Patent Grant
11021521
In recent years, antibiotic-resistant Gram-negative bacterial species emerged in clinics and cause life-threatening infections that are effectively untreatable by antibiotic monotherapy. These species are intrinsically resistant to antibiotics, albeit to a varying degree, and gain further resistance when exposed to antibiotic treatments. The differences in antibiotic susceptibilities among Gram-negative bacteria are attributed to various factors including the presence of chromosomally encoded enzymes that modify antibiotics, mutations, and variations in activities or amounts of antibiotic targets. Additionally, in all Gram-negative species, the low permeability barrier of the outer membranes and multidrug efflux play key roles in resisting antibiotic challenges.
The outer membrane (OM) of Gram-negative bacteria is an asymmetric bilayer composed of lipopolysaccharides (LPS) in the outer leaflet and glycerophospholipids (PL) in the inner leaflet. The major features of the LPS structure, such as the presence of lipid A, the core and O-antigen chains, are conserved among various species while specific chemical structures vary broadly (
The inner membrane (IM) is relatively permeable for a majority of amphiphilic drug molecules. However, it contains multidrug efflux pumps responsible for active non-specific extrusion of toxic compounds from cells. Two types of efflux pumps operate and affect drug concentrations in different bacterial cell compartments. Some efflux transporters transport drugs across the IM and affect the cytoplasmic drug accumulation. Other transporters, such as those belonging to the Resistance-Nodulation-cell Division (RND) superfamily, associate with additional proteins located in the periplasm and in the OM and function as trans-envelope (across the two membranes) efflux pumps. These efflux pumps bind various substrates on the periplasmic side of the IM and translocate them across the OM into the external medium. Inactivation of trans-envelope efflux increases bacterial susceptibility to various antibiotics, whereas their overexpression is a recognized cause of the clinical antibiotic resistance. Studies that included such Gram-negative bacteria as Haemophilus influenzae, E. coli and P. aeruginosa, revealed that antibacterial activities of the very polar and low molecular weight (MW) compounds on one hand, and zwitterionic and high MW compounds on the other, tend to be the least affected by efflux pumps, suggesting that such compounds are poor substrates for multidrug transporters. In contrast, an increase in hydrophobicity was found to correlate with increased propensity of a compound to be a substrate of efflux pumps in studies of Salmonella typhimurium.
The exceptional efficiency of trans-envelope efflux pumps is the result of a complex interplay between the two opposing fluxes of drugs across the two membranes. The experimental data and kinetic modeling agree that Gram-negative cell envelopes serve to dramatically reduce the intracellular concentration of many antibiotics unless breached by either efflux inactivation or an increase in the transmembrane flux (Krishnamoorthy G, Wolloscheck D, Weeks J W, Croft C, Rybenkov V V, Zgurskaya H I. 2016, Breaking the Permeability Barrier of Escherichia coli by Controlled Hyperporination of the Outer Membrane. Antimicrob Agents Chemother 60:7372-7381; Nichols W W. 2017, Modeling the kinetics of the permeation of antibacterial agents into growing bacteria and its interplay with efflux. Antimicrob Agents Chemother doi:10.1128/AAC.02576-16). This synergistic character and effectiveness of cell envelopes create a major hurdle in the discovery and development of new therapeutics against Gram-negative pathogens. Significant efforts are presently directed at gaining a fundamental understanding of the permeability properties of the OM and at finding correlations between physicochemical properties of compounds and their permeation across cell envelopes. The task is complicated by difficulties in separation of contributions of diffusion and active efflux in antibacterial activities. Furthermore, heuristics established using model organisms, such as E. coli, tend to be poorly applicable to other Gram-negative bacteria and clinical isolates.
Several embodiments of the present disclosure are hereby illustrated in the appended drawings. It is to be noted however, that the appended drawings only illustrate several embodiments and are therefore not intended to be considered limiting of the scope of the present disclosure. The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.
Gram-negative bacteria are notoriously resistant to antibiotics, but the extent of the resistance varies broadly between species. Multidrug resistant strains of Gram-negative pathogens rapidly spread in clinics. Significant efforts worldwide are currently directed to finding the rules of permeation of antibiotics across two membrane envelopes of these bacteria. We have developed an approach that separates the contributions of active efflux and passive barrier in activities of antibiotics and thereby sidesteps many of the aforementioned difficulties (Krishnamoorthy et al., 2016, op cit.). In this approach, a modified FhuA siderophore uptake channel (EcPore) is expressed from the chromosome and used to create a plurality of large non-specific pores in the OM of E. coli. EcPore is large enough for a passage of small proteins and does not discriminate between compounds based on their hydrophilicity (Krishnamoorthy et al., 2016, op cit.).
In the present disclosure additional results regarding the permeability barriers of four Gram-negative species P. aeruginosa, Acinetobacter baumannii, Burkholderia cepacia and B. thailandensis are provided. These bacteria were chosen because they are difficult to treat clinically and differ significantly in antibiotic susceptibilities, the structure and composition of their OM and in the activities and repertoire of trans-envelope efflux pumps. Thus, they represent a diverse spectrum spanning the types of Gram-negative cell envelopes. We constructed hyperporinated P. aeruginosa and A. baumannii using EcPore. Hyperporinated strains of B. thailandensis and B. cepacia were constructed using a mutant OrbA protein. We analyzed the contributions of the OM permeability and intrinsic active efflux in antibacterial activities of antibiotics belonging to different classes in all strains. Antibacterial activities were then correlated with permeability barriers that differ in chemical structures and properties.
The present disclosure thus describes work wherein major differences in antibacterial activities that distinguish the permeability barriers of P. aeruginosa, A. baumannii, B. thailandensis and B. cepacia were identified. We unexpectedly found that synergistic interplays between active efflux pumps and passive barriers (the OM barrier) universally protect Gram-negative bacteria from structurally diverse antibiotics, even those previously thought to be privileged in efflux avoidance. We report that in significant human pathogens including Acinetobacter baumannii, Pseudomonas aeruginosa and Burkholderia spp, the differences in antibiotic resistance are largely defined by their penetration into the cell. For all tested antibiotics, the intracellular penetration was determined by a synergistic relationship between active efflux and the permeability barrier. We found that the outer membrane and efflux pumps select compounds based on distinct properties and together universally protect bacteria from structurally diverse antibiotics. Based on their permeation properties, antibiotics can be divided into four clusters. Within each cluster, antibiotics are characterized by their own sets of structural rules, which are defined by their interactions with the permeability barrier. The identified specificities in the permeability barriers can be used to design successful therapeutic strategies against antibiotic resistant pathogens.
The diversity of the outer membrane structures and efflux capacities included in this study broaden the diversity of antibiotics affected by active efflux and outer membrane barriers and define the clustering of antibiotics according to specific biological determinants such as requirement of specific porins in the OM, targeting the OM or specific recognition by efflux pumps. Despite the lack of apparent chemical similarities, antibiotics within each cluster are likely to share structural characteristics that are recognized by distinct permeability barriers. These characteristics define the rules of antibiotic permeation into Gram-negative bacteria.
