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

被引:45
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
[11]   Quantification of the copy number of nor-1, a gene of the aflatoxin biosynthetic pathway by real-time PCR, and its correlation to the cfu of Aspergillus flavus in foods [J].
Mayer, Z ;
Bagnara, A ;
Färber, P ;
Geisen, R .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2003, 82 (02) :143-151
[12]   Detection of transcripts of the aflatoxin genes aflD, af10, and aflP by reverse transcription-polymerase chain reaction allows differentiation of aflatoxin-producing and non-producing isolates of Aspergillus flavus and Aspergillus parasiticus [J].
Scherm, B ;
Palomba, M ;
Serra, D ;
Marcello, A ;
Migheli, Q .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2005, 98 (02) :201-210
[13]   Detection of aflatoxigenic molds in grains by PCR [J].
Shapira, R ;
Paster, N ;
Eyal, O ;
Menasherov, M ;
Mett, A ;
Salomon, R .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (09) :3270-3273
[14]   PCR-restriction fragment length analysis of aflR gene for differentiation and detection of Aspergillus flavus and Aspergillus parasiticus in maize [J].
Somashekar, D ;
Rati, ER ;
Chandrashekar, A .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2004, 93 (01) :101-107
[15]   TRANSFORMATION OF ASPERGILLUS-NIDULANS BY USING A TRPC PLASMID [J].
YELTON, MM ;
HAMER, JE ;
TIMBERLAKE, WE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (05) :1470-1474
[16]   Detection of aflatoxigenic fungi in feeds using the PCR method [J].
Zachová, I ;
Vytrasová, J ;
Pejchalová, M ;
Cervenka, L ;
Tavcar-Kalcher, G .
FOLIA MICROBIOLOGICA, 2003, 48 (06) :817-821