- Research article
- Open Access
Molecular characterization of a DNA fragment harboring the replicon of pBMB165 from Bacillus thuringiensis subsp. tenebrionis
© Huang et al; licensee BioMed Central Ltd. 2006
- Received: 23 May 2006
- Accepted: 23 October 2006
- Published: 23 October 2006
Bacillus thuringiensis belongs to the Bacillus cereus sensu lato group of Gram-positive and spore-forming bacteria. Most isolates of B. thuringiensis can bear many endogenous plasmids, and the number and size of these plasmids can vary widely among strains or subspecies. As far as we know, the replicon of the plasmid pBMB165 is the first instance of a plasmid replicon being isolated from subsp. tenebrionis and characterized.
A 20 kb DNA fragment containing a plasmid replicon was isolated from B. thuringiensis subsp. tenebrionis YBT-1765 and characterized. By Southern blot analysis, this replicon region was determined to be located on pBMB165, the largest detected plasmid (about 82 kb) of strain YBT-1765. Deletion analysis revealed that a replication initiation protein (Rep165), an origin of replication (ori165) and an iteron region were required for replication. In addition, two overlapping ORFs (orf6 and orf10) were found to be involved in stability control of plasmid. Sequence comparison showed that the replicon of pBMB165 was homologous to the pAMβ1 family replicons, indicating that the pBMB165 replicon belongs to this family. The presence of five transposable elements or remnants thereof in close proximity to and within the replicon control region led us to speculate that genetic exchange and recombination are potentially responsible for the divergence among the replicons of this plasmid family.
The replication and stability features of the pBMB165 from B. thuringiensis subsp. tenebrionis YBT-1765 were identified. Of particular interest is the homology and divergence shared between the pBMB165 replicon and other pAMβ1 family replicons.
- Transposable Element
- Plasmid Stability
- Insecticidal Crystal Protein
- Replication Initiation Protein
- Replication Fragment
B. thuringiensis, belonging to the Bacillus cereus sensu lato group, is a gram-positive and spore-forming bacterium that produces parasporal crystals during sporulation. The proteinaceous parasporal crystals show toxicity against insect larvae. The toxin protein genes, usually insecticidal crystal protein (ICP) genes, are mainly located on large conjugative plasmids .
B. thuringiensis strains appear to contain plasmid DNA in proportion of 10–20% of total cell DNA . Generally, plasmids of different B. thuringiensis strains vary in number and size, with the number between 1–12 and the size from 2 to > 250 kb [3, 4]. In addition to harboring ICP genes, B. thuringiensis plasmids can also bear insertion sequences and transposons that are commonly associated with crystal protein genes , or biosynthesis genes of the heat-stable toxin thuringiensin .
These plasmids consist of two groups: (1) the small plasmids (< 15 kb), which perform rolling-circle replication (RCR) using a single-stranded (ssDNA) intermediate , and (2) the large plasmids that normally follow a theta-replicating mode . Theta replicons are currently divided into six groups (Group A-F) . Although there have been relatively few studies focusing on the characterization of Gram-positive theta replicons, as opposed to their Gram-negative counterparts, plasmids pertaining to the broad-host-range pAMβ1 family (group D) have been mostly studied from Gram-positive bacteria [10–13]. To date, only four plasmids from the B. cereus group have been analyzed and reported to belong to the pAMβ1 family. Of these, p43 (65 kb) comes from B. thuringiensis subsp. kurstaki HD263, and a 2,828 bp replication region of p43 has been cloned . The broad-host-range conjugative plasmid pAW63 (71,777 bp) has been isolated from B. thuringiensis subsp. kurstaki HD73, and a 4.1 kb replicon of pAW63 has been characterized . pBT9727 (77,112 bp) is the sole plasmid in the pathogenic strain B. thuringiensis subsp. konkukian 97-27, and its replication protein and the predicted origin have been analyzed by sequence comparison . pXO2 (96,231 bp) is the second virulence plasmid of Bacillus anthracis, and a 2,429 bp replication region has been identified .
