- Research article
- Open Access
A Mycobacterium avium subsp. paratuberculosis relA deletion mutant and a 35 kDa major membrane protein elicit development of cytotoxic T lymphocytes with ability to kill intracellular bacteria
© The Author(s) 2018
Received: 9 January 2018
Accepted: 31 May 2018
Published: 26 June 2018
Efforts to develop live attenuated vaccines against Mycobacterium avium subspecies paratuberculosis (Map), using indirect methods to screen Map deletion mutants for potential efficacy, have not been successful. A reduction in the capacity to survive in macrophages has not predicted the ability of mutants to survive in vivo. Previous studies for screening of three deletion mutants in cattle and goats revealed one mutant, with a deletion in relA (ΔMap/relA), could not establish a persistent infection. Further studies, using antigen presenting cells (APC), blood dendritic cells and monocyte derived DC, pulsed with ΔMap/relA or a 35 kDa Map membrane protein (MMP) revealed a component of the response to ΔMap/relA was directed towards MMP. As reported herein, we developed a bacterium viability assay and cell culture assays for analysis and evaluation of cytotoxic T cells generated against ΔMap/relA or MMP. Analysis of the effector activity of responding cells revealed the reason ΔMap/relA could not establish a persistent infection was that vaccination elicited development of cytotoxic CD8 T cells (CTL) with the capacity to kill intracellular bacteria. We demonstrated the same CTL response could be elicited with two rounds of antigenic stimulation of APC pulsed with ΔMap/relA or MMP ex vivo. Cytotoxicity was mediated through the perforin granzyme B pathway. Finally, cognate recognition of peptides presented in context of MHC I and II molecules to CD4 and CD8 T cells is required for development of CTL.
Mycobacterium avium subspecies paratuberculosis (Map) is a pathogen with a broad host range. It is the causative agent of Johne’s disease (JD) in cattle, a major disease problem in the US and other countries . Cumulative studies now show humans are susceptible to infection with Map. Studies have revealed some infected subjects develop clinical disease manifestations varying from an ileitis in humans referred to as Crohn’s disease, to other diseases associated with autoimmunity [2–5]. To reduce exposure of the public to Map, there is a need to find ways to clear dairy herds of Map. This has proven difficult, however, because efforts to date have not yielded a vaccine that elicits a protective immune response. This is attributable in part to the lack of methods to accurately predict the efficacy of candidate vaccines before testing in the field.
As illustrated by results from a standardized multi-institutional vaccine study, the use of macrophages and mice as indirect approaches to screen a set of candidate Map mutant vaccines for efficacy were not successful [6, 7]. The conclusion drawn from the study suggested more direct methods are needed to fully evaluate the immune response to candidate vaccines in the natural host [7, 8]. Many of the mutants submitted for evaluation in the study were excluded from a vaccine trial in the natural host because they did not exhibit efficacy in macrophage and mouse model systems . This was the fate of the three mutants our group submitted for evaluation in the study. Studies in cattle and goats, however, had shown deletion of one gene, relA, interfered with the capacity of Map to establish a persistent infection, indicating the mutant was a good candidate for further evaluation . An immune response to the mutant cleared infection and limited the capacity of wild type Map to establish an infection .
In light of the problems of using indirect methods of assessing the potential efficacy of candidate vaccines, we focused on development of methods to examine the immune response to candidate vaccines in the natural host. We developed an ex vivo platform to study the functional activity of T lymphocytes proliferating in response to live-attenuated and peptide-based candidate vaccines. The first studies conducted with steers vaccinated with ΔMap/relA demonstrated a CD4 and CD8 T cell recall response could be elicited ex vivo from peripheral blood mononuclear cells (PBMC) stimulated with ΔMap/relA [9, 11]. Development of a monoclonal antibody (mAb) to CD209, uniquely expressed on blood APC, dendritic cells (bDC), monocyte derived dendritic cells (MoDC), and monocyte derived macrophages (MoMΦ), allowed us to extend the studies and characterize the response in greater detail using APC pulsed with Ag for Ag presentation to T cells . Analysis revealed the recall response could be elicited by antigenic peptides presented by APC pulsed with ΔMap/relA. Presentation of antigens by APC was blocked by mAbs specific for MHC class I and II molecules showing the recall response was MHC restricted .
