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Genomic Characterization of the Filamentous Integrative Bacteriophages RSS1 and RSM1, Which Infect Ralstonia solanacearum

Department of Molecular Biotechnology, Graduate School of Advanced Sciences of Matter, Hiroshima University, Higashi-Hiroshima 739-8530, Japan

Received 10 April 2007/ Accepted 30 May 2007

	ABSTRACT

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The genomic DNA sequences were determined for two filamentous integrative bacteriophages, RSS1 and RSM1, of the phytopathogen Ralstonia solanacearum. The 6,662-base sequence of RSS1 contained 11 open reading frames (ORFs). In the databases, this sequence showed high homology (95% identity) to the circular double-stranded DNA plasmid pJTPS1 (6,633 bp) isolated from a spontaneously occurring avirulent mutant of R. solanacearum. Two major differences between the two sequences were observed within RSS1 ORF7, corresponding to pIII, a minor coat protein required for host adsorption, and at the RSS1 intergenic (IG) region. The 9,004-base sequence of RSM1 showed 12 ORFs located on the same strand (plus strand) and 2 ORFs on the opposite strand. Compared with Ff-type phages, two insertions are obvious in the RSM1 replication module. Genomic DNA fragments containing the RSM integration junctions were cloned and sequenced from RSM lysogenic strain R. solanacearum MAFF211270. The att core sequence was identified as 5'-TGGCGGAGAGGGT-3', corresponding to the 3' end of the serine tRNA (UCG) gene. Interestingly, ORF14, located next to the attP site on the RSM1 genome, showed high amino acid sequence homology with bacterial DNA recombinases and resolvases, different from XerCD recombinases. attP of RSS1 is within a sequence element of the IG region.

	INTRODUCTION

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Ralstonia solanacearum is a soil-borne gram-negative bacterium known to be the causative agent of bacterial wilt in many important crops (14, 38). This bacterium has an unusually wide host range, with more than 200 species belonging to more than 50 botanical families (14). R. solanacearum strains represent a heterogeneous group subdivided into five races on the basis of their host range or six biovars on the basis of their physiological and biochemical characteristics (14). Recently, the complete genome sequence of R. solanacearum GMI1000 was reported (31). The 5.8-Mbp genome is organized into two replicons, a 3.7-Mbp chromosome and a 2.1-Mbp megaplasmid. The genome encodes a total of 5,129 predicted proteins, many of which are potentially associated with a role in pathogenicity. To accelerate comprehensive functional analyses of the pathogenicity of this pathogen, efficient molecular biological tools for R. solanacearum are required.

Very recently, Yamada et al. (39) detected and isolated various kinds of bacteriophage that specifically infect races of R. solanacearum. These phages may be useful as a tool for molecular biological studies of R. solanacearum pathogenicity. They could also be used for specific and efficient detection of harmful pathogens in cropping ecosystems, as well as growing crops. Two of them, RSM1 and RSS1, were characterized as Ff-like phages (inoviruses) on the basis of their particle morphology, genomic single-stranded DNA (ssDNA), and infection cycle. Despite their similar filamentous morphology, their genome sizes (9.0 kb for RSM1 and 6.6 kb for RSS1) and genome sequences were different. Strains of R. solanacearum that were sensitive to RSM1 were resistant to RSS1 and vice versa. Interestingly, all 15 strains of R. solanacearum tested contained RSS1-related sequences in their genomes and the RSS1 hybridization patterns coincided well with the taxonomical grouping of these strains. RSS1 infection was shown to enhance the virulence of strain C319 (race 1). Similarly, 6 of the 15 strains tested showed strong hybridization signals for RSM1-related sequences in their genomes. There were two types of RSM1-related sequences, A and B, distinguished by restriction fragmentation pattern, and only strains of type B could serve as hosts for RSS1 infection. Of these, at least one strain, MAFF211270 (type A), contained a lysogenic RSM1-like phage and occasionally produced phage particles (39). These results clearly demonstrate the temperate phage nature of RSM1. Other filamentous Ff-like phages known to have a lysogenic cycle include Xanthomonas campestris phages Cf1c (22), Cf1t (20, 21), Cf16v1 (7), and Lf (24); Xylella fastidiosa phage Xff1 (35); Yersinia pestis phage CUS-2 (11); and Vibrio cholerae phages VGJ (5) and CTX (18). These host bacteria are pathogenic for plants and animals, and the phages are frequently involved in pathogenesis.

