Patent Grant
11136358
The contents of the electronic sequence listing (sequencelisting.txt; Size: 12,789 bytes; and Date of Creation: Jun. 14, 2019) is herein incorporated by reference in its entirety.
The present invention relates to a plasmid-based CTX phage replication system and Vibrio cholerae strain that can be infected by CTX phage and can be used for cholera toxin production.
Toxigenic Vibrio cholerae (V. cholerae) is generated by inserting a lysogenized CTX phage having a toxin gene into the chromosome of V. cholerae. Serotype O1 and O139 strains, which can be classified into three biotypes such as classical, El Tor and atypical El Tor, produce toxins, and thus epidemic cholera is developed. Classical biotype strains have the CTX-cla phage, prototype El Tor strains have CTX-1, and atypical El Tor strains are Wave 2 strains harboring CTX-2 and Wave 3 strains harboring CTX-3 to CTX-6. The O139 serotype strains have CTX-1 or CTX-O139. Toxigenic strains are generated through infection by a CTX phage, which is a virus having the cholera toxin gene, and subsequent lysogenization thereof. While a model for an evolutionary mechanism through which a strain producing a toxin is generated by infection by each biotype strain has been suggested, the infection and replication of the CTX phage are not limited by biotypes of a host strain. Recently, atypical El Tor strains having CTX phages appearing to be formed by mosaics of CTX-cla and CTX-1 have become mainstream worldwide.
The evidence that replication of CTX-1 and CTX-O139 phages is possible under laboratory conditions and the evidence of mechanisms for generating Wave 2, 3 atypical El Tor strains suggest that replication of a CTX-cla phage and a similar phage CTX-2 occurs in nature, but is not proved experimentally.
Meanwhile, conventional CTX phage replication was performed using El Tor biotype V. cholerae, in which the CTX phage had been previously lysogenized (Brigid M Davis et al. Current Opinion in Microbiology, 2003, 6: 35-42), and it has been known that CTXE1 Tor (CTX-1) can be made into a replicative form in a prophage state and can also be transduced. However, a CTX-CTX repeat or CTX-RS1 array is needed, and at this time, the replicated CTX-1 has been known to be only transduced in a classical biotype strain. The replicative form of CTX-1 has a plasmid-like form (pCTX-1), and the replicative form of CTX-1 transduced into a classical biotype strain may replicate a CTX phage and transduce a different classical strain with the CTX phage.
On the other hand, it has been known that CTXcla has no CTX-CTX array, and does not replicate because of no transducible E1 Tor strain, and replication of CTXcla and CTX-2 under laboratory conditions has not been proven.
The present invention is directed to providing a recombinant plasmid for replicating a CTX phage which includes the genomic sequence of a Vibrio cholera CTX phage and is replicable in host cells.
The present invention is also directed to providing a host cell transformed by the plasmid.
The present invention is also directed to providing a method of producing a Vibrio cholerae CTX phage from the host cells transformed by the plasmid.
The present invention is also directed to providing a V. cholerae variant strain which can be used as a recipient strain for CTX phage infection.
The present invention is also directed to providing a method of improving the infection efficiency of a CTX phage using the V. cholerae variant strain.
The present invention is also directed to providing a method of improving the production yield of cholera toxin using a V. cholerae variant strain harboring a recombinant plasmid for replicating a CTX phage or a CTX prophage.
To achieve the above-described objects, the present invention provides a recombinant plasmid for replicating a CTX phage, which includes the genomic sequence of a CTX phage in which the full-length sequence of a ctxA gene represented by SEQ ID NO: 1, and the full-length sequence of a ctxB gene represented by SEQ ID NO: 2, or fragments thereof are substituted with the base sequence of a selection marker gene.
The present invention also provides a host cell transformed by the recombinant plasmid for replicating a CTX phage.
The present invention also provides a method of preparing a CTX phage, which includes isolating and purifying a CTX phage from a culture of the host cell.
The present invention also provides a V. cholerae variant strain, which expresses a toxT protein in which tyrosine (Tyr) at amino acid 139 is substituted with phenylalanine (Phe) through the point mutation of a toxT gene, and the substituted toxT protein includes the amino acid sequence of SEQ ID NO: 7.
The present invention also provides a V. cholerae variant strain, which contains the recombinant plasmid for replicating a CTX phage and expresses the toxT protein in which Tyr at amino acid 139 is substituted with Phe through the point mutation of the toxT gene, and the substituted toxT protein includes the amino acid sequence of SEQ ID NO: 7.
The present invention also provides a V. cholerae variant strain, which is infected by a V. cholerae strain harboring one or more CTX prophages selected from the group consisting of CTX-1, CTX-cla, CTX-2, CTX-env and CTX-O139 to insert the genomic sequence of a CTX phage into its chromosome, and expresses a toxT protein in which Tyr at amino acid 139 is substituted with Phe through the point mutation of a toxT gene, and the substituted toxT protein includes the amino acid sequence of SEQ ID NO: 7.
The present invention also provides a method of preparing a V. cholerae variant strain, which includes inducing a UAU to UUU point mutation at the 139th codon of a toxT gene of a V. cholerae strain to express a toxT protein in which Tyr at amino acid 139 is substituted with Phe.
The present invention also provides a method of improving the infection efficiency of a CTX phage, which includes transducing the V. cholerae variant strain by the recombinant plasmid for replicating a CTX phage, or performing infection using a V. cholerae strain harboring one or more CTX prophages selected from the group consisting of CTX-1, CTX-cla, CTX-2, CTX-env and CTX-O139 as a donor strain and the V. cholerae variant strain as a recipient strain.
The present invention also provides a method of improving the production yield of cholera toxin, which includes single-phase culturing the V. cholerae variant strain under conditions of 30 to 37° C. and pH 6 to 8.
The present invention can improve the CTX phage infection efficiency for a V. cholerae variant strain expressing a toxT protein in which Tyr at amino acid 139 is substituted with Phe through the point mutation of a toxT gene as a recipient strain using a plasmid-based CTX phage replication system, simultaneously infect a plurality of CTX prophages, and increase the production yield of cholera toxin.
