Siva R. Uppalapati1*
Andres Vazquez-Torres1,2*- 1Department of Immunology & Microbiology, University of Colorado School of Medicine, Aurora, CO, United States
- 2Veterans Affairs Eastern Colorado Health Care System, Denver, CO, United States
The metal ion manganese (Mn2+) is equally coveted by hosts and bacterial pathogens. The host restricts Mn2+ in the gastrointestinal tract and Salmonella-containing vacuoles, as part of a process generally known as nutritional immunity. Salmonella enterica serovar Typhimurium counteract Mn2+ limitation using a plethora of metal importers, whose expression is under elaborate transcriptional and posttranscriptional control. Mn2+ serves as cofactor for a variety of enzymes involved in antioxidant defense or central metabolism. Because of its thermodynamic stability and low reactivity, bacterial pathogens may favor Mn2+-cofactored metalloenzymes during periods of oxidative stress. This divalent metal catalyzes metabolic flow through lower glycolysis, reductive tricarboxylic acid and the pentose phosphate pathway, thereby providing energetic, redox and biosynthetic outputs associated with the resistance of Salmonella to reactive oxygen species generated in the respiratory burst of professional phagocytic cells. Combined, the oxyradical-detoxifying properties of Mn2+ together with the ability of this divalent metal cation to support central metabolism help Salmonella colonize the mammalian gut and establish systemic infections.
Introduction
A rich microbiome, cellular and abiotic mucosal barriers, as well as cellular and humoral effectors of the innate and adaptive immune system may limit the colonization, growth and spread of pathogenic bacteria in mammalian hosts (Rosales and Uribe-Querol, 2017; Levinson et al., 2018; Uribe-Querol and Rosales, 2020). Hosts use metal transporters, calprotectins, siderocalins and a variety of other metal-sequestering proteins to limit the availability of Mg2+, Fe2+, Mn2+ and Zn2+ ions from bacteria, a phenomenon known as nutritional immunity (Bellamy, 2003; Loomis et al., 2014; Hennigar and McClung, 2016; Wang et al., 2018; Cunrath and Bumann, 2019; Monteith and Skaar, 2021). Bacteria display sophisticated transport systems that counteract metal restrictions imposed by hosts (Porcheron et al., 2013; Chandrangsu et al., 2017). Among the bioactive metal ions, Mn2+ plays a salient role in bacterial physiology and the adaptation of prokaryotic cells to stress (Papp-Wallace and Maguire, 2006). Mn2+ is a cofactor of enzymes involved in carbon and nucleotide metabolism, DNA replication, and protein translation (Lovley and Phillips, 1988; Martin and Imlay, 2011; Culotta and Daly, 2013; Torrents, 2014; Kaur et al., 2017; Tong et al., 2017; Daniel et al., 2018; Li and Yang, 2018; Hutfilz et al., 2019). Mn2+ is also a cofactor of superoxide dismutase (SOD) and catalase (KatN) family members, and this divalent metal is utilized by carbon utilization enzymes such as phosphoglycerate mutase (PGM) and fructose-1,6-bisphosphate phosphatase, or envelope stress phosphatases (Shi et al., 2001; Miriyala et al., 2012; Whittaker, 2012; Radin et al., 2019). The MntR repressor coordinates a Mn2+ ion and the ferric uptake regulator (Fur) can bind to Fe2+ or Mn2+ (Hiemstra et al., 1999; Kehres et al., 2002a; Ikeda et al., 2005; Waters, 2020).
Salmonella enterica serovar Typhimurium is a facultative intracellular pathogen associated with intestinal and invasive diseases in humans and animals (Galan, 2021). The success of Salmonella as a pathogen can be directly ascribed to its capacity to overcome colonization resistance by resident gut microbiota, invade epithelial cells, and establish intracellular infections within host enterocytes and macrophages (Winter and Bäumler, 2011; Lorkowski et al., 2014; Lhocine et al., 2015; Aljahdali et al., 2020; Jiang et al., 2021; Powers et al., 2021). During their associations with host cells, Salmonella are exposed to acid pH, oxidative and nitrosative stress, and nutritional deprivation (Fang et al., 2016). A variety of adaptive mechanisms are used by Salmonella to fight the hostile host environment (Bernal-Bayard and Ramos-Morales, 2018; Tanner and Kingsley, 2018; Gogoi et al., 2019), and a few reviews have examined the contribution of Mn2+ in Salmonella pathogenesis (Kehres and Maguire, 2003; Papp-Wallace and Maguire, 2006; Osman and Cavet, 2011). Despite these advances, many unanswered questions and occasional contradictory findings warrant a review of our current understanding of Mn2+-mediated stress responses in Salmonella pathogenesis. In this review, we discuss the adaptive mechanisms that allow Salmonella to compete with the host for Mn2+, and present ways by which this divalent metal contributes to metabolic programs associated with resistance of Salmonella to oxidative and nitrosative stress.
