Skip to main content

Strategy for mass production of lytic Staphylococcus aureus bacteriophage pSa-3: contribution of multiplicity of infection and response surface methodology

Abstract

Background

Antibiotic-resistant bacteria have emerged as a serious problem; bacteriophages have, therefore, been proposed as a therapeutic alternative to antibiotics. Several authorities, such as pharmacopeia, FDA, have confirmed their safety, and some bacteriophages are commercially available worldwide. The demand for bacteriophages is expected to increase exponentially in the future; hence, there is an urgent need to mass-produce bacteriophages economically. Unlike the replication of non-lytic bacteriophages, lytic bacteriophages are replicated by lysing host bacteria, which leads to the termination of phage production; hence, strategies that can prolong the lysis of host bacteria in bacteria–bacteriophage co-cultures, are required.

Results

In the current study, we manipulated the inoculum concentrations of Staphylococcus aureus and phage pSa-3 (multiplicity of infection, MOI), and their energy sources to delay the bactericidal effect while optimizing phage production. We examined an increasing range of bacterial inoculum concentration (2 × 108 to 2 × 109 CFU/mL) to decrease the lag phase, in combination with a decreasing range of phage inoculum (from MOI 0.01 to 0.00000001) to delay the lysis of the host. Bacterial concentration of 2 × 108 CFU/mL and phage MOI of 0.0001 showed the maximum final phage production rate (1.68 × 1010 plaque forming unit (PFU)/mL). With this combination of phage–bacteria inoculum, we selected glycerol, glycine, and calcium as carbon, nitrogen, and divalent ion sources, respectively, for phage production. After optimization using response surface methodology, the final concentration of the lytic Staphylococcus phage was 8.63 × 1010 ± 9.71 × 109 PFU/mL (5.13-fold increase).

Conclusions

Therefore, Staphylococcus phage pSa-3 production can be maximized by increasing the bacterial inoculum and reducing the seeding phage MOI, and this combinatorial strategy could decrease the phage production time. Further, we suggest that response surface methodology has the potential for optimizing the mass production of lytic bacteriophages.

Background

Antibiotic-resistant bacteria, such as vancomycin-resistant Enterococci, methicillin-resistant Staphylococcus aureus, and carbapenem-resistant Enterobacteriaceae, are a global, emerging problem [1,2,3]. With the emergence of these antibiotic-resistant bacteria, an alternative treatment strategy is urgently required. One of the most anticipated alternatives is the use of lytic bacteriophages (phages), which are effective against bacterial infections [4,5,6]. Numerous phages are commercially available, and their therapeutic application is reported from East European countries, such as Georgia, Russia, Poland, and Belgium [7]; several phages have also been approved by the US FDA, as they have been proven to have no adverse effects during phase 1 clinical trials [8, 9]; hence, phage therapy has attracted attention as a potential alternative to antibiotics.

The most important aspect in phage therapy is the isolation and selection of effective phages against antibiotic-resistant bacteria [10,11,12]. Mass production of these phages is the next pivotal step based on increasing demands in the future [13,14,15,16]. It is well known that host bacterial cells and their phages have different optimal conditions for replication. As described in previous reports, replication of phages is dependent on the physiology of their hosts [17, 18]. In particular, the specific growth rate (μ) of host bacteria is an important factor for the replication of phages [19, 20].

Temperate or filamentous phages replicate in proportion to the growth of the host, without a significant effect on the host [21, 22]. In contrast, the replication of lytic phages causes lysis of their host, which means there will be no “factory” to produce phages in the end. Thus, keeping host bacteria alive for longer periods by manipulating the physiology or the interaction between phage and bacteria can be a strategy for increasing the yield of lytic phages [23]. In addition to manipulating the nature of bacteria, scale-up trials (i.e. flask to fermenter) are being widely researched [24, 25].

Previously, we isolated the obligatory lytic phage pSa-3 which effectively lysed S. aureus cells at low concentration (MOI 0.1) [26, 27]. The phage pSa-3 which has 137,836 base pair (bp) of genomic DNA was classified in the genus Kayvirus, family Herelleviridae. With the co-application of a surfactant, the Staphylococcus phage pSa-3 could effectively degrade the aggregations of S. aureus including biofilms in vitro and in vivo [26]. As this phages does not possess any antibiotic resistance- or virulence-related genes, or lysogeny-related genes, pSa-3 has the potential to be used as a therapeutic agent for the treatment of S. aureus-associated atopic dermatitis [27].

This study was designed to optimize the phage yield by altering the physiology of bacteria by controlling the energy source and by manipulating the bacterial inoculum and phage concentration to keep the host alive for a longer period. Carbon, nitrogen, ion sources, and surfactant were supplemented in the growth medium, and the multiplicity of infection (MOI) was modified for the maximization of the phage production yield. Response surface methodology (RSM) was also adopted for the optimization of the combined effect.

