Bradley D. Jones
Matthew Faron2
Jed A. Rasmussen
Joshua R. Fletcher- 1Department of Microbiology, The University of Iowa Carver College of Medicine, Iowa City, IA, USA
- 2The Genetics Program, The University of Iowa Carver College of Medicine, Iowa City, IA, USA
- 3The Midwest Regional Center for Excellence in Biodefense and Emerging Infectious Disease Research, Washington University, St. Louis, MO, USA
Over the last decade, studies on the virulence of the highly pathogenic intracellular bacterial pathogen Francisella tularensis have increased dramatically. The organism produces an inert LPS, a capsule, escapes the phagosome to grow in the cytosol (FPI genes mediate phagosomal escape) of a variety of host cell types that include epithelial, endothelial, dendritic, macrophage, and neutrophil. This review focuses on the work that has identified and characterized individual virulence factors of this organism and we hope to highlight how these factors collectively function to produce the pathogenic strategy of this pathogen. In addition, several recent studies have been published characterizing F. tularensis mutants that induce host immune responses not observed in wild type F. tularensis strains that can induce protection against challenge with virulent F. tularensis. As more detailed studies with attenuated strains are performed, it will be possible to see how host models develop acquired immunity to Francisella. Collectively, detailed insights into the mechanisms of virulence of this pathogen are emerging that will allow the design of anti-infective strategies.
Introduction
Bacterial pathogens adopt a variety of different strategies to infect and grow within a chosen host. In general, opportunistic pathogens take advantage of a compromised host environment to employ their virulence factors to generate a productive infection. Overt pathogens, such as Francisella tularensis, have developed sophisticated strategies to alter and/or avoid recognition and antimicrobial killing mechanisms to reach or create a privileged growth site within a “normal” or healthy host, causing the disease tularemia. This organism causes disease by diverse routes, including oral, subcutaneous, and pneumonic; the respiratory route is of particular concern because infection with 50 or less organisms is associated with mortality rates of 30–60%, if untreated (Tarnvik and Berglund, 2003; McLendon et al., 2006). Regardless of the route of infection, the virulence strategy of F. tularensis involves entering host cells, escaping from the phagosome and growing within the cytosol of the infected host. Surprisingly, the host immune responses to these activities are delayed and significantly less than expected (Jones et al., 2012). Cells infected with F. tularensis quickly disseminate throughout the host to the liver and spleen. Uncontrolled growth in systemic organs causes host cell damage, hypersecretion of cytokines and death by “cytokine storm” (Sharma et al., 2011). Due to the extreme virulence and ease of aerosol dissemination of F. tularensis, the US Centers for Disease Control and Prevention have classified this organism as a Tier 1 select agent because of its potential development into a bioweapon (Dennis et al., 2001).
Here we review the literature describing the work that is characterizing the intracellular strategy of this organism as well as the interactions that occur between these organisms and a wide variety of different host cell types (Conlan and North, 1992; Forestal et al., 2003; Lindemann et al., 2007; Schulert et al., 2009; Horzempa et al., 2010). We will highlight studies that have used virulent F. tularensis strains since it is becoming clear that work with model organisms (i.e., F. tularensis subsp. holarctica LVS and F. novicida) have sometimes provided results that are different than those obtained with the virulent strains, perhaps not surprisingly since LVS is an attenuated vaccine strain. In addition, we discuss recent work in which mutagenesis studies have identified mutants with significantly altered virulence phenotypes that are yielding important insights into the immune evasion mechanisms of virulent F. tularensis. We will discuss the virulence roles of the unique F. tularensis LPS and capsule and we also report the presence of glycoproteins that carry O-antigen. In addition, we will discuss various aspects of Francisella immunology and how attenuated F. tularensis strains are providing opportunities to study adaptive immune in a murine model of infection. Finally, we will attempt to provide insights into how this accumulating body of work may direct efforts to develop strains that can provide protective immunity against F. tularensis infection.
Genetic Approaches to Discover Fcrancisella tularensis Virulence Mechanisms
Efforts to understand the molecular details of the F. tularensis virulence strategy have progressed rapidly in the last decade. These research efforts have relied on genetic approaches to identify Francisella genes that are required for various aspects of pathogenesis. Qin and Mann (reference) performed transposon mutagenesis in the Schu S4 strain and identified numerous genes required for growth in HepG2 cells, including metabolic genes (i.e., car and pur genes, ggt, etc.) and hypothetical genes that have been found in screens by numerous groups, including our own. Weiss et al. identified F. novicida genes required for systemic mouse disease by creating a library of random transposon insertions in the chromosome of F. novicida (Weiss et al., 2007). This work identified the genes on the Francisella Pathogenicity Island (FPI, required for phagosomal escape), LPS O-antigen biosynthetic genes and 44 previously unidentified genes as important for F. novicida virulence. Many of the genes found in these screens are important for modifying the intracellular growth niche of the organism, acquiring nutrients or in modifying the host immune response to the presence of the bacteria.
