|Home | About | Journals | Submit | Contact Us | Français|
Sialic acids are negatively charged nine carbon backbone sugars expressed on mammalian cell surfaces. Sialic acids are part of a larger family of nonulosonic acid (NulO) molecules that includes pseudaminic and legionaminic acids. Microbial expression of sialic acids and other nonulosonic acids has been shown to contribute to host-microbe interactions in a variety of contexts, including participation in colonization, immune subversion, and behaviors such as biofilm formation, autoagglutination and motility. Previous research has suggested that some spirochetes may also express these molecules.
Here we use a combination of molecular tools to investigate the presence of NulO biosynthetic gene clusters among clinical and saprophytic isolates of the genus Leptospira. Polymerase chain reaction and Southern blotting suggested that a variety of leptospires encoded NulO biosynthetic pathways. High performance liquid chromatography and mass spectrometry analyses provided biochemical evidence that di-N-acetylated NulO molecules are expressed at relatively high levels by L. interrogans serovar Lai strain 55601, and at lower levels by L. alexanderi serovar Manhao and L. fainei serovar Hurstbridge. Endogenous expression of N-acetylneuraminic acid (Neu5Ac, the most common sialic acid) was documented in L. interrogans serovar Copenhageni strain L1-130. Neu5Ac biosynthesis is also supported by a unique gene fusion event resulting in an enzyme with an N-terminal N-acetylneuraminic acid synthase domain and a C-terminal phosphatase domain. This gene fusion suggests that L. interrogans uses a Neu5Ac biosynthetic pathway more similar to animals than to other bacteria. Analysis of the composition and phylogeny of putative NulO biosynthetic gene clusters in L. interrogans serovar Lai and serovar Copenhageni revealed that both strains have complete biosynthetic pathways for legionamimic acid synthesis, a molecule with the same stereochemistry as sialic acid. Lectin-based affinity purification of NulO-modified molecules, followed by mass spectrometric identification suggests post-translational modification of surface lipoproteins, including Loa22.
Leptospira species encode NulO biosynthetic pathways and synthesize multiple NulO molecules including sialic acid. Additional studies are needed to clarify the exact context and functional significance of NulO expression. These findings have implications for immune evasion during systemic leptospirosis.
Leptospirosis, the most common zoonotic illness affecting humans, is caused by spirochetes of the genus Leptospira[1,2]. Some Leptospira species live exclusively in water or soil, while others cycle between environmental and mammalian reservoirs. Leptospira can colonize/infect renal tubules of a wide variety of wild and domesticated mammals. Human disease follows exposure to water or soil contaminated with urine of infected animals. Leptospirosis can be asymptomatic, or manifest as a mild flu-like illness. In another subset of individuals (5-10% of patients) Leptospira can produce more serious systemic infections resulting in pulmonary hemorrhage, jaundice, renal failure, refractory shock, myocarditis, and/or aseptic meningitis.
Despite its medical importance, few virulence determinants of pathogenic Leptospira have been characterized in any detail. Investigation of the organism is hampered by its fastidiousness, slow growth in culture and the lack of available genetic tools. To date, only Omp-A like lipoprotein Loa22 has been demonstrated to be necessary for virulence, appearing to be cytotoxic and capable of inducing apoptosis. [3-5] LipL32, a major outer membrane protein of pathogenic Leptospira, is expressed in vivo and, although it has been shown to bind to host extra-cellular membrane, LipL32 does not seem to be required for acute or chronic infection in vivo in animal models. [6,7] Other potential virulence leptospiral factors include LigA and LigB that contain immunoglobulin-like repeats associated with adhesion to host cells in other gram-negative bacteria. Other proteins shown to have laminin binding activity in-vitro include LenA/LfhA/Lsf24 and related proteins LenBCDEF. LenA seems to also bind factor H of complement, so it might have more than one role in virulence. [8,9]. Leptospiral LPS, although not characterized in detail, has some unique characteristics which could explain why it is poorly recognized by the TLR4- MD2 complex. This diminished recognition could contribute to leptospiral survival in the bloodstream and dissemination. Other potential virulence factors for which more evidence remains to be published include mediators of motility and chemotaxis, including chemotaxis towards hemoglobin .
