Lactoferrin (LF) is an iron binding glycoprotein found in the milk of all mammals that acts as a protective factor in milk, and is thought to provide antimicrobial activity to the infant (Chandan et al., Reference Chandan, Kilara and Shah2015). Bovine LF is a large protein of circa 80 kDa, depending on the degree of glycosylation (Korhonen and Marnila, Reference Korhonen, Marnila and Fuquay2011). It is comprised of a simple polypeptide chain folded into two symmetrical lobes, the N- and C-lobes (García-Montoya et al., Reference García-Montoya, Cendón, Arévalo-Gallegos and Rascón-Cruz2012), and contains around 690 amino acids, with a considerable proportion of them being branched chain amino acids of leucine, isoleucine and valine at 18.6% combined. The quantity of LF ranges from 20 to 200 mg/l in bovine milk, with fluctuations due to the stage of lactation and with the highest quantity recorded in colostrum, the milk produced in the first few days of lactation (Cheng et al., Reference Cheng, Wang, Bu, Liu, Zhang, Wei, Zhou and Wang2008).
The antimicrobial activity of LF has been extensively reviewed (Superti, Reference Superti2020; Gruden and Poklar Ulrih, Reference Gruden and Poklar Ulrih2021; Rascón-Cruz et al., Reference Rascón-Cruz, Espinoza-Sánchez, Siqueiros-Cendón, Nakamura-Bencomo, Arévalo-Gallegos and Iglesias-Figueroa2021) including its effectiveness against viruses (Ammendolia et al., Reference Ammendolia, Agamennone, Pietrantoni, Lannutti, Siciliano, De Giulio, Amici and Superti2012; Redwan et al., Reference Redwan, Uversky, El-Fakharany and Al-Mehdar2014) and potential efficiency against SARS-CoV-2 or Covid-19 (Kell et al., Reference Kell, Heyden and Pretorius2020; Wang et al., Reference Wang, Wang, Wang, Luo, Wan, Jiang and Chu2020). Both LF and the antimicrobial peptide lactoferricin (LFcin) have been shown to exhibit host-protective effects to the gastrointestinal tract when consumed orally in various in-vivo animal and human studies, as reviewed by Tomita et al. (Reference Tomita, Wakabayashi, Yamauchi, Teraguchi and Hayasawa2002). A more recent review reported the positive effect of LF on the gut microbiome, detailing how LF can affect the growth of intestinal bacteria by promoting the growth of selected probiotic strains (Vega-Bautista et al., Reference Vega-Bautista, de la Garza, Carrero, Campos-Rodríguez, Godínez-Victoria and Drago-Serrano2019).
The generation of bioactive peptides from LF after in-vitro simulated digestion has shown ACE-inhibitory activity (Wada and Lönnerdal, Reference Wada and Lönnerdal2015; Tu et al., Reference Tu, Xu, Xu, Cheng, Wu, Liu and Du2021) as well as anticoagulation properties (Tu et al., Reference Tu, Xu, Xu, Cheng, Wu, Liu and Du2021) and antioxidation activity (Wada and Lönnerdal, Reference Wada and Lönnerdal2015). LF has also been shown to exhibit antimicrobial activity in its native state against a range of pathogenic bacteria (Tian et al., Reference Tian, Maddox, Ferguson and Shu2010; Murata et al., Reference Murata, Wakabayashi, Yamauchi and Abe2013) including Escherichia coli (Yen et al., Reference Yen, Shen, Hsu, Chang, Lin, Chen and Chen2011) and Cronobacter sakazakii (Harouna et al., Reference Harouna, Carramiñana, Navarro, Pérez, Calvo and Sánchez2015). However, LF antibacterial bioactivity is mainly associated with peptides generated by hydrolysis (Tomita et al., Reference Tomita, Bellamy, Takase, Yamauchi, Wakabayashi and Kawase1991). For example, an in-vitro simulation of human digestion produced antibacterial peptides from LF that were affective against C. sakazakii (Abad et al., Reference Abad, Serrano, Graikini, Pérez, Grasa and Sánchez2023). Much investigation has gone into the antibacterial activity of small LF peptides generated by pepsin hydrolysis, located in the N1-domain of the LF molecule including LFcin, f(17–41) (Bellamy et al., Reference Bellamy, Takase, Yamauchi, Wakabayashi, Kawase and Tomita1992b) and lactoferricin B (LFcin B), f(17–30) (Hwang et al., Reference Hwang, Zhou, Shan, Arrowsmith and Vogel1998). Also located in the N1-domain is the LF peptide lactoferrampin (LFampin) f(265–284) which has shown antifungal activity (van der Kraan et al., Reference van der Kraan, Groenink, Nazmi, Veerman, Bolscher and Nieuw Amerongen2004). These well characterised peptides have also been shown to be active against a wide range of bacteria including Staphylococcus aureus and E. coli (Flores-Villaseñor et al., Reference Flores-Villaseñor, Canizalez-Román, Reyes-Lopez, Nazmi, de la Garza, Zazueta-Beltrán, León-Sicairos and Bolscher2010, Huertas et al., Reference Huertas, Monroy, Medina and Castañeda2017), including E. coli O157:H7 (Haiwen et al., Reference Haiwen, Rui, Bingxi, Qingfeng, Jifeng, Xuemei and Beibei2019), Listeria monocytongenes (Longhi et al., Reference Longhi, Conte, Ranaldi, Penta, Valenti, Tinari, Superti and Seganti2005), Bacillus subtilis and Pseudomonas aeruginosa (van der Kraan et al., Reference van der Kraan, Groenink, Nazmi, Veerman, Bolscher and Nieuw Amerongen2004) and Pseudomonas syringae (Kim et al., Reference Kim, Kim and Shimazaki2016). The C-terminal end of LF is reportedly more resistant to hydrolysis, however, Rastogi et al. (Reference Rastogi, Singh, Pandey, Sinha, Bhushan, Kaur, Sharma and Singh2014b) successfully used trypsin to partially hydrolyse this region, and reported large fragments of approximately 21, 38 and 45 kDa which were shown to be antibacterial against the Gram-negative bacteria E. coli and Yersinia enterocolitica (Rastogi et al., Reference Rastogi, Nagpal, Alam, Pandey, Gautam, Sinha, Shin, Manzoor, Virdi, Kaur, Sharma and Singh2014a).