Manganese Limitation in the Host
Hosts sequester transition metals in their fight against pathogenic organisms (Hennigar and McClung, 2016). Metal sequestration is mediated by calprotectin, lipochalin 2, metallothioneins, ferritin and transport systems including NRAMP1. Mn2+ limitation is mostly mediated by calprotectin and NRAMP1.
Calprotectin
The host protein calprotectin, a member of the calcium-binding S100 family, limits Mn2+ from extracellular Salmonella. Human calprotectin is a heterooligomer with a dedicated Zn2+-binding site-1 and a versatile Mn2+-, Fe2+-, Zn2+- and Ni2+-binding site-2 (Hayden et al., 2013; Zygiel and Nolan, 2018). Calprotectin is secreted by infiltrating neutrophils at sites of inflammation, reaching extracellular concentrations of about 40 μM, but is also expressed by epithelial cells and keratinocytes (Johne et al., 1997; Zygiel and Nolan, 2018; Jukic et al., 2021). Calprotectin limits metal bioavailability from bacteria, thus inhibiting bacterial growth, and its expression in epithelial cells diminishes binding of Salmonella to host cells (Nisapakultorn et al., 2001). Infection of gut mucosa by Salmonella attracts neutrophils, which secrete calprotectin in extracellular traps (Urban et al., 2009; Patel and McCormick, 2014). Fecal calprotectin levels in diarrheic children correlate with the severity of bacterial infection, and the concentration of calprotectin is increased in plasma during acute salmonellosis (Chen et al., 2012; De Jong et al., 2015). The acidic pH typical of infectious sites disrupts the tetramerization of calprotectin, not only attenuating its capacity to bind Mn2+ but also impairing its growth-inhibiting properties (Menkin, 1956; Rosen and Nolan, 2020). Although calprotectin inhibits Salmonella growth in vitro, its effectiveness in the intestinal lumen is severely limited by Salmonella’s Zn2+ and Mn2+ metal transporters (Liu et al., 2012; De Jong et al., 2015; Diaz-Ochoa et al., 2016).
NRAMP1
The integral membrane protein NRAMP1, which is also known as SLC11A1, transports divalent transition metals such as Fe2+, Mn2+, Co2+ and Mg2+ (Canonne-Hergaux et al., 1999; Forbes and Gros, 2003; Cellier et al., 2007; Cunrath and Bumann, 2019). The expression of NRAMP1 is restricted to lysosomal compartments of monocytes and macrophages, whereas the highly homologous NRAMP2 protein is widely distributed on most cells (Vidal et al., 1995; Gunshin et al., 1997). The expression of NRAMP1 is maximal at late stages in the maturation of phagosomes (Gruenheid et al., 1997). NRAMP1 can import or efflux metals into the phagosome (Atkinson and Barton, 1999; Kuhn et al., 1999; Zwilling et al., 1999; Jabado et al., 2000), although recent structural studies have suggested a strong unidirectional efflux movement under physiological conditions (Bozzi and Gaudet, 2021). The directionality of NRAMP1-mediated ion transport is dependent on pH (Goswami et al., 2001). Although the affinity of human or mouse NRAMP1 to Mn2+ has not been determined, a homologous transporter from Arabidopsis has a Km of 28 nM, (i.e., about 4-fold higher than the affinity of the Salmonella transporters MntH and SitABCD for Mn2+) (Kehres et al., 2000; Kehres et al., 2002b; Cailliatte et al., 2010).
Nutritional immunity imposed by NRAMP1 is a significant defense determinant against Salmonella as vividly illustrated by the high resistance of Sv129S6 or C3H/HeN mice carrying an intact nramp1 locus and the propensity of BALB/c or C57BL/6 mice bearing the mutant allele nramp1G169D to develop severe Salmonella infections (Brown et al., 2013; Wendy P.; Loomis et al., 2014). Recent work argued that NRAMP1 contributes to Salmonella pathogenesis by depriving phagosomes of Mg2+ (Cunrath and Bumann, 2019). However, the latter model appears to be in conflict with the observation that the attenuation of Salmonella bearing mutations in the Mn2+ transport system SitABCD or the Mn2+-dependent SpoT enzyme are contingent on the expression of a functional NRAMP1 (see below). More investigations are needed to definitively identify the metal specificity of NRAMP1 in different tissues and different times in the course of the Salmonella infection.