Our research group has performed a similar screen to identify genes in virulent F. tularensis Schu S4 required for growth in human macrophages (Lindemann et al., 2011). Using a transposon system similar to that of Weiss et al., pools of F. tularensis Schu S4 mutants were screened for strains that were significantly reduced in their ability to grow within human monocyte-derived macrophages (MDMs). That work identified F. tularensis Schu S4 mutants that were defective in production of capsule and O-antigen, defective in FPI gene expression, nutritional mutants, as well as many other mutants in genes with unknown functions. These mutants are yielding important insights into Francisella mechanisms of virulence and are providing avenues to study host immune responses to Francisella strains that have lost some of their virulence properties.
Factors Important in the Uptake of Francisella tularensis into Phagocytic Cells
The virulence of Francisella is dependent upon the ability of the organisms to enter, persist and replicate within host cells as strains that have lost these abilities are avirulent (Brotcke and Monack, 2008; Charity et al., 2009). While it is not known which host cells provide growth niches that are essential to Francisella virulence, it is known that Francisella infects multiple cell types including phagocytes such as MDMs and polymorphonuclear leukocytes (PMN) as well as non-phagocytic epithelial and endothelial cells (Golovliov et al., 2003; Lauriano et al., 2004; Nano et al., 2004; McCaffrey and Allen, 2006; Qin and Mann, 2006; Schulert and Allen, 2006; Lindemann et al., 2007; Moreland et al., 2009). Upon contact with a phagocytic cell, F. tularensis can interact with different receptors, depending upon the opsonization state of the organism. In studies performed with non-opsonized Francisella, the mannose receptor plays an important role as non-opsonized Schu S4 had reduced uptake into macrophages acquired from mannose receptor knockout mice compared to macrophages from wild type mice (Geier and Celli, 2011). Consistent with this observation, blocking the mannose receptor with antibodies or soluble mannan significantly inhibits Francisella uptake (Balagopal et al., 2006; Schulert and Allen, 2006; Geier and Celli, 2011). However, deletion or blockade of the mannose receptor does not completely inhibit Francisella uptake, indicating that other receptors are involved in the uptake of the bacteria (Geier and Celli, 2011). While the reasons for the ability of this organism to use some many different receptors for internalization into phagocytic cells is not well understood, it does give the organism the capability to be internalized into a wide variety of different cell types. Entry into cells via different receptors doubtlessly activates different signaling cascades that elicit different cytokine responses from the host cells. Research efforts, by different groups, are aimed at understanding how the use of different receptors for internalization of F. tularensis impacts the infection dynamics between the pathogen and the host.
Studies of opsonized Francisella have demonstrated that the type of opsonization (serum vs. antibody) can alter the receptor employed for internalization of the organisms. In addition, independent of the method of opsonization, internalization of opsonized Francisella is significantly increased compared to non-opsonized organisms (Ben Nasr et al., 2006; Pierini, 2006; Geier and Celli, 2011). The targets of complement opsonization appear to be LPS and capsule, which protect the organism from the killing activity of complement while simultaneously stimulating the uptake of the bacteria into host cells (Clay et al., 2008). Several studies have implicated complement receptors in the uptake of Francisella strains (Schulert and Allen, 2006; Clay et al., 2008; Geier and Celli, 2011; Schwartz et al., 2012). Knockout of the CR3 receptor significantly reduces internalization of serum-opsonized Schu S4 in macrophages (Clay et al., 2008; Geier and Celli, 2011) whereas, serum-opsonized LVS utilizes CR4 to enter MDMs and dendritic cells (Ben Nasr et al., 2006; Schwartz et al., 2012). Both F. tularensis Schu S4 and LVS (serum opsonized) can use CR1 and CR3 for internalization into neutrophils (Schwartz et al., 2012). Additionally, both strains can utilize scavenger receptor A (SRA) for uptake into MDMs (Pierini, 2006). In contrast, IgG antibody-opsonized organisms have been shown to interact almost exclusively with Fc receptor (FcγR), since MDMs isolated from FcγR knockout mice are significantly reduced in their ability to internalize antibody opsonized Schu S4 (Geier and Celli, 2011). Antibody opsonization of Schu S4 has been associated with production of superoxide and decreased intracellular growth compared to non-opsonized bacteria (Geier and Celli, 2011). These data indicate that Francisella has evolved multiple mechanisms of internalization, which appear to be equally important, to take advantage of different host conditions and it is likely that the mechanism of uptake is important role in the subsequent interactions of the organism with its host.