In general, the genomes of Ff phage are organized in a module structure in which functionally related genes are grouped (15, 30). Three functional modules are always present. The replication module contains the genes encoding rolling-circle DNA replication and ssDNA binding proteins, gII, gV, and gX (27). The structural module contains genes for the major (gVIII) and minor (gIII, gVI, gVII, and gIX) coat proteins, and gene gIII encodes the host recognition or adsorption protein pIII (2). The assembly-and-secretion module contains the genes (gI and gIV) for morphogenesis and extrusion of the phage particles (26). Gene gIV encodes protein pIV, an aqueous channel (secretin) in the outer membrane through which phage particles exit from the host cells. Some phages encode their own secretins, but others use host products (8). In addition, some phages encode transcriptional repressors, like RstR of CTX and vpf122 of Vf22, which regulate the expression of other phage genes (6, 19). In the lysogenic filamentous phages such as CTX, two chromosome-encoded site-specific recombinases (XerC and XerD) are known; they catalyze recombination between the phage attachment site (attP) and the chromosome attachment site (attB) inside the site-specific recombination site dif of the host chromosome (18). Other lysogenic filamentous phages, including those described above, seem to use XerCD recombinases in a similar way.

	MATERIALS AND METHODS

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Bacteria and phages. Strains of R. solanacearum were obtained from the following culture collections. Strains M4S, MAFF106611, and MAFF211270 were from the Leaf Tobacco Research Center, Japan Tobacco Inc., and the National Institute of Agrobiological Sciences, Japan, respectively. Strain C319 (10) was kindly donated by N. Furuya, Kyushu University, Fukuoka, Japan. The bacterial cells were cultured in CPG medium (17) at 28°C with shaking at 200 to 300 rpm. Phages were propagated and purified from single-plaque isolates. Routinely, phages RSS1 and RSM1 were propagated with strains C319 and M4S as the host, respectively. An overnight culture of bacterial cells grown in CPG medium was diluted 100-fold with 100 ml fresh CPG medium in a 500-ml flask. To collect sufficient amounts of phage particles, a total of 2 liters of bacterial culture was grown. When the cultures reached an optical density at 600 nm of 0.1, the phage was added at a multiplicity of infection of 0.01 to 0.05. After further growth for 16 to 18 h, the cells were removed by centrifugation with an R12A2 rotor in a Hitachi himac CR21E centrifuge at 8,000 x g for 15 min at 4°C. The supernatant was passed through a 0.45-µm-pore-size membrane filter, followed by precipitation of the phage particles in the presence of 0.5 M NaCl and 5% polyethylene glycol 6000. Phage preparations were stored at 4°C until use. Escherichia coli XL10 Gold and pBluescript II SK(+) were obtained from Stratagene (La Jolla, CA).

DNA manipulations and sequencing. Standard molecular biological techniques for DNA isolation, digestion with restriction enzymes and other nucleases, and construction of recombinant DNAs were used according to Sambrook and Russell (32). Phage DNA was isolated from the purified phage particles by phenol extraction. In some cases, extrachromosomal DNA was isolated from phage-infected R. solanacearum cells by the minipreparation method (3). Replicative-form (RF) DNA for sequencing was isolated from host bacterial cells infected with RSS1 or RSM1 and partially digested with Sau3AI. DNA fragments of 1.0 to 4.0 kbp were recovered from the agarose gels after electrophoretic separation and ligated to the BamHI site of pBluescript II SK(+). After transformation into E. coli XL10 Gold cells, random clones were isolated for nucleotide sequencing. The DNA sequences of both strands were determined throughout, with a total coverage of 5.0x. Computer-aided assembly of the nucleotide sequence data was performed with a DNASIS (version 3.6) program (Hitachi Software Engineering Co., Ltd.). Potential ORFs larger than 80 bp were identified with the online program Orfinder (http://www.ncbi.nlm.nih.gov/gorf/gorf.html) and the DNASIS program. Sequence alignment was performed with the ClustalW program. To search for signal peptide cleavage sites and transmembrane domains, the online programs SignalP (http://genome.cbs.dtu.dk) and SOSUI (http://sosui.proteome.bio.tuat.ac.jp) were used. For prediction of RNA and DNA secondary structures, the Pairfold software was used (http://www.rnasoft.ca/). To assign possible functions to the ORFs, searches of the databases were done with the FASTA, FASTX, BLASTN, and BLASTX programs (1).

