key: cord-1036033-0vcuqpqo authors: Bhargava, Kanika; Nath, Gopal; Bhargava, Amit; Aseri, G. K.; Jain, Neelam title: Phage therapeutics: from promises to practices and prospectives date: 2021-11-25 journal: Appl Microbiol Biotechnol DOI: 10.1007/s00253-021-11695-z sha: 448d4fbdf92c8fc5baec3deb5b185280283a237d doc_id: 1036033 cord_uid: 0vcuqpqo The rise in multi-drug resistant bacteria and the inability to develop novel antibacterial agents limits our arsenal against infectious diseases. Antibiotic resistance is a global issue requiring an immediate solution, including the development of new antibiotic molecules and other alternative modes of therapy. This article highlights the mechanism of bacteriophage treatment that makes it a real solution for multidrug-resistant infectious diseases. Several case reports identified phage therapy as a potential solution to the emerging challenge of multi-drug resistance. Bacteriophages, unlike antibiotics, have special features, such as host specificity and do not impact other commensals. A new outlook has also arisen with recent advancements in the understanding of phage immunobiology, where phages are repurposed against both bacterial and viral infections. Thus, the potential possibility of phages in COVID-19 patients with secondary bacterial infections has been briefly elucidated. However, significant obstacles that need to be addressed are to design better clinical studies that may contribute to the widespread use of bacteriophage therapy against multi-drug resistant pathogens. In conclusion, antibacterial agents can be used with bacteriophages, i.e. bacteriophage-antibiotic combination therapy, or they can be administered alone in cases when antibiotics are ineffective. Key points • AMR, a consequence of antibiotic generated menace globally, has led to the resurgence of phage therapy as an effective and sustainable solution without any side effects and high specificity against refractory MDR bacterial infections. • Bacteriophages have fewer adverse reactions and can thus be used as monotherapy as well as in conjunction with antibiotics. • In the context of the COVID-19 pandemic, phage therapy may be a viable option. GRAPHICAL ABSTRACT: [Image: see text] "The role of the infinitely small in nature is infinitely great…". The prevailing global pandemic COVID-19 reminds us of this quote by the Father of Microbiology-Louis Pasteur. The current pandemic makes us realize and reimagine the immense power of the tiniest microorganisms. Phages are viruses that infect prokaryotic (bacteria) cells but have no effect on eukaryotic (human or animal) cells; hence, they can be employed to manage infections caused by bacteria (Domingo-Calap and Delgado-Martínez 2018) . The administration of bacteriophages for treatment traces back almost a century, and the widespread availability of effective and safe antibacterial medications following WWII led to scepticism of bacteriophage use until the 1990s (Abedon et al. 2011) . Over the last three decades, the global spread of multidrug resistant (MDR), pan-drug resistant (PDR), and extreme-drug resistant (XDR) bacteria, as well as the decreased availability of new effective antibacterial agents, has rekindled the scientific community's interest in bacteriophage as an alternate antibacterial agent (Perros 2015; WHO 2018) . Phage particles are natural and versatile. Furthermore, owing to their (phages) lack of affinity for eukaryotic cells, their modifications contribute to their prospective use in gene therapy and medicinal applications (Hashemi et al. 2010; Robertson et al. 2011; Yata et al. 2014; Bardy et al. 2016 ). According to Biset et al. (2020) and Folliero et al. (2020) , the most commonly reported resistant bacteria were Escherichia coli (56.67%), Klebsiella pneumoniae (50%), Enterobacter cloacae (100%), Staphylococcus aureus (45.45%), Coagulase-negative Staphylococcus aureus (76.47%), Enterococcus spp. (97.50%), Acinetobacter baumannii (100%), and Pseudomonas aeruginosa (96.80%). If corrective measures are not implemented, MDR infection mortality may exceed 10 million by 2050 (WHO 2020). Antibiotic resistance (AR) has been continuously increasing and has primarily been addressed from the perspective of human misuse, whereas in veterinary and agricultural context, their overuse leading to MDR has not received the requisite attention. Antimicrobial resistance (AMR) poses a significant threat to the ecosystem, which must be acknowledged and addressed when designing effective AMR plans (O'Neill 2014) . The global problem of MDR bacterial infections necessitates immediate actions, and one such infection control option could be bacteriophage therapy (Chanishvili and Aminov 2019) . Besides, in addition to engineered phages, bacteriophageproduced lytic enzymes also exhibit properties that can be marketed in medical and industrial sectors. With the current advent of AMR throughout the world and the dried pipelines of pharmaceutical industries, phage therapy could be the answer. In this review, we emphasize the aspects of phage therapy that make it a promising solution to MDR infectious diseases and also delineate some of the hurdles that must be addressed in the designing and implementation of clinical research to determine the effectiveness of phage therapy in humans against MDR infections and briefly discuss the prospects of phage therapy in COVID-19 pandemic. Most of the mini-reviews that have been published before discuss how phages were discovered? Where were they practiced before? Why they were abandoned and their advantages compared to antibiotics? To break the cycle of resistance and circumvent this silent global epidemic, the pharmacokinetics of phage therapy must be adopted which is being used in some instances that we have summarized in this manuscript based on different clinical infections. The clinical cases outlined in this manuscript focuses on major systemic diseases in which phage therapy experiments have contributed to the fight against resistant bacterial infections caused by MDR bacteria. This manuscript has not nullified antibiotics use but has stipulated an approach where bacteriophages can be used synergistically, as evident from some practical clinical case studies. In a natural ecosystem, antibiotics play a critical part in the regulatory processes of the microbes (Aminov 2009 ), where they serve as signalling molecules in small quantities (Davies et al. 2006) . However, when used in an appropriate concentration, antibiotics act as bacteriolytic and bacteriostatic agents in the management of bacterial