FormalPara Key Summary Points
The soaring crisis of antibiotic resistance has directed research towards the development of alternatives to antibiotics.
The use of engineered phages as therapy that is helpful in killing resistant bacteria is a promising tool to confront antibiotic resistance.
Pre-screening of phage-encoded proteins may be performed before in vitro or in vivo analysis of the candidate protein.
Bacteriophage lysins target only specific bacteria and do not damage the microflora as do antibiotics, thus phage therapy has an advantage over antibiotics.
Bacteriophages and associated proteins have been suggested as promising antibacterials, and may have a wide range of applications in humans, animals, and agriculture.
In future, further experimental and clinical investigations are essential regarding the safety profile, half-life, dose, and site specificity of the bacteriophages or their proteome to be used as novel therapeutic candidates.

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In the current era, antibiotic resistance has become an emerging and important threat, globally jeopardizing healthy living. The non-judicious use of antibiotics is leading to the emergence of multidrug-resistant superbugs. Antibiotic resistance is posing huge economic and health losses in both the developing and the developed world. According to WHO estimates, multidrug-resistant infections account for approximately 25,000 deaths every year, which will increase to 10 million by 2050. Overall, it costs about €55 billion/year in the US, which could rise to US$100 trillion by 2050. The stay of patients suffering from such resistant infections is approximately 13 days, which costs about $29,000/patient treated with such resistant bacterial infections. In this regard, a total annual economic loss (productivity loss) of about $35 billion has been reported [1,2,3,4]. The global nature of this issue emphasizes the need to control the antibiotic resistance crisis [1, 5].

At present, there is increasing interest in the use of bacteriophages as well as their lytic proteins to treat resistant bacterial infections. Bacteriophages are known as natural enemies of bacteria, their self-replicating particles having stringent host specificity to recognize and kill bacteria by hijacking the cell machinery [6]. Phages destroy the pathogenic bacteria without destroying the microflora, hence prevent the side effects that are usually associated with antibiotic treatment, for example, antibiotic-associated diarrhea [7].

Phage-associated peptidoglycan hydrolasinges are potential antibacterials. During the last decade, bacteriophage research has evolved from basic to applied and up to clinical trials, e.g., use of endolysins as antibacterials. These hydrolases destroy the peptidoglycan layer of a host bacterial cell, which results in rapid killing of the host and the exit of phage progeny [8]. This useful killing ability of endolysins may be utilized by employing these hydrolases as chimeric proteins to destroy the resistant and pathogenic bacterial strains [9, 10]. This plan proved to work well against Gram-positive bacterial pathogens, which have no external protection for their cell walls, permitting direct access of recombinant endolysins to the peptidoglycan layer of the cells. Additionally, many studies to make lytic enzymes effective against Gram-negative bacteria have been reported in recent times [11].

The World Health Organization (WHO) has proclaimed the urgent need for antibiotics against ESKAPE (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter spp.) pathogens [12]. These pathogens are associated with severe nosocomial infections, especially in critical patients [13]. Several studies have reported the effectiveness of phage therapy in humans. Previously, a patient with P. aeruginosa-associated septicemia was treated with phage therapy [14], and another patient with P. aeruginosa-associated aortic graft infection has also been managed successfully by employing phage therapy [15].

Additionally, the role of bacteriophages in the food industry and as potential sanitizing agents against multidrug-resistant pathogens has also been recognized [16]. Antibiotics are unable to penetrate the matrix of biofilms to kill or destroy the bacterial species; however, the phages have been found to be very effective in killing bacterial biofilms, making them a viable alternative to antibiotics [17]. The prevalence rate of antimicrobial resistance has increased remarkably in food-borne pathogens, and the emergence of resistance in the food chain is an increasing public health concern across the globe. Phage therapy has profound beneficial effects on human and animal health, and can lead to a greater productivity rate in the livestock industry. Meeting the increasing demand for meat can be possible only by adopting alternative approaches to antibiotics, like phage therapeutics, to control infections in intensified production systems [18].

The increase of multidrug-resistant bacterial strains and the lack of new antibiotics calls for the development of new antibacterial drugs or alternative strategies, like phage therapy and the use of phage lytic proteins [19]. Moreover, a few pathogens can evade the action of antibiotics by hiding themselves in safe niches within the host, e.g., S. aureus, a recognized pathogen that may survive in the intracellular environment, biofilms, or abscesses, resulting in persistent infections. Thus, the development of novel, target-specific, safe, and effective antibacterials is urgently required [20,21,22].

