INTRODUCTION

Top Abstract Introduction Materials & Methods Results Discussion References

A key primary event in bacterial colonization of the host is adherence mediated by adhesins which recognize either carbohydrate or peptide structures (15, 21, 22, 26). Adhesins also participate in adherence-associated events, such as bacterial uptake into cells and host cell signaling (10, 23). Moreover, multiple adhesin families and heterologous specificities among each adhesin family lead to specific animal and tissue tropisms (39, 42, 44, 45).

Actinomyces naeslundii genospecies 1 and 2 and Actinomyces odontolyticus are common oral species displaying specific tissue and animal host tropisms (12-14, 25, 32, 34, 38). The intraoral tropism of A. naeslundii genospecies 1 and 2 involves two antigenically and functionally distinct fimbriae, type 1 and type 2 (8, 9). The amino acid sequences of the type 1 and type 2 major fimbrial subunits as deduced from the corresponding fimP and fimA genes of strains T14V (genospecies 2) (48) and ATCC 12104^T (genospecies 1) (11, 49), respectively, have 34% sequence identity (50). Recently, the biogenesis and function of type 1 fimbriae were found to involve six genes (open reading frames 1 through 6), in addition to the fimP gene (51). Moreover, the adhesive capacity of type 2 fimbriae has been associated with a 95-kDa protein or protein complex, although the genetic basis for this is unclear (27). The corresponding genes for adhesion of A. odontolyticus to oral surfaces remain unknown (18).

Type 1 fimbriae, present mainly on genospecies 2 (8, 39), mediate attachment to salivary acidic proline-rich proteins (APRPs) and statherin adsorbed onto hydroxyapatite surfaces (15, 16). Allelic (e.g., PRP-1, PRP-2, Db, Pa, and PIF) and posttranslational (e.g., PRP-3 and PRP-4) variants of APRPs and four statherin variants (3, 20) and variant binding patterns of Actinomyces to APRPs and statherin (18, 41) have been demonstrated. The genospecies 2 strains LY7 and ATCC 19246, both expressing type 1 fimbriae (16, 47) and isolated from human sites, display preferential binding to APRPs and statherin, respectively (40, 41). Type 2 fimbriae, expressed by both genospecies (8, 39), mediate binding to 1-3-linked galactose or galactosamine structures (referred to as GalNAc specificity) (33, 43) in cell surface glycolipids and glycoproteins (5, 40), salivary glycoproteins (41), and streptococcal capsular polysaccharides (1). However, the genospecies 1 strain ATCC 12104^T and the genospecies 2 strain LY7 display different binding patterns to a panel of saccharides containing -linked galactose or galactosamine structures (39, 40). Consequently, these two strains display different lactose- and GalNAc1-3Gal-O-ethyl-inhibitable adherence patterns to epithelial cells (5, 39-41), polymorphonuclear leukocytes (36, 39), and streptococci (7, 28, 29, 39, 40). The adherence (or coaggregation) of Actinomyces-Streptococcus involves heterogeneous interaction modes (coaggregation groups A through F) which are either inhibitable or unaffected in the presence of lactose (28, 29). However, the genetic basis for the different types of APRP and GalNAc specificity is unknown.

Recently, we surveyed the expression of APRP and GalNAc binding specificities among a collection of Actinomyces isolates from defined individual and tissue sites of the human oral cavity (18, 19, 39). The survey revealed (i) different types of GalNAc specificity, as measured by coaggregation with streptococci, in genospecies 1 (type 2:1 specificity) and genospecies 2 (type 2:2 specificity); (ii) different prevalence rates of APRP binding, but preferential binding to APRPs over statherin, for isolates of genospecies 1 and 2; (iii) tongue isolates of A. odontolyticus expressing fimbriae and coaggregating with streptococci in a fashion that was not inhibited in the presence of GalNAc1-3Gal-O-ethyl.

The aim of this study was to generate full-length and central DNA fragments specific for the fimP (type 1) and fimA (type 2) fimbrial subunit genes and to use these fragments as probes in DNA-DNA hybridization assays with our collection of Actinomyces isolates and representative strains of the Actinomyces coaggregation groups A through F. Using this approach, we identified genetic variation among the fimP and fimA fimbrial subunit genes that correlated with the different types of APRP and GalNAc specificity displayed by Actinomyces species. Furthermore, we provide evidence that A. odontolyticus may exhibit a genetically related but functionally distinct adhesin binding specificity.

