The spleen plays an integral protective role against encapsulated bacterial infections. Our understanding of the associated mechanisms is limited to thymus-independent (TI) antibody production by the marginal zone (MZ) B cells, leaving the contribution of other splenic compartments such as the red pulp (RP) largely unexplored despite asplenic patients succumbing to the infection in the first 24 h, suggesting important antibody-independent mechanisms. In this study, using time-lapse intravital imaging of the spleen, we identify a tropism for Streptococcus pneumoniae in this organ mediated by tissue-resident MZ and RP macrophages and a protective role for two distinct splenic neutrophil populations (Ly6Ghi and Ly6Gintermediate) residing in the splenic RP. Splenic mature neutrophils mediated pneumococcal clearance in the spleen by plucking bacteria off the surface of RP macrophages that caught the majority of bacteria in a complement-dependent manner. This neutrophil phagocytic capacity was further enhanced after TI antibody production. Resident immature neutrophils (Ly6Gintermediate) in the spleen undergo emergency proliferation and mobilization from their splenic niche after pneumococcal stimulation to increase the effector mature neutrophil pool. We demonstrate that splenic neutrophils together with two macrophage populations and MZ B cells regulate systemic S. pneumoniae clearance through complementary mechanisms.
The spleen is important for protection against encapsulated bacteria including Streptococcus pneumoniae, a major cause of morbidity and mortality worldwide. Invasive pneumococcal disease, detected in 10–30% of pneumococcal pneumoniae cases, has long been known to increase the mortality substantially beyond that seen with pneumonia alone (Chiou and Yu, 2006; Blasi et al., 2012). It is estimated to directly cause >1.6 million deaths annually (World Health Organization Geneva, 2007; O’Brien et al., 2009). Invasive disease is particularly serious in splenectomized or asplenic patients. These individuals have a 50-fold higher risk of developing a fulminant septic infection to encapsulated bacteria, and a 50–70% mortality rate is associated with these cases (Holdsworth et al., 1991; Di Sabatino et al., 2011). Importantly, the majority of deaths occur within the first 24 h (Gransden et al., 1985; Di Sabatino et al., 2011), highlighting the importance of some very rapid as yet unknown innate immune mechanisms within the spleen in providing protection during the acute stages of i.v. infection before antibody production.
To date, the major protective mechanism of the spleen against S. pneumoniae is believed to be dependent on thymus-independent (TI) antibody production by specialized B cells within the marginal zone (MZ). After stimulation, MZ B cells rapidly differentiate into plasmablasts and secrete pathogen-binding serum IgM antibodies that are detectable in the serum only starting at 72–96 h after infection (Martin et al., 2001; Belperron et al., 2005; Moens et al., 2007), meaning other cells must keep the pathogen in check until antibodies are made. Once made, these antibodies are thought to enhance recognition and facilitate clearance of S. pneumoniae. Indeed, splenectomized patients display impaired IgM antibody responses to polysaccharide antigen (Amlot and Hayes, 1985; Kruetzmann et al., 2003). As a result, pneumococcal research in the spleen has focused almost exclusively on the cells that regulate B cell–dependent antibody production. However, considering the kinetics of i.v. pneumococcal disease in splenectomized patients, we hypothesize that other very rapid innate immune mechanisms within the spleen must not only contribute to early protection, but also stave off the infection until antibodies can be made.
Neutrophils are first responders in the innate immune response to infection. Their multiple defense mechanisms, such as their phagocytic capacity, reactive oxygen species production, and ability to degranulate and form neutrophil extracellular traps, contribute to the effective clearance of pathogens (Kolaczkowska and Kubes, 2013). Neutrophils typically access sites of infection via the circulation, following chemoattractant cues and responding to local inflammatory mediators (Kolaczkowska and Kubes, 2013). In addition to these circulating neutrophils, a large pool of neutrophils can be found in the bone marrow, and marginated pools of neutrophils may also exist within peripheral organs. These sources of neutrophils are thought to mobilize in response to stimulation (Athens et al., 1961a,b). There is some evidence to suggest that the spleen might function as a reservoir. Neutrophils, upon reinjection into humans and mice, appear to accumulate within the spleen (Peters et al., 1985; Ussov et al., 1995; Suratt et al., 2001). Whether this is related to an artifact of neutrophil isolation and reinjection or a bona fide physiological event remains unclear. Recently, a B helper neutrophil subset has been described to reside in the perifollicular zone of the spleen in humans and mice to promote antibody production by MZ B cells (Puga et al., 2012; Magri et al., 2014; Chorny et al., 2016). However, evidence on splenic neutrophil turnover, behavior, and additional functions during basal and infectious conditions is lacking and would require live cell imaging of these cells in the spleen, something that has to date not been done to our knowledge.
In this study, we used a combination of spinning-disk intravital microscopy (IVM [SD-IVM]) and two-photon IVM to evaluate the behavior of neutrophils in the spleen under steady state and after S. pneumoniae infection. Using this platform, we found that much but not all of the S. pneumoniae bypassed the MZ macrophages and were caught by red pulp (RP) macrophages. We also identified two neutrophil populations within the splenic RP: an immobilized, immature Ly6G-intermediate (Ly6Gint) population of neutrophils and a mature Ly6G-high (Ly6Ghi) population of neutrophils that scan the tissue. Mature neutrophils mediated pneumococcal clearance by removing the bacteria from the surface of RP macrophages. During an emergency response to infection, the immobilized Ly6Gint immature neutrophils increased their proliferative capacity and took on features of the resident mature neutrophils. Circulating neutrophils recruited to the splenic MZ helped increase TI antibody production by MZ B cells, which further enhanced the ability of mature splenic neutrophils to fully eradicate systemic pneumococcal infection.
