Spatial variability of Aspergillus flavus soil populations under different crops and corn grain colonization and aflatoxins

2004 ◽  
Vol 82 (12) ◽  
pp. 1768-1775 ◽  
Author(s):  
H K Abbas ◽  
R M Zablotowicz ◽  
M A Locke

Aflatoxin contamination in corn caused by Aspergillus flavus Link is a serious constraint on economical corn (Zea mays L.) production in the Mississippi Delta. The ecology of A. flavus was evaluated in a 3-year study assessing the spatial variability of soil populations of A. flavus in a Mississippi Delta field under different crops. A 1.07-ha section of the field was laid out in 126 9.2-m2 plots, and soil was sampled in May 2000, March 2001, and April 2002. Aspergillus flavus populations were determined by plating on selective media, and A. flavus colonization was assessed in corn during 2000. Aspergillus flavus populations in soil were significantly (P < 0.01 level) influenced by previous crop. The highest propagule density (794 cfu·g–1) was found following the corn crop in 2001 versus 251 cfu·g–1 soil in 2000 following cotton and 457 cfu·g–1 following wheat in 2002. Aspergillus flavus populations in 2001 and 2002 exhibited a moderate degree of spatial structure, described by spherical and exponential models, respectively, but populations in 2000 exhibited little spatial structure. Colonization of corn kernels by A. flavus in 2000 ranged from 0% to 100% (mean = 15% colonized kernels), and aflatoxin levels ranged from 0 to 1590 ppb (mean = 57 ppb). Aflatoxin levels were randomly distributed in the field and not correlated with A. flavus colonization. Aflatoxin production was found in 43% to 59% of A. flavus soil isolates with the highest incidence in soil populations following corn in 2001. However, 84% of A. flavus isolated from corn kernels produced aflatoxin. Results indicate that within a single field there was a wide range of A. flavus soil propagule densities varying in potential to produce aflatoxin.Key words: Aspergillus flavus, aflatoxins, soil, corn (Zea mays), cotton, wheat, spatial variability.

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Hamed K. Abbas ◽  
Nacer Bellaloui ◽  
Robert M. Zablotowicz ◽  
H. Arnold Bruns ◽  
Anne M. Gillen

The effect of corn-soybean rotation on mycotoxin contamination in corn (Zea maysL.) and soybean (Glycine maxL. Merrill.) grains has not been fully evaluated. Therefore, this research investigated the effect of corn-soybean rotation on aflatoxin and fumonisin contamination in respective grains. The results showed that aflatoxin levels in soybean averaged 2.3,<0.5, 0.6, and 6.8 ng/g in 2005, 2006, 2007, and 2008, while corn aflatoxin levels were 16.7, 37.1, 2.4, and 54.8 ng/g, respectively.Aspergillus flavuscolonization was significantly greater (P≤0.05) in corn (log 1.9, 2.9, and 4.0 cfu/g) compared to soybean (<1.3, 2.6, and 2.7 cfu/g) in 2005, 2007, and 2008, respectively. AflatoxigenicA. flavusisolates were more frequent in corn than in soybean in all four years. Higher fumonisin levels were found in corn (0.2 to 3.6 μg/g) than in soybean (<0.2 μg/g). Rotating soybean with corn reduces the potential for aflatoxin contamination in corn by reducingA. flavuspropagules in soil and grain and reducing aflatoxigenicA. flavuscolonization. These results demonstrated that soybean grain is less susceptible to aflatoxin contamination compared to corn due to a lower level of colonization byA. flavuswith a greater occurrence of non-aflatoxigenic isolates.


1999 ◽  
Vol 65 (6) ◽  
pp. 2738-2740 ◽  
Author(s):  
Sui-Sheng T. Hua ◽  
James L. Baker ◽  
Melanie Flores-Espiritu

ABSTRACT The nor mutant of Aspergillus flavus has a defective norsolorinic acid reductase, and thus the aflatoxin biosynthetic pathway is blocked, resulting in the accumulation of norsolorinic acid, a bright red-orange pigment. We developed a visual agar plate assay to monitor yeast strains for their ability to inhibit aflatoxin production by visually scoring the accumulation of this pigment of the nor mutant. We identified yeast strains that reduced the red-orange pigment accumulation in the normutant. These yeasts also reduced aflatoxin accumulation by a toxigenic strain of A. flavus. These yeasts may be useful for reducing aflatoxin contamination of food commodities.