In this study, a DNA fragment was shown to contain a plasmid replicon capable of supporting replication and maintaining stability in B. thuringiensis. The location of this replicon was identified as being on pBMB165, the largest detected plasmid (about 82 kb) from B. thuringiensis subsp. tenebrionis YBT-1765. Sequence analysis revealed that the replicon of pBMB165 shared significant homology to the replicons of pAMβ1 family plasmids, suggesting that pBMB165 also belongs to this plasmid family. Moreover, the characterization of the replicon region of pBMB165 provided additional information on the evidence of genetic exchange, molecular evolution and distribution of these closely related plasmids in their various isolates of origin.
Isolation and localization of a plasmid replicon from YBT-1765
Identification and characterization of the minireplicon
Consequently, the pBMB165 mini-replicon (as harbored in pBMB165-F4A) was reduced to a 3.6 kb fragment with a single intact ORF, orf1 (rep165) encoding a 518-amino acids (aa) Rep protein (Rep165, in Fig. 2). Furthermore, a 266 bp fragment (from the Sca I site to the stop codon in rep165) was deleted by PCR amplification with the primer pair orf5-1 and orf5-4, which led the Rep165 protein to be truncated (deletion of 88 codons in rep165); and the corresponding construct pBMB165-F1B was unable to replicate in B. thuringiensis (Fig. 2).
Amino acid sequence comparison showed that Rep165 displayed similarity to the Rep proteins of the pAMβ1 family of theta-replicating plasmids, such as Rep of pBT9727 (97% identity), Rep63A of pAW63 (82% identity) and Rep of p43 (27% identity) from B. thuringiensis [8, 14, 15], RepS of pXO2 (81% identity) from B. anthracis , RepE of pAMβ1 (38% identity) from Enterococcus faecalis , RepR of pIP501 (38% identity) from Streptococcus agalactiae  and RepS of pSM19035 (38% identity) from Streptococcus pyogenes .
Taken together, the conservation among these Rep proteins and ori regions thus provided significant evidence that pBMB165 belongs to the pAMβ1 family of Gram-positive theta-replicating plasmids.
To assess the involvement of these iterons in the replication of pBMB165, a deletion experiment was performed. The results obtained with pBMB165-F6B, which lacked the iterons, suggested that these repeated sequences are required for replication (Fig. 2). In contrast, the iterons sequences present upstream of rep from pAMβ1 have been shown to be non-essential to pAMβ1 replication .
orf6 and orf10 are required for plasmid stability
As shown in Fig. 2, the recombinant plasmid pBMB1651 and its derivatives pBMB1652, pBMB1653, pBMB1654, pBMB165-F4A, pBMB165-F5C and pBMB165-F6A were unable to be properly maintained (after 40 generations at 30°C) in B. thuringiensis BMB171. This result showed that the 12 kb EcoR I replication fragment harbored only the factors required for replication and lacked some elements necessary for retaining plasmid stability.
To investigate the missing elements, a random YBT-1765 plasmid library was constructed by inserting Bam HI-partially digested plasmid DNA from YBT-1765 into the vector pBeloBAC11. In this small library, a recombinant plasmid, designated pBMB165B8, contained a 20 kb insert consisting of two Bam HI fragments of 16 kb and 4 kb; and further sequence analysis revealed that the 12 kb Eco RI replication region was located on the 16 kb Bam HI fragment (Fig. 2).
At the 3' end of this 20 kb fragment cloned from pBMB165, there were two intact overlapping putative ORFs, named orf6 and orf10 (Fig. 2), respectively. The same structural organization was also found in the corresponding location (between the two iterons) of plasmids pBT9727 (ORF47 and ORF48), pXO2 (ORF40 [repB] and ORF41) and pAW63 (ORF48 [rep63B] and ORF49) (Fig. 5).
ORF6 from pBMB165 shared sequence similarity with ORF47 (94% identity) from pBT9727 and RepB (ORF40, 89% identity) from pXO2, as well as copy control protein RepB (35% identity) from the E. faecalis plasmid pAD1 . But while it resembled Rep63B (ORF48) from pAW63 in terms of location and size, they did not share any significant sequence similarity. These proteins, including Rep63B, were all shown to have conserved ATPase motif of ParA protein involved in chromosome or plasmid partitioning.