Mn2+ Import Promotes Salmonella Pathogenesis
Entry of Mn2+ into the periplasmic space is mostly mediated by non-specific porins on the outer membrane, whereas transporters in the cytoplasmic membrane actively influx this divalent metal cation into the bacterial cytoplasm (Figure 1A). MntH, a proton-dependent NRAMP1 homolog, actively imports Mn2+ with a Km of 0.1 μM (Kehres et al., 2000). Salmonella upregulate MntH expression in response to both low Mn2+ concentrations and oxidative stress (Kehres et al., 2002a; Cunrath and Palmer, 2021). MntH mutant Salmonella grow poorly in mouse macrophages, but replicate rather well in mice (Boyer et al., 2002; Zaharik et al., 2004; Diaz-Ochoa et al., 2016). The slight attenuation of mntH deficient Salmonella suggests the existence of redundant transport systems. Genetic analyses revealed the presence of a Mn2+ responsive element in the promoter of the sitABCD operon that is encoded within the Salmonella pathogenicity island-1 gene cluster (Janakiraman and Slauch, 2000; Kehres et al., 2002b). The SitABCD transporter is a typical ABC transporter consisting of a periplasmic-binding protein SitA, an ATP-binding protein SitB and two integral membrane permeases, SitC and SitD. Initially, the SitABCD transporter was thought to function as a Fe2+ transport system, as this locus is regulated by Fur under iron-limiting conditions (Janakiraman and Slauch, 2000; Ikeda et al., 2005). However, metal ion uptake studies have shown that SitABCD mediates influx of Mn2+ with an apparent affinity of 0.1 μM, transporting Fe2+ with 30–100 times lower efficiency (Kehres et al., 2002b). A third transporter with broad cation specificity, ZupT, has also been implicated in Mn2+ transport in Salmonella during nitrosative stress (Yousuf et al., 2020).
FIGURE 1. Manganese transport systems in Salmonella. (A) While the outer membrane is permeable to Mn2+ ions, the inner membrane imports this metal ion via specific and non-specific transporters like MntH, SitABCD and ZupT. A type VI secretion system dependent Mn2+ acquisition mechanism observed in pathogens such as Burkholderia, Vibrio, and Yersinia is proposed. (B) Neighbor-joining tree of MnoT-like proteins identified in Salmonella genome by Pattern Hit Initiated BLAST. (C) Genetic organization of mnTH and sitABCD operons with regulatory elements in the promoter regions. (D) Clustal alignment of Burkholderia MnoT (WP_171466016) and Salmonella YncD (ACY88391.1) proteins by Clustal Omega aligner. The alignment results were extracted and reformatted in MView command line utility. All protein identities were normalized by aligned length and the residues are colored using the default built-in colormap.
Low Mn2+ concentrations activate the expression of MntH and SitABCD (Kehres and Maguire, 2003; Chandrangsu et al., 2017; Bosma et al., 2021). The mntH gene is repressed by both MntR and Fur in response to high Mn2+ and iron replete conditions, respectively (Kehres et al., 2000; Kehres et al., 2002a; Troxell et al., 2011; Powers et al., 2021). Expression of mntH is also induced by peroxide via H2O2-sensing OxyR regulatory protein (Kehres et al., 2002a) (Figure 1C). The persistence of Mn2+-dependent repression of mntH in ΔmntR Salmonella points to the existence of MntR-independent control. Analysis of the mntH 5′ UTR identified an Mn2+-sensing riboswitch that forms a Rho-independent terminator (Shi et al., 2014; Scull et al., 2020) (Figure 1C). The presence of several transcriptional breakpoints suggests dynamic expression of MntH in diverse host niches. MntR, Fur and OxyR elements are also present in the sitABCD promoter (Ikeda et al., 2005). The sitABCD operon does not contain, however, a riboswitch-like sequence at the 5′ UTR. Despite the similarities in transcriptional control and their identical affinity for Mn2+, MntH and SitABCD have specialized functions. MntH primarily transports Mn2+ at acidic pH, whereas SitABCD preferentially works at alkaline pH (Kehres et al., 2002b), suggesting that Salmonella may preferentially utilize MntH or SitABCD at different anatomical locations or times during infection (Ikeda et al., 2005).
mntH mutant Salmonella display little attenuation, whereas sitABCD mutants are attenuated in systemic models of infection (Janakiraman and Slauch, 2000; Boyer et al., 2002; Zaharik et al., 2004). Attenuation of sitABCD mutant Salmonella is contingent on the presence of host NRAMP1 (W. P. Loomis et al., 2014; Zaharik et al., 2004). Additionally, the non-specific transporter ZupT also competes with the host NRAMP1 for Mn2+ metal ions in phagosomes, contributing to Salmonella virulence (Karlinsey et al., 2010). By competing for Mn2+ with host cell calprotectin, MntH and SitABCD Mn2+ transport systems help Salmonella overgrow commensals in the inflamed gut (Diaz-Ochoa et al., 2016). Acquisition of Mn2+ also powers detoxification of ROS produced by inflammatory neutrophils in the gut mucosa (Diaz-Ochoa et al., 2016). The role of MntH and SitABCD may not be limited to extracellular bacteria, as genes encoding these Mn2+ transporters are transcribed in Salmonella residing in the cytosol of epithelial cells, and mntH and sitA Salmonella mutants grow poorly in the cytosol of epithelial cells (Powers et al., 2021). The acquisition of Mn2+ by cytosolic Salmonella may counteract oxidative stress, while facilitating utilization of sugars (Powers et al., 2021).
