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1 School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK
2 Cardiff School of Biosciences, Cardiff University, PO Box 915, Cardiff CF1 3TL, UK
Correspondence
Christopher M. Thomas
c.m.thomas{at}bham.ac.uk
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ABSTRACT |
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 TOP ABSTRACT INTRODUCTIONMETHODSRESULTSDISCUSSIONREFERENCES |
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subgroup. The complete nucleotide sequence of pQKH54 was determined, revealing it to have a complete IncP-1 backbone but belonging to a new distinct subgroup which was designated IncP-1
. The results emphasize the ubiquity and diversity of IncP-1 plasmids in the environment but demonstrate that plasmids of as yet unknown groups are also able to retrotransfer IncQ plasmids efficiently.
A supplementary table of biologically relevant reading frames identified in the pQKH54 sequence is available with the online version of this paper.
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INTRODUCTION |
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TOPABSTRACTINTRODUCTIONMETHODSRESULTSDISCUSSIONREFERENCES |
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), enables capture of chromosomal genes or non-conjugative plasmids by the host bearing the conjugative plasmid. The mechanism of this process, whether it occurs as an indirect consequence of conjugation or is a distinct genetically determined process, has proved controversial (Blanco et al., 1991; Top et al., 1992; Heinemann & Ankenbauer, 1993a, b; Perkins et al., 1994; Ramos-González et al., 1994; Szpirer et al., 1999), but for IncP-1 plasmid RK2 it has been demonstrated that the plasmid must transfer into the recipient before it can mobilize the captured plasmid back to the donor (Sia et al., 1996). Consistent with this model of retromobilization involving two unidirectional steps, it has been proposed that low surface exclusion is important in the mobilizing plasmid (Szpirer et al., 1999), presumably because strong surface exclusion would disrupt mating pairs before transfer back from the recipient had occurred. In addition it seems likely that retromobilization specificity is determined by the VirD/TraG-like coupling proteins (Gomis-Ruth et al., 2002). However, it is not clear how widespread this ability is among uncharacterized plasmids and whether this phenomenon is environmentally important.
Attempts have also been made to link retrotransfer to certain plasmid incompatibility groups. So far, retrotransfer has been demonstrated for the plasmid groups IncP-1 (Mergeay et al., 1987; Powell et al., 1989; Blanco et al., 1991; Heinemann & Ankenbauer, 1993a, b; Smit et al., 1993; Perkins et al., 1994; Hill et al., 1995; Top et al., 1995), IncM and IncN (Thiry et al., 1984; Mergeay et al., 1985), IncF and IncW (Heinemann & Ankenbauer, 1993a, b; Wlodarczyk & Piechucka, 1995) and IncP-9 (Ramos-González et al., 1994; Ronchel et al., 2000) in a variety of different bacteria as well as some plasmids that do not belong to well-established groups (Szpirer et al., 1999). The majority of these groups are recognized as broad host range, possessing mechanisms which allow them to transfer extensively (Mergeay et al., 1990; Szpirer et al., 1999). IncP-1 plasmids have been specifically implicated in retrotransfer and can transfer to an exceptionally wide range of cell types, showing DNA mobilization to Gram-positive bacteria (Trieu-Cuot et al., 1987), cyanobacteria (Kreps et al., 1990) and yeasts (Heinemann & Sprague, 1989).
Allocating plasmids to specific incompatibility groups often proves difficult. Traditional methods of testing are laborious and rely on transfer of a known incompatibility group plasmid into the strain bearing the plasmid under study and checking for displacement of either plasmid (Stanisich, 1988). Displacement occurs as a consequence of two plasmids sharing similar replication control and/or partitioning systems (Kittell & Helinski, 1993; Novick, 1987). So far about 30 incompatibility groups are known for plasmids studied in Enterobacteriaceae (Jacob, 1977) and 14 in Pseudomonas species (Boronin, 1992). Specific DNA sequences corresponding to genes involved in replication control have been identified for the Enterobacteriaceae plasmid groups (Couturier et al., 1988; Davey et al., 1984) and have proved useful in characterizing plasmids of medical importance by replicon typing.
