L. O. Henderson1
B. J. Erazo Flores1,2
J. Skeens1
D. Kent1
S. I. Murphy1
M. Wiedmann1
V. Guariglia-Oropeza1*- 1Department of Food Science, Cornell University, Ithaca, NY, United States
- 2Universidad de Puerto Rico, Mayagüez, Puerto Rico
The growth of Listeria monocytogenes on refrigerated, ready-to-eat food products is a major health and economic concern. The natural antimicrobial nisin targets the bacterial cell wall and can be used to inhibit L. monocytogenes growth on cheese. Cell wall composition and structure, and therefore the efficacy of cell wall acting control strategies, can be severely affected by environmental and stress conditions. The goal of this study was to determine the effect of a range of pH and temperatures on the efficacy of nisin against several strains of L. monocytogenes in a lab-scale, cheese model. Cheese was made with or without the addition of nisin at different pH and then inoculated with L. monocytogenes; L. monocytogenes numbers were quantified after 1, 7, and 14 days of incubation at 6, 14, or 22°C. While our data show that nisin treatment is able to reduce L. monocytogenes numbers, at least initially, growth of this pathogen can occur even in the presence of nisin, especially when cheese is stored at higher temperatures. Several environmental factors were found to affect nisin efficacy against L. monocytogenes. For example, nisin is more effective when cheese is stored at lower temperatures. Nisin is also more effective when cheese is made at higher pH (6 and 6.5), compared to cheese made at pH 5.5, and this effect is at least partially due to the activity of cell envelope modification genes dltA and mprF. Serotype was also found to affect nisin efficacy against L. monocytogenes; serotype 4b strains showed lower susceptibility to nisin treatment compared to serotype 1/2 strains. Overall, our results highlight the importance of considering environmental conditions specific to a food matrix when developing and applying nisin-based intervention strategies against L. monocytogenes.
Introduction
Controlling Listeria monocytogenes in food is essential to food safety due to the high mortality rate associated with listeriosis, especially among susceptible populations, such as pregnant women, newborns, the elderly, and those with compromised immune systems (Farber and Peterkin, 1991; Jackson et al., 2018). L. monocytogenes can also cause disease in animals and is found in both natural and food-processing environments (Nightingale et al., 2004). L. monocytogenes can be classified into different serotypes, which are associated with specific environments and differ in their ability to cause disease (Orsi et al., 2011). Each serotype belongs to at least one of four lineages: I, II, III, and IV (Piffaretti et al., 1989; Rasmussen et al., 1995; Wiedmann et al., 1997; Roberts et al., 2006; Ward et al., 2008); however, the majority of L. monocytogenes isolates commonly associated with human clinical cases belong to lineages I (serotype 1/2b and 4b) (Orsi et al., 2011), whereas lineage II (serotypes 1/2a) isolates are more prevalent in food products and natural and farm environments (Kabuki et al., 2004; Manfreda et al., 2005).
L. monocytogenes is of particular concern in ready-to-eat (RTE) dairy foods that allow L. monocytogenes growth, such as Hispanic-style fresh cheese (Jackson et al., 2018). High water activity, low salt content, and near neutral pH make Hispanic-style fresh cheese an ideal environment for survival and growth of a number of foodborne pathogens (Leggett et al., 2012), including L. monocytogenes (Uhlich et al., 2006; Ibarra-Sánchez et al., 2017). Furthermore, L. monocytogenes can tolerate a number of environmental stressors associated with foods, including a wide range of temperatures (0–45°C), pH (4.4–9.4), and high salt concentrations (13–14 w/v%) (Swaminathan et al., 2007). The ability of L. monocytogenes to survive adverse environmental conditions increases the likelihood of transmission from the environment to humans via contaminated food products. Critical points for controlling L. monocytogenes in the food supply are prevention of post-processing contamination and/or reformulation of RTE foods using antimicrobials (Ilsi Research Foundation/Risk Science Institute and Expert Panel on Listeria monocytogenes in Foods, 2005).
One control strategy currently used for L. monocytogenes on RTE foods is the addition of bacteriocins. Bacteriocins are ribosomally synthesized cationic antimicrobial peptides (CAMPs) produced by bacteria that inhibit the growth of a broad spectrum of pathogens (Heng et al., 2007). Some bacteria that produce bacteriocins are considered food grade by the United States Food and Drug Administration (FDA) (Chen and Hoover, 2006), making them useful for food preservation (Hu et al., 2015). Although, there are a number of bacteriocins that have been studied for their antimicrobial properties, nisin and pediocin are the only commercially available, FDA-approved bacteriocins used in a variety of food products (Chen and Hoover, 2006; Garsa et al., 2014). Of these two bacteriocins, nisin is the most widely used (Ross et al., 2002). Nisin is produced by Lactococcus lactis and is active against a broad number of Gram-positive bacteria (O’Connor et al., 2015). Nisin has two modes of action: (i) binding to lipid II, a precursor molecule in cell-wall synthesis, thus preventing synthesis of the cell-wall component peptidoglycan (Wiedemann et al., 2001; Hasper et al., 2006) and (ii) aggregating in complexes that create pores in the bacterial cell membrane, subsequently causing cell lysis (Brotz et al., 1998; Hasper et al., 2006). Previous studies have shown that nisin can inhibit growth of L. monocytogenes on cheese (Van Tassell et al., 2015), hotdogs (Vijayakumar and Muriana, 2017), and smoked meats (Nilsson et al., 1997), suggesting that the use of nisin or other bacteriocins can reduce pathogen prevalence and/or levels and may consequently reduce the incidence of foodborne disease cases.
The bacterial cell envelope provides structural integrity to the cell, but also protects these organisms from unpredictable or sometimes hostile environments (Silhavy et al., 2010). Maintaining the integrity and function of the cell envelope under fluctuating environmental conditions is essential for bacterial survival. Bacteria can sense and respond to cell envelope stressors through alternative sigma factors and/or two-component systems (TCS) (Jordan et al., 2008). L. monocytogenes harbors at least 15 TCS, four of which have been reported to play a critical role in regulating the cell envelope stress response (liaRS, lisRK, cesRK, and virRS) (Nielsen et al., 2012; Kang et al., 2015). A number of genes associated with resistance to nisin and other CAMPs are a part of TCS regulons, including dltABCD (Kramer et al., 2008; McBride and Sonenshein, 2011a) and mprF (Staubitz and Peschel, 2002; Thedieck et al., 2006; Samant et al., 2009). The gene products of the dltABCD operon modify the cell wall by the addition of D-alanine to lipoteichoic acids (LTAs), while the MprF protein modifies the cell membrane by the addition of lysine to phospholipids, resulting in a net positive charge of the cell envelope (Fischer, 1988; Peschel et al., 2001; Thedieck et al., 2006). Mutants lacking these modifications allow for increased binding of CAMPs. For example, in some Gram-positive bacteria, mutations in the dlt operon cause the strain to be more sensitive to nisin and other CAMPs such as polymyxin B and gallidermin, presumably due to the lack of D-alanine on the LTAs and the creation of an overall negatively charged cell wall (Kramer et al., 2008; McBride and Sonenshein, 2011a, b).
The environment in which bacteria are grown can affect the efficacy of CAMPs (Jordan et al., 2008; Bergholz et al., 2012, 2013; Nielsen et al., 2012; Kang et al., 2015). For example, exposure of L. monocytogenes to salt (NaCl) (Bergholz et al., 2013) and pre-exposure of L. monocytogenes to the organic acid potassium lactate (Kang et al., 2015) increased subsequent resistance to nisin. Furthermore, the antimicrobial effect of nisin varies with the food matrix and under different environmental conditions (Jung et al., 1992; Davies et al., 1997; Chen and Hoover, 2006; Khan and Oh, 2016).
Given that the characteristics of Hispanic fresh-style cheese allow for L. monocytogenes growth, the objective of this study was to investigate the effects of temperature and pH on nisin treatment efficacy against L. monocytogenes in a lab-scale cheese model. Understanding the effects of the environment on antimicrobial treatments will allow for development and application of new strategies or optimization of current control strategies to prevent Listeria-related foodborne outbreaks and infections.
