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The biopreservation of foods using bacteriocinogenic lactic acid bacteria (LAB) isolated directly from foods is an innovative approach. The objectives of this study were to isolate and identify bacteriocinogenic LAB from various cheeses and yogurts and evaluate their antimicrobial effects on selected spoilage and pathogenic microorganisms in vitro as well as on a food commodity.
LAB were isolated using MRS and M17 media. The agar diffusion bioassay was used to screen for bacteriocin or bacteriocin-like substances (BLS) producing LAB using Lactobacillus sakei and Listeria innocua as indicator organisms. Out of 138 LAB isolates, 28 were found to inhibit these bacteria and were identified as strains of Enterococcus faecium, Streptococcus thermophilus, Lactobacillus casei and Lactobacillus sakei subsp. sakei using 16S rRNA gene sequencing. Eight isolates were tested for antimicrobial activity at 5°C and 20°C against L. innocua, Escherichia coli, Bacillus cereus, Pseudomonas fluorescens, Erwinia carotovora, and Leuconostoc mesenteroides subsp. mesenteroides using the agar diffusion bioassay, and also against Penicillium expansum, Botrytis cinerea and Monilinia frucitcola using the microdilution plate method. The effect of selected LAB strains on L. innocua inoculated onto fresh-cut onions was also investigated.
Twenty percent of our isolates produced BLS inhibiting the growth of L. innocua and/or Lact. sakei. Organic acids and/or H2O2 produced by LAB and not the BLS had strong antimicrobial effects on all microorganisms tested with the exception of E. coli. Ent. faecium, Strep. thermophilus and Lact. casei effectively inhibited the growth of natural microflora and L. innocua inoculated onto fresh-cut onions. Bacteriocinogenic LAB present in cheeses and yogurts may have potential to be used as biopreservatives in foods.
Lactic acid bacteria (LAB) are generally recognized as safe (GRAS microorganisms) and play an important role in food and feed fermentation and preservation either as the natural microflora or as starter cultures added under controlled conditions. The preservative effect exerted by LAB is mainly due to the production of organic acids (such as lactic acid) which result in lowered pHs ([Daeschel 1989]). LAB also produce antimicrobial compounds including hydrogen peroxide, CO2, diacetyl, acetaldehyde, D-isomers of amino acids, reuterin and bacteriocins (Cintas et al. ).
Bacteriocins are ribosomally synthesized antimicrobial peptides that are active against other bacteria, either of the same species (narrow spectrum), or across genera (broad spectrum) (Bowdish et al. ; Cotter et al. ). Bacteriocins may be produced by both gram negative and gram positive bacteria (Savadogo et al. ). In recent years, bacteriocin producing LAB have attracted significant attention because of their GRAS status and potential use as safe additives for food preservation (Diop et al. ). Nisin, produced by Lactococcus lactis, is the most thoroughly studied bacteriocin to date and has been applied as an additive to certain foods worldwide (Delves-Broughton et al. ). Substantial work has been done on the effectiveness of nisin on various spoilage and pathogenic microorganisms such as L. monocytogenes and its application in different food products ([Staszewski and Jagus 2008]; Freitas et al. ; Schillinger et al. ). Other bacteriocins such as pediocin, may also have potential applications in foods, though they are not currently approved as antimicrobial food additives (Naghmouchi et al. ).
Fresh fruits and vegetables harbor various microorganisms, some of which are psychrotrophic. L. monocytogenes is one of the pathogenic bacteria capable of growing at refrigeration temperatures. Moreover, it is also tolerate to acidic pH and salt concentrations up to 10% ([Tasara and Stephan 2006]; Vescovo et al. ). Therefore, it is important to seek biopreservatives that control both spoilage and pathogenic microorganisms including L. monocytogenes. Although several studies have indicated the presence of LAB species with antagonistic activity for improving the quality and safety of meat and dairy products (Gagnaire et al. ; [Stiles and Holzapfel 1997]), few reports have involved fresh produce (Trias et al. [2008a,b]). Since the isolation and screening of microorganisms from natural sources has always been the most powerful means for obtaining useful and genetically stable strains for industrially important products (Ibourahema et al. ), in the prsent study, we isolated and identified bacteriocinogenic LAB from cheeses and yogurts, then further evaluated their antimicrobial effects in vitro and on fresh-cut produce inoculated with L. innocua, a surrogate bacteria for L. monocytogenes.
