1 Introduction
Since the original discovery of bacteriophages by William Twort in 1915, and Félix d'Hérelle in 1917, there have been numerous reports describing the use of these “filterable viruses” in phage therapy, and interest in this area continues to grow as the frequency of human infections with multidrug resistant bacteria escalates. In addition, a growing list of significant historic moments in science were only made possible through the study of phages. These achievements include the first demonstration that DNA is the genetic material [leading to the Nobel Prize in Physiology or Medicine in 1969 (Hershey and Chase, )]; the first SDS-PAGE separating phage T4 proteins performed by Laemmli [and among the top 10 most cited papers of all time (Laemmli, )]; the first DNA sequencing ever to be performed by Sanger on the phage φX174 genome [and leading to his second Nobel Prize in Chemistry in 1980 (Sanger et al., 1977)]; the first isolation of a bacterial restriction enzyme capable of cleaving phage T7 DNA [and a joint Nobel Prize in Physiology or Medicine in 1978 (Smith and Wilcox, 1970)]; and the first description of gene editing through the use of a phage defense mechanism known as CRISPR/Cas9 [and again a Nobel Prize in Chemistry in 2023 (Barrangou et al., ; Jinek et al., )]. These and several additional studies have emerged demonstrating that phages are an invaluable resource to scientists and that their individual components have a plethora of functions beyond the usage of intact phages for bacterial therapy and gene transduction [for an excellent review, see Salmond and Fineran (2015)]; although new applications for phages even in gene cloning and expression have emerged through the discovery of phage N15's ability to deliver linearized vectors into bacteria, and now also engineered for use in eukaryotic cells (Wong et al., 2023). Additional phage applications include the use of their receptor binding proteins for bacterial detection, or engineering intact phages for bacterial viability reporting [using phage cocktails or synthetic approaches to expand host ranges (Sun et al., 2023)], and even uses in tumor detection, targeted therapeutic delivery (Shen et al., 2023), or reducing cancer progression (Sanmukh et al., 2021a,b); the exploitation of filamentous phages for phage display (Franca et al., ) traditionally for antibody screening and more recently for antibacterial development (Zhao et al., 2023); exogenous addition of phage endolysins (Fischetti, ; Cahill and Young, ; Abdelrahman et al., ) as a method for killing of Gram-positive (Mursalin et al., ), and more recently, Gram-negative microbes (Gondil et al., ) [together with outer membrane permeabilizers (Kocot et al., )]; phage-based vaccines (more on this below) (Palma, 2023); and the use of phage depolymerases as adjuvant therapy to disperse microbial biofilms (Topka-Bielecka et al., 2021). Bacteria have also retained phage proteins such as their toxins (typically in lysogenic conversion) to help with dissemination (Kumar et al., ), or permanently adapted phage tail-like structures in Type VI secretions systems for injection of toxic effectors into eukaryotic or bacterial hosts (Leiman et al., ), or co-opted holins coupled with cell-wall editing enzymes in Type X secretion systems (Palmer et al., 2021).
In this opinion article, I will discuss re-emerging trends to exploit phages for glyco-tool discovery, glycan display and vaccine development. Although phage display was first described in 1985 by George Winter (who subsequently received the Nobel Prize together with Gregory Smith in 2018), the use of phages to display sugars, either linked enzymatically or chemically, is more recent. Also, since phages are genetically tractable and three-dimensional, they provide many advantages that inert glycan arrays cannot provide. Similarly, one of the first reports of antibody Fab binding to a carbohydrate, the Salmonella O-antigen oligosaccharide, was published in the seminal paper by Cygler et al. () and phage display was subsequently used to select for the infamous carbohydrate-binding monoclonal antibody Se155-4 (Deng et al., ). It was 6 years later that the same O-antigen was crystallized with the Salmonella phage P22 tailspike protein (TSP), a protein that also possessed endoglycosidase activity (Steinbacher et al., 1997). However, this was not the first report of a phage polysaccharide depolymerase, these activities were already described in the 1950s (Maxted, ; Adams and Park, ). Both phage binding to carbohydrates and hydrolase/lyase activities have been described on an individual lectin/enzyme basis, similar to the P22 TSP example given above. However, functional assays for screening for broad phage activities within a population or data mining through genome databases is only now being considered.