The use of engineered phages as a therapy that helps to kill bacteria could be the next step to confront antibiotic resistance. Engineered phages precisely detect and control bacteria, serving as a new source of antimicrobials as well as a vehicle for the delivery of vaccine antigens and drugs. For example, endolysins have a modular structure that may be exploited for phage engineering by substituting and recombining the functional domain of diverse species, which could lead to the development of chimeric proteins with the desired features. This practice may also be a good option for other phage lytic proteins like virion-associated peptidoglycan hydrolases (VAPGHs). Additionally, it could be a promising tool for proteins with non-phage origins, like bacteriocins and autolysins [23]. The specificity of such engineered proteins would be a key advantage when used as antibacterials, for further bactericidal activity, with a negligible risk of resistance development, and good efficacy against persister cells, multidrug-resistant strains, and biofilms [9]. In this review, an attempt is made to explore the hidden potential of bacteriophage proteins, which may be a practical alternative approach to manage the threat of antibiotic resistance.

This article is based on previously conducted studies, and does not contain any new studies with human participants or animals performed by any of the authors.

Bacteriophage Proteins

Bacteria are all around the world, good ones and bad ones. The dominance of bad bacteria leads to infections and disease in the susceptible host. Antibiotics not only kill the bad bacteria but are also harmful to the good ones, and overuse of antibiotics introduces resistance in exposed bacterial populations. The development of bacterial resistance to many antibiotics has become a crucial therapeutic challenge across the globe. Often, these multidrug-resistant bacteria are associated with the community as well as with hospital-acquired infections. Because of the alarming situation of antibiotic resistance among bacterial species and complications in treatment, possible support or alternatives are required to reduce the infection rate [24].

Bacteriophages have been suggested as antibacterial agents to combat bacterial infections in humans, animals, and crops. Since bacteriophages encode a variety of proteins that play a vital role in the bacteriophage replication cycle, from the recognition of the host to the lysis of the cell (Fig. 1), phage-encoded proteins like receptor binding proteins, VAPGHs, endolysins, and holins are being considered as a possible means to fight antibiotic-resistant bacteria [25].

Fig. 1
figure 1

A Various phage-associated proteins located at different structural components of a bacteriophage. B Key structural components of the bacterial host related to phage infection. C Attachment of bacteriophage to the host (bacterium); attachment initiates after long-term facilitation binds (reversibly) to host receptors, leads to conformational changes to the base plates and allows rotation, resulting in short-term facilitation binding (irreversibly) to the host receptors. Sheath contraction allows gp27-associated DNA translocation, while gp5 and gp29 play roles in channel formation. DF Various steps along with different phage-encoded proteins in the lytic phase of the infection. D Ribosylation of host RNAp by phage-encoded gp Alt recruits RNAp to early gene transcription, while the MotA transcriptional regulator inhibits transcription from the host (bacterial) DNA and initiates middle transcription by binding to the MotA box. Middle phase transcription product, gp55, along with proteins of DNA polymerase enhancer complex and gp33 initiates late transcription, while subsequent products play an important role in phage assembly. E Phage DNA replication through phage-encoded DNA polymerase (gp43) depends on the DNA polymerase enhancer complex, while replisome-associated proteins include a DNA polymerase enhancer complex (clamp loader), Primase gp 61 (produces primers for DNA elongation), gp41 (helicase activity), gp30 (ligation), Rnh gene (RNase H), and gp32 (ssDNA binding activity). F Assembly of phage components takes place right after the formation of the gp20–gp40 initiation complex followed by head recruitment, while the DNA is transferred to head domain via ATPase-dependent gp16–gp17 DNA translocation activity, wile phage-encoded holins and spanins assist the phage existing from the host cell. G The CI repressor binds with the oL and oR operators and represses the transcription from pL and pR, retaining the virus in a prophage state, while SOS leads to CI de-attaching from the operators. Modification of RNAp by the N and Q proteins allows it to pass through the terminators tR1, tL1, and tR’, leading to lytic genes transcription, while the N protein-associated CII expression leads to the expression of Int and the integration of phage DNA into the host DNA

Receptor Binding Proteins (RBPs)

The role of RBPs as detecting tools for bacterial pathogens has been described, and they have also been suggested as probes for bacterial O-serotyping [26,27,28]. RBs-encoded depolymerases have been proposed to be applied in pathogen-specific targeting. Thus, a depolymerase has been used as a host immune system adjuvant against bacterial infection by inhibiting the bacterial capsule [29, 30]. On the other hand, the amazing capsule specificity of these depolymerases may be employed for diagnostics and capsular typing, particularly for K. pneumoniae [31, 32]. Thorough knowledge regarding the structural and molecular phenomena controlling the RBPs and phage–host interaction would substantially improve the applicability of phage-derived tools in the medical and biotechnological fields.

These proteins are particularly valuable for identifying particular receptors, like the membrane surface-anchored protein gamma phage receptor, GamR, on the surface of the cell wall of Bacillus anthracis, thus making it possible to detect particular bacteria [33]. RBPs can identify glycosylation patterns of O signature antigens (determinants of the immunogenicity of bacteria and disease spread). The binding affinity and specificity of these proteins have a major role in the detection of bacterial endotoxin contaminants [28]. The binding specificity of phages is mediated by RBPs, which form spikes or tail fibers at the caudal end. A monomeric RBP located at the T5 tail tip, called Pb5, showed irreversible binding with FhuA receptors of the bacterial host during the infection, i.e., E. coli [34, 35]. The outer membrane protein, FhuA has a key role in iron acquisition by E. coli from the environment as it transports the siderophore–ferrichrome very actively.

