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Applied and Environmental Microbiology, August 2005, p. 4696-4702, Vol. 71, No. 8
0099-2240/05/$08.00+0     doi:10.1128/AEM.71.8.4696-4702.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Study of Spanish Grape Mycobiota and Ochratoxin A Production by Isolates of Aspergillus tubingensis and Other Members of Aspergillus Section Nigri

Angel Medina,¹ Rufino Mateo,² Laura López-Ocaña,³ Francisco Manuel Valle-Algarra,² and Misericordia Jiménez^1*

Departamento de Microbiología y Ecología, Facultad de Biología, Universidad de Valencia, Dr. Moliner 50, E-46100 Burjasot, Valencia, Spain,¹ Departamento de Química Analítica, Facultad de Química, Universidad de Valencia, Dr. Moliner 50, E-46100 Burjasot, Valencia, Spain,² Colección Española de Cultivos Tipo (CECT), Universidad de Valencia, Dr. Moliner 50, E-46100 Burjasot, Valencia, Spain³

Received 10 January 2005/ Accepted 10 March 2005

The native mycobiota of five grape varieties grown in Spain has been studied. Four (Bobal, Tempranillo, Garnacha, and Monastrell) were red varieties and one (Moscatel) was white. The main fungal genera isolated were Alternaria, Cladosporium, and Aspergillus. The isolation frequency of Aspergillus spp. section Nigri in contaminated samples was 82%. Ochratoxin A (OTA) production was assessed using yeast extract-sucrose broth supplemented with 5% bee pollen. Cultures of 205 isolates from this section showed that 74.2% of Aspergillus carbonarius and 14.3% of Aspergillus tubingensis isolates produced OTA at levels ranging from 1.2 to 3,530 ng/ml and from 46.4 to 111.5 ng/ml, respectively. No Aspergillus niger isolate had the ability to produce this toxin under the conditions assayed. Identification of the A. niger aggregate isolates was based on PCR amplification of 5.8S rRNA genes and its two intergenic spacers, internal transcribed spacer 1 (ITS1) and ITS2, followed by digestion with restriction endonuclease RsaI of the PCR products. The restriction patterns were compared with those from strains of A. niger CECT 2807 and A. tubingensis CECT 20393, held at the Spanish Collection of Type Cultures. DNA sequencing of the ITS1-5.8S rRNA gene-ITS2 region of the OTA-producing isolates of A. tubingensis matched 99 to 100% with the nucleotide sequence of strain A. tubingensis CBS 643.92. OTA determination was accomplished by liquid chromatography with fluorescence detection. OTA confirmation was carried out by liquid chromatography coupled to ion trap mass spectrometry. The results showed that there are significant differences with regard to the isolation frequency of ochratoxinogenic fungi in the different grape varieties. These differences were uncorrelated to berry color. The ability of A. tubingensis to produce OTA and the influence of grape variety on the occurrence of OTA-producing fungi in grapes are described in this report for the first time.

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* Corresponding author. Mailing address: Departamento de Microbiología y Ecología, Facultad de Biología, Universidad de Valencia, Dr. Moliner 50, E-46100 Burjasot, Valencia, Spain. Phone: 34-96-3543144. Fax: 34-96-3543099. E-mail: misericordia.jimenez{at}uv.es.

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Applied and Environmental Microbiology, August 2005, p. 4696-4702, Vol. 71, No. 8
0099-2240/05/$08.00+0     doi:10.1128/AEM.71.8.4696-4702.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.