Therefore, disclosed herein are novel bacterial mutants (i.e., mutants which are pore-modified and/or efflux-pump-modified) which have been sensitized, for example for drug discovery, drug screening, structure-activity relationships and development purposes. More particularly, the present disclosure includes embodiments of Gram-negative bacteria which have been sensitized to biologically active compounds by introducing modified nanopores in the outer membranes thereby modulating permeability properties of the outer membranes without compromising active efflux. The present disclosure also includes embodiments of Gram-negative bacteria which have been sensitized to biologically active compounds by introducing modified efflux pumps thereby modulating active efflux properties of the cells without compromising OM permeability. Other embodiments include Gram-negative bacteria which have been sensitized by introducing modified nanopores in the outer membranes thereby modulating permeability properties of the outer membranes and which include modified efflux pumps thereby modulating active efflux properties of the cells. Certain embodiments of the present disclosure are directed to P. aeruginosa, A. baumannii, B. thailandensis and B. cepacia strains, as well as other strains that are sensitized to antibiotics in a controlled manner due to increased rates of antibiotic uptake without compromising the active efflux and cell viability. This was carried out by inserting into bacterial chromosomes genes encoding modified protein nanopores. These nanopores can be produced in a tightly controlled manner so that the outer membranes of the bacterial cells have different total numbers of nanopores depending on the concentration of an inducer present in the external medium. In at least one non-limiting embodiment, the nanopore is OrbA ΔC/Δ4L, a genetically modified OrbA variant without its N-terminal plug (cork) domain and without four of its large external loops. These nanopores, when present in the outer membrane, remove restrictions on the size and physico-chemical properties of compounds that can penetrate the outer membrane without compromising drug efflux activities or physiological states of cells. We demonstrated the modulation of the outer membrane permeability by: (i) measuring changes in susceptibilities of bacterial cells with nanopores to antibiotics as a dependence on the concentration of an inducer; (ii) measuring accumulation of radioactive chemicals of different sizes and fluorescent probes in cells containing nanopores. Thus, described herein is the development of bacterial strains, in which permeation properties of the outer membrane and hence uptake of antibiotics and other molecules can be controlled.
The present patent application contains subject matter related to U. S. Provisional Patent Application Ser. No. 62/138,781, filed on Mar. 26, 2015, and to U.S. patent application Ser. No. 15/081,021, filed Mar. 25, 2016, the entire contents of which are hereby expressly incorporated herein by reference.
Before describing various embodiments of the present disclosure in more detail by way of exemplary description, examples, and results, it is to be understood that the present disclosure is not limited in application to the details of methods and compositions as set forth in the following description. As such, the language used herein is intended to be given the broadest possible scope and meaning; and the embodiments are meant to be exemplary, not exhaustive. Also, it is to be understood that the phraseology and terminology employed herein is for the purpose of description and should not be regarded as limiting unless otherwise indicated as so. Moreover, in the following detailed description, numerous specific details are set forth in order to provide a more thorough understanding of the disclosure. However, it will be apparent to a person having ordinary skill in the art that other embodiments of the inventive concepts may be practiced without these specific details. In other instances, features which are well known to persons of ordinary skill in the art have not been described in detail to avoid unnecessary complication of the description.
While the compositions and methods of the present disclosure have been described in terms of particular embodiments, it will be apparent to those of skill in the art that variations may be applied to the compositions and/or 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 inventive concepts. All such similar substitutes and modifications apparent to those of skilled in the art are deemed to be within the spirit, scope and concept of the present disclosure as described herein.
Unless otherwise defined herein, scientific and technical terms used in connection with the present disclosure shall have the meanings that are commonly understood by those having ordinary skill in the art. Further, unless otherwise required by context, singular terms shall include pluralities and plural terms shall include the singular. As utilized in accordance with the methods and compositions of the present disclosure, the following terms, unless otherwise indicated, shall be understood to have the following meanings:
The use of the word “a” or “an” when used in conjunction with the term “comprising” in the claims and/or the specification may mean “one,” but it is also consistent with the meaning of “one or more,” “at least one,” and “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 when the alternatives are mutually exclusive, although the disclosure supports a definition that refers to only alternatives and “and/or.” The use of the term “at least one” will be understood to include one as well as any quantity more than one, including but not limited to 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 30, 40, 50, 100, or any integer inclusive therein. The term “at least one” may extend up to 100 or 1000 or more, depending on the term to which it is attached; in addition, the quantities of 100/1000 are not to be considered limiting, as higher limits may also produce satisfactory results. In addition, the use of the term “at least one of X, Y and Z” will be understood to include X alone, Y alone, and Z alone, as well as any combination of X, Y and Z.
As used in this specification and claims, the words “comprising” (and any form of comprising, such as “comprise” and “comprises”), “having” (and any form of having, such as “have” and “has”), “including” (and any form of including, such as “includes” and “include”) or “containing” (and any form of containing, such as “contains” and “contain”) are inclusive or open-ended and do not exclude additional, unrecited elements or method steps.
The term “or combinations thereof” as used herein refers to all permutations and combinations of the listed items preceding the term. For example, “A, B, C, or combinations thereof” is intended to include at least one of: A, B, C, AB, AC, BC, or ABC, and if order is important in a particular context, also BA, CA, CB, CBA, BCA, ACB, BAC, or CAB. Continuing with this example, expressly included are combinations that contain repeats of one or more item or term, such as BB, AAA, AAB, BBC, AAABCCCC, CBBAAA, CABABB, and so forth. The skilled artisan will understand that typically there is no limit on the number of items or terms in any combination, unless otherwise apparent from the context.
Throughout this application, the term “about” is used to indicate that a value includes the inherent variation of error for the composition, the method used to administer the composition, or the variation that exists among the study objects. Further, in this detailed description and the appended claims, each numerical value (e.g., temperature or time) should be read once as modified by the term “about” (unless already expressly so modified), and then read again as not so modified unless otherwise indicated in context. As used herein, the term “substantially” means that the subsequently described event or circumstance completely occurs or that the subsequently described event or circumstance occurs to a great extent or degree. For example, the term “substantially” means that the subsequently described event or circumstance occurs at least 90% of the time, or at least 95% of the time, or at least 98% of the time.
Also, any range listed or described herein is intended to include, implicitly or explicitly, any number within the range, particularly all integers, including the end points, and is to be considered as having been so stated. For example, “a range from 1 to 10” is to be read as indicating each possible number, particularly integers, along the continuum between about 1 and about 10. Thus, even if specific data points within the range, or even no data points within the range, are explicitly identified or specifically referred to, it is to be understood that any data points within the range are to be considered to have been specified, and that the inventors possessed knowledge of the entire range and the points within the range.
As used herein, all numerical values or ranges include fractions of the values and integers within such ranges and fractions of the integers within such ranges unless the context clearly indicates otherwise. Thus, to illustrate, reference to a numerical range, such as 1-10 includes 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, as well as 1.1, 1.2, 1.3, 1.4, 1.5, etc., and so forth. Reference to a range of 1-50 therefore includes 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, etc., up to and including 50, as well as 1.1, 1.2, 1.3, 1.4, 1.5, etc., 2.1, 2.2, 2.3, 2.4, 2.5, etc., and so forth. Reference to an integer with more (greater) or less than includes any number greater or less than the reference number, respectively. Thus, for example, reference to less than 100 includes 99, 98, 97, etc. all the way down to the number one (1); and less than 10 includes 9, 8, 7, etc. all the way down to the number one (1). Reference to a series of ranges includes ranges which combine the values of the boundaries of different ranges within the series. Thus, to illustrate reference to a series of ranges, for example, of 1-10, 10-20, 20-30, 30-40, 40-50, 50-60, 60-75, 75-100, 100-150, 150-200, 200-250, 250-300, 300-400, 400-500, 500-750, 750-1,000, 1,000-1,500, 1,500-2,000, 2,000-2,500, 2,500-3,000, 3,000-3,500, 3,500-4,000, 4,000-4,500, 4,500-5,000, 5,500-6,000, 6,000-7,000, 7,000-8,000, or 8,000-9,000, includes ranges of 1-20, 10-50, 50-100, 100-1,000, 1,000-3,000, 2,000-4,000, etc.