Generally, CTXEl Tor (CTX-1) is able to be generated from a prophage state to a replicative form and also generated by transduction. However, it has been known that a CTX-CTX repeat or CTX-RS1 array is required, and only classical biotype strains can be transduced by replicative-form CTX-1 phages. In addition, the replication of CTXcla (CTX-cla) has not been demonstrated under laboratory conditions because of no CTX:CTX or CTX:RS1 array and no El Tor strain to be transduced.
Therefore, the inventors constructed a plasmid-based CTX phage replication system for CTX-cla under laboratory conditions and an El Tor variant strain to be transduced by a CTX phage to demonstrate a replication process.
Accordingly, the present invention relates to a recombinant plasmid for replicating a CTX phage, which includes the genomic sequence of a CTX phage in which the full-length sequence of a ctxA gene of SEQ ID NO: 1 and the full-length sequence of a ctxB gene of SEQ ID NO: 2 or fragments thereof are substituted with the base sequences of selection marker genes.
In the present invention, a plasmid is constructed as a unit for replicating a CTX phage, amplified in E. coli, and then injected into V. cholerae to be replicated. The CTX phage generated from the plasmid is the same as a phage generated in nature. The genome of the CTX phage injected into a plasmid is capable of being artificially synthesized. Since the CTX replication can occur in a plasmid, both CTXEl Tor and CTXcla can be produced. This suggests that different CTX phages (CTX-2, CTX-O139 and CTX-env) may be produced. As the El Tor strain capable of being transduced by CTXcla was newly found, it can be confirmed that CTXcla can be transduced.
El Tor strains have been previously known to be transduced by CTX-1 in a living body (specifically, in the intestine of a mouse), but were not demonstrated to be transduced under laboratory conditions. Therefore, it can be expected that, only when suitable laboratory conditions are provided, the El Tor strains may be transduced by CTX-1 as well as CTX-cla or CTX-2. Since CTX-2 having rstRcla, as a tandem repeat, was contained on chromosome 2 of a Wave 2 atypical El Tor strain, CTX-2 replication can be expected, but had not been experimentally demonstrated. It can also be considered that this is because there was no El Tor strain transduced by CTX-2 or CTX-cla.
The recombinant plasmid for replicating a CTX phage of the present invention will be described in detail as follows.
The recombinant plasmid for replicating a CTX phage includes the genomic sequence of a CTX phage in which the full-length sequence of a ctxA gene and the full-length sequence of a ctxB gene or fragments thereof are substituted with a selection marker gene.
The genomic sequence of the CTX phage may be one or more genomic sequences of CTX-1, CTX-cla, CTX-2, CTX-env and CTX-O139.
In one exemplary embodiment of the present invention, the genome of the CTX-1 phage consists of rstR, rstA, rstB, cep, orfU, ace, zot, ctxA and ctxB genes.
In the recombinant plasmid for replicating a CTX phage of the present invention, the full-length sequence of the ctxA gene and the full-length sequence of the ctxB gene or fragments thereof may be substituted with a selection marker gene cassette.
The full-length sequence of the ctxA gene may be the base sequences of SEQ ID NO. 1. In addition, the full-length sequence of the ctxB gene may be the base sequences of SEQ ID NO: 2. The fragment of the ctxB gene may include the base sequences of SEQ ID NO: 3.
In addition, a selection marker gene such as a drug-resistance gene facilitates the detection of a transductant due to a phenotype of the selection marker gene in the transductant. As the selection marker gene, an ampicillin-resistance gene, a kanamycin-resistance gene, a streptomycin-resistance gene, a tetracycline-resistance gene, an erythromycin-resistance gene or a chloramphenicol acetyl transferase gene may be used. More specifically, in the present invention, the kanamycin-resistance gene may be substituted for the full-length sequence of the ctxA gene and the full-length sequence of the ctxB gene or fragments thereof. More specifically, the substituted kanamycin-resistance gene may include base sequences represented by SEQ ID NO: 4.
According to one embodiment of the present invention, the part in which the full-length sequence of the ctxA gene and the full-length sequence of the ctxB gene or fragments thereof are substituted with the kanamycin-resistance gene further includes 5′ and 3′-non-coding sequences, and represented by sequences of SEQ ID NO: 5.
The recombinant plasmid for replicating a CTX phage of the present invention may contain a region essential for self-replication of the plasmid (a replication regulatory region, or a gene expression cassette). Even when a region other than the replication regulatory sequence, that is, a region excluding a replication origin and a region including genes necessary for replication, is deleted, the recombination plasmid may be replicated in host cells.
The replication regulatory region is a nucleic acid sequence including a promoter, and having an expression activity of regulating the expression, that is, transcription and translation, of a gene after being functionally linked to the gene subjected to expression.
The recombinant plasmid for replicating a CTX phage may be derived from a E. coli-derived plasmid for transformation selected from the group consisting of pUC19, pUC18, pBR322, pHSG299, pHSG298, pHSG399, pHSG398, RSF1010, pMW119, pMW118, pMW219 and pMW218.
The recombinant plasmid for replicating a CTX phage may be constructed in the same manner as known constructs such as conventional cloning vectors, expression vectors, etc.
For the preparation of plasmid DNA, the cleavage and binding of DNA and transformation, methods known by those skilled in the art may be used. The methods are disclosed in the literature [Sambrook, J., Fritsch, E. F., and Maniatis, T., “Molecular Cloning: A Laboratory Manual, Second Edition”, Cold Spring Harbor Laboratory Press (1989)].
According to one embodiment of the present invention, the recombinant plasmid for replicating a CTX phage may be prepared by operably linking a selection marker gene cassette to the genomic sequence of a CTX phage from which the full-length sequence of a ctxA gene and the full-length sequence of a ctxB gene or fragments thereof are removed, and inserting the DNA fragment into the replication origin of the plasmid.
