Investigation of a Novel DNase of Streptococcus suis Serotype 2

Strains, media, and culture conditions.The virulent S. suis isolate SX332 was obtained from F. Blecha (College of Veterinary Medicine, Kansas State University), the type strains for serotypes 1 through 9 (19, 27) were obtained from A. Crichlow (Western College of Veterinary Medicine, University of Saskatchewan), and 258 field isolates were collected from swine in North America (primarily western Canada). All strains were stored frozen at −70°C in 15% glycerol. Field strains were classified by recovery from a surface (nasal mucosa or palatine tonsil of clinically normal swine) or internal (joint, brain, or other internal organ of diseased swine) location. Escherichia coli strains were routinely cultured in Luria-Bertani medium (Difco, Detroit, Mich.) supplemented with the appropriate antibiotics at 37°C. S. suis strains were cultured statically in a 5% CO₂ atmosphere at 30 or 37°C either in Todd-Hewitt broth (Difco) supplemented with 0.5% (wt/vol) yeast extract (THYB), on Mueller-Hinton agar (MHA) plates (Difco), or on tryptic soy agar plates containing 5% (vol/vol) sheep blood (PML Microbiologicals, Mississauga, Ontario, Canada). Media were supplemented with erythromycin for plasmid-containing S. suis and E. coli strains, to 2 and 350 μg/ml, respectively. For detection of nuclease activity of bacterial colonies on plates, toluidine blue agar (TBA) (28) was used; TBA contains a DNA source that when degraded by nuclease results in a change in pH and a concomitant change in color of TBA from blue to pink.

Molecular biological techniques.Unless otherwise specified, restriction endonuclease digestions, DNA ligations, agarose and sodium dodecyl sulfate-polyacrylamide (SDS-PA) gel electrophoreses, and Southern and Western blotting were performed according to standard protocols (30). Restriction endonucleases and modifying enzymes were purchased from Amersham Pharmacia Biosciences, Ltd. (Baie d'Urfé, Québec, Canada). The broad-host-range, temperature-sensitive, gram-positive shuttle plasmid pG⁺host 9 (26) and its derivative pGh9:ISS1 (26) were donated by E. Maguin (Institut National de la Recherche Agronomique, Paris, France). Manipulation of pG⁺host 9-based plasmids was carried out in E. coli TG1-dev, a recA-deficient derivative of TG1 containing a transposon-borne, chromosomally located copy of the wild-type repA gene (E. Maguin, personal communication). Electrocompetent E. coli was prepared and transformed as described previously (18), and electrocompetent S. suis was prepared and transformed by using a method previously described for Streptococcus agalactiae (17), with the omission of glycine. Genomic DNA was extracted and purified from streptococci by using the NucleoSpin tissue kit (Clontech, Palo Alto, Calif.), and plasmid DNA for miniprep analysis was extracted from E. coli by using the QIAquick spin miniprep kit (Qiagen Inc., Mississauga, Ontario, Canada). Plasmid DNA for sequencing was purified by using the Qiagen plasmid minikit. PCR and sequencing primers are described in Table 1. Automated DNA sequencing was carried out at the National Research Council of Canada sequencing facility (Plant Biotechnology Institute, University of Saskatchewan, Saskatchewan, Canada). For isolation of RNA, S. suis cultures from different time points, corresponding to early exponential, mid-exponential, late exponential, and stationary growth phases (optical densities at 600 nm of ca. 0.2, 0.5, 0.9, and 1.2, respectively), were treated with RNAprotect bacterial reagent (Qiagen), and then total RNA was extracted by using the RNeasy minikit (Qiagen) according to the manufacturer's instructions, following a prelysis incubation of cells in 100 μl of Tris-EDTA (pH 8.0) buffer containing 10 mg of lysozyme per ml and 250 U of mutanolysin at 37°C for 10 min. DNA contamination was removed from RNA during purification by treatment with RNase-free DNase (Qiagen) and following purification by digestion with amplification-grade DNase I (Invitrogen Canada Inc., Burlington, Ontario, Canada). Synthesis of cDNA was performed with SuperScript II RNase H⁻ reverse transcriptase (Invitrogen) according to the manufacturer's supplied protocol, using a random nanomer primer. Reverse transcription-PCR experiments were performed with the ssnA-specific PCR primers XII(HindIII) 01 and XII(HindIII) 02; control PCRs with non-reverse-transcribed RNA samples failed to generate any products, confirming the absence of DNA contamination.