As used herein any reference to “one embodiment” or “an embodiment” means that a particular element, feature, structure, or characteristic described in connection with the embodiment is included in at least one embodiment and may be included in other embodiments. The appearances of the phrase “in one embodiment” in various places in the specification are not necessarily all referring to the same embodiment and are not necessarily limited to a single or particular embodiment.
Specific amino acids may be referred to herein by the following designations: alanine: ala or A; arginine: arg or R; asparagine: asn or N; aspartic acid: asp or D; cysteine: cys or C; glutamic acid: glu or E; glutamine: gln or Q; glycine: gly or G; histidine: his or H; isoleucine: ile or I; leucine: leu or L; lysine: lys or K; methionine: met or M; phenylalanine: phe or F; proline: pro or P; serine: ser or S; threonine: thr or T; tryptophan: trp or W; tyrosine: tyr or Y; and valine: val or V.
For purposes of classifying amino acids substitutions as conservative or nonconservative, amino acids are grouped in one embodiment as follows: Group I (hydrophobic side chains): met, ala, val, leu, ile; Group II (neutral hydrophilic side chains): cys, ser, thr; Group III (acidic side chains): asp, glu; Group IV (basic side chains): asn, gln, his, lys, arg; Group V (residues influencing chain orientation): gly, pro; and Group VI (aromatic side chains): trp, tyr, phe. Conservative substitutions involve substitutions between amino acids in the same group. Nonconservative substitutions constitute exchanging a member of one of these groups for a member of another.
Tables of conservative amino acid substitutions have been constructed and are known in the art. In other embodiments, examples of interchangeable amino acids include, but are not limited to the following: arginine and lysine; glutamate and aspartate; serine and threonine; glutamine and asparagine; and valine, leucine and isoleucine. In other embodiments, the following substitutions can be made: Ala (A) by leu, ile, or val; Arg (R) by gln, asn, or lys; Asn (N) by his, asp, lys, arg, or gln; Asp (D) by asn, or glu; Cys (C) by ala, or ser; Gln (Q) by glu, or asn; Glu (E) by gln, or asp; Gly (G) by ala; His (H)by asn, gln, lys,or arg; Ile (I) by val, met, ala, phe, or leu; Leu (L) by val, met, ala, phe, or ile; Lys (K) by gln, asn, or arg; Met (M) by phe, ile, or leu; Phe (F) by leu, val, ile, ala, or tyr; Pro (P) by ala; Ser (S) by thr; Thr (T) by ser; Trp (W) by phe, or tyr; Tyr (Y) by trp, phe, thr, or ser; and Val (V) by ile, leu, met, phe, or ala.
Other considerations for amino acid substitutions include whether or not the residue is located in the interior of a protein or is solvent—(i.e., externally) exposed. For interior residues, conservative substitutions include for example: Asp and Asn; Ser and Thr; Ser and Ala; Thr and Ala; Ala and Gly; Ile and Val; Val and Leu; Leu and Ile; Leu and Met; Phe and Tyr; and Tyr and Trp. For solvent-exposed residues, conservative substitutions include for example: Asp and Asn; Asp and Glu; Glu and Gln; Glu and Ala; Gly and Asn; Ala and Pro; Ala and Gly; Ala and Ser; Ala and Lys; Ser and Thr; Lys and Arg; Val and Leu; Leu and Ile; Be and Val; and Phe and Tyr.
The term “nucleic acid” is well known in the art. A “nucleic acid” as used herein will generally refer to a molecule (i.e., a strand) of DNA, RNA or a derivative or analog thereof, comprising a nucleobase. A nucleobase includes, for example, a naturally-occurring purine or pyrimidine base found in DNA (e.g., an adenine “A,” a guanine “G,” a thymine “T” or a cytosine “C”) or RNA (e.g., an “A,” a “G,” a uracil “U” or a “C”). The term nucleobase also includes non-natural bases as described below. The term “nucleic acid” encompasses the terms “oligonucleotide” and “polynucleotide,” each as a subgenus of the term “nucleic acid.”
As used herein, the terms “complementary” or “complement” also refer to a nucleic acid comprising a sequence of consecutive nucleobases or semiconsecutive nucleobases (e.g., one or more nucleobase moieties are not present in the molecule) capable of hybridizing to another nucleic acid strand or duplex even if less than all the nucleobases do not base pair with a counterpart nucleobase. In certain embodiments, a “complementary” nucleic acid comprises a sequence in which about 70%, about 71%, about 72%, about 73%, about 74%, about 75%, about 76%, about 77%, about 77%, about 78%, about 79%, about 80%, about 81%, about 82%, about 83%, about 84%, about 85%, about 86%, about 87%, about 88%, about 89%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, about 99%, or about 100%, and any range derivable therein, of the nucleobase sequence is capable of base-pairing with a single or double stranded nucleic acid molecule during hybridization. In certain embodiments, the term “complementary” refers to a nucleic acid that may hybridize to another nucleic acid strand or duplex in stringent conditions, as would be understood by one of ordinary skill in the art.
The term “homologous” or “% identity” as used herein means a nucleic acid (or fragment thereof), or a protein (or a fragment thereof) having a degree of homology to the corresponding natural reference nucleic acid, or protein, that is at least 70%, or at least 75%, or at least 80%, or at least 85%, or at least 90%, or at least 91%, or at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% identical thereto. For example, in regard to peptides or polypeptides, the percentage of homology or identity as described herein is typically calculated as the percentage of amino acid residues found in the smaller of the two sequences which align with identical amino acid residues in the sequence being compared, when four gaps in a length of 100 amino acids may be introduced to assist in that alignment (as set forth by Dayhoff, in Atlas of Protein Sequence and Structure, Vol. 5, p. 124, National Biochemical Research Foundation, Washington, D.C. (1972)). In one embodiment, the percentage homology as described above is calculated as the percentage of the components found in the smaller of the two sequences that may also be found in the larger of the two sequences (with the introduction of gaps), with a component being defined as a sequence of four, contiguous amino acids. Also included as substantially homologous is any protein product which may be isolated by virtue of cross reactivity with antibodies to the native protein product. Sequence identity or homology can be determined by comparing the sequences when aligned so as to maximize overlap and identity while minimizing sequence gaps. In particular, sequence identity may be determined using any of a number of mathematical algorithms. A non-limiting example of a mathematical algorithm used for comparison of two sequences is the algorithm of Karlin & Altschul, Proc. Natl. Acad. Sci. USA 1990, 87, 2264-2268, modified as in Karlin & Altschul, Proc. Natl. Acad. Sci. USA 1993, 90, 5873-5877.
Percentage sequence identities can be determined with protein sequences maximally aligned by the Kabat numbering convention. After alignment, if a particular polypeptide region is being compared with the same region of a reference polypepetide, the percentage sequence identity between the subject and reference polypeptide region is the number of positions occupied by the same amino acid in both the subject and reference polypeptide region divided by the total number of aligned positions of the two regions, with gaps not counted, multiplied by 100 to convert to percentage.
In one embodiment “% identity” represents the number of amino acids which are identical at corresponding positions in two sequences of a protein having the same or similar activity. For example, two amino acid sequences each having 100 residues will have at least 90% identity when 90 of the amino acids at corresponding positions are the same. Similarly, in one embodiment “% identity” represents the number of nucleotides which are identical at corresponding positions in two sequences of a nucleic acid encoding the same or similar polypeptides. For example, two nucleic acid sequences each having 100 nucleotides will have 90% identity when 90 of the nucleotides in homologous positions are the same.