The spleen is integral for protection against systemic
S. pneumoniae infection
A pneumococcal bacteremia model was used to evaluate individual components of immunity during S. pneumoniae infection. Intravenous infection with a very small dose (104 CFU) of S. pneumoniae resulted in a fivefold preferential sequestration by the spleen compared with the lung and liver within 60 min (Fig. 1 a). Bacterial counts in the brain, heart, and kidneys were below detection limit (not depicted). This splenic tropism is unique to S. pneumoniae infection, as our previous work has shown tremendous preferential sequestration of circulating Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa by the liver (Kolaczkowska et al., 2015 and unpublished data). In fact, removal of the spleen did not increase blood levels or dissemination of S. aureus (unpublished data). The course of S. pneumoniae infection was tracked in the spleen and blood over a 5-d period (Fig. 1 b). Bacterial counts decreased in blood and spleen for the first 8 h after infection. This was followed by a rebound in levels at 24 and 48 h before complete clearance by 5 d after infection.
The spleen was integral for clearance, as a pneumococcal challenge in splenectomized mice resulted in 100% mortality by 48 h, even at a fivefold decrease in infection dose (Fig. 1 c). Much focus has been placed on the MZ B cells and MZ macrophages as contributors to antibody production and pneumococcus clearance. Specific depletion of MZ B cells via an antibody-mediated protocol (Lu and Cyster, 2002) resulted in 40% mortality but only in the later phase (72 h) after S. pneumoniae infection (Fig. 1 d), coinciding with the MZ B cell–dependent production of IgM and IgG antibodies capable of binding S. pneumoniae (Fig. 1 e). Low-dose clodronate liposome (CLL) treatment, which depleted 80–90% of MZ macrophages but not RP macrophages (McGaha et al., 2011), resulted in a nearly identical temporal outcome (Fig. 1 d). Combined MZ macrophage and MZ B cell depletion did not further increase susceptibility to S. pneumoniae infection (Fig. 1 d), suggesting a single collaborative protective mechanism of these two cell types via TI antibody production. Importantly, the combined depletion of these two cell populations only partially recapitulated the effect of a splenectomy but with a delayed time frame, indicating that other earlier splenic innate immune mechanisms independent of these two cell types (and their ability to stimulate TI antibody production) are involved in splenic protection to pneumococcus.
S. pneumoniae localizes to both the MZ and the RP of the spleen
Dynamics of S. pneumoniae distribution in the spleen were determined using time-lapse two-photon IVM and SD-IVM of the spleen. First, evaluation of S. pneumoniae movement in the MZ revealed that, upon i.v. infection, the GFP-expressing bacteria flowed across the MZ, with some tethering interactions to MZ macrophages or other structures in this area (Fig. 2 a and Video 1). Quantification over the first 20 min after infection revealed that the vast majority of bacteria visualized had a short transit time through this area with only a few bacteria (<20%) being detained permanently in the MZ (>5 min in Fig. 2 b). Depletion of MZ macrophages by low-dose CLL treatment resulted in increased localization of bacteria in the RP at 60 min after infection (Fig. 2 c). Visualization of the splenic RP revealed a progressive accumulation of bacteria in this region over the first 20 min (Fig. 2, d and e; and Video 2). RP macrophages are at least in part responsible for this retention, as their depletion through high-dose CLL treatment significantly impaired the number of bacteria in the compartment (Fig. 2 e). This is despite increased bacteria migrating to the RP as a result of the concurrent depletion of MZ macrophages. Localization of bacteria in both splenic regions over time was also determined using fresh sections of spleen with labeled RP (F4/80+) and MZ (CD209b+) macrophages. This approach revealed a preferential localization of S. pneumoniae in the MZ at 20 min after infection (Fig. 2, f and g), whereas at 1 h after infection, bacteria load increased in the RP (Fig. 2 g).
Flow cytometry was used to identify the main cell types involved in S. pneumoniae capture in the spleen. Analysis of splenic S. pneumoniae-GFP–positive cells from spleens harvested at 30 min after infection revealed that >60% of bacteria were in populations that resided within the RP of the spleen, whereas MZ macrophages contributed a smaller portion to overall capture (20.1 ± 0.9%; Fig. 2 h). However, RP macrophages only accounted for 18.5 ± 2.1% of the total (Fig. 2 h). Systematic assessment of the remaining population of cells harboring S. pneumoniae using flow cytometry revealed that the majority were neutrophils (42 ± 2.9%; Fig. 2 h). The S. pneumoniae uptake appeared to be preferential to splenic neutrophils, as the number of total S. pneumoniae-GFP–positive neutrophils was significantly higher in the spleen than the blood (Fig. 2 i). Furthermore, neutrophil numbers in the spleen did not increase within the first 30 min after S. pneumoniae infection (Fig. 2 j), suggesting that a resident neutrophil population within the spleen is responsible for this bacterial uptake.
Neutrophil populations reside in the splenic RP
Time-lapse SD-IVM of the spleen was performed to study resident neutrophils in this organ. Under basal conditions, the spleen contained a large population of neutrophils that were localized in the RP compartment (Video 3). Based on their morphology and behavior, two neutrophil populations could be identified: those that crawled around scanning the tissue (mobile neutrophils) and those that formed large immobile colonies (immobilized neutrophils) that could be as large as 30–50 cells (Fig. 3, a and b). Mobile neutrophils (Fig. 3 a, white arrowheads) migrated throughout the RP at varied velocities (Fig. 3 c), and individual cells could be tracked for up to 1 h within the same field of view (Fig. 3, a–c). Neither of these populations was in the blood vessels. Immobilized neutrophils (Fig. 3 a, green arrowheads) were stationary (Fig. 3 b and Video 3), displayed a rounded morphology, and had a perivascular localization (Fig. 3 a). Aside from these two populations, neutrophils could also be seen rolling within blood vessels, but they rarely stopped, and none emigrated out of the vasculature (Video 3).
