Two Newly Isolated Enterobacter-Specific Bacteriophages: Biological Properties and Stability Studies

In an era of antibiotic therapy crisis caused by spreading antimicrobial resistance, and when recurrent urinary tract infections constitute a serious social and medical problem, the isolation and complex characterization of phages with a potential therapeutic application represents a promising solution. It is an inevitable, and even a necessary direction in the development of current phage research. In this paper, we present two newly isolated myoviruses that show lytic activity against multidrug-resistant clinical isolates of Enterobacter spp. (E. cloacae, E. hormaechei, and E. kobei), the genomes of which belong to a poorly represented phage group. Both phages were classified as part of the Tevenvirinae subfamily (Entb_43 was recognized as Karamvirus and Entb_45 as Kanagawavirus). Phage lytic spectra ranging from 40 to 60% were obtained. The most effective phage-to-bacteria ratios (MOI = 0.01 and MOI = 0.001) for both the phage amplification and their lytic activity against planktonic bacteria were also estimated. Complete adsorption to host cells were obtained after about 20 min for Entb_43 and 10 min for Entb_45. The phage lysates retained their initial titers even during six months of storage at both −70 °C and 4 °C, whereas storage at 37 °C caused a complete loss in their activity. We showed that phages retained their activity after incubation with solutions of silver and copper nanoparticles, which may indicate possible synergistic antibacterial activity. Moreover, a significant reduction in phage titers was observed after incubation with a disinfectant containing octenidinum dihydrochloridum and phenoxyethanol, as well as with 70% ethanol. The observed maintenance of phage activity during incubation in a urine sample, along with other described properties, may suggest a therapeutic potential of phages at the infection site after intravesical administration.


Introduction
Bacteria of the Enterobacter species were first described in 1960 by Hormaeche and Edwards as Gram-negative, facultative anaerobic bacilli with the ability to move [1]. They belong to the ESKAPE (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter spp.) group of pathogens, which include bacteria that are characterized by a constantly increasing resistance to antibiotics-this is a huge problem, particularly for hospital environments [2,3]. The name of this group of microorganisms is related to their "escape" from the effects of antibiotics and other antimicrobial agents [4,5]. According to a report by the World Health Organization (WHO) published in 2017 on the need to search for new antibiotics and ways to combat multidrug-resistant pathogens, bacteria from the Enterobacteriaceae family (including Enterobacter spp.) belong to the highest priority group [6]. Infections with these pathogens are especially dangerous in immunocompromised patients, e.g., in solid organ transplant recipients on chronic immunosuppressive therapy [7] or in hemodialysis patients [8]. Enterobacter cloacae, the main representative of Enterobacter spp., colonizes the mucosa of the human intestine in a physiological state; however, it is also described as the source of many different disorders, including bacteremia [9,10], urinary tract infections (UTIs) [11,12], wound infections [13][14][15], osteoarticular infections [16][17][18], and pneumonia/lower respiratory tract infections [19][20][21]. These bacteria also commonly colonize in various hospital wards, including neonatal intensive care units, which may result in the development of life-threatening infections such as meningitidis [22]. Moreover, it has been suggested that the presence of E. cloacae in the colon environment may be associated with the initiation and progression of colorectal cancer [23].
A significant proportion of clinical bacterial isolates are extended-spectrum β-lactamase (ESBL)-producing strains. The principal described genes responsible for this mechanism of resistance to β-lactam antibiotics (penicillins, cephalosporins, and monobactams) include bla TEM , bla CTX-M , and bla SHV [20,24,25]. Broad-spectrum antibiotic resistance also includes resistance to carbapenems, known as last-resort antibiotics, and to colistin, which often causes a wide range of side effects [26,27]. Related genes that have increasingly been found in clinical strains are, among others, bla KPC−2 , as well as bla NDM , and the presence of efflux pumps is also important [25,27,28]. Recent studies describing Enterobacter-induced UTIs indicate the involvement of extensive drug resistant (XDR), multidrug resistant (MDR), as well as carbapenem-resistant Enterobacterales (CRE) strains in the pathogenesis of infection in hospitalized patients in Eastern Europe [29].
In an era of increasing antibiotic resistance, the search for new alternative infection treatment strategies is a major medical challenge. Although antibiotics are losing their effectiveness, one way to combat bacterial pathogens is bacteriophage therapy. Bacteriophages (phages)-viruses specific to their bacterial host-after penetrating into the host pathogen, amplify and destroy them, and should not negatively impact the physiological microbiota [30]. Various environmental samples are used to search and isolate new therapeutic bacteriophages [31]. Despite the ubiquitous presence of phages in the environment, there may be many obstacles in their isolation, as well as the possibility of using them as therapeutic agents. There is a constant need to obtain preclinical data on new phages in order to assess their efficacy and safety, both in vitro and in vivo [32], especially in the case of urinary tract infections in which Enterobacter strains are etiological agents. In our study, we have isolated and characterized two new bacteriophages which are specific for multidrug-resistant (MDR) Enterobacter spp. strains, and which are meant to be applicable in phage therapy.

Bacterial Strains
In the study, we used twenty clinical strains of antibiotic-resistant Enterobacter, which were isolated from patients with infections of the genitourinary system (n = 7); ears (n = 2); and wounds, ulcers, or purulent lesions (n = 11); who applied to qualify for experimental bacteriophage therapy at the Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences (HIIET PAS) in the years 2017-2021. The species of bacterial strains were determined using matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF/TOF) mass spectrometry (Bruker Daltonics, Billerica, MA, USA). Antibiotic sensitivity was determined by the microdilution method using the MicroScan

Assessment of the Lytic Spectrum of Phages
For the evaluation of the lytic spectrum of each phage, the bacterial suspensions of each of 20 Enterobacter spp. strains were used, with the subsequent procedure being very similar to that used in the search for new bacteriophages. Each amplified phage lysate (40 µL), at a titer of approximately 10 7 -10 8 PFU/mL, was spotted on the plates with a bacterial lawn, incubated under the same conditions, and assessed the next day according to the signs: CL-confluent lysis, SCL-semiconfluent lysis, +++-60 and more confluent plaques, ++-20-60 separate plaques, +-10-20 separate plaques, +/−-single plaques, OL-opaque lysis. The percentage of bacterial strains that were sensitive to specific phages made it possible to determine their lytic spectrum.