Reviews on the specific mechanisms of the antibacterial activity of LF such as iron binding (Kell et al., Reference Kell, Heyden and Pretorius2020), and specific antibacterial activity against E. coli (Yen et al., Reference Yen, Shen, Hsu, Chang, Lin, Chen and Chen2011), including against the Shiga-like toxin producing Escherichia coli O157:H7 which causes severe intestinal infections in humans (Rybarczyk et al., Reference Rybarczyk, Kieckens, Vanrompay and Cox2017), have been recently examined. A well-documented antibacterial mechanism is the transferrin ability of LF to bind iron and, therefore, reduce iron availability, which is an essential nutrient for bacterial growth, resulting in a bacteriostatic activity (Chandan et al., Reference Chandan, Kilara and Shah2015; Kell et al., Reference Kell, Heyden and Pretorius2020; Gruden and Poklar Ulrih, Reference Gruden and Poklar Ulrih2021). LF is the only transferrin with the ability to bind iron over a wide range of pH, with iron ions still strongly attached at pH 3 whereas other transferrins dissociate the attached ferric ions at pH 5 (Korhonen and Marnila, Reference Korhonen, Marnila and Fuquay2011). This iron binding ability has also been associated with the prevention of biofilm formation for example against the pathogen Pseudomonas aeruginosa (Singh et al., Reference Singh, Parsek, Greenberg and Welsh2002). Another antibacterial mechanism of LF is direct interaction with bacterial cell membranes, particularly Gram-negative bacterial cell membranes which contain lipopolysaccharides, as LF was found to bind to the lipid part A of bacterial cell wall lipopolysaccharides characteristic of Gram-negative bacteria including E. coli (Orsi, Reference Orsi2004). This disruption to the bacterial cell walls increases the membrane permeability and decreases the membrane integrity resulting in a bactericidal activity (Rybarczyk et al., Reference Rybarczyk, Kieckens, Vanrompay and Cox2017; Gruden and Poklar Ulrih, Reference Gruden and Poklar Ulrih2021). Examples of this include direct bactericidal activity of the peptide LFcin recorded as a result of lipopolysaccharide membrane damage (Yamauchi et al., Reference Yamauchi, Tomita, Giehl and Ellison1993). Cell wall disruption was also observed by Flores-Villaseñor et al. (Reference Flores-Villaseñor, Canizalez-Román, Reyes-Lopez, Nazmi, de la Garza, Zazueta-Beltrán, León-Sicairos and Bolscher2010) for the peptides LFcin B, LFampin and particularly by a chimaeric construct of both peptides against E. coli O157:H7 at low concentrations. Additionally, bovine LF was recorded to reduce adhesion of E. coli O157:H7 to human Caco-2 cells (Atef Yekta et al., Reference Atef Yekta, Verdonck, van den Broeck, Goddeeris, Cox and Vanrompay2010). Other factors that contribute to the antibacterial activity of LF include environmental factors of pH, temperature and the food matrix composition which can reportedly lead to variability in antibacterial activity within in-vitro studies (Rybarczyk et al., Reference Rybarczyk, Kieckens, Vanrompay and Cox2017).
The antimicrobial effect of LF fragments generated after hydrolysis with protease enzymes naturally found within the digestive system has been established. The digestive enzymes pepsin (Tomita et al., Reference Tomita, Bellamy, Takase, Yamauchi, Wakabayashi and Kawase1991; Bellamy et al., Reference Bellamy, Takase, Wakabayashi, Kawase and Tomita1992a, Reference Bellamy, Takase, Yamauchi, Wakabayashi, Kawase and Tomita1992b; Yamauchi et al., Reference Yamauchi, Tomita, Giehl and Ellison1993; Jones et al., Reference Jones, Smart, Bloomberg, Burgess and Millar1994; Murata et al., Reference Murata, Wakabayashi, Yamauchi and Abe2013; Kim et al., Reference Kim, Kim and Shimazaki2016), and trypsin (Tomita et al., Reference Tomita, Bellamy, Takase, Yamauchi, Wakabayashi and Kawase1991; Rastogi et al., Reference Rastogi, Nagpal, Alam, Pandey, Gautam, Sinha, Shin, Manzoor, Virdi, Kaur, Sharma and Singh2014a, Reference Rastogi, Singh, Pandey, Sinha, Bhushan, Kaur, Sharma and Singh2014b) have been commonly used. The enzymes are used at their optimum hydrolysis conditions rather than those that would simulate digestion, therefore the effect of digestive processes and natural conditions of these enzymes within a gastrointestinal simulation is less well characterised, as only very recent studies have examined in-vitro digestion of dairy products on either Staphylococcus aureus or Cronobacter sakazakii (Abad et al., Reference Abad, Serrano, Graikini, Pérez, Grasa and Sánchez2023, Abad et al., Reference Abad, Bailac, Pérez, Carramiñana, Calvo and Sánchez2024).