Results

Effect of MOI on phage amplification

The effect of MOI on phage amplification is shown in Fig. 1. The experiment was conducted with various bacterial inoculum concentrations to analyze the effect of increased bacterial load on phage production yield. As shown in Fig. 1a, the host bacteria were lysed 9 h after phage injection in all groups. In the 1% bacterial inoculum group (initial concentration: 2 × 108 CFU/mL), the phage yield was negatively correlated with the phage inoculum, whereas the final phage yield was positively correlated with the bacterial optical density (OD; Fig. 1b). In the 5% bacterial inoculum group (initial concentration: 1 × 108 CFU/mL), the lower MOI groups (MOI 0.00000001 and 0.000001) showed bacterial growth, while the other groups showed inhibition of bacterial growth (Fig. 1c). As shown in Fig. 1d, MOI 0.01 and 0.0001 groups showed the highest phage yield (approximately 1010 PFU/mL), while the lowest MOI group (MOI 0.000001) showed lower phage production (approximately 108 PFU/mL) than the other groups. In the 10% bacterial inoculum group (initial concentration: 2 × 109 CFU/mL), the two lower MOI groups (MOI 0.000001 and 0.00000001) showed bacterial growth rather than replication of phages similar to the 5% bacterial inoculum–MOI 0.000001 group (Fig. 1e), and only the MOI 0.01 group showed lysis of the host bacteria. The MOI 0.01 group showed the highest phage production (approximately 1010 PFU/mL), while the lower MOI groups produced phages fewer than 109 PFU/mL (Fig. 1f). As the MOI (phage inoculum) was lowered, an increase in the time at which the inhibition of bacterial growth began was observed, and the final concentration of phages did not increase after reaching the highest concentration for 24 h. The summary of the maximum phage production yield in each bacterial inoculum group is presented in Table 1. The group with 5% bacterial inoculum–MOI 0.0001, which showed the highest phage yield, was used for further experiments.

Fig. 1
figure 1

Growth curve of the microorganisms in the bacteria–phage co-culture. Bacterial growth was measured using optical density (a, c, e). Phage growth was measured in PFU count (b, d, f). 2 × 108 CFU/mL of initial Staphylococcus aureus concentration (a, b), 1 × 109 CFU/mL of S. aureus concentration (c, d), and 2 × 109 CFU/mL of S. aureus concentration (e, f). The experiment was performed in triplicate

Table 1 Effects of MOI on lytic Staphylococcus aureus phage pSa-3 production

Effect of growth medium source on phage amplification

The effect of medium supplements on bacteriophage production was analyzed using 5% bacterial inoculum with MOI of the phage being 0.0001, as the combination resulted in maximum production. As a medium supplement, different carbon sources, nitrogen sources, ions, and surfactants were supplemented in Luria–Bertani (LB) broth and analyzed using a one-factor-at-a-time method. As a carbon source, 0.5% (w/v) of glucose, sucrose, fructose, galactose, or glycerol was supplemented. Galactose and glycerol showed an upregulation of phage production, and glycerol supplementation led to a significant increase (p < 0.05), i.e., 100% increased value in phage production compared to that of the control (Fig. 2a). As a nitrogen source, 0.1% (w/v) of casamino acid, peptone, gelatin, or glycine was supplemented. Among the nitrogen sources, only glycine showed 18% increase in phage yield and was selected as a nitrogen source for further experiments (Fig. 2b). A divalent ion source, such as magnesium chloride or calcium chloride, was supplemented in the culture medium for the amplification test, and calcium chloride was selected as the ion supplement, as it revealed the highest (28% increase) yield (Fig. 2c). For the surfactant screening, tween 20, triton X-100, and SDS were examined, and these were found to downregulate phage amplification (Fig. 2d). Thus, glycerol, glycine, and calcium chloride were selected as carbon, nitrogen, and ion sources, respectively, for RSM analysis. And each supplement influenced the growth of the host bacteria, as well (Additional file 1: Fig. S1). Especially, SDS showed the deteriorating effect on host growth.

Fig. 2
figure 2

Media supplement screening for maximizing the lytic Staphylococcus aureus phage pSa-3 production with carbon sources (a), nitrogen sources (b), divalent ion sources (c), and surfactants (d). The experiment was performed in triplicate. Statistical significance was calculated using Student’s t-test, and p < 0.05 was considered as statistically significant

Optimization of bacteriophage pSa-3 production by RSM

RSM based on central composite design (CCD) technique was used to examine the effect of the selected media supplements on the amplification of the lytic phage pSa-3. A total of 20 coded levels are represented in Table 2. The experimental design and results obtained from RSM are shown in Table 3. By employing analysis of variance (ANOVA), the following equation was obtained, describing the relationship between phage yield (Y), and glycerol (X1), glycine (X2), and calcium chloride (X3):

$$\begin{aligned} {\text{Y}} & = 46287782214 - 7470787473{\text{X}}_{1} + 89924699{\text{X}}_{2} - 125989578{\text{X}}_{3} - 6578793992{\text{X}}_{1}^{2} + 2964876080{\text{X}}_{2}^{2} \\ & \quad + 1314889898{\text{X}}_{3}^{2} - 5212500000{\text{X}}_{1} {\text{X}}_{2} + 4745833333{\text{X}}_{1} {\text{X}}_{3} + 5879166667{\text{X}}_{2} {\text{X}}_{3} , \\ \end{aligned}$$

