Figures
Abstract
Sophisticated genetic tools to modify essential biological processes at the molecular level are pivotal in elucidating the molecular pathogenesis of Clostridium difficile, a major cause of healthcare associated disease. Here we have developed an efficient procedure for making precise alterations to the C. difficile genome by pyrE-based allelic exchange. The robustness and reliability of the method was demonstrated through the creation of in-frame deletions in three genes (spo0A, cwp84, and mtlD) in the non-epidemic strain 630Δerm and two genes (spo0A and cwp84) in the epidemic PCR Ribotype 027 strain, R20291. The system is reliant on the initial creation of a pyrE deletion mutant, using Allele Coupled Exchange (ACE), that is auxotrophic for uracil and resistant to fluoroorotic acid (FOA). This enables the subsequent modification of target genes by allelic exchange using a heterologous pyrE allele from Clostridium sporogenes as a counter-/negative-selection marker in the presence of FOA. Following modification of the target gene, the strain created is rapidly returned to uracil prototrophy using ACE, allowing mutant phenotypes to be characterised in a PyrE proficient background. Crucially, wild-type copies of the inactivated gene may be introduced into the genome using ACE concomitant with correction of the pyrE allele. This allows complementation studies to be undertaken at an appropriate gene dosage, as opposed to the use of multicopy autonomous plasmids. The rapidity of the ‘correction’ method (5–7 days) makes pyrE− strains attractive hosts for mutagenesis studies.
Citation: Ng YK, Ehsaan M, Philip S, Collery MM, Janoir C, Collignon A, et al. (2013) Expanding the Repertoire of Gene Tools for Precise Manipulation of the Clostridium difficile Genome: Allelic Exchange Using pyrE Alleles. PLoS ONE 8(2): e56051. https://doi.org/10.1371/journal.pone.0056051
Editor: Michel R. Popoff, Institute Pasteur, France
Received: August 10, 2012; Accepted: January 8, 2013; Published: February 6, 2013
Copyright: © 2013 Ng et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The authors acknowledge the financial support of the MRC (G0601176), the European Community's Seventh Framework Programme ‘HYPERDIFF’ (HEALTH-F3-2008-223585), the Biotechnology and Biological Sciences Research Council (BB/G016224/1), and TMO686 Renewables Ltd. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: One of the authors, Muhammad Ehsaan is a PhD student sponsored by TMO Renewables Ltd. His stipend and fee is received by the University from TMO and administered by them. Neither he nor Nigel P. Minton have any other association with this company (neither in terms of salary, consultancy or shares). The work has not been patented. The funding of Muhammad Ehsaan's studentship does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials.
Introduction
Clostridium difficile is the major cause of nosocomial diarrhoea and a major burden to healthcare services worldwide. The organism is resistant to various broad-spectrum antibiotics and capitalises on the disruption of the normal intestinal flora to cause disease symptoms ranging from asymptomatic carriage to a fulminant, relapsing and potentially fatal colitis [1], [2]. Sophisticated genetic tools to modify essential biological processes at the molecular level are pivotal in enabling the systematic study of the basis of colonization, virulence and pathogenesis of C. difficile. The requisite systems ideally need to be able to both make precise, in situ alterations to existing alleles, as well as introduce entirely new alleles to progress hypothesis driven research. The former include the generation of in-frame deletions and the introduction or correction of single or multiple nucleotide substitutions, deletions and insertions. The latter is required both to add entirely new, or altered alleles or provide the facility for the complementation of distal mutant alleles at chromosomal gene dosage.
For many years the required level of sophistication has been unavailable. Thus, directed mutants could only be made using insertional mutagens, reliant either on replication deficient [3] or defective [4], [5] plasmids, or on the deployment of the ClosTron and group II intron re-targeting [6], [7]. Recently, however, the cytosine deaminase gene (codA) of Escherichia coli was developed as a negative/counter selection marker for C. difficile, which enabled precise manipulation of the C. difficile chromosome for the first time [8]. In parallel, a second method (Allele-Coupled Exchange, ACE) has been formulated that allows the rapid insertion of heterologous DNA, of any size or complexity, into the genome [9]. Whilst a number of different genetic loci may be used to insert heterologous DNA via ACE, one exemplification of the method exploits the native pyrE gene, bringing about its inactivation by replacement of the wild type allele with a mutant allele lacking the codons from both the 5′ and 3′ end of the structural gene. The pyrE gene encodes orotate phosphoribosyltransferase [E.C.2.4.2.10]), which is an enzyme involved in de novo pyrimidine biosynthesis. It may be used as a positive/negative selection marker as it is essential in the absence of exogenous pyrimidines and it also renders 5-fluoro-orotate (FOA) toxic to cells. Toxicity occurs via a series of steps which result in misincorporation of fluorinated nucleotides into DNA and RNA and hence, cause cell death.
Mutant strains defective in pyrE created using ACE become auxotrophs requiring exogenous uracil to grow. They also lends themselves to the use of a functional pyrE allele as a negative/counter selection marker in a similar way to codA [8].The functionally equivalent gene, URA5, and URA3 (encoding orotidine-phosphate decarboxylase) have been widely used as negative selection markers in Saccharomyces cerevisiae [10]. Indeed, this approach has allowed homologous gene replacement in a range of different microbes [11]–[14], including most recently Clostridium thermocellum [15] using the organisms own pyrF gene (equivalent to URA3) in a specifically created ΔpyrF mutant. Not unexpectedly, the ΔpyrF strain created required the addition of exogenous uracil to achieve equivalent cell density to the wild type in the rich media employed. With supplementation, whilst growth was slightly delayed, the eventual the growth rate was comparable to wildtype [15].
In this study, we have developed a procedure for the generation of allelic exchange mutants in pyrE mutants of two different strains of C. difficile (strain 630Δerm and a BI/NAP1/PCR-Ribotype 027 strain, R20291) using a heterologous pyrE allele from Clostridium sporogenes as a negative/counter-selection marker. Use of a heterologous pyrE allele avoids homologous recombination with the native pyrE locus of C. difficile. The system has been used to make in-frame deletions in three different genes, spo0A (the master regulator of sporulation), cwp84 (which encodes a cysteine protease) and mtlD (which encodes mannitol-1-phosphate 5-dehydrogenase). Crucially, having created these mutants, a specific ACE-vector is used to rapidly (within 5–7 days) restore the chromosomal pyrE allele to wild-type, allowing the specific in-frame deletion mutant to be characterised in a clean, wild-type background. Moreover, variants of the same vector may be used to deliver the wild-type allele of the deleted gene, either under the control of its native promoter or the strong fdx promoter, into the genome. The former allows complementation studies to be performed at an appropriate gene dosage, while the latter potentially allows the assessment of the effect of overexpressing the gene.