To evaluate the turnover of these splenic populations with blood neutrophils, parabiosis experiments pairing a LysMGFP mouse, in which neutrophils express GFP, with a nonfluorescent wild-type mouse (C57) were undertaken. After 2 wk, chimerism within the blood was 20–30%, as determined by flow cytometry (Fig. 3 d), values consistent with that of previous studies (Sawanobori et al., 2008; Guilliams et al., 2013). However, in the spleen, there was a dichotomy. IVM of the spleen in these same animals revealed that 35% of the mobile subset was derived from the parabiotic partner (Fig. 3 d and Video 4), indicating that, under steady state, this population was primarily replenished by neutrophils from the circulation. Interestingly, only 10% of the immobilized clustered neutrophils appeared to derive from the parabiotic partner (Fig. 3 d and Video 4), suggesting the majority of this population was primarily resident.
Intriguingly, analyzing all cells in the spleen, there were clearly two populations of neutrophils: a large population of Ly6Ghi neutrophils and a second smaller population of Ly6Gint neutrophils. High concentrations of Ly6G (1A8) antibody were given to deplete neutrophils. IVM revealed that all mobile neutrophils were depleted and only immobilized neutrophils remained (Fig. 4 a). Flow cytometric analysis of these spleens revealed a significant decrease in Ly6Ghi neutrophils, whereas Ly6Gint neutrophils remained unaffected (Fig. 4 a). When spleens from parabiosis animals were examined, the percentage of Ly6Ghi neutrophils of partner origin was akin to that of blood overall, whereas the percentage of Ly6Gint neutrophils was significantly reduced (Fig. 4 b), suggesting the Ly6Gint neutrophils are the resident population. These results support the view that the mobile neutrophils are Ly6Ghi and the immobilized resident neutrophils were the Ly6Gint population. This was not dissimilar to mature and immature neutrophils, respectively, in bone marrow.
To further characterize whether the Ly6Gint neutrophils expressed other markers of immaturity, we examined the expression of c-KIT (CD117) as well as other maturity markers for neutrophils. Expression of CD117 was seen only on Ly6Gint neutrophils (Fig. 4 c). CD117 staining was confirmed on immobilized neutrophils by IVM (Fig. 4 d). A portion of clustered Ly6Gint neutrophils also displayed increased CD49d (consistent with immature neutrophils) and lower l-selectin expression (Fig. 4 c). No difference was noted in any of the other markers between the two neutrophil populations (Fig. 4 c). Nuclear morphology assessment of immobilized neutrophils in situ demonstrated the presence of banded (Fig. 4 e, white arrowheads) and segmented (Fig. 4 e, blue arrowheads) neutrophils. Collectively, these data further support the view that there are two phenotypically distinct neutrophil populations in the RP, one immature expressing intermediate Ly6G levels and remaining immobilized in large colonies mostly as band cells and a second mature neutrophil population that is Ly6G high and that scans the splenic RP under steady-state conditions.
Mature splenic neutrophils mediate uptake of
S. pneumoniae in the RP
Next, we examined the behavior of the two populations of neutrophils in the splenic RP by SD-IVM. S. pneumoniae uptake by neutrophils in the RP was predominantly limited to mature neutrophils, as the immobilized immature neutrophils bound very little bacteria (Fig. 5, a and b; and Video 5). RP macrophages also bound the bacteria during this time period. Visualization at a higher magnification revealed that S. pneumoniae first bound to the surface of an RP macrophage, and the mature neutrophil subsequently migrated over and plucked the bacteria off the macrophage surface (Fig. 5 c and Video 6). At no point were mature neutrophils able to catch S. pneumoniae freely flowing in the splenic RP. Three-dimensional (3D) reconstruction of neutrophil-bound bacteria further confirmed intracellular localization of the pathogen. Increasing the transparency of Ly6G staining (Fig. 5 d, I–III) revealed GFP-expressing bacteria. Neutrophil phagocytosis of S. pneumoniae was complement dependent, as capture was completely abrogated in C3-deficient mice (Fig. 5 e and Video 5). This was not because of the RP macrophage not being able to catch the bacteria, as the C3−/− RP macrophages caught the S. pneumoniae, as well as wild-type RP macrophages (Fig. 5 e). Intriguingly, in C3−/− mice, where neutrophils were not able to remove the bacteria from the surface of the macrophage, huge numbers of bacteria associated with the RP macrophage and resulted in 100% mortality within the first 18 h of infection (Fig. 5 f). This suggested the macrophages were not able to directly kill the bacteria and required the immediate presence of the neutrophils. Even in the presence of complement, the macrophages were not able to kill bacteria, as depletion of mature neutrophils using a Ly6G (1A8) antibody resulted in increases in splenic bacterial counts at 24 h after infection (Fig. 5 g). Neutrophil-mediated respiratory burst has long been regarded as an important intracellular killing mechanism for pathogens. To evaluate this capacity in mature splenic neutrophils, S. pneumoniae was labeled with an OxyBURST probe that fluoresces green in the presence of oxidants. Visualization of OxyBURST-labeled bacteria upon neutrophil phagocytosis demonstrated a very rapid oxidative burst (Fig. 5, h and i). This rapid response was NADPH (nicotinamide adenine dinucleotide phosphate reduced) oxidase dependent, as the oxidant production was not seen in Cybb−/− mice within this timeframe (Fig. 5 i). However, oxidation was not the predominant killing mechanism, as Cybb-deficient animals were able to effectively clear and control the pneumococcal infection (Fig. 5 j). Previous in vitro work with human neutrophils has noted an important contribution of the serine proteases (e.g., cathepsin G [CatG]) and neutrophil elastase in intracellular pneumococcal killing (Standish and Weiser, 2009). In our in vivo model, animals with a deficiency in CatC, a central regulator of serine proteases including CatG and neutrophil elastase, displayed nearly a log-fold increase in mean bacterial load in the spleen, compared with wild-type animals, which was bordering on significant (P = 0.0628; Fig. 5 j). A significant difference in bacterial loads was observed between CatC- and Cybb-deficient mice (Fig. 5 j). The increased clearance of S. pneumoniae observed in Cybb-deficient animals likely results from increased proteolytic activity that has previously been reported in phagocytes from this mouse strain (Rybicka et al., 2010, 2012). These data suggest an important role for the local mature neutrophils in removing the bacteria from the RP macrophage and helping in bacterial clearance.