infections (Leekha et al. 2011) . Antibiotics are also commonly used at sub-therapeutic concentrations in the livestock feed for metaphylaxis (Manyi-Loh et al. 2018) . Antibacterial agents, which are imprudently used in the medical, aquaculture, agricultural, and other industries, are hotspots for their continual entry into the ecosystem, leading to the selection and amplification of antibiotic-resistant genes (ARG) (Yadav and Kapley 2021) . ARG is incorporated into the commensal flora at this stage, and the expense of "fitness" of an organism carrying ARG is reduced (Beceiro et al. 2013) . As a result, even in the absence of antibacterial agent-induced selective pressure, AR bacterium persists (Andersson and Hughes 2011; Brown and Wright 2016) . The pool of amplified ARG is subsequently discharged into other compartments of the ecosystem, along with the accompanying antibacterial medications, from whence it is further distributed to even more distant ecological compartments via horizontal gene transfer (HGT) processes [ Fig. 1 ] (Aminov 2011; Duran et al. 2016; Brown et al. 2017 ). Bacteriophages bind to and adsorb on specific receptors on the surface of their hosts (bacteria) before introducing their genetic material to begin viral propagation; their relationship ranges from parasitic to mutualistic (Weinbauer 2004; Sime-Ngando 2014) . In lytic infection, the phage adheres to the bacterial surface [ Fig. 2A Antibiotics gained popularity due to their broadspectrum activity (Fair and tor 2014) , however, with the increase in the understanding of the human microbiome, this broad-spectrum killing potential is rapidly revealing itself as a significant disadvantage (Cho and Blaser 2012) . Being natural bacteria predators, bacteriophages have an advantage over antibiotics as they are specific, targeting only their host bacteria, implying a gentler approach to local microflora (Divya Ganeshan and Hosseinidoust 2019). However, another factor to consider is the interaction of the polyvalent lytic phages with the commensal flora (Ly-Chatain 2014). This is especially true in the case of gut flora if the phage is administered orally. Therefore, the impact of bacteriophages on any microbiome, (Fabijan et al. 2020) particularly gut microbiota, must be regarded as an essential component that governs the microbiome and should be further researched (Sutton and Hill 2019) . Drug resistance is a worrisome and widespread problem worldwide, with the emergence of MDR, PDR and XDR strain containing novel ARGs and the paucity of new medicines for treating bacterial diseases (Fair and Tor 2014) . Bacterial defence mechanisms evolved as a result of the fight for survival between bacteria and the phages that infect them; yet, phage counteracting mechanisms are little understood and unexplored (Rostøl and Marraffini 2019) . Phages can evolve in tandem with their hosts, increasing their chances of infecting their host. Lysogenic phages/temperate phages insert their DNA into the bacterial genome and may act as vehicles for HGT and ARG dissemination, making them ineffective in acute infections (Principi et al. 2019; Lin et al. 2017) . Hence for bacteriophage therapy, lytic phages should be employed. ARG can be carried by phages and spread to other bacterial pathogens; however, utilizing DNA sequencing methods assures that therapeutic phage is clear of any virulent genes (Taati Moghadam et al. 2020 ). Many experimental data have demonstrated the potential role of phage-antibiotic synergistic effects and efficacy of bacteriophage alone on different models for different indications. The concept of bacteriophage therapy, which was used to treat bacterial diseases at the turn of the twentieth century, has garnered attention in the current period of rising AMR (Schooley et al. 2017; Furfaro et al. 2018; ). However, due to the unavailability of validated and adequately controlled clinical trials, phage therapy faces many challenges in its progression in the present scenario. Additional care needs to be taken in the organising and designing such trials where therapeutic variables such as the dose (Payne and Jansen 2003) and concoction of phage cocktails are required ). Some of those systemic studies of antimicrobial agents and chemotherapy, of diseases caused by MDR organisms, successful treatments with adjunctive bacteriophage therapy are described below (Fig. 3 ). Bone and joint infection (BJI) pose significant management challenges and cause severe morbidity [ Table 1 ]. If ignored, BJIs induce acute sepsis with bone and joint deterioration, severe pain, sinuses, and permanent impairment, necessitating exceptional microbiological examination to allow for targeted antibiotic therapy (Colston and Atkins, 2018) . A recent study suggested that local phage administration into the joints, with hardware removal, systemic antibiotics, and antibiotic spacers, successfully managed MDR P. aeruginosa infection of prosthetic joint (PJ) and osteomyelitis (Tkhilaishvili et al. 2020) . In vitro, the authors discovered phage-antibiotic synergistic effect against P. aeruginosa biofilm. Several other studies in the publication endorse the use of supplementary bacteriophage therapy in the management of resistant BJIs. Ferry et al. (2018) reported a recent case study of recurring S. aureus PJ infection treated with a phage cocktail and antibiotic combination instilled locally. Another case report documented treatment via bacteriophage and antibiotics of left tibial infection caused due to XDR A. baumannii and MDR K. pneumoniae, thereby resulting in tissue healing and limb preservation (Nir-Paz et al. 2019). Yilmaz et al. (2013) investigated the therapeutic efficacy of MRSA (methicillin-resistant Staphylococcus aureus) and P. aeruginosa induced rat tibiae infection utilizing a phage cocktail and an antibiotic in combination and/ or alone, resulting in the reduction of bacterial colonyforming units. Another animal model study for the management of S. aureus osteomyelitis was undertaken, where the potential of bacteriophage therapy alone in the treatment of chronic infections caused by MDR bacteria was demonstrated by Kishor et al. (2016) . As a result, phage application in orthopaedic surgery as an adjuvant to antibiotic therapy or alone against drug-resistant bacteria holds a lot of promise. BJIs have a significant impact on healthcare resources due to growing urbanization and an ageing population, necessitating well organized, novel multidisciplinary collaboration for successful therapy. The prevalence of urinary tract infection (UTI) is high, resulting