Likewise, ORF10 from pBMB165 displayed similarity to ORF48 from pBT9727 (86% identity) and ORF41 from pXO2 (66% identity), and although their predicted protein products did not display any sequence similarity to other known proteins, their size and location matched those of RepC, a protein involved in the stability of pAD1 , as did those of ORF49 from pAW63.
In order to conclusively identify the region responsible for the plasmid stability, the recombinant plasmid pBMB165-F6D (derived from pBMB165-F5C, additionally containing orf6 and orf10), and its derivatives pBMB165-F6E (obtained by deleting the fragment from position 311 to the stop codon of orf10) and pBMB165-F6G (a frame-shift mutation in orf6 due to the deletion of 7 bp from position 737 to 743) were constructed. The pBMB165-F6D construct was found to be highly stable in B. thuringiensis (almost 100 %), whereas pBMB165-F6E and pBMB165-F6G were not (Fig. 2), suggesting that orf6 and orf10 were both essential for plasmid stability.
Interestingly, previous studies have demonstrated that repB of pXO2 is not required for replication . While in contrast, rep63B of pAW63 has previously been found to be indispensable for replication . In this study, orf6 and orf10 were not essential for replication, but they were important for the stable maintenance of pBMB165. This result was consistent with previous observations on repB and repC of the E. faecalis plasmid pAD1, which is a member of another family of theta-replicating plasmids (group E). Nevertheless, the mechanism by which orf6 and orf10 contribute to plasmid stability control remains unclear.
Transposable elements or their remnants
Three ORFs (orf2, orf3 and orf4) were found encoding putative transposases in the vicinity of rep165 (Fig. 5). An IS231-like element was identified downstream of rep165 and named IS231 U. It harbored a single open reading frame encoding a 477-aa transposase (orf2) that displayed highest similarity to the transposases of IS231 O-Q and F (81–87% identity).
Intriguingly, ORF3 (971-aa) and a downstream 59 bp sequence were similar to the transposase (TnpA) and right-side IR of several class II transposons from the B. cereus group, such as TnXO1 (71 % TnpA identity) from B. anthracis pXO1, Tn4430 (39 % TnpA identity) and Tn5401 (26 % TnpA identity) from B. thuringiensis [19–21], as well as of an unnamed transposon from pBtoxis (ORFs pBt072 to pBt077, temporarily named TnBtoxis in this paper) and a novel transposon (tentatively named Tn13001) from the B. thuringiensis subsp.pakistani strain T13001 (J. Mahillon, personal communication) (Fig. 5). These sequence features may be the transposase and right-side IR of a remnant class II transposon (tentatively named TnBMB165). Furthermore, the IS231 U described above had inserted just before the last bp (C) of this proposed IR, a peculiar structural association also seen in the case of IS231 A insertion within Tn4430 , IS231 F within TnBtoxis and IS231 L within TnBt9727 .
Another intact transposable element, designated ISBth165 was found upstream of rep165. ISBth165 contained a 289-aa putative transposase (ORF4) that displayed similarity with putative transposases from various bacterial species. It was tentatively grouped into the IS5 family of transposable elements . It is particularly interesting to note that the replication control center of pBMB165 is divided into two parts by ISBth 165 (Fig. 4, Fig. 5): one part harboring rep165 and ori165, the other containing the iterons region and the two proposed stability-control elements (orf6 and orf10). Surprisingly, the presence of ISBth 165 in the intervening region between rep165 and orf6 apparently has little or no disruptive effect on the function of these replication-related factors (Fig. 4). An experiment involving the interruption of orf4 (pBMB165-F4A) showed that it was not implicated in plasmid replication (Fig. 2).
Finally, upstream of the replication region were two additional insertion sequences, designated ISBth 166 (with orf13) and ISBth 167 (with orf14 and orf15), that were tentatively classified as belonging to the IS110 and IS3 family of transposable elements , respectively, on the basis of their sequence similarities.
