The Glaesserella parasuis phosphoglucomutase is partially required for lipooligosaccharide synthesis

Lipooligosaccharides (LOSs) are virulence determinants of Glaesserella parasuis, a pathogen of the respiratory tract of pigs. We previously reported that disruption of the galU or galE gene in G. parasuis results in increased sensitivity to porcine serum, indicating that the galactose catabolism pathway is required for polysaccharide formation in G. parasuis. Here, we evaluated the role of the HAPS_0849 gene in LOS synthesis. The G. parasuis SC096 HAPS_0849 mutant produced a highly truncated LOS molecule, although a small fraction of intact LOS was still observed, and this mutant was found to be more sensitive to serum than the parental strain. HAPS_0849 was overexpressed and purified for biochemical assays, and this protein exhibited phosphoglucomutase (PGM) activity. Heterologous expression of a pgm gene from Escherichia coli in the HAPS_0849 mutant led to restoration of the wild-type LOS glycoform, further demonstrating the PGM function of HAPS_0849 in G. parasuis. The autoagglutination and biofilm formation ability of this strain were also investigated. Disruption of HAPS_0849 led to an increased tendency to autoagglutinate and form more biofilms, and these enhanced phenotypes were observed in the absence of glucose. In addition, LOSs from HAPS_0849, galU and lgtB mutants had similar truncated glycoforms, while LOSs from the galE and lex-1 mutants exhibited another type of defective LOS pattern. These findings imply that HAPS_0849 may function upstream of GalU in the generation of glucose 1-phosphate. In conclusion, our results preliminarily described the functions of HAPS_0849 in G. parasuis, and this gene was partially required for LOS synthesis.


Introduction
Glaesserella parasuis is a pathogen of the upper respiratory tract of conventional swine herds and the aetiological factor of Glässer's disease, causing fibrinous polyserositis, arthritis, and meningitis. G. parasuis has emerged as one of the major causes of high mortality rates in piglets, resulting in significant economic losses to the swine industry worldwide [1,2]. The complement system is part of the innate immune system and is a first line of defence. The cascade of reactions that follows complement activation can lead to the formation of the membrane attack complex (MAC), resulting in lysis of the pathogen [3]. The complement susceptibility of G. parasuis strains of different clinical origins is highly variable. In general, isolates from the nares of healthy piglets are sensitive to the bactericidal effect of the complement system, while strains from systemic diseases of swine tend to be resistant to serum [4]. In a previous study, the capD gene, encoding a capsular polysaccharide biosynthesis protein, was identified as a virulence-associated factor, indicating that surface polysaccharides may participate in virulence, particularly in the context of serum resistance in G. parasuis [5].
Bacterial polysaccharides (PCs), including capsular polysaccharides (CPSs) and lipooligosaccharides (LOSs), are widespread structures found on the cell surfaces of a broad range of Haemophilus species and have been confirmed as major complement resistance factors in these bacteria [6][7][8][9][10]. Capsules were previously observed in some G. parasuis strains by precipitation with hexadecyl trimethylammonium bromide (CTAB), and the presence of acidic polysaccharides in some types of capsules was observed. However, capsules from other strains did not coprecipitate with CTAB, suggesting that the compositions of these capsules may be quite different or that CPS is not synthesized by these strains [11]. This finding may be attributed to the genetic diversity of the capsular biosynthetic locus in strains of different serotypes [12]. Furthermore, three heptosyltransferase genes (opsX, rfaF, and waaQ) are required for lipooligosaccharide (LOS) synthesis. Disruption of these genes resulted in serumsensitive mutants, indicating that LOSs are also needed for virulence of G. parasuis [13].