	MATERIALS AND METHODS

Top Abstract Introduction Materials & Methods Results Discussion References

Bacterial strains, culture conditions, and characterization. Strains of Actinomyces were isolated from different intraoral sites and subjects and characterized as previously described (18, 19). Representative reference strains of coaggregation group A (A. naeslundii T14V), group B (A. naeslundii PK19), group C (A. naeslundii PK947), group D (A. naeslundii PK606), group E (A. odontolyticus PK984), and group F (A. naeslundii PK1259) were obtained from P. Kolenbrander, National Institutes of Health, Bethesda, Md. A. naeslundii LY7 was obtained from R. J. Gibbons, Forsyth Dental Center, Boston, Mass. A. naeslundii ATCC 19246 and ATCC 12104^T were obtained from the National Bacteriology Laboratory, Stockholm, Sweden. Strains LY7 and ATCC 19246 and reference strains for coaggregation groups A through F were characterized by multivariate statistical analysis of phenotypic characteristics, serotyping, and sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) as previously described (18). Streptococcus oralis MPB1 was obtained from the Department of Cariology, Göteborg University, Göteborg, Sweden, and S. oralis Ss34 was obtained from P. Kolenbrander. Escherichia coli HB101 and K-12 and Actinomyces ATCC 10048^T, ATCC 12102^T, ATCC 35568^T, ATCC 23860^T, and ATCC 49285^T were all obtained from the Culture Collection, Göteborg University (CCUG). All Actinomyces and streptococcal strains were cultured at 37°C for 24 h in 5% CO₂-10% H₂ in nitrogen on Columbia II agar base plates (Becton Dickinson and Co., Cockeysville, Md.) supplemented with 30 ml of a human erythrocyte suspension per liter. E. coli strains were cultured on Luria-Bertani (LB) agar plates at 37°C for 24 h. Bacteria were metabolically labeled by mixing 10 µl of [³⁵S]methionine (10 mCi/ml; Amersham, Little Chalfont, United Kingdom) with bacteria suspended in 100 µl of 10 mM phosphate-buffered saline (pH 7.2) prior to growth for 24 h.

Chromosomal DNA isolation. Chromosomal DNA was isolated essentially as described previously (6), except for the following minor modifications: (i) the concentration of lysozyme was increased to 20 mg/ml; (ii) bacterial lysis was induced by the addition of 60 µl of 10% SDS and 150 µl of pronase (25 mg/ml; Sigma Chemical Co., St. Louis, Mo.) prior to overnight incubation at 37°C; and (iii) after lysis, DNA was extracted with an equal volume of phenol, followed by chloroform-isoamyl alcohol (24:1, vol/vol), and precipitated with 2 volumes of ethanol (95%)-1 M NaCl at 20°C. Following treatment with 0.5 mg of RNase (Boehringer GmbH, Mannheim, Germany) at 37°C for 45 min, DNA was finally recovered with 375 µl of cold ethanol (95%) in the presence of 50 µl of 7.5 M ammonium acetate for 30 min at 20°C.

Oligonucleotide primer pairs. The PCR primer sequences used to generate DNA probes specific for fimP (type 1), fimA (type 2:1), and fimA (type 2:2) fimbrial subunit genes were as follows: P1, 5'-ACA GCA ATG CAC TCC CTC AA-3', and P2, 5'-TG CTT GGC AAC GTG ACG GC-3' (used to generate a 1,603-bp type 1 full-length probe); P3, 5'-ACC CTC TCC GGT GTG GAC AA-3', and P4, 5'-ACC TCG TTC TGA CCG ACG AT-3' (a 208-bp type 1 central probe); P5, 5'-G AAG TAC AAC ACC AGC ACG C-3', and P6, 5'-GAG GTC CCG GTT CCG CTT-3' (a 1,576-bp type 2:1 full-length probe); P7, 5'-AGA AGA TCG AAG TCG CCA AGA-3', and P8, 5'-CTG TAG CCG TCA CCT GCT TCA-3' (a 176-bp type 2:1 central probe); P9, 5'-G AAG TAC AAC ACC AGC ACG C-3', and P10, 5'-CTT GGC ACC AGT GAG GGG-3' (a 1,506-bp portion of the type 2:2 fimbrial subunit gene); and P11, 5'-AGG CCA TCA GCG TTG AGA AGA-3', and P12, 5'-AGA CCT CAG TGG CGG TCA-3' (a 182-bp type 2:2 central probe). The locations of these primer sequences with respect to the type 1 and type 2 fimbrial subunit genes are indicated in Fig. 1.