Detection of S. suis nuclease activity. (i) Assay of whole cells.Nuclease activity in whole cells was detected by using a slightly modified version of a previously described method (28). Initially, SX332 was screened for nuclease production; bacteria were streaked on MHA plates and incubated to allow colony formation. The plates were overlaid with 3.5 ml of TBA supplemented with 1 mM (each) CaCl₂ and MgCl₂. Following incubation at 37°C for no longer than 2 h, nuclease activity was determined as the presence of pink halos surrounding colonies. Subsequently, the nuclease phenotypes of the type strains for S. suis serotypes 1 to 9 and of 258 clinical isolates were evaluated by placing 2 μl of culture of each strain on the surfaces of MHA plates, using a grid template with 50 designated locations per 100-mm-diameter circle. The plates were incubated to allow bacterial growth before the nuclease phenotype was determined as described above.

(ii) Assay of cell fractions.The nuclease activity of proteins electrophoresed in PA gels containing sonicated, single-stranded salmon sperm DNA (5s DNA) was determined by using a modified version of a previously described method (29). Briefly, denaturing or native PA gels were prepared, with the resolving gel portions supplemented with 5 μg of 5s DNA per ml. Spent media from exponentially growing cultures (optical density at 600 nm of ca. 0.4) were sterilized through 0.2-μm-pore-size syringe filters (Gelman Sciences, Ann Arbor, Mich.) and supplemented with complete EDTA-free protease inhibitor cocktail (Roche Diagnostics, Laval, Québec, Canada) to a 1× final concentration. Supernatants were concentrated ca. 50-fold in Ultrafree-15 BIOMAX-30 K filters (Millipore, Bedford, Mass.) by centrifugation at 2,000 × g at 4°C and buffer exchanged in 40 mM Tris-HCl (pH 7.5). Cell wall proteins were extracted from S. suis as described previously (22) and buffer exchanged as described above. Following electrophoresis of samples, gels were rinsed briefly in water and immersed in 20 mM Tris-HCl (pH 7.5) with or without 1 mM (each) CaCl₂ and MgCl₂. The gels were then incubated at 37°C for up to 8 h, with occasional replacement of buffer, before addition of ethidium bromide to 1 μg/ml. After continued incubation at 37°C, gels were analyzed with UV transillumination. Proteins with nuclease activity (which degraded surrounding DNA, preventing ethidium bromide staining) appeared as dark bands against the fluorescing background.

Construction of S. suis plasmid insertion mutants and determination of insertion loci.A random pGh9:ISS1 insertion library of S. suis SX332 was constructed as described previously for other gram-positive species (26, 37), and targeted chromosomal integration of plasmids (other than pGh9:ISS1) by homologous recombination was also performed as described previously (7). Colonies resistant to erythromycin at 37°C (the nonpermissive temperature for plasmid replication) were considered likely to have undergone plasmid integration into the chromosome. Sequences flanking the sites of chromosomally integrated plasmids were obtained by using the sequence rescue (SR) technique, essentially as described previously (26). Briefly, genomic DNAs from integrant strains were digested with restriction endonucleases for which a single recognition site was present within the inserted vector (Fig. 1). Following ligation, circularized genomic fragments flanked by vector sequences (containing the erythromycin resistance gene) were recovered after transformation of E. coli TG1-dev and selection in the presence of erythromycin.

