Vegetative compatibility and phenotypic characterization as a means of determining genetic diversity of Aspergillus flavus isolates.

Fungal Biol

Department of Molecular and Cell Biology, Plant Stress Laboratory 204/207, MCB Building, Upper Campus, University of Cape Town, Private Bag X3, Rondebosch, 7701 Cape Town, South Africa. Electronic address:

Published: April 2018

AI Article Synopsis

  • Toxigenic Aspergillus species are harmful fungi that produce mycotoxins, causing serious health issues like cancer and liver damage in both humans and animals, particularly seen in outbreaks like the deadly one in Kenya in 2010.
  • A study focused on the diversity and characteristics of Aspergillus flavus across different Kenyan agricultural regions identified 20 unique vegetative compatibility groups, with some groups being more prevalent than others.
  • The research offered new insights into aflatoxin distribution in counties like Nandi, Homa Bay, and Kisumu, providing valuable data for future biocontrol strategies to combat aflatoxin contamination.

Article Abstract

Toxigenic Aspergillus species produce mycotoxins that are carcinogenic, hepatotoxic and teratogenic immunosuppressing agents in both human and animals. Kenya frequently experiences outbreaks of aflatoxicosis with the worst occurring in 2010, which resulted in 215 deaths. We examined the possible reasons for these frequent aflatoxicosis outbreaks in Kenya by studying Aspergillus flavus diversity, phenotypes and mycotoxin profiles across various agricultural regions. Using diagonal transect random sampling, maize kernels were collected from Makueni, Homa Bay, Nandi, and Kisumu counties. Out of 37 isolates, nitrate non-utilizing auxotrophs complementation test revealed 20 vegetative compatibility groups. We designated these groups by the prefix "KVCG", where "K" represented Kenya and consequently assigned numbers 1-20 based on our findings. KVCG14 and KVCG15 had highest distribution frequency (n = 13; 10.8 %). The distribution of the L-, S- and S-/L-morphotypes across the regions were 57 % (n = 21); 7 % (n = 3) and 36 % (n = 13), respectively. Furthermore, a unique isolate (KSM015) was identified that had characteristics of S-morphotype, but produced both aflatoxins B and G. Coconut agar medium (CAM) assay, TLC and HPLC analyses confirmed the presence or absence of aflatoxins in selected toxigenic and atoxigenic isolates. Diversity index (H') analyses ranged from 0.11 (Nandi samples) to 0.32 (Kisumu samples). Heterokaryon compatibility ranged from 33 % (for the Makueni samples, n = 3) to 67 % (Nandi samples, n = 6). To our knowledge, this is the first reported findings for A. flavus diversity and distribution in Nandi, Homa Bay and Kisumu counties and may assist current and future researchers in the selection of biocontrol strategies to mitigate aflatoxin contamination as has been researched in Makueni and neighbouring counties.

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http://dx.doi.org/10.1016/j.funbio.2017.11.005DOI Listing

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