Patent Application
20140220632
In order to ensure effective colonization and transmission, meningococcus bacteria adapt and respond to different microenvironments through differential expression of genes involved in pathogenesis. In Neisseria meningitidis, the presence or absence of pathogenic determinants is regulated at the transcriptional level, while more fine-tuning of the determinant level can be made at both transcriptional and translational levels. Gene activation is typically associated with reversible changes within simple DNA sequence tracts (repeats in some instances) located in promoter, coding, and/or transcription terminator sequence regions. The number of repeats can be modified during replication through mechanisms such as slipped strand mis-pairing, and can consequently influence transcription or translation by introducing frame-shift mutations or changing critical promoter spacing. The loss or gain of repeat units results in high frequency on-off switching (in the case of frame-shift/translational control) or modulation of the level (in the case of promoter control) of expression of genes typically associated with surface antigens.
PorA is an example of a surface antigen whose promoter strength is regulated at least partially by changes in a poly-G tract that is located between base pairs −35 and −10 relative to the transcription start site. NadA is an example of a surface antigen whose promoter strength is regulated in part by phase variation. A tract of repeated TAAA sequences, located upstream of the nadA promoter, together with the binding of nadR transcriptional repressor to three different operator elements, dictates the frequency of phase variation of nadA. Over-expressing a surface antigen from a strong native promoter in a Neisseria meningitidis host therefore presents difficulties when producing vaccines, as these mechanisms can result in inconsistent expression of surface antigens.
The present disclosure generally provides engineered polynucleotide sequences that facilitate high-level expression of one or more gene products (e.g., polypeptides) of interest in Neisseria meningitidis. Methods of use of such sequences, e.g., use in vaccine production, are also provided.
In some embodiments, an engineered polynucleotide sequence is a promoter, including a 5′ portion of a native N. meningitidis porA promoter comprising the sequence ATGGTT, a spacer portion, and a 3′ portion of a native N. meningitidis porA promoter comprising the sequence TATAAT, wherein the spacer comprises a sequence of the formula N1-TTTCA-N2, wherein N1 is Xa(T/A)(T/A)(T/A)(T/G)(C/G)(C/G)(C/G/A)(G/T)CXb and N2 is XcXdXe, wherein: Xa is present or absent, and when present is T or A, Xb is present or absent, and when present is A or C, Xc is present or absent, and when present is T or G, Xd is present or absent, and when present is A or G; and Xe is present or absent, and when present is G, wherein the 5′ portion, the spacer, and the 3′ portion are operably linked to provide for transcription in N. meningitidis.
In some embodiments, the spacer comprises the sequence ATATGCCTCCTTTCATA. In some embodiments, the spacer comprises the sequence TATATGCCTCCTTTCATA. In some embodiments, the spacer comprises the sequence ATAATGCCTCCTTTCATA. In some embodiments, the spacer comprises the sequence ATATGCATCATTTCATA. In some embodiments, the spacer comprises the sequence TTTTGCGGGCTTTCATA. In some embodiments, the spacer comprises the sequence TTTTGCGGGCTTTCAGGG. In some embodiments, the spacer comprises the sequence TTTTGCGGGCTTTCAG.
In some embodiments, an engineered polynucleotide sequence is a promoter comprising the formula, from 5′ to 3′: TFB-X-E-ATG, wherein TFB refers to a transcription factor binding sequence of a native nmb1523 promoter; E refers to a 66 base pair extension sequence of a native nmb1523 promoter; and X refers to a spacer sequence of a native nmb1523 promoter positioned between TFB and E, wherein portions TFB, X, and E are operably linked to provide for transcription in N. meningitidis, with the proviso that when E is present, TFB is absent, and when TFB is present, E is absent. In certain embodiments, both TFB and E are absent.
In some embodiments, an engineered polynucleotide sequence is a nucleic acid construct comprising the promoter described above operably linked to a polynucleotide sequence encoding a Neisseria meningitidis surface antigen.
In some embodiments, an isolated Neisseria meningitidis bacterium comprises a promoter described above, or a nucleic acid construct described above. In some embodiments, an isolated Neisseria meningitidis bacterium comprises a promoter that is operably positioned in the genome of the bacterium to facilitate expression of an endogenous polynucleotide. In some embodiments, the endogenous polynucleotide encodes a Neisseria meningitidis surface antigen.
Some embodiments relate to a method of expressing a Neisseria meningitidis surface antigen, the method comprising: culturing an isolated Neisseria meningitidis bacterium as described above, wherein said culturing facilitates expression of the surface antigen.
Some embodiments relate to a method of expressing a Neisseria meningitidis surface antigen, the method comprising operably inserting a promoter sequence as described above into the genome of a Neisseria meningitidis host upstream of a native surface antigen gene, and culturing the Neisseria meningitidis host, wherein said culturing facilitates expression of the surface antigen.
Some embodiments relate to a method of expressing a Neisseria meningitidis surface antigen, the method comprising inserting a nucleic acid construct comprising a promoter sequence as described above operably linked to a polynucleotide sequence encoding a surface antigen into the genome of a Neisseria meningitidis host; and culturing the Neisseria meningitidis host, wherein said culturing facilitates expression of the surface antigen.
Some embodiments relate to a method of expressing a Neisseria meningitidis surface antigen, the method comprising operably inserting a first promoter sequence as described above into the genome of a Neisseria meningitidis host upstream of a native surface antigen gene, inserting a nucleic acid construct comprising a second promoter sequence as described above operably linked to a polynucleotide sequence encoding a surface antigen into the genome of a Neisseria meningitidis host, and culturing the Neisseria meningitidis host, wherein said culturing facilitates expression of the surface antigen. In some embodiments, the first and second promoters are the same. In other embodiments, the first and second promoters are different.
In some embodiments, nucleic acid constructs include a promoter that is operably linked to a first polynucleotide that encodes a gene product of interest, and the first polynucleotide is operably linked to a second polynucleotide that encodes a gene product of interest, such that the promoter drives expression of the first and the second polynucleotides. In some embodiments, nucleic acid constructs include a first polynucleotide and a second polynucleotide that encode the same gene product of interest. In some embodiments, nucleic acid constructs include a first polynucleotide and a second polynucleotide that encode different gene products of interest. In some embodiments, one or both of the gene products of interest is a Neisseria meningitidis surface antigen. In some embodiments, nucleic acid constructs include a transcription terminator that is operably linked to the 3′ end of the second polynucleotide.
In some embodiments, nucleic acid constructs include a promoter that is operably linked to a first polynucleotide that encodes a gene product of interest, and the first polynucleotide is operably linked to a second polynucleotide that encodes a gene product of interest, and the second polynucleotide is operably linked to a third polynucleotide that encodes a gene product of interest, such that the promoter drives expression of the first, the second, and the third polynucleotides. In some embodiments, nucleic acid constructs include a first, a second, and a third polynucleotide that encode the same gene product of interest. In some embodiments, the gene product of interest is a Neisseria meningitidis surface antigen. In some embodiments, two of the polynucleotides encode a first gene product of interest, and one of the polynucleotides encodes a second gene product of interest that is different from the first gene product of interest. In some embodiments, the first gene product of interest is a Neisseria meningitidis surface antigen. In some embodiments, the second gene product of interest is a Neisseria meningitidis surface antigen. In some embodiments, the first, the second, and the third polynucleotides each encode a different gene product of interest. In some embodiments, each of the gene products of interest are Neisseria meningitidis surface antigens. In some embodiments, nucleic acid constructs include a transcription terminator that is operably linked to the 3′ end of the third polynucleotide.
Before the present invention is further described, it is to be understood that this invention is not limited to particular embodiments described, as such may, of course, vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting, since the scope of the present invention will be limited only by the appended claims.
Where a range of values is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit unless the context clearly dictates otherwise, between the upper and lower limit of that range and any other stated or intervening value in that stated range, is encompassed within the invention. The upper and lower limits of these smaller ranges may independently be included in the smaller ranges, and are also encompassed within the invention, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included in the invention.
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although any methods and materials similar or equivalent to those described herein can also be used in the practice or testing of the present invention, the preferred methods and materials are now described. All publications mentioned herein are incorporAted herein by reference to disclose and describe the methods and/or materials in connection with which the publications are cited.
It must be noted that as used herein and in the appended claims, the singular forms “a,” “an,” and “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to “the promoter” includes reference to one or more promoters, and so forth. It is further noted that the claims may be drafted to exclude any optional element. As such, this statement is intended to serve as antecedent basis for use of such exclusive terminology as “solely,” “only” and the like in connection with the recitation of claim elements, or use of a “negative” limitation.
The publications discussed herein are provided solely for their disclosure prior to the filing date of the present application. Nothing herein is to be construed as an admission that the present invention is not entitled to antedate such publication by virtue of prior invention. Further, the dates of publication provided may be different from the actual publication dates which may need to be independently confirmed.
The following terms have the following meanings unless otherwise indicated. Any undefined terms have their art recognized meanings.
“Polynucleotide” as used herein refers to an oligonucleotide, nucleotide, and fragments or portions thereof, and to DNA or RNA of genomic or synthetic origin which can be single- or double-stranded, and represent the sense or antisense strand.
“Promoter” refers to a DNA regulatory region having a sequence capable of initiating transcription of a downstream (3′ direction) sequence.
“Transcriptional terminator” refers to a DNA regulatory region capable of terminating transcription of an upstream (5′ direction) sequence.
A “codon” is a series of three contiguous nucleotides that encode a specific amino acid residue in a polypeptide chain or encode the termination of translation (e.g. a “stop” codon).
“Translationally optimized sequence” refers to a non-natural DNA sequence wherein the codons have been altered based on the preferences of the organism expressing the sequence for one of the several codons that encode the same amino acid in order to facilitate more efficient expression of the DNA sequence.
A “deletion” is defined as a change in nucleotide sequence in which one or more nucleotide bases are absent as compared to a nucleotide sequence of a naturally occurring reference polynucleotide.
An “insertion” or “addition” is that change in a nucleotide sequence which has resulted in the addition of one or more nucleotide bases as compared to a nucleotide sequence of a naturally occurring reference polynucleotide.
A “substitution” results from the replacement of one or more nucleotides by different nucleotides as compared to a nucleotide sequence of a naturally occurring reference polynucleotide.
By “construct” or “polynucleotide construct” is meant a nucleic acid sequence that has been constructed to comprise one or more functional units not found together in nature.
By “operably linked” is meant that a DNA sequence and a regulatory sequence (e.g. a promoter) are connected in such a way as to permit gene expression when the appropriate molecules (e.g., transcriptional activator proteins) are bound to the regulatory sequence. Operably linking a DNA sequence and a regulatory sequence can be accomplished by operably inserting the regulatory sequence upstream (e.g. in the 5′ direction) of the DNA sequence, or by operably inserting the DNA sequence downstream (e.g. in the 3′ direction) of the regulatory sequence.
The term “endogenous” refers to any naturally-occurring component of a cell.
The term “exogenous” refers to any non-naturally-occurring component of a cell that originates outside the cell.
The term “heterologous” or “chimeric” refers to two components that are defined by structures derived from different sources. For example, where “heterologous” is used in the context of a chimeric promoter, the chimeric promoter can include operably linked nucleotide sequences that can be derived from different polynucleotide reference sequences (e.g., a first component from an alpha and a second component from a beta reference nucleotide sequence). A chimeric polynucleotide containing two or more defined segments, each of which is from a different reference sequence, can be naturally-occurring or man-made (non-naturally-occurring). Non-naturally occurring chimeric polynucleotide sequence refers to “man-made chimeras” and may encompass, e.g., a promoter with heterologous components that are not found together in nature.