Emergency neutrophil maturation occurs in response to
Neutrophil populations were further evaluated at later time points after infection. Flow cytometric analysis revealed an increase in Ly6Ghi neutrophils within the first 24 h after S. pneumoniae infection (Fig. 6 a). Conversely, Ly6Gint neutrophil numbers did not significantly change within this time period (Fig. 6 a). Although 10% of Ly6Gint neutrophils were positive for the proliferative marker Ki67 at baseline, this value increased by 24 h after S. pneumoniae administration (Fig. 6 b) and only in the Ly6Gint neutrophil population, as none of the Ly6Ghi neutrophils were Ki67 positive after infection.
To see whether during infection the immature Ly6Gint neutrophils could take on the more mature mobile phenotype, a photoactivatable (UBC-PaGFP) transgenic mouse system was used. This allowed the tracking of the cells over time. When immobilized immature neutrophils were photoactivated under control conditions, ∼10% of the population mobilized over a 1-h period, so now, photoactivatable immobilized GFP-positive neutrophils became GFP-positive mature neutrophils (Fig. 6 c and Video 7), suggesting some immature neutrophils are always maturing in the spleen. After 6-h pneumococcal stimulation, a significantly larger proportion of immobilized progenitor neutrophils were able to start mobilizing and scan the RP over 1 h after photoactivation (Fig. 6 c and Video 7) and contribute to the pool of mature neutrophils within the spleen. Collectively, these data support that proliferation, maturation, and mobilization of the immature Ly6Gint into the mature Ly6Ghi neutrophil population occurred within the first 24 h after S. pneumoniae infection.
Neutrophils from the blood stream are sequestered into the MZ by MZ macrophages and influence TI antibody production
Under basal conditions, very few neutrophils could be found in the MZ. However, at 24 and 48 h after infection, a very dramatic infiltration of neutrophils occurred into the MZ (Fig. 7 a). Two-photon imaging of this area revealed that, after pneumococcal infection, neutrophils leaving the main circulation in the marginal sinus were tethered right out of the mainstream of blood by the MZ macrophages, where they remained rather than moving to the splenic RP (Fig. 7 b). Tracking individual neutrophils in the MZ under basal conditions revealed that the few cells that crawled within the area did so at speeds ranging from 2 to 10 µm/min (Fig. 7 c and Video 8). After the infection, the neutrophils that were recruited from the main stream of blood did not move like the local neutrophils in the RP, but rather, many were not crawling at all at 24 and 48 h after S. pneumoniae sequestration in the MZ, and the remainder crawled at the lowest detectable velocity (2–4 µm/s; Fig. 7 c). Indeed, the dwell time (Fig. 7 d) and number of firm interactions of neutrophils with MZ macrophages (Fig. 7 e) were both increased during infections. Depletion of MZ macrophages using low-dose CLL treatment resulted in a significant decrease in MZ localization of neutrophils (Fig. 7 f). These data support a role for MZ macrophages in the retention of splenic neutrophils after pneumococcal infection. Blocking antibodies against various integrins revealed that neutrophil retention in the MZ was partially β1 but not β2 integrin dependent (Fig. 7 g). This decrease in retention could be recapitulated by VCAM-1 blockade (Fig. 7 g), supporting an α4β1–VCAM-1–mediated retention mechanism. It is worth mentioning that other as yet unidentified adhesion molecules make up a significant portion of this retention.
A consequence of this sequestration mechanism into the MZ of the spleen was that the neutrophils localized not only with MZ macrophages, but also with MZ B cells (Fig. 7 h). To see whether this impacted antibody output by these neutrophils, we attempted to deplete neutrophils with Ly6G (1A8) antibody. The results were somewhat ambiguous. Although there was a decreased density of neutrophils in the MZ and RP areas of the spleen after infection (not depicted) when anti-Ly6G was used, the MZ B cell–dependent IgM and IgG antibody responses occurred in a dichotomous fashion (Fig. 7 i). A portion of the animals displayed low antibody production similar to MZ B cell depletion (Fig. 1 e), whereas normal responses were detected in other animals (Fig. 7 i). It became very clear that although neutrophil depletion efficiency was ∼90% at 24 h, at 72 h it was highly variable in the spleen ranging from as little as 30 to as high as 80%. This likely accounts for much of the antibody variability. Consistent with these data, a similar dichotomy was also observed in both blood and spleen bacterial counts at 72 h after infection (Fig. 7 j). Clearly, the more effective the neutrophil depletion was, the fewer antibodies were produced and the more bacteria were noted. Correlational analysis of these mixed responses revealed that splenic bacterial titers in neutrophil-depleted animals negatively correlated with both IgM (r = −0.6950; P = 0.0402) and IgG (r = −0.813 and P = 0.0092) serum antibody levels (not depicted). These data suggest that retained neutrophils in the MZ participate in the TI antibody response after S. pneumoniae infection, but one has to be cautious when trying to deplete neutrophils in the spleen long term.