In addition to the replication/stability-related and transposable features, other elements were found in this cloned fragment. Downstream of the rep165 gene, an open reading frame (orf5) encoding a 250-aa hypothetical protein (Fig. 2) of unknown function displayed similarities with ORFs found in pBT9727, pXO2 and pAW63 in equivalent locations (Fig. 5).
The segment of pBMB165 spanning from orf7 to orf12, flanked on either side by transposable elements, was found to be remarkably similar to a corresponding segment on pBtoxis (ORFs pBt145 to pBt150). None of the sequences involved were found in pBT9727, pXO2 and pAW63 (Fig. 5). Based on their similarities, several of the genes carried by these segments were related to sporulation genes . ORF12 of pBMB165 and pBt145 of pBtoxis were homologous to a putative spore coat-associated protein from Bacillus. ORF8 of pBMB165 and pBt148 of pBtoxis were homologous to the regulatory protein AbrB, which has been shown in B. subtilis to regulate sporulation , as well as being involved in an important example of chromosome-plasmid crosstalk in the B. cereus group [15, 26]. ORF9 of pBMB165 and pBt149 of pBtoxis were homologous to members of the transcriptional regulator ArsR family.
Sequence variability in the pAMβ1 family replicons
The pAMβ1 family replicons that have so far been identified from the B. cereus group (pBMB165, pBT9727, pXO2 and pAW63) have been shown to share the same organization (Fig. 5); however, this organization scheme is distinctly different from the one found in the pAMβ1 family replicons that are of enterococcal (pAMβ1) or streptococcal (pIP501 and pSM19035) origin (Fig. 5). The genetic divergence that led to the establishment of these two types of replicon apparently affected all the components upstream of the rep gene, including the iteron region and the stability-control genes of plasmids. It is of significant interest that the same organization of stability-associated genes found upstream of the rep genes in the B. cereus group replicons is also present in the group F family of theta-replicating plasmids (a novel family of theta plasmids from Gram-positive bacteria) which includes, most notably, plasmids pAD1 and pCF10  from E. faecalis. It would therefore seem reasonable to speculate that a genetic exchange between the theta replicons of the group D family (pAMβ1 family) and those of the group F family may have been responsible for the evolution of the peculiar pAMβ1 family replicons found in the B. cereus group. For these reasons, we proposed that the pAMβ1 family replicons should be divided into two subfamilies with those from the B. cereus group forming a subfamily of their own.
The detailed sequence analysis performed on the pAMβ1 family replicons of the B. cereus group also showed that the iterons region and the two overlapping plasmid stability-associated genes constituted the highest source of sequence variability among these plasmid replicons, and that the major divergence from the general consensus was seen in the replicon of pAW63, a result consistent with the recent report of Van der Auwera et al.  which also suggested that these iterons region may act as recombination nodes participating in genetic plasticity.
The mini-replicon of pBMB165 from B. thuringiensis subsp. tenebrionis YBT-1765 was determined. This study demonstrated that the determinants rep165, ori165 and the iterons region are indispensable for plasmid replication; and that orf6 and orf10 are involved in stable maintenance of the plasmid.
The exploration of sequence conservation among the pAMβ1 family replicons led to the suggestion that the pAMβ1 family replicons from the B. cereus group should be grouped into a subfamily that may have diverged mainly in the iterons and stability control regions. Comparative sequence analysis of additional such replicons may yield further insight into the genetic relationship of these divergent groups.
Bacteria, plasmids and media
B. thuringiensis subsp. tenebrionis YBT-1765 was isolated from a warehouse in China by our research group. The strain BMB171 was a plasmid-cured derivative of B. thuringiensis subsp. kurstaki YBT-1463  isolated and preserved in our lab, which was used as the recipient strain in electroporation. The Escherichia coli TG1 strain (supE, hsd Δ5, thi, Δ (lac-proAB)/F' [traD 36, proAB+, lacIq, lacD ΔM15]) was used for plasmid amplification. All strains were grown at 30 or 37°C in Luria-Bertani (LB) medium. Antibiotics were added at the following concentrations: ampicillin (100 μg/mL), kanamycin (50 μg/mL). Plasmid pUC19 was used for cloning and sequencing. Plasmid pDG780 was used as B. thuringiensis plasmid replicon cloning vector; it bears a replicon and an ampicillin resistance marker for selection in E. coli and a kanamycin resistance marker for selection in Bacillus .