The biosynthesis of surface polysaccharides is closely related to carbohydrate metabolism in pathogens [14][15][16]. In our previous study, two galactose metabolismrelevant genes, denoted galU and galE, were found to affect virulence and biofilm formation in G. parasuis SC096 [17]. The metabolism of galactose may affect the synthesis of CPS or LOS, as galU and galE mutants are notably more sensitive to killing by porcine serum than their parent strain. As shown in Figure 1, exogenous glucose or amino acids can be converted to glucose 1-phosphate (G1P) by glycolysis then converted to uridine diphosphate glucose (UDP-glucose) by UDPglucose pyrophosphorylase (GalU) and further converted to UDP-galactose by UDP-glucose-4-epimerase (GalE). These monosaccharide derivatives can then be utilized for the synthesis of various polysaccharides by glycosyltransferases, such as lgtB and lex-1, as described in our previous study [18]. To date, the genome sequences of many G. parasuis strains have been determined [19][20][21][22], and several virulence factors involved in the evasion of immune responses have been identified [5,13,17,[23][24][25]. However, the correlation between UDP-sugars biosynthesis and virulence has yet to be further investigated. The gene HAPS_0849 (NCBI accession no. ACL32480.1) in the sequenced strain SH0165 is annotated as encoding phospho-sugar mutase. This mutase may be an upper-pathway enzyme involved in the generation of G1P, which is further used for LOS synthesis by GalU as described above (Figure 1). The phosphohexomutase family includes several homologous enzymes that catalyse the reversible conversion of 1-phospho-sugar substrates to 6-phospho-sugar substrates. The proteins in this superfamily play important roles in carbon source metabolism in bacteria. At least three related proteins constitute the majority of this superfamily: the highly specific phosphoglucomutase (PGM) protein, which uses only glucose as a substrate, the mannose specific phosphomannomutase (PMM) protein, and the less specific PMM/PGM protein, a bifunctional protein that can use either mannose or glucose [26]. HAPS_0849 is homologous to the gene pgmB, which is predicted to encode a PGM and is involved in LOS synthesis in Haemophilus influenzae [27]. However, the biochemical functions of these genes in Haemophilus species are still unclear. Importantly, the correlation between PGM and the source of G1P mentioned above, as well as the roles of PGM in G. parasuis, remain poorly understood. Surface polysaccharides of G. parasuis are important virulence factors and key antigens for vaccine development. The pathway pgm-galU-galE may be a key node for these polysaccharides biosynthesis based on our studies although it is yet to be investigated further. How these polysaccharides synthesis affected by metabolism, and how to improve the yield of these key antigens? Understanding of G. parasuis pgm may provide some hints to answer these questions.
In the present study, we identified the gene HAPS_0849, encoding a PGM, as a virulence factor in G. parasuis. Phenotypes of its mutant affected by concentration of glucose are different from that of other reported LOS mutants in G. parasuis, and interestingly the HAPS_0849 gene is partially required for lipooligosaccharide synthesis. To our best knowledge, it may be the first report to show these findings in Pasteurellaceae species and even in other bacteria. We have attempted to explain the relevance between PGM and polysaccharide synthesis in G. parasuis and pinpoint the molecular basis of this link.

