|Home | About | Journals | Submit | Contact Us | Français|
Two inducible temperate bacteriophages ΦS9 and ΦS63 from Clostridium perfringens were sequenced and analyzed. Isometric heads and long non-contractile tails classify ΦS9 and ΦS63 in the Siphoviridae family, and their genomes consist of 39,457 bp (ΦS9) and 33,609 bp (ΦS63) linear dsDNA, respectively. ΦS63 has 3′-overlapping cohesive genome ends, whereas ΦS9 is the first Clostridium phage featuring an experimentally proven terminally redundant and circularly permuted genome. A total of 50 and 43 coding sequences were predicted for ΦS9 and ΦS63, respectively, organized into 6 distinct lifestyle-associated modules typical for temperate Siphoviruses. Putative functions could be assigned to 26 gene products of ΦS9, and to 25 of ΦS63. The ΦS9 attB attachment and insertion site is located in a non-coding region upstream of a putative phosphorylase gene. Interestingly, ΦS63 integrates into the 3′ part of sigK in C. perfringens, and represents the first functional skin-element-like phage described for this genus. With respect to possible effects of lysogeny, we did not obtain evidence that ΦS9 may influence sporulation of a lysogenized host. In contrast, interruption of sigK, a sporulation associated gene in various bacteria, by the ΦS63 prophage insertion is more likely to affect sporulation of its carrier.
Clostridium perfringens is an anaerobic Gram-positive spore-forming rod, frequently isolated from soil, freshwater sediments, sewage and the gastrointestinal tract of both humans and animals. It is the causative agent of food poisoning and gas gangrene in humans, and enteric diseases in these hosts. Fourteen types of toxins are known so far;1 among them, α- (phospholipase C), β-, ε- and ι-toxins are used to classify C. perfringens into five biotypes (A–E). Others include θ-toxin (perfringolysin O), µ-toxin (hyaluronidase), κ-toxin (collagenase), a sporulation-associated (food-poisoning) enterotoxin (CPE), the structure of which was recently solved,2,3 and others.1 The TpeL-toxin, which is produced during sporulation, is another addition to that family.4,5 Phenotypic variations among the isolates, such as different toxins produced and various degrees of symptoms severity could mainly be attributed to a high degree of genomic variability, as evidenced from comparative genomic studies using three complete C. perfringens (biotype A strains) genome sequences (a food poisoning strain S13, a CPE-negative gas gangrene isolate ATCC13124 and a CPE-negative and gas gangrene-causing strain (SM101)).6,7 In addition to the variation in chromosome-encoded toxin/virulence genes, large plasmids with strain-specific genes8,9 were identified, offering insights into a wide range of environmental adaptations and virulence traits.6 Interestingly, no clear explanation regarding the extremely diverse sporulation efficiencies among the isolates could yet be found. Many of the above mentioned genes appear to be located in mobile elements, or are transferred via conjugational processes.6
Bacterial chromosomes contain a significant proportion of prophage sequences, as mobilizable elements. For example, Streptococcus pyogenes features a genome with more than 10% phage-related sequences,10 and in Escherichia coli O157:H7 strain Sakai, prophage elements account for 16% of the total genome.11 These elements are involved in horizontal gene transfer and their characteristics offer insights into evolutionary processes of the host.12 In addition, prophages often encode virulence genes such as toxins, and provide an explanation for various bacterial virulence characteristics among the different strains.10,12 Thus far, only 12 C. perfringens phage sequences are available from public databases. Prophage Φ362613 was the first C. perfringens phage sequence published, later followed by episomal prophage ΦSM101 identified in sequenced C. perfringens genomes.6 Recently, sequences of phages ΦCP39O and ΦCP26F, as well as ΦCP9O, ΦCP13O and ΦCP3O were reported.14,15 The Podovirus ΦCPV1 was described as the smallest C. perfringens phage isolated so far, both in terms of particle dimensions and DNA size.16 Three recently described virulent podoviruses feature slightly bigger genomes of approximately 18 kb.17 Some trials using C. perfringens specific bacteriophages (CPAS-cocktail) to counteract necrotic enterocolitis have been published.18 Phage ΦCP24R was described as a small virulent podovirus featuring an 18.92 kb genome.19
We here report the sequence and analysis of temperate phages ΦS9 (vB_CpeS-PhiS9) and ΦS63 (vB_CpeS-PhiS63), induced from C. perfringens strains S9 and S63, respectively. We determined and compared their physical genome structures and phage integration sites. ΦS9 was previously reported to influence sporulation of C. perfringens,20 which prompted us to investigate the effects of lysogenic conversion of C. perfringens by ΦS9 and ΦS63.