2 A bottomless toolbox for glycobiologists
I recently attempted to summarize the complexity in the composition of bacterial surface glycans in Gram-negative, Gram-positive and acid-fast microbes, like Mycobacterium tuberculosis (Szymanski, 2022). I subsequently used Campylobacter jejuni as the model to emphasize that each bacterial strain within this Gram-negative species possesses separate pathways for the biosynthesis of several glycoconjugate structures including N- and O-linked glycoproteins, capsular polysaccharides (CPS) and lipooligosaccharides (Szymanski, 2022). In addition, the set of enzymes required for synthesis of the three latter conjugates differs from strain to strain resulting in different carbohydrate structures and serotypes; and even within a single strain, many of the enzymes can vary in expression (on or off) leading to the possibility of one in >1,000 different glycan compositions (for CPS alone) on each individual cell. Now considering that (1) NMR has been used to solve glycoconjugate structures for a miniscule number of bacterial strains to inform our understanding of the vastness of unique monosaccharides that the domain of Bacteria are capable of synthesizing, and (2) phages predominantly express receptor binding proteins recognizing specific bacterial surface glycan structures and glycoside hydrolases/lyases capable of degrading polysaccharides in order to gain access to the bacterial cell surface (Simpson et al., 2015), it is obvious to conclude that the estimated 1031 phages on Earth (Mushegian, ) provide an enormous repertoire for discovering proteins (glyco-tools) involved in glycan binding and degradation as a consequence of this evolutionary arms race (Figure 1A). However, the possibilities do not end with simply the identification of novel lectins and enzymatic functions [now also including glycosyltransferases modifying capsids and tail tubes (Freeman et al., )], since many enzymes can also be manipulated to maintain the lectin binding domain while inactivating the enzymatic activity, or optimized through methods such as phage display to exhibit improved activity. This would provide the scientific community with a limitless number of reagents for bacterial glycan labeling and structural characterization to better define the carbohydrate receptors necessary for phage therapy and enable researchers to screen pathogenic isolates to assess the conservation of specific glycan structures for glycoconjugate vaccine design.
Figure 1
Furthermore, phage genomes are not static, but rather quick to acquire new mutations and recombination events and are capable of also adapting to bind to human glycans, such as fucosylated mucins, when coevolved together with the bacterial host and gut-on-a-chip environment (Chin et al., ). The binding of human glycans was also observed by Green et al. when they demonstrated that the phage tail fiber could bind to human heparan sulfate proteoglycans co-localizing the phage to the epithelial cell surface in proximity to the Escherichia coli bacterial host (Figure 1A). The authors concluded that their new findings provide the opportunity to target phages to mucosal surfaces to selectively remove pathogens from these sites (Green et al., ). It will also be interesting to explore whether the phage expresses two different phage tail fibers with different carbohydrate specificities, or whether these fibers possess two separate glycan binding sites, similar to the CTX-phage encoded cholera toxin B-subunit (Heim et al., ). These observations further expand the toolbox to include reagents of value for eukaryotic glycobiologists alike.
3 Phage glycan display
Phages can serve as templates for glycan display to allow for screening of scrambled protein sequons permissible for glycosyltransferase recognition (Durr et al., ), or to rapidly screen for genetically altered transferases capable of protein modification. More recently, phages have been used for density-controlled, multivalent display of varying glycan structures, as an alternative to glycan arrays, to screen glycan binding interactions (Sojitra et al., 2021; Lin et al., ). To accomplish this, genetically bar-coded M13 filamentous phages are chemically functionalized with different glycan structures in a process known as LiGA (for liquid glycan array, shown in Figure 1B in comparison to more commonly used glycan arrays). Incubation with a cocktail of phages, each displaying a different carbohydrate structure, allows investigators to characterize glycan binding preferences of purified proteins, or glycan recognition by adhesins on specific cell types, or glycan enrichment correlated with known organ functions in mouse models (Sojitra et al., 2021; Lin et al., ). Another application of this method would be to investigate bacterial binding to various glycan structures which very few laboratories have been able to assess through the use of standard glycan arrays (Day et al., ; Semchenko et al., 2019; Sanchez et al., 2023).