Results
Construction of a pyrE− mutant of R20291
The pyrE− mutant of strain 630Δerm was previously made using Allele-Coupled Exchange (ACE) and the purpose built, replication defective vector pMTL-JH18::lambda6.5 [9]. It is based on the replicon of plasmid pCB102 [16], previously shown to be the least effective (most unstable in terms of segregation into daughter cells) in strain 630Δerm of the four replicons available in the pMTL80000 modular vector series [17]. In strain R20291, however, the plasmid pBP1 replicon is the most defective, ie., plasmids that use this replication region are more rapidly lost in the absence of antibiotic selection [18]. Accordingly, pMTL-YN18 was constructed in order to generate a pyrE mutant of C. difficile R20291 (Figure 1). pMTL-YN18 is equivalent to the pMTL-JH18::lambda6.5 vector used to construct a ΔpyrE mutant in C. difficile 630Δerm, except the pCB102 replicon is substituted with that of pBP1 and the 6.5 kb fragment of phage lambda DNA is absent. It carries two asymmetric homology arms that flank a lacZ' multiple cloning site (MCS) region. The shorter, 300 bp left-hand homology arm (LHA) is composed of a variant pyrE allele that lacks 50 nucleotides from the 5′-end of the gene and is devoid of 235 bp from the 3′-end of the gene. The larger 1200 bp right-hand homology arm (RHA) encompasses the region residing immediately downstream of the pyrE gene in the C. difficile genome.
The ACE vector pMTL-YN18 is designed to create a deletion mutant specifically in the C. difficile strain R20191. Plasmid components are: CatP, the catP gene of Clostridium perfringens conferring thiamphenicol resistance; ColE1, the replication region of the E.coli plasmid ColE1; TraJ, transfer function of the RP4 oriT region; RepA and Orf2, the replication region of the Clostridium botulinum plasmid pBP1; LHA, left-hand homology arm encompassing a 300 bp internal fragment of the R20291 pyrE gene lacking 50 nucleotides from the 5′-end, and 235 bp from the 3′-end; RHA, right-hand homology arm comprising encompassing the 1200 bp region of DNA immediately downstream of pyrE, and; lacZ', gene encoding the alpha fragment of the E.coli β-galactosidase (and containing a multiple cloning site region derived from plasmid pMTL20 [19]).
Plasmid pMTL-YN18 was used to generate a pyrE mutant of C. difficile R20291. Five independent fluoroorotic acid (FOA) resistant colonies were chosen and shown to be pyrE deletion mutants. Thus, they all required exogenous uracil for growth on minimal media, were no longer thiamphenicol resistant, consistent with plasmid loss, and generated a PCR fragment of the expected size (623 bp) using primers that flanked the pyrE locus (Supporting Information File S1). Nucleotide sequence of the 623 bp fragment generated confirmed the presence of the expected deletion.
Restoration of pyrE+ phenotype in 630Δerm and R20291
With pyrE mutants of both C. difficile 630Δerm and R20291, it was desirable to demonstrate that they could be converted back to uracil prototrophy, through restoration of the pyrE locus to wild-type. Accordingly, ACE plasmids pMTL-YN1 and pMTL-YN2 were constructed to correct the pyrE mutations in C. difficile 630Δerm and R20291, respectively (Figure 2). These plasmids were broadly equivalent to pMTL-JH14, used to correct a similar pyrE mutation in C. acetobutylicum [9], with a pyrE allele that lacked the first 50 nucleotides of the open-reading-frame forming the short 300 bp LHA. Crucially, they differed from pMTL-JH14 in that they did not carry the lacZ' region present in this plasmid between the LHA and RHA. As a consequence, the strains generated using them would be indistinguishable from the wild-type at the pyrE locus. Both plasmids were conjugated into their respective pyrE mutants from an E. coli CA434 donor and, following the procedure outlined in MATERIALS AND METHODS, several dozen colonies were obtained that were able to grow without uracil supplementation. Six random colonies from each strain were screened by PCR using primers which annealed to the chromosomal genes that reside up- and down-stream of the pyrE gene. In all cases, the expected 2,058 bp band was generated, equivalent to the wild-type control, whereas no band was generated when the template DNA was derived from the pyrE mutant (Supporting Information File S1). Nucleotide sequencing of the fragment generated confirmed that the cells carried a wild type pyrE gene.
Both vectors carry identical components between their FseI and SbfI restriction sites. These are: CatP, the catP gene of Clostridium perfringens conferring thiamphenicol resistance; ColE1, the replication region of the E.coli plasmid ColE1, and; TraJ, transfer function of the RP4 oriT region. Plasmids pMTL-YN1C and pMTL-YN2C have an additional segment of DNA inserted between the left-hand homology arm (LHA) and the right-hand homology arm (RHA) which carries: a transcriptional terminator (T1) of the ferredoxin gene of Clostridium pasteurianum; a copy of the lacZ' gene encoding the alpha fragment of the E.coli β-galactosidase, and; a multiple cloning site (MCS) region derived from plasmid pMTL20 [19]. Plasmids pMTL-YN1X and pMTL-YN2X differ from pMTL-YN1C and pMTL-YN2C, respectively, in that they carrying the promoter region (Pfdx) of the Clostridium sporogenes ferredoxin gene.
Formulation of the components of an Allelic Exchange vector
Aside from the gene specific knock-out cassettes, the two most important components of the desired allelic exchange vector are the pyrE allele, to be used as the negative/counter-selection marker, and the clostridial plasmid replicon. In the case of the pyrE allele, it is desirable that the gene used is heterologous, to avoid recombination at the native chromosomal pyrE locus of C. difficile. Therefore, we selected the pyrE gene of Clostridium sporogenes, which shares only 65% identity with its C. difficile equivalent. The pyrE gene was cloned into pMTL83151 and the resultant plasmid (pMTL-ME2, Figure 4) shown to be able to restore the C. difficile pyrE mutants to prototrophy, ie., they were able to grow on minimal media lacking uracil supplementation (data not shown).
The isolation of the initial, single cross-over plasmid integrants required for the creation of allelic exchange mutants is facilitated by the use of ‘pseudo-suicide’ vectors [8], [18]. These are plasmids carrying catP (encoding resistance to thiamphenicol) that are sufficiently replication defective for there to be a significant growth disadvantage in the presence of thiamphenciol compared to cells in which the plasmid, together with catP, has integrated. Such integrated clones grow faster, and produce larger colonies, on agar media supplemented with thiamphenicol, because all of the progeny carry a copy of catP. Cells carrying catP on a non-integrated, defective autonomous plasmid, in contrast, grow slower because in the presence of antibiotic they are limited by the rate at which the plasmid is segregated amongst the daughter population. Previously, the pCB102-based plasmid had been made more defective in strain 630Δerm by increasing the size of the final vector through the insertion of 6.5 kb of DNA derived from phage lambda [9]. Here we took a different strategy, and explored the effect of introducing a frame-shift mutation into the 3′-end of putative repH gene of the pCB102 replication region. Accordingly, the modular plasmid pMTL83251 was cleaved with NsiI, treated with T4 polymerase and subjected to self-ligation, yielding pMTL83*251. Nucleotide sequencing confirmed that the expected modification had occurred, altering the sequence ATGCAT to AT. The resulting deletion of 4 nucleotides (TGCA) causes a frame-shift in the coding sequence, replacing the COOH-terminal region of RepH (CIKYYARSFKKAHVKKSKKKK) with LNIMGALKKLM. The effect on segregational stability was tested by growing cells of 630Δerm carrying either pMTL83251 or pMTL83*251 in the absence of antibiotic selection and measuring plasmid loss. The results are shown in Figure 3, and demonstrate that the frame-shift has caused a significant reduction in the segregational stability of the plasmid.