Transmission electron microscopy revealed an icosahedral head (60.4 nm in size) and a long non-contractile tail (Figs. 1A–C) for ΦS9, placing it into the family Siphoviridae in the order of the Caudovirales.21 The tail structure is rather unusual since that it lacks a typical baseplate structure and features a tail fiber cover-like structure (TFC) instead (Fig. 1B, black arrows and and1C).1C). This component was found to quite easily separate from the tail during particle preparation for EM. The tail shaft is 191 nm long and 11 nm wide, and the prominent central tail fiber itself is 46.6 nm long, 3.2 nm wide. Dimension of the TFC is approximately 102 nm long and 10 nm wide (Fig. 1C).
Phage ΦS63 also belongs to the Siphoviridae, featuring a 170 nm tail with a diameter of 11 nm and a head of 62 nm diameter (Fig. 1D–G). In contrast to ΦS9, the ΦS63 tail features a classical baseplate structure (Fig. 1F and G). Putative baseplate spikes are visible at the lower end of the base plate (Fig. 1G). It is interesting to note that in all negatively stained ΦS63 particles, very unusual and satellite bubble-like structures are present, arranged around the lower part of the tail just above the base plate, and at the upper portion of the tail just below the head-tail connector (Fig. 1D, black arrows). These structures most likely represent curled tail fibers and/or long whiskers, likely involved in the recognition of and/or interaction with the host cells surface.
The complete unit genome (not considering possible redundancy of the packaged DNA molecule) of ΦS9 features 39,457 bp, which agrees well with the overall size predicted from restriction analysis (Figs. 2 and 3).3). The GC content of 28.1 mol% is identical to C. perfringens (28.1–28.4% as determined from sequenced C. perfringens genomes; results not shown). A total of 50 open reading frames with a minimum length of 150 nt were identified in the ΦS9 genome (coding capacity 92.0%) (Table 1), which is organized into distinct functional modules (Fig. 2). One putative tRNAAsn gene was found at nt position 10,367 to 10,439. A putative function could be assigned to 26 gene products.
The ΦS63 unit genome is 33,609 bp in size, which matches very well with PFGE analysis of full-length phage DNA (data not shown), and reflects the physical size of the packaged molecule (see below). It features a GC-content of 27.5 mol%, slightly less than ΦS9 and the Clostridium host strains. A total of 43 open reading frames could be annotated (89.9% of the coding capacity) (Table 1) and a putative function could be assigned to 25. The ΦS63 genome is also organized in a lifestyle specific, modular fashion (Fig. 2).
We determined the genome structure of both phages ΦS9 and ΦS63. Runoff Sanger sequencing reactions with primers complementary to the ends of the ΦS9 single large contig produced sequence complementary to the other end of the contig (data not shown). Ligation of ΦS9 DNA prior to digestion and heat treatment (75°C for 10 min) did not alter restriction patterns (Fig. 3A). In addition, Bal31 exonuclease treatment of ΦS9 DNA followed by EcoRI or NsiI digestion simultaneously decreased the intensity of all restriction fragments over time (Fig. 3B),22,23 and no specific fragment was shortened. These findings clearly indicated that ΦS9 DNA represents a collection of terminally redundant and circularly permuted DNA molecules.
In contrast, when full length ΦS63 DNA was subjected to pulsed field gel electrophoresis, it yielded a pattern of unit-size genomes joined in a concatemeric fashion (data not shown), indicating the presence of self-ligating cohesive (cos) genome ends in these DNA molecules. Heating prior to electrophoresis changed the restriction pattern in a characteristic fashion (Fig. 3C), which also perfectly matched the in silico predictions. Sequencing of a PCR product generated from C. perfringens S63, using primers cos_fw and cos_rev (Table S1), and comparison to sequence generated with the same primer pair using linear ΦS63 DNA yielded the precise structure and sequence of the terminal single-stranded cos site region (Fig. 3D), featuring 3′-overhangs of 11 nt (CGCAGTGTCTA).