Other exemplary “heterologous” nucleic acids include expression constructs in which a nucleic acid comprising a coding sequence is operably linked to a regulatory element (e.g., a promoter) that has a genetic origin different from that of the coding sequence (e.g., to provide for expression in a host cell of interest, which may be of different genetic origin relative to the promoter, the coding sequence or both). For example, a chimeric promoter operably linked to a polynucleotide encoding an fHbp polypeptide or domain thereof is said to be a heterologous nucleic acid.
“Domain deletion promoter” as used herein refers to a polynucleotide promoter sequence that is derived from a native promoter sequence, but in which one or more domains (e.g. a transcription factor binding domain and/or a base pair extension domain) has been deleted.
“Recombinant” as used herein refers to a nucleic acid encoding a gene product, a gene product (e.g., polypeptide) encoded by such a nucleic acid, or a cell (e.g. a bacterial cell) that has been manipulated by the hand of man, and thus is provided in a context or form in which it is not found in nature. “Recombinant” thus encompasses, for example, a polynucleotide sequence encoding a gene product operably linked to a heterologous promoter (such that the construct that provides for expression of the gene product from an operably linked promoter is not found in nature). For example, a “recombinant fHbp” encompasses an fHbp encoded by a construct that provides for expression from a promoter heterologous to the fHbp coding sequence, fHbp polypeptides that are modified relative to a naturally-occurring fHbp (e.g., as in a fusion protein), and the like. It should be noted that a recombinant fHbp polypeptide can be endogenous to or heterologous to a Neisseria meningitidis strain in which such a recombinant fHbp-encoding construct is present. A recombinant organism (e.g. a recombinant bacterium) can be created by incorporating exogenous DNA into an organism to achieve a permanent or transient genetic change. Genetic change can be accomplished either by incorporation of the exogenous DNA into the genome of the host cell, or by transient or stable maintenance of the exogenous DNA as an episomal element.
A “knock-out” or “knockout” of a target gene refers to an alteration in the sequence of the gene that results in a decrease of function of the target gene, e.g., such that target gene expression is undetectable or insignificant, and/or the gene product does not function or is not significantly functional. For example, a “knockout” of a gene involved in LPS synthesis means that function of the gene has been substantially decreased so that the expression of the gene is not detectable or is only present at insignificant levels and/or a biological activity of the gene product (e.g., an enzymatic activity) is significantly reduced relative to prior to the modification or is not detectable. “Knock-outs” encompass conditional knock-outs, where alteration of the target gene can occur upon, for example, exposure to a predefined set of conditions (e.g., temperature, osmolarity, exposure to substance that promotes target gene alteration, and the like).
As used herein, the term “isolated” is meant to describe a molecule of interest (e.g., a promoter) that is in an environment different from that in which the molecule naturally occurs. Thus, for example, “isolated” encompasses a naturally-occurring promoter that is isolated from its natural environment and operably linked to a heterologous polynucleotide sequence. “Isolated” may also include compounds that are within samples in which the compound of interest is partially or substantially purified, e.g., isolated surface antigen proteins.
“Enriched” means that a compound of interest in a sample is manipulated by an experimentalist or a clinician so that it is present in at least a three-fold greater concentration by total weight, usually at least 5-fold greater concentration, more preferably at least 10-fold greater concentration, more usually at least 100-fold greater concentration than the concentration of that antigen in the strain from which the antigen composition was obtained. Thus, e.g., if the concentration of a particular antigen is 1 microgram per gram of total bacterial preparation (or of total bacterial protein), an enriched preparation would contain at least 3 micrograms per gram of total bacterial preparation (or of total bacterial protein).
As used herein, the term “substantially purified” refers to a compound (e.g., a surface antigen) that is removed from its natural environment and is at least 60% free, preferably 75% free, and most preferably 90% free from other components with which it is naturally associated.
The term “native” when used in the context of a polynucleotide sequence (e.g. a promoter or a polynucleotide sequence encoding a surface antigen) refers to naturally-occurring sequences (e.g. naturally-occurring porA or nadA promoter sequences, or naturally-occurring fHbp-encoding sequences) as they are typically found in Neisseria meningitidis bacteria.
“Derived from” in the context of a polynucleotide sequence (e.g., a polynucleotide sequence derived from a native Neis serial promoter) is meant to indicate that the polynucleotide has a sequence that is modified relative to a reference polynucleotide, e.g., a naturally-occurring polynucleotide sequence, and is not meant to be limiting as to the source or method by which the polynucleotide is made. A polynucleotide sequence derived from another polynucleotide sequence may include, for example, multiple additions, deletions, or substitutions of specific nucleic acids.
The phrase “a disease caused by Neisseria meningitidis” encompasses any clinical symptom or combination of clinical symptoms that are present in an infection with Neisseria meningitidis bacteria. These symptoms include but are not limited to: colonization of the upper respiratory tract (e.g. mucosa of the nasopharynx and tonsils) by a pathogenic strain of Neisseria meningitidis, penetration of the bacteria into the mucosa and the submucosal vascular bed, septicemia, septic shock, inflammation, haemmorrhagic skin lesions, activation of fibrinolysis and of blood coagulation, organ dysfunction such as kidney, lung, and cardiac failure, adrenal hemorrhaging and muscular infarction, capillary leakage, edema, peripheral limb ischaemia, respiratory distress syndrome, pericarditis and meningitis.
The phrase “elicit an immunological response in a subject” means that there is a detectable difference between an immunological response indicator measured before and after administration of a particular antigen preparation. Immune response indicators include but are not limited to: antibody titer or specificity, as detected by an assay such as enzyme-linked immunoassay (ELISA), bactericidal assay, flow cytometry, immunoprecipitation, Ouchter-Lowny immunodiffusion; binding detection assays of, for example, spot, Western blot or antigen arrays; cytotoxicity assays, etc.
A “surface antigen” is an antigen that is present in a surface structure of Neisseria meningitidis (e.g. the outer membrane, inner membrane, periplasmic space, capsule, pili, etc.).
“Serogroup” or “capsular group” as used herein refers to classification of Neisseria meningitidis by virtue of immunologically detectable variations in the capsular polysaccharide. About 12 serogroups are known: A, B, C, X, Y, Z, 29-E, W-135, H, I, K and L. Any one serogroup can encompass multiple serotypes and multiple serosubtypes.
“Serotype” as used herein refers to classification of Neisseria meningitidis strains based on monoclonal antibody defined antigenic differences in the outer membrane protein Porin B. A single serotype can be found in multiple serogroups and multiple serosubtypes.
“Serosubtype” as used herein refers classification of Neisseria meningitidis strains based on antibody defined antigenic variations on an outer membrane protein called Porin A, or upon VR typing of amino acid sequences deduced from DNA sequencing (Sacchi et al., 2000, J. Infect. Dis. 182:1169; see also the Multi Locus Sequence Typing web site). Most variability between PorA proteins occurs in two (loops I and IV) of eight putative, surface exposed loops. The variable loops I and IV have been designated VR1 and VR2, respectively. A single serosubtype can be found in multiple serogroups and multiple serotypes.
A “monovalent vaccine” refers to a vesicle vaccine prepared from a single strain. The strain may be a mutant strain (i.e., genetically modified) or a wildtype strain (naturally occurring). Such vaccines may be combined with other immunogenic or antigenic components to provide a vaccine composition (e.g., combined with one or more recombinant protein antigens).
A “bivalent vaccine” refers to a vesicle vaccine prepared from two different strains. The two strains may be mutant strains or wildtype strains or a combination of a mutant and a wildtype strain. Such vaccines may be combined with other immunogenic or antigenic components to provide a vaccine composition (e.g., combined with one or more recombinant protein antigens).
The term “subject” as used herein can refer to a human or to a non-human animal, e.g. a mammal, including humans, primates, domestic and farm animals, and zoo, sport, laboratory, or pet animals, such as horses, cows, dogs, cats, rodents, and the like.
The present disclosure generally provides engineered polynucleotide sequences that facilitate consistent, high-level expression of one or more gene products (e.g., polypeptides, RNA) of interest in recombinant host cells. Methods of use of such sequences, e.g., use in vaccine production, are also provided.
As described in more detail below, some of the polynucleotide sequences of the present disclosure function as promoters, while others function as transcription terminators. The polynucleotide sequences described herein may be operably linked to one or more polynucleotide sequences encoding one or more gene products (e.g., polypeptides, RNA) of interest, and the resulting construct may be introduced into host cells, e.g., Neisseria meningitidis cells, to create recombinant hosts capable of expressing the one or more gene products of interest at high levels. Polynucleotide sequences of the present disclosure that encode a protein of interest may be codon-optimized to increase expression of the protein of interest in recombinant host cells.
The present disclosure generally provides engineered polynucleotide sequences that can act as promoters in host cells, e.g, Neisseria cells, e.g., N. meningitidis, N. gonorrhoeae or related N. flavescens, N. lactamica, N. polysaccharea, N. cinerea, N. mucosa, N. subflava, N. sicca, N. elongata, or Haemophilus spp. The disclosed promoter sequences facilitate high-level expression of gene products (e.g., proteins of interest, e.g. surface antigens), in host cells. Engineered promoters can be, for example, chimeric promoters that incorporate sequences from two or more different native Neisserial promoters (or variants thereof). Engineered promoters may also be, for example, domain deletion promoters that are derived from a native Neisserial promoter in which one or more functional domains of the promoter have been deleted (e.g., where a transcription factor binding domain and/or a base pair extension domain have been deleted).
The engineered promoters of the present disclosure can provide for an increase in expression of a gene product of interest to which it is operably linked of about 5%, about 10%, about 25%, about 50%, about 75%, or more relative to expression of the gene product from its native promoter. The engineered promoters of the present disclosure can provide for an increase in expression of a gene product of interest that is at least about 2-fold, about 3-fold, about 4-fold, about 5-fold, about 8-fold, about 10-fold or at least about 15-fold relative to expression of the gene product from its native promoter.
When combined with a transcription terminator of the present disclosure, the engineered promoters with the transcription terminator can provide for a further increase in expression of a gene product of interest above that provided by an engineered promoter without a transcription terminator, e.g, by at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30% or more relative to the engineered promoter without the transcription terminator.
Chimeric Promoters
The engineered promoters of the present disclosure that contain combinations of native Neisserial promoter sequences (or variants thereof) are referred to herein as chimeric promoters.
In general, the chimeric promoters contain 1) a 5′ portion of a native porA promoter having the contiguous nucleotide sequence ATGGTT (referred to as a “−35 region” due to its location relative to the transcription start site), 2) a spacer portion, and 3) a 3′ portion of a native PorA promoter having the contiguous nucleotide sequence TATAAT (referred to as a “−10 region” due to its location relative to the transcription start site).
The spacer portion generally includes a 5′ portion containing a sequence of 10 to 11 contiguous nucleotides derived from a native PorA and/or NadA promoter, 5 contiguous nucleotides having the sequence TTTCA, and a 3′ portion containing a sequence of 1 to 3 contiguous nucleotides derived from a native PorA or NadA promoter. As used herein, the term “analogous” is used to describe a heterologous portion of a chimeric promoter that originates from the same geographical region of the reference or source promoter. For example, a sequence of 10 contiguous nucleotides located adjacent to the −35 region of a NadA promoter would be “analogous” to a sequence of 10 contiguous nucleotides located adjacent to the −35 region of a PorA promoter.