Sialic acids are a diverse family of acidic nine-carbon backbone (nonulosonic) monosaccharides found in abundance on the surfaces of mammalian cells and are sometimes expressed by microbial pathogens. The most common sialic acid in nature is N-acetylneuraminic acid (Neu5Ac). Expression of Neu5Ac by pathogenic bacteria has been linked mechanistically to complement and neutrophil evasion in disseminated infections with Streptococcus and Neisseria and with the induction of autoimmune neuropathy following infection with Campylobacter. Sialic acids are part of an even wider family of di-N-acetylated nonulosonic acid (NulO) sugars, which also includes pseudaminic and legionaminic acids. Legionaminic acid was first described as part of the Legionella lipopolysaccharide O-antigen , which is thought to have roles in environmental and host associations . Legionaminic and pseudaminic acids are also found as post-translational modifications of flagellin, best studied in Campylobacter and Helicobacter[13,14]. Even further, recent data suggest that in Helicobacter proteins other than flagellins may also undergo glycosylation . Our recent genomic and phylogenetic analyses indicated the presence of NulO biosynthetic gene clusters in the available genomes of L. interrogans. In this study, we sought to investigate the presence of NulO biosynthetic gene clusters in other Leptospira species and to determine whether these genes produced functional biosynthetic pathways. Here we define the presence of putative nonulosonic acid biosynthetic gene clusters in a variety of Leptospira species. Further biochemical investigations show that some Leptospira are capable of endogenous synthesis of nonulosonic acids, including sialic acids.
The genome sequences of L. interrogans serovar Copenhageni strain L1-130 and L. interrogans serovar Lai strain 55601 contain genes predicted to synthesize sialic acids or related molecules (Figure (Figure1A).1A). Using PCR and Southern blotting, we evaluated the presence of this gene cluster in other isolates of Leptospira, including pathogenic, saprophytic, and intermediate strains. Polymerase chain reactions using primers designed from the genome strains amplified genes in the pathogenic strains L. interrogans serovar Copenhageni and Lai but not in the saprophyte L. biflexa (Figure (Figure11B). Interestingly, one of the intermediate strains, L. licerasiae, gave a negative result, while the other, L. fainei, gave a faint positive. Control reactions using primers designed from 16S rRNA gene showed amplification in all the samples, verifying DNA integrity. A probe based on the neuA2 gene of L. interrogans was used for southern blotting of genomic DNA from a number of Leptospira reference strains and isolates. These experiments confirm and extend the PCR data. Of particular interest is a pair of wild rodent isolates of Leptospira in lanes 6 and 7 (MMD4847 identifies as L. licerasiae and MMD3731 identified as L. interrogans serovar Copenhageni). Whereas the intermediately pathogenic L. licerasiae strain did not give a positive result, the pathogenic serovar Copenhageni isolate gave a strong positive band. Also, the intermediate strain L. fainei gave a positive result in southern blotting, further confirming the faint positive result observed by PCR for this strain. Since low sequence identity between primers or probes and the target sequences from less closely related species could produce a negative result in these experiments, other more functional assays were utilized next.