Another example of a mathematical algorithm used for comparison of sequences is the algorithm of Myers & Miller, CABIOS 1988, 4, 11-17. Such an algorithm is incorporated into the ALIGN program (version 2.0) which is part of the GCG sequence alignment software package. When utilizing the ALIGN program for comparing amino acid sequences, a PAM120 weight residue table, a gap length penalty of 12, and a gap penalty of 4 can be used. Yet another useful algorithm for identifying regions of local sequence similarity and alignment is the FASTA algorithm as described in Pearson & Lipman, Proc. Natl. Acad. Sci. USA 1988, 85, 2444-2448.
Another algorithm is the WU-BLAST (Washington University BLAST) version 2.0 software (WU-BLAST version 2.0 executable programs for several UNIX platforms). This program is based on WU-BLAST version 1.4, which in turn is based on the public domain NCBI-BLAST version 1.4 (Altschul & Gish, 1996, Local alignment statistics, Doolittle ed., Methods in Enzymology 266, 460-480; Altschul et al., Journal of Molecular Biology 1990, 215, 403-410; Gish & States, Nature Genetics, 1993, 3: 266-272; Karlin & Altschul, 1993, Proc. Natl. Acad. Sci. USA 90, 5873-5877; all of which are incorporated by reference herein).
In addition to those otherwise mentioned herein, mention is made also of the programs BLAST, gapped BLAST, BLASTN, BLASTP, and PSI-BLAST, provided by the National Center for Biotechnology Information. These programs are widely used in the art for this purpose and can align homologous regions of two amino acid sequences. In all search programs in the suite, the gapped alignment routines are integral to the database search itself. Gapping can be turned off if desired. The default penalty (Q) for a gap of length one is Q=9 for proteins and BLASTP, and Q=10 for BLASTN, but may be changed to any integer. The default per-residue penalty for extending a gap (R) is R=2 for proteins and BLASTP, and R=10 for BLASTN, but may be changed to any integer. Any combination of values for Q and R can be used in order to align sequences so as to maximize overlap and identity while minimizing sequence gaps. The default amino acid comparison matrix is BLOSUM62, but other amino acid comparison matrices such as PAM can be utilized.
As used herein, “hybridization,” “hybridizes” or “capable of hybridizing” is understood to mean the forming of a double or triple stranded molecule or a molecule with partial double or triple stranded nature. The term “anneal” as used herein is synonymous with “hybridize.” The term “hybridization,” “hybridize(s)” or “capable of hybridizing” encompasses the terms “stringent condition(s)” or “high stringency” and the terms “low stringency” or “low stringency condition(s).”
As used herein “stringent condition(s)” or “high stringency” are those conditions that allow hybridization between or within one or more nucleic acid strand(s) containing complementary sequence(s), but precludes hybridization of random sequences. Stringent conditions tolerate little, if any, mismatch between a nucleic acid and a target strand. Non-limiting applications include isolating a nucleic acid, such as a gene or a nucleic acid segment thereof, or detecting at least one specific mRNA transcript or a nucleic acid segment thereof, and the like. Stringent conditions may comprise low salt and/or high temperature conditions, such as provided by about 0.02 M to about 0.15 M NaCl at temperatures of about 50° C. to about 70° C. It is understood that the temperature and ionic strength of a desired stringency are determined in part by the length of the particular nucleic acid, the length and nucleobase content of the target sequence, the charge composition of the nucleic acid, and to the presence or concentration of formamide, tetramethylammonium chloride or other solvent in a hybridization mixture.
It is also understood that these ranges, compositions and conditions for hybridization are mentioned by way of non-limiting examples only, and that the desired stringency for a particular hybridization reaction is often determined empirically by comparison to one or more positive or negative controls. Depending on the application envisioned varying conditions of hybridization to achieve varying degrees of selectivity of a nucleic acid towards a target sequence are used. In a non-limiting example, identification or isolation of a related target nucleic acid that does not hybridize to a nucleic acid under stringent conditions may be achieved by hybridization at low temperature and/or high ionic strength. Such conditions are termed “low stringency” or “low stringency conditions,” and non-limiting examples of low stringency include hybridization performed at about 0.15 M to about 0.9 M NaCl at a temperature range of about 20° C. to about 50° C. Of course, it is within the skill of one in the art to further modify the low or high stringency conditions to suit a particular application.
Herein certain embodiments, a “gene” refers to a nucleic acid that is transcribed. In certain aspects, the gene includes regulatory sequences involved in transcription, or message production or composition. In particular embodiments, the gene comprises transcribed sequences that encode for a protein, polypeptide or peptide. As will be understood by those in the art, this function term “gene” includes both genomic sequences, RNA or cDNA sequences or smaller engineered nucleic acid segments, including nucleic acid segments of a non-transcribed part of a gene, including but not limited to the non-transcribed promoter or enhancer regions of a gene. Smaller engineered gene nucleic acid segments may express, or may be adapted to express using nucleic acid manipulation technology, proteins, polypeptides, domains, peptides, fusion proteins, mutants and/or such like.
Where used herein in reference to a bacterium, the term “mutant” is intended to refer to a bacterium comprising a mutation in a “wild-type” or parental bacterium. “Wild-type” refers to the typical form (genotype and/or phenotype) of a bacterium, gene, nucleic acid, or protein as it occurs in nature and/or is the most common form in a natural population. In reference to a gene or nucleic acid, the term “mutation” refers to a gene or nucleic acid comprising an alteration in the wild type, such as but not limited to, a nucleotide deletion, insertion, and/or substitution. A mutation in a gene or nucleic acid generally results in either inactivation, decrease in expression or activity, increase in expression or activity, or another altered property of the gene or nucleic acid in the mutant bacterium comprising the mutation. In reference to a protein, the term “mutation” refers to protein comprising an alteration in the wild type, such as but not limited to, one or more amino acid deletions, insertions, and/or substitutions. A mutation in a protein generally results in either inactivation, decrease in activity or effect, increase in activity or effect, or another altered property or effect of the protein in the mutant bacterium comprising the mutation. A mutant bacterium may comprise a gene or nucleic acid comprising a mutation. A mutant bacterium may also comprise a deletion of one or more entire genes, the deletion of the one or more genes comprising the mutation in the mutant bacterium. A mutant bacterium may also comprise an insertion of one or more additional genes, the insertion of the one or more additional genes comprising the mutation in the mutant bacterium. The additional one or more genes may be duplicates of a native gene already present in the wild-type bacterium, or may be non-native genes. A mutant bacterium may also comprise a substitution of one or more native genes by one or more non-native genes or mutated genes, the substitution comprising the mutation in the mutant bacterium.
Where used herein, the terms “hyperporinated” or “hyperporination” or “pore-modified” refer to bacterial mutants comprising genes encoding modified protein nanopores, e.g., a genetically modified OrbA nanopore, that result in increased cell outer membrane permeability in the mutant bacteria.
Where used herein, the term “efflux-proficient” refers to bacteria which comprise non-modified efflux pumps that function in a manner equal to or similar to the wild type efflux pump.
Where used herein, the term “efflux-deficient” refers to bacterial mutants (e.g., AbΔ3, PΔ3, ΔTolC and BtΔ2) which comprise genes encoding modified efflux pumps that have impaired active efflux activity as compared to the efflux-proficient pump of the wild type.