Few studies have assessed the potential of plasmids from natural environments to carry out retrotransfer. However, some retrotransfer-proficient plasmids showing broad-host-range characteristics have been isolated from natural sources (Hill et al., 1992). In this study we aimed to determine whether plasmids capable of retrotransfer within an aquatic environment are limited to incompatibility groups known already to be capable of retrotransfer. The only known plasmid group identified was the IncP-1 family, although members of this group represented a minority of the plasmids tested. One plasmid, pQKH54, which appeared to be IncP-1 by some tests but not others was characterized by determining its complete genome sequence and proved to belong to a new subgroup of this ubiquitous plasmid family, which we have designated IncP-1.
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METHODS |
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TOPABSTRACTINTRODUCTIONMETHODSRESULTSDISCUSSIONREFERENCES |
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and Table 2 respectively. Strains were maintained on nutrient agar (NA) or L agar (LA) and grown in nutrient broth (NB) or Luria Broth (LB) containing the appropriate selective markers (Sambrook et al., 1989). Other media used are mentioned in context. Supplements were as follows: nalidixic acid (Nal), 200 µg ml–1; rifampicin (Rif), 100 µg ml–1; streptomycin (Sm), 1000 µg ml–1; kanamycin (Km), 50 µg ml–1; tetracycline (Tc), 40 µg ml–1; mercuric chloride (Hg), 27.5 µg ml–1 in nutrient agar or 13.5 µg ml–1 in casein hydrolysate medium. An exception was matings involving Cytophaga heparina, where Hg concentrations of 10 µg ml–1 were used.
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. For smaller plasmids the alkaline SDS procedure was used (Birnboim & Doly, 1979; Kado & Liu, 1981). Further purification was by CsCl gradient for larger-scale preparations (Sambrook et al., 1989). Both standard and pulsed-field gel electrophoresis (PGFE) were carried out to obtain accurate size measurements for restriction bands. PFGE was performed by the CHEF DR II system with 0.5x TBE (Sambrook et al., 1989) at 8 °C using 1.2 % pulsed-field-grade agarose gels (Bio-Rad pulsed-field certified). Gels were run for 18 h, 150 V at 4 s pulse times, followed by 6 h, 110 V at 2.5 s pulse times. Ethidium-bromide-stained gels were scanned using a scanning densitometer and similarity between plasmid profiles was calculated by matching of peak positions using GelManager for Windows (BioSystematica). Dendrogram plots were produced as a result of clustering by UPGMA (unweighted pair group method using averages) on SphI digests of each plasmid, performed in buffers according to the manufacturer's instructions. The multiple regression method (Rochelle et al., 1985) was used to calculate fragment sizes based on migration of known molecular mass markers.
Conjugative transfer.
Overnight NB cultures of donor (100 µl) and recipient (1000 µl) strains were mixed and mating allowed to proceed on a 0.45 µm cellulose nitrate filter which was placed on a NA plate for 24 h at 20 °C or 30 °C. The bacteria were then resuspended in 2–5 ml 1/10x NB and c.f.u. enumerated by standard techniques on NA at 30 °C containing appropriate antibiotics (Bale et al., 1987). Frequencies of conjugal transfer and retrotransfer were determined from isogenic matings between Pseudomonas putida UWCB20, bearing the conjugative plasmids, and UWC7(R300B). Transconjugants were selected on NA+Nal+Sm+Hg and retrotransconjugants on NA+Rif+Sm+Hg. In mobilization UWC7 was the donor, containing both the conjugative plasmid and R300B. Transfer of R300B to UWCB20 was selected on NA+Rif+Sm. For plasmid host-range studies, PaW340 bearing the Hgr plasmid was mixed with a range of recipients. Casein hydrolysate medium (Oxoid L41), which is deficient in tryptophan, was used to select against PaW340, with additions of Hg to select for transconjugants. Donors were enumerated on Pseudomonas selective medium (Oxoid CM559) plus cetrimide and nalidixic acid (Oxoid CN selective supplement SR102) and Hg. Representative colonies of putative transconjugants and retrotransconjugants were checked for the relevant plasmids. Transfer frequencies were compared by analysis of variance using log10-transformed data to ensure homogeneity of variance and normality of error distribution. All means are expressed as geometric means and transfer frequencies as transconjugants per recipient. Mean values were compared by least significant difference (LSD) or minimum significant difference (MSD), using the Tukey–Kramer test for the latter, as appropriate.
Probes used in hybridization studies.