Materials and Methods
Bacterial Strains and Growth Conditions
Four recent outbreak strains, encompassing the L. monocytogenes serotypes most commonly associated with human clinical cases (4b, 1/2a and 1/2b), and the reference strain 10403S were used in this study (Table 1). To assess the role of cell wall modification genes on the effect of environmental conditions over nisin efficacy, a non-polar, in-frame deletion mutation of mprF was constructed from the L. monocytogenes 10403S parent strain using the splicing by overlap extension (SOE) method as previously described (Horton et al., 1990; Wiedmann et al., 1998). Additionally, a ΔdltAmprF mutant was constructed by deleting the mprF open reading frame (ORF) from a ΔdltA mutant strain (Tokman et al., 2016) using SOE. All mutations were confirmed by PCR and sequencing of the chromosomal copy of the deletion allele. Strains were streaked from frozen brain heart infusion (BHI; Difco, Becton Dickinson and Co., Sparks, MD, United States) stocks, stored at −80°C in 15% glycerol, onto a BHI agar plate, followed by incubation at 37°C for 24 h. A single colony was subsequently inoculated into 5 mL of BHI broth in 16 mm tubes, followed by incubation at 37°C with shaking (230 rpm) for 16 h (Series 25 Incubator, New Brunswick Scientific, Edison, NJ, United States). After 16 h, 50 μL BHI culture was inoculated into fresh 5 mL BHI broth and grown at 30°C until it reached an OD600 = 1.0.
Table 1. Strains and plasmids used in this study.
Minimal Inhibitory Concentration Assay
The broth microdilution method described by Van Tassell et al., 2015 was used to measure the minimal inhibitory concentration (MIC) of nisin for all strains of L. monocytogenes (wildtype, cheese outbreak isolates, and cell wall mutants), as well as the Pediococcus cerevisiae E66 (nisin sensitive strain) as a reference. Overnight cultures were inoculated at approximately 105 cfu/mL into 96-well microtiter plates containing serial 2-fold dilutions of nisin in BHI broth starting at 5 mg/mL. Plates were prepared in triplicate and OD600 measurements were made in a Synergy H1 Hybrid plate reader (BioTek, Winooski, VT, United States). The MIC was recorded as the lowest concentration of nisin that inhibited visible growth (Wiegand et al., 2008) after a 24 h incubation period at 37°C, and it is reported in Table 1.
Growth of L. monocytogenes in a Lab-Scale Cheese Model Containing Nisin
To test the effect of dairy-relevant conditions on the efficacy of nisin treatment against L. monocytogenes, different pH and temperatures were selected to represent the range of pH and temperature that can be found in cheese environments (e.g., pH of different types of cheese as well as temperatures used during cheese make, aging, and storage). We used a method previously described (Henderson et al., 2019) to make approximately 10 g miniature cheese at different pH (6.5, 6.0, or 5.5) and stored at different temperatures (6, 14, or 22°C). Bacteria, including L. monocytogenes, present in the milk before cheese was made, were quantified by plating milk samples on plate count agar (PCA; Difco, Becton Dickson and Co.) and on L. monocytogenes plating medium (LMPM; Difco, Becton Dickson and Co.). After 48 h of incubation at 32°C for PCA plates and 24 h of incubation at 30°C for LMPM plates, colonies (if present) were counted using a Q Count Colony Counter (Advanced Instruments, Norwood, MA, United States). No L. monocytogenes colonies were found (data not shown).
For treated cheese, 50 mg NisaplinTM (Danisco) was added to 600 mL of pasteurized, whole milk (equivalent to 2 μg/mL or 2 ppm nisin, since Nisaplin contains 2.5% nisin), prior to acidification, to ensure even distribution throughout the final product (Fowler and McCann, 1971). Immediately after cheese was made, it was surface inoculated with 100 μL of a stationary phase (OD600 = 1.0) culture of L. monocytogenes for a target level of inoculation of approximately 107 cfu/g. For pH and temperature experiments, four selected L. monocytogenes outbreak strains were used (Table 1). For cell wall mutant experiments, three L. monocytogenes 10403S isogenic deletion mutants (ΔdltA, ΔmprF, and ΔdltAmprF) were used (Table 1). Plates of six cheese per plate were covered and incubated at 6, 14 or 22°C for 1, 7, or 14 days. For cell wall deletion mutant experiments, cheese was incubated at 6°C for 1 day. All plates included a lab strain (10403S), as well as an un-inoculated cheese control.
On the day of sampling, cheese was diluted 1/10 with PBS and homogenized using a Stomacher (Seward., Worthing, United Kingdom). Homogenates were then serially diluted and plated on modified Oxford agar (MOX; Difco, Becton Dickinson and Co.) using an Autoplate spiral plating system (Advanced Instruments., Norwood, MA, United States). After 48 h of incubation at 30°C (Curtis et al., 1989), L. monocytogenes colonies were quantified using a Q Count Colony Counter (Advanced Instruments). Experiments were performed in biological triplicate.
Nisin Extraction and Activity Assay
To evaluate whether a different amount of nisin was lost during preparation of cheese at different pH, nisin was extracted from cheese using a modified acid extraction method as previously described (Bouksaim et al., 2000). While 2 ppm nisin was enough to inhibit L. monocytogenes growth on our cheese experiments, it was an insufficient amount to extract from cheese; therefore, for nisin extraction experiments, cheese was made with 25 ppm nisin at each pH (6.5, 6.0, or 5.5). To extract nisin, each 10 g cheese was added to 40 mL 0.02 N HCl. The pH was then adjusted to 2.0 with 6 N HCl and the samples were heated to 100°C for 5 min. Samples were then cooled to 20°C and the volume was adjusted to 40 mL with 0.02 N HCl. Samples were centrifuged for 20 min at 4000 × g at 4°C. The supernatant was held at 4°C for 30 min and then filtered through a 0.22 μm sterile filter. The extracts were adjusted to pH 5.5 using 6 N NaOH to ensure high nisin solubility and stored at 4°C until nisin activity testing.
For nisin activity assessment, a well agar diffusion method (Balouiri et al., 2016) was used in which wells (8.8 mm in diameter) were cut out of De Man, Rogosa and Sharpe (MRS) (Difco, Becton Dickinson and Co.) agar plates, and a total volume of 500 μL of nisin extracted from the cheese was added to each well. A control well was made using 500 μL of a 25 ppm nisin stock preparation. The nisin was allowed to diffuse into the agar, then 6 mL of MRS soft agar (0.75%) seeded with ∼105 cfu/mL of P. cerevisiae E66 (nisin sensitive strain) was overlaid onto the plates. After the agar solidified, the plates were incubated at 30°C for 24 h. The diameter of zones of inhibition were measured to determine nisin activity. Experiments were performed as two independent biological replicates.
Statistical Analysis
All statistical analyses were carried out in R Statistical Programming Environment (R Core Team, 2015). We constructed individual linear mixed effects models for temperature and pH using “lmer” function in the “lme4” package (Bates et al., 2015). For each model, the response was the log cfu/g of the number of L. monocytogenes, defined as log count and random effects were (i) replicate and (ii) plate nested within cheese make and milk batch. Fixed effects were (i) temperature or pH, (ii) day, (iii) nisin, (iv) strain, (v) age of the milk (based on a 21-day code date), (vi) log of the aerobic plate counts (bacterial counts in the milk before cheese was made; milk apc), and (vii) inoculum (log cfu/g of L. monocytogenes inoculated on each cheese). We also included interactions between (i) nisin and temperature or pH, (ii) nisin and strain, and (iv) nisin and day. To address multicollinearity, variance inflation factors were investigated and brought into an acceptable range, resulting in the exclusion of “age of the milk” from both the temperature model and the pH model (Zuur et al., 2010). To address an issue of singularity for the temperature model, the random effect of “replicate” was excluded. To address a model convergence issue, a single outlier was identified and removed from the pH model. Model assumptions were verified for the final version of both the temperature model and the pH model.
A one-way analysis of variance (ANOVA) was calculated for the effect of pH on nisin extracted from cheese. A two-way ANOVA was calculated for the effect of strain and pH on L. monocytogenes log reduction for experiments using the mutant strains; post hoc analysis was performed using Tukey’s honestly significant difference. The cut-off for significance for all statistics was set at P < 0.05. Raw data and the R code used for all statistical analyses are available on GitHub1.
Results
Temperature Affects L. monocytogenes’ Susceptibility to Nisin
Nisin (2 ppm) was added to pasteurized milk prior to production of a lab-scale cheese model (pH 6.5) to assess the effect of different cheese incubation temperatures on the ability of nisin to reduce L. monocytogenes numbers on cheese. Cheese was surface inoculated with one of four recent L. monocytogenes outbreak strains or reference strain 10403S and then incubated at either 6, 14, or 22°C prior to quantification of L. monocytogenes numbers at day 1, 7, and 14. In general, nisin-treated cheese showed lower numbers of L. monocytogenes compared to untreated cheese at each temperature tested; however, higher L. monocytogenes numbers were observed for nisin-treated cheese stored at 14 and 22°C compared to nisin-treated cheese stored at 6°C. Figure 1 represents the observed data for each strain individually, while Figure 2 shows L. monocytogenes counts averaged for all strains. A linear mixed effects model was used to specifically determine whether (i) temperature, (ii) day of incubation, (iii) presence or absence of nisin, and (iv) strain as well as interactions between (v) temperature and nisin, (vi) strain and nisin, and (vii) nisin and day showed significant effects on log transformed bacterial numbers (Table 2).