4 Vaccine development—Manipulation of nucleobases
Many researchers have shown that the successful breakthrough in the use of mRNA vaccines to treat SARS CoV-2 viral infections hinged on the use of the modified nucleobase, N1-methyl-pseudouridine (Morais et al., ; Nance and Meier, ). And Karikó and Weissman subsequently received the Nobel Prize in Physiology or Medicine in 2023 for demonstrating the benefits of this modified nucleoside base in protein expression and immune recognition (Karikó et al., ). The application of this new mRNA vaccine platform and the encapsulation into lipid nanoparticles (see below), has caused an explosion in vaccine development targeting a number of infectious agents, and phages may provide new alternatives for the biopharmaceutical industries. For example, there are currently 40 DNA and 150 RNA modifications known, and many of these are found in phages (Nielsen et al., ). Furthermore, we and others have identified several new single-stranded (ss)RNA and double-stranded (ds)RNA phages and their RNA compositions have yet to be explored (Crippen et al., ; Thongchol et al., 2023). Also, some phages, including the C. jejuni Firehammervirus phages, possess mechanisms to precisely exchange canonical nucleotides with non-canonical nucleotides with 100% efficiency into an existing DNA strand (Crippen et al., ). Such enzymes would have great utility in creating novel DNA/RNA templates for functional studies and potentially engineering mRNA vaccines against a variety of pathogens more efficiently and/or with novel properties.
5 Vaccine development—Self-assembling lipid nanoparticles
Pseudomonas syringae phage ϕ6 was the first enveloped dsRNA Cystovirus identified more than 50 years ago (Gottlieb and Alimova, ) and has served as the model phage to understand phage RNA biosynthesis, packaging and host lipid bilayer recruitment. Reminiscent of eukaryotic viruses, the phages use protein-triggered membrane fusion for entry into their bacterial hosts (Bamford et al., ) and the phages exit surrounded by host phospholipid bilayers from the inner membrane (Heymann, ). These envelopes are generated through the insertion of one specific phage protein (that must be expressed together with its chaperone) and vesicles of similar buoyant density as ϕ6 phospholipid precursors can be generated independently through the sole expression of these proteins (Johnson and Mindich, ). More recently, P. aeruginosa enveloped RNA viruses were discovered (Yang et al., 2016; Antonova et al., ), followed by similar viruses described by our group targeting Acinetobacter radioresistens (Crippen et al., ). Not only is the mechanism of membrane acquisition and assembly around the RNA-core require further elucidation for these Cystoviruses (Sun et al., 2017), but it is currently unknown whether the glycolipid intermediates normally assembled on the bacterial inner membrane are being excluded or whether the bacterial membranes can be manipulated to include specific glycans to target immune cell receptors or to include glycan antigens of interest (Crippen et al., ) (Figure 1C). It would be interesting to determine whether naturally enveloped phages such as those described for Pseudomonas, and more recently for Acinetobacter, can be engineered to form self-assembling lipid nanoparticles displaying specific bacterial polysaccharides (Figure 1C). This would be reminiscent of glycoconjugate expressing outer membrane vesicles (OMVs) that have been successfully used in many studies (Dull and McIntosh, ; Sinha et al., 2015; Chen et al., ; Liu et al., ; Price et al., 2016; Banerjee et al., ). There would be several added advantages to using the enveloped phages including the presence of a phospholipid bilayer rather than the use of an endotoxin containing outer membrane, homogeneous particle sizes, facile generation of particles from bacterial fermentor growth, etc. Similarly, these lipid nanoparticles can potentially be engineered to carry different cargo including select protein antigens or modified mRNA, perhaps by taking advantage of some of the mechanisms that phages have evolved to alter their own nucleoside bases. Not discussed, but equally interesting, there are extensive efforts in using well-characterized phage proteins such as the Salmonella phage P22 capsid as a carrier, reactor or vaccine (Wang and Douglas, 2022; Essus et al., ), or the phage Qβ system (Sungsuwan et al., 2022), among others (Yuan et al., 2023).