Strains were evaluated biochemically to determine whether nonulosonic acid biosynthetic pathways were functional in different species and strains of Leptospira. Bacteria were hydrolyzed with mild acetic acid to release nonulosonic acid species, and low molecular weight fractions were fluorescently derivatized with 1,2-diamino-4,5-methylene dioxybenzene (DMB), a molecule that specifically reacts with alpha keto acids, including NulOs. DMB-derivatized reaction products were separated by high performance liquid chromatography (HPLC) with a tandem electrospray ionization mass spectrometer. As expected by the Gram-negative-like structure of Leptospira, all samples displayed an early-eluting HPLC peak corresponding to the retention time and mass of 2-keto-3-deoxy-D-manno-octulosonic acid (Kdo). Kdo is an 8-carbon α-keto acid present in the core region of lipopolysaccharide in most Gram-negative bacteria. It serves as an internal positive control in these assays (Figure (Figure22 peak b, m/z 355) and allowed comparison between different HPLC runs. Masses of some DMB-derivatized peaks did not readily correspond to masses of known varieties of nonulosonic acids (for example Figure Figure22 peak a, 407 and peak d, 440). It is not known whether these masses represent nonulosonic acids. In contrast, a consistent m/z of 433 (peak c) indicates the presence of di-N-acetylated nonulosonic acids and was found in pathogenic L. interrogans serovar Lai and L. alexanderi, and intermediate strain L. fainei. In all cases, the DMB-derivatized di-N-acetylated masses were accompanied with characteristic masses corresponding to the hydrated and hydrated sodium salt (m/z 451 and 473 respectively). These biochemical data show that pathogenic and intermediately pathogenic strains of Leptospira are capable of expressing di-N-acetylated nonulosonic acids. However, in contrast, the pathogenic strain L. santarosai was not found to synthesize identifiable nonulosonic acid species at detectable levels (Figure (Figure2).2). We also performed analyses on L. biflexa serovar Patoc. In this case, we observed the presence of Kdo by HPLC and mass spectrometry, but identifiable NulO molecules were not present at detectable levels (not shown).
Interestingly, HPLC analysis of the two different genome strains of L. interrogans (serovar Copenhageni strain L1-130 and serovar Lai strain 56601) gave distinct results. While L. interrogans serovar Lai expresses di-N-acetylated nonulosonic acid (Figure (Figure2,2, m/z 433), strain L1-130 (serovar Copenhagenii) exhibited a peak with mass and retention time consistent with Neu5Ac (m/z 408, hydrated 426, and hydrated sodium salt 448) (Figure (Figure3A-B).3A-B). Additional MS2 analysis consistently reduced this trio of masses almost exclusively to the parent mass of 408 (Figure (Figure3B),3B), as expected based on the behavior of standard Neu5Ac derivatized in parallel (Figure (Figure3C).3C). Since the common animal sialic acids Neu5Ac and Neu5Gc were found in the standard culture media used for Leptospira (EMJH, Figure Figure4A),4A), experiments were designed to exclude the possibility that L. interrogans strain L1-130 may incorporate exogenous sialic acid from the culture media. Unfortunately, the lack of a readily available genetic system for Leptospira rules out gene deletion as an approach to demonstrate endogenous synthesis. However, leptospires grown in defined serum-free media without sialic acids (as confirmed by HPLC) still produced a Neu5Ac peak, confirming that L. interrogans strain L1-130 synthesizes Neu5Ac and this sugar is not acquired from growth media (Figure (Figure44B).
Next we performed analysis of the composition and phylogeny of the putative NulO biosynthetic gene clusters and the enzymes they encode in L. interrogans serovars Lai (strain 56601) and Copenhageni (strain L1-130). Consistent with the biochemical analysis of L. interrogans, genomic analysis of the NulO gene cluster reveals that the organism encodes a complete pathway for di-N-acetylated nonulosonic acid biosynthesis (see Table Table11 in comparison with Figure Figure5).5). There are multiple distinct open reading frames encoding synthesis of aminotransferases, NulO synthases, and CMP-NulO synthetases (see Table Table11 and Figure Figure5),5), suggesting that L. interrogans may express multiple nonulosonic acid species, a conclusion supported by our biochemical investigations (Figure (Figure22 and Figure Figure33).