where Y represents the predicted phage yield; X1, X2, and X3 are the concentrations of supplemented glycerol, glycine, and calcium chloride, respectively. The experimental value varied from 2.00 × 1010 to 6.30 × 1010 PFU/mL (119% to 375% yield increase compared to that of the yield of MOI optimization), which fits in with the predicted value calculated from the equation. Figure 3 graphically represents the equation in 2D contour (Fig. 3a, c, e) and 3D response surface plot (Fig. 3b, d, f), which suggests the optimum range of the factors for the maximum phage yield response. The optimum conditions for increased phage yield are as follows: (a) glycerol concentration: − 1.3 to − 0.8, (b) glycine concentration at both ends: − 1.633 to 0 and 0 to 1.633, and (c) decrease of calcium chloride concentration from 1.633 to − 1.633.

Table 2 The Central Composite Design (CCD) of experiments and response of Staphylococcus aureus phage pSa-3 production
Table 3 The experimental design and response of lytic Staphylococcus aureus phage pSa-3 production
Fig. 3
figure 3

Response surface contour plots of media supplements for lytic Staphylococcus aureus phage pSa-3 production in 3D (a, c, e) and 2D (b, d, f). The effect of glycerol and calcium chloride on phage production (a, b). The effect of glycine and calcium chloride on phage production (c, d). The effect of glycerol and glycine on phage production (e, f)

Analysis of variance

To validate the models used in this study, ANOVA was performed for the phage production yield. The significance of the models was determined by p-value less than 0.05. A low p-value of 0.023 with a high F value of 4.51 implied that the model was credible (Table 4). The analysis represented that the determination coefficient (R2) value of 0.84 and a p-value for lack of fit (0.084) were higher than the significance value (0.05). Overall, these statistical values suggested that RSM can be an effective tool for the optimization of lytic phage production, indicating that the model for the phage pSa-3 production in this study was a good fit.

Table 4 Analysis of variance (ANOVA) of the experimental results for the lytic Staphylococcus aureus phage pSa-3 production

Validation of the optimized conditions

Based on the RSM analysis, the optimal phage yield was predicted to be 7.63 × 1010 PFU/mL when the code levels of glycerol, glycine, and calcium chloride were − 0.610313 (around 347 mg/mL of glycerol), 1.633 (90 mg/mL of glycine), and 1.633 (18 mM of calcium chloride), respectively. The validation experiment was conducted to confirm the predicted result. The observed average phage yield under the optimal value was 8.63 × 1010 ± 9.71 × 109 PFU/mL, which was in good agreement with the predicted value.

Discussion

The emergence of super-bacteria with resistance to multiple commonly used antibiotics has drawn the attention of scientists to bacteriophages as an alternative for antibiotics [28,29,30]. For therapeutic purposes, rapid eradication of pathogenic bacteria is important. Therefore, phage therapy research focused on isolating and selecting phages that can effectively control multidrug-resistant bacteria is gaining popularity [10,11,12, 31, 32]. On the contrary, for phage mass production, host bacteria are essential and should survive longer as “phage-producing factories.” In this study, the modification of the initial inoculum concentrations of the host and lytic phage improved the production rate of the phages. Meanwhile, the selected supplements successfully enhanced the lytic phage production after optimization by response surface methodology at bench scale (flask).

One approach to slowly lyse the “factory,” the host bacteria, is to lower the inoculum of phages pSa-3. In this study, we focused on the fact that S. aureus is gradually eradicated or partially suppressed at a low MOI of pSa-3, as described in the in vitro phage therapy studies [11, 33,34,35,36]. To verify that a lower phage inoculum results in higher phage production, we designed the study as follows [37, 38]. We used MOI 0.01 as the highest phage inoculum for the experiments, as MOI 0.1 was sufficient for the eradication of the host bacteria in our previous study [26]. In the first test with 2 × 108 CFU/mL of bacteria and MOI 0.01 to 0.000001 of the phage, the lowest MOI resulted in the highest final phage production and delayed eradication of the host bacteria (Fig. 1). As the inoculum size and lag phase has a negative correlation in general, we expanded the initial bacterial concentration to 2 × 109 CFU/mL for the reduction in production time and validation of the hypothesis “lower phage inoculum is good for production.” We observed that there might be a negative correlation between the initial phage inoculum and the final phage production or the phage production time; however, this was not always the case (Fig. 1). Although more detailed kinetics between the inoculum quantity of phage and bacteria should be elucidated through further studies, we observed that there was a lower limit of MOI (i.e., MOI 0.0001 and 0.01 for 1 × 109 CFU/mL and 2 × 109 CFU/mL initial concentration, respectively) for the final phage production. Simple manipulation of the initial phage and bacterial inoculum could regulate the production time and the final yield of the phage, without any other complicated alterations in culture conditions.

The optimal environments for the growth of phages and bacteria can be different; however, phages can control their life cycle in response to the physiology of the host [17,18,19,20, 39]. We examined the amplification rate by manipulating the inoculum dose and medium substrates such as carbon and nitrogen sources, divalent cations, and surfactants.