The novel constructed bacterial mutants and strains of the present disclosure can be used for example in methods comprising, but not limited to: (i) high-throughput screening programs to identify compounds with anti-bacterial activities; (ii) counter-screens to separate contributions of active efflux and uptake to a given compound cell permeation and accumulation; (iii) lead development efforts to build structure-activity relationships separately for active efflux and uptake for a given compound; (iv) improvement of the intracellular compound accumulation without inhibiting efflux; and (v) improvement of the intracellular compound accumulation by bypassing efflux pumps.
The sensitization/permeabilization methods of the present disclosure can be applied to all Gram-negative bacteria containing a typical outer membrane composed of lipids, lipopolysaccharides and porins, including but not limited to those shown below in Table 1, which is a list of clinically important human pathogens that are most commonly targeted in current drug discovery programs.
Several embodiments of the present disclosure, having now been generally described, will be more readily understood by reference to the following examples and embodiments, which are included merely for purposes of illustration, and are not intended to be limiting. The following detailed examples of the present disclosure are to be construed, as noted above, only as illustrative, and not as limitations of the embodiments described herein in any way whatsoever. Those skilled in the art will promptly recognize appropriate variations from the various compositions, structures, components, procedures and methods.
EXPERIMENTAL
Construction of Plasmids and Strains
Bacterial strains and plasmids used in this study are listed in Table 2.
P. aeruginosa PAO1
B. thailandensis E264
B. cepacia 25416
A. baumanii 17978
1
1
1
4
4
2
3
3
5
6
a Apr, Gmr, Telr, Tpr genes encoding resistance to ampicillin, gentamicin, tellurite, and trimethoprim, respectively.
b Plac, ParaBAD, PTAC, PrhaBAD, encode the E. coli lac, arabinose, lac/trp hybrid, and rhamnose promoters; P1 encodes the P1 integron promoter; PS12 encodes the B. thailandensis ribosomal protein S12 promoter; PCS12 encodes the B. cenocepacia rpsL promoter driving transcription of Telr or Tpr genes; Pλ encodes the λ repressor promoter.
1 Choi K-H, Schweizer H P. 2006. mini-Tn7 insertion in bacteria with single attTn7 sites: example Pseudomonas aeruginosa. Nat Protocols 1: 153-161.
2 Mohammad M M, Howard K R, Movileanu L. 2011. Redesign of a plugged beta-barrel membrane protein. J Biol Chem 286: 8000-13.
3 Tucker A T, Nowicki E M, Boll J M, Knauf G A, Burdis N C, Trent M S, Davies B W. 2014. Defining Gene-Phenotype Relationships in Acinetobacter baumannii through One-Step Chromosomal Gene Inactivation. mBio 5.
4 Krishnamoorthy G, Wolloscheck D, Weeks J W, Croft C, Rybenkov V V, Zgurskaya H I. 2016. Breaking the Permeability Barrier of Escherichia coli by Controlled Hyperporination of the Outer Membrane. Antimicrob Agents Chemother 60: 7372-7381.
5 Amin I M, Richmond G E, Sen P, Koh T H, Piddock L J, Chua K L. 2013. A method for generating marker-less gene deletions in multidrug-resistant Acinetobacter baumannii. BMC Microbiol 13: 158.
6 Damron F H, McKenney E S, Barbier M, Liechti G W, Schweizer H P, Goldberg J B. 2013. Construction of mobilizable mini-Tn7 vectors for bioluminescent detection of gram-negative bacteria and single-copy promoter lux reporter analysis. Appl Environ Microbiol 79: 4149-53.
P. aeruginosa (Pae) Strains
To construct pGK-LAC-fhuA ΔC/Δ4L (Gmr), the gene encoding FhuA ΔC/Δ4L (EcPore) was amplified from the pPR-IBA1-FhuA ΔC/Δ4L plasmid. The PCR product was ligated with the pUC18-mini-Tn7T-LAC suicide delivery vector restricted with SacI and KpnI enzymes and transformed into E. coli DH5α competent cells and plated on LB agar plates containing Gentamycin (30 μg/ml). The colonies were screened for the insertion of FhuA ΔC/Δ4L gene into the vector by restriction digest analysis.
Insertion of mini-Tn7T-LAC-FhuA ΔC/Δ4L (Gmr) onto the chromosome of P. aeruginosa PAO1 strain was achieved as described by Choi and Schweizer(1). Briefly, the suicide delivery vector carrying the fhuA ΔC/Δ4L gene and the helper plasmid pTNS3 were electroporated into PAO1 and PaΔ3 strains and grown for 1 h in LB medium containing 1 mM glucose. The cells were then plated onto LB agar containing gentamicin at 30 μg/ml (PAO1) or 15 μg/ml (PaΔ3) and incubated for 16 h at 37° C. Resulting colonies were selected and confirmed for the insertion by PCR using glmS down and glmS UP primers (see Table 3 in U.S. Provisional Patent Application Ser. No. 62/560,999).
B. thailandesis (Bt) and B. cepacia (Bc) Strains
The B. thailandensis orbA gene was modified to delete the coding sequence for the periplasmic cork domain and the four extracellular loops of OrbA protein. This synthetic (mutant) orbA (OrbA ΔC/Δ4L) gene was cloned into pUC57 between the SacI/HindIII sites. The DNA coding sequence (SEQ ID NO:1) for the OrbA mutant BtPore is shown in Table 3, this sequence includes the Thrombin cleavage site and a deca-histidine affinity tag. The amino acid sequence (SEQ ID NO:2) of the OrbA mutant BtPore protein is shown in Table 4. The mutant OrbA protein can be made without the Thrombin cleavage site or histidine affinity tag at the C-terminal end (e.g., see Table 5, SEQ ID NO:3), or with an alternate affinity tag which substitutes for the His tag of SEQ ID NO:2. A NcoI site was engineered to encode the Start Codon for cloning into pUC18T-mini-Tn7T-RHA, which encode optimized Shine-Dalgarno sequences in frame to their NcoI sites. To construct pUC18T-mini-Tn7T-Tp-RHA, the rhaRS-PrhaBAD promoter was amplified with primers RhaR NsiI REV and P-rhaBAD SpeI/NcoI REV (see Table 3 in U.S. Provisional Ser. No. 62/560,999). PCR product and pUC18T-miniTn7T-Tp were digested with NsiI/SpeI and ligated using T4 ligase, following manufacturer's protocols (NEB). The DNA sequence of the pUC18T-mini-Tn7-Tp-RHA-orbA plasmid encoding the BtPore protein is shown in Table 6 (SEQ ID NO:4). SEQ ID NO:4 includes the pUC18T-mini-Tn7-Tp core, a BtPore sequence, a Prha promoter for rhamnose-dependent expression of the BtPore sequence, and RhaR and RhaS sequences for rhamnose-dependent activation of the Prha promoter sequence. As noted, the BtPore-encoding plasmid could be constructed without a sequence for encoding an affinity tag in the BtPore protein.
Mini Tn7 cassettes were routinely integrated onto the chromosome of B. thailandensis or B. cepacia by tri-parental mating with recipient B. thailandensis or B. cepacia with the donors RHO3/pTNS3 and SM10λpir+ carrying pUC18T-based mini Tn7 cassettes. Mating was carried out by growing strains on LBA plates with appropriate selection markers. Overnight cultures were diluted, 1 to 100 for recipient and RHO3/pTNS3 or 1:20 for SM10λpir+ carrying pUC18T-based mini Tn7 cassettes, into fresh LB containing appropriate selection markers and grown at 37° C. to OD ˜0.2. Cells were collected by centrifugation at 3220×g for 20 min and gently resuspended in LB to concentrate 100×. 10 μl of each strain was mixed in a sterile centrifuge tube and 10 μl of tri-parental mixture was spotted and allowed to adsorb onto a dried LBA plate containing 0.3 mM diamino palmitic acid. Mating reactions were incubated at 37° C. for 16 hours. Spots were scraped off the LBA plates and resuspended in 500 μl of LB. 100 μl of resuspended mating reaction was plated onto LBA containing 25 μg/ml polymyxin B and 100 μg/ml trimethoprim. Integrants were screened by stable growth on LBA plates containing 25 μg/ml polymyxin B and 100 μg/ml trimethoprim for Bt and 10 μg/ml polymyxin B and 10 μg/ml trimethoprim, pigment production on LBA for B. cepacia, as well as PCR confirmation of integration into either or both attTn7 sites at gimS1 or glmS2.