Recombinant phage-derived proteins have also been designed which introduced specific tags (Cys-tag) to the receptor binding proteins, which significantly improved their capturing performance and their efficiency as detection probes [36]. It has been identified that the C-terminal domain of these receptor binding proteins is responsible for the binding and recognition to the host receptors, such as cell wall teichoic acids [37]. Due to the higher affinity and specificity of receptor binding proteins, many of their applications are directed towards pathogen detection rather than pathogen control [38]. Therefore, the use of such proteins to detect bacterial pathogens can help to manage bacterial infections, including antibiotic-resistant bacteria.

Long Tail Fiber (gp37-gp38)

To infect the bacterial host cell by targeting specific receptors, tailed bacteriophages use their molecular machinery, having a wide range of RBPs, like tail spikes, central tail spikes, and tail fibers. After the recognition of the host, these tail fibers penetrate the cell and deliver the phage DNA into the host cytoplasm. Different receptors for these fibers include porins, lipopolysaccharides (LPS), outer membrane protein C (OmpC), and teichoic acids. The first contact of a long-tail fiber with any of the mentioned receptors is followed by a second contact of another long-tail before the dissociation of the first one. It is a repetitive process until the phage finds the proper site for permanent adsorption followed by DNA ejection [35, 39] (Fig. 2).

Fig. 2
figure 2

Schematic of the endolysin structure of Gram-positive and Gram-negative bacteria. A The endolysin of Gram-positive bacteria possesses two domains, namely the N-terminus catalytic domain and the C-terminus cell wall binding domain. Some endolysins also have a 2nd catalytic domain which is different from the 1st one. The cell wall binding domain contains binding motifs which may be single or multiple. B Endolysin of Gram-negative bacteria exhibit a catalytic domain. In those which contain a cell wall binding domain, this domain is situated on the N-terminus rather than the C-terminus of the protein. Artilysin, an engineered lysin, can be made by adding hydrophobic or amphipathic sequences at either the N-terminus or the C-terminus, and are effective only when applied externally

The molecular mechanisms used by myophages for the adsorption and infection of Gram-positive bacteria have been described previously. Phage phi812 uses its tail fibers to contact the host bacteria (S. aureus), which alters the shape of the base plate [40]. However, phi812 has a distinct base plate conformation as compared to T4; it possesses heavy ‘legs’, a trimer of RBPs and tripod proteins. These all lead to base plate reorganization by binding with specific receptors (receptor–tripod complex). The phi812 myophage with double-layered base plate machinery can infect both Gram-negative and Gram-positive bacteria [41, 42].

The long tail fiber proteins have been demonstrated as high-affinity molecules for the detection of Salmonella. The long tail fiber proteins have a great capability for diagnosing a broad spectrum of bacteria. These proteins are made particularly useful by coating them with paramagnetic particles for capturing S. typhimurium from food samples. A new method, enzyme-linked long tail fiber assay (EELTA), has now been suggested that detects as low as 102 CFU/ml of S. typhimurium. It has been observed that phage S16 long tail fiber paramagnetic beads have a great capability to bind and immobilize all strains of Salmonella. A 98% detection rate of S. typhimurium cells from tested suspensions has been demonstrated. It is suggested that the microflora does not affect these proteins, as these are also able to tolerate variable concentrations of salt and pH. These factors promote in situ detection of Salmonella by these proteins. Tail fibers may be used as a promising diagnostic tool for pathogen detection in health care settings [43]. The LPS of P. aeruginosa are of two types: the A-band (common polysaccharide antigen) and the B-band (O-specific antigen) [44]. The LKA1 phage of Pseudomonas primarily utilizes the LPS B-band O-specific antigen as a receptor. The tail spike protein LKAI gp49 has three basic domains: β-helix, β-barrel, and β-sandwich. This protein has a strong enzymatic activity and can degrade the LPS binding protein and ultimately destroy the biofilm matrix, allowing small molecules to rapidly diffuse across the membrane. Owing to its high specificity and enzymatic activity, LKA1gp49 can be used for various microbiological as well as biotechnological applications. The tail spike protein LKA1gp49 can act as a powerful antimicrobial agent [45]. The depolymerase activity of LKA1gp49 is considered a potential antibacterial. The LKA1 is a lyase and specifically degrades O5 serotype LPS molecules, thus disrupting the biofilm matrix [45].

