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Associations between the expression of virulence factors and bacteriocins have been demonstrated in several bacterial pathogens, and in some instances, their genetic determinants have been localized to the same plasmid. For instance, it was shown that both botulinum toxin type G and bacteriocin production could be eliminated from certain Clostridium botulinum strains in association with the loss of an 81-MDa plasmid when cultures were grown at 44°C (6). Hemocin production in Haemophilus influenzae is found in 98% of strains producing type b capsule and not in any nontypeable strains (14). It was suggested that hemocin may play a role in nasopharyngeal colonization by assisting competition against commensal Haemophilus spp. In another study, pathogenic human Enterococcus faecalis strains were demonstrated to frequently produce both hemolysin and bacteriocin activities and the determinants were shown to be encoded by a transmissible plasmid (13). A unique feature of this two-component peptide system is its cytolytic activity against both prokaryotic and eukaryotic cells (2).

The simultaneous elimination of bacteriocin (BacR1) and exfoliative toxin B (ET-B) production from the phage group II strain Staphylococcus aureus U0007 was demonstrated by Warren and associates (26) by either incubation of the bacteria at elevated temperatures or treatment with ethidium bromide. They concluded that both products are encoded by a 37-kb plasmid. The same group of researchers then demonstrated in vitro transduction of the plasmid encoding ET-B into other S. aureus strains and suggested the possibility that a similar transfer occurs within the mixed microflora of the skin (18). They were later able to clone and sequence the gene responsible for the production of ET-B (9, 12). However, the determinant for BacR1 production was not identified.

Production of bacteriocin-like inhibitory activity by S. aureus has been reported on many occasions (21, 24), but primary-structure details are only available for staphylococcins C55 and C55, isolated from S. aureus C55 (16). The production of antibacterial activity by strain C55 was first reported by Dajani's group in 1970 (3). Those researchers partially purified an inhibitory agent from strain C55 and described it as a nondialyzable proteinaceous substance. We have recently reported that the majority of the inhibitory activity of strain C55 is due to the synergistic activity of the lantibiotics staphylococcins C55 and C55 (16). In the same communication, we demonstrated that the production of staphylococcins C55 and C55 is dependent on the presence of a 32-kb plasmid. Staphylococcins C55 and C55 have molecular masses of 3,339 and 2,993 Da, respectively. Amino acid composition analyses confirmed the presence of lanthionine and/or -methyllanthionine in both peptides, but the specific location and orientation of these unusual amino acids in lantibiotic molecules cannot be determined by conventional N-terminal amino acid sequencing.

In the present report, we establish that the bacteriocins produced by Dajani's strain C55 and Rogolsky's strain U0007 are identical and that this type of bacteriocin is widely distributed in phage group II S. aureus. Moreover, we demonstrate that the bacteriocin structural genes are closely associated with the ET-B determinant and are located on the same plasmid.

Cloning of genes encoding strain C55 lantibiotic production. The N-terminal sequence of the C55 peptide has previously been shown to be XXDhbNXFDhaLXDYWGNKGNWCTA, where X represents an unidentified amino acid residue and Dhb and Dha represent dehydrobutyrine and dehydroalanine, respectively (16). From this sequence, amino acids 10 to 15 (i.e., DYWGNK) were used to design a wobbled 17-mer oligonucleotide probe [5'-GA(CT) TA(CT) TGG GG(AGTC) AA(CT) AA-3']. The probe was labelled with [³²P]ATP by using T4 polynucleotide kinase as described by Sambrook et al. (20). Strain C55 was found to contain two plasmids with sizes of approximately 3.5 and 32 kb. A 6.5-kb PstI fragment of the 32-kb plasmid hybridized with the staphylococcin C55 probe by Southern hybridization. This fragment was cloned in pUC19 with Escherichia coli Dh5' as the host, and both strands of the plasmid insert were sequenced by the dideoxy-chain termination method.

Nucleotide sequence of strain C55 lantibiotic genes. The cloned fragment comprised 6,276 bp, and computer analysis revealed four open reading frames (ORFs) in the same orientation designated sacA, sacA, sacM1, and sacT (Fig. 1). Putative ribosomal binding sites were identified in front of sacA, sacA, and sacM1, and only a single base was found between sacM1 and sacT (Fig. 2).

View larger version (6K): [in this window] [in a new window]   FIG. 1.   Comparison of the organization of staphylococcin C55 ORFs with that of the putative gene cluster of lacticin 3147. (A) Organization of the ORFs designated sacA, sacA, sacM1, and sacT in a 6,276-bp PstI fragment. (B) Putative lacticin 3147 gene cluster (5).

View larger version (34K): [in this window] [in a new window]   FIG. 2.   Nucleotide sequence of the structural genes of staphylococcins C55 and C55. The deduced amino acid sequences of the ORFs are shown below the nucleotide sequence. Vertical arrows indicate the cleavage sites of propeptides. The termination codons are indicated by asterisks. Primers used for amplifications are underlined.