Salmonella deficient of MntH, SitA and ZupT transporters still acquire trace levels of Mn2+ in vitro, indicating the presence of other import systems (Karlinsey et al., 2010; Yousuf et al., 2020). The search for other modes of Mn2+ import into Salmonella is still underway, and examples from other bacteria may lead to the discovery of novel Mn2+ uptake systems in Salmonella. Burkholderia pseudomallei import Mn2+ via a type VI secretion system (T6SS) and the TonB cell envelope protein (Si et al., 2017; DeShazer, 2019). B. pseudomallei undergoing oxidative stress secrete the Mn2+-binding T6SS effector TseM, and low Mn2+ concentrations induce expression of the Mn2+ specific, TonB-dependent MnoT integral protein (Figure 1A). TseM scavenges extracellular Mn2+ and actively shuttles the metal via MnoT. Salmonella T6SS is activated by oxidative stress and our bioinformatics analysis has revealed a conserved locus in the Salmonella genome with high similarity to Burkholderia MnoT (Figures 1B,D) (Kroger et al., 2013). Additional T6SS substrates with Mn2+-scavenging capacities are still being uncovered, including the TssS micropeptide from Yersinia pseudotuberculosis that chelates Mn2+ and sabotages bacterial clearance by inhibiting STING-mediated innate immune response (Zhu et al., 2021).
Mn2+ Export in Salmonella Pathogenesis
Paradoxically, excessive Mn2+ evokes oxidative stress in E. coli, affecting protein stability, interfering with envelope biogenesis, disrupting iron homeostasis and diminishing both tricarboxylic acid cycle and electron transport chain functions (Kaur et al., 2017). Bacteria excrete excessive Mn2+ using both the LysE superfamily MntP protein, and the cation diffuser facilitator (CDF) family member MntE (Martin et al., 2015). The Xanthomonas MntP homolog has two DUF204 domains that are conserved in Salmonella MntP protein (Li et al., 2011). MntP is regulated at transcriptional and posttranscriptional levels via MntR, mismetallated Fur and a yybP-ykoY riboswitch (Dambach et al., 2015; Bosma et al., 2021). The expression of the small RNA rybA, which encodes the small protein MntS, is repressed by MntR (Waters et al., 2011; Martin et al., 2015). The accumulation of apo-MntR in Mn2+ starving cells activates production of MntS, which represses MntP efflux activity and thus enlarges the intracytoplasmic pool of Mn2+ (Martin et al., 2015). On the other hand, the yybP-ykoY riboswitch directly binds to Mn2+, stabilizing a secondary structure that prevents sequestration of the mntP ribosome-binding site during translation (Dambach et al., 2015). MntP mediates efflux of Mn2+ ions in Salmonella following nitrosative stress (Ouyang et al., 2022).
The second efflux pump MntE is widely distributed in Gram-positive bacteria (Chandrangsu et al., 2017; Lam et al., 2020). Streptococci bearing mutations in mntE harbor excessive intracellular Mn2+ and experience attenuation of virulence (Rosch et al., 2009). Our bioinformatic analysis shows that Salmonella FieF (Yiip) protein belonging to CDF family has around 26%–64% sequence similarity with Streptococcus MntE, although it mediates zinc and iron export (Grass et al., 2005; Huang et al., 2017).
Mn2+ Helps Salmonella Adapt to Oxidative Stress
Salmonella are exposed to ROS generated in the innate host response. Sulfur-containing cysteine and methionine amino acids are primary targets of H2O2 (Bin et al., 2017). In addition, ROS carbonylate arginine, lysine, proline and threonine residues, and oxidize metal prosthetic groups and histidine residues (Ortiz de Orue Lucana et al., 2012; Chang et al., 2020). Salmonella have evolved diverse mechanisms to counter ROS generation, prevent formation of hydroxy radicals, inhibit delivery of ROS into Salmonella-containing vesicles, detoxify and scavenge ROS, or repair the resultant protein and DNA modifications (Buchmeier et al., 1995; De Groote et al., 1997; Vazquez-Torres et al., 2000a; Vazquez-Torres et al., 2000b; Gallois et al., 2001; Vazquez-Torres and Fang, 2001; Waterman and Holden, 2003; Halsey et al., 2004; Aussel et al., 2011; Bogomolnaya et al., 2013; Song et al., 2013; Rhen, 2019; Bogomolnaya et al., 2020; Shome et al., 2020). Of particular interest to this review, Mn2+ protects Salmonella from ROS-mediated cytotoxicity by serving as a cofactor for SOD and KatN enzymes, replacing Fe2+ in the active sites of mononuclear iron-containing enzymes, and acting as a nonproteinaceous antioxidant (Culotta and Daly, 2013; Imlay, 2014; Ighodaro and Akinloye, 2018).