6 Conclusion
There is no doubt that bacteriophages will continue to inform our understanding of a multitude of biological and chemical processes, and lead to key discoveries and additional Nobel Prizes for years to come. Since Félix d'Hérelle's first realization that phages can be used to manage microbial infections, researchers have continued to make improvements in this approach and are also exploring the use of several phage components as their unique functions are being realized. In this article, I emphasized that phages will act as a constant source of reagents for glycobiologists since it is known that as bacteria adapt and change their carbohydrate structures for phage evasion, phages alter the specificities of their receptor binding proteins and polysaccharide depolymerases for bacterial infection. Similarly, phages will also be more commonly used in glycan display platforms to better understand the binding specificities in carbohydrate-protein interactions. Lastly, enveloped phages have the potential to replace OMVs, lipid nanoparticles and virus-like particles in various vaccine platforms and I anticipate this will be a topic for future development.
Statements
Author contributions
CS: Conceptualization, Writing—original draft, Writing—review & editing.
Funding
The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.
Acknowledgments
Author would like to thank Bibi Zhou for providing the illustrations shown in Figure 1 and Harald Nothaft for critically reviewing this manuscript.
Conflict of interest
The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
1
AbdelrahmanF.EaswaranM.DaramolaO. I.RagabS.LynchS.OduseluT. J.et al. (2021). Phage-encoded endolysins. Antibiotics10:124. 10.3390/antibiotics10020124
2
AdamsM. H.ParkB. H. (1956). An enzyme produced by a phage-host cell system. II. The properties of the polysaccharide depolymerase. Virology2, 719–736. 10.1016/0042-6822(56)90054-X
3
AntonovaD.BelousovaV. V.ZhivkopliasE.SobininaM.ArtamonovaT.VishnyakovI. E.et al. (2023). The dynamics of synthesis and localization of jumbo phage RNA polymerases inside infected cells. Viruses15:2096. 10.3390/v15102096
4
BamfordD. H.RomantschukM.SomerharjuP. J. (1987). Membrane fusion in prokaryotes: bacteriophage phi 6 membrane fuses with the Pseudomonas syringae outer membrane. EMBO J.6, 1467–1473. 10.1002/j.1460-2075.1987.tb02388.x
5
BanerjeeS.HalderP.DasS.MaitiS.BhaumikU.DuttaM.et al. (2023). Pentavalent outer membrane vesicles immunized mice sera confers passive protection against five prevalent pathotypes of diarrhoeagenic Escherichia coli in neonatal mice. Immunol. Lett.263, 33–45. 10.1016/j.imlet.2023.09.009
6
BarrangouR.FremauxC.DeveauH.RichardsM.BoyavalP.MoineauS.et al. (2007). CRISPR provides acquired resistance against viruses in prokaryotes. Science315, 1709–1712. 10.1126/science.1138140
7
CahillJ.YoungR. (2019). Phage lysis: multiple genes for multiple barriers. Adv. Virus Res.103, 33–70. 10.1016/bs.aivir.2018.09.003
8
ChenL.ValentineJ. L.HuangC. J.EndicottC. E.MoellerT. D.RasmussenJ. A.et al. (2016). Outer membrane vesicles displaying engineered glycotopes elicit protective antibodies. Proc. Natl. Acad. Sci. U. S. A.113, E3609–3618. 10.1073/pnas.1518311113