The two plasmids differ only in that pMTL83*251 has a frame shift in the pCB102 RepH gene, introduced by blunt-end ligation following cleavage with NsiI. Cells carrying the two plasmids were grown in BHIS media in the absence of antibiotic and then CFUs estimated on agar media supplemented with thiamphenicol after 6, 12 and 24 h of growth. The illustrated data was derived from three independent experiments.
Accordingly, the NsiI site of plasmid pMTL-ME2 was similarly frame-shifted, and the resulting plasmid was designated pMTL-YN3 (Figure 4). For manipulations in R20291, the pCB102 replication region of pMTL-YN3 was simply replaced with that of pBP1, by cleaving pMTL-YN3 with AscI and FseI and replacing the excised fragment carrying the pCB102 replicon with the equivalent fragment from the pBP1-based plasmid pMTL82251 [17]. The resulting plasmid was designated pMTL-YN4 (Figure 4).
Common plasmid components are: CatP, the catP gene of Clostridium perfringens conferring thiamphenicol resistance; PyrE, the pyrE gene of Clostridium sporogenes; ColE1, the replication region of the E.coli plasmid ColE1, and; TraJ, transfer function of the RP4 oriT region; Z, the lacZ' gene encoding the alpha fragment of the E.coli β-galactosidase (and containing a multiple cloning site, MCS, region derived from plasmid pMTL20); T1, a transcriptional terminator isolated from downstream of the Clostridium difficile strain 630 CD0164 gene, and; T2, a transcriptional terminator of the ferredoxin gene of Clostridium pasteurianum. The position of the frame-shift generated at the NsiI site is indicated by an asterick. Plasmid pMTL-ME2 is identical to plasmid pMTL-YN3, except it carries an NsiI site at the 3′-end of RepH at the position marked by an asterick.
Exemplification of the System to create spo0A mutants of strains 630Δerm and R20291
To test the system, we made in-frame deletions in the spo0A gene of both C. difficile 630Δerm and R20291 using plasmids pMTL-YN3::630spo0A* and pMTL-YN4::R20291spo0A*, respectively, as detailed in the allele exchange procedure outlined in MATERIALS AND METHODS. After two (630Δerm) and four (R20291) passages of the transconjugants on BHIS selective media, one of the six visibly larger colonies derived from 630Δerm, and four of the six visibly larger colonies derived from R20291, were found to be pure single crossover mutants by PCR (data not shown). Subsequently, single colonies were re-streaked onto minimal medium supplemented with FOA and uracil to select for cells in which the integrated plasmid had excised. The isolated FOA resistant colonies (four in the case of 630Δerm and twelve in the case of R20291) were then screened by PCR using primers spo0A-YN-F2 and spo0A-YN-R2 that anneal to the upstream and the downstream sequence of spo0A, respectively. Of the four 630Δerm colonies screened, one yielded the expected 1,845 bp DNA fragment, indicative of an in-frame deletion (Supporting Information File S1). The other colonies yielded a 2,331 bp DNA fragment, consistent with the presence of a wild-type copy of the gene. In the case of R20291, two of the twelve colonies screened yielded the 1,845 bp DNA fragment indicative of an in-frame deletion (Supporting Information File S1). Nucleotide sequencing of the 1,845 bp DNA fragments confirmed that the expected allelic exchange event had taken place in all three putative mutants.
The sporulation minus phenotype of the mutants was confirmed by assaying colony forming units (cfu) on BHIS supplemented with 0.1% [w/v] sodium taurocholate before and after heat shock (65°C for 30 min), as previously described [20]. In each case, no colonies were obtained after heat shock, whereas the wild type controls gave counts of 1.28×104 and 9.17×104 cfu for CRG2548 (R20191ΔpyrE) and CRG2547 (630ΔermΔpyrE), respectively. Phase contrast microscopy confirmed that unlike the wild type strains, phase-bright spores were absent in the mutant cultures.
Creation and in situ complementation of in-frame deletion mutants of cwp84
To further test the system, we constructed mutants of the cwp84 gene of both 630Δerm and R20291. Cwp84 is a cysteine protease responsible for the post-translational cleavage of SlpA into the two proteins High Molecular Weight (HMW) and Low Molecular Weight (LMW) SlpA, which are the major components of the C. difficile surface layer. ClosTron mutants of cwp84 have been made elsewhere in C. difficile 630Δerm [21], [22], and in the one study [22] complemented using an autonomous plasmid. cwp84 in-frame deletion mutants were constructed following an identical procedure to that used to isolate the spo0A mutants, using plasmids pMTL-YN3::630cwp84* and pMTL-YN4::R20291cwp84*. One of the three 630Δerm FOA resistant colonies screened yielded a 1,218 bp PCR product, indicative of the desired in-frame deletion (Supporting Information File S1). In the case of R20291, three of four FOA resistant colonies screened yielded the 1,218 bp PCR product, indicative of the desired in-frame deletion (Supporting Information File S1). Nucleotide sequencing of the 1,218 bp fragments confirmed that the desired in-frame deletion had been obtained.
A second round of pyrE-based allele exchange was carried out in the 630Δerm and R20291 cwp84 mutants, using pMTL-YN3::630cwp84c and pMTL-YN4::R20291cwp84c, respectively, to restore the mutant alleles back to wild-type, in situ. A conservative base substitution was made to introduce a ScaI restriction site into the restored cwp84 sequence (Figure 5A). Three 630Δerm FOA resistant colonies were screened and yielded a 1.1 kb PCR product with primers cwp84-F4 and cwp84-R4, indicating that the cwp84 allele had been successfully restored (Figure 5B). Subsequent digestion of the PCR products with ScaI confirmed that restoration of the cwp84 allele had been successful in each of the three clones screened (Figure 5C). Similar analysis was carried out on nine R20291 FOA resistant clones. Successful restoration of cwp84 was confirmed in each of the nine clones, as evidenced by a 1.1 kb PCR product which was cleaved by Sca I (data not shown).