Manganese-Based Detoxification of ROS
Salmonella confronts exogenous ROS generated by either host NADPH oxidase in phagocytes or dual oxidase 2 in epithelial cells (Vazquez-Torres and Fang, 2001; Behnsen et al., 2014). Superoxide anion (O2.-) formed by the vectorial transfer of electrons from flavoproteins and semiquinones to molecular oxygen is also a source of endogenous oxidative stress (Imlay, 2013). SODs and catalases expressed basally scavenge endogenously produced O2•- and H2O2, which accumulate at steady-intracellular concentrations of ∼0.2 and ∼50 nM, respectively (Imlay, 2013). Cytoplasmic membranes are semipermeable to exogenous H2O2, but at neutral pH prevent entry of O2•- (Bienert et al., 2006; Imlay, 2019). However, the HO2• acid conjugate readily reaches the bacterial cytoplasm (Imlay, 2019). Salmonella synthesizes two structurally distinct classes of SOD enzymes that catalyze the disproportionation of O2•- to O2 and H2O2 (Perry et al., 2010; Rhen, 2019). Both Mn and Fe-dependent SODs (SodA and SodB, respectively) are cytoplasmic, whereas Cu,Zn-dependent SodC-I and SodC-II are periplasmic (Tsolis et al., 1995; Canvin et al., 1996; Taylor et al., 2009; Perry et al., 2010; Bismuth et al., 2021). Cu,Zn-SOD protect periplasmic or inner membrane targets from O2•- toxicity, and limit peroxynitrite formation from the reaction of O2•- and nitric oxide (NO•) (De Groote et al., 1997; Gort et al., 1999). Mutants devoid of cytoplasmic Mn-SOD and Fe-SOD are auxotrophic for branched chain amino acids, sulfur-containing amino acids, and aromatic amino acids, and, due to defects in aconitase and fumarase, can only grow on fermentable carbon sources (Carlioz and Touati, 1986; Imlay and Fridovich, 1992). Salmonella lacking Mn-SOD are susceptible to early killing by J774 macrophages but are virulent in an acute mouse model of Salmonella infection, likely reflecting the existence of redundant antioxidant systems (Tsolis et al., 1995). However, a Salmonella strain deficient in Mn-SOD is at a competitive disadvantage in the gut because of the Mn2+ limitation imposed by calprotectin (Diaz-Ochoa et al., 2016). Collectively, these investigations indicate that the role played by Mn-SOD in Salmonella pathogenesis is tissue specific.
Salmonella degrade H2O2 with the aid of the catalase activity of KatG, KatE, and KatN, of which KatN uses Mn2+ as cofactor. H2O2 induces transcription of katG in an OxyR-dependent manner, whereas katE and katN are members of the RpoS regulon (Buchmeier et al., 1995; Ibanez-Ruiz et al., 2000; Seaver and Imlay, 2001; Pardo-Este et al., 2018). Under oxidative stress and Mn2+ deplete conditions, KatN seems to be dispensable for Salmonella growth, likely reflecting redundancy of multiple peroxide degrading enzymes such as the alkyl/thiol hydroperoxide reductases AhpC and TsaA as well as peroxiredoxin Tpx (Hebrard et al., 2009; Horst et al., 2010; Diaz-Ochoa et al., 2016). Independently, H2O2-induced protein damage can be effectively repaired by thioredoxin and glutathione systems (Agbor et al., 2014; Song et al., 2016). The redundancy of antioxidant defenses in Salmonella attest to the tremendous selective pressure this intracellular pathogen faces during the respiratory burst of professional phagocytes.
