Improved Viability of Spray-Dried Pantoea agglomerans for Phage-Carrier Mediated Control of Fire Blight

Fire blight, caused by Erwinia amylovora, is a devastating bacterial disease that threatens apple and pear production. It is mainly controlled by using antibiotics, such as streptomycin. Due to development of E. amylovora resistant strains and the excessive agricultural use of antibiotics, there is an increased awareness of the possibility of antibiotic resistance gene transfer to other microbes. Urgent development of biocontrol agents (BCAs) is needed that can be incorporated into integrated pest management programs as antibiotic alternatives. A novel phage-carrier system (PCS) that combines an antagonistic bacterium, Pantoea agglomerans, with its ability to act as a phage-carrier bacterium for Erwinia phages has been developed. The low viability of P. agglomerans cells following spray-drying (SD) has been a challenge for the industrial-scale production of this PCS. Here, an SD protocol was developed for P. agglomerans by modifying the growth medium and bacterial cell formulation using D(+)-trehalose and maltodextrin. The developed protocol is amenable to the industrial-scale production of the BCA/PCS. The P. agglomerans viability was greater than 90% after SD and had a shelf life at 4 °C of 4 months, and reconstituted cells showed a 3 log reduction in E. amylovora counts with a pear disc assay.


Introduction
Fire blight, caused by Erwinia amylovora, is a devastating bacterial disease that threatens apple and pear production worldwide [1].Apple and pear infection by E. amylovora occurs during blossom opening, and the bacterial populations increase on the stigma.In the presence of dew droplets and rainwater, the bacterial cells flow down into the hypanthium and reach the natural flower openings.Bacterial cells then invade the plant tissue, resulting in the infection of blossoms and shoots [2].Antibiotics, such as streptomycin and kasugamycin, have been noted to have a superior blossom blight control efficacy, with significant population reductions in E. amylovora on apple flower stigmas [3].In Canada and the US, streptomycin and kasugamycin are the most commonly used pesticides against fire blight [4].However, streptomycin-resistant strains of E. amylovora have been identified in different countries around the world [5][6][7].This trend is concerning, as there is an increasing awareness of the possibility of antibiotic resistance gene transfer to human and animal Viruses 2024, 16, 257 2 of 16 pathogenic microbes due to the excessive use of antibiotics in agriculture [8][9][10][11].Currently, the European Union regulatory agencies have restricted the use of streptomycin in agriculture, while Canada and the USA have only prohibited its use for organic farms [12].
Commercial biocontrol agents (BCAs) using antagonistic bacteria or lytic bacteriophages are available [8,13,14].The bacterial BCA mode of action relies on competition for niches, nutrients and/or induction of plant defenses [15].Bacterial-dependent BCAs against fire blight are commercially available, such as BlightBan TM A506 (Nufarm, IL, USA) and Bloomtime Biological TM (Verdesian Life Sciences LLC, Cary, NC, USA [16].Lytic phage-dependent BCAs are also commercially available (e.g., AgriPhage-Fireblight by OmniLytics, West Sandy, UT, USA) and have been authorized by the US Environmental Protection Agency (EPA) for fire blight treatment [17][18][19].The phage-carrier system (PCS) is a new form of BCA that combines antagonistic bacteria with phages as a double-pronged treatment that was developed for fire blight control [20][21][22][23].The phages used in these treatments are able to infect both the antagonistic bacteria, Pantoea agglomerans (i.e., the phage carrier) and E. amylovora (i.e., the pathogen).A study using PCS with P. agglomerans and E. amylovora phages showed a 56% reduced infection on flowers of potted apple trees, and this treatment was comparable to the application of the antibiotic streptomycin [24].Thus, PCS systems like this offer an opportunity to move away from using antibiotics and the resultant antibiotic resistance that develops in these agricultural sectors.
Spray-drying and freeze-drying are the most widely used methods for producing BCA powders.The spray-drying approach is preferable, as it is characterized by a high production rate and open production mode, as well as being easily scaled to industrial levels.Furthermore, the spray-drying operation time and production costs are 30-50 fold lower when compared to the costly and time-consuming freeze-drying approach [25,26].However, a significant drawback of spray-drying is the loss of cell viability due to the use of high temperature and rapid dehydration during the spray-drying process.
Previous spray-drying trials with P. agglomerans showed low viability (e.g., 3-29% viability) after spray-drying due to the heat sensitivity of these cells [27].The research presented herein describes an optimized formulation and protocol that leads to the improved viability of spray-dried P. agglomerans.Notably, the protocol demonstrated that greater than 90% viability remained following spray-drying for both the P. agglomerans cells alone and the same cells infected with Erwinia phages as a PCS.In follow-up experiments, a green fruit disc assay confirmed the high efficacy of the spray-dried P. agglomerans to control E. amylovora growth.Thus, the spray-drying protocol developed herein provides a viable avenue to make industrial-scale production of P. agglomerans as a BCA or PCS possible.Moreover, this protocol has broader implications for other antagonistic bacteria that are known to be sensitive to spray-drying, given the easily adaptable formulation and protocol.

Bacterial Isolates
All bacterial strains used in this study are listed in Table 1.Cultures were stored at −80 • C in Microbank cryobeads (Pro-Bank Diagnostics, Richmond Hill, ON, Canada).To prepare the working culture stock, one Microbank cryobead was mixed with one drop of PBS buffer (10 mM, pH 7.2) and plated on 2.3% (w/v) Difco TM nutrient agar (NA) plates (BD, Sparks, MD, USA).The plates were incubated for 16-18 h at 27 • C and then stored at 4 • C for 1 to 2 wks.Working cultures were obtained from the initial cultures by streaking single colonies onto NA and incubating at 27 • C for 16-18 h.

Bacteriophages
The two lytic E. amylovora bacteriophages used in this study are ϕEa21-4 (Myovirus) and ϕEa46-1-A1 (Podovirus) as listed in Table 2. To propagate each phage, a bacterial host (Table 2) suspension was prepared by suspending 5-6 colonies in 3 mL of 0.8% (w/v) nutrient broth (NB) (BD, Sparks, MD, USA) to obtain an OD 600 of ~0.6.Using a 250 mL baffled Erlenmeyer flask, 100 µL of the bacterial suspension was added to 75 mL of NB, which was then incubated at 27 • C with 150 rpm shaking (New Brunswick Innova ® 42, Eppendorf, Hamburg, Germany) for 3-4 h.A 100 µL aliquot of phage stock (5.0 × 10 9 PFU/mL) was added and the mixture was incubated for 16-18 h at 27 • C with 150 rpm shaking.Following incubation, 1 mL of chloroform was added to the culture and incubated with shaking for 5 min.The bacterial culture was subjected to centrifugation at 8500× g at 4 • C for 15 min, the pellet discarded, and the supernatant filtered through a 0.22 µm Steriflip filter (Millipore, Burlington, MA, USA).The working phage stocks were stored at 4 • C in dark amber glass vials until needed and the titers were determined by using qPCR (Section 2.3) [23].