View larger version (15K): [in this window] [in a new window]   FIG. 1.   Schematic illustration of the fimP and fimA fimbrial subunit genes from A. naeslundii. DNA probes representing full-length and central (gray area) gene segments specific for different adhesin specificities were PCR amplified by using synthetic oligonucleotide primers specific for fimP from A. naeslundii T14V (genospecies 2), fimA from ATCC 12104T (genospecies 1), and fimA from P-1-N (genospecies 2, strain CCUG 33910). The nucleotide positions of all primers are indicated by arrowheads and labeled p1 through p12 (see Materials and Methods). Primers set as superscripts to position numbers were used to amplify full-length gene segments; primers set as subscripts to position numbers were used to amplify central gene segments. The central DNA probes were generated from a region of the gene sequences having comparably low homology and being devoid of highly conserved proline-containing segments. The overall nucleotide sequence identities between the three fimbrial subunit genes are indicated on the right. An asterisk marks the position of the BamHI cleavage site in the type 2:1 fimbrial subunit gene.

PCR. The PCRs were performed in 50-µl reaction mixtures containing 100 ng of DNA; 50 ng of each oligonucleotide primer; 2 U of Taq polymerase (Boehringer); 100 µM each dATP, dGTP, dCTP, and dTTP (deoxynucleoside triphosphate [dNTP] mixture; Boehringer); and 1× PCR buffer (10 mM Tris-HCl [pH 8.3], 50 mM KCl, 1.5 mM MgCl₂). DNA fragments were labeled with digoxigenin by replacing the dNTP mixture with the digoxigenin dNTP labeling mixture (Boehringer) in the second PCR amplification. Chromosomal DNA isolated from A. naeslundii T14V (type 1), ATCC 12104^T (type 2:1), and P-1-N (type 2:2) was used as the template for probe construction. The full-length gene fragments were amplified by using an initial cycle with denaturation at 94°C for 5 min, annealing at 59°C for 150 s, and extension at 72°C for 150 s, followed by a repeat of 33 cycles with denaturation at 94°C for 75 s, annealing at 59°C for 150 s, extension at 72°C for 150 s, and a final hold at 72°C for 7 min. The type 1 and type 2:1 central gene segments were amplified by using an initial cycle with denaturation at 94°C for 4 min, annealing at 63°C for 2 min, and extension at 72°C for 2 min, followed by a repeat of 29 cycles with denaturation at 94°C for 75 s, primer annealing at 63°C for 75 s, primer extension at 72°C for 75 s, and a final hold at 72°C for 7 min. The type 2:2 central gene segments were amplified in the same way except that the annealing temperature was decreased to 50°C.

Slot blot hybridization assay. Chromosomal DNA (3 µg) was transferred to nylon membranes (Hybond N+; Amersham) with a slot blot manifold filter system (Milliblot-S; Millipore, Västra Frölunda, Sweden) as described previously (2). Membranes were prehybridized in 5× SSC (0.75 M sodium chloride, 0.075 M sodium citrate)-0.02% N-lauroylsarcosine-0.1% SDS-1% blocking reagent (Boehringer) at 80°C for 5 h (high-stringency conditions). Following overnight hybridization in prehybridization solution containing probe DNA, the membranes were washed twice in 2× SSC-0.1% SDS for 5 min at room temperature and twice in 0.5× SSC-0.1% SDS (for type 1 and type 2:1 full-length and central probes) or 0.3× SSC-0.1% SDS (for type 2:2 central probe) for 15 min at 80°C. Additional rounds of hybridization and stringency washes were also performed under the same conditions except that the temperature was lowered from 80 to 50°C (low-stringency conditions). Hybridization was detected by using a digoxigenin DNA detection kit, as recommended by the manufacturer (Boehringer), scanned in a densitometer (GS-700 imaging densitometer; Bio-Rad, Hercules, Calif.), and analyzed with Molecular Analyst software (Bio-Rad). The degree of hybridization was scored from 0 to 6 according to the following densitometric values: score of 0 = a densitometric value of <0.01, 1 = 0.01 to <0.04, 2 = 0.04 to <0.10, 3 = 0.10 to <0.16, 4 = 0.16 to <0.22, 5 = 0.22 to <0.27, and 6 = 0.27.