2002 ◽  
Vol 65 (12) ◽  
pp. 1984-1987 ◽  
Author(s):  
J. E. MELLON ◽  
P. J. COTTY

Soybean lines lacking lipoxygenase (LOX) activity were compared with soybean lines having LOX activity for the ability to support growth and aflatoxin B1 production by the fungal seed pathogen Aspergillus flavus. Whole seeds, broken seeds, and heat-treated (autoclaved) whole seeds were compared. Broken seeds, irrespective of LOX presence, supported excellent fungal growth and the highest aflatoxin levels. Autoclaved whole seeds, with or without LOX, produced good fungal growth and aflatoxin levels approaching those of broken seeds. Whole soybean seeds supported sparse fungal growth and relatively low aflatoxin levels. There was no significant difference in aflatoxin production between whole soybean seeds either with or without LOX, although there did seem to be differences among the cultivars tested. The heat treatment eliminated LOX activity (in LOX+ lines), yet aflatoxin levels did not change substantially from the broken seed treatment. Broken soybean seeds possessed LOX activity (in LOX+ lines) and yet yielded the highest aflatoxin levels. The presence of active LOX did not seem to play the determinant role in the susceptibility of soybean seeds to fungal pathogens. Seed coat integrity and seed viability seem to be more important characteristics in soybean seed resistance to aflatoxin contamination. Soybean seeds lacking LOX seem safe from the threat of increased seed pathogen susceptibility.


mBio ◽  
2020 ◽  
Vol 11 (4) ◽  
Author(s):  
Milton T. Drott ◽  
Tatum R. Satterlee ◽  
Jeffrey M. Skerker ◽  
Brandon T. Pfannenstiel ◽  
N. Louise Glass ◽  
...  

ABSTRACT The apparent rarity of sex in many fungal species has raised questions about how much sex is needed to purge deleterious mutations and how differences in frequency of sex impact fungal evolution. We sought to determine how differences in the extent of recombination between populations of Aspergillus flavus impact the evolution of genes associated with the synthesis of aflatoxin, a notoriously potent carcinogen. We sequenced the genomes of, and quantified aflatoxin production in, 94 isolates of A. flavus sampled from seven states in eastern and central latitudinal transects of the United States. The overall population is subdivided into three genetically differentiated populations (A, B, and C) that differ greatly in their extent of recombination, diversity, and aflatoxin-producing ability. Estimates of the number of recombination events and linkage disequilibrium decay suggest relatively frequent sex only in population A. Population B is sympatric with population A but produces significantly less aflatoxin and is the only population where the inability of nonaflatoxigenic isolates to produce aflatoxin was explained by multiple gene deletions. Population expansion evident in population B suggests a recent introduction or range expansion. Population C is largely nonaflatoxigenic and restricted mainly to northern sampling locations through restricted migration and/or selection. Despite differences in the number and type of mutations in the aflatoxin gene cluster, codon optimization and site frequency differences in synonymous and nonsynonymous mutations suggest that low levels of recombination in some A. flavus populations are sufficient to purge deleterious mutations. IMPORTANCE Differences in the relative frequencies of sexual and asexual reproduction have profound implications for the accumulation of deleterious mutations (Muller’s ratchet), but little is known about how these differences impact the evolution of ecologically important phenotypes. Aspergillus flavus is the main producer of aflatoxin, a notoriously potent carcinogen that often contaminates food. We investigated if differences in the levels of production of aflatoxin by A. flavus could be explained by the accumulation of deleterious mutations due to a lack of recombination. Despite differences in the extent of recombination, variation in aflatoxin production is better explained by the demography and history of specific populations and may suggest important differences in the ecological roles of aflatoxin among populations. Furthermore, the association of aflatoxin production and populations provides a means of predicting the risk of aflatoxin contamination by determining the frequencies of isolates from low- and high-production populations.


