Patent Application
20160348088
The present invention relates to bacterial genes and enzymes involved in the synthesis of polymyxin E, an antiobiotic molecule used in therapy against infections with gram-negative bacteria.
Polymyxins are antibiotic molecules isolated from Bacillus species or from Paenibacillus species. These molecules are lipopeptides, consisting:
At least 16 types of polymyxins have been identified since the discovery of polymyxin B in 1947. Among them, polymyxins B and E have antimicrobial activity on most of the strains of Escherichia coli and of Pseudomonas aeruginosa, and also on all strains of Salmonellae and Shigellae, and of numerous gram-negative bacteria. These antiobiotics have therefore been used as therapeutic agents in many cases. Unfortunately, their toxic effects are such that they have been gradually replaced by antiobiotics that are better tolerated.
Because of the increasing demand for new antibiotics for which there is not yet any resistance in the population, new antiobiotic agents are sought, and polymyxins are again used clinically in combating multiresistant gram-negative bacteria.
Colistin or polymyxin E, identified under CAS number 1264-72-8, and as described in patent application WO 1998/020836, is an antibiotic of the polymyxin family, making it possible to treat infections due to multiresistant gram-negative bacteria. Its peptide structure is indicated in
Colistin is responsible for numerous unwanted effects, in particular nephrotoxic and neurotoxic effects. These toxic effects are attributable to the cationic nature of this molecule, which contains five positive charges, but also to the low degree of purity of the molecule, produced in a fermenter by culturing the original bacterial strain which synthesizes it, and purified from the fermentation medium.
Indeed, polymyxins are currently obtained by isolation and purification from culture media of bacterial strains which produce these molecules, in particular strains of Paenibacillus polymyxa. The purification of the molecule from fermentation media is unsatisfactory, and this is why new production techniques are envisioned. In particular, studies are carried out to identify and clone the genes encoding polymyxin synthetases.
Polymyxin synthetases are part of the “Non-Ribosomal Peptide Synthetase” (NRPS) family; the genes encoding these synthetases are organized in a cluster comprising several modules, the order and specificity of which determine the structure of the peptide product. NRPSs allow the synthesis of peptides which exhibit a broader structural variety than that which could be obtained if these peptides were translated from messenger RNA by ribosomes. Furthermore, the peptides thus produced can undergo modifications, in particular through the creation of bonds with hydroxylated acids, and oxidations in the peptide chain making it possible to obtain cyclic structures and also acylations, glycosylations, and an N-methylation of the residues.
Such NRPS complexes have been described in many microorganisms and are involved in the production of tyrocidine, gramicidin, vancomycin, penicillin, and fusaricidins.
NRPS synthetases consist of various modules. Each module is capable of activating an amino acid, optionally of modifying it and of subsequently transferring it onto the activated amino acid in the adjacent module so as to constitute a peptide. Each module is composed of several domains and allow the incorporation of a particular amino acid into the peptide undergoing elongation. Each module contains a minimum of 3 domains:
The release of the peptide is induced by a specific domain, the Te (thioesterase) domain. This domain will cleave the thioester bond which links the synthesized peptide to the final T domain. This domain also allows the cyclization of certain peptides.
There are also optional secondary domains which make it possible to carry out modifications on the amino acids, such as epimerization (conversion of an amino acid of the L series to an isomer of the D series), methylation (addition of a methyl group) or else formylation (addition of a formyl group).
In the case of polymyxins, and as indicated in
The article by Choi et al. (Journal of Bacteriology, 2009) and also patent U.S. Pat. No. 8,329,430 describe the isolation of a cluster (group) of genes of the gram-positive strain Paenibacillus polymyxa E681 secreting polymyxin A. Five genes constitute this cluster: pmxA, pmxB, pmxC, pmxD and pmxE. The pmxC and pmxD genes encode transport proteins, while the other three genes, pmxA, pmxB and pmxE, encode synthetases. This is in particular demonstrated by a mutant strain which has undergone a mutation by insertion into the pmxE gene: this strain no longer produces polymyxin. Conversely, a strain of Bacillus subtilis transformed by the introduction of this gene cluster becomes capable of producing polymyxin A, but only in the presence of L-2,4-diaminobutyric acid (Dab, major residue of the polymyxin peptide chain).
