based on fold-change expression of APEC-bearing cells compared to their PBS controls, with red indicating higher expression and blue lower expression.
Transcriptomic Response of APEC Harboring CSF1R-tgneg/low Cells
Lung CSF1R-tglow cells from uninfected birds were sorted and analyzed in an independent study. As expected, these cells formed a heterogenous group of cells, including heterophils, B cells and T cells (data not shown). Since there is no relevant uninfected control for the CSF1R-tgneg/low samples the only comparison that could be made was directly between APEC O1-GFPpos and APEC O2-GFPpos CSF1R-tgneg/low cells. Between these cell populations, 91 genes showed differential expression, 59 of which were annotated, suggesting that the overall response of APEC O1-GFP and APEC O2-GFP infected CSF1R-tgneg/low cells are similar. In line with the transcriptomic analysis of CSF1R-tghigh cells, both APEC strains induced an inflammatory response, but many genes showed lower expression after APEC O2-GFP inoculation, in a direct comparison between APEC O1-GFPpos and APEC O2-GFPpos CSF1R-tgneg/low cells (Supplementary Table 4). Two genes with the highest gene count difference between the APEC strains were involved in apoptosis, DTHD1 and EVA1A, suggesting that apoptosis may be modulated differently between the APEC strains. The other genes showing the largest difference with higher expression in APEC O1-GFP infected samples, were FABP2 which is involved in fatty acid metabolism, a chicken-specific chemokine receptor (CCR8L), two cytokines (CCL19, IL22), TRPC6, which is involved in calcium channel activity, and the SAMD9L homolog.
To further examine the difference between APEC O1-GFP and APEC O2-GFP infected CSF1R-tgneg/low cells, a pathway comparison was made (Figure 7). The pathways enriched in APEC O1-GFPpos CSF1R-tgneg/low cells included “granulocyte adhesion and diapedesis” (CCL19, CX3CL1, CXCL8, VCAM1), “Pattern Recognition Receptors in Recognition of Bacteria” (CXCL8 and PTX3), “Role of cytokines in mediating communication” (CXCL8, IL22), and “IL15 and HMGB1 signaling” (CXCL8, VCAM1). Similar to the pathways enriched in the CSF1R-tghigh infected cells, the pathways showed more enrichment in the APEC O1-GFP infected cells relative to the APEC O2-GFP infected cells.
Figure 7. Pathway analysis of APEC O1-GFP vs. APEC O2-GFP infected CSF1R-tgneg/low cells based on DEGs between the two populations (log fold-change). Stronger coloring indicates enrichment of genes associated with the given pathway.
Bacterial Invasion Contributes to APEC Uptake in vitro
in vitro phagocytosis and killing assays were performed using primary lung cells of CSF1R-reporter transgenic birds and APEC O1-GFP or APEC O2-GFP (MOI = 10), revealing differences in cell tropism and intracellular survival between the APEC strains (Figure 8). The total number of viable intracellular bacteria detected after infection and ceftazidime treatment at the “zero hpi” interval did not differ significantly between the APEC strains (Figure 8A). At this time, APEC O1-GFP infected around 20% of CSF1R-tgneg, CSF1R-tglow, and CSF1R-tghigh cells. In contrast, APEC O2-GFP infected around 80% of CSF1R-tghigh cells (Figures 8B–D). Interestingly, APEC O2-GFP survived longer in lung cells than APEC O1-GFP, with statistically significant differences in recovery of the strains from 4 hpi (Figure 8A). The percentage of APEC O2-GFPpos CSF1R-tghigh cells did not significantly decrease post-inoculation (Figure 8D; P = 0.053 between 0 and 6 hpi; in addition to significant differences between the strains at each time point as indicated), whilst the percentage of APEC O1-GFPpos CSF1R-tghigh cells significantly decreased over time (P = 0.0006 between 0 and 6 hpi). Confocal microscopy of adherent CSF1R-tghigh cells confirmed the higher number of APEC O2-GFP infected cells (Figure 8E), and that bacteria were intracellular (Supplementary Figure 2). The relative proportions of CSF1R-tgneg, CSF1R-tglow, and CSF1R-tghigh cells in the isolated cell populations used for these in vitro studies is shown in Supplementary Figure 3, and shows a large CSF1R-tgneg population and small CSF1R-tglow and CSF1R-tghigh populations as expected. This indicates that APEC O2-GFP were phagocytized by, or actively invaded, the CSF1R-tghigh cells as a higher percentage of CSF1R-tghigh cells were APEC O2-GFPpos compared to the other cell populations whilst the CSF1R-tghigh cells represent the smallest population. To determine if APEC were phagocytized or actively invading the CSF1R-tghigh and CSF1R-tglow cells, the assay was repeated with live and heat killed bacteria. Heat killed bacteria were phagocytosed at low levels, whereas up to 60% of CSF1R-tghigh and CSF1R-tglow cells contained the live bacteria suggesting that active invasion is the primary route of entry (Figure 9).