in significant loss of man hours, financial burden on society, and a strain on health-care infrastructure. UTI complications frequently result in sepsis and can be fatal if caused by AMR pathogens, and various studies demonstrate the effectiveness of bacteriophages in the management of it [ Table 2 ] (Bhargava et al. 2021 ). Leitner et al. (2017) reported lytic activity, as well as the resilience of phages to resistance, can be a useful option for the treatment of the world's ever-increasing AR. To treat recurrent UTI caused by ESBL (extended spectrum beta-lactamase)-positive K. pneumoniae in a subject with an indwelling urostomy and uretral stent, Kuipers et al. (2020) employed a personalized phage-antibiotic combination. Valerio et al. (2017) investigated the efficacy of bacteriophages and antibiotics alone or in combination in managing E. coli-induced UTI and also the susceptibility of the bacteria to the screened antibacterial agents in the presence and absence of bacteriophages. The effectiveness of combination therapy is determined by the AR, the bacteria in question, and the type of antibiotic employed (bactericidal or bacteriostatic). In another case study, bacteriophage therapy against P. aeruginosa UTI in humans was documented where combination therapy of phage and antibiotic was well tolerated resulting in treatment of the patient (Khawaldeh et al. 2011) . The high bacterial inactivation efficiency of phage alone or in conjunction with antibiotics, as well as their self-limitation property, lay the groundwork for future comprehensive studies into UTI and AMR management and control. Biofilm formation by multiple microorganisms causes persistent tissue and foreign body infections which become highly resistant to the antibiotics [ Table 3 ]. Bacteria in biofilm flourishes in slime-encased aggregations that affect millions of individuals, and it is sometimes difficult to treat, resulting in a chronic infection that medical practitioners struggle to control (Harper et al. 2014) . As biofilms are difficult to treat in general, a novel technique is required; currently, antibiotics and basic disinfectants have shown a limited ability to successfully remove biofilms. Fong et al. (2019) conducted an experimental investigation on an animal model in which P. aeruginosa biofilm-induced frontal sinusitis was reduced by phage cocktail and concluded that it was effective and safe. Bacteriophages reproduce within the host bacterium and synthesize enzymes that disintegrate the bacterial biofilm extracellular polymeric substance, resulting in pathogen eradication. In their research, Coulter et al. (2014) documented that a combination of bacteriophage and antibiotics resulted in the complete eradication of biofilm and the reduction of bacteria resistant to both phages and antibiotics. Similar studies conducted using antibiotics combined with phage have resulted in the eradication of Klebsiella pneumoniae and Staphylococcus aureus biofilms (Verma et al. 2010; Rahman et al. 2011) . Chaudhry et al. (2017) conducted an in vitro experiment in which P. aeruginosa biofilms were treated alone and in combination with bacteriophages and bacteriolytic antibiotics. The findings delineated that combination therapy of bacteriophage and antibiotics for the treatment of biofilm infections are more effective and a better therapeutic option. Furthermore, Rahman et al. (2011) demonstrated in their study that combining a bacteriophage and an antibiotic effectively combats Staphylococcus aureus biofilm. In another investigation paired lytic bacteriophage with an antibacterial agent, which resulted in increased biofilm eradication compared to either alone, reinforcing the concept that when combined, they are more efficient (Verma et al. 2010) . Bacteriophages have tremendous potential for the management of biofilms; nevertheless, such applications are still in their early phases because the processes of killing by drugs and phages differ significantly, necessitating additional experimental investigation. The emergence of MDR bacteria has entailed the search for novel therapeutic designs or strategies [ Table 4 ]. Heart and pulmonary infections are highly challenging as they often lead to septicemia. If left ignored, they might affect other organs as well. When pathogenic microorganisms evolve and gain resistance to potential treatments, novel therapeutic approaches would preferably target them, resulting in infection management. As an illustration of such a technique, Chan et al. (2018) isolated a lytic bacteriophage against MDR P. aeruginosa with multi-drug systemic porin M on its outer membrane, where phages bind. It culminated in the process of evolution in which the phage altered the bacteria's efflux pumping mechanism, making the pathogen susceptible to several classes of antibacterial drugs. Antibiotics alone are frequently ineffective in treating these resistant infections due to AR, poor biofilm permeability, and other factors; however, phages are host specific, killing the intended bacterium, and the development of phage resistance may lead to an increase in antibiotic sensitivity (Chan et al. 2018) . In a patient with Pseudomonas aeruginosa, Oechslin et al. (2017) demonstrated that a single dose of bacteriophage had a high synergistic activity with an antibiotic and phage-resistant bacteria had decreased infectivity. Phage therapy, when used alone or in combination with antibiotics, warrants further clinical investigation to improve the efficacy of existing methodologies or develop innovative approaches. Cao et al. (2015) found that administering phage intranasally to mice with a Klebsiella pneumoniae pulmonary infection reduced pathogenicity and pro-inflammatory cytokine levels. An in vivo investigation was conducted in mice in which MDR A. baumannii lung infection was treated with a newly isolated phage cocktail, resulting in a higher rate of survival after infection as compared to the untreated group (Cha et al. 2018) . As AR among bacteria is a problematic issue that necessitates the creation of next-generation treatment approaches in which phage can thrive and soon be at the forefront of clinical care in the management of heart and pulmonary infections. The causes of gastrointestinal infection (GI) are many; however, bacterial causes are often responsible for severe cases of infectious diarrhoea than other infectious aetiologies [ They further stipulated that in the case of fulminant AR infections, antibiotics combined with phages will provide significant benefit in both the immediate and delayed outcomes, with