In the polymyxins described in the literature, it is very rare to observe the presence of D-Dab residues, except for polymyxins A, C and P.
Shaheen et al. (Chemistry and Biology, 2011) have described the identification and sequencing of a gene cluster derived from the Paenibacillus polymyxa PKB1 strain. The involvement of this genes in polymyxin B biosynthesis is demonstrated by insertional mutation in the pmxE gene: the mutated strain no longer produces polymyxin. During the characterization of the cluster, Shaheen et al. identified an epimerization domain in the third module of the pmx cluster. This suggests the integration of a D-Dab in position 3. Thus, these genes are involved in the biosynthesis of polymyxin B variants, comprising, in position 3, not a D-2,4-diaminobutyrate residue, but its enantiomer, L-2,4-diaminobutyrate.
Other gene clusters derived from Paenibacillus polymyxa strains have been isolated, but their functions and specificities are only predicted and in no way functionally demonstrated.
Moreover, “variant” molecules exhibiting slight structural differences with the known polymyxins, and lesser toxic effects, have been reported. Thus, patent application WO 2009/098357 and also the article by Vaara and Vaara (Peptides, 2010) describe polymyxin B variants comprising only three positive charges and having reduced toxic effects. Polymyxin B variants have also been described in the article by Shaheen et al. (2011).
The technique currently used to produce colistin, based on the fermentation of bacterial producer strains in rich media, is not satisfactory, in particular in terms of purity of the molecule, which must be purified from the fermentation medium.
The identification of the genes involved in colistin synthesis would make it possible, by means of genetic engineering processes, to produce a purer polymyxin E molecule, and also to create derived synthetic molecules, having fewer harmful side effects and/or better activity.
The present invention describes the isolation of a gene cluster derived from a strain of Paenibacillus alvei isolated from the environment, producing polymyxin E, and uses thereof.
The present invention relates to a PmxA synthetase involved in polymyxin E synthesis, comprising four adenylation domains, characterized in that the second adenylation domain comprises or has a particular peptide sequence represented in SEQ ID NO 1, this sequence forming a binding pocket specific for a leucine, isoleucine or valine residue.
The present invention also relates to a PmxE synthetase involved in polymyxin E synthesis, comprising five adenylation domains and one epimerization domain.
The present application also relates to a group of genes encoding enzymes involved in polymyxin E synthesis, comprising a gene encoding the PmxA synthetase, genes encoding the PmxB and PmxE synthetases, and genes encoding the PmxC and PmxD transport proteins.
The present invention also relates to transformed microorganisms expressing at least the modified or nonmodified pmxA, pmxB and pmxE genes, said transformed microorganisms producing polymyxin E or variant molecules of this polymyxin.
Polypeptides and Polynucleotides
The invention relates to the isolation and identification of new genes encoding polymyxin E synthetases, in particular of a gene encoding the “PmxA” synthetase having a particular adenylation site, forming a specific binding pocket allowing the integration into the polymyxin molecule of a leucine or isoleucine residue.
All the technical terms used in the present application are well known to the person skilled in the art and are defined in the reference book by Sambrook et al. “Molecular Cloning: a Laboratory Manual”.
The term “polynucleotide” denotes a chain of covalently bonded nucleotides. For the purposes of the invention, this term denotes nucleic acids such as ribonucleic acid (RNA) and deoxyribonucleic acid (DNA).
For the purposes of the present invention, the “percentage identity” between two nucleic acid sequences is determined by comparing the two optimally aligned sequences through a comparison window.
The part of the nucleotide sequence in the comparison window may comprise additions or deletions (for example gaps) compared with the reference sequence (which does not comprise these additions or these deletions) so as to obtain optimal alignment between the two sequences.
The percentage identity is calculated by determining the number of positions at which an identical nucleic base is observed for the two sequences compared, then by dividing the number of positions at which there is identity between the two nucleic bases by the total number of positions in the comparison window, then by multiplying the result by one hundred in order to obtain the percentage nucleotide identity of the two sequences with respect to one another.
The optical alignment of the sequences for the comparison may be carried out by a computer using known algorithms.