Quantitative PCR (qPCR)
Phage titers and P. agglomerans cell numbers were determined using qPCR with a protocol described by Gayder and coworkers (2019).Briefly, phage working solutions (or lysate) were treated with DNase I to remove non-encapsulated phage DNA prior to qPCR.DNase I treatments contained 10 µL of phage lysate, 1 µL of 2000 U/mL DNase I (NEB, Ipswich, MA, USA), 2 µL of 10× DNase I buffer (NEB, Ipswich, MA, USA), and 7 µL of sterile distilled water.The solution was incubated for 40 min at 37 • C and then 20 min at 80 • C to inactivate the DNase I.For qPCR, the 20 µL reactions consisted of 4 µL of 5× EVOlution Probe qPCR Mix (Montreal Biotech Inc., Montreal, QC, Canada), 200 nM of each primer (Table 3), 100 mM of the probe, and 2 µL of the template.
The reaction conditions began with 10 min at 95 • C, followed by 40 cycles of 10 s at 95 • C and 45 s at 54 • C. Dilutions of the standard plasmid, pTotalStdA (10 11 , 10 8 , and 10 5 copies/mL), which contains amplicons for E. amylovora and P. agglomerans, as well as the phages ϕEa21-4 and ϕEa46-1-A1, were included in every run to generate a standard curve.A linearly fit standard curve of Ct value vs. copies/mL of the pTotalStdA was used to calculate the sample population quantities (genomes/mL).Populations of bacteria and phage were directly interpreted from this curve with the assumption that each cell or phage capsid contained a single genome.All qPCR quantification was performed with a Bio-Rad CFX96 qPCR System (Bio-Rad, Hercules, CA, USA).

Bacterial Counting by Platting
Bacterial cell cultures or reconstituted suspensions were serially diluted in PBS and a 100 µL volume of these dilutions was spread on NA and then incubated for 16-18 h at 27 • C. Bacterial colonies were enumerated, and the final CFU/mL was calculated accordingly by taking into account the dilution and plating factors.For all enumerations, the plating was carried out in at least triplicate.

Carrier Preparation
P. agglomerans was subcultured weekly on NA and, after 20 h at 27 • C, the plates were stored at 4 • C until needed that week.P. agglomerans cells were grown in NB as an initial rich-nutrient growth condition.For growth under stress conditions (i.e., osmoticadaptation to increase the cell's tolerance to heat stress and desiccation during spraydrying), P. agglomerans was grown on medium containing 5.0 g/L yeast extract, 10.0 g/L sucrose, and 35.5 g/L NaCl (YSN media) or in NB with the same amount of NaCl to reach a water activity (a w ) in the medium of 0.98 a w (where a w is the ratio between the vapour pressure of a sample compared to a control) [27,29].Cells were harvested by centrifugation (8500× g for 10 min at 4 • C), resuspended in 10 mM PBS at pH 7.2, and enumerated using the serial dilution and spread plating techniques on NA (outlined in Section 2.4).The colonies on the plates were counted after incubation for 16-18 h at 27 • C.
2.6.Phage-Carrier Formulation 2.6.1.Material Screening and Formulation Optimization Different concentrations and combinations of carbohydrates (all from Sigma-Aldrich, St. Louis, MO, USA) were used for formulations to explore with spray-drying (Table 4).These include D(+)-trehalose dihydrate, maltodextrin (dextrose equivalents 4.0-7.0 and 16.5-19.5),gum Arabic (from acacia tree), and carboxymethylcellulose sodium salt (CMC) with talc.P. agglomerans cell pellets (growth conditions mentioned in Section 2.5) were resuspended in a formulation mixture for 30 min to produce the formulated cells (fPa).The effect of different formulation chemicals on the P. agglomerans' carrier infectivity by Erwinia phages was tested before selecting the suitable formulation for spray-drying.Different concentrations of formulation chemicals were prepared in NB, as outlined in Table 4, and inoculated with P. agglomerans Pa39-7 (10 3 CFU/mL) together with the ϕEa21-4 phage (10 5 PFU/mL) in 96-well plates prior to incubation at 27 • C in a Synergy H1 BioTek microplate reader (Agilent, Santa Clara, CA, USA) for 24 h.Readings of the plates at an OD 600 were taken every 15 min and compared with the control sample (no phage added) in order to monitor growth/infectivity.After the initial trials, further optimization was carried out using different concentrations and combinations of the selected formulation chemicals as shown in Table 5. Osmotically stressed or non-stressed P. agglomerans strain Pa39-7 cells (sPa or nsPa, respectively) were prepared by mixing cell pellets with a formulation solution (1 g/100 mL) for 30 min before spray-drying to form formulated stressed (sfPa) or formulated nonstressed (nsfPa) samples.For phage-infected cells (i.e., the phage-carrier system), P. agglomerans cell pellets were resuspended in PBS and mixed with the phage (ϕEa21-4 or ϕEa46-1-A1) at an MOI of 1.0 for 30 min.The cells were then harvested by centrifugation (8500× g for 10 min at 4 • C) and resuspended in the formulation mixture (1 g/100 mL) for spray-drying.The spray-drying process was carried out using a Yamato ADL311S model (Yamato Scientific Co., Tokyo, Japan) with a feeding rate of 11-14 mL/min, inlet temperature of 160 • C, and an outlet temperature of 60 • C. The spray-dried powder was collected and stored in white plastic polyethylene high density tubes [30] at 4 • C or room temperature (RT) with activated Silica gel packets (5 g each) (Millipore Sigma, Oakville, ON, Canada).

Storage Stability of the Spray-Dried Preparations
Spray-dried powder of phage-infected and non-infected carrier cells was collected and stored in polyethylene tubes (as mentioned above), then enclosed in Statshield ® Moisture Barrier Al-bags (DESCO, Chino, CA, USA) and sealed with an Impulse Sealer, model AIE 300 (American International Electric, City of Industry, CA, USA).Spray-dried samples in sealed tubes were stored at RT or 4 • C for 16 wks (~4 months).At the time of sampling (biweekly), one tube was taken, and three technical replicates were prepared by reconstitution of the powder in sterile distilled water (0.9 g/3 mL).P. agglomerans cells were enumerated by plating on NA, and the logarithmic cell counts were plotted versus time.To test the presence of phage particles in the PCS powder and the capability of the phage to propagate (i.e., lyse the carrier cells) after reconstitution, 100 µL of reconstituted powder was used to inoculate 10 mL of NB and incubated at 27 • C with shaking at 180 rpm (New Brunswick Innova ® 42, Eppendorf, Hamburg, Germany).The phages were enumerated by qPCR (according to Section 2.3) at time intervals of 0, 2, 4, and 18 h (T 0 , T 2 , T 4 , and T O/N ).The viability of the phage following spray-drying and reconstitution of the PCS powder was also tested by plating 100 µL of a 1/10 dilution of this resuspension on NA plates and incubating it for 16-18 h at 27 • C.These plates have a lawn of Pantoea growth from the reconstituted powder and any plaques on these plates were an indication that the phage (which had infected some of the Pantoea) were still viable.The PFU/mL was calculated after taking into account the dilution and plating factors.