An autonomously replicating plasmid was constructed from RSS1 DNA as follows. Approximately 2,160 bases of RSS1 DNA lacking the modules for structural proteins and morphogenesis (ORF4 to ORF11) was amplified by PCR with a forward primer, 5'-CGG AAT TCT ATC CGG AGT AAC GA AAA G, corresponding to the 3' end of orf11 and a reverse primer, 5'-ATG GAA TTC TCC TTG AGA TGG AGG TTG AG, corresponding to the 5' end of orf4. Twenty-five rounds of PCR were performed with RF DNA (1 ng) of RSS1 as a template under the standard conditions in a MY Cycler (Bio-Rad). After digestion with EcoRI at the primer sites, the amplified fragment was connected to a Km^r cassette cut out with EcoRI from plasmid pUC4-KIXX (Amersham Biosciences). It was then introduced into cells of R. solanacearum MAFF106611 by electroporation by using a Gene Pulser Xcell (Bio-Rad) with a 2-mm cell at 2.5 kV according to the manufacturer's instructions. Transformants were selected on CPG plates containing 15 µg/ml kanamycin (Meiji Seika, Tokyo, Japan).

In a similar way, an autonomously replicating plasmid (pRSM11) was constructed from RSM1 DNA as follows. An approximately 2.4-kb portion of RSM1 DNA containing ORF1 to ORF8 was amplified by PCR with a 21-base forward primer (P1), 5'-CTG CTG CAG CAG GAA TTC AAG, corresponding to the 3' end of orf14 (with an EcoRI site added) and a 21-base reverse primer (P2), 5'-GTA CCA CCG GTC GTG GTC TGA, corresponding to the 3' end of orf8 (Fig. 1C). Another fragment of RSM1 DNA approximately 3.2 kb in size, containing orf11 and orf12, was amplified by PCR. The primers were a 20-base forward primer (P3), 5'-CAG TCC GCG TTC AAC TCG TT, corresponding to the 3' end of orf10 and a 21-base reverse primer (P4), 5'-CGC GAT CCG AAT TCA AAT GAG, corresponding to the 5' end of orf13 (with an EcoRI site added). Both 2.4-kb and 3.2-kb PCR products were blunt ended with T4 DNA polymerase and phosphorylated with T4 polynucleotide kinase. After digestion with EcoRI at the primer sites, the DNA fragments were mixed with a Km^r cassette (with EcoRI sites at both ends) and treated with T4 DNA ligase. The reaction mixture was introduced into the cells of R. solanacearum M4S by electroporation as described above.

View larger version (16K): [in this window] [in a new window]   FIG. 1. Genomic organization of bacteriophages RSS1 and RSM1. Linear ORF maps of E. coli phages M13 (A), RSS1 (B), and RSM1 (C) are compared. ORFs or genes are represented by arrows oriented in the direction of transcription. The functional modules for replication (R), structure (S), and assembly-secretion (A-S) are indicated according to the M13 model (26). ORF sizes (in amino acids) are in parentheses. The region containing the attP sequence is also indicated. Most of the gene function assignments for RSS1 and RSM1 are still putative. Arrows P1 and P2 in panel B and P1 to P4 in panel C indicate primers used in PCR.

Southern blot hybridization. Genomic DNA of R. solanacearum cells was prepared by a standard method according to Ausubel et al. (3). After digestion with various restriction enzymes, DNA fragments were separated by agarose gel electrophoresis and blotted onto a nylon membrane (Biodyne; Pall Gelman Laboratory, Closter, NJ). They were then hybridized with a probe (RSS1 or RSM1 genomic DNA), labeled with fluorescein (Gene Images Random Prime labeling kit; Amersham Biosciences, Uppsala, Sweden), and detected with a Gene Images CDP-Star detection module (Amersham Biosciences). Hybridization was performed in buffer containing 5x SSC (1x SSC is 0.15 M NaCl plus 0.015 M sodium citrate), 0.1% sodium dodecyl sulfate (SDS), and 5% dextran sulfate for 16 h at 65°C. The filter was washed at 60°C in 1x SSC-0.1% SDS for 15 min and then in 0.5% SSC-0.1% SDS for 15 min with agitation according to the manufacturer's protocol. The hybridization signals were detected by exposing the filter to X-ray film (RX-U; Fuji Film, Tokyo, Japan).