Long-Tail Fiber Protein gp37

Phage T4 of E. coli has long tail fibers through which they interact with the LPS of their host, and thus recognizes and binds to it. Long-tail fibers consist of four different proteins: gp34, gp35, gp36, and gp37 [46]. The tip of the tail fiber protein gp37 comprises a length of 1600 Angstroms and divides into two portions (proximal and distal) of about 70 nm [47]. The distal portion of the long tail fiber interacts with the LPS of bacteria, thus determining the phage’s host range against Gram-negative bacteria [47]. Overall, gp37 is one of the key proteins in the distal segment of the phage tail, forming a needle-like foot containing the receptor-binding site at the C terminus. It is interlaced with a globular collar, an elongated needle, and head. It is the iron ions that hold the interlaced strand and residues in the head domains, which facilitate the binding to LPS, OmpC, or porins of the host [47, 48].

Tail Spikes

P22 typically infects serotype S. typhimurium, has icosahedral symmetry, and has a short tail. It is almost 60 nm in diameter, and belongs to the Podoviridae family. P22 has a tail spike gp9 protein which forms a homotrimer, and each unit contains three domains. The N terminus binding domain has two central β-sheets used to attach the tail of the phage [49]. The C terminus receptor binding domain facilitates the attachment with the O antigen and shows endorhamnosidase hydrolyzing activity which cuts the O polysaccharide chain [28, 50]. Bacteriophage infection occurs as the gp9 tail spike protein of bacteriophage P22 binds to the O antigen of S. typhimurium. This spike protein hydrolyzes the alpha-1, 3-O-glycosidic linkage of the O antigen polysaccharide. It then enters either in the lytic phase (in which the virus replicates itself and ultimately releases its progeny cells through cell lysis) or in the lysogenic phase (in which the cell divides by integrating the phage’s DNA into the chromosomes of the host) [50]. Also, the Det7 (myophage) and SP6 (podophage) display the same tail spikes (gp49 and gp207 respectively) and host specificity, as they both can infect Salmonella species [51].

Although tail spikes may vary in their host specificity or receptor binding domains, they generally contain conserved structures. Moreover, these proteins frequently carry different enzymes which destroy the host cell wall and expedite the ejection of phage DNA. Thus, these proteins are useful for serotyping purposes. and also helpful in visualizing phase variations during vaccine production [25].

Penetrating Proteins

There are some proteins, which are different both structurally and functionally from tail fibers and spikes, known as membrane-penetrating proteins. The exact mechanism of penetration into the inner membrane is not known, but it has been suggested that these proteins have the ability to breach the boundary of the host bacterium. In addition, a membrane-penetrating protein of λ phage80, i.e., gpJ, may have a role in adsorption or in determining the host range of the phage. The T4 myophage central spike protein, i.e., gp5, is a lysozyme; it hydrolyzes the glycosidic bonds in peptidoglycans. This gp5 forms a complex with gp27 and looks like a long torch. The cylindrical portion of the structure is made up of the gp27 trimer and contains three N terminus domains of gp5 trimers. The C terminus domain of gp5 is attached to these which then is folded into a β-helix [34, 52]. The neighboring three gp5 lysozyme domains are attached to the N-terminus and C-terminus domains via two linkers (long peptide) [34]. The binding of the substrate to the lysozyme is prevented by these linkers, while the polysaccharide binding site is blocked by the β-helix. Consequently, β-helix dissociation restores the activity of the lysozyme which causes the digestion of peptidoglycan, hence assisting in the tail tube penetration [34]. Although the puncturing mechanism of the inner membrane is vague, it is assumed that gp27 or gp29 are involved in the DNA ejection [34, 53].


Endolysins are bacteriophage lysins or peptidoglycan hydrolases that degrade the peptidoglycan layer of the bacterial host during the lytic cycle. Since the outer membrane is absent in the cell walls of Gram-positive bacteria, purified endolysins when applied from outside directly gain access or reach the peptidoglycan layer, suggesting them as potent antimicrobials [54].

The endolysin structure of Gram-positive bacteria differs slightly from those of Gram-negative bacteria (Fig. 1). The endolysin of Gram-positive bacteria have two domains: the N-terminal enzymatically active domains, and the C-terminal cell wall binding domain (see Fig. 2A). An enzymatically active domain contains certain enzymes that are endopeptidases, L-amidases, glucosaminidase, muramidase, or transglycosylase. Cell wall binding domains contain binding motifs which may be single or multiple [55]. Enzymatically active domains cleave the particular bonds in bacterial peptidoglycan, while the cell wall binding domain specifically targets the protein to its substrate. After lysis of the bacterial cell, it binds tightly to the cell wall debris, thereby preventing diffusion and destruction of those intact bacterial cells that have not been infected by phage cell [54]. Table 1 presents an overview of the endolysins which have been purified and tested against Gram-positive bacteria.