The carbon source can affect phage multiplication by physically modifying the host cell, such as by altering the receptors required for phage infection. Depending on the carbon supplement, the host cell surface area, which is positively correlated with phage adsorption and composition of receptors for phage infection, can be modified [17]. Previously, glycerol enhanced the size of plaques, indicating an increased number of the phage progeny in the multiplication process (Fig. 2a) [40].

While carbon supplement influences the physical factors involved in adsorption, the nitrogen source is also a major contributor to phage multiplication from a physiological perspective. A lack of a proper nitrogen source prevents the propagation of phages, whereas the carbon source does not [41]. Accordingly, numerous nitrogen sources such as amino acids, peptides, and proteins were used as supplemental nitrogen sources; a very small amount of these supplements was sufficient to increase the adsorption rate or the number of the phage progeny: glycine (13 mM) increased propagation (4.2-fold); tryptophan (1 g/L) increased adsorption (1.8-fold); peptone (0.4 g/L) increased propagation (100-fold); tryptone (1%) increased adsorption and propagation (two- to threefold); and gelatin (0.5 g/L) increased propagation (four- to sixfold) [42,43,44,45,46]. Positive results were observed only for glycine, as numerous differences including the microorganisms, culture media, or supplementation concentration were affected (Fig. 2b). Particularly, modifications with glycine supplement can upregulate the phage production because glycine showed synergistic effects with various materials (inorganic salts, purines, carbon dicarboxylic acids, and phosphorylated compounds) [47].

Metal ions such as divalent cations are well-known to affect phage multiplication [46]. Particularly, Ca2+ and Mg2+ examined in the present study are associated with the adsorption, penetration, and growth of virion progeny in host cells [48, 49]. Calcium is generally considered as a more dominant factor than magnesium; the burst size of the Ca2+-supplemented group was superior to that of the Mg2+-supplemented group (Fig. 2c) [50]. To exert the same effect on the burst size, much more Mg2+ is required [46]. Further, a reduced burst size was observed in some phages after supplementation with Mg2+, as shown in our result (Fig. 2c) [51]. In some cases, combined use of Ca2+ and Mg2+ had synergistic effects on the burst size [50]. Thus, combinations of divalent cations should be tested after RSM optimization to upregulate phage production.

Staphylococcus aureus cells aggregate into a grape pattern and form micro-colonies, decreasing the surface area of the individual cells. As described for the carbon source, a larger host surface area has greater chance of enabling a collision between a phage and its host [17]. Thus, it is necessary to reduce the adhesive form to increase phage multiplication. As surfactants possess anti-adhesive potential, they may be useful as therapeutic agents for S. aureus [52]. In our previous research, we observed that the use of a surfactant effectively reduced the size of the S. aureus micro-colonies [27]. Thus, we tested several surfactants, and found that they were not effective for phage multiplication (Fig. 2d). The mechanisms of phage multiplication facilitated by the surfactant should be further evaluated except the SDS which negatively influenced the host growth (Additional file 1: Fig. S1).

Each of the above-mentioned optimal parameters (except for the surfactants), when applied in combination, increased the final phage production, eventually showing a high production of 10.93 ± 0.9 log10PFU/mL (500% increase). However, the production of large phages from the Herelleviridae family is not as easy as the production of small phages of the Podoviridae and Siphoviridae families, which show a large propagation potential (burst size > 100 PFU/cell) [26, 5355]. As they can propagate with small burst sizes, K (60 PFU/cell), pSa-3 (40 PFU/cell, this study), and phiPLA-RODI (25 PFU/cell), philPLA-RODI were propagated to a low concentration of 8.9 ± 0.1 log10PFU/mL using conventional methods [56,57,58]. Similarly, pSa-3 showed a low yield of approximately 5–6 log10PFU/mL before MOI optimization (Fig. 1). After RSM modification, philPLA-RODI and pSa-3 reached high concentrations (9.25 ± 0.9, and 10.93 ± 0.9 log10PFU/mL), with around 270% and 500% increase in yield. Although the two studies with the two phages used different factors for optimization, RSM analysis was reliable for the mass production of phages. Thus, a combined RSM experimental design using various factors may further increase the yield. In future, the demand for phages is expected to increase rapidly; therefore, economical mass production of phages is essential, and studies should focus on the optimization of phage mass production.

Conclusions

This study aimed to develop an economical method for the mass production of lytic bacteriophages. We found that the manipulation of the initial inoculation ratio of the phage and its host can significantly influence the phage pSa-3 yield. However, the common belief that low MOIs guarantee high yields is untrue: there exists a lower limit of the inoculum ratio between the host and phage. After screening several substrates using the one-factor-at-a-time method, we were able to achieve more than 500% increase in the phage yield using RSM. Although we could not elucidate a correlation between the results from previous studies and those of the current study, we established that the manipulation of the bacterial inoculum and MOI will help in ensuring economically efficient mass production of phages in the future.