The spacer portion of the chimeric promoters of the present disclosure, in general, has a structure of the formula, from 5′ to 3′:
N1-TTTCA-N2,
where N1 is contiguous with TTTCA and is of the formula
Xa(T/A)(T/A)(T/A)(T/G)(C/G)(C/G)(C/G/A)(G/T)CXb
wherein
Xa is present or absent, and when present is T or A; and
Xb is present or absent, and when present is A or C; and
where N2 is contiguous with TTTCA and is of the of the formula
XcXdXe,
wherein
Xc is present or absent, and when present is T or G,
Xd is present or absent, and when present is A or G, and
Xe is present or absent, and when present is G.
The components of the spacer were selected by replacing a portion of a native Neisserial promoter (e.g., a native PorA promoter) with an analogous portion of another native Neisserial promoter (e.g., a native NadA promoter). In some embodiments, variants of the analogous sequence were used, including nucleotide substitutions, eliminations, or additions.
In some embodiments, the spacer portion is of the sequence ATATGCCTCCTTTCATA. In some embodiments, the spacer portion is of the sequence TATATGCCTCCTTTCATA. In some embodiments, the spacer portion is of the sequence ATAATGCCTCCTTTCATA. In some embodiments, the spacer portion is of the sequence ATATGCATCATTTCATA. In some embodiments, the spacer portion is of the sequence TTTTGCGGGCTTTCATA. In some embodiments, the spacer portion is of the sequence TTTTGCGGGCTTTCAGGG. In some embodiments, the spacer portion is of the sequence TTTTGCGGGCTTTCAG.
The chimeric promoters of the present disclosure can provide for an increase of expression of a gene product of interest of at least about 5%, about 10%, about 15%, about 20%, about 25%, about 50%, about 75%, or more relative to the expression level of the gene product from its native promoter. The engineered promoters of the present disclosure can provide for an increase in expression of a gene product of interest of at least 2-fold, about 3-fold, about 4-fold, about 5-fold, about 8-fold, about 10-fold, about 15-fold or more relativeot the expression level of the gene product from its native promoter.
When combined with a transcription terminator of the present disclosure, the chimeric promoter and transcription terminator can provide for a further increase in expression of a gene product of interest above that provided by a chimeric promoter without a transcription terminator, e.g, by at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30% or more relative to the chimeric promoter without the transcription terminator.
Domain Deletion Promoters
The engineered promoters of the present disclosure that are derived from native promoter sequences wherein one or more functional domains of the native promoter have been deleted are referred to herein as domain deletion promoters. In general, the domain deletion promoters of the present disclosure are derived from a native Neisserial promoter. In some embodiments, a domain deletion promoter is derived from a native Neisserial nmb1523 promoter. The native nmb1523 promoter is approximately 580 nucleotides in length, and has a transcription factor binding domain located between nucleotides 105 and 369. The native nmb1523 promoter also has a 66 base pair extension domain located between nucleotides 511 and 577.
Domain deletion promoters are of the general formula, from 5′ to 3′:
TFB-X-E-ATG
wherein TFB refers to a transcription factor binding sequence of a native nmb1523 promoter, E refers to a 66 bp extension sequence of a native nmb1523 promoter, and X refers to a spacer sequence positioned between a TFB sequence and an E sequence of a native nmb1523 promoter, with the proviso that when TFB is present, E is absent, and when E is present, TFB is absent, e.g., so as to provide for domain deletion promoters of the following formulae, from 5′ to 3′: TFB-X-ATG, X-E-ATG. In some embodiments, both TFB and E are absent, so as to provide for domain deletion promoters having the formula X-ATG.
In some embodiments, the domain deletion promoter is of the formula, from 5′ to 3′ TFB-X-ATG such that the promoter includes a native nmb1523 promoter sequence containing the transcription factor binding domain, but lacks the 66 base pair extension domain. In one example, the sequence of this domain deletion promoter comprises:
In other embodiments, the domain deletion promoter is of the formula, from 5′ to 3′ X-E-ATG such that the promoter includes a nucleotide sequence of a native nmb1523 promoter sequence containing the 66 base pair extension domain, but lacks the transcription factor binding domain. In one example, the sequence of the domain deletion promoter comprises:
In other embodiments, the domain deletion promoter is of the formula, from 5′ to 3′ X-ATG such that the promoter includes the spacer element, but lacks the transcription factor binding domain and the 66 base pair extension domain of the native nmb1523 promoter. In one example, the sequence of the domain deletion promoter comprises:
The domain deletion promoters of the present disclosure can provide for an increase in expression of a gene product of interest by at least about 5%, about 10%, about 15%, about 20%, about 25%, about 50%, about 75%, or more relative to an expression level of the gene product from its native promoter. The domain deletion promoters of the present disclosure can provide for an increase in expression of a gene product of at least about 2-fold, about 3-fold, about 4-fold, about 5-fold, about 8-fold, about 10-fold or more relative to an expression level of the gene product from its native promoter.
When combined with a transcription terminator of the present disclosure, the domain deletion promoter and transcription terminator can provide for a further increase in expression of a gene product of interest above that provided by a domain deletion promoter without a transcription terminator, e.g, by at least about 5%, about 10%, about 15%, about 20%, about 25%, about 30% or more relative to the domain deletion promoter without the transcription terminator.
The present disclosure generally provides polynucleotide sequences that function as transcription terminators, which can further facilitate efficient expression of gene products in a host cell, e.g., a Neisseria cell. Without being held to theory, the transcription terminator sequences generally function by dissociating RNA polymerase from the DNA template sequence, thus terminating the transcription process.
The present disclosure generally provides transcription terminator sequences that can be operably linked to the 3′ end of a polynucleotide sequence encoding a surface antigen to facilitate efficient expression. In some embodiments, polynucleotide constructs comprising a transcription terminator sequence are provided in which the transcription terminator sequence is heterologous to the promoter sequence, the coding sequence, or both. In other embodiments, a transcription terminator sequence can be a native sequence that is found operably attached to the 3′ end of a coding sequence in nature. Transcription terminator sequences can be naturally-occurring transcription terminators of native surface antigen coding sequences, e.g., fHbp coding sequences, especially native fHbp coding sequences that naturally exhibit increased expression relative to other fHbp coding sequences.
The polynucleotide sequences of the present disclosure that function as transcription terminators generally have at least about 85% sequence identity to the following sequence:
In some embodiments, the transcription terminator sequence has up to about 90%, up to about 95%, or up to about 98% sequence identity to the sequence disclosed above.
As shown in
The polynucleotide sequences of the present disclosure can be provided in a variety of forms, such as a construct, e.g., an expression construct, for use in the methods described herein. Examples include circular, linear, double-stranded, extrachromosomal DNA molecules (plasmids), cosmids (plasmids containing COS sequences from lambda phage), viral genomes comprising non-native nucleic acid sequences, and the like. A “vector” is any molecule or agent capable of transferring gene sequences to target cells. Typically, “vector construct,” “expression vector,” and “gene transfer vector,” mean any polynucleotide construct capable of directing the expression of a gene of interest and which can transfer gene sequences to target cells, which can be accomplished by genomic integration of all or a portion of the vector, or transient or inheritable maintenance of the vector as an extrachromosomal element. Thus, the term includes cloning and expression vehicles, as well as integrating vectors.
The constructs of the present disclosure may include expression constructs comprising an engineered promoter operably linked to, for example, one or more polynucleotides encoding one or more gene products of interest (e.g., a polypeptide or mRNA). In some embodiments, an expression construct may also include a transcription terminator sequence operably linked to the 3′ end of a coding sequence of interest. An “expression cassette” comprises any nucleic acid construct capable of directing the expression of one or more coding sequences of interest, which are operably linked to a promoter of the expression cassette. Such cassettes can be constructed into a “vector,” “vector construct,” “expression vector,” or “gene transfer vector,” in order to transfer the expression cassette into target cells. Thus, the term includes cloning and expression vehicles, as well as viral vectors.
The nucleic acid constructs of the present disclosure may also include specific nucleotide sequences (e.g., restriction enzyme recognition sequences or homologous recombination sequences) that can facilitate the transfer of nucleic acid sequences between constructs or into the genome of a host. For example, constructs may be provided in which an engineered promoter (or expression construct comprising an engineered promoter) is flanked by homologous recombination sequences to facilitate genomic insertion of the target sequence into the genome of a host cell (e.g., a Neisseria cell) by homologous recombination at a desired location in the genome of the cell.
The present disclosure generally provides expression constructs that may comprise an engineered promoter sequence of the present disclosure operably linked to one or more polynucleotide sequences that encode a gene product of interest (e.g., a protein of interest, e.g., an antigen of interest, such as a surface antigen (e.g., fHbp)). In some embodiments, the expression constructs of the present disclosure also include a transcription terminator sequence that is operably linked to the 3′ end of a polynucleotide sequence that encodes a gene product (e.g., a protein) of interest. In some embodiments, expression constructs of the present disclosure may contain a plurality of polynucleotide sequences that encode one or more gene products (e.g., proteins) of interest. In such embodiments, the polynucleotide sequences that encode the gene products (e.g., proteins) of interest may encode different gene products (e.g., proteins) of interest, or may encode the same gene products (e.g., proteins) of interest.
In some embodiments, expression constructs of the present disclosure may include an engineered promoter sequence that is operably linked to a polynucleotide sequence that encodes a gene product (e.g., a protein) of interest, such that a single engineered promoter sequence drives expression of a single gene product (e.g., protein) of interest.
In some embodiments, expression constructs of the present disclosure may include an engineered promoter sequence that is operably linked to a plurality of polynucleotide sequences that encode one or more gene products (e.g., proteins) of interest, such as two or more, or such as three or more, polynucleotide sequences that encode gene products (e.g., proteins) of interest, such that a single engineered promoter sequence drives expression of a plurality of polynucleotide sequences that encode one or more gene products (e.g., proteins) of interest. In such embodiments, the polynucleotide sequences that encode the gene products (e.g., proteins) of interest may encode the same gene product, or may encode different gene products (e.g., may encode different surface antigens). As described above, in some embodiments, the expression constructs of the present disclosure may include a transcription terminator sequence that is operably linked to the 3′ end of one of the gene product of interest-encoding polynucleotide sequences. Expression constructs of the present disclosure may also contain restriction enzyme recognition sequences and/or homologous recombination sequences that facilitate transfer of the polynucleotide sequences between constructs or into a suitable host.
In general, the present disclosure involves the use of recombinant hosts for the replication and expression of nucleic acid constructs. Any of a variety of suitable host cells (e.g., various suitable Neisserial strains) may be used with the constructs and methods of the present disclosure, including but not limited to naturally-occurring strains and genetically modified strains.
In some embodiments, replication hosts are used to replicate nucleic acid constructs of the present disclosure. Constructs are introduced into the replication host using any suitable technique, and the host cells are then cultured under appropriate conditions that facilitate replication of the construct. After the host cells have been cultured for a sufficient time, the cells are lysed and the replicated nucleic acid constructs are isolated and purified for further use in the methods of the present disclosure.
Suitable replication hosts are well known in the art, and include, e.g. DH5 alpha competent cells, DH10B cells, XL-1 Blue cells, JM109 cells, and the like.