Bacterial strains, plasmids, and growth conditions
The bacterial strains and plasmids used in this study are listed in Additional files 1 and 2. Escherichia coli strains were routinely grown in Luria-Bertani (LB) broth or on LB agar plates at 37 °C. G. parasuis strains were cultured on trypticase soy agar (TSA) or trypticase soy broth (TSB) with or without dextrose (BD Biosciences, USA) and supplemented with 0.005% nicotinamide adenine dinucleotide (NAD) (Sigma Aldrich, USA) and 5% inactivated bovine serum at 37 °C in 5% CO 2 as previously described [17]. When required, the media were supplemented with kanamycin (30 µg/mL) or gentamicin (30 µg/mL).

Molecular biology methods
Plasmid isolation was performed using the QIAprep Spin Miniprep Kit (Qiagen, Germany). Restriction enzymes were purchased from New England BioLabs Inc. T4 DNA ligase, Taq polymerase and high-fidelity DNA polymerase were purchased from Takara Bio Inc., Japan. Restriction enzyme digestion, ligation, and transformation of E. coli were performed using standard methods. Genomic DNA was extracted with the E.Z.N.A. Bacterial Genomic DNA Kit (Omega Bio-Tek, USA). PCRs were used to produce DNA fragments and evaluate mutants.

Construction of plasmids and strains
The primers used in this study are listed in Additional file 3. Mutants were constructed as previously described [17] with some modification. To mutate the G. parasuis HAPS_0849 gene, regions of homology flanking the HAPS_0849 locus were amplified by PCR using SC096 genomic DNA as a template. The upstream region was amplified using primers P1 and P2, while the downstream fragment was amplified using primers P3 and P4. The KanR gene was amplified from the plasmid template pK18mobsacB with primers P11 and P12, and these three fragments were joined by overlap PCR with the primer pair P1 and P4. This PCR product was then cloned into pMD19-T (Takara Bio Inc., Japan) to generate pSF251. The constructed plasmid was then used for natural transformation, and the HAPS_0849 mutant was generated with the method described previously [23]. Briefly, bacteria were cultivated overnight at 37 °C on TSA plates and then washed and resuspended in TSB supplemented with newborn calf serum and NAD at 5 × 10 9 CFU/mL. A 20-µL bacterial suspension was pipetted onto TSA supplemented with inactivated serum and coenzyme and spread onto a small area. One microgram of the plasmid DNA was then added and mixed, followed by cultivation for 5 h at 37 °C. Cultures were scraped off and plated on TSA with 30 µg/mL kanamycin and then incubated at 37 °C for 2 days. Positive clones were evaluated by PCR and sequencing. The wclP and wcaJ mutant strains were constructed by a similar method with the primers P5-P8 and P33-P36 listed in Additional file 3.
Complemented strains were constructed using the method published previously [28] with some modifications. Intact HAPS_0849 was amplified with primers P13 and P14. This PCR fragment was digested with SalI and SphI, subjected to agarose gel electrophoresis followed by purification with the QIAquick Gel Extraction Kit (Qiagen, Germany), and ligated into pSF116, a complementation vector for inserting target genes between ompP5 and msrB, to generate pSF254. This recombinant plasmid was transformed into the HAPS_0849 mutant by natural transformation, and selection of the complemented G. parasuis ΔHAPS_0849 strain (SF415) was accomplished using TSA containing gentamycin. Transformants were confirmed by PCR and sequencing using primers P5 and P10. The ΔwclP and ΔwcaJ complemented strains (SF416 and SF417, respectively) were constructed using a similar method as that described above with the corresponding primers (Additional file 3).
The ΔHAPS_0849 strain expressing E. coli pgm was constructed as follows: the pgm gene fragment was amplified from E. coli MG1655 genomic DNA by PCR with primers P19 and P20. After purification and digestion with SalI and SphI, Ecpgm was ligated into pSF116 to create pSF257. This plasmid was then transformed into the ΔHAPS_0849 strain by natural transformation and selected using gentamicin (Gm). Positive clones were confirmed by PCR amplification and sequencing using primers P5 and P10.
To construct the G. parasuis strain overexpressing HAPS_0849, complete open reading frame of HAPS_0849 was amplified by PCR using the primer pair P39 and P40. After gel extraction, the PCR product and pET28(a) vector were digested with NdeI and HindIII, gel purified, and ligated together to corresponding sites using DNA ligase, generating the expression plasmid pSF258. The correct recombination was confirmed by PCR and sequencing.

Overexpression and purification of G. parasuis HAPS_0849
pET28-HAPS_0849 was transformed into E. coli BL21 (DE3) for overexpression. A single colony was selected and cultured in a flask overnight and then used to inoculate 200 mL of LB broth supplemented with kanamycin at a concentration of 50 µg/mL. The cells were cultivated at 37 °C, and then isopropyl-β-d-thiogalactoside (IPTG) was added at a concentration of 1 mM when the absorbance OD 600 reached 0.8. The induced cells were incubated for another 4 h and then centrifuged to obtain a bacterial pellet. Next, the cells were resuspended in 1/5 volume of lysis buffer (50 mM NaH 2 PO 4 , 300 mM NaCl, 10 mM imidazole, pH 8.0) and lysed by ultrasonic treatment for 20 min. Supernatants were collected after centrifugation at 13,400 × g for 10 min, and then the lysate was filtered with a 0.22 µm Millipore polyethersulfone filter. Nickelnitrilotriacetic acid (Ni-NTA) matrices (GE Healthcare) were used for protein purification. The Ni-NTA column was preequilibrated with ten volumes of lysis buffer, and then the samples were loaded onto the column by gravity. After washing with ten volumes of washing buffer (50 mM NaH 2 PO 4 , 300 mM NaCl, 20 mM imidazole, pH 8.0), target proteins were then eluted with 2 mL of elution buffer (50 mM NaH 2 PO 4 , 300 mM NaCl, 500 mM imidazole, pH 8.0) in 4 fractions. The purified proteins were analysed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). The fractions with pure protein were pooled and dialyzed against dialysis buffer (lysis buffer without imidazole). The protein concentrations were determined with a Quick Start Bradford Protein Assay kit (Biorad, USA) and then diluted to 1 mg/mL with dialysis buffer for further enzyme activity analysis.