Phylogenetic comparisons were performed to provide additional insights into the potential functions of Leptospira nonulosonic acid biosynthesis enzymes. We included in the phylogenetic analysis the well-characterized enzymes of Campylobacter jejuni that participate in parallel pathways of legionamimic, pseudaminic, and neuraminic acid synthesis [14,17-21]. A schematic of these biosynthetic pathways is shown in Figure Figure5,5, noting the structural differences between neuraminic (sialic), legionamimic, and pseudaminic acids. These different NulOs are used by C. jejuni to modify a variety of different surface structures including the O-antigen of lipooligosaccharides, flagellin, and other surface proteins. To add further resolution to our phylogenetic analysis, we also included NulO biosynthetic enzymes from two Photobacterium profundum genome strains (3TCK and SS9), previously demonstrated to synthesize legionamimic and pseudaminic acids respectively . In addition, homologous enzymes from other Leptospira genomes (L. noguchii str. 2006001870, L. biflexa serovar Patoc, L. santarosai str. 2000030832, L. borgpetersenii serovar Hardjo-bovis str. L550) were included in the phylogenetic analysis to better place the L. interrogans NulO enzymes into context with other putative leptospiral NulO biosynthetic enzymes.
The phylogenetic analysis of L. interrogans NulO biosynthetic enzymes demonstrates that a subset of these enzymes is more closely related to the C. jejuni legionaminic acid biosynthetic enzymes and more distantly related to the pseudaminic acid biosynthetic enzymes (Figure (Figure6).6). Specifically, the aminotransferases YP_002110 and NP_711788 and the NulO synthetases YP_002108 and NP_711790 in L. interrogans serovars Copenhageni and Lai respectively, are more closely related to legionaminic acid synthesis enzymes and more distantly related to C. jejuni and P. profundum pseudaminic acid synthesis enzymes (Figure (Figure6A-B,6A-B, note green and pink shading indicates legionaminic acid pseudaminic acid pathways respectively). A similar relationship was found for the predicted epimerase/NDP-sugar hydrolases YP_002107 and NP_711791(not shown). Moreover, we find that both homologs of the putative CMP-NulO synthetases in L. interrogans (YP_002102 and YP_002112 in L1-130 and NP_711786 and NP_711796 in 56601) are more closely related to legionaminic acid and neuraminic acid synthetases than to CMP-pseudaminic acid synthetases (Figure (Figure6C).6C). Note in this figure that CMP-Kdo synthases were included to provide contrast and distinguish between enzymes that likely participate in CMP activation of eight carbon sugars (i.e. Kdo) and nine carbon sugars (i.e. NulOs). The sequences retrieved by BLAST of these Leptospira genomes, together with their phylogeny, suggest that a number of leptospires do not encode homologs of CMP-NulO synthetases. In contrast, some leptospires encode putative NulO biosynthesis enzymes that are more closely related to the C. jejuni and P. profundum pseudaminic acid biosynthesis enzymes and more distantly related to the legionaminic acid enzymes (e.g. L. noguchii Figure Figure66A-B).
In contrast to bacterial NulO biosynthetic pathways that synthesize Neu5Ac from ManNAc (N-acetyl mannosamine), the mammalian pathway relies on a NulO synthase with unique specificity for 6-phosphate-modified ManNAc, to generate 9-phosphate-modified Neu5Ac . A set of adapter enzymes precede (kinase) and follow (phosphatase) the NulO synthase in the animal pathway (see Figure Figure7).7). In some cases, ‘adapter’ enzymes have become fused into the same open reading frame with one of the other nonulosonic acid biosynthesis genes. One example is the mammalian UDP-GlcNAc-2-epimerase, which is fused to a kinase that phosphorylates ManNAc to generate the substrate for the next step of the pathway, ManNAc-6-P. Interestingly, when performing analyses of L. interrogans NulO biosynthetic pathway, we noted that one of the NulO synthases encoded by L. interrogans (YP_002104 in serovar Copenhageni and NP_711794 in serovar Lai) has a unique C-terminal domain that is homologous to endonucleases that cleave phosphodiester bonds. By inference, we suggest that the route for N-acetylneuraminic acid biosynthesis in L. interrogans may be very similar to the animal pathway, condensing phosphoenolpyruvate with a phosphorylated 6-carbon intermediate to generate a phosphorylated 9-carbon sugar, followed by dephosphorylation catalyzed by the fused C-terminal phosphatase domain (Figure (Figure7).7). This enzyme is distantly related to other NulO synthases and did not cluster with animal neuraminic acid synthases when these enzymes were included in the analysis (not shown), suggesting that this biosynthetic route may be ancestral. This conclusion is supported by previous evolutionary analyses of NulO pathways .