Efficacy Testing of Phage-Carrier with a Green Pear Disc Assay
A pathogenicity test was carried out using a green pear disc assay [31,32].Briefly, green pears were purchased from a local grocery store, washed, rinsed, surface sterilized with 70% (v/v) ethanol, and rinsed twice with sterile distilled water.Under sterile conditions, a copper borer was used to cut into the fruit and produce pear plugs from which discs were cut measuring 1.5 mm in diameter and 1 mm in depth.The discs were placed into 2 mL sterile Eppendorf tubes using sterile forceps.Treatments consisted of formulated P. agglomerans Pa39-7, formulated P. agglomerans plus phages (strain Pa39-7 + phage ϕEa21-4), a positive control (1:1 ratio of E. amylovora strains Ea6-4 and EaD7), and a negative control (non-infected formulated P. agglomerans).Two biological replicates, containing eight technical replicates were set up for each treatment.To each pear plug, 10 µL of treatment was added and sample tubes were collected at 0, 24, and 48 h.A 10 µL volume of pathogen was added at 10 6 CFU/mL at 24 h and allowed to incubate for an additional 24 h.Following this time period, 500 µL of 0.01 M phosphate buffer pH 7.0 was added to the tubes containing the disc and sonicated for 3 min at high power for 3 min.A 200 µL volume of the sonicated supernatant was removed into 2 mL sterile Eppendorf tubes and the cells were heat-killed at 80 • C for 10 min (Figure 1).The heat-treated supernatant was frozen at −20 • C prior to evaluation by qPCR (Section 2.3).A Student's t-test was performed comparing the means between the 24 and 48 h experimental data.Statistical analyses were performed using the JMP programme (JMP Statistical Discovery LLC, Cary, NC, USA).A three-way random analysis of variance (ANOVA) was performed on natural log (ln) + 1 transformed data comparing the effects of the two formulated products in suppressing the population of E. amylovora in vitro on green pear discs over time.

Efficacy Testing of Phage-Carrier with a Green Pear Disc Assay
A pathogenicity test was carried out using a green pear disc assay [33,34].Briefly, green pears were purchased from a local grocery store, washed, rinsed, surface sterilized with 70% (v/v) ethanol, and rinsed twice with sterile distilled water.Under sterile conditions, a copper borer was used to cut into the fruit and produce pear plugs from which discs were cut measuring 1.5 mm in diameter and 1 mm in depth.The discs were placed into 2 mL sterile Eppendorf tubes using sterile forceps.Treatments consisted of formulated P. agglomerans Pa39-7, formulated P. agglomerans plus phages (strain Pa39-7 + phage фEa21-4), a positive control (1:1 ratio of E. amylovora strains Ea6-4 and EaD7), and a negative control (non-infected formulated P. agglomerans).Two biological replicates, containing eight technical replicates were set up for each treatment.To each pear plug, 10 µL of treatment was added and sample tubes were collected at 0, 24, and 48 h.A 10 µL volume of pathogen was added at 10 6 CFU/mL at 24 h and allowed to incubate for an additional 24 h.Following this time period, 500 µL of 0.01 M phosphate buffer pH 7.0 was added to the tubes containing the disc and sonicated for 3 min at high power for 3 min.A 200 µL volume of the sonicated supernatant was removed into 2 mL sterile Eppendorf tubes and the cells were heat-killed at 80 °C for 10 min (Figure 1).The heat-treated supernatant was frozen at −20 °C prior to evaluation by qPCR (Section 2.3).A Student's t-test was performed comparing the means between the 24 and 48 h experimental data.Statistical analyses were performed using the JMP programme (JMP Statistical Discovery LLC, Cary, NC, USA).A three-way random analysis of variance (ANOVA) was performed on natural log (ln) + 1 transformed data comparing the effects of the two formulated products in suppressing the population of E. amylovora in vitro on green pear discs over time.Testing BCA/PCS efficacy using a pear disc assay.Pear slices were inoculated with 10 µL of reconstituted BCA/PCS powder, separately, then incubated at 21 °C for 24 h.A mixture of the plant pathogens (E.amylovora strains Ea6-4 and EaD7, 1:1 mixture of 1 × 10 6 CFU/mL each) was added and then incubated for an additional 24 h.At sampling times T0, T24, and T48, the pear disc was mixed with 500 µL buffer, sonicated for 3 min, and then 200 µL of this solution was heated at 80 °C for 10 min and then stored at −20 °C for qPCR analysis (red arrows).

Water Activity (aw)
Carrier and PCS powder water activities were measured by using an Aqualab 4TE water activity meter according to the manufacturer's instructions [35].Three technical replicates of powders were prepared and tested for the shelf-life experiment.Testing BCA/PCS efficacy using a pear disc assay.Pear slices were inoculated with 10 µL of reconstituted BCA/PCS powder, separately, then incubated at 21 • C for 24 h.A mixture of the plant pathogens (E.amylovora strains Ea6-4 and EaD7, 1:1 mixture of 1 × 10 6 CFU/mL each) was added and then incubated for an additional 24 h.At sampling times T 0 , T 24 , and T 48 , the pear disc was mixed with 500 µL buffer, sonicated for 3 min, and then 200 µL of this solution was heated at 80 • C for 10 min and then stored at −20 • C for qPCR analysis (red arrows).
2.9.Powder Physical Properties 2.9.1.Water Activity (a w ) Carrier and PCS powder water activities were measured by using an Aqualab 4TE water activity meter according to the manufacturer's instructions [33].Three technical replicates of powders were prepared and tested for the shelf-life experiment.

Transmission Electron Microscopy (TEM)
Copper-rhodium (150-mesh) grids were covered with a thin layer of amorphous carbon made hydrophilic by a 45 s vacuum glow-discharge.PCS powder was rehydrated in filtered MilliQ water and then 4-6 µL was placed on individual grids and left for 2 min to adsorb.Excess sample was gently removed by filter paper.The grid was then washed three times with water.Sample on the grids were stained with 2% (w/v) uranyl acetate.A Tecnai G2 transmission electron microscope (FEI Company, Hillsboro, OR, USA) at the University of Guelph Electron Microscopy Unit (Guelph, ON, Canada) was used for visualization, operating at 200 kV under variable magnification (×50,000).Images were acquired using the Gatan Ultascan 4K CCD (Gatan Inc., Pleasanton, CA, USA) and Gatan Digital Micrograph software imaging system (version 3.5).

Material Selection for the Phage-Carrier Formulation
To exclude the possibility of interference of the formulation chemicals on the phage infectivity of the carrier cells after reconstitution, the lytic activity on P. agglomerans strain Pa39-7 cells by the ϕEa21-4 phage was assessed by turbidity measurements of cultures in the presence of each formulation chemical being tested.Phage infectivity and the growth of carrier cells was not significantly affected by the presence of D(+)-trehalose (Figure 2A) or maltodextrin (Figure 2B).Interestingly, the presence of D(+)-trehalose or maltodextrin actually augmented the ability of the phage to infect the host cells.Similarly, the presence of talc/CMC did not affect the growth of the carrier cells or their infectivity by ϕEa21-4 phage (Figures S1 and S2).

