scholarly journals Aspergillus Colonization and Aflatoxin Contamination in Peanut Genotypes with Resistance to Other Fungal Pathogens

Plant Disease ◽  
1997 ◽  
Vol 81 (12) ◽  
pp. 1429-1431 ◽  
Author(s):  
C. Corley Holbrook ◽  
David M. Wilson ◽  
Michael E. Matheron ◽  
William F. Anderson

Indirect selection tools would be valuable in the development of peanut (Arachis hypogaea) cultivars with resistance to aflatoxin contamination. The objective of this study was to determine whether resistance to other fungi could be used as an indirect selection tool for resistance to colonization of peanut by Aspergillus flavus group fungi or aflatoxin contamination. Nine peanut genotypes with resistance to late leaf spot (Cercosporidium personatum) or white mold (Sclerotium rolfsii) were evaluated for 2 years at Tifton, GA, and Yuma, AZ. Plots were subjected to late-season heat and drought stress. None of the genotypes exhibited less colonization of shells or kernels by A. flavus group fungi than cv. Florunner when tested in Georgia or Arizona. None of the genotypes showed a reduced level of aflatoxin contamination in comparison to Florunner at either location. These results indicate that the mechanisms of resistance to other fungi operating in these genotypes are not effective in providing resistance to colonization by A. flavus group fungi or reducing aflatoxin contamination. Therefore, resistance to these fungi cannot be used as an indirect selection tool for resistance to aflatoxin contamination.

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.


1982 ◽  
Vol 75 (2) ◽  
pp. 265-269 ◽  
Author(s):  
W. D. Guthrie ◽  
E. B. Lillehoj ◽  
D. Barry ◽  
W. W. McMillian ◽  
W. F. Kwolek ◽  
...  

2017 ◽  
Vol 3 (3) ◽  
pp. 22-29 ◽  
Author(s):  
Chancy B. Sibakwe ◽  
Trust Kasambara-Donga ◽  
Samuel M. C. Njoroge ◽  
W. A. B. Msuku ◽  
Wezi G. Mhango ◽  
...  

2019 ◽  
Author(s):  
Jake C. Fountain ◽  
Liming Yang ◽  
Manish K. Pandey ◽  
Prasad Bajaj ◽  
Danny Alexander ◽  
...  

AbstractThe primary and secondary metabolites of fungi are critical for adaptation to environmental stresses, host pathogenicity, competition with other microbes, and reproductive fitness. Drought-derived reactive oxygen species (ROS) have been shown to stimulate aflatoxin production and regulate development in Aspergillus flavus, and may function in signaling with host plants. Here, we have performed global, untargeted metabolomics to better understand the role of aflatoxin production in oxidative stress responses, and also explore isolate-specific oxidative stress responses over time. Two field isolates of A. flavus, AF13 and NRRL3357, possessing high and moderate aflatoxin production, respectively, were cultured in medium with and without supplementation with 15mM H2O2, and mycelia were collected following 4 and 7 days in culture for global metabolomics. Overall, 389 compounds were described in the analysis which were examined for differential accumulation. Significant differences were observed in both isolates in response to oxidative stress and when comparing sampling time points. The moderate aflatoxin-producing isolate, NRRL3357, showed extensive stimulation of antioxidant mechanisms and pathways including polyamines metabolism, glutathione metabolism, TCA cycle, and lipid metabolism while the highly aflatoxigenic isolate, AF13, showed a less vigorous response to stress. Carbohydrate pathway levels also imply that carbohydrate repression and starvation may influence metabolite accumulation at the later timepoint. Higher conidial oxidative stress tolerance and antioxidant capacity in AF13 compared to NRRL3357, inferred from their metabolomic profiles and growth curves over time, may be connected to aflatoxin production capability and aflatoxin-related antioxidant accumulation. The coincidence of several of the detected metabolites in H2O2-stressed A. flavus and drought-stressed hosts suggests their potential role in the interaction between these organisms and their use as markers/targets to enhance host resistance through biomarker selection or genetic engineering.Author SummaryAspergillus flavus is a fungal pathogen of several important crops including maize and peanut. This pathogen produces carcinogenic mycotoxins known as aflatoxins during infection of plant materials, and is particularly severe under drought stress conditions. This results in significant losses in crop value and poses a threat to food safety and security globally. To combat this, understanding how this fungus responds to environmental stresses related to drought can allow us to identify novel methods of mitigating aflatoxin contamination. Here, we analyzed the accumulation of a broad series of metabolites over time in two isolates of A. flavus with differing stress tolerance and aflatoxin production capabilities in response to drought-related oxidative stress. We identified several metabolites and mechanisms in A. flavus which allow it to cope with environmental oxidative stress and may influence aflatoxin production and fungal growth. These may serve as potential targets for selection in breeding programs for the development of new cultivars, or for alteration using genetic engineering approaches to mitigate excessive aflatoxin contamination under drought stress.