(A) Schematic diagram of the complementation of cwp84, with a single nucleotide change to base 2280 of cwp84 from a T to an A, without changing the corresponding valine amino acid residue and at the same time creating a ScaI site. The purpose of this single nucleotide change was to prove the occurrence of the complementation event. (B) PCR screening of candidate clones of the complemented cwp84 gene. Primers cwp84-F4 and cwp84-R4 anneal to the internal sequence of the knockout cassette and the downstream sequence of cwp84, respectively, resulting in a 1, 026 bp PCR product from double-crossover complemented clones and wild-type, while no PCR product is expected from Δcwp84 mutants. MW is a 2-Log DNA Ladder (NEB) molecular weight marker, WT is a wild-type C. difficile DNA control, and 1–3 are the candidate clones. All candidates 1 to 3 show the expected complemented 1, 026 bp band, thereby confirmed as cwp84 complemented clones, as seen in the wildtype control. (C) PCR products amplified using primers cwp84-F4 and cwp84-R4 from candidates clones and wildtype were analysed by RE digestion with ScaI. PCR products amplified from cwp84 complemented clones were cut into two fragments (786 and 240 bp), whereas PCR products amplified from the wildtype control did not.
Before carrying out any phenotypic characterisation, the cwp84 mutants and their restored derivatives were converted back to a pyrE-positive (uracil prototrophy) phenotype using pMTL-YN1 and pMTL-YN2 for the 630Δerm-derived strains and the R20291-derived strains, respectively. In keeping with previous observations [21], [22], the mutants grew poorly on anaerobic blood agar compared to the wild-type and the complemented strains (Supporting Information File S1). S-layer extracts from the WT, mutant and complemented strains were prepared by the glycin acid method. The absence of the Cwp84 protease in the 630Δerm and R20291 mutant strains was confirmed by immunoblot analysis with anti-Cwp84 antibodies (Figure 6A). Furthermore, while glycin extracts of both the 630Δerm wild type strain and the complemented mutant contained two bands corresponding to the cleaved HMW and LMW S-layer proteins, only a band corresponding to the unprocessed SlpA precursor was evident in the cwp84 mutant strain (Figure 6B). Interestingly, whilst broadly equivalent results were obtained with the R20291 strains, it was clear that the cwp84 mutant contained two lower intensity bands, most likely corresponding to the HMW and LMW, in addition to the SplA precursor (Figure 6B). The identity of the HMW-SLP band was further confirmed by immunoblot (Figure 6C). This suggests that some proteolytic cleavage of SlpA may have occurred in the R20219 mutant, despite the absence of Cwp84.
(A) Immunoblot analysis with anti-Cwp84 antibodies of glycin extracts, showing complete absence of Cwp84 in the mutants compared to WT and complemented strains. (B) SDS-PAGE of glycin extracts of 630Δerm and R20291 WT, mutant and complemented strains, showing no processing of SlpA precursor in the 630Δcwp84 mutant, and in contrast, an incomplete processing of SlpA in the R20291Δcwp84 mutant. (C) Identification of the HMW-SLP in the glycin extract of the R20291Δcwp84, showing that a partial processing of SlpA takes place in this mutant even in absence of the Cwp84 protease. Lanes 1, 630Δerm; lanes 2, 630ΔermΔcwp84; lanes 3, 630ΔermΔcwp84 complemented; lanes 4, R20291; lanes 5, R20291ΔermΔcwp84; lanes 6, R20291ΔermΔcwp84 complemented; MW, molecular weight standard.
Creation and rapid in trans complementation of in-frame deletion mutants
Whilst the in situ complementation of mutant alleles represents the ‘gold standard’, the procedure required is lengthy (approx. 3–4 weeks), and therefore adds to the time needed to characterise a mutant. An alternative strategy would be, having made a specific in-frame deletion in a pyrE strain, to use ACE to introduce a wild type copy of the gene into the chromosome at the pyrE locus concomitant with the correction of this allele back to a PyrE-positive phenotype. Accordingly, complementation vectors (pMTL-YN1C and pMTLYN2C, for strains 630 and R20291, respectively) were constructed (MATERIALS AND METHODS) especially for this purpose, together with derivatives (pMTL-YN1X and pMTLYN2X, for strains 630 and R20291, respectively) carrying a strong promoter (the fdx promoter) to direct the over expression of the complementing gene. In contrast to in situ complementation, and as a consequence of being able to directly select for uracil prototrophy without the need to isolate pure single crossover clones, the successful introduction of genes using these vectors takes between 5 and 7 days.
To test the utility of this approach, we targeted the mtlD gene which forms part of the operon responsible for mannitol metabolism in C. difficile strain 630Δerm, using plasmid pMTL-YN3::630mtlD. The ability of C. difficile to ferment mannitol is a distinguishing feature and forms the basis of CDSA (Clostridium difficile Selective Agar) developed by Becton Dickinson [23]. Fermentation of mannitol in this medium causes a pH drop, which causes the indicator present to change in color, from red to yellow. In many bacteria mannitol is transported into the cell via a typical phosphotransferase system (PTS), and therefore couples transport to phosphorylation of the sugar [24]. The mtl operon in E. coli consists of the mtlA, mtlR, and mtlD genes that respectively encode the mannitol transporter (enzyme IICBAmtl), a transcriptional regulator, and mannitol-1-phosphate dehydrogenase [25]. The arrangement of genes in C. difficile 630Δerm is predicted to be equivalent to that of B. stearothermophilus and comprises four putative genes: mtlA (enzyme IICBmtl), mtlR, mtlF (enzyme IIAmtl), and mtlD [26], [27].
Following transfer of the knock-out plasmid pMTL-YN3::630mtlD into C. difficile 630Δerm, three FOA resistant clones were isolated. PCR screening using primers mtlD-F3 and mtlD-R3, that anneal to the upstream and the downstream sequence of mtlD, demonstrated that two clones were ΔmtlD mutants, yielding a PCR product of 1,418 bp, while the third clone was a wild type revertant, yielding a PCR product of 2,582 bp (Supporting Information File S1). Nucleotide sequencing of the 1,418 bp products confirmed that the desired mtlD in-frame deletion had been created.
On isolation of the mtlD mutant, the pyrE− gene was converted back to pyrE+ using plasmid pMTL-YN1 as described above. In addition, two further derivatives of pMTL-YN1 were employed which simultaneously delivered a functional copy of the mtlD wild type gene into the genome immediately downstream of the corrected pyrE gene. Plasmid pMTL-YN1CmtlD introduced the mtlD structural gene into the chromosome together with its native promoter. In contrast, pMTL-YN1XmtlD placed the inserted gene under the control of the strong fdx promoter. In both instances, the inserted mtlD gene was followed by the transcriptional terminator sequence [6] derived from the ferredoxin gene of Clostridium pasteurianum. The purpose of the terminator was to prevent polar effects being exerted by the inserted gene on the downstream gene, CD0188. In both cases, six independent PyrE+ clones able to grow on minimal media in the absence of uracil were screened for the presence of the wild type allele by PCR using primers Cdi630-pyrD-sF1 and Cdi630-CD0189-SR3. All twelve clones gave the expected 2,058 bp DNA product, equivalent to a wild type control. Nucleotide sequencing confirmed its identity as a wild type pyrE allele.