Transmission Electron Microscopy (TEM)
Copper-rhodium (150-mesh) grids were covered with a thin layer of amorphous carbon made hydrophilic by a 45 s vacuum glow-discharge.PCS powder was rehydrated in filtered MilliQ water and then 4-6 µL was placed on individual grids and left for 2 min to adsorb.Excess sample was gently removed by filter paper.The grid was then washed three times with water.Sample on the grids were stained with 2% (w/v) uranyl acetate.A Tecnai G2 transmission electron microscope (FEI Company, Hillsboro, OR, USA) at the University of Guelph Electron Microscopy Unit (Guelph, ON, Canada) was used for visualization, operating at 200 kV under variable magnification (×50,000).Images were acquired using the Gatan Ultascan 4K CCD (Gatan Inc., Pleasanton, CA, USA) and Gatan Digital Micrograph software imaging system (version 3.5).

Material Selection for the Phage-Carrier Formulation
To exclude the possibility of interference of the formulation chemicals on the phage infectivity of the carrier cells after reconstitution, the lytic activity on P. agglomerans strain Pa39-7 cells by the ϕEa21-4 phage was assessed by turbidity measurements of cultures in the presence of each formulation chemical being tested.Phage infectivity and the growth of carrier cells was not significantly affected by the presence of D(+)-trehalose (Figure 2A) or maltodextrin (Figure 2B).Interestingly, the presence of D(+)-trehalose or maltodextrin actually augmented the ability of the phage to infect the host cells.Similarly, the presence of talc/CMC did not affect the growth of the carrier cells or their infectivity by ϕEa21-4 phage (Figures S1 and S2).Based on the formulation screening results, 20% (w/v) D(+)-trehalose with 2% (w/v) talc and 0.1% (w/v) CMC was selected as Formula I for cell preparations before spraydrying.Despite the promising results, there were downstream application troubles using Formula I. Following reconstitution of the spray-dried powders for the biocontrol assay, Based on the formulation screening results, 20% (w/v) D(+)-trehalose with 2% (w/v) talc and 0.1% (w/v) CMC was selected as Formula I for cell preparations before spraydrying.Despite the promising results, there were downstream application troubles using Formula I. Following reconstitution of the spray-dried powders for the biocontrol assay, the atomizer nozzle became clogged by the talc particles.Hence, further optimization was carried out using different mixtures of carbohydrates, as shown in Table 5, to solve the issue of nozzle clogging (Figure 3, Table S1).Accordingly, Formula II was a modified version containing 15% (w/v) of D(+)-trehalose and 15% (w/v) maltodextrin 16.5-19.5.This represented the final formulation that was used in all other experiments.the atomizer nozzle became clogged by the talc particles.Hence, further optimization was carried out using different mixtures of carbohydrates, as shown in Table 5, to solve the issue of nozzle clogging (Figure 3, Table S1).Accordingly, Formula II was a modified version containing 15% (w/v) of D(+)-trehalose and 15% (w/v) maltodextrin 16.5-19.5.This represented the final formulation that was used in all other experiments.

Optimization of Spray-Drying and Reconstitution Protocols
Several trials were carried out to determine the optimal spray-drying temperatures and reconstitution times of the spray-dried powders.Experiments were conducted at different inlet (150-160 °C) and outlet (50-60 °C) temperatures to assess the parameters that minimize the loss in viability of the carrier cells during the spray-drying process.According to this optimization, the best combination of inlet and outlet temperatures was determined to be 160 and 60 °C, respectively.The water activity of the powder (aw) was found to be 0.18 ± 0.002.After spray-drying, the powder produced was dissolved in sterile distilled water to 0.3 g/mL to retain the same weight/volume ratio used before the spraydrying process.The optimum reconstitution time was assessed by the powder solubility and cell plating on NA across a time course.

Confirmation of Cell Viability and Phage Infectivity after Spray-Drying
Once the formulation and spray-drying process was determined, the viability of formulated P. agglomerans carrier cells that grew in NB (nsfPa) was compared to osmotically adapted cells grown in NB plus NaCl medium.The nsfPa formulation displayed a 30% reduction in cell viability after spray-drying (Figure 4).However, osmotically adapted cells showed ≥95% of cell viability for carrier cells (sfPa) and about 90% for the PCS infected carrier (sfPa-P), as shown in Figure 4.The presented results are for the P. agglomerans strain Pa39-7 and ϕEa21-4 phage; however, the cell viability after spray-drying of the Pa39-7 strain infected with ϕEa46-1-A1 was similar to that infected with the ϕEa21-4 phage (Tables S2, S4 and S5).Also, the strain Pa31-4 showed a similar cell viability to Pa39-7 after spray-drying (Table S3).

Optimization of Spray-Drying and Reconstitution Protocols
Several trials were carried out to determine the optimal spray-drying temperatures and reconstitution times of the spray-dried powders.Experiments were conducted at different inlet (150-160 • C) and outlet (50-60 • C) temperatures to assess the parameters that minimize the loss in viability of the carrier cells during the spray-drying process.According to this optimization, the best combination of inlet and outlet temperatures was determined to be 160 and 60 • C, respectively.The water activity of the powder (a w ) was found to be 0.18 ± 0.002.After spray-drying, the powder produced was dissolved in sterile distilled water to 0.3 g/mL to retain the same weight/volume ratio used before the spray-drying process.The optimum reconstitution time was assessed by the powder solubility and cell plating on NA across a time course.