9
ChinW. H.KettC.CooperO.MuselerD.ZhangY.BamertR. S.et al. (2022). Bacteriophages evolve enhanced persistence to a mucosal surface. Proc. Natl. Acad. Sci. U. S. A.119:e2116197119. 10.1073/pnas.2116197119
10
CrippenC. S.LeeY. J.HutinetG.ShajahanA.SacherJ. C.AzadiP.et al. (2019). Deoxyinosine and 7-deaza-2-deoxyguanosine as carriers of genetic information in the DNA of Campylobacter viruses. J. Virol.9, e01111-19. 10.1128/JVI.01111-19
11
CrippenC. S.ZhouB.AndresenS.PatryR. T.MuszynskiA.ParkerC. T.et al. (2021). RNA and sugars, unique properties of bacteriophages infecting multidrug resistant Acinetobacter radioresistens strain LH6. Viruses13:1652. 10.3390/v13081652
12
CyglerM.RoseD. R.BundleD. R. (1991). Recognition of a cell-surface oligosaccharide of pathogenic Salmonella by an antibody Fab fragment. Science253, 442–445. 10.1126/science.1713710
13
DayC. J.KingR. M.ShewellL. K.TramG.NajninT.Hartley-TassellL. E.et al. (2016). A direct-sensing galactose chemoreceptor recently evolved in invasive strains of Campylobacter jejuni. Nat. Commun.7:13206. 10.1038/ncomms13206
14
DengS. J.MackenzieC. R.SadowskaJ.MichniewiczJ.YoungN. M.BundleD. R.et al. (1994). Selection of antibody single-chain variable fragments with improved carbohydrate binding by phage display. J. Biol. Chem.269, 9533–9538. 10.1016/S0021-9258(17)36914-4
15
DullP. M.McIntoshE. D. (2012). Meningococcal vaccine development–from glycoconjugates against MenACWY to proteins against MenB–potential for broad protection against meningococcal disease. Vaccine30 (Suppl. 2), B18–B25. 10.1016/j.vaccine.2012.01.062
16
DurrC.NothaftH.LizakC.GlockshuberR.AebiM. (2010). The Escherichia coli glycophage display system. Glycobiology20, 1366–1372. 10.1093/glycob/cwq102
17
EssusV. A.Souza JuniorG. S. E.NunesG. H. P.OliveiraJ. D. S.De FariaB. M.RomaoL. F.et al. (2023). Bacteriophage P22 capsid as a pluripotent nanotechnology tool. Viruses15:516. 10.3390/v15020516
18
FischettiV. A. (2011). Exploiting what phage have evolved to control gram-positive pathogens. Bacteriophage1, 188–194. 10.4161/bact.1.4.17747
19
FrancaR. K. A.StudartI. C.BezerraM. R. L.PontesL. Q.BarbosaA. M. A.BrigidoM. M.et al. (2023). Progress on phage display technology: tailoring antibodies for cancer immunotherapy. Viruses15:1903. 10.3390/v15091903
20
FreemanK. G.RobothamA. C.ParksO. B.AbadL.Jacobs-SeraD.LauerM. J.et al. (2023). Virion glycosylation influences mycobacteriophage immune recognition. Cell Host Microbe. (2023)31, 1216–1231.e6. 10.1016/j.chom.2023.05.028
21
GondilV. S.HarjaiK.ChhibberS. (2020). Endolysins as emerging alternative therapeutic agents to counter drug-resistant infections. Int. J. Antimicrob. Agents55:105844. 10.1016/j.ijantimicag.2019.11.001
22
GottliebP.AlimovaA. (2023). Discovery and classification of the phi6 bacteriophage: an historical review. Viruses15:1308. 10.3390/v15061308
23
GreenS. I.Gu LiuC.YuX.GibsonS.SalmenW.RajanA.et al. (2021). Targeting of mammalian glycans enhances phage predation in the gastrointestinal tract. MBio12:e03474-20. 10.1128/mBio.03474-20
24