Mature splenic neutrophils mediate TI antibody–dependent pneumococcal clearance
To assess whether MZ B cell–dependent TI antibodies enhanced mature neutrophil function, serum transfer experiments were performed (Fig. 8 a). Transfer of pneumococcus-immunized serum (72 h) resulted in an increased phagocytosis of S. pneumoniae by mature neutrophils at 30 min after infection, compared with both control serum (72 h) and pneumococcus-immunized serum from MZ B cell–depleted animals (TI antibody deficient, 72 h; Fig. 8 b). This antibody-dependent mechanism was limited to neutrophils, as no differences in RP macrophage uptake of bacteria were noted between serum transfers (Fig. 8 b). This enhanced neutrophil phagocytic capacity resulted in rapid removal of pneumococcus from the bloodstream (Fig. 8 c). Next, to determine whether these TI antibodies could enhance killing in the absence of the splenic environment, they were injected into splenectomized mice. The data reveal that benefit of the antibodies required splenic neutrophils, as injection of these antibodies into splenectomized mice provided no survival benefit (Fig. 8 d). Collectively, these data highlight the important phagocytic role of mature splenic neutrophils for antibody-mediated clearance of S. pneumoniae.
This study used imaging to track the dynamic progression of S. pneumoniae infection in spleen and has revealed previously unknown mechanisms that increase our understanding of spleen-specific protective mechanisms against this pathogen. This includes the collaboration of local neutrophils and macrophages as early innate immune components in the splenic RP helping to dampen bacterial proliferation. Indeed, we visualized the macrophage of the splenic RP being able to capture and present bacteria to local mature neutrophils. Based on our parabiosis experiments, these local mature neutrophils are recruited constantly from the mainstream of blood under basal conditions. Furthermore, we identify the presence of a second local population of splenic neutrophils that appear to be an immature population that, based on photoactivation experiments, can rapidly mature and mobilize during emergency situations, and this turns out to be key for helping to control the infection until antibodies are made. We also determine the requirement for the TI antibody response by MZ B cells aiding neutrophil phagocytosis for final clearance.
Tissue-resident macrophages play important homeostatic roles including immune surveillance for pathogens. In the context of encapsulated bacterial infection, MZ macrophages have been suggested to be important with their ability to bind the capsule of S. pneumoniae via the c-type lectin SIGN-R1 expressed on its surface (Kang et al., 2004). Our data support this work but also provide new information on a second population of splenic macrophages, the RP macrophages, which appear to contribute in a major way to initial binding and tropism of S. pneumoniae to the spleen. This macrophage function appears to be limited to the spleen, as Kupffer cells in the liver were less effective at catching encapsulated S. pneumoniae in the sinusoidal circulation (unpublished data). Although both splenic macrophage populations sequestered pneumococcus early, they contributed to S. pneumoniae infection defense by distinct mechanisms. MZ macrophages contributed to TI antibody production by MZ B cells, consistent with another study (Koppel et al., 2008). This is likely by facilitating the direct interaction of MZ B cells with the pathogen on the surface of the macrophages and indirectly enhancing MZ B cell activation through recruitment of neutrophils at the MZ. Interestingly, MZ macrophages displayed only a small amount of catching of S. pneumoniae as observed by intravital imaging. In fact, RP macrophages had a larger contribution to initial binding and subsequent clearance of S. pneumoniae mediated by mature neutrophils. RP macrophage binding of S. pneumoniae in our model was not dependent on complement and was not enhanced with passive immunization, suggesting an alternative mechanism.
In addition to resident macrophages, the spleen also serves as an important reservoir for other myeloid cells. Swirski et al. (2009) described a pool of monocytes that reside within the RP under steady-state conditions and that can be mobilized to the sites of injury. We demonstrate that mature neutrophils are also present within the RP compartment under basal conditions and carry out an important filtering function within the organ by mediating phagocytosis of bacteria. This protective mechanism is not restricted to encapsulated bacteria, as phagocytosis of S. aureus and Listeria monocytogenes has also been observed with our system (unpublished data), supporting an immune surveillance role for this pool of neutrophils. The spleen also has the capacity to increase both neutrophil and monocyte numbers by facilitating extramedullary hematopoiesis during inflammation (Swirski et al., 2009; Robbins et al., 2012). This is thought to occur by mobilization of hematopoietic stem and progenitor cells from the bone marrow to the spleen, where they seed preestablished niches and undergo expansion (Swirski et al., 2009). Intriguingly, the recently described hematopoietic niche in the splenic RP (Dutta et al., 2015; Inra et al., 2015) shares common features with the local environment surrounding our described Ly6Gint immature neutrophils, including the perivascular location and the presence of VCAM-1–positive macrophages around the colonies (unpublished data). It is likely that our immature neutrophils represent the consequence of continuous extramedullary hematopoiesis during the steady state, albeit at a very slow rate. Upon inflammatory stimulation, these immature neutrophils can mobilize as observed and contribute to the mature neutrophil population.