Only few similarities were found among ΦS9 and ΦS63, and also to other C. perfringens prophages. The two apparently unrelated viruses feature significant similarities only in the lysogeny control region (integrase and repressor), and the endolysin enzymes. However, proteins of both phages feature several homologies to Siphoviruses of other Firmicutes, such as Listeria, Streptococcus and Bacillus,24,25 as well as to (often cryptic) prophages identified in the genomes of these organisms. Some of the ΦS9 structural genes show sequence homology to Brochothrix phage BL3 (e.g., gp38),25 while some of the early genes feature homologies to Listeria phages A118, A006 and A500.22,24
All predicted gene products encoded by the two phages and putative functional assignments are listed in Tables S2 and S3.
A phylogenetic tree of large terminase subunit amino acid sequences can serve as measure of similarity in DNA packaging strategy and relatedness between phages.26 A tree generated of 109 terminase sequences (Fig. S1) placed ΦSM101 with Φ3626 in close relation to ΦS63 in the branch of 3′ cos-phages. ΦS9 and ΦCP39O cluster in the headful packaging branch and phages ΦCP9O, ΦCP13O, ΦCP26F and ΦCP34O form an own branch in the tree. These findings confirm experimentally evaluated packaging strategies and overall relatedness of the phages. No terminase sequences were available for phages ΦCP7R, ΦCP24R, ΦCPV4 and ΦZP2 and none could be predicted by homology searches.
Because genome sequences of C. perfringens strains S9 and S63 have not been available, the insertion sites used by ΦS9 and ΦS63 were identified by inverse PCR from self-ligated C. perfringens S9 or S63 genomic DNA fragments (Fig. 4), and comparison to non-lysogenic host DNA. In the case of ΦS9, the sequence matched a region located next to a different prophage-like element (referred to as Φ13124). Phage ΦS9 integrates into the non-coding intergenic sequence, 541 nt downstream of a gene encoding a putative phosphorylase, and 157 nt upstream of a hypothetical protein. The core sequence of ΦS9 integration is TTACATATTTG (Fig. 4A), which is similar in length to those used by Clostridium phages Φ3626 (12 bp), ΦC2 (11 bp) and ΦCD119 (14 bp).13,27,28
The same approach was used to identify the insertion site for ΦS63 in C. perfringens S63 (Fig. 4B). The GTAATGAAAT 10 nt core of the attB sequence is located at nt position 427 from the the 5′ end and nt 265 from the 3′ end, and the insertion region features significant homology to sigK from C. perfringens S13,7 ATCC 131246 and SM101.6
In the course of our in silico analyses, we identified region 1088991–1128198 (corresponding to CPF_0926–CPF_0977) of strain ATCC131246 as a putative 39,208 bp prophage genome, which was designated Φ13124. Surprisingly, a putative Φ13124 integrase (CPF_0926) was found 100% identical to the ΦS9 integrase. Moreover, the beginning and end of the Φ13124 attP sequence matched the ΦS9 attP, and overall good sequence homologies were found between the two phages. Sequence alignment with ΦS63 indicated another putative prophage sequence in ATCC 13124 (termed Φ13124_2), located on a genomic island6 in between positions 1783746 to 1820131 of the ATCC 13124 genome.6 The putative Φ13124_2 genome is 36,385 bp in size, and this prophage sequence is also flanked by the attachment site used by ΦS63.
The high degree of genomic variation and phenotypic diversities among bacteria appears to be mediated by mobile elements such as conjugative plasmids, transposons and insertion elements. Although lysogenic conversion was established for numerous bacterial species including Clostridia, it has not yet been observed for C. perfringens, possibly due to a lack of data regarding temperate C. perfringens phage.