Phenotypic analysis confirmed that the mtlD mutant was no longer able to ferment mannitol. Thus, in contrast to the wild type and complemented strain, no growth was evident on minimal media containing mannitol as the sole carbon source (Figure 7A). Moreover, growth of the mutant in liquid media comprising a mannitol-rich complex media (BD Diagnostics, USA) was severely retarded (Figure 7B), and only a slight decrease in the pH of the culture was evident (Figure 7C). The complemented mutant, on the other hand grew at the same rate as the wild type, as did the complemented mutant in which the native mtlD promoter had been replaced with the strong fdx promoter. In this instance, at least, any phenotypic benefit of increasing the expression of mtlD could not be measured.
(A) Clock-wise from top-left, C. difficile 630Δerm (1) 630ΔermΔmtlD mutant (2), and 630ΔermΔmtlD-complemented (3) and 630ΔermΔmtlD-overexpressed (4) were streaked onto minimal media agar with mannitol as the sole carbon source and incubated for 48 h to observe growth. In contrast to the wild type, complemented and overexpressed strains, no growth was evident for the 630ΔermΔ mtlD mutant. (B) The growth of ΔmtlD was limited in mannitol broth, while growth of the ΔmtlD complemented and mtlD overexpressed strains were restored to wildtype levels. (C) The pH of the media broth showed a dip in pH caused by the fermentation of mannitol for the wildtype, ΔmtlD complemented and ΔmtlD overexpressed strains, which correlate to their growth. The 630 Δerm ΔmtlD mutant strain grew very weakly in mannitol broth, which was reflected in the sustained pH levels of the media. All experiments were undertaken in triplicate. The data, complete with error bars is provided in the Supporting Information File S1.
Finally, to confirm the utility of this approach to complementation, we created the complementation plasmids pMTL-YN1Cspo0A and pMTL-YN2Cspo0A (MATERIALS AND METHODS) and used them to insert a functional copy of the strain 630Δerm spo0A gene into the genomes of the spo0A mutants of strains 630Δerm and R20291 concomitant with restoration of the pyrE mutant allele back to wild type. The sporulation phenotypes of the resultant strains were restored to that of the wildtype (Supporting Information File S1).
Discussion
For many years the gene tools available to bring about specific, directed modifications of C. difficile at the genetic level were scant indeed. In the present study we have capitalised on the development of ACE technology to devise and exemplify methods for the generation and complementation of precise allelic exchange mutants in the C. difficile genome based on the use of various pyrE alleles. The use of genes involved in uracil metabolism, such as pyrE and pyrF, as a negative-/counter- selection marker has previously been demonstrated in a number of different bacteria and yeast [10]–[15], where it is reliant on the initial creation of a mutant defective in the chosen gene to act as the host for mutant construction. The deployment of ACE technology ensures this is a relatively simple and rapid undertaking. More important, as demonstrated here, ACE may be used to rapidly convert the host back to pyrE+, allowing the assessment of the mutant phenotype in a ‘clean’, wild type background. Such an undertaken has not generally been applied in other systems. Thus, for instance, the mutants created in C. thermocellum [15] using the organisms own pyrF gene as a counter-selection marker were always analysed in the ΔpyrF strain in which they were created. Similarly, a mutagenesis system developed in Bacillus subtilis, based on the use of the upp gene [28], has been adapted for use in C. acetobutylicum (P Soucaille, pers comm.) and is always undertaken, and the resultant mutants made analysed in, a upp- background. The use of a background defective in nucleoside metabolism can complicate the assessment of the effect of the mutation under analysis. This is particularly the case in the investigation of pathogens and virulence, where mutants in nucleoside metabolism are considered a form of disablement in their own right [29]. This has considerable impact on studies designed to assess the effect of mutation of other loci on virulence, particularly in vivo.
We have demonstrated the robustness and reliability of this pyrE method of mutagenesis in both C. difficile 630 Δerm and C. difficile R20291, through the creation of in-frame deletion mutants in spo0A, cwp84 and mtlD. We have re-affirmed the value of strategies based on pseudo-suicide vectors, and in the case of 630Δerm improved the options available through the further disablement of the pCB102 replicon used by the introduction of a frameshift in the repH gene. This was found to facilitate the ease with which single crossover integrants were isolated, which tend to emerge after just two passages of transconjugants on selective media. This is in contrast to strain R20291 allelic exchange vectors, which make use of the pBP1 vector. During the course of this work we have confirmed that the annotated mtlD locus is indeed involved in mannitol utilisation and re-affirmed that Cwp84 plays a role in the processing of SlpA. Intriguingly, we found that despite the introduction of the cwp84 frame-shift in R20291, unlike 630Δerm, some processing of SlpA was still occurring in this strain. The in-frame deletion of both strains results in an internal deletion of 406 amino acids from the protein (total 804 amino acids). Whilst the truncated protein that results still contains Cys116, an important residue in the active site of the protease [22], it seems unlikely that the protein retains proteolytic activity, particularly as the truncated protein in the 630Δerm mutant is identical. Moreover, no signal was detected by immunoblot analysis in the two mutant strains, suggesting that there is no expression at all of the protease, even in a truncated form, or that this form is quickly degraded in the cell. Perhaps strain R20291 produces a secondary protease also able to process SlpA? At this stage no one explanation can be ruled out. Here our focus has been on the development and description of the mutagenesis method, and our data on individual mutants remains observational.
The method developed here is in many respects equivalent to our recent description of the use of codA as a counter selection [8]. Indeed, the allelic exchange cassettes and methodological procedures are the same, except counter-selection is based on differential resistance to FOA (PyrE) rather than FC (CodA). Accordingly, the isolation of mutants using either protocol takes around 3–4 weeks to accomplish once the allelic exchange vectors have been constructed, and both methods may be subsequently employed to undertake in situ complementation of the mutated allele (exchange of the mutant allele with the wild type gene). A pivotal difference is that codA-based mutagenesis [8] can be undertaken in a wild type background (provided the host does not carry a native codA gene, as is the case in C. botulinum, C. sporogenes and C. ljungdahlii), whereas the method described here requires the initial creation of a pyrE mutant which needs to be corrected back to wild type once a mutant at a distal locus has been created. However, using ACE, this is rapid (5 days), and provides the opportunity to complement the mutant in parallel, through concomitant insertion of a wild type copy of the gene either under the control of its native promoter, or the strong fdx promoter.