Southern blot analysis. Chromosomal DNA (8 µg) was digested with BamHI or PstI, and DNA fragments were separated on 0.7% agarose gels. DNA was transferred to nylon membranes (Hybond N+; Amersham) as described previously (35). Membranes were prehybridized in 5× SSC-0.02% N-lauroylsarcosine-0.1% SDS-1% blocking reagent (Boehringer) at 80°C for 5 h (high-stringency conditions). Following overnight hybridization in prehybridization solution containing probe DNA, the membranes were washed twice in 2× SSC-0.1% SDS for 5 min at room temperature and twice in 0.5× SSC-0.1% SDS (for type 1 and type 2:1 full-length and central probes) or 0.3× SSC-0.1% SDS (for type 2:2 central probe) for 15 min at 80°C. Hybridization was detected by using a digoxigenin DNA detection kit, as recommended by the manufacturer (Boehringer).

Subcloning and nucleotide sequencing. PCR-amplified DNA fragments were purified with the Jetpure PCR purification kit (Saveen, Malmö, Sweden). Type 1 and type 2 full-length and central DNA fragments were cloned directly into the pGEM-T vector system (Promega, Madison, Wis.) in accordance with the manufacturer's instructions. The ligation mixture was transformed into E. coli JM109 competent cells, and appropriate transformants were selected on LB agar plates containing ampicillin (50 µg/ml), 5-bromo-4-chloro-3-indolyl--D-galactopyranoside (40 µg/mL; X-Gal), and isopropyl--D-thiogalactopyranoside (0.1 mM; IPTG). Plasmid DNA was isolated by miniprep DNA purification systems (Wizard; Promega) and sequenced by using the Pharmacia (Uppsala, Sweden) T7 sequencing system (37) and analyzed in 8 M urea-6% polyacrylamide gels.

Computer analysis. DNA and deduced amino acid sequence comparisons were performed by using the Sequence Analysis software package, version 8.1, from the Genetics Computer Group, University of Wisconsin, Madison.

Coaggregation. The coaggregation of streptococci (3 × 10⁹ cells/ml) and Actinomyces cells (3 × 10⁹ cells/ml), both suspended in coaggregation buffer (1.0 mM Tris-HCl, 0.1 mM Ca²⁺, 0.1 mM Mg²⁺, 0.02% NaN₃), was determined by visual inspection after mixing the cells as described previously (18).

Isolation of APRPs and statherin. Freshly collected parotid saliva from one individual homozygous for allelic APRP variants (PRP-1 and PIF-s) was separated on a DEAE-Sephacel column (15 by 1.6 cm; Pharmacia) by using a linear gradient of 25 mM to 1.0 M NaCl in 50 mM Tris-HCl (pH 8.0). The peak containing APRPs and statherin was concentrated by ultrafiltration on a Centriprep 10 concentrator (Amicon Inc., Beverly, Mass.) and separated by gel filtration (HiLoad 26/60 Superdex S-200 Prepgrade; Pharmacia) in 20 mM Tris-HCl-0.5 M NaCl (pH 8.0). Each of the resolved PRP-1-PIF-s, PRP-3-PIF-f, and statherin proteins were then finally purified on a Macroprep high Q column (15 by 1.6 cm; Bio-Rad) by using a linear gradient of 25 mM to 1.0 M NaCl in 50 mM Tris-HCl (pH 8.0). The purity and identity of APRPs and statherin were confirmed by SDS-PAGE, native alkaline electrophoresis, NH₂-terminal amino acid sequencing, and bacterial binding properties.

Hydroxyapatite assay. The adherence of [³⁵S]methionine-labeled bacteria (6 × 10⁴ cpm/ml; 5 × 10⁸ cells/ml) to purified proteins (5.0 µg/ml) adsorbed onto hydroxyapatite beads (BDH Chemicals Ltd., Poole, United Kingdom) was measured as described previously (16, 41).

