Patent Application
20170080080
The sequence listing that is contained in the file named “UTFB1044WO_ST25.txt”, which is 10_KB (as measured in Microsoft Windows®) and was created on May 11, 2015, is filed herewith by electronic submission and is incorporated by reference herein.
1. Field of the Invention
The present invention relates generally to the field of microbiology. More particularly, it concerns bacterial cell engineering.
2. Description of Related Art
In 1892, Richard Pfeiffer introduced the revolutionary concept of bacterial endotoxin in his description of a non-proteinaceous, non-secreted toxin bound to the surface of Vibrio cholerae (Pfeiffer et al., 1892). This toxin, now known as lipopolysaccharide (LPS), is the major surface molecule of Gram-negative bacteria that triggers the host immune response during infection (Poltorak et al., 2000; Raetz et al., 2002). LPS is composed of lipid A, core oligosaccharide, and O-antigen (Raetz et al., 2007). Lipid A is recognized by the innate immune system through the conserved pattern recognition receptor, Toll-like receptor 4/myeloid differentiation factor 2 (TLR4/MD-2) complex, which initiates a robust signal cascade that leads to production of inflammatory cytokines. This signaling is crucial for detection and clearance of infection, but can be potent enough to result in lethal endotoxic shock (Raetz et al., 2002). Such tremendous immunogenicity makes lipid A an attractive therapeutic tool as an adjuvant, but its toxicity is a major concern.
Efforts have been made to dampen the toxicity of whole bacteria by altering the degree of Lipid A acylation. One approach has been to inactivate lpxM, a gene encoding the acyltransferase responsible for converting lipid A from a penta-acylated to a hexa-acylated species. LpxM mutants are under investigation in the development of meningococcal vaccines, oncolytic Salmonella strains that specifically target tumors, and bacterial strains designed for gene therapy. Other efforts to detoxify cells or outer membrane vesicles have included acyl chain modification by the enzymes PagL or PagP. However, no bacterial strains have been previously generated using a complex combinatorial approach to yield a diverse library of in bacterium linked lipid A moieties and antigens.
Provided herein are engineered E. coli strains that produce a lipid A moiety linked to an antigen and methods for producing these E. coli strains. In some embodiments, an engineered E. coli strain is provided that comprises one or more lipid modification polynucleotides selected from the group consisting of lpxE, lpxF, lpxO, lpxR, pagL, and pagP polynucleotides and one or more antigen associated polynucleotides. The lpxE, lpxF, lpxO, lpxR, pagL, and pagP polynucleotides include those described in the Examples below, those described in U.S. Patent Application Publication No. 20130230555, which is hereby incorporated by reference in its entirety, and their homologs, orthologs, and paralogs. In some embodiments, the engineered E. coli strain comprises lpxE, pagL and pagP polynucleotides. In other embodiments, the engineered E. coli strain comprises lpxE, lpxO, pagL and pagP polynucleotides.
U.S. Patent Application Publication No. 20130230555 describes that combinations of the LpxE, LpxF, LpxO, LpxR, PagL, and PagP endotoxin modification enzymes are used to generate a library of E. coli strains, each presenting unique lipid A moieties on its surface. These engineered bacterial cells and lipid A moieties stimulated a wide range of TLR4 activation, resulting in differential cytokine induction. Thus, U.S. Patent Application Publication No. 20130230555 provided the ability to select from a range of inflammation and cytokine induction by lipid A that prior adjuvant options could not provide.
The present disclosure significantly advances this previously described technology by describing compositions and methods for linking an antigen with a lipid A moiety within a bacterium such as E. coli and thereby producing a “whole vaccine” from a bacterium. Prior glycoconjugate vaccine production has been tedious because of laborious chemical synthesis, purification, and production costs. The present disclosure reduces these costs dramatically as it allows the generation of an antigen and an adjuvant in parallel and linked with one another in less time with lower costs. In addition, many complex carbohydrate antigens cannot be synthesized in vitro. The present disclosure not only provides compositions and methods for the synthesis of complex carbohydrate antigens in a bacterium such as E. coli, but also provides for their synthesis in parallel with numerous lipid A adjuvants.
According to the present disclosure, the lipid modification polynucleotides can reside within a vector introduced into the engineered E. coli strain. In some embodiments, the vector is a plasmid and the E. coli strain is transformed with the plasmid. In some embodiments, the plasmid is a pACYC184 plasmid, for example, the pACYC184 plasmid as shown in
The antigen associated polynucleotides can also reside within a vector introduced into the engineered E. coli strain. This vector can be the same or different from the vector containing the lipid modification polynucleotides. In some embodiments, the vector containing the antigen associated polynucleotides is a plasmid and the E. coli strain is transformed with the plasmid. It is to be understood, however, that the present description also encompasses antigen associated polynucleotides that are integrated into the E. coli chromosome. Accordingly, the present invention includes an engineered E. coli strain having either or both intra-chromosomal and extrachromosomal antigen associated polynucleotides.
The antigen associated polynucleotides can be peptide antigen encoding or polysaccharide antigen generating polynucleotides. Peptide antigen encoding polynucleotides include, but are not limited to, those associated with peptide vaccines for the treatment of anthrax, brucellosis, cholera, diphtheria, Hib, Lyme disease, meningococcal infection, pertussis, plague, pneumococcal infection (PCV and PPSV), tetanus, tuberculosis, typhoid, adenovirus, influenza, hantavirus, hepatitis A, hepatitis B, human papilloma virus, encephalitis, measles, mumps, polio, rabies, rotavirus, and related cancers. In one embodiment, the peptide antigen encoding polynucleotides are viral Influenza polynucleotides such as hemagglutinin and/or neuraminidase polynucleotides.
In some embodiments, an Lpp targeting polynucleotide, a transmembrane polynucleotide, and, if necessary, a linker sequence are introduced into the engineered E. Coli strain in addition to the one or more lipid modification polynucleotides and the one or more peptide antigen encoding polynucleotides. In these embodiments, the peptide antigen is produced as a fusion protein with the transmembrane polypeptide, which thereby directs the peptide antigen to the outer membrane of an E. coli cell. The lipid A moiety and the peptide antigen are thereby co-localized at the outer membrane and can be isolated together in an outer membrane vesicle.
An Lpp targeting polynucleotide comprises nucleotides that encode an Lpp targeting sequence, which targeting sequence includes a signal sequence and about the first nine amino acids of a mature Lpp protein. See U.S. Pat. No. 5,348,867, which is hereby incorporated by reference in its entirety, for exemplary descriptions and sequences of Lpp targeting sequences, transmembrane polypeptides, and linker sequences. One exemplary transmembrane polynucleotide is an ompA polynucleotide. The Lpp targeting polynucleotide, a transmembrane polynucleotide, and, if necessary, the linker sequence can be introduced to the E. coli strain in any vector. In some embodiments, these sequences are contained within the same vector that contains the one or more antigen encoding polynucleotides in a position downstream of the transmembrane polynucleotide such that translation of the vector results in a fusion polypeptide comprising an Lpp targeting polypeptide/linker peptide/transmembrane polypeptide/antigen polypeptide.
In some embodiments related to the expression of peptide antigen encoding polynucleotides, the engineered E. coli strain is a wild-type E. coli such as W3110 (F−1−rph-1InV(rmD, rrnE)1 rph-1). In other embodiments, the engineered E. coli strain is a W3110 strain having a deletion of one or more of a pagP, lpxT, eptA, and 1pp polynucleotide. One exemplary and non-limiting 1pp polynucleotide is provided in GenBank Accession No. NC_07779. In still other embodiments, the engineered E. coli strain is a W3110 strain having a deletion of one or more of a pagP, lpxT, eptA, 1pp, and lpxM polynucleotides.
Accordingly, in some embodiments, an engineered E. coli strain is provided that comprises a plasmid containing one or more lipid modification polynucleotides selected from the group consisting of lpxE, lpxF, lpxO, lpxR, pagL, and pagP polynucleotides; an Lpp targeting polynucleotide; a linker polynucleotide; a transmembrane polynucleotide; and one or more peptide antigen encoding polynucleotides; wherein the E. coli strain has a deletion of a pagP, lpxT, eptA, and a 1pp polynucleotide. In one embodiment, an engineered E. coli strain is provided that comprises a plasmid containing one or more lipid modification polynucleotides selected from the group consisting of lpxE, lpxF, lpxO, lpxR, pagL, and pagP polynucleotides; an Lpp targeting polynucleotide; a linker polynucleotide; an ompA polynucleotide; a hemagglutinin polynucleotide, and/or a neuraminidase polynucleotide; wherein the E. coli strain has a deletion of a pagP, lpxT, eptA, and a 1pp polynucleotide.