Phosphoglucomutase activity assay
The activity of HAPS_0849 was confirmed with a Glucose-6-Phosphate Assay Kit (Sigma, MAK014) according to the manufacturer's manual, with some modifications. Briefly, 10 µL of 1 mM G1P was added to a 96-well plate, and then G6P assay buffer was added to each well to bring the volume to 50 µL. Another 50-µL reaction mix containing 45 µL of G6P Assay Buffer, 2 µL of G6P Enzyme Mix, 2 µL of G6P Substrate Mix and 1 µL of protein sample or phosphate buffered saline (PBS) as a negative control was prepared. Next, 50 µL of the reaction mix was added to 50 µL of the 1 mM G1P solution described above and mixed well by pipetting. The reaction was incubated for 30 min at room temperature, and then the absorbance was measured at 450 nm (A450). To eliminate the effect of background NADH or NADPH, a blank sample was prepared for each sample by omitting the glucose-6-phosphate enzyme mix. The blank readings were subtracted from the sample readings. Activity was calculated as U (units) of sample after 30 min; A b , A450 of sample without G6P enzyme mix as a blank; T 1 , time reaction was stopped; T 0 , time reaction began; df, dilution factor of protein). Phosphoglucomutase from rabbit muscle (Sigma Aldrich, USA) was used as positive control.

Autoagglutination assay
The ability of G. parasuis strains to autoagglutinate was tested by a modified method as previously reported [17]. Briefly, G. parasuis strains were cultured overnight in 100 mL of TSB broth with or without glucose and supplemented with 0.005% NAD and 5% inactivated serum and diluted to an optical density at 600 nm of one. The bacterial cultures were then transferred to 15 mL tubes and allowed to remain static at room temperature. The turbidity of the culture was determined every 60 min for 12 h.

Biofilm formation assay
The biofilm formation test was performed as previously reported with some modifications [29,30]. Briefly, 20 µL of overnight culture of the wild-type strain and its mutants were inoculated into 2 mL of fresh TSB broth containing NAD and inactivated serum with or without glucose in 6-well plates, and then incubated for 24 h or 72 h at 37 °C. Supernatants were removed by pipetting; then, biofilms were rinsed with sterile distilled water and stained with 0.1% crystal violet for 30 min. Afterwards, excess staining was gently washed off with dH 2 O, and the biofilms were dried. Bound crystal violet was dissolved in 1 mL of 33% (v/v) acetic acid, and 200 µL of solution was transferred to a 96-well microtiter plate. Then, the optical density was measured at 600 nm. All experiments were performed independently three times.

Serum sensitivity assay
The serum bactericidal assay was carried out as previously described with 50% porcine serum, which was also obtained from a previous study [17]. Serum inactivated at 56 °C for 30 min was used as a control in all experiments. The wild-type strain and mutants were cultured to midlogarithmic phase, and then, 100 μL of porcine serum or inactivated serum was added to 100 μL of a bacterial dilution (10 8 CFU), followed by incubation at 37 °C for 1 h. The bacterial cells were then serially diluted tenfold and plated on TSA plates supplemented with serum and NAD. The plates were cultivated at 37 °C in an atmosphere containing 5% CO 2 for 48 h. The survival percentage was determined according to the ratio of bacterial colonies in natural serum to those in heat-inactivated serum. All strains were tested in at least three independent experiments.

Preparation of LOSs and electrophoresis
Bacterial polysaccharides were prepared from G. parasuis strains as described previously [18]. Bacterial cells were grown on TSA supplemented with NAD and 5% newborn calf serum (NBS) and washed with PBS, and LOSs were extracted with a concentration of 50% phenol at 70 °C for 15 min. The resulting aqueous phase was dialyzed against distilled water until phenol was removed (molecular weight cutoff, 1000 Da). The samples were separated by 15% SDS-PAGE, and the gels were visualized using silver staining.

Statistical analysis
All experiments were performed at least three times, and the standard deviations were calculated with GraphPad Prism. Student's t-test was used to evaluate the significance of differences. A P-value < 0.05 was considered statistically significant.