LAB were isolated from 7 commercial cheeses: [Tre Stelle® bocconcini cheese (TSB); Tre Stelle® fromage romano cheese (TSR); Saputo® feta cheese (SF); Agropur® signature rondoux pure goat cheese (ASR); Agropur® signature OKA cheese (OKA); Arla® fontina cheese (Arla) and Jarlsberg® firm ripened cheese (JFR)]; plus 3 commercially available yogurts: (Danone, Activia®; Astro® BioBest yogurt; and Bioghurt® Liberte yogurt), and one in- house produced yogurt.
A 25g sample of cheese was weighed into filtered stomacher bags (Fisher Scientific, Nepean, ON, Canada) and mixed with 225ml of sterile 0.1% (w/v) peptone water (Fisher Scientific). Samples were blended at 280rpm for 3min (400C stomacher circulator, Seward, England). For yogurt samples, 1ml of sample was added to 99ml of sterile 0.1% peptone water. All samples were serially diluted and 50uL of each dilution was spiral plated onto de Man, Rogosa and Sharp (MRS) agar, (Oxoid, Basingstoke, UK) and M17 agar (Oxoid). MRS plates were incubated at 37°C under both aerobic and anaerobic conditions for 48h and M17 plates at 44°C under anaerobic condition for 48h. All gram positive, catalase negative (3%v/v H2O2) isolates were purified and observed under a light microscope. All isolates were coded and stored in MRS or M17 broth containing equal amounts of 30% sterile glycerol at - 80°C.
The agar diffusion bioassay described by Herreros et al. () was used to screen for bacteriocin producing LAB among the 138 isolates. L. innocua (ATCC 33090TM) and Lact. sakei (ATCC 15521TM) were used as indicator bacteria. L. innocua was incubated overnight in Brain Heart Infusion broth (BHI, Fisher Scientific, ON, Canada) at 37°C and Lact. sakei was cultured anaerobically in MRS broth at 37°C.
One ml of each indicator organism (5×105cfuml-1) was inoculated into 15ml of semisolid BHI or MRS agar (BHI or MRS broth plus 0.7% bacteriological agar) maintained at 50°C and then poured into a petri dish. After solidification, three wells (5mm diameter) were cut and 35μl of cell-free supernatant (CFS) from each LAB isolate and appropriately adjusted was added to each well. CFS were prepared as follows: one ml of frozen LAB isolate was cultured overnight in 20ml MRS or M17 broth then 1ml culture was sub-cultured overnight in 20ml MRS broth. Cells were removed by centrifuging at 14,000g for 5min (Sorvall RC6 PLUS, Thermo-electron Corporation, Asheville, NC, USA). The supernatant was filtered through a sterile 0.22μm syringe filter (Chromatographic Specialties Inc., ON, Canada) and 35 μl of the unadjusted aliquot of CFS was added to the first well. The remaining CFS was adjusted to pH 6.0 with 1moll-1 NaOH in order to rule out possible inhibition effects due to organic acids. 35 μl of the pH adjusted CFS was filtered and added to the second well. The neutralized CFS was then treated with 1mgml-1 of catalase (Sigma-Aldrich Corporation, USA) at 25°C for 30min to eliminate the possible inhibitory action of H2O2 and filtered, then was placed in the third well. If inhibitions zones were found in the third well, the isolates were considered to be able to produce BLS.
The BHI or MRS plates were incubated at 37°C aerobically for 24h or at 37°C anaerobically for 24h, respectively. Inhibition zones were measured using an electronic caliper with digital display (MastercraftMD, Miami, FL, USA). Screenings for bacteriocin producing LAB were repeated twice for each isolate.
To confirm production of a proteinaceous compound, CFS displaying antimicrobial potential after acid neutralization and H2O2 elimination were treated with 1mgml-1 of proteolytic enzymes, including proteinase K (33 U mg-1), α-chymotripsin (66 U mg-1), and trypsin (105 U mg-1) (Sigma- Aldrich Corporation, USA) at 37°C for 2h (Bonadè et al. , Herreros et al. ). Antimicrobial activity of treated CFS was determined by the agar diffusion bioassay as described above.