As stated above, the antigen associated polynucleotides included herein can be peptide antigen encoding or polysaccharide antigen generating polynucleotides. Polysaccharide antigen generating polynucleotides include, but are not limited to, capsular antigen generating polynucleotides. Capsular antigen generating polynucleotides include, but are not limited to, O antigen generating polynucleotides and non-O antigen generating polynucleotides. Non-limiting examples of O antigens are those from V. cholerae, S. typhimurium, and Shigella sonnei and flexneri species. Non-limiting examples of non-O antigens are those from Streptococcus pneumonia, Staphylococcus aureus, and Neisseria meningitidis. Although not wanting to be bound by the following theory, it is believed that upon expression of the various lipid A moieties and the O antigen in the E. coli, the E. coli O antigen ligase WaaL covalently conjugates the synthesized V. cholerae O antigen to the lipid A core region of the modified E. coli lipid A. In a manner similar to the V. cholerae O antigen, the conserved O antigen genetic coding region of Salmonella typhimurium and Shigella spcs. are cloned and expressed in E. coli for covalent attachment to lipid A. Accordingly, in some embodiments, the engineered E. coli produces a lipid A moiety that is covalently attached to a polysaccharide antigen.
In some embodiments related to the expression of polysaccharide antigen generating polynucleotides, the engineered E. coli strain is a wild-type E. coli such as W3110 (F−1−rph-1InV(rmD, rrnE)1 rph-1). In other embodiments, the engineered E. coli strain is a W3110 strain having a deletion of one or more of a pagP, lpxT, eptA, and 1pp polynucleotide. One exemplary and non-limiting 1pp polynucleotide is provided in GenBank Accession No. NC_07779. Included herein are a homolog, ortholog, or paralog of the 1pp polynucleotide provided in GenBank Accession No. NC_07779. In still other embodiments, the engineered E. coli strain is a W3110 strain having a deletion of one or more of a pagP, lpxT, eptA, 1pp, and lpxM polynucleotides.
In some embodiments, an engineered E. coli strain is transformed with a vector containing one or more V. cholerae O antigen generating polynucleotides. This vector can be a pPM1001 plasmid. The V. cholerae O antigen generating polynucleotides include, but are not limited to, a wzm polynucleotide, a wzt polynucleotide, a wzx polynucleotide, a wzy polynucleotide, a rml polynucleotide, a galE polynucleotide, a wbeW polynucleotide, a wecC polynucleotide, a wecE polynucleotide, a wecB polynucleotide, a rfbT polynucleotide, a wbf region polynucleotide, and a homolog, ortholog or paralog thereof Further, V. cholerae O antigens include, but are not limited to, O antigens of the following serogroups: O1, O22, O139, and O140. In some embodiments, the V. cholerae O antigen is an O1 serogroup antigen selected from the group of an Inaba, Ogawa and Hikojima serotype. In some embodiments, the V. cholerae O antigen is an O1 serogroup antigen of the Inaba serotype. In some embodiments, the vector comprises one or more genes provided in GenBank Accession No. AE003852.1 (Vibrio cholerae O1 biovar El Tor str. N16961), or a homolog, ortholog or paralog thereof. In some embodiments, the vector comprises a polynucleotide having about 80%, about 85%, about 90%, about 95%, about 96%, about 97%, about 98%, or about 99% sequence identity with one or more genes provided in GenBank Accession No. AE003852.1.
Accordingly, in some embodiments, an engineered E. coli strain is provided that comprises a plasmid containing one or more lipid modification polynucleotides selected from the group consisting of lpxE, lpxF, lpxO, lpxR, pagL, and pagP polynucleotides; and one or more polysaccharide antigen generating polynucleotides; wherein the E. coli strain has a deletion of an rfbD polynucleotide and a 1pp polynucleotide. In other embodiments, an engineered E. coli strain is provided that comprises a plasmid containing one or more lipid modification polynucleotides selected from the group consisting of lpxE, lpxF, lpxO, lpxR, pagL, and pagP polynucleotides; and one or more polysaccharide antigen generating polynucleotides; wherein the E. coli strain has a deletion of a 1pp polynucleotide and a polynucleotide region spanning an rfbB polynucleotide to a wbbL polynucleotide. In other or further embodiments, an engineered E. coli strain is provided that comprises a plasmid containing one or more lipid modification polynucleotides selected from the group consisting of lpxE, lpxF, lpxO, lpxR, pagL, and pagP polynucleotides; and one or more V. cholerae, S. enterica, or Shigella spcs. O antigen generating polynucleotides; wherein the E. coli strain has a deletion of an rfbD polynucleotide and a 1pp polynucleotide.
In some embodiments, an engineered E. coli strain is transformed with a vector containing one or more S. enterica O antigen generating polynucleotides. In some embodiments, the O antigen is an S. enterica enterica subspecies antigen. In some embodiments, the vector comprises one or more genes provided in GenBank Accession No. AE006468 (Salmonella enterica subsp. enterica serovar Typhimurium str. LT2), or a homolog, ortholog or paralog thereof. In some embodiments, the vector comprises a polynucleotide having about 80%, about 85%, about 90%, about 95%, about 96%, about 97%, about 98%, or about 99% sequence identity with one or more genes provided in GenBank Accession No. AE006468. The S. enterica O antigen generating polynucleotides include, but are not limited to, a wzx polynucleotide, a wzy polynucleotide, a rml polynucleotide, a wba polynucleotide, a man polynucleotide, wda polynucleotide, a wcm polynucleotide, a wfb polynucleotide, a gmm polynucleotide, a wbd polynucleotide, a wbu polynucleotide, a wbe polynucleotide, a fcl polynucleotide, a wcl polynucleotide, a wej polynucleotide, a wdc polynucleotide, a wek polynucleotide, a qdt polynucleotide, a gmd polynucleotide, an fdt polynucleotide, a wcn polynucleotide, a wdc polynucleotide, a wpb polynucleotide, a wei polynucleotide, a gna polynucleotide, a gne polynucleotide, a wbb polynucleotide, a rfbA polyulceotide, a rfbB polynucleotide, a rfbD polynucleotide, a rfbF polynucleotide, a rfbG polynucleotide, a rfbK polynucloeitde, a rfbM polynucleotide, a rfbP polynucleotide, and a homolog, ortholog or paralog thereof.
In some embodiments, an engineered E. coli strain is transformed with a vector containing one or more Shigella sonnei and/or Shigella flexneri O antigen generating polynucleotides. The S. sonnei O antigen generating polynucleotides include, but are not limited to, a wzz polynucleotide, a wbgT polynucleotide, a wbgU polynucleotide, a wzx polynucleotide, a wzy polynucleotide, an IS630 polynucleotide, a wbgV polynucleotide, a wbgW polynucleotide, a wbgX polynucleotide, a wbgY polynucleotide, a wbgZ polynucleotde and an aqpZ′ polynucleotide. In some embodiments, the vector comprises one or more genes provided in GenBank Accession No. CP001383.1 (Shigella flexneri 2002017), or a homolog, ortholog, or paralog thereof. In some embodiments, the vector comprises a polynucleotide having about 80%, about 85%, about 90%, about 95%, about 96%, about 97%, about 98%, or about 99% sequence identity with one or more genes provided in GenBank Accession No. CP001383.1. In other or further embodiments, the vector comprises one or more genes provided in GenBank Accession No. AE005674.2 (Shigella flexneri 2a str. 301) or a homolog, ortholog, or paralog thereof. In some embodiments, the vector comprises a polynucleotide having about 80%, about 85%, about 90%, about 95%, about 96%, about 97%, about 98%, or about 99% sequence identity with one or more genes provided in GenBank Accession No. AE005674.2. The S. flexneri O antigen generating polynucleotides include, but are not limited to, a wzx polynucleotide, a wzy polynucleotide, an rml polynucleotide, a wbu polynucleotide, a gnd polynucletode, a galF polynucleotide, a wfd polynucleotide, a glf polynucleotide, a wbd polynucleotide, a man polynucleotide, a wba polynucleotide, a psb polynucleotide, a wbg polynucleotide, a wbs polynucleotide, a wbw polynucleotide, a fnl polynucleotide, a qnl polynucleotide, a wfe polynucleotide, a wfa polynucleotide, a wbb polynucleotide, and a wff polynucleotide.