SDS-polyacrylamide gel electrophoresis (SDS-PAGE) and peptide sequencing. Purified phage particles were subjected to SDS-PAGE according to Laemmli (23). For the separation of small proteins, Tricine-SDS-PAGE was performed according to the method of Schagger and von Jagow (33). The separated proteins were transferred to polyvinylidene difluoride nylon membranes (Immobilon; Nihon Millipore K.K., Tokyo, Japan) with a semidry transfer cell (Bio-Rad, Hercules, CA). Each protein band was subjected to N-terminal peptide sequence analysis on a protein sequencer (model 492; Applied Biosystems) as described by Songsri et al. (36). The UniProt and GenBank databases were searched for sequences homologous to the amino acid sequences obtained.

Nucleotide sequence accession numbers. The sequence data for RSS1 and RSM1 have been deposited in the DDBJ database under accession no. AB259124 and AB259123, respectively.

	RESULTS

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Nucleotide sequence analysis of the RSS1 genomic DNA. The genome of RSS1 was 6,662 nucleotides (nt) long (DDBJ accession no. AB259124) with a GC content of 62.6%, which is comparable to that of R. solanacearum GMI1000 (66.97%) (31). There were 11 ORFs located on the same strand (Fig. 1B). Frequently, the termination codon of the preceding gene overlapped the initiation codon of the following gene. The coding sequence occupied by these ORFs accounted for 91.6% of the total RSS1 sequence. The 11 ORFs showed similarity to known gene sequences, as shown in Table 1. The circular double-stranded DNA plasmid pJTPS1 found in one strain of R. solanacearum (DDBJ accession no. AB015669) showed significant nucleotide sequence similarity to the RSS1 DNA. The size of pJTPS1 is 6,633 bp, 29 bp smaller than that of RSS1. The nucleotide sequence identity of the two DNAs was 95%. Figure 2A shows the alignment of ORFs and a matrix comparison of the RSS1 and pJTPS1 sequences, indicating two major differences located around RSS1 nucleotide positions 2674 to 3014 and 6632 to 6657. The former region was included in the large ORF7 coding region (pIII), and the latter corresponded to the intergenic (IG) region.

View this table: [in this window] [in a new window]   TABLE 1. Predicted ORFs found in the RSS1 genome

View larger version (27K): [in this window] [in a new window]   FIG. 2. Comparison of the RSS1 genomic DNA and plasmid pJTPS1 DNA. (A) ORF alignment and matrix comparison between RSS1 genomic DNA (6,662 bases) and plasmid pJTPS1 DNA (6,633 bp; from position 3947 in the complementary sequence with DDBJ accession no. AB015669) sequences. Gray shading indicates the significant amino acid or nucleotide sequence similarity between the two DNAs. In a matrix comparison between RSS1 (across) and modified pJTPS1 (down), 15 matches between 15 nucleotide sequences are marked by dots (DNASIS). The nucleotide sequence identity between the two DNAs was 95%. Two regions containing extended changes are shown by circles (RSS1 positions 2674 to 3014 and 6632 to 6657). ORFs are indicated along the RSS1 sequence. (B) Nucleotide sequence alignment of the RSS1 (positions 6505 to 20) and pJTPS1 (positions 3772 to 3966 in the complementary sequence) DNA IG regions. The coding region of ORF1 is boxed. Underlined are the Shine-Dalgarno sequences. Arrows indicate the regions having potential to form hairpin structures. (C) A model to show repetition of sequence elements (arrow) in the IG region changed between the RSS1 and pJTPS1 DNAs. The asterisk on the RSS1 sequence shows the position of integration on the C319 genomic DNA. (D) Formation of an autonomously replicating plasmid from RSS1 DNA. All Kmr transformants (lanes 1 to 4) harbored plasmid pRSS11, from which a 1.5-kbp Kmr cassette was cut out by EcoRI digestion. ssDNA molecules that were sensitive to S1 nuclease digestion were also observed. ccc, covalently closed circular; oc, open circular.