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FIG. 1.

Schematic representation of the ssnA locus. The ca. 4.5-kb region between the EcoRI and HindIII recognition sites was obtained by SR from integrated pGh9:ISS1. The ca. 1.3-kb region between the HindIII site and the 3′ end, including the hatched portion of ssnA, was obtained by SR from integrated pMF1012i. Nuclease-deficient mutants were constructed by disruption of ssnA by random insertion of pGh9:ISS1 (SX435), and targeted insertion of pMF1012i (SX436) and pMF1015i (SX437).

SR was performed from the pGh9:ISS1 integrant mutant, SX435, using EcoRI for upstream and HindIII for downstream sequence retrieval. Subsequently, ca. 1.6 kb of the upstream flanking region was recovered in a ca. 6.2-kb plasmid, designated pXII(EcoRI), and ca. 2.9 kb of the downstream flanking region was recovered in a ca. 7.5-kb plasmid, designated pXII(HindIII). The junctions between pGh9:ISS1 and cloned inserts were initially determined with the primers 5′ISS1(rev) plus pGh9 02 for pXII(EcoRI) and 3′ISS1(fwd) plus pGh9 01 for pXII(HindIII). The pXII(EcoRI) sequence was completed with primers XII(EcoRI) 01 and XII(EcoRI) 02, and the pXII(HindIII) sequence was completedwith the primers XII(HindIII) 01 and XII(HindIII) 02. Sequence data determined the presence of an 8-bp duplicated sequence (ATATCTAC) on either side of the pGh9:ISS1 insertion site, allowing the upstream and downstream sequences to be joined in frame, resulting in a contiguous sequence (contig) of 4,499 bp.

To determine chromosomal sequences downstream of the region obtained by SR from pXII(HindIII), an internal fragment of ssnA was cloned into pG⁺host 9. PCR with the primers XII(HindIII) 01 plus pGh9 01 amplified a DNA product from pXII(HindIII) which was digested with PvuI and HindIII to liberate a 414-bp fragment corresponding to the central portion of the ssnA gene. The ssnA fragment was blunt ended by using the PCR polishing kit (Stratagene, La Jolla, Calif.) and cloned into the SmaI site of pG⁺host 9. Subsequently, a clone containing the ssnA fragment in the opposite orientation to the pG⁺host 9 repA(Ts) gene was identified and designated pMF1012i. A mutant, designated SX436, was identified following homologous recombination of pMF1012i into the SX332 chromosome (Fig. 1). Plasmid integration at the desired locus was confirmed by PCR with the primers XII(HindIII) 01 plus XII(HindIII) 02 and XII(HindIII) 01 plus pGh9 01 (data not shown); as expected, the former control PCR amplified a fragment of ca. 1.2 kb from the ssnA gene of SX436 and wild-type SX332 DNA (the amplified region lay upstream of the pMF1012i insertion site), while the latter PCR amplified a product of ca. 1.85 kb from SX436 but failed to amplify any product from SX332, due to the pGh9 01 primer's specificity for the integrated plasmid. SR was performed from SX436 with EcoRI, and a clone containing a plasmid of ca. 5.6 kb was identified and designated pMF1013i. pMF1013i was sequenced with XII(HindIII) 03 and MF1013i 01; when combined with the above sequence, a 5,821-bp contig was obtained.