More specifically, the recombinant plasmid for replicating a CTX phage may include:
a replication origin fragment of a plasmid;
a DNA fragment including a sequence spanning nucleotide 245 of zot upstream of the genome of a CTX phage to the termination codon of rstR downstream thereof, a part of the zot gene, a selection marker gene cassette, and a partial sequence up to 3′UTR of the ctxB gene in a cholera strain having a CTX:RS1 or CTX:CTX array; and a DNA fragment including 5′UTR of a CTX phage, rstR, rstA, rstB, cep, orfU and a sequence up to nucleotide 244 of zot may be included in a cholera strain having an array with CTX at the very front. The DNA fragment may be amplified in a different type of CTX phage (CTX-1, CTX-cla, CTX-2, CTX-O139 or CTX-env) and linked to two different fragments such that different types of CTX phage genomes may be contained, respectively.
An example of the recombinant plasmid for replicating a CTX phage of the present invention is illustrated in the cleavage map of
The recombinant plasmid for replicating a CTX phage of the present invention may be replicated in E. coli, the genus Salmonella, the genus Shigella, the genus Klebsiella, the genus Pseudomonas or the genus Vibrio. More specifically, the recombinant plasmid for replicating a CTX phage of the present invention may be E. coli or the genus Vibrio.
The genus Vibrio may include a classical biotype, an E1 Tor biotype, an atypical E1 Tor, an O139 serotype, or any serotype of V. cholerae. Most specifically, CTX phages can be replicated by transducing a classical biotype strain by a CTX-1 genome-cloned plasmid. A CTX-cla or CTX-2 genome-cloned plasmid can be introduced into any El Tor strain through transformation, thereby replicating a CTX-cla or CTX-2 phage, and the replicated CTX phage can be introduced into a Vibrio cholera strain in which a Tyr139Phe mutation is present at a toxT gene by transduction to replicate the CTX phage. Such variant strains may include an A213-toxTY139F strain or an IB4122-toxTY139F strain, but the present invention is not limited thereto.
Therefore, the present invention provides a host cell transformed with a recombinant plasmid for replicating a CTX phage.
A method of transforming host cells with the recombinant plasmid for replicating a CTX phage may be selected from all transformation methods known in the art without limitation, for example, selected from bacterial protoplast fusion, electroporation, and infection using a viral vector.
The host cells may be selected from E. coli, the genus Salmonella, the genus Shigella, the genus Klebsiella, the genus Pseudomonas or the genus Vibrio.
The culture of the transformed host cells may be performed in suitable media by various methods known in the art. Examples of the culture method include batch, continuous and fed-batch cultures. The fed-batch culture may include injection batch and repeated injection batch cultures, but the present invention is not limited thereto.
The medium used herein generally includes one or more of carbon sources, nitrogen sources, inorganic salts, vitamins and/or trace elements. A preferable carbon source is a saccharide such as a monosaccharide, a disaccharide or a polysaccharide. A nitrogen source is generally an organic or inorganic nitrogen compound, or a material including a compound thereof. Examples of the nitrogen sources include an ammonia gas, an ammonium salt such as ammonium sulfate, ammonium chloride, ammonium phosphate, ammonium carbonate or ammonium nitride, a nitrate, urea, an amino acid, or a complex nitrogen source, such as a corn steep liquor, soybean powder, a soy protein, a yeast extract or a meat extract. The nitrogen source may be used alone or in combination. Inorganic compounds that can be contained in media include chlorides, phosphates or sulfates of calcium, magnesium, sodium, cobalt, molybdenum, potassium, manganese, zinc, copper and iron. As a phosphorous source, phosphoric acid, potassium dihydrogen phosphate or dipotassium hydrogen phosphate, or a sodium-containing salt corresponding thereto may be used. To maintain a metal ion in a solution, a chelating agent may be added to the medium. More specifically, to enhance the replication of the CTX phage, nanomoles of mitomycin C may be added. All components in the medium are sterilized by heating (at 1.5 bar and 121° C. for 20 minutes) or sterile filtration. These components may be sterilized together or independently as needed. All components of the medium may be present at the beginning of the culture, or may be arbitrarily added by way of continuous or batch culture.
The CTX phages may be produced by isolating and purifying CTX phages from the transformed cell mass, culture or lysate of the host cells or the lysate of the culture.
Therefore, the present invention provides a method of producing CTX phages, which includes isolating and purifying CTX phages from a culture of the host cells.
In addition, the present invention relates to a V. cholerae variant strain, which expresses a toxT protein in which Tyr at amino acid 139 is substituted with Phe through the point mutation of a toxT gene, and the substituted toxT protein includes the amino acid sequence of SEQ ID NO: 7.
The present invention provides a method of preparing a V. cholerae variant strain, which includes inducing a UAU to UUU point mutation at the 139th codon of toxT gene of a V. cholerae strain to express toxT protein of SEQ ID NO: 7 in which Tyr is substituted with Phe at amino acid 139.
According to one embodiment of the present invention, the inventors found out a strain transduced by CTX-2 and CTX-cla among El Tor biotype strains. Compared with other V. cholerae strains, the El Tor strain has one single nucleotide polymorphism (SNP) at a toxT gene, which is a transcription activator of tcpA and ctxAB. Other El Tor strains have Tyr at amino acid 139 (SEQ ID NO: 6), whereas this strain has Phe at amino acid 139 of the toxT gene (SEQ ID NO: 7). Due to such a mutation, the strain may be transduced by a CTX phage and thus produce cholera toxin under laboratory conditions. When SNP of toxT has changed from 139Phe to the toxT allele (139Tyr) of a different El Tor strain, the stain of the present invention does not act as a transduction recipient strain. When SNP (139Phe) is introduced into toxT of other El Tor strains, these strains may be infected by CTX phages. Since toxT is directly involved in transcriptional activation of both tcp expression and ctxAB expression, when El Tor strains were cultured in a single phase, it was confirmed that toxin expression was also increased. In addition, using a plurality of recombinant plasmids for replicating a CTX phage, an E1 Tor strain having all of multiple CTX prophages can be constructed.
As a strain used to manufacture the V. cholerae variant strain of the present invention, a classical biotype, E1 Tor biotype, atypical E1 Tor biotype or O139 serotype V. cholerae strain may be used.
