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Brazilian Archives of Biology and Technology

Print version ISSN 1516-8913

Braz. arch. biol. technol. vol.56 no.4 Curitiba July/Aug. 2013

https://doi.org/10.1590/S1516-89132013000400012 

BIOLOGICAL AND APPLIED SCIENCES

 

Role of killer factors in the inhibitory activity of bio-control yeasts against Penicillium expansum and Aspergillus ochraceus

 

 

Ciro da Silva Portes; Andriélen Virke de Oliveira; Patrícia Simer; Alessandra Machado Lunkes; Alexandre Rodrigo Coelho*

Universidade Tecnologica Federal do Paraná; Linha Santa Bárbara s/n; 85061-970; Francisco Beltrão - PR - Brasil

 

 


ABSTRACT

This work evaluated the antagonism of killer positive yeast strains (isolated from 11 samples of different frozen fruit pulps) against  the strains of Penicillium expansum and Aspergillus ochraceus.  Of the total 41 killer yeasts tested in YM agar, 19 showed antibiosis against P. expansum and A. ochraceus, with inhibition zone ranging from 10 to 18 mm and 10 to 19 mm, respectively. In the following step, the extracellular activity of Kluyveromyces sp. FP413 was tested performing the assay in YM broth. The antifungal activity of Kluyveromyces sp. FP413 cell-free culture supernatant (25oC/96 h) was more effective against the conidia germination, showing inhibition rates of 93.33 and 86.44% for P. expansum and A. ochraceus, respectively. The micelial growth inhibition was 28.45 and 21.0%, respectively. The antagonism showed by the selected yeasts could be used as a promising alternative tool to reduce and control the postharvest fungal spoilage of the fruits. However, further studies should be carried out in order to better elucidate the role of innocuous characters in antagonistic microorganisms, as well as the purification and characterization of new killer toxins.

Key words: Moulds, Killer yeasts, Biocontrol, Antibiosis


 

 

INTRODUCTION

Efforts have been made to improve the competitiveness in the area of agri-food system in Brazil. Brazilian fresh fruit exports had a growth of 13% during 2003/2007. Fruit productivity has been over 39 million tons, with the country ranking among the four largest fruit-producers worldwide, along with China, India and the USA (IBRAF 2010; FAO 2010). However, considerable losses occur in the commercial crops due to fruit susceptibility to infection by fungi, such as Penicillium expansum (Janisiewicz et al. 1998), Colletotrichum gloeosporioides (Rezende and Fancelli 1997), Aspergillus ochraceus, Fusarium spp., and Alternaria spp. (Hussein and Brasel 2001; Nielsen et al. 2006). Thus, raw material productivity is dependent on fungicide application, leading to levels of undesirable chemical contaminants in the final product. Biological methods are viable alternatives to the traditional chemical methods, since no toxic residues remain on the fruit (Wilson and Wisniewski 1994). Biological products currently available, such as BIOSAVE II ® (Pseudomonas syringae), ASPIRE (Candida oleophila), and YIELD PLUS ® (Cryptococcus albidus) have been used in the control of postharvest fruit diseases (Janisiewicz and Korsten 2002; Wisniewski et al. 2007; Droby et al. 2002). This is in agreement with the use of yeasts in bio-control, based on the mycotoxigenic character of this group of microorganisms (Janisiewicz et al. 2003) and the presence of the killer factor in some strains. The killer factor is an extra-cellular peptide capable of inhibiting the growth of other microorganisms.

Biological control of the postharvest fruit diseases caused by mycotoxigenic moulds, combined with the investigation of bioactive compounds compatible with practical application, are necessary to ensure fruit  quality and safety (Coelho et al. 2003). Thus, the aim of this work was to study the antagonism of killer positive yeasts against Penicillium expansum and Aspergillus ochraceus strains.