Assessment of Optimal Multiplicity of Infection (MOI) for Phages
During the experiments, the best MOI was assessed to optimize bacteriophage amplification. In the first stage, plots of dependence of bacterial concentration (colony-forming unit per milliliter-CFU/mL) on the OD 600 that were determined spectrophotometrically were made for bacterial hosts. Briefly, different dilutions (0, 2, 3, 5, 8, and 10-fold) of the bacterial suspension were prepared and the OD 600 of each sample was measured. Then, serial dilutions of each sample (from 10 0 to 10 −8 ) were made and 100 µL of the selected samples was spotted on an agar plate and spread over the entire surface. Plates were incubated at 37 • C for 11 h, then bacterial colonies were counted and bacterial titers that depend on optical density (OD 600 ) were determined. In the next step, two-hour bacterial suspensions were made, and the bacterial concentrations were tested using the formulas generated from the plots (dependence of the bacterial titer in CFU/mL on OD 600 ). Dilutions were then made to obtain a titer of about 3.0 × 10 6 CFU/mL. Different titers of phage lysates were also prepared. To 10 mL of peptone water, we added 200 µL of a suspension of the appropriate bacterial strain and 200 µL of a specific phage dilution (10 3 , 10 4 , 10 5 , 10 6 , 10 7 , 10 8 , or 10 9 PFU/mL) and mixed them. After overnight incubation at 37 • C, all samples were filtered and RTD in triplicate were performed for each of them to determine phage titers.

Planktonic Bacterial Lysis Assay
The experiment was performed similarly to those described elsewhere [38]. The lytic efficiency of the two new bacteriophages was determined using suspensions with different phage and bacteria ratios (at the most effective MOI determined in the previous experiment: 0.001, 0.01, 0.1, and 1.0). Briefly, the two-hour bacterial suspension was diluted to a titer of 10 6 CFU/mL and samples with different MOIs were prepared. In these samples, as well as the samples with bacterial suspension (positive control) and only phage lysates (negative control), the OD 600 were measured spectrophotometrically at 0, 1, 2, 3, 4, 6, 8, and 10 h of incubation at 37 • C. Two independent experiments were conducted, and in each of them, sample measurements were performed in triplicate.

Determination of the Phage Adsorption Time
To determine the kinetics of phage adsorption to their hosts and to estimate the adsorption rate constant, we used the procedures described elsewhere [39,40], with some modifications. Briefly, 10 mL of phage lysate (10 7 PFU/mL) was added to 10 mL of bacterial suspension (10 8 CFU/mL) at MOI = 0.1, and then incubated at 37 • C. At time 0 and after specified time intervals, 1 mL of the sample was taken and filtered through a syringe filter. Its serial dilutions were made and the titer of free, unadsorbed phages in the solution was determined. The number of phage particles at time 0 (immediately after mixing bacteria and viruses) represented 100% of the unadsorbed phages. Two independent experiments were conducted, and in each of them, sample measurements were performed in triplicate. The adsorption rate constants were calculated according to the following mathematical formula: where k is the adsorption rate constant (in mL/min); B is the concentration of bacterial cells; and t is the time interval in which the titer falls from P0 (original phage titer) to P (final phage titer) [41].

Long-Term Study of Phage Stability under Various Temperature Conditions
Phage lysates in the determined titers (1.62 × 10 10 PFU/mL for Entb_43; 3.67 × 10 7 PFU/mL for Entb_45-the difference is that a higher titer could not be obtained at the beginning of the experiment) were placed in different temperature conditions: 37 • C, 22-24 • C (room temperature-RT), 4 • C, and frozen at −70 • C with or without addition of 20% glycerol (Difco). Experiments were performed over 6 months, and samples were taken after 1, 2, 4, 10, 14, 18, and 24 weeks, respectively. Additionally, to assess if defrosting affected the titer of bacteriophages stored at −70 • C, the same sample was defrosted several times at different time intervals. Phage titers were determined using RTD and the double-layer agar method in triplicate.

Investigation of Phage Stability in Solutions of Different pH and Disinfectants
To evaluate the stability of phages in solutions with a different pH, we tested the liquid culture medium-peptone water at a different pH, at a range from 3 to 12 (established with 5 M HCl or 10 M NaOH). Phage suspensions in pH = 7.2 (standard culture medium) were used as controls. For this purpose, 200 µL of phage lysate (10 9 PFU/mL) was added to 1800 µL of a specific solution (at 1:9 ratio) and incubated for 1 h at 37 • C in a water bath. After this period, serial dilutions of phages were prepared, and their titers were determined using RTD in triplicate. In addition, the stability of bacteriophages in various disinfectants or surfactants (including 70% ethanol, 10% dish soap, 10% liquid soap, 10% hand wash gel, and two antibacterial and antiviral liquid skin disinfectants diluted 2 times) was assessed. Using a similar method to that presented above, 200 µL of phage lysates were added to 1800 µL of specific solution and incubated at room temperature. Phage titers were determined after 5, 10, 20, and 30 min of incubation. All experiments were performed in triplicate. Results are presented as a percentage of active phages [40]. A similar method was used to test the phage stability with commercially available colloidal silver and copper solutions (Nano-Tech, Polska) at a concentration of 50 mg/kg (ppm), also used as antibacterial and antifungal agents. In this case, an additional 24 h of incubation was performed.

Stability of Phage Lysates in Urine Sample In Vitro
The fresh urine sample collected from the midstream was obtained from a healthy donor. The urine sample presented pH = 6, and a density of 1.015. The glucose, ketones, proteins, and nitrites were absent from the urine sample, and flat epithelial cells were sparse. The sample was filtered through 0.22 µm pore size filters. As in previous experiments, phages were incubated with the sample with a ratio of 1:9 at 37 • C for 30 min, 1 h, and 24 h. Phage titers after defined incubation times were determined by RTD. The experiment was performed in triplicate. Phage titer at the start of the experiment (time zero) was used as a comparison for the statistical analysis.