Finally, efforts were made to identify the type of molecule(s) modified with sialic acids in L. interrogans strain L1-130. Immobilized sialic acid-binding lectins from Sambucus nigra agglutinin (SNA) and Maackia amurensis lectin (MAL), which recognize sialic acids in α2-6 and α2-3-linked sialic acids respectively, were used to affinity purify sialic acid-modified molecules in lysates of the L1-130 strain. Wheat germ agglutinin (WGA) also recognizes sialic acids, but is less specific, and also recognizes N-acetylglucosamine residues. As a control, buffers used in the solid phase assay were analyzed in parallel lanes of the gel, revealing that the faint bands present at ~60kDa were part of the supplied buffers and not specific for sialylated L. interrogans molecules. Silver staining after SDS-Page gel electrophoresis of the eluted material from the affinity columns shows clear bands at ~21kDa and ~25kDa that are present at similar intensities in the MAL and SNA lanes (Figure (Figure8A).8A). Other bands appear to be enriched by affinity purification using one or the other lectin. For example, a faint band at ~43kDa is apparent in the material isolated by MAL, but not by SNA. Alternatively, bands at ~15, ~37, and ~41kDa are much stronger in the SNA-purified sample. These finding suggests that L. interrogans may modify surface structures with both α2-3- and α2-6-linked nonulosonic acids (Figure (Figure8A).8A). However, future studies should further investigate the molecule(s) modified by nonulosonic acids in leptospires, as well as their exact context and importance.
The affinity-purified material was subjected to DMB-derivatization and HPLC analysis, which showed the Neu5Ac peak, but not the Kdo peak (data not shown), strongly suggesting that this material was free of LPS-components. This does not rule-out that LPS may be modified with NulOs, just that LPS was not present in this affinity-purified preparation. We performed mass spectrometry to identify protein components in the affinity-purified material. Three proteins were identified by mass spectrometry (Figure (Figure8B):8B): Loa22, LipL32, and LipL41, all of which have been described in previous publications as surface-exposed lipid-linked outer membrane proteins of L. interrogans[23-27]. Indeed, Loa22 and LipL31 are among the most abundant proteins expressed on the Leptospira cell surface . Loa22 was identified with the highest number of peptide matches. Loa22 is an outer membrane protein encoded within all Leptospira genomes sequenced to date. It has been observed to be upregulated in vivo and it is one of very few leptospiral proteins so far that has been shown to be necessary for virulence . Additional studies are needed to define the precise context of NulO expression on L. interrogans and understand its potential significance in virulence.
Based on a combination of experimentation and in silico genomic analysis, we have demonstrated the function of NulO biosynthetic gene clusters in pathogenic and intermediately pathogenic species of Leptospira, several of which are capable of synthesizing di-N-acetylated NulO species, as well as the true sialic acid, N-acetyneuraminic acid, a finding of considerable consequence for the leptospirosis field. This finding expands the number of important human pathogens that utilize endogenous biosynthetic pathways to elaborate surface structures containing sialic acids and related NulO molecules . Sialic acids have proven roles in complement evasion, intracellular survival, and biofilm formation , and evidence is emerging that some human pathogens with Neu5Ac on their surfaces can engage sialic acid-binding receptors (Siglecs) on leukocyte cell surfaces, resulting in phagocytosis or dampening of bactericidal activities [30-32]. The roles of other NulO molecules such as legionaminic and pseudaminic acids are less well defined, but these molecules have been shown to play roles in behaviors such as autoagglutination, motility, and host colonization [33-37]. Curiously, disease caused by L. interrogans includes bacteremia and meningitis as components of the clinical disease spectrum, similar to the well-characterized Neu5Ac-expressing human bacterial pathogens Group B StreptococcusNeisseria meningitidisE. coli K1, and Haemophilus influenzae. As genetic tools and small animal infection systems for study of Leptospira are further refined, analysis of the contribution of NulO biosynthesis to the virulence of this neglected disease can be further elucidated.