Near full-length 16S rRNA gene sequencing was used to identify unknown bacteriocin producing LAB strains based on the method of Abnous et al. (). Briefly, genomic DNA was extracted from isolates using the UltraCleanTM Microbial DNA Isolation kit (MO Bio laboratories, Inc., Carlsbas, CA, USA). Universal primers F44 (5’RGTTYGATYMTGGCTCAG-3’) and R1543 (5’-GNNTACCTTKTTACG ACTT-3’) (Abnous et al., ) were used for the amplification of the 16S rRNA gene by PCR. PCR reactions were carried out using a Biometra thermal cycler (Montreal Biotech Inc., Kirkland, QC, Canada) with the following cycle parameters: an initial denaturation at 94°C for 2min, followed by 35cycles of denaturation at 94°C for 30s, annealing at 52°C for 30s, and elongation at 72°C for 1min. A final elongation step was performed at 72°C for 5min. PCR amplicons were separated by agarose gel electrophoresis (0.8%w/v) and visualized by staining with ethidium bromide.
The PCR products were cloned into the psc-A-amp/kan vector using the StrataClone PCR Cloning kit (Stratagene, La Jolla, CA) and transformed into E. coli according to the manufacturer’s instructions. Transformants were grown overnight in Luria-Bertani broth supplemented with 100μgml-1 ampicillin. Plasmids were extracted and purified from selected E. coli clones with the UltraClean TM mini plasmid prep kit (MO Bio Laboratories) according to the manufacturer’s recommendations and then sequenced using the Big Dye Terminator v3.1cycle sequencing kit. A homology search of the sequences was conducted using the BLAST program at the NCBI database.
Based on identified LAB species, isolation source and the size of inhibition zones, eight LAB isolates were chosen for thermal stability tests. The pH adjusted and H2O2 eliminated CFS described above were treated at 80 and 100°C for both 60 and 90min, and at 121°C for 15min. pH adjusted and H2O2 eliminated CFS without any heat treatments served as a controls. Residual antimicrobial activity of heat-treated CFS was determined by the agar diffusion bioassay compared to the control using L. innocua as the indicator bacteria.
The antibacterial effects of eight selected LAB isolates on six common food borne pathogens or spoilage organisms at 5 and 20°C were investigated using the agar diffusion bioassay described above. Targeted indicator organisms and their respective media used were as follows: L. innocua (BHI, DifcoTM, Spark, MD), E. coli K-12 (ATCC 10798TM) (Tryptic Soy Broth, DifcoTM), B. cereus (ATCC 14579TM) (Nutrient Broth (NB), DifcoTM), Ps. fluorescens (A7B) (NB), Erw. carotovora (ATCC 15713TM) (NB) and Leuc. mesenteroides subsp. mesenteroides (ATCC 8293TM) (MRS, DifcoTM). All strains were cultured aerobically for 24h at their optimal growth temperatures: 26°C for Erw. carotovora, Ps. fluorescens and Leuc. mesenteroides; 30°C for B. cereus; and 37°C for E. coli and L. innocua. LAB isolates were sub-cultured and the CFS was prepared as previously described. Following inoculation, plates were incubated at 5 and 20°C for 7 d and 24h, respectively. Inhibition zones were measured as before.
The microdilution method described by Lavermicocca et al. () with some modifications was used to test the eight LAB isolates against P. expansum (Pex 03–10.1), B. cinerea (B94-b) and M. fructicola (Mof 03–25) at 5 and 20°C. Fungi were obtained from the culture collection at our Research Centre, AAFC. The stock cultures were stored as spore or mycelial suspensions in 15% glycerol (v/v) at −80°C. Conidia of P. expansum were collected from 4 d-old cultures grown on potato dextrose agar (PDA) at 25°C. Conidia of B. cinerea were collected from 12 d-old cultures grown under a 12h light/dark cycle on Pseudomonas Agar F at 22°C. Conidia of M. fructicola were collected from 12 d-old cultures grown on modified V-8TM medium at 25°C. Using sterile distilled water, the density of spore suspensions were diluted to 2×105 spores ml-1 as determined using a haemocytometer (Hausser Scientific, PA, USA).