Figure 8. In vitro analysis of APECpos lung cells. (A) Enumeration of viable bacteria within freshly isolated gradient purified lung cells inoculated with an MOI = 10 at 0, 2, 4, and 6 hpi, (B–D) quantification of APECpos cells within the CSF1R-tgneg, CSF1R-tglow, and CSF1R-tghigh cells of the same samples by flow cytometry, and (E) visualization of APEC infection post MOI = 10 inoculation of adherent CSF1R-tghigh cells by confocal microscopy. (A–D) n = 7 birds from two independent studies, the mean with SEM is shown, *P < 0.05, ***P < 0.001. (E) Data from one representative bird.
Figure 9. In vitro flow cytometric analysis of APECpos lung cells after inoculation with live or heat killed APEC. Gradient purified lung cells were isolated from 6 to 8 weeks old CSF1R-reporter transgenic birds and inoculated with an MOI = 10 of either live or heat killed APEC O1-GFP or APEC O2-GFP. (A–C) Quantification of APECpos cells in the CSF1R-tgneg, CSF1R-tglow, and CSF1R-tghigh cells. O1 is APEC O1-GFP, O2 is APEC O2-GFP. n = 4 birds from two independent studies. The mean with SEM is shown. *P < 0.05.
In this study the interactions between GFP-expressing strains of APEC serotypes O1:K1:H7 and O2:K1:H5 and phagocytic cells in the lung of CSF1R-reporter transgenic chickens at 6 hpi were investigated. When analysing events early after inoculation it is essential to deliver consistent doses to avoid dose-related differences in innate responses. The intra-air sac route was chosen in this study as it was previously shown to produce reproducible bacterial loads chicken lungs (5, 10, 25). In our study CSF1R-reporter transgenic chickens were inoculated with 109 CFU. While this is unlikely to reflect natural exposure, our pilot dose-titration studies indicated that this dose of APEC was a prerequisite to detect >1% APECpos leukocytes in the lung (data not shown). We were also mindful that cloning vectors and fluorescent proteins have been reported to attenuate bacterial pathogens, including pFVP25.1 used in this study and which had a modest impact on Salmonella invasion in vitro (26). However, no impact of pFVP25.1 on APEC invasion or in vitro growth was detected (data not shown) and we observed that the APEC O1-GFP and APEC O2-GFP strains rapidly induced pathology similar to that of the parent strains and that they were capable of efficient systemic translocation.
Flow cytometry analysis of lung cells from CSF1R-trangenic chickens indicate the presence of three cell phenotypes based on transgene expression, CSF1R-tghigh, CSF1R-tglow, and CSF1R-tgneg. In this study the CSF1R-tgneg/low cells were identified as the main cell population associated with APEC O1-GFP or APEC O2-GFP in vivo and flow cytometric and transcriptomic analysis identified them as heterophils, the chicken counterpart of mammalian neutrophils. Significantly lower numbers of bacteria were associated with CSF1R-tghigh cells, identified as macrophages and DCs. Compared to CSF1R-tghigh cells from uninfected birds many DC related genes were not upregulated in APEC-infected birds (FLT3, CADM1, CIITA, CCR7, XCR1), indicating that APECpos CSF1R-tghigh cells were enriched for macrophages, likely recruited from the circulation due to strong inflammatory signals produced by epithelial cells and resident innate cells in the lung to limit the infection. These data indicate an important role for the early cellular innate immune response in the control of colibacillosis, driven primarily by heterophils and to a lesser extent by macrophages, both cells known to be important in bacterial clearance and immunomodulation.