Probes for replicon typing as defined by Couturier et al. (1988) were prepared by digestion of purified plasmid DNA with appropriate restriction enzymes, separated by gel electrophoresis and eluted from low-melting agarose using the Geneclean II kit (Bio Inc.). Probes for the following incompatibility groups were used: IncY (1245 bp), IncT (304 bp), IncX (942 bp), IncL/M (800 bp), IncU (950), IncQ (357 bp), IncFIA (917 bp), IncFIB (1202 bp), IncB/O (1600 bp), rep9 (539 bp), IncHI1 (2250 bp), IncHI2 (1800 bp) and IncP (750 bp). Probes were denatured in a boiling water bath for 10 min and labelled by random priming using dioxigenin (DIG)-dUTP (Boehringer Mannheim) according to the manufacturer's instructions. Additional probes were prepared from the plasmids R751 and pQKH6. R751 (Thorsted et al., 1998) DNA was digested with PstI, producing five fragments corresponding to: (i) Tra2/Tra3/trfA region; (ii) Tra1/oriT/primase; (iii) Tn5090/404, encoding trimethoprim resistance; (iv) oriV/Tn4321; and (v) korA/korB. These were separated by gel electrophoresis and purified as specified using the Glassmax DNA Isolation Spin Cartridge system (Gibco-BRL). As Tn4321 has shown some homology to the mercury-resistance transposon Tn501 it was separated from the oriV fragment by digestion with EcoRI and purification of the two smallest fragments. Plasmid pQKH6 DNA was digested with EcoRI and the largest six fragments were separated by the same technique. These probes were denatured as above and labelled with 32P using Amersham Multiprime according to the manufacturer's instructions. After labelling, unincorporated 32P was removed using Sephadex G50 columns (Sambrook et al., 1989).
Southern blotting and colony hybridization.
Extracted plasmid DNA was digested with EcoRI and separated by gel electrophoresis with appropriate replicon controls. Chromosomal DNA of the plasmid host strain was extracted (Austubel et al., 1989) and included to show any background hybridization. Gels were washed and blotted overnight onto nylon membrane (Hybond-N, Amersham) using standard procedures (Sambrook et al., 1989). DNA was fixed by UV irradiation. Membranes were hybridized with DIG-labelled incompatibility probes following the Boehringer Mannheim DIG Nucleic Acid Detection kit instructions. The chemiluminescent detection technique was carried out using Lumigen PPD. Membranes were exposed to X-ray film at room temperature for 30 min to 3 h. For colony hybridization NB cultures were used to inoculate circular membranes on tryptone-based medium, incubated overnight at 30 °C; then the cells were lysed and the DNA was denatured, neutralized and fixed by standard techniques (Sambrook et al., 1989). After washing and prehybridization, 32P-labelled probes were used to detect related sequences and signals detected by exposure to X-ray film.
PCR amplification and sequencing of selected IncP-1 regions.
Degenerate oligonucleotide primers for IncP-1 control regions were designed previously (Thomas & Thorsted, 1994). A 241 bp trfA product (based on plasmid RK2) was expected using the forward primer 5'-CGA AAT TCR TRT GGG AGA AGTA-3' and reverse primer 5'-CGY TTG CAA TGC ACC AGG TC-3'. For the korA gene, a 294 bp (based on RK2) sequence was amplified by the forward primer 5'-ATG AAG AAA CGG CTN ACC GA-3' and reverse primer 5'-TTC CTG TTT YYT CTT GGC GTC-3'. All primer sequences were compared with GenBank nucleotide sequence data for possible homologies with other non-target sequences. Total DNA extracts were from 1.5 ml overnight cultures as described by Austubel et al. (1989). Amplification and analysis of products used standard procedures (Sambrook et al., 1989). Products were sequenced directly using the PCR primers or cloned into pGEMT-Easy and then at least three clones were sequenced from universal primers to eliminate errors that might have occurred during amplification.
IncP-1 incompatibility testing.