1987 ◽  
Vol 22 (4) ◽  
pp. 307-310 ◽  
Author(s):  
W. W. McMillian ◽  
N. W. Widstrom ◽  
D. M. Wilson

The use of plants that resist insects has been suggested as a potential means of reducing aflatoxin contamination in some crops. Dent corn, Zea mays L., germplasm possessing the characteristic of a relatively tight, complete husk cover and germplasm possessing the characteristic of a relatively loose, incomplete husk cover on the ear were evaluated for 3 years at Tifton, GA, for aflatoxin contamination. In two of the three test years, corn ears with tight, complete husk cover sustained significantly lower mean amounts of aflatoxin than ears with loose, incomplete husk cover following artificial inoculation with Aspergillus flavus Link spores. Ears hand-infested with maize weevils, Sitophilus zeamais (Motschulsky), sustained significantly higher amounts of aflatoxin (329 ng·g−1) than ears infested with fall armyworms, Spodoptera frugiperda (J. E. Smith), (80 ng·g−1), European corn borers, Ostrinia nubilalis (Hübner), (71 ng·g−1), or corn earworms Heliothis zea (Boddie) (60 ng·g−1). Overall, ears in the check (inoculated with A. flavus only) sustained significantly lower aflatoxin (37 ng·g−1) amounts than ears from plots supplemented with insects. Although insects were not applied in the check plots, some damage was observed on the ears.


2010 ◽  
Vol 11 (1) ◽  
pp. 18 ◽  
Author(s):  
H. Arnold Bruns ◽  
Hamed K. Abbas

Aflatoxin research in corn (Zea mays L.) usually requires application of inoculum of Aspergillus flavus to soil or plant ears. The pin-bar vs. side-needle or spray vs. solid material inoculations using A. flavus isolate F3W4 (NRRL 30798) were compared in 2004, 2006, and 2007 using three hybrids in two irrigated experiments each year at Stoneville, MS. Both were planted on a silty clay soil in randomized complete block designs with four replications of treatments. Mature ears inoculated by the pin-bar, side-needle, or spray methods were analyzed for aflatoxin. Ears from controls and solid material inoculum treatments were sampled for analysis at plot harvest. Pin-bar inoculation had more aflatoxin in 2004 (551.9 ng/g) and 2006 (305.8 ng/g) than side-needle inoculation (342.2 ng/g and 151.1 ng/g for 2004 and 2006, respectively), which was greater than controls (76.8 ng/g and 21.6 ng/g for 2004 and 2006, respectively). Solid material inoculation did not differ in aflatoxin from controls. Spraying produced the most aflatoxin (344.1 ng/g) only in 2004. Aflatoxin was low in 2007 when timely rainfall, irrigation, and no temperatures ≥ 35°C resulted in only the pin-bar (20.8 ng/g) and solid material (20.6 ng/g) treatments having > 2.0 ng/g of aflatoxin. Accepted for publication 26 March 2010. Published 1 June 2010.


1998 ◽  
Vol 88 (4) ◽  
pp. 276-281 ◽  
Author(s):  
Z.-Y. Chen ◽  
R. L. Brown ◽  
A. R. Lax ◽  
B. Z. Guo ◽  
T. E. Cleveland ◽  
...  

Corn genotypes resistant or susceptible to Aspergillus flavus were extracted for protein analysis using a pH 2.8 buffer. The profile of protein extracts revealed that a 14-kDa protein is present in relatively high concentration in kernels of seven resistant corn genotypes, but is absent or present only in low concentration in kernels of six susceptible ones. The N-terminal sequence of this 14-kDa protein showed 100% homology to a corn trypsin inhibitor. The 14-kDa protein purified from resistant varieties also demonstrated in vitro inhibition of both trypsin activity and the growth of A. flavus. This is the first demonstration of antifungal activity of a corn 14-kDa trypsin inhibitor protein. The expression of this protein among tested genotypes may be related to their difference in resistance to A. flavus infection and subsequent aflatoxin contamination.