Any of a variety of suitable host cells may be used as expression hosts to express an antigen of interest using various combinations of the polynucleotide sequences of the present disclosure. In some embodiments, pathogenic or commensal Haemopilus spp. or Neisseria spp. or strains derived from pathogenic Neisseria spp., particularly strains pathogenic for humans or derived from strains pathogenic or commensal for humans, are used as expression hosts. Exemplary Nessserial spp. include N. meningitidis, N. flavescens, N. gonorrhoeae, N. lactamica, N. polysaccharea, N. cinerea, N. mucosa, N. subflava, N. sicca, N. elongata, and the like. “Derived from” in the context of bacterial strains is meant to indicate that a strain was obtained through passage in vivo, or in in vitro culture, of a parental strain and/or is a recombinant cell obtained by modification of a parental strain.
N. meningitidis strains can be divided into serologic capsular groups (also called serogroups), PorB serotypes and PorA serosubtypes on the basis of reactions with polyclonal (Frasch, C. E. and Chapman, 1973, J. Infect. Dis. 127: 149-154) or monoclonal antibodies that interact with different surface antigens. Serogrouping is based on immunologically detectable variations in the capsular polysaccharide. About 12 serogroups (A, B, C, X, Y, Z, 29-E, and W-135) are known. PorA serosubtypes can also be classified by differences in DNA sequences of two variable regions (VR1 and VR2), and are referred to VR types (see, e.g., Russell et al. Emerging Infect Dis 2004 10:674-78; Sacchi C T, et al. Clin Diagn Lab Immunol 1998; 5:845-55; Sacchi et al, J. Infect Dis 2000; 182:1169-76).
The Neisserial strain to be used as an expression host can be selected according to a number of different characteristics that may be desired. For example, the strain may be selected according to a desired serogroup, serotype, serosubtype, and the like; decreased capsular polysaccharide production, and the like.
Alternatively or in addition, a suitable expression host strain can be a capsule deficient strain. Capsule deficient strains can be used to produce vesicle-based vaccines that provide for a reduced risk of eliciting a significant autoantibody response in a subject to whom the vaccine is administered (e.g., due to production of antibodies that cross-react with sialic acid on host cell surfaces). “Capsule deficient” or “deficient in capsular polysaccharide” as used herein refers to a level of capsular polysaccharide on the bacterial surface that is lower than that of a naturally-occurring strain or, where the strain is genetically modified, is lower than that of a parental strain from which the capsule deficient strain is derived. A capsule deficient strain includes strains that are decreased in surface capsular polysaccharide production by at least 10%, 20%, 25%, 30%, 40%, 50%, 60%, 75%, 80%, 85%, 90% or more, and includes strains in which capsular polysaccharide is not detectable on the bacterial surface (e.g., by whole cell ELISA using an anti-capsular polysaccharide antibody).
Capsule deficient strains include those that are capsule deficient due to a naturally-occurring or recombinantly-generated genetic modification. Naturally-occurring capsule deficient strains (see, e.g., Dolan-Livengood et al. J. Infect. Dis. (2003) 187(10):1616-28)), as well as methods of identifying and/or generating capsule-deficient strains (see, e.g., Fisseha et al. (2005) Infect. Immun. 73(7):4070-4080; Stephens et al. (1991) Infect Immun 59(11):4097-102; Frosch et al. (1990) Mol. Microbiol. 1990 4(7):1215-1218)) are known in the art.
Modification of a Neisserial host cell to provide for decreased production of capsular polysaccharide may include modification of one or more genes involved in capsule synthesis, where the modification provides for, for example, decreased levels of capsular polysaccharide relative to a parent cell prior to modification. Such genetic modifications can include changes in nucleotide and/or amino acid sequences in one or more capsule biosynthesis genes rendering the strain capsule deficient (e.g., due to one or more insertions, deletions, substitutions, and the like in one or more capsule biosynthesis genes). Capsule deficient strains can lack or be non-functional for one or more capsule genes.
Strains that are deficient in sialic acid biosynthesis may also be used as expression hosts. Such strains can provide for production of vesicles that have reduced risk of eliciting anti-sialic acid antibodies that cross-react with human sialic acid antigens, and can further provide for improved manufacturing safety. Strains having a defect in sialic acid biosynthesis (due to either a naturally occurring modification or an engineered modification) can be defective in any of a number of different genes in the sialic acid biosynthetic pathway. Of particular interest are strains that are defective in a gene product encoded by the N-acetylglucosamine-6-phosphate 2-epimerase gene (known as synX AAF40537.1 or siaA AAA20475), with strains having this gene inactivated being of special interest. For example, in one embodiment, a capsule deficient strain is generated by disrupting production of a functional synX gene product (see, e.g., Swartley et al. (1994) J. Bacteriol. 176(5):1530-4).
Capsular deficient strains can also be generated from naturally-occurring strains using non-recombinant techniques, e.g., by use of bactericidal anti-capsular antibodies to select for strains that are reduced in capsular polysaccharide.
Where the use of two or more expression hosts is involved (e.g., to produce antigenic compositions of vesicles from different strains), the hosts can be selected so as to differ in on or more strain characteristics.
Methods suitable for the growth and maintenance of recombinant Neisserial strains are well known in the art. In general, bacterial cells are grown at approximately 35-37° C. in appropriate growth media (e.g. Mueller-Hinton broth (BD Biosciences, Franklin Lakes, N.J., US) supplemented or not with 0.25% glucose (w/v) and 0.02 mM cytidine 5′-monophospho-N-acetylneuraminic acid (Sigma-Aldrich, St, Louis, Mo., US), Regular or modified Frantz Media, Minimal media, Catling Media, etc).
Gene Products Suitable for Expression from an Engineered Promoter
The polynucleotide sequences and methods of the present disclosure generally facilitate consistent, high-level expression of any gene product of interest (e.g., a protein of interest, e.g., a surface antigen of interest) in a recombinant host. The promoter sequences and/or transcription terminator sequences of the present disclosure can be operably linked to a polynucleotide sequence encoding any gene product of interest in order to facilitate its expression in a recombinant host. In some embodiments, the polynucleotide coding sequences of the present disclosure comprise translationally optimized sequences, wherein the codons in the coding sequence have been optimized to facilitate efficient expression in the host organism. This technique is described in more detail below.
The following are examples of gene products that are contemplated by the compositions and methods of the present disclosure. The following examples of gene products are in no way limiting, and those of skill in the art will readily appreciate that the sequences and methods of the present disclosure may be used to express any gene product of interest.
Gene products of interest that are suitable for expression include, but are not necessarily limited to, naturally-occurring polypeptides (e.g., as encoded by an endogenous genomic sequence), and recombinant polypeptides, where a recombinant polypeptide may be a polypeptide having an amino acid sequence endogenous or exogenous to the host cell. Where the polypeptide is an exogenous polypeptide, the polypeptide may have an amino acid sequence of a naturally-occurring polypeptide that is not endogenous to the host cell and/or have an amino acid sequence that is non-naturally occurring (e.g., a man-made polypeptide having an amino acid sequence that does not occur in nature). Polypeptides can be of any of a variety of classes, including but not limited to e.g., secreted proteins, outer membrane proteins, (e.g., surface antigens), and intracellular proteins. Gene products of interest also include protein-encoding and non-protein-encoding RNAs, where the RNAs may be either endogenous or exogenous to the host cell.
The polynucleotides and methods of the present disclosure find use in facilitating expression of gene products such as those provided herein, e.g., to facilitate vaccine production in a recombinant host. As set out in the examples in more detail below, various gene products, including but not limited to Neisserial outer membrane proteins and their variants and subvariants, are well known in the art and find use in connection with the sequences and methods of the present disclosure.
fHbp
Factor H binding protein (fHbp), also known in the literature as GNA1870, ORF2086, rLP-2086, and “741”, is a Neisseria meningitidis surface antigen.
Nucleic acids encoding fHbp polypeptides for use in the present disclosure are known in the art. Suitable fHbp polypeptides are described in, for example, WO 2004/048404; Masignani et al. 2003 J Exp Med 197:789-799; Fletcher et al. Infect Immun 2004 2088-2100; Welsch et al. J Immunol 2004 172:5606-5615; and WO 99/57280. Nucleic acid (and amino acid sequences) for fHbp variants and subvariants are also provided in GenBank as accession nos.: NC—003112, GeneID: 904318 (NCBI Ref. NP—274866) (from N. meningitidis strain MC58); AY548371 (AAT01290.1) (from N. meningitidis strain CU385); AY548370 (AAT01289.1) (from N. meningitidis strain H44/76); AY548377 (AAS56920.1) (from N. meningitidis strain M4105); AY548376 (AAS56919.1) (from N. strain M1390); AY548375 (AAS56918.1) (from N. meningitidis strain N98/254); AY548374 (AAS56917.1) (from N. meningitidis strain M6190); AY548373 (AAS56916.1) (from N. meningitidis strain 4243); and AY548372 (AAS56915.1) (from N. meningitidis strain BZ83).
fHbp polypeptides useful in the present disclosure include non-naturally occurring (artificial or mutant) fHbp polypeptides that differ in amino acid sequence from a naturally-occurring fHbp polypeptide, but which are present in the membrane of a Nesserial host so that vesicles prepared from the host contain fHbp in a form that provides for presentation of epitopes of interest, preferably a bactericidal epitope, and provides for an anti-fHbp antibody response. In one embodiment, the fHbp polypeptide is a variant 1 (v.1) or variant 2 (v.2) or variant 3 (v.3) fHbp polypeptide, with subvariants of v.1 v.2 and v.3 being of interest, including subvariants of v.1 (see, e.g., Welsch et al. J Immunol 2004 172:5606-5615). Subvariants are defined by peptide alleles or identification numbers (ID) as specified on the website: pubmlst.org/neisseria/fHbp/. In one embodiment, the fHbp polypeptide comprises an amino acid sequence of a fHbp polypeptide that is most prevalent among the strains endemic to the population of a subject to be vaccinated.
fHbp polypeptides useful in the present disclosure also include fusion proteins, where the fusion protein comprises a fHbp polypeptide having a fusion partner at its N-terminus or C-terminus. Fusion partners of interest include, for example, glutathione S transferase (GST), maltose binding protein (MBP), His-tag, and the like, as well as leader peptides from other proteins, particularly lipoproteins (e.g., the amino acid sequence prior to the N-terminal cysteine may be replaced with another leader peptide of interest).
Other fHbp polypeptide-encoding nucleic acids can be identified using techniques well known in the art, where fHbp polypeptides can be identified based on amino acid sequence similarity to a known fHbp polypeptide. Such fHbp polypeptides generally share at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or greater sequence identity at the nucleotide or amino acid level. Sequence identity can be determined using methods for alignment and comparison of nucleic acid or amino acid sequences, which methods are well known in the art. Comparison of longer sequences may require more sophisticated methods to achieve optimal alignment of two sequences. Optimal alignment of sequences for aligning a comparison window may be conducted by the local homology algorithm of Smith and Waterman (1981) Adv. Appl. Math. 2:482, by the homology alignment algorithm of Needleman and Wunsch (1970) J. Mol. Biol. 48:443, by the search for similarity method of Pearson and Lipman (1988) Proc. Natl. Acad. Sci. (USA) 85:2444, by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package Release 7.0, Genetics Computer Group, 575 Science Dr., Madison, Wis.), or by inspection, and the best alignment (i.e. resulting in the highest percentage of sequence similarity over the comparison window) generated by the various methods is selected.