Confirmation of Cell Viability and Phage Infectivity after Spray-Drying
Once the formulation and spray-drying process was determined, the viability of formulated P. agglomerans carrier cells that grew in NB (nsfPa) was compared to osmotically adapted cells grown in NB plus NaCl medium.The nsfPa formulation displayed a 30% reduction in cell viability after spray-drying (Figure 4).However, osmotically adapted cells showed ≥95% of cell viability for carrier cells (sfPa) and about 90% for the PCS infected carrier (sfPa-P), as shown in Figure 4.The presented results are for the P. agglomerans strain Pa39-7 and ϕEa21-4 phage; however, the cell viability after spray-drying of the Pa39-7 strain infected with ϕEa46-1-A1 was similar to that infected with the ϕEa21-4 phage (Tables S2, S4 and S5).Also, the strain Pa31-4 showed a similar cell viability to Pa39-7 after spray-drying (Table S3).The viability of spray-dried P. agglomerans Pa39-7 was measured as a percentage by comparing before and after spray-drying cell counts.All tested P. agglomerans cells were formulated by the resuspension of cell pellets in Formula II.Both versions of the osmotically adapted cells that grew in NB plus NaCl medium (i.e., either phageuninfected (sfPa) or ϕEa21-4-phage-infected (sfPa-P)), showed greater than 90% viability after spraydrying compared to osmotically non-adapted cells (nsfPa), which showed about 70% cell viability.Assays were carried out in triplicate and the data averages and standard deviation were plotted.Using a t-test, the significance (p < 0.05) between sfPa and nsfPa (*), as well as between sfPa-P and nsfPa (**), was noted.
A 1/10 dilution of reconstituted PCS powder (i.e., from the sfPa-P cells) was plated onto NA to mimic the double-layer plaque overlay assay to test the phage infectivity in the phage-carrier powder.After a 24 h incubation at 27 °C, plaques were observed, indicating the presence of active phage in the powder of spray-dried infected carrier cells.Furthermore, the phage titer increased by more than 4.5 log (PFU/mL) after 24 h when the reconstituted PCS powder was used to inoculate 10 mL of NB, as shown in Figure 5.   7 was measured as a percentage by comparing before and after spray-drying cell counts.All tested P. agglomerans cells were formulated by the resuspension of cell pellets in Formula II.Both versions of the osmotically adapted cells that grew in NB plus NaCl medium (i.e., either phage-uninfected (sfPa) or ϕEa21-4-phage-infected (sfPa-P)), showed greater than 90% viability after spray-drying compared to osmotically non-adapted cells (nsfPa), which showed about 70% cell viability.Assays were carried out in triplicate and the data averages and standard deviation were plotted.Using a t-test, the significance (p < 0.05) between sfPa and nsfPa (*), as well as between sfPa-P and nsfPa (**), was noted.
A 1/10 dilution of reconstituted PCS powder (i.e., from the sfPa-P cells) was plated onto NA to mimic the double-layer plaque overlay assay to test the phage infectivity in the phage-carrier powder.After a 24 h incubation at 27 • C, plaques were observed, indicating the presence of active phage in the powder of spray-dried infected carrier cells.Furthermore, the phage titer increased by more than 4.5 log (PFU/mL) after 24 h when the reconstituted PCS powder was used to inoculate 10 mL of NB, as shown in Figure 5.Both versions of the osmotically adapted cells that grew in NB plus NaCl medium (i.e., either phageuninfected (sfPa) or ϕEa21-4-phage-infected (sfPa-P)), showed greater than 90% viability after spraydrying compared to osmotically non-adapted cells (nsfPa), which showed about 70% cell viability.Assays were carried out in triplicate and the data averages and standard deviation were plotted.Using a t-test, the significance (p < 0.05) between sfPa and nsfPa (*), as well as between sfPa-P and nsfPa (**), was noted.
A 1/10 dilution of reconstituted PCS powder (i.e., from the sfPa-P cells) was plated onto NA to mimic the double-layer plaque overlay assay to test the phage infectivity in the phage-carrier powder.After a 24 h incubation at 27 °C, plaques were observed, indicating the presence of active phage in the powder of spray-dried infected carrier cells.Furthermore, the phage titer increased by more than 4.5 log (PFU/mL) after 24 h when the reconstituted PCS powder was used to inoculate 10 mL of NB, as shown in Figure 5. TEM images were taken to compliment the P. agglomerans viability and phage plaque assays with reconstituted PCS powder.The images show assembled phage capsid heads A volume of 100 µL of the reconstituted PCS powder (P.agglomerans Pa39-7 strain infected with ϕEa21-4) was used to inoculate 10 mL of NB and incubated at 27 • C with shaking at 180 rpm for 18 h before determining PFU/mL using qPCR.The graph displays the phage titer (log PFU/mL) increased with incubation time and that the phages were viable.Assays were carried out in triplicate and the data averages and standard deviation were plotted.
TEM images were taken to compliment the P. agglomerans viability and phage plaque assays with reconstituted PCS powder.The images show assembled phage capsid (heads) (red arrows) inside and outside of the carrier cells (Figure 6A,B, respectively).Overall, these results further confirm that osmotic adaptation in combination with Formula II act to protect the phage and carrier cells during the spray-drying process so that they are present and viable after storage and reconstitution (Figures 5 and 6).
Viruses 2024, 16, x FOR PEER REVIEW 10 of 16 (red arrows) inside and outside of the carrier cells (Figure 6A,B, respectively).Overall, these results further confirm that osmotic adaptation in combination with Formula II act to protect the phage and carrier cells during the spray-drying process so that they are present and viable after storage and reconstitution (Figures 5 and 6).

Shelf-Life of the Carrier and Phage-Carrier Spray-Dried Powders
Cell count and phage infectivity assays were conducted every 2 wks for 4 months to assess the carrier and phage viability in the powder following storage.The viability of the P. agglomerans strain Pa39-7 in the carrier powder was reduced by more than 2 log (CFU/g) after 16 wks of storage at RT.However, only a 1-1.5 log reduction in bacterial counts was observed in powder stored at 4 °C (Figure 7A).For the PCS powder, P. agglomerans viability was reduced by 4 log CFU/g after 16 wks at RT and maintained an approximate 2.5 log reduction when stored at 4 °C (Figure 7B).Inoculation of reconstituted PCS powders in NB to test phage infectivity gave a similar pattern to that mentioned before in Figure 5.

Shelf-Life of the Carrier and Phage-Carrier Spray-Dried Powders
Cell count and phage infectivity assays were conducted every 2 wks for 4 months to assess the carrier and phage viability in the powder following storage.The viability of the P. agglomerans strain Pa39-7 in the carrier powder was reduced by more than 2 log (CFU/g) after 16 wks of storage at RT.However, only a 1-1.5 log reduction in bacterial counts was observed in powder stored at 4 • C (Figure 7A).For the PCS powder, P. agglomerans viability was reduced by 4 log CFU/g after 16 wks at RT and maintained an approximate 2.5 log reduction when stored at 4 • C (Figure 7B).Inoculation of reconstituted PCS powders in NB to test phage infectivity gave a similar pattern to that mentioned before in Figure 5.
(red arrows) inside and outside of the carrier cells (Figure 6A,B, respectively).Overall, these results further confirm that osmotic adaptation in combination with Formula II act to protect the phage and carrier cells during the spray-drying process so that they are present and viable after storage and reconstitution (Figures 5 and 6).

Shelf-Life of the Carrier and Phage-Carrier Spray-Dried Powders
Cell count and phage infectivity assays were conducted every 2 wks for 4 months to assess the carrier and phage viability in the powder following storage.The viability of the P. agglomerans strain Pa39-7 in the carrier powder was reduced by more than 2 log (CFU/g) after 16 wks of storage at RT.However, only a 1-1.5 log reduction in bacterial counts was observed in powder stored at 4 °C (Figure 7A).For the PCS powder, P. agglomerans viability was reduced by 4 log CFU/g after 16 wks at RT and maintained an approximate 2.5 log reduction when stored at 4 °C (Figure 7B).Inoculation of reconstituted PCS powders in NB to test phage infectivity gave a similar pattern to that mentioned before in Figure 5. Changes in the cell viability of carrier cells in PCS powder stored at 4 °C (○) or at RT (•).Assays were carried out in triplicate and the data averages and standard deviation were plotted.