Plasmid DNA was prepared from E. coli strains by alkaline lysis procedure . Plasmid DNA was obtained from B. thuringiensis strains by the modified method of Andrup et al. . Plasmid DNA bands were separated by electrophoresis on a 0.8% agarose gel. Gel extraction of DNA was performed using AxyPrep DNA Gel Extraction Kit (Axygen Scientific, Inc).
DNA samples were electrophoresed in agarose gel and transferred to Hybond N+ (Amersham). Probe labeling was performed by the random primer method with digoxigenin according to the kit manufacture's protocol (Roche). Hybridization was carried out in 5 × SSC overnight at 65°C.
Construction of recombinant plasmids
To determine the pBMB165 minireplicon, a number of deletion constructs were made by sub-cloning all deletion fragments into the vector pDG780 (Fig. 2). Because pDG780 lacked available restriction enzyme sites to clone some of these fragments, the vectors pUC19, pEG-28a (+) or pMD18-T Simple vector (a T-A cloning vector with no multiple cloning sites; TaKaRa Biotechnology [Dalian] Co., Ltd) were used to obtain sites suitable for cloning in pDG780. The details of the constructions are described below.
The vector pDG780 carrying the cloned 12 kb Eco RI fragment was designated pBMB1651 (Fig. 2). The 12 kb Eco RI fragment was partially digested with Sau 3AI and ligated into pDG780 linearized with Bam HI. The ligation mixture was electroporated into the B. thuringiensis BMB171 strain. One transformant was obtained, and a plasmid preparation of this transformant was introduced into E. coli competent cells for further analysis. The resulting plasmid, named pBMB1652, harbored an 8.0 kb insert from pBMB1651 (Fig. 2).
A 5.9 kb Kpn I-Sac I fragment (Sac I site is present in the vector) from pBMB1652 was first inserted into pUC19, and then was cut by Bam HI and Eco RI and cloned into the corresponding sites of pDG780, generating plasmid pBMB1653. In the same way, a 3.0 kb Hap II fragment from pBMB1652 was sub-cloned into pUC19 at the site of Acc I, and then the fragment was digested with Bam HI and Pst I to be inserted into pDG780, resulting in plasmid pBMB1657. The insertion orientation of the 3.0 kb Hap II fragment was established by digestion with Sca I.
A 4.8 kb Sph I-Sac I fragment was cut from the plasmid pBMB1652 and the resulting 3' overhang of the Sph I site was rendered blunt with T4 DNA polymerase. The fragment was ligated into pDG780 between the Sma I and Sac I sites to form the plasmid pBMB1654. Plasmid pBMB1659 was constructed by ligating the 3.9 kb Eco RI-Bgl II fragment of pBMB1654 and Eco RI-Bam HI fragment of pDG780. Plasmid pBMB1658 was constructed by sub-cloning a 3.5 kb Sca I-Sac I fragment from the plasmid pBMB1652 into the Sma I-Sac I sites of pDG780.
A 598 bp fragment was amplified from pBMB1651 by the primer pair orf4-1 and orf6-2. The fragment was cloned into pBM1657 between the Bam HI and Sac I sites to generate plasmid pBMB165-F4A. A 704 bp fragment, contained the Sca I site in rep165, was amplified from pBMB1651 with the primer pair orf5-1 and orf5-2 and cloned into the vector pEG-28a (+) at the Bam HI and Sac I sites to produce plasmid pBMB165-F5A. Then, the 5.9 kb Sca I-Sac I pBMB165-F5A fragment and the 3.5 kb Sca I-Sac I pBMB1652 fragment were ligated to generate plasmid pBMB165-F5B. Finally, pBMB165-F5C was constructed by sub-cloning the 4.0 kb Bam HI-Sac I fragment of pBMB165-F5B into pDG780. Plasmids pBMB165-ORIB and pBMB165-F1B were constructed in the same manner.