	RESULTS

Top Abstract Introduction Materials & Methods Results Discussion References

Genetically related Actinomyces adhesin specificities. To determine the genetic relatedness of different binding specificities in A. naeslundii and A. odontolyticus, DNA fragments which span the known fimP and fimA fimbrial subunit genes of strains T14V (genospecies 2) and ATCC 12104^T (genospecies 1), respectively, were amplified by PCR (Fig. 1) and hybridized with DNA from Actinomyces isolates with defined binding specificities (Table 1). Isolates of A. naeslundii were positive for hybridization with the fimP and fimA full-length probes, irrespective of genospecies 1 or 2, type of APRP and GalNAc specificity, or tissue origin (teeth or buccal mucosa) (Table 1 and see Table 3). Isolates of genospecies 1 displayed stronger hybridization signals with the fimA probe than genospecies 2 did, while the opposite was true for the fimP probe. Isolates of A. odontolyticus, which binds to unknown structures, were positive with both probes, whereas Actinomyces israelii, Actinomyces meyeri, Actinomyces gerencseriae, Actinomyces georgiea, and E. coli were negative. Thus, A. naeslundii and A. odontolyticus may express a family of genetically related but distinct adhesin specificities.

A. naeslundii genospecies 1 exhibits a variant fimA gene associated with type 2:1 GalNAc specificity. To investigate the genetic basis for different types of GalNAc specificity, a DNA probe which spans the central segment of the fimA gene of strain ATCC 12104^T (genospecies 1) was amplified by PCR (Fig. 1) and hybridized with DNA from isolates of A. naeslundii with different types of GalNAc specificity (Tables 1 and 2). Isolates of A. naeslundii genospecies 1, which display GalNAc1-3Gal-O-ethyl-inhibitable coaggregation with S. oralis Ss34 and MPB1 (type 2:1 specificity), were positive with the probe irrespective of tooth (18 isolates) or buccal mucosa (2 isolates) origin. In contrast, isolates of A. naeslundii genospecies 2, which harbor APRP and another GalNAc specificity, were negative with the probe (63 of 63 isolates). Thus, A. naeslundii genospecies 1 appears to encode a variant fimA gene that confers type 2:1 GalNAc specificity.

A. naeslundii genospecies 2 exhibits a variant fimA gene associated with type 2:2 GalNAc specificity. To investigate the molecular basis for the variant GalNAc specificity of genospecies 2, essentially the entire fimA gene from the genospecies 2 strain P-1-N (CCUG 33910) was amplified by PCR, cloned, and sequenced (Fig. 1). This gene segment showed 74% nucleotide sequence identity to the known fimA gene of the genospecies 1 strain ATCC 12104^T (data not shown).

Variant fimP genes correspond to different types of type 1 APRP specificity. To characterize the molecular basis for different types of APRP specificity, a DNA probe which spans the central segment of the fimP gene was generated by PCR from the genospecies 2 strain T14V (Fig. 1). When used in hybridization assays, this central DNA probe hybridized with DNA from virtually all A. naeslundii isolates characterized by a preferential binding to APRPs over statherin (67 of 68 isolates), irrespective of genospecies (62 genospecies 2 isolates and 5 genospecies 1 isolates) or tissue origin (45 tooth, 21 buccal mucosa, and 1 tongue isolate). In contrast, the genospecies 2 strain ATCC 19246, displaying preferential binding to statherin over APRPs, was positive with the fimP full-length, but not with the central, probe (Table 3). Thus, A. naeslundii genospecies 2 may contain variant fimP genes that correspond to different types of APRP specificity.

APRP and GalNAc specificity in A. odontolyticus. Since we have demonstrated that genetic diversity within the fimP and fimA fimbrial structural genes correlates with different types of binding specificity, we aimed to use hybridization analysis with specific probes to characterize APRP and GalNAc specificity in A. odontolyticus (Tables 1 and 2). Isolates of A. odontolyticus were positive with both fimP and fimA full-length probes (19 of 19 isolates), irrespective of binding to unknown structures (17 tongue isolates), APRP and GalNAc (1 buccal mucosa and 1 tooth isolate), or to APRP alone (1 tongue isolate). However, only the isolate from buccal mucosa with APRP and type 2:2 GalNAc specificity was positive with the fimP and fimA central probes. These data suggest a further genetic heterogeneity in fimbrial subunit genes in A. odontolyticus.