Figure 1. Average counts (log cfu/g) of L. monocytogenes in the presence (blue line) and absence (red line) of nisin treatment in a lab-scale cheese model. Each cheese was inoculated with a single strain of L. monocytogenes (10403S, FSL R9-5621, FSL R9-5623, FSL R9-5624, or FSL R9-5625) to a level of approximately 7 log cfu/g. These results represent the effect of temperature (6, 14, and 22°C) on L. monocytogenes’ sensitivity to nisin. The data points are slightly offset such that the reader can clearly see each point; however, the points still correspond to 1, 7, and 14 days. All values are the arithmetic mean of three independent experiments, and error bars denote standard error. For some data points, error bars are not visible because standard error was too low to yield a visible error bar. All cheese was made at pH 6.5.
Figure 2. Average counts (log cfu/g) of L. monocytogenes in the presence (blue line) and absence (red line) of nisin treatment in a lab-scale cheese model. Calculated initial (day 0) L. monocytogenes numbers based on the average inoculum level (approximately 7 log cfu/g) are shown in black. Each cheese was inoculated with a single strain of L. monocytogenes (10403S, FSL R9-5621, FSL R9-5623, FSL R9-5624, or FSL R9-5625) to a level of approximately 7 log cfu/g. These results represent the effect of temperature (6, 14, and 22°C) on L. monocytogenes’ sensitivity to nisin. The data points are slightly offset such that the reader can clearly see each point; however, the points still correspond to 1, 7, and 14 days. All values are the arithmetic mean of three independent experiments, and error bars denote standard error. All cheese was made at pH 6.5.
Table 2. Model parameters for all fixed effects in the temperature model for L. monocytogenes counts.
A significant effect (P < 0.001) on L. monocytogenes numbers was found for presence of nisin with a model-estimated effect size of −3.44, indicating 3.44 log cfu/g lower L. monocytogenes numbers in the presence of nisin (Table 2). The significance of the factor “nisin” supports that nisin significantly reduces L. monocytogenes numbers in the cheese model, as evidenced by the data shown in Figures 1, 2. For cheese incubated at 6°C, average L. monocytogenes numbers (across all sampling days and strains) were 6.69 and 8.95 log cfu/g for cheese made with and without nisin, respectively (Supplementary Table 1). Nisin-treated cheese also consistently showed lower bacterial numbers at day 1 as compared to untreated cheese (2.26, 2.78, and 2.03 log cfu/g lower average L. monocytogenes numbers [across the 5 strains tested] for 6, 14, and 22°C) (Figure 2, Supplementary Table 1).
The interaction between nisin and day 7 and 14 also had significant effects on L. monocytogenes numbers with higher numbers at both days as compared to the reference (i.e., day 1) (Table 2). The significance of this interaction is not surprising considering that L. monocytogenes showed growth over time even in the presence of nisin (average log counts (cfu/g) across strains were 6.4 and 7.5 for day 1 and 14, respectively, at 6°C; Figure 2, Supplementary Table 1).
We also found a significant interaction effect between nisin and storage at 14 and 22°C with an effect size of 0.97 and 1.39, respectively, indicating 0.97 and 1.39 log cfu/g higher L. monocytogenes numbers relative to nisin treatment at 6°C (Table 2). While on average, nisin-treated cheese showed lower L. monocytogenes numbers across all temperatures, the difference between L. monocytogenes numbers on treated and untreated cheese varied considerably by temperature (Figure 2). For example, the lowest log difference between nisin-treated and untreated cheese for day 1 (0.58 log) was found for strain 5621 grown on cheese incubated at 22°C, with higher corresponding log differences of 2.22 and 2.59 for 6 and 14°C, respectively (Figure 1 and Supplementary Table 1). Importantly, however, growth of L. monocytogenes was still observed in nisin-treated cheese, particularly those stored at 14 and 22°C (Figures 1, 2) where, for a number of strains, by day 7 and 14, L. monocytogenes numbers were similar for nisin-treated and untreated cheese and differed by <0.5 log. For example, at 6°C, only strains 10403S, 5621, and 5624 (both day 7 and 14) showed >0.5 log difference between nisin-treated and untreated cheese.
Lastly, we found a significant interaction effect between presence of nisin and strains 5621 (serotype 1/2a), 5623 (serotype 4b), and 5625 (serotype 4b) (P = 0.007; effect size of 0.45, P = 0.043; effect size of 0.33 and P < 0.001; effect size of 0.66, respectively) (Table 2). This indicates that these strains have reduced sensitivity to nisin with 0.45, 0.33, and 0.66 log cfu/g higher L. monocytogenes numbers in the presence of nisin as compared to the reference strain 10403S. While strain 5625 showed a higher broth MIC compared to 10403S (Table 1), strains 5621 and 5623 did not.
pH Affects L. monocytogenes’ Susceptibility to Nisin Treatment
Nisin (2 ppm) was added to the milk, and cheese was made at pH 5.5, 6.0, and 6.5 to assess the effect of different pH on nisin inhibition of L. monocytogenes. Bacterial numbers were quantified after storage at 6°C for 1, 7, and 14 days (Figure 3). In general, nisin-treated cheese showed lower numbers of L. monocytogenes compared to untreated cheese at each pH tested; however, higher L. monocytogenes numbers were observed for nisin-treated cheese made at pH 5.5 compared to nisin treated cheese made at pH 6.0 and 6.5. Figure 3 represents the observed data for each strain individually, while Figure 4 shows L. monocytogenes counts averaged for all strains. A linear mixed effects model was used to determine whether (i) pH, (ii) day of incubation, (iii) presence or absence of nisin, and (iv) strain as well as interactions between (v) pH and nisin, (vi) strain and nisin, and (vii) nisin and day showed significant effects on log transformed bacterial numbers (Table 3).
Figure 3. Average counts (log cfu/g) of L. monocytogenes in the presence (blue line) and absence (red line) of nisin treatment in a lab-scale cheese model. Each cheese was inoculated with a single strain of L. monocytogenes (10403S, FSL R9-5621, FSL R9-5623, FSL R9-5624, or FSL R9-5625) to a level of approximately 7 log cfu/g. These results represent the effect of pH (5.5, 6.0, and 6.5) on L. monocytogenes’ sensitivity to nisin. The data points are slightly offset such that the reader can clearly see each point; however, the points still correspond to 1, 7, and 14 days. All values are the arithmetic mean of three independent experiments, and error bars denote standard error. For some data points, error bars are not visible because standard error was too low to yield a visible error bar. All cheese was stored at 6°C.
Figure 4. Average counts (log cfu/g) of L. monocytogenes in the presence (blue line) and absence (red line) of nisin treatment in a lab-scale cheese model. Calculated initial (day 0) L. monocytogenes numbers based on the average inoculum level (approximately 7 log cfu/g) are shown in black. Each cheese was inoculated with a single strain of L. monocytogenes (10403S, FSL R9-5621, FSL R9-5623, FSL R9-5624, or FSL R9-5625) to a level of approximately 7 log cfu/g. These results represent the effect of pH (5.5, 6.0, and 6.5) on L. monocytogenes’ sensitivity to nisin. The data points are slightly offset such that the reader can clearly see each point; however, the points still correspond to 1, 7, and 14 days. All values are the arithmetic mean of three independent experiments, and error bars denote standard error. All cheese was stored at 6°C.
Table 3. Model parameters for all fixed effects in the pH model for L. monocytogenes counts.
A significant effect (P < 0.001) was found for presence of nisin with an effect size of −1.89, which indicates L. monocytogenes numbers are 1.89 log cfu/g lower in the presence of nisin treatment (Table 3). For cheese made at pH 6.0, average bacterial numbers (across all sampling days and strains) were 6.14 and 8.61 log cfu/g for cheese made with and without nisin, respectively (Figure 4 and Supplementary Table 1). Although nisin-treated cheese showed lower L. monocytogenes numbers across pH, the difference between L. monocytogenes numbers on treated and untreated cheese varied considerably by pH; for example, the lowest log difference between nisin-treated and untreated cheese for day 1 (0.14 log) was found for strain 5621 on cheese made at pH 5.5, with higher corresponding log differences of 1.39 and 2.22 for pH 6.0 and 6.5, respectively (Figure 3 and Supplementary Table 1). Differences between L. monocytogenes numbers on treated and untreated cheese made at pH 5.5 were minimal and ranged from 0.14 to 1.73 log cfu/g, based on observed data across strains as compared to 0.33–3.63 log cfu/g and 0.49–3.47 log cfu/g for pH 6.0 and pH 6.5, respectively (Supplementary Table 1 and Figure 4). Similar to results obtained from the temperature model, L. monocytogenes still grew in nisin-treated cheese, but only in cheese made at pH 6.5 (Figure 3) where, by day 14, all L. monocytogenes strains had higher numbers for nisin-treated cheese compared to day 7.
