High genetic variability in non-aflatoxigenic A. flavus strains by using Quadruplex PCR-based assay

被引:46
作者
Criseo, Giuseppe [1 ]
Racco, Cosimo [1 ]
Romeo, Orazio [1 ]
机构
[1] Univ Messina, Dept Microbiol Genet & Mol Sci, I-98166 Messina, Italy
关键词
aflatoxin; Aspergillus flavus; nor-1; omt-A; ver-1 and aflR genes; aflatoxin non-producing A. flavus strains;
D O I
10.1016/j.ijfoodmicro.2008.04.020
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Aflatoxigenic Aspergillus flavus isolates always show, by using a multiplex PCR-system, four DNA fragments specific for aflR, nor-1. ver-1. and omt-A genes. Non-aflatoxigenic A. flavus strains give variable DNA banding pattern lacking one, two, three or four of these genes. Recently, it has been found and reported that some aflatoxin non-producing A. flavus strains show a complete set of genes. Because less is known about the incidence of structural genes aflR, nor-1, ver-1 and omt-A in aflatoxin non-producing strains of A. flavus, we decided to study the frequencies of the aflatoxin structural genes in non-aflatoxigenic A. flavus strains isolated from food and feed commodities. The results can be summarized as following: 36.5% of the examined non-aflatoxigenic A. flavus strains showed DNA fragments that correspond to the complete set of genes (quadruplet pattern) as found in aflatoxigenic A. flavus. Forty three strains (32%) showed three DNA banding patterns grouped in four profiles where nor-L ver-1 and omt-A was the most frequent profile. Twenty five (18.7%) of non-aflatoxigenic A. flavus strains yielded two DNA banding pattern whereas sixteen (12%) of the strains showed one DNA banding pattern. In one strain, isolated from poultry feed, no DNA bands were found. The nor-1 gene was the most representative between the four aflatoxin structural assayed genes. Lower incidence was found for aflR gene. Our data show a high level of genetic variability among non-aflatoxigenic A. flavus isolates that require greater attention in order to design molecular experiment to distinguish true aflatoxigenic from non-aflatoxigenic A. flavus strains.
引用
收藏
页码:341 / 343
页数:3
相关论文
共 16 条
[1]   Mycotoxins [J].
Bennett, JW ;
Klich, M .
CLINICAL MICROBIOLOGY REVIEWS, 2003, 16 (03) :497-+
[2]   Understanding the genetics of regulation of aflatoxin production and Aspergillus flavus development [J].
Bhatnagar, Deepak ;
Cary, Jeffrey W. ;
Ehrlich, Kenneth ;
Yu, Jiujiang ;
Cleveland, Thomas E. .
MYCOPATHOLOGIA, 2006, 162 (03) :155-166
[3]   Gene duplication, modularity and adaptation in the evolution of the aflatoxin gene cluster [J].
Carbone, Ignazio ;
Ramirez-Prado, Jorge H. ;
Jakobek, Judy L. ;
Horn, Bruce W. .
BMC EVOLUTIONARY BIOLOGY, 2007, 7 (1)
[4]   Aflatoxigenicity in Aspergillus:: molecular genetics, phylogenetic relationships and evolutionary implications [J].
Cary, Jeffrey W. ;
Ehrlich, Kenneth C. .
MYCOPATHOLOGIA, 2006, 162 (03) :167-177
[5]   Sequence breakpoints in the aflatoxin biosynthesis gene cluster and flanking regions in nonaflatoxigenic Aspergillus flavus isolates [J].
Chang, PK ;
Horn, BW ;
Dorner, JW .
FUNGAL GENETICS AND BIOLOGY, 2005, 42 (11) :914-923
[6]   Differentiation of aflatoxin-producing and non-producing strains of Aspergillus flavus group [J].
Criseo, G ;
Bagnara, A ;
Bisignano, G .
LETTERS IN APPLIED MICROBIOLOGY, 2001, 33 (04) :291-295
[7]   A multiplex RT-PCR approach to detect aflatoxigenic strains of Aspergillus flavus [J].
Degola, F. ;
Berni, E. ;
Dall'Asta, C. ;
Spotti, E. ;
Marchelli, R. ;
Ferrero, I. ;
Restivo, F. M. .
JOURNAL OF APPLIED MICROBIOLOGY, 2007, 103 (02) :409-417
[8]   Detection of aflatoxinogenic fungi in figs by a PCR reaction [J].
Farber, P ;
Geisen, R ;
Holzapfel, WH .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 1997, 36 (2-3) :215-220
[9]   Multiplex polymerase chain reaction for the detection of potential aflatoxin and sterigmatocystin producing fungi [J].
Geisen, R .
SYSTEMATIC AND APPLIED MICROBIOLOGY, 1996, 19 (03) :388-392
[10]   Detection of aflatoxigenic fungi in selected food commodities by PCR [J].
Manonmani, HK ;
Anand, S ;
Chandrashekar, A ;
Rati, ER .
PROCESS BIOCHEMISTRY, 2005, 40 (08) :2859-2864