To allow targeted disruption of ssnA, a 1,143-bp PCR fragment corresponding to the region directly downstream of the predicted secretion signal peptide-encoding sequence of ssnA was amplified from SX332 genomic DNA with the primers pETssnA 01 and pETssnA 02. The fragment was ligated into pPCR-SCRIPT by using the PCR-SCRIPT cloning kit (Stratagene), and a recombinant plasmid containing the ssnA fragment in the opposite orientation to the pPCR-SCRIPT lacZ gene was identified and designated pMF1005i. Following NotI and XhoI digestion of pMF1005i, a fragment containing bp 106 to 1236 of ssnA and adjacent vector sequences was cloned into pG⁺host 9 to create plasmid pMF1015i. Following chromosomal integration of pMF1015i (Fig. 1), confirmation of integration at the desired locus was obtained by PCR with XII(HindIII) 01 plus pGh9 01 and pGh9 02 plus XII(HindIII) 04. Both pG⁺host 9 primers are specific for the pG⁺host 9 backbone of pGh9:ISS1, and as expected, the former primer pair amplified a ca. 2.2-kb fragment (corresponding to the region directly upstream of the inserted plasmid) from SX437, whereas no product was obtained from wild-type SX332 DNA (data not shown). The second primer pair amplified an expected product of ca. 3.2 kb (corresponding to the region directly downstream of the inserted plasmid) from SX437, while the control SX332 PCR was negative (data not shown). SX437 was screened with TBA and found to be nuclease deficient.

Expression and purification of a truncated SsnA derivative.A DNA fragment, corresponding to the sequence encoding amino acid residues Thr₃₆ to Asp₄₁₂ of SsnA (377 amino acids [aa] immediately following the predicted signal peptide cleavage site), was liberated from pMF1005i with NdeI and BamHI and cloned into the pET-15b expression plasmid (Novagen, Madison, Wis.). The resulting construct, designated pMF1025, was used to transform E. coli BL21(DE3). Expression of the N-terminally six-histidine-residue-tagged, truncated SsnA protein (rSsnA_Δ) was induced by addition of IPTG (isopropyl-β-d-thiogalactopyranoside) to exponentially growing cultures to a concentration of 1 mM. Following induction, cultures were incubated at 30°C for 1 h, and then rifampin was added to 400 μg/ml. Incubation was continued for a further 3 h, prior to protein purification by immobilized metal affinity chromatography with Ni-nitrilotriacetic acid agarose (Qiagen) according to the manufacturer's instructions.

Generation of immune sera.Anti-SsnA polyclonal antibodies were raised in New Zealand White rabbits. An initial subcutaneous immunization (day 0) was performed with 1 ml of PBS containing 25 μg of rSsnA_Δ and 30% oil-in-water emulsion (VSA3; MVP Laboratories, Ralston, Nebr.). Booster vaccinations were performed, as described above, at days 20 and 27, and rabbits were bled out to obtain immune serum on day 33. Porcine anti-S. suis SX323 immune sera were obtained from pigs challenged intrapharyngeally with live SX332 (performed as part of an unrelated study [24]). Nonimmune sera were also obtained from unchallenged control animals from the same experiment.

Computational analyses.Sequence manipulations were performed with the Clone Manager Suite software (Scientific & Educational Software, Durham, N.C.). Translated sequences were identified by comparison with protein sequences in the National Center for Biotechnology Information database, using the Clone Manager Blastx interface. Further sequence analyses were performed with the Prosite database of families and domains (http://www.expasy.ch/prosite ) and applications of the European Molecular Biology Open Software Suite package (http://www.hgmp.mrc.ac.uk/Software/EMBOSS/ ) via the Canadian Bioinformatics Resource web interface (http://bioinfo.pbi.nrc.ca/ ). Analysis of the statistical significance of nuclease phenotypes in clinical field isolates was performed by using cross-tabulation in the SYSTAT 10 software package (SPSS Science, Chicago, Ill.).

Nucleotide sequence accession number.The 5,821-bp contig containing the S. suis SX332 ssnA gene was submitted to GenBank under accession number AY254322 .

Screening of S. suis isolates for nuclease activity.Pink halos were observed surrounding growth of the virulent S. suis isolate SX332 and each of the type strains of serotypes 1 through 9, indicating expression of nuclease (data not shown). As shown in Table 2, most of the field strains isolated from internal sites (87.5%) expressed a nuclease phenotype, whereas fewer than half (40.2%) of the surface isolates displayed an equivalent phenotype. This difference in proportion was found to be highly statistically significant (P < 0.001), with an odds ratio of 10.4 (95% confidence interval, 4.7 to 23.0).