 

MATERIALS AND METHODS

Moulds

Single-spored A. ochraceus A152 and P. expansum n. 2 were isolated from naturally-decaying fruit. The culture was stored in Potato Dextrose Agar (PDA) at 4ºC and cultivated on PDA slants at 21ºC for 120 h before use. A spore suspension was prepared by inoculating the culture into 3.0 mL sterile distilled water containing 0.1% (v/v) Tween 80, and the cell number was adjusted to 1 x 105 spores mL-1 (Newbauer chamber).

Antagonistic Agents

Yeasts were isolated from the samples of 11 flavors of frozen fruit pulp by using Yeast Medium Agar–YM agar (2.0% glucose, 0.5% yeast extract; 0.23% NaH2PO4; 1.0% NaCl; 0.5% (NH4)2SO4; 1.8% agar).The frozen fruit pulp used was obtained by a unique processing industry. The yeast isolates were maintained in GYMP Agar slant (2.0% glucose, 1.0% malt extract, 0.5% yeast extract, 0.2% NaHPO4 and 1.8% agar) at 4oC.  Yeast isolates showing potential antifungal activity, based on the antibiosis were identified by the commercial Kit RapidTM Yeast Plus System (Remel, Lenexa, USA). Yeasts were encoded and submitted to computerized identification system (Electronic Rapid Compendium–ERIC, Remel). For subsequent assay, the strains were activated in YM agar at 25ºC/48 h.

Killer Toxin Assay

Isolated yeasts were submitted to killer toxin assay by using the killer sensitive reference strains of Candida glabrata NCYC 366, C. glabrata NCYC 388, C. albicans 12A, Pichia kluyveri CAY 15 and Saccharomyces cerevisiae NCYC 1006. The cell suspension of each reference strain (100 µL, 3 x 106 cells mL-1) was pour-plated in Methylene Blue Agar (MBA) following the method modified by Polonelli et al. (1983). A loop of the test strain reactivated in YM agar was inoculated (four testing strains/plate) onto the surface (2 mm diameter) of previously prepared MBA, and the plate was incubated at 20ºC for 72 h. The killer positive strain was characterized as the colony with a clear surrounding zone, or the surrounding pour-plated reference culture was blue-stained (Walker et al. 1995). MBA was prepared in citrate-phosphate buffer, pH 4.5 with the addition of 2.0% agar, 2.0% glucose, 1.0% peptone and 0.003% methylene blue, and autoclaved at 121ºC for 15 min. A killer strain of Saccharomyces cerevisiae NCYC-738 was used as positive control. The experiment was carried out in triplicate.

Antifungal Assay in Solid Medium

For the antifungal assay in solid medium, the inoculum of 105 spores of A. ochraceus and P. expansum was pour-plated in 25mL YM agar. After solidification, an 8 mm diameter well was made in the center of the plate, followed by inoculation of 100 μL yeast cultivate (YM broth at 25oC/48 h), corresponding to 3.0 x 106 cells
mL-1. Plates were incubated at 25oC and the inhibition zone was measured after 5 days.

The antifungal assay in solid medium was used for screening the yeasts with potential activity against the fungal strains. This method allowed observing two types of inhibition, i.e., competition for the nutrients, identified by yeast growth pumping through the edge of the well and/or extra-cellular compound production by antibiosis, characterized by the inhibition zone with no growth of spoilage mould (Coelho et al. 2007).

Antifungal Assay in Broth Culture

The antifungal assay in broth culture was essentially based on the methods described by Janisiewicz et al. (2000) and Chen et al. (1999), followed by the microscopic analysis. The yeast isolates showing potential activity against the fungal tests in the solid medium assay were submitted to antifungal assay in broth culture. Kluyveromyces sp. FP413 was activated in YM broth at 25ºC for 24 h (150 rpm), and 100 mL of cell suspension (3.0 x 106 cells) were inoculated in five Erlenmeyer flasks with 50mL of YM broth. After 24, 48, 72, 96, and 120 h incubation at 25ºC under static condition, one yeast culture flask was centrifuged (6,500 x g for 15 min) and filter sterilized (0.20 µm, Millipore Corporation, Bedford, MA, USA). An aliquot (1.0 mL) of the sterilized supernatant was added to 1 mL of YM broth (120 x 13 mm tube), and inoculated with fungal tests (105 spores). Tubes were incubated at 25ºC for 12h, and conidial germination percentage and fungal growth were determined by an optical microscope. Negative control was performed in the tubes without yeast culture supernatant (105 spores of fungal test in 1.0mL sterile water plus 1mL YM broth). The conidial germination percentage in the culture with supernatant (X) was calculated as:

X=100 x mean conidia germination in the supernatant

           mean conidial germination in the control

The inhibition percentage of conidial germination was calculated as 100% inhibition – X.

The hyphal length in the culture with the supernatant (Y) was calculated as:

Y = 100 x mean hyphal length in the supernatant
mean hyphal length in the control

 

The inhibition percentage of hyphal growth was calculated as 100% inhibition – Y.

The experiment was carried out in three replications (at three different time) over eight months; for each replication, the mean hyphal lengths were obtained by measuring 40 random hyphae in mm. Conidial germination data were based on two counts of 100 conidia per repetition (Chen et al. 1999). The data from three replications were analyzed by comparing the mean values obtained from 120 data for hyphal length and 6 data for conidial percentage.

Statistical Analysis

The 120 data for hyphal lengths and the six data for conidia germination percentage, obtained from three replications, were evaluated by Tukey test (p < 0.05) using the Anova/Manova program (Statistica version 7.0, Inc. Tulsa ,OK, USA, 2005).

 

RESULTS AND DISCUSSION

Isolation and Identification of Killer Yeast

Forty-one yeasts were isolated from 11 samples of different frozen fruit pulps, as shown in Table 1. Table 2 shows the killer positive yeast isolates against the standard yeast strains. Of the total yeasts tested, 31 (75.6%) were positive for the killer character. Of these, 24 yeasts (77.4%) showed killer activity against more than one standard sensitive strain, with six being against two standard sensitive strains; 13 against three; four against four; and one against all standard sensitive strains. Seven yeast isolates showed killer factor against only one standard sensitive strain (Table 2).

Figure 1 showed the killer positive strains against the reference strain S. cerevisiae NCYC 1006, which showed a clear surrounding zone on methylene blue agar surface. This work presented more results than the study conducted by Coelho et al. (2011) using 44 yeast strains isolated from different natural sources in northern Parana, which showed only 29.55% with positive outcome for the killer factor. However, Oliveira et al. (2011) obtained 100% positivity to the killer factor in 24 yeasts isolated from the commercial and organic strawberry.

The yeast isolates that showed killer factor against more than one sensitive strain suggested that the killer toxin produced could have a large spectrum of action. On the other hand, yeasts could produce more than one killer toxin, such as killer toxins K1, K2, and K28, produced by S. cerevisiae (Schmitt and Breinig 2002). Also, the yeast strains FP21 and FP42 showed killer factor against
C. glabrata NCYC 366 and C. glabrata NCYC 388, indicating the possible production of a unique antagonistic substance (Poloneli et al. 1983). Similar results were also found by Coelho et al. (2011) and Oliveira et al. (2011) against the same standard sensitive strains.

Yeast strains FP23, FP41, and FP413 were identified by using the commercial kit RapidTM Yeast Plus System (Remel, Lenexa, USA). According to the results, starin FP23 was S. cerevisiae and FP41
and FP413 were Kluyveromyces sp., whose probabilities were >99.9, 99.88 and 99.88%, respectively.

The results of this work suggested that the killer phenomenon showed by S. cerevisiae FP23 and Kluyveromyces sp. strains FP41 and FP413 could be similar to that reported by other works, such as the production of K1, K2, and K28 killer toxins by S. cerevisiae and killer toxins from K. lactis and K. wickerhamii (Philliskirk and Young 1975; Golubev 1998; Schmitt and Breinig 2002; Comitini et al. 2004).