According to the homology shown in Table 1, a putative module organization of RSS1 can be depicted as shown in Fig. 1B. The RSS1 genes fit well with the general arrangement of Ff-like phages. A survey of the databases for amino acid sequences of some RSS1 ORFs revealed significant homology to Ff-like phage proteins such as ORF2 (pII homologue), ORF4 (pVIII homologue), ORF7 (pIII homologue), ORF8 (pVI homologue), and ORF9 (pI homologue). ORF11 might be involved in the virulence-enhancing effects (39) because pJTPS1 with a corresponding ORF disrupted by an insertion transforms bacterial cells to nonpathogenicity (28). Further information is required to exactly assign a biological function to each ORF of RSS1.

The six ORFs detected on the opposite strand of plasmid pJTPS1 (Fig. 2A) overlap the possible functional phage modules of RSS1 and do not accord with the codon usage that is well conserved among the RSS1 plus strand genes. For example, codons AAG (Lys), GAG (Glu), and ACG (Thr) are predominant in the phage genes (accounting for 82.2%, 70.8%, and 60.8% of the corresponding amino acids, respectively), whereas they are relatively rare in the opposite ORFs (42.9%, 30.1%, and 37.9%, respectively). These ORFs did not show any significant sequence homology with known proteins in the databases. These results suggest that pJTPS1 may have been derived from a RSS1-like phage, followed by changes in the phage DNA.

Relationship between RSS1 and pJTPS1. Compared with pJTPS1, two major different regions in the RSS1 DNA were recognized (Fig. 2B). One region (RSS1 positions 2674 to 3014) corresponded to ORF7, putatively encoding pIII, which is a minor coat protein at one end of the phage particle required to recognize and adsorb to host cells (26, 27). The other extended change was found at positions 6632 to 6657, corresponding to the IG region highly conserved in other Ff-like phages (27). This region may be involved in the rolling-circle DNA replication mechanism, producing phage genomic ssDNA molecules. Nucleotide changes in the corresponding region between the RSS1 and pJTPS1 DNAs are not simple; within a 30-base region of the RSS1 DNA, 17 bases are added and 4 bases are substituted in pJTPS1 (Fig. 2A). This addition can be explained by repetition of a RSS1 sequence element in pJTPS1, as shown in Fig. 2C. Downstream of this changed region, there is a possible Shine-Dalgarno sequence (GCGA/GTGG), followed by ORF1, suggesting that this region may function as a promoter of ORF1 and affect its expression in pJTPS1.

Formation of an autonomously replicating plasmid from the RSS1 DNA. To verify the replication origin possibly present around this IG region, an autonomously replicating plasmid was derived from the RSS1 DNA. A one-third portion (approximately 2,160 bases) of the RSS1 DNA that lacks the modules for structural proteins and morphogenesis (ORF4 to ORF11) was amplified by PCR with a 27-base forward primer corresponding to the 3' end of orf11 and a 29-base reverse primer corresponding to the 5' end of orf4. After digestion with EcoRI at the primer sites, the amplified fragment was connected to a Km^r cassette of approximately 1.5 kbp cut out from pUC4-KIXX with EcoRI. The resulting plasmid of approximately 3.7 kbp (pRSS11) was introduced into R. solanacearum cells by electroporation. It was stably maintained (100% retained after 100 generations without kanamycin) in a single copy in these cells, indicating that the region between the 3' end of orf11 and the 5' end of orf2 may contain the RSS1 DNA replication origin. Interestingly, nuclease S1-sensitive ssDNA molecules of the plasmid were detected in some of the transformed cells (Fig. 2D).

Integration of RSS in R. solanacearum strain C319. In our previous Southern blot hybridization experiments, we detected RSS1-related sequences in the genomic DNAs of all 15 strains of R. solanacearum (39). To characterize such sequences, 2.7-kbp and 1.2-kbp HincII bands of strain C319 which showed strong hybridization signals were cloned and sequenced. Their sequences exactly coincided with that of RSS1 (data not shown), indicating an integration of RSS1 in strain C319. The RSS1 integration site was determined by inverse PCR as follows. After cyclization with DNA ligase of EcoRI fragments of C319 genomic DNA (there is no EcoRI site in the RSS1 DNA), 27-mer oligonucleotides of the RSS1 sequence were arbitrarily set for forward and reverse primers in PCR. When the forward primer was S-6450F (5'-GCC GAT GCT ACG CTG CTC AGA ACA ACC-3') and the reverse primer was S-1399R (5'-CAT CCA TGT TGC CAA CCC ACG TCT TGG-3'), a 3.7-kbp PCR product was obtained. The nucleotide sequence determined for this fragment revealed that this 3.7-kbp sequence contained both junctions of RSS1 integration, as shown in Fig. 3A and B. There is only one overlapping base (A) of the RSS1 sequence between the two junctions. The RSS1 sequence at the integration site corresponds to position 6629 in the IG region, 34 nt upstream from ORF1, which is within the region different from pJTPS1 (indicated by an asterisk in Fig. 2C).