PorA
PorA is another Neisseria meningitidis surface antigen. “PorA polypeptide” as used herein encompasses naturally-occurring and synthetic (non-naturally occurring) polypeptides which share at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or greater sequence identity at the nucleotide or amino acid level with a naturally-occurring PorA polypeptide, and which are capable of eliciting antibodies that specifically bind a naturally-occurring PorA polypeptide present on a Neisseria meningitidis bacterium. “PorA polypeptide” also encompasses fusion proteins, e.g., a PorA polypeptide having a heterologous polypeptide at the N- and/or C-terminus.
Nucleic acids encoding PorA polypeptides for use in the present disclosure are known in the art. Suitable PorA polypeptides include those that confer a serosubtype of P1.7,16; P1.19,15; P1.7,1; P1.5,2; P1.22a,14; P1.14; P1.5,10; P1.7,4; P1.12,13; as well as variants of such PorA polypeptides which may or may not retain reactivity with conventional serologic reagents used in serosubtyping.
Also of interest are PorA polypeptides characterized according to PorA variable region (VR) typing (see, e.g., Russell et al. Emerging Infect Dis 2004 10:674-678; Sacchi C T, et al, Clin Diagn Lab Immunol 1998; 5:845-55; Sacchi et al, J. Infect Dis 2000; 182:1169-1176). A substantial number of distinct VR types have been identified, which can be classified into VR1 and VR2 family “prototypes”. A web-accessible database describing this nomenclature and its relationship to previous typing schemes is found at neisseria.org/nm/typing/porA. Alignments of exemplary PorA VR1 and VR2 types is provided in Russell et al. Emerging Infect Dis 2004 10:674-678.
Exemplary PorA polypeptides as characterized by PorA serosubtypes include P1.5,2; P1.5a,2a; P1.5a,2c; P1.5a,2c; P1.5a,2c; P1.5b,10; P1.5b,10; P1.5b, C; P1.7,16; P1.7d,1; P1.7d,1; P1.7d,1; P1.7d,1; P1.7b,3; P1.7b,4; P1.7b,4; P1.12,16; P1.12a,13a; P1.22,9; P1.23,14; P1.23,14; P1.19,15; P1.B,1; P1.C,1; P1.E,A; P1.E,A; P1.E,A; P1.5,2; P1.5,2; P1.5a,10a; P1.5b,10; P1.5b,10; P1.5b,10b; P1.7,16; P1.7,16; P1.7b,1; P1.7b,13e; P1.7b,4; P1.7b,4; P1.7d,1; P1.7d,1; P1.7b,13a; P1.23,3; P1.23,3; P1.23,3; P1.19,15; P1.19,1; P1.19,15; P1.19,15; P1.19,15; P1.19,15; P1.19,15; P1.19,15; P1.19,15; P1.E,A; P1.E,A; P1.E,16a; P1.E,4a; P1.E,4a; P1.Ea,3; P1.Eb,9; P1.Eb,9; P1.Eb,9; P1.Eb,9; P1.Eb,9; P1.F,16; P1.7a,1; P1.7b,3; P1.7d,1; P1.Ea,3; P1.5b,10; P1.5b,10; P1.5b,10; P1.5b,10; P1.5b,10; P1.5b,10; P1.5b,10b; P1.5b,10; P1.22,14a; P1.F,16; P1.D,2d; P1.D,2; P1.D,2d; P1.19c,2c; P1.D,10f; P1.A,10e; P1.A,10g; P1.A,10; P1.19,15; P1.19,15; P1.19,15; P1.19,15; P1.7b,16; P1.7,16b; P1.7,16; P1.19,15; P1.Eb,9; P1.5,2e; P1.E,A; P1.7b,13d; P1.Ea,3; P1.7,16b; P1.Ec,1; P1.7b,4; P1.7b,4; P1.7,9; P1.19,15; P1.19,15; P1.19,15; P1.19,15a; P1.19a,15b; P1.19,15; P1.5b,16; P1.19b,13a; P1.5,16; P1.5,2; P1.5,2b; P1.7b,16; P1.7,16b; P1.7b,3; P1.Ea,3; P1.5a,2c; P1.F,16; P1.5a,9; P1.7c,10c; P1.7b,13a; P1.7,13a; P1.7a,10; P1.20,9; P1.22,B; P1.5b,del; P1.5b,10; P1.7,13a; P1.12a,13f; P1.12a,13; P1.12a,13a; P1.12a,13a; P1.12a,13; P1.12a,13; P1.E,13b; P1.7b,13a; P1.7b,13; P1.5,2; P1.5,2; P1.Ea,3; P1.22,9; P1.5,2; P1.5,2; P1.19,15; P1.5,2; P1.12b,13a; P1.5c,10a; P1.7e,16e; P1.B,16d; P1.F,16e; P1.F,16e; P1.7b,13e; P1.B,16d; P1.7e,16e; P1.7b,13g; P1.B,16f; P1.7,16c; P1.22,14b; P1.22,14c; P1.7,14; P1.7,14; and P1.23,14.
Amino acid sequences of exemplary PorA polypeptides are found at GenBank accession nos. X57182, X57180, U92941, U92944, U92927, U92931, U92917, U92922, X52995, X57184, U92938, U92920, U92921, U92929, U92925, U92916, X57178, AF051542, X57181, U92919, U92926, X57177, X57179, U92947, U92928, U92915, X57183, U92943, U92942, U92939, U92918, U92946, U92496, U97260, U97259, AF042541, U92923, AF051539, AF051538, U92934, AF029088, U92933, U97263, U97261, U97262, U92945, AF042540, U92935, U92936, U92924, AF029086, AF020983, U94958, U97258, U92940, AF029084, U92930, U94959, U92948, AF016863, AF029089, U92937, AF029087, U92932, AF029090, AF029085, AF051540, AF051536, AF052743, AF054269, U92495, U92497, U92498, U92499, U92500, U92501, U92502, U92503, AF051541, X12899, Z48493, Z48489, Z48485, Z48494, Z48487, Z48488, Z48495, Z48490, Z48486, Z48491, Z48492, X66478, X66479, X66477, X66480, X81110, X79056, X78467, X81111, X78802, Z14281/82, Z14273/74, Z14275/76, Z14261/62, Z14265/66, Z14277/78, Z14283/84, Z14271/72, Z14269/70, Z14263/64, Z14259/60, Z14257/58, Z14293/94, Z14291/92, Z14279/80, Z14289/90, Z14287/88, Z14267/68, Z14285/86, L02929, X77423, X77424, X77433, X77426, X77428, X77430, X77427, X77429, X77425, X77432, X77431, X77422, Z48024/25, Z48032/33, Z48020/21, Z48022/23, Z48028/29, Z48016/17, Z48012/13, Z48014/15, Z48018/19, Z48026/27, U31060, U31061, U31062, U31063, U31064, U31065, U31066, U31067, U93898, U93899, U93900, U93901, U93902, U93903, U93904, U93905, U93906, U93907, and U93908.
NspA
NspA is another Neisseria meningitidis surface antigen. “NspA polypeptide” as used herein encompasses naturally-occurring and synthetic (non-naturally occurring) polypeptides which share at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or greater sequence identity at the nucleotide or amino acid level with a naturally-occurring NspA polypeptide, and which are capable of eliciting antibodies that specifically bind a naturally-occurring NspA polypeptide present on a Neisseria meningitidis bacterium. “NspA polypeptide” also encompasses fusion proteins, e.g., a NspA polypeptide having a heterologous polypeptide at the N- and/or C-terminus.
Nucleic acids encoding NspA polypeptides for use in the present disclosure are known in the art. Suitable NspA polypeptides are described in, for example, Martin et al., J Exp Med, Apr. 7, 1997, 185(7).
Nucleic acid (and amino acid sequences) for NspA variants and subvariants are also provided in GenBank as accession nos.: U52069, GQ293900.1, AF175678.1, AF175683.1, AF175682.1, AF175681.1, AF175680.1, AF175679.1, AF175677.1, AF175676.1.
TbpB
TbpB is a Neisseria surface antigen. “TbpB polypeptide” as used herein encompasses naturally-occurring and synthetic (non-naturally occurring) polypeptides that share at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or greater sequence identity at the nucleotide or amino acid level with a naturally-occurring TbpB polypeptide, and which are capable of eliciting antibodies that specifically bind a naturally-occurring TbpB polypeptide present on a Neisseria meningitidis bacterium. “TbpB polypeptide” also encompasses fusion proteins, e.g., a TbpB polypeptide having a heterologous polypeptide at the N- and/or C-terminus.
Nucleic acids encoding TbpB polypeptides for use in the present disclosure are known in the art. Suitable TbpB polypeptides are described in, for example, Rokbi, B. et al., “Heterogeneity of tbpB, the transferrinbinding protein B gene, among serogroup B Neisseria meningitidis strains of the ET-5 complex,” Clinical and Diagnostic Laboratory Immunology 4(5): 522-529 (1997).
Nucleic acid (and amino acid sequences) for TbpB variants and subvariants are also provided in GenBank as accession nos.: DQ355978.1, AJ704760.1, AJ704759.1, AJ704758.1, AJ704757.1, AJ704756.1, AJ704755.1, AJ704754.1, AJ704753.1, AJ704752.1, AJ704751.1.
TbpA
TbpA is a Neisseria surface antigen. “TbpA polypeptide” as used herein encompasses naturally-occurring and synthetic (non-naturally occurring) polypeptides which share at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or greater sequence identity at the nucleotide or amino acid level with a naturally-occurring TbpA polypeptide, and which are capable of eliciting antibodies that specifically bind a naturally-occurring TbpA polypeptide present on a Neisseria bacterium. “TbpA polypeptide” also encompasses fusion proteins, e.g., a TbpA polypeptide having a heterologous polypeptide at the N- and/or C-terminus.
Nucleic acids encoding TbpA polypeptides for use in the present disclosure are known in the art. Suitable TbpA polypeptides are described in, for example, J. Med. Microbiol. 1998 September; 47(9): 757-60.
Nucleic acid (and amino acid sequences) for TbpA variants and subvariants are also provided in GenBank as: Accession: EU339282.1 GI: 166863281, Accession: M96731.1 GI: 150360, Accession: AF240638.1 GI: 9719359, Accession: AF241227.1 GI: 9719361, Accession: AF124338.1 GI: 8439550, Accession: X94533.1 GI: 2764816, Accession: X99615.1 GI: 2764959, Accession: X99614.1 GI: 2764957, Accession: X99613.1 GI: 2764956, Accession: X99612.1 GI: 2764955, Accession: X99611.1 GI: 2764954, Accession: X99610.1 GI: 2764952.
LbpA
LbpA is a Neisseria surface antigen. “LbpA polypeptide” as used herein encompasses naturally-occurring and synthetic (non-naturally occurring) polypeptides which share at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or greater sequence identity at the nucleotide or amino acid level with a naturally-occurring LbpA polypeptide, and which are capable of eliciting antibodies that specifically bind a naturally-occurring LbpA polypeptide present on a Neisseria bacterium. “LbpA polypeptide” also encompasses fusion proteins, e.g., a LbpA polypeptide having a heterologous polypeptide at the N- and/or C-terminus.
Nucleic acids encoding LbpA polypeptides for use in the present disclosure are known in the art. Suitable LbpA polypeptides are described in, for example, Vaccine (2006) Vol. 24 Issue 17, pp. 3545-57.