Incompatibility tests were performed in P. putida strains. Transfer frequencies into plasmid-bearing bacteria at 30 °C for both RP4 and the mercury-resistance plasmids were determined as described above, selecting for the incoming plasmid only (Stanisich, 1988). After overnight incubation, four colonies were removed from each of the transconjugant plates, either NA+Rif+Km in the case of RP4 transfer or NA+Sm+Hg for mercury-resistance plasmid transfer. Cells were resuspended in 2 ml 1/10x NB, and 40 µl aliquots of each colony suspension were pipetted into 48 wells of a microtitre plate followed by replica plating to NA plates and separate NA plates containing individual and both selective markers. After overnight incubation at 30 °C replica plating from growth on NA plates was repeated to determine if growth in non-selective conditions would allow the plasmids to segregate. This was repeated to give over 100 generations of unselected growth. Failure to grow on one or other of the selective plates then indicated incompatible plasmids. DNA was regularly extracted and checked for the correct plasmids and absence of interplasmid recombination. To differentiate surface exclusion effects from true incompatibility, control matings were performed with RP4 and mercury-resistance plasmids into plasmidless recipients of PaW340 or UWCB20. Additional controls were performed by mating known IncP-1 plasmids together and examining the degree of segregation.
Sequencing of pQKH54 and sequence accession number.
Subclone libraries of pQKH54 in pUC18 vector were initially generated by cloning SphI fragments, and partial TaqI or Sau3AI digests of the two large SphI fragments. These were sequenced using an ABI373 automated sequencer. Later, subclones were generated using randomly sheared fragments with the TOPO Shotgun Subcloning kit from Invitrogen, using an ABI3700 sequencer. Finishing reads used custom primers on clones or PCR products. A few PCR products were cloned using the Promega pGEM-T Easy vector system. The sequence was produced and assembled using the Phred/Phrap/Consed package (Ewing & Green, 1998; Ewing et al., 1998; Gordon et al., 1998, 2001). Analysis and annotation of the sequence used Artemis and ACT (Rutherford et al., 2000) and WU-BLAST2 (http://blast.wustl.edu/). The nucleotide sequence of pQKH54 has been submitted to the EMBL database (GenBank/EMBL/DDBJ accession no. AM157767). After consultation with the IS database in Toulouse, France (http://www-is.biotoul.fr/), the two new IS elements identified in the DNA sequence have been designated ISUnCu3 (position 13002 to 15597 in the sequence) and ISUnCu4 (position 39749 to 40861 in the sequence) because the identity of the original bacterial host for the plasmid was not known and uncultured.
Construction of phylogenetic tree.
To generate the phylogenetic tree for IncP-1 plasmids, protein sequences were aligned using PILEUP (Wisconsin Package, Devereux et al., 1984) and the alignments concatenated. A neighbour-joining tree was generated using CLUSTALX, with gaps excluded and correction for multiple substitutions.
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RESULTS |
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TOPABSTRACTINTRODUCTIONMETHODSRESULTSDISCUSSIONREFERENCES |
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). Five of the nine plasmids isolated from epilithon showed significant retrotransfer frequencies, ranging from 2.1x10–4 to 1.8x10–5, which were generally 2–3 orders of magnitude lower than the respective conjugation frequencies. The highest retrotransfer frequency detected among the plasmids studied (3.6x10–3) was shown by the IncP-1 plasmid pSS50, which was 15–30 fold higher than the epilithic plasmids pQKH6, pQM705 and pQM719. For plasmids pQM1, pQM62, pQM125 and pQM714, retrotransfer was either undetectable or was just within the limits of detection. All plasmids able to retrotransfer well (at frequencies >10–5) could also mobilize R300B at frequencies of >10–4. Plasmids showing low or undetectable retrotransfer generally had a lower mobilization frequency. An exception was pQM714, which showed similar conjugation and mobilization frequencies but retrotransfer could not be detected.
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as recipients: Escherichia coli, Alcaligenes eutrophus, Agrobacterium tumefaciens and Cytophaga heparina. Transfer to the C. heparina strain could not be detected for any of the plasmids tested (Table 3). However, the RP4 derivative plasmid pQM899 and the IncP-1 plasmids showed a broad host range, being transferred and maintained in all subgroups of the Proteobacteria. Epilithic plasmids pQKH6 and pQM719 showed a pattern of transfer similar to that of the IncP-1 plasmids pJP4 and pSS50, with higher transfer frequencies to A. tumefaciens. The transfer frequency of pQKH54 was somewhat lower to this alphaproteobacterial species but high transfer frequencies, as shown by pQKH6 and pQM719, were detected to the gamma- and betaproteobacteria subgroups. The remaining plasmid tested, pQKH33, only showed a higher transfer frequency to P. putida, with transfer to the other strains at or below the limit of detection.