Entirely preferably, the percentage sequence identity is determined using the CLUSTAL W software (version 1.82), the parameters being fixed as follows: (1) CPU MODE=ClustalW mp; (2) ALIGNMENT=“full”; (3) OUTPUT FORMAT=“aln w/numbers”; (4) OUTPUT ORDER=“aligned”; (5) COLOR ALIGNMENT=“no”; (6) KTUP (word size)=“default”; (7) WINDOW LENGTH=“default”; (8) SCORE TYPE=“percent”; (9) TOPDIAG=“default”; (10) PAIRGAP=“default”; (11) PHYLOGENETIC TREE/TREE TYPE=“none”; (12) MATRIX=“default”; (13) GAP OPEN=“default”; (14) END GAPS=“default”; (15) GAP EXTENSION=“default”; (16) GAP DISTANCES=“default”; (17) TREE TYPE=“cladogram” and (18) TREE GAP DISTANCES=“hide”.
The term “polypeptide” denotes a chain of covalently bonded amino acids.
The term “polymyxin E synthetases” denotes the enzymes capable of integrating a specific amino acid into the chain of amino acids forming polymyxin E, and where appropriate of converting the amino acid so as to form a cyclic structure.
The term “adenylation site” or “adenylation domain” denotes, in the polymyxin synthetase molecule, the domain which plays a role in the choice and activation of the amino acid, while the “condensation domain” catalyzes the formation of a peptide bond and the “thiolation domain” is responsible for the transport of the compounds undergoing formation between the modules.
The term “epimerization site” denotes, in a synthetase, a domain which makes it possible to convert a residue which has a levorotary chirality “L” into its enantiomer of dextrorotary chirality “D”, in particular an L-α,γ-diaminobutyric acid (L-Dab) into a D-α,γ-diaminobutyric acid (D-Dab).
The term “binding pocket” denotes a zone of the protein which has a three-dimensional structure in the form of a “pocket”, in which high-specificity interactions with a substrate or, in the present case, an amino acid, will make it possible to select and activate this amino acid.
The expression “the underlined amino acids being conserved” means that, even if slight sequence variations may be observed between two proteins having the same catalytic activity, the amino acids indicated are essential to the specificity and to the activity of this protein and may not therefore be modified, without risk of losing or reducing the specificity and/or the activity of this protein.
The present invention relates to a PmxA synthetase involved in polymyxin E synthesis, comprising four adenylation sites, characterized in that the second adenylation site has at least 90% identity with the following peptide sequence:
the underlined amino acids DGFFLGVVYK being conserved and forming a binding pocket specific for a leucine, isoleucine or valine residue.
According to one particular aspect of the invention, the second adenylation site of PmxA has 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% identity with the peptide sequence SEQ ID NO 1, the underlined amino acids DGFFLGVVYK being conserved and forming a binding pocket specific for a leucine, isoleucine or valine residue.
According to one particular aspect of the invention, the second adenylation site of PmxA has a peptide sequence comprising or consisting of the peptide sequence SEQ ID NO 27, the underlined amino acids DGFFLGVVYK being conserved and forming a binding pocket specific for a leucine, isoleucine or valine residue.
According to one particular aspect of the invention, the PmxA synthetase comprises four specific binding pockets comprising the following amino acids:
It is clearly understood that these sequences SEQ ID NO 2, 3, 4 and 5 group together the essential amino acids forming a functional binding pocket in a three-dimensional structure, but are not consecutive amino acids in a peptide sequence.
According to one particular aspect of the invention, the PmxA synthetase comprises the polypeptide sequence presented in SEQ ID NO 6, and shown in
According to one particular aspect, the polypeptide sequence of the PmxA synthetase consists of the polypeptide sequence presented in SEQ ID NO 6.
According to another aspect of the invention, the PmxA synthetase has the sequence which comprises, or consists of, the peptide sequence presented in SEQ ID NO 25.
The PmxA synthetase has four adenylation sites at the following positions:
It is understood that these positions are identified according to a particular peptide sequence, in this case according to SEQ ID NO 6 comprising 4967 amino acids, and may be redefined for sequences of larger size.
In particular, when the PmxA synthetase has a sequence consisting of the sequence SEQ ID NO 25, the four adenylation sites are in the following positions:
The present invention also relates to a PmxE synthetase involved in polymyxin E synthesis, comprising five adenylation sites and one epimerization site, characterized in that the epimerization site has at least 90% identity with the peptide sequence as presented in SEQ ID NO 30.