Microdilution tests were performed in sterile 96-well micro dilution plates (Costar 3370, Corning Incorporated, Corning, NY, USA). 200μl of test solution consisting of 185μl LAB CFS inoculated with 15μl of conidial suspension was dispensed into the wells. Microdilution plates were incubated at either 20 or 5°C and the optical density (OD) at 580nm was recorded at specific time intervals using a microtiter plate reader/ spectrophotometer (Spectra MAX 190, Molecular Devices, CA, USA). For the 20°C plates, OD values were measured at 0, 24, 40, 48 or 72h, while at 5°C, they were measured at 0, 48, 72, 96 or 120h. For each fungus, both positive controls containing 185μl MRS broth and 15μl conidial suspension and negative controls containing 185μl LAB CFS and 15μl dead conidial suspension were prepared and monitored. Experiments were repeated three times.
Ent. faecium, Strep. thermophilus and Lact. casei were chosen for in vivo tests. Fresh-cut yellow onions processed at a commercial facility were supplied by Nova Agri Inc. (Canning, NS). Ent. faecium and Lact. casei were incubated anaerobically in MRS broth at 37°C for 16h. Strep. thermophilus was incubated anaerobically in M17 broth at 43°C for 16h. LAB were sub-cultured twice and then centrifuged at 14,000g for 5min. Pellets of LAB were washed using sterile distilled water, centrifuged, re-suspended and inoculated onto the batches of diced onions using a calibrated TLC sprayer to give a final concentration of 5×105cfug-1. Diced onions inoculated with sterile distilled water served as a control. Samples were left to dry for 10min, then 100g was transferred to food grade bags (Golden Eagle-VH-62 190) and sealed using an electric sealer (FoodSaver V2490, Tilia International Inc. US). The densities of naturally occurring (indigenous) LAB, Pseudomonas sp., yeasts and moulds, Listeria sp. and Enterobacteriaceae were enumerated following 0, 3, 6, 9 and 12 d of storage at 4°C. LAB were cultured anaerobically on MRS Agar at 37°C for 48h; Pseudomonas sp. on Pseudomonas selective medium at 30°C for 48h; yeasts and moulds on PDA supplemented with chloramphenicol (DifcoTM) at 25°C for 48h; and Enterobacteriaceae on Violet Red Bile Agar (VRBG)(DifcoTM) at 37°C for 48h. Colonies were counted using an aCOLyte automated colony counter (Synbiosis, Cambridge, England) and expressed as cfug-1 of diced onions.
L. innocua was sub-cultured into BHI broth and incubated at 37°C for 24h. The selected LAB strains and inoculation procedures were the same as described above. The final density of L. innocua inoculated on fresh-cut onions was 5×103cfug-1. After drying for 10min, the LAB species were inoculated respectively onto the fresh-cut onions at a density of 5×105cfug-1. A batch of fresh-cut onions inoculated with L. innocua alone was used as the control. Samples (100g/ bag) were stored at 4°C and Listeria sp. and LAB were enumerated following 0, 3, 6, 9 and 12 d. Listeria sp. was cultured on Listeria selective medium at 35°C for 48h and LAB on MRS agar at 37°C for 48h anaerobically.
The initial screening for bacteriocin producing LAB from 138 LAB isolates was repeated twice. For antimicrobial tests, a three repetition split-split plot design was used with the eight LAB isolates on the main plot versus the six bacteria (or three fungi) on the sub plot, which was then split into two temperatures (5 and 20°C). For the in vivo testing, non-inoculation or inoculation of L. innocua was designed on the main plot with the three LAB strains used to investigate the treatment effect on naturally occurring microflora and introduced L. innocua on the onions. The sub plot was represented by sample removal at days 0, 3, 6, 9 and 12. Data were analyzed using the ANOVA directive and standard errors of mean (SEM) option of GenStat® (12th Edition, VSN International Ltd, Hemel Hempstead UK, 2009). The results of a Principal Components Analysis (PCA) were discussed in terms of component scores.
A total of 160 potential LAB strains were isolated from 11 different cheeses and yogurts. Eighty seven isolates were obtained from MRS agar and 73 from M17 medium. Of these, 138 were gram positive and catalase negative, and were cocci or rod in shape. Twenty percent of isolates showed antimicrobial activity against at least one indicator that is presumed to be attributable to BLS, which was determined after the neutralization of pH, and the elimination of H2O2 from the CFS (Table (Table1).1). All 28 LAB isolates had BLS inhibitory effect on L. innocua, while BLS produced by 20 isolates were effective against Lact. sakei.