Complementation is essential to unequivocally confirm the role of a genetic determinant in a specific phenotype [30]. Complementation is traditionally achieved using multicopy plasmids. The consequent abnormal gene dosage can, however, frequently fail to restore phenotype to wildtype levels. Thus, CwpV was over produced in a plasmid complemented cwpV mutant of C. difficile [31], the perfringolysin O titre of a virR mutant of the C. perfringens strain 56 was approximately 3-fold higher than the wild type strain when complemented with a multicopy plasmid carrying the virRS genes [32], while in a study of Clostridium septicum ‘haemolytic activity of the complemented strain was higher than the parent strain …‥ presumably a reflection of the presence of the csa gene on a multicopy plasmid.’ [33]. In the study of Dingle and co-workers [34], ‘although the wild-type 630Δerm strain and the fliC mutant strain produced FliD, the fliC-complemented strain did not, suggesting that there was a reduction in fliD gene expression when FliC is expressed in trans off a plasmid rather than in cis from the chromosomal gene’. Similarly, plasmid complemented agr mutants of Clostridium perfringens failed to completely regain wild-type sporulation levels [35], a phenomenon attributed by the authors to ‘complementation involving a multicopy plasmid carrying the cloned agr locus’.
Ancillary effects can also arise when using plasmids for complementation studies due to the need to maintain plasmids, and the complementing gene, through supplementation with antibiotics. Thus, for instance, complementation of the a sleC mutation using a plasmid-located gene did not restore the phenotype to wild type [20], but did restore germination to the reduced level obtained in a vector only control. The presence of the plasmid alone, and most likely the effect of the added thiamphenicol needed to maintain the plasmid, detrimentally effected spore germination. Consequently, the use of plasmid complementation systems may require the inclusion of a vector only control [20]. This is not required when using ACE-based complementation at the pyrE locus. Crucially, the intrinsic stability of chromosomal complementation makes it the method of choice in those situations where plasmid maintenance through antibiotic supplementation is not a viable option, such as when complementation in an in vivo model is required.
The use of plasmids pMTL-YN1C and pMTL-YN2C positions the complementing gene in the genome immediately downstream of the pyrE gene (CD0187). This allows read through from the upstream promoter responsible for transcription of pyrE, the identity of which is unknown but may reside immediately upstream of CD0187 or, more likely, CD0184. The availability of transcriptional read through is important in those cases where the identity of the natural promoter of the complementation gene is not defined, and cannot be guaranteed to be cloned along with the structural gene, allowing, for instance, a promoter-less copy of the structural gene to be cloned. In those instances where the promoter is defined, and the operator wishes to exclude read through, a transcriptional terminator may simply be added during the cloning of the complementation gene and its promoter.
In certain instances it may be desirable to bring about ‘overexpression’ of the complementing gene. For this purpose, two further vectors were constructed (pMTL-YN1X and pMTLYN2X, for strains 630 and R20291, respectively) carrying the promoter of the ferredoxin gene (fdx) of Clostridium sporogenes. As a consequence of its central role in anaerobic electron transfer, the ferredoxin gene is highly expressed in Clostridium, with the ferredoxin protein representing, for instance, up to 2% of the soluble protein in Clostridium pasteurianum [36]. Indeed the fdx promoter of C. perfringens has been used to derive a highly effective clostridial expression system [37], while the C. sporogenes fdx promoter used here was employed to maximise expression of a nitroreductase gene in C. sporogenes [38].
Whichever vectors are used, their deployment involves only marginal additional effort compared to the use of autonomous complementation vectors. Thus, both methods (plasmid-based and ACE-based complementation) involve the assembly of the requisite vector in E. coli and its transformation into the appropriate clostridial mutant and the selection of transconjugants on antibiotic supplemented plates. ACE-mediated complementation merely requires re-streaking of the primary transconjugant onto minimal media lacking uracil. All those colonies that develop represent complemented strains in which the pyrE allele has been corrected to wildtype. The additional time required, therefore, equates to merely the 2 days needed for uracil prototrophic colonies to develop on the minimal media.
Conclusion
We have demonstrated the use of a pyrE-based allele exchange system to make precise alterations to the genome of C. difficile. In using a pyrE- strain as the host, by whatever means a mutant is made (e.g., allelic exchange or ClosTron), the facility to insert a wild type copy of the gene at the pyrE locus provides a rapid mechanism for generating a stable complementation clone that is not compromised by inappropriate gene dosage effects. As such, the pyrE mutants made here are available to the scientific community for mutagenesis studies, along with the requisite pyrE correction vectors. The genomes of both strains have been subjected to genome re-sequencing and found to be devoid of any additional SNPs or Indels compared to the progenitor 630Δerm strain or R20291 parental strains.
Materials and Methods
Bacterial strains and growth conditions
Escherichia coli TOP10 (Invitrogen) and E. coli CA434 [39] were cultured in Luria-Bertani (LB) medium, supplemented with chloramphenicol (25 µg/ml), where appropriate. Routine cultures of C. difficile 630 Δerm [40] and C. difficile R20291 were carried out in BHIS medium (brain heart infusion medium supplemented with 5 mg/ml yeast extract and 0.1% [wt/vol] L-cysteine) [41]. C. difficile medium was supplemented with D-cycloserine (250 µg/ml), cefoxitin (8 µg/ml), lincomycin (20 µg/ml), and/or thiamphenicol (15 µg/ml) where appropriate. A defined minimal media [18] was used as uracil-free medium when performing genetic selections. A basic nutritive mannitol broth for growth assays of C. difficile strains were prepared as follows : Proteose peptone no. 2 4% [wt/vol] (BD Diagnostics, USA), sodium phosphate dibasic 0.5%[wt/vol], potassium phosphate monobasic 0.1%[wt/vol], sodium chloride, 0.2% [wt/vol], magnesium sulfate, 0.01% [wt/vol], mannitol, 0.6% [wt/vol] with final pH at +/−7.35. For solid medium, agar was added to a final concentration of 1.0% (wt/vol). Clostridium sporogenes ATCC 15579 was cultivated in TYG media [7]. All Clostridium cultures were incubated in an anaerobic workstation at 37°C (Don Whitley, Yorkshire, United Kingdom). Uracil was added at 5 µg/ml, and 5-Fluoroorotic acid (5-FOA) at 2 mg/ml. All reagents, unless noted, were purchased from Sigma-Aldrich.
Conjugation into C. difficile
Plasmids were transformed into E. coli donor, CA434 and then conjugated into C. difficile [42]. Thiamphenicol (15 µg/ml) was used to select for catP-based plasmid. D-cycloserine (250 µg/ml) and cefoxitin (8 µg/ml) were used to counter select against E. coli CA434 after conjugation.