According to one particular aspect of the invention, the peptide sequence of the PmxE synthetase comprises or consists of the sequence represented in sequence SEQ ID NO 14.
This synthetase is responsible for the integration of residues 1 to 5 (see
The present invention also relates to a nucleic acid comprising an open reading frame, encoding a synthetase involved in polymyxin E synthesis, having at least 90% identity with the nucleotide sequence SEQ ID NO 7, with the proviso that the nucleotides encoding the underlined amino acids DGFFLGVVYK of the sequence SEQ ID NO 1 are conserved.
According to one particular aspect of the invention, the nucleic acid encoding a synthetase involved in polymyxin E synthesis has 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% identity with the nucleotide sequence SEQ ID NO 7, with the proviso that the nucleotides encoding the underlined amino acids DGFFLGVVYK of the sequence SEQ ID NO 1 are conserved.
The expression “the nucleotides [ . . . ] are conserved” indicate that these nucleotides encoding the amino acids DGFFLGVVYK of the sequence SEQ ID NO 1 must be either identical to those observed in the same position in the sequence SEQ ID NO 7, or different but with the proviso that the codons formed by these nucleotides encode the amino acids DGFFLGVVYK underlined in the sequence SEQ ID NO 1.
This is because, and as indicated above, these amino acids are essential to the specificity and to the activity of this synthetase and may not therefore be modified, without the risk of losing or reducing the specificity of this binding pocket.
According to another particular aspect of the invention, the nucleic acid encoding a PmxA synthetase involved in polymyxin E synthesis comprises a nucleotide sequence encoding the second adenylation site of this PmxA synthetase, consisting of the nucleotide sequence presented in sequence SEQ ID NO 28. This sequence encodes the peptide sequence represented in SEQ ID NO 27 and also encodes the peptide sequence represented in SEQ ID NO 1 which has two amino acids fewer than SEQ ID NO 27 at the C-terminal end of the domain.
The present invention also relates to a group of genes encoding enzymes involved in polymyxin E synthesis, comprising in particular:
According to one preferred aspect of the invention, this group of genes comprises the pmxE gene encoding a PmxE synthetase comprising an epimerization domain, the peptide sequence of which comprises or consists of the sequence represented in SEQ ID NO 30.
According to one preferred aspect of the invention, this group of genes also comprises genes encoding respectively the PmxC and PmxD transport proteins. The sequences of the PmxC and PmxD proteins isolated from the Paenibacillus alvei strain are shown in sequences SEQ ID NO 12 and NO 13, respectively.
According to another particular aspect of the invention, this group of genes involved in polymyxin E synthesis comprises:
According to another aspect of the invention, this group of genes involved in polymyxin E synthesis comprises:
According to another aspect of the invention, this group of genes involved in polymyxin E synthesis comprises:
The present invention also relates to a nucleic acid comprising or consisting of a sequence SEQ ID NO 10, or a sequence SEQ ID NO 29, representing the complete sequence of the cluster derived from the Paenibacillus alvei strain, comprising the pmxA, pmxB, pmxC, pmxD and pmxE genes involved in polymyxin E synthesis.
Table 1 below presents the various nucleic acid and protein sequences referenced in the present application:
Paenibacillus alvei strain
alvei strain; see also FIG. 5
Paenibacillus alvei
alvei strain
Paenibacillus alvei strain
Paenibacillus alvei
Paenibacillus alvei strain
a Paenibacillus alvei strain
Paenibacillus alvei
Expression Vectors
The present invention also relates to an expression vector comprising a gene encoding a PmxA synthetase as defined above, or a nucleic acid encoding a PmxA synthetase as defined above, and/or a gene encoding a PmxE synthetase as defined above.
In the context of the invention, the terms “vector”, “expression vector” and “plasmid” are equivalent and are used in accordance with the usual acceptance in the molecular biology, genetic engineering and microbiology field. Very briefly, it is a non-viral DNA molecule housed by a host cell, distinct from the natural chromosomal DNA of said host cell and capable of autonomous replication. A “vector” is obtained by conventional molecular biology and genetic engineering techniques, and is a molecule into which one or more exogenous nucleotide sequences have been inserted (or cloned). The present invention relates to a vector for the expression, by a host cell, of exogenous nucleotide sequences, comprising:
The choice of the vector and, more particularly, of the origin of replication that it carries depends on the host cell that will house it. Depending on the type of host cells, several copies of a vector and/or several different vectors may be introduced into the same host cell, simultaneously or sequentially.