Adhesin specificities among an independent reference collection of Actinomyces strains. We next characterized the binding properties present in an independent reference collection of Actinomyces strains, i.e., Actinomyces coaggregation groups A through F, which represent the different adherence properties of isolates of largely subgingival origin (28). Representative strains of groups A through F bound to APRPs, GalNAc, and unknown structures, and DNA from these isolates hybridized to the fimP and fimA full-length probes (Table 3).

Single type 1 and type 2 fimbrial gene copies. To exclude the possibility of multiple fimP and fimA genes contributing to genetic diversity, Southern blot hybridizations were used to demonstrate single fimP and fimA gene copies among randomly selected isolates (Fig. 2). The type 1 and type 2:2 central probes hybridized to single BamHI or PstI DNA fragments of chromosomal DNA from several isolates of A. naeslundii genospecies 2. The type 2:1 central probe hybridized to two BamHI DNA fragments of chromosomal DNA from four isolates of A. naeslundii genospecies 1. This is expected since a BamHI restriction site is located within the central region of the fimA gene of the genospecies 1 strain ATCC 12104^T (Fig. 1).

View larger version (59K): [in this window] [in a new window]   FIG. 2.   The type 1 and type 2 fimbrial subunits are encoded by single gene copies in Actinomyces isolates. Southern blot hybridization of chromosomal DNA from A. naeslundii isolates with the fimP type 1 central DNA probe (left panel: lane 1, strain B-1-K; lane 2, P-1-K; lane 3, T14V; and lane 4, LY7), the fimA type 2:1 central DNA probe (middle panel: lane 1, strain Pn-22-E; lane 2, Pn-6-GA; lane 3, P-5-N; and lane 4, ATCC 12104T), and the fimA type 2:2 central DNA probe (right panel: lane 1, strain P-1-K; lane 2, P-1-N; and lane 3, LY7). Chromosomal DNA was digested with BamHI prior to hybridization with either type 1 or type 2:1 DNA probes and with PstI prior to hybridization with the type 2:2 DNA probe. The sizes (in kilobases) of HindIII-digested bacteriophage lambda DNA standards (lanes kb) are indicated on the right.

The variant fimA and fimP genes conferring a given binding specificity are highly conserved within each Actinomyces genospecies. To gain further insights into the genetic diversity of fimA and fimP genes, central fimA and fimP gene fragments from isolates of A. naeslundii were amplified by PCR, cloned, and sequenced (Fig. 3). The fimP genes from five isolates of A. naeslundii genospecies 2, which bind preferentially to APRPs over statherin, displayed central gene segments with 98 to 100% nucleotide and deduced amino acid sequence identity to the known fimP gene. Similarly, the fimA genes from six isolates of A. naeslundii genospecies 1, which display type 2:1 GalNAc specificity, displayed central gene segments with 90 to 100% nucleotide and deduced amino acid sequence identity to the known fimA gene. The fimA genes of three isolates of genospecies 2, which display type 2:2 GalNAc specificity, had central gene segments with 92 to 100% nucleotide and deduced amino acid identity to each other. The fimP and fimA type 2:1 central gene segments had 42 to 51% nucleotide sequence identity and 28 to 43% deduced amino acid sequence identity; the fimP and fimA type 2:2 central gene segments had 44 to 50% nucleotide sequence identity and 26 to 38% deduced amino acid sequence identity. In contrast, the nucleotide and deduced amino acid sequence identities between the fimA type 2:1 and type 2:2 central segments were 70 to 75% and 71 to 81%, respectively. These data reveal a direct correlation between genetic diversity among fimP and fimA genes and the binding specificity mediated by the protein product encoded by these genes.

View larger version (12K): [in this window] [in a new window]   FIG. 3.   Alignment of the deduced amino acid sequences (in single-letter code) of central segments of the fimP and fimA type 2:1 and type 2:2 fimbrial subunit genes (see Fig. 1). Identical amino acids are indicated by gray shading, and those conserved in structure are indicated by a colon (:). Amino acids in boldface type are variable in fimbrial subunit sequences corresponding to the same binding specificity. The type 1 sequence data were collected from five isolates of genospecies 2 (strains B-10-K, B-1-K, P-1-K, P-3-K, and LY7), the type 2:1 sequence data are from six strains of genospecies 1 (strains P-3-N, P-5-N, Pn-1-GA, Pn-6-N, Pn-20-E, and Pn-22-E), and the type 2:2 sequence data are from a comparison of three strains of genospecies 2 (strains P-1-N, P-1-K, and LY7).