DNA manipulations
DNA manipulations were carried out according to standard techniques. C. difficile genomic DNA for use in cloning and PCR analysis was prepared as described previously [9]. Polymerase chain reactions (PCR) used Failsafe™ PCR system (Epicentre) and Taq polymerase (Promega) in accordance with the manufacturers' protocols using primers detailed in Table 1. Primer design for amplification of DNA from C. difficile 630 Δerm and R20291 strains were based on the available C. difficile genomes from the EMBL/GenBank databases with accession numbers AM180356 and FN545816 respectively. The oligonucleotides and the plasmids/strains used in this study are listed in Table 1 and Table 2, respectively. All DNA manipulations and cloning procedures were performed as per Sambrook [43].
Vector Construction
Plasmid pMTL-YN18 (accession number; JX465728), used to create a pyrE− mutant in R20291, is an equivalent vector to pMTL-JH18 [9] in which the pCB102 replicon was replaced with that of pBP1 (isolated from pMTL82251), using the flanking AscI and FseI sites specifically created for this purpose [17]. Plasmid pMTL-YN1 (accession number; JX465729) was made by cloning a 1,753 bp SbfI/AscI fragment between the corresponding restriction sites of plasmid pMTL-JH20 [9]. This fragment was generated from the 630Δerm genome by PCR using the primers pyrE-int-SbfI-F and pyrEcomplement-Asc1-R, and carries a truncated copy of pyrE, lacking the first 50 nucleotides of the structural gene, together with 1200 bp from immediately 3′ to the stop codon of pyrE, which includes the entire coding sequence of CD0188 of 630Δerm. To generate the equivalent pyrE correction vector (pMTL-YN2, accession number; JX465732) for R20291, the pCB102 replicon of pMTL-YN1 was replaced with that of pBP1 from pMTL82251 (using the AscI and FseI sites) and the 630Δerm DNA between the SbfI and AscI sites replaced with the equivalent region from the R20291 genome. In this case, the DNA was synthesized by DNA2.0 specific to the R20291 chromosome by PCR as two contiguous SbfI/NdeI and NdeI/AscI fragments. The PyrE complementation vector pMTL-ME2 was constructed by inserting the C. sporogenes ATCC 15579 pyrE gene into pMTL83151. The pyrE gene was amplified by PCR from genomic DNA prepared from Clostridium sporogenes ATCC 15579 using primers Csp-pyrE-HpaI-sF1 and Csp-pyrE-HpaI-sR1. The PCR product was digested with HpaI and gel purified followed by cloning in same orientation as catP in pMTL83151 [17] linearized with the same enzyme.
To construct the ACE overexpression plasmids pMTL-YN1X (accession number; JX465731) and pMTL-YN2X (accession number; JX465734), a 214 bp NotI/NdeI fragment encompassing the C. sporogenes fdx promoter was isolated from plasmid pMTL82253 and inserted between the equivalent sites of pMTL-JH14 [9]. The plasmid obtained (pMTL-JH14::Pcspfdx) was cleaved with NheI, and ligated to two, annealed oligonucleotides (Cpa-TT-Oligo-1 and Cpa-TT-Oligo-2) which encompassed the transcriptional terminator of the Clostridium pasteurianum ferredoxin gene. A 517 bp NotI/NheI fragment (encompassing the fdx promoter, lacZ' and multiple cloning sites, and the transcriptional terminator of the C. pasteurianum ferredoxin gene) was then isolated from the resultant plasmid (pMTL-ME6X) and inserted between the equivalent sites in pMTL-YN1 and pMTLYN2, to yield pMTL-YN1X and pMTL-YN2X, respectively. In parallel, pMTL-ME6X was digested with EcoRI and NheI and the released 293 bp fragment inserted between the equivalent sites of pMTL-JH14 [9] to make pMTL-ME6C. This plasmid was then cleaved with NotI and NheI, and the released 323 bp fragment inserted between the equivalent sites of pMTL-YN1 and pMTLYN2, to yield the complementation vectors pMTL-YN1C (accession number; JX465730) and pMTL-YN2C (accession number; JX465733), respectively.
Allelic Exchange Cassettes
Allele exchange cassettes were assembled, specific to the three target loci (spo0A, cwp84 and mtlD) of the two strains, composed of a left-hand homology arm (LHA) and a right-hand homology arm (RHA), each of approximately 500 to 800 bp in size. Each cassette was cloned between the SbfI and AscI restriction recognition sites in pMTL-YN3 (accession number; JX465735) to create pMTL-YN3::630spo0A*, pMTL-YN3::630cwp84* and pMTL-YN3::630mtlD*. Similarly, pMTL-YN3::R20291spo0A* and pMTL-YN3::R20291cwp84* were made by cloning the allelic exchange cassettes between the AscI and SbfI sites in pMTL-YN4 (accession number; JX465736).
The spo0A knockout cassette was synthesized by DNA2.0 which consists of a 672 bp LHA (bases 1412012 to 1412789 on the forward strand of C. difficile 630 Δerm genome) fused to a 800 bp RHA (bases 1413275 to 1414074 on the forward strand of C. difficile 630 Δerm genome) which were designed to make an in-frame deletion removing codons 65 to 226, inclusive, out of a total of 275 codons). For the equivalent in C. difficile R20291, a 778 bp LHA (bases 1319650 to 1320427 on the forward strand of the C. difficile R20291 genome) was fused to a 800 bp RHA (bases 1320913 to 1321712 on the forward strand of the C. difficile R20291 genome). Each cassette was designed to incorporate a SbfI site at the 5′ end and an AscI site at the 3′ end to facilitate cloning into the pMTL-YN3 plasmid. The cwp84 knockout cassette consists of a 653 bp LHA (bases 1045907 to 1046559 on the reverse strand of the C. difficile 630 Δerm genome) fused to a 558 bp RHA (bases 1047778 to 1048335 on the reverse strand of the C. difficile 630 Δerm genome) which were designed to remove codons 214 to 629, inclusive, representing the removal of 417 codons from a total of 814). For the equivalent in C. difficile R20291, a 713 bp LHA (bases 1067119 to 1067771 on the reverse strand of the C. difficile R20291 genome) was fused to a 558 bp RHA (bases 1068990 to 1069547 on the reverse strand of the C. difficile R20291 genome). The mtlD knockout cassette consists of a 654 bp LHA (bases 1593564 to 1594217 on the reverse strand of the C. difficile 630 Δerm genome) fused to a 654 bp RHA (bases 1595353 to 1596006 on the reverse strand of the C. difficile 630 Δerm genome) which were designed to make an in-frame deletion between codon 3 and codon 387 of mtlD (total codons 388).
Complementation Vectors
Plasmids for the complementation of the spo0A mutants of strains R20291 and 630Δerm were constructed as follows. The spo0A of strain C. difficile 630Δerm was PCR amplified as a 1216 bp DNA fragment using the two primers spo0A-SpeI-F and spo0A-BamHI-R and cloned in pCR2.1 vector (Invitrogen) and verified by sequencing. The spo0A was re-isolated as a 1.2 kb EcoRI and BamHI fragment and inserted between the equivalent sites of pMTL-YN2C to give the R20291 complementation plasmid pMTL-YN2Cspo0A. To derive an equivalent plasmid for strain 630Δerm, the spo0A gene was excised from pMTL-YN2Cspo0A as a 1.2 kb DNA fragment following cleaved with NotI and BamHI and inserted into the appropriate sites of pMTL-YN1C to give the complementation plasmid pMTL-YN1Cspo0A.