We here describe the two heterogeneous Siphoviridae ΦS9 and ΦS63. Compared with the other studied C. perfringens phages, ΦS9 and ΦS63 feature significantly larger head diameter and tail length. Interestingly, both also feature unusual tail-associated appendices, which probably assume functions comparable to tail fibers and whiskers. ΦS9 possess the second-largest genome of all known C. perfringens phages, and has been shown to represent a collection of terminally redundant and circularly permuted DNA molecules. In contrast, ΦS63 features identical unit-length genomes with cohesive ends, similar to Φ3626.13 Most of the sequence-based similarities exist to proteins of other (putative) prophages infecting members of the Firmicutes, namely Streptococcus, Lactococcus, Bacillus, Staphylococcus, Listeria, Brochothrix and other Clostridium species (Tables S2 and S3). Altogether, these findings clearly indicate horizontal gene transfer among the ancestors of the bacterial host and their mobile genome element, i.e., the prophages. Likewise, the surprisingly few homologies between ΦS9 and ΦS63, and to other known C. perfringens phages can be explained by divergent evolution of these phages from a distant ancestor. Interestingly, ΦS9 and ΦS63 feature a virtually identical endolysin (95.3% amino acid identity), which has most likely been acquired by a more recent horizontal gene exchange. Also, the endolysin of ΦS63 is 98% identical to the murein hydrolase of the episomal C. perfringens phage ΦSM101, strongly suggesting a modular exchange of functional units. Altogether, the significant heterogeneity among C. perfringens phages emphasizes the need for more sequences in order to obtain a better overview of this probably large and diverse group of viruses infecting and interacting with an important pathogen.
Homology searches with ΦS9 sequences identified prophage Φ13124 in the genome of C. perfringens ATCC 13124. Based on significant homology over wide areas of the genome, the two phages appear to have a common origin, and are clearly different from ΦS63 and Φ3626. Similarities of ΦS9 and Φ13124 include almost identical integrases and repressors, tail structural components, the holin-endolysin dual lysis module, and the major capsid protein. Φ13124 is inserted within the largest genomic island (243 kb) of the host bacterium, which also contains genes responsible for iron transport, fucose utilization, and glycolytic activities,6 enabling this strain to exploit various environments.6 Interestingly, it also contains the sporulation-related genes cotJB and cotJC, as well as some putative virulence factors such as a sialidase located near the right arm of Φ13124.6 Whether prophage Φ13124 is able to mobilize these closely positioned genes by either a faulty phage excision or generalized transduction is, however, speculative and needs more investigation.
Another putative prophage Φ13124_2 in the ATCC 13124 genome6 was identified using sequence alignment with the ΦS63 genome, sharing extensive sequence similarity among most of the structural proteins. The lack of homology in lysogeny control or DNA replication proteins suggested a more distinct evolution of these two phage sequences. However, it remains to be determined if Φ13124_2 is a functional virus, in contrast to the frequent occurrence of defective or cryptic remnants of inserted phage.
Lysogenic conversion may result from expression of genes located on an inserted phage genome,10,29 or by integration and disruption of coding sequence.22,27 The putative effect of C. perfringens phage ΦS9 on sporulation of its lysogenized host has been subject of discussion over many years. Stewart and Johnson (1977) claimed that curing of ΦS9 from C. perfringens strain S9 delayed sporulation, while a re-lysogenized strain S9CR restored the sporulation competent phenotype.20 This suggested possible lysogenic conversion of C. perfringens by ΦS9. Unfortunately, we were unable to confirm this hypothesis, i.e., we found no indication for lysogenic conversion of C. perfringens by phage ΦS9. The presence or absence of prophage ΦS9 in the C. perfringens strain S9 genome did not significantly influence the onset of production of heat-resistant spores or the total number of spores produced under experimental conditions similar to those published previously20 (Kim K.-P., unpublished data).
The integration site of ΦS9 is different from the Φ362613 and ΦS63 attachment sites, and lies in an intergenic region upstream of a gene encoding a putative membrane protein of unknown function (homologous to CPF_0925 in ATCC 13124), and downstream of a putative phosphorylase-encoding gene.