The V. cholerae variant strain may be any one of V. cholerae strains expressing the toxT protein of SEQ ID NO: 7 in which Tyr at amino acid 139 is substituted with Phe through the point mutation of a toxT gene without limitation, and may be, for example, a MG116025 (Matlab type III)-toxTY139F strain, a B33-toxTY139F strain, an A213-toxTY139F strain or an IB4122-toxTY139F strain, but the present invention is not limited thereto.
The V. cholerae variant strain of the present invention may include a CTX prophage selected from CTX-1, CTX-cla, CTX-2, CTX-env, CTX-O139 and a combination thereof.
One or more of the CTX prophages may be included by transducing a V. cholerae variant strain by the above-described recombinant plasmid for replicating a CTX phage selected from the group consisting of CTX-1, CTX-cla, CTX-2, CTX-env and CTX-O139; or infecting a V. cholerae variant strain using a V. cholerae strain which contains one or more CTX prophages selected from the group consisting of CTX-1, CTX-cla, CTX-2, CTX-env and CTX-O139 as a donor strain.
Accordingly, the present invention provides a V. cholerae variant strain, which includes the recombinant plasmid for replicating a CTX phage and expresses a toxT protein in which Tyr at amino acid 139 is substituted with Phe through the point mutation of a toxT gene, wherein the substituted toxT protein includes the amino acid sequence of SEQ ID NO: 7.
In addition, the present invention provides a V. cholerae variant strain, which is infected using a V. cholerae strain harboring one or more CTX prophages selected from the group consisting of CTX-1, CTX-cla, CTX-2, CTX-env and CTX-O139 such that the genomic sequence of the CTX phage is inserted into the chromosome of the strain, and expresses a toxT protein in which Tyr at amino acid 139 is substituted with Phe through the point mutation of a toxT gene, wherein the substituted toxT protein includes the amino acid sequence of SEQ ID NO: 7.
The “prophage” used herein may be a non-infectious type, and present in a phage state maintained in V. cholerae cells.
The “replicative-form CTX phage (pCTX)” is not inserted into a specific region of the V. cholerae chromosome and present in the form of a plasmid outside the chromosome.
The “donor strain or donor” used herein is a donor of a V. cholerae CTX phage, and refers to a V. cholerae strain in which a CTX phage is inserted into the chromosome as a lysogenic phage (lysogen), or a V. cholerae strain harboring a replicative-form CTX phage.
The term “recipient strain” used herein refers to a V. cholerae strain infected by a CTX phage produced from a donor.
The V. cholerae variant strain of the present invention may be increased in expression of a TcpA protein, compared with a V. cholerae strain expressing a wild-type toxT protein, and allows transcriptional activation of ctxAB expression, and thus the expression of cholera toxin may be increased.
The V. cholerae variant strain of the present invention may be used as a recipient strain for CTX phage infection to improve transduction efficiency.
Therefore, the present invention provides a method of improving the infection efficiency of a CTX phage, which includes transducing a V. cholerae strain with the recombinant plasmid for replicating a CTX phage of the present invention, or infecting the V. cholerae variant strain as a recipient strain using a V. cholerae strain harboring one or more CTX prophages selected from the group consisting of CTX-1, CTX-cla, CTX-2, CTX-env and CTX-O139 as a donor strain.
Generally, E1 Tor strains may not induce the production of cholera toxin under general experimental conditions. Therefore, conditions for producing the cholera toxin are induced using a method of reducing an oxygen partial pressure and increasing a CO2 partial pressure under AKI conditions (biphasic culture, method of performing culture in a stationary state for 16 hours and then further culture by changing the culture condition to shaking culture), but the cholera toxin is not produced by single phase culture (condition for culturing stains only by shaking culture).
On the other hand, the V. cholerae variant strain of the present invention may produce the cholera toxin through single phase culture under conditions of 30 to 37° C. and pH 6 to 8.
The V. cholerae variant strain may be any V. cholerae strain expressing the toxT protein of SEQ ID NO: 7 in which Tyr at amino acid 139 is substituted with Phe through the point mutation of a toxT gene without limitation, and may be, for example, a MG116025 (Matlab type III)-toxTY139F strain, B33-toxTY139F strain, A213-toxTY139F strain or IB4122-toxTY139F strain. In addition, a classical biotype strain may also be used.
A medium that can be used according to the present invention has been described above, and will be omitted to avoid excessive duplication.
The transformed strain is single phase-cultured, and then the cholera toxin is isolated and purified from the cell mass, culture or lysate of the strain, or the lysate of the culture, thereby obtaining the cholera toxin.
Hereinafter, the present invention will be described in detail with reference to examples. However, the following examples are merely provided to illustrate the present invention, and the scope of the present invention is not limited by the following examples.
By using a plasmid-based CTX phage replication system, the replication of various CTX phages was performed under laboratory conditions. To this end, CTX phages may be replicated from the plasmid-cloned CTX phage genome. An E. coli- and V. cholerae-compatible recombinant plasmid was constructed by linking the replication origin of pUC18, the CTX-1 phage genome in which total ctxA and a part of ctxB were substituted with a kanamycin cassette and upstream and downstream non-coding sequences of the CTX phage (
The inventors disclosed strain PM8 in an article published in 2014 (Kim, E. J., et al. (2014) Molecular insights into the evolutionary pathway of V. cholerae O1 atypical El Tor variants. PLoS Pathog. 10, e1004384), three types of host strains for the recombinant plasmid were PM14 (N16961 derivative that has lost a lysogenic CTX-1 prophage in a N16961 strain, which is a V. cholerae El Tor biotype strain, thus having TLC:RS1 array), O395 (classical biotype strain) and A213 (U.S. Gulf Coast strain harboring only the TLC element on chromosome 1). The transduction efficiency of CTX-1kan produced from plasmids using the host was investigated (Table 2).