In still other embodiments, an engineered E. coli strain is provided that comprises a vector containing one or more lipid modification polynucleotides selected from the group consisting of lpxE, lpxF, lpxO, lpxR, pagL, and pagP polynucleotides; and one or more Streptococcus pneumoniae, Staphylococcus aureus, or Neisseria meningitidis capsular antigen generating polynucleotides (non-O antigen); wherein the E. coli strain has a deletion of an rfbD polynucleotide. In some embodiments, the vector comprises one or more genes provided in GenBank Accession No AE005672.3 (Streptococcus pneumoniae TIGR4 or a homolog, ortholog or paralog thereof. The S. pneumoniae capsular (non-O) antigen generating polynucleotides include, but are not limited to, a wzg polynucleotide, a wzh polynucleotide, a wzd polynucleotide, a wze polynucleotide, a wch polynucleotide, a wci polynucleotide, a wzy polyncueltodie, a wzx polynucleotide, and a rml polynucleotide. In other or further embodiments, the vector comprises one or more genes provided in GenBank Accession No. CP000255.1 (Staphylococcus aureus subsp. aureus USA300_FPR3757) or a homolog, ortholog or paralog thereof. The S. aureus capsular (non-O) antigen generating polynucleotides include, but are not limited to, a cap1A polynucleotide, a cap1B polynucleotide, a cap1C polynucleotide, a cap 1D polynucleotide, a cap1E polynucleotide, a caplF polynucleotide, cap1G polynucleotide, cap1H polynucleotide, cap1I polynucleotide, cap1J polynucleotide, cap1K polynucleotide, cap1L polynucleotide, cap1M polynucleotide, cap1N polynucleotide, and cap1O polynucleotide. The N. meningitides capsular (non-O) antigen generating polynucleotides include, but are not limited to, a myn polynucleotide, a sia polynucleotide, a lip polynucleotide, and an mtr polynucleotide.
The compositions and methods described herein advantageously provide a means for producing a whole vaccine (an antigen and an adjuvant) from a bacterium. The compositions and methods further provide a broad range of lipid A moiety and antigen combinations, and thereby allows for selection and creation of lipid A and antigen combinations that are specifically tailored to generate a desired immune response. Accordingly, the compositions produced by the E. coli strains are highly useful as vaccines or vaccine components.
Therefore, included herein is a composition isolated from an engineered E. coli strain as described above or below, wherein the composition comprises one or more lipid A moieties linked to one or more antigens. In some embodiments, the one or more lipid A moieties are covalently attached to one or more polysaccharide antigens in the composition. In other or further embodiments, the one or more lipid A moieties are co-localized with the one or more peptide antigens at the outer membrane of an E. coli cell or an outer membrane vesicle in the composition.
Also included herein is a pharmaceutical composition comprising one or more lipid A moieties linked to one or more antigens isolated from an engineered E. coli strain as described above or below. The pharmaceutical compositions include a therapeutically effective amount of the isolated lipid A-antigen compounds described herein in combination with a pharmaceutically acceptable carrier and, in addition, can include other medicinal agents, pharmaceutical agents, carriers, or diluents.
As used herein, the term “carrier” encompasses any excipient, diluent, filler, salt, buffer, stabilizer, solubilizer, lipid, stabilizer, or other material well known in the art for use in pharmaceutical formulations. The choice of a carrier for use in a composition will depend upon the intended route of administration for the composition. The preparation of pharmaceutically acceptable carriers and formulations containing these materials is described in, e.g., Remington's Pharmaceutical Sciences, 21st Edition, ed. University of the Sciences in Philadelphia, Lippincott, Williams & Wilkins, Philadelphia Pa., 2005. Examples of physiologically acceptable carriers include saline, glycerol, DMSO, buffers such as phosphate buffers, citrate buffer, and buffers with other organic acids; antioxidants including ascorbic acid; low molecular weight (less than about 10 residues) polypeptides; proteins, such as serum albumin, gelatin, or immunoglobulins; hydrophilic polymers such as polyvinylpyrrolidone; amino acids such as glycine, glutamine, asparagine, arginine or lysine; monosaccharides, disaccharides, and other carbohydrates including glucose, mannose, or dextrins; chelating agents such as EDTA; sugar alcohols such as mannitol or sorbitol; salt-forming counterions such as sodium; and/or nonionic surfactants such as TWEEN™ (ICI, Inc.; Bridgewater, N.J.), polyethylene glycol (PEG), and PLURONICS™ (BASF; Florham Park, N.J.). To provide for the administration of such dosages for the desired therapeutic treatment, compositions disclosed herein can advantageously comprise between about 0.1% and 99% by weight of the total of one or more of the lipid A-antigen compounds based on the weight of the total composition including carrier or diluent.
It should also be understood that the foregoing relates to preferred embodiments of the present invention and that numerous changes may be made therein without departing from the scope of the invention. The invention is further illustrated by the following examples, which are not to be construed in any way as imposing limitations upon the scope thereof. On the contrary, it is to be clearly understood that resort may be had to various other embodiments, modifications, and equivalents thereof, which, after reading the description herein, may suggest themselves to those skilled in the art without departing from the spirit of the present invention and/or the scope of the appended claims. All patents, patent applications, and publications referenced herein are incorporated by reference in their entirety for all purposes.
As used herein, “essentially free,” in terms of a specified component, is used herein to mean that none of the specified component has been purposefully formulated into a composition and/or is present only as a contaminant or in trace amounts. The total amount of the specified component resulting from any unintended contamination of a composition is therefore well below 0.05%, preferably below 0.01%. Most preferred is a composition in which no amount of the specified component can be detected with standard analytical methods.
As used herein the specification, “a” or “an” may mean one or more. As used herein in the claim(s), when used in conjunction with the word “comprising,” the words “a” or “an” may mean one or more than one.
The use of the term “or” in the claims is used to mean “and/or” unless explicitly indicated to refer to alternatives only or the alternatives are mutually exclusive, although the disclosure supports a definition that refers to only alternatives and “and/or.” As used herein “another” may mean at least a second or more.
Throughout this application, the term “about” is used to indicate that a value includes the inherent variation of error for the device, the method being employed to determine the value, or the variation that exists among the study subjects.
Other objects, features and advantages of the present invention will become apparent from the following detailed description. It should be understood, however, that the detailed description and the specific examples, while indicating preferred embodiments of the invention, are given by way of illustration only, since various changes and modifications within the spirit and scope of the invention will become apparent to those skilled in the art from this detailed description.
The following drawings form part of the present specification and are included to further demonstrate certain aspects of the present invention. The invention may be better understood by reference to one or more of these drawings in combination with the detailed description of specific embodiments presented herein.
Provided herein are engineered Escherichia coli strains that create lipid A moieties linked with antigen and methods for producing these E. coli strains. In some embodiments, the lipid A moiety is covalently linked to the antigen. In other embodiments, the lipid A moiety is linked to the antigen via a co-localization in an outer membrane of the E. coli. The compositions and methods described herein advantageously provide a means for producing a whole vaccine (a linked antigen and an adjuvant) from a bacterium. The compositions and methods further provide a broad range of possible lipid A moiety and antigen combinations, and thereby allows for selection and creation of lipid A and antigen combinations that are specifically tailored to generate a desired immune response. Accordingly, the compositions created by the E. coli strains are highly useful as vaccines or vaccine components.