A. baumannii (Ab)
A suicide vector harboring a tellurite-resistance marker pMo130-TelR was first created by inserting a gentamicin-resistance cassette to replace a kanamycin-resistance marker. To construct the suicide plasmid for deletion of efflux pumps, a 1 kb (for adeIJK) and 0.5 kb (for adeFGH and adeAB) DNA fragment located upstream and downstream of the efflux pump operons were amplified from genomic DNA. The constructed pIL118, pIL119 and pIL121 plasmids were used as templates to amplify ΔadeIJK::Gm, ΔadeFGH::Gm and ΔadeAB::Gm fragments, correspondingly.
The inactivation of adeIJK gene was done by cloning AadeIJK::Gm PCR product into pEX18Ap. The resulting plasmid construct pIL127 was first introduced into E. coli SM10λpir and subsequently delivered into A. baumannii by biparental conjugation. A. baumannii transconjugants (first crossovers) were selected on LB agar containing 30 μg/ml gentamicin and 100 μg/ml trimethoprim. During the second cross-over, mutants with gene deletion were selected for loss of sacB by passaging the first cross-over recombinants in LB agar containing 10% sucrose.
The inactivation of adeAB and adeFGH genes were done using RecAB as described in Nikaido H. 2003, Molecular basis of bacterial outer membrane permeability revisited. Microbiol Mol Biol Rev 67:593-656. We used electrocompetent cells at a density of 1010 CFU/reaction and 5 μg of PCR product with 0.5 kb of flanking homology. We obtained approximately 10-50 colonies from each transformation, depending on the gene being targeted for replacement. The gentamicin resistance cassette was removed by transformation of the pAT03 plasmid and activation of the FLP recombinase enzyme. Genomic deletions of the adeAB, adeFGH and adeIJK operons in the mutants were verified by comparing the PCR amplimers obtained from the wild type strain and corresponding pump gene deletion mutants.
Mini Tn7 cassettes were routinely integrated onto the chromosome of A. baumannii WT and AbΔ3 strains by tri-parental mating with recipient A. baumannii, RHO3/pTNS3, and SM10λpir+ carrying pTJ1 or pDW-araC-ParaBAD-fhuA ΔC/Δ4L (see Table 2). Mating was carried out by growing strains on LBA plates with appropriate selection markers. Overnight cultures were diluted, 1 to 100 for recipient and RHO3/pTNS3 or 1:20 for SM10λpir+ carrying pDW-araC-ParaBAD-fhuA ΔC/Δ4L, into fresh LB containing appropriate selection markers and grown at 37° C. to OD ˜0.5. Cells were collected by centrifugation at 4000×g for 20 min and gently resuspended in LB to concentrate 100×. 10 μl of each strain was mixed in a sterile centrifuge tube and 10 μl of tri-parental mixture was spotted and allowed to adsorb onto a dried LBA plate containing 0.3 mM diaminopimelic acid. Mating reactions were incubated at 37° C. for 16 hours. Spots were scraped off the LBA plates and resuspended in 500 μl of LB. 100 μl of resuspended mating reaction was plated onto LBA containing 100 μg/ml streptomycin and 100 μg/ml trimethoprim. Integrants were screened by stable growth on LBA plates containing 100 μg/ml streptomycin and 100 μg/ml trimethoprim. Resulting colonies were selected and confirmed for the insertion of EcPore by PCR. We also found that pTJ1-based plasmids used for the chromosomal integration in this and previous studies can self-replicate in this Abau strain (data not shown). This plasmid is also the reason for the β-lactam resistance of the constructed Abau strains (see Table 9). Primers used in the construction of plasmids are listed in Table 3 in U. S. Provisional Ser. No. 62/560,999.
Experimental Conditions
Luria-Bertani (LB) broth (10 g of Bacto tryptone, 5 g of yeast extract, and 5 g of NaCl per liter, pH 7.0) or LB agar (LB broth with 15 g of agar per liter) were used for bacterial growth. When indicated, cultures were induced with 0.1 mM isopropyl β-D-1-thiogalactopyranoside (IPTG), 1% L-arabinose, or 0.2% L-rhamnose to induce expression of “Pore” proteins. For selection, gentamicin (P. aeruginosa-30 μg/ml or 15 μg/ml, A. baumannii 30 μg/ml), trimethoprim (B. thailandensis, B. cepacia, E. coli and A. baumannii 100 μg/ml), tellurite (E. coli 10 μg/ml), ampicillin (100 μg/ml), carbenicillin (200 μg/ml), streptomycin (100 μg/ml) and polymyxin B (10 μg/ml or 25 μg/ml) were used. Susceptibility to different classes of antibiotics were determined by two-fold broth dilution method. (Krishnamoorthy et al., 2016, op cit.)
Uptake assay was performed in a temperature controlled micro-plate reader (TECAN SPARK 10 M multimode microplate reader) equipped with a sample injector, in fluorescence mode.(24) Cells from frozen stocks were inoculated into LB medium incubated for 16 h at 37° C. Cells were then sub-cultured into fresh 30 ml of LB medium and grown at 37° C. up to OD600-0.3. The cells were then induced with 0.1 mM IPTG or 0.2% rhamnose or 1% arabinose and grown until OD600 is 1.0, collected by centrifugation at 4,000 rpm for 40 min at room temperature and washed in 25 ml HEPES-KOH buffer 50 mM (pH 7.0) containing 1 mM magnesium sulfate and 0.4 mM glucose (HMG buffer). The cells in HMG buffer were adjusted to OD˜1.0 and kept at room temperature during the experiment. Fluorescence intensities from HT and NPN uptake experiments were plotted against time in Microsoft Excel and normalized to the emission before cells were added. The data was imported into MATLAB (MathWorks) to be fitted to a simple exponential equation in the form of F=A1+A2(1−exp(−kt)).
For protein analyses, membrane fractions were isolated from Pae or Bt or Bc cells by ultracentrifugation. Outer membrane fractions were enriched by solubilization of inner membrane proteins in buffer containing 50 mM Tris-HCl (pH 8.0), 150 mM NaCl, 1 mM PMSF, and 0.2% Triton X-100 and separated from the insoluble outer membrane fractions by ultracentrifugation. The resulting pellet was further solubilized in 50 mM Tris-HCl (pH 8.0), 150 mM NaCl, 1 mM PMSF, and 5.0% Triton X-100 followed by ultracentrifugation to remove insoluble components. The supernatant was incubated with His⋅Bind Resin (Novagen), which was previously charged with 50 mM CuSO4. The pore protein was eluted with 20 mM Tris-HCl (pH 8.0), 500 mM NaCl, 1 mM PMSF, 0.2% Triton X-100, and 400 mM imidazole. The eluted fractions were analyzed by 12% SDS-PAGE followed by immunoblotting with primary monoclonal anti-Histidine tag antibodies (Thermofisher Inc.) and a secondary alkaline phosphatase-conjugated anti-mouse antibody (Sigma). The 5-bromo4-chloro-3-indoyl phosphate (BCIP) and nitroblue tetrazolium (NBT) substrates were used to visualize the bands. The pore was quantified using the Quantity One software (Bio-Rad) with a His tagged P. aeruginosa protein TriC as a standard.