Little is understood of the Francisella factors that mediate uptake into host cells. Recent data from our lab has demonstrated that the Francisella capsule and/or LPS are important in reducing uptake by phagocytes (Lindemann et al., 2011). Mutants in the waaY and waaL genes, which produce no capsule and lack the O-antigen side chain, displays ~10 fold increase in uptake into MDMs compared to wild type Schu S4 (Lindemann et al., 2011; Rasmussen et al., 2014). One of these mutants also displays slightly increased uptake into epithelial cells (unpublished observation). The mechanism for this increased uptake is unknown but it is tempting to speculate that mutations that result in disruptions of capsule and LPS biosynthesis either change the charge of the bacterial surface or uncover other surface molecules that mediate uptake. While not much is known about the bacterial factors that facilitate entry of Francisella into various host cells, strains that display increased uptake may be valuable in uncovering the mechanism of entry.
The Intracellular Interactions of Francisella tularensis
After entry, F. tularensis is located within a phagosome that begins to mature into a phagolysosome. Although maturation of the phagosome progresses significantly, Francisella has the ability to prevent fusion of the phagosome with the lysosome (Anthony et al., 1991; Checroun et al., 2006). During this process, the Francisella-containing phagosome (FCP) becomes decorated with both early and late endosomal markers: EEA-1, CD63, LAMP-1, LAMP-2, and Rab5 (Golovliov et al., 2003; Clemens et al., 2004; Checroun et al., 2006; Santic et al., 2006). Instead of fusing with the lysosome, the bacteria degrade the phagosomal membrane and egress into the host cytosol between 1 and 4 h post entry into the cell (Clemens et al., 2004, 2009; Chong et al., 2008). Interestingly, inhibition of phagosomal acidification delays F. tularensis escape and replication (Chong et al., 2008). The molecular mechanism that allows the bacteria to escape the phagosome is still uncharacterized but several studies have established that disruption of FPI genes renders the bacteria unable to escape the phagosome (Nano et al., 2004; Barker and Klose, 2007; de Bruin et al., 2007; Nano and Schmerk, 2007; Ludu et al., 2008; Buchan et al., 2009). In F. tularensis type A and type B strains both copies of the FPI must be mutated to inhibit phagosomal escape.
As Francisella reaches the cytosol the bacteria begin to replicate quickly, with data showing that virulent Schu S4 has an intracellular doubling time of ~1 h (Chong et al., 2008). This intracellular growth appears to last up to 48 h in vitro. Depending upon the host cell type, the organisms can replicate 50–1500 fold (Lai et al., 2001; Qin and Mann, 2006; Bonquist et al., 2008; Schulert et al., 2009; Edwards et al., 2010). Eventually host cell resources are consumed and the cell dies, releasing bacteria into the extracellular environment (Lai and Sjostedt, 2003; Lai et al., 2004; Celli and Zahrt, 2013).
Several bacterial factors that are essential for cytosolic growth have been identified through genetic approaches. Many of these genes are involved in metabolic pathways such as purine biosynthesis (purMCD) or uracil biosynthesis (pyrF) (Pechous et al., 2006, 2008; Horzempa et al., 2010). Recent work using F. novicida demonstrated that the FTN1586 open reading frame, an ortholog of ansP, encodes an asparagine transporter that is important for cytosolic growth (Gesbert et al., 2013). Similar roles in cytosolic growth have been identified for other transport proteins in the LVS strain, including, FTL1645, FTL1586, and FTL0129 (Marohn et al., 2012). Other genes have been identified that are involved in cytosolic replication including dipA, FTT0989, ripA, and the γ-glutamyl transpeptidase, ggt (Brotcke et al., 2006; Fuller et al., 2008; Alkhuder et al., 2009; Wehrly et al., 2009; Chong et al., 2012).