HeimJ. B.HodnikV.HeggelundJ. E.AnderluhG.KrengelU. (2019). Crystal structures of cholera toxin in complex with fucosylated receptors point to importance of secondary binding site. Sci. Rep.9:12243. 10.1038/s41598-019-48579-2
25
HersheyA. D.ChaseM. (1952). Independent functions of viral protein and nucleic acid in growth of bacteriophage. J. Gen. Physiol.36, 39–56. 10.1085/jgp.36.1.39
26
HeymannJ. B. (2023). Structural studies of bacteriophage phi6 and its transformations during its life cycle. Viruses15:2404. 10.3390/v15122404
27
JinekM.ChylinskiK.FonfaraI.HauerM.DoudnaJ. A.CharpentierE. (2012). A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity. Science337, 816–821. 10.1126/science.1225829
28
JohnsonM. D.III.MindichL. (1994). Plasmid-directed assembly of the lipid-containing membrane of bacteriophage phi 6. J. Bacteriol.176, 4124–4132. 10.1128/jb.176.13.4124-4132.1994
29
KarikóK.MuramatsuH.WelshF. A.LudwigJ.KatoH.AkiraS.et al. (2008). Incorporation of pseudouridine into mRNA yields superior nonimmunogenic vector with increased translational capacity and biological stability. Mol. Ther.16, 1833–1840. 10.1038/mt.2008.200
30
KocotA. M.BriersY.PlotkaM. (2023). Phages and engineered lysins as an effective tool to combat gram-negative foodborne pathogens. Compr. Rev. Food Sci. Food Saf.22, 2235–2266. 10.1111/1541-4337.13145
31
KumarA.DasB.KumarN. (2020). Vibrio pathogenicity island-1: the master determinant of cholera pathogenesis. Front. Cell. Infect. Microbiol.10:561296. 10.3389/fcimb.2020.561296
32
LaemmliU. K. (1970). Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature227, 680–685. 10.1038/227680a0
33
LeimanP. G.BaslerM.RamagopalU. A.BonannoJ. B.SauderJ. M.PukatzkiS.et al. (2009). Type VI secretion apparatus and phage tail-associated protein complexes share a common evolutionary origin. Proc. Natl. Acad. Sci. U. S. A.106, 4154–4159. 10.1073/pnas.0813360106
34
LinC. L.SojitraM.CarpenterE. J.HayhoeE. S.SarkarS.VolkerE. A.et al. (2023). Chemoenzymatic synthesis of genetically-encoded multivalent liquid N-glycan arrays. Nat. Commun.14:5237. 10.1038/s41467-023-40900-y
35
LiuQ.LiuQ.YiJ.LiangK.LiuT.RolandK. L.et al. (2016). Outer membrane vesicles derived from Salmonella Typhimurium mutants with truncated LPS induce cross-protective immune responses against infection of Salmonella enterica serovars in the mouse model. Int. J. Med. Microbiol.306, 697–706. 10.1016/j.ijmm.2016.08.004
36
MaxtedW. R. (1952). Enhancement of streptococcal bacteriophage lysis by hyaluronidase. Nature170, 1020–1021. 10.1038/1701020b0
37
MoraisP.AdachiH.YuY. T. (2021). The critical contribution of pseudouridine to mRNA COVID-19 vaccines. Front. Cell Dev. Biol.9:789427. 10.3389/fcell.2021.789427
38
MursalinM. H.AstleyR.CoburnP. S.BagarukaE.HuntJ. J.FischettiV. A.et al. (2023). Therapeutic potential of Bacillus phage lysin PlyB in ocular infections. mSphere8:e0004423. 10.1128/msphere.00044-23
39
MushegianA. R. (2020). Are There 1031 Virus Particles on Earth, or More, or Fewer?J Bacteriol.202, e00052-20. 10.1128/JB.00052-20
40
NanceK. D.MeierJ. L. (2021). Modifications in an emergency: the role of N1-methylpseudouridine in COVID-19 vaccines. ACS Cent. Sci.7, 748–756. 10.1021/acscentsci.1c00197
41