To construct a CTX phage plasmid shown in
An experiment was carried out to examine whether a CTX phage can be transferred to a recipient strain through transduction after the transformation of a V. cholerae strain containing no CTX prophage or a strain containing no replicative-form CTX phage with the recombinant plasmid and the replication of the CTX phage from the strain. Briefly, 0.5 mL of the supernatant of a donor strain culture grown overnight in the presence of 20 ng/mL mitomycin C was mixed with 3×108 CFU of agglutinated recipient strains (grown at 30° C., pH 6.5 in LB). The transduction efficiency of each recipient strain was calculated by the number of transductants per 6×108 CFU recipient cells per 1 mL of the supernatant of the donor strain. Since the recipient strains have different transduction efficiencies, the transduction efficiency of each recipient strain does not reflect the actual titer of the CTX phage produced from the recipient strain. The transduction efficiency was presented as the average of at least three independent experiments.
As shown in Table 2, although there was a difference between host strains, when O395 was used as a recipient, ˜105 transductants were obtained per 1 mL of the donor strain supernatant. This was similar to CTX-1 phage production from the lysogenic CTX-1:RS2 array of N16961. This shows that the replication and propagation of CTX phages do not depend on a host bacterial biotype. Since similar numbers of transductants were obtained from plasmids containing the entire intergenic region 1 (ig-1) sequence and the last 119 nucleotides, respectively, the 119 nucleotides upstream of rstR were sufficient to initiate CTX-1 replication in this system. Afterward, CTX phages were produced from the recombinant plasmid containing the last 119 nucleotides of ig-1.
The replication origin of pUC18 was no longer present in the transformed CTX-1kan phage genome, and the DNA sequence of CTX-1kan produced from the recombinant plasmid was identical to CTX-1kan produced from the lysogenic CTX-1kan. PM20 is the strain in which CTX-1-kan phages can be replicated from a prophage-type CTX genome, the CTX phage genome replicated from the recombinant plasmid and the CTX phage genome replicated from PM20 have the same base sequence, demonstrating that CTX phages replicated from the plasmid-cloned CTX phage genome and naturally-replicated CTX phages are the same.
Based on the confirmation that CTX-1 could be replicated from a plasmid-cloned CTX phage genome in V. cholerae, the replication of CTX-2 and CTX-cla using the plasmid-based replication system could be predicted. Recombinant plasmids containing CTX-clakan and CTX-2kan genomes were constructed by the method described in Example 1 to transform PM14. Due to phage immunity, it was expected that classical biotype strains could not be transduced by CTX-clakan or CTX-2kan PM14, and thus it was tested whether CTX-clakan and CTX-2kan phages produced from the pUC-CTX plasmids could be used to transduce various El Tor biotype strains. Recipient El Tor strains were prepared for transduction in the same manner as the classical strains (agglutinated, that is, grown in LB (pH 6.5) at 30° C.).
+pCTX-clakan-P: pCTX-clakan is produced from plasmidpUC-CTX-clakan.
++pCTX-2kan-VL: pCTX-2kan is produced from lysogenic CTX-2 in PM9, which is a derivative of a V212-1 strain.
As shown in Table 3, no El Tor strains were transduced by CTX-clakan and CTX-2kan except Wave 2 El Tor strain MG116025. This strain was transduced by CTX-clakan and CTX-2kan phages replicated using the plasmid-based replication system. Approximately 100 and 20 transductants were obtained from the plasmid-cloned CTX-clakan and CTX-2kan genomes, respectively. The replication of CTX-clakan and CTX-2kan was confirmed by secondary transduction. Based on these results, the replication of CTX-2 and CTX-cla was confirmed with a suitable recipient strain, demonstrating the proper operation of the plasmid-based CTX phage replication system. Similarly, CTX-O139kan phages were also produced using the plasmid-based replication system.
The replication of CTX-2 from a tandem repeat of lysogenic CTX-2 present on chromosome 2 of a Wave 2 El Tor (Tor 2) strain was also demonstrated. PM9 and PM22, and V212-1 and B33 were constructed as described previously. Approximately 103 transductants were obtained through primary transduction of PM9 and PM22. Secondary transduction from the transductants containing replicative forms of pCTX-clakan and pCTX-2kan to CTX-cla and CTX-2 was further demonstrated. Since no classical strain containing the CTX-cla:RS1 array or the tandem repeat of CTX-cla has been reported yet, the replication of lysogenic CTX-cla in the classical biotype strains could not be proved.
To identify genetic changes facilitating the susceptibility of the MG116025 strain to a CTX phage, genetic changes in the tcp gene cluster of MG116025, which was caused by TCP-mediated CTX phage infection, was examined.
Compared with other El Tor strains, two SNPs specific to the tcp gene cluster of MG116025 were identified from genome sequencing data. Ala56 (C269) of tcpA is changed to Asp (A269), and Tyr139 (A416) of toxT is substituted with Phe (T416) in MG116025. When Asp56 of tcpA of MG116025 is switched to Ala, the transduction efficiency was not changed or increased by up to 10 fold depending on a CTX phage, indicating that this change is not significant to the transduction-competent phenotype of MG116025. When Phe139 of toxT of MG116025 was substituted with Tyr, the transduction efficiency was decreased, suggesting that the SNPs mediate the ability of MG116025 transformed by CTX phages (Table 3-7).
Subsequently, the toxT allele (Tyr139) of two El Tor strains which were not transduced by CTX phages such as A213 and IB4122 (Wave 3 El Tor strain containing RS1:CTX-3 on chromosome 1) was substituted with the toxT allele (Phe139) of MG116025, and the ability of the strains to be transduced by CTX phages was examined.
To this end, from MG116025 and N16961 strains, a DNA fragment from 50 nucleotides upstream of the ATG initiation codon to nucleotide 793 of toxT was amplified by PCR using toxT-XbaIF (5′-CCG GCC TCT AGA TAC GTG GAT GGC TCT CTG CG-3′: SEQ ID NO: 16) and toxTSacIR (5′-CCG GCC GAG CTC CAC TTG GTG CTA CAT TCA-3′: SEQ ID NO: 17) primers, and inserted into suicide plasmid pCVD442. The SNP position at nucleotide 416 (A416 of N16961 and T416 of MG116025) was placed in the center of the fragment. The MG116025 toxT 139Phe allele was replaced with the toxT 139Tyr allele by an allelic exchange method, and similarly, IB4122 and A213 toxT 139Tyr alleles were replaced with the toxT 139Phe allele.