Due to its relevance in clinical microbiology, E. coli, a Gram-negative rod-shaped bacterium, is one of the most characterised bacteria of the Enterobacteriaceae family. Some strains are pathogenic and are associated with gastrointestinal infections, fevers and diarrhoeal diseases, while other strains naturally inhabit the intestinal tracts of human and animals and are important for facilitating nutrition by synthesising vitamins particularly vitamin K (Madigan et al., Reference Madigan, Bender, Buckley, Slattley and Stahl2019). Recent outbreaks of pathogenic enterohaemorrhagic E. coli O157:H7 have occurred in the UK (Gobin et al., Reference Gobin, Hawker, Cleary, Inns, Gardiner, Mikhail, McCormick, Elson, Ready, Dallman, Roddick, Hall, Willis, Crook, Godbole, Tubin-Delic and Oliver2018), while outbreaks of the Shiga toxin-producing E. coli are increasingly common (European Food Safety Authority et al., 2021).
Therefore, the aim of the present work was to use the simulated gastro-intestinal digestion protocol (SGID) developed by the COST INFOGEST Network (Brodkorb et al., Reference Brodkorb, Egger, Alminger, Alvito, Assunção, Ballance, Bohn, Bourlieu-Lacanal, Boutrou, Carrière, Clemente, Corredig, Dupont, Dufour, Edwards, Golding, Karakaya, Kirkhus, Le Feunteun, Lesmes, Macierzanka, Mackie, Martins, Marze, McClements, Ménard, Minekus, Portmann, Santos, Souchon, Singh, Vegarud, Wickham, Weitschies and Recio2019) to generate digesta at several time points and to examine their antibacterial activity against the common food pathogen E. coli using the broth micro-dilution assay. This method allowed for the study of the microbial growth curve throughout a 24-h period to determine both the extent of a lag phase and the microbial load after 24 h.
Materials and methods
Materials
Lactoferrin (Lactoferrin, Bioferrin 2000, ≥95% protein containing 15 mg Iron/100 g), was kindly donated by Glanbia Nutritionals. The digestive enzymes used were of porcine origin, pepsin (EC 3.4.23.1) and trypsin (EC 3.4.21.4) obtained from Sigma-Aldrich (Ireland), supplied as powders, and stored at −20°C. The salts (KCl, KH2PO4, NaHCO3, NaCl, MgCl2(H2O)6, (NH4)2CO3, CaCl2(H2O)2,) used in the simulated digestive fluids were of general-purpose reagent grade and obtained from Sigma-Aldrich (Ireland), along with HCl and NaOH. The bacterial strain used was Escherichia coli (Migula) Castellani and Chalmers (ATCC 8739™). Müeller-Hinton (MH) broth, maximum recovery diluent (MRD) and plate count agar (PCA) were obtained from Sparks Laboratory Supplies (Ireland). Sterile consumables were obtained from VWR International. Simulated salivary (SSF), gastric (SGF) and intestinal digestive fluids (SIF) were prepared prior to the digestion according to Brodkorb et al. (Reference Brodkorb, Egger, Alminger, Alvito, Assunção, Ballance, Bohn, Bourlieu-Lacanal, Boutrou, Carrière, Clemente, Corredig, Dupont, Dufour, Edwards, Golding, Karakaya, Kirkhus, Le Feunteun, Lesmes, Macierzanka, Mackie, Martins, Marze, McClements, Ménard, Minekus, Portmann, Santos, Souchon, Singh, Vegarud, Wickham, Weitschies and Recio2019) and were used in the procedure at a ratio of 1:1 wt/wt sample/digestive fluid. The enzyme preparations of pepsin at 2000 Units/ml and trypsin at 100 Units/ml of final volume were prepared on the day of digestion according to Brodkorb et al. (Reference Brodkorb, Egger, Alminger, Alvito, Assunção, Ballance, Bohn, Bourlieu-Lacanal, Boutrou, Carrière, Clemente, Corredig, Dupont, Dufour, Edwards, Golding, Karakaya, Kirkhus, Le Feunteun, Lesmes, Macierzanka, Mackie, Martins, Marze, McClements, Ménard, Minekus, Portmann, Santos, Souchon, Singh, Vegarud, Wickham, Weitschies and Recio2019).