Generation and screening of a nuclease-deficient mutant.A pGh9:ISS1 random insertion library of SX332 was constructed, and comparison of total CFU per milliliter with erythromycin-resistant CFU per milliliter at 37°C revealed a pGh9:ISS1 chromosomal integration frequency of 5 × 10⁻². Approximately 10,000 individual colonies were screened for nuclease activity by TBA overlay. A single colony which was not surrounded by a pink halo was identified, indicating the absence of nuclease activity. Subsequently, this clone, designated SX435, was restreaked on selective agar plates, tested for nuclease activity, and confirmed to be nuclease deficient. Southern blot analysis of SX435 with a probe corresponding to the ermAM gene of pGh9:ISS1 determined the presence of a single band (data not shown), confirming that a single integration of pGh9:ISS1 had occurred.

Analysis of the region containing the nuclease-encoding gene.The locus of pGh9:ISS1 insertion in SX435 was determined following SR (Fig. 1). The presence of coding regions within the 4,499-bp contig was determined, and translated open reading frames (ORFs) were compared with the GenBank sequence database. Homologues of genes described previously for other species were annotated accordingly. At the extreme 5′ end of the chromosomal fragment, a 558-bp partial reading frame was found, encoded by the positive strand. The translated 186-aa product showed 73% identity and 82% similarity to aa 566 to 750 of a 754-aa putative glutamate-cysteine ligase enzyme of Streptococcus mutans UA159 (accession no. AAN58035 ). Approximately 0.8 kb further downstream lay a second ORF encoded by the positive DNA strand, starting at bp 1384 and extending throughout the remainder of the sequence. The translated 1,057-aa product showed the most extensive homology, at 59% identity and 73% similarity, to a 910-aa conserved hypothetical protein of Streptococcus pyogenes (group A Streptococcus [GAS]) M1 (accession no. AAK33693 ) and MGAS8232 (accession no. AAL97472 ). The protein also shared 38% identity and 52% similarity over aa 114 to 787 of a putative member of the Bacillus anthracis AP endonuclease 1 family (accession no. NP_654986 ). Furthermore, regions of the predicted ORFs in the S. suis sequence shared homology with regions of extracellular nuclease proteins of several bacteria (Fig. 2), including those of a Synechosystis sp. (accession no. BAA16955 ), Aeromonas hydrophila (accession no. AAB39273 ), Vibrio cholerae (accession no. AAF95762 ), and Deinococcus radiodurans (accession no. AAF12592 ). This gene, apparently encoding an S. suis nuclease, was designated ssnA (for S. suis secreted nuclease A).

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FIG. 2.

Schematic representation of homology between S. suis SsnA and nucleases from other species. The numbers shown with each protein denote the amino acid residues at which regions of homology (hatched boxes) begin and end.

To determine the remaining ssnA sequence, SR was performed from chromosomally integrated pMF1012i. Analysis of the resulting sequence revealed that the ssnA ORF extended a further 67 bp downstream of the previously determined sequence (Fig. 1). In addition, a second, 867-bp ORF, encoded by the positive DNA strand, was identified 80 bp downstream of ssnA, the translated 288-aa product of which shared 79% identity and 90% similarity over its entire length to the 290-aa, 33-kDa heat shock protein (Hsp33) of Streptococcus pneumoniae (accession no. AAK76239 ). The S. suis gene has been designated hsp33.

