Biotechnology Research International

Volume 2014 (2014), Article ID 397167, 6 pages

http://dx.doi.org/10.1155/2014/397167

Research Article

Biocontrol Activity of the Local Strain of Metschnikowia pulcherrima on Different Postharvest Pathogens

Sezai Türkel,¹ Mihriban Korukluoğlu,² and Mümine Yavuz²

¹Department of Molecular Biology and Genetics, Faculty of Arts and Sciences, Uludag University, 16059 Bursa, Turkey

²Department of Food Engineering, Faculty of Agriculture, Uludag University, 16059 Bursa, Turkey

Received 21 November 2013; Revised 18 March 2014; Accepted 31 March 2014; Published 17 April 2014

Academic Editor: Shengwu Ma

Copyright © 2014 Sezai Türkel et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

The strains of the yeast Metschnikowia pulcherrima have strong biocontrol activity against various microorganisms. Biocontrol activity of M. pulcherrima largely depends on its iron immobilizing pigment pulcherrimin. Biocontrol activity of pulcherrimin producing strain, M. pulcherrima UMY15, isolated from local vineyards, was tested on different molds that cause food spoilage. M. pulcherrima UMY15 was a very effective biocontrol agent against Penicillium roqueforti, P. italicum, P. expansum, and Aspergillus oryzae in in-vitro plate tests. However, the inhibitory activity of M. pulcherrima UMY15 was less effective on Fusarium sp. and A. niger species in biocontrol assays. In addition, M. pulcherrima UMY15 strain completely inhibited the germination and mycelia growth of A. oryzae, A. parasiticus, and Fusarium sp. spores on artificial wounds of apples when they coinoculated with M. pulcherrima UMY15. Moreover, when coinoculated, M. pulcherrima UMY15 strain also inhibited the growth of P. roqueforti, P. italicum, P. expansum, A. oryzae, Fusarium sp., and Rhizopus sp. in grape juice, indicating that M. pulcherrima UMY15 can be used as a very effective biocontrol yeast against various species of postharvest pathogens, including   Penicillium, Aspergillus, Fusarium, and Rhizopus.

1. Introduction

Postharvest spoilage of fruits and vegetables by various molds results in substantial economic loss every year [1]. Certain species of Aspergillus, Penicillium, Fusarium, and Rhizopus are the major molds that can be found regularly on food stuff throughout the world. Some species or varieties of these molds also produce mycotoxins [2, 3]. Use of traditional fungicidal chemicals in postharvest disease control results in the formation of drug resistant microorganisms and large scale environmental pollution, which also causes severe health problems in human populations [4, 5]. Biological control of postharvest diseases caused by various fungal pathogens seems to be the best alternative to chemical fungicidal agents [6–8].

Different yeast species have been used as effective biocontrol agents against certain fungal pathogens [8–11]. Some of these yeasts are Metschnikowia pulcherrima, Trichosporon pullulans, Rhodotorula glutinis, Pichia membranifaciens, and Pichia anomala. Each one of these biocontrol or antagonistic yeasts can effectively inhibit growth of the various fungal pathogens on different fruits and vegetables. Some of these yeasts or their products have been commercially produced by different companies as biocontrol agents [9, 12]. Biocontrol yeasts inhibit the growth of targeted pathogens by different mechanisms. Competition for nutrient and space, secretion of specific lytic enzymes, and synthesis and secretion of specific inhibitory secondary metabolites are the only few examples of the mechanisms of the action for the biocontrol yeasts [8, 13].

Different strains of the yeast M. pulcherrima have been used as a highly effective biocontrol agent against different fungal species such as Penicillium expansum and Botrytis cinerea [14, 15]. Antagonistic effects of different M. pulcherrima strains on different species of Candida, Aspergillus, E. coli, Proteus vulgaris, Trichosporon mucoides, and on Trichoderma spp., were also reported [16]. M. pulcherrima produces a secondary metabolite pulcherrimin and secretes it to the growth medium [17]. Pulcherrimin forms a chelate complex and immobilizes the iron ions in the growth medium [15, 18]. Hence, it seems that M. pulcherrima strains exert their antagonistic effects on the other microorganisms by the depletion of iron in the growth medium [15, 16, 18]. In addition to the pulcherrimin pigment, there is evidence indicating that M. pulcherrima also secretes lytic enzymes such as chitinase that contribute to the overall antagonistic effects of related M. pulcherrima strains [19].