Methods

Microbial culture, growth conditions, and phage preparation

Staphylococcus aureus ATCC25923 and previously isolated phage pSa-3 were used for the experiments in this study [26, 27]. LB broth and agar media were used for the culture of the host bacteria and bacteriophages pSa-3. For phage preparation, 1% (2 × 108 CFU) of overnight (approximately 18 h) bacterial culture adjusted to 2 × 108 CFU and serial dilutions of the phage solution (102–107 PFU/mL) were co-inoculated in fresh LB broth and incubated overnight at 37 °C under shaking conditions (150 rpm). The culture was centrifuged (14,000×g), filtered (0.45 μm), and purified using the PEG precipitation method [59]. A high concentration (approximately 1010 PFU/mL) of the phage solution was stored at 4 °C for further use.

Growth of bacteria and enumeration of bacteriophages

Bacterial growth and the concentration of the phages were examined periodically (0, 1, 3, 5, 7, 9, 12, and 24 h). For bacterial growth, OD was measured at 600 nm using a spectrophotometer (Biorad SmartSpecTM Plus, USA), and the number of phages was determined using a standard double layer agar plaque assay. Briefly, 100 μL of each of the diluted samples and the overnight bacterial culture were inoculated in the top agar (0.4% agar) and poured onto the bottom agar (1.5% agar) plate. After overnight incubation at 37 °C, the number of plaques was counted.

Effect of MOI on phage amplification

The effect of MOI on phage amplification was examined with various combinations of bacterial inoculum and phage MOI after maintaining the bacteria–bacteriophage co-culture for 24 h. Briefly, 100 mL of fresh LB broth was inoculated with an overnight bacterial culture (adjusted to 2 × 108, 1 × 109, and 2 × 109 CFU/mL) and phage with different MOI (0.01, 0.0001, 0.000001, and 0.00000001 at each bacterial inoculum concentration). At each time point (0, 1, 3, 5, 7, 9, 12, and 24 h), the bacterial growth and phage amplification were calculated as mentioned above.

Effect of growth medium source on phage amplification

To select the optimal nutritional sources, we adapted the one-factor-at-a-time method, which is used in conventional scale-up processes. This approach is conducted by replacing one nutritional factor in the basal medium, while all the other factors are kept constant. In the experiments for the optimization of the carbon source, basal medium was supplemented with 0.5% (w/v) of glucose, sucrose, fructose, glycerol, and galactose, individually. To assess the effect of nitrogen sources, LB was supplemented with 0.1% (w/w) of casamino acid, peptone, gelatin, and glycine, individually. We also examined different surfactants (Tween 20, triton X-100, and SDS) at a concentration of 0.01% (v/v) to maximize the host strain surface for easy phage adherence. The influence of divalent cations on bacteriophage production was investigated by supplementing 0.01 M of calcium chloride or magnesium chloride to the LB medium.

Experimental design for optimization of phage amplification

To determine the optimal levels of the selected variables, the experimental design was as per the central composite design method of RSM coded in Minitab (v16.2) software. Among the variables, glycerol, glycine, and calcium chloride were selected as the carbon, nitrogen, and ion source, respectively, as they displayed the highest phage production. The experimental setup consisted of 20 trials (Table 2), and all the experiments were conducted in triplicate. A second order polynomial equation was used for the analysis of phage production:

$${\text{Y}} = {\text{b}}\_0 + \sum {\text{b}}_{{\text{i}}} {\text{X}}_{{\text{i}}} + \sum {\text{b}}_{{{\text{ii}}}} {\text{X}}_{{\text{i}}}^{2} + \sum {\text{b}}_{{{\text{ij}}}} {\text{X}}_{{\text{i}}} {\text{X}}_{{\text{j}}} ,$$

where Y is the predicted response, b0 is the constant, bi is the linear coefficient, bii is the quadratic coefficient, bij is the interaction coefficient, Xi is the independent variable, Xi2 is the squared effect, and XiXj is the interaction effect. The quadratic model was visualized as counterplots and the response surface curve was generated using Minitab (v16.2) for each variable. The correlation between μ and yield was analyzed using the regression model in the same software. Statistical analysis of the model was conducted using ANOVA and p < 0.05 was considered as significant.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Abbreviations

MOI:

Multiplicity of infection

RSM:

Response surface methodology

CCD:

Central composite design

PFU:

Plaque forming unit

OD:

Optical density

LB:

Luria–Bertani

ANOVA:

Analysis of variance

References

  1. Flokas ME, Karageorgos SA, Detsis M, Alevizakos M, Mylonakis E. Vancomycin-resistant enterococci colonisation, risk factors and risk for infection among hospitalised paediatric patients: a systematic review and meta-analysis. Int J Antimicrob Agents. 2017;49:565–72.

    Article  CAS  PubMed  Google Scholar 

  2. Wenzel RP, Bearman G, Edmond MB. Community-acquired methicillin-resistant Staphylococcus aureus (MRSA): new issues for infection control. Int J Antimicrob Agents. 2007;30:210–2.

    Article  CAS  PubMed  Google Scholar 

  3. Interagency Coordination Group on Antimicrobial Resistance. No Time to Wait: securing the future from drug-resistant infections Report to the Secretary-General of the United Nations. 2019. https://www.who.int/antimicrobial-resistance/interagency-coordination-group/final-report/en/. Accessed 5 Oct 2020.

  4. Kakasis A, Panitsa G. Bacteriophage therapy as an alternative treatment for human infections. A comprehensive review. Int J Antimicrob Agents. 2019;53:16–21.