Results
The HAPS_0849 mutant has defects in LOS synthesis and is sensitive to serum To investigate the function of HAPS_0849, a kanamycin resistance cassette with flanked regions of this gene was used to disrupt HAPS_0849 on the chromosome of strain SC096, and the generation of the complemented strain is described in "Materials and methods" section (Additional file 4). Our previous studies have shown that the heptosyltransferase genes opsX, rfaF, and waaQ are required for the transfer of heptoses I, II, and III, respectively, in G. parasuis [13], and these heptoses are derived from UDP-glucose, which is generated through the galUE pathway. Therefore, we sought to determine whether HAPS_0849 was involved in lipooligosaccharide synthesis and participated in the generation of UDP-glucose ( Figure 1). The LOSs from the HAPS_0849 mutant, along with the wild-type strain SC096, were visualized by SDS-PAGE and silver staining. Figure 2A shows that SC096 expressed a single LOS band (lane 1), and ΔHAPS_0849 produced two types of LOS glycoforms (lane 2) when these strains were cultured in TSB with 0.25% glucose. The principal LOS glycoform of ΔHAPS_0849 migrated faster than the wild-type LOS, which suggests that the HAPS_0849 mutant synthesized a highly truncated LOS molecule. Notably, ΔHAPS_0849 also partially produced intact LOS, with a banding pattern corresponding to that of the wild-type LOS. However, the proportion of complete LOS was obviously lower when this mutant was cultured in TSB without glucose ( Figure 2B, lane 2). In addition, LOS glycoforms from the complemented HAPS_0849 mutant displayed a migration profile that was consistent with the migration profile of LOS from the wild-type strain (lane 3 in Figures 2A, B).
LOSs and outer membrane proteins have been proposed to play a role in serum resistance in G. parasuis [13,23]. To investigate whether HAPS_0849 also contributes to serum resistance, the sensitivity of ΔHAPS_0849 to 50% swine serum was investigated. The survival rates of wild-type strain SC096, HAPS_0849 mutant and complemented strain were 73.16 ± 4.26%, 0.052 ± 0.046% and 76.68 ± 4.06% respectively. The bactericidal activity of swine serum with the HAPS_0849 mutant was significantly greater than that of the parent strain G. parasuis SC096 (P < 0.01), whereas the serum resistance phenotype was restored in the complemented strain (Figure 3). It should be noted that there was negligible variance in the doubling times between ΔHAPS_0849 and the wild-type strain SC096 (Additional file 5). These results suggest that HAPS_0849 was partially required for LOS synthesis and that the HAPS_0849 mutant was sensitive to the bactericidal effects of porcine serum.

HAPS_0849 encodes a phosphoglucomutase
In order to confirm the biochemical functions of HAPS_0849, we constructed a pET28-HAPS_0849 plasmid and transformed it into E. coli strain BL21 (DE3) for overexpression. After IPTG induction and ultrasonication, the concentration of target protein in the soluble fraction was high. Afterwards, we purified the proteins from the supernatant solution directly with Ni-NTA resin. After affinity chromatography, the HAPS_0849 protein was diluted to the appropriate concentration, analysed by SDS-PAGE ( Figure 4A) and further confirmed by matrix-assisted laser desorption ionization time of flight mass spectrometry (MALDI-TOF MS) analysis (data not shown). For enzyme activity analysis, a modified phosphoglucomutase assay was performed as described in "Materials and methods" section. The purified protein had a significant ability (P < 0.05) to convert glucose 1-phosphate to glucose 6-phosphate generation compared to the negative control ( Figure 4B), indicating that HAPS_0849 may have phosphoglucomutase activity.
The E. coli pgm gene (Ecpgm) encodes phosphoglucomutase, which is specifically essential for the conversion of glucose 6-phosphate to glucose 1-phosphate [31]. To further assess whether G. parasuis HAPS_0849 is a phosphoglucomutase, we constructed an Ecpgm-expressing strain derived from the HAPS_0849 mutant (Additional  file 6). LOSs were extracted and analysed by electrophoresis; as shown in Figure 4C, a principal LOS glycoform from the pgm-expressing strain was disrupted in HAPS_0849 (lane 3), with an apparent molecular weight equivalent to that of the major LOS profile expressed by the wild-type strain (lane 1). Moreover, a small LOS glycoform was mainly observed in ΔHAPS_0849, as predicted (lane 2). Complementation of the HAPS_0849 mutant with the Ecpgm gene also implied that HAPS_0849 may mainly function as a phosphoglucomutase in G. parasuis.