In contrast, phage ΦS63 integrates into a B. subtilis sigK-like gene, which encodes a RNA polymerase sigma factor involved in the late stage of spore formation. SigK directs the Stage IV to Stage V transition, i.e., the spore coat formation in the sporulation cascade (reviewed in refs. 30, 31). sigK is encoded on two gene fragments (spoIVCB and spoIIIC) in B. subtilis and is created by splicing and the excision of a sigK intervening sequence (skin element). Interruption of sigK by these prophage-like sequences has been reported not only for B. subtilis (skinBs), but also for C. difficile (skinCd) and C. tetani (skinCt).30,32-34 It should be noted that ΦS63 is the first functional phage reported that inserts into a sigK gene of its host. Also, the presence of a skin element has never been reported in C. perfringens. Phage ΦS63 int is oriented in the opposite direction of sigK, similar to the situation in B. subtilis and C. tetani,35 but different to C. difficile.32 There also seems to be some variability regarding the exact insertion locus; while the integration sites of ΦS63, skinCd and skinCt are at a similar location within the coding sequence, skinBs is located in a different region of sigK.35 It was found that a specific recombinase can excise the B. subtilis skin element from sigK.36 Our findings also demonstrate precise excision, resulting in reconstitution of native sigK (Fig. 4). Altogether, these observations point to an important role of this insertion element for control of sigK function and a potential influence on sporulation. While it was reported, that insertion is not required for sporulation in B. subtilis,33 it is needed in C. difficile. A possible explanation is a missing sigK pro-sequence in C. difficile, which lacks an N-terminal portion that needs to be cleaved in order to activate SigK.32 sigK of strain S63 is not different from other C. perfringens strains (the pro-sequence is present), similar to the situation in B. subtilis.32,33 This would suggest that its interruption might not be strictly required for successful sporulation of the host cell. However, the sequenced C. perfringens strains do not contain a protease SpoIVFB homolog, which is necessary to remove the pro-sequence in B. subtilis.37 A reliable sporulation model for strain S63 is not available, and the precise sporulation phenotype of the ΦS63 sigK integration remains to be elucidated.
C. perfringens strains used in this study included S9, S13,38 S9ΔΦS9 (cured of the prophage), S63, and ATCC 13124. Strains were anaerobically grown in TGY medium (3%, tryptone peptone; 2%, glucose; 1%, yeast extract; 0.1% cysteine, pH 7.4) at 37°C in a flexible vinyl glove chamber (Coy Laboratories), containing a 95% N2 and 5% H2 atmosphere. Escherichia coli DH5α MCR and XL1-blue MRF` (Invitrogen) were grown in Luria-Bertani medium (LB) (1%, tryptone peptone; 1%, NaCl; 0.5%, yeast extract) at 37°C. If required, media were supplemented with ampicillin (100 μg/ml). or tetracycline (18 µg/ml).
To induce temperate phages ΦS9 and ΦS63, C. perfringens S9 and S63 were grown to exponential growth phase, and exposed to UV light (254 nm) in a UVC500 Crosslinker (Amersham) for 4 min at 2 J/cm2. An equal volume of TGY medium was added to the culture, and bacteria were incubated for 2 h at 37°C, followed by centrifugation (14,000 ×g, 5 min) and filter-sterilization (0.2 µm pore size). Serially diluted phage-containing lysates were mixed with C. perfringens strain S13 indicator cells, and plated using soft-agar overlays.39 After overnight incubation, distinct plaques were picked and eluted with SM buffer (50 mM TRIS-HCl (pH 7.5), 100 mM NaCl, 8 mM MgSO4). The procedure was repeated twice. Initial stocks of ΦS9 or ΦS63 were prepared by plating the single plaque eluates onto C. perfringens S13, and elution of the entire soft agar layer with SM buffer. Cell debris was removed by centrifugation, and the phage suspension was filter-sterilized and stored at 4°C.
For phage ΦS9, exponentially growing cells of C. perfringens strain S13 in broth culture were infected with ΦS9 at a multiplicity of infection (MOI) of 1, and incubated for 8 h at 37°C. Phage ΦS63 was propagated by the agar overlay method and removed by eluting the phage particles with 4 ml SM-buffer per plate.
Following centrifugation of the lysates at 6,000 ×g for 10 min, 8% (w/v), polyethylene glycol (PEG, MW 8,000) and 0.5 M NaCl were added to the supernatant and incubated overnight at 4°C.40 After centrifugation (10,000 × g, 10 min), the supernatant was removed and precipitated phage particles resuspended in SM buffer, followed by stepped CsCl density gradient centrifugation (76,000 × g, 18 h, L-60 Ultracentrifuge, Beckman) as previously described.23 Finally, virus particles were removed and dialyzed against SM buffer (pore size 50,000 Da, Spectrum) overnight at 4°C.
Purified phage particles were negatively stained with either 2% uranyl acetate, or 2% Na-phosphotungstic acid, or 2% ammonium molybdate.41 Samples were observed in a Philips CM100 transmission electron microscope at 100 kV acceleration voltage (FEI Company), equipped with a TVIPS Fastscan CCD camera (Tietz Systems), or in a Tecnai G2 Spirit electron microscope at 120 kV equipped with an EAGLE CCD camera (FEI Company).