Cambialistic Enzymes
Because of the high binding affinity and ready availability in anoxic environments of the primitive Earth, Fe2+ was incorporated as cofactor of many primordial metabolic enzymes (Imlay, 2014). However, Fe2+ bound to a polypeptide can reduce H2O2, generating reactive hydroxyl and ferryl radicals in situ (Touati, 2000). This feature predisposes the Feα in [4Fe-4S] clusters of dehydratases and mononuclear Fe2+ to H2O2 attack, and Fe2+-mediated reduction of H2O2 in proximity to DNA inflicts genotoxicity (Winterbourn, 1995; Henle et al., 1999; Park and Imlay, 2003; Anjem and Imlay, 2012). Iron and manganese exist in two interchangeable redox forms, 2+ and 3+. Due to the symmetry of half-filled d5 electron shells, Mn2+ and Fe3+ (3d5) are more thermodynamically stable than Mn3+ (3d4) and Fe2+ (3d6) (Lingappa et al., 2019). The Mn3+/Mn2+ and Fe3+/Fe2+ redox couples have potentials of 1.51 and 0.77 V, respectively. Therefore, Mn2+ is less likely to donate electrons than Fe2+ (Guillemet-Fritsch et al., 2005). It is for this reason that, under most biological conditions, Mn2+ is less reactive than Fe2+ (Nealson and Myers, 1992). The thermodynamic stability of Mn2+, lower reactivity, and identical coordination geometry favor the mismetallation of Fe2+ by Mn2+. Replacement of Fe2+ with Mn2+ prevents oxidative damage of metalloenzymes (Emerson et al., 2008; Puri et al., 2010; Hood and Skaar, 2012). Accordingly, members of the Enterobacteriaceae shift from an iron- to a manganese-centric metabolism following oxidative stress (Anjem et al., 2009; Aguirre and Culotta, 2012). Examples of cambialistic enzymes include Rpe in the pentose phosphate pathway as discussed below. Incorporation of Mn2+ in place of Fe2+ allows metabolic flow during exposure to oxidative stress.
Mn2+-Dependent Nonproteinaceous Antioxidants
Manganese ions render bacteria resistant to oxidative stress, even in the absence of Mn-SOD (Horsburgh et al., 2002). This protection may be mediated by the Mn2+-dependent degradation of O2•- and H2O2 (Archibald and Fridovich, 1981, 1982; Berlett et al., 1990; Yocum and Pecoraro, 1999). Mn2+ reacts with O2•- to form transient MnO2+, which converts to manganous phosphate, H2O2 and H2O (Barnese et al., 2012). In turn, Mn2+ disproportionates H2O2 to H2O and O2 (Stadtman et al., 1990).
Mn2+-Driven Central Metabolism in Salmonella Virulence
Growth of Salmonella in host cells relies on a versatile metabolism. Relevant to this review, Mn2+ impacts glycolysis, reductive TCA and the pentose phosphate pathway in Salmonella sustaining oxidative stress.
Metabolism of Mn2+ in Glycolysis and Reductive TCA During Oxidative Stress
The electron transport chain is a source of ATP and a dominant pathway for balancing NADH/NAD+ redox. The oxidative inhibition of NDH-I NADH dehydrogenase in Salmonella undergoing oxidative stress decreases the energetic and redox outputs of the respiratory chain (Husain et al., 2008; Chakraborty et al., 2020). Thus, Salmonella experiencing oxidative stress favor glycolysis and fermentation (Figure 2A) to rescue ATP homeostasis and to balance redox. Glycolysis and associated fermentation generate ATP via substrate-level phosphorylation, produce intermediates for a variety of biosynthetic pathways, and balance redox (Figure 2A). Glycolysis is indispensable for the successful survival of Salmonella in host cells and is an essential component in resistance of Salmonella to the phagocyte NADPH oxidase (NOX2) (Bowden et al., 2009; Paterson et al., 2009; Götz and Goebel, 2010; Fitzsimmons L. et al., 2018; Chakraborty et al., 2020). Salmonella activate overflow metabolism in macrophages, partially to utilize the glycolytic products 3-phosphoglycerate (3PG) and 2-phosphoglycerate (2PG) as carbon sources (Jiang et al., 2021). Phosphoglycerate mutase (PGM) plays a unique role in controlling the overflow metabolism that mitigates oxidative stress in Salmonella. PGM, the third enzyme in the payoff phase of glycolysis, converts 3PG to 2PG. Many bacteria encode two analogous PGM enzymes with no sequence or structural similarity (Foster et al., 2010; Radin et al., 2019). The dPGM isoform utilizes the cofactor 2,3-bisphosphoglycerate, whereas the iPGM isoform requires Mn2+. While dPGM functions as a dimer or trimer, iPGM is active as a monomer (Foster et al., 2010). These Non-homologous I Sofunctional Enzymes (NISE) evolved independently to undertake the crucial metabolic conversion 3PG and 2PG, and bacteria may have accrued them via lateral gene transfer or non-orthologous gene displacement (Omelchenko et al., 2010). The genome of Salmonella enterica encodes two Mn2+-dependent iPGMs (GpmB and GpmI) and one Mn2+-independent dPGM (GpmA) (Figures 2B,C). The two Mn2+-dependent iPGMs are unique in sequence and structure. Our bioinformatic analysis revealed that Salmonella GpmB, which is structurally similar to Bacillus stearothermophilus phosphatase, PhoE, is conserved among major Enterobacteriaceae members, while two-domain monomer GpmI has around 50% sequence similarity with Staphylococcus aureus orthologue (Figure 2C), suggesting a common evolutionary origin (Figure 2B). Strikingly, Salmonella exposed to ROS produced in inflammation preferentially utilize the Mn2+-independent GpmA isoform over the Mn2+-cofactored GpmB enzyme (Chakraborty et al., 2020). The preferential utilization of the Mn2+-independent GpmA by Salmonella during resistance to NADPH oxidase-mediated host defense may be explained by the high demand for Mn2+ during periods of oxidative stress as hinted by the negative selection of mntH mutants after H2O2 treatment (Chakraborty et al., 2020). In addition to the constraints imposed by Mn2+ limitation, the NOX2-dependent acidification of the cytoplasm of intracellular Salmonella may also explain the preferential utilization of the acid phosphatase family member GpmA over its alkaline GpmB counterpart.