NeelameghamS.Aoki-KinoshitaK.BoltonE.FrankM.LisacekF.LuttekeT.et al. (2019). Updates to the symbol nomenclature for glycans guidelines. Glycobiology29, 620–624. 10.1093/glycob/cwz045
42
NielsenT. K.Forero-JuncoL. M.KotW.MoineauS.HansenL. H.RiberL. (2023). Detection of nucleotide modifications in bacteria and bacteriophages: Strengths and limitations of current technologies and software. Mol. Ecol.32, 1236–1247. 10.1111/mec.16679
43
PalmaM. (2023). Aspects of phage-based vaccines for protein and epitope immunization. Vaccines11:436. 10.3390/vaccines11020436
44
PalmerT.FinneyA. J.SahaC. K.AtkinsonG. C.SargentF. (2021). A holin/peptidoglycan hydrolase-dependent protein secretion system. Mol. Microbiol.115, 345–355. 10.1111/mmi.14599
45
PriceN. L.Goyette-DesjardinsG.NothaftH.ValguarneraE.SzymanskiC. M.SeguraM.et al. (2016). Glycoengineered outer membrane vesicles: a novel platform for bacterial vaccines. Sci. Rep.6:24931. 10.1038/srep24931
46
SalmondG. P.FineranP. C. (2015). A century of the phage: past, present and future. Nat. Rev. Microbiol.13, 777–786. 10.1038/nrmicro3564
47
SanchezH.O'tooleG. A.BerwinB. (2023). Assessment of the glycan-binding profile of Pseudomonas aeruginosa PAO1. Microbiol. Spectr.11:e0166723. 10.1128/spectrum.01667-23
48
SangerF.AirG. M.BarrellB. G.BrownN. L.CoulsonA. R.FiddesC. A.et al. (1977). Nucleotide sequence of bacteriophage phi X174 DNA. Nature265, 687–695. 10.1038/265687a0
49
SanmukhS. G.Dos SantosN. J.BarquilhaC. N.CucieloM. S.De CarvalhoM.Dos ReisP. P.et al. (2021a). Bacteriophages M13 and T4 increase the expression of anchorage-dependent survival pathway genes and down regulate androgen receptor expression in LNCaP prostate cell line. Viruses13:1754. 10.3390/v13091754
50
SanmukhS. G.SantosN. J.BarquilhaC. N.Dos SantosS. a,.ADuranB. O. S.et al. (2021b). Exposure to bacteriophages T4 and M13 increases integrin gene expression and impairs migration of human PC-3 prostate cancer cells. Antibiotics10:1202. 10.3390/antibiotics10101202
51
SemchenkoE. A.Everest-DassA. V.JenF. E.MubaiwaT. D.DayC. J.SeibK. L. (2019). Glycointeractome of Neisseria gonorrhoeae: identification of host glycans targeted by the gonococcus to facilitate adherence to cervical and urethral epithelial Cells. MBio10:e01339-19. 10.1128/mBio.01339-19
52
ShenY.WangJ.LiY.YangC. T.ZhouX. (2023). Modified bacteriophage for tumor detection and targeted therapy. Nanomaterials13:665. 10.3390/nano13040665
53
SimpsonD. J.SacherJ. C.SzymanskiC. M. (2015). Exploring the interactions between bacteriophage-encoded glycan binding proteins and carbohydrates. Curr. Opin. Struct. Biol.34, 69–77. 10.1016/j.sbi.2015.07.006
54
SinhaR.KoleyH.NagD.MitraS.MukhopadhyayA. K.ChattopadhyayB. (2015). Pentavalent outer membrane vesicles of Vibrio cholerae induce adaptive immune response and protective efficacy in both adult and passive suckling mice models. Microbes Infect.17, 215–227. 10.1016/j.micinf.2014.10.011
55
SmithH. O.WilcoxK. W. (1970). A restriction enzyme from Hemophilus influenzae. I. Purification and general properties. J. Mol. Biol.51, 379–391. 10.1016/0022-2836(70)90149-X
56
SojitraM.SarkarS.MagheraJ.RodriguesE.CarpenterE. J.SethS.et al. (2021). Genetically encoded multivalent liquid glycan array displayed on M13 bacteriophage. Nat. Chem. Biol.17, 806–816. 10.1038/s41589-021-00788-5