2015 ◽  
Vol 8 (2) ◽  
pp. 235-244 ◽  
Author(s):  
K.E. Damann Jr.

The term ‘competitive exclusion’ involving physical blockage of growth or access of the toxigenic strain to the seed target has been used to describe the mechanism of biological control of aflatoxin contamination. However, recent evidence suggests that a form of intraspecific aflatoxin inhibition requiring growth of the competing strains together during the infection process in such a way that hyphae physically interact or touch is the trigger for preventing induction of aflatoxin synthesis. This direct touch-based inhibition of aflatoxin synthesis is posited to be the mechanistic basis of biological control in this system. Evidence for this idea comes from the published observations that co-culture of toxigenic and atoxigenic strains in a suspended disc system, in which the hyphae physically interact, prevents aflatoxin production. However, growth of the same strains in the same medium in the two compartments of a filter insert plate well system, separating the atoxigenic and toxigenic strains with a 0.4 μm or 3.0 μm filter, allows aflatoxin production approaching that of the toxigenic strain alone. When the strains are mixed and placed in both the insert and the well compartments, the intraspecific aflatoxin inhibition occurs as it did in the suspended disc culture system. This further suggests that neither nutrient competition nor soluble signal molecules, which should pass through the filter, are involved in intraspecific aflatoxin inhibition. When the two strains are separated by a 12 μm filter that would allow some passage of conidia or hyphae between the compartments the aflatoxin synthesis is approximately half that of the toxigenic strain alone. This phenomenon could be termed ‘competitive inclusion’ or ‘competitive phenotype conversion’. Work of others that relates to understanding the phenomenon is discussed, as well as an Aspergillus flavus population biology study from the Louisiana maize agro-ecosystem which has biological control implications.


2014 ◽  
Vol 668-669 ◽  
pp. 1550-1553 ◽  
Author(s):  
Chu Shu Zhang ◽  
Qin Zhao ◽  
Jian Xiong Feng ◽  
Jie Sun ◽  
Li Na Yu ◽  
...  

Single factor and Plackett-Burman design were used to determine the key environmental factors for Aspergillus flavus growth and aflatoxin production. The results showed that the key factors were culture time, moisture content. So Controling of moisture was crucial for Aflatoxin contamination prevention and control.


2004 ◽  
Vol 31 (2) ◽  
pp. 134-141 ◽  
Author(s):  
H. Q. Xue ◽  
T. G. Isleib ◽  
H. T. Stalker ◽  
G. A. Payne ◽  
G. OBrian

Abstract Anatoxins are carcinogenic and extremely toxic secondary metabolites produced primarily by two fungi, Aspergillus flavus Link ex Fries and A. parasiticus Speare. Elimination of aflatoxin contamination in peanut (Arachis hypogaea L.) is a high priority of the peanut industry. Resistant cultivars should be an effective and low-cost part of an integrated aflatoxin management program. To date, no cultivated peanut has been reported with stable high levels of resistance to aflatoxin production. Arachis species and interspecific tetraploid lines have been evaluated for resistance to several peanut diseases and insect pests, and highly resistant accessions have been reported. Seven accessions of A. cardenasii Krapov. and W.C. Gregory, 29 of A. duranensis Krapov. and W.C. Gregory, and 17 interspecific tetraploid lines derived from A. hypogaea × A. cardenasii were inoculated with A. flavus strain NRRL 3357 and analyzed for aflatoxin content after incubation. On average, A. duranensis and A. cardenasii accumulated significantly less aflatoxin than A. hypogaea checks. The mean difference between the two wild species was not significant. Arachis duranensis accessions PI 468319 (GKBSPSc 30073), PI 468200 (GKBSPSc 30064), and PI 262133 (GKP 10038 sl.); and A. cardenasii accessions PI 262141 (GKP 10017) and PI 475997 (KSSc 36018) had reduced levels of aflatoxin accumulation and should be valuable sources of resistance to aflatoxin contamination. Of the interspecific tetraploid lines, only GP-NC WS 2 supported aflatoxin production not significantly different from resistant parent A. cardenasii GKP 10017, and it appears to be a line with reduced capacity for aflatoxin accumulation.


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