Three genes, migR, trmE, and cphA have been identified from genetic screens and shown to be involved in modulating FPI expression and growth inside of MDMs (Buchan et al., 2009; Charity et al., 2009; Lindemann et al., 2011). It has recently been shown by our research group that each of these genes affects FPI expression by indirectly altering intracellular concentrations of the alarmone ppGpp (Faron et al., 2013). The ppGpp alarmone has been shown to strengthen the interaction of FevR and RNA polymerase to induce expression of FevR-dependent genes (Charity et al., 2009). Despite each of these mutants having reduced ppGpp concentrations, each mutant has a unique growth pattern in different in vitro infection models. The LVS ΔtrmE strain did not grow inside of MDM cells, but replicated in both A549 and HEp-2 cells while the LVS ΔmigR mutant only replicated in HEp-2 cells. The LVS ΔcphA strain was unable to grow in any of the three cell types (Faron et al., 2013). These data indicate that different host cells present different intracellular growth challenges to Francisella; the bacteria appear to respond to these challenges via different homeostatic feedback pathways that contribute to the intracellular ppGpp pools.
Evidence is accumulating that significant differences exist between virulent F. tularensis strains and LVS. For instance, mutation of migR decrease F. tularensis LVS virulence for mice but deletion of migR in Schu S4 has a very minor effect on mouse virulence (Buchan, 2009). It is possible that this virulence difference is due to steady-state FPI gene expression levels between Schu S4 and LVS, as iglA-lacZ reporter activity in Schu S4 is about 3-fold higher than that observed in the LVS strain (Faron et al., 2013).
We have recently identified another difference between F. tularensis Schu S4 and F. tularensis LVS. Using recently immortalized human AT-II cells (ABM), we have compared the ability of virulent Schu S4 and LVS to enter and replicate within these cells. Interestingly, Schu S4 grows ~100-fold better in these airway epithelial cells than does LVS, suggesting that LVS attenuation may be partly due to an inability to effectively grow within epithelial lung cells (manuscript in preparation). To our knowledge, this is the first cell type in which such a stark difference in intracellular growth is observed between Schu S4 and LVS. These results indicate that it may be important to identify host cells that are key growth sites for the bacteria prior to efficient dissemination to distal organs. This knowledge may be vital in efforts to produce live attenuated vaccine strains.
The Atypical Lipopolysaccharide of Francisella tularensis
An important contributing factor to the high virulence of this pathogen is that its early intracellular growth appears to be unchecked by significant host responses (Bosio, 2011). A factor that is important in F. tularensis immune evasion is the lipid A component of LPS. Francisella lipid A species are unusual in that they are asymmetrical, tetraacylated and have longer than normal fatty acids chains (16–18 carbons). This is in contrast to the lipid A from most Gram-negative bacteria that contain six acyl chains of 12–14 carbons in length and phosphate groups available for interactions with TLR-4 that stimulate strong proinflammatory responses (Raetz, 1990; Poltorak et al., 1998; Beutler and Poltorak, 2000). For Francisella, the non-prime phosphate on the di-glucosamine backbone can be shielded by a galactosamine while the phosphate on the prime side of the sugar backbone is often missing (Vinogradov et al., 2002; Phillips et al., 2004; Gunn and Ernst, 2007). Multiple species of lipid A with some or all of these differences may be present in the outer membrane of a single organism (reference). The differences in the Francisella lipid A make the endotoxin of F. tularensis unable to bind to LBP and therefore unable to activate TLR-4 signaling pathways, rendering it inert compared to typical endotoxins (Hajjar et al., 2006; Gunn and Ernst, 2007). Several research groups are working to understand how acylation, length of fatty acid side chains and shielding the phosphates of the endotoxin contribute to the lack of bioactivity of the F. tularensis LPS (Kanistanon et al., 2012). These studies are providing important insights into how bacteria can modify their LPS to lessen the ability of the host to recognize their presence and activate key host cytokine pathways.
Characteristics of the Francisella tularensis Capsule and its Role in Bacterial Virulence
The role of the Francisella capsule in immune evasion and pathogenesis is an active area of investigation. Early work aimed at characterization of a crude preparation of the Francisella capsule revealed that it was composed of mannose, rhamnose, and dideoxy sugars (Hood, 1977). Sandstrom et al. created an acapsular Francisella strain and found that it was more sensitive to antibody-mediated killing (Sandstrom et al., 1988), although unfortunately this strain was not preserved for additional studies. Recent work using a monoclonal antibody directed against purified capsular material of Francisella has helped to characterize some aspects of this structure (Apicella et al., 2010). The capsule ranges in size from 100 to 250 kDa and it is present in all type A and B strains of F. tularensis that have been examined (Apicella et al., 2010). Immunization of mice with purified capsular material elicited circulating anti-capsule antibodies that protected from challenge with F. tularensis LVS but did not protect from F. tularensis Schu S4 challenge (Apicella et al., 2010).