57
SteinbacherS.MillerS.BaxaU.WeintraubA.SecklerR. (1997). Interaction of Salmonella phage P22 with its O-antigen receptor studied by X-ray crystallography. Biol. Chem.378, 337–343. 10.1515/bchm.1997.378.3-4.337
58
SunQ.ShenL.ZhangB. L.YuJ.WeiF.SunY.et al. (2023). Advance on engineering of bacteriophages by synthetic biology. Infect. Drug Resist.16, 1941–1953. 10.2147/IDR.S402962
59
SunZ.El OmariK.SunX.IlcaS. L.KotechaA.StuartD. I.et al. (2017). Double-stranded RNA virus outer shell assembly by bona fide domain-swapping. Nat. Commun.8:14814. 10.1038/ncomms14814
60
SungsuwanS.WuX.ShawV.KavunjaH.Mcfall-BoegemanH.RashidijahanabadZ.et al. (2022). Structure guided design of bacteriophage qbeta mutants as next generation carriers for conjugate vaccines. ACS Chem. Biol.17, 3047–3058. 10.1021/acschembio.1c00906
61
SzymanskiC. M. (2022). Bacterial glycosylation, it's complicated. Front. Mol. Biosci.9:1015771. 10.3389/fmolb.2022.1015771
62
ThongcholJ.LillZ.HooverZ.ZhangJ. (2023). Recent advances in structural studies of single-stranded RNA bacteriophages. Viruses15:1985. 10.3390/v15101985
63
Topka-BieleckaG.DydeckaA.NecelA.BlochS.Nejman-FalenczykB.WegrzynG.et al. (2021). Bacteriophage-derived depolymerases against bacterial biofilm. Antibiotics10:175. 10.3390/antibiotics10020175
64
WangY.DouglasT. (2022). Bioinspired approaches to self-assembly of virus-like particles: from molecules to materials. Acc. Chem. Res.55, 1349–1359. 10.1021/acs.accounts.2c00056
65
WongY. C.NgA. W. R.ChenQ.LiewP. S.LeeC. W.SimE. U. H.et al. (2023). Phage N15-based vectors for gene cloning and expression in bacteria and mammalian cells. ACS Synth. Biol.12, 909–921. 10.1021/acssynbio.2c00580
66
YangY.LuS.ShenW.ZhaoX.ShenM.TanY.et al. (2016). Characterization of the first double-stranded RNA bacteriophage infecting Pseudomonas aeruginosa. Sci. Rep.6:38795. 10.1038/srep38795
67
YuanB. C.LiuY.LvM. L.SuiY. L.HouS. H.YangT. H.et al. (2023). Virus-like particle-based nanocarriers as an emerging platform for drug delivery. J. Drug Target31, 433–455. 10.1080/1061186X.2023.2193358
68
ZhaoH.NieD.HuY.ChenZ.HouZ.LiM.et al. (2023). Phage display-derived peptides and antibodies for bacterial infectious diseases therapy and diagnosis. Molecules28:2621. 10.3390/molecules28062621
Summary
Keywords
bacteriophages, glycan binding proteins, glycoside hydrolases, glycosyltransferases, modified nucleobases, self-assembling nanoparticles, vaccines
Citation
Szymanski CM (2024) Bacteriophages and their unique components provide limitless resources for exploitation. Front. Microbiol. 15:1342544. doi: 10.3389/fmicb.2024.1342544
Received
22 November 2023
Accepted
22 January 2024
Published
06 February 2024
Volume
15 - 2024
Edited by
Jamshid Tanha, National Research Council Canada (NRC), Canada
Reviewed by
Swapnil Ganesh Sanmukh, Université Clermont Auvergne, France
Lone Brøndsted, University of Copenhagen, Denmark
Updates
Copyright
© 2024 Szymanski.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Christine M. Szymanski cszymans@uga.edu
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.