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Ciência Rural

Print version ISSN 0103-8478On-line version ISSN 1678-4596

Cienc. Rural vol.45 no.8 Santa Maria Aug. 2015  Epub June 16, 2015

http://dx.doi.org/10.1590/0103-8478cr20140581 

Microbiologia

Identification of toxigenic Aspergillus species from diet dairy goat using a polyphasic approach

Identificação de espécies toxigênicas de Aspergillus isoladas da dieta de cabras leiteiras utilizando uma abordagem polifásica

Janaina Lara da Silva 1  

Christiane Ceriani Aparecido 2  

Daiane Hansen 1  

Tacila Alves Muniz Pereira 1  

Joana D'arc Felicio 1  

Edlayne Gonçalez

1Centro de Pesquisa e Desenvolvimento de Sanidade Animal (CPDSA), Instituto Biológico, Av. Conselheiro Rodrigues Alves, 1252, 04014-002, São Paulo, SP, Brasil.

2 Centro de Pesquisa e Desenvolvimento de Sanidade Vegetal (CPDSV), Instituto Biológico, São Paulo, SP, Brasil.


ABSTRACT

Some species of filamentous fungi that infest agricultural commodities are able to produce mycotoxins, contaminating feed and animal products. The aim of this research was to identify the mycoflora present in the feed and forage for dairy goat and to isolate and characterize the Aspergillus flavusand A. parasiticus strains based on a morphological and molecular characterization and mycotoxigenic ability. The goat dairy diets were collected monthly from 11 goat milk farms, totaling 129 and 106 samples of concentrate and forage, respectively. For the isolation of the mycobiota the surface plating method was used. Aspergillus, Penicillium,and Fusarium were the main fungi producing mycotoxins isolated. The morphological and molecular characterization and mycotoxigenic ability were used for A. flavus and A. parasiticusidentification. The Aspergillus spp. from feed 39% produced aflatoxins B1 and B2, 17% produced cyclopiazonic acid (CPA), 18% produced both toxins, and 42% had no toxigenic ability. Only 2.0% of the strains produced aflatoxins B1, B2, G1, and G2, but no CPA. The strains from forage were producers of aflatoxins B1 and B2 (37%), CPA (14%), 14% of both mycotoxins, whereas 49% have shown no toxigenic ability. The aflD and aflR genes were used by PCR and PCR-RFLP, respectively. The presence of toxigenic species in samples of feed for lactating goats indicates a potential risk of contamination of dairy products, if they are exposed to environmental conditions favorable to fungal growth and mycotoxin production.

Key words: toxigenic fungi; aflatoxin; cyclopiazonic acid; feed; molecular characterization.

RESUMO

Algumas espécies de fungos filamentosos que infestam os produtos agrícolas e ração são capazes de produzir micotoxinas. O objetivo deste trabalho foi identificar a micoflora presente nos concentrados e volumosos utilizados na dieta de cabras leiteiras e isolar as espécies Aspergillus flavuse A. parasiticus, com base em uma caracterização morfológica e molecular e capacidade micotoxigênica. Os alimentos foram coletados mensalmente em 11 fazendas produtoras de leite de cabra, totalizando 129 e 106 amostras de concentrado e volumoso, respectivamente. Para o isolamento da micobiota, foi utilizado o método de plaqueamento de superfície.Aspergillus, Penicillium e Fusarium foram os principais gêneros de fungos produtores de micotoxinas isolados das amostras. A caracterização morfológica e molecular e capacidade micotoxigênica foram utilizadas para identificação de A. flavus e A. parasiticus. Das cepas Aspergillus spp isoladas do concentrado, 39% produziram aflatoxinas B1 e B2, 17% produziram ácido ciclopiazônico (ACP), 18% produziram ambas as toxinas e 42% não tinham capacidade toxigênica. Apenas 2,0% das cepas produziram aflatoxinas B1, B2, G1 e G2. As cepas de Aspergillus spp. isoladas do volumoso foram produtores de aflatoxinas B1 e B2 (37%), ACP (14%), sendo que 14% produziram ambas toxinas e 49% não foram produtoras. Os genes aflD e aflR foram utilizados para a PCR e a PCR-RFLP, respectivamente. A presença de espécies toxigênicas em amostras de alimentos destinados a caprinos em lactação indica um risco potencial de contaminação dos produtos lácteos por aflatoxinas e ACP, caso estes sejam expostos a condições ambientais favoráveis ao crescimento de fungos e produção de micotoxinas.