a good survival rate. Chaturvedi and Nath (2018) reported that when K. pneumoniae (MDR)-specific phages were administered orally in the gut of albino mice, they eliminated MDR bacteria that had the potential to cause additional nosocomial infections upon translocation. Furthermore, Green et al. (2017) demonstrated that phages isolated from the environment could be effective in combating even the most serious of infections caused by Escherichia coli superbugs found in intestinal tracts of immunocompromised patients, which when translocate, pose a considerable threat. Despite the favourable findings of phage therapy, multiple studies have demonstrated that phage-host interactions are more complicated and that the majority of attention is focused on them and less on the phage-human interaction. As a result, more research is needed to make this medication broadly available for human usage. Bloodstream infection (BSI) due to bacteria (bacteremia) is a severe multisystem disease that is strenuous to treat due to its high mortality rates and manifestation [ Table 6 ]. Bacteremia can have several serious health repercussions, and the haematogenous spread of bacteria may result in diseases like endocarditis or osteomyelitis (Holland et al. 2016; Agarwal and Aggarwal 2016) . Jennes et al. (2017) described the first contemporary report of bacteriophage monotherapy against MDR P. aeruginosa septicaemia in a patient, which resulted in the eradication of the pathogen. Hung et al. (2011) concluded in an experimental study of phage therapy that liver abscess and bacteremia in mice due to K. pneumoniae could be a prospective mode of therapeutic intervention. In a study conducted by Vinodkumar et al. (2008) , a single dosage of lytic phage administered to mice suffering from MDR Pseudomonas aeruginosa-induced septicemia resulted in its redemption. The phage strain utilized in this study displayed broad-spectrum lytic activity against other isolated MDR strains of Pseudomonas aeruginosa, implying that phage therapy might be employed as a stand-alone treatment for AR infections. In an original research work, Sunagar et al. (2010) investigated the effect of bacteriophage therapy on fatal S. aureus-induced bacteremia in non-diabetic and streptozotocin-induced-diabetic mice. They concluded that bacteriophages could also be used to prevent Staphylococcus aureus infections in immunocompromised patients. Furthermore, Watanabe et al. (2007) ascertained the effectiveness of phage in an animal model of P. aeruginosa-induced sepsis. The results of this experiment showed that newly isolated lytic phage strain administration was extremely effective against sepsis caused by P. aeruginosa. Although bacteriophage therapy is thought to have significant potential in the treatment of a variety of topical and localized infections, this interest has not extended to the treatment of BSIs, which is surprising given that phages are likely to be safe and efficient when delivered in a controlled manner. Skin and soft tissue infections (SSTIs) are caused by microbial infiltration of the epidermis, dermis, subcutaneous tissue, superficial fascia, or muscles and can present with a wide range of symptoms, etiological agents, and severity (Ki and Rotstein 2008) . The advent of AR bacteria has complicated the management of SSTIs, with MRSA, VRE, and ESBL positive isolates of Escherichia coli and Klebsiella spp. being the most common (Moet et al. 2007) , necessitating a reconsideration of the use of phage for its treatment [ Table 7 ]. Chhibber et al. (2017) investigated the efficiency of a transfersomal phage cocktail in the treatment of MRSAinduced SSTIs. They concluded that using transfersome as a delivery vehicle improves the stability and persistence of the enclosed bacteriophages in vivo. Similarly, when an animal model burn wound was infected with Klebsiella pneumoniae, bacteriophage was applied topically, which reduced mortality and resulted in an insignificant decrease in phage titre, indicating its stability (Kumari et al. 2011 ). An original clinical study reported by Gupta et al. (2019) stated that topical bacteriophage application for treatment of chronic non-healing wounds is highly effective. Chronic wounds are often recalcitrant to medication due to MDR pathogens and biofilm formation; however, phage cocktail was an excellent alternative to drugs (Jault et al. 2019 ). Wills et al. (2005) reported a wound infection caused by S. aureus, where staphylococcal phage managed to prevent abscess formation when injected simultaneously with the bacterium. Phage multiplied in the tissues. Therefore, the authors concluded that phages might also be valuable prophylaxis against staphylococcal infection (Wills et al. 2005) . Superficial bacterial infections impose significant emotional and economic burdens on healthcare systems worldwide and are frequently worsened by AR, for which phage therapy is a viable potential antibacterial option (Abedon et al. 2011 ). Antibiotic resistance is a cause of concern, and phage has been advocated as one feasible therapeutic alternative for therapy and antibiotic potency enhancement. Bacteriophage is presently the recommended therapeutic modality, either alone or combined with an antibacterial agent, with the latter is expected to boost efficiency (Gkartziou et al. 2021) . The combination of phage with antibiotics could have a variety of outcomes, including additive, synergistic, ineffective, or antagonistic effects (Abedon 2019; Gu Liu et al. 2020) . Principi et al. (2019) suggested that bacteriophages reduce the minimum inhibitory concentration of AR bacteria to the level of sensitive bacteria. Antibacterial agents are frequently chosen based on antibiotics susceptibility data and the patient's medical condition so that when phages are coupled, a "phage adjuvation" effect can be produced (Gu Liu et al. 2020) . Antibiotic concentration must also be optimized since they increase the rate of bacterial cell mutation when used at sub-lethal concentrations, rendering coupled strainspecific phage useless (Saha and Mukherjee 2019). Several phage-antibiotic combinations have been assessed in vitro. However, due to inconsistent results with the combinatorial treatment, a customized in vitro assessment approach is required for optimal therapeutic effect in vivo against distinct bacterial species (Torres- Barceló et al., 2018) . Currently, phage therapy does not replace antibiotics, but with the emergence of MDR, the concurrent use of personalized phage alone or in combination with antibiotics may be the way to