Provided herein are new bacterial vaccine production platforms where nonpathogenic bacteria produce antigen and adjuvant on the cell surface or where the adjuvant and antigen are purified from whole bacteria using OMVs. Previously, a bacterial system was developed in nonpathogenic E. coli that expressed lipid A modification genes from a plasmid. This work resulted in 61 distinct E. coli strains that each generated a unique lipid A adjuvant molecule on the surface of the cell (Needham et al., 2013). In this work, this new adjuvant technology is built on by adapting both protein and carbohydrate antigens to express coordinately with a bacterial-derived lipid adjuvant on the cell surface. Initial pilot vaccines were produced with a HA2-domain protein that was tested in mice to understand the efficacy of this system. The influenza vaccine successfully induced an antibody response specific to the HA protein, resulted in reduced viral titers after lethal challenge, and protected vaccinated mice from influenza. In addition, this vaccine platform has also been engineered to directly link carbohydrate antigens onto a lipid adjuvant, such as MPL, to produce glycoconjugate vaccines. Carbohydrate antigens and lipid adjuvants are produced on the cell surface and purified as a vaccine to protect from cholera infections.
As used in the specification and claims, the singular form “a,” “an,” and “the” include plural references unless the context clearly dictates otherwise. For example, the term “a cell” includes a plurality of cells, including mixtures thereof.
The terms “about” and “approximately” are defined as being “close to” as understood by one of ordinary skill in the art. In one non-limiting embodiment the terms are defined to be within 10%. In another non-limiting embodiment, the terms are defined to be within 5%. In still another non-limiting embodiment, the terms are defined to be within 1%.
As used herein, the term “comprising” is intended to mean that the compositions and methods include the recited elements, but not excluding others. “Consisting essentially of” when used to define compositions and methods, shall mean excluding other elements of any essential significance to the combination. Thus, a composition consisting essentially of the elements as defined herein would not exclude trace contaminants from the isolation and purification method and pharmaceutically acceptable carriers, such as phosphate buffered saline, preservatives, and the like. “Consisting of” shall mean excluding more than trace elements of other ingredients and substantial method steps for administering the compositions of this invention. Embodiments defined by each of these transition terms are within the scope of this invention.
The expression “control sequences” refers to DNA sequences necessary for the expression of an operably linked coding sequence in a particular host organism. The control sequences that are suitable for prokaryotes, for example, include a promoter, optionally an operator sequence, and a ribosome binding site. DNA for a presequence or secretory leader may be operably linked to DNA for a polypeptide if it is expressed as a preprotein that participates in the secretion of the polypeptide; a promoter or enhancer is operably linked to a coding sequence if it affects the transcription of the sequence; or a ribosome binding site is operably linked to a coding sequence if it affects the transcription of the sequence; or a ribosome binding site is operably linked to a coding sequence if it is positioned so as to facilitate translation. Generally, “operably linked” means that the DNA sequences being linked are contiguous, and, in the case of a secretory leader, contiguous and in reading phase. However, enhancers do not have to be contiguous.
The term “deletion,” when referring to a polynucleotide sequence or a gene, is used herein to refer to an effective deletion of the function of the polynucleotide sequence or gene. More specifically, a deletion includes a complete removal, a partial removal, and one or more mutations that render the polynucleotide sequence, the gene, or a polypeptide encoded by the polypeptide or gene, inactive or ineffective for its desired purpose.
As used herein, “expression” refers to the process by which polynucleotides are transcribed into mRNA and/or the process by which the transcribed mRNA is subsequently being translated into peptides, polypeptides, or proteins.
A “gene” refers to a polynucleotide containing at least one open reading frame that is capable of encoding a particular polypeptide or protein after being transcribed and translated.
The terms “link,” “linked,” and “linkage” refer to a close proximity and do not require a physical touching. In some embodiments, these terms refer to a covalent bond. In other embodiments, these terms refer to a co-localization such as at an outer membrane.
A “pharmaceutical composition” is intended to include the combination of an active agent with a pharmaceutically acceptable carrier, inert or active, making the composition suitable for diagnostic or therapeutic use in vivo or ex vivo.
The term “pharmaceutically acceptable carrier” means a carrier or excipient that is useful in preparing a pharmaceutical composition that is generally safe and non-toxic, and includes a carrier that is acceptable for veterinary and/or human pharmaceutical use. As used herein, the term “pharmaceutically acceptable carrier” encompasses any of the standard pharmaceutical carriers, such as a phosphate buffered saline solution, water, and emulsions, such as an oil/water or water/oil emulsion, and various types of wetting agents. As used herein, the term “carrier” encompasses any excipient, diluent, filler, salt, buffer, stabilizer, solubilizer, lipid, stabilizer, or other material well known in the art for use in pharmaceutical formulations and as described further below. The pharmaceutical compositions also can include preservatives. A “pharmaceutically acceptable carrier” as used in the specification and claims includes both one and more than one such carrier.
The terms “polynucleotide” and “oligonucleotide” are used interchangeably, and refer to a polymeric form of nucleotides of any length, either deoxyribonucleotides or ribonucleotides, or analogs thereof. Polynucleotides may have any three-dimensional structure, and may perform any function, known or unknown. The following are non-limiting examples of polynucleotides: a gene or gene fragment, exons, introns, messenger RNA (mRNA), transfer RNA, ribosomal RNA, ribozymes, cDNA, recombinant polynucleotides, branched polynucleotides, plasmids, vectors, isolated DNA of any sequence, isolated RNA of any sequence, nucleic acid probes, and primers. A polynucleotide may comprise modified nucleotides, such as methylated nucleotides and nucleotide analogs. If present, modifications to the nucleotide structure may be imparted before or after assembly of the polymer. The sequence of nucleotides may be interrupted by non-nucleotide components. A polynucleotide may be further modified after polymerization, such as by conjugation with a labeling component. The term also refers to both double- and single-stranded molecules.
A polynucleotide is composed of a specific sequence of four nucleotide bases: adenine (A); cytosine (C); guanine (G); thymine (T); and uracil (U) for thymine (T) when the polynucleotide is RNA. Thus, the term “polynucleotide sequence” is the alphabetical representation of a polynucleotide molecule. This alphabetical representation can be input into databases in a computer having a central processing unit and used for bioinformatics applications such as functional genomics and homology searching.
As used herein, an “antigen associated polynucleotide” includes a polynucleotide that encodes the antigen polypeptide and a polynucleotide that encodes a polypeptide, which polypeptide functions to create or modify the antigen. In some embodiments, an antigen associated polynucleotide encodes an enzyme that creates or modifies a polysaccharide antigen such as a capsular antigen. Capsular antigens include O antigens and non-O antigens. These antigen associated polynucleotides are referred to herein as “polysaccharide generating.”
The term “polypeptide” is used in its broadest sense to refer to a compound of two or more subunit amino acids, amino acid analogs, or peptidomimetics. A peptide of three or more amino acids is commonly called an oligopeptide if the peptide chain is short. If the peptide chain is long, the peptide is commonly called a polypeptide or a protein.
A polynucleotide or polynucleotide region (or a polypeptide or polypeptide region) has a certain percentage (for example, 80%, 85%, 90%, or 95%) of “sequence identity” to another sequence means that, when aligned, that percentage of bases (or amino acids) are the same in comparing the two sequences. This alignment and the percent homology or sequence identity can be determined using software programs known in the art, for example those described in CURRENT PROTOCOLS IN MOLECULAR BIOLOGY (F. M. Ausubel et al., eds., 1987) Supplement 30, section 7.7.18, Table 7.7.1. Preferably, default parameters are used for alignment. A preferred alignment program is BLAST, using default parameters. In particular, preferred programs are BLASTN and BLASTP, using the following default parameters: Genetic code=standard; filter=none; strand=both; cutoff=60; expect=10; Matrix=BLOSUM62; Descriptions=50 sequences; sort by=HIGH SCORE; Databases=non-redundant, GenBank+EMBL+DDBJ+PDB+GenBank CDS translations+SwissProtein+SPupdate+PIR. Details of these programs can be found at the following Internet address: ncbi.nlm.nih.gov/cgi-bin/BLAST.
“Transformation” of a cellular organism with DNA means introducing DNA into an organism so that at least a portion of the DNA is replicable, either as an extrachromosomal element or by chromosomal integration.