    Article  CAS  PubMed  Google Scholar 

  5. Fabijan AP, Lin RC, Ho J, Maddocks S, Zakour NLB, Iredell JR. Safety of bacteriophage therapy in severe Staphylococcus aureus infection. Nat Microbiol. 2020;5:465–72.

    Article  CAS  Google Scholar 

  6. Abedon ST, Kuhl SJ, Blasdel BG, Kutter EM. Phage treatment of human infections. Bacteriophage. 2011;1:66–85.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Moelling K, Broecker F, Willy C. A wake-up call: we need phage therapy now. Viruses. 2018;10:688.

    Article  CAS  PubMed Central  Google Scholar 

  8. Lang LH. FDA approves use of bacteriophages to be added to meat and poultry products. Gastroenterology. 2006;131:1370.

    PubMed  Google Scholar 

  9. Rhoads D, Wolcott R, Kuskowski M, Wolcott B, Ward L, Sulakvelidze A. Bacteriophage therapy of venous leg ulcers in humans: results of a phase I safety trial. J Wound Care. 2009;18:237–43.

    Article  CAS  PubMed  Google Scholar 

  10. Merabishvili M, De Vos D, Verbeken G, Kropinski AM, Vandenheuvel D, Lavigne R, et al. Selection and characterization of a candidate therapeutic bacteriophage that lyses the Escherichia coli O104: H4 strain from the 2011 outbreak in Germany. PLoS ONE. 2012;7:e52709.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Kokkari C, Sarropoulou E, Bastias R, Mandalakis M, Katharios P. Isolation and characterization of a novel bacteriophage infecting Vibrio alginolyticus. Arch Microbiol. 2018;200:707–18.

    Article  CAS  PubMed  Google Scholar 

  12. Chang Y, Shin H, Lee JH, Park CJ, Paik SY, Ryu S. Isolation and genome characterization of the virulent Staphylococcus aureus bacteriophage SA97. Viruses. 2015;7:5225–42.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Sauvageau D, Cooper DG. Two-stage, self-cycling process for the production of bacteriophages. Microb Cell Fact. 2010;9:81.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  14. Smrekar F, Ciringer M, Jančar J, Raspor P, Štrancar A, Podgornik A. Optimization of lytic phage manufacturing in bioreactor using monolithic supports. J Sep Sci. 2011;34:2152–8.

    Article  CAS  PubMed  Google Scholar 

  15. Bourdin G, Schmitt B, Guy LM, Germond JE, Zuber S, Michot L, et al. Amplification and purification of T4-like Escherichia coli phages for phage therapy: from laboratory to pilot scale. Appl Environ Microbiol. 2014;80:1469–76.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  16. Jurač K, Nabergoj D, Podgornik A. Bacteriophage production processes. Appl Microbiol Biotechnol. 2019;103:685–94.

    Article  PubMed  CAS  Google Scholar 

  17. Hadas H, Einav M, Fishov I, Zaritsky A. Bacteriophage T4 development depends on the physiology of its host Escherichia coli. Microbiology. 1997;143:179–85.

    Article  CAS  PubMed  Google Scholar 

  18. You L, Suthers PF, Yin J. Effects of Escherichia coli physiology on growth of phage T7 in vivo and in silico. J Bacteriol. 2002;184:1888–94.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Kick B, Hensler S, Praetorius F, Dietz H, Weuster-Botz D. Specific growth rate and multiplicity of infection affect high-cell-density fermentation with bacteriophage M13 for ssDNA production. Biotechnol Bioeng. 2017;114:777–84.

    Article  CAS  PubMed  Google Scholar 

  20. Nabergoj D, Modic P, Podgornik A. Effect of bacterial growth rate on bacteriophage population growth rate. MicrobiologyOpen. 2018;7:e00558.

    Article  PubMed  CAS  Google Scholar 

  21. Grieco SHH, Lee S, Dunbar WS, MacGillivray RT, Curtis SB. Maximizing filamentous phage yield during computer-controlled fermentation. Bioprocess Biosyst Eng. 2009;32:773–9.

    Article  CAS  PubMed  Google Scholar 

  22. Grieco SHH, Wong AY, Dunbar WS, MacGillivray RT, Curtis SB. Optimization of fermentation parameters in phage production using response surface methodology. J Ind Microbiol Biotechnol. 2012;39:1515–22.

    Article  CAS  PubMed  Google Scholar 

  23. Almeida GM, Laanto E, Ashrafi R, Sundberg LR. Bacteriophage adherence to mucus mediates preventive protection against pathogenic bacteria. Mbio. 2019. https://0-doi-org.brum.beds.ac.uk/10.1128/mBio.01984-19.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Krysiak-Baltyn K, Martin GJ, Gras SL. Computational modelling of large scale phage production using a two-stage batch process. Pharmaceuticals. 2018;11:31.

    Article  PubMed Central  CAS  Google Scholar 

  25. Nabergoj D, Kuzmić N, Drakslar B, Podgornik A. Effect of dilution rate on productivity of continuous bacteriophage production in cellstat. Appl Microbiol Biotechnol. 2018;102:3649–61.