The intact ssnA ORF was observed to be 3,186 bp, encoding a predicted protein of 1,061 aa; however, within the first 70 bp of the DNA sequence were two other potential ATG codons, each in frame with the first. Only the last of the three start codons exhibited a potential ribosome-binding site (GGAG), 10 bp immediately upstream. Analysis of the predicted SsnA sequence, translated from the first start codon, by using the SPScan application predicted three different putative signal peptides, with identical cleavage sites but with lengths of 55, 46, and 35 aa, respectively, corresponding to each of the three translational start codons. Typical gram-positive signal peptides are usually approximately 30 aa in length, so it is likely that the last of the three start codons corresponds to the translational start site of SsnA. While a longer signal peptide is possible (for example, the staphylococcal nuclease gene, nuc, encodes a 60-aa signal peptide [33]), the 35-aa sequence is in keeping with the observed ribosome-binding site. Therefore, the 1,041-aa SsnA is encoded by a 3,126-bp ORF, with a predicted 35-aa signal peptide cleavage site between amino acid residues Ala₃₅ and Thr₃₆. Sequence data revealed the pGh9:ISS1 insertion locus to be downstream of bp 634 of ssnA. A putative nucleic acid binding domain (ITETNIAQLATQAQATLVSLKN) was predicted within SsnA between aa 256 and 277 by using the Helixturnhelix application (12). Comparison of SsnA with the Prosite database revealed a typical gram-positive cell wall sorting signal between aa 1011 and 1041. This sequence fulfilled all criteria proposed for gram-positive surface proteins, including a conserved hexapeptide (LPKTG) motif followed by a hydrophobic domain and finally a cluster of basic residues (16). Nonquantitative reverse transcription-PCR analysis consistently generated a DNA fragment of the expected size of ca. 1.2 kb, confirming that the ssnA gene is expressed throughout all growth stages examined (data not shown).

Porcine immune recognition of SsnA.Western blotting was performed to determine whether SsnA was expressed during in vivo infection with S. suis. Pooled immune sera, obtained from pigs challenged experimentally with S. suis, were used to probe nitrocellulose-bound rSsnA_Δ. A strong band of ca. 44 kDa was observed, corresponding to rSsnA_Δ (data not shown). Conversely, sera from naive pigs failed to detect rSsnA_Δ, confirming the specificity of the immune reaction. These combined data confirmed that SsnA is expressed by S. suis in vivo and that it appears to be a strongly immunogenic protein.

Serum neutralization of SsnA.The ability of rabbit anti-rSsnA_Δ antibodies to neutralize SsnA activity was determined. Single colonies of SX332 on THYB agar plates were overlaid with TBA, and 25-μl drops of anti-rSsnA_Δ serum were placed directly on the TBA at different locations on the plates. After incubation at 37°C for up to 18 h, no nuclease activity was observed surrounding colonies in the immediate vicinity of the antiserum drops, whereas pink halos surrounded all outlying colonies (data not shown). Similar assays performed with nonimmune rabbit serum failed to inhibit SsnA activity, confirming that SsnA is specifically neutralized by anti-rSsnA_Δ antibodies.

Targeted disruption of ssnA.To confirm that ssnA was in fact the nuclease-encoding gene, targeted disruption was carried out by homologous recombination of pMF1015i into the chromosome (Fig. 1), and a nuclease-deficient mutant, designated SX437, was identified following screening with TBA. Interestingly, the mutant SX436 (see above) was derived from the insertion of pMF1012i ca. 0.3 kb upstream of the putative cell wall sorting signal; conveniently, this mutant was theoretically deficient in its capacity to be cell wall anchored. Screening with TBA confirmed a nuclease-positive phenotype, and thus the final ca. 100 aa of SsnA is not required for enzymatic activity.