Palavras-Chave: fungos toxigênicos; aflatoxinas; ácido ciclopiazônico; ração; caracterização molecular.

INTRODUCTION:

The complex diet of ruminants, consisting of forages, concentrates, and silages, can be a source of diverse mixture of mycotoxins that contaminate individual feed components (SMITH KOROSTELEVA, 2012). Both, feed grains (e.g. corn, wheat, barley, cottonseed) and forages support fungal growth that leads to mycotoxin production (OSWEILER, 2012). MORETTI et al. (2013) emphasize the importance of knowledge of biodiversity of toxigenic fungi to better understand factors that contribute to mycotoxin production, assessment of risks posed by mycotoxigenic fungi, and reduction of mycotoxin contamination in feed and food crops. The mycotoxigenic fungi involved in the food and feed chain belong mainly to the Aspergillus, Penicillium,Fusarium and Alternaria genera.Aspergillus section Flavi includes three species, A. flavus, A. parasiticus and A. nomius, producers of aflatoxins, highly toxic compounds of concern in food safety. A. flavus also produces other mycotoxin such as cyclopiazonic acid (CPA) (VAAMONDE et al., 2003). The identification of Aspergillus Section Flavi has been traditionally based on morphological and biochemical characterization. Conidial wall ornamentation is regarded as the primary morphological diagnostic character for separation ofAspergillus flavus and A. parasiticus. The mycotoxigenic profile (regarding aflatoxins B and G and CPA) of these strains has been routinely used for identification (RODRIGUES et al., 2009). Molecular techniques have been used to differentiate these two species (SOMASHEKAR et al., 2004; RODRIGUES et al., 2009). However, it is to be emphasized that the PCR detection of A. flavus, A. parasiticus or A. nomius is no guarantee of aflatoxin production since gene other than those involved in the biosynthesis of aflatoxins are not target for amplification (LEVIN, 2012). The State of São Paulo has environmental factors conducive to the consolidation of goat and sheep production, and the scientific and technological advances contribute to increased rates of production and productivity of animals. Since the aflatoxins and CPA can be toxic compounds of concern in milk, it is very important to offer a quality feed for dairy goats. So, the aim of this work was to identify the mycoflora present in the feed and forage for dairy goat and isolate and characterize the A. flavus and A. parasiticus strains based on a polyphasic approach involving morphological and molecular characterization, and mycotoxigenic ability.

MATERIAL AND METHODS:

Samples

The samples of dairy goat feed (129) and forage (106) were collected from May, 2010 to September, 2011, once a month from 11 farms producing goat milk located in the cities of Ibiúna, Piedade, Alambari, Capão Bonito, Guareí, and Porto Feliz, in São Paulo State, Brazil. In the properties, feed and forage were packed in barrels with a capacity of 20 kg each. Samples of the feed and forage were collected at nine different points of each barrel: three points of the upper third, three points of the middle third and three points of the lower third (SASSAHARA et al., 2003). Each sample contained a minimum of 500 g. The collected material was homogenized and stored in plastic packaging and sent to the laboratory for isolation and identification of the mycoflora and water activity analysis.

Identification and enumeration of the mycobiota from goat feed and forage

The animal feed and forage samples were apportioned in 10g aliquots and homogenized for 30 minutes in bottles containing 90mL of sterile distilled water. Aliquots with 0.1mL of the dilutions in serial from 10-1 to 10-6 of the samples were plates in duplicate using the surface methods in potato agar dextrose (PDA) medium. The plates were incubated at 25oC for 5 days, but the observations were made daily. The colonies were identified at the genus level, and those belonging to the genus Aspergillus were identified at the species level according to PITT HOCKING (1997).

Molecular Characterization of A. flavus and A. parasiticus

DNA extraction

The strains characterized as the genus Aspergillus (233) were submitted to molecular identification. The strains of A. favus andA. parasiticus were maintained in a tube containing PDA at 25oC at 7 days, and a loop full of spores from each strain was transferred to 1.5mL of lysis buffer with 1.0g of sterile acid-washed 0.4 to 0.6mm diameter glass beads and vortexed for 5.0 min at maximum speed. Proteins and polysaccharides were precipitated by 750µL of cold 3M sodium acetate, pH 5.5. The solution was mixed, placed at -20oC for 10min and centrifuged at 5000g for 10min (4oC) for twice. The supernatant was precipitated with one volume of cold isopropanol. The solution was mixed gently, incubated for 1.0h at -20oC and centrifuged at 5000g for 10min at 4oC. DNA pellet was washed twice with 1.0mL of cold 70% ethanol, centrifuged at 5000g for 5min at 4oC. DNA was diluted in 100µL of ultrapure water and stored at -20oC (RODRIGUES et al., 2009). The DNA was quantified by measuring the absorption at 260nm in a Hitachi U-2000 spectrophotometer.