Nucleic acid (and amino acid sequences) for LbpA variants and subvariants are also provided in GenBank as: Accession: DQ058017.1 GI: 68359439, Accession: U16260.1 GI: 915277, Accession: AF049349.1 GI: 3582727, Accession: DQ058018.1 GI: 68359441, Accession: X79838.1 GI: 509053.
LbpB
LbpB is a Neisseria surface antigen. “LbpB polypeptide” as used herein encompasses naturally-occurring and synthetic (non-naturally occurring) polypeptides which share at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or greater sequence identity at the nucleotide or amino acid level with a naturally-occurring LbpB polypeptide, and which are capable of eliciting antibodies that specifically bind a naturally-occurring LbpB polypeptide present on a Neisseria bacterium. “LbpB polypeptide” also encompasses fusion proteins, e.g., a LbpB polypeptide having a heterologous polypeptide at the N- and/or C-terminus.
Nucleic acids encoding LbpB polypeptides for use in the present disclosure are known in the art. Suitable LbpB polypeptides are described in, for example, Vaccine (2006) Vol. 24 Issue 17, pp. 3545-57.
Nucleic acid (and amino acid sequences) for LbpB variants and subvariants are also provided in GenBank as: Accession: AF123382.1 GI: 4884690, Accession: AF072890.1 GI: 4106392, Accession: AF031432.1 GI: 3213214, Accession: AF022781.1 GI: 2843172, Accession: AF123380.1 GI: 4884686, Accession: AF123383.1 GI: 4884692, Accession: AF123381.1 GI: 4884688.
GNA2132
GNA2132 is a Neisseria surface antigen. “GNA2132 polypeptide” as used herein encompasses naturally-occurring and synthetic (non-naturally occurring) polypeptides which share at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or greater sequence identity at the nucleotide or amino acid level with a naturally-occurring GNA2132 polypeptide, and which are capable of eliciting antibodies that specifically bind a naturally-occurring GNA2132 polypeptide present on a Neisseria bacterium. “GNA2132 polypeptide” also encompasses fusion proteins, e.g., a GNA2132 polypeptide having a heterologous polypeptide at the N- and/or C-terminus.
Nucleic acids encoding GNA2132 polypeptides for use in the present disclosure are known in the art. Suitable GNA2132 polypeptides are described in, for example, Proc Natl Acad Sci U.S.A. 2010 Feb. 23; 107(8): 3770-5.
Nucleic acid (and amino acid sequences) for GNA2132 variants and subvariants are also provided in GenBank as: Accession: FJ750981.1 GI: 224830211, Accession: AY315195.1 GI: 32455020, Accession: AY315194.1 GI: 32455018, Accession: AY315193.1 GI: 32455016, Accession: AY315192.1 GI: 32455014, Accession: GQ302857.1 GI: 254547346, Accession: AY315196.1 GI: 32455022, Accession: AF226448.1 GI: 7228725, Accession: AF226447.1 GI: 7228723, Accession: AF226446.1 GI: 7228721, Accession: AF226445.1 GI: 7228719, Accession: FN908855.1 GI: 308814886, Accession: FN908854.1 GI: 308814884, Accession: FJ615459.1 GI: 222107907, Accession: FJ615446.1 GI: 222107881.
NadA
NadA is a Neisseria surface antigen. “NadA polypeptide” as used herein encompasses naturally-occurring and synthetic (non-naturally occurring) polypeptides which share at least about 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or greater sequence identity at the nucleotide or amino acid level with a naturally-occurring NadA polypeptide, and which are capable of eliciting antibodies that specifically bind a naturally-occurring NadA polypeptide present on a Neisseria bacterium. “NadA polypeptide” also encompasses fusion proteins, e.g., a NadA polypeptide having a heterologous polypeptide at the N- and/or C-terminus.
Nucleic acids encoding NadA polypeptides for use in the present disclosure are known in the art. Suitable NadA polypeptides are described in, for example, Infection and Immunity, July 2004, Vol. 72, No. 7, pp. 4217-23.
Nucleic acid (and amino acid sequences) for NadA variants and subvariants are also provided in GenBank as: Accession: FJ750979.1 GI: 224830207, Accession: DQ239933.1 GI: 83616362, Accession: DQ239932.1 GI: 83616360, Accession: DQ239931.1 GI: 83616359, Accession: DQ239930.1 GI: 83616357, Accession: DQ239929.1 GI: 83616355, Accession: DQ239928.1 GI: 83616354, Accession: DQ239927.1 GI: 83616353, Accession: DQ239926.1 GI: 83616351, Accession: FJ619647.1 GI: 222159590.
Further Examples of Gene Products of Interest
Other examples of gene products that find use with the sequences and methods of the present disclosure include the following:
Opacity outer membrane protein (see, e.g., Hobbs et al., Microbiology 144:157-66 (1998)), Genbank Accession Numbers: U03412.1, U37255.1, U37256.1, U37257.1, AF016292.1, AF016285.1, AF001204.1, AF001203.1;
FetA (see, e.g., Biegel et al, J. Bacteriology 181(9):2895-901 (1999)), Genbank Accession Numbers: JN182195.1 GI: 343174597, EF157665.1 GI: 120971583, EF153764.1 GI: 120971579, EF153762.1 GI: 120971576;
MafB, MspA, App, Opa, Opc, NhhA, MafA-1, MafA2, NalP, Mip, NMB1483, HmbR (see, e.g., Echenique-Rivera et al., PLoS Pathog 7(5): 1-18 (2011));
The foregoing gene products are in no way intended to limit the scope of the present disclosure, and merely serve as examples of antigens that may be expressed using the polynucleotide sequences and methods disclosed herein.
Polynucleotide sequences encoding gene products of interest encompass naturally-occurring sequences as well as codon-optimized sequences. Naturally-occurring sequences may be codon-optimized in order to further facilitate increased expression levels based on known codon preferences of the host organism selected for expression. For example, a known polynucleotide sequence encoding a surface antigen (e.g., fHbp) may be altered to replace those codons that are not preferred by the host organism with redundant codons that encode the same amino acid residue, but which are preferred by the host organism and therefore facilitate more efficient expression of the coding sequence in the host organism.
A variety of computer algorithms that facilitate codon optimization are publicly available via the internet. See, e.g., Puigb P., Guzman E., Romeu A., and Garcia-Vallv S., OPTIMIZER: A web server for optimizing the codon usage of DNA sequences. Nucleic Acids Research, 35:W126-W131 (2007). Such algorithms generally allow a user to input a known polynucleotide sequence encoding a gene product. Once the sequence has been provided, the user may specify any desired codon-usage preferences (e.g., the most frequently-used codons for each amino acid residue in the chosen expression host) and the computer algorithm will then provide the user with a codon-optimized sequence. For example,
Polynucleotide sequences of the present disclosure may be generated by any means known in the art, including but not limited to mutagenesis techniques, including chemical mutagenesis, polymerase chain reaction (PCR), site-directed mutagenesis of one or more nucleotides, and the like. Polynucleotide sequences may also be chemically synthesized using reagents and techniques known in the art. Expression constructs according to the present disclosure may be generated by using techniques known in the art, including but not limited to PCR, cloning, and the like. Practicing the present invention may involve the use of conventional molecular biology, microbiology, recombinant DNA, and immunology techniques that are well known in the art. Such techniques are fully explained in the literature, e.g. Sambrook Molecular Cloning; A Laboratory Manual, Second Edition (1989); DNA Cloning, Volumes I and II (D. N. Glover ed. 1985); Oligonucleotide Synthesis (M. J. Gait ed, 1984); Nucleic Acid Hybridization (B. D. Hames & S. J. Higgins eds. 1984); Transcription and Translation (B. D. Hames & S. J. Higgins eds. 1984); Immobilized Cells and Enzymes (IRL Press, 1986); B. Perbal, A Practical Guide to Molecular Cloning (1984); the Methods in Enzymology series (Academic Press, Inc.); Mayer and Walker, eds. (1987), Immunochemical Methods in Cell and Molecular Biology (Academic Press, London).
In general, the polynucleotide sequences of the present disclosure may be cloned into a suitable vector or expression construct for use in the methods of the present disclosure. In some embodiments, an engineered promoter sequence is operably linked to a polynucleotide sequence encoding a surface antigen, which is operably linked to a transcription terminator sequence. The resulting sequence (comprising a promoter sequence, a surface antigen-encoding sequence, and a transcription terminator sequence) may then be isolated, e.g., by PCR or with restriction enzymes, and cloned into a suitable vector or construct. In some embodiments, constructs may contain polynucleotide sequences that can be used to introduce a target sequence into the genome of a host, e.g., by homologous recombination.
In general, the present disclosure provides methods for expressing one or more gene products of interest, e.g., one or more proteins of interest, e.g., one or more surface antigens of interest, in recombinant host organsims at high levels. The methods involve combining the polynucleotide sequences of the present disclosure in ways that facilitate high-level expression of a gene product (e.g., a protein) of interest in a selected recombinant host organism, e.g., a Neisseria meningitidis bacterium. The methods of the present disclosure find use in, e.g., production of vaccines, where consistent, high-level expression of surface antigens is desirable.
As described above, some of the polynucleotide sequences of the present disclosure function as promoters in host organisms. Unlike some naturally-occurring promoter sequences, the present promoters do not cause variable expression, but instead provide consistent, high-level expression of one or more gene product-encoding polynucleotide sequences to which they are operable linked. Other polynucleotide sequences of the present disclosure function as transcription terminators that facilitate efficient transcription, and therefore enhanced expression of gene product-encoding sequences to which they are operably linked. Various combinations of the polynucleotide sequences of the present disclosure may be used to facilitate high-level expression ofone or more gene products of interest (e.g., surface antigens) in recombinant hosts. In addition, the present disclosure provides for codon-optimization of polynucleotide sequences encoding a protein product to be expressed, e.g., a surface antigen, based on the codon preferences of the recombinant organism chosen for expression. The methods of the present disclosure involve combining these polynucleotide sequences in various ways to facilitate consistent, high-level expression of one or more gene product of interest in a selected recombinant host organism.
Introduction of Promoters Upstream of Endogenous Host Sequences
In some embodiments, the methods of the present disclosure involve inserting a polynucleotide promoter sequence of the present disclosure into the genome of a suitable host organism, e.g., a Neisseria host cell, upstream (e.g., in the 5′ direction) of a native gene, e.g., a native surface antigen gene. The recombinant host cells are then cultured under conditions that facilitate expression of the native gene. In embodiments where N. meningitidis are chosen as the host organsims, vesicles produced by the host cells can then be isolated and used to prepare vaccine compositions that can be administered to a subject in order to induce an immunological response in the subject.
For example, in some embodiments, a chimeric promoter (e.g., X1-X7) or a domain deletion promoter (e.g., S1-S3) is inserted into the genome of a Neisserial strain upstream of a native fHbp gene. Introduction of the engineered promoter sequence facilitates high levels of expression of the fHbp gene.
Introduction of Expression Constructs
In some embodiments, the methods of the present disclosure involve inserting an expression construct comprising an engineered promoter operably linked to one or more polynucleotide sequences that encode a gene product of interest, e.g., a protein of interest into the genome of a host organism. In some embodiments, a transcription terminator sequence is operably linked to the 3′ end of the polynucleotide sequence encoding a gene product of interest. For example, in some embodiments, an expression construct comprising a chimeric promoter (e.g., X1-X7) or a domain deletion promoter (e.g., S 1-S3) operably linked to a polynucleotide sequence encoding fHbp and operably linked to a transcription terminator having the sequence described above is inserted into a suitable region of the genome of the Neisserial host cell (e.g., the lpxL1 locus).