Antifungal Assay

Yeasts were submitted to antifungal assay in solid medium against P. expansum n. 2 and A. ochraceus A152 as a screening method. Of the total 41 yeasts tested, 24 (58.5%) showed antifungal activity against P. expansum n. 2, out of which 19 (79.2%) showed antagonism, based exclusively on antibiosis (clear inhibition zone due to production of extracellular substances), with inhibition zone ranging from 10 to 18 mm. Three yeasts (12.5%) showed antagonism based on nutrient competition (evidenced as cellular mass growth on the surface of the YM agar), and four (16.7%) based on synergism (nutrient competition and antibiosis), between 48 and 120 h incubation at 25oC (Table 3). Geng et al. (2011) reported significant antagonistic effect by K. marxianus 1.0 x 108 CFU/mL against P. digitatum, showing 95.6% inhibition of spore germination.

The antagonism focused in this study was shown by the antibiosis, i.e., the production of extracellular substances that inhibited the growth of other microorganisms. Thus, yeast strains FP23, FP26, FP41, FP413, FP84, FP93, FP102, FP133, FP135, FP144, FP166 and FP167 showed greater antagonism against P. expansum n. 2, with inhibition zone ranging from 12 to 18 mm (Table 3). Coelho et al. (2011) found positive results for antagonism in 20 (45.5%) out of the 44 yeasts tested against P. expansum, with 15 being for nutrient competition and 5 with indications of antibiosis, with inhibition diameters ranging from 10 to 31 mm and 13 to 17 mm, respectively.

As for antagonism against Aspergillus ochraceus A152, out of the 41 yeasts tested, 25 (61.0%) showed antagonism, with 19 (76.0%) being exclusively by the antibiosis, with inhibition zone ranging from 10 to 19 mm; one yeast isolate (4.0%) inhibited the mould by nutrient competition; and five yeasts (20%) showed synergistic effect against A. ochraceus A152. Yeast strains FP11, FP22, FP23, FP26, FP41, FP46, FP413, FP84, FP91 and FP93 showed greater antagonism based on the antibiosis, with inhibition zone ranging from 13 to 19mm (Table 3). However, some yeasts that were antagonistic by the antibiosis against one, or both spoilage mould did not show positivity to the killer factor (strains FP22, FP88, FP91, FP144, FP167 and FP168). This could be explained by the production of other extra-cellular substances, such as the detection of exoquitinase [N-acetyl-D-glucosaminidase (Nagase)] and β-1-3-glucanase produced by Aureobasidium pullulans (LS-30) against the development of B. cinerea, P. expansum, Rhizopus stolonifer and A. niger conducted in vitro and in apple wounds (Castoria et al. 2001). Wickerhamomyces anomalus, grown on acidified medium, showed mycotoxigenic activity against P. digitatum resulting from β-glucanase activity (Platania et al. 2012).

In general, S. cerevisiae strain FP23 and Kluyveromyces sp. strains FP41 and FP413 showed satisfactory results against the development of the spoilage mould tested. According to the results, Kluyveromyces sp. FP413 was selected for the subsequent tests in antifungal assay in YM Broth.

The antifungal assay in YM Broth has been proved to be a more sensitive test than the solid medium, since it is a quantification method that allows counting conidial germination and measuring fungal hyphal length (Janisiewicz et al. 2000). For this stage, Kluyveromyces sp. FP413 was used since it presented a good performance in the antifungal assay in YM agar, as shown in Table 3. Tests were conducted with cell-free culture supernatant from the yeast cultivation with a growing control of the tested moulds. The antifungal activity was more effective against the conidial germination than the inhibition of hyphal growth for P. expansum and A. ochraceus (Table 4, Fig. 2).

