Genetic relationships among strains of the Aspergillus niger aggregate

We analyzed the genetic relationships between 51 fungal isolates previously identified as A. niger aggregate, obtained from dried fruit samples from worldwide origin and 7 A. tubingensis obtained from Brazilian coffee beans samples. Greater fungal diversity was found in black sultanas. Aspergillus niger sensu stricto was the most prevalent species. It was found in all fruit substrates of all geographical origins. Based on Random Amplification of Polymorphic DNA (RAPD) and β-tubulin sequences data two groups of A. niger were found. In spite of the small number of isolates from Group IV an association between extrolite patterns and molecular clustering is speculated. A. tubingensis were the second most frequent species and this species were clearly subdivided into two groups. The finding of two groups for A. tubingensis strains could not yet explain the contradictions found in the literature about the capability this species for ochratoxin production, because both of them were formed by only non-ochratoxin-producing strains.

[1]  A. Visconti,et al.  Mycotoxins: Detection Methods, Management, Public Health and Agricultural Trade , 2008 .

[2]  Y. Ueno,et al.  A comparison between enzyme immunoassay and HPLC for ochratoxin A detection in green, roasted and instant coffee , 2007 .

[3]  P. Martínez-Culebras,et al.  An ITS-RFLP method to identify black Aspergillus isolates responsible for OTA contamination in grapes and wine. , 2007, International journal of food microbiology.

[4]  A. Logrieco,et al.  Ochratoxin A Production and Amplified Fragment Length Polymorphism Analysis of Aspergillus carbonarius, Aspergillus tubingensis, and Aspergillus niger Strains Isolated from Grapes in Italy , 2006, Applied and Environmental Microbiology.

[5]  M. Taniwaki,et al.  Incidence of toxigenic fungi and ochratoxin A in dried fruits sold in Brazil , 2005, Food additives and contaminants.

[6]  M. Jiménez,et al.  Study of Spanish Grape Mycobiota and Ochratoxin A Production by Isolates of Aspergillus tubingensis and Other Members of Aspergillus Section Nigri , 2005, Applied and Environmental Microbiology.

[7]  C. Magnoli,et al.  Survey of mycoflora and ochratoxin A in dried vine fruits from Argentina markets , 2004, Letters in applied microbiology.

[8]  C. Magnoli,et al.  Mycoflora and ochratoxin‐producing strains of Aspergillus section Nigri in wine grapes in Argentina , 2003, Letters in applied microbiology.

[9]  F. Accensi,et al.  Aspergillus carbonarius as the main source of ochratoxin A contamination in dried vine fruits from the Spanish market. , 2003, Journal of food protection.

[10]  S. Mínguez,et al.  What is the source of ochratoxin A in wine? , 2002, International journal of food microbiology.

[11]  F. Accensi,et al.  Distribution of Ochratoxin A producing strains in the A. niger aggregate , 2001, Antonie van Leeuwenhoek.

[12]  J. Visser,et al.  Combined Molecular and Biochemical Approach Identifies Aspergillus japonicus and Aspergillus aculeatus as Two Species , 2001, Applied and Environmental Microbiology.

[13]  R. Massey,et al.  Ochratoxin A in dried vine fruit: method development and survey. , 1999, Food additives and contaminants.

[14]  M. Vieira,et al.  Diversity among soil and insect isolates of Metarhizium anisopliae var. anisopliae detected by RAPD , 1996 .

[15]  N. L. Glass,et al.  Development of primer sets designed for use with the PCR to amplify conserved genes from filamentous ascomycetes , 1995, Applied and environmental microbiology.

[16]  J. Thompson,et al.  CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. , 1994, Nucleic acids research.

[17]  M. Castegnaro Mycotoxins, endemic nephropathy and urinary tract tumours. , 1991, IARC scientific publications.

[18]  J. Frisvad,et al.  Standardized high-performance liquid chromatography of 182 mycotoxins and other fungal metabolites based on alkylphenone retention indices and UV-VIS spectra (diode array detection). , 1988, Journal of chromatography.

[19]  F. Rohlf NTSYS-pc: Microcomputer Programs for Numerical Taxonomy and Multivariate Analysis , 1987 .

[20]  R. Sokal,et al.  Numerical Taxonomy: The Principles and Practice of Numerical Classification. , 1975 .

[21]  F. Verstraete,et al.  European Union legislation on mycotoxins in food and feed: overview of the decision-making process and recent and future developments. , 2008 .

[22]  J. Frisvad,et al.  Diagnostic tools to identify black aspergilli , 2007, Studies in mycology.

[23]  Jens Christian Frisvad,et al.  New ochratoxin A or sclerotium producing species in Aspergillus section Nigri. , 2004 .

[24]  Agra Europe European Union Legislation on Dairy Products. , 2000 .

[25]  T. A. Hall,et al.  BIOEDIT: A USER-FRIENDLY BIOLOGICAL SEQUENCE ALIGNMENT EDITOR AND ANALYSIS PROGRAM FOR WINDOWS 95/98/ NT , 1999 .

[26]  M. Nakajima,et al.  Use of monoclonal antibodies, enzyme-linked immunosorbent assay and immunoaffinity column chromatography to determine ochratoxin A in porcine sera, coffee products and toxin-producing fungi. , 1991, IARC scientific publications.

[27]  T. White Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics , 1990 .

[28]  Thomas J. White,et al.  PCR protocols: a guide to methods and applications. , 1990 .

[29]  J. Frisvad,et al.  Standardized high-performance liquid chromatography of 182 mycotoxins and other fungal metabolites based on alkylphenone retention indices and UV—VIS spectra (diodearray detection) , 1987 .