The choice of the vector will also depend on the size of the nucleic acid sequence to be expressed. In particular, for sequences greater than 20 kilobase pairs, fosmids, which are vectors capable of containing large nucleic acid sequences (up to 40 kilobase pairs), will be preferred. It is also possible to use several vectors, each comprising a portion of a set of genes, and to transfer several vectors into the same host cell, this making it possible to express an entire set of genes in the same strain.
Other vectors that may contain sequences of large sizes are cosmids and bacterial artificial chromosomes (BACs).
According to one preferred aspect of the invention, the expression vector totally or partly comprises a group of genes as defined above.
According to another preferred aspect of the invention, the expression vector totally or partly comprises a nucleic acid as defined above, in particular comprising the sequence presented in SEQ ID NO 10 or in SEQ ID NO 29. Preferably, the expression vector is a fosmid comprising all of the DNA sequence encoding the complete cluster comprising the pmxA, pmxB, pmxC, pmxD and pmxE genes derived from Paenibacillus alvei, having the sequence SEQ ID NO 10.
Other Enzymes Involved in Polymyxin Synthesis
Other enzymes are involved in polymyxin synthesis, in particular polymyxin E synthesis. These are enzymes which allow the biosynthesis of the Dab residue, this residue being the residue predominantly integrated into the peptide chain of polymyxin E, and enzymes which allow the bonding of the fatty acid on the peptide part.
An enzyme for biosynthesis of the α,γ-diaminobutyric acid (Dab) residue has been identified and isolated from the bacterial strain of Paenibacillus alvei described in the examples. In particular, the peptide sequence of this enzyme comprises or consists of the peptide sequence presented in sequence SEQ ID NO 31. The nucleic acid encoding this enzyme comprises or consists of the nucleotide sequence presented in sequence SEQ ID NO 32.
Preferably, this enzyme with transaminase activity may be expressed in a microorganism intended to produce polymyxin E, in combination with the PmxA, PmxB and PmxE synthetases, and preferably also with the PmxC and PmxD transport molecules.
This transaminase comprising 431 residues has a sequence homology with enzymes exhibiting similar functions, derived from other microorganisms, as is shown in Table 2 below:
P. polymyxa
P. alvei
P. polymyxa
Halobacillus
halophilus
Enzymes which allow the bonding of the fatty acid on the peptide chain of polymyxin E, said enzymes therefore having acyl transferase activity, have also been identified and isolated from the bacterial strain of Paenibacillus alvei described above.
Preferably, at least one acyl transferase will be expressed in a microorganism intended for producing polymyxin E, in combination with the PmxA, PmxB and PmxE synthetases, and preferably also with the PmxC and PmxD transport molecules, and more preferably also with an enzyme for the biosynthesis of the α,γ-diaminobutyric acid (Dab) residue.
Alternatively, the bonding of the fatty acid on the peptide chain of polymyxin E may also be carried out by chemical coupling, according to one of the techniques well known to those skilled in the art.
Host Cells
The term “host cell” or “host microorganism” is used in the context of the present invention to denote a cell which has been transformed, i.e. into which the exogenous DNA has been introduced, this exogenous DNA being in particular in the form of an expression vector comprising a sequence of interest, which will be expressed by means of the cellular machinery of the host cell, capable of synthesizing, from the exogenous DNA, the messenger RNAs and the proteins corresponding to this DNA.
The present application relates in particular to a microorganism transformed by introducing a gene or group of genes as defined above, or one or more expression vectors as presented above.
The invention relates in particular to a microorganism transferred by introducing:
The invention also relates to a microorganism transformed by introducing a group of genes as defined above, or a nucleic acid encoding all or part of the pmxA, pmxB and pmxE genes, as defined above, or at least one expression vector comprising a gene encoding all or part of the pmxA, pmxB and pmxE genes, as defined above.
According to one particular aspect of the invention, the microorganism is in addition transformed so as to comprise at least one nucleic acid encoding an enzyme involved in the biosynthesis of the Dab residue, and in particular a nucleic acid comprising a sequence comprising or consisting of the sequence SEQ ID NO 32.