In-vitro digestion of LF
LF was digested using the in-vitro simulated gastrointestinal digestion (SGID) method of Brodkorb et al. (Reference Brodkorb, Egger, Alminger, Alvito, Assunção, Ballance, Bohn, Bourlieu-Lacanal, Boutrou, Carrière, Clemente, Corredig, Dupont, Dufour, Edwards, Golding, Karakaya, Kirkhus, Le Feunteun, Lesmes, Macierzanka, Mackie, Martins, Marze, McClements, Ménard, Minekus, Portmann, Santos, Souchon, Singh, Vegarud, Wickham, Weitschies and Recio2019) with modifications. As the study was designed to examine the digestion of a sample containing ≥95% protein, protease enzymes were used exclusively with no lipase or bile salts (Minekus et al., Reference Minekus, Alminger, Alvito, Ballance, Bohn, Bourlieu, Carrière, Boutrou, Corredig, Dupont, Dufour, Egger, Golding, Karakaya, Kirkhus, Le Feunteun, Lesmes, Macierzanka, Mackie, Marze, McClements, Ménard, Recio, Santos, Singh, Vegarud, Wickham, Weitschies and Brodkorb2014). LF was prepared at 25 g/l in deionised water. SSF was added, and the mixture incubated for 2 min at 37°C in a shaking water bath at 160 movements/min, to simulate the oral phase. For the gastric phase, after addition of the SGF the pH was reduced to pH 3 ± 0.05 using 1 M HCl. Pepsin at 2000 U/ml final digesta volume was added and the sample was incubated for two hours. Aliquots were removed at different time points, at 30, 60 and 120 min, labelled LF G30, G60 and G120 respectively and the pH increased to pH 8 using 1 M NaOH to terminate the gastric digestion of these aliquots. For the intestinal phase, SIF was added to the remaining digesta, and the pH adjusted to pH 7 ± 0.05 using 1 M NaOH. Trypsin at 100 U/ml of final digesta volume was then added and the sample incubated for another two hours. Aliquots were removed at the end of the 2-h intestinal phase (240 min in total, labelled LF GI240). Undigested LF samples were prepared at 25 g/l containing the relevant digestive fluids of SSF and SGF to ensure that ion concentration was maintained, with no enzyme added. All digesta were stored at 4°C until use.
Fractionation of LF digesta
The digesta sample obtained after 30 min of gastric digestion (G30) was fractionated by ultrafiltration (UF) using different molecular weight cut off (MWCO) filter units (Amicon® Ultra-15 Centrifugal Filters) and a Hettich Rotofix 32A centrifuge. An aliquot of digesta (15 ml) was placed in the upper chamber of an UF unit fitted with a 30 kDa MWCO membrane and centrifuged at 4000 rpm for 20 min. The permeate fraction was collected and subjected to further fractionation using a 10 kDa MWCO filter. The respective retentates and filtrates were collected and yielded the following large (Mw > 30 kDa), intermediate (30 < Mw kDa < 10), and small (Mw < 10 kDa) peptide fractions. The protein content of each fraction was determined by measuring absorbance at 280 nm using UV spectroscopy and the samples were appropriately diluted to 1 mg/ml in MRD before antibacterial activity was assessed.
Antibacterial activity
Antibacterial activity of undigested LF and LF digesta samples were examined using spectrophotometric analysis (Rautenbach et al., Reference Rautenbach, Gerstner, Vlok, Kulenkampff and Westerhoff2006), involving standardised sterile techniques used in microbiology. The test strain, Escherichia coli ATCC 8739, was cultured in sterile MH broth at 37°C for 30 h under aerobic conditions (i.e., stationary phase), resulting in a cell density of approximately 109 CFU/ml. The bacterial culture was then diluted in sterilised MH to achieve approximately 105 CFU/ml, with enumerations completed using a standard plate count technique and PCA agar. This was done on each experimental day to validate the bacterial concentration (CFU/ml) of the culture. The antimicrobial activity of samples of undigested LF G0 and LF digesta G30, G60, G120, GI240, at a pH of 7 ± 0.5, were evaluated by appropriately diluting them in sterile MRD to achieve different protein concentrations (8, 4, 2, 1, 0.5, 0.25, 0.125 mg/ml), and sterilised by filtration through sterile Whatman 0.2 μm membrane PES filters (Sigma-Aldrich). 100 μl of each LF test sample and concentration were placed into individual wells on a PCR 96-well plate followed by 100 μl of 105 CFU/ml bacterial cell suspension in MH, obtaining a final bacterial concentration of approximately 5 × 104 CFU/ml. Relevant growth controls including a positive control of E. coli (+Ctrl) and negative growth controls (sterilised LF in medium, and sterilised medium) were included in each plate. Using a Thermo Scientific™ Multiskan™ FC Microplate Photometer, Absorbance values at 620 nm (Abs620) over 24-h, at 37°C were recorded every 20 min after prior minor shaking. Antibacterial activity of the samples was determined on separate days to give at least three replicates.
Antibacterial measurements
Antibacterial activity was determined by plotting bacterial growth curves and examining the effect of LF against E. coli by plotting Abs620 values recorded over a 24-h period. Two measures of antibacterial activity were determined using the bacterial growth curves. The lag phase (LP), which is the phase prior to the start of exponential growth (Madigan et al., Reference Madigan, Bender, Buckley, Slattley and Stahl2019), was measured as the period of time during which the Abs620 value did not increase by more than 5% from the value immediately post inoculation (Peleg and Corradini, Reference Peleg and Corradini2011). A significant increase in LP may be described as a delay to bacterial growth or a delay to the exponential phase and would indicate bacteriostatic activity of the relative LF sample (Fig. 1). If no increase from the initial Abs620 value was observed over 24-h, samples were assigned a LP value of 25-h for data analysis purposes and antibacterial activity was assumed to be bactericidal due to no recorded bacterial growth. A second measure of antibacterial activity was evaluated as % inhibition, which was calculated as a percentage difference between the final recorded Abs620 value after 24-h of the E. coli + Ctrl vs. the test LF sample, taking into consideration the background absorbance values of each. Significant % inhibition would indicate that the bacterial load of E. coli had been reduced, indicating a bacteriostatic effect of the sample (Fig. 1).