View larger version (14K): [in this window] [in a new window]   FIG. 3. Junctions of integrated RSS1 DNA in the lysogenic strain R. solanacearum C319 genome. (A) Partial sequence of the 3.7-kbp PCR product containing the right junction of RSS1 integration on the strain C319 genomic DNA. The sequence is compared with the RSS1 sequence. (B) Partial sequence of the 3.7-kbp PCR product containing the left junction of RSS1 integration on the strain C319 genomic DNA. The sequence is compared with the RSS1 sequence. (C) PCR primers for the production of pJTPS1 DNA from M4S chromosomal DNA and ligation for self-cyclization. According to the sequence of the RSS1 host integration site, a 41-base forward primer and a 45-base reverse primer were set. After PCR, a band with the expected size was isolated, phosphorylated with polynucleotide kinase, ligated with DNA ligase, and introduced into the cells of strain M4S by electroporation.

pJTPS1 corresponds to the RF of a RSS-type phage.

Nucleotide sequence analysis of the RSM1 genomic DNA. The genome of RSM1 was 9,004 nt long (DDBJ accession no. AB259123) with a GC content of 59.9%, which is lower than that of R. solanacearum GMI1000 (66.97%) (31). There were 12 putative ORFs located on the same strand and two on the opposite strand (Fig. 1C). In contrast to RSS1, overlapping between the termination codon of the preceding gene and the initiation codon of the following gene was rare. The coding sequences occupied by these ORFs accounted for 83.0% of the total RSM1 sequence. Assignment of gene functions to these ORFs by FASTA, FASTX, BLASTN, and BLASTX searches revealed that 10 ORFs showed homology to known gene sequences (Table 2). Since RSM1 ORF1 corresponded to p12J ORF1, which was described as a possible ssDNA-binding protein, we designated this ORF the first ORF in the possible gene organization according to the Ff phage model (27). On the basis of homology, three ORFs were included in a putative replication module and seven ORFs (ORF4 to ORF10) were included in the structure module, as shown in Fig. 1C. There was homology between RSM1 ORF12 and Rep proteins of various bacteria and plasmids. It was found that the plus-strand ssDNA was generated from plasmid pHT926 by a rolling-circle mechanism like phages (9). Because no ORF with obvious homology with pII was found on the RSM1 genome, a protein encoded by ORF12 may have an equivalent function. There is a wide gap (IG region) between ORF11 and ORF12. Two remaining ORFs (ORF13 and ORF14) are on the opposite strand and show amino acid sequence similarity to a proline-rich transmembrane protein and a DNA recombinase, respectively (Table 2). Compared with the conserved gene arrangement of Ff-like phages, the RSM1 genes can be drawn as shown in Fig. 1C. Here, ORF13 and ORF14 are inserted between ORF11, corresponding to pII as a replication protein, and ORF1, corresponding to an ssDNA-binding protein like pV in the putative replication module. There are two additional ORFs (ORF2 and ORF3) between the replication and structural modules. No functions are known for these ORF-encoded proteins.

View this table: [in this window] [in a new window]   TABLE 2. Predicted ORFs found in the RSM1 genome

Formation of an autonomously replicating plasmid from RSM1 DNA.