Low percentages of APECpos CSF1R-tgneg/low and CSF1R-tghigh cells after APEC O1-GFP or APEC O2-GFP inoculation may be explained by the possible ability of APEC to evade phagocytosis due to the expression of surface polysaccharides, fimbriae and other APEC virulence factors. In particular, the E. coli K1 polysialic acid capsule, expressed by both APEC strains selected for this study, is hypothesized to contribute toward the evasion of phagocytosis (6), although in vivo data confirming this are lacking. Our in vivo data show the percentage of APEC uptake by CSF1R-tglow and CSF1R-tghigh cells was similar to those observed after in vitro inoculation of lung leukocytes with heat killed APEC. However, the percentage of APEC uptake in vitro using live bacteria was significantly higher and APEC O2-GFP seem to preferentially be taken up by the CSF1R-tghigh cells. This demonstrates a clear discrepancy between APEC uptake in vivo and in vitro, and studies that predict the outcome of APEC infections in poultry from in vitro data alone must therefore be interpreted with caution.
In our study the response of heterophils, macrophages and DCs to APEC O1-GFP and O2-GFP infection in birds was overall similar. This response involved inflammatory pathways including IL-8, IL-6 and Th1 pathway signaling, suggesting a robust innate immune response at 6 hpi. Previous transcriptome studies analysing bone marrow, thymus, bursa, spleen and blood derived leukocytes, in birds with differing susceptibility to APEC O1:K1:H7 infection, also revealed an important role for the innate immune response (25, 27). At 1 dpi differences in β-defensins, CD74, and IL8 expression between challenged and control birds were observed. However, in contrast to our study these studies did not analyse lung tissue or individual immune cells and focused on the adaptive immune response at later time points post 108 CFU APEC O1. A direct comparison was therefore not feasible, and we chose a higher dose of inoculation which seemed ideal to induce a strong cellular innate immune response 6 hpi based on our pilot data. Strikingly in our study investigating the very early cellular innate immune response, many pathways were more highly repressed or less activated in APEC O2-GFP inoculated birds compared to APEC O1-GFP, in both heterophils, macrophages and DCs. Most notably pathways associated with the Aryl Hydrocarbon Receptor (AhR), an important emerging modulator of inflammatory signaling, IL-17 and STAT3 associated signaling were more highly repressed or less activated during APEC O2-GFP infection.
AhR is a ligand-dependent transcription factor that not only senses environmental toxins, but also bacterial virulence factors. In mice it was shown to be an intracellular pattern recognition receptor that regulates immune and degradation pathways in myeloid and epithelial cells (28). AhR is evolutionarily conserved amongst many species including birds (29, 30). AhR sensing leads to transcription of canonical detoxifying genes of which CYP1A1 and CYP1A2 are key members and in our study amongst the most repressed genes post-APEC O2-GFP inoculation compared to APEC O1-GFP (Figure 6). In addition, AhR regulates cytokine and chemokine production, inflammatory leukocyte recruitment and control of bacterial replication and LPS-induced inflammatory responses (28, 31). Inflammatory pathways such as Th1, NF-κB, and STAT3 pathways and their associated cytokines were generally more highly repressed or less activated post-APEC O2-GFP inoculation compared to APEC O1-GFP in our study. The pro-inflammatory cytokines IL-6 and IL-1β were strongly induced post-APEC O1-GFP and slightly higher post-APEC O2-GFP infection in macrophages.