The BLS from all 28 LAB isolates lost their anti-listerial activity following treatment with proteinase K, α-chymotripsin and/or trypsin (Table (Table2).2). However, when Lact. sakei was used as an indicator, the BLS produced by the different LAB stains had varying activity following treatment with these enzymes. Nevertheless, the lost antimicrobial ability following treatment with proteolytic enzymes indicated the proteinaceous nature of the BLS.
Near-full length sequencing of the 16S rRNA gene for the 28 bacteriocin producing LAB identified the isolates as follows: 24 strains of Ent. faecium, two strains of Strep. thermophilus, one strain of Lact. casei and one strain of Lact. sakei subsp. sakei.
The BLS produced by the eight selected LAB isolates were heat-treated at 80 and 100°C for 60 and 90min, respectively. BLS were thermal stable at these heat conditions above as their inhibitory effects against L. innocua were retained (Table (Table3).3). However, BLS were sensitive to autoclaving at 121°C for 15min displaying either smaller or no inhibition zones compared to the control. Isolates Strep. thermophilus (ASR-1) and Lact. casei (JFR-5) totally lost their anti-listerial activity subsequent to exposure to 121°C for 15min.
The CFS from the eight LAB isolates significantly inhibited the growth of all bacteria tested (p<0.05) at 5 and 20°C with the exception of E. coli (Table (Table4).4). Neutralized CFS from isolates Arla-18, ASR-6, JFR-1, OKA-14, and Yog-3S continued to inhibit the growth of Leuc. mesenterioides at 5°C. After pH neutralization and H2O2 elimination, the CFS from the eight LAB isolates had inhibitory effects only on L. innocua but not the other test bacteria suggesting that organic acids and /or H2O2 produced by LAB had strong antimicrobial effects on bacteria tested.
In conducting a principal components analysis, we intended to figure out that the principal component had as high a variance as possible (accounted for as much of the variability in our data as possible). It was found that score 1 was a contrast between L. innocua (control), L. innocua (pH neutralized), Leuc. mesenteroides (pH neutralized), Erw. carotovora (control), B. cereus (control) vs Ps. fluoresecens (control) (Figure (Figure1).1). A high score 1 was dominated by the values (inhibitory zones) at 5°C except for Strep. thermophilus and Lact. casei. All the CFS produced by Ent. faecium (Arla-18, ASR-6, JFR-1, OKA-14, and Yog-3S) had a similar antibacterial activity towards all the bacteria tested at both temperatures. The effects of untreated CFS and neutralized CFS from the eight LAB isolates on L. innocua highly correlated at 5 and 20°C.
No significant difference among the eight LAB isolates was observed with respect to inhibition of spore germination of M. fructicola, B. cinerea and P. expansum at either 5 or 20°C (p>0.05). Therefore, data for antifungal ability of untreated CFS, pH neutralized CFS, and pH neutralized and H2O2 eliminated CFS from the eight isolates were averaged, respectively, and compared to the positive controls. At 5 and 20°C, untreated CFS was the most effective at inhibiting fungal growth compared to their controls (Figure (Figure2).2). Neutralized CFS also had an inhibitory effect on the growth of these fungi (p <0.001). However, pH neutralized and H2O2 eliminated CFS showed no significant effect on fungal growth at 20°C (Figure (Figure2a1,2a1, a1,2b1,2b1, and and2c1).2c1). Similar results were found at 5°C as the CFS, but not the BLS, produced by the eight LAB were effective in controlling the fungal growth (Figure (Figure2a2,2a2, a2,2b2,2b2, and and22c2).