In this study, we have tested the antagonistic effects of the recently isolated M. pulcherrima strain on different fungal species involved in food spoilage. We have found that the M. pulcherrima UMY15 strain, isolated from a local vineyard in Turkey, is a very effective biocontrol agent against different species of Penicillium, Aspergillus, and Fusarium on synthetic growth medium and also on apple.

2. Materials and Methods

2.1. Microorganisms and Growth Medium

Isolation and characterization of M. pulcherrima UMY15 strain were described previously [16]. M. pulcherrima UMY15 strain was cultivated in YPD medium (1% yeast extract, 2% peptone, and 2% glucose) for antagonistic activity tests.

Food spoilage molds used in this study are P. roqueforti, P. italicum, P. expansum, Fusarium sp., Rhizopus sp., A. niger, A. oryzae, and A. parasiticus. All of the molds are held in the culture collection of the Food Engineering Department of Uludag University (Bursa, Turkey). Molds were sporulated on malt extract agar (MEA) plates for 7 days at 30°C. Then, spores were collected aseptically into filter-sterilized 10 mL 0.1% Tween 80. The numbers of mold spores in Tween suspensions were adjusted to 10⁵ spores/mL using sterile 0.1% Tween solution [20]. Spore concentrations were determined microscopically using Thoma slides. Spore suspensions were used immediately after preparations for antagonistic activity tests.

2.2. Antagonistic Activity Tests

First, M. pulcherrima UMY15 strain was cultivated in 10 mL YPD medium overnight at 30°C in an incubator shaker with 130 rev/min at 30°C to obtain saturated precultures. Then, from these precultures, 200 μL of yeast sample was inoculated into 10 mL YPD medium and grown to the midlog stage (OD₆₀₀ : 1.0) under same growth conditions. Yeast cells were harvested by centrifugation (1500 g for 5 min) and washed once with 10 mL of sterile distilled water and resuspended in 10 mL of sterile distilled water. This M. pulcherrima suspensions are used in antagonistic activity tests as described below.

For antagonistic activity tests, 100 μL of spore suspensions from each mold species (approximately 10⁴ spores) was taken from the stock spore suspensions and spread evenly on synthetic dextrose (SD) medium (1.67 g/L yeast nitrogen base, 5 g/L ammonium sulfate, 20 g/L glucose, and 20 g/L agar). When the surface of spore-spread plates dried, 4 μL of M. pulcherrima UMY15 strain (prepared as described) was planted on the plates in duplicates, and then the plates were incubated at 30°C for spore germination and growth for 1-2 days. All of the antagonistic activity tests were repeated at least twice. Inhibition zones were measured manually and defined as the distance extending from the edges of the M. pulcherrima UMY15 colonies to the beginning of the fungal lawn on the plates and expressed in millimeters.

Antagonistic effects of M. pulcherrima UMY15 on germination of fungal spores were also tested when these molds were grown on apple. For this assay, apple (Malus domestica Borkh, cv. Golden Delicious) slices with dimensions of 4 cm L × 2 cm W × 1 cm H were prepared aseptically from the fully matured Golden Delicious apples. Then 3 holes (3-4 mm diameter, 3-4 mm deep) were prepared on these slices with sterile pipette tips. To these three holes on apple slices, 10 μL of spore suspensions only, 10 μL of M. pulcherrima UMY15 together with 10 μL of spore suspensions, and 10 μL of M. pulcherrima UMY15 samples were added, respectively. Apple slices were placed in sterile petri dishes and incubated at 25°C for 2 days for spore germination and fungal growth. At the end of incubation period, spoilage zones on the apple slices caused by the germination and the growth of molds were measured manually. Percentage of the biocontrol activity of M. pulcherrima UMY15 strain on the above given fungal species was expressed as the ratio of infection zones (mm) developed on apples when these molds coexist with M. pulcherrima UMY15 strain over the zone of infection formed by these molds alone on apple wounds [21].