Transmission Electron Microscopy (TEM)
Phage lysates were prepared in a LB (Luria-Bertani) medium in high titers (Entb_43: 2.3 × 10 10 PFU/mL; Entb_45: 1.22 × 10 9 PFU/mL) and filtered two times. Samples were concentrated using ultracentrifugation (1 h, 7 • C, 25,000 × g) and, after removing the supernatant, 0.1 M ammonium acetate was added and centrifuged in the same conditions. In the next step, a drop of phage lysate was placed on a 400 mesh copper grid (Athene). After being contrasted with 2% uranyl acetate, preparations were dried and analyzed using the Zeiss EM900 TEM (at an acceleration voltage 80 kV). Images of phages were obtained using Kodak/Carestream Electron Microscope Film 4489. Phages' morphology and dimensions were defined.

Phage DNA Isolation Procedure and DNA Sequencing
Phage lysates at a volume of 20 mL in high titers (Entb_43: 2.3 × 10 10 PFU/mL; Entb_45: 1.22 × 10 9 PFU/mL) were concentrated with the use of Amicon Ultra Centrifugal Filters (Merck, NJ, USA). To isolate the phage nucleic acid (dsDNA), QIAamp MinElute Virus kits (Qiagen, Germantown, MD, USA) were used. Analysis of dsDNA concentrations was prepared using QuantiFluor dsDNA System (Quantus, Promega, Madison, WI, USA), which uses a fluorescent DNA-binding dye. The Illumina DNA Prep system was used to construct the sequencing library, following the assessment of their quality using a high sensitivity D1000 ScreenTape Assay for TapeStation System (Agilent, Santa Clara, CA, USA). Sequencing of phage genomic DNA was performed with MiSEQ Reagent Kit Nano V2 or MiSEQ Reagent Kit V3 (New Generation Sequencing, Illumina system).
Read sequences (fastq) (from Illumina technology sequencing) for both phages were subjected to the same general pipeline. Quality assessment was completed with the Trimmomatic software [42]. Reads passing the quality check were used by SPAdes software (3.12) to assemble reads into contigs and scaffolds [43][44][45][46][47]. For the Entb_43 phage, k-mer size was detected automatically, but for Entb_45 it was set to 21, 33, and 55 with additional coverage cutoff set to 50. Assembly artifacts were checked and removed if recognized as bacterial contamination. This allowed one dominant scaffold to be assembled which relates to other phages, and this was used as a partial genome for further analysis. BLASTn (megablast) was used to evaluate similarity to prokaryotic and phage genomes in currently existing databases.
Genome annotations were performed with the Prokka software [48,49] and PGAP (Prokaryotic Genome Assembly Pipeline) [50][51][52] using prokaryotic databases. This forced adherence to International Nucleotide Sequence Database Collaboration (NCBI, ENA and DDBJ) standards and up-to-date databases. The PGAP annotation process is described in detail on the NCBI webpage (https://www.ncbi.nlm.nih.gov/genome/annotation_ prok/process/, accessed on 12 May 2022) and both processes result in functional annotation of genomes. In short, this approach mixes alignment-based methods, functional assessments of elements directly from the sequence (with the help of hidden Markov Models), representative reference proteins/genomes, and software (such as GeneMarkS2+). Alignments of closely related genomes were calculated by Geneious Prime 2022.1.1 (http: //www.geneious.com, accessed on 12 May 2022) [53] and progressiveMauve [54]. SD motifs (ribosome binding sites) were found by the XSTREME [55] tool connecting the MEME, STREME, and SEA software to perform comprehensive motif discovery in accordance with guidelines for bacteriophage annotation [56].

Statistical Analysis
The statistical analysis was performed using the GraphPad Prism 9 software. A oneway ANOVA was used to determine if any changing factors (stability in nanoparticles, in solutions with different pH and in urine) influenced the phage titer and a Dunnett's multiple comparisons test determined the statistical significance of differences between groups. Statistical significance was considered at p < 0.05. All experiments were performed in at least three repetitions.

Characterization of the Bacterial Strains
The twenty bacterial strains used in the experiments were mainly identified as E. cloacae (15/20), but also as E. hormaechei (4/20) and E. kobei (1/20) (Table 1). All tested strains were resistant to amoxicillin/clavulanic acid. The host strains turned out to be multidrug resistant (resistance to several antibiotics simultaneously)-e.g., E. cloacae 30345, which has been shown to be resistant to amoxicillin/clavulanic acid, ciprofloxacin, levofloxacin, and tobramycin, and E. cloacae 29796, which, in addition to the antibiotics mentioned above, is resistant to cefotaxime, cefepime, gentamicin, and trimethoprim/sulfamethoxazole. Single bacterial strains also showed resistance to fosfomycin (E. cloacae 3344 and E. hormaechei 30550), as well as to a wider range of antibiotics from different pharmacological groups-e.g., ciprofloxacin, cefepime, ertapenem, gentamicin, levofloxacin, piperacillin/ tazobactam, and tobramycin (E. cloacae 30342).

Isolated Bacteriophages
After screening over 300 environmental samples, we isolated three new, potentially lytic bacteriophages, specific for Enterobacter spp.: Entb_43 (vB_EclM-43), Entb_44 (vB_EclM-44), and Entb_45 (vB_EclM-45). As a result of genetic analysis, we proved that the Entb_44 phage has an almost identical genome to Entb_43, so we decided to further characterize only the Entb_43 and Entb_45 phages. Both phages show species-specificity for Enterobacter spp. only-no lysis of other Gram-negative and Gram-positive strains from the ESKAPE group was observed ( Table 2). The broadest lytic spectrum was determined for the Entb_45 phage, which also had the highest species specificity-causing lysis on various species belonging to Enterobacter (E. cloacae, E. hormaechei, E. kobei) ( Table 3).
For two strains, which were hosts for phages: E. cloacae 30345 (host for Entb_43) and E. cloacae 29796 (host for Entb_45), plots of dependence of the bacterial titer (CFU/mL) on the OD 600 were prepared.