Hierarchical clustering was done using Matlab Statistics toolbox using unweighted average euclidean distances between logarithms of measured MIC ratios. Principle component analysis (PCA) revealed that the first two components describe the effect of hyperporination and active efflux and are responsible for 77% of the overall variance, 93% for four components (Table 10). The coordinates of the PCA vectors are shown in Table 10 together with the percent explained variance for each vector. The R-squared index analysis suggested the existence of three clusters in the distribution. PCA coordinates were then fit to a Gaussian mixture model using expectation maximization (EM) algorithm. Both the hierarchical and EM algorithms produced the same separation of data into clusters, which did not change upon the removal of up to 20% of constituent points from each cluster.
Results
Hyperporination of the outer membrane is well tolerated by various species.
Contributions of the diffusion barrier and active efflux in antibacterial activities can be separated by inserting a large non-specific pore into the OM to allow unrestricted influx of antibiotics (Krishnamoorthy et al., 2016, op cit.). To construct certain hyperporinated strains, the gene encoding the recombinant EcPore (FhuA ΔC/Δ4L) was integrated onto the chromosomes of P. aeruginosa PAO1 (Pae), A. baumannii ATCC17978 (Abau), B. thailandensis E264 (Bt) and B. cepacia ATCC25416 (Bc) (Table 2). As negative controls, empty expression cassettes were integrated into respective strains as well. Herein and hereinbelow, the names of the strains comprise the strain abbreviation followed by the inducible promoter used for the induction (ARA for arabinose, LAC for IPTG and RHA for rhamnose) and the name of the pore, if present. Genetic tests, the hypersusceptibility to the OM-impermeable antibiotic vancomycin and immunoblotting analyses confirmed the successful integration onto chromosomes and the inducer-dependent expression of the protein in PAO1-LAC-EcPore and Ab-ARA-EcPore (
We next designed a pore (BtPore) using the OrbA siderophore uptake channel (Sokol P A, Darling P, Lewenza S, Corbett C R, Kooi C D. 2000, Identification of a Siderophore Receptor Required for Ferric Ornibactin Uptake in Burkholderia cepacia Infection and Immunity 68:6554-6560.) from Bt as a template. To improve the expression, a synthetic gene encoding BtPore protein was cloned downstream of the rhamnose-inducible promoter (RHA). Genetic tests showed that the gene encoding BtPore was integrated into gimS sites present on the Bt (Bt-RHA-BtPore) and Bc (Bc-RHA-BtPore) chromosomes. The protein was expressed in a rhamnose-dependent manner, was localized to the OM fractions and enabled vancomycin-dependent killing of cells (
The genes encoding EcPore and BtPore were further integrated onto the chromosomes of efflux-deficient variants of Pae, Abau and Bt, correspondingly. PaΔ3-LAC and PaΔ3-LAC-EcPore cells are deficient in mexAB, mexCD and mexXY, the inner membrane components of the major RND pumps of this species. BtΔ2-RHA and BtΔ2-RHA-BtPore strains lack the two RND type pumps AmrAB-OpmA and BpeAB-OpmB that were previously reported to be constitutively expressed and to contribute to the intrinsic antibiotic resistance in Burkholderia spp. To analyze the role of efflux in Abau, we constructed an isogenic strain AbΔ3 lacking AdeIJK, AdeAB and AdeFGH, the three characterized RND efflux pumps of this species. For all constructed strains (Table 2), incubation of cells in the presence of respective inducers did not affect growth rates or cell densities suggesting that hyperporination of all four species and their efflux-deficient strains does not result in significant growth defects (
Intracellular Accumulation of Fluorescent Probes is defined by Differences in Permeability Barriers.
Active efflux is effective because drugs are expelled across the low permeability barrier of the OM. Hence, increased influx across the OM could significantly diminish or even obliterate the contribution of active efflux. On the other hand, inactivation of efflux is expected to completely eliminate the permeability barrier in non-growing cells, because the outer membrane slows down but does not prevent the diffusion. To analyze the interplay between passive influx and active efflux in permeation of compounds and to establish whether hyperporination affects diverse species in the same manner, we measured kinetics of intracellular accumulation of two fluorescent probes Hoechst 33342 (HT) and N-phenyl-1-naphthylamine (NPN). The two probes are known substrates of bacterial efflux pumps, but have different physicochemical properties and intracellular binding sites. HT is an inhibitor of DNA topoisomerases with MICs in a low micromolar range in efflux-deficient strains (Tables 7-9). The fluorescence of water-soluble HT is significantly enhanced when the compound is bound to lipids and DNA. NPN is a lipophilic, non-toxic compound, which is fluorescent when bound to biological membranes.
In these experiments, induced cells were suspended in buffered glucose solution, supplemented with either HT or NPN. In all four species, the overall kinetics of HT accumulation was similar (
Inactivation of efflux led to a smaller, up to 2-fold increase of intracellular HT accumulation in Bt and Abau, whereas PΔ3-LAC cells accumulated HT at the levels lower than those in the parent PAO1-LAC. Thus, inactivation of efflux and hyperporination have different effects on the penetration of HT across the cell envelope. However, in all species, efflux-deficient hyperporinated cells accumulated the highest amounts of HT and were the most susceptible to the antibacterial activity of HT with MICs at 25-50 nM in AbΔ3-ARA-EcPore and 0.5 M and 2.0 μM in BtΔ2-RHA-BtPore and PΔ3-LAC-EcPore, respectively.
Thus, in all species, active efflux remains functional in hyperporinated cells and reduces intracellular accumulation of HT despite increased influx of the probe across the outer membrane. At the same time, inactivation of efflux reduces the permeability barrier only partially and the slow uptake across the outer membrane defines the rates of penetration. The changes in rates of uptake in hyperporinated cells without active efflux appear to be different from the uptake rates in cells either producing the pore or lacking efflux pumps, suggesting synergistic relationships. The exact changes in MICs of HT could be calculated only in the case of Abau (Table 9). Impressively, inactivation of efflux in Abau reduces the MIC of HT by 32 fold, hyperporination by 8 fold, whereas AbΔ3-ARA-EcPore are 1000-fold more susceptible to HT than Ab-ARA. Thus, the effect of the active efflux and the permeability barrier on the HT uptake and its antibacterial activity is synergistic.
The results described above also show that the effect of hyperporination and efflux inactivation on HT accumulation is species-specific, as can also be seen in accumulation of NPN, a membrane-binding dye (
Taken together, these results show that the four Gram-negative species are protected by permeability barriers that differ significantly in their properties. Either hyperporination or efflux inactivation lead to species-specific changes in the kinetics of intracellular accumulation of fluorescent probes. The interplay between active efflux and the permeability barrier of the OM generate strong synergistic effects.
Synergism of Active Efflux and Passive Uptake in Antibacterial Activities.