FIGURE 2. Manganese dependent metabolic adaptations in Salmonella. (A) Schematic representation of central metabolites and enzymes involved in glycolysis and TCA cycle. Enzymes in red are Mn2+ dependent. Glycolytic conversion of 3PG to 2PG is catalyzed by GpmA, a Mn2+-independent protein or its non-homologous isofunctional Mn2+-dependent GpmB and GpmI. During oxidative stress induced Mn2+ limitation, Salmonella utilizes the GpmA isoform to synthesise 2PG. The Mn2+-dependent phosphoenolpyruvate carboxylase (Ppc) shunts PEP into the reductive TCA cycle. Ribulose-5-PO4, 3-epimerase (Rpe), which catalyzes the conversion of ribulose-5PO4 to xylulose-5-PO4, is mismetallated during oxidative stress. As a result, Salmonella metabolism shifts into the production of reductive intermediates of the TCA cycle by Ppc and compromised non-oxidative phase of pentose phosphate pathway. (B) Phylogenetic analysis of Salmonella GpmA, B and I enzymes reveal that GpmI is similar to S. aureus GpmI. Differences between sequences are estimated by the scale shown at the bottom of the panel. (C) Clustal alignment of Salmonella GpmA (ACY87394.1), GpmB (ACY91834.1) and GpmI (ACY90848.1) with S. aureus GpmI (WP_001085507). Same scheme as in Figure 1D was followed to represent the alignment.
A knowledge-based and mathematical model of carbon flux in Salmonella revealed the importance of anaplerotic reactions around phosphoenolpyruvate (PEP) to oxaloacetate (OAA) conversion (Thiele et al., 2011; Dandekar et al., 2012). When modeled with glucose as sole C-source, the Mn2+-dependent PEP carboxylase enzyme (Ppc) seemed essential for fluxing glycolytic substrates into the reductive TCA cycle (Matsumura et al., 1999). Salmonella deficient of Ppc is virulent in BALB/c mouse model of infection (Tchawa Yimga et al., 2006). However, the combination of mutations in Ppc, acetate kinase (AckA) and phosphotransacetylase (Pta) results in a dramatic attenuation of Salmonella virulence (Chakraborty et al., 2020). Thus, generation of ATP via substrate-level phosphorylation together with the balancing of redox in the reductive TCA that is facilitated by fluxing PEP to oxaloacetate by the Mn2+-dependent Ppc contribute to Salmonella pathogenesis.
Pentose-Phosphate Pathway
The mononuclear iron in ribulose-5-PO4, 3-epimerase (Rpe) in the pentose-phosphate pathway can be poisoned by submicromolar H2O2 concentrations (Sobota and Imlay, 2011). The inactive form of Rpe, however, can rapidly metallate with Mn2+ ions and revert to its active form (Sobota and Imlay, 2011). Metallation of Rpe with oxidative stress-resistant Mn2+ may allow for carbon flow through the pentose phosphate pathway, thereby generating NADPH reducing power that is needed to maintain antioxidant defenses such as glutathione or thioredoxin reductase (Song et al., 2016).
Mn2+-Based Antinitrosative Defenses
Reactive nitrogen species synthesized by inducible nitric oxide (NO) synthase are bacteriostatic against Salmonella (Vazquez-Torres et al., 2000a; Thiele et al., 2011; Henard and Vázquez-Torres, 2012; Fitzsimmons L. F. et al., 2018). RNS modify biomolecules containing radicals, heme prosthetic groups, mononuclear iron, [Fe-S] clusters or redox active thiols in cysteine residues (Mikkelsen and Wardman, 2003; Forman et al., 2004; Poole, 2005; Husain et al., 2008; Pearce et al., 2009; Crawford et al., 2016; Jones-Carson et al., 2016; Jones-Carson et al., 2020). Salmonella mutants lacking Mn2+ transporters are more sensitive to RNS (Frawley et al., 2018; Yousuf et al., 2020; Ouyang et al., 2022). The intracellular concentrations of Mn2+ increase in Salmonella undergoing nitrosative stress, likely reflecting the upregulation of Mn2+ importers (Richardson et al., 2011; Yousuf et al., 2020). Regulation of Mn2+ transport systems is under the control of the transcription factor DksA (Crawford et al., 2016). Maintaining the homeostasis of intracellular Mn2+ in Salmonella after exposure to NO also involves the MntP and FieF efflux pumps (Ouyang et al., 2022). It remains unknown if these Mn2+ efflux systems contribute to the antinitrosative defenses of Salmonella.