The term “vector” means a DNA construct containing a DNA sequence which is operably linked to a suitable control sequence capable of effecting the expression of the DNA in a suitable host. Such control sequences include a promoter to effect transcription, an optional operator sequence to control such transcription, a sequence encoding suitable mRNA ribosome binding sites, and sequences which control the termination of transcription and translation. The vector may be a plasmid, a phage particle, or simply a potential genomic insert. Once transformed into a suitable host, the vector may replicate and function independently of the host genome, or may in some instances, integrate into the genome itself. A plasmid is the most commonly used form of vector, however, the invention is intended to include such other forms of vectors which serve equivalent function as and which are, or become, known in the art.
Influenza virus is a highly transmissible respiratory pathogen that results in about 40,000 deaths annually and kills millions during pandemic years (Fan et al., 2004). Influenza viruses are classified into two epidemiologically interesting types including A and B. While only one serologically distinct influenza B virus exists, influenza A viruses are highly variable and strains are subtyped based on two antigenic surface glycoproteins called hemagglutinin (HA) and neuraminidase (Lamb and Krug, 2001). While influenza A viruses include 16 different HA proteins (H1-H16) and nine neuraminidase (N1-N9), Human-infectious influenza viruses are primarily A-type H1N1, H2N2, H3N2, and B-type viruses, but cross-species infections from avian-associated H5N1 and H7N7, and H9N2 and swine-associated strains have recently emerged. These avian influenza outbreaks are extremely worrisome because of close human interaction with birds present the possibility of a new influenza pandemic (Horimoto and Kawaoka, 2005).
Currently, vaccination is considered the most effective way to prevent influenza transmission. The most common influenza vaccine consists of heat-inactivated H1N1, H3N2, and B-type viruses that are grown in chicken eggs, but recently, a cold-adapted live virus has been developed that actively replicates in the nasal passages to generate immunity. While each of these vaccination methods produce protective antibodies to protect from influenza, each has drawbacks. Due to antigenic drift and shift of the A-type viruses, influenza vaccines require regular modifications based on emergent viral strains. However, production of each virus strain takes at least six months. Therefore, quick production of vaccines in epidemics/pandemics is not possible with current technology. Furthermore, a recombinant vaccine that can be produced in a timeframe of days or weeks that offers long-term protection from influenza would be ideal for controlling viral outbreaks.
Influenza HA is a highly immunogenic protein that coats the surface of the virus and it has been the target of many vaccines (Cox, 2005). HA is required for influenza infection by promoting fusion with host cells. Cellular proteases cleave the HA protein into HA1 and HA2 domains, which comprise a necessary step for viral infection (Skehel and Wiley, 2000). Viral entry is mediated by the HA1 domain binding to salic acid receptors on the surface of the host cell. Through endocytosis the virion enters the cell where it is transported to the endosome where the acidic pH promotes structural changes in the HA protein. Conformational shifts expose the HA2 domain, and promote fusion of the viral and endosomal membranes. The crystal structures of HA have revealed that cleavage of the HA1 and HA2 domains and the low pH of the endosome are required for structural alterations that promote viral infection (Chen et al., 1998; Bullough et al., 1994; Sauter et al., 1992).
While the HA2 domain of HA is considerably more conserved than the HA1 domain, neutralizing antibodies directed at both protein domains offer protection from influenza challenge (Skehel and Wiley, 2000; Gocnik et al., 2008; Smirnov et al., 2000; Okuno et al., 1994). In fact, several neutralizing antibodies has been isolated that target the conserved HA2 domain. These antibodies target conserved epitopes in the HA2 protein of several influenza A subtypes to offer broad protection (Ekiert et al., 2009; Sui et al., 2009; Throsby et al., 2008; Okuno et al., 1993; Sancheck-Fauquier et al., 1987). Mechanistically, the antibodies presumably inhibit the conformational changes that are necessary for viral and host membrane fusion at low pH. Blocking viral entry by targeting the conserved HA domain could offer widespread protection from influenza viruses in human, chickens, and swine, which are the major reservoirs for these viruses.
A bacterial-based vaccine was engineered that targets the conserved domain of HA2 to offer widespread protection against influenza A viruses. A mouse model was used to demonstrate the efficacy of the influenza protein-based vaccine. The benefits of this new technology are that it is a quick, low cost, high yield production of influenza vaccines that does not require growth of viruses in chicken eggs. Incorporating a conserved antigenic HA2 epitope into a bacterial based vaccine system could be valuable against the threat of epidemics/pandemics.
In addition to this protein-based vaccine, this system has also been adapted to produce glycoconjugate vaccines that target carbohydrate epitopes of pathogenic bacteria. The efficacy of this system has been demonstrated by generating a vaccine against the conserved O-antigen of Vibrio cholerae. Cholera disease is a potentially lethal diarrheal disease that affects millions of people every year (Harris et al., 2012; Kaper et al., 1995). The well-conserved Vibrio cholerae O-antigen has been shown to provide a protective immune response against infection (Seed et al., 2012). Therefore, a bacterium was engineered to produce the V. cholerae O -antigen as the antigen in the bacterial-based vaccine system.
A wide range of nucleic acid-based expression systems may be used for the expression of polypeptide antigens or genes controlling synthesis of polysaccharide antigens of the embodiments. For example, one embodiment of the invention involves transformation of bacteria with the coding sequences of fusion polypeptides comprising a polypeptide antigen linked to a membrane anchor sequence (and section signal). Numerous expression systems exist that comprise some or all of the sequence components discussed below.
The term “expression vector” refers to a vector containing a nucleic acid sequence coding for at least part of a gene product capable of being transcribed and then translated into a polypeptide. Expression vectors can contain a variety of “control sequences,” which refer to nucleic acid sequences necessary for the transcription and possibly translation of an operably linked coding sequence in a particular host organism (e.g., gram positive or gram negative bacteria). In addition to control sequences that govern transcription and translation, vectors and expression vectors may contain nucleic acid sequences that serve other functions as well and are described infra.
1. Promoters and Enhancers
A “promoter” is a control sequence that is a region of a nucleic acid sequence at which initiation and rate of transcription are controlled. It may contain genetic elements at which regulatory proteins and molecules may bind such as RNA polymerase and other transcription factors. The phrases “operatively positioned,” “operatively linked,” “under control,” and “under transcriptional control” mean that a promoter is in a correct functional location and/or orientation in relation to a nucleic acid sequence to control transcriptional initiation and/or expression of that sequence. A promoter may or may not be used in conjunction with an “enhancer,” which refers to a cis-acting regulatory sequence involved in the transcriptional activation of a nucleic acid sequence.
Preferably a promoter a promoter for use according to the embodiments is a recombinant or heterologous promoter, which refers to a promoter that is not normally associated with a nucleic acid sequence in its natural environment. A recombinant or heterologous enhancer refers also to an enhancer not normally associated with a nucleic acid sequence in its natural environment. Such promoters or enhancers may include promoters or enhancers of other genes, and promoters or enhancers isolated from any other prokaryotic, viral, or eukaryotic cell, and promoters or enhancers not “naturally occurring,” i.e., containing different elements of different transcriptional regulatory regions, and/or mutations that alter expression. Furthermore, it is contemplated that the control sequences that direct transcription and/or expression of sequences within non-nuclear organelles such as mitochondria, chloroplasts, and the like, can be employed as well.
In preferred aspects, a promoter (or promoter enhancer system) for use according to the embodiments is an inducible promoter that provides expression of a sequence based on an external stimulus. For example, the inducible promoter may be a promoter that provides expression only in the presence of a particular compound (e.g., IPTG), at a particular pH, or in specific environmental (e.g., lighting) conditions.
2. Initiation Signals and Internal Ribosome Binding Sites
A specific initiation signal also may be required for efficient translation of coding sequences. These signals include the ATG initiation codon or adjacent sequences. Exogenous translational control signals, including the ATG initiation codon, may need to be provided. One of ordinary skill in the art would readily be capable of determining this and providing the necessary signals. It is well known that the initiation codon must be “in-frame” with the reading frame of the desired coding sequence to ensure translation of the entire insert. The exogenous translational control signals and initiation codons can be either natural or synthetic. The efficiency of expression may be enhanced by the inclusion of appropriate transcription enhancer elements.