Further studies were conducted to dissect the recall response and determine which antigens were presented by the APC. This approach revealed a major component of the response was directed towards a 35 kDa membrane protein of Map, termed MMP . The recall response to MMP was equivalent to the response elicited by ΔMap/relA . As reported herein, further analysis of the immune response to ΔMap/relA and MMP required development of two assays: (1) a bacterium viability assay that was faster than the colony forming unit (CFU) assay for assessment of CTL activity against Map and (2) a method to characterize the functional activity of CD4 and CD8 T cells ex vivo. These newly developed assays demonstrated that vaccination with ΔMap/relA elicits the development of CTL with the ability to kill intracellular bacteria. Further analysis revealed the CTL activity was directed towards MMP. Follow up studies with MMP, ex vivo, demonstrated the same CTL response could be elicited with APC from unvaccinated cattle pulsed with MMP. Analysis the CTL activity revealed cytotoxicity was mediated through the perforin granzyme B (GrzB) pathway.
Materials and methods
Eight Holstein steers were obtained from the Map free Washington State University (WSU) dairy herd from 2013 to 2017. In the first phase of the study, two of the steers were vaccinated with the ΔMap/relA mutant and maintained as a source of blood to characterize cell responses elicited by ΔMap/relA and MMP. Two additional age-matched naïve steers were maintained as controls. In the second phase of the study, four additional unvaccinated naïve steers were used as a source of blood to conduct the ex vivo studies on the immune response to ΔMap/relA and MMP. The vaccinated steers were kept in an open feed lot since initial studies demonstrated the mutant ΔMap/relA was immune eliminated and did not present a health risk to other cattle under study . All the steers were maintained by the college staff. The steers were in good health during the studies. Midway through the initial studies, however, one of the vaccinated steers had to be euthanized because he was unruly and an injury risk to the staff. All protocols were approved by the WSU Institutional Animal Care and Use Committee (ASAFs 3360 and 04883).
Preparation of Map K10, K10GFP, ΔMap/relA, and MMP
The ΔMap/relA mutant was constructed in the K-10 and K10GFP strains of Map using site directed allelic exchange, as previously described . Cultures of Map K10, K10GFP, and ΔMap/relA were prepared from single colonies and used to inoculate Middlebrook 7H9 broth flasks (Difco, BD biosciences, USA) supplemented with 6.7% para-JEM GS (Trek Diagnostic Systems, OH, USA), 2 μg/mL mycobactin J (Allied Monitor, MO, USA), and 0.05% Tween 80 (Sigma-Aldrich Corp.) [9, 14]. The cultures were expanded on a shaking stand at 37 °C. When the broth cultures reached an OD600 of 0.6–0.8, master stocks were prepared in 1.5 mL micro-centrifuge screw-cap tubes for immediate use in each experiment. To ensure a single-cell suspension, bacterial stocks were disaggregated by passages through a 26-gauge needle three times, then the bacterial numbers were estimated based on the final OD600 values .
Bacterium viability assay
The Map viability assay was adapted from a method developed by Kralik et al.  to distinguish and quantify the concentration of live Map present in food products and samples from the environment. The method involves the use of propidium monoazide (PMA), a membrane impermeant fluorescent compound similar to propidium iodide. It only enters dead cells and intercalates into DNA . When it is activated by light, it binds covalently to DNA and blocks binding of probes used to detect Map genes. The concentration of live Map in a mixture of live and dead bacteria is determined from a standard curve generated with known concentrations of pure DNA from live Map. The number of live bacteria present in a sample preparation is determined by using quantitative PCR (qRT-PCR) with a probe specific for a single copy gene, F57, specific for Map . Two types of controls were used to adapt the PMA method for measuring Map killing. The first set of controls was used to demonstrate the concentration of live Map in a defined mixture of live and dead bacteria, which was determined from a standard curve generated with DNA from a known number of live Map. The controls were prepared from pure DNA from live Map for use as reference standards for extrapolating the extent of killing mediated by Ag-specific CTL. In the first set of controls, tubes were prepared to contain 2 × 107 Map/ tube. One set was heat-killed by incubating Map at 90 °C for 15 min. Tubes were then prepared to contain 100% live, 50% live/50% killed and 100% killed Map suspended in 400 μL of H2O in 1.5 mL translucent Eppendorf tubes and stored at −20 °C until processed. The second set of controls was used to quantitate the number of live Map present in Map-infected MoMΦ (generation of MoMΦ described below). This set of controls was essential for determining the extent of killing by CTLs since it covered the dynamic range for detection of live vs dead Map obtained from infected MoMΦ before and after incubation with CTL. Aliquots of Map mixed in four ratios, 100% live, 75% live/25% killed, 25% live/75% killed, and 100% killed, were prepared and added to the cultures of MoMΦ at a MOI of 10 respectively and incubated for 3 h. The cultures were then washed to remove free bacteria. In this set of controls, cells were lysed following infection and incubation with Map by adding 2 mL of 0.01% saponin in H2O and incubating at 37 °C for 15 min. The cell lysates were centrifuged for 30 min at 4500 rpm to pellet the bacteria. The supernatants were discarded and the pellets re-suspended in 1 mL H2O and transferred into micro-centrifuge tubes. The second centrifugation step was performed to harvest the washed bacteria at 14 000 rpm for 10 min. The supernatants were discarded, and the pellets re-suspended in 400 μL of H2O in 1.5 mL translucent Eppendorf tubes and stored at −20 °C until used.