Table 1 Some important endolysins against Gram-positive bacteria

Endolysins of Gram-negative bacteria have a single domain of globular proteins, particularly without a cell wall binding domain. This means that phage endolysins against Gram-negative bacteria comprise only the catalytic domain (Fig. 2B). Since the outer membrane is present in Gram-negative bacteria, so phage endolysins against Gram-negative bacteria cannot access peptidoglycan, and are not active when applied externally against Gram-negative bacteria. To overcome this issue, endolysins have been engineered. One of the most important engineered endolysin is Artilysin, which is developed by adding hydrophobic/polycationic peptide sequences to the N-terminal portion or C-terminal portion of endolysins, which enables penetration to the outer membrane of Gram-negative bacteria [56]. Innolysins is a T5 endolysin combined with RBP Pb5, and it showed significant lytic activity against E. coli when Pb5 specific receptors FhuA are present. Additionally, innolysins displayed activity against other bacterial hosts carrying FhuA receptors, such as P. aeruginosa and Shigella sonnei [57]. Endolysins have a three-dimensional crystalline structure, and two endolysins have been successfully crystallized, namely pneumococcal phage lysin Cp1-1 and Listeria phage PSA [58, 59]. Various purified endolysins active against Gram-negative bacteria are listed in Table 2.

Table 2 Some important endolysins against gram negative bacteria

There is growing interest in the field of engineered phage-encoded lytic proteins, called enzybiotics, since their discovery. Lytic enzymes make a significant impact in therapeutics, such as endocarditis and bloodstream infection. Exebacase (CF-301) which is a prophage endolysin has good lytic activity against S. aureus [9, 60]. Recently, it has been observed that human serum albumin and serum lysozyme have a synergistic effect with CF-301 [61]. A hydrolase called SAL200 is currently under investigation for the treatment of bacterial-associated pneumoniae caused by P. aeruginosa, A. baumannii, S. pneumoniae, B. anthracis, and S. aureus. Likewise, a selected endolysin for Gram-negative bacteria, i.e., PlyPa91, showed 70% challenge protection in animal models against P. aeruginosa-induced pneumonia [62]. One commercially available pharmaceutical gel product, Staphefekt, is an engineered endolysin that is used to treat skin infections [63]. CF-301 was used systemically to treat experimental osteomyelitis, and showed a significant reduction in bone localization of S. aureus [64]. A phage-encoded protein, PlyCD, has been used to develop a chimeric protein, LHD, which showed strong lytic activity against C. difficile, mitigated C. difficile-associated diarrhea, and reduced the toxin concentration in patient feces [65].

Endolysins are considered as novel antibacterials; therefore, in vivo safety of endolysins is critically important. It has been observed that the phage-encoded endolysin, PlyC, has lytic activity [66] against S. uberis, showing no cytotoxicity, and did not affect the production of reactive oxygen species in leukocytes of lactating cows [67]. The advantage of endolysins over antibiotics is that they are highly specific for peptidoglycan and bind to the most conserved regions in the cell walls of bacteria which are immobile. This high specificity limits the risk of developing antimicrobial resistance. Bacteriophage lysins target only specific bacteria and do not damage the microflora as do antibiotics, thus phage therapy has an advantage over antibiotics [54].

An experimental study has reported that antibodies conjugated with bacteriophage-derived lysins or bacterial autolysins to form a functional homodimer called a lysibody have a protective effect against methicillin-resistant S. aureus (MRSA). Although the Gram-positive bacterial cell wall contains highly conserved carbohydrate molecules, these are considered poor immunogens. Autolysins or phage lysins have distinct high-affinity binding domains for carbohydrates present in the cell wall. Lysibodies may be produced by combining lysin binding domains with the Fc portion of human IgG, and it has ben observed that lysibodies have fixed the complement on the bacterial cell surface and augmented the phagocytic activity of macrophages and neutrophils. Based on these results, it is suggested that lysibodies could be potential antibacterials [62].

Endolysin activity can be measured both by quantitative and qualitative methods, namely turbidity reduction analysis, zymogram assays, viable count assays, minimal inhibitory concentration assays, or plate agar lysis assays [54]. The endolysins have a vast range of lytic activity displaying species specificity, thus avoiding selective pressure on commensals. Here are some possible reasons due to which resistance against endolysins is unlikely to develop. Endolysins bind to and cleave highly conserved bonds and linkages in the structures of the cell wall, and bacteria are unable to modify this property of phage endolysin, thus minimizing the chances of the development of resistance against endolysins. The majority of endolysins have two catalytic domains in their structure that cleave bonding within the peptidoglycan layer, which is unfavorable in the development of antibiotic resistance. Since most of the phage lysins are used externally and target the cell wall without entering the bacterial cells, the endolysins avoid possible mechanisms of antibacterial resistance, such as active efflux from the cell and reduced membrane permeability. It has also been suggested that, to increase their therapeutic property and to minimize the development of antimicrobial resistance, endolysins can be used in combination with antibiotics to treat infections. Thus, endolysins have been suggested as potential antibacterials to fight antibiotic-resistant bacteria [68].