Integration of RSM in R. solanacearum strain MAFF211270. In our previous experiments, 6 of the 15 strains of R. solanacearum tested showed RSM1-related sequences on the genomic DNA in Southern blot analysis (39), suggesting the temperate phage nature of RSM1. In fact, RSM1 phage plaques appeared spontaneously from strain MAFF211270, one of the hybridizing strains. Southern blot analysis of HincII fragments of strain MAFF211270 genomic DNA revealed five RSM1-hybridizing bands, two of which (a 4.3-kbp band and a 3.5-kbp band) were expected to contain junctions of integrated RSM1-like DNA, judging by the relative intensities of the hybridization signals and their large sizes. These bands were cut from the gel, ligated to pBluescript II SK+, and cloned into E. coli, and their entire nucleotide sequences were determined. By comparing their nucleotide sequences with that of RSM1 DNA, it was found that one junction was located on the 4.3-kbp fragment (approximately 1.5 kbp from one end, Fig. 4A) and the other was located at a position approximately 1.4 kbp from one end of the 3.5-kbp fragment (Fig. 4B). The two junction sequences of the RSM1-like phage overlapped by the 13-bp sequence 5'-TGGCGGAGAGGGT-3' (Fig. 4C). This sequence (attP) corresponds to positions 8544 to 8556 of the RSM1 DNA, located between ORF14 and ORF1. Its nucleotide sequence showed no similarity to att sequences known for various Ff-like phages, including CTX, VGJ, VSK, Vf33, f237, LF, and Cf1c (5), but is identical to the 3' end of the host R. solanacearum gene for serine tRNA (UCG) in the reverse orientation (Fig. 4D), suggesting that this tRNA gene serves as attB on the host genome. This RSM-R. solanacearum integration system is obviously different from that mediated by host XerCD recombinases (18) suggested for other lysogenic filamentous phages (5).

View larger version (19K): [in this window] [in a new window]   FIG. 4. Junctions of integrated RSM1 DNA in the lysogenic strain R. solanacearum MAFF211270 genome. (A) Partial sequence of the 4.3-kbp HincII fragment containing attL of the strain MAFF211270 genomic DNA. The sequence is compared with the RSM1 sequence. (B) Partial sequence of the 3.5-kbp HincII fragment containing attR of the strain MAFF211270 genomic DNA. The sequence is compared with the RSM1 sequence. (C) Comparison of the attB, attP, attL, and attR sequences. The core sequences are shown by capital letters. (D) For sequence comparison, the serine tRNA (UCG) structure is also shown, along which a part of the attB sequence is aligned (indicated by shaded letters).

Characterization of the coat proteins and identification of their genes on the RSS1 and RSM1 genomes.

When purified RSM1 particles were subjected to SDS-PAGE on a 10% polyacrylamide gel, six bands (80 kDa, 66 kDa, 40 kDa, 27 kDa, 25 kDa, and 10 kDa) were separated (data not shown). The major band (10 kDa) was separated into two bands by Tricine (16%)-SDS-PAGE. The major capsid band corresponding to 6.0 kDa was subjected to N-terminal peptide sequence analysis. The first seven amino acid residues could be determined as QTTTGGT, which coincided with the amino acid sequence of RSM1 ORF8 (positions 22 to 27). This result confirmed the gene arrangement inferred from the homology search data (Fig. 1C). Mature molecules of the major coat protein of 6.0 kDa consisted of 51 aa, and a possible leader sequence of 20 aa was cleaved from the precursor protein, which coincided with the prediction of the SignalP program (data not shown).

	DISCUSSION

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Integration of phage genomes into the host genome. Compared with the RSS1 genome, the RSM1 genome (9,004 bases) is approximately 33% larger. This is mainly a result of an extended IG region between ORF11 (pI) and ORF12 and the presence of two additional ORFs (ORF13 and ORF14) located in reversed orientation in the putative regulatory module (Fig. 1C). No information is available about the biological significance of the IG region, which has an 80-bp region containing 80% GC (positions 5951 to 6030). The RSM1 attP sequence determined as 5'-TGGCGGAGAGGGT-3', identical to the 3' end of the host serine tRNA (UCG) gene in the reversed orientation, was shown to be located next to ORF14. To our knowledge, the integration process of lysogenic filamentous phages generally involves site-specific recombination between the attP site of the phage and the attB sequence inside the dif site of the host chromosome. Phages exploit the XerC and XerD recombinase/resolvase of their host to integrate themselves into the bacterial genome (18). Most lysogenic filamentous phages, such as CTX and VGJ of V. cholerae; Cf1c, Cf1t, and Lf of X. campestris; Xff1 of X. fastidiosa; and CVS-2 of Y. pestis, seem to use XerCD recombinases of their hosts and share attP sites with similar sequences (5). However, the RSM1 attP core sequence is quite different from that of these phages, for example, 5'-TTTCGCATAATGTATA-3' for Lf (accession no. X70328). This may suggest a different mechanism involved in the RSM1-R. solanacearum integration system. It is well established that various kinds of temperate phages and plasmids use tRNA genes as their integration sites on host bacterial chromosomes (4, 12, 34). In such cases, a phage- or plasmid-encoded site-specific recombinase or integrase mediates integrative recombination. As seen in many P2-like phages, including P4, 186, R73, and CTX, the 3' ends of tRNA genes serve as attP genes and are closely associated with the integrase (int) gene (13, 25, 29, 37). For RSM1, we suggest a possible involvement of phage-encoded functions for recombination such as ORF14 located next to the attP site. This ORF showed significant amino acid sequence homology to the resolvase of Pelodictyon phaeoclathratiforme (accession no. Q3VJH7, FASTA score of 582, E value of 4.4e-32) and the DNA invertase/recombinase of Marinobacter aquaeolei (accession no. Q36TJ9, FASTA score of 556, E-value of 2.8e-30). This is the first case of possible integration of a filamentous phage into a host tRNA gene (attB) by a phage-encoded integrase.