PCR amplification of aflD gene

The gene aflD was tested for all strains and theaflD primers were specifically designed according to the described by RODRIGUES et al. (2009). The PCR amplifications were performed using about 1µg of fungal template DNA, 200 pmol of each primer (Nor1-Forward: 5´-ACC GCT ACG CCG GCA CTC TCG GCA C-3´ and Nor2-Reverse: 5´-GTT GGC CGC CAG CTT CGA CAC TCC G-3´), MgCl2-free reaction buffer, 2.0mM MgCl2, 2.5U of Taq polymerase and 0.2mM of each dNTP. PCR was carried out under the following conditions: one cycle at 94oC for 3min; 30 cycles at 94oC for 1min, at 55oC for 1min and at 72oC for 1min; and at 72oC for 10min in a final extension.

Restriction site analysis of PCR products

After analysis of PCR products by amplification of aflD gene, only the samples positive for Aspergillus fungi were used in the restriction site analysis. First, a new PCR was used to amplify two target fragments on A. flavus and A. parasiticus, and theaflR primer sequences were designed according to the described by SOMASHEKAR et al. (2004) to amplify a fragment of 796pb (aflR1-Forward: 5´-AAC CGC ATC CAC AAT CTC AT-3´ and aflR2-Reverse: 5´-AGT GCA GTT CGC TCA GAA CA-3´). The reaction mixture consisted of 1.0µg of fungal template DNA, 50pmol of each primer, MgCl2-free reaction buffer, 2.0mM MgCl2, 0.5U of Taq polymerase and 0.2mM of each dNTP. PCR was carried out under the following conditions: one cycle at 94oC for 5min; 30 cycles at 94oC for 3min, at 50oC for 1.25min and at 72oC for 1.40min; and at 72oC for 10min in a final extension. Then, the PCR products were digested with HincII to analyze the restriction site. Each restriction reaction contained 10µL of PCR product (about 50µg DNA), 10 units of HincII enzyme and 2.0µL of 10x digestion buffer as recommended by the manufacturer. The reaction mixture was incubated at 37oC for 4h. The sample was frozen and dried in nitrogen gas. After, the precipitate was dissolved in 10µL of water, and the resulting fragments were separated by electrophoresis on a 1.5% agarose gel. The primers were synthetized by Bioneer Corporation, South Korea, and all other reagents used in PCR and restriction analysis were purchased by Fermentas, Lithuania, part of Thermo Fisher Scientific.

Toxigenic potential ofA. flavus and A. parasiticusstrains for aflatoxins

The production of aflatoxins was tested using the method of LIN DIANESE, 1976. The A. flavus strains isolated from goat feed (130) and from forage (70) were maintained in a tube containing PDA at 25oC for 5 days. A fragment of each colony was then inoculated into a place containing coconut agar medium and incubated at 25oC for 10 days. After growth, the whole content of each plate was removed, and chloroform was added, 30mL for each 10g of culture. After shaking, the sample was filtered through filter paper with diatomaceous earth and sodium sulfate. The filtrated was evaporated, and the extract was suspended in chloroform and then submitted to thin layer chromatography (TLC).

Aflatoxin analyses

The aflatoxins identification and quantification were performed by TLC using an aliquot (40μL) of each sample, which was spotted on silica gel-G thin layer plate (Merck, Germany) and then developed with chloroform:acetone 9:1 (v/v) as a solvent system. The concentration of aflatoxins was determined by photodensitometry (Shimadzu, CS 9000) comparing the area and density of the spot samples with aflatoxins B1, B2, G1, and G2 standards (Sigma Aldrich, USA) (GONÇALEZ et al., 2001). The detection e quantification limits were established how the lowest fluorescence detectable signal and the lowest concentration measured, respectively. The detection and quantification limits for AFB1 were 0.8ng g-1 and 1.6ng g-1, respectively. Recovery for standard aflatoxin B1 should be at least 94%.