Intermediately pathogenic strains L. licerasiae serovar Varillal strains MMD3731, MMD4847 and CEH008 (isolated from rodents in Peru), L. fainei serovar Hurstbridge strain BUT 6T and the saprophyte L. biflexa serovar Patoc were used for these experiments. Pathogenic Leptospira used in this study included L. interrogans serovar Copenhageni strain L1-130, L. interrogans serovar Lai strain 55601, and L. interrogans serovar Icterohaemorrhagiae wild rodent isolate MMD 3731 that were passaged fewer than 5 times in vitro after re-isolation from hamster liver to maintain virulence. L. santarosai and L. alexanderi serovar Manhao were originally isolated from clinical cases of leptospirosis and now serve as reference laboratory strains. Generally, Leptospira were cultivated at 30°C in Ellinghausen-McCullough-Johnson-Harris (EMJH) medium (catalog #279510, Becton Dickinson, Sparks, Maryland). Chemically-defined, sialic acid-free medium, prepared as previously described and verified by HPLC to be sialic acid free, was used to cultivate Leptospira in experiments where the lack of exogenous sialic acids was a necessary condition .
Primers based on the genome of L. interrogans L1-130 were designed for the detection of genes in the sialic acid cluster as follows: sasfrontF (5′- TCC GGA AAT GCG AAT GAT G-3′), sasfrontR (5′- CAC CGG GCA AAA GAC TAA CCT - 3′), sasendF (5′- CGG ATA TAG CGG ACG ATG TAA - 3′), sasendR (5′- CGC CAA AAA GCC AAG GAA - 3′), neuA2F (5′- TGA AGC GGC AAA AAG AGC - 3′), neuA2R (5′- TGA AAT AAC ATG CCG ACA AAT A - 3′), neuCfrontF (5′- CGC TAC GGG AAT GCA TCT GTC TC - 3′), neuCfrontR (5′- CCC ATT CCC CCA ACC AAA AA - 3′), neuCendF (5′- GGC GAG GAT CCT TCT AAT GTT TTT - 3′) and neuCendR (5′- ACT CGC TCC GCC TTC ACC A - 3′). PCR reactions were prepared using 0.2mM of each primer in a 20 μL reaction with DNA from the pathogens L. interrogans Lai, L. interrogans L1-130, the intermediates L. licerasiae and L. fainei and the saprophyte L. biflexa serovar Patoc. NeuA2 and neuBfront reactions used an annealing temperature of 52°C. NeuCfront, neuCend, sasfront and sasend were run using an annealing temperature of 58°C. A 16S gene PCR reaction using previously published primers fLIP and rLIP1 was used as a control for integrity of DNA.
Genomic DNA samples of Salmonella enterica, L. interrogans serovar Lai str. 56601, L. interrogans serovar Copenhageni str. L1-130, L. biflexa serovar Patoc, L. licerasiae strains CEH008 and MMD4847, L. interrogans serovar Icterohaemorrhagiae str.MMD3731 and L. fainei serovar Hurstbridge were prepared into plugs using 1% agarose and 0.5x TBE. These were subjected to depurination and denaturing conditions. DNA was then transferred to a positively charged membrane via overnight capillary transfer with 20x SSC. Finally the DNA was cross-linked to the membrane using short wave DNA for 15min. 10mL of pre-hybridization solution (QuikHyb, Stratagene) were warmed to 40°C prior to hybridization. Hybridization was done overnight at 40-42°C using the same solution and adding 10mL of DIG-labeled PCR product of primer neuA2F (5′ - TGA AGC GGC AAA AAG AGC - 3′) and neuA2R (5 ′- TGA AAT AAC ATG CCG ACA AAT A - 3′). 2xSSC at room temperature and 1x SSC at 68°C were used for stringency washes. A chemiluminescent substrate and an alkaline phosphatase conjugated anti-DIG antibody were used to demonstrate binding of the probe.