Treatment with PMA to block binding of the F57 probe
The basic procedure for PMA treatment was carried out according the manufacturer’s instructions. 1 µL of 20 mM PMA working stock solution was added to 400 µL of the previously prepared preparations of cell controls to reach a final dye concentration of 50 µM. The translucent PMA-treated tubes were incubated at room temperature for 5 min in the dark on a rocker followed by brief spinning. To avoid overheating during exposure to the halogen light, a plastic tray was prepared with a frozen ice pack wrapped in aluminum foil. The tubes were placed in a diagonal slant position on top of the ice pack. The tray was then set on a rocking platform to ensure continuous mixing during light exposure. Light exposure was performed for 5 min using a halogen lamp with a 650 W bulb placed at a distance of ~20 cm from the tubes. Cells were subsequently harvested by centrifugation at 10 000 × g for 5 min. The supernatants were discarded and the cell pellets from the two sets of controls processed for isolation of DNA .
DNA was extracted using the protocol for Gram-positive bacteria using DNeasy® Blood and Tissue kit (Qiagen, USA) following enzymatic lysis to facilitate breakdown of the Map cell wall as described by Park et al. . In all cases, DNA extraction was performed in duplicate. The DNA was eluted in 100 μL of the designated elution buffer in the kits. DNA yield was measured by a NanoDrop® ND-1000 Spectrophotometer (Thermo Fisher Scientific Inc., Waltham, USA) using A260/280 ratio with 1 μL of sample.
Quantitative real-time PCR
Ex vivo assays to characterize the functional activity of CD4 and CD8 T cells
Generation of MoDC and CTL from PBMC from the vaccinated and unvaccinated control steers
As illustrated in Figure 1, the first blood draw from the vaccinated and unvaccinated control steers was used to generate MoDC for antigen (Ag) presentation to monocyte depleted PBMC (mdPBMC). Magnetic microbeads coated with a cross-reactive anti-human CD14 mAb were used to isolate monocytes per the manufacturer’s instructions (Miltenyi Biotec) . The average purity of isolated CD14+ cells was greater than 98%, as determined by FC analysis using an anti-bovine CD14 mAb, CAM36A [11, 22]. Monocytes (2 × 106) were added to wells of six well culture plates and cultured in 3 mL of complete culture medium (cRPMI) [RPMI-1640 medium with GlutaMAX™ (Life Technologies, CA, USA) supplemented with 10% calf bovine serum (CBS), 1 mM β-mercaptoethanol, 100 units/mL of penicillin G, and 100 μg/mL of streptomycin sulfate] in the presence of a DC growth cocktail containing bovine GM-CSF and IL-4 (Kingfisher Biotech, MN, USA). On the 3rd day, 1.4 mL of the medium was replaced with 1.8 mL of fresh medium containing the cocktail. The cultures were incubated for an additional 3 days to obtain MoDC. ΔMap/relA (5 × 106 Map/well) or MMP (5 μg/mL) were added to the cultures of MoDC and incubated for 3 h at 37 °C, 5% CO2. The adherent MoDC were then carefully washed 3 times with warm RPMI (without antibiotics) to remove free bacteria or MMP.
Following preparation of fresh PBMC from the second blood draw of the vaccinated and control steers, one portion was used to prepare monocyte depleted PBMC (mdPBMC), as described, using magnetic beads coated with anti-CD14 to remove monocytes. The mdPBMC, were added to their respective autologous MoDC pulsed with ΔMap/relA or MMP (2 × 106/mL in 5 mL of cRPMI). Following 6 days of culture, the cells were collected and used in FC and the Map killing assay. The second portion of fresh PBMC was used to generate MoMΦ as described below for use in the ex vivo studies.
Generation of MoDC and CTL from PBMC from the unvaccinated steers
Two rounds of antigenic stimulation were used to generate CTL from mdPBMC from the unvaccinated steers. The same general protocol was used as illustrated in Figure 1. The main difference is that the first blood draw from the unvaccinated steers was used for (1) the first round of stimulation of mdPBMC with ΔMap/relA and MMP, processed and presented by bDC (present in the mdPBMC) and (2) to generate MoDC for use in the second round of antigen (Ag) presentation to mdPBMC by MoDC pulsed with ΔMap/relA or MMP. The second blood draw was used to generate MoMΦ for use as target cells. The rest of the protocol was identical to the protocol described in Figure 1.