Toxigenic potential of A. flavus strains for CPA

The methodology of GONÇALEZ et al. (2013) was employed to evaluate the CPA production by A. flavus strains. The A. flavus strains isolated from goat feed (130) and from forage (70) were maintained in a tube containing PDA at 25˚C for 7 days. Spore solutions (1.0mL) of each sample were inoculated into 25mL of Czapec-Dox broth (Difco) and incubated for 12 days at 25oC. The cultures were filtrated, and the CPA was extracted twice with 25mL of chloroform. The chloroform was evaporated and the extract was diluted in 1.0mL of methanol HPLC grade and then submitted to high performance liquid chromatography (HPLC).

HPLC conditions

The mobile phase consisted of methanol:water/zinc sulfate 4.0mM 7:3 (v/v) at a flow rate of 0.6mL min-1. A C18 column, 250mm x 4.6mm (Shimadzu, Japan) was used, and the analyses were done with a UV detector at 284nm. The calibration curve was established by the external standard method with five concentrations: 0.611; 1.223; 2.446; 4.892, and 9.798mg mL-1 (r 2=0.998). The HPLC quantification and detection limits for a standard CPA were 0.030mg mL-1 and 0.005mg mL-1, respectively. Recovery for standard CPA was 97%.

Water activity determination

The water activity (aw) of goat feed and forage samples was determined by automatic analysis using Aqualab 4TE (Decagon Devices Inc., Pullman, WA).

Statistical analysis

The results were analyzed by ANOVA and Tukey's multiple range tests with a significance level P < 0.05 to determine differences between feed and forage using the variables: fungi isolation, A. flavus and A. parasiticus identification, mycotoxigenic ability and aw.

RESULTS AND DISCUSSION:

An important component of efforts to control mycotoxin contamination problems is the study of the morphological, molecular genetics, metabolic and plant pathological diversity of mycotoxigenic fungi (MORETTI et al., 2013).

The mycoflora of the animal feed and forage samples are shown in table 1. Toxigenic fungi belonging to the genera Aspergillus, Penicillium,and Fusarium were isolated from most samples (Table 1). Other studies also reported the presence ofAspergillus spp., Penicillium spp., Fusariumspp., and Eurotium spp. in animal feed (PEREYRA et al., 2010; ASTORECA et al., 2011). Among representatives of the genusAspergillus , were isolated from animal feed: A. flavus (69%),A. fumigatus (2.30%), A. niger (1.50%) and A. parasiticus (0.80%). The highest incidence of A. flavus was shown in animal feed and in their ingredients (PEREYRA et al., 2010 and 2011; ASTORECA et al., 2011). The Aspergillus species isolated from forage were: A. flavus (49%), A. fumigatus (5.70%), and A. niger (1.0%). The forage samples showed highest incidence ofAspergillus spp. than in feed. Same results were found by ACCENSI et al. (2004). The identification ofAspergillus Section Flavi has been traditionally based on morphological and biochemical characterization (RODRIGUES et al., 2009).

Table 1: Relative frequency (%) of the genera fungi contamination of animal feed (129 samples) and forage (106 samples) collected in 11 dairy goat farms in the period May, 2010 to September, 2011.  

*NSF: Non-sporulating fungi.

The morphological and molecular characterization and mycotoxigenic ability were used for A. flavus and A. parasiticus identification. Morphologically, A. flavus has finely roughened conidia mostly produced from heads bearing both metulae and phialides, whereas conidia of A. parasiticus are usually conspicuously roughened and most heads bear phialides alone (PITT HOCKING, 1997). Based on these morphological characters, it was possible to identify A. flavus in 64% of the Aspergillus spp. isolated from feed and 37% from the forage. The identification was confirmed by molecular characterization and mycotoxigenic ability of the A. flavus and A. parasiticus strains.