Figure 1. Idealised dose–response curves. Predicted bacterial growth curves plotting absorbance at 620 nm recorded every 20 min, over 24 h of (A) E. coli, with no LF, and (B) response of E. coli with LF. (**) 5% increase from initial Abs indicating exponential growth. ↕: % inhibition of LF sample compared to the +Ctrl.
Statistical analysis
Results presented are the mean of triplicate measurements for each sample. Statistical analysis was carried out using IBM SPSS 27 Statistics software. Multiple comparison tests were carried out using one-way analysis of variance (ANOVA), with least-significant difference (LSD) used post-hoc. Values of P < 0.05 were significant, and values of P < 0.001 were very significant. Results are expressed as mean ± standard deviation (sd) of n = 3 unless stated otherwise.
Results and discussion
All samples examined exhibited typical microbial growth curves characterised by a lag phase (LP), followed by an exponential growth phase where the absorbance of the medium increased to a plateau after 24-h, characteristic of the stationary phase. The LP for the positive control E. coli at initial inoculation level of 5 × 104 CFU/ml was 3.8 ± 0.3 h (n = 12). As readings were taken every 20 min, or every 0.3 h, the growth of the bacterial strain was shown to be highly reproducible across different plates and different days.
Antibacterial activity of undigested LF
Firstly, the antibacterial activity of native LF before undergoing SGID digestion was determined. Results displayed in Table 1 show the effect of undigested LF concentration on both LP and % inhibition.
Table 1. Antibacterial effect of undigested LF examining LP and % inhibition, as measured by Abs620nm after 24 h
LP, lag phase
a–dMean values with different letter indices indicate significant difference at P < 0.05.
Undigested LF did not significantly increase LP at concentrations up to 4 mg/ml inclusive (Table 1). However, at a concentration of 8 mg/ml, LP doubled to 8.1 ± 3 h, with this concentration being the only one of statistical significance, showing that high concentrations of undigested LF greater than 4 mg/ml can delay E. coli growth significantly. This effect was assumed to be bacteriostatic as bacterial growth was delayed rather than totally suppressed. For % inhibition, undigested LF significantly reduced bacterial load after 24 h at all examined concentrations (1 to 8 mg/ml), as evident from Table 1. These results demonstrate that to delay the time until exponential phase, a concentration greater than 4 mg/ml of undigested LF is required, whereas to reduce bacterial load, lower concentrations of 1 mg/ml can be significant.
Concentrations of intact bovine LF greater than 5 mg/ml have been similarly observed to alter bacterial growth by Tian et al. (Reference Tian, Maddox, Ferguson and Shu2010) against both Gram-positive and Gram-negative food pathogens including E. coli. This occurred in a dose-dependent manner when concentrations of up to 40 mg/ml were examined. LF concentrations below 5 mg/ml have been shown to be effective, as LF showed bacterial inhibition against the pathogenic strain E. coli O111 with an MIC of 2 mg/ml recorded (Tomita et al., Reference Tomita, Bellamy, Takase, Yamauchi, Wakabayashi and Kawase1991). In addition, activity has been shown against non-pathogenic E. coli strains such as E. coli K-12 (where 2 mg/ml reduced colony forming units two-fold: Murata et al., Reference Murata, Wakabayashi, Yamauchi and Abe2013) and E. coli O157:H7 strain (when a lethal concentration 50 (LC50) of LF at 1.9 mg/ml was recorded: Rastogi et al., Reference Rastogi, Nagpal, Alam, Pandey, Gautam, Sinha, Shin, Manzoor, Virdi, Kaur, Sharma and Singh2014a). As shown in Table 1, LF at 1 mg/ml exhibited a significant bacterial inhibition of 35%. Similar inhibition scores were recorded by Flores-Villaseñor et al. (Reference Flores-Villaseñor, Canizalez-Román, Reyes-Lopez, Nazmi, de la Garza, Zazueta-Beltrán, León-Sicairos and Bolscher2010) for intact LF against three different E. coli strains at this same concentration, where a minimum inhibition of 36.7% was recorded. A maximum inhibition of 81% against the enterohaemorrhagic E. coli O157:H7 strain was observed (Flores-Villaseñor et al., Reference Flores-Villaseñor, Canizalez-Román, Reyes-Lopez, Nazmi, de la Garza, Zazueta-Beltrán, León-Sicairos and Bolscher2010). In an exposure-based study on E. coli, the same concentration of LF at 1 mg/ml resulted in a bactericidal activity, as a result of bacterial membrane breakdown observed using scanning electron microscopy (Yen et al., Reference Yen, Shen, Hsu, Chang, Lin, Chen and Chen2011). Extended exposure time from 2 to 4 h resulted in more significant membrane damage than the 2 h exposure which was still significant (Yen et al., Reference Yen, Shen, Hsu, Chang, Lin, Chen and Chen2011). Our study supports the bacteriostatic properties of intact LF against Gram-negative bacteria as seen by an extended lag phase and decreased bacterial load (at 24 h) observed at low concentrations.
Effect of in-vitro digestion of LF on antibacterial activity
After undergoing SGID, the antibacterial properties of the various LF digesta were tested and compared to the undigested LF. All concentrations greater than 1 mg/ml showed significant antibacterial activity in terms of both LP and % inhibition for LF gastric digesta (2 mg/ml, 4 mg/ml). The LP effect of SGID LF digesta (Fig. 2) and the % inhibition (Table 2) are shown at a concentration of 1 mg/ml. Digested LF significantly increased LP compared to its undigested counterpart, indicating an increase of LF bacteriostatic activity upon SGID.