Analysis of nuclease in cell fractions.Concentrated culture supernatants of SX332 were prepared in denaturing sample loading buffer (containing SDS and β-mercaptoethanol) or in native loading buffer (without SDS or β-mercaptoethanol). Duplicate samples were prepared in each buffer, and one of each was boiled for 3 min prior to gel loading (the experiment was repeated on several occasions). Following electrophoresis of proteins on 5s DNA-containing SDS-PA gels, nuclease activity was restored by incubation in buffer containing MgCl₂ and CaCl₂. Ethidium bromide staining at 37°C was performed for a minimum of 1 h; however, it was occasionally necessary to continue incubation for up to 8 h to allow visualization of nuclease activity. Samples loaded in nondenaturing buffer revealed numerous high-molecular-mass dark bands, visible as a smear against the fluorescent background of the stained gel (data not shown); this was attributed to inadequate disruption of protein aggregates in the native buffer. Samples loaded in denaturing sample buffer revealed a major band with an apparent molecular mass of ca. 80 kDa and two lower-molecular-mass bands of ca. 68 and 63 kDa (Fig. 3), indicating that all had nuclease activity; the two lower-molecular-mass bands most likely derived from proteolytic degradation of the higher-molecular-mass moiety (see Discussion). Boiling of SX332 samples failed to reduce the extent of the observed nuclease activity, confirming the heat-stable nature of SsnA (data not shown); however, samples prepared in denaturing buffer revealed less nuclease activity than those prepared in native buffer (data not shown), suggesting incomplete refolding prior to detection of activity. Nuclease activity was detected only in the presence of Mg²⁺ and Ca²⁺ together (Fig. 3), suggesting that SsnA has an absolute requirement for both ions for activity. Furthermore, in addition to 5s DNA, SDS-PA gels were also prepared with either 5 μg of linear, double-stranded DNA (unboiled, sonicated salmon sperm DNA) per ml, 20 μg of yeast tRNA per ml, or 10 μg of double-stranded, closed circular plasmid DNA (pPCR-SCRIPT) per ml. Nuclease activity equivalent to that in 5s DNA was observed in gels containing linear, double-stranded DNA fragments; however, with all other substrates no nuclease activity was evident (data not shown), even following extended incubation (>48 h) prior to staining.

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FIG. 3.

Nuclease in S. suis supernatant extracts was detected in 5s DNA-containing SDS-PA gels. In the presence of Ca²⁺ and Mg²⁺, three protein bands of ca. 80, 68, and 63 kDa were observed to possess nuclease activity.

Equivalent quantities of cell wall extracts, prepared from SX332 and derived mutants, were analyzed on native 5s DNA-containing PA gels (Fig. 4). Samples were not boiled prior to electrophoresis, and nondenaturing sample loading buffer was used. Nuclease activity was detected for SX332 in the form of two distinct bands. No activity was observed for SX435 and SX437, while a faint, single band was observed for SX436, corresponding approximately in size to the lower-molecular-mass band of SX332. Western blot analysis of cell wall fractions was also performed (Fig. 5). SX332 samples revealed two dominant bands of ca. 112 kDa and 108 kDa, corresponding to the predicted sizes of SsnA with and without signal peptide. Equivalent bands were completely absent from SX435 and SX437 samples. The ca. 112-kDa band was also absent from SX436 samples; however, there was the suggestion of an extremely faint band, of ca. 100 kDa, in place of the 108-kDa band of SX332, corresponding to the predicted 98-kDa truncated SsnA with an intact signal peptide.

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FIG. 4.

Determination of nuclease activity in S. suis subcellular fractions. Proteins were analyzed on 5s DNA-containing native PA gels, and samples correspond to supernatant fractions (lanes 1 to 4) and cell wall fractions (lanes 5 to 8). Samples 1 and 5 derive from SX332, 2 and 6 derive from SX435, 3 and 7 derive from SX436, and 4 and 8 derive from SX437. Arrowheads indicate bands with nuclease activity. No activity was observed for SX435 and SX437, while the upper nuclease band was absent in SX436 samples.

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FIG. 5.

Western blot analysis of mutanolysin-extracted S. suis cell wall proteins. Two nuclease bands were detected in SX332 which were absent from SX435 and SX437. A very faint band of approximately 100 kDa was observed for SX436.