Antagonistic effects of M. pulcherrima on the germination and hyphal growth of various molds in grape juice were also analyzed in shake-flask culture. For these assays, approximately 10⁵ of mold spores and 10⁴ colony forming unit (CFU) from M. pulcherrima samples were coinoculated into 20 mL of additive-free grape juice in 100 mL flask. Grape juice samples inoculated with M. pulcherrima and/or mold spores were incubated at 30°C in an incubator shaker with 130 rev/min. Cultures were visually inspected for mold sporulation after 48 hours. Efficacy of spore germination in grape juices was estimated by comparing the amount of mycelia growth in the grape juice cultures to the cultures that contain only spores of relevant molds (control group without M. pulcherrima).

The numbers given for inhibition and spoilage zones in Tables 1 and 2 are the average values of at least 4 independent experiments. The standard deviations for the zones of inhibitions were less than 10%.

Table 1: Antagonistic effects of M. pulcherrima UMY15 strains on the spore germination and the mycelia growth of different fungal species.

Fungal species
Zone of inhibitions (mm)a

24 h
48 h

P. roqueforti
4
3

P. italicum
3
3

P. expansum
3
3

Fusarium sp.
1
0.5

Rhizopus sp.
1
1

A. niger
1
0

A. oryzae
3
2

A. parasiticus
2
1.5

Inhibition zones were measured as the distance from the edges of M. pulcherrima colonies to the beginning of the fungal lawns on SD plates at the 24th and 48th hours of incubations. Standard deviations were less than 10% in zones of inhibition.

Table 2: Inhibition of spore germination and fungal growth on the artificial wounds on apple by M. pulcherrima UMY15 strain.

Fungal species
Inoculations and zones (mm) of fungal growtha
% Biocontrol

Fungal spores only
Fungal spores + M. pulcherrima

P. roqueforti
NG
NG
NA

P. italicum
15
5
67

P. expansum
NG
NG
NA

Fusarium sp.
12
0
100

Rhizopus sp.
Full growth
Full growth
0

A. niger
15
6
60

A. oryzae
8
0
100

A. parasiticus
10
3
70

Zones of fungal growth were measured as the distance from the center of artificial wounds to the ends of fungal growths (rots) on apples at the end of 48th hours of incubations.

NG: no growth on apple wounds, NA: not applicable. Standard deviations were less than 10% in zones of inhibition.

3. Results

3.1. Testing the Inhibitory Effects of M. pulcherrima UMY15 Strain on Fungal Growth

The inhibitory or antagonistic effects of M. pulcherrima UMY15 strain on the spore germination and the growth of eight different mold species were first investigated by plate tests. M. pulcherrima UMY15 strain’s suspensions were applied onto the spores of molds used in this study as described. Germinations and hyphal growth of P. roqueforti, P. italicum, and P. expansum spores were significantly inhibited by M. pulcherrima UMY15 strain on SD petri plates (Table 1 and Figures 1(a) and 1(b)). At the end of 24 hours incubation period, 3-4 mm of inhibition zones were clearly visible on the spore germination plates of Penicillium species used in this study. However, unlike Penicillium species, germination of Fusarium sp., Rhizopus sp., and A. niger spores was inhibited at low levels by M. pulcherrima strain. Inhibition zones on the spore germination plates of these three fungal strains were approximately 1 mm (Table 1). Nonetheless, there is a significant level of inhibitory effect of M. pulcherrima strain on two other Aspergillus species, A. oryzae and A. parasiticus, respectively (Table 1 and Figures 1(c) and 1(d)). Inhibition zones on the spore germination plates of A. oryzae and A. parasiticus were 2-3 mm after 24 hours of incubation period.

(a)

(b)

(c)

(d)

Figure 1: M. pulcherrima inhibits the growth of different molds on SD plates. Lawns on plate (a) P. expansum, plate (b) P. roqueforti, plate (c) A. oryzae, and plate (d) A. parasiticus.