Classification of plasmids by hybridization with labelled probes
The only replicon probe that gave a positive signal was that for IncP-1, which showed strong Southern hybridization with plasmids pQKH6, pQM719 and pQKH33 at both high and low stringency using RP4 as a positive control (Table 3). No other probes reacted with any of the plasmids under study, even at low stringency, with the probes for the broad-host-range plasmid groups IncN, IncW and IncQ. Plasmid pQM1 has previously been shown to belong to the IncP-13 group of the pseudomonads (Bale et al., 1988) so is unlikely to produce a signal by E. coli replicon typing.
Plasmids belonging to the IncP-1 subgroup have previously been differentiated from the IncP-1
subgroup based on characteristic SphI fragment pattern (Burlage et al., 1990). After SphI digestion a number of identical bands were observed between pQKH6 and pQM719 and the IncP-1 plasmids R751 and pSS50 (data not shown), amounting to a similarity of 50–60 % as indicated in the dendrogram in Fig. 1, which shows just those plasmids that we suspected of being IncP-1 and an outlier, pQM705. RP4, which belongs to the IncP-1 subgroup, did not show these characteristic fragments, indicating a lack of similarity of pQKH6 and pQM719 to the IncP-1 subgroup. Plasmid pQKH33 was not examined because it was much larger than the other plasmids (>300 kb) but additional resistance markers it carries to Ap, Tc and Km are common to the IncP-1 subgroup and suggest that it may belong to this group. No significant similarities were observed in the SphI digestion patterns of pQKH54, pQM85, pQM705 and the known IncP-1 plasmids.
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). As expected from the results above, pSS50, pQKH6 and pQM719 hybridized with almost all of the R751 fragments. Regions of common homology were shown for the fragments containing the Tra1 and oriV regions of the different IncP-1 subgroup plasmids RP4 and R751. Of the remaining plasmids only RP4, pQKH54 and pQM62 hybridized strongly with more than one R751 fragment. Plasmids pQM719 and pSS50 also showed a high degree of similarity with the majority of pQKH6 fragments, all of which hybridized to pQKH54. The other epilithic plasmids failed to hybridize with most of the pQKH6 fragments with the exception of the smallest two fragments (5/6). Hybridization of these latter fragments with 9 out of 10 (now including pQKH33) epilithic plasmids and pNMM1 indicated that they encode mercury-resistance genes possessing some homology to Tn501 present on this vector; such genes are widespread and abundant in the environment (Barkay et al., 2003).
IncP-1 incompatibility testing
Since the only group identified by hybridization is IncP-1 we determined whether this genetic relatedness was manifest as classical incompatibility. Transfer of the epilithic plasmids to PaW340(RP4) identified three, pQKH6, pQM719 and pQKH54, which could displace RP4 (Table 3). Reduction in transfer due to surface exclusion was also exerting an effect, as transfer of these plasmids to a plasmidless PaW340 recipient was up to 250-fold higher. As results for the IncP-1 plasmid pJP4 were very similar, pQKH6, pQM719 and pQKH54 were classified as IncP-1 plasmids by this approach. The other plasmids showed no sign of incompatibility to RP4 in this direction although a small degree of surface exclusion was detected for pQM1 and pQM125. Displacement of the epilithic plasmids by RP4 (Table 3) only identified one plasmid, pQKH6, as belonging to the IncP-1 group. Plasmids pQM1, pQM62, pQM125 and pQM714 were again clearly compatible. For the remaining plasmids, pQM705, pQM719, pQKH54 and pQM85, it took some time before a compatible coexistent relationship could be established and both plasmids were clearly visible with no signs of cointegrate formation after extraction and electrophoresis. This suggested a degree of similarity between the replication control genes of these plasmids. Unfortunately pQKH33 could not be tested by this procedure due to its additional markers, Ap, Tc and Km, which prevented selection for RP4.
PCR using trfA and korA primers
PCR amplification using the trfA primers was detected in only 2 out of 10 (including pQKH33) of the plasmids isolated from epilithon (Table 3). A 241 bp product was obtained for plasmid controls from the IncP-1 group, RP4 and pUZ8, and the IncP-1 subgroup, R751, pSS50. A product of the same size was detected for plasmids pQKH6 and pQM719 but not for any of the other plasmids under study. Amplification using the korA primers again resulted in two plasmids producing a similar sized product to the controls, namely pQKH6 and pQKH33. Plasmid pQM719 showed no product, supporting results of colony hybridization with the korA/korB R751 probe, which gave only a weak signal, whereas pQKH33 gave a strong hybrization signal with this probe and a korA PCR product (Table 3). The origin of the PCR products for trfA and korA products from R751, pSS50 and pQKH6 was confirmed by sequencing. Sequence alignment showed that pSS50 and pQKH6 were indistinguishable on this basis and that their closest sequenced IncP-1 relative was pJP4 (Smith & Thomas, 1987; Trefault et al., 2004), to which they showed >99 % identity, whereas they were clearly different from R751, as expected from the described diversity for this IncP-1 subgroup (Droge et al., 2000).