Three LAB species inoculated on fresh-cut onions significantly inhibited Pseudomonas sp. (p=0.02) (Figure (Figure3a)3a) and lactose-positive (Lac+) Enterobacteriaceae (p=0.042) (Figure (Figure3b)3b) during 12 d when stored at 5°C compared to non-LAB inoculated controls. On day 12, Lac+Enterobacteriaceae increased to 4.5 log cfug-1 on control samples while levels of 0.3, 2.2 and 1.1 log cfug-1 were obtained in Strep. thermophilus, Lact. casei and Ent. facium treated samples, respectively. However, no significant differences were found in yeast and mould levels between LAB inoculated and control samples (Figure (Figure3c).3c). Moreover, no dramatic decrease in the LAB inoculated on the fresh-cut onions was observed over the 12 d storage period (Figure (Figure3d)3d) and no naturally occurring Listeria sp. was detected in this study.
The initial density of L. innocua subsequent to their introduction onto fresh-cut onions was 3.2 log cfug-1 on day 0. During the following 12 d at 5°C, the growth of L. innocua was significantly inhibited by the LAB (p=0.042, Figure4a) as its levels were reduced by 1.0, 1.6, and 1.6 log cfug-1 in samples treated with Strep. thermophilus, Lact. casei and Ent. faecium, respectively. In contrast, levels of LAB inoculated on the fresh-cut onions remained at the initial inoculation level of 5×105cfug-1 over the 12 d storage at 5°C (Figure (Figure44b).
In the present work we isolated, identified and characterized bacteriocinogenic LAB indigenous to cheese and yogurt and explored their potential as biopreservatives. Two types of media were chosen for the isolation of LAB. First, MRS was used as a medium for LAB which gave a general scope of the flora present in the samples ([Reuter 1985]). M17 agar was also used as a selective medium for the isolation of Streptococci sp. Twenty percent of our isolates produced BLS effective against L. innocua and 16S rRNA gene sequencing determined that these isolates belonged to four LAB species. ([Sharpe 2009]) reported detecting 8.7% bacteriocinogenic strains among 92 LAB isolated from fresh-cut vegetable products, whereas Sezer and Güven () screened 12,700 LAB isolates from milk and meat products and found only 35 exhibited bacteriocin production. Therefore, the choice of food source and media are important for the successfully isolation of bacteriocinogenic LAB.
Using 16S rRNA gene sequencing to identify the 28 bacteriocinogenic LAB isolates, we found that the genus Enterococcus was predominant representing 85.7% of the isolates. Another 7.1% were Streptococcus sp. whereas the other 7.1% were Lactobacillus sp. Furthermore, all the Enterococcus sp. were identified as Ent. faecium, which was also found to be the most frequently isolated species in cured and semi-cured cheese (Cogan et al. ). López-Díaz et al. () found that 40.4% of nearly 500 strains isolated from Valdeón cheese were Enterococcus sp.
Bacteriocins can be broken down by some proteolytic enzymes leading to a loss in their antimicobial activity. In our study, we used L. innocua or Lact. sakei as indicators, and the BLS produced by different LAB stains had various inhibitory effects following treatment with proteolytic enzymes (Table (Table2).2). Similar behavior was observed by Khalil et al. () with a Bacillus megaterium19 strain isolated from a mixture of fermented vegetable wastes. They found that pepsin and trypsin treatment inhibited the bacteriocin activity against Staphylococcus aureus more than Salmonella typhimurium. Cherif et al. () used pepsin, papain, trypsin, chymotrypsin, proteinase K, lysozyme, catalase, DNase and RNase to treat thuricin 7, a bacteriocin produced by Bacillus thuringiensis BNG 1.7. They found that the inhibitory activity was only susceptible to proteinase K.
The thermal stability at 80 and 100°C (up to 90min) (Table (Table3)3) of BLS produced by our bacteriocinogenic LAB isolates may constitute an advantage for potential use as biopreservatives in combination with thermal processing in order to preserve food products. However, it should be noted that the antimicrobial effect of these BLS on L. innocua and/or Lact. sakei was markedly decreased or completely lost after treatment at 121°C for 15min. [Todorov and Dicks (2009]) reported that bacteriocin ST44AM remained stable at 25, 30, 45, 60 and 100°C for 120min. However, the activity of this bacteriocin against L. ivanovii subsp. ivanovii ATCC 19119 was reduced from 3.3×106AUml-1 to 4.1×105AUml-1 after exposure at 121°C for 20min. Similar results were reported for a bacteriocin produced by Lactobacillus CA44 (Joshi et al. ) and also thuricin 7 from B. thuringiensis BMG1.7 (Cherif et al. ).