Morphology of Entb_43 and Entb_45 Phages and Their Plaques
Bacteriophage Entb_43 formed small, clear plaques on the solidified agar plates (less than 1 mm in diameter) with no apparent "halo" effect. The Entb_45 phage created slightly larger clear plaques on the agar plates (approximately 1-2 mm in diameter), and after about 3 days a slight "halo" effect was noticeable.
Studies with the use of TEM revealed that both newly isolated bacteriophages had the A2 morphotype. The morphology of the phages corresponds to that of myoviruses ( Figure 1), which are characterized by contractile tails and icosahedral heads [57][58][59]. Entb_43, but not Entb_45, had a visible belt structure at the level of one-third of the tail. Dimensions of the capsids, tails, and base plates of each phage are included in Table 4. Studies with the use of TEM revealed that both newly isolated bacteriophages had the A2 morphotype. The morphology of the phages corresponds to that of myoviruses ( Figure 1), which are characterized by contractile tails and icosahedral heads [57][58][59]. Entb_43, but not Entb_45, had a visible belt structure at the level of one-third of the tail. Dimensions of the capsids, tails, and base plates of each phage are included in Table 4.

Influence of Different MOI on the Effectiveness of Phage Amplification and Antimicrobial Effect
As shown in Table 5, the phage titers, after overnight cultivation at 37 °C , varied

Influence of Different MOI on the Effectiveness of Phage Amplification and Antimicrobial Effect
As shown in Table 5, the phage titers, after overnight cultivation at 37 • C, varied depending on the phage-to-bacteria ratio used (different MOI). In general, the lower MOI used (lower phage titer than bacterial titer), the higher final phage titer obtained. For both phages, the best phage-to-bacteria ratio was either 0.01 or 0.001. The MOI-dependent ability of phages to lyse planktonic bacteria was determined. As shown on Figure 2, each of the bacteriophages significantly inhibited the growth of the host bacteria. Bacterial lysis varied slightly on the used MOI; however, even a low MOI is sufficient to successfully eliminate bacterial cells, whereas the OD 600 of the phage-untreated bacterial strains (positive controls) clearly increased over time. The optical density of the only phage lysates (negative controls) oscillated around 0.00 and did not change during the measurements (not shown in the graphs).

Phage Adsorption to Bacterial Cells
After the infection of E. cloacae 30345 with the Entb_43 phage (at MOI = 0.1), we obtained about 84% adsorption of the phage particles to the host cells at 37 °C in 20 min. However, the adsorption time of Entb_45 to E. cloacae 29796 was much faster, and after 10 min, almost 90% adsorption was achieved ( Figure 3 and Supplementary Figure S1). The adsorption rate constants, which are included in Table 6, were also calculated.

Phage Adsorption to Bacterial Cells
After the infection of E. cloacae 30345 with the Entb_43 phage (at MOI = 0.1), we obtained about 84% adsorption of the phage particles to the host cells at 37 • C in 20 min. However, the adsorption time of Entb_45 to E. cloacae 29796 was much faster, and after 10 min, almost 90% adsorption was achieved ( Figure 3 and Supplementary Figure S1). The adsorption rate constants, which are included in Table 6, were also calculated.

Genome Sequencing
We present the genomes of two new phages: Enterobacter phage Entb_43 (174 kbp, acc. No. ON585039) and Enterobacter phage Entb_45 (173 kbp, acc. No. ON630910). Both phages were sequenced with Illumina technology and assembled into a single, gapless contig from reads passing through a quality check (see Materials and Methods for details). Phage genomes show a high degree of diversity between each other, with only 12% of the genome showing high similarity between two of them. These similarities were, however, limited (up to 75% of identity) and they were found mainly in regions coding for structural phage proteins. The presented genomes show poor genomic similarity to already known phages. In databases accessible through the International Nucleotide Sequence Database Collaboration (https://www.insdc.org/, accessed on 10 June 2022), only 8 and 7 phage genomes show a similarity above 70% to Entb_43 and Entb_45, respectively (Supplementary Tables S1 and S2). The first one is most closely related to the Klebsiella phage vB_KaeM KaAlpha (93% identical at the nucleotide level, acc. no. MN013084) and the second one is most closely related to the Enterobacter phages ENC9 (93% identical at the nucleotide level,