DNA sequencing and the IncP-1 backbone of pQKH54
The results described above indicated that pQKH54 is related to IncP-1 plasmids but differs with respect to incompatibility reactions, backbone restriction fragment profiles and sequence similarity since it gave negative results with the Couturier IncP-1 probe and the PCR test with trfA and korA primers (Table 3). This suggested that pQKH54 may represent a new branch of the IncP-1 family. Therefore its DNA sequence was determined as described in Methods, resulting in a complete genome of 69 966 bp. The results are summarized in supplementary Table S1, available with the online version of this paper. They confirmed that pQKH54 is indeed a typical IncP-1 plasmid on the basis that it carries all the key gene blocks of the IncP-1 group: the minimal replicon oriV and trfA; the transfer origin oriT and associated transfer gene blocks tra and trb; the central control/partitioning region korA-korB, and associated auxiliary operons kfr, kle and klc. In general the promoter regions for these transcriptional units are typical of other IncP-1 plasmids and have obvious candidate operators for the IncP-1 global regulators, so it seems that the essential features of the regulatory network coordinating the genes for the basic plasmid functions of replication, stable inheritance and transfer are intact.
The G+C content of the backbone is generally lower than for the other subgroups. If the trb region is excluded beyond the end of trbL (as the majority of these genes are unique to pQKH54), then the mean G+C content of the backbone is 56.5 mol%, while it is 63.1 mol% for RK2 (Pansegrau et al., 1994), 66.6 mol% for R751 (Thorsted et al., 1998) and 62.0 mol% for pEST4011 (Vedler et al., 2004). Thus it appears that pQKH54 has spent a considerable proportion of its recent evolutionary history in species with a lower G+C content than the other branches of the IncP-1 family. While the overall structure of the backbone is conserved, there are several differences at the gene level, with genes common to the other IncP-1 groups either being deleted or replaced, or a novel gene inserted. In particular a new operon apparently comprising three small genes was identified upstream of, and reading towards, the klc region. The predicted promoter has KorC and KorA binding sites. Therefore this appears to be part of the IncP-1 KorA/C regulon for this plasmid. Of the kle region, only kleE remains, preceded by a new gene we have called kleH. klcB is divided into two, and may be inactivated but may also simply provide the multiple functions associated with this region by way of two polypeptides rather than one, since there is a reasonable putative ribosome-binding site preceding the second ORF, klcB2. The downstream end of the trb operon is the most drastically changed. Starting from the promoter end of the operon, a new gene, trbQ, replaces trbM. trbR replaces trbO, with OB7 (typically at the start of trbO) being found at the end of trbR; a completely new terminus for the operon follows trbP, consisting of four or five genes. An IS element appears to have inactivated what may be the last gene. The novel genes in this region are generally of a lower G+C content than the rest of the backbone. The tra operon carries only two new genes: a small potential regulator traP (on the basis of similarity to a phage regulatory protein) replacing traA, and a new gene traQ (that has no significant matches to anything in the database) between traF and G.
In the standard IncP-1 replication origin the iterons to which the Rep protein binds are organized as groups of 1, 3, 5 and 1 (in reverse), whereas in pQKH54 they are 1, 2, 5 and 2 (in reverse). Only the group of 5 is essential in RK2 (Thomas et al., 1981; Stalker et al., 1981). The number of auxiliary (non-essential) iterons is thus constant, which may be important since this has been shown to affect copy number control and incompatibility (Cross et al., 1984; Shah et al., 1995). The consensus sequence for the iterons has also changed – most significantly with the GC of the conserved TGAGGGGC motif being replaced by AT (Fig. 2), which may correlate with changes in the putative HTH motif of TrfA observed in pairwise alignments (data not shown).