	DISCUSSION

Top Abstract Introduction Materials & Methods Results Discussion References

In the present study, we have used two independent Actinomyces reference collections of supra- and subgingival origin to extend our previous demonstration of two types of both APRP and GalNAc specificity in A. naeslundii and a yet-uncharacterized binding specificity in A. odontolyticus. We show that variant fimP and fimA fimbrial subunit genes confer the two types of APRP and GalNAc specificity and that a genetically related fimbrial adhesin may account for the binding of A. odontolyticus to unknown structures. Thus, structural variation in fimbria-associated proteins conferring adhesin specificity may account for the many tissues and animal hosts being colonized by Actinomyces species.

Our findings provide the following evidence that genetic variation in the fimP and fimA genes of A. naeslundii corresponds to different types of both APRP and GalNAc specificity. First, isolates with different types of APRP and GalNAc specificity were distinguished by DNA probes spanning the central portions of the fimA and fimP genes, while full-length probes were positive for hybridization with the isolates irrespective of type of binding specificity. Second, inverse hybridization signals with fimA and fimP full-length probes occurred between isolates with differing binding specificities (i.e., genospecies 1 versus 2). Third, the sequences of the fimA and fimP central gene segments were highly conserved among isolates with the same, but diversified between those with a variant, binding specificity. Furthermore, the different binding specificities observed were not due to a contribution of multiple genes, since randomly selected isolates contained only single fimA and fimP gene copies.

The present finding of variant fimA and fimP genes corresponding to different types of both APRP and GalNAc specificity may suggest the presence of a binding domain in the fimbrial subunit. This is reminiscent of the E. coli K88 and K99 major fimbrial subunits, both of which contain a domain for binding to host carbohydrate or protein structures (4, 24). Many bacterial adhesins constitute minor proteins distinct from the major structural subunit (21, 22), and similar to the situation for the minor Sfa adhesin of S fimbriae (17), structural variations in the major subunit could modulate the specificity of a separate, as-yet-uncharacterized adhesin in Actinomyces. Both extensive structural differences, as observed for PapG adhesins recognizing different glycolipid conformations (21, 22, 31, 44, 45), and single amino acid substitutions, similar to those described for different influenza virus binding specificities (46), could confer different binding specificities to Actinomyces species.

The binding of tongue isolates of A. odontolyticus to unknown structures in coaggregation with streptococci (18) may reflect a genetically related but functionally distinct fimbrial adhesin. Evidence for this is that all tongue isolates of A. odontolyticus, which produce fimbriae (18, 47), were positive with the full-length but not the central fimP and fimA probes. The fact that three A. odontolyticus isolates expressing APRP and GalNAc specificity were positive with the full-length probes while only one of those was positive with the central probes provides further arguments for a genetic variability among fimbrial subunit genes in A. odontolyticus.

The present association of variant fimbrial subunit genes with different types of APRP and GalNAc specificity may explain the intraoral tissue and animal tropisms of Actinomyces species (40, 41). For example, the different GalNAc1-3Gal-O-ethyl-inhibitable adherence patterns of genospecies 1 (ATCC 12104^T) and genospecies 2 (LY7) to oral epithelial cells (40) may suggest variation in GalNAc specificity as a contributing factor to the relative dominance of genospecies 2 on the buccal mucosa and that of genospecies 1 on the tongue (12, 32). Furthermore, the differing appearances of genospecies 1 and 2 in plaque formation and their distinct patterns of coaggregation with streptococci irrespective of tissue origin (teeth or buccal mucosa) may suggest variation in GalNAc binding specificity as a tool to establish specific ecological niches (28). Although the role of variation in APRP specificity is less well understood, APRPs and statherin are polymorphic proteins displaying allelic and posttranslational variants. Therefore, the weak binding of some isolates (group C and D strains and one tooth isolate) to the allelic APRP-1 variant but positive fimP hybridization signals may suggest either binding to other APRP variants or a repressed fimbrial gene expression. Nonetheless, in line with the absence of preferential binding to statherin of strain 19246, which originated from a human case of actinomycosis, in both Actinomyces collections, statherin binding seems to be a characteristic of Actinomyces isolates from the oral cavity of rats and hamsters (30).