According to another aspect of the invention, the microorganism is in addition transformed so as to comprise at least one nucleic acid encoding an enzyme with acyl transferase activity, catalyzing the bonding of a fatty acid on the peptide chain of polymyxin E.
The transformation of microorganisms is a technique commonly used in molecular biology laboratories, which makes it possible to introduce exogenous DNA into the microorganism. Various techniques enable the transformation of a microorganism, and in particular of a competent bacterium, and are all well known to those skilled in the art. Mention may in particular be made of electroporation, and the use of calcium chloride followed by a heat shock.
In one preferred aspect of the invention, in the transformed microorganism, the gene or the group of genes introduced is overexpressed.
The overexpression of a gene may be defined by an increased expression of this gene, i.e. a greater production of messenger RNA and the protein encoded by this gene, in the cell. The expression of the protein will in particular be increased by 50%, by 100%, by 150%, by 200%, or even by 300% compared with the level of endogenous expression observed in a bacterium expressing this gene naturally, before any transformation.
The overexpression of a gene may be obtained in several ways, all well known to those skilled in the art. Mention will in particular be made of: using strong promoters for controlling the level of gene expression and increasing the number of copies of the gene in the cell. Preferably, the vector used will comprise a strong promoter under the control of which the gene will be inserted, and said vector will be present in a high number of copies, in particular 10, 20, 50 or 100 copies in the host cell.
Those skilled in the art will know how to choose the host microorganism most suitable for the expression of a vector comprising the gene(s) according to the invention. In particular, gram-positive bacteria will be preferred. A microorganism which is particularly suitable is a bacterium belonging to the Bacillus or Paenibacillus genus. The species B. subtilis and Paenibacillus polymyxa are particularly suitable for the expression of polymyxin synthetases and the production of polymyxin E. The strains of the Paenibacillus genus, and in particular of Paenibacillus alvei, and more particularly the Paenibacillus alvei strain isolated from the environment by the inventors, may also be used as host microorganism to be transformed with the vector or the nucleic acid as defined above. Finally, synthetic bacteria may also be used in the context of the present invention, as host cells.
Method for Producing Polymyxin E
The present application also relates to a method for producing polymyxin E, comprising:
The term “appropriate mineral medium” denotes a culture medium which allows the growth of microorganisms, and which comprises in particular mineral salts and nutrients. A preferred medium has the following specific composition: 0.45% (w/v) anhydrous KH2PO4, 1.13% (w/v) K2HPO4. 3H2O, 0.6% (w/v) (NH4)2SO4, 0.6% (w/v) glucose, 0.001%0 (w/v) thiamine, 0.02% (w/v) MgSO4.7H2O. This medium may also comprise, where appropriate, a precursor required for polymyxin synthesis, in particular diaminobutyric acid.
According to one preferred aspect of the invention, the culturing is carried out at a temperature of 30° C., and lasts at least 25 hours.
Preferably, the culturing takes place in 200 ml of mineral medium in 1 L flasks, with shaking, for 30 h at 30° C.
The present invention also relates to a method for producing polymyxin E variants, comprising culturing a microorganism as defined above, in an appropriate mineral medium, and purifying, from the culture medium, the polymyxin E variant(s).
The present invention also relates to polymyxin E variants obtained according to the production method as described above.
The “polymyxin E variants” denote molecules derived from the structure of polymyxin E (see
In particular, the types of molecules detected in the culture medium for the Paenibacillus alvei strain BL-R are polymyxin E variants which have the following structural difference: the residue in position 3 may be a D-Dab residue in place of an L-Dab residue observed in the conventional structure of polymyxin E.
The variant forms may be natural or synthetic. The term “natural variants” is intended to mean variants synthesized by non-transformed microorganisms; the term “synthetic variants” is intended to mean variant forms synthesized by transformed microorganisms, which have not been identified in the natural state.
In particular, the polymyxin synthetases encoded by the pmxA, pmxB and pmxE genes may be modified so as to become specific for the binding of certain amino acids which are part of the composition of polymyxin E, in order to synthesize polymyxin E variants which have fewer cationic charges and which are therefore less toxic to the human organism.
These polymyxin E variants have advantages and in particular a lower toxicity than polymyxin E.