Phage genomic DNA was prepared by proteinase K (Fermentas) treatment of purified phage particles, and subsequent organic extraction as described elsewhere.42 Genomic shotgun libraries of ΦS9 and ΦS63 were constructed as previously described.13,23 Briefly, partial restriction digestion (Tsp509I) (New England Biolabs) or complete digestion with HindIII (Fermentas) or TaqI (Fermentas) were performed, fragments of 1 to 2.5 kb in length were separated on agarose gels (0.8%), eluted using QIAquick Gel Extraction kit (Qiagen), and ligated into pBluescript SK II (-) (Stratagene), followed by transformation into E. coli XL-1 Blue and blue-white screening on agar plates containing ampicillin (100 µg/ml), X-Gal (40 µg/ml) and IPTG (3 mM). Plasmids bearing inserts of the desired size were confirmed by restriction enzyme digestion and the inserts sequenced. Following assembly of the sequences, gaps were closed by primer walking directly on ΦS9 and ΦS63 chromosomal DNA, with the aid of specific primers as sequences became available.
Phage genomic DNA was treated with restriction enzymes as recommended by the manufacturers. The fragments were heat-treated (62°C, 10 min) and separated in 1.0% agarose gels.
For exonuclease treatment, phage genomic DNA was first incubated with Bal31 nuclease (New England Biolabs) (1.5 unit per 1 μg DNA) for 0, 10, 20 and 30 min as directed by the manufacturer, followed by phenol-chloroform extraction and ethanol precipitation.42 Following restriction enzyme digestion, fragment patterns were analyzed electrophoretically.
Identification of ΦS9 attP was performed as previously described,43 using two divergent primers inv3a and inv10 (Table S1), derived from the 3′ end of the putative ΦS9 integrase (int). The S9 template DNA was first digested with TasI (Fermentas), and self-ligated using T4 DNA ligase (New England Biolabs). The PCR product was cloned into the pGEMT-easy TA vector (Promega), yielding pS9att3. Alignments of the inserts with available C. perfringens genomes enabled precise identification of the attachment site locus. Primers inv8 (corresponding to to phage sequence) and S9attBP-3 (homologous to C. perfringens ATCC 13124 sequence facing the integration site) were used to confirm the prophage location. For confirmation of prophage presence or absence in the identified locus, PCR with S9attBP-3 and S9attBP1-1 was performed on genomic DNA of the ΦS9 lysogen, and of a ΦS9-cured strain (S9ΔΦS9) (Fig. 4).
A similar strategy was used to identify the attB and attP of phage ΦS63. After digestion of S63 DNA with MboI (Fermentas) and self-ligation, inverse PCR was performed using primers orf23_fw, orf23_rev, both homologous to downstream sequence of the putative ΦS63 integrase gene. Using alignments with sequence obtained by inverse PCR with primer pair int_fw and int_rev corresponding to the phage integrase, the transition point from phage to host DNA was identified. Results were confirmed by sequencing of PCR products generated with primer combinations S63_att23 + orf23_fw and S63_att24 + int_fw, as well as sigK_upstr and sigK_dstr on C. perfringens lysogen DNA (Fig. 4).
CLC Genomics Workbench Version 5.1 (CLC, Aarhus, Denmark) was used for analysis of nucleotide (nt) and amino acid (aa) sequences. The BLAST algorithms44 were used for similarity searches in the non-redundant protein and nucleotide sequence databases available through the NCBI website (http://www.ncbi.nlm.nih.gov). HHPred (http://toolkit.tuebingen.mpg.de/hhpred) was used for additional homology and structure predictions. The integrated ClustalW algorithm of CLC Genomics Workbench was used for multiple sequence alignments and comparisons.45 InterProScan (http://www.ebi.ac.uk/InterProScan/) was used to identify conserved domains in translated Orfs, and TmHMM protein analysis software (version 2.0) was used to predict transmembrane domains.46 Putative tRNAs genes were identified using tRNAScan SE.47
The DNA sequences reported here appear in GenBank under accession number AY082069 (ΦS9), JQ660954 (ΦS63) and JQ660953 (partial sequence of sigK gene of strain S63).
No potential conflicts of interest were disclosed.
We are grateful to D. Mahony, Dalhousie University, Halifax, Canada for the gift of C. perfringens strains S9 and S63.
Supplemental materials may be found here:
Previously published online: www.landesbioscience.com/journals/bacteriophage/article/21363