3.2. Inhibition of Fungal Growth on Apple by M. pulcherrima UMY15 Strain

We have shown that M. pulcherrima UMY15 strain has a significant inhibitory effect on the spore germination and mycelial growth of certain molds such as Penicillium and Aspergillus on petri plates. Next, we wanted to test whether M. pulcherrima strain will also inhibit the germination of these fungal species when their spores seeded on artificial wounds on Golden Delicious apples. Hence, spore suspensions of certain species of Penicillium, Fusarium, Rhizopus, and Aspergillus were applied on small holes on apples with or without M. pulcherrima strain.

Coexistence or cocultivation of M. pulcherrima strain UMY15 with Fusarium sp. spores completely inhibited the germination of Fusarium sp. spores and spoilage of artificially wound apples (Table 2, Figure 2(a)). In the absence of M. pulcherrima strain, Fusarium sp. spores germinated and mycelia growth led to the formation of 12 mm spoilage zones on apple wounds. However, when M. pulcherrima strain and Fusarium spores coinoculated on same wound, there were no spoilage zones on artificial wounds on apples (Table 2, Figure 2(a)). Biocontrol activity of M. pulcherrima on Fusarium was determined as 100%.

(a)

(b)

(c)

(d)

Figure 2: Examples of the inhibitory effects of M. pulcherrima UMY15 strain on different fungal species on artificially wound apples. Infection assays for Fusarium sp. (a), A. Oryzae (b), A. niger (c), and A. parasiticus (d) were done on artificial wounds on apple slices. Inoculations on artificial wounds are 1: mold spores only, 2: M. pulcherrima only, and 3: mold spores and M. pulcherrima inoculations.

Cocultivation of M. pulcherrima strain with A. oryzae on apple wounds also prevented the spore germination, mycelia growth, and spoilage of apple slices. As seen in Figure 2(b) and Table 2, when spore suspensions of A. oryzae were applied on apple wounds, spore germination and mycelia growth resulted in the development of an 8–10 mm wide zone of infection. However, in the presence of M. pulcherrima strain together with the spores of these molds, there were no spoilage zones on apples, indicating that M. pulcherrima strain has very strong inhibitory effects (100% biocontrol) on the germination of the spores of these fungal pathogens.

We have also tested the inhibitory effects of M. pulcherrima UMY15 strain on the germination of P. roqueforti, P. italicum, P. expansum, Rhizopus sp., A. parasiticus, and A. niger ’s spores’ germinations and their efficacy in the formation or development of rotting zones on artificial apple wounds. Since apple is not a natural habitat for P. roqueforti, there was no spore germination and fungal growth on apple holes that contain P. roqueforti spores at the end of a 2-day incubation period. In a similar manner, we were unable to detect any spore germination and fungal growth on apple wounds which contain P. expansum spores at the end of a 2-day incubation period. However, M. pulcherrima strain had a significant level of biocontrol activity (50–70% inhibition) on the germination and mycelia development of P. italicum, A. niger, and A. parasiticus (Figures 2(c) and 2(d)). Germination and the development of P. italicum and A. niger spores on apple wounds in the absence of M. pulcherrima strain resulted in the formation of an approximately 15 mm wide zone of infection. However, cocultivation of the spores of these molds with M. pulcherrima strain led to the formation of about a 5-6 mm wide zone of infection on apple wounds (Table 2, Figure 2(c)). In addition, we further tested the inhibitory effects of M. pulcherrima on spore germination in grape juice (Table 3). The results indicated that M. Pulcherrima is also very effective on P. roqueforti, Fusarium sp., and A. oryzae, with 100% biocontrol activity (Table 3).

Table 3: Inhibition of spore germination and fungal growth in grape juice by M. pulcherrima UMY15 strain.

Fungal species
% mycelial growtha
% Biocontrol

Fungal spores only
Fungal spores + M. pulcherrima

P. roqueforti
100
0
100

P. italicum
100
50
50

P. expansum
100
25
75

Fusarium sp.
100
0
100

Rhizopus sp.
100
25
75

A. niger
100
70
30

A. oryzae
100
0
100

A. parasiticus
100
40
60

Mycelial growth in grape juice was determined visually. Spore germination and growth of mycelia in control groups that do not contain M. pulcherrima UMY15 were accepted as %100 growth. %biocontrol activity was estimated by comparing the mycelial growth of mold spores coinoculated with M. pulcherrima UMY15 strains to the growth of controls.