We found a significant interaction effect between nisin and pH 5.5 with an effect size of 1.44, indicating 1.44 log cfu/g higher L. monocytogenes numbers relative to nisin treatment at pH 6.5 (Table 3). The fact that nisin seemed less effective against L. monocytogenes in cheese made at pH 5.5 is surprising considering that nisin is more stable at lower pH (Tan et al., 2015); thus, one could have hypothesized that nisin would have effectively killed L. monocytogenes at this pH.
We also found significant interaction effects between presence of nisin and strain 5625, one of the two 4b strains used here (P < 0.001; effect size 0.61) (Table 3); this indicates that this strain shows 0.61 log cfu/g higher numbers in the presence of nisin as compared to the reference strain 10403S. Strain 5625, as mentioned above, also showed a higher MIC in broth compared to 10403S (Table 1).
L. monocytogenes Reduced Sensitivity to Nisin on Lab-Scale Cheese Made at pH 5.5 Is at Least Partially dltA- and mprF-Dependent
As mentioned before, the reduced nisin sensitivity effect observed for strains growing in cheese made at pH 5.5 was surprising given the fact that nisin should be stable at this pH (Tan et al., 2015). We hypothesized that this effect could be due to (i) a more pronounced loss of nisin in the whey for cheese made at pH 5.5 compared to pH 6.5 as nisin is more soluble at lower pH (Liu and Hansen, 1990) or (ii) a response in cells grown at pH 5.5 that involves the nisin resistance genes dltA and mprF.
To test whether nisin loss was responsible for the reduced sensitivity of L. monocytogenes to nisin on cheese made at pH 5.5, 25 ppm nisin was added to the milk, and cheese was made at pH 5.5, 6.0, and 6.5. After extracting nisin from each cheese, soft agar diffusion assays were performed using the nisin sensitive strain P. cerevisiae E66 and the diameter of the zones of inhibition caused by the extracted nisin were measured (Figure 5). A one-way ANOVA was used to determine differences in zones of inhibition between the nisin-extracted samples; the results show there was no significant difference among diameters of the zones of inhibition (P = 0.31; Supplementary Table 2), indicating that nisin loss in the whey is similar regardless of the pH (5.5, 6.0, or 6.5) at which the cheese was made, therein nisin loss does not explain the decreased ability of nisin to kill L. monocytogenes in cheese made at pH 5.5.
Figure 5. Average size (mm) of zone of inhibitions of nisin extracted from cheese made at pH 5.5, 6.0, and 6.5 against P. cerevisiae. Results are of two independent biological replicates. Error bars denote standard error.
To determine whether the significant interaction effect between nisin and pH 5.5 involves the activity of nisin resistance genes (dltA and mprF), nisin (2 ppm) was added to the milk, and cheese was made at pH 5.5, 6.0, and 6.5 prior to L. monocytogenes (10403S, ΔdltA, ΔmprF, and ΔdltAmprF) surface inoculation. Bacterial numbers were quantified after storage at 6°C for 1 day and the log reduction (between untreated cheese and nisin-treated cheese) was calculated (Figure 6). A two-way ANOVA was calculated for the effect of strain and pH on L. monocytogenes log reduction and post hoc analysis was performed using Tukey’s HSD (Supplementary Tables 3, 4, respectively).
Figure 6. Log reduction of L. monocytogenes strains on cheese made at pH 5.5, 6.0, and 6.5 between untreated and treated cheese. These results represent the effect of pH on L. monocytogenes’ (10403S, ΔdltA, ΔmprF, and ΔdltAmprF) sensitivity to nisin. Bar groups (i.e., 10403S, ΔdltA, ΔmprF, and ΔdltAmprF) that do not share any letters represent values that are significantly different between strains. Asterisks denote a significant difference between pH 5.5 and pH 6.0 or 6.5 within a strain. Results are an average of three biological replicates. The log reduction was calculated separately for each replicate and then averaged. Error bars denote standard error.
As expected, the cell wall mutant strains ΔdltA, ΔmprF, and ΔdltAmprF showed an increased sensitivity to nisin, consistent with their lower broth MIC (Table 1), compared to the parental strain 10403S (Figure 6). Interestingly, pH 5.5 still led to significantly reduced nisin sensitivity in the ΔdltA and ΔmprF single mutants, when compared to pH 6.0, and in the ΔdltA when compared to pH 6.5, however, this was not observed in the double mutant ΔdltAmprF, suggesting that the reduced nisin susceptibility observed at pH 5.5 involves both of these genes (Figure 6 and Supplementary Table 4).
Discussion
Overall, our results indicate that nisin can reduce L. monocytogenes numbers on a lab-scale cheese model, however, L. monocytogenes growth was still observed, even in the presence of nisin. Furthermore, pH, temperature, and strain serotype showed significant effects on the efficacy of nisin treatment. These findings highlight the need to consider environmental conditions, including those specific to the product (e.g., pH), to optimize the effectiveness of nisin treatment on foods. While an initial log reduction, as that we observed with nisin, may reduce the overall risk of human listeriosis cases linked to fresh cheese, a formal risk assessment considering several of these parameters would be needed to more precisely assess the public health impact of nisin application on cheese. Importantly, a previous risk assessment focused on surface ripened soft raw milk cheeses did, however, suggest that even log reductions less than 5 log can have a considerable public health impact with regard to human listeriosis cases in the US (FDA, 2015).
Nisin Efficacy Is Enhanced at Lower Storage Temperatures
Our data showed that nisin can significantly decrease L. monocytogenes numbers in cheese and that its efficacy is enhanced when cheese is stored at lower temperatures. However, L. monocytogenes was able to grow on nisin-treated cheese, and more rapid growth is seen when cheese is stored at higher temperatures.
We found that L. monocytogenes numbers were approximately 1 log lower at day 14 on nisin-treated cheese stored at 6°C compared with nisin-treated cheese stored at 14 or 22°C (Figure 2). Others have shown that nisin is more effective at killing L. monocytogenes at lower temperatures. For example, Li et al. (2002) reported that L. monocytogenes grown in BHI broth at 10°C was more sensitive to nisin than cells grown at 30°C, likely due to membrane modifications in the cells grown at lower temperature, which cause an increase in fluidity (Li et al., 2002). It is therefore possible that L. monocytogenes cells growing on cheese at 6°C have increased membrane fluidity that in turns increases sensitivity to nisin as observed in our results.
In addition to the temperature effect observed on nisin efficacy, our data also show that L. monocytogenes growth occurs, even in the presence of nisin, and more rapid growth is seen when cheese is stored at higher temperatures. This finding is consistent with other studies that have shown that L. monocytogenes can grow in the presence of nisin on cheese (Ferreira and Lund, 1996; Martinez and Rodriguez, 2005). Additionally, a transient bactericidal effect against L. monocytogenes, followed by regrowth of cells in food matrices and laboratory media supplemented with nisin has also been previously reported (Davies et al., 1996). There are a number of possible reasons for re-growth of L. monocytogenes after an initial significant reduction, including, but not limited to (i) conditions intrinsic to the cheese matrix that decrease nisin availability or activity, and (ii) the physiological state of the cells that could increase the survival rate of the culture. For example, binding of nisin to food matrix components, such as fat (Jung et al., 1992), decrease nisin availability and therefore, its ability to bind and kill L. monocytogenes. In addition, nisin is known to be less stable at near neutral pH (such as that of queso fresco) (Gharsallaoui et al., 2016), which could possibly affect its activity in this food matrix. Emergence of nisin resistant cells (Gandhi and Chikindas, 2007) and/or cells that have acclimated to the presence of nisin (Chi-Zhang et al., 2004), could also explain a subsequent regrowth after an initial reduction. It would be interesting to test whether cells recovered from our cheese model made with nisin show any evidence of developing a higher resistance to this bacteriocin after 14 days compared to the original culture. Given the potential for regrowth of L. monocytogenes during long-term refrigerated storage, even after an initial reduction due to nisin treatment, studies over product shelf-life that consider storage time and temperature are essential to appropriately assess nisin treatment efficacy and evaluate the usefulness of nisin applications and their impact for public health. In addition, alternate strategies could be used to overcome the limitations of nisin when used in fresh cheese (Ibarra-Sánchez et al., 2020) including nisin encapsulation (Feng et al., 2019) as well as combination with other antimicrobials (Ibarra-Sánchez et al., 2018).