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), which showed clearly that pQKH54 is well separated from the IncP-1 and groups. We therefore designated this plasmid as belonging to IncP-1. The existence of this third group has already been referred to as ‘personal communication’ on the basis of conference presentations (Adamczyk & Jagura-Burdzy, 2003). Because of this prior designation, another recently described IncP-1 plasmid, pEST4011, was designated IncP-1
(Vedler et al., 2004) after the authors of that paper had compared their sequence with that of TrfA of pQKH54 supplied by us. One key point is that pQKH54 lacks evidence of the blocks of inverted repeats and restriction sites typical of the inter-backbone segment regions of IncP-1 plasmids (Thorsted et al., 1998). Comparison with IncP-1 and plasmids indicates that these repeats are confined to the group, which raises further questions about their origin and functional significance. It seems that they are a recent acquisition rather than an ancestral remnant.
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,1995). The rest of this mobile element is mosaic in structure, with only a terminal match to Tn5053, suggesting that it is probably not self-transposable, being dependent on another element to provide the transposase function. Most remarkably, it contains a segment that is a very close match to part of traC of the IncP-1 plasmid R751. This appears to have been acquired by the transposon through an inexact transfer or recombination event from an ancestor of pADP-1 because this plasmid contains the appropriate conjunction of transposable element and IncP-1 backbone. A possible scheme for how this might have occurred is shown in Fig. 4. This proposed scheme is important because it suggests that IncP-1 plasmids are sufficiently common in the environment as to have a reticulated history. Adjacent to this, in the mosaic region, are two more apparently complete genes. One of these shows some similarity to a sterol desaturase, while divergent from this is an AraC-family regulator (Gallegos et al., 1997).
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). This probably represents the remnants of a previous insertion. Between oriV and trfA there is a large segment of non-backbone material. Despite a region of homology including a two-component transposase on pB4 and an adjacent orphan gene, we were unable to identify matching termini for a transposon in this region. Neighbouring the pB4 homologous region is what appears to be an operon of genes and a divergently expressed AraC-family regulator. |
DISCUSSION |
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TOPABSTRACTINTRODUCTIONMETHODSRESULTSDISCUSSIONREFERENCES |
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). However, at least for IncP-1 plasmids, the self-transmissible plasmid must move from the donor to the recipient before promoting retromobilization (Sia et al., 1996), so one would predict that retromobilization should obey the specificity rules of the TraG/VirD4 coupling protein family (Llosa et al., 2003). This does hold to the extent that plasmids that retromobilize efficiently are also generally good at mobilization, although it might be expected that mobilization frequency would be higher than retromobilization, which is not the case for pQM85 and pQM705 (Table 3). Therefore additional factors may be involved and, as with certain examples of mobilization, retrotransfer may reveal plasmid-pair specific properties (Willetts, 1981; Willetts & Crowther, 1981). Where mobilization is efficient but retromobilization is not, it may be that surface exclusion, as suggested by Szpirer et al. (1999), can explain the results, so that pQM719 expresses proteins that cause the mating bridge to break down before the reverse transfer can occur. Detailed comparison of pQM719 with other IncP-1 plasmids may reveal differences in surface exclusion proteins that explain why it does not behave as expected from its apparent classification.
Reinforcing their importance as agents of retromobilization, the screening identified new IncP-1 plasmids, although not all of them initially gave clear-cut results. For pQM719, the mating technique used to examine plasmid incompatibility did not produce bidirectional incompatibility, which may be due to a second replicon in this plasmid. This would be consistent with pQM719 not being a completely typical IncP-1 plasmid, as already suggested in the previous paragraph. However, SphI restriction profiles, colony hybridization and the PCR suggest that both pQM719 and pQKH6 are related to the IncP-1 subgroup (Table 3) and have host ranges similar to the IncP-1 plasmids examined.
By contrast pQKH54 showed inconsistent plasmid grouping by the phenotypic and genotypic tests used, suggesting a degree of similarity with IncP-1 plasmids but insufficient sequence identity to react with the repP probe from the Couturier collection (Couturier et al., 1988). Similar problematic results were obtained for incompatibility testing of plasmids pQM705 and pQM85 (Table 3), indicating that although similarities may exist to the replication and maintenance genes of RP4, enough differences are present to allow maintenance of both systems after continuous growth in non-selective conditions. Explanations for such asymmetric incompatibility include the occurrence of a replicon fusion followed by deletion events to leave P-1 group incompatibility determinants on plasmids with alternative replication systems (Smith & Thomas, 1989). Because the divergence of pQKH54 from RK2 and R751 made it difficult to use hybridization or PCR to assess its relatedness to the IncP-1 group, sequencing the whole genome proved an efficient analytical approach. The sequence revealed a surprisingly conserved IncP-1 backbone. It is therefore surprising that it showed efficient transfer but relatively inefficient retrotransfer (Table 3). The sequence may provide the basis for a detailed analysis of the surface exclusion functions as discussed above.