Genome Sequencing
We present the genomes of two new phages: Enterobacter phage Entb_43 (174 kbp, acc. No. ON585039) and Enterobacter phage Entb_45 (173 kbp, acc. No. ON630910). Both phages were sequenced with Illumina technology and assembled into a single, gapless contig from reads passing through a quality check (see Materials and Methods for details). Phage genomes show a high degree of diversity between each other, with only 12% of the genome showing high similarity between two of them. These similarities were, however, limited (up to 75% of identity) and they were found mainly in regions coding for structural phage proteins. The presented genomes show poor genomic similarity to already known phages. In databases accessible through the International Nucleotide Sequence Database Collaboration (https://www.insdc.org/, accessed on 10 June 2022), only 8 and 7 phage genomes show a similarity above 70% to Entb_43 and Entb_45, respectively (Supplementary Tables S1 and S2). The first one is most closely related to the Klebsiella phage vB_KaeM KaAlpha (93% identical at the nucleotide level, acc. no. MN013084) and the second one is most closely related to the Enterobacter phages ENC9 (93% identical at the nucleotide level, acc. no. OL355124.1) and vB_EclM_CIP9 (94% identical at the nucleotide level, acc. no. NC_048849.1). Basic features of the presented phages are described in Table 7.  43 40 For the genomes of Entb_43 and Entb_45, revealed after annotation 298 and 289 coding sequences, respectively, 44% and 58% of the proteins are designated as "hypothetical proteins". One hypothetical protein is present in a tail gene cluster of Entb_43, but not in the Entb_45 phage (protein ID: M8345145). The highest similarity (except for hypothetical proteins) is shown for a putative GIY-YIG homing endonuclease (Yersinia phage vB_Yem_TG1, acc. no.: NC_028820.1), but no significant similarity to well-described proteins was found. Typically for Tevenvirinae, our annotation in both phages revealed no apparent integrase gene, suggesting a lytic life cycle. Genomes were linearized to the presumed position at the beginning of the identified gene coding the rIIA/B gene, as is standard for Tevenvirinae. Analysis of the Entb_43 genome revealed 19 tRNA, but only 9 tRNA in Entb_45. No similarity to antibiotic resistance genes were found in the CARD database (no strict hits) [60].
Based on genomic similarity, we classified phage Entb_43 to genus Karamvirus and Entb_45 phage to genus Kanagawavirus [61,62], which classifies both phages to the Tevenvirinae subfamily (Straboviridae family) in accordance with current ICTV guidelines [63]. Each phage genome showed a similarity of over 70% to representatives of only one genus. Similarity to the most closely similar phage is shown in Figures 4 and 5. Similarity of the marker genes recommended by ICTV for Tevenvirinae shows that Entb_43 and Entb_45 are closely related to other representative phages from the Karamvirus and Kanagawavirus genera, respectively (Supplementary Tables S3 and S4) [64]. We identified Shine-Dalgarno sequences (ribosome binding site) in fragments 100 bp upstream of the START codon ( Figures 6 and 7) according to the recommendation by Turner et al. in the "Phage Annotation Guide: Guidelines for Assembly and High-Quality Annotation" [56].

Stability Studies of New Enterobacter-Specific Phages
In order to assess the effect of commonly used disinfectants and cleaning agents on the stability of bacteriophages, six different commercially available substances were used in the experiment (Table 8). In general, a significant reduction in phage titers was observed after incubation with the disinfectant that contained the active substances octenidinum dihydrochloridum and phenoxyethanol (1) (titer reduction of over 90% for phage Entb_43 and by 99.9% in the case of phage Entb_45, after 30 min of incubation), and was slightly less pronounced with 70% ethanol (reduction in the titer by nearly 70% for Entb_43 and by 97% for phage Entb_45, after 30 min of incubation). The remaining disinfectants and surfactants influenced the phage titers, but this was less significant. Metal nanoparticles such as copper and silver are used in a variety of ways as disinfectants. We decided to evaluate the stability of phage lysates in these solutions to assess if applying them together was possible. As shown in Figure 8, both bacteriophages retain a lot of active particles for 30 min of incubation with nanoparticle solutions at room temperature. On the other hand, 24 h incubation caused more significant reductions in phage titers in the case of silver colloid than copper.

Stability Studies of New Enterobacter-Specific Phages
In order to assess the effect of commonly used disinfectants and cleaning agents on the stability of bacteriophages, six different commercially available substances were used in the experiment (Table 8). In general, a significant reduction in phage titers was observed after incubation with the disinfectant that contained the active substances octenidinum dihydrochloridum and phenoxyethanol (1) (titer reduction of over 90% for phage Entb_43 and by 99.9% in the case of phage Entb_45, after 30 min of incubation), and was slightly less pronounced with 70% ethanol (reduction in the titer by nearly 70% for Entb_43 and by 97% for phage Entb_45, after 30 min of incubation). The remaining disinfectants and surfactants influenced the phage titers, but this was less significant. Metal nanoparticles such as copper and silver are used in a variety of ways as disinfectants. We decided to evaluate the stability of phage lysates in these solutions to assess if applying them together was possible. As shown in Figure 8, both bacteriophages retain a lot of active particles for 30 min of incubation with nanoparticle solutions at room temperature. On the other hand, 24 h incubation caused more significant reductions in phage titers in the case of silver colloid than copper.