Neutrophils in the spleen have previously been shown to contribute to MZ B cell activation and subsequent production of anti-capsular polysaccharide antibodies (Puga et al., 2012; Magri et al., 2014; Chorny et al., 2016). Pentraxin 3 has recently been identified as a natural adjuvant produced and released by these B helper neutrophils to help mediate this response (Chorny et al., 2016). Although, some have not been able to confirm these observations in humans (Nagelkerke et al., 2014), our data does support a role for newly recruited splenic neutrophils in promoting anti-pneumococcal TI antibody production during systemic mouse pneumococcal infection. Although it is very easy to deplete circulating neutrophils to determine their function, the resident mature population in the spleen was extremely difficult to eradicate during infection, and the immature population was resistant to 1A8 depletion. In fact, similar depletion inefficiency of splenic neutrophils has previously been noted in a chronic inflammatory setting of tumor-bearing mice (Moses et al., 2016). It was unclear whether this resident population could impact on B cell antibody production. Nevertheless, in those mice where we obtained good depletion, we also got better inhibition of antibody production and increased bacterial load, consistent with a potential role for regulation of antibody production by neutrophils within the spleen.
Although most tissues rely on circulating neutrophils for recruitment, the spleen appeared to compartmentalize its recruitment; in the MZ, there was classical recruitment of neutrophils from the vasculature, whereas the RP had its own population of immature and mature neutrophils that were key for local eradication of S. pneumoniae. The obvious advantage of this type of system is that, at the first sign of infection, neutrophils are already in the RP ready to help kill bacteria caught by the macrophage. Without the neutrophils there, the bacteria were able to increase their numbers dramatically within the spleen, killing the host. Although at this point we can only conclude that it is the immediate presence of neutrophils in spleen that helped to eradicate bacteria, an additional possibility is that the circulating neutrophils that enter the RP further mature to perform a necessary function that circulating neutrophils are incapable of doing. In fact, under steady-state conditions, we do note a more activated phenotype for mature splenic neutrophils compared with circulating neutrophils (unpublished data). Many of these features are reminiscent of B helper neutrophils, which are proposed to polarize locally in response to bacterial factors and GM-CSF, which is released locally by innate lymphoid cells (Magri et al., 2014; Chorny et al., 2016). It will also be interesting to know whether during systemic infections such as sepsis, where most neutrophils are recruited to lungs and other infectious sites and in some instances patients become neutropenic, this local pool helps to maintain neutrophil presence in the spleen for critical innate immune purposes.
Materials and methods
8–12-wk-old male and female mice were used for experiments. C57BL/6, Pep BoyJ(B6), LysM-eGFP/eGFP, UBC-PaGFP, and Cybb-deficient (Cybb−/−) mice were obtained from The Jackson Laboratory, and CatC-deficient (CatC−/−) mice were a gift from GlaxoSmithKline. All mice were housed under a specific pathogen–free, double-barrier unit at the University of Calgary. Mice were fed autoclaved rodent feed and water ad libitum. All protocols used were in accordance with the guidelines drafted by the University of Calgary Animal Care Committee and the Canadian Council on the Use of Laboratory Animals.
Multichannel spinning-disk confocal and two-photon confocal microscopes were used to image mouse spleens. Mice were anaesthetized (10 mg/kg xylazine hydrochloride and 200 mg/kg ketamine hydrochloride). The right jugular vein was cannulated to administer fluorescent dyes and additional anesthetic. After skin incision, the mouse was placed in a left lateral position, and the spleen was exteriorized onto a glass coverslip on the inverted microscope stage. The stage was kept at 37°C to maintain the mouse body temperature.
Image acquisition of the splenic RP was performed using an inverted microscope (IX81; Olympus), equipped with a focus drive (Olympus) and a motorized stage (Applied Scientific Instrumentation) and fitted with a motorized objective turret equipped with 4×/0.16 UPLANSAPO, 10×/0.40 UPLANSAPO, and 20×/0.70 UPLANSAPO objective lenses and coupled to a confocal light path (WaveFx; Quorum Technologies) based on a modified CSU-10 head (Yokogawa Electric Corporation). Cells of interest were visualized using fluorescently labeled antibodies, fluorescent reporter mice, and fluorescent reporter bacteria. Typically, RP macrophages and neutrophils were stained by i.v. injection of 2.5 µg anti–F4-80 and 1 µg anti-Ly6G fluorescent conjugated mAbs, respectively. Laser excitation wavelengths of 491, 561, 642, and 730 nm (Cobolt) were used in a rapid succession together with the appropriate band-pass filters (Semrock). A back-thinned electron-multiplying charge-coupled device 512 × 512–pixel camera (Hamamatsu Photonics) was used for fluorescence detection. Volocity software (PerkinElmer) was used to drive the confocal microscope and for 3D rendering, acquisition, and analysis of images. Bacteria and neutrophil behavior was evaluated using Volocity software. Both populations were identified and tracked using the Find Object and Track functions, respectively, within the measurement modality. For each animal, tracking data were averaged for multiple fields of view and considered an n = 1.
Image acquisition of the splenic MZ was performed using an inverted multiphoton microscope (TCS SP8; Leica Biosystems) or upright multiphoton microscope (TCS SP8; Leica Biosystems). Typically, MZ macrophages were stained by i.v. injection of 1 µg anti-CD209b fluorescent conjugated mAbs. i.v. injection of 2 µg anti-MARCO (macrophage receptor with collagenous structure) fluorescent conjugated mAbs was also used to label MZ macrophages in preliminary experiments to confirm that 1 µg anti-CD209b did not affect S. pneumoniae binding. The dynamic behaviors of immune cells and bacteria were visualized simultaneously with a single-pulsed laser (Ti-Sapphire; Spectra-Physics or Coherent) at 950 nm or 1,040 nm in combination with appropriate bandpass emission filters (Semrock). The fluorescence was detected by HyD hybrid or high-sensitivity photomultiplier non-descanned detectors. Leica Biosystems software was used to drive the confocal microscope and for 3D rendering and acquisition of images. Files were converted from LIF format into multiple TIFFs using Volocity and subsequently imported into ImageJ (National Institutes of Health) for analysis. The plugin StackReg was used for movement correction purposes. Both bacteria and neutrophil tracking were completed using the Manual Tracking plugin. For each animal, tracking data were averaged for multiple images and considered an n = 1. For photoactivation experiments, multiphoton excitation at 800 nm was used to activate neutrophil populations of interest, and images were acquired using a spinning-disk microscope as described in the previous paragraph.