the future. However, because some antibiotics can interfere with phage therapy by killing their host (bacterium) and blocking their reproduction, more rigorous sophisticated preclinical clarifications are essential prior to in vivo administration (Abedon 2019) . There are significant gaps in how bacteriophages, bacteria, and antibiotics interact. Antibiotics can modify phage features such as growth rate, infectivity, and burst size, and their fate is mostly unknown and unexplored (Cairns et al. 2017) . Torres-Barceló et al. (2018) findings imply that the effects of antibacterial medications on bacteriophages, and the combined effects of phages and antibiotics on bacteria, can alter substantially as interactions evolve. Although multiple studies have demonstrated a synergistic link between phages and antibiotics, the focus is often on bacteria, with little knowledge about the influence on phages. Therefore, further research is required to test it in its entirety. In various medical and biotechnological areas, innovations in genetic engineering and molecular biology for the application of phages have been observed. One of the phage modifications, "modus operandi", is based on the integration of bacteriophage coat protein genes with foreign molecules (Bardy et al. 2016) . It results in the creation of numerous bacteriophage variants. Currently, engineered bacteriophages have generated little proof of robust efficacy (Nair and Khairnar 2019) . It has contributed to inconsistent outcomes in the treatment of diseases, as it has been less explored. Contrary to antibiotics, modified phages conflicted results are due to their unknown detailed molecular composition (Pizarro-Bauerle and Ando 2020). When bacteriophages are introduced into the food chain, they progress into the environment uncontrollably. When they infect bacteria, altering those would alter associated microbiota that may or may not be governable (Nair and Khairnar 2019) . Engineered bacteriophages can pose an issue in terms of public acceptance due to a lack of knowledge and understanding (Sybesma et al. 2018) . They are themselves living entities that are allowed to thrive on their host, which is thriving on another living organism. Hence, phage therapy via modified phages further derails its approval as a mainstream treatment option. For its concrete establishment in the world of medicine, there is a need for thorough research with extensive clinical trials (Pizarro-Bauerle and Ando 2020; Kutter et al. 2010; Miedzybrodzki et al. 2012; Carvalho et al. 2017) . Unlike antibiotics, phages have genomes and replicate while parasitising on their host; engineering them may result in further complications and would lead to the addition of clauses of legislation regarding the ethical concerns related to genetic modifications (Abdelkader et al. 2019) . Bacteriophage recombinant lytic proteins can be used as enzybiotics (Schuch et al. 2002) . For gram-positive bacteria, external administration of endolysin results in cell disruption (Young 2013) . Moreover, for gram-negative bacteria, lysins are unable to cross the bacterial outer cytoplasmic membrane (Fischetti 2018) . Therefore, endolysin therapy is futile since it can also lead to the release of a large amount of endotoxin. Furthermore, it is a significant constituent of lipopolysaccharide, which, when released in the bloodstream of an infected host, would result in gram-negative septic shock causing hemodynamic and metabolic anomalies (Bardy et al. 2016; Prins et al. 1994) . Also, when lysins are put up for therapeutic use, the production of neutralising antibodies is induced, which subsequently hinder their antibacterial activity on multiple administrations. Hence their use as an antimicrobial agent in human treatment raises concerns as they possess relatively short plasma life, immunogenicity and possible toxicity, proinflammatory response to bacterial debris and its inadequacy to lyse intracellular bacteria (Vazquez et al. 2018) . Furthermore, the transfer of toxin-producing genes by genetically engineered phages puts them on the downside. However, new strategies are being implemented to safely use such phages after the risk of recombination and horizontal gene transfer among bacteriophages is thoroughly investigated. The successful launch of modified bacteriophages cannot be implemented by putting health, safety and environment at risk (Bardy et al. 2016 ). Currently, no framework (Verbeken et al. 2014) exists that could define phage as a medicinal product for human use. However, institutes in Georgia, Poland, provide customized phage cocktails to chronically ill patients for whom all other options of authorized treatment get exhausted (Yilmaz et al. 2013) . Although in other parts of the world, bacteriophage therapy is still controversial, hence a dedicated legal framework is essential for its smooth introduction into western medicine. Regulatory cells in western countries have been debating about norms and steps to pioneer guidelines for phage therapy (Vandenheuvel et al. 2015) . For safety purposes, legislation nowadays is heavily controlled for the production and administration of drugs by having strict quality control procedures. For the safety of bacteriophage therapy, a monitoring system needs to be implemented for data collection and analysis to follow the development of bacterial resistance to phages along with the installation of dedicated public structures that could pioneer more clinical trials (Sybesma et al. 2018; Kortright et al. 2019; Pirnay et al. 2018; Svircev et al. 2018 ). For bacteriophage stability and effectiveness, good manufacturing practice level facilities are necessary for phage production and prospective research investigations (Brown et al. 2017; Kutter et al. 2010) . This would allow for the storage of bacteriophage concoctions in retail pharmacies. Bacteriophage therapy is currently being developed in two directions. The first is the development of broadhost-range "off-the-shelf" solutions that may be utilised for infections caused by specific bacteria, and the second is a customized approach, such as the isolation and production of specific phage cocktails against a specific strain isolated from a patient. Bacteriophages isolated from the environment are the initial step toward bacteriophage therapeutics; many research investigations are currently underway to increase efficiency and optimise biofilm disruption, employing genetically altered phages (Bradley et al. 2016; Haellman and Fussenegger 2016; Wang et al. 2011) in situations when antibiotics become