Mild (2N) acetic acid hydrolysis was performed to release surface nonulosonic acids from Leptospira. 4N acetic acid was added to an equal volume of extensively washed and resuspended pellets followed by 3h of incubation at 80°C. The resulting soluble fraction was filtered to remove large molecular weight components and derivatized with DMB (1,2-diamino-4,5-methylene dioxybenzene), a reagent that reacts with the α-keto acid portion of nonulosonic acids. Final reaction conditions were 7mM DMB, 18mM sodium hydrosulfite, 1.4M acetic acid, and 0.7 M 2-mercaptoethanol. Derivatization was carried out for 2 hours at 50°C in the dark.
DMB-NulO derivatives were resolved by HPLC using a reverse phase C18 column (Varian) eluted isocratically at a rate of 0.9ml/min over 50 minutes using 85% MQ-water, 7% methanol, 8% acetonitrile as previously described [16,39,40]. In some experiments, HPLC was performed without online mass spectrometry and detection of fluorescently labeled NulO sugars was achieved using an online fluorescence detection using excitation and emission wavelengths of 373nm and 448nm respectively. In other experiments HPLC was combined with online mass spectrometry using a Thermo-Finnigan model LCQ ion trap mass spectrometer system. When mass spectrometry was performed, the mobile phase also included 0.1% formic acid, and online UV detection of DMB-NulO molecules preceded mass spectrometric analysis. We note that similar HPLC-MS analyses have been described previously DMB-derivatized α-keto acids [39-41].
We performed BLAST searches (blastp) against the NCBI genome database using as seeds the sequences of 1) proteins encoded by Campylobacter jejuni pseudaminic, legionaminic, and neuraminic acid biosynthetic pathways or 2) enzymes encoded in the Leptospira interrogans NulO biosynthetic gene cluster (Figure (Figure1A).1A). NCBI accession numbers are provided in Table Table11 and a schematic of the biosynthetic pathways is illustrated in Figure Figure5.5. Complete protein sequences of homologous amino acids were aligned using ClustalW in MacVector 11.1.1 software and alignments were checked manually. The Neighbor Joining (NJ) method was utilized for phylogenetic tree construction using MacVector 11.1.1 software, including 1000 Bootstrap replications to obtain confidence values for branches of the NJ trees.
Whole cell lysates were prepared using three cycles of freeze-thawing of PBS washed L. interrogans serovar Copenhageni strain L1-130. In order to probe the abundance and nature of the sialylated molecules on L. interrogans, these lysates were fractionated using a lectin-based solid phase assay (Q Proteome Sialic Acid kit, Qiagen) using three immobilized sialic acid binding lectins: wheat germ agglutinin (WGA), Sambucus nigra agglutinin (SNA), and Maackia amurensis lectin (MAL), according to manufacturer’s instructions. Molecules captured by each of these lectins were eluted according to the manufacturers instructions. then analyzed by SDS-PAGE followed by silver staining (SilverQuest Silver Staining Kit, Invitrogen).
To determine whether L. interrogans uses nonulosonic acids for post-translational modification of proteins, pooled affinity-purified material from above mentioned experiment was subjected to denaturation, reduction, and alkylation, followed by trypsin digestion and MS/MS analysis using a nano-flow LC- tandem mass spectrometer. Peptide mass fingerprints identified in the affinity-purified material were used to identify L. interrogans proteins by searching against the NCBInr bacterial genome database.
The authors declare that they have no competing interests.
JNR, MAM, JMV and ALL conceived and designed experiments, JNR and ALL acquired data, JNR, MAM and ALL analyzed and interpreted data, JNR and ALL drafted manuscript, JNR, MAM, JMV, and ALL revised manuscript critically for important intellectual content. All authors read and approved the final manuscript.
We thank Ajit Varki and Victor Nizet for valuable advice and Sandra Diaz for technical assistance with HPLC-MS. The Scripps Research Institute’s Center for Mass Spectrometry performed nano-flow MS/MS data and provided results of the NCBInr database search (http://masspec.scripps.edu/). This work was supported in part by U.S. Public Health Service grants from the National Institutes of Health 1D43TW007120 and 1RO1TW05860.