The Effect of pH 5.5 to Decrease Nisin Efficacy Against L. monocytogenes Is Partially Due to the Activity of dltA and mprF
Our data showed that when cheese is formulated at pH 5.5, nisin is less effective at killing L. monocytogenes compared to when cheese is made at pH 6.5. L. monocytogenes encounters many stresses in a food environment, and tolerance to a stress condition could lead to cross-protection against a subsequent stress (van Schaik et al., 1999; Bergholz et al., 2013; Kang et al., 2015). Furthermore, transcriptome profiling in L. monocytogenes under acid-induced conditions shows up-regulation of the VirR regulon (Tessema et al., 2012), which regulates at least 12 genes, including dltABCD and mprF, both of which confer resistance to a variety of CAMPs, including nisin. Wall teichoic acids (WTAs) are a main component of the Gram-positive bacterial cell wall and are highly negatively charged due to deprotonized phosphate groups. It has been shown experimentally, that Gram-positive bacteria, such as Staphylococcus aureus (Peschel et al., 1999), Clostridium difficile (McBride and Sonenshein, 2011b), Bacillus cereus (Abi Khattar et al., 2009), and L. monocytogenes (Reichmann et al., 2013) can resist interactions with bacteriocins by upregulating the dlt operon, which encodes proteins that incorporate D-alanine residues onto teichoic acids, reducing the net negative charge of the cell wall (Fischer, 1988). Additionally, the product of the mprF gene is required for the synthesis of lysylphosphatidylglycerol and the addition of L-lysine to phosphatidylglycerol, which also reduce the net negative charge of the cell membrane (Peschel et al., 2001; Thedieck et al., 2006). As bacteriocins are positively charged, the activity of dltA and mprF, will result in inhibition of nisin action on the cell wall. We hypothesized that the decreased effect of nisin against L. monocytogenes in cheese formulated at pH 5.5 is at least partially dependent on the presence of nisin-resistance genes dltA and mprF. While our results show a greater sensitivity to nisin in ΔdltA and ΔmprF mutant strains compared to 10403S, pH 5.5 still showed a protective effect in the single mutants but not in the double mutant (ΔdltAmprF). Therefore, the reduced sensitivity to nisin at pH 5.5 could be partially due to the activity of dltA and mprF from upregulation of the VirR regulon at pH 5.5. It would be interesting to test if the VirR regulon, along with dltA and mprF, is induced in L. monocytogenes growing on our cheese model made at pH 5.5.
Reduced sensitivity to nisin, independent of dltA and mprF, has also been associated with changes in cell membrane fatty acid composition, resulting in more rigid membrane fluidity (Ming and Daeschel, 1993; van Schaik et al., 1999). Changes in cell membrane composition can be attributed to acid tolerance in L. monocytogenes, in which diffusion of fatty acids across the membrane is inhibited, resulting in more rigid cell membranes (Beales, 2004), and subsequently, partially decreasing sensitivity to nisin. Furthermore, it has been shown that L. monocytogenes uses a glutamate decarboxylase system to survive acid stress (Cotter et al., 2001; Begley et al., 2010; Lourenco et al., 2017). GadD1 catalyzes the breakdown of glutamate into -aminobutyrate and carbon dioxide, forming ATP, which could restore intracellular levels of ATP that are depleted by nisin activity on the cell (van Schaik et al., 1999), and thus lead to reduced sensitivity to nisin. It is likely that the increased resistance to nisin observed in L. monocytogenes growing on cheese made at pH 5.5 is a result of a combination of processes including dltA- and mprF- mediated modifications of the cell membrane, changes in membrane fluidity, and acid tolerance. Overall, our data suggest that pH can significantly affect the efficacy of nisin against L. monocytogenes on cheese, therefore, the pH of cheese should be considered for L. monocytogenes control strategies, especially given the range in pH of different cheese types. Our results also highlight the importance of considering the intrinsic characteristics of a product when assessing the efficacy of L. monocytogenes control strategies. Follow up studies would be needed to explore the role of other intrinsic cheese characteristics, such as salt concentration, on nisin treatment on cheese.
L. monocytogenes Serotype Affects Nisin Efficacy
In addition to the effects of environmental conditions, our data also indicate that both serotype 4b strains showed reduced sensitivity to nisin across temperature and that serotype 4b strain 5625 also showed reduced sensitivity to nisin across pH. Interestingly, while strain 5625 (serotype 4b) showed a higher MIC in broth compared to the reference strain 10403S, strain 5623 (serotype 4b) did not (Table 1), which again highlights the importance of considering the environmental conditions specific to the food matrix when studying the efficacy of an antimicrobial strategy. Our findings are consistent with previous work that shows that the L. monocytogenes Scott A (4b) strain appeared to be more resistant to nisin compared to strains other serotypes (Ukuku and Shelef, 1997). However, others have shown no correlation between the differences in nisin sensitivity and serotype (Ferreira and Lund, 1996; Martinez and Rodriguez, 2005). In contrast, Buncic et al., 2001, showed that serotype 1/2a isolates were more resistant to two antilisterial bacteriocins (Lb 265 and Lb706) than serotype 4b isolates (Buncic et al., 2001). More recently, a screen of 282 L. monocytogenes isolates from German RTE food products and food-processing environments revealed various degrees of nisin sensitivity between strains, however, isolates derived from milk/cheese and other dairy products (which were predominantly serotype 1/2a) showed significantly higher resistance to nisin concentrations than isolates from other sources (p < 0.002) (Szendy et al., 2019). It seems plausible that the overrepresentation of isolates from dairy products with higher resistance to bacteriocins could be explained by the intrinsic advantage these isolates would have in environments where bacteriocin-producing organisms are found.
Our data are also consistent with a previous study that found that serotype also affects the effectiveness of phage treatment against L. monocytogenes in a lab-scale cheese model (Henderson et al., 2019) where the same 4b strains used in this study were also more resistant to phage treatment. Although, different serotypes (1/2a, 1/2b, and 4b) have been linked to a number of Hispanic-style cheese outbreaks (CDC, 2012, 2013, 2014, 2015, 2017), historically, isolates of serotype 4b strains have caused the greatest proportion of listeriosis outbreaks and the largest number of outbreak-associated cases compared to serotype 1/2a and 1/2b strains (Cartwright et al., 2013). Differences in nisin sensitivity among L. monocytogenes serotypes highlight the importance of validating nisin-based treatment strategies using different L. monocytogenes serotypes and environmental conditions relevant to a given application.
Conclusion
This study shows the critical role of temperature, pH, and L. monocytogenes serotype can have over the efficacy of antimicrobials intended for food preservation. Improved understanding of how environmental conditions affect antimicrobial efficacy could facilitate the development and/or effective implementation of control strategies. Additionally, the potential for cross-protection induced by food-relevant stress (e.g., pH) should be considered to avoid overestimation of antimicrobial strength in a food product. Our data suggest that nisin-based control strategies could be successful when cheese is formulated at near neutral pH and stored at low temperature (6°C). However, it is likely that other intrinsic characteristics of cheese (e.g., salt concentration) may also affect nisin efficacy against L. monocytogenes on this food matrix.
Data Availability Statement
All datasets generated for this study are included in the article/Supplementary Material.
Author Contributions
LH, BE, and JS performed experiments. LH, DK, and SM performed statistical analysis. MW and VG-O conceived the study. LH, MW, and VG-O wrote the manuscript. All authors read and approved the final manuscript.
Funding
This work was made possible by the research funding provided by the National Dairy Council and administered by Dairy Research Institute.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We would like to thank Dr. Erika Mudrak (Cornell University Statistical Consulting Unit) for help with experimental design and statistical consulting, and Dr. Shelley Clark (Food Safety Laboratory – Cornell University) for construction of the L. monocytogenes mutant strains. We also thank Dr. Randy Worobo (Food Science Department – Cornell University) for many insightful discussions and providing the P. cerevisiae strain, and the Centers for Disease Control and Prevention (CDC) for providing L. monocytogenes strains associated with recent cheese outbreaks.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmicb.2020.00635/full#supplementary-material
Footnotes
References
Abi Khattar, Z., Rejasse, A., Destoumieux-Garzon, D., Escoubas, J. M., Sanchis, V., Lereclus, D., et al. (2009). The dlt operon of Bacillus cereus is required for resistance to cationic antimicrobial peptides and for virulence in insects. J. Bacteriol. 191, 7063–7073. doi: 10.1128/JB.00892-09
Balouiri, M., Sadiki, M., and Ibnsouda, S. K. (2016). Methods for in vitro evaluating antimicrobial activity: a review. J. Pharm. Anal. 6, 71–79. doi: 10.1016/j.jpha.2015.11.005
Bates, D., Machler, M., Bolker, B. M., and Walker, S. C. (2015). Fitting linear mixed-effects models using lme4. J. Stat. Softw. 67, 1–48.