Most bacterial capsules are large structures formed of repeating sugar subunits that are held together by glycosidic bonds and these structures associate with the bacterial outer membrane either directly or indirectly. There are four general classes of capsules for Gram-negative bacteria based upon biochemical, genetic, serological, and physical properties (Orskov et al., 1977; Daly et al., 1997). Of particular interest to this discussion of Francisella virulence factors are Group 4 capsules. Group 4 capsules are composed of similar (often identical) O-antigen sugars as those found in the LPS, contain acetimido sugars in their repeat unit structures, and are greater than 100 kDa in size (Whitfield, 2006). The capsule of Francisella has been shown to have a molecular weight of 100–250 kDa and contain the core sugar tetrasaccharide repeat of <2-acetamido-2,6-dideoxy-o-glucose (o-QuiNAc), 4,6-dideoxy-4-formamido-D-glucose (o-Qui4NFm), and 2-acetamido-2-deoxy-o-galacturnoamide (o-GalNAcAN), with the o-GalNAcAN unit present at twice the concentration of the other two sugars (Apicella et al., 2010; Wang et al., 2011). This is the exact composition of the sugars present in the Francisella repeating O-antigen subunits of the LPS (Vinogradov et al., 2002; Thomas et al., 2007). In a report characterizing the purified Francisella capsule, it was found that neither lipid A nor 2-keto-3-deoxyoctulsonic acid (KDO) were attached to the purified capsular structure, providing additional support that the LPS and capsule are distinct from each other (Apicella et al., 2010). These observations indicate that the Francisella capsule is similar to capsules produced by some strains of the Gram-negative bacteria Vibrio cholera, Escherichia coli, and Salmonella enterica which produce capsules that incorporate the LPS O-antigen (Jayaratne et al., 1993; Zhang et al., 2002; Peleg et al., 2005; Barak et al., 2007; Chen et al., 2007). Work to identify capsule biosynthetic genes has produced mutant strains that are disrupted for both capsule and LPS biosynthesis, indicating that the LPS and capsule biosynthetic pathways share many components for their assembly (unpublished observation). Efforts are still underway to identify the genes responsible for the unique biosynthetic steps in each pathway, such as the anchoring mechanism of capsule to the outer membrane, which is apparently distinct from the lipid A anchor of LPS (Bandara et al., 2011; Lindemann et al., 2011; Rasmussen et al., 2014).
One research group (Zarrella et al., 2011) has published data demonstrating that an alternate non-O-antigen capsule is present when Francisella is grown in brain heart infusion media (BHI). This high molecular weight alternate capsule species can be detected by PAGE in a F. tularensis LVS wbtA mutant that is unable to produce O-antigen. This indicates that this alternate capsule is distinct from the O-antigen capsule our research group has described. However, the composition of this structure was not reported. Another group also described the existence of a high molecular weight capsule-like material present in an F. tularensis LVS wbtI mutant strain, which is unable to produce O-antigen (Bandara et al., 2011). The authors reported that this capsule-like material was composed of glucose, galactose and mannose sugars. While it is not known if the structures reported by Zarella et al. and Bandara et al. are the same, both appear to be high molecular weight capsule-like molecules and both are present in strains with O-antigen defects.
F. tularensis Produces Proteins that are Glycosylated with the O-antigen
Efforts to understand the roles of bacterial glycoproteins have gained momentum from recent data indicating that some bacterial glycoproteins may play roles in host-pathogen interactions (Straskova et al., 2009; Egge-Jacobsen et al., 2011; Balonova et al., 2012). Francisella species have recently been shown to produce significant amounts of glycoproteins, many of which appear to be outer membrane proteins (Balonova et al., 2010). We have recently discovered that both virulent type A and B strains of F. tularensis produce O-antigen glycoproteins, detectable in whole cell lysates that bind to a monoclonal antibody specific for the O-antigen subunit (FB11, QED Biosciences). Interestingly, the F. tularensis LVS strain does not produce detectable quantities of these glycosylated proteins (Figure 1A). Furthermore, when the glycoprotein profiles of Schu S4 LPS O-antigen mutants [FTT1236 (waaY) and FTT1238c (waaB)] were compared to the orthologous LVS mutants (FTL0708 and FTL0706, respectively), we found that the LVS mutants lacked detectable O-antigen reactive protein bands that are present in the Schu S4 mutants (Figure 1B). Early work with these mutants obscured O-antigen protein reactivity due to proteinase K digestion during sample preparation (Lindemann et al., 2011). More recent work with non-proteinase K treated whole cell lysates has revealed that these strains do produce O-antigen reactive bands which can be detected by Western blots (Figure 1C).