3. Multiple Cloning Sites
Vectors can include a multiple cloning site (MCS), which is a nucleic acid region that contains multiple restriction enzyme sites, any of which can be used in conjunction with standard recombinant technology to digest the vector (see Carbonelli et al., 1999, Levenson et al., 1998, and Cocea, 1997, incorporated herein by reference.) “Restriction enzyme digestion” refers to catalytic cleavage of a nucleic acid molecule with an enzyme that functions only at specific locations in a nucleic acid molecule. Many of these restriction enzymes are commercially available. Use of such enzymes is understood by those of skill in the art. Frequently, a vector is linearized or fragmented using a restriction enzyme that cuts within the MCS to enable exogenous sequences to be ligated to the vector. “Ligation” refers to the process of forming phosphodiester bonds between two nucleic acid fragments, which may or may not be contiguous with each other. Techniques involving restriction enzymes and ligation reactions are well known to those of skill in the art of recombinant technology.
4. Termination Signals
The vectors or constructs prepared in accordance with the present invention will generally comprise at least one termination signal. A “termination signal” or “terminator” is comprised of the DNA sequences involved in specific termination of an RNA transcript by an RNA polymerase. Thus, in certain embodiments, a termination signal that ends the production of an RNA transcript is contemplated. A terminator may be necessary in vivo to achieve desirable message levels.
Terminators contemplated for use in the invention include any known terminator of transcription described herein or known to one of ordinary skill in the art, including but not limited to, for example, rhp dependent or rho independent terminators. In certain embodiments, the termination signal may be a lack of transcribable or translatable sequence, such as due to a sequence truncation.
5. Origins of Replication
In order to propagate a vector in a host cell, it may contain one or more origins of replication sites (often termed “ori”), which is a specific nucleic acid sequence at which replication is initiated. Alternatively an autonomously replicating sequence (ARS) can be employed if the host cell is yeast.
6. Selectable and Screenable Markers
In certain embodiments of the invention, cells containing a nucleic acid construct of the present invention may be identified in vitro or in vivo by including a marker in the expression vector. Such markers would confer an identifiable change to the cell permitting easy identification of cells containing the expression vector. Generally, a selectable marker is one that confers a property that allows for selection. A positive selectable marker is one in which the presence of the marker allows for its selection, while a negative selectable marker is one in which its presence prevents its selection. An example of a positive selectable marker is a drug resistance marker, such an antibiotic resistance marker.
7. Fusion Polypeptides
As described above, in some aspects a vector of the embodiments comprises a sequence for expression, which comprises a fusion of a membrane anchor sequence and an antigen polypeptide. Furthermore, in some aspects, the fusion polypeptide comprises a secretion signal that directs the fusion protein to the bacterial (outer) membrane. Optionally, the fusion polypeptide further comprises a linker positions between the antigen polypeptide sequence and the membrane anchor sequence.
a. Signal Sequences
In some aspects, a fusion polypeptide of the embodiments comprises a signal sequence that targets the fusion polypeptide to the membrane (and may be cleaved away from the fusion). In certain aspects, the signal sequence can be from a gram negative bacteria (e.g., E. coli). For example, the signal sequence can be from Lpp. In further aspects, the signal sequence can be a signal sequence from an autotransporter polypeptide of a gram negative bacteria. For example, the signal sequence can be from AIDA-I, EstA, MisL, Hbp, Ag43, BrkA, OmpA, OmpC, OmpX, LamB, FhuA, PfaI, EspP, IgAP, Pet or Yfal (see, e.g., Nicolay et al., 2015 and van Bloois et al., 2011, each incorporated herein by reference).
b. Membrane Anchor Sequence
Certain aspect of the embodiments concern fusion polypeptides that comprise a bacterial membrane anchor sequence. For example, the membrane anchor sequence can be composed of all or part of an integral membrane protein from a gram negative bacteria. In further aspects, the membrane anchor sequence can be a non-integral membrane polypeptide, such as a lipoprotein or a component of a bacterial surface appendage. In particular aspects, the bacterial membrane anchor sequence can be an outer membrane anchor sequence. In some aspects, the sequence can be a beta-barrel domain from an autotransporter polypeptide of a gram negative bacteria. For example, the membrane anchor sequence can comprise a membrane anchor domain from AIDA-I, EstA, MisL, Hbp, Ag43, BrkA, OmpA, OmpC, OmpX, LamB, FhuA, PfaI, EspP, IgAP, Pet, Yfal or MraY (see, e.g., Nicolay et al., 2015 and van Bloois et al., 2011, each incorporated herein by reference). In further aspects, the bacterial membrane anchor sequence comprises the membrane anchor sequence from OmpA.
c. Linker Sequence
It will be understood that in certain cases, a fusion polypeptide may comprise additional amino acids positioned between the antigen polypeptide sequence and the membrane anchor sequence. In general these sequences are interchangeably termed “linker sequences” or “linker regions.” One of skill in the art will recognize that linker regions may be one or more amino acids in length and often comprise one or more glycine residue(s) which confer flexibility to the linker. A variety of linkers can be used as part of fusion polypeptide of the embodiments. In preferred aspects, the optional linker sequence is positioned between the membrane anchor sequence and the antigen polypeptide sequence. In certain aspects the linker sequence comprises at least or about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 or 20 amino acids. In still further aspects the linker comprises between about 10 and 200, 10 and 100, 20 and 100, 40 and 100 or 50 and 90 amino acids. In certain aspects, the linker sequence may comprise two, three, four or more Gly positions or a poly Gly sequence having two or more consecutive Gly positions.
The following examples are included to demonstrate preferred embodiments of the invention. It should be appreciated by those of skill in the art that the techniques disclosed in the examples which follow represent techniques discovered by the inventor to function well in the practice of the invention, and thus can be considered to constitute preferred modes for its practice. However, those of skill in the art should, in light of the present disclosure, appreciate that many changes can be made in the specific embodiments which are disclosed and still obtain a like or similar result without departing from the spirit and scope of the invention.
Bacterial strains and growth. For all experiments, E. coli strains were initially grown from freezer stocks on LB agar overnight at 37° C. After initial growth, isolated colonies were inoculated into 10 ml cultures and incubated overnight at 37° C. for use in experiments. Ampicillin was used at 100 ng/ml, while chloramphenicol was used at 15 ng/ml for all experiments. IPTG was used at a concentration of 100 μM.
Immunoblot analysis. To detect 6×-his tagged proteins, E. coli preparations were grown and diluted to OD600 of 1.0 for whole cell lysates. 5 ng of total protein from whole bacterial cells or isolated OMVs was separated by SDS-PAGE and transferred onto nitrocellulose Immunoblotting was performed with mouse-anti-5×-his antibody (Qiagen) at a dilution of 1:2000 or anti-Vibrio antibody at a dilution of 1:40,000 (KPL-seracare). Anti-mouse or anti-rabbit conjugated-HRP secondary antibody (GE Healthcare) or was used at a concentration of 1:10,000, respectively. Detection was performed using Pierce® ECL Western Blotting Substrate (Thermo Scientific).
Fluorescent analysis. E. coli cells were examined as previously described with some modifications (Lam et al., 1994). In brief, cells were grown to mid log phase OD600 of 0.5 and 1 ml was fixed in 4% paraformaldehyde for 20 minutes at 25° C. Samples were washed twice with 2 ml of PBS and then incubated in 10% BSA resuspended in PBS for 20 minutes. Cells were resuspended in 10% BSA-PBS with a 1:100 dilution of mouse-anti-5×-his antibody (Qiagen) or anti-Vibrio antibody (KPL-seracare) and incubated at 25° C. for 1 h. Samples were washed three times in PBS and a fluorescein-conjugated anti-mouse or an anti-rabbit secondary antibody was diluted 1:200 in 10% BSA-PBS and incubated at 25° C. for 1 h. The cells were washed four times with PBS. 10 μl of cells were mounted on glass slides under a coverslip and examined on a Nikon Eclipse 80i microscope.
Mass spectrometry. For mass spectrometry, lipid A was analyzed using a MALDI-TOF/TOF (ABI 4700 Proteomics Analyzer) mass spectrometer in the negative mode as previously described (Hankins et al., 2011).