Figure 2. The effect of LF after undergoing SGID on the LP of E. coli, presented at 1 mg/ml, showing differences with digestion stage and time points within. Black: E. coli + Ctrl, White: Undigested LF, Diagonal Stripes: Gastric stage, Vertical Stripes: Intestinal stage. *No change in absorbance recorded after 24 h for some replicates, assigned a value of 25 h for data analysis purposes. a–dMean values with different letter indices indicate significant difference at P < 0.05. LP, lag phase.
Table 2. % inhibition by LF digesta samples detailing undigested LF and SGID LF samples at 1 mg/ml after 24 h, with negative values indicating an increase above the +Ctrl
a–dMean values with different letter indices indicate significant difference at P < 0.05.
All LF digesta at 1 mg/ml (G30, G60, G120) resulted in significantly increased LP, as shown in Fig. 2. A maximum LP of 18.7 ± 6 h was observed in the initial digestion stage after 30 min of gastric digestion (G30) which thereafter declined over time. This LP effect was lost when LF SGID samples were exposed to the intestinal digestion stage (GI240), as these samples showed no significant difference from the positive control. This transient antibacterial effect was equally observed at higher LF concentrations of 2 mg/ml and 4 mg/ml, with LP likewise peaking for the LF G30 sample and decreasing with increased digestion time until no longer statistically significant for the GI240 samples (results not shown). These results demonstrate the effectiveness of gastric generated LF peptides in delaying growth of E. coli at concentrations of 1 mg/ml and greater, albeit that this antibacterial activity decreases on extended digestion.
As can also be seen in Fig. 2, the exposure of the LF samples to a 2-h intestinal phase as part of the SGID protocol resulted in the loss of the extension of LP observed on gastric digestion. The time at which this antibacterial activity was lost during the intestinal stage was further investigated by removing additional aliquots at 15, 30 and 60 min within the intestinal digestion stage. After 15 min of in-vitro intestinal digestion, no antibacterial LP effect was observed, with all subsequent aliquots similarly exhibiting no LP effect (results not shown). This indicates that the stage of digestion can influence LF antibacterial activity, as only gastric samples altered the LP of E. coli to a significant level.
In Table 2 the effect of digestion phase on % inhibition is shown. Significant inhibition after 24-h was observed for all LF gastric digesta (G30, G60, G120) at 1 mg/ml. A twofold increase was observed when compared to the intact LF, as a maximal inhibition of 65.7% was observed for the LF G30 sample which decreased thereafter. A significant % inhibition was not observed for LF GI240, suggesting that any antimicrobial effect observed for both intact LF or any additional effect generated within the gastric stage were lost upon sample exposure to intestinal digestion conditions. This may be due to the exposure to a second hydrolysis step upon addition of the trypsin enzyme within the SGID. Results showing antibacterial activity of LF increasing after hydrolysis with a single enzyme have been previously reported. Pepsin has been used to generate antimicrobial peptides from LF over the last few decades, with the peptide LFcin B (generated by pepsin hydrolysis of bovine LF: Yamauchi et al., Reference Yamauchi, Tomita, Giehl and Ellison1993; Tomita et al., Reference Tomita, Wakabayashi, Yamauchi, Teraguchi and Hayasawa2002) showing strong antibacterial activity first being recorded against the food pathogen E. coli O111 (Tomita et al., Reference Tomita, Bellamy, Takase, Yamauchi, Wakabayashi and Kawase1991). LFcin was found to bind to lipopolysaccharides on the outer membrane of Gram-negative cells and affect bacterial growth via this direct interaction (Yamauchi et al., Reference Yamauchi, Tomita, Giehl and Ellison1993). Further investigation into this peptide shows that LFcin B has a molecular mass of 6.6 kDa (Jones et al., Reference Jones, Smart, Bloomberg, Burgess and Millar1994) and has effective antibacterial activity against a wide range of both Gram-positive and -negative bacteria (Bellamy et al., Reference Bellamy, Takase, Wakabayashi, Kawase and Tomita1992a, Reference Bellamy, Takase, Yamauchi, Wakabayashi, Kawase and Tomita1992b; Jones et al., Reference Jones, Smart, Bloomberg, Burgess and Millar1994). LFcin B is thought to exhibit bactericidal activity against E. coli by interacting with the lipopolysaccharides and causing depolarisation of the bacterial membranes (Ulvatne et al., Reference Ulvatne, Haukland, Olsvik and Vorland2001, Ulvatne and Vorland, Reference Ulvatne and Vorland2001). In a recent animal study, Haiwen et al. (Reference Haiwen, Rui, Bingxi, Qingfeng, Jifeng, Xuemei and Beibei2019) examined LFcin B against E. coli O157:H7, showing that intestinal damage caused by this enterohaemorrhagic bacteria was attenuated in the animals consuming this LF peptide at a dose of 0.5 mg/kg body weight. Another Gram-negative bacteria, Pseudomonas syringae, has also been shown to be inhibited by bovine LF hydrolysates generated by pepsin at pH 3 and 37°C, with this antibacterial activity shown to be associated with small peptides generated from the N-terminal region of the bovine LF molecule (Kim et al., Reference Kim, Kim and Shimazaki2016). When trypsin was used to hydrolyse LF, the tryptic hydrolysates of LF were more effective than the intact LF counterpart against the Gram-negative bacteria E. coli and Yersinia enterocolitica (Rastogi et al., Reference Rastogi, Nagpal, Alam, Pandey, Gautam, Sinha, Shin, Manzoor, Virdi, Kaur, Sharma and Singh2014a).