The lysis mechanism of bacteriophages exhibits two different strategies: murein hydrolase activity, namely endolysin, and a membrane protein known as holin. Holins include a vast group of small proteins (Table 3). They form pores in the cell membrane of the host, through which lysins move to the murein layer and degrade the peptidoglycan layer which induces cell death and measures the timing of the infection cycle [69, 70]. Holins perform a distinct established function which includes (1) release of gene transfer agents, (2) facilitate various processes required for differentiation, like spore germination, (3) have a role in biofilm formation, (4) release toxins and related proteins, and (5) help in different responses to stress conditions [71]. In animals, programmed cell death is facilitated by Bax and Bak (holin-like proteins), which may have a bacterial origin. It has been suggested that holins are ubiquitous in the three domains of life as they have also been characterized from archaea.

Table 3 Description of important holins proteins present in bacteriophage proteome

Structurally holins have been classified into three major classes. Holins of Class I have three hydrophobic transmembrane domains. The N-terminal portion is present inside the periplasm while the C-terminal portion is present inside the cytoplasm. Lambda phage holins and the S. aureus phage P68 Hol 15 protein have been categorized to belong to this group. Holins of Class II have two hydrophobic transmembrane domains, as well as – and C-terminal portions, but both terminals are found in cytoplasmic portions. The S protein of the lambda phage 21 and Hol 3626 holin protein from the Clostridium perfringens phage 3626 are examples of Class II holins. Holins of Class III also have – and C-terminal portions with the N-terminus inside the cytoplasm and the C inside the periplasm. Examples of this category include T4 holins and holins from phage CP 26F and phage CP390 [72, 73].

Mostly, genes encoded for holins are located adjacent to a gene encoding for endolysin. During the late phase of the phage infection, before activation holins accumulate in the plasma membrane, a gradual increase in holin concentration is required to achieve the threshold level, which, once it is achieved, leads to the formation of holes that permit the release of endolysins from the cytoplasm which destroys the peptidoglycan [74]. Canonical holins form large oligomer holes through which protein molecules of about 500 kDa can pass, thus allowing endolysins to escape and subsequently gain access to the peptidoglycan layer, and ultimately cleave various bonds in the peptidoglycan layer and digest it [75]. Pinholins form small pores, thus depolarizing the membrane. They are mostly associated with signal arrest release endolysins. In periplasm, they are present as an inactive-enzymatic form.

Due to the increased development of multidrug-resistant strains, holin proteins have been suggested as potent antibacterial agents for fighting against resistant strains of bacteria. The S. aureus GH15 phage-associated holin, i.e., HolGH15, has shown significant lytic activity against a wide host range [76]. Recently, the lytic activity of HolGH15 was observed against L. monocytogenes. HolGH15 showed significant lytic activity against the tested pathogen, and it was observed that HolGH15 showed a 240-µg/mL minimal bactericidal concentration against L. monocytogenes. It was concluded that HolGH15 displayed a similar sort of lytic activity against various serotypes of L. monocytogenes. Additionally, the antibacterial activity of HolGH15 has also been observed at refrigerator temperature against L. monocytogenes. Such abilities of HolGH15 make it a potential antibacterial agent against L. monocytogenes, and it may be used as a spray in the course of the handling and processing of various food items, like fruits, eggs, meat products, and vegetables [77]. Holins do not disturb the microflora and thus ultimately reduces the risk of the development of antimicrobial resistance [78].


Since lysins and holins disrupt the cell wall and inner membrane, respectively, disruption of the Gram-negative bacterial outer membrane is also very necessary with the help of the third type of holin proteins, called spanins. Spanins disrupt the outer membrane by catalyzing both the outer and inner membranes. Without these spanin proteins, the lysis mechanism is supposed to be blocked, and viral particles would remain trapped inside the dead cells instead of being released [79]. There are two types of spanins used by phages during the last step in the course of host Gram-negative bacteria lysis, i.e., unimolecular spanin and bicomponent spanins [8, 80]. Structural details of the lambda phage Rz-Rz1 spanin (a bi-component spanin) revealed that it contains a basic internal membrane protein, i.e., I-spanin, and a lipoprotein of the external membrane, i.e., o-spanin, which produces a complex spanning the gel-like matrix called periplasm. Three different genetic configurations of bi-component spanins include separated units, embedded parts, or overlapped components. On the other hand, T1 gp11 (unimolecular spanin) has an N-terminal lipoylation sequence and a C-terminal domain, e.g., U-spanins have N-terminal signal protruding towards the outer membrane lipoproteins as well as the C-terminus transmembrane domain [81].

Holin proteins act as the clock in the phage lytic cycle. During phage assembly in the cytoplasm, these holin proteins disturb the integrity of the whole membrane with the help of spanins, create holes in the membrane, and allow phage lysins to get access to the cell wall which cleaves the bacterial peptidoglycan, hence allowing the release of phages from host bacterial cells. Holin also reduces the chances of biofilm development by incorporating an extracellular polymeric substances layer while antibiotics do not penetrate the biofilm layers. Thus, phage holins in conjunction with endolysins could be powerful alternative lytic proteins in confronting antibiotic-resistant bacteria [78].