Age-matched female mice were housed together for 2 wk before surgery. Parabiotic pairs of mice were generated surgically as previously described (Ajami et al., 2007). In brief, a skin incision running from elbow to knee along the flank was generated on opposite sides of the mice to be paired. The mice were first joined with a suture through the shoulder and thigh muscles, and next, the inside faces of the skin flaps were juxtaposed and sutured. Complete blood sharing was monitored between 12 and 17 d by tail vein blood sampling. 24 h after chimerism detection in the blood, pairs were separated and prepared for subsequent intravital imaging of the spleen and/or flow cytometry of the spleen, blood, and bone marrow.
Bacterial growth and infection
The S. pneumoniae D39-GFP strain was grown on blood agar plates overnight at 37°C with 95% O2/5% CO2. Single colonies were picked from plates and grown in brain-heart infusion broth at 37°C with CO2 until an OD 600 of 0.5 was reached. Bacteria were resuspended in saline and diluted to achieve appropriate dose with a 100-µl volume. For long-term infection and acute bacteria infection, doses of 2 × 103 CFU or 104 CFU and 5 × 106 CFU were administered i.v., respectively. Generation of reporter bacteria for oxidation was performed as previously described (Surewaard et al., 2016). In brief, fresh streptococcal cultures were washed twice in saline, resuspended at 5 × 108 CFU in 500 µl in carbonate, pH 8.3, buffered saline, and labeled for 30 min with 20 µg ml−1 AF647 N-hydroxysuccinimide ester (Thermo Fisher Scientific) and 60 µg ml−1 OxyBURST Green H2DCFDA SE (DMSO stock; Thermo Fisher Scientific) under vigorous agitation. Activation of OxyBURST was accomplished by adding 250 µl of 1.5 M hydroxylamine, pH 8.5, and incubating for 30 min on ice. Reporter bacteria were washed twice with PBS and injected i.v. into mice at 5 × 106–107 CFU.
Anesthetized mice were washed with 70% ethanol under aseptic conditions. Blood was collected in a heparinized syringe by cardiac puncture. The lungs, liver, heart, kidneys, and spleen were removed after thoracotomy, weighed, and homogenized. For determination of CFUs, 50 µl of blood and 100 µl of tissue homogenate were serially diluted, plated onto blood agar plates, and incubated at 37°C with 5% CO2 for 18 h, and bacterial colonies were counted.
Serum antibody measurement
Blood was collected by cardiac puncture at multiple time points after either saline or S. pneumoniae injection and spun down at 400 g for 10 min. Then, serum was collected, and 25 µl was diluted with an equal volume of FACS wash buffer (1× PBS, 2% FBS, and 0.2% EDTA) and subsequently incubated with 106 CFU of freshly cultured S. pneumoniae for 30 min on ice. After a wash step, 1 µg of APC-conjugated anti–mouse IgG or IgM antibody was added in a resuspension volume of 50 µl and incubated for an additional 30 min. Antibody concentration used was determined by a preliminary serial dilution experiment to ensure optimal signal saturation. Samples were subsequently fixed with 0.5% paraformaldehyde in flow cytometry wash buffer and run using a flow cytometer (LSRII; BD). Samples were first gated on GFP+ bacteria, and then, the median fluorescence intensities were determined for APC-labeled anti-IgG or IgM. Values were normalized to control animal (saline injected) levels within each experiment and then averaged among multiple experiments.
Serum transfer experiments
Serum was collected as described in the previous paragraph at 72 h after injection (saline or S. pneumoniae). After confirmation of antibody production, serum from multiple animals (same treatment) was combined and heat inactivated at 56°C for 20 min. 100 µl of the control, immunized, or immunized (MZ B cell depletion) heat-inactivated serum was administered i.v. 20–30 min before infection with S. pneumoniae.