In the assay carried out against P. expansum, there was a significant difference (p < 0.05) between the control and the treatment with the cell-free culture supernatant after 24-120h; spore germination inhibition was not very efficient when the cell-free culture supernatant was used after 24h (13.85% inhibition), increasing considerably with the cell-free culture supernatant after 48-72h (50-53.2%), and reaching the maximum inhibition level after 96h incubation (93.33% spore germination inhibition). After 120 h incubation time, antifungal activity slightly decreased to 76.62% inhibition level (Fig. 2C). As for  hyphal growth inhibition, there was a significant difference (p < 0.05) between the cell-free culture supernatant treatment after 72-120h and the control treatment, showing the highest hyphal growth inhibition after 96h incubation time (28.45%, Fig. 2A). These results suggested that the use of cell-free culture supernatant from Kluyveromyces sp. FP413 cultivate during 96h could efficiently control the hyphal growth and conidial germination of P. expansum.

Tests conducted against the hyphal growth of A. ochraceus showed a significant difference (p < 0.05) between the treatment and the control of the yeast cultivate after 48-72 h (Table 4). However, inhibition percentage was not higher than 21% (Fig. 2B). The conidial germination results were similar to that found against P. expansum, i.e., there was a significant difference between the treatment and the control of the yeast cultivated for 24h (16.5% inhibition level), increasing after 48-72h (inhibition of 72.6-76.39%), and reaching maximum activity after 96h incubation (inhibition of 86.44%). After 120 h, antifungal activity was drastically reduced to 56.7% (Fig. 2D). Thus, based on the results, the use of cell-free culture from yeast cultivate at 25oC for 96 h could efficiently control spore germination of
A. ochraceus.

In the YM broth assay, antifungal activity was evidenced as the presence of an extra-cellular substance that could efficiently inhibit spore germination of both the filamentous fungi. The antagonism of Kluyveromyces sp. FP413 against P. expansum and A. ochraceus based on the antibiosis suggested the involvement of such factor with killer positive phenomenon shown in this work.  As the killer toxin was capable of inhibiting the conidial germination and hyphal growth, the effect was probably associated with rapid loss of cellular integrity rather than inhibition of the cell division cycle. Mechanisms associated with the cell surface have been reported in S. cerevisiae K1 toxin, which was linked to cell wall receptor (De La Peña et al. 1981), such as in Pichia membranifaciens killer toxin (Santos and Marquina 2004). Walker et al. (1995) reported the susceptibility of yeast and filamentous fungi caused by the killer positive strains of S. cerevisiae, P. anomala and Williopsis mrakii. Studies by Coelho et al. (2006, 2007) showed 58.15% inhibition of spore germination of P. expansum with supernatant of C. guilliermondii cultivate obtained after 72 h of incubation at 25oC, whereas Pichia ohmeri (25oC/48 h) inhibited the hyphal length development  in 64.37%, both associated with the killer factor.

Although there had not been any reports on the action of killer toxins produced by Kluyveromyces sp. against molds, Comitini et. al (2004) reported the fungicidal effect of Kwkt killer toxin by K. wickerhamii (DBVPG 6077) against Dekkera/Brettanomyces spp. spoilage yeasts in wine and concluded that this killer toxin could have great potential as a bio-preservative agent in wine ageing. 

 

CONCLUSION

Of the 41 yeasts tested, 75.6% showed killer phenomenon against at least one sensitive standard yeast used as reference, indicating a good number of yeasts producing extra-cellular substance. The antagonism showed by the yeasts tested against P. expansum and A. ochraceus based on the antibiosis rendered them promising biocontrol agents against the spoilage mould in postharvest fruit. The killer positive isolate FP413 of Kluyveromyces sp. significantly inhibited the conidial germination of P. expansum and

A. ochraceus
, reaching about 93.33 and 86.44% inhibition, respectively. However, further studies on the antagonistic microorganisms with innocuous characters would be needed and purification and characterization of new killer toxins must be carried out to improve the quality and safety of agro-industrial products.

 

ACKNOWLEDGEMENTS

The authors would like to thank National Council of Scientific and Technological Development (CNPq, Brazil) for financial support.

 

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Received: October 10, 2012;
Accepted: June 18, 2013.

 

 

* Author for correspondence: arcoelho@utfpr.edu.br

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