inadequate (Tagliaferri et al. 2019; . For further commercialization of phage and its products, there is a need for extensive research of bacteriophage metagenomics and metaproteomics. Metagenomics is a concept that refers to the examination of genetic data from environmental samples in order to identify microbial communities (de Abreu et al. 2021) . A high-throughput sequence (HTS) based functional metagenomics technique is useful for identifying and understanding resistance mechanisms detecting ARG and examining the internal dynamics (DNA or RNA level) of the cell (Churko et al. 2013; Sukhum et al. 2019) . Because of the significant growth in data creation, new bioinformatics tools have been developed to deal with the massive volume of sequencing reads gathered during genome sequencing investigations (Pereira et al. 2020 ). There are two types of metagenomic analyses: sequence-based and functional-based (de Abreu et al. 2021) . Numerous fragment sequences are generated and analysed using software, allowing for the development of structural and functional diversity in a microbiome by finding genes and metabolic pathways of bacterial genomes (Bharti and Grimm 2021) . Genomic analysis also determines the relationship between the bacteriophage and its host, genomic content, and genetic linkage between the most sensitive and most resistant strains obtained to evaluate phage therapy viability by ensuring they did not encode for toxins and/or lysogenic characteristics (Haines et al. 2021) . Furthermore, genetic analysis of isolates with polar opposite phage sensitivity could provide additional insight into resistance mechanisms, contributing to cocktail formulation design. Pirnay (2020) further discussed in "the future Earth 2035", in which he shared Dr John Iverian's experience and work on the technology Phage BEAM (Bedside Energized Anti-Microbial). First, a metagenome analysis of the entire sample was performed, and the results were stored in the "Phage Xchange" server, where an intricate artificial intelligence-driven algorithm predicted the sequence of the phage that would most likely infect the infecting bacteria. Then the predicted phage genome data was transferred to the Phage-BEAM device, which manufactured the phage genome and, eventually, the phage itself for clients using patented technology (Pirnay 2020) . Antibiotic overuse and abuse in the medical, agriculture, and aquaculture sectors has aided the world into a silent pandemic of AMR. The most common cause of opportunistic infections worldwide is a group of ESKAPE (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter spp.) organisms, the majority of which are MDR isolates (Mulani et al. 2019) . The upsurge may be seen in the number of bacteriophage therapy publications (more than 600) covered by PubMed from 2016 to 2020, compared to around 285 articles published between 2010 and 2015 (Azam et al. 2021) . It is worth noting that these data from the recent decade reflect a significant increase over those from two decades before when there were few papers published. The rise in the number of articles published in the last two decades indicates that the scientific industry's focus is returning to phage therapy; however, physicians are wary of phages because they are a living organism that is introduced into a sick patient, and their complete mechanism of action is still underexplored. COVID-19 is one of the most prominent disaster-induced pandemics of our century (World Health Organization 2020). The prevalence, occurrence and manifestations of bacterial infections in patients already diagnosed with SARS-CoV-2 (COVID-19) are currently not well documented and pose many questions (Cox et al. 2020; Huttner et al. 2020; Langford et al. 2020 ). It has been reported that over 70% of patients were administered broad-spectrum fluoroquinolones and third-generation cephalosporins, despite a significant low rate of bacterial infections (Langford et al. 2020) . While antibiotics are inadequate for the treatment of COVID-19, patients with suspected or confirmed secondary bacterial infections and/or co-infections are still administered antibiotics. This assumption, however, poses the question of antibiotic overuse and eventual global bacterial resistance. The increasing number and our decreasing ability to eradicate AMR bacteria not only makes us more prone to bacterial infections but also weakens us during viral pandemics (Vaillancourt and Jorth 2020) . New antibiotics or alternative therapies for secondary bacterial infections are required for the recurrent waves of COVID-19 and the imminent future pandemic. Alternative therapies such as phage therapy can be explored as it shows promise. Although data for COVID-19 is still scarce, an integrative approach is proposed where bacterial infections, together with delayed production of antibodies results in a significant contributing factor to COVID-19 mortality rate. Therefore the implementation of phage therapy might lead to microbiota homeostasis accelerated development of therapeutic antibodies via "Phage display" (Blanco-Picazo et al. 2020 ) and also decrease the pathogenic bacterial load in the respiratory tract of the infected persons (Wojewodzic 2020) . Also, phages tend to compete with virus for cellular receptors when introduced after a primary viral infection and thus reduce the harmful activities of it (Meek and Takahashi 1968) . Inflammation and cell destruction resulting from excessive reactive oxygen species (ROS) are often associated with a respiratory virus infecting the lungs (Gorski et al. 2020) . Phage and phage proteins, however, inhibit the development of ROS and thus demonstrate antiviral activities by anti-oxidant therapy (Miedzybrodzki et al. 2005; Centifanto 1968 ). The same types and dosage of drugs are used in both techniques, the prophylactic and therapeutic: but the prophylactic use of antibiotics is not approved by most health institutions and policy makers globally due to the reported rise in AMR rates, which correlate with the overuse and misuse of antibiotics (Manohar et al. 2020; Holshue et al., 2020; Wang et al. 2020) . However, that is not the case with bacteriophages as they do not affect any eukaryotic cells and therefore can be used both prophylactically and therapeutically (Adhya et al. 2014; Lin et al. 2017 ). With the emerging AR bacterial infections, the activity of bacteriophages against resistant bacteria with no major serious side effects makes them a promising solution in recalcitrant bacterial infections since bacteriophages are specific for their host. As