Transient drops in intracellular amino acids during NO stress induce RelA-catalyzed synthesis of the (p)ppGpp alarmone, and the hydrolytic activity of SpoT is essential for reestablishing ppGpp homeostasis (Richardson et al., 2011; Fitzsimmons L. F. et al., 2018). A Mn2+ ion is coordinated by at least two carboxylates from aspartate and glutamate residues in the hydrolase domain of SpoT (Hogg et al., 2004). Histidine along with H2O molecules coordinate the rest of the four electrons of Mn2+. Studies in E. coli and Streptococcus revealed that ppGpp hydrolysis is strictly dependent on Mn2+ ions (Heinemeyer et al., 1978; Mechold et al., 1996). The nucleotidyltransferase domain (cd05399) of SpoT has a metal binding region dominated by aspartate and glutamate residues. Interestingly, the aspartate and glutamic acid residues of CD05399 are conserved in the synthetase domain rather than the hydrolase domain of SpoT, raising the possibility that Mn2+ may catalyze ppGpp synthesis rather than hydrolysis in Salmonella’s SpoT proteins. However, studies in Streptococcus revealed that intramolecular signal transmission between the two domains in the presence of ppGpp creates an allosteric shift in the synthetase domain, resulting in coordination of Mn2+ by an additional aspartate (Hogg et al., 2004). The additional coordination suppresses synthetase enzymatic activity. Interestingly, intracellular Salmonella lacking the non-catalytic regulatory C-terminal domain of SpoT (i.e., SpoT-ΔCTD) transcribe abnormally low levels of the Mn2+ importer SitABCD in macrophages (Fitzsimmons et al., 2020). SpoT-ΔCTD-expressing Salmonella are attenuated in NRAMP1+ C3H/HeN mice but not in NRAMP1- C57BL/6 mice, suggesting that the SpoT-dependent regulation of SitABCD combats the Mn2+ restrictions associated with a functional NRAMP1 transporter (Fitzsimmons et al., 2020).
Conclusion
Mn2+ homeostasis plays a poorly understood, but vital role in Salmonella pathogenesis. The elaborate transcriptional and posttranscriptional regulation of expression of diverse Mn2+ uptake and efflux systems help Salmonella navigate different metal-restricted anatomical sites in the vertebrate host. Historically, Mn2+ has been recognized as a cofactor of critical antioxidant defenses of Salmonella. Mn2+-dependent SOD protects Salmonella from oxidative stress; a function for Mn2+-dependent catalase in Salmonella virulence remains to be determined. Recent investigations have revealed the intricate relations between Mn2+ homeostasis, central metabolism, and antioxidant defenses of Salmonella. Salmonella rely on Mn2+ independent glycolysis during their adaptations to oxidative killing, but use Mn2+ to power anapleurotic pentose phosphate pathway reactions involved in redox balance necessary for central metabolism and synthesis of reductive power that fuels classical antioxidant defenses, such as glutathione reductase. Many unanswered questions still exist about the involvement of Mn2+ in the adaptations that promote Salmonella pathogenesis, providing a myriad of opportunities for future research.
Author Contributions
SRU and AV-T conceived the structure of this review and wrote the manuscript. SRU elaborated figures. All authors revised the manuscript and approved the final version.
Funding
These studies were supported by a VA Merit Grant BX0002073, and NIH grants R01AI54959 and R01AI136520.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s Note
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Keywords: manganese, Salmonella, virulence, mismetallation, carbon metabolism, central metabolism, oxidative stress, nitrosative stress
Citation: Uppalapati SR and Vazquez-Torres A (2022) Manganese Utilization in Salmonella Pathogenesis: Beyond the Canonical Antioxidant Response. Front. Cell Dev. Biol. 10:924925. doi: 10.3389/fcell.2022.924925
Received: 20 April 2022; Accepted: 22 June 2022;
Published: 12 July 2022.
Edited by:
Mathieu F. Cellier, Université du Québec, CanadaReviewed by:
Erik Thomas Yukl, New Mexico State University, United StatesCélia Valente Romão, Universidade Nova de Lisboa, Portugal
Andrea Battistoni, University of Rome Tor Vergata, Italy
Copyright © 2022 Uppalapati and Vazquez-Torres. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Siva R. Uppalapati, siva.uppalapati@cuanschutz.edu; Andres Vazquez-Torres, andres.vazquez-torres@cuanschutz.edu