Generation of MoMΦ for use as target cells
At the times indicated in the protocol, fresh PBMC were re-suspended in cRPMI, placed in 150 mm tissue culture plates and incubated overnight. The majority of the non-adherent cells were then removed the following day. The adherent cells were cultured in fresh medium for 4 days then brought into suspension by incubating them on ice in the presence of EDTA in PBS [4 mL EDTA (250 mM stock in H2O), 5 mL CBS, 91 mL PBS]. The cells were re-suspended in cRPMI, counted, and then used to prepare MoMΦ for scanning confocal microscopy or use in the viability assay.
Infection of MoMΦ with Map K10GFP for scanning confocal microscopy
A two chamber culture slide was used to prepare cultures of MoMΦ infected with Map K10GFP to determine whether a 3 h incubation time is sufficient for preparing infected MoMΦ for use in the intracellular killing assay. MoMΦ were added to the two chambers (~2 × 104 MoMΦ/well) of the culture slide. After 2 days of additional culture, the MoMΦs were infected with K10GFP at a MOI of 10:1 (2 × 105 K10GFP to ~2 × 104 MoMΦ) in antibiotic free cRPMI. The slide was incubated at 37 °C, 5% CO2 for 3 h. Immediately following incubation, the medium containing free bacteria was washed away with warm cRPMI. The cells were then treated with a saponin-based permeabilization and wash reagent (BD Pharmingen) for 30 min at room temperature, then washed once with 1 mL of PBS. The cells were counter stained for 5 min with 500 µL of diluted (1:3000) propidium iodide stain (1 mg/mL stock solution, Invitrogen). Subsequently, the cells were rinsed several times in PBS then fixed with 2% formaldehyde in PBS overnight at 4 °C. After fixation the cells were covered with Vectasheild antifade agent and imaged on a Leica SP8 scanning confocal microscope, using the Leica Application Suite X software 1.10.12420.
Infection of MoMΦ for use in the viability assay
MoMΦ were distributed into six well culture plates (2 × 106 cells/well) and cultured for an additional 2 days and then used as target cells.
MoMΦ were infected with Map at a multiplicity of infection (MOI) of 10:1 (2 × 107 Map to ~2 × 106 MoMΦ/well) in antibiotic free cRPMI. The culture plates were centrifuged at 700 × g for 5 min, then incubated at 37 °C, 5% CO2 for 3 h. Extracellular bacteria were removed by washing 5 times with warm RPMI with no antibiotics. A vacuum source, equipped with a side-arm flask, rubber tubing and a pipette tip, was used for liquid removal in culture wells to avoid detaching the adherent MoMΦ. Two wells from each of the respective sets of 6 wells, containing Map infected MoMΦ, were used as controls, without addition of primed or unprimed preparations of mdPBMC.
Incubation of mdPBMC from the vaccinated and the control steers with MoMΦ alone or infected with Map
mdPBMC prepared from the vaccinated and control steers as outlined in Figure 1, were added to the cultures of MoMΦ alone or MoMΦ infected with Map (2 × 106 cells/well). After incubation for 6 h, the non-adherent cells were washed away with warm RPMI. The remaining MoMΦ were collected and processed for the Map viability assay.
Incubation of mdPBMC from unvaccinated steers with MoMΦs, alone or infected with Map
mdPBMC preparations from the unvaccinated steers prepared according to the protocol, were added to the preparations of MoMΦ alone or infected with Map (2 × 106 cells/well) and incubated for 24 h. The non-adherent cells were collected and held separately until collection of the adherent cells and then recombined for analysis of Map viability.
Cell processing for the Map viability assay
Cells in one control well of infected MoMΦ were lysed immediately following infection with Map using 0.01% saponin in H2O as described. The pellets were re-suspended in 400 μL of H2O in 1.5 mL translucent Eppendorf tubes and stored at −20 °C for later analysis. The other control well was incubated for 6 or 24 h concurrent with infected MoMΦ cultures overlaid with Ag-primed or unprimed preparations of mdPBMC. At the end of respective incubation times, all cultures were lysed as described. All lysed cells were treated with PMA and subjected to DNA extraction followed by qPCR as previously described in the viability assay to determine the extent of intracellular killing.