    Article  CAS  PubMed  Google Scholar 

  26. Kim SG, Giri SS, Yun S, Kim HJ, Kim SW, Kang JW, et al. Synergistic phage-surfactant combination clears IgE-promoted Staphylococcus aureus aggregation in vitro and enhances the effect in vivo. Int J Antimicrob Agents. 2020;56(1):105997.

    Article  CAS  PubMed  Google Scholar 

  27. Kim SG, Jun JW, Giri SS, Yun S, Kim HJ, Chi C, Kim SW, Park SC. Complete genome sequence of Staphylococcus aureus bacteriophage pSa-3. Genome Announc. 2017;5:e00182-e217.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Abedon ST, García P, Mullany P, Aminov R. Phage therapy: past, present and future. Front Microbiol. 2017;8:981.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Pirnay JP, De Vos D, Verbeken G, Merabishvili M, Chanishvili N, Vaneechoutte M, et al. The phage therapy paradigm: pret-a-porter or sur-mesure? Pharm Res. 2011;28:934–7.

    Article  CAS  PubMed  Google Scholar 

  30. Górski A, Jończyk-Matysiak E, Międzybrodzki R, Weber-Dąbrowska B, Łusiak-Szelachowska M, Bagińska N, Borysowski J, et al. Phage therapy: beyond antibacterial action. Front Med. 2018;5:146.

    Article  Google Scholar 

  31. Han SH, Lee D, Im J, Na H, Ryu S, Yun CH. The novel Enterococcus phage vB_EfaS_HEf13 has broad lytic activity against clinical isolates of Enterococcus faecalis. Front Microbiol. 2019;10:2877.

    Article  PubMed  PubMed Central  Google Scholar 

  32. Ong SP, Azam AH, Sasahara T, Miyanaga K, Tanji Y. Characterization of Pseudomonas lytic phages and their application as a cocktail with antibiotics in controlling Pseudomonas aeruginosa. J Biosci Bioeng. 2020;129:693–9.

    Article  CAS  PubMed  Google Scholar 

  33. Chen L, Liu Q, Fan J, Yan T, Zhang H, Yang J, et al. Characterization and genomic analysis of ValSw3-3, a new Siphoviridae bacteriophage infecting Vibrio alginolyticus. J Virol. 2020;94:e00066-e120.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. Ciacci N, D’Andrea MM, Marmo P, Demattè E, Amisano F, Pilato VD, et al. Characterization of vB_Kpn_F48, a newly discovered lytic bacteriophage for Klebsiella pneumoniae of sequence type 101. Viruses. 2018;10:482.

    Article  PubMed Central  CAS  Google Scholar 

  35. Huang C, Virk SM, Shi J, Zhou Y, Willias SP, Morsy MK, et al. Isolation, characterization, and application of bacteriophage LPSE1 against Salmonella enterica in ready to eat (RTE) foods. Front Microbiol. 2018;9:1046.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Yazdi M, Bouzari M, Ghaemi EA, Shahin K. Isolation, characterization and genomic analysis of a novel bacteriophage vB_EcoS-Golestan infecting multidrug-resistant Escherichia coli isolated from urinary tract infection. Sci Rep. 2020;10:1–13.

    Article  CAS  Google Scholar 

  37. Gašić K, Ivanović MM, Ignjatov M, Calić A, Obradović A. Isolation and characterization of Xanthomonas euvesicatoria bacteriophages. J Plant Pathol. 2011;93:415–23.

    Google Scholar 

  38. Czajkowski R, Ozymko Z, de Jager V, Siwinska J, Smolarska A, Ossowicki A, et al. Genomic, proteomic and morphological characterization of two novel broad host lytic bacteriophages ΦPD10. 3 and ΦPD23. 1 infecting pectinolytic Pectobacterium spp. and Dickeya spp. PLoS ONE. 2015;10:e0119812.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  39. Marcó MB, Reinheimer JA, Quiberoni A. Phage adsorption to Lactobacillus plantarum: influence of physiological and environmental factors. Int J Food Microbiol. 2010;138:270–5.

    Article  PubMed  Google Scholar 

  40. Santos SB, Carvalho CM, Sillankorva S, Nicolau A, Ferreira EC, Azeredo J. The use of antibiotics to improve phage detection and enumeration by the double-layer agar technique. BMC Microbiol. 2009;9:148.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  41. Marcó MB, Reinheimer J, Quiberoni A. Phage adsorption and lytic propagation in Lactobacillus plantarum: could host cell starvation affect them? BMC Microbiol. 2015;15:1–7.

    Google Scholar 

  42. Spizizen J. Biochemical studies on the phenomenon of virus reproduction: I. Amino acids and the multiplication of bacteriophage. J Infect Dis. 1943;73:212–21.

    Article  CAS  Google Scholar 

  43. Storms ZJ, Arsenault E, Sauvageau D, Cooper DG. Bacteriophage adsorption efficiency and its effect on amplification. Bioprocess Biosyst Eng. 2010;33:823–31.

    Article  CAS  PubMed  Google Scholar 

  44. Lepper EH. The reproduction of bacteriophage when the sensitive organism is grown in a synthetic medium. Br J Exp Pathol. 1924;5:40.