Stability Studies of New Enterobacter-Specific Phages
In order to assess the effect of commonly used disinfectants and cleaning agents on the stability of bacteriophages, six different commercially available substances were used in the experiment (Table 8). In general, a significant reduction in phage titers was observed after incubation with the disinfectant that contained the active substances octenidinum dihydrochloridum and phenoxyethanol (1) (titer reduction of over 90% for phage Entb_43 and by 99.9% in the case of phage Entb_45, after 30 min of incubation), and was slightly less pronounced with 70% ethanol (reduction in the titer by nearly 70% for Entb_43 and by 97% for phage Entb_45, after 30 min of incubation). The remaining disinfectants and surfactants influenced the phage titers, but this was less significant. Metal nanoparticles such as copper and silver are used in a variety of ways as disinfectants. We decided to evaluate the stability of phage lysates in these solutions to assess if applying them together was possible. As shown in Figure 8, both bacteriophages retain a lot of active particles for 30 min of incubation with nanoparticle solutions at room temperature. On the other hand, 24 h incubation caused more significant reductions in phage titers in the case of silver colloid than copper. The isolated bacteriophages were also tested for stability in the culture medium (peptone water) with different pH values. As a control for comparisons, samples with peptone water with pH = 7.2 were used, which were treated the same as the other samples. As a result of the statistical analysis, it was observed that the most significant differences in phage titers after incubation occurred in the case of the most extreme pH values (pH = 12 for phages Entb_43 and Entb_45, pH = 11 for phage Entb_45, and pH = 3 for both phages). Interestingly, higher phage titers were obtained as a result of incubation with a medium for which the pH was 8, which may suggest more effective results of phage amplification in slightly more alkaline media than before (Figure 9). The isolated bacteriophages were also tested for stability in the culture medium (peptone water) with different pH values. As a control for comparisons, samples with peptone water with pH = 7.2 were used, which were treated the same as the other samples. As a result of the statistical analysis, it was observed that the most significant differences in phage titers after incubation occurred in the case of the most extreme pH values (pH = 12 for phages Entb_43 and Entb_45, pH = 11 for phage Entb_45, and pH = 3 for both phages). Interestingly, higher phage titers were obtained as a result of incubation with a medium for which the pH was 8, which may suggest more effective results of phage amplification in slightly more alkaline media than before (Figure 9). Stability of phages over six months (24 weeks) was clearly dependent on the temperature at which they were stored. As was shown in Figure 10, storage of bacteriophages at 4 °C , as well as in frozen form at −70 °C (with or without the addition of cryoprotective glycerol), did not significantly affect their titers (only the titer of Entb_45 stored at 4 °C , which initially had a lower titer, decreased by one order of magnitude on a logarithmic scale at the end of the experiment). Phage titers decreased successively at both room temperature and 37 °C . No active phage particles were found in the Entb_45 phage lysate after 18 weeks of storage at 37 °C , whereas the titer of the Entb_43 phage decreased from 10 10 to 10 1 PFU/mL after 24 weeks. Moreover, the thaw-resistance of frozen phage lysates was demonstrated, because after defrosting the same samples five times and refreezing, the phage titers only decreased by about one order of magnitude ( Figure 11). Stability of phages over six months (24 weeks) was clearly dependent on the temperature at which they were stored. As was shown in Figure 10, storage of bacteriophages at 4 • C, as well as in frozen form at −70 • C (with or without the addition of cryoprotective glycerol), did not significantly affect their titers (only the titer of Entb_45 stored at 4 • C, which initially had a lower titer, decreased by one order of magnitude on a logarithmic scale at the end of the experiment). Phage titers decreased successively at both room temperature and 37 • C. No active phage particles were found in the Entb_45 phage lysate after 18 weeks of storage at 37 • C, whereas the titer of the Entb_43 phage decreased from 10 10 to 10 1 PFU/mL after 24 weeks. Moreover, the thaw-resistance of frozen phage lysates was demonstrated, because after defrosting the same samples five times and refreezing, the phage titers only decreased by about one order of magnitude ( Figure 11). Stability of phages over six months (24 weeks) was clearly dependent on the temperature at which they were stored. As was shown in Figure 10, storage of bacteriophages at 4 °C , as well as in frozen form at −70 °C (with or without the addition of cryoprotective glycerol), did not significantly affect their titers (only the titer of Entb_45 stored at 4 °C , which initially had a lower titer, decreased by one order of magnitude on a logarithmic scale at the end of the experiment). Phage titers decreased successively at both room temperature and 37 °C . No active phage particles were found in the Entb_45 phage lysate after 18 weeks of storage at 37 °C , whereas the titer of the Entb_43 phage decreased from 10 10 to 10 1 PFU/mL after 24 weeks. Moreover, the thaw-resistance of frozen phage lysates was demonstrated, because after defrosting the same samples five times and refreezing, the phage titers only decreased by about one order of magnitude ( Figure 11).  . Figure 11. Influence of repeated defrosting on titers of phage lysates with or without 20% glycerol. Error bars represent the standard deviation (±SD) of the mean phage titers.

Phage Stability in a Urine Sample
As mentioned before, Enterobacter spp. can cause severe urinary tract infections. A key feature of phage therapy in the intravesical administration of phages is their stability at the site of action, so we examined their ability to remain active in a urine sample (pH = 6) obtained from a healthy donor (Figure 12). It was noted that, after both half an hour and an hour of incubation in a fresh sample of urine, the phage titers remained at the same level as at the beginning of the experiment, which may suggest their potential efficacy without loss of activity at the infection site after intravesical administration.  Figure 11. Influence of repeated defrosting on titers of phage lysates with or without 20% gly Error bars represent the standard deviation (±SD) of the mean phage titers.

Phage Stability in a Urine Sample
As mentioned before, Enterobacter spp. can cause severe urinary tract infectio key feature of phage therapy in the intravesical administration of phages is their sta at the site of action, so we examined their ability to remain active in a urine sample 6) obtained from a healthy donor (Figure 12). It was noted that, after both half an and an hour of incubation in a fresh sample of urine, the phage titers remained at the level as at the beginning of the experiment, which may suggest their potential eff without loss of activity at the infection site after intravesical administration. Figure 11. Influence of repeated defrosting on titers of phage lysates with or without 20% glycerol. Error bars represent the standard deviation (±SD) of the mean phage titers.

Phage Stability in a Urine Sample
As mentioned before, Enterobacter spp. can cause severe urinary tract infections. A key feature of phage therapy in the intravesical administration of phages is their stability at the site of action, so we examined their ability to remain active in a urine sample (pH = 6) obtained from a healthy donor (Figure 12). It was noted that, after both half an hour and an hour of incubation in a fresh sample of urine, the phage titers remained at the same level as at the beginning of the experiment, which may suggest their potential efficacy without loss of activity at the infection site after intravesical administration.

Discussion
Because Enterobacter strains are one of the etiological factors of various life-threatening conditions, we decided to isolate and characterize new phages specific to these bacteria. Our characteristics concerned not only the standard life cycle parameters, the lytic spectrum, and the stability under various conditions, but also the detailed genomic characteristics (as suggested by Suh et al., 2021 [65]).
As a result of typing 339 samples from various sources, we were able to find three new bacteriophages (Entb_43, Entb_44, and Entb_45) showing an ability to lyse clinical Enterobacter strains. Despite the fact that the bacteriophages Entb_43 and Entb_44 were isolated from different environmental samples, a genetic analysis showed that they were too similar to be considered separate phages. Therefore, we decided to further characterize only Entb_43 and Entb_45.
Currently, 85 genomes of Enterobacter phages have been deposited in the gene bank (https://www.ncbi.nlm.nih.gov/nuccore, accessed on 26 May 2022), which may indicate the potential and the need to conduct research on these phages and their comprehensive characteristics. Bioinformatic analysis of the genomes of two of our new bacteriophages allowed us to describe them as double-stranded DNA and to determine their sizes, respectively, as 174,681 bp for Entb_43 and 172,771 bp for Entb_45. Similar results have already been reported for the Enterobacter-specific phage vB_EclM_CIP9 (defined as myovirus) with a 174,924 bp genome [66], as well as the EBP bacteriophage (also myovirus), which has a 179.1 kb genome size [67]. Interestingly, a phage active against E. cloacae was recently reported with a genome size of 51,894 bp and was assigned to a new genus, Eclunavirus [68]. Moreover, no rRNA or tRNA were found in its genome, whereas our phages had 19 and 9 tRNAs in their genomes, respectively. The similarity of Entb_43 to the Klebsiella-specific phage may be related to the similarity of these two types of bacteria. Until recently, Klebsiella aerogenes was considered Enterobacter aerogenes [9,69]. Moreover, genomic analyses provide data on the genetic relationships of these bacteria, as described, for example, for strains isolated from patients with a bloodstream infection (69% shared genes) [70].
The host range of phages estimated on the basis of the spot test was 40% and 60%, respectively. Both phages were also tested simultaneously: immediately after mixing, 24