Disruption of HAPS_0849 enhances autoagglutination and biofilm formation
The serum-sensitive phenotype and LOS truncation of ΔHAPS_0849 indicate that HAPS_0849 may be a virulence gene in G. parasuis. To further investigate the role of this gene, autoagglutination and biofilm formation assays were carried out as previously described.
The aggregation results showed no obvious difference between SC096 and ΔHAPS_0849 cultured in TSB with 0.25% glucose in the first 10 h; however, slight precipitation was observed after incubation was prolonged for 2 h (Figure 5A, D). The decrease in the optical density of ΔHAPS_0849 dramatically accelerated when the strain was precultured in the same medium with a lower concentration (0.05%) of glucose ( Figure 5B). Meanwhile, no apparent decrease in absorbance was observed in the wild-type and complemented strains. Furthermore, the aggregation of ΔHAPS_0849 cultured in a lower glucose concentration was more obvious than that cultured in a higher glucose concentration, as shown in Figure 5E. The absorbance of ΔHAPS_0849 at 600 nm drastically declined and reached its lowest value in 6 h when the strain was cultivated in TSB broth without glucose compared to the absorbance of SC096 ( Figure 5C). The accumulation amount of ΔHAPS_0849 cells in this condition was similar to that in 0.05% glucose after 12 h of incubation, while the phenotype of the complement strain was consistent with that of the parent strain ( Figure 5F). The results indicated that the HAPS_0849 mutant was inclined to autoagglutination and that the sedimentation rate was influenced by the concentration of glucose.
The biofilm formation abilities of the wild-type and ΔHAPS_0849 strains were assessed, and the results are depicted in Figure 6. After 24 h or 72 h, a significant gradual increase (P < 0.05) in biofilm biomass of ΔHAPS_0849 was observed compared to the biofilm formed by SC096 or the complemented strain in the absence of glucose ( Figure 6A, B). The absorbance of ΔHAPS_0849 at 600 nm was close to 1.0 after 24 h and 2.0 after 72 h, while the absorbance values of the wild-type and complemented strains were less than 0.5 at both time points. The absorbance values of the stained biofilms of all strains Figure 5 Autoagglutination of G. parasuis SC096, ΔHAPS_0849 and the HAPS_0849 complementation strain. A Autoagglutination rates of the SC096, ΔHAPS_0849 and ΔHAPS_0849-comp strains cultured in TSB with 0.25% glucose. D A photograph was taken at the end of the assay, as shown in panel A, and the results were from a representative experiment. Lane 1, SC096; lane 2, HAPS_0849 mutant; lane 3, complemented strain. B, E Assays were performed under the same conditions corresponding to panels A and D except that strains were cultivated in TSB broth with 0.05% glucose. C, F Tests were carried out in the same conditions corresponding to panels A and D except that strains were cultured without glucose. With the decrease in glucose, the rates of autoagglutination increased gradually. did not exceed 0.5 when the strains were incubated in the presence of 0.25% glucose at different time intervals ( Figure 6C, D). Hence, this evidence further supported the influence of glucose on the ΔHAPS_0849 strain, and disruption of the HAPS_0849 gene may increase biofilm formation in the absence of glucose.