4. Discussion

Crop protection is the major problem in the production of fresh fruits and vegetables. Large amounts of fruits and vegetables (up to 40%) are rotten by food pathogens after harvesting from the production fields [22]. One of the commonly used methods for the postharvest protection of fresh fruits is to apply antifungal chemicals. Apart from their hazards to human health, fungal pathogens develop resistance to fungicidal chemicals [4]. Hence, biocontrol of postharvest diseases by antagonistic yeasts is the best alternative to antifungal chemicals [4, 12]. Several yeast species are currently used as biocontrol agents for postharvest preservation of fruits and vegetables [23]. M. pulcherrima is one of the best biocontrol yeasts that are used in the prevention of the postharvest spoilage of fresh fruits [14, 24]. Biocontrol activity of M. pulcherrima largely depends on its pulcherrimin pigment that immobilizes free iron ions in the growth medium [18, 21].

Previously, we had isolated a new strain of M. pulcherrima from the local vineyards of the Düzce province of Turkey [16]. Antagonistic effects of this new M. pulcherrima strain on human pathogen yeasts and bacteria have been shown in that previous study [16]. Certain species of Penicillium sp., Fusarium sp., Rhizopus sp., and Aspergillus sp. are the major cause of spoilage of fresh fruits. In addition, certain species of Aspergillus also produce highly toxic aflatoxins [3]. In this study, we have analyzed the biocontrol activity of one of these new M. pulcherrima strains (UMY15) on aforementioned postharvest pathogens both on plate tests and also on artificial wounds on apples. Our biocontrol activity tests showed that the M. pulcherrima UMY15 strain has very effective antagonistic activities on P. roqueforti, P. italicum, and P. expansum on plate tests. However, M. pulcherrima UMY15 is less effective on other fungal pathogens such as Fusarium sp. and Rhizopus sp. Furthermore, M. pulcherrima UMY15 did not have any inhibitory effect on the growth of A. niger at the end of a 48 hour incubation period. Although there was an inhibitory zone on the A. niger lawn at the end of a 24 h incubation period, A. niger overcomes the antagonistic effects of M. pulcherrima UMY15 at the end of 48 h of growth on plates. Different fungal species transport and acquire free iron from the growth medium by different mechanisms [25]. Hence it is possible that the differential antagonistic effects of M. pulcherrima UMY15 on different pathogenic molds might result from the differences of iron requirements of these molds for their growth and development.

Cocultivation of M. pulcherrima UMY15 strain with different mold spores on artificial wounds of apples indicates that this yeast is also a very effective inhibitor of fungal spore development. M. pulcherrima UMY15 completely inhibited (100% biocontrol) the development of Fusarium sp. and A. oryzae spores on apple wounds (Figures 2(a) and 2(b), Table 2). It is less effective on A. parasiticus, A. niger, and P. italicum spore germination and mycelia development on apple. However, M. pulcherrima UMY15 is a better inhibitor of A. niger on apples than the petri tests. This indicates that M. pulcherrima UMY15 is a better competitor for pathogenic molds when it grows on apples. This was also shown by Janisiewicz et al. [26], that M. pulcherrima is a highly effective antagonistic yeast for long term storage of apples (up to 6 months). In our in-vivo analyses, we have used only one dose of M. pulcherrima UMY15 samples (approximately 10³ yeasts cells/inoculums on apple wounds). Efficacy of M. pulcherrima can be further improved by increasing the concentration of yeast samples applied on mold spores. In addition to our results, Oro et al. [27] reported that different isolates of M. pulcherrima have significant lethal effects on the non-Saccharomyces yeast when they are coinoculated into grape must. Sisti and Savini [28] also showed that local isolates of M. pulcherrima strain are highly effective as antifungal agents on human related dermatophytes. They have pointed out that strains of M. Pulcherrima have great potential to be used in the natural treatment of certain fungal infections.

5. Conclusion

Results of this study clearly indicated that M. pulcherrima UMY15 strain is a very effective biocontrol agent that can be used in the prevention of postharvest diseases caused by molds. This M. pulcherrima strain can be developed as a commercial product for postharvest protection of fruits and vegetables from fungal pathogens.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

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