Discussion
Because Enterobacter strains are one of the etiological factors of various life-threatening conditions, we decided to isolate and characterize new phages specific to these bacteria. Our characteristics concerned not only the standard life cycle parameters, the lytic spectrum, and the stability under various conditions, but also the detailed genomic characteristics (as suggested by Suh et al., 2021 [65]).
As a result of typing 339 samples from various sources, we were able to find three new bacteriophages (Entb_43, Entb_44, and Entb_45) showing an ability to lyse clinical Enterobacter strains. Despite the fact that the bacteriophages Entb_43 and Entb_44 were isolated from different environmental samples, a genetic analysis showed that they were too similar to be considered separate phages. Therefore, we decided to further characterize only Entb_43 and Entb_45.
Currently, 85 genomes of Enterobacter phages have been deposited in the gene bank (https://www.ncbi.nlm.nih.gov/nuccore, accessed on 26 May 2022), which may indicate the potential and the need to conduct research on these phages and their comprehensive characteristics. Bioinformatic analysis of the genomes of two of our new bacteriophages allowed us to describe them as double-stranded DNA and to determine their sizes, respectively, as 174,681 bp for Entb_43 and 172,771 bp for Entb_45. Similar results have already been reported for the Enterobacter-specific phage vB_EclM_CIP9 (defined as myovirus) with a 174,924 bp genome [66], as well as the EBP bacteriophage (also myovirus), which has a 179.1 kb genome size [67]. Interestingly, a phage active against E. cloacae was recently reported with a genome size of 51,894 bp and was assigned to a new genus, Eclunavirus [68]. Moreover, no rRNA or tRNA were found in its genome, whereas our phages had 19 and 9 tRNAs in their genomes, respectively. The similarity of Entb_43 to the Klebsiella-specific phage may be related to the similarity of these two types of bacteria. Until recently, Klebsiella aerogenes was considered Enterobacter aerogenes [9,69]. Moreover, genomic analyses provide data on the genetic relationships of these bacteria, as described, for example, for strains isolated from patients with a bloodstream infection (69% shared genes) [70].
The host range of phages estimated on the basis of the spot test was 40% and 60%, respectively. Both phages were also tested simultaneously: immediately after mixing, 24 h after, 48 h after, and one week after mixing, but no significant changes in the lytic spectrum were observed. The phage cocktail retained its lytic properties on strains against which at least one phage was active (data not presented herein). Interestingly, the myPSH1140 phage, described by Manohar et al. (2019), showed a much wider host range, reaching 100% of E. cloacae and 75% of E. hormaechei strains [71]. There are also Enterobacter-specific phages with an extremely narrow range of activity, lysing only one bacterial strain [72]. Instead, phages are also described as polyvalent, as presented by Finney et al. (2022), with phages lysing both Enterobacter spp. and Klebsiella aerogenes [73], or by Addablah et al. (2021), with phages infecting E. cloacae and E. coli simultaneously [74]. Jamal et al. (2018) reported the phage MJ2, which was able to inhibit the growth of E. cloacae, Achromobacter xylosoxidans, K. pneumoniae, and P. aeruginosa [75]. However, determination of the host range is not always clear and repeatable due to the different determination methods and the ability of phages to form plaques on the specific bacterial lawn [76].
Similar morphological characterization, as well as host range, was described for a lytic EBP bacteriophage by Asif et al. (2021) [67] and for three phages reported by Gibson et al. (2019) [77]. Nair et al. (2021) also described a myovirus, which was able to lyse both the planktonic form of bacteria and the biofilm produced by E. cloacae [78].
The best phage-to-bacteria ratio, both for estimating the optimal conditions for bacteriophage amplification and for lytic activity against planktonic bacteria, turned out to be 1:1000 or 1:100 (MOI = 0.001 or MOI = 0.01). Interestingly, studies using the new phage against Enterococcus faecalis producing biofilm in Foley catheters initially reported more efficacy of phage lytic activity at a higher MOI (MOI = 10). On the other hand, after 6 h and 24 h of exposing the bacterial biofilm to the phage, the preparations with a lower phage-to-bacteria ratio (MOI = 0.01 and MOI = 0.0001) were more effective [80]. However, we describe the MOI as the ratio of the number of phages to the number of bacteria at the start of the experiment, and it is suggested to also consider, inter alia, the changing densities of bacteria during the course of the experiment [81].
In the case of long-term storage of phage preparations, a temperature of 4 • C is usually recommended [82]. Our phage lysates (in peptone water) remained stable at this temperature throughout the six-month period of the experiment. The maintenance of stability by phages in frozen forms (−70 • C) indicates such a possibility for their storage. Interestingly, over the course of a month, only the titers of phages stored at the highest temperature (37 • C) decreased by only one order of magnitude. It is worth noting that studies on adaptive evolution regarding various thermal conditions are being designed to increase phage stability [83].
The ability of phages to remain active under unfavorable conditions may be very important for people working with these viruses, as well as for the industrial or pharmaceutical applications of phages [84]. An example of the industrial use of E. cloacae-specific bacteriophages is the attempt to use them as factors to reduce the bloating defect caused by these bacteria in cucumber fermentation [85]. The different values of acidity/alkalinity of the environment are of particular importance in the context of the human organism and other animals in the processes of health and disease. From the point of view of phage therapy, factors such as changes in the pH of skin and wounds [86], unfavorable pH in the stomach [87], or changes in the pH of the environment caused by growth of bacteria [88] can determine the effectiveness of treatments. Relatively good stability was observed in our phages after incubation in peptone water with a pH ranging from 4 to 11. Moreover, the observed decrease in titers as a result of a large deviation from physiological pH has been confirmed for most phages, including Enterobacter-specific [71,[89][90][91][92] and other species (e.g., Escherichia coli-specific) [93]. Very similar tolerance to a wide pH range was also shown by the phages KKP 3262 and KKP 3263 described by Wójcicki et al. (2021) [94]. Interestingly, two of five E. hormaechei-specific phages isolated by Chen and coworkers (2022) showed an almost complete resistance to a more alkaline environment (such as pH = 12) [95].