Phage-Carrier Efficacy Assessment with the Pear Disc Assay
A pear disc was used as an in vitro assay to assess the protection that the BCA and PCS powder formulations can afford to plants when challenged with E. amylovora (Figure 1).In these trials, the BCA (only P. agglomerans strain Pa39-7) and PCS (P.agglomerans strain Pa39-7 and phage фEa21-4) were not significantly different from each other in population growth during the 24 h and 48 h sampling on the pear discs (Figure 8; c and a, respectively).Using this assay, E. amylovora was also noted to grow on the pear discs and increased significantly by 2 logs between the 24 h to 48 h time points (Figure 8; f and b, respectively).When the myovirus фEa21-4 population was monitored on the pear discs, a slight reduction in titer at 48 h after being exposed to E. amylovora for 24 h was noted (Figure 8; d to e statistical comparison).When the E. amylovora population was followed by qPCR, both the BCA (Pa39-7) and PCS (Pa39-7 + фEa21-4) led to significant reductions in E. amylovora numbers at the 48 h timepoint (Figure 8; g and h compared to b).Interestingly, the BCA was noted to have a slightly more significant effect in suppressing the E. amylovora pathogen on the green pear discs than PCS under these assay conditions (Figure 8; g and h, respectively).and E. amylovora on green pear discs measured at 24 and 48 h.On the x-axis, the initial individual application to the pear discs is noted in black text, where the BCA (i.e., containing spray-dried P. agglomerans strain Pa39-7) and PCS (i.e., containing spray-dried фEa21-4 phage-infected P. agglomerans strain Pa39-7) formulations were tested and E. amylovora alone served as a positive control (+veC).The red text on the x-axis denotes what was enumerated by qPCR from the trial and is shown in the bar graph above.Grey bars represent populations on the pear discs at 24 h.For the statistically noted c and d samples, this is the bacterial count before inoculation with E. amylovora, while in the +veC (f) represents the E. amylovora numbers at the time of E. amylovora inoculations.All bars at 48 h (black) represent the growth of each organism in each formulation after 24 h of additional growth in the presence of E. amylovora.Statistical analyses showed that the interactions between all variable combinations in the experiment were highly significant (p < 0.0001), as denoted by the letters a-h above the bars.Replicate and random effects in the analysis were not significant (p > 0.05), indicating there was no variability between replicates of individual groups.and E. amylovora on green pear discs measured at 24 and 48 h.On the x-axis, the initial individual application to the pear discs is noted in black text, where the BCA (i.e., containing spray-dried P. agglomerans strain Pa39-7) and PCS (i.e., containing spray-dried ϕEa21-4 phage-infected P. agglomerans strain Pa39-7) formulations were tested and E. amylovora alone served as a positive control (+veC).The red text on the x-axis denotes what was enumerated by qPCR from the trial and is shown in the bar graph above.Grey bars represent populations on the pear discs at 24 h.For the statistically noted c and d samples, this is the bacterial count before inoculation with E. amylovora, while in the +veC (f) represents the E. amylovora numbers at the time of E. amylovora inoculations.All bars at 48 h (black) represent the growth of each organism in each formulation after 24 h of additional growth in the presence of E. amylovora.Statistical analyses showed that the interactions between all variable combinations in the experiment were highly significant (p < 0.0001), as denoted by the letters a-h above the bars.Replicate and random effects in the analysis were not significant (p > 0.05), indicating there was no variability between replicates of individual groups.

Discussion
In fire blight management, BCAs and phages (registered in the USA) are commercially available as alternatives to antibiotic utilization [8,16,17].Subsequently, PCS has been developed as an additional approach that combines the biological activity of an-tagonistic bacteria, P. agglomerans, and Erwinia phages that specifically target and kill the fire blight pathogen [20,21,34].An optimized and economical production protocol is required for industrial-scale production of the PCS, and spray-drying or freeze-drying are the most widely used methods for production [25].However, freeze-drying is costly, time-consuming, and operates as a closed system, which means that it cannot be used in a continuous large-scale production mode.In contrast, spray-drying has a higher powder production rate, continuous production mode, is easily scalable to industrial levels, and is 30-50-fold more cost effective compared to freeze-drying [25,26].The major drawback of spray-drying is the loss of bacterial and/or phage viability due to exposure to high temperatures during preparation.For example, P. agglomerans carrier cells are thermally sensitive and have exhibited a significant reduction in cell viability (only 3-29% cell viability following spray-drying) [27,35,36].Bacterial growth under osmotically adapted conditions is known to increase tolerance to desiccation.More specifically, osmotically adapted P. agglomerans can accumulate glycine-betaine, ectoine, and D(+)-trehalose [29,36,37].Under this premise, osmotically adapted (i.e., grown in a standard medium with NaCl to a water activity of 0.97-0.98)and spray-dried Pantoea were able to consistently display cell viabilities around 30% [27].However, these low viability numbers remain a hindrance to industrial-scale production.
This study established an improved P. agglomerans viability protocol by optimizing the formulation mixtures, spray-drying temperatures, nozzle clogging, and reconstitution times.The culmination of this work indicates that P. agglomerans (either under non-stressed or osmotically non-adapted conditions) treated with Formula II have an approximately 70% survival after spray-drying.Further optimization of this protocol was carried out by growing P. agglomerans Pa39-7 on NB with NaCl at an a w of 0.98 for 18-20 h.This osmotic adaptation further improved cell viability to more than 95% for P. agglomerans alone (BCA) or more than 90% for PCS, which far exceeds the previously published results of ~30% for osmotically adapted [36] and 3% for non-adapted [27].Thus, this enhanced protocol represents a very promising approach for industrial-scale production of P. agglomerans as a BCA or PCS application to control fire blight but also more widely as an avenue to explore for other bacteria recalcitrant to these processes.
For the PCS, the modified protocol was also assessed for the survival and infectivity of the phage in the carrier bacteria.In the presence of D(+)-trehalose and maltodextrin, the survival of P. agglomerans with the phage was markedly lower, thereby suggesting that not only had the phage ϕEa21-4 survived the spray-drying process, but that the presence of Formula II components enhanced its infectivity (Figure 2A,B).The presence of formulation compounds has been suggested in the literature to increase the viscosity and hence phage adsorption and/or can lead to changes in bacterial metabolism [38,39].While plausible as a reason for the observed increase, further research would be needed to confirm these possibilities in our studies.
Maintaining the viability of the carrier and the ability of these cells to be infected with E. amylovora phages are important factors for a suitable PCS.In this work, Formula II was noted to protect both phage-infected and non-infected cells, as shown by a combination of plaque assays and NB inoculation with reconstituted powder, as well as electron microscopy imaging results (Figures 5 and 6).In addition, the powder storage protocol used in this study utilized low O 2 -permeability tubes, silica gel packets to control humidity, and enclosure of the bottle in Statshield ® Moisture Barrier Al-bags, along with different storage temperatures.Combing these storage conditions led to the high cell viability of both carrier and PCS powders for almost 4 months (i.e., only 1-2 log reductions in viability over this period).By this process, the high humidity content in the powder, which can cause the crystallization of the amorphous trehalose matrix and decrease the cell viability [40,41], appears to have been mitigated.Our low temperature results are also consistent with other studies that demonstrated that the powder storage temperature has previously been noted to be an important factor that can affect the viability of the cells during storage due to membrane lipid oxidation [42,43].Thus, by combining all of these factors we have been able to generate a PCS that has proven longevity that is amenable to production and delivery for field applications in future studies with expanded trials.
As an initial in vitro test of the efficacy of the BCA and PCS powders in mitigating E. amylovora infections, reconstituted powders were used on pear slices as a model system of infection.Both the BCA and PCS preparations were able to decrease E. amylovora growth by a 3 log reduction compared to untreated samples after 24 h of infection time with E. amylovora (Figure 8).While the pear disc assay represents initial analyses in plants, future work will build on this in a full workup with greenhouse and field trials (e.g., with potted apples and field-grown trees at the blossom stage).
Interestingly, the populations of carrier and phage (in the case of PCS) were not significantly different from each other over the entire 48 h experiment.These results are in contrast to our separate experiment where reconstituted PCS in NB led to a doubling of the phage counts after 24 h with shaking at 27 • C (Figure 5).It is plausible that there are alterations or delays in the infection process for the phage in the pear disc assay given that these environmental conditions are likely to be different than the rich NB media.Indeed, published data have noted that there are several factors that can contribute to discrepancies in phage counts between assays.For example, the bacterial carrier metabolic state can play a vital role in phage adsorption/infectivity and consequently phage propagation.For instance, the burst size of T4 phage is dependent on the cell state of the E. coli strain B23 [44].The T4 burst size can vary between 1 and 40 progeny/cell depending on whether they are in the mid-log or stationary phase of growth, where the latter may produce only one phage per cell since the cells have entered a hibernation of scavenger response mode [45].The cell's metabolic state can also influence the sigma factors present within cells, which can differentially orchestrate the activity of the DNA-dependent RNA polymerase (RNAP) holoenzyme (Eσ) during the transcription process [46].For example, E. coli contains six σ factors, including σ 70 that is present during exponential growth and σ S that is found during the stationary phase [46,47] and activated by various stress signals, including hyperosmolarity [48].In the present spray-drying protocol, P. agglomerans was exposed to salt stress during osmotic adaptation and stationary-phase growth, which combined with further phyllosphere pressures/responses led to a slower/lower release of phages and concomitantly higher numbers of P. agglomerans.While the PCS and BCA both showed antagonistic behavior towards E. amylovora, the pear disc assay highlights the importance of assaying beyond the typical in vitro rich culture scenarios and provides a future avenue to explore observations over longer time periods, MOI concentrations, reconstitution variables, and more.