1998 ◽  
Vol 61 (1) ◽  
pp. 98-102 ◽  
Author(s):  
B. Z. GUO ◽  
R. L. BROWN ◽  
A. R. LAX ◽  
T. E. CLEVELAND ◽  
J. S. RUSSIN ◽  
...  

Mechanisms of resistance to infection by the fungus Aspergillus flavus and accumulation of aflatoxin were studied in kernels of resistant (GT-MAS:gk, Mp420) and susceptible (Pioneer 3154, Deltapine G-4666) corn genotypes. Proteins from kernel extracts of corn genotypes were analyzed by several methods of polyacrylamide gel electrophoresis. Consistent differences in protein profiles were detected among genotypes. Several proteins were unique to or present in greater concentration in resistant genotypes, whereas others were present only in susceptible genotypes. Extracts of resistant kernels showed markedly greater antifungal activity against A. flavus than did susceptible kernel extracts. Results from the present study suggest a role for kernel proteins in resistance to A. flavus infection and aflatoxin contamination in corn genotypes GT-MAS:gk and Mp420.


2018 ◽  
Vol 11 (2) ◽  
pp. 215-224 ◽  
Author(s):  
V. Garrido-Bazan ◽  
G. Mahuku ◽  
M. Bibbins-Martinez ◽  
A. Arroyo-Bacerra ◽  
M. Ángel Villalobos-López

Aspergillus flavus induced ear rots and subsequent contamination of maize (Zea mays L.) by aflatoxin is a serious food safety issue, especially in developing countries where the crop is mostly cultivated by smallholder famers for own consumption and income generation. A better understanding of the mechanisms of resistance could help breeders to develop resistant maize varieties. In this study, a set of six tropical maize inbred lines previously identified as resistant or susceptible under natural field conditions were evaluated for response to A. flavus colonisation and aflatoxin contamination. Fungal biomass was significantly higher (P<0.05) in susceptible than resistant maize inbred lines, and this was highly correlated (P=0.001) to aflatoxin levels. Maize inbred lines MRI, MR2 and MR3 had low fungal biomass and low aflatoxin levels, suggesting that resistance in these lines was mediated through restricted fungal colonisation and establishment. Among the three putatively resistant inbred lines mentioned above, MR2 had a relatively high colonisation compared to the other two lines, revealing that A. flavus could establish and colonise kernels that were injured during inoculation, but did not contain high levels of aflatoxin. This could signify the presence of host genes that interfere with the aflatoxin biosynthetic pathway.


Agro-Science ◽  
2021 ◽  
Vol 20 (1) ◽  
pp. 1-8
Author(s):  
F.T. Obani ◽  
B. Ikotun