The inactivation of phages as a result of contact with various disinfectants/surfactants may be of great importance in the quality of work involving them, and may also have an impact on the field of therapeutics when the use of surface disinfectants can support phage action (e.g., skin surface disinfection or coating the surface of catheters with metal nanoparticles). Compounds based on silver were applied in antimicrobial therapy until the 1940s when antibiotics were implemented [96]. The observed antimicrobial activity of silver may be the result of a direct toxic effect on bacterial cell walls [97]. When silver ions are released, the bacterial cell membrane and a variety of intracellular functions are disrupted. The small size of their particles, together with the large surface area of the dressing's integrated silver nanoparticles, increase their solubility and cause a sustained release of silver ions in relatively nontoxic concentrations [96]. Coating the catheter's surface with silver nanoparticles resulted in significant in vitro antimicrobial activity and also prevented biofilm formation by E. coli, Enterococcus, S. aureus, coagulase-negative staphylococci, P. aeruginosa, and Candida albicans [98]. Studies by Thomas et al. (2015) indicate a high potential in applying silver nanoparticles to urinary catheters for preventing catheter-associated infections, especially the attachment and colonization of bacteria [99,100]. The scientific literature also indicates that copper nanoparticles have antibacterial properties [101,102]. Therefore, it is important to evaluate phage-nanoparticle interactions due to data about the possibility of irreversible inactivation of phages (e.g., E. coli-specific) by nanoparticles [103,104]. The activity of our new phages, despite a statistically significant difference compared to the beginning of incubation, was well maintained for about 30 min of incubation at RT with both types of nanoparticles. This may indicate the possibility of a synergistic antibacterial effect and the need for further research into this phenomenon. Similarly, Abdelsattar et al. (2021) showed no significant differences in the titer of a Salmonella-specific phage after 4 h incubation at 37 • C with synthesized silver nanoparticles [105]. The 24 h incubation, especially in the case of silver, led to a more significant inactivation of our phages.
We also decided to test the phage stability in 10% dish soap and 10% liquid hand soap. In similar experiments, Necel et al. (2020) [40] found no decrease in two E. coli phage titers after 2 min and 5 min of incubation at RT, respectively. Our results indicated an initial reduction in titers for both phages by approximately 20-25% (after 5 min), while for half an hour, despite fluctuations in the titers, no reduction was observed. The commonly used skin disinfectant based on octenidinum dihydrochloridum and phenoxyethanol, as well as 70% ethanol, had the strongest effect in reducing the number of active phage particles, which may be important in skin or wound disinfection before phage administration. For ECML-117 and vB_Eco4M-7 phages, active phage particles were described as 0% and 0.01%, respectively, after one hour of incubation in 63% ethanol [40]. Likewise, such conditions caused a significant decrease in vB-EcoS-95 phage survival (0.8% active particles) [79]. Interestingly, Tomat et al. (2018) [106] reported E. coli phages that remained active after 24 h of incubation in 100% ethanol (decrease of titer by 2.5 PFU/mL). Recently, the possible negative effects of the uncontrolled spread of phages in food production processes have also been emphasized [107]. Information about the factors that deactivate them may therefore be useful in industrial fields.
Beta-lactam antibiotics, as well as fluoroquinolones and aminoglycosides, are the most common antimicrobials prescribed to treat infections caused by Enterobacteriaceae [108]. The bacteria we used demonstrated ESBL+ resistance, a mechanism that is characteristic of uropathogenic Enterobacter strains [109,110] and other Gram-negative bacteria [111]. More relevant data are emerging on the prospects of managing UTIs through the use of lytic bacteriophages, phage cocktails, enzymes derived from them, and genetically modified phages, as well as by using the synergistic effect of phages and antibiotics [112][113][114][115][116]. Promising clinical trials in this area are slowly emerging [117,118], but many issues still need to be refined [119]. There are reports of clinical successes in the treatment of UTIs as a result of intravenous phage cocktail administration, which, although it did not completely eradicate the pathogen, its succession resulted in a significant improvement in the patient's condition [120]. As a preliminary study determining the possibility of using our phages in the treatment of UTI, we decided to evaluate their stability in a urine sample. The results turned out to be promising as bacteriophages were not inactivated by the components of the previously filtered urine. Pereira et al. (2016) described not only the good stability of Enterobacter-specific phages in a urine sample, but also an increase in their titer in the presence of bacteria [113].
The results described in this paper strongly suggest the therapeutic potential of the presented Enterobacter-specific bacteriophages.
Supplementary Materials: The following supporting information can be downloaded at: https: //www.mdpi.com/article/10.3390/v14071518/s1, Figure S1. Kinetics of Entb_43 phage adsorption on E. cloacae 30345 and Entb_45 phage on E. cloacae 29796 at MOI = 0.1. Table S1. List of all genomes with over 70% similarity to Enterobacter phage Entb_43 genome. Table S2. List of all genomes with over 70% similarity to Enterobacter phage Entb_45 genome. Table S3. Similarity of each protein product of marker genes from Enterobacter phage Entb_43 to the closest relative classified by ICTV. Table S4. Similarity of each protein product of marker genes from Enterobacter phage Entb_45 to the closest relative classified by ICTV.