Beales, N. (2004). Adaptation of microorganisms to cold temperatures, weak acid preservatives, low pH, and osmotic stress: a review. Comp. Rev. Food Sci. Food Saf. 3, 1–20. doi: 10.1111/j.1541-4337.2004.tb00057.x
Begley, M., Cotter, P. D., Hill, C., and Ross, R. P. (2010). Glutamate decarboxylase-mediated nisin resistance in Listeria monocytogenes. Appl. Environ. Microbiol. 76, 6541–6546. doi: 10.1128/AEM.00203-10
Bergholz, T. M., Bowen, B., Wiedmann, M., and Boor, K. J. (2012). Listeria monocytogenes shows temperature-dependent and -independent responses to salt stress, including responses that induce cross-protection against other stresses. Appl. Environ. Microbiol. 78, 2602–2612. doi: 10.1128/AEM.07658-11
Bergholz, T. M., Tang, S., Wiedmann, M., and Boor, K. J. (2013). Nisin resistance of Listeria monocytogenes is increased by exposure to salt stress and is mediated via LiaR. Appl. Environ. Microbiol. 79, 5682–5688. doi: 10.1128/AEM.01797-13
Bishop, D. K., and Hinrichs, D. J. (1987). Adoptive transfer of immunity to Listeria monocytogenes. The influence of in vitro stimulation on lymphocyte subset requirements. J. Immunol. 139, 2005–2009.
Bouksaim, M., Lacroix, C., Audet, P., and Simard, R. E. (2000). Effects of mixed starter composition on nisin Z production by Lactococcus lactis subsp. lactis biovar. diacetylactis UL 719 during production and ripening of Gouda cheese. Int. J. Food Microbiol. 59, 141–156. doi: 10.1016/s0168-1605(00)00295-6
Brotz, H., Josten, M., Wiedemann, I., Schneider, U., Gotz, F., Bierbaum, G., et al. (1998). Role of lipid-bound peptidoglycan precursors in the formation of pores by nisin, epidermin and other lantibiotics. Mol. Microbiol. 30, 317–327. doi: 10.1046/j.1365-2958.1998.01065.x
Buncic, S., Avery, S. M., Rocourt, J., and Dimitrijevic, M. (2001). Can food-related environmental factors induce different behaviour in two key serovars, 4b and 1/2a, of Listeria monocytogenes? Int. J. Food Microbiol. 65, 201–212. doi: 10.1016/s0168-1605(00)00524-9
Cartwright, E. J., Jackson, K. A., Johnson, S. D., Graves, L. M., Silk, B. J., and Mahon, B. E. (2013). Listeriosis outbreaks and associated food vehicles, United States, 1998-2008. Emerg. Infect. Dis. 19, 1–9. doi: 10.3201/eid1901.120393
CDC (2012). Multistate Outbreak of Listeriosis Linked to Imported Frescolina Marte Brand Ricotta Salata Cheese (Final Update). Available online at: https://www.cdc.gov/listeria/outbreaks/cheese-09-12/index.html (accessed February 6, 2019).
CDC (2013). Multistate Outbreak of Listeriosis Linked to Crave Brothers Farmstead Cheeses (Final Update). Available online at: https://www.cdc.gov/listeria/outbreaks/cheese-07-13/index.html (accessed February 6, 2019).
CDC (2014). Multistate Outbreak of Listeriosis Linked to Roos Foods Dairy Products (Final Update). Available online at: https://www.cdc.gov/listeria/outbreaks/cheese-02-14/index.html (accessed February 6, 2019).
CDC (2015). Multistate Outbreak of Listeriosis Linked to Soft Cheeses Distributed by Karoun Dairies, Inc. (Final Update) [Online]. Available online at: https://www.cdc.gov/listeria/outbreaks/soft-cheeses-09-15/index.html (accessed February 6, 2019).
CDC (2017). Listeria Outbreaks. Available online at: https://www.cdc.gov/listeria/outbreaks/ (accessed February 6, 2019).
Chen, H., and Hoover, D. G. (2006). Bacteriocins and their food applications. Comp. Rev. Food Sci. Food Saf. 2, 82–100. doi: 10.1111/j.1541-4337.2003.tb00016.x
Chi-Zhang, Y., Yam, K. L., and Chikindas, M. L. (2004). Effective control of Listeria monocytogenes by combination of nisin formulated and slowly released into a broth system. Int. J. Food Microbiol. 90, 15–22. doi: 10.1016/s0168-1605(03)00168-5
Cotter, P. D., O’reilly, K., and Hill, C. (2001). Role of the glutamate decarboxylase acid resistance system in the survival of Listeria monocytogenes LO28 in low pH foods. J. Food Prot. 64, 1362–1368. doi: 10.4315/0362-028x-64.9.1362
Curtis, G. D. W., Nichols, W. W., and Falla, T. J. (1989). Selective agents for Listeria can inhibit their growth. Lett. Appl. Microbiol. 8, 169–172. doi: 10.1111/j.1472-765x.1989.tb00240.x
Davies, E. A., Bevis, H. E., and Delves-Broughton, J. (1997). The use of the bacteriocin, nisin, as a preservative in ricotta-type cheeses to control the food-borne pathogen Listeria monocytogenes. Lett. Appl. Microbiol. 24, 343–346. doi: 10.1046/j.1472-765x.1997.00145.x
Davies, E. A., Falahee, M. B., and Adams, M. R. (1996). Involvement of the cell envelope of Listeria monocytogenes in the acquisition of nisin resistance. J. Appl. Bacteriol. 81, 139–146. doi: 10.1111/j.1365-2672.1996.tb04491.x
Farber, J. M., and Peterkin, P. I. (1991). Listeria monocytogenes, a food-borne pathogen. Microbiol. Rev. 55, 476–511. doi: 10.1128/mmbr.55.3.476-511.1991
FDA (2015). Joint FDA / Health Canada Quantitative Assessment of the Risk of Listeriosis from Soft-Ripened Cheese Consumption in the United States and Canada: Report. Available online at: https://www.fda.gov/media/90488/download (accessed March 8, 2020.)Google Scholar
Feng, Y. M., Ibarra-Sanchez, L. A., Luu, L., Miller, M. J., and Lee, Y. (2019). Co-assembly of nisin and zein in microfluidics for enhanced antilisterial activity in Queso Fresco. LWT Food Sci. Technol. 111, 355–362. doi: 10.1016/j.lwt.2019.05.059
Ferreira, M. A., and Lund, B. M. (1996). The effect of nisin on Listeria monocytogenes in culture medium and long-life cottage cheese. Lett. Appl. Microbiol. 22, 433–438. doi: 10.1111/j.1472-765x.1996.tb01197.x
Fischer, W. (1988). Physiology of lipoteichoic acids in bacteria. Adv. Microb. Physiol. 29, 233–302.
Fowler, G. G., and McCann, B. (1971∗). The growing use of nisin in the dairy industry. Aust. J. Dairy Technol. 26, 44–46. doi: 10.1186/s12934-018-0974-z
Gandhi, M., and Chikindas, M. L. (2007). Listeria: a foodborne pathogen that knows how to survive. Int. J. Food Microbiol. 113, 1–15. doi: 10.1016/j.ijfoodmicro.2006.07.008
Garsa, A. K., Kumariya, R., Kumar, A., Lather, P., Kapila, S., and Sood, S. K. (2014). Industrial cheese whey utilization for enhanced production of purified pediocin PA-1. LWT Food Sci. Technol. 59, 656–665. doi: 10.1016/j.lwt.2014.07.008
Gharsallaoui, A., Oulahal, N., Joly, C., and Degraeve, P. (2016). Nisin as a food preservative: part 1: physicochemical properties, antimicrobial activity, and main uses. Crit. Rev. Food Sci. Nutr. 56, 1262–1274. doi: 10.1080/10408398.2013.763765
Hasper, H. E., Kramer, N. E., Smith, J. L., Hillman, J. D., Zachariah, C., Kuipers, O. P., et al. (2006). An alternative bactericidal mechanism of action for lantibiotic peptides that target lipid II. Science 313, 1636–1637. doi: 10.1126/science.1129818
Henderson, L. O., Cabrera-Villamizar, L. A., Skeens, J., Kent, D., Murphy, S., Wiedmann, M., et al. (2019). Environmental conditions and serotype affect Listeria monocytogenes susceptibility to phage treatment in a laboratory cheese model. J. Dairy Sci. 102, 9674–9688. doi: 10.3168/jds.2019-16474
Heng, N. C., Wescombe, P. A., Burton, J. P., Jack, R. W., and Tagg, J. R. (2007). The Diversity of Bacteriocins in Gram-Positive Bacteria. Berlin: Springer.