In some embodiments, an expression construct may be inserted into the genome of the host in a location that disrupts expression of one or more host genes. For example, in some embodiments, an expression construct may be inserted into the genome of a host in a location that disrupts expression of a gene that facilitates production of endotoxin (lipopolysaccharide, LPS). The resulting recombinant host is an endotoxin knockout host, which may be useful in the production of vaccines with reduced endotoxin.
In some embodiments, a first engineered promoter sequence is inserted into the genome of a host cell upstream of a native gene, e.g., a native surface antigen gene, and an expression construct comprising a second engineered promoter sequence operably linked to a polynucleotide sequence encoding a gene product of interest is inserted into the genome of the host cell in a suitable location within the genome of the host cell (e.g., the lpxL1 locus).
In some embodiments, the first and second promoter sequences are the same, while in other embodiments, the first and second promoter sequences are different. For example, in some embodiments, chimeric promoter X1 is inserted into the genome of a Neisserial cell upstream of a native fHbp gene and an expression construct comprising chimeric promoter X1 operably linked to a polynucleotide sequence encoding fHbp is inserted into the lpxL1 locus of the host Neisserial cell. In other embodiments, chimeric promoter X1 is inserted into the genome of a Neisserial strain upstream of a native fHbp gene and an expression construct comprising domain deletion promoter S1 operably linked to a polynucleotide sequence encoding fHbp is inserted into the lpxL1 locus of the host Neisserial cell.
Introduction of an engineered promoter upstream of a native gene, e.g., a native surface antigen gene, results in increased expression of the gene, while introduction of a second copy of the gene driven by an engineered promoter at another location within the host genome can facilitate increased expression even further. In some embodiments, additional expression constructs comprising one or more polynucleotide sequences that encode one or more gene products of interest (e.g., one or more proteins of interest) may be inserted into the host cell genome as well. In some embodiments, introduction of a third, fourth, or fifth copy of a gene product of interest (e.g., a surface antigen of interest) driven by an engineered promoter increases expression of the gene product of interest even further.
In some embodiments, several different gene products of interest may be expressed in the same host cell. For example, in some embodiments, an engineered promoter is inserted upstream of a first native surface antigen gene (e.g., fHbp), and one or more expression constructs comprising different surface antigen genes (e.g., NspA) driven by the same or different engineered promoter sequences are also inserted into the genome of the host cell. The resuling host cell expresses two or more different surface antigens, and may be useful in the production of vaccines.
Vectors and Methods for Introducing Genetic Material into Neisserial Host Cells
Methods and compositions that can be readily adapted to provide for genetic modification of a host cell with a nucleic acid construct of the present disclosure are known in the art. Exemplary vectors and methods are provided in, e.g., WO 02/09746 and O'Dwyer et al. Infect Immun 2004; 72:6511-80.
Methods for transfer of genetic material into a host cell include, for example, conjugation, transformation, electroporation, calcium phosphate methods and the like. In general, the method for transfer should provide for stable expression of the introduced construct. The construct can be provided as an inheritable episomal element (e.g., plasmid) or can be genomically integrated.
Suitable vectors will vary in composition depending on what type of recombination event is to be performed. Integrative vectors can be conditionally replicative or can be suicide plasmids, bacteriophages, transposons or linear DNA fragments obtained by restriction hydrolysis or PCR amplification. Selection of the recombination event can be accomplished by use of selectable genetic markers such as genes conferring resistance to antibiotics (for instance kanamycin, erythromycin, chloramphenicol, or gentamycin), genes conferring resistance to heavy metals and/or toxic compounds, or genes complementing auxotrophic mutations (for instance pur, leu, met, aro).
Antigenic compositions contemplated by the present disclosure generally include vesicles prepared from Neisserial cells that express a surface antigen. As referred to herein, “vesicles” is meant to encompass outer membrane vesicles as well as microvesicles (which are also referred to as blebs).
Antigenic compositions for use in the production of vaccines can contain outer membrane vesicles (OMV) prepared from the outer membrane of a cultured strain of Neisseria meningitidis spp. genetically modified to express a surface antigen, e.g. fHbp. OMVs may be obtained from Neisseria meningitidis grown in broth or solid medium culture, preferably by separating the bacterial cells from the culture medium (e.g. by filtration or by a low-speed centrifugation that pellets the cells, or the like), lysing the cells (e.g. by addition of detergent, osmotic shock, sonication, cavitation, homogenization, or the like) and separating an outer membrane fraction from cytoplasmic molecules (e.g. by filtration; or by differential precipitation or aggregation of outer membranes and/or outer membrane vesicles, or by affinity separation methods using ligands that specifically recognize outer membrane molecules; or by a high-speed centrifugation that pellets outer membranes and/or outer membrane vesicles, or the like); outer membrane fractions may be used to produce OMVs.
Antigenic compositions can contain microvesicles (MV) (or “blebs”) containing surface antigens, where the MV or blebs are released during culture of a Neisseria meningitidis strain genetically modified to express a surface antigen. For example, MVs may be obtained by culturing a strain of Neisseria meningitidis in broth culture medium, separating whole cells from the broth culture medium (e.g. by filtration, or by a low-speed centrifugation that pellets only the cells and not the smaller blebs, or the like), and then collecting the MVs that are present in the cell-free culture medium (e.g. by filtration, differential precipitation or aggregation of MVs, or by a high-speed centrifugation that pellets the blebs, or the like). Strains for use in production of MVs can generally be selected on the basis of the amount of blebs produced in culture (e.g., bacteria can be cultured in a reasonable number to provide for production of blebs suitable for isolation and administration in the methods described herein). An exemplary strain that produces high levels of blebs is described in PCT Publication No. WO 01/34642. In addition to bleb production, strains for use in MV production may also be selected on the basis of production of other surface antigens, where strains that produce higher levels of specific surface antigens may be of particular interest (for examples of N. meningitidis strains having different NspA production levels, see, e.g., Moe et al. (1999 Infect. Immun. 67: 5664)). Other strains of interest for use in production of blebs include strains having an inactivated GNA33 gene, which encodes a lipoprotein required for cell separation, membrane architecture and virulence (see, e.g., Adu-Bobie et al. (2004) Infect Immun. 72:1914-1919).
The antigenic compositions of the present disclosure can contain vesicles from one strain, or from 2, 3, 4, 5 or more strains, which strains may be homologous or heterologous, usually heterologous, to one another. For example, the strains may be homologous or heterologous with respect to a particular surface antigen, such as porA and/or fHbp. The vesicles can be prepared from strains that express more than one variant or subvariant of a specific surface antigen (e.g., 1, 2, 3, or more variants of fHbp) which may be composed of fHbp amino acid sequences from different variants (v.1, v.2, or v.3) or subvariants (e.g., a subvariant of v.1, v.2, or v.3).
The antigenic compositions can comprise a mixture of OMVs and MVs presenting the same or different surface antigens, where the surface antigens may optionally present epitopes from different combinations of variants and/or subvariants and where the OMVs and/or MVs may be from the same or different strains. Vesicles from different strains can be administered as a mixture, or can be administered serially.
Where desired (e.g., where the strains used to produce vesicles are associated with endotoxin or particularly high levels of endotoxin), the vesicles can optionally be treated to reduce endotoxin, e.g., to reduce toxicity following administration. Although potentially less desirable, reduction of endotoxin can be accomplished by extraction with a suitable detergent (for example, BRIJ-96, sodium deoxycholate, sodium lauroylsarcosinate, Empigen BB, Triton X-100, TWEEN 20 (sorbitan monolaurate polyoxyethylene), TWEEN 80, at a concentration of 0.1-10%, preferably 0.5-2%, and SDS). Where detergent extraction is used, it is preferable to use a detergent other than deoxycholate.
The vesicles of the antigenic compositions can be prepared without detergent, e.g., without use of deoxycholate. Although detergent treatment is useful to remove endotoxin activity, it may negatively impact the surface antigen proteins in preparation. Thus it may be particularly desirable to decrease endotoxin activity using technology that does not require a detergent. In one approach, strains that are relatively low producers of endotoxin (lipopolysaccharide, LPS) are used so as to avoid the need to remove endotoxin from the final preparation prior to use in humans. For example, the vesicles can be prepared from Neisseria mutants in which lipooligosaccharide or other antigens that may be undesirable in a vaccine (e.g. Rmp) is reduced or eliminated.
Vesicles can be prepared from N. meningitidis strains that contain genetic modifications that result in decreased or no detectable toxic activity of lipid A. For example, such strain can be genetically modified in lipid A biosynthesis (Steeghs et al. (1999) Infect Immun 67:4988-93; van der Ley et al. (2001) Infect Immun 69:5981-90; Steeghs et al. (2004) J Endotoxin Res 10:113-9; Fissha et al, (2005) Infect Immun 73:4070). The immunogenic compositions may be detoxified by modification of LPS, such as downregulation and/or inactivation of the enzymes encoded by lpxL1 or lpxL2, respectively. Production of a penta-acylated lipid A made in lpxL1 mutants indicates that the enzyme encoded by lpxL1 adds the C12 to the N-linked 3-OH C14 at the 2′ position of GlcN II. The major lipid A species found in lpxL2 mutants is tetra-acylated, indicating the enzyme encoded by lpxL2 adds the other C12, i.e., to the N-linked 3-OH C14 at the 2 position of GlcN I. Mutations resulting in a decreased (or no) expression of these genes (or decreased or no activity of the products of these genes) result in altered toxic activity of lipid A (van der Ley et al. (2001) Infect Immun 69:5981-90). Tetra-acylated (lpxL2 mutant) and penta acylated (lpxL1 mutant) lipid A are less toxic than the wild-type lipid A. Mutations in the lipid A 4′-kinase encoding gene (lpxK) also decrease the toxic activity of lipid A. Of particular interest for use in production of vesicles (e.g., MV or OMV) are N. meningitidis strains genetically modified so as to provide for decreased or no detectable functional lpxL1-encoded protein, e.g., where the Neisseria bacterium (e.g., N. meningitidis strain) is genetically modified to provide for decreased or no activity of a gene product of the lpxL1 gene. For example, the Neisseria bacterium can be genetically modified to have an lpxL1 gene knockout, e.g., where the lpxL1 gene is disrupted. See, e.g., US Patent Publication No. 2009/0035328. The Neisseria bacterium can be genetically modified to provide for decreased or no activity of a gene product of the lpxL1 gene and/or the lpxL2 gene. Such vesicles provide for reduced toxicity as compared to N. meningitidis strains that are wild-type for LPS production, while retaining immunogenicity of a surface antigen, e.g., fHbp.
LPS toxic activity can also be altered by introducing mutations in genes/loci involved in polymyxin B resistance (such resistance has been correlated with addition of aminoarabinose on the 4′ phosphate of lipid A). These genes/loci could be pmrE that encodes a UDP-glucose dehydrogenase, or a region of antimicrobial peptide-resistance genes common to many enterobacteriaciae which could be involved in aminoarabinose synthesis and transfer. The gene pmrF that is present in this region encodes a dolicol-phosphate manosyl transferase (Gunn J. S., Kheng, B. L., Krueger J., Kim K., Guo L., Hackett M., Miller S. I. 1998. Mol. Microbiol. 27: 1171-1182).