Figure 1. F. tularensis strains produce O-antigen glycosylated proteins. One ml of F. tularensis broth cultures was centrifuged at 8000 × g for 2 min before resuspending the pellet in Buffer Part A, (6 mM Tris, 10 mM EDTA, and 2% [wt/vol] sodium dodecyl sulfate [pH 6.8]) and heated to 65°C to sterilize cultures. Bacterial lysates were incubated with, or without, proteinase K (New England Biolabs, Ipswitch, MA) at 37°C for 24 h before lyophilizing. Approximately 14 mg of bacterial material from each sample was mixed with NuPage (Life Technologies, Carlsbad, CA) sample reducing agent and buffer, boiled, and loaded into a 4–12% Bis-Tris NuPage gel and electrophoresed using NuPage MES SDS running buffer (Life Technologies, Carlsbad, CA). For immunoblots, samples were transferred to nitrocellulose and probed with FB11 primary antibody to detect O-antigen attached to LPS or to protein (QED Bioscience, San Diego, CA). Bands were visualized using goat anti-mouse IgG (H+L) conjugated to horseradish peroxidase (Jackson ImmunoResearch, West Grove, PA) and SuperSignal West Pico chemiluminescent substrate (Pierce Biotechnology, Rockford, IL). (A) Western blot analysis of LPS preparations from F. tularensis LVS, virulent type B F. tularensis subsp.holarctica strains (1547 and 1623) and virulent type A F. tularensis subsp. tularensis strains (Schu S4, MA00, and WY96) using the O-antigen FB11 antibody for detection of bands containing O antigen, without or with proteinase K (pk) treatment. (B) Western blot of whole cell lysates of F. tularensis Schu S4, F. tularensis Schu S4 waaY::TrgTn and F. tularensis Schu S4 waaL::TrgTn, F. holarctica LVS, F. holarctica LVS waaY::TrgTn and F. holarctica LVS waaL::TrgTn probed with the anti-O antigen monoclonal antibody FB11 to detect the presence of LPS O antigen laddering in these strains. (C) Western blot analysis of F. tularensis Schu S4, F. tularensis Schu S4 waaY::TrgTn and F. tularensis Schu S4 waaL::TrgTn whole cell lysates without or with (pk) proteinase K treatmenst, using O-antigen FB11 antibody.
Another group has reported findings that are consistent with these observations. Balonova et al. (2012) reported the presence of a Francisella lipoprotein that is glycosylated with O-antigen sugars and that the glycosylated lipoprotein was absent in an F. tularensis subsp. holarctica FSC200 wbtDEF mutant (Balonova et al., 2012). We believe that protein O-antigen glycosylation, unique to virulent F. tularensis strains, may play a role in either the virulence of the organism or aid in evading the host immune response. Future work in the lab is focused on understanding the significance of O-antigen glycosylated proteins in F. tularensis pathogenesis.
Differences in Adaptive Immune Responses to Virulent F. tularensis and F. tularensis LVS
One of the key features of the murine pneumonic tularemia model is the rapid time to death (~5 days post infection), which precludes the development of a robust adaptive immune response. This aspect of Francisella virulence has made vaccine development a daunting challenge, and many labs have used F. tularensis LVS as a less virulent substitute to study aspects of B and T cell biology in sublethal infection and immunization. Evidence is accumulating that the host response to Francisella infection is strain-specific and responses that occur to F. tularensis LVS or F. novicida infection may be different than those observed for virulent F. tularensis (i.e., Schu S4) (Kurtz et al., 2013; Laws et al., 2013). This is logical; the LVS strain was purposefully selected as a vaccine strain based upon its attenuated virulence phenotype (Sandstrom, 1994; Elkins et al., 2003). A vaccine against fully virulent Francisella strains will almost certainly require stimulation of cellular immunity, though the mechanisms by which these processes can be directed against Francisella remain elusive (Ray et al., 2009; Conlan, 2011).