HAPS_0849 may be an upper-pathway enzyme in uridine diphosphate galactose synthesis
We presented evidence that HAPS_0849 is a phosphoglucomutase that is responsible for producing G1P from G6P. Moreover, autoagglutination and biofilm phenotypes of ΔHAPS_0849 indicated that HAPS_0849 may correlate with surface polysaccharides biosynthesis. Thus, given our previous findings, we investigated whether HAPS_0849 was an upper-pathway gene in the galUE pathway, as mentioned in "Introduction" section and Figure 1. Several mutants involved in polysaccharide synthesis were selected for LOS pattern comparison to explain the functional relationship between these genes. Two galUE pathway mutants of G. parasuis strain SC096, namely, ZY001 (galU) and ZY005 (galE), defective in serum resistance have previously been reported [17]. Analysis of the ZY001 and ZY005 LOSs by silverstained PAGE revealed that loss of galU or galE alone in SC096 resulted in the truncation of the LOS core (Figure 7A). The LOS core from the galU mutant strain (lane 2) was smaller than that isolated from the galE mutant strain (lane 4). In general, the patterns of LOSs from the complemented strains were the same as those of the LOSs isolated from the parent strain SC096 (lanes 1, 3 and 5), except that the truncation of the LOS core was not completely eliminated in the ΔgalU-complemented strain ZY002 (ΔgalU-c) (lane 3), but the serum resistance phenotype was restored [17]. These findings suggested that galU and galE are required for LOS completeness, and disruption of galU or galE resulted in different LOS patterns.
Our previous data demonstrated that mutants of two additional glycosyltransferases, lgtB or lex-1, exhibited alterations in the LOS core [18]. To investigate the LOS patterns of these G. parasuis mutants, LOSs from the Biofilm formation by SC096 and the HAPS_0849 mutant and complementation strains. A Quantification of biofilm production from 24-h or 72-h cultures in TSB broth without glucose. This graph indicated that disruption of HAPS_0849 significantly increased the ability of the strain to form biofilms (*P < 0.05), while the biofilm formation phenotype of the complemented strain was restored to that of the wild-type strain SC096. B A photograph was taken at the end of the assay after cultivation in TSB with 0.25% glucose for 24 h or 72 h. C, D Experiments were performed under the same conditions except that strains were cultured with 0.25% glucose. These results showed that no obvious variance in the tested strains was observed when they were cultivated with adequate glucose. Error bars represent the standard deviations of three independent experiments. galU, galE, lgtB, lex-1, and HAPS_0849 mutants and wild-type strain SC096 were extracted and visualized by SDS-PAGE. As shown in Figure 7B, the mutant lacking galE exhibited a LOS molecule (lane 2) with a migration band identical to that of the major glycoform produced by the lex-1 mutant (lane 3). The LOSs from these two mutants migrated with an increased mobility compared to the LOS from the wild-type strain (lane 1) based on SDS-PAGE. This result suggests that lex-1, encoding a glycosyltransferase, may utilize UDP-galactose for LOS synthesis because galE is responsible for the production of this substrate. The galU mutant (lane 4) produced a highly truncated LOS molecule that migrated identically to the LOS produced by ΔlgtB (lane 5) or the lower band of ΔHAPS_0849 (lane 6) and migrated more rapidly than the LOSs produced by ΔgalE, Δlex-1 and the wild-type strain. It should be noted that all the tested mutants exhibited complete LOS truncation, except ΔHAPS_0849, and a small amount of wild-type LOS was produced by this strain.
Only two structures of LOSs from G. parasuis serovar 5 and serovar 15 have been previously reported, and they share the same structure [32] (Additional file 7). The completely deacylated LOS contains heptoses which are supposed to be transferred by opsX, rfaF, and waaQ [13] and multiple glucose and galactose provided by GalU for UDP-glucose and GalE for UDP-galactose, respectively. galU is also required for UDP-galactose synthesis because UDP-galactose is generated from UDP-glucose by GalE. This is consistent with the fact that the ΔgalU strain produced a smaller LOS molecule than the galE mutant. We infer that GalU and HAPS_0849 may be contiguous in the UDP-galactose synthesis pathway, and then LgtB or Lex-1 transfer these glycosyl substrates to the LOS core. This finding may explain why there are mainly two types of LOS patterns, defects in both glucose and galactose or only a defect in galactose, in these mutants. Our previous studies showed that most of glycosyltransferases (GTs) genes such as opsX, rfaF, waaQ, lgtB and lex-1 are involved in LOS synthesis [13,18]. In order to confirm if all the GTs were participated in LOS formation, two GT genes wcaJ and wclP in G. parasuis were also chosen for LOS inspection. These two GT genes were predicted to lie in CPS synthesis locus, and their GenBank Accession numbers are KC795356 and KC795359 respectively. However, LOS from either mutant was intact as wildtype strain although these mutants were serum sensitive (Additional file 8).
Our data provide evidence that HAPS_0849 in G. parasuis may be an upper-pathway enzyme involved in the generation of glucose-1-phosphate; however, HAPS_0849 is not the only source of G1P based on the incomplete truncation of LOS in the HAPS_0849 mutant strain.