In our study, the immunomodulatory cytokine genes IL17 and IL22 were less upregulated in APEC O2-GFP infected birds' macrophages and heterophils, respectively, whereas IL-10 was upregulated in macrophages to the same extent after APEC O1-GFP and O2-GFP inoculation. In mammalian studies with LPS-stimulated murine peritoneal macrophages, loss of AhR resulted in inhibited IL-10 production (31, 32), and attenuated IL-17 and no IL-22 production was linked to impairment of the Th17 response (33). We observed significantly less pathology in APEC O2-GFP infected birds whilst the bacterial load was similar to APEC O1-GFP, possibly a consequence of dampened IL-17 related signaling. In addition, the induction of systemic responses via the acute-phase response and increasing serum concentrations of CSF3 and CSF2 is linked to an increase in neutrophil and macrophage numbers at the site of infection in mice, and is regulated by IL-17 amongst other cytokines (34). This observation merits further study over a wider series of sampling intervals. It should also be appreciated that differences at transcript level cannot be taken to mean differences in the abundance or processing of individual proteins, which require further validation prior to in-depth follow-on studies. Overall it draws a complex picture of AhR induced signaling in cellular innate immunity in response to bacterial challenge and indicates that after APEC inoculation, AhR plays a complex role in the pro- and anti-inflammatory cytokine production and its effect on the immune system is modulated by the APEC strain.
Notably in our data, PTX3 was less expressed in APEC O2-GFP infected heterophils compared to APEC O1-GFP infected cells. PTX3 is rapidly produced and released by mononuclear phagocytes and DCs in response to inflammatory signals (35). In chickens, it was shown to be strongly upregulated post-APEC O1:K1:H7 inoculation (36). Recent findings in mammals have shown that pentraxins are involved in complement activation and amplification via communication with complement initiation pattern recognition molecules, but also via recruitment of complement regulators (37). In our data, the complement component, C4A and complement regulator, CSMD2 were downregulated in APEC O2-GFP infected macrophages and DCs compared to APEC O1-GFP. A role for PTX3 in the complement-mediated clearance of apoptotic cells was also suggested where it limits C1q-mediated complement activation and binds to apoptotic cells and inhibits their clearance by DCs (38, 39).
In our data, CASP7 and the chicken homolog of ZNF420 were less expressed in APEC O2-GFP infected macrophages and DCs, and DTHD1 and EVA1A were less expressed in APEC O2-GFP infected heterophils. All these genes are important in the apoptotic response. Other genes and pathways less expressed in APEC O2-GFP infected heterophils included the granulocyte adhesion and diapedesis pathway, and particularly CCL19, CX3CL1, CXCL8, and VCAM1 expression, with important roles in attracting heterophils to the site of infection and promoting adhesin to endothelial cells. Overall, lower expression of IL17, IL22, PTX3, and heterophil attracting cytokines, such as CXCL8 and VCAM1 in our data suggests a dampened innate immune response post APEC O2-GFP infection. This could at least partially explain the higher bacterial loads observed in the left lung, opposite the inoculation site, and liver post-APEC O2-GFP inoculation.
In conclusion, our data identified heterophils and macrophages as the main APEC-bearing lung phagocytes post-APEC O1-GFP or APEC O2-GFP inoculation of chickens, in an innate immune response dominated by heterophils. Transcriptomic analysis identified many inflammatory pathways including IL-8, IL-6, and Th1 were strongly upregulated post-APEC O1-GFP or APEC O2-GFP inoculation. Strikingly our analysis revealed many pathways and genes, particularly related to AhR, IL17 and STAT3 signaling, heterophil recruitment and the acute phase response, were more highly repressed or less activated in APEC O2-GFP inoculated birds compared to APEC O1-GFP. Given the huge genetic diversity of APEC, observations made in this study stress the potential for observed responses to be specific to the host-pathogen combination under study. Moreover, genetic differences can also occur within an APEC serotype (40), and differences in the clinical outcome of disease after inoculation with different APEC strains of the same serotype were shown (41). Thus, it will be important not to assume that responses detected with single strains will necessarily apply to other strains of a different or the same serotype. In primary lung leukocytes in vitro, APEC O2-GFP exhibited higher net intracellular survival over time compared to APEC O1-GFP. However, we observed a clear discrepancy between APEC uptake in vivo and in vitro. Our data revealed important differences in the cellular innate immune response between APEC strains O1:K1:H7 and O2:K1:H5 and suggest that APEC O2-GFP may subvert or evade immune responses in phagocytic cells to a greater extent than APEC O1-GFP. Future experiments will focus on the functional consequences of the APEC-cell interactions and include time series leading to resolution or distinct pathologies.