Mice were anesthetized, and the spleen was removed and placed in PBS on ice. Then, blood was collected in a heparinized syringe by cardiac puncture. The spleen was passed through a 70-µm filter. For S. pneumoniae–GFP+ detection experiments, cells were immediately stained for 20 min with fluorescently labeled antibodies and subsequently incubated in 1× Fix/Lyse buffer (eBioscience). For the remainder of experiments, residual red blood cells were lysed using ACK lysing buffer (Invitrogen). The cells were blocked using anti-CD16/32 antibody (2.4G2 clone; Bio X Cell) for 20–30 min. Then, cells were stained for 30 min with specified markers including FITC-labeled B220 (RA3-6B2; BD), CD18 (C71/16; BD), CD62P (RB40.3; BD), CD45.2 (104; BD), CD43 (eBioR2/60; eBioscience), PE-labeled anti–mouse Ly6G (1A8; eBioscience), F4/80 (BM8; eBioscience), CD 21/35 (4E3; eBioscience), CD117 (2B8; eBioscience), CD49d (R1-2; eBioscience), CxCR4 (2B11; eBioscience), CD62L (MEL-14; eBioscience), CD169 (3D6.112; BioLegend), APC-labeled anti–mouse CD209b (22D1; eBioscience), CD23 (B3B4; eBioscience), CD45.1 (A20; eBioscience), PerCP Cy5.5-labeled Ly6C (HK 1.4; eBioscience), PE-Cy7–labeled CD11b (M1/70; eBioscience), Pacific blue–labeled Ly6G (1A8; eBioscience), AF647-labeled CD54 (YN1/1.7.4; BioLegend), efluor 660–labeled CD11c(N418; eBioscience), Brilliant violet 510–labeled CD45 (30-F11; BioLegend), and APC-Cy7–labeled CD45 (30-F11; eBioscience). Appropriate isotype control antibodies were used to confirm positive signals. Nonviable cells were identified using propidium iodide or viability dye efluor 780 (eBioscience). Samples were run using a flow cytometer (FACSCanto; BD) and analyzed using FlowJo software (Tree Star). Neutrophils were identified as CD11b+ Ly6Ghi Ly6Cint or LysM GFPhi SSChi (for depletion experiments). Proinflammatory monocytes were identified as CD11b+ Ly6G− Ly6Chi. RP macrophages were identified as CD11b+/lo CD209b− F4/80hi. MZ macrophages were identified as CD11b+ CD209bhi F4/80−. Metallophilic macrophages were identified as CD11b+ CD169+ F4/80−/lo. Follicular B cells were identified as B220+ CD23hi CD21/35int, MZ B cells as B220+ CD23lo CD21/35int/hi, and B1 B cells as B220+ CD23lo CD21/35lo CD43+.
Depletion and blocking antibody protocols
Depletion protocols for various cell types have been used as previously described (Lu and Cyster, 2002; McGaha et al., 2011; Kolaczkowska et al., 2015). In brief, transient MZ B cell depletion was achieved by intraperitoneal injection of 100 µg of both anti-CD11a (M17/4; Bio X Cell) and anti-CD49d (PS/2; Bio X Cell) 96 h before S. pneumoniae infection. Depletion of MZ macrophages was completed by i.v. delivery of a low-dose clodronate treatment (100 µg) 96 h before infection. Neutrophils were depleted using an anti-Ly6G (1A8; Bio X Cell) antibody. For acute infection experiments, a single 500-µg dose was given intraperitoneally 24 h before infection. For long-term infection, supplemental 200-µg doses were given daily. Isotype antibodies or control liposomes were given as control injections. The specificity of all three depletion protocols was verified using both flow cytometry and in some instances immunohistochemistry. LysM-GFP reporter mice for our depletion studies were used to evaluate neutrophil depletion. Ly6Ghi neutrophils were identified as Ly6Cint GFPhi, Ly6Gint neutrophils as Ly6Cint GFPint, and Ly6C hi monocytes as Ly6Chi GFPint. These gates were established in experiments performed with control and isotype antibody–treated LysM-GFP mice with the inclusion of the Ly6G antibody (1A8 clone).
For blocking antibody experiments, 100 µg of purified anti-CD18 (clone M18/2; BioLegend), anti-CD29 (clone HMβ1-1; BioLegend), or anti-CD106 (clone 429; eBioscience) was added i.v. 10 min before S. pneumoniae infection. Appropriate isotype control antibodies were used for control experiments.
Statistical comparisons were performed using Prism (v6.0; GraphPad Software). Data are represented as mean ± SEM unless otherwise specified. Data, with the exception of bacterial CFUs, were compared either by unpaired two- tailed Student’s t test or one-way or two-way ANOVA followed by Bonferroni posthoc test for multiple comparisons adjustment. Bacterial CFU data were compared by Mann-Whitney test or Kruskal-Wallis test followed by Dunn’s multiple comparisons test. Survival curves were compared using log-rank (Mantel-Cox) test. Statistical significance was set at P < 0.05. The applied statistical analyses and the numbers of independent replicates (n) are reported in the figure legends.
Online supplemental material
Video 1 displays the movement of S. pneumoniae in the splenic MZ after infection. Video 2 shows S. pneumoniae accumulation in the splenic RP after infection. Video 3 demonstrates in vivo behavior of splenic neutrophil populations under steady-state conditions. Video 4 shows chimerism of both mature and immature splenic neutrophils after parabiosis. Video 5 displays in vivo capture of S. pneumoniae by splenic neutrophils in the presence or absence of complement. Video 6 shows neutrophil-mediated removal and phagocytosis of S. pneumoniae after initial binding to RP macrophages. Video 7 shows mobilization of photoactivated immature neutrophils after S. pneumoniae infection. Video 8 displays the in vivo behavior of circulating neutrophils in the splenic MZ.
We thank Trecia Nussbaumer and Dr. Robin Yates for the breeding of mice. We thank Dr. Craig Jenne and Dr. Bryan Yipp for use of their multiphoton microscopes. We thank Dr. Pina Colarusso at the Snyder Live Cell Imaging Facility for technical support for photoactivation experiments and Dr. Karen Poon (Snyder Institute Molecular Core) for assistance with flow cytometry.
P. Kubes is supported by a foundation grant from the Canadian Institutes of Health Research and a Heart and Stroke Foundation of Canada grant. J.F. Deniset is financially supported by a postgraduate fellowship from Alberta Innovates–Health Solutions. B.G. Surewaard is partially funded by Marie Curie Actions (FP7-PEOPLE-2013-IOF; grant no. 627575) and a postgraduate fellowship from Alberta Innovates–Health Solutions.
The authors declare no competing financial interests.
Author contributions: J.F. Deniset and B.G. Surewaard conceived the study, performed experiments, analyzed data, and wrote the manuscript. W.-Y. Lee contributed to parabiosis experiments. P. Kubes wrote the manuscript and directed the study.