Mutations in the PhoP-PhoQ regulatory system, which is a phospho-relay two component regulatory system (e.g., PhoP constitutive phenotype, PhoPc), or low Mg++ environmental or culture conditions (that activate the PhoP-PhoQ regulatory system) lead to the addition of aminoarabinose on the 4′-phosphate and 2-hydroxymyristate replacing myristate (hydroxylation of myristate). This modified lipid A displays reduced ability to stimulate E-selectin expression by human endothelial cells and TNF secretion from human monocytes.
Polymyxin B resistant strains are also suitable for use, as such strains have been shown to have reduced LPS toxicity (see, e.g., van der Ley et al. (1994) In: Proceedings of the ninth international pathogenic Neisseria conference. The Guildhall, Winchester, England). Alternatively, synthetic peptides that mimic the binding activity of polymyxin B may be added to the antigenic compositions to reduce LPS toxic activity (see, e.g., Rustici et al. (1993) Science 259:361-365; Porro et al. (1998) Prog Clin Biol Res. 397:315-25).
Endotoxin can also be reduced through selection of culture conditions. For example, culturing the strain in a growth medium containing 0.1 mg-100 mg of aminoarabinose per liter medium provides for reduced lipid toxicity (see, e.g., WO 02/097646).
Also provided by the present disclosure are kits for using the polynucleotide sequences disclosed herein to practice the methods described above. Kits may contain one or more polynucleotide sequences of the present disclosure in the form of vectors or expression constructs to be used in the production of additional expression constructs and/or recombinant Neisseria meningitidis strains. Kits may also contain one or more polynucleotide sequences encoding an antigen to be expressed in a Neisseria meningitidis host strain in the form of a vector or an expression construct. Kits may further include one or more recombinant Neisseria meningitidis strains that comprise one or more of the engineered promoter sequences disclosed herein and/or a polynucleotide sequence encoding an antigen and/or a transcription terminator sequence.
In addition to the above-mentioned components, the kits can further include instructions for using the components of the kit to practice the subject methods. The instructions for practicing the subject methods are generally recorded on a suitable recording medium. For example, the instructions may be printed on a substrate, such as paper or plastic, etc. As such, the instructions may be present in the kits as a package insert, in the labeling of the container of the kit or components thereof (i.e., associated with the packaging or subpackaging), etc. In other embodiments, the instructions are present as an electronic storage data file present on a suitable computer readable storage medium, e.g. CD-ROM, diskette, etc. In yet other embodiments, the actual instructions are not present in the kit, but means for obtaining the instructions from a remote source, e.g. via the internet, are provided. An example of this embodiment is a kit that includes a web address where the instructions can be viewed and/or from which the instructions can be downloaded. As with the instructions, this means for obtaining the instructions is recorded on a suitable substrate.
The following examples are put forth so as to provide those of ordinary skill in the art with a complete disclosure and description of how to make and use the present invention, and are not intended to limit the scope of what the inventors regard as their invention nor are they intended to represent that the experiments below are all or the only experiments performed. Efforts have been made to ensure accuracy with respect to numbers used (e.g. amounts, temperature, etc.) but some experimental errors and deviations should be accounted for. Unless indicated otherwise, parts are parts by weight, molecular weight is weight average molecular weight, temperature is in degrees Celsius, and pressure is at or near atmospheric. Standard abbreviations may be used, e.g., bp, base pair(s); kb, kilobase(s); pl, picoliter(s); s or sec, second(s); min, minute(s); h or hr, hour(s); aa, amino acid(s); nt, nucleotide(s); and the like.
The following methods and materials were used in the Examples below.
Bacterial Strains
The six N. meningitidis strains used in the examples that follow are listed in Table 1.
N. meningitidis strains used in the following examples.
Measurement of fHbp Expression by Western Blot
fHbp expression was measured by a quantitative Western blot, which was performed as previously reported (Pajon, Vaccine 2010 Feb. 25; 28(9):2122-9) with minor changes. For fHbp sequences in variant group 1, anti-fHbp mAb JAR 3 was used for detection of fHbp sequence variants ID 1, 4 or 9, and JAR 5 was used for ID 74. For fHbp in variant groups 2 or 3, anti-fHbp mAb JAR 31 was used (Beernink, Infect Immun. 2008 September; 76(9):4232-40). The results for the test strains were reported as percentages of the amount of fHbp expressed by bacterial cells from the corresponding reference strains H44/76 or 8047 with high expression of fHbp variant 1 (ID 1) and 2 (ID 77), respectively.
Flow Cytometry
Binding of mouse anti-fHbp mAbs to live meningococci was measured to assess the relative amounts of fHbp on the bacterial surface accessible to antibody in mutants engineered to have increased or decreased fHbp relative to a control. Flow cytometry was performed as described previously using a combination of two mouse anti-fHbp mAbs, JAR4 and JAR5 (Welsch, J Infect Dis. 2008 Apr. 1; 197(7):1053-61), each at a final concentration of 10 μg/mL. Controls in the assay included a mouse mAb, specific for group A (JW-A1) or B (SEAM 12) polysaccharides (Moe, Mol. Immunol. 2006 March; 43(9):1424-31).
Neisseria meningitidis strain CH21A, which is a serogroup A strain expressing fHbp ID 5, was used to test the ability of the engineered promoters of the present disclosure to drive expression. Chimeric promoters and domain deletion promoters were operatively inserted into the genome of the CH21A host strain upstream of the fHbp gene, and subsequent expression of fHbp was measured by quantitative Western blot. The results are shown in
Chimeric promoter X1 was operably inserted upstream of the fHbp gene in Neisseria meningitidis strain CH21A. In addition, an expression construct comprising the chimeric promoter X1 or domain deletion promoter S1 operably linked to a copy of the fHbp gene was inserted into the lpxL1 locus of the host strain to provide a second copy of the fHbp gene. Subsequent expression of fHbp was measured by a quantitative Western blot. The results are shown in
Neisseria meningitidis strain CH38W, a serogroup W-135 strain expressing fHbp ID 9, was used to test the ability of the chimeric promoters of the present disclosure to drive expression. Chimeric promoters X1-X4 were operatively inserted into the genome of the CH38W host strain upstream of the fHbp gene, and subsequent expression of fHbp was measured by quantitative Western blot. The results are shown in
Chimeric promoter X1 was operably inserted upstream of the fHbp gene in Neisseria meningitidis strain CH38W. In addition, an expression construct comprising the chimeric promoter X1 or domain deletion promoter S1 operably linked to a copy of the fHbp gene was inserted into the lpxL1 locus of the host strain to provide a second copy of the fHbp gene. Subsequent expression of fHbp was measured by quantitative Western blot. The results are shown in
X1-X1, a mutant containing X1-fHbp in the fHbp native locus and a second copy of the X1-fHbp genetic cassette inserted into the lpxL1 locus. Values are mean percentages (+/− ranges in replicate experiments) compared with expression of fHbp by the reference group B strain H44/76, which is a relatively high expresser of fHbp ID 1 (variant group 1).
Neisseria meningitidis strain CH248B, a capsular group B strain, was used to test the ability of the chimeric promoters of the present disclosure to drive expression. This strain also is referred to as H44/76. Chimeric promoter X1 was operatively inserted into the genome of the CH248B host strain upstream of the fHbp gene, and subsequent expression of fHbp was measured by quantitative Western blot. The results are shown in
Neisseria meningitidis strain CH253B, a capsular group B strain expressing fHbp ID 14, was used to test the ability of chimeric promoter X1 to drive expression. Chimeric promoter X1 was operatively inserted into the genome of the CH253B host strain (also known as NZ98/254) upstream of the fHbp gene, and subsequent expression of fHbp was measured by quantitative Western blot. The results are shown in
Neisseria meningitidis strain CH164X, a capsular group X strain expressing fHbp ID 74, was used to test the ability of chimeric promoter X1 to drive expression. Chimeric promoter X1 was operatively inserted into the genome of the CH164X host strain upstream of the fHbp gene, and subsequent expression of fHbp was measured by quantitative Western blot. The results are shown in
Neisseria meningitidis strain CH36W, a capsular group W135 strain expressing fHbp ID 23 (variant 2), was used to test the ability of chimeric promoter X1 to drive expression. Chimeric promoter X1 was operatively inserted into the genome of the CH36W host strain upstream of the fHbp ID 23 gene, and subsequent expression of fHbp was measured by quantitative Western blot. The results are shown in
Neisseria meningitidis strain CH21A, a capsular group A strain, was used to evaluate the influence of a transcription terminator sequence on the expression level of fHbp ID 5. An X1 promoter sequence was inserted into the genome of the CH21A strain upstream of a sequence encoding fHbp ID 5. In a first recombinant host, the native transcription terminator having the sequence TAACCATTGTGAAAATGCCGTCCGAACACGATAATTTACCGTTCGGACGG CATTTTGTA was operably linked to the 3′ end of the fHbp ID 5 coding sequence. In a second recombinant host, the native transcription terminator sequence was deleted. Both recombinant hosts were then cultured under the same conditions, and the expression level of fHbp ID 5 was compared between the two hosts. Results are shown in
Codon usage frequency was determined in FAM18 and Z2491, two different Neisseria meningitidis strains. Codon usage mean and standard deviation results for the two strains are shown in
Codon optimization was also performed for polynucleotide sequences encoding fHbp ID 23, ID 4, ID 28, ID 1, ID 14, ID 45, ID 55, ID 19, ID 77, NspA (nmb0663), NspA (nmc0612, nma0862), NHbp (nmb2132), TbpB (Tbp2, nmb0461), TbpA (tbp1, nmb0461), LbpB (nmb1541), LbpA (nmb1540), Opacity protein (Class 5, nmb1053), NadA (nmb1994), PorA (nmb1429), and feta (nmb1988). The codon-optimized sequences are shown in
Engineered promoter sequences were used to drive expression of multiple polynucleotides encoding surface antigens that were organized in an operon-like fashion. FIG. 39, Panel A. This allowed for over-expression of multiple surface antigens under the control of a single copy of the engineered promoter. The system can be used to express a plurality of polynucleotides at the same time due to the high output of the engineered promoters. Examples of tested surface antigen-encoding polynucleotide sequence configurations are provided in
To further illustrate this approach, engineered promoter X1 was operably inserted upstream of an fHbp-encoding polynucleotide sequence in Neisseria meningitidis strain CH38W, a capsular W-135 strain expressing fHbp ID 9 and NspA, both at low levels. The NspA-encoding polynucleotide sequence was operably inserted just downstream of the fHbp-encoding sequence. The transcription terminator sequence from fHbp was operably linked to the 3′ end of the NspA-encoding polynucleotide sequence. Subsequent expression of both fHbp and NspA was measured by quantitative Western blot using monoclonal antibodies specific to each of the antigens.
This application claims priority benefit of U.S. Provisional Patent Application Ser. No. 61/529,776, filed Aug. 31, 2011, which application is incorporated herein by reference in its entirety.
This invention was made with government support under Grant No. AI 046464, and AI 082263, awarded by the National Institutes of Health. The government has certain rights in the invention.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/US2012/053142 | 8/30/2012 | WO | 00 | 4/4/2014 |
| Number | Date | Country | |
|---|---|---|---|
| 61529776 | Aug 2011 | US |
