Abstract

Infestation of cereals such as wheat by pathogenic Fusarium species (Fusarium spp.) is associated with over 25% weight loss of the grain and accumulation of hazardous mycotoxins. Potential management strategies against the pathogens include the development of more resistant wheat genotypes and the development of rapid and accurate Fusarium spp. identification methods, among other control measures. This study evaluated the toxigenic potential in populations of Fusarium spp. isolated from seeds of locally developed wheat genotypes and levels of fumonisins in the grains at harvest in three counties in Kenya. The sampling of the wheat grains took place between September 2016 and October 2017. Determination of toxigenic potential was PCR based using Tri13F/Tri13DONR and FUM1F/FUM1R specific primer pairs while detection of fumonisin levels was done using Total Fumonisin Assay 0.25/5.0 ELISA kit. Data were analyzed using ANOVA and the Tukey HSD test. FUM1 gene was detected in 60% of the Fusarium spp. analyzed. The distribution of the gene within the isolates across the three regions was as follows: Narok: 54%, Uasin Gishu: 25%, and Nakuru: 21%. Tri13DON gene was not detected in the assessed potential deoxynivalenol (DON) producers. Fumonisin levels in the wheat samples from the three counties were significantly different ( p < 0.001 ). The highest fumonisin levels, 9.6 ppm, occurred in 30.7% of the grains of the studied wheat genotypes. Relatively high fumonisin levels occurred in Njoro II, Eagle 10, Robin, and Korongo wheat genotypes with no significant difference at 0.05 confidence interval. In conclusion, the toxigenic potential amongst the Fusarium spp. studied was confirmed based on the occurrence of FUM1 gene and the detection of fumonisins in 76% of the sampled wheat grains. More research is recommended to ascertain the prevalence of the genes determining the production of DON and the other trichothecenes in Fusarium spp. prevalent in the developed wheat genotypes in the different agroecological regions in Kenya. In addition, the assessment of the occurrence and levels of the respectful mycotoxins also needs further research. These would provide additional information for the improvement of strategies put in place to manage the effects of the pathogenic Fusarium spp. in the crop and to ensure mycotoxin safety of the wheat food chain for both livestock and human consumption. It also shows the need for the development of more disease-resistant wheat varieties by wheat seed-producing companies.

Highlights

  • Introduction e negative effect of pathogenicFusarium spp. in agriculture is due to the secondary metabolites they produce [1]. e toxigenic properties of mycotoxins are wide and vary in their effects ranging from phytotoxic to zootoxic activities

  • Fusarium spp. identification to determine the potential producers of mycotoxins among the isolates was based on internal transcribed spacer (ITS) region of the rDNA amplified by PCR using the described universal primers ITS1 (5’- TCCGTAGGTGGAACC TGCGG-3’) and ITS4 (5 -TCCTCCGCTTATTGATATGC3’) [29]. e ITS regions targeted for amplification were between the small nuclear 18S rDNA and large nuclear 28S rDNA, including 5.8S rDNA

  • Due to the existence of cryptic populations or intraspecific diversity, forecast of the toxigenic potential of Fusarium spp. may not necessarily depend on the accurate identification of the phytopathogenic species. e findings from this study ascertained the mycotoxigenic potential in populations of Fusarium spp. infecting varieties of wheat genotypes in three of the major wheat-producing counties in Kenya. e prevalence of the FUM1 and Tri13DON biosynthesis pathway genes determining the production of the respective mycotoxins was verified based on the results obtained from PCR reactions

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Summary

Introduction

Introduction e negative effect of pathogenicFusarium spp. in agriculture is due to the secondary metabolites (mycotoxins) they produce [1]. e toxigenic properties of mycotoxins are wide and vary in their effects ranging from phytotoxic to zootoxic activities. Fusarium spp. in agriculture is due to the secondary metabolites (mycotoxins) they produce [1]. E most frequently detected Fusarium spp. contaminants in wheat are DON, fumonisins (Fs), and Zearalenones [3,4,5]. Deoxynivalenol is a mycotoxin in the category of trichothecenes. It is produced by certain pathogenic Fusarium spp. infecting cereal crops in the field and in stores depending on the storage conditions. Other DON’s effects in animals are characterized by feed refusal and reduced weight gain [9, 10]. Fumonisins are another category of toxigenic compounds produced by certain pathogenic Fusarium spp. such as F. verticillioides, F. proliferatum, and F. oxysporum. Fumonisins are another category of toxigenic compounds produced by certain pathogenic Fusarium spp. such as F. verticillioides, F. proliferatum, and F. oxysporum. e toxins have been reported to cause diverse diseases in animals such as pigs and rats and have been implicated in the etiology of human esophageal cancer [11] and WHO [12]

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