reflected from prior clinical case studies, instead of replacing antibiotics altogether, the combination of both, i.e. bacteriophage and antibiotic or phage alone, could result in potentially viable therapeutic options against bacterial pathogens. Enhanced bacterial clearance, more efficient adsorption into biofilms and a lower likelihood of the development of bacteriophage resistance are the potential advantages of bacteriophage therapy. Furthermore, they have pronounced prospective for treating secondary bacterial infections or co-infections during viral pandemics like the prevailing Covid-19 pandemic. We are in the midst of a significant shift in the medical industry, and we are failing to combat various diseases caused by AMR organisms. Looking at the current scenario, more research that sheds light on the nature of host-phage interactions in the context of commensal flora is required that would aid in elucidating and accelerating the concept of bacteriophage therapy and advocating its regulatory approval in modern medicine. The preclinical and clinical progress of bacteriophages and their lytic enzymes: the parts are easier than the whole Phage-antibiotic combination treatments: antagonistic impacts of antibiotics on the pharmacodynamics of phage therapy? Phage Treatment of Human Infections Therapeutic and prophylactic applications of bacteriophage components in modern medicine Bone and Joint Infections in Children: Acute Hematogenous Osteomyelitis The role of antibiotics and antibiotic resistance in nature Horizontal gene exchange in environmental microbiota Persistence of antibiotic resistance in bacterial populations Early clinical experience of bacteriophage therapy in 3 lung transplant recipients What's Old Is New Again: Bacteriophage Therapy in the 21 st century Genetically modified bacteriophages in applied microbiology Antimicrobial resistance and virulence: a successful or deleterious association in the bacterial world? Urinary tract infections and phage therapy to tackle antimicrobial resistance (AMR) Current challenges and best-practice protocols for microbiome analysis Multi-drug resistant and extended-spectrum β-lactamases producing bacterial uropathogens among pregnant women in Northwest Ethiopia Unravelling the consequences of the bacteriophages in human samples Tools and principles for microbial gene circuit engineering Antibacterial drug discovery in the resistance era Phage engineering: how advances in molecular biology and synthetic biology are being utilized to enhance the therapeutic potential of bacteriophages Sublethal streptomycin concentrations and lytic bacteriophage together promote resistance evolution Evaluation of the efficacy of a bacteriophage in the treatment of pneumonia induced by multi-drug resistance Klebsiella pneumoniae in mice Bacteriophages and their derivatives for the treatment and control of food-producing animal infections Intestinal microbiota and antibiotic resistance: perspectives and solutions Antiviral Agent from λ-infected Escherichia coli K-12: I Isolation Characterization of two novel bacteriophages infecting multidrug-resistant (MDR) Acinetobacter baumannii and evaluation of their therapeutic efficacy in vivo Phage treatment of an aortic graft infected with Pseudomonas aeruginosa Bacteriophage therapy: coping with the growing antibiotic resistance problem Oral administration of Klebsiella pneumoniae-specific bacteriophage eradicates the bacteria in albino mice Synergy and order effects of antibiotics and phages in killing Pseudomonas aeruginosa biofilms Transfersomal phage cocktail is an effective treatment against methicillin-resistant Staphylococcus aureus-mediated skin and soft tissue infections The human microbiome: at the interface of health and disease Overview of high throughput sequencing technologies to elucidate molecular pathways in cardiovascular diseases Effect of bacteriophage infection in combination with tobramycin on the emergence of resistance in Escherichia coli and Pseudomonas aeruginosa biofilms Co-infections: potentially lethal and unexplored in COVID-19 The world of sub inhibitory antibiotic concentrations Metagenomic Approaches to Analyze Antimicrobial Resistance: An Overview Phage therapy with a focus on the human microbiota Bacteriophages: protagonists of a post-antibiotic era Successful Treatment of a Recalcitrant Staphylococcus epidermidis Prosthetic Knee Infection with Intraoperative Bacteriophage Therapy Silver nanoparticles: A new view on mechanistic aspects on antimicrobial activity Safety of bacteriophage therapy in severe Staphylococcus aureus infection Antibiotics and bacterial resistance in the 21 st century DAIR") with local injection of a selected cocktail of bacteriophages: is it an option for an elderly patient with relapsing Staphylococcus aureus prosthetic-joint infection? Development of phage lysins as novel therapeutics: a historical perspective Prevalence and Antimicrobial Susceptibility Patterns of Bacterial Pathogens in Urinary Tract Infections in University Hospital of Campania "Luigi Vanvitelli Safety and efficacy of a bacteriophage cocktail in an in vivo model of Pseudomonas aeruginosa sinusitis Bacteriophage therapy: clinical trials and regulatory hurdles Combined bacteriophages and antibiotics as an efficient therapy against VRE Enterococcus faecalis in a mouse model Antimisiaris SG (2021) Nanobiosystems for Antimicrobial Drug-Resistant Infections Phage therapy: current status and perspectives Bacteriophages from ExPEC reservoirs kill pandemic multidrug-resistant strains of clonal group ST131 in animal models of bacteremia Phage-antibiotic synergy is driven by a unique combination of antibacterial mechanism of action and stoichiometry Bacteriophage therapy of chronic non-healing wound: clinical study Synthetic biology-toward therapeutic solutions Analysis of Selection Methods to Develop Novel Phage Therapy Cocktails Against Antimicrobial Resistant Clinical Isolates of Bacteria Evaluation of humoral and cellular immune responses against HSV-1 using genetic immunization by filamentous phage particles: a comparative approach to conventional DNA vaccine Washington State 2019-nCoV Case Investigation Team (2020) First Case of 2019 Novel Coronavirus in the United States Experimental phage therapy in treating Klebsiella pneumoniae-mediated liver abscesses and bacteremia in mice COVID-19: don't neglect antimicrobial stewardship principles! Efficacy and tolerability of a cocktail of bacteriophages to treat burn wounds infected by Pseudomonas aeruginosa (PhagoBurn): a randomised, controlled, double-blind