The results of the molecular analysis showed that 97% of the Aspergillusspp. isolated from feed was PCR positive for A. flavus and A. parasiticus. The molecular identification using the geneaflD (PCR) was a good maker for differentiating the A. flavus and A. parasiticus species (fragment of 400pb) from the other Aspergillus spp., but it was not possible to differentiate them from each other. Of 131 strains isolated from feed and confirmed by PCR, 65.60% were A. flavus and 0.76% was A. parasitcus, using the geneaflR (PCR-RFLP). Among the Aspergillus spp. isolated from forage (98 strains) 71.40% were positive by PCR analysis and 51.40% of them were identified with A. flavus, however A. parasiticus was not isolated. The results obtained in this work are in agreement with SOMASHEKAR et al. (2004), who showed that PCR-RFLP patterns obtained with HincII can be used to distinguish the two species. A. flavus cleaved into 3 fragments of 385, 250, 161bp whereas A. parasiticus, having one restriction site for theHincII, produced 2 fragments of 546 and 250bp. TheaflD and aflR genes were not able to identify the ability of the strains to produce aflatoxins (SOMAHEKAR et al., 2004; RODRIGUES et al., 2009). In addition, the genomic structural genes involved in aflatoxins biosynthesis do not guarantee the production of aflatoxins by all isolates of A. flavus and A. parasiticus (LEVIN, 2012), so their mycotoxigenic ability was investigated. The 131 Aspergillus spp. strains confirmed by PCR from feed and 70 strains from the forage were evaluated as having ability to produce aflatoxins and CPA (Table 2). A. flavus is able to produce aflatoxins and CPA, and A. parasiticus can produce only aflatoxins. The results showed that of theAspergillus spp. from feed 39% produced aflatoxins B1and B2, 17% produced CPA, 18% produced both toxins, and 42% had no toxigenic ability. Only 2.0% of the strains produced aflatoxins B1, B2, G1, and G2, but no CPA, and, based on all characteristics analyzed, they were identified with A. parasiticus. Almost all A. parasiticus isolated produce both aflatoxins B and G, but not CPA (HORN DORNER, 1999). The strains from forage were producers of aflatoxins B1 and B2 (37%), CPA (14%), 14% of both mycotoxins, and 49% did no show toxigenic ability. The concentrations of aflatoxins B1 and B2, and CPA were showed in the table 2. The results showed the great variability in the mycotoxins producing potential by A. flavus in the culture conditions. Our results agree with the literature that also found difference in the mycotoxigenic ability of theA. flavus (VAAMONDE et al., 2003; ASTORECA et al., 2011). VAAMONDE et al. (2003) proposed five chemotypes for A. flavus species, based on the mycotoxins produced by them: chemotype I for aflatoxin B and CPA producers; II for AFB, AFG and CPA producers; III for AFB producers; IV for CPA producers and V for non mycotoxin producers. TheA. flavus strains isolated from feed and forage belong to the following chemotypes, respectively: type I (18% and 14%); type III (39% and 37%); type IV (17% and 14%) and type V (25% and 35%). The chemotype II was not isolated.ASTORECA et al. (2011), also isolatedA. flavus belonging to chemotypes I, III, IV and V, but no type II from poultry feed. By comparing the chemotypes isolated from feed and forage, there was no statically significant difference between them (P<0.05).

Table 2: Aflatoxins B1 and B2 and CPA production in culture medium by Aspergillus spp. isolated from feed (131 strains) and forage (70 strains) collected in 11 dairy goat farms in the period May, 2010 to September, 2011.  

1 AFB: aflatoxin B1; AFB2: aflatoxin B2; CPA: cyclopiazonic acid.

The average aw values of the samples ranged from 0.51 to 0.75 for feed and from 0.46 to 1.0 for forage. The minimum aw values required for growingA. fla vus and A. parasiticus as well as for producing aflatoxins are 0.80 and 0.83, respectively (PITT HOCKING, 1997). The aw did not influence the A. flavus andA. parasiticus isolation from feed and also forage (P<0.05) since these species were isolated in all samples analyses. Therefore, the feed did not have water enough for the fungal activity. On the other hand, the forage is not a good substrate, because it has high fiber concentration and low nutrients to the fungi.

According to SMITH MOSS (1985), feed with good microbiological quality should present a maximum of 105 colony-forming units g-1 (CFU g-1). The results showed that only 17% of the feed and 2.8% of forage samples had more than 105CFU g-1, therefore most of goat feeding had good quality in all farms studied.

CONCLUSION:

The results obtained in this study indicate that, to distinguish the A. flavus and A. parasiticus species, it is necessary more than one technique of identification. The presence of A. flavus capable of producing CPA and aflatoxins indicates a risk of contamination in dairy goat feed and forage if they are exposed to environmental conditions that allow fungal growth.

ACKNOWLEDGEMENTS

The authors are grateful to the Fundação de Amparo a Pesquisa do Estado de São Paulo (FAPESP) for financial support.

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Received: April 16, 2014; Accepted: September 04, 2014

Corresponding author: Edlayne Gonçalez, email:goncalez@biologico.sp.gov.br

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