In addition to RSM1, we also demonstrated the integration of RSS1-like phages. The RSS1 sequence at the integration site determined in strain C319 corresponds to position 6629 in the IG region, 34 nt upstream from ORF1. This phage site for integration appears to be specific because pJTPS1 is also integrated at the same approximate position in strain M4S. The nucleotide sequence around this position in RSS1, 5'-CGC CTG CTA GAA TAT AAC CGA TTA, is not repeated at the junctions in the host genome and does not show any significant homology with the core sequence of att sites involved in the XerCD recombinase/resolvase integration (18). The detailed mechanism for host integration of RSS-type phages is largely unknown.

Host selection by RSS1 and RSM1. Bacteriophages RSS1 and RSM1 recognize different strains of R. solanacearum as hosts. Selective recognition of hosts with different types of pili was also reported for filamentous phages Pf1 and Pf3 of Pseudomonas aeruginosa (16). Phage Pf1 was shown to bind to the type IV PAK pilus, whereas the RP4 pilus is the target of Pf3. The amino acid sequences of the pIII proteins, which are responsible for pilus recognition, are quite different between the two phages. However, the D1-D2-D3 domain structure conserved in Ff phages is also retained in both Pf1 and Pf3, indicating the conserved mechanisms of phage-host pilus interaction among a wide range of filamentous phages. Putative ORFs for pIII of RSS1 (ORF7) and RSM1 (ORF9) were identified in the structural module of their genomes (Fig. 1). Characteristic D1 and D3 domains were predicted in both ORFs, but the amino acid sequences were different from each other. These pIII proteins may interact with different (exclusive) receptors, pili on the host cells, resulting in the unique host specificity. In this context, it is interesting that the pJTPS1 phage, as demonstrated in this work, infects R. solanacearum strains that are also sensitive to RSM1 but does not infect host strains of RSS1. The overall nucleotide sequence of phage pJTPS1 is very similar to that of RSS1 DNA, with variations in the pIII region and the IG region. In the pJTPS1 pIII coding region, approximately 360 nt in the middle portion are changed. This results in a pIII (ORF C5) with 15 fewer aa and more than 100 aa substitutions in the D2 domain of the protein. The N-terminal and C-terminal regions are unchanged. The changed domain of pIII might be responsible for discriminating the pilus type. Our previous Southern blot hybridization experiments revealed the frequent occurrence of RSS1-related sequences in the genome of R. solanacearum strains irrespective of phage RSS1 sensitivity. The hybridizing band patterns coincided well with phylogenetic groups of the bacterial strains. From these results, we speculate that RSS-type phages with different host specificities (or a different pIII genes) frequently infect and are integrated into a variety of strains of R. solanacearum. The RSS1-R. solanacearum system may provide a good opportunity to understand the molecular mechanism of pIII-pilus interaction and dynamic changes in their structures.

	ACKNOWLEDGMENTS

 
We thank Naruto Furuya and the Leaf Tobacco Research Center, Japan Tobacco Inc., for providing R. solanacearum strains C319 and M4S, respectively.

This study was supported by the Industrial Technology Research Grant Program in 04A09505 from the New Energy and Industrial Technology Development Organization (NEDO) of Japan.

	FOOTNOTES

 
* Corresponding author. Mailing address: Department of Molecular Biotechnology, Graduate School of Advanced Sciences of Matter, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima 739-8530, Japan. Phone and fax: 81-82-424-7752. E-mail: tayamad{at}hiroshima-u.ac.jp

Published ahead of print on 8 June 2007.

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