Conclusions
An improved viability protocol for spray-dried P. agglomerans as a BCA and PCS was established.This protocol can be used for industrial-scale production of a P. agglomerans BCA or PCS that is ready for greenhouse and field trials.Given the efficacy of this protocol, it is likely to also have broader applicability to other thermal-sensitive BCAs in development as an example of iterative optimization that can have drastically different yields and improved cell viability from 3-30% to over 90%.

Figure 1 .
Figure 1.Testing BCA/PCS efficacy using a pear disc assay.Pear slices were inoculated with 10 µL of reconstituted BCA/PCS powder, separately, then incubated at 21 °C for 24 h.A mixture of the plant pathogens (E.amylovora strains Ea6-4 and EaD7, 1:1 mixture of 1 × 10 6 CFU/mL each) was added and then incubated for an additional 24 h.At sampling times T0, T24, and T48, the pear disc was mixed with 500 µL buffer, sonicated for 3 min, and then 200 µL of this solution was heated at 80 °C for 10 min and then stored at −20 °C for qPCR analysis (red arrows).

Figure 1 .
Figure 1.Testing BCA/PCS efficacy using a pear disc assay.Pear slices were inoculated with 10 µL of reconstituted BCA/PCS powder, separately, then incubated at 21 • C for 24 h.A mixture of the plant pathogens (E.amylovora strains Ea6-4 and EaD7, 1:1 mixture of 1 × 10 6 CFU/mL each) was added and then incubated for an additional 24 h.At sampling times T 0 , T 24 , and T 48 , the pear disc was mixed with 500 µL buffer, sonicated for 3 min, and then 200 µL of this solution was heated at 80 • C for 10 min and then stored at −20 • C for qPCR analysis (red arrows).

Figure 2 .
Figure 2. Determination of ϕEa21-4 phage infection of P. agglomerans cells in the presence of different formulation chemicals.(A) Survival of the P. agglomerans strain Pa39-7 after phage ϕEa21-4 infection in the presence (○) and absence (△) of D(+)-trehalose.Uninfected P. agglomerans Pa39-7 growth in the presence (•) and absence (▼) of D(+)-trehalose was also measured as controls.(B) Survival of the P. agglomerans strain Pa39-7 after phage ϕEa21-4 infection in the presence (○) and absence (△) of maltodextrin.In the absence of phage, P. agglomerans Pa39-7 growth in the presence (•) or absence (▼) of maltodextrin was similar.Assays were carried out in triplicate and the data averages and standard deviation were plotted.The final concentration of D(+)trehalose and maltodextrin was 5.0% each.

Figure 2 .
Figure 2. Determination of ϕEa21-4 phage infection of P. agglomerans cells in the presence of different formulation chemicals.(A) Survival of the P. agglomerans strain Pa39-7 after phage ϕEa21-4 infection in the presence ( ) and absence (△) of D(+)-trehalose.Uninfected P. agglomerans Pa39-7 growth in the presence (•) and absence (▼) of D(+)-trehalose was also measured as controls.(B) Survival of the P. agglomerans strain Pa39-7 after phage ϕEa21-4 infection in the presence ( ) and absence (△) of maltodextrin.In the absence of phage, P. agglomerans Pa39-7 growth in the presence (•) or absence (▼) of maltodextrin was similar.Assays were carried out in triplicate and the data averages and standard deviation were plotted.The final concentration of D(+)trehalose and maltodextrin was 5.0% each.

Figure 3 .
Figure 3. Visual representation of the spray-drying optimization process.One of the optimization criteria was the powder distribution during the spray-drying process.Using Formulation I (20% D(+)-trehalose and 2% talc/CMC), in addition to nozzle clogging by talc particles, collecting the powder was a challenge due to its adhesion to the drying chamber and the wall of the spray-dryer, as shown in (A,B).Using Formulation II (15% of D(+)-trehalose and 15% maltodextrin (16.5-19.5 dextrin equivalent) resulted in enhanced powder collection as shown in (C,D), as well as a reduced reconstitution time of 30 min instead of 3 h that was needed with the first formulation.

Figure 3 .
Figure 3. Visual representation of the spray-drying optimization process.One of the optimization criteria was the powder distribution during the spray-drying process.Using Formulation I (20% D(+)trehalose and 2% talc/CMC), in addition to nozzle clogging by talc particles, collecting the powder was a challenge due to its adhesion to the drying chamber and the wall of the spray-dryer, as shown in (A,B).Using Formulation II (15% of D(+)-trehalose and 15% maltodextrin (16.5-19.5 dextrin equivalent) resulted in enhanced powder collection as shown in (C,D), as well as a reduced reconstitution time of 30 min instead of 3 h that was needed with the first formulation.

Figure 4 .
Figure 4. Viability of P. agglomerans after spray-drying.The viability of spray-dried P. agglomerans Pa39-7 was measured as a percentage by comparing before and after spray-drying cell counts.All tested P. agglomerans cells were formulated by the resuspension of cell pellets in Formula II.Both versions of the osmotically adapted cells that grew in NB plus NaCl medium (i.e., either phageuninfected (sfPa) or ϕEa21-4-phage-infected (sfPa-P)), showed greater than 90% viability after spraydrying compared to osmotically non-adapted cells (nsfPa), which showed about 70% cell viability.Assays were carried out in triplicate and the data averages and standard deviation were plotted.Using a t-test, the significance (p < 0.05) between sfPa and nsfPa (*), as well as between sfPa-P and nsfPa (**), was noted.