The outcome seen here of LF digesta exhibiting maximal antibacterial effect in a time-dependent manner, with a short 30 min digesta sample exhibiting the highest activity when compared to 60 and 120 min digestion, is novel. Tomita et al. (Reference Tomita, Bellamy, Takase, Yamauchi, Wakabayashi and Kawase1991) examined the antibacterial activity of peptic digests of LF against E. coli O111. Similar to the findings of the present study, the authors found that antibacterial activity was generated after only 30 min of digestion. However, in contrast to the present findings, they found that the activity persisted after 4 h of pepsin hydrolysis, with no transient decrease observed. More recent investigations have examined only one time point of the relevant LF hydrolysis for the generation of antibacterial LF peptides. For example, in a recent study examining a lactoferrin supplemented milk fat globule membrane, gastric digesta showed bacteriostatic activity against a Cronobacter sakazakii strain, although only an aliquot at the end of the 120 min gastric phase was examined (Abad et al., Reference Abad, Serrano, Graikini, Pérez, Grasa and Sánchez2023). The duration of the hydrolysis varies dramatically between experiments, from 30 min with human gastric juices (Furlund et al., Reference Furlund, Ulleberg, Devold, Flengsrud, Jacobsen, Sekse, Holm and Vegarud2013), 90 min with trypsin (Rastogi et al., Reference Rastogi, Nagpal, Alam, Pandey, Gautam, Sinha, Shin, Manzoor, Virdi, Kaur, Sharma and Singh2014a, Reference Rastogi, Singh, Pandey, Sinha, Bhushan, Kaur, Sharma and Singh2014b), 240 min with pepsin (Kim et al., Reference Kim, Kim and Shimazaki2016) and even 5hrs when the enzymes Proteinase K, thermolysin, trypsin, and chymotrypsin were used (Salami et al., Reference Salami, Moosavi-Movahedi, Ehsani, Yousefi, Haertlé, Chobert, Razavi, Henrich, Balalaie, Ebadi, Pourtakdoost and Niasari-Naslaji2010), with intermediate aliquots not examined. Hence, the observed transient change in LF antibacterial activity seen within this SGID experiment has not been indicated before.
When Furlund et al. (Reference Furlund, Ulleberg, Devold, Flengsrud, Jacobsen, Sekse, Holm and Vegarud2013) used human gastric juice followed by human duodenal juices in an in-vitro digestion system to digest bovine LF, large peptides were produced after 30 min of gastric digestion step which were degraded to smaller peptides following the 30 min intestinal digestion step. This could explain the loss of antibacterial activity of the LF digesta observed for the gastric sample in this experiment, as upon entering the intestinal SGID phase (LF GI240), the peptides with antibacterial activity may have been degraded in such a manner that the potency reduced over time, as observed with the maximal LF G30 sample which decreased in a transient manner and terminated after the SGID intestinal phase. Therefore, the complete loss of antibacterial activity in the LF digesta samples after exposure to SGID intestinal conditions may be as a result of tryptic degradation of the antibacterial peptides produced during the gastric stage of the SGID. This result is in contrast to a recent study that showed that the intestinal digesta of a lactoferrin supplemented milk fat globule membrane resulted in a greater antibacterial effect than the gastric digesta (Abad et al., Reference Abad, Bailac, Pérez, Carramiñana, Calvo and Sánchez2024), although this was seen against S. aureus which is a Gram-positive bacteria. As seen in this study, digestion of LF resulted in significantly increased LP and % inhibition compared to its undigested counterpart, indicating an increase of LF bacteriostatic activity due to the generation of antibacterial peptides from bovine LF hydrolysis during SGID. Notably, this antibacterial effect was observed at a high inoculation level of <104 CFU/ml, showing the potential of LF to provide antibacterial activity to the host due to the generation of antimicrobial peptides during the digestive process.
LF G30 concentration effect
Since the maximum antibacterial effect was observed for the LF G30 digesta sample, a more detailed analysis was carried out to establish if a dose–response relationship existed (Fig. 4) and an attempt to identify the fraction responsible for the antibacterial activity within this sample was also completed. Figure 3 shows a classic dose response on the effect of increasing concentration of LF G30 on the LP, where a direct relationship between the increase in concentration and the increase in the antibacterial effect was observed. Concentrations less than 0.5 mg/ml did not significantly alter LP, while all concentrations of 1 mg/ml or greater showed significant and substantial delay to E. coli growth. At concentrations of 2 mg/ml and above, E. coli failed to grow over the 24-h incubation period. Whether these observed antibacterial effects at these higher concentrations were bacteriostatic or bactericidal was investigated by re-plating in fresh media. Results were not consistent as some re-plated replicates exhibited bactericidal activity (no growth observed), while others exhibited bacteriostatic activity only, therefore, further investigation is needed to fully establish the true nature of antibacterial activity.
Figure 3. Effect of LF G30 concentration on LP of E. coli. a–cMean values with different letter indices indicate significant difference at P < 0.05.