Protective antibodies were an early target of research into immunity to Francisella. In studies utilizing a Type A strain, Foshay (1946) showed that transfer of hyperimmune serum from horses or goats provided protection to ~70–90% of rats infected subcutaneously, although the written details of these experiments are vague. More recent studies utilizing the mouse model have found contradictory results (Foshay, 1946; Kirimanjeswara et al., 2008). Kirimanjeswara et al. found that immune serum from LVS-immunized mice did not provide protection against Schu S4. In vitro, however, they observed that murine alveolar macrophages stimulated with interferon-γ were able to kill immune serum opsonized Schu S4 (Kirimanjeswara et al., 2008). While the latter result is intriguing, Crane et al. have shown that Schu S4 may be able to avoid this fate in vivo by interacting with the host serine protease plasmin. Schu S4 can bind to active plasmin, which can degrade Francisella-specific antibodies (Crane et al., 2009). The authors found that while antibody opsonization of both Schu S4 and LVS resulted in an increase in TNF-α, the presence of active plasmin on Schu S4, but not LVS, inhibited the induction of TNF-α in infected cells (Crane et al., 2009). These results highlight a difference between the two strains that may have important implications for how virulent Francisella species avoid early detection and control. To that end, plasminogen knockout mice might be an interesting model to examine the role of antibody opsonization and plasmin during Schu S4 infection in vivo (Berri et al., 2013).
As with antibodies, the role of B cell activity in providing immunity to Francisella species is complex; however, it is clear that mice lacking B cells are less able to control or survive a Francisella infection (Crane et al., 2012). Data is emerging that a specific subset of B cells (B1a) can have almost opposite effects in the host response, depending on the infecting strain and the model of infection (Cole et al., 2009; Crane et al., 2013). Cole et al. demonstrated that immunization with lipopolysaccharide from LVS generated a B1a cell-dependent protective response against an intraperitoneal challenge with ~103 CFU of LVS (Cole et al., 2009). In contrast, Crane et al. utilized a short-term low dose antibiotic treatment after intranasal infection with Schu S4 (the convalescent model) and observed that mice largely deficient in B1a cells (XID mice) survived better than did wild type mice (Crane et al., 2013). The increased survival in these mice was found to be associated with a reduction in the anti-inflammatory cytokine IL-10, which is a potent inhibitor of IL-12. The latter cytokine stimulates interferon-γ production, and is necessary for the survival of tularemia (Crane et al., 2012). Curiously, Metzger et al. reported that IL-10−/− mice succumb to standard intranasal Schu S4 infection similar to wild type mice, though it should be noted that the time scales of infection are different between these studies and direct comparisons may not be appropriate (Metzger et al., 2013). The immune responses observed in the convalescent model would not have time to develop in a standard intranasal infection, although it would be of interest to see if IL-10−/− mice phenocopy XID mice in the convalescent model of Schu S4 infection.
One possible target of the anti-inflammatory activity of IL-10 may be at the interface of antigen presenting cells and T lymphocytes. Hunt et al. identified a factor released by Francisella infected cells that stimulated IL-10-dependent degradation of MHC class II molecules in macrophages (Hunt et al., 2012). Importantly, supernatants from Schu S4 infected macrophages have also been shown to stimulate the downregulation of MHC class II molecules (Wilson et al., 2009). These data suggest that antigen presentation to CD4+ T cells may be reduced in vivo. This research group, as well as others, has also shown that F. novicida and LVS induce prostaglandin E2 (PGE2) production in infected macrophages (Woolard et al., 2007; Wilson et al., 2009). PGE2 has been shown to inhibit macrophage maturation, and might play a similar role in downregulating pathways important for intracellular killing of Francisella, as in Burkholderia pseudomallei infections (Zaslona et al., 2012; Asakrah et al., 2013). Interestingly, these groups showed that PGE2 induced by Francisella infection inhibited T cell proliferation and interferon-γ production in vitro. It has long been known that T cells are important for bacterial control and immunity to Francisella; for an excellent summary of this literature, see Cowley and Elkins' 2011 review (Cowley and Elkins, 2011; Crane et al., 2012; Eneslatt et al., 2012). Both CD4+ T cells and CD8+ T cells were required for survival of a primary Schu S4 infection in the convalescent model of tularemia, but only partial protection against a secondary challenge was observed for wild type mice (66% survival) (Crane et al., 2012). It is intriguing to speculate that the partial protection may be a function of a less than optimal T cell response mediated by PGE2, both in terms of antigen presentation and T cell proliferation. The use of knockout mice lacking various aspects of PGE2 production or signaling may be useful in testing this hypothesis. Our lab has preliminarily identified Schu S4 mutants that provide some protection against wild type Schu S4; it would be interesting to compare PGE2 levels during infection with our strains to those of other groups that have also shown protection (Conlan et al., 2010; Rockx-Brouwer et al., 2012). Additionally, we are developing vectors to express recombinant Francisella proteins fused to known CD4+ and CD8+ epitopes from lymphocytic choriomeningitis virus (LCMV) in an effort to quantify the magnitude of T cell proliferation and maturation state during both the immunization and challenge phases of protection studies.