Figure 5 .
Figure 5. Infectivity of the ϕEa21-4 phage following reconstitution of the spray-dried powder.A volume of 100 µL of the reconstituted PCS powder (P.agglomerans Pa39-7 strain infected with ϕEa21-4) was used to inoculate 10 mL of NB and incubated at 27 °C with shaking at 180 rpm for 18 h before determining PFU/mL using qPCR.The graph displays the phage titer (log PFU/mL) increased with incubation time and that the phages were viable.Assays were carried out in triplicate and the data averages and standard deviation were plotted.TEM images were taken to compliment the P. agglomerans viability and phage plaque assays with reconstituted PCS powder.The images show assembled phage capsid heads

Figure 4 .
Figure 4. Viability of P. agglomerans after spray-drying.The viability of spray-dried P. agglomerans Pa39-7 was measured as a percentage by comparing before and after spray-drying cell counts.All tested P. agglomerans cells were formulated by the resuspension of cell pellets in Formula II.Both versions of the osmotically adapted cells that grew in NB plus NaCl medium (i.e., either phage-uninfected (sfPa) or ϕEa21-4-phage-infected (sfPa-P)), showed greater than 90% viability after spray-drying compared to osmotically non-adapted cells (nsfPa), which showed about 70% cell viability.Assays were carried out in triplicate and the data averages and standard deviation were plotted.Using a t-test, the significance (p < 0.05) between sfPa and nsfPa (*), as well as between sfPa-P and nsfPa (**), was noted.

Figure 4 .
Figure 4. Viability of P. agglomerans after spray-drying.The viability of spray-dried P. agglomerans Pa39-7 was measured as a percentage by comparing before and after spray-drying cell counts.All tested P. agglomerans cells were formulated by the resuspension of cell pellets in Formula II.Both versions of the osmotically adapted cells that grew in NB plus NaCl medium (i.e., either phageuninfected (sfPa) or ϕEa21-4-phage-infected (sfPa-P)), showed greater than 90% viability after spraydrying compared to osmotically non-adapted cells (nsfPa), which showed about 70% cell viability.Assays were carried out in triplicate and the data averages and standard deviation were plotted.Using a t-test, the significance (p < 0.05) between sfPa and nsfPa (*), as well as between sfPa-P and nsfPa (**), was noted.

Figure 5 .
Figure 5. Infectivity of the ϕEa21-4 phage following reconstitution of the spray-dried powder.A volume of 100 µL of the reconstituted PCS powder (P.agglomerans Pa39-7 strain infected with ϕEa21-4) was used to inoculate 10 mL of NB and incubated at 27 °C with shaking at 180 rpm for 18 h before determining PFU/mL using qPCR.The graph displays the phage titer (log PFU/mL) increased with incubation time and that the phages were viable.Assays were carried out in triplicate and the data averages and standard deviation were plotted.

Figure 5 .
Figure 5. Infectivity of the ϕEa21-4 phage following reconstitution of the spray-dried powder.A volume of 100 µL of the reconstituted PCS powder (P.agglomerans Pa39-7 strain infected with ϕEa21-4) was used to inoculate 10 mL of NB and incubated at 27 • C with shaking at 180 rpm for 18 h before determining PFU/mL using qPCR.The graph displays the phage titer (log PFU/mL) increased with incubation time and that the phages were viable.Assays were carried out in triplicate and the data averages and standard deviation were plotted.

Figure 6 .
Figure 6.Electron microscopy of ϕEa21-4 after reconstitution of the spray-dried powder.Transmission electron microscopy images of the PCS reconstituted powder samples showed phage capsid heads (red arrows) assembled inside (A), or phage attached to P. agglomerans strain Pa39-7 cells (B).

Figure 7 .Figure 6 .
Figure 7. Changes in cell viability of P. agglomerans Pa39-7 cells in BCA or PCS powders after storage.(A) Changes in the cell viability of carrier cells in BCA powder stored at 4 °C (○) or at RT (•).(B)

Figure 6 .
Figure 6.Electron microscopy of ϕEa21-4 after reconstitution of the spray-dried powder.Transmission electron microscopy images of the PCS reconstituted powder samples showed phage capsid heads (red arrows) assembled inside (A), or phage attached to P. agglomerans strain Pa39-7 cells (B).

Figure 7 .Figure 7 .
Figure 7. Changes in cell viability of P. agglomerans Pa39-7 cells in BCA or PCS powders after storage.(A) Changes in the cell viability of carrier cells in BCA powder stored at 4 °C (○) or at RT (•).(B) Figure 7. Changes in cell viability of P. agglomerans Pa39-7 cells in BCA or PCS powders after storage.(A) Changes in the cell viability of carrier cells in BCA powder stored at 4 • C ( ) or at RT (•).(B) Changes in the cell viability of carrier cells in PCS powder stored at 4 • C ( ) or at RT (•).Assays were carried out in triplicate and the data averages and standard deviation were plotted.

Figure 8 .
Figure 8. Populations of P. agglomerans, фEa21-4,and E. amylovora on green pear discs measured at 24 and 48 h.On the x-axis, the initial individual application to the pear discs is noted in black text, where the BCA (i.e., containing spray-dried P. agglomerans strain Pa39-7) and PCS (i.e., containing spray-dried фEa21-4 phage-infected P. agglomerans strain Pa39-7) formulations were tested and E. amylovora alone served as a positive control (+veC).The red text on the x-axis denotes what was enumerated by qPCR from the trial and is shown in the bar graph above.Grey bars represent populations on the pear discs at 24 h.For the statistically noted c and d samples, this is the bacterial count before inoculation with E. amylovora, while in the +veC (f) represents the E. amylovora numbers at the time of E. amylovora inoculations.All bars at 48 h (black) represent the growth of each organism in each formulation after 24 h of additional growth in the presence of E. amylovora.Statistical analyses showed that the interactions between all variable combinations in the experiment were highly significant (p < 0.0001), as denoted by the letters a-h above the bars.Replicate and random effects in the analysis were not significant (p > 0.05), indicating there was no variability between replicates of individual groups.

Figure 8 .
Figure 8. Populations of P. agglomerans, ϕEa21-4,and E. amylovora on green pear discs measured at 24 and 48 h.On the x-axis, the initial individual application to the pear discs is noted in black text, where the BCA (i.e., containing spray-dried P. agglomerans strain Pa39-7) and PCS (i.e., containing spray-dried ϕEa21-4 phage-infected P. agglomerans strain Pa39-7) formulations were tested and E. amylovora alone served as a positive control (+veC).The red text on the x-axis denotes what was enumerated by qPCR from the trial and is shown in the bar graph above.Grey bars represent populations on the pear discs at 24 h.For the statistically noted c and d samples, this is the bacterial count before inoculation with E. amylovora, while in the +veC (f) represents the E. amylovora numbers at the time of E. amylovora inoculations.All bars at 48 h (black) represent the growth of each organism in each formulation after 24 h of additional growth in the presence of E. amylovora.Statistical analyses showed that the interactions between all variable combinations in the experiment were highly significant (p < 0.0001), as denoted by the letters a-h above the bars.Replicate and random effects in the analysis were not significant (p > 0.05), indicating there was no variability between replicates of individual groups.

Table 1 .
Bacterial strains used for optimizing the spray-drying method.

Table 2 .
E. amylovora phages used to generate a PCS.

Table 3 .
Primers and probes used for qPCR enumeration.

Table 4 .
Carbohydrates used for screening.

Table 5 .
Concentration ranges used for optimization of the carrier formulation.