Intracellular labeling for perforin and GrzB
MAbs used in the present study
Alexa Fluor® 647
Alexa Fluor® 647
Alexa Fluor® 488; PE
Alexa Fluor® 647
Granzyme B R&D Systems
Aliquots of Map infected MoMΦ incubated with Ag-primed mdPBMC for 24 h were collected and used to examine the role of apoptosis in intracellular killing of Map, using a PE Annexin V Apoptosis kit (BD Pharmingen). [The kit includes Annexin V conjugated with phycoerythrin (PE) and 7AAD, a fluorescent membrane impermeant dye that is taken up by dead cells with a permeant membrane. Annexin V detects the changes in the membrane during the early stages of apoptosis. As apoptosis progresses with disruption in the integrity of the membrane, cells become double positive, necrotic]. Non-adherent cells comprised of lymphocytes and MoMΦ, from each culture were collected and held in suspension. The adherent cells from each cell culture were suspended and added to the corresponding preparation of non-adherent cells. The cells were pelleted by low speed centrifugation and re-suspended in PBS. Approximately 1 × 106 cells were transferred into 5 mL tubes and washed twice with cold PBS. Cells were then labeled according to the manufacturer’s instructions. Two types of controls were included in this assay (1) uninfected MoMΦ alone and (2) uninfected MoMΦ incubated with MMP-primed mdPBMC. The cell preparations were analyzed by FC within 1 h of labeling by gating only on MoMΦ. At least 105 gated events were collected for each cell preparation.
One set of the cultures used for the apoptosis study, as described above, was maintained for 3 days after initiation of co-culture of mdPBMC, to determine whether necrosis or apoptosis increased over time.
Flow cytometry (FC)
Data were imported into JMP software (version 12.0.1; SAS Institute Inc., Cary, NC, USA) for statistical analysis and graphical presentation (means and standard deviations). Two-way ANOVA was used to conduct statistical analyses and included an interaction term expect for the analysis of data represented in Figure 6B. In this instance, the second factor (blood donor) was instead considered a blocking factor. Post-hoc multiple comparisons were conducted using Tukey HSD (overall α = 0.05).
Development of a PMA-based viability assay to quantify the relative concentration of live Map in a mixed population of live and dead bacteria
We next determined if a sufficient number of bacteria were taken up by MoMΦ in a 3 h time frame to be quantitated using the PMA method. A two well culture slide was prepared with MoMΦ and infected with Map K10GFP under the same culture conditions used to set up infected MoMΦ for the viability assay (see "Materials and methods"). Confocal microscopy showed efficient bacterial uptake following 3 h of incubation (Figure 3B), even without a centrifugation step to concentrate the bacteria to the cell surface of MoMΦ for uptake.
The qPCR assay showed the number of bacteria taken up was sufficient to consistently determine the relative percent of live Map present within MoMΦ after 3 h of incubation (Figure 3D). Importantly, the study showed there was minimal killing of bacteria mediated by MoMΦ during the 6 h incubation period with MoMΦ cultured alone or in the presence of mdPBMC from control steers. (Figure 3D). We concluded that the dynamic range between live and dead bacteria isolated from MoMΦ was adequate for studying the intracellular killing activity of effector CD4 and CD8 T cells proliferating in response to stimulation with MoDC, pulsed with ΔMap/relA or MMP.
Analysis of the proliferative response and functional activity of mdPBMC from the vaccinated and control steers stimulated by MoDC pulsed with ΔMap/relA or MMP
As reported previously, extensive studies with PBMC from the vaccinated steers showed a CD4 CD8 T cell recall response could be elicited ex vivo by stimulation with ΔMap/relA [11, 12]. The studies demonstrated an equivalent recall response could be elicited with mdPBMC using bDC or MoDC pulsed with ΔMap/relA or MMP. The response was MHC restricted . As reported here, studies were extended to determine if the functional activity of the proliferating cells could be determined using a modification of the intracellular killing assay described by Worku and Hoft  and a PMA-based method to distinguish live from dead Map present in Map-infected MoMΦ .