To generate the two required allelic exchange cassettes need for complementation of the cwp84 in-frame deletions, the portion of cwp84 missing in the two plasmids (pMTL-YN4::R20291cwp84* and pMTL-YN3::630cwp84*) originally used to make the in-frame deletions were synthesised (DNA2.0) as a 1,082 bp NdeI-KpnI fragment (R20291) and a 1,255 bp NdeI-XbaI fragment (630Δerm) generated by cloned into the appropriate allelic exchange vectors to yield plasmids pMTL-YN4::R20291cwp84c and pMTL-YN3::630cwp84c. In order to be able to distinguish the complementation allele from wild type, the synthesised region included a single nucleotide change (T to A) to base 2280 of cwp84 which retains the codon specificity (codon 760, Valine) but creates a ScaI restriction enzyme recognition site.
The complementation plasmid pMTL-YN1CmtlD was constructed by the PCR amplification of the C. difficile 630Δerm mtlD gene, together with its 5′ non-coding region, as a 1,779 bp fragment (using primers mtlD-NotI-F and mtlD-BamHI-R), and its subsequent insertion, following cleaved with NotI and BamHI, between the NotI and BamHI sites of pMTL-YN1C. pMTL-YN1XmtlD was derived by the PCR amplification of the C. difficile 630Δerm mtlD structural gene alone (ie., lacking its native promoter), as a 1,161 bp fragment (using primers mtlD-NdeI-F and mtlD-BamHI-R), cleaved with NdeI and BamHI, and insertion between the NdeI and BamHI sites of pMTL-YN1X. This positioned the mtlD gene under the transcriptional and translational (RBS) control of fdx promoter.
ACE Procedure
The procedure adopted was as previously described [9]. For inactivation of pyrE, E. coli CA434 donor cells carrying pMTL-YN18 were conjugated with R20291 and transconjugants selected on BHIS media supplemented D-cycloserine (250 µg/ml), cefoxitin (8 µg/ml), thiamphenicol (15 µg/ml) and uracil (5 µg/ml). A single transconjugant was re-streaked onto the same medium and then a ‘large’ representative colony streaked onto minimal agar medium agar supplemented with FOA (2 mg/ml) and uracil (5 µg/ml). The colonies that arose were re-streaked twice onto the same media, and analyzed by PCR to confirm deletion of pyrE (as detailed in Results), and Sanger sequencing was used to confirm the expected genotype. Confirmation that the plasmid had been lost, was obtained by patch plating onto BHIS agar supplemented with thiamphenicol and establishing that no growth occurred. For correction of the pyrE mutation (ie., plasmids pMTL-YN1, 1C, 1X, 2, 2C and 2X) transconjugants were streaked onto minimal media without uracil or FOA supplementation and those colonies that developed analysed as above.
Allelic exchange procedure
The adopted protocol resembles that used for the isolation of allelic exchange mutants using codA as a negative selection marker [8], except counter-selection was based on differential resistance to FOA rather than FC. It in essence involves the initial isolation of pure single crossovers clones, and their subsequent transfer onto selective plates to identify those cells in which the plasmid has excised. These clones correspond to colonies that are resistant to FOA as a consequence of loss of the heterologous PyrE+ allele and reversion to a pyrE minus phenotype. Depending which homology arm undergoes recombination, plasmid excision can result in either the desired double crossover mutant, or a wild type cell. In the absence of any bias, the wild type cells and desired mutants should be present in equal proportions, ie., 50∶50.
Each plasmid was conjugated into the appropriate host and plated onto BHIS media (supplemented with cycloserine, cefoxotin, thiamphenicol and uracil) and the transconjugants restreaked onto fresh media to allow the identification of putative single crossover mutants. These were readily identified as visibly larger colonies after 16–24 hr. Such colonies were sequentially restreaked from single colonies and after 2–4 passages, their identify and purity confirmed by an appropriate PCR. Unlike ACE, where powerful selection allows the purification of the desired double crossover excision event, it is crucial that the single cross-over integrants are pure, and not contaminated with wild type cells, ie., cells in which integration has not occurred. Otherwise, the contaminating wild type cells, which are all resistant to FOA, will cause unacceptable high background when cells are plated on FOA media during the screen for the desired double crossover events. To establish that no wild type cells were present, an appropriate primer pair (spo0A-YN-F2/spo0A-YN-R2 in the case of spo0A, cwp84-F3/cwp84-R4 in the case of cwp84, and mtlD-F3/mtlD-R3 the case of mtlD) was used that annealed to the chromosome at positions that flanked the site of the in-frame deletion but that were both distal to the regions that comprised the homology arms of the plasmid borne allelic exchange cassette. The absence of a DNA product of a size consistent with the wild type indicated clonal purity, and that wild type cells were not present. To confirm that they were indeed single crossover integrants, two different primers (M13F and M13R) were used that annealed to plasmid specific sequences together with the appropriate flanking primers. The presence of a DNA fragment indicated that the clones were indeed single crossover integrants, while the size was diagnostic of at which homology arm (LHA or RHA) recombination had occurred.
Following the isolation of pure single crossover integrants of the two strains, a single colony was re-streaked onto minimal medium supplemented with FOA and uracil to select for cells in which the integrated plasmid had excised. The isolated FOA resistant colonies were then screened by PCR using primers that anneal to the upstream and the downstream sequence of the respective target. DNA products of the predicted size were subjected to Sanger sequencing to confirm their genotype.
Cwp84 Analysis Methods
S-layer extracts from the WT, mutant and complemented strains were prepared by the glycin acid method [44]. Proteins were separated by SDS-PAGE and transferred onto a PVDF membrane for immunoblotting. Blocking of the membrane was followed by incubation with either anti-Cwp84 (1/2,000 dilution) or anti-HMW-SLP (1/10,000 dilution). Washing was done as previously described [45], and bound antibodies were detected using goat anti-rabbit immunoglobulin G alkaline phosphatase conjugate (1/20,000 dilution; Sigma) with the substrates nitroblue tetrazolium and 5-bromo-4-chloro-3-indolylphosphate (Sigma). Anti-HMW-SLP antibodies were a kind gift from Pr. Neil Fairweather, Imperial College, London.
Author Contributions
Conceived and designed the experiments: YKN AC STC NPM. Performed the experiments: YKN ME SP MMC CJ. Analyzed the data: YKN CJ AC NPM. Contributed reagents/materials/analysis tools: ME SP. Wrote the paper: YKN CJ SC NPM.
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