Horton, R. M., Cai, Z. L., Ho, S. N., and Pease, L. R. (1990). Gene splicing by overlap extension: tailor-made genes using the polymerase chain reaction. Biotechniques 8, 528–535.
Hu, Y. C., Kang, C. K., Tang, C. H., and Lee, T. H. (2015). Transcriptomic analysis of metabolic pathways in milkfish that respond to salinity and temperature changes. PLoS One 10:e0134959. doi: 10.1371/journal.pone.0134959
Ibarra-Sánchez, L. A., El-Haddad, N., Mahmoud, D., Miller, M. J., and Karam, L. (2020). Invited review: advances in nisin use for preservation of dairy products. J. Dairy Sci. 103, 2041–2052. doi: 10.3168/jds.2019-17498
Ibarra-Sánchez, L. A., Van Tassell, M. L., and Miller, M. J. (2017). Invited review: hispanic-style cheeses and their association with Listeria monocytogenes. J. Dairy Sci. 100, 2421–2432. doi: 10.3168/jds.2016-12116
Ibarra-Sánchez, L. A., Van Tassell, M. L., and Miller, M. J. (2018). Antimicrobial behavior of phage endolysin PlyP100 and its synergy with nisin to control Listeria monocytogenes in Queso Fresco. Food Microbiol. 72, 128–134. doi: 10.1016/j.fm.2017.11.013
Ilsi Research Foundation/Risk Science Institute and Expert Panel on Listeria monocytogenes in Foods (2005). Achieving continuous improvement in reductions in foodborne listeriosis–a risk-based approach. J. Food Prot. 68, 1932–1994. doi: 10.4315/0362-028x-68.9.1932
Jackson, K. A., Gould, L. H., Hunter, J. C., Kucerova, Z., and Jackson, B. (2018). Listeriosis outbreaks associated with soft cheeses, United States, 1998-2014(1). Emerg. Infect. Dis. 24, 1116–1118. doi: 10.3201/eid2406.171051
Jordan, S., Hutchings, M. I., and Mascher, T. (2008). Cell envelope stress response in Gram-positive bacteria. FEMS Microbiol. Rev. 32, 107–146. doi: 10.1111/j.1574-6976.2007.00091.x
Jung, D. S., Bodyfelt, F. W., and Daeschel, M. A. (1992). Influence of fat and emulsifiers on the efficacy of nisin in inhibiting Listeria monocytogenes in fluid milk. J. Dairy Sci. 75, 387–393. doi: 10.3168/jds.s0022-0302(92)77773-x
Kabuki, D. Y., Kuaye, A. Y., Wiedmann, M., and Boor, K. J. (2004). Molecular subtyping and tracking of Listeria monocytogenes in latin-style fresh-cheese processing plants. J. Dairy Sci. 87, 2803–2812. doi: 10.3168/jds.s0022-0302(04)73408-6
Kang, J., Wiedmann, M., Boor, K. J., and Bergholz, T. M. (2015). VirR-mediated resistance of Listeria monocytogenes against food antimicrobials and cross-protection induced by exposure to organic acid salts. Appl. Environ. Microbiol. 81, 4553–4562. doi: 10.1128/AEM.00648-15
Khan, I., and Oh, D. H. (2016). Integration of nisin into nanoparticles for application in foods. Innov. Food Sci. Emerg. Technol. 34, 376–384. doi: 10.1016/j.foodchem.2019.02.044
Kramer, N. E., Hasper, H. E., Van Den Bogaard, P. T., Morath, S., De Kruijff, B., Hartung, T., et al. (2008). Increased D-alanylation of lipoteichoic acid and a thickened septum are main determinants in the nisin resistance mechanism of Lactococcus lactis. Microbiology 154, 1755–1762. doi: 10.1099/mic.0.2007/015412-0
Leggett, L. N., Tomasula, P. M., Van Hekken, D. L., Porto-Fett, A. C. S., Shoyer, B., Renye, J. A., et al. (2012). Effect of storage at 4 and 10C on the growth of Listeria moncytogenes in and on queso fresco. J. Food Saf. 32, 236–245. doi: 10.1111/j.1745-4565.2012.00373.x
Li, J., Chikindas, M. L., Ludescher, R. D., and Montville, T. J. (2002). Temperature- and surfactant-induced membrane modifications that alter Listeria monocytogenes nisin sensitivity by different mechanisms. Appl. Environ. Microbiol. 68, 5904–5910. doi: 10.1128/aem.68.12.5904-5910.2002
Liu, W., and Hansen, J. N. (1990). Some chemical and physical properties of nisin, a small-protein antibiotic produced by Lactococcus lactis. Appl. Environ. Microbiol. 56, 2551–2558. doi: 10.1128/aem.56.8.2551-2558.1990
Lourenco, A., Kamnetz, M. B., Gadotti, C., and Diez-Gonzalez, F. (2017). Antimicrobial treatments to control Listeria monocytogenes in queso fresco. Food Microbiol. 64, 47–55. doi: 10.1016/j.fm.2016.12.014
Manfreda, G., De Cesare, A., Stella, S., Cozzi, M., and Cantoni, C. (2005). Occurrence and ribotypes of Listeria monocytogenes in Gorgonzola cheeses. Int. J. Food Microbiol. 102, 287–293. doi: 10.1016/j.ijfoodmicro.2004.11.045
Martinez, B., and Rodriguez, A. (2005). Antimicrobial susceptibility of nisin resistant Listeria monocytogenes of dairy origin. FEMS Microbiol. Lett. 252, 67–72. doi: 10.1016/j.femsle.2005.08.025
McBride, S. M., and Sonenshein, A. L. (2011a). The dlt operon confers resistance to cationic antimicrobial peptides in Clostridium difficile. Microbiology 157, 1457–1465. doi: 10.1099/mic.0.045997-0
McBride, S. M., and Sonenshein, A. L. (2011b). Identification of a genetic locus responsible for antimicrobial peptide resistance in Clostridium difficile. Infect. Immun. 79, 167–176. doi: 10.1128/IAI.00731-10
Ming, X. T., and Daeschel, M. A. (1993). Nisin resistance of foodborne bacteria and the specific resistance responses of Listeria monocytogenes Scott-A. J. Food Prot. 56, 944–948. doi: 10.4315/0362-028X-56.11.944
Nielsen, P. K., Andersen, A. Z., Mols, M., Van Der Veen, S., Abee, T., and Kallipolitis, B. H. (2012). Genome-wide transcriptional profiling of the cell envelope stress response and the role of LisRK and CesRK in Listeria monocytogenes. Microbiology 158, 963–974. doi: 10.1099/mic.0.055467-0
Nightingale, K. K., Schukken, Y. H., Nightingale, C. R., Fortes, E. D., Ho, A. J., Her, Z., et al. (2004). Ecology and transmission of Listeria monocytogenes infecting ruminants and in the farm environment. Appl. Environ. Microbiol. 70, 4458–4467. doi: 10.1128/aem.70.8.4458-4467.2004
Nilsson, L., Huss, H. H., and Gram, L. (1997). Inhibition of Listeria monocytogenes on cold-smoked salmon by nisin and carbon dioxide atmosphere. Int. J. Food Microbiol. 38, 217–227. doi: 10.1016/s0168-1605(97)00111-6
O’Connor, P. M., Ross, R. P., Hill, C., and Cotter, P. D. (2015). Antimicrobial antagonists against food pathogens: a bacteriocin perspective. Curr. Opin. Food Sci. 2, 51–57. doi: 10.1016/j.cofs.2015.01.004
Orsi, R. H., Den Bakker, H. C., and Wiedmann, M. (2011). Listeria monocytogenes lineages: genomics, evolution, ecology, and phenotypic characteristics. Int. J. Med. Microbiol. 301, 79–96. doi: 10.1016/j.ijmm.2010.05.002
Peschel, A., Jack, R. W., Otto, M., Collins, L. V., Staubitz, P., Nicholson, G., et al. (2001). Staphylococcus aureus resistance to human defensins and evasion of neutrophil killing via the novel virulence factor MprF is based on modification of membrane lipids with l-lysine. J. Exp. Med. 193, 1067–1076. doi: 10.1084/jem.193.9.1067
Peschel, A., Otto, M., Jack, R. W., Kalbacher, H., Jung, G., and Gotz, F. (1999). Inactivation of the dlt operon in Staphylococcus aureus confers sensitivity to defensins, protegrins, and other antimicrobial peptides. J. Biol. Chem. 274, 8405–8410. doi: 10.1074/jbc.274.13.8405
Piffaretti, J. C., Kressebuch, H., Aeschbacher, M., Bille, J., Bannerman, E., Musser, J. M., et al. (1989). Genetic characterization of clones of the bacterium Listeria monocytogenes causing epidemic disease. Proc. Natl. Acad. Sci. U.S.A. 86, 3818–3822.