The four fragments upstream of orf4 were amplified with the primer pairs orf6-1 and orf6-2, orf6-1 and orf6-3, orf6-1 and orf6-4, orf6-1 and orf6-5, respectively. The four amplified fragments were digested with Bgl II-Sac I and ligated to the 7.6 kb Bgl II-Sac I fragment of pBMB165-F5C, resulting in plasmids pBMB165-F6A, pBMB165-F6B, pBMB165-F6D and pBMB165-F6E, respectively.
Using the Eco RI site in orf6, a frame-shift mutation was introduced in orf6 by PCR amplification with the primer pair orf6-6 and orf6-4. The amplified fragment, deleted of the 7 bp following the Eco RI site in orf6, was digested with Eco RI-Sac I and ligated to the 4.0 kb Eco RI-Sac I fragment of pBMB165-F6T which was constructed by cloning the 1,974 bp fragment amplified with the primer pair orf6-1 and orf6-4 into the pMD18-T Simple vector, generating plasmid pBMB165-F6F. Then, a 1,926 bp Bgl II-Sac I fragment, cut from pBMB165-F6F, was ligated into the 7.6 kb Bgl II-Sac I fragment of pBMB165-F5C to generate plasmid pBMB165- F6G.
Primers used in this study
Nucleotide sequence (5'-3')
forward primer, to construct pBMB165-F4A
forward primer, to construct pBMB165-F5C, pBMB165-F1B
reverse primer, to construct pBMB165-F5C, pBMB165-ORIB
forward primer, to construct pBMB165-ORIB
reverse primer, to construct pBMB165-F1B
forward primer, to construct pBMB165-F6A, pBMB165-F6B, pBMB165-F6D, pBMB165-F6E
reverse primer, to construct pBMB165-F6A, pBMB165-F4A
reverse primer, to construct pBMB165-F6B
reverse primer, to construct pBMB165-F6D, pBMB165-F6G
reverse primer, to construct pBMB165-F6E
forward primer, to construct pBMB165-F6G
Transformation of E. coli and B. thuringiensis
Transformation of E. coli was carried out using CaCl2-treated competent cells, as described by Sambrook and Russell (2001). Transformation of B. thuringiensis plasmid-cured strain BMB171 was performed by electroporation with the Bio-Rad gene pulser set as previously described .
The stability of the recombinant plasmids in B. thuringiensis was tested under nonselective conditions at 30°C according to the method of Sanchis et al. . One hundred single colonies of each recombinant were transferred onto LB plates and LB plates with kanamycin (50 μg/mL). Plasmid stability was estimated as the number of resistant colonies after about 40 generations. Each experiment was repeated three times.
DNA sequence analysis
The replicon fragments of pBMB165 were sub-cloned into the vector pUC19 and DNA sequencing was performed using a primer walking strategy. Sequence homology searches were accomplished with a series of BLAST programs  in GenBank and EMBL sequence databases. Putative ORFs were predicted using ORF-finder  and Clone Manager 5 software. Multiple sequences were aligned based on Clustal W service at the European Bioinformatics Institute website  using the default parameters. For the comparative analysis among the plasmids, the sequences of pBT9727 [GenBank: CP000047], pAW63 [GenBank: DQ025752], pXO2 [GenBank: AE017335], pAMβ1 [GenBank: AF007787], p43 [GenBank: M60513], pBtoxis [GenBank: AL731825] and pAD1 [GenBank: L01794] were used. The nucleotide sequence of the pBMB165 replicon has been submitted to GenBank databases under the accession number DQ242517 [GenBank: DQ242517].
The work was supported by National Basic Research Program of China (2003CB114201), Chinese National Program for High Technology Research and Development and National Natural Science Foundation of China. We are grateful to Fang Wei for her contribution in the early stage of this research.
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