Characterization of sacA and sacA. The previously determined C55 peptide sequence was consistent with the deduced amino acid sequence of the sacA ORF (Fig. 3). The C55 propeptide starts at the first Cys residue in the predicted prepeptide. The presence of a Thr codon corresponding to the third amino acid residue in the propeptide and a Ser codon at the seventh amino acid residue agrees with the locations of Dhb and Dha residues on N-terminal sequencing of the mercaptoethanol-modified C55 peptide (16). The blank cycles (denoted by the letter X) for amino acid residues 1, 2, 5, and 9 probably represent components of lanthionine and -methyllanthionine residues, since they correlate with the presence of Thr, Ser, or Cys codons in the nucleotide sequence. The presence of a Cys component of lanthionine or -methyllanthionine at the N terminus of C55 differs from the arrangement of these modified amino acids in all other known class I lantibiotics. In all other cases, the Cys component is toward the C terminus. The calculated mass of C55, based on the predicted amino acids and the presence in the peptide of four lanthionine and/or -methyllanthionine amino acids and three dehydro amino acids, is 3,336 Da, which agrees closely with the actual mass of 3,339 Da determined by mass spectrometry.

View larger version (13K): [in this window] [in a new window]   FIG. 3.   Elucidation of the primary structure of staphylococcins C55 and C55. The first and third lines show the sequences derived by N-terminal amino acid sequencing (16). Dhb and Dha represent dehydrobutyrine and dehydroalanine. X represents unidentified cycles during Edman degradation. The second and fourth lines represent the amino acid sequences deduced from the DNA sequences. The arrows indicate cleavage sites.

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Comparison of sacA and sacA with the structural genes of other lantibiotics. Marked differences were observed when the structural genes sacA and sacA were compared with those of other known staphylococcal lantibiotics. All of the well-studied staphylococcal lantibiotics (epidermin, gallidermin, epilancin, Pep5, and epicidin) (8, 19) can be classified as class AI (4) or type FNLD (19) lantibiotics and neither staphylococcin C55 nor C55 is related to any of the lantibiotics in this group. However, the presence of Gly and Ala in the 2 and 1 positions of the C55 prepeptide is consistent with the cleavage sites of class AII or double-Gly-type lantibiotics (4, 19). The presence of Ala in positions 1 and 2 at the cleavage site of the C55 prepeptide has not been described before in double-Gly-type lantibiotics but does occur in mersacidin, a type B lantibiotic (1). A computer-aided homology search indicated that these two peptides have no homologies with other lantibiotics listed in the data banks, but both have very high homology with two putative lantibiotic peptides encoded by Lactococcus lactis DPC3147 plasmid pMRC01 (5, 15). Comparison of the deduced amino acid sequences of the sacA and ltnA ORFs gave 65.5% identity and 77.6% similarity. Also, the sacB- and ltnB-encoded peptides showed 44.6% identity and 63.1% similarity. These results indicate that strains C55 and DPC 3147 produce closely related two-component lantibiotic systems.

ORFs downstream of sacA and sacA. An ORF encoding a putative protein comprising 965 amino acids was found in the same orientation and 18 bp 3' to sacA (Fig. 2). This ORF, named sacM1, has some homology (20% identity and 38% similarity) with the lctM gene, located downstream of lctA, the structural gene for lactococcin DR (17) (now called lacticin 481). lctM encodes the protein that modifies the lacticin 481 propeptide. Based on the comparison of lantibiotic M genes done by Siezen et al. (22), some residues within the amino acid sequence of C55M1 correlate with conserved amino acids and segments found in other lantibiotic M gene products. A further ORF, sacT, identified downstream of sacM1 encodes a protein of 720 amino acids. This has strong homology with the genes for several transporters, including lctT, which have been shown to be involved in both the transport and the processing of this type of lantibiotic (7, 22).

Screening for etb and for bacteriocin production similar to that of strain C55. Fifty strains previously reported to be ET producers and belonging to phage group II (and including Rogolsky's strain U0007) and 15 phage group II strains negative for ET production were tested for bacteriocin production and for the presence of cross-immunity to the bacteriocin produced by strain C55 (Table 1). For specific amplification of sacA and sacA, primers AGC GTG GTG ATT CTT ATG and TCT GAT TTA TTT AGT TCT GGA T were designed by using the sequence given in Fig. 2. DNA extraction for PCR was done by the method of Unal et al. (25). The PCR amplification was performed in a total volume of 100 µl with each deoxyribonucleotide triphosphate at 200 µM and each primer at 1 µM in 1× reaction buffer. Each reaction mixture was heated to 72°C for 5 min before the addition of 2.5 U of Taq polymerase. A total of 30 cycles (1 cycle being 30 s at 94°C, 30 s at 48°C, and 1 min at 72°C) and a 5-min final extension at 72°C were performed on a DNA thermal cycler. The PCR products (499 bp) were analyzed by electrophoresis using a 2% agarose gel in Tris-acetate electrophoresis buffer and then stained with ethidium bromide. The ET-A and ET-B genes, eta and etb, were amplified by use of the primers described by Johnson et al. (10).

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Nucleotide sequence accession number. The nucleotide sequence reported here has been deposited in the GenBank nucleic acid sequence database under accession no. AF147744.