Summary
Significant advances have been made in understanding the virulence of F. tularensis over the last decade. The development of genetic tools has been critical in creating F. tularensis mutants that are defective in various aspects of virulence. The study of mutants has provided insights into the pathogenic mechanisms of Francisella and is pushing forward efforts to understand the mechanisms that this pathogen uses to evade host detection. The virulence strategy of F. tularensis has a two-pronged approach (Figure 2). A primary thrust of the Francisella virulence strategy is to reach the host cell cytosol as a privileged site for growth. The organism possesses a phagosomal escape mechanism, encoded on the FPI, which allows the organisms to disrupt the phagosomal membrane and enter the cytosol for growth. The FPI genes, which encode the capacity to lyse the phagosomal membrane, are central to the ability of the pathogens to reach the cytosol. Several labs are continuing work aimed at elucidating the molecular details of both the host and bacterial components of this process.
Figure 2. Comparison of the intracellular growth strategies of wild type F. tularensis and a F. tularensis capsule/LPS mutant. Both wild type and mutant organisms are internalized into a host cell, although the absence of capsule and LPS allows increased internalization. Both strains can escape from the phagosome. The wild type strain grows to high numbers in the host cell cytosol before inducing death of the cell. At late stages, organisms can be found in Francisella-containing vacuoles (FCVs). In contrast, after mutant organisms escape the phagosome, they grow for a short time in the cytosol before the cell dies preventing additional growth of the organisms.
A second component of the Francisella virulence strategy employs the capsule and its unique LPS to avoid detection by host innate immunity mechanisms. The capsule and LPS provide protection from the host complement system by protecting the organism from complement opsonization and killing. Perhaps even more importantly, the unique F. tularensis LPS provides stealth to the overall virulence strategy as the lipid A does not activate the TLR4 cytokine response pathway.
We have also highlighted in this review some of the differences between laboratory strains of F. tularensis and virulent strains of F. tularensis. F. tularensis Schu S4 and LVS display significant differences in FPI gene expression levels with Schu S4 FPI expression being about 3-fold higher than LVS. Antibodies generated against F. tularensis LPS and capsule provide significant protection against murine challenge with F. tularensis LVS while little protection against Schu S4 challenge is observed. We also observe that virulent Schu S4 produces significant amounts of proteins glycosylated with O-antigen while LVS has almost undetectable levels of those glycosylated proteins, although the significance of these observations is still unknown. Finally, we have evidence in our lab that LVS does not grow well in a human airway epithelial cell while Schu S4 grows to high levels (manuscript in preparation).
Importantly, there are many research groups actively trying to understand how virulent F. tularensis suppresses a variety of host immune responses including neutrophil and macrophage activation mechanisms. The molecular and cellular details of these virulence mechanisms continue to be pursued in detail with the goal of understanding the mechanisms which lead to the extreme virulence of this bacterial pathogen as well as to develop methods to create effective immune responses against Francisella infection.
Conflict of Interest Statement
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.
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Keywords: Francisella tularensis, FPI virulence genes, phagosome escape, unique LPS, stealth strategy, capsule mutant, virulent Schu S4
Citation: Jones BD, Faron M, Rasmussen JA and Fletcher JR (2014) Uncovering the components of the Francisella tularensis virulence stealth strategy. Front. Cell. Infect. Microbiol. 4:32. doi: 10.3389/fcimb.2014.00032
Received: 09 December 2013; Accepted: 17 February 2014;
Published online: 07 March 2014.
Edited by:
Max Maurin, Université Aix-Marseille II, FranceReviewed by:
Andrey P. Anisimov, State Research Center for Applied Microbiology and Biotechnology, RussiaThomas Henry, Institut National de la Santé et de la recherche médicale, France
Copyright © 2014 Jones, Faron, Rasmussen and Fletcher. 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) or licensor 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.
*Correspondence: Bradley D. Jones, Department of Microbiology, The University of Iowa Carver College of Medicine, 3-330 Bowen Science Building, 51 Newton Road, Iowa City, IA 52242-1109, USA e-mail: bradley-jones@uiowa.edu