R Core Team (2015). R: A Language and Environment for Statistical Computing. Vienna: R Foundation for Statistical Computing.
Rasmussen, O. F., Skouboe, P., Dons, L., Rossen, L., and Olsen, J. E. (1995). Listeria monocytogenes exists in at least three evolutionary lines: evidence from flagellin, invasive associated protein and listeriolysin O genes. Microbiology 141(Pt 9), 2053–2061.
Reichmann, N. T., Cassona, C. P., and Grundling, A. (2013). Revised mechanism of D-alanine incorporation into cell wall polymers in Gram-positive bacteria. Microbiology 159, 1868–1877. doi: 10.1099/mic.0.069898-0
Roberts, A., Nightingale, K., Jeffers, G., Fortes, E., Kongo, J. M., and Wiedmann, M. (2006). Genetic and phenotypic characterization of Listeria monocytogenes lineage III. Microbiology 152, 685–693.
Ross, R. P., Morgan, S., and Hill, C. (2002). Preservation and fermentation: past, present and future. Int. J. Food Microbiol. 79, 3–16.
Samant, S., Hsu, F. F., Neyfakh, A. A., and Lee, H. (2009). The Bacillus anthracis protein MprF is required for synthesis of lysylphosphatidylglycerols and for resistance to cationic antimicrobial peptides. J. Bacteriol. 191, 1311–1319. doi: 10.1128/JB.01345-08
Silhavy, T. J., Kahne, D., and Walker, S. (2010). The bacterial cell envelope. Cold Spring Harb. Perspect. Biol. 2:a000414. doi: 10.1101/cshperspect.a000414
Smith, K., and Youngman, P. (1992). Use of a new integrational vector to investigate compartment-specific expression of the Bacillus subtilis spoIIM gene. Biochimie 74, 705–711.
Staubitz, P., and Peschel, A. (2002). MprF-mediated lysinylation of phospholipids in Bacillus subtilis–protection against bacteriocins in terrestrial habitats? Microbiology 148, 3331–3332.
Swaminathan, B., Cabanes, D., Zhang, W., and Cossart, P. (2007). “Listeria monocytogenes,” in Food Microbiology: Fundamentals and Frontiers, 3rd Edn, eds M. P. Doyle and L. R. Beuchat (Washington, DC: ASM Press).
Szendy, M., Kalkhof, S., Bittrich, S., Kaiser, F., Leberecht, C., Labudde, D., et al. (2019). Structural change in GadD2 of Listeria monocytogenes field isolates supports nisin resistance. Int. J. Food Microbiol. 305:108240. doi: 10.1016/j.ijfoodmicro.2019.108240
Tan, Z., Luo, J., Liu, F., Zhang, Q., and Jia, S. (2015). “Effects of pH, temperature, storage time, and protective agents on Nisin Antibacterial stability,” in Advances in Applied Biotechnology Lecture Notes in Electrical Engineering, eds T. C. Zhang and M. Nakajima (Berlin: Springer), 305–312.
Tessema, G. T., Moretro, T., Snipen, L., Heir, E., Holck, A., Naterstad, K., et al. (2012). Microarray-based transcriptome of Listeria monocytogenes adapted to sublethal concentrations of acetic acid, lactic acid, and hydrochloric acid. Can. J. Microbiol. 58, 1112–1123. doi: 10.1139/w2012-091
Thedieck, K., Hain, T., Mohamed, W., Tindall, B. J., Nimtz, M., Chakraborty, T., et al. (2006). The MprF protein is required for lysinylation of phospholipids in listerial membranes and confers resistance to cationic antimicrobial peptides (CAMPs) on Listeria monocytogenes. Mol. Microbiol. 62, 1325–1339.
Tokman, J. I., Kent, D. J., Wiedmann, M., and Denes, T. (2016). Temperature significantly affects the plaquing and adsorption efficiencies of Listeria phages. Front. Microbiol. 7:631. doi: 10.3389/fmicb.2016.00631
Uhlich, G. A., Luchansky, J. B., Tamplin, M. L., Molina-Corral, F. J., Anandan, S., and Porto-Fett, A. C. S. (2006). Effect of storage temperature on the growth of Listeria monocytogenes on queso blanco slices. J. Food Saf. 26, 202–214.
Ukuku, D. O., and Shelef, L. A. (1997). Sensitivity of six strains of Listeria monocytogenes to nisin. J. Food Prot. 60, 867–869. doi: 10.4315/0362-028X-60.7.867
van Schaik, W., Gahan, C. G., and Hill, C. (1999). Acid-adapted Listeria monocytogenes displays enhanced tolerance against the lantibiotics nisin and lacticin 3147. J. Food. Prot. 62, 536–539.
Van Tassell, M. L., Ibarra-Sanchez, L. A., Takhar, S. R., Amaya-Llano, S. L., and Miller, M. J. (2015). Use of a miniature laboratory fresh cheese model for investigating antimicrobial activities. J. Dairy Sci. 98, 8515–8524. doi: 10.3168/jds.2015-9967
Vijayakumar, P. P., and Muriana, P. M. (2017). Inhibition of Listeria monocytogenes on ready-to-eat meats using bacteriocin mixtures based on mode-of-action. Foods 6:22. doi: 10.3390/foods6030022
Ward, T. J., Ducey, T. F., Usgaard, T., Dunn, K. A., and Bielawski, J. P. (2008). Multilocus genotyping assays for single nucleotide polymorphism-based subtyping of Listeria monocytogenes isolates. Appl. Environ. Microbiol. 74, 7629–7642. doi: 10.1128/AEM.01127-08
Wiedemann, I., Breukink, E., Van Kraaij, C., Kuipers, O. P., Bierbaum, G., De Kruijff, B., et al. (2001). Specific binding of nisin to the peptidoglycan precursor lipid II combines pore formation and inhibition of cell wall biosynthesis for potent antibiotic activity. J. Biol. Chem. 276, 1772–1779.
Wiedmann, M., Arvik, T. J., Hurley, R. J., and Boor, K. J. (1998). General stress transcription factor sigmaB and its role in acid tolerance and virulence of Listeria monocytogenes. J. Bacteriol. 180, 3650–3656.
Wiedmann, M., Bruce, J. L., Keating, C., Johnson, A. E., Mcdonough, P. L., and Batt, C. A. (1997). Ribotypes and virulence gene polymorphisms suggest three distinct Listeria monocytogenes lineages with differences in pathogenic potential. Infect. Immun. 65, 2707–2716.
Wiegand, I., Hilpert, K., and Hancock, R. E. (2008). Agar and broth dilution methods to determine the minimal inhibitory concentration (MIC) of antimicrobial substances. Nat. Protoc. 3, 163–175. doi: 10.1038/nprot.2007.521
Keywords: Listeria monocytogenes, cell wall, dltA, mprF, nisin
Citation: Henderson LO, Erazo Flores BJ, Skeens J, Kent D, Murphy SI, Wiedmann M and Guariglia-Oropeza V (2020) Nevertheless, She Resisted – Role of the Environment on Listeria monocytogenes Sensitivity to Nisin Treatment in a Laboratory Cheese Model. Front. Microbiol. 11:635. doi: 10.3389/fmicb.2020.00635
Received: 30 October 2019; Accepted: 20 March 2020;
Published: 09 April 2020.
Edited by:
Arun K. Bhunia, Purdue University, United StatesReviewed by:
Michael Joseph Miller, University of Illinois at Urbana-Champaign, United StatesStephanie Clark, Iowa State University, United States
Copyright © 2020 Henderson, Erazo Flores, Skeens, Kent, Murphy, Wiedmann and Guariglia-Oropeza. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: V. Guariglia-Oropeza, dmc5M0Bjb3JuZWxsLmVkdQ==