Anti-CRISPR Proteins

From the origin of life, the fight between phages and bacteria never ends. The bacterial system uses an adaptive immune system, CRISPR-Cas, to destroy the phage’s attack and, in turn, the bacteriophages produce anti-CRISPR proteins to fight back. The CRISPR-Cas system is divided into two groups, the Class I and Class II CRISPR-Cas systems. The Class I system includes types I and III, as well as IV, with multiple subunits of ribonucleoproteins, while the Class II CRISPR-Cas system comprises the II, V, and VI types with a single ribonucleoprotein. Bacteriophages in turn develop anti-CRISPR protein systems to combat the CRISPR-Cas system of bacteria. These proteins also belong to two classes based on the classification of the target CRISPR-Cas system, namely Classes 1 and 2 anti-CRISPR proteins [82].

The most important and notable feature of anti-CRISPR proteins (Acr) is a lack of sequence similarity with any other protein. The most important anti-CRISPR proteins are AcrF1, AcrF2, and AcrF3. The first two proteins, AcrF1 and AcrF2, bind to the type I-F CRISPR-Cas system with the help of a binding complex formed by multiple subunits. AcrF1 binds to Csy3 subunits while AcrF2 binds to the Csy complex (Csy1 and Csy2). However, AcrF3 binds to the Cas-3 helicase-nuclease protein, preventing its recruitment to the DNA–Csy complex [83].

One of the possible approaches to manage antibiotic resistance is a genetic strategy that seems to include sensitization of bacteria to antibiotics and selective killing of antibiotic-resistant bacteria. Towards this approach, temperate phages have proved to be very helpful. By using temperate phages, the CRISPR-Cas system is inserted within the genome of the resistant bacteria and this engineered CRISPR-Cas system protects from lytic phages by degrading both lytic phages (genetically modified) as well as destroys plasmids having antibiotic-resistant genes. These lytic phages selectively destroy antibiotic-resistant bacteria and protect antibiotic-sensitive bacteria. A transferable CRISPR-Cas system has been designed to sensitize the bacteria having an antibiotic resistance gene. The CRISPR-Cas genes are amplified by PCR and introduced in lambda prophage via homologous recombination. The CRISPR array that specifically targets the conserved regions of resistant genes has also been introduced within the same lysogen. Then, induction of prophage and lysogenization of resistant bacteria with a lambda CRISPR-Cas and lambda-Cas is carried out to determine plasmid loss. Plasmid curing occurs with lambda CRISPR-Cas, but not with lambda-Cas (Fig. 3). It has also been seen that the transferable CRISPR-Cas system prevents horizontal gene transfer of antibiotic resistance elements, as well as protects bacteria from an engineered T7 phage, thus linking bacterial sensitization to antibiotics with resistance to lytic phages. This transferable system prevents the transformation of plasmids and protects lysogenized bacteria from the lytic phages. This lysogenization is then used to sensitize antibiotic-resistant bacteria. This genetic strategy may be used in hospital settings as well as in hand sanitizers to replace resistant bacteria with antibiotic-sensitive bacteria. The benefit of using this genetic strategy is that there is no need to administer the phages within the host tissue [84].

Fig. 3
figure 3

CRISPR-CAS-based mechanism for re-sensitizing antibiotic-resistant bacteria. A vector phage is used to insert a CRISPR system into a targeted population of bacteria. The Cas9 RNA-guided nuclease is conveyed along with a guide RNA to cut a target sequence. The target carried on plasmids leads to a plasmid-curing phenomenon, i.e., re-sensitization to antibiotics, while the target carried on the chromosome leads to the death of the cell due to degradation of the chromosome

Virion-Associated Peptidoglycan Hydrolases (VAPGH’s)

Unlike endolysins, the VAPGHs (endopeptidases, glucosaminidase, etc.) facilitate the bacteriophage entry into the host cell by developing a hole in the bacterial cell wall. However, both these lytic proteins have a similar mode of action (the same catalytic domains), which degrades the bacterial cell wall, called the peptidoglycan layer [80, 85]. The exact location of these enzymes is not fixed, and they may be located at any place in the phage. They have been observed in the capsid, head, tail, and phage membrane [86, 87]. Hydrolases are appropriate to perform the activity against Gram-positive as well as Gram-negative bacteria [88]. VAPGHs have numerous benefits which make these proteins potential antibacterial agents against multidrug resistant bacteria. Additionally, they are very useful food decontaminants, particularly in processed foods and dairy products [87]. Recently, activity of VAPGHs against Agrobacterium tumefaciens-associated plant diseases has been observed [89]. The bactericidal activity of VAPGHs may be enhanced by creating chimeric proteins by exchanging the functional domains of various enzymes or via combining different proteins. Chimeric proteins have shown promising results against S. aureus infections [87].