Data Availability Statement
The datasets generated and analyzed for this study are included in the published article (and its additional files) or in the following data repository; RNA-seq data has been submitted to the European Nucleotide Archive (PRJEB35225) (https://www.ebi.ac.uk/ena/data/view/PRJEB35225).
The animal study was reviewed and approved by the Animal Welfare and Ethical Review Board of The Moredun Research Institute, Scotland, United Kingdom. Animals were bred and housed in premises licensed under UK Home Office Establishment Licenses (PEL X212DDDBD and XA40CEF03) in full compliance with the requirements of the Animals (Scientific Procedures) Act 1986. Procedures were conducted under project license PPL 70/7860, with CSF1R-reporter transgenic birds bred under PPL 60/4253, with the consent of the Animal Welfare and Ethical Review Board of The Moredun Research Institute.
AA, LV, and MS conceptualized the study. AA, KB, CC-U, DB, and LV performed or assisted with the animal experiments. KM and MM performed the transcriptomic data analysis. KS performed the confocal staining and analysis. PK, MS, LV, CS, and SL secured the funding. CS provided resources. AA, KM, and LV wrote the manuscript. All authors contributed to, read and approved the final manuscript.
This work was supported by the BBSRC funding via the ERA-NET Animal Health and Welfare (ANIHWA) initiative under grant BB/M028305/1 and the Biotechnology and Biological Sciences Research Council (BBSRC) as part of the joint NIFA-BBSRC Animal Health and Disease program under grant BB/M028208/1 and USDA-NIFA AFRI under grant 2015-67015-23093. We also acknowledge strategic investment by BBSRC in The Roslin Institute via a National Capability Grant to the NARF (BB/J004219/1) and Institute Strategic Programme grants (BBS/E/D/20002173 and BBS/E/D/20002174).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
We would like to dedicate this paper to our late colleague and friend PK. We express our gratitude to Professor Lisa Nolan for providing the APEC O1 strain. We express our gratitude to Dr. Sonja Härtle for providing the CD11 and K1 antibodies. We would like to thank Graeme Robertson and Bob Fleming for support with the cell sorting and Dr. Sungwon Kim for fruitful discussions and technical support. We wish to thank the animal caretakers of the National Avian Research Facility and The Moredun Research Institute for the supply of birds and support during the studies. Sequencing work (library preparation, sequencing, and data generation and initial analysis) was carried out by Edinburgh Genomics at The University of Edinburgh.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2019.03055/full#supplementary-material
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Keywords: APEC, chicken, immunomodulation, macrophage, dendritic cell, heterophil, granulocyte, CSF1R
Citation: Alber A, Morris KM, Bryson KJ, Sutton KM, Monson MS, Chintoan-Uta C, Borowska D, Lamont SJ, Schouler C, Kaiser P, Stevens MP and Vervelde L (2020) Avian Pathogenic Escherichia coli (APEC) Strain-Dependent Immunomodulation of Respiratory Granulocytes and Mononuclear Phagocytes in CSF1R-Reporter Transgenic Chickens. Front. Immunol. 10:3055. doi: 10.3389/fimmu.2019.03055
Received: 11 November 2019; Accepted: 13 December 2019;
Published: 10 January 2020.
Edited by:Tamás Laskay, Universität zu Lübeck, Germany
Reviewed by:Michael Kogut, Agricultural Research Service (USDA), United States
Song Gao, Yangzhou University, China
Copyright © 2020 Alber, Morris, Bryson, Sutton, Monson, Chintoan-Uta, Borowska, Lamont, Schouler, Kaiser, Stevens and Vervelde. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
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