Moreover, the clinical use of various polymyxin E variants makes it possible to reduce the appearance of antiobiotic resistance.
It is probable that, for the variants comprising D-Dab residues in place of L-Dab residues, the antimicrobial activity of these molecules is increased compared with the antimicrobial properties observed with the conventional polymyxins.
The present invention relates to these variants, and also to the use thereof in the treatment of bacterial infections with gram-negative bacteria.
The examples below illustrate the invention claimed, but are not limiting.
A microorganism (B-LR) producing colistin (polymyxins E1 and E2), belonging to the Paenibacillus alvei species, was isolated from the environment and cultured. A genomic DNA library was constructed in Escherichia coli using fosmid vectors (900 clones). The search for the genes encoding the enzymes which synthesize colistin was carried out by degenerate PCRs. The primers used were defined with the aim of amplifying the domains specializing in the integration of diaminobutyric acid (Dab), which is the amino acid most representing the structure of colistin (6 amino acids/12). Three clones of interest were selected from the sequence (Roche GS FLX). The sequences obtained could be assembled over 50 kb. The open reading frames were sought. Five of them called A, B, C, D and E describe a cluster of approximately 41 kb with A (14.9 kb), B (3.3 kb), C (1.8 kb), D (1.7 kb) and E (18.9 kb), which is represented in
The A, B and E genes were identified, by sequence homology, as encoding synthetases. An in silico study made it possible to predict the involvement of these synthetases in the assembly of colistin (http://nrps.informatik.uni-tuebingen.de/ and http://nrps.igs.umaryland.edu/nrps/). The C and D genes could, for their part, be involved in the export and resistance of the producer microorganism with respect to colistin.
The enzymes involved in polymyxin production belong to the non-ribosome synthetase (NRPS) family. These synthetases are capable of producing a particular peptide without relying on the translation of an mRNA template. The specificity of the peptide chain produced depends on a precise sequence of amino acids of the synthetase constituting an adenylation domain. Four adenylation domains were identified in silico for the synthetase A of B-LR, one for B and five for E. Each adenylation domain contains a signature of ten amino acids which confers it on the specificity of integrating a precise amino acid into the non-ribosomal peptide during elongation. These signatures were identified in silico and compared to those described in the literature (Table 4) using the program available at the following web address: http://nrps.informatik.uni-tuebingen.de/.
The E681 and ATCC21830 strains are described in patent U.S. Pat. No. 8,329,430.
The PKB1 strain is described in the article by Shaheen et al., 2011.
The M-1 strain is described in the article by Niu et al., 2013.
The synthetases of B-LR differ at the level of the second adenylation domain of the PmxA synthetase and of the third domain of the PmxE synthetase.
The comparisons with the protein sequences derived from the BL-R strain with the protein sequences already known are presented in Table 5 below:
A sequence of 1650 bp beginning at the end of pmxD and finishing at the start of pmxE was selected and amplified. It has the particularity of possessing a unique SacII enzyme restriction site. The amplified sequence was cloned into the pGEM® 7Z plasmid. The gene encoding apramycin resistance was integrated at the SacII restriction site. This construct was introduced into B-LR by electroporation. The selection of the mutants having undergone a double recombination event was carried out by culturing on agar medium supplemented with apramycin. The antiomicrobial activity of the supernatant of the mutants was compared with that of B-LR. The culture supernatant of mutant 5 is less active than that of the wild-type B-LR bacterium on P. aeruginosa (
The peptide sequence of the PmxE synthetase is presented in sequence SEQ ID NO 14. The sequence of the epimerization domain is presented in SEQ ID NO 30; it comprises at least 461 residues comprised between and including the residues Val3205 to Leu3665 of the sequence SEQ ID NO 14. One of the characteristics of non-ribosomal peptides is the presence of amino acids with (L) stereoisomerism. Usually, an (L) amino acid is activated by the A domain, which then incorporates it directly. However, sometimes, this amino acid of the (L) series may be converted into its (D) form by any epimerization domain, before the formation of the peptide bond. According to the in silico predictions, two epimerization domains were identified in modules 3 and 6 of the pmx cluster. This suggests that a stereochemical change in the amino acids present at these sites is possible. Thus, the amino acids present in position 3 (Dab-3) and in position 6 (Leu-6) would be incorporated into the peptide chain in their (D) form. This was known for Leu-6, incorporated in its (D) form into all polymyxins E, but is unusual for the Dab-3 residue.