In the present study, eight BLS producing LAB isolates were tested for their antimicrobial effects on three gram-negative, and three gram-positive bacteria, as well as three common spoilage fungi. The results showed that untreated CFS inhibited all test bacteria and fungi except for E. coli. However, after pH neutralization and H2O2 elimination, the CFS inhibited only L. innocua. Similar results were reported by [Sharpe (2009]) as they found that the BLS produced by Lact. lactis and Ent. faecium were able to control Lact. sakei and L. innocua. However, the strong antimicrobial effects associated with Lact. lactis and Ent. faecium in our study appeared to be a direct result of the organic acids and the H2O2 present in the CFS rather than the BLS. In other research, the antimicrobial activity of 12 enterococci strains was confirmed by Hajikhani et al. (), showing that Ps. aeruginosa and Proteus vulgaris were sensitive to compounds produced by enterococci but E. coli and Yersinia enterocolitica were not affected. Trias et al. ([2008a] ) treated apple wounds and lettuce cuts with the LAB strains resulting in reduced counts of Salmonella typhimurium and E. coli by 1 to 2 log cfug-1, whereas the growth of L. monocytogenes was completely inhibited. Cheikhyoussef et al. () investigated bifidin I from Bifidobacterium infantis BCRC 14602, and reported an increase in bacteriocin activity from 2. 6×102 AUmg-1 for neutralized CFS to 3.7×105 AUmg-1 for the purified bacteriocin. Simova et al. () achieved a 105 -fold increase in bacteriocin activity after a single peak was assessed upon C2/C18 reversed-phase liquid chromatography purification. The relative low concentration of bacteriocin in the CFS likely contributed to the BLS not being able to inhibit all bacteria and fungi examined in this study. Further investigation is needed to establish the method of direct use of LAB as protective cultures or that of purified bacteriocins on foods.
It has been hypothesized that organic acids act on the cytoplasmic membrane by neutralizing its electrochemical potential and increasing its permeability, thus leading to bacteriostasis and eventual death of susceptible bacteria (Dalié et al. ). The same hypothesis could also explain the susceptibility of some fungal cultures to organic acids (Batish et al. ). However, [Elsanhoty (2008]) suggested that the antifungal effect of LAB could not simply be the result of low pH but is most probably due to the formation and secretion of pH dependent antifungal metabolites. Magnusson and Schnürer () found that the antifungal metabolite produced by the Lact. coryniformis subsp. coryniformis Si3 strain was a small highly heat stable peptide and its activity was stable at pHs between 3.0 and 4.5, but rapidly decreased between 4.5 and 6.0. No inhibitory activity was detected above pH 6.0.
In the present study, selected LAB strains were also inoculated onto fresh-cut onions to investigate in vivo application of these isolates. These isolates significantly inhibited the growth of Pseudomonas sp. and Lac+Enterobacteriaceae during storage at 5°C (Figure (Figure3a,3a, a,3b).3b). Similar results were reported by [Sharpe (2009]); when L. lactis and Ent. faecium were inoculated onto fresh-cut salads, the growth of Pseudomonas sp., yeasts and total coliforms were remarkably reduced. Vescovo et al. ([1995,1996]) reported that the inoculation of ready-to-use vegetables with selected strains of LAB effectively controlled the growth of undesirable bacteria. In our challenge tests, L. innocua inoculated onto fresh-cut onions was reduced by 1 to 1.6 log cfug-1 after 12 d storage at 5°C due to the presence of selected LAB strains. Although the inoculated LAB loads did not increase during the storage period, they still significantly inhibited the growth of L. innocua. Further investigations into the mechanisms of inhibition and determination of the optimal growth conditions for LAB to produce BLS are necessary. Moreover, more studies are required to envisage the effectiveness of LAB and BLS on other food products.
The authors declare that they have no competing interests. Contribution no. 2379 of the Atlantic Food and Horticulture Research Centre, Agriculture and Agri-Food Canada (AAFC).
Authors would like to thank Drs. Greg Bezanson and Tim Ells at AAFC for their critical review and helpful suggestions in preparing the manuscript, thank Judy Kwan and Steve Brooks at Health Canada for doing the gene sequencing, and thank the MOE-AAFC Ph.D training program for supporting Ph.D students.