It has been reported that VAPGHs have no certain cell wall binding domain as have endolysins. Also, it has been suggested that VAPGHs have highly conserved regions, but modification of these conserved regions is very rare. Thus, the development of bacterial resistance against these VAPGHs is a remote possibility, suggesting VAPGHs as novel and alternative antibacterials. VAPGHs derived from Gram-negative infecting phages have a broad host range compared to VAPGHs from Gram-positive infecting phages.

The VAPGHs proteins are highly thermostable, which could be exploited against extremophile bacteria. The VAPGH HydH5 is a novel VAPGH protein, produced from staphylococcal phage vB-SauS-PhilLA88. This protein, when combined with lysostaphin, exhibits augmented lytic activity against S. aureus in milk. HydH5 is a potential antibacterial that may be used in the dairy industry [87, 90]. VAPGH proteins act extracellularly, and can avoid the intracellular bacterial mechanism of resistance, i.e., as an efflux pump, and can also share a similar mode of action as for endolysins, this suggests them as promising antimicrobial agents to counter drug resistance. On the other hand, VAPGH-derived enzybiotics may be a significant tool that can be employed to cope with intracellular bacterial pathogens, as, due to the absence of receptors, the phage may encounter hurdles to obtain entry inside the eukaryotic cell.

Challenges to Face with Possible Solutions

In the past, enzymes used in experiments conducted for therapeutic evaluation of phage-encoded proteins were chosen randomly and are not suitable for particular applications. Additionally, in vivo experimental conditions are crucial to obtain good therapeutic efficacy [10]. To solve this problem, pre-screening of phage-encoded proteins may be performed before advance (in vitro or in vivo) analysis of suitable therapeutic candidate proteins. It has been successfully demonstrated in the case of engineered staphylococcal peptidoglycan hydrolases characterized from a collection that they showed significant efficacy in milk, human blood, and the inner environment of the cell [91,92,93].

The therapeutic efficacy of phage-encode proteins is dependent on the serum half-life, as most of the proteins feature a short half-life ranging from minutes to hours [94,95,96]. Generally, a long half-life is considered suitable because in this case boosting is not required, but the associated risk of anaphylaxis is also considerable in such cases. Recently, engineered PGH-ABD demonstrated a long half-life and augmented distribution, improved efficacy in human blood [93].

Some bacteria, like E. coli, S. aureus, and L. monocytogenes, can evade therapy and immunity by surviving inside the cells. Few phage proteins have the penetrating features to target these intracellular pathogens. Significant development has been made to solve this problem by combining lytic enzymes with cell-penetrating peptides, which facilitates the penetration of lytic enzymes into the host. For instance, short peptides which identify specific cells by surface markers and can deliver the biomolecules to a specific site are called homing peptides (HPs). These HPs have been used in cancer therapeutics and have been considered for clinical trials (e.g., NGR015) [97]. The same function of HPs may be exploited in phage-engineered therapeutics.

Preclinical development of phage-encoded proteins is dependent on different important concerns, like therapeutic safety, immunogenicity, and cell toxicity. A study conducted in the recent past described the safety of endolysins Pal and Cpl-1: experimental mice exposed to these endolysins showed an augmented IgG response and decreased level of IgE, which suggested that these enzymes have an adequate profile of safety and toxicity to be considered for therapeutic use [98]. Endolysins like lysostaphin may also be used to construct lysibodies by fusing them with the Fc portion of human IgG. It has been observed that lysibodies play a significant role in the opsonization of S. aureus, which facilitates the phagocytosis of this pathogen [99].

Industrial production is also a substantial contributing factor in the therapeutic application of phage-encoded proteins. Safety protocols and cost-effectiveness are most important concerns which should be kept in consideration during the production process. This should be related to the whole process, starting from the selection of the host, e.g., yeast bacteria or plants, to the removal of the endotoxins. In the end, regulatory approval for phage-encoded proteins to be used as therapeutics is mandatory [23, 95]. The approval process should be that followed in the case of therapeutic proteins. This authorization approach was successful in the past for the approval of recombinant therapeutic proteins as compared to the approval of new antibiotics, which is a lengthy process [100, 101].


The soaring crisis of antibiotic resistance has directed research towards the development of alternatives to antibiotics. In this context, bacteriophages and phage-encoded proteins are promising, effective, and novel classes of therapeutic agents to fight antibiotic resistance. Despite the novelty and aspiration to use bacteriophage proteome as an alternative to antibiotic therapy, it has also been proved to be worthy of further research for clinical applications of these therapeutic engineered proteins. Since the world is facing a serious threat of antimicrobial resistance, it is necessary and timely to look afresh at this approach with practical applications. In the future, further experimental and clinical investigations are essential regarding the safety profile, half-life, dose, and site-specificity of the bacteriophages or their proteome for them to be used as novel therapeutic candidates.