A213-toxTY139F and IB4122-toxTY139F were transduced by CTX phages when grown in LB (pH 6.5) at 30° C. (Tables 4 to 7), and A213 and IB4122 were not transduced by a CTX phage.
1 × 102
The CTX phage infection in V. cholerae strains was mediated by TCP as a CTX phage recipient. Phenotypes enabling transduction of strains harboring the toxT 139Phe allele may be mediated by the high expression of TCP. TcpA expression was assessed by western blotting to monitor a TCP level.
For western blotting, bacterial strains were grown overnight in a LB medium at 30° C., subcultured in a LB medium (pH 6.5) at 30° C. or in LB diluted 1:100 at 37° C., and grown overnight again. Cells were pelleted, resuspended in 1×sample buffer, and boiled for 5 minutes. Approximately 5×107 cells were loaded onto each lane in an SDS-PAGE gel. Proteins were transferred to a Protran nitrocellulose membrane (GE Healthcare) and probed with rabbit anti-CT (Sigma) or rabbit anti-TcpA (W. F. Wade, Dartmouth University, Hanover, N.H.).
As shown in
Primary and secondary transduction of various CTX phages was evaluated for O395, MG116025, A213-toxTY139F and IB4122-toxTY139F recipients. Briefly, El Tor strains having the toxT-Phe139 allele may be transduced by CTX phages, but efficiencies vary depending on a strain. Compared with a lysogenic or plasmid-cloned CTX phage genome (primary transduction), the production of CTX phages was ˜102-fold (CTX-1 and CTX-cla) to 104-fold (CTX-2 and CTX-O139) higher by replicative-form pCTXs (secondary transduction). Electron microscopy images of CTX-1kan, CTX-2kan and CTX-O139kan were obtained when the viral titer exceeded 106 particles per mL (
CTX-1: When O395, A213-toxTY139F and MG116025 (and IB4122-toxTY139F) were recipients, approximately 105, 104 and 102 transductants were obtained from PM14-U1 (PM14 transformed with pUC-CTX-1kan) (Table 4). When O395 was a recipient, secondary transduction efficiency by pCTX-1kan in the O395 transductant increased up to 5×107, indicating that ˜10% of the recipient cells were transduced by CTX-1kan. When MG116025 was a recipient, 104 transductants may be obtained with the same CTX-1kan phage titer because of the phage immunity by lysogenic CTX-1 and RS1 (described below). The replication efficiency of pCTX-1kan also varied depending on a host strain. 5×107 transductants were obtained from O395 (pCTX-1kan), whereas fewer transductants (5×106 and 5×104, respectively) were produced from MG116025 (pCTX-1kan) and A213-toxTY139F (pCTX-1kan). The replication efficiency of the CTX-1kan phages produced from lysogenic CTX-1 (PM20 strain) was similar to that from the pUC-CTX-1kan plasmid. Electron microscopy images of the CTX-1kan phages were obtained from the culture supernatant of O395 (pCTX-1kan) as shown in
CTX-2: pCTX-2kan replicated from a pUC-CTX-2kan plasmid was transferred to MG116025 and IB4122-toxTY139F at an efficiency of 20 and 10 transductants, respectively (Table 5). Approximately 2×104 transductants were obtained in secondary transduction from the primary transductant MG116025, which harbored pCTX-2kan-P. The replication efficiency of lysogenic CTX-2 varied depending on a recipient strain. Approximately 5×103 transductants were obtained from PM22 (B33 derivative), and 103 transductants were obtained from PM9 (V212-1 derivative). No CTX phage was produced from the second CTX-2 prophage of V212-1 (PM10).
A213-toxTY139F was also transduced at a slightly lower efficiency than MG116025, but the transduction efficiency of IB4122-toxTY139F was significantly lower. O395 classical biotype strains were also transduced by the supernatant of PM9, but pCTX transferred to O395 contained rstRE1 Tor, which was expected to be generated by the recombination between CTX-2kan produced from the plasmid and CTX-1 on chromosome 1 and caused by the immunity imparted by rstRcla in lysogenic CTX-cla. Perhaps, since classical biotype strains already have the rstRcla gene, the efficiency of transducing CTX-2 containing rstRcla may be expected to be reduced.
The secondary transduction efficiency of pCTX-2kan produced from PM9 or PM22 exceeded 106 when MG116025 was a recipient. A213-toxTY139F and IB4122-toxTY139F were transduced by a high CTX-2kan phage titer. The classical strain O395 was not transduced by a low CTX-2kan phage titer, but by a high CTX-2kan phage titer. Among several hundred transductants, approximately ⅔ of O395 transductants were transduced by a CTX phage containing rstRE1 Tor, and ⅓ were transduced by CTX-2. Electron microscopy images of CTX-2kan phages in the culture supernatant of MG116025 (pCTX-2kan) were taken (
CTX-cla: The transduction efficiency of CTX-clakan from pUC-CTX-clakan into MG116025 was 102 transductants, and 104 transductants were formed in the secondary transduction (Table 6). A213-toxTY139F and IB4122-toxTY139F were also transduced by CTX-clakan in the primary and secondary transduction at a slightly lower efficiency than MG116025. Due to the low CTX-clakan titer, electron microscopy images of CTX-clakan phages were not obtained.
CTX-O139: The replication and production of infectious CTX-O139 from a lysogenic CTX-O139 genome were reported, and thus CTX-O139 replication from plasmid-cloned CTX-0139 was demonstrated. When O395 and MG116025 were recipients, ˜200 and 10 transductants may transfer CTX-O139kan phages which were produced in PM14-U4 by transduction, respectively (Table 7). The secondary transduction efficiency increased up to 106 transductants, and electron microscopy images of CTX-O139kan phages were taken (
To measure the degree of inhibition of superinfection of the CTX-1 phage by lysogenic CTX-1 and RS1, a set of isogenic strains of MG116025 was constructed by stepwise removal of CTX-1 and RS1 (strains PM25˜PM29). To this end, MG116025, PM25 (TLC:CTX-1:RS1), PM26 (TLC:RS1:RS1), PM27 (TLC:RS1), PM28 (TLC) and PM29 (no TLC, no element) were constructed by stepwise removal of CTX-1 and RS1 on chromosome 1. pCVDrstRET which contained a DNA fragment including rstRE1 Tor (339 bp) and the first 226 bp of rstA was inserted independently into rstRE1 Tor of CTX-1 and RS1 of MG116025. The removal of CTX-1 and RS1 was verified by analyzing the genetic structure of strains selected from LB plates containing 15% (wt/vol) sucrose.
