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. 2020 Mar 18;86(7):e02312-19.
doi: 10.1128/AEM.02312-19. Print 2020 Mar 18.

Competitive Exclusion Is a Major Bioprotective Mechanism of Lactobacilli against Fungal Spoilage in Fermented Milk Products

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Competitive Exclusion Is a Major Bioprotective Mechanism of Lactobacilli against Fungal Spoilage in Fermented Milk Products

Solvej Siedler et al. Appl Environ Microbiol. .

Abstract

A prominent feature of lactic acid bacteria (LAB) is their ability to inhibit growth of spoilage organisms in food, but hitherto research efforts to establish the mechanisms underlying bioactivity focused on the production of antimicrobial compounds by LAB. We show, in this study, that competitive exclusion, i.e., competition for a limited resource by different organisms, is a major mechanism of fungal growth inhibition by lactobacilli in fermented dairy products. The depletion of the essential trace element manganese by two Lactobacillus species was uncovered as the main mechanism for growth inhibition of dairy spoilage yeast and molds. A manganese transporter (MntH1), representing one of the highest expressed gene products in both lactobacilli, facilitates the exhaustive manganese scavenging. Expression of the mntH1 gene was found to be strain dependent, affected by species coculturing and the growth phase. Further, deletion of the mntH1 gene in one of the strains resulted in a loss of bioactivity, proving this gene to be important for manganese depletion. The presence of an mntH gene displayed a distinct phylogenetic pattern within the Lactobacillus genus. Moreover, assaying the bioprotective ability in fermented milk of selected lactobacilli from 10 major phylogenetic groups identified a correlation between the presence of mntH and bioprotective activity. Thus, manganese scavenging emerges as a common trait within the Lactobacillus genus, but differences in expression result in some strains showing more bioprotective effect than others. In summary, competitive exclusion through ion depletion is herein reported as a novel mechanism in LAB to delay the growth of spoilage contaminants in dairy products.IMPORTANCE In societies that have food choices, conscious consumers demand natural solutions to keep their food healthy and fresh during storage, simultaneously reducing food waste. The use of "good bacteria" to protect food against spoilage organisms has a long, successful history, even though the molecular mechanisms are not fully understood. In this study, we show that the depletion of free manganese is a major bioprotective mechanism of lactobacilli in dairy products. High manganese uptake and intracellular storage provide a link to the distinct, nonenzymatic, manganese-catalyzed oxidative stress defense mechanism, previously described for certain lactobacilli. The evaluation of representative Lactobacillus species in our study identifies multiple relevant species groups for fungal growth inhibition via manganese depletion. Hence, through the natural mechanism of nutrient depletion, the use of dedicated bioprotective lactobacilli constitutes an attractive alternative to artificial preservation.

Keywords: Lactobacillus; bioprotection; food spoilage; genome editing; lactic acid bacteria; manganese starvation.

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Figures

FIG 1
FIG 1
Growth of D. hansenii in aqueous phase (AQ) of reference (REF) yogurt (red bars) and bioprotective strains (BioP) containing yogurt (blue bars). (A) The REF AQ and BioP AQ were diluted with tap water (clear bars) or MilliQ water (striped bars). Growth of D. hansenii was measured at 600 nm after 4 days of incubation at 17°C. (B) Effect of complementation BioP AQ with metals found in milk on the growth of D. hansenii (light blue bars). Growth was measured after 5 days of incubation at 17°C and compared to REF AQ without any addition of metal ions. Metal concentrations were used as found in milk (0.3 mg/liter Fe2+, 0.1 mg/liter Cu2+, 4.2 mg/liter Zn2+, 60 mg/liter Mg2+, and 0.03 mg/liter Mn2+). Mean and standard deviation of three replicates are indicated by the bars and error bars. Hashtags (#) indicate data being statistically significantly different (P < 0.0001) from REF AQ (A, Student's t test; B, one-way ANOVA), and asterisks (*) indicate data being different from BioP AQ diluted with MilliQ water (A, two-way ANOVA) or undiluted/nonsupplemented BioP AQ (B, one-way ANOVA).
FIG 2
FIG 2
Yeast growth in BioP AQ without (dark blue) and with (light blue) the addition of 0.6 mg/liter manganese and in REF AQ (red) after 5 days of incubation at 17°C. The following yeasts were tested: D. hansenii strain 1 (A), D. hansenii strain 2 (B), S. cerevisiae (C), R. mucilaginosa (D), C. fragicola (E), and T. delbrueckii (F). Individual data points for the 6 to 9 replicates are shown along with indications of mean ± standard deviation. Hashtags (#) indicate data being statistically significantly different (P < 0.05) from REF AQ, and asterisks (*) indicate data being different from nonsupplemented BioP AQ (one-way ANOVA).
FIG 3
FIG 3
Growth of 3 different molds: P. brevicompactum (A), P. crustosum (B), and P. solitum (C) on plates prepared from milk fermented with starter culture alone (REF) or both starter and bioprotective culture (BioP). Different manganese concentrations were added as indicated. The spoilage molds were added in concentrations of 500 spores/spot. The plates were incubated at 22°C for 8 days.
FIG 4
FIG 4
Overall and mntH1-specific gene count distribution. (A) Sample-normalized gene count distribution of BioP L. rhamnosus and L. paracasei during coculture after 6 h milk fermentation. A white circle denotes the mntH1 count level. (B) Temporal, sample-normalized mntH1 count levels of BioP strains during 37°C milk fermentation (4 h, 6 h), and after 6 h of 37°C milk fermentation and 18 h of 7°C storage (6 + 18 h). (C) Normalized mntH1 count levels after 6 h of coculture (strains A and B) and individual culture (strain A, strain B, and strain C) in milk. Normalization is here performed individually for each strain, also for coculture. Included are the BioP strains (strains A and B) and an L. paracasei strain with a lower level of bioprotective activity (strain C).
FIG 5
FIG 5
Effect of mntH1 deletion on yeast growth inhibition. Yeast growth in AQ of milk fermented by wild-type L. paracasei strain B (WT) and ΔmntH1 L. paracasei strain B, without (full bars) and with 0.6 mg/liter manganese addition (dashed bars). Two yeast, D. hansenii 1 (A) and D. hansenii 2 (B), were included, and the growth was measured after 5 days of incubation at 17°C. Means and standard deviations of two biological replicates are indicated by bars and error bars. Hashtags (#) indicate data being statistically significantly different (P < 0.0001) from WT with manganese (Student's t test).
FIG 6
FIG 6
Growth scores of D. hansenii after 4 days of incubation at 17°C in fermented milk with a strain containing (blue) and not containing (red) an mntH gene. The addition of 6 mg/liter manganese restored the yeast growth in all cases (black). The average and standard deviation of two biological independent experiments are shown (n = 2).

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