Analysis of the proliferative and functional activity of naïve mdPBMC from unvaccinated steers stimulated with bDC and MoDC pulsed with ΔMap/relA and MMP
The essential need for CD4 and CD8 T cell cognate recognition of MMP peptides presented by APC for development of CD8 CTL against Map
All the previous studies up to this time were conducted with mdPBMC because it was unknown whether the response to Ag peptides, processed and presented by APC pulsed with ΔMap/relA or MMP, required cognate recognition of Ag peptides by CD4 and CD8 T cells to generate CTL activity. Also, it was assumed but not verified that CTL activity was primarily associated with CD8 T cells. To address these unknowns, a series of experiments were conducted with freshly isolated mdPBMC from the 2 steers. The first experiments focused on determining whether both CD4 and CD8 T cells needed to be present at the time of Ag presentation to generate CTL activity. The second set of experiments were focused on demonstrating whether CTL activity was primarily associated with CD8 T cells proliferating in response to Ag presented by APC. mdPBMC from 2 of the unvaccinated steers were depleted of either CD4 or CD8 T cells and then subjected to 2 rounds of stimulation with APC pulsed with MMP. Preparations of unseparated mdPBMC, unstimulated and stimulated, were used as controls. There was limited cell proliferation in cultures of mdPBMC depleted of CD4 or CD8 T cell following two rounds of stimulation with APC pulsed with MMP (data not shown). In contrast, there was robust proliferation of CD4 and CD8 T cells in the unseparated preparations of mdPBMC following two rounds of stimulation (results similar to those shown in Figure 5C). Following demonstration that both CD4 and CD8 T cells must be present for generation of a proliferative and CTL response to MMP, we used the two steers to determine which cell subset(s) possessed CTL activity. Negative and positive selection were used to obtain preparations of Ag-primed mdPBMC containing CD4 and CD8 T cells, CD4 T cells, CD8 T cells alone or only γδ T cells. Preparations of unseparated unstimulated and stimulated mdPBMC were used as controls. The proliferation (not shown) and killing activity of unseparated preparations mdPBMC stimulated with APC, pulsed with MMP, were similar to the results obtained with all 4 steers (compare Figure 6C with Figure 6B). Killing activity was less but clearly evident in cell preparations containing both CD4 and CD8 T cells and CD8 T cells alone (Figure 6C). Little or very limited killing activity was evident in cell preparations containing CD4 T cells. No killing activity was evident in the cell preparations containing γδ T cells (Figure 6C).
Role of the perforin/ GnzB pathway in intracellular killing of Map
Infected cells do not undergo apoptosis during intracellular killing of Map
The studies presented here were focused on analysis of the immune response to Map using the natural host. The initial studies leading up to the present studies showed all animals exposed to Map under experimental conditions at birth, develop an infection that elicits an immune response that controls but doesn’t eliminate the pathogen [38, 39]. Flow cytometric analysis of the immune response to Map and soluble Map Ags ex vivo demonstrated an immune response to Map could be detected 3–5 months post exposure that included CD4 and CD8 T cells . γδ T cells did not exhibit an Ag specific response. Further analysis with a cannulated ileum model demonstrated that Map introduced directly into the ileum are rapidly taken up and disseminated to other sites without establishing detectable lesions in the ileum containing Map, as detected by biopsy. In fact, no lesions were detectable up to 18 months post exposure . A follow up study comparing the immune response to human and bovine isolates of Map showed no difference in the immune response to Map. The one interesting comparative observation was that it appeared the CD8 T cell response in experimentally infected calves was delayed, reaching a maximum at 12 months . Development of a method to use site directed mutagenesis provided opportunity to look at the immune response to Map in greater detail and determine if any gene product was essential for establishing a persistent infection. Three genes were selected for analysis: relA, demonstrated to impair survival of Mtb in a mouse model ; pknG, shown to affect survival of BCG in macrophages ; and lsr2, shown to be involved in mediating multi-drug resistance to antibiotics . In vivo studies revealed, similar to the studies in mice with Mtb, that deletion of relA impaired survival [9, 10]. Comparison of survival with Map at necropsy showed wild type Map was readily detected in multiple tissues whereas ΔMap/relA was not detected in any tissue using culture and PCR. These findings and the ex vivo studies indicated there was a clear difference in the immune response to the ΔMap/relA mutant and suggested that deletion of the gene allowed for the development of an effector T cell response that cleared the infection. To investigate the immunological mechanisms accounting for clearance of the mutant, two steers were vaccinated with ΔMap/relA and maintained as a source of cells to characterize the effector T cells ex vivo. We hypothesized the difference in the immune response to Map and ΔMap/relA might involve signaling mediated through antigen presenting cells (APC). To examine this possibility we developed and used a mAb to CD209 (uniquely expressed on bDC, MoDC, and MoMΦ) to phenotypically identify and compare the capacity of bDC, MoDC, and MoMΦ to process and present Ags to effector memory T cells, elicited by vaccination with ΔMap/relA . The studies revealed the complexity of the immune response to the mutant. The study revealed bDC, MoDC, and MoMΦ were essentially equal in their capacity to process and present Ag to naïve T cells. Of special interest, all three APCs presented antigenic peptides in context of MHC I and II molecules simultaneously and provided signaling that elicited a CD4 and CD8 proliferative response.