The PmxE synthetase according to the invention therefore has the property of converting the L-Dab residue into its stereoisomer (D), and of integrating it in position 3 (see
Said polymyxin E molecules comprising a D-Dab residue in position 3 are polymyxin E variants.
The microorganism (B-LR) produces several types of polymyxin E molecules comprising a leucine, isoleucine or valine residue in position 7.
These various types of molecules could be detected in the culture medium by mass spectrometry, according to the protocol detailed below:
A control solution of colistin sulfate at 0.0002% was prepared in the microorganism culture medium (M63T medium). Four fractions were recovered and analyzed by UPLC-MS (Ultra Performance Liquid Chromatography—tandem mass spectrometry). The two peaks corresponding to the polymyxins E1 and E2 present in the positive control were found in the fourth extraction fraction.
The B-LR strain exhibits a maximum level of antimicrobial activity at 30 hours of culture. At this time, the culture supernatant was recovered and filtered (0.22 μm) before being subjected to a solid-phase extraction step. The peptides of the fourth fraction were analyzed by UPLC-MS. Seventeen elution peaks were observed in this fourth fraction. Among them, the main peaks exhibiting retention times of 1.61 and 1.52 minutes have [M+H]+ molecular masses respectively of 1169.7727 and 1155.7555. They correspond respectively to the known polymyxins E1 and E2, which have the same peptide structure and differ by their fatty acids, respectively of formulae C9H17O and C8H15O.
MS/MS analyses were carried out in order to confirm these structures, as have previously been presented in the articles by Govaerts et al., 2002; and by DeCrescenzo et al., 2007. Tandem mass spectrometry (MS/MS) is used to determine the series of amino acids through fragmentation of the peptide bond. This technique consists in combining two analyzers separated by a collision cell. A first step consists in selecting an ion derived from the source of ionization in the quadrupole: this is the parent or precursor ion. This ion undergoes fragmentation in the collision cell under the effect of a bombardment by argon atoms, and gives “daughter” or “product” ions that will be analyzed and protected by the time-of-flight (TOF) analyzer. The TOF analyzer is based on the measurement of the time taken by the ions to cover a given distance, thereby making it possible to detect the m/z ratios and thus to determine the mass of the corresponding ions.
During these experiments, the leucine and isoleucine residues cannot be differentiated, because of their identical molecular masses.
Three decapeptides with a ring containing seven amino acids were purified from the B-LR supernatant. Their molecular weights range from 1140.74 Da to 1168.77 Da. The comparison of these molecules shows homologies at the level of residues 1 to 6 and 8 to 10 and differences at the level of residue 7 and also at the level of the fatty acid. These three molecules correspond to polymyxins (colistins) E1, E2 and to Val-colistin E2. The deduced chemical formulae thereof are presented in Table 6 below.
The mass spectra obtained for colistin E1, colistin E2 and val-colistin E2 have respective [M+2H]2+ values of 585.39, 578.38 and 571.38. The fragmentation of the parent ions of colistins E1 and E2 give daughter ions of m/z 829, 728, 628, 427, 327 and 227 (
These daughter ions obtained are identical to those described in the literature during the fragmentation of colistins E1, E2 and Val-E2 (Govaerts et al., 2002; DeCrescenzo et al., 2007). Colistins E1 and E2 have the same amino acid sequences with a molecular mass difference of 14 Da which corresponds to the loss of a CH2 at the level of the fatty acid.
In conclusion, these results show that the B-LR strain produces colistin E1, colistin E2 and valine-colistin E2 (Val-E2).
Bacillus is a heterologous expression host that is phylogenetically close to B-LR. The fosmid manipulated to house all of the colistin production cluster is transferred into the recipient strain by electroporation. The transformed strains are selected on agar medium supplemented with an antibiotic. The colistin production is carried out in liquid medium supplemented with diaminobutyric acid (synthesis precursor). The colistin is detected after separation of the biomass from the culture supernatant. Extractions make it possible to isolate the colistin before characterization thereof by mass spectrometry.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1450641 | Jan 2014 | FR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IB2015/050571 | 1/26/2015 | WO | 00 |