Melon (Citrullus colocynthis L.) is an important crop used mainly for soups in Nigeria. Egusi: as it is commonly called in Nigeria is contaminated by many fungal pathogens which reduce quality of seeds during storage. Use of botanicals can be a safe method to manage fungal contamination instead of chemicals which pose a threat to human health. Therefore, efficacy of Piper guineense, Xylopia aethiopica and Ocimum gratissimum on fungi in shelled Egusi seed kernels (EK) were evaluated. One market in each of six South-western Nigerian states where Egusi is sold was purposively selected in 2012 and 2013. Egusi kernels (1⁄2kg, n = 162) were purchased from selected traders for fungi isolation, identification and incidence (%) determination. Clean EK treated with botanical powder (10, 20 and 40 g kg–1) were inoculated with Aspergillus flavus, A. niger, A. tamarii, Rhizopus sp., Penicillium aurantiogriseum, P. citrinum and Fusarium solani bi-weekly for 14-week storage period to evaluate growth reduction (%). Control was inoculated with sterile distilled water. Aspergillus flavus, A. niger, A. tamarii, Penicillium citrinum, P. aurantiogriseum, Fusarium solani and Rhizopus sp. were frequently encountered in EK. Aspergillus (32.4±1.6%) was the most predominant fungus followed by Rhizopus (21.5±2.0%) in all States. Piper guineense (40 g kg–1), X. aethiopica (20 g kg–1) and O. gratissimum (10 g kg–1) powders significantly reduced aflatoxin contamination by 42.5%, 56.5% and 45.0%, respectively; fungi growths were progressively reduced by P. guineense (5.5-90.0%), X. aethiopica (6.7-100.0%) and O. gratissimum (7.4 66.7%) up to 12 weeks of storage. Egusi kernels were highly infected with postharvest fungi especially Aspergillus species. Xylopia aethiopica at 20 g kg–1, O. gratissimum (40.0%) and P. guineense (40.0%) reduced fungi growth on Egusi considerably and therefore could be used as a safe management option to mitigate storage fungi contamination in Egusi kernels.


1989 ◽  
Vol 16 (2) ◽  
pp. 109-113 ◽  
Author(s):  
H. A. Azaizeh ◽  
R. E. Pettit ◽  
O. D. Smith ◽  
R. A. Tabef

Abstract Seven peanut genotypes (Arachis hypogaea L.) were tested in greenhouse and microplot experiments during two consecutive years to determine peanut peg colonization by Aspergillus flavus and to determine the effect of two drought stress treatments on the susceptibility of peanut shells and kernels to Aspergillus colonization and aflatoxin contamination. Moisture tensions within the soil and temperatures of the soil and air were monitored during these experiments. Colonization of peanut pegs was inconsistent among genotypes and between years. In general, low soil moisture tension enhanced colonization of peanut shells and kernels. Shells of most genotypes were highly colonized after harvest from each moisture regime. Kernels of all genotypes were more susceptible to A. flavus and A. parasiticus colonization under both long and short drought stress conditions compared to non-stressed conditions. However, no significant differences were obtained in the degree of Aspergillus infestation of kernels from PI 337409, Starr, and J-11 in the greenhouse experiments. Under microplot conditions, acomparison of several genotypes revealed that kernels from plants of genotypes TX811956 and TX798736 (short stress treatments) contained significantly lower Aspergillus infestation and kernels from the genotypes PI 337409 and TX811956 and TX798736 contained significantly less aflatoxin.


2020 ◽  
Vol 8 (11) ◽  
pp. 1633
Author(s):  
Mohamed F. Abdallah ◽  
Kris Audenaert ◽  
Sarah De Saeger ◽  
Jos Houbraken

The aflatoxin type B and G producer Aspergillus novoparasiticus was described in 2012 and was firstly reported from sputum, hospital air (Brazil), and soil (Colombia). Later, several survey studies reported the occurrence of this species in different foods and other agricultural commodities from several countries worldwide. This short communication reports on an old fungal strain (CBS 108.30), isolated from Pseudococcus sacchari (grey sugarcane mealybug) from an Egyptian sugarcane field in (or before) 1930. This strain was initially identified as Aspergillus flavus; however, using the latest taxonomy schemes, the strain is, in fact, A. novoparasiticus. These data and previous reports indicate that A. novoparasiticus is strongly associated with sugarcane, and pre-harvest biocontrol approaches with non-toxigenic A. novoparasiticus strains are likely to be more successful than those using non-toxigenic A. flavus strains. Further studies on the association between A. novoparasiticus and Pseudococcus sacchari might shed light on the distribution (and aflatoxin contamination) of this species in sugarcane. Additionally, the interaction between A. novoparasiticus, Pseudococcus sacchari, and sugarcane crop under different scenarios of climate change will be critical in order to get more insight into the host–pathogen interaction and host resistance and propose appropriate prevention strategies to decrease mycotoxin contamination and crop loss due to A. novoparasiticus attack.


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