Ancillary studies conducted to determine which Map proteins might be involved in the immune response to Map, included examining the proliferative response to the whole and truncated forms of the 35 kDa membrane protein, MMP [13, 44]. A proliferative response was obtained with the whole and truncated forms of the protein (unpublished). As reported here, further studies conducted to determine if MMP was a component of the recall response, elicited with ΔMap/relA, demonstrated it was included as a component of the immune response. Comparative studies demonstrated equivalent recall responses were obtained with ΔMap/relA and MMP with all three APCs . The recall response was MHC restricted .
In the present study, we initially used the vaccinated and control unvaccinated steers to examine the functional activity of memory T cells proliferating in response to Ag presentation by MoDC pulsed with ΔMap/relA and MMP. To conduct these studies, a viability assay was developed based on studies by Worku and Hoft, using patients with tuberculosis and control subjects vaccinated with the BCG . In addition, we adapted an expedient method for distinguishing live from dead bacteria to obviate the problem of using CFU as a read out of bacterial viability . Although the conditions for blocking all gene sites was not optimal for PMA, it was sufficient to be able to detect differences in live vs dead bacteria. The scale showed where the residual DNA from dead cells falls on the curve. The wide dynamic range between live and dead cells was consistent for distinguishing between DNA from live and dead bacteria. Comparison of the recall and functional activity of memory CD4 and CD8 T cells proliferating in response to Ag presentation by MoDC pulsed with ΔMap/relA and MMP revealed equivalent CTL activity was elicited with ΔMap/relA and MMP. The results proved highly reproducible using APC pulsed with either ΔMap/relA or MMP. A singular observation made throughout the studies was, regardless of the route of exposure to Map, ΔMap/reA, or MMP, exposure resulted in development of a CD4 CD8 T cell response [9, 12, 39, 40]. This raised two questions. Is cognate recognition of Ags by CD4 and CD8 a requirement for development of CTL activity? And, do both CD4 and CD8 T cells develop CTL activity? Only one of these questions could be answered with further studies using vaccinated animals. This prompted us to explore the possibility of developing an assay to study the full CTL response ex vivo. The results showed equivalent Ag presentation could be achieved with bDC and MoDC pulsed with either ΔMap/reA, or MMP. This suggested APC could be used to develop a method to study the full immune response to Ags ex vivo. If successful, it would be possible to study mechanisms of Ag processing and presentation by APC to a relevant pathogen. It would also make it possible to study the importance of cognate recognition of antigenic peptides presented in context of MHC class I and II molecules in development of CTL activity.
As reported here, four unvaccinated steers were used to modify the protocol for studying the recall response starting with stimulation of naïve T cells with bDC pulsed with ΔMap/relA or MMP followed by a second round of stimulation with MoDC pulsed with ΔMap/relA or MMP. After demonstrating equivalent responses occurred with ΔMap/relA and MMP, further studies were focused on analysis of the immune response to MMP. The first question of interest was whether the CD4 and CD8 T cells needed to be present in a culture to generate CTL. The studies conducted to this point in the investigation involved use of mdPBMC. Little or no response was observed if CD4 and CD8 T cells were separated from preparations of mdPBMC before primary Ag presentation by bDC followed by secondary stimulation with MoDC. In contrast, a full CTL response was consistently obtained if unseparated mdPBMC were used. The second question of interest was which T cell subset possessed the CTL activity. The unproven supposition was that CTL activity was primarily attributable to CD8 T cells. To answer this question, mdPBMC primed with APC pulsed with MMP, were separated into 4 populations before incubating with infected MoMΦ target cells. Cell preparations containing CD4, CD8, and CD4/CD8 were obtained by negative selection. The cell preparation containing CD8+ and CD8− γδ T cells was obtained by positive selection. Comparison of CTL activity showed unseparated mdPBMC contained the highest level of CTL activity followed by the cell preparations containing both CD4 and CD8 T cells and CD8 T cells. Minimal or no activity was observed with separated CD4 T cells or γδ T cells. NK cells were not evaluated for potential CTL activity in this study. Repeat studies showed they only comprised ~5% of cells present in mdPBMC stimulated with Ag-pulsed bDC and MoDC. The results demonstrated the importance of the interaction of CD4 and CD8 T cells in the generation of CTL. Further studies are needed to detail the signaling associated with interaction of CD4 and CD8 T cells during Ag presentation.