In addition, to measure phage immunity, the inhibition of CTX-1 superinfection by lysogenic CTX-1 or RS1 was monitored by measuring the transduction efficiency of isogenic strains of MG116025. MG116025 and PM25˜PM29 were transfected by pCTX-1kan phages produced from O395 transductants by pCTX-1kan. The immunity against CTX-2 was tested in the same strain as the pCTX-2kan phage produced from the MG116025 transductant by pCTX-2kan.
PM28 and PM29, which do not contain CTX-1 or RS1, were transduced by CTX-1 at ˜80% efficiency; when 6×108 recipient cells were used, 5×108 transductants were obtained (Table 8), which was 10-fold higher than the classical strain O395. When PM27 containing one RS1 (thus, 1 rstREl Tor) was used as a recipient, transduction efficiency was almost the same. The transduction efficiency was reduced by ˜10−3-fold in PM26 and PM25 strains as well as the MG116025 strain. These results show that CTX-1 superinfection was limited by rstRE1 Tor of lysogenic CTX-1 or RS1. However, one rstR is not sufficient to inhibit superinfection, and at least two rstR genes are needed to inhibit the superinfection. While the superinfection of the CTX-1kan phage was restricted by the preexisting RS1 and CTX-1, the infection of rstRcla-containing CTX-2kan was not influenced by rstRE1 Tor (heteroimmunity).
ToxT is a 32-kDa AraC family transcriptional activator. ToxT contains a conserved C-terminal DNA-binding domain including 100 amino acids, and its 176-amino acid N terminus is a dimerized domain. ToxT directly controls the expression of the tcp gene cluster and ctxAB. The toxT-F139 allele of El Tor strains up-regulated TCP at 30° C., pH 6.5, enabling the bacteria to be transduced by CTX phages. This result indicates that the toxT-F139 allele increases the expression of cholera toxin. The production of cholera toxin in V. cholerae strains was assessed by Western blotting (
While no cholera toxin was produced in 37° C. culture, production was observed at 30° C., pH 6.5 in O395, MG116025 and IB4122-toxTY139F. The expression of cholera toxin was shut off in MG116025-toxTF139Y, demonstrating that SNP in toxT mediates the increased expression of TCP and cholera toxin of El Tor biotypes under laboratory conditions.
In addition, since El Tor strains may not induce toxin production under general laboratory conditions, conditions for producing a toxin were induced using a method of lowering an oxygen partial pressure and increasing a CO2 partial pressure under AKI conditions (biphasic culture, method of culturing for 16 hours in a stationary state and then culturing under different culture conditions), but no toxin was produced in single phase culture (condition for culturing a strain only in shaking culture). However, the results show that the cholera toxin can also be produced in toxT variant strains in single phase culture.
Since the replication and propagation methods of CTX-2 and CTX-cla, which were used in the above-describe examples, had been setup in laboratories, strains having more various CTX phages and arrays were designed and constructed. The CTX phages were transferred by transduction and inserted, and a plasmid form was removed, such that El Tor strains having both CTX-1 and CTX-2 were constructed. In addition to El Tor biotype strains, a non-typical classical strain in which CTX-1 was inserted into a classical biotype strain was also constructed. The cholera strains used in this example have been listed in Table 1.
(Construction of pCTX Phages)
pCTX-1-kan-N1 is authentic pCTX-1 having a non-coding sequence which is the same as pCTX-1, and having a kanamycin cassette which is substituted for ctxA and the first 166 bp of ctxB (Table 1). pCTX-1-kan-N1 may be generated by replication of lysogenic CTX-1-kan in a strain such as PM20, or from a plasmid-based CTX phage replication system. pCTX-1-kan-N2 may be constructed by recombination between CTX-1 and CTX-2 in a PM9 strain. pCTX-1-kan-N2 has a non-coding sequence of pCTX-2/pCTX-cla. pCTX-1-cm-N1, like CTX-1-kan-N1, may be generated using a plasmid-based CTX phage replication system. In this system, a chloramphenicol cassette is substituted instead of the kanamycin cassette. pCTX-1-cm-N2 is generated from PM48.
pCTX-cla-kan-N1 has the non-coding sequence of pCTX-1, and is generated from a plasmid-based CTX phage replication system. pCTX-2-kan-N1 is generated from a plasmid-based CTX phage replication system. pCTX-2-kan-N1 has the non-coding sequence of pCTX-1. pCTX-2-kan-N2 is generated from the CTX-2 tandem repeat of PM22 generated in B33.
The pCTX phages generated from a plasmid-based CTX phage replication system or a lysogenic CTX prophage were maintained by transduction of suitable recipient strains for maintenance, that is, transduction of an O395 classical strain using pCTX-1 or a PM27-toxT-139F strain using pCTX-2, to produce more progeny phages, and used for secondary transduction.
(Construction of MG116025 and B33 Derivative Strains)
Isogenic strains of MG116025 and PM25 to PM29 were constructed by stepwise removal of CTX-1 and RS1. PM21, which is a derivative strain of B33, contained only one CTX-2 on chromosome 2, which was similar to PM6. These strains were used to construct strains having various CTX arrays.
(Construction of CTX Phage Transduction Recipient Strains)
When cultured under agglutination conditions (LB, pH6.5, 30° C.), a pCTX-1 phage was inserted into a classical biotype strain O395. When El Tor biotype strains harbored the toxT-139F allele, the strains were transduced by CTX phages. Strains such as A213, B33, MG116025, etc. were prepared to serve as a transduction recipient by substitution with toxT-139F.