*Included replicates of 25 h. LP, lag phase.
Table 3 reveals a similar concentration-dependent effect for LF G30 on % inhibition of E. coli. A concentration as low as 0.25 mg/ml showed a significant (P < 0.05) % inhibition of 28.6% ± 4.9, observing a maximum % inhibition of 99.6% ± 0.09 at the highest concentration tested (4 mg/ml). These results highlight that LF after 30 min of gastric digestion can delay the onset of bacterial growth at LF concentrations over 1 mg/ml, while significantly reducing the final bacterial load at much lower concentrations as an IC50 (Rautenbach et al., Reference Rautenbach, Gerstner, Vlok, Kulenkampff and Westerhoff2006) which was achieved at 1 mg/ml.
Table 3. The effect of LF G30 concentration on the % inhibition of E. coli over 24 h
a–dMean values with different letter indices indicate significant difference at P < 0.05.
Fractionation of antibacterial digesta by ultrafiltration (UF)
An attempt was made to isolate the peptide fraction responsible for the increased antibacterial activity seen in the LF G30 digesta using filtration of digesta through 30 and 10 kDa MWCO filters (Amicon® Ultra Centrifugal Filters). The following peptide fractions were isolated: A retentate with large molecular weight, Mw > 30 kDa, an intermediate fraction between 30 and 10 kDa, and a small molecular weight fraction in the filtrate Mw < 10 kDa. All three fractions were tested for antibacterial activity examining LP effect (Fig. 4) and % inhibition (data not shown).
Figure 4. Size fractionation of LF G30 sample using MWCO units and the effect on LP, to identify the size of the fraction associated with antibacterial activity within this gastric digested sample. Different letter indices indicate significant difference at P < 0.05. MWCO, molecular weight cut off; LP, lag phase.
The large molecular weight peptide fraction at 0.5 mg/ml was the only isolated peptide fraction to increase LP significantly to 10.7 h ± 0.9 (P < 0.001). The two other two peptide fractions of lower molecular weight showed no significant effect on LP at the concentration studied, as seen in Fig. 4. In terms of % inhibition, none of the three isolated peptide fractions reduced the bacterial load after 24 h, with no significant % inhibition observed. These results might suggest that LF peptides within the large peptide fraction >30 kDa at the concentration tests were mostly responsible for the antibacterial activity of the LF G30 sample. The antibacterial activity of this sample was observed at half the concentration (0.5 mg/ml) at which the non-fractionated LF G30 showed significant antibacterial activity (1 mg/ml). Another instance where peptides of Mw ~30 kDa, derived from LF hydrolysis, showed antibacterial activity against E. coli was when tryptic derived bovine LF fractions 21, 38 and 45 kDa exhibited a significant reduction in E. coli viability at 1.5 mg (Rastogi et al., Reference Rastogi, Nagpal, Alam, Pandey, Gautam, Sinha, Shin, Manzoor, Virdi, Kaur, Sharma and Singh2014a). Thus, it appears that the >30 kDa fraction within this study was effective at much lower concentrations (0.5 mg/ml), than those previously reported.
Our antibacterial activity against E. coli was only observed in the high molecular weight fraction of >30 kDa. This contrasts with much of the reported literature in which antimicrobial activity of LF hydrolysates against both Gram-negative and -positive bacteria is largely attributed to relatively small peptides such as LFcin f(17–41) (Bellamy et al., Reference Bellamy, Takase, Yamauchi, Wakabayashi, Kawase and Tomita1992b), LFcin B f(17–30) (Hwang et al., Reference Hwang, Zhou, Shan, Arrowsmith and Vogel1998), and LFampin f(265–284))(van der Kraan et al., Reference van der Kraan, Groenink, Nazmi, Veerman, Bolscher and Nieuw Amerongen2004). These would be expected to have been found within the smallest peptide fraction of <10 kDa in the present study. In addition to this, previous studies report that the antibacterial activity of hydrolysed LF was due to the presence of small peptides generated from the N-terminal region of the bovine LF molecule (Kim et al., Reference Kim, Kim and Shimazaki2016). The expectation of finding previously characterised antibacterial LF peptides within samples after undergoing digestive hydrolysis was similarly not observed by Furlund et al. (Reference Furlund, Ulleberg, Devold, Flengsrud, Jacobsen, Sekse, Holm and Vegarud2013) who could not identify LFcin f(17–41) during either in-vitro or in-vivo digestion. Therefore, these results suggest that there may be a large peptide fraction generated from LF by hydrolysis within an in-vitro digestion system that can exhibit significant antibacterial activity against a Gram-negative bacterium, which has yet to be fully characterised.
In conclusion, bovine LF significantly inhibited growth of E. coli at high concentrations. This microbial inhibitory potential significantly increased upon exposure to gastric digestive conditions for short periods of 30 min but declined on continued SGID, disappearing completely upon exposure to intestinal conditions. LF G30 digesta showed concentration dependent effects on both LP and % inhibition. The largest peptide fraction isolated from the LF G30 sample of Mw > 30 kDa appeared to be chiefly responsible for the observed antibacterial effect, particularly on the extension of LP, which was significant at a low concentration of 0.5 mg/ml. These results point towards a transient generation of large antibacterial LF peptides within the digestive process that peaks in the early gastric stage and need further characterisation. These findings suggest that a small concentration of intact LF within a contaminated food could provide antibacterial protection to the host acting as a bacteriostatic agent.
Open access