Extensive studies conducted to elucidate the mechanisms used by CTL to kill intracellular bacteria and protozoan parasites have shown perforin, GrzB, and granulysin play a role in killing [30, 45]. Our studies clearly show perforin and GrzB are involved in killing of Map. Further studies should show granulysin is also involved. An immune synapse develops on contact of CTL with the infected cells. Cytotoxic granules migrate to the synapse allowing perforin molecules to intercalate into the membrane of the target cell and form pores through which granzymes and granulysin are introduced into the cytoplasm. Granulysin disrupts the integrity of the bacterial cell membrane allowing entrance of GrzB and death of the bacteria . Analysis of effector cells after incubation with uninfected and infected MoMΦ showed CTL contact with infected MoMΦ is essential for killing. Newly synthesized perforin was present in CD8 CTL incubated with infected MoMΦ. Only a few CD4 T cells contained newly synthesized perforin. In contrast, there was minimal or no increase in newly synthesized perforin in primed CD8 CTL incubated with uninfected MoMΦ. GrzB was detectable in half of the CD8 CTL with no detectable level in CD4 T cells. These results indicate the intracellular killing of Map is associated with upregulation of both perforin and GrzB, mainly in CD8 CTL.
It has remained unclear as to whether apoptosis of the target cells, mediated by the perforin–granzyme pathway, is an essential component of the mechanisms of intracellular killing of bacteria. Studies by Thoma-Uszynski et al.  have suggested killing of Mtb is independent of apoptotic death of infected target cells. We conducted studies to examine this issue. Analysis of apoptosis showed the majority of infected MoMΦ were still viable after incubation with primed mdPBMC. The average percentages of apoptotic cells observed in infected MoMΦ co-cultured with Ag-primed mdPBMC was 13% compared to ~4% in infected MoMΦ co-cultured with control mdPBMC and ~2% in uninfected MoMΦ co-cultured with Ag-primed mdPBMC. This is in contrast to CTL mediated killing of virus infected and cancer cells where apoptosis is clearly involved . Introduction of GnzB leads to immediate initiation of apoptosis and death of the target cell. The majority of target cells infected with Map were still alive even after 3 days of incubation with Ag-primed mdPBMC. Further studies are needed to explain this apparent paradox. The interaction between Map and macrophages is a complex process affected by the lethal signals released by the CTL involved in the bacterial killing and cell apoptosis. Further studies of the roles of apoptosis in defense against Map infection are needed to fully explain the results obtained by Thoma-Uszynski et al.  and the results obtained in the present study.
In summary, we have used the natural host to gain a better understanding of the immune response to Map and candidate vaccines. Data obtained thus far have shown relA plays a central role in the ability of Map to establish a persistent infection and that deletion of relA leads to immune elimination of the mutant. Ex vivo analysis has shown MMP is a component of the immune response to ΔMap/relA. An equivalent CD8 CTL response is elicited with APC pulsed with ΔMap/relA or MMP. Simultaneous presentation of antigenic peptides to CD4 and CD8 by Ag pulsed bDC and MoDC is essential for generation of CTL. CTL activity is mediated through the perforin/granzyme pathway. In contrast to CTL activity against virus infected cells and cancer cells, intracellular killing of bacteria occurs with limited induction of apoptosis. The assays developed to conduct the studies ex vivo provide opportunities to study the potential efficacy of candidate vaccines as well as opportunities to study Ag presentation by DC and consequent proliferation and differentiation of CD4 and CD8 T cells with different functional activity.
The authors declare that they have no competing interests.
GSA, MME, KTP, SAK, HAT and WCD conceived the study. GSA and WCD participated in the design of the protocol to conduct the studies. JPB participated in the development and use of the ΔMap/relA mutant and the Map major membrane protein (MMP). GSA conducted the experiments. MME, BB and VH participated in the conduct of the experiments. GSA and DAS participated in statistical analysis of the data. GSA, MME, KTP, WCD, JPB, DAS, CDS, and LMF participated in the writing and interpretation of the results. WCD and JPB obtained the funding for the project. WCD oversaw and participated in all aspects of the study. All authors read and approved the final manuscript.
The authors wish to acknowledge the excellent technical support and animal care provided by Emma Karol and her staff. The results of this study were presented in part at the IVIS2016, the Gold Coast Convention Centre, The Gold Coast, Australia, and at the 2016 Student and Post-Doctoral Research Symposium, College of Veterinary Medicine, WSU, USA, and at the 2016 Global Veterinary Microbiology and Veterinary Medicine Summit, Chicago, USA. Finally the Authors would like to acknowledge and give thanks to the Franceschi Microscopy and Imaging Center and its staff.
The studies were supported by the WSU CVM Animal Health Research Center, the WSU Monoclonal Antibody Center (WSUMAC) and a gift from the Robert R. Fast Food Animal Research endowment. Gaber S. Abdellrazeq was supported by the WSUMAC. Mahmoud M. Elnaggar was supported in part by a fellowship from the Egyptian government and the WSUMAC. Portions of this work were also supported by the USDA-Agricultural Research Service. Mention of trade names or commercial products in this article is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the US Department of Agriculture.
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