Discussion
PGM is responsible for the conversion of G6P to G1P and functions upstream of the galUE pathway. This protein is important for the virulence of a number of bacterial pathogens, including Neisseria meningitidis [33], Brucella abortus [34], Bordetella bronchiseptica [35] and Salmonella enterica serovar Typhimurium [36] and is a critical enzyme connecting glycolysis with the synthesis of polysaccharides, such as CPS, LPS and EPS (exopolysaccharides). Based on our previous findings that galU and galE contribute to serum resistance and biofilm formation in G. parasuis [17], we hypothesize that the HAPS_0849 mutant may have similar phenotypes as the galU mutant based on the known pathway. However, the observation that the LOS pattern of ΔHAPS_0849 was not completely consistent with that of ΔgalU and shared a partially identical band with the LOS of the parent strain was unexpected. Unlike the phenotypes observed for ΔgalU, glucose clearly affected autoagglutination and biofilm formation in the ΔHAPS_0849 strain. This finding pointed out the main difference between ΔgalU and the HAPS_0849 mutant. The UDP-glucose generated by GalU appeared to be the sole source for LOS synthesis because the LOS in ΔgalU was completely truncated. However, the substrate G1P converted by HAPS_0849 was not the only substrate according to our data provided here.
We highlight the importance of G1P because it is a central node involved in multiple carbon source pathways, including glycolysis, a central system of glucose metabolism. Because there are many phenotypes related to glucose, we suspect that there is another pathway to bypass the deficiency of G1P synthesis in the HAPS_0849 mutant. G1P can be derived from at least four routes based on Kyoto Encyclopedia of Genes and Genomes (KEGG) database analysis. As shown in Additional file 9, (1) G1P can be derived from endogenous glycogen that can be degraded by glycogen phosphorylase (GlgP); however, it should be noted that endogenous glycogen is derived from G1P, and glycogen synthesis can occur only when G1P is present. (2) G1P can be derived from the metabolism of galactose, catalysed by galactokinase (GalK) and galactose-1-phosphate uridylyl transferase (GalT); however, no phenotypic variation was observed in mutants lacking these enzymes (data not shown). (3) G1P can be derived from exogenous glycogen, such as dextrin, which can also be converted by GlgP. The metabolic fingerprint of SC096 shows that dextrin is an ideal carbon source for G. parasuis (unpublished observation), and dextrin has been proposed as a potential source for G1P supplementation. Finally, (4) G1P can be derived from G6P produced by HAPS_0849, which should be the principal source for G1P generation according to the data presented above.
Several studies have demonstrated that CPS and LOS are important virulence factors and confer serum resistance in G. parasuis [5,12,13,37]. However, the correlation between these polysaccharides and carbon source metabolism still awaits experimental investigation. Our previous work reported that two glycosyltransferases annotated as lgtB and lex-1 are involved in the synthesis of LOS, and the absence of one of these genes can lead to a serum-sensitive phenotype [18]. Analysis of the LOSs of the mutants in this study showed that the LOS migration patterns of galE and lex-1 were consistent, while the LOSs produced by lgtB, HAPS_0849 and galU showed another glycoform. These results suggest that UDP-glucose may serve as a substrate for lgtB, while lex-1 may use UDP-galactose as a donor for LOS synthesis, as the products of GalE and GalU are UDP-galactose and UDPglucose, respectively. To date, only one study has performed structural analysis of the LOSs and CPSs of G. parasuis, and the results showed that multiple glucose and galactose residues do indeed exist in LOS molecules [32]. This finding may explain why the absence of galU or galE resulted in LOS truncation. In addition, these UDP sugars may also be involved in the synthesis of capsules because disruption of CPS genes reduced the resistance of G. parasuis to serum, and these genes are clearly not related to LOS expression. There are at least two types of polysaccharides that protect this bacterium from the effects of serum, and G1P could be a critical junction between glucose and UDP-sugars for these polysaccharides synthesis in G. parasuis.
In summary, we have identified HAPS_0849 as a phosphoglucomutase gene that is correlated with the biosynthesis of LOS in G. parasuis SC096. The HAPS_0849 mutant is not resistant to serum, and the complemented strain displayed a restored phenotype corresponding to that of the parent strain. Autoagglutination and biofilm formation were significantly increased in the ΔHAPS_0849 strain. Moreover, the LOS profile of the HAPS_0849 mutant was partially consistent with that of ΔgalU, and HAPS_0849 may act upstream of galU in the generation of G1P. Altogether, our observations highlight the fact that PGM is a key node for LOS synthesis in G. parasuis.