    PubMed Central  Google Scholar 

  45. Egermeier ER. Studies of methods for controlling bacteriophage in lactic cultures. Degree thesis. Oklahoma State University, Dairy Manufacturing Department. 1956.

  46. Kay D. The effect of divalent metals on the multiplication of coli bacteriophage T5st. Br J Exp Pathol. 1952;33:228.

    CAS  PubMed  PubMed Central  Google Scholar 

  47. Spizizen J. Biochemical Studies on the phenomenon of virus reproduction: II. Studies on the influence of compounds of metabolic significance on the multiplication of bacteriophage. J Infect Dis. 1943;73:222–8.

    Article  CAS  Google Scholar 

  48. Tucker RG. The role of magnesium ions in the growth of Salmonella phage anti-R. Microbiology. 1961;26:313–23.

    CAS  Google Scholar 

  49. Kay D. Methods for studying the infectious properties and multiplication of bacteriophage. In: Norris JR, Ribbons DW, editors. Methods in microbiology. London: Academic Press; 1972. p. 191–262.

    Google Scholar 

  50. Potter NN, Nelson FE. Role of calcium and related ions in proliferation of lactic Streptococcus bacteriophage. J Bacteriol. 1953;66:508.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  51. Rountree PM. The role of divalent cations in the multiplication of Staphylococcal bacteriophages. Microbiology. 1955;12:275–87.

    CAS  Google Scholar 

  52. Seethalakshmi PS, Rajeev R, Kiran GS, Selvin J. Promising treatment strategies to combat Staphylococcus aureus biofilm infections: an updated review. Biofouling. 2020;36:1–23.

    CAS  Google Scholar 

  53. Cha Y, Chun J, Son B, Ryu S. Characterization and genome analysis of Staphylococcus aureus podovirus CSA13 and its anti-biofilm capacity. Viruses. 2019;11:54.

    Article  CAS  PubMed Central  Google Scholar 

  54. Rahman M, Kim S, Kim SM, Seol SY, Kim J. Characterization of induced Staphylococcus aureus bacteriophage SAP-26 and its anti-biofilm activity with rifampicin. Biofouling. 2011;27:1087–93.

    Article  CAS  PubMed  Google Scholar 

  55. Matsuzaki S, Yasuda M, Nishikawa H, Kuroda M, Ujihara T, Shuin T, et al. Experimental protection of mice against lethal Staphylococcus aureus infection by novel bacteriophage ϕMR11. J Infect Dis. 2003;187:613–24.

    Article  CAS  PubMed  Google Scholar 

  56. Rees PJ, Fry BA. The morphology of staphylococcal bacteriophage K and DNA metabolism in infected Staphylococcus aureus. J Gen Virol. 1981;53:293–307.

    Article  CAS  PubMed  Google Scholar 

  57. Gutiérrez D, Vandenheuvel D, Martínez B, Rodríguez A, Lavigne R, García P. Two phages, phiIPLA-RODI and phiIPLA-C1C, lyse mono-and dual-species staphylococcal biofilms. Appl Environ Microbiol. 2015;81:3336–48.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  58. González-Menéndez E, Arroyo-López FN, Martínez B, García P, Garrido-Fernández A, Rodríguez A. Optimizing propagation of Staphylococcus aureus infecting bacteriophage vB_sauM-phiIPLA-RODI on Staphylococcus xylosus using response surface methodology. Viruses. 2018;10:153.

    Article  PubMed Central  CAS  Google Scholar 

  59. Kwon J, Kim SG, Kim HJ, Giri SS, Kim SW, Lee SB, Park SC. Isolation and characterization of Salmonella jumbo-phage pSal-SNUABM-04. Viruses. 2021;13:27.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

This research was funded by the Rural Development Administration, Republic of Korea (PJ04965022020) and Brain Pool Program’ through the National Research Foundation of Korea (NRF) funded by the Ministry of Science and ICT (KRF: 2016H1D3A1909005).

Author information

Authors and Affiliations

Authors

Contributions

Conceptualization: SGK; methodology: SGK, SY, and HJK; software: SGK and JWK; validation: SGK and SSG; formal analysis: SGK and SY; investigation: SGK; resources: SSG, SWK, JK, WJJ, and HJK; data curation: SGK and SCP; writing—original draft preparation: SGK; writing—review and editing: SGK, SSG and SCP; visualization: SGK, and SBL; supervision: SCP; project administration: SCP; funding acquisition: SCP. All authors have agreed to the published version of the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Se Chang Park.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1.

Influence of the media supplement on the growth of host bacteria examined with carbon sources (a), nitrogen sources (b), divalent sources (c), and surfactants (d). The experiment was performed in triplicate.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kim, S.G., Kwon, J., Giri, S.S. et al. Strategy for mass production of lytic Staphylococcus aureus bacteriophage pSa-3: contribution of multiplicity of infection and response surface methodology. Microb Cell Fact 20, 56 (2021). https://0-doi-org.brum.beds.ac.uk/10.1186/s12934-021-01549-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://0-doi-org.brum.beds.ac.uk/10.1186/s12934-021-01549-8

Keywords