While pQKH54 clearly belongs to the IncP-1 family it is distinct from IncP-1 plasmids and appears to be somewhat less broad host range than pQKH6 and pQM719. This would also be consistent with the lower G+C content of the genome since it suggests adaptation to a different group of hosts. The restriction map of pQKH54 predicted from the DNA sequence (data not shown) exhibited clustered regions of sites, coincident with the insertions of transposable elements or phenotypic determinants, a characteristic of all typical IncP-1 plasmids (Thomas & Smith, 1987; Smith & Thomas, 1989). Nevertheless pQKH54 does not possess the clusters of repeats associated with restriction sites (Thorsted et al., 1998; Heuer et al., 2004) that are now clearly associated only with IncP-1 plasmids. Despite the absence of these putative hot-spots for acquisition of transposable elements the only insertion into the backbone of pQKH54 occurs in one of these regions. The contiguous oriV-rep region confirms the nature of the ancestral backbone backbone as previously predicted by Smith et al. (1993) and first observed by Heuer et al. (2004).
Preliminary analysis for pQKH6 (data not shown) indicated one larger clustered region, containing both the mercury-resistance genes and genetic information homologous to the oriV region of RK2. This is consistent with the pQKH6 backbone being only interrupted in one place as found for the recently sequenced plasmids pJP4 (Trefault et al., 2004) and pB3 (Heuer et al., 2004) and as suggested for IncP-1 plasmids pSS50 and pSS60 (Burlage et al., 1990). While using PCR primers for trfA and korA did not identify any additional IncP-1 plasmids it did provide a simple basis to assess relatedness of backbone genes, showing that indeed pQKH6 and pSS50 are indistinguishable on the basis of the sequence determined.
The clearest phenotype conferred by pQKH54 is mercury resistance, which has been found previously in IncP-1 plasmids (Smith & Thomas, 1987). The particular version of mer genes related to those in Tn501 is environmentally widespread, having been reported in 35–100 % of Hgr bacteria isolated from terrestrial environments (Osborn et al., 1993). In addition, the pQKH54 sequence identified four genes in two transposon-associated regions which may encode hitherto unsuspected phenotypic properties. The closest sequence database matches are a choline dehydrogenase, a hydratase, a taurine dioxygenase and a sterol desaturase (Supplementary Table S1). Both operons are divergently transcribed from AraC-family regulators. While we have not studied them experimentally, it is tempting to speculate that these may all be involved in catabolism of bile salts.
Overall the capacity of these aquatic plasmids to retrotransfer the small non-conjugative IncQ plasmid R300B and other IncQ plasmids (Hill et al., 1995) has important implications not only in the release of genetically engineered sequences, which are frequently encoded on non-conjugative cloning vectors (Bolivar et al., 1977), but also in terms of the role of plasmids in promoting horizontal gene transfer in natural microbial communities. This study shows that bacteria harbouring plasmids indigenous to freshwater biofilms are capable of capturing such genes and this can potentially occur from a wide range of bacterial hosts. Almost certainly completely new incompatibility groups have yet to be identified. Evidence for this comes from plasmid pQM85 studied here, which could capture R300B efficiently by retrotransfer, but could not be placed into any known retrotransfer proficient incompatibility group. Plasmids of the IncP-1 family appear to be the commonest for which good identification methods exist (Pukall et al., 1996; Smalla et al., 2000). Our data indicate that within natural aquatic systems a whole spectrum of IncP-1-like plasmids may be present with differing degrees of similarity to clinical IncP-1 plasmids, and probably adapted to particular hosts. This suggests a broad IncP-1 group rather than a closely defined one (Smith & Thomas, 1989) and this point is reinforced by the recent report of a fourth IncP-1 subgroup designated IncP-1 (Vedler et al., 2004). Sequencing and classification of plasmids from a whole range of environmental sources is required to determine the true plasmid diversity found in nature and to determine whether new plasmids are related to known groups or represent completely new sequence families.
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REFERENCES |
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