(Insertion of CTX Phages into Cholera Strains)
The CTX phages replicated in a CTX phage donor strain are transferred through transduction to a recipient strain according to a standard protocol. The insertion of pCTX into chromosome 1 or chromosome 2 and the final CTX array were confirmed by various PCR combinations. pCTX was inserted into the chromosome, and a pCTX-cured strain was screened.
The non-coding sequences (the sequence between ctxB and rstR) of pCTX-1 and pCTX-cla differ from each other. The difference in base sequence of the non-coding sequences of pCTX-1 and pCTX-cla determines the orientation of inserting CTX phages into either chromosome 1 or chromosome 2 of cholera strains. When a phage has the non-coding sequence of pCTX-1, it has been known that the sequence is inserted only into chromosome 1, and when a phage has the non-coding sequence of pCTX-cla, the sequence may be inserted into both chromosome 1 and chromosome 2. The non-coding sequences of pCTX-1 and pCTX-2 may be interchangeable. CTX-1-kan-N1 contains the non-coding sequence of authentic pCTX-1, and CTX-1-kan-N2 contains the non-coding sequence of pCTX-cla. Therefore, pCTX-1-kan-N2 can be expected to integrate into both chromosome 1 and chromosome 2, and PM34 (also PM45, 49 and 50) was indeed constructed by inserting pCTX-1-kan-N2 into chromosome 2.
The non-coding sequence of pCTX is derived from RS1 downstream of a CTX phage during the replication of CTX prophages or a different prophage. Since most El Tor strains have a CTX-1:CTX-1 array or CTX-1:RS1 array, pCTX-1 has the non-coding sequence of authentic CTX-1. However, if there are CTX-1:CTX-2 and CTX-1:CTX-cla arrays, CTX-1 having the non-coding sequence of CTX-cla may be generated while CTX-1 is replicated. Therefore, the pCTX-1-N2 phage having both the pCTX-1 genome and the non-coding sequence of CTX-cla may be present like pCTX-1-N1. When the pCTX-1-N2 phage is inserted downstream of CTX-1 of a different strain, another pCTX-1-N2 phage may be generated. In this study, pCTX-1-cm-N2 was actually generated from PM48 (Table 1).
A mechanism of generating mosaic CTX phages by recombination between two different CTX phages present on different chromosomes in a single cholera strain had been previously demonstrated. Similarly, recombination between pCTX and a prophage could be possible. pCTX-1-kan-N1 is transferred to a B33-toxT-139F strain, thereby generating B33 (pCTX-1-kan-N1), and the phage progeny pCTX-1-kan-N1 generated from this strain may be transduced to O395 to avoid phage immunity. However, the recombination between pCTX-1-kan-N1 and a CTX-2 prophage may occur in B33 (pCTX-1-kan-N1), and when the recombination between rstA and a non-coding sequence, which are present at both sides of rstR of each CTX phage, occurs, pCTX-2-kan-N1 may be produced (
While atypical El Tor strains (Wave 2) harboring CTX-2 have been found, no classical strain having CTX-1 containing rstREl Tor and ctxBEl Tor has been found. Classical biotype strains are transduced by CTX-1, and while pCTX-1 is maintained in a classical biotype strain, a strain prepared by inserting CTX-1 into the chromosome of a classical biotype strain has not been found yet. As shown in
Toxigenic El Tor-type strains are generated by the integration of TLC, CTX-1 and RS1 in the dif1 base sequence of chromosome 1. In addition, it has been previously reported that strains that do not generate a toxin are generated by removing CTX-1 and RS1 from El Tor biotype strains. For example, the MG116025 strain has the TLC:RS1:CTX-1:RS1 array on chromosome 1, and a process of generating isogenic strains of the MG116025 strain, which are generated by stepwise removal of RS1, CTX-1 and even TLC (PM25˜PM29), has been previously reported. In this study, various types of pCTXs are transferred to MG116025 and strains generated therefrom, El Tor strains such as B33, A213, etc., thereby constructing strains having various CTX arrays.
MG116025 and derivative strains thereof: As shown in
PM30 and PM31 strains are strains generated by inserting CTX-2 into chromosome 1 and chromosome 2 of MG116025 (
B33 and derivative strains thereof: As shown in
A213 and derivative strains thereof: A213 is a strain which is classified as a US Gulf Coast strain or a pre-seventh pandemic strain and does not harbors CTX, which might be lost during isolation or storage. This study has more focused on constructing various strains from A213, which is to demonstrate a principle for a method of constructing a strain having various CTX phage arrays since A213 is a strain harboring only TLC.
As shown in
The present invention can be applied in the field of producing a cholera vaccine. In addition, the present invention can be applied in order to produce cholera toxin or a toxoid.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2016-0172681 | Dec 2016 | KR | national |
| 10-2016-0172684 | Dec 2016 | KR | national |
| 10-2017-0144851 | Nov 2017 | KR | national |
This application is a Continuation of International Application No. PCT/KR2017/014782 filed Dec. 15, 2017, which claims benefit of priority to Korean Patent Application No. 10-2016-0172681 filed Dec. 16, 2016, Korean Patent Application No. 10-2016-0172684 filed Dec. 16, 2016, and Korean Patent Application No. 10-2017-0144851 filed Nov. 1, 2017, the entire content of which is incorporated herein by reference.
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| 5631010 | Mekalanos | May 1997 | A |
| 20080305125 | Hirst | Dec 2008 | A1 |
| Entry |
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| Brigid M Davis et al.; “Filamentous Phages Linked to Virulence of Vibrio cholerae”; Current Opinion in Microbiology; 2003; pp. 35-42; vol. 6. |
| Eun Jin Kim; “A Study on the Evolution of Atypical Vibrio cholerae O1 El Tor Variants”; Doctoral Thesis, Department of Pharmacy, The Graduate School of Hanyang University; Aug. 2015; pp. 1-116. |
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| Number | Date | Country | |
|---|---|---|---|
| 20190315813 A1 | Oct 2019 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/KR2017/014782 | Dec 2017 | US |
| Child | 16442164 | US |