phase ½ trial Use of bacteriophages in the treatment of colistin-only-sensitive Pseudomonas aeruginosa septicaemia in a patient with acute kidney injury-a case report Bacterial skin and soft tissue infections in adults: A review of their epidemiology, pathogenesis, diagnosis, treatment and site of care Phage therapy of staphylococcal chronic osteomyelitis in experimental animal model Phage therapy: a renewed approach to combat antibiotic-resistant bacteria A Dutch case report of successful treatment of chronic relapsing urinary tract infection with bacteriophages in a renal transplant patient Bacteriophage versus antimicrobial agents for the treatment of murine burn wound infection caused by Klebsiella pneumoniae B5055 Phage therapy in clinical practice: treatment of human infections Bacterial co-infection and secondary infection in patients with COVID-19: a living rapid review and meta-analysis General principles of antimicrobial therapy Bacteriophages for treating urinary tract infections in patients undergoing transurethral resection of the prostate: a randomised, placebo-controlled, double-blind clinical trial Kessler TM (2021) Intravesical bacteriophages for treating urinary tract infections in patients undergoing transurethral resection of the prostate: A randomised, placebo-controlled, double-blind clinical trial Phage therapy: An alternative to antibiotics in the age of multi-drug resistance The factors affecting effectiveness of treatment in phages therapy Secondary Bacterial Infections During Pulmonary Viral Disease: Phage Therapeutics as Alternatives to Antibiotics? Front Microbiol 11:1434 Antibiotic use in agriculture and its consequential resistance in environmental sources: potential public health implications Differential inhibition by phagicin of DNA synthesis in cells infected with vaccinia Clinical aspects of phage therapy Bacterial viruses against viruses pathogenic for man? Contemporary causes of skin and soft tissue infections in North America Emerging Strategies to Combat ESKAPE Pathogens in the Era of Antimicrobial Resistance: A Review Genetically engineered phages for therapeutics: proceed with caution Successful treatment of antibiotic-resistant, poly-microbial bone infection with bacteriophages and antibiotics combination Review on Antimicrobial Resistance Antimicrobial Resistance: Tackling a crisis for the health and wealth of nations Synergistic interaction between phage therapy and antibiotics clears Pseudomonas aeruginosa infection in endocarditis and reduces virulence Pharmacokinetic principles of bacteriophage therapy Bioinformatics and Computational Tools for Next-Generation Sequencing Analysis in Clinical Genetics A sustainable model for antibiotics Phage Therapy in the Year 2035 The Magistral Phage Engineered Bacteriophages for Practical Applications Advantages and limitations of bacteriophages for the treatment of bacterial infections Clinical relevance of antibiotic-induced endotoxin release Characterization of induced Staphylococcus aureus bacteriophage SAP-26 and its anti-biofilm activity with rifampicin T4 viral nanoparticles for cellular imaging and flow cytometry Ph)ighting Phages: How Bacteria Resist Their Parasites Bacteriophage therapy for critical infections related to cardiothoracic surgery Ameliorating the antimicrobial resistance crisis: phage therapy Oral phage therapy of acute bacterial diarrhea with two coliphage preparations: a randomised trial in children from Bangladesh Development and use of personalised bacteriophage-based therapeutic cocktails to treat a patient with a disseminated resistant Acinetobacter baumannii infection A bacteriolytic agent that detects and kills Bacillus anthracis Environmental bacteriophages: viruses of microbes in aquatic ecosystems Genomic and Metagenomic Approaches for Predictive Surveillance of Emerging Pathogens and Antibiotic Resistance Bacteriophage therapy for Staphylococcus aureus bacteremia in streptozotocin-induced diabetic mice Gut bacteriophage: current understanding and challenges Framing the future with bacteriophages in agriculture Silk route to the acceptance and re-implementation of bacteriophage therapy-part II How phages overcome the challenges of drug resistant bacteria in clinical infections Fighting pathogenic bacteria on two fronts: phages and antibiotics as combined strategy Bacteriophages as adjuvant to antibiotics for the treatment of periprosthetic joint infection caused by multidrug-resistant Pseudomonas aeruginosa Transient negative effects of antibiotics on phages do not jeopardise the advantages of combination therapies The Unrecognized Threat of Secondary Bacterial Infections with COVID-19 Effects of single and combined use of bacteriophages and antibiotics to inactivate Escherichia coli Bacteriophage therapy: advances in formulation strategies and human clinical trials Phage lysins for fighting bacterial respiratory infections: a new generation of antimicrobials Call for a dedicated European legal framework for bacteriophage therapy Structural changes induced by a lytic bacteriophage make ciprofloxacin effective against older biofilm of Klebsiella pneumoniae Utility of lytic bacteriophage in the treatment of multidrug-resistant Pseudomonas aeruginosa septicemia in mice Engineering modular and orthogonal genetic logic gates for robust digital-like synthetic biology Clinical characteristics of 138 hospitalized patients with 2019 novel coronavirus-infected pneumonia in Wuhan Efficacy of bacteriophage therapy against gut-derived sepsis caused by Pseudomonas aeruginosa in mice Ecology of prokaryotic viruses Experimental bacteriophage protection against Staphylococcus aureus abscesses in a rabbit model Bacteriophages could be a potential game changer in the trajectory of coronavirus disease (COVID-19) Antimicrobial resistance and primary health care Global antimicrobial resistance surveillance system (GLASS) report: early implementation 2020 Coronavirus disease 2019 (COVID-19): situation report, 73. World Health Organization Antibiotic resistance: Global health crisis and metagenomics Hybrid nanomaterial complexes for advanced phage-guided gene delivery Bacteriophage therapy in implant related infections: an experimental study Phage lysis: do we have the whole story yet? Acknowledgements We gratefully acknowledge the facilities provided by Amity University Rajasthan (Jaipur) and Viral Research and Diagnostic Laboratory, Department of Microbiology, Institute of Medical Sciences, Banaras Hindu University, India. Authors' contribution NJ, GN and KB hypothesised and designed the