The results described above show that hyperporination and efflux inactivation have different effects on compound accumulation and that these effects are also specific to bacterial species. We next analyzed interplay between active efflux and transmembrane diffusion in antibacterial activities of compounds with widely diverse physicochemical properties and mechanisms of action. We found that antibacterial activities of all tested antibiotics were affected in a species-specific manner by efflux inactivation, hyperporination or both (Tables 7-9).
aAt least three independent measurements
aAt least three independent measurements
MIC ratios of parental and either efflux-deficient or hyperporinated cells, were calculated as appropriate. When grouped according to the effects of efflux inactivation (efflux ratios) and hyperporination (OM ratios), the MIC ratios displayed broad, species- and antibiotic-dependent variations (
To reveal potentially hidden features in the accumulated data, we performed cluster analysis of the measured ratios. These analyses also included the MIC ratios determined previously in efflux-deficient and hyperporinated E. coli strains (Krishnamoorthy et al., 2016, op cit.). Strikingly, the tested antibiotics separated into several groups, which could be seen both in linkage analysis (
The four clusters of antibiotics revealed by distance analysis were as follows. Group 1 comprises antibiotics that are strongly potentiated by hyperporination but not efflux inactivation in all species with the exception Bt that will be discussed below. This group includes vancomycin, bacitracin and rifampicin, as well as some beta-lactams (
Group 2 includes antibiotics, the antibacterial activities of which are strongly affected by both efflux inactivation and hyperporination. The Group 2 antibiotics are macrolides erythromycin and azithromycin, novobiocin, cloxacillin and zeocin (
Group 3 antibiotics were modestly affected by efflux or porination. This group comprises fluoroquinolones, tetracycline and chloramphenicol as well as polycationic aminoglycosides and polymyxin. These antibiotics either have small efflux and OM ratios, because they are able to penetrate permeability barriers of all species by avoiding efflux and diffusing across the OMs, or because they target the OM itself by binding and disintegrating the OMs in susceptible species. We found accordingly that neither inactivation of efflux nor hyperporination of OM, separately and combined, only weakly affected the bacterial susceptibilities to these antibiotics (Tables 7-9).
Finally, Group 4 was represented by only one antibiotic, triclosan, which uniquely showed a strong effect of efflux inactivation in all tested bacteria and a moderate effect of hyperporination. In general, a single point would not qualify to be called a cluster. However, triclosan (i) is well outside of the other three clusters, (ii) displays unique pattern of behavior, and (iii) is the furthest away from the rest of antibiotics on the clustering dendrogram. Analyses of a wider range of compounds will likely identify other members of this group. Thus, the found clusters produced clearly discernible patterns in respect to effects of efflux inactivation and hyperporination.
Clusterization based on, separately, the effects of the pore (
Notably, the found clusters were broadly distributed across the physicochemical space of the tested antibiotics (
Discussion
In the present work we analyzed contributions of the OM permeability and active efflux in the intracellular accumulation and antibacterial activities in four divergent bacterial species. We found that Pae, Abau, Bt and Bc differ significantly from each other in specificities and capacities of their active efflux pumps and how these pumps interact with the OM barriers. As seen from the increased accumulation of fluorescent probes (
First, in agreement with intracellular accumulation experiments, the effects of efflux and OM on antibacterial activities cluster separately, indicating that these two barriers affect antibiotics independently from each other, and hence, are mechanistically unrelated (
The mechanistic separation between efflux and OM effects is apparent despite significant interspecies differences in the structures of OMs and specificities of efflux pumps. The overall structural organization of all Gram-negative OMs is thought to be similar and comprises an asymmetric bilayer of LPS-phospholipids with general and specific porins and channels embedded into it. Undoubtedly, structural features and variability of both lipids and proteins of OMs contribute to antibiotic permeation. The Pae lipid A is structurally the closest to that of E. coli (
RND pumps are the major contributors to intrinsic and clinical antibiotic resistance in Gram-negative bacteria and are effective against a broad range of structurally unrelated compounds. We unexpectedly found that the functions of RND pumps universally affect activities of all tested antibiotics, even those previously considered to be outside of the efflux recognition space. The effect of efflux on large antibiotics could not be assessed before, because such antibiotics as zeocin, bacitracin or vancomycin penetrate the OM too slowly and do not accumulate significantly in cells. However, hyperporination enabled penetration of these large antibiotics into periplasm and their active efflux. These results demonstrate that the chemical space affected by active efflux is much broader than previously thought and that the size of a compound is not a predictive characteristic of an efflux substrate. This result has further implications for the mechanism of efflux pumps, as the substrate binding sites and tunnels of transporters must be able to accommodate significantly larger than previously thought substrates.
There are also significant species-specific efflux effects. The efflux contribution in Abau is largely defined by the activity of AdeIJK, the major constitutively expressed efflux pump of this species. Although the strains used in this study are susceptible to most of the antibiotics, Abau is notorious for rapid development of multidrug resistance in clinical settings. Overproduction of AdeABC efflux system is observed with a high incidence in multidrug-resistant Abau isolates and results in increased resistance to several antibiotics of choice for the treatment of infections caused by this nosocomial pathogen. Our results predict that the overexpression of these pumps must be very efficient, in order to compensate for the “leaky” OM of Abau and provide antibiotic resistance. MexAB-OprM is the major efflux pump of Pae with broad substrate specificity and likely to be responsible for the observed efflux effects (Table 7). MexCD-OprJ and MexXY-OprM also lacking in PΔ3 strain, are commonly overproduced in clinical isolates. While inactivation of efflux made Pae hypersusceptible to various antibiotics, the OM of PΔ3 became less permeable to fluorescent probes, as seen from the reduced initial rates of HT uptake (
Bc and Bt differ dramatically from each other and other species in their efflux capacities. Our results further suggest that even the limited, 3-4 pores per cell (
It will be understood from the foregoing description that various modifications and changes may be made in the various embodiments of the present disclosure without departing from their true spirit. The description provided herein is intended for purposes of illustration only and is not intended to be construed in a limiting sense. Thus, while the present disclosure has been described herein in connection with certain embodiments so that aspects thereof may be more fully understood and appreciated, it is not intended that the present disclosure be limited to these particular embodiments. On the contrary, it is intended that all alternatives, modifications and equivalents are included within the scope of the present disclosure as defined herein. Thus the examples described above, which include particular embodiments, will serve to illustrate the practice of the present disclosure, it being understood that the particulars shown are by way of example and for purposes of illustrative discussion of particular embodiments of the present disclosure only and are presented in the cause of providing what is believed to be a useful and readily understood description of procedures as well as of the principles and conceptual aspects of the inventive concepts. Changes may be made in the formulation of the various components and compositions described herein, the methods described herein or in the steps or the sequence of steps of the methods described herein without departing from the spirit and scope of the present disclosure.
All patents, published patent applications, and non-patent publications referenced in any portion of this application are herein expressly incorporated by reference in their entirety to the same extent as if each individual patent or publication was specifically and individually indicated to be incorporated by reference.
The present patent application is a continuation-in-part of U.S. patent application Ser. No. 15/081,021, filed Mar. 25, 2016, which claims priority to U.S. Provisional Patent Application U.S. Ser. No. 62/138,781, filed on Mar. 26, 2015. The present patent application also claims priority to U.S. Provisional Patent Application U.S. Ser. No. 62/560,999, filed on Sep. 20, 2017. The entire contents of each of said applications is hereby expressly incorporated herein by reference.
This invention was made with government support under Grant number HDTRA1-14-1-0019-P00002 awarded by the Defense Threat Reduction Agency of the Department of Defense. The government has certain rights in the invention.
| Number | Name | Date | Kind |
|---|---|---|---|
| 8916684 | Movileanu et al. | Dec 2014 | B2 |
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| Number | Date | Country | |
|---|---|---|---|
| 20190002508 A1 | Jan 2019 | US |
| Number | Date | Country | |
|---|---|---|---|
| 62138781 | Mar 2015 | US | |
| 62560999 | Sep 2017 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 15081021 | Mar 2016 | US |
| Child | 16134696 | US |