Immunization and challenge studies. Female Balb/C mice were immunized orally with 1×108 bacterial cfu or intranasal administration with OMVs containing 20 μg of total protein. All bacterial strains were expression enzymes from the pELOP plasmid (Needham et al., 2013) to generate MPL. All animals were boosted four weeks later with equivalent amounts. At week six, the mice were challenged with 35×LD50 of A/PR/8/1934 (H1N1). At day seven, five mice from each group were sacrificed for lung viral titers, while the rest were monitored for seventeen days. Serum was collected two weeks after the last vaccination for antibody analysis.
Lung viral titers. A confluent layer of MDCK cells was washed with PBS and lung homogenate was added at 1:10, 1:100, 1:1000 etc. dilutions. Cells were incubated at 33° C. for 1 h with shaking every 15 minutes to ensure an equal distribution of virus throughout the plate. After 1 h the media was removed and the cells were overlayed with 25 ml of 2% DMEM containing 2% penicillin/streptomycin, 2.5 μg/ml of NAT, and 2% agarose. Solidified plates were inverted and incubated at 33° C. for three days. Plaques were reported as viral forming units/lung. All titers were performed in triplicate and averaged.
ELISAs. For antibody analysis, 3 μg of recombinant soluble HA2 was purified and immobilized on a 96-well plate. Wells were probed with serial dilutions of mouse serum diluted in PBS. After washing, anti-mouse conjugated-HRP secondary antibody (GE Healthcare) was used at a concentration of 1:10,000. Detection was performed using Pierce® ECL Western Blotting Substrate (Thermo Scientific). The absorbance was read at 405 nm.
Six genes, lpxE, lpxF, lpxO, lpxR, pagL, and pagP, were cloned individually into pQLinkN and expressed in wild-type E. coli for co-expression as described in U.S. Patent Application Publication No. 2013/0230555, which is hereby incorporated by reference in its entirety. The six genes originated from the following species: pagP from E. coli; pagL, lpxR, and lpxO from Salmonella enterica serovar Typhimurium; and lpxE and lpxF from Francisella tularensis. Specifically, the primers listed below in Table 1 were used for said cloning.
Transformation of wild-type E. coli with pQlinkN-derived plasmids that contained various combinations of the lpxE, lpxF, lpxO, lpxR, pagL, and pagP genes yielded E. coli strains that produce diverse lipid A species. The lipid A species are described in U.S. Patent Application Publication No. 2013/0230555. However, for E. coli expression of linked lipid A/polysaccharide antigen compositions, the lipid A modification genes (lpxE, lpxF, lpxO, lpxR, pagL, and pagP) and their IPTG inducible promoters were transferred to a pACYC184 plasmid and two plasmids were employed. First, the lipid A modification genes (lpxE, lpxF, lpxO, lpxR, pagL, and pagP) and their promoters were amplified from the pQlinkN-derived plasmid with engineered Sall sites and the digested fragments were cloned into SaII-digested pACYC184, which contains a p15A replicon. A schematic of the pACYC184 plasmid is provided in
Next, a plasmid, pPM1001, was obtained from Monash University that contains the genes required to synthesize the O1 O-antigen from Vibrio cholerae (Manning et al., 1986). More specifically, the plasmid contained one or more of: gmhD gene, a manC gene, a manB gene, a gmd gene, a wbeE gene, a wbeG gene, a wzm gene (ABC transport), a wzt gene (ABC transport), a wbeK gene, a wbeL gene, a wbeM gene, a wbeN gene, a wbeO gene, a wbeP gene, a wbeT gene, a wbeU gene, a wbeV gene, a gale gene, and a wbeW gene, and a wbf region gene. For optimal expression of O antigen genes in E. coli, either the rfbD gene (Eck2034; see, for example, GenBank Accession No. NC_007779) or the entire E. coli O antigen biosynthetic genetic region from ribB to wbbL (Eck2025-Eck2035) were chromosomally deleted by P1 vir phage transduction using Keio mutants or lambda red recombination, respectively (Baba et al., 2006; Touze et al., 2008). E. coli manifesting one of these deletions were then transformed with the plasmid pPM1001 and a pACYC184 plasmid selected from the group of plasmids containing the various combinations of the lpxE, lpxF, lpxO, lpxR, pagL, and pagP genes.
All Escherichia coli W3110 strains were grown from freezer stock on Luria-Bertani Broth (LB) or 2× Nutrient broth with 5 g/L of NaCl at 25° C., 30° C., or 37° C. and supplemented with 100 mg/mL ampicillin, 15 mg/mL chloramphenicol, or 30 mg/mL kanamycin when appropriate. When required, 50 μM-1mM isopropyl β-D-1-thiogalactopyranoside (IPTG) was added as determined by TLC analysis of lipid A enzyme activity. To increase production of outer membrane vesicles (OMVs), the gene Eck1673, which encodes the major outer membrane lipoprotein Lpp, was deleted from the E. coli genome. The Eck1673 gene is also known as lpp. One exemplary lpp polynucleotide is provided in GenBank Accession No. NC_007779. Deletion of the Lpp lipoprotein resulted in a 100- to 1000-fold increased production of OMVs in E. coli strains.
It is believed that upon expression of the various lipid A species and the O antigen in the E. coli, the E. coli O antigen ligase WaaL covalently conjugated the synthesized V. cholerae O antigen to the lipid A core region of the modified lipid A adjuvant. In a manner similar to the V. cholerae O antigen, the conserved O antigen genetic coding region of Salmonella typhimurium and Shigella spcs. are cloned and expressed in E. coli for covalent attachment to lipid A. In addition, capsule biosynthesis genetic coding regions from Streptococcus pneumoniae and Staphylococcus aureus including, but not limited to, a wzm gene (ABC transport), a wzt gene (ABC transport), a wzx gene (flippase) and/or a wzy gene (polymerase), are cloned in a similar manner and ligated to engineered E. coli lipid A molecules.
The above-described glycolipids were then isolated in outer membrane vesicles, or OMVs. Outer membrane vesicles from E. coli were purified as previously described (Hug and Feldman, 2011; Mashburn and Whiteley, 2005; Schertzer and Whiteley, 2012). In brief, E. coli strains were grown to stationary phase and pelleted. The cell supernatants were filtered using a 0.45 nm syringe filter and centrifuged at 346249×g for 1 h at 4° C. The pellet was resuspended in MV buffer (50 mM Tris pH=7.2, 5 mM NaCl, and 1 mM MgSO4) and centrifuged at 346249×g for 1 h at 15° C. The vesicles were then washed in MV buffer and protein concentration was quantified using Coomassie Plus (Bradford) assay (Thermo).
While most infectious agents express surface proteins that can be targeted in vaccines, most pathogens also express carbohydrates on their surface. Glycoconjugate vaccines, such as those to Streptococcus pneumoniae capsule can prevent bacterial infections (De Roux et al., 2008). Using the bacterial adjuvant system described in patent US20130230555 A1, a system was developed to directly conjugate carbohydrates to the core region of E. coli lipopolysaccharide (
The pQLinkN plasmids containing the various combinations of the lipid A modification genes lpxE, lpxF, lpxO, lpxR, pagL, and pagP as described in U.S. Patent Application Publication No. 2013/0230555 and Example 1 above were provided. Genes encoding the influenza hemagglutinin (HA) protein from Influenza strain A/PR/8/34 H1N1 (ACCESSION NP 040980.1 and NP 040981.1) and A/HK/03V6205/2003 H3N2 (ACCESSION EU502208 and EU516332.1) were introduced into these Lipid A modification enzyme encoding pQLinkN plasmids along with genes encoding Lpp signal sequence and OmpA polypeptides. See U.S. Pat. No. 5,348,867, which is hereby incorporated by reference in its entirety, for descriptions and sequences of the Lpp signal sequence and OmpA polypeptides.
More specifically, the genes encoding the above-described HA proteins were codon optimized by Genescript for optimal expression in E. coli. In order to target the conserved regions of the HA proteins, the genes included polypeptides encoding the HA2 domains for the H1N1 and H3N2 influenza viruses that were codon optimized by Genescript as previously described (Bommakanti et al., 2010; Bommakanti et al., 2012). The HA2 subunit of the hemagglutinin protein is well known to those of ordinary skill in the art as being created upon cleavage of hemagglutinin by cellular proteases. In some embodiments, a codon optimized polypeptide encoding amino acid residues 1-172 or 1-160 of HA2 is introduced into the pQLinkN plasmid. All genes were engineered with a 5′ EcoRI site, a 3′ BamHI site, and a C-terminal 6×-histidine tag.
After amplification of the coding sequences, DNA fragments were digested with EcoRI and BamHI and cloned into EcoRI- and BamHI-digested pTX101. Plasmid pTX101 is disclosed in U.S. Pat. No. 5,348,867, which is hereby incorporated by reference in its entirety. pTX101 fuses the target influenza protein to the C-terminus of an Lpp-OmpA protein fusion (Francisco et al., 1992). The tripartite fusion protein localizes to the E. coli outer membrane and surface displays the C-terminal influenza protein to the extracellular environment. The tripartite Lpp-OmpA-influenza protein coding sequence was amplified from pTX101 with primers that engineer 5′ BamHI and 3′ NotI restriction sites. Following the BamHI/NotI digestion, genes encoding the complete tripartite influenza fusion were cloned into BamHI/NotI-digested pQlinkN plasmid to allow expression from an IPTG-inducible promoter, resulting in co-expression of the Lipid A modification enzymes and the tripartite Lpp-OmpA-influenza protein.
These pQLinkN plasmids, which encode both the lipid A modification enzymes and the tripartite influenza fusion, were transformed into a W3110 E. coli strain mutated as follows. Deletions of pagP, lpxT and eptA resulted in a strain producing >95% of the prototypical, hexa-acylated bis-phosphorylated lipid A species (Needham et al., 2013). To increase production of outer membrane vesicles (OMVs), the gene Eck1763, which encodes the major outer membrane lipoprotein Lpp was also deleted from the E. coli genome. Deletion of the Lpp lipoprotein resulted in a 100- to 1000-fold increased production of OMVs in E. coli strains. E. coli W3110 gene deletions and antibiotic cassette removals were performed by P1 vir phage transduction using Keio mutants, as previously described (Baba et al., 2006; Touze et al., 2008). All Escherichia coli W3110 strains (mutated or wild-type) were grown from freezer stock on Luria-Bertani Broth (LB) or 2× Nutrient broth with 5 g/L of NaCl at 25° C., 30° C., or 37° C. and supplemented with 100 μg/mL ampicillin, 15 μg/mL chloramphenicol, or 30 μg/mL kanamycin when appropriate. When required, 50 μM-1 mM isopropyl β-D-1-thiogalactopyranoside (IPTG) was added as determined by TLC analysis of lipid A enzyme activity (Needham et al., 2013).
The above-described E. coli strain produced surface-exposed influenza proteins that were packaged into OMVs with the modified lipid A species. Outer membrane vesicles from E. coli were purified as previously described (Mashburn and Whiteley, 2005; Schertzer and Whiteley, 2012). In brief, E. coli strains were grown to stationary phase and pelleted. The cell supernatants were filtered using a 0.45 μm syringe filter and centrifuged at 346249×g for 1 h at 4° C. The pellet was resuspended in MV buffer (50 mM Tris pH=7.2, 5 mM NaCl, and 1 mM MgSO4) and centrifuged at 346249×g for 1 hour at 15° C. The vesicles were then washed in MV buffer and protein concentration was quantified using Coomassie Plus (Bradford) assay (Thermo).
Nonpathogenic E. coli have been engineered to co-produce lipid A adjuvants and either protein or carbohydrate antigens on the surface of the bacterial cell. These vaccine components can be purified from the bacteria as OMVs and used as vaccines. Influenza was used herein to demonstrate the efficacy of this system. As a model for the vaccine, the HA2 domain of influenza hemagglutinin protein was co-localized to the surface of the bacterial strain by fusing it with an N-terminal Lpp sorting sequence and an OmpA domain (
Either whole bacteria or purified OMVs were used to vaccinate eight week old mice on day 0 and boost on day 28. A subset of mice were used to collect serum before challenge and all other mice were challenged with a lethal dose of mouse-adapted H1N1 influenza virus on day 44. Animals were sacrificed seven days post infection and homogenized lung tissue was used to determine viral infectivity (
First, mice (n=5) were orally vaccinated with either PBS and whole E. coli that were producing the MPL adjuvant only or MPL and the HA2 expression construct. Upon sacrifice, titers indicted almost a 100-fold decrease in infectious viral load of the lungs suggesting that oral vaccination with whole bacteria could protect from influenza infection (
The weight of all mice groups was monitored for up to seventeen days post-challenge. The PBS and MLP-vaccinated groups rapidly lost weight and infection manifested as a ruffled coat, lethargy, and dehydration post challenge (
To engineer glycoprotein vaccines, acrA (cjj0390) and pglB (cjj1143) genetic coding sequences are amplified from Campylobacter jejuni 81-176 with BamHI and NotI sites and cloned into BamHI and NotI-digested pQlinkN for expression from an IPTG-inducible promoter (Scheich et al., 2007). A C-terminal 6×-histidine tag is engineered onto the acrA coding sequence. AcrA is an acceptor protein that is glycosylated by the ligase Pg1B in C. jejuni (Feldman et al., 2005). The two genes, acrA and pglB are linked into the same vector for co-expression as previously described (Scheich et al., 2007; Ihssen et al., 2010). The acrA and pglB genes and their IPTG-inducible promoters are then amplified from the pQlinkN-derived vector with SaII sites and cloned into SaII-digested pACYC184.
The V. cholerae O-antigen plasmid pPM1001 described in Example 1 above is then provided and both the pPM1001 plasmid and the pACYC184 plasmid containing acrA and pglB genes are transformed into an E. coli strain having the following characteristics: All E. coli W3110 strains are grown from freezer stock on Luria-Bertani Broth (LB) or 2× Nutrient broth with 5 g/L of NaCl at 25° C., 30° C., or 37° C. and supplemented with 100 μg/mL ampicillin, 15 μg/mL chloramphenicol, or 30 μg/mL kanamycin when appropriate. When required 50 μM-1 mM isopropyl β-D-1-thiogalactopyranoside (IPTG) is added as determined by TLC analysis of lipid A enzyme activity (Needham et al., 2013). For optimal expression of O-antigen/capsule genes in E. coli, either the rfbD gene (Eck2034) or the entire E. coli O-antigen biosynthetic genetic region from rfbB to wbbL (Eck2025-Eck2035) are chromosomally deleted by P1 vir phage transduction using Keio mutants or lambda red recombination, respectively (Baba et al., 2006; Touze et al., 2008). For production of all glycoprotein vaccines, efficient ligation of polysaccharides (O-antigen or capsule) onto an acceptor protein, called AcrA (Cjj0390) by the ligase Pg1B (Cjj1143) requires deletion of the E. coli gene encoding WaaL (Eck3612).
Once transformed into the E. coli as described above, the V. cholerae O-antigen plasmid pPM1001 is co-expressed with the pACYC-derived plasmid with IPTG to ligate the V. cholerae O-antigen onto the AcrA protein. AcrA glycoproteins are purified using Ni-affinity chromatography and size exclusion chromatography for use as glycoconjugate vaccines. A similar method is used to generate other O-antigen (S. typhimurium, Shigella) and capsule (S. pneumoniae, S. aureus) glycoprotein vaccines using their respective plasmids, which plasmids are described in the Examples above.
All of the methods disclosed and claimed herein can be made and executed without undue experimentation in light of the present disclosure. While the compositions and methods of this invention have been described in terms of preferred embodiments, it will be apparent to those of skill in the art that variations may be applied to the methods and in the steps or in the sequence of steps of the method described herein without departing from the concept, spirit and scope of the invention. More specifically, it will be apparent that certain agents which are both chemically and physiologically related may be substituted for the agents described herein while the same or similar results would be achieved. All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope and concept of the invention as defined by the appended claims.
The following references, to the extent that they provide exemplary procedural or other details supplementary to those set forth herein, are specifically incorporated herein by reference.
The present application claims the priority benefit of U.S. provisional application No. 62/000,254, filed May 19, 2014, the entire contents of which is incorporated herein by reference.
The invention was made with government support under Grant No. R01 A1076322 awarded by the National Institutes of Health. The government has certain rights in the invention.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2015/031325 | 5/18/2015 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62000254 | May 2014 | US |
