The Development of a qPCR Assay to Measure Biomass in Maize and the Use of a Biocontrol Strategy to Limit Aflatoxin Production.

Toxins (Basel)

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

Published: March 2019

colonisation of maize can produce mycotoxins that are detrimental to both human and animal health. Screening of maize lines, resistant to infection, together with a biocontrol strategy, could help minimize subsequent aflatoxin contamination. We developed a qPCR assay to measure biomass and showed that two African maize lines, GAF4 and KDV1, had different fungal loads for the aflatoxigenic isolate (KSM014), fourteen days after infection. The qPCR assay revealed no significant variation in biomass between diseased and non-diseased maize tissues for GAF4, while KDV1 had a significantly higher biomass ( < 0.05) in infected shoots and roots compared to the control. The biocontrol strategy using an atoxigenic isolate (KSM012) against the toxigenic isolate (KSM014), showed aflatoxin production inhibition at the co-infection ratio, 50:50 for both maize lines (KDV1 > 99.7% and GAF ≥ 69.4%), as confirmed by bioanalytical techniques. As far as we are aware, this is the first report in Kenya where the biomass of from maize tissue was detected and quantified using a qPCR assay. Our results suggest that maize lines, which have adequate resistance to together with the appropriate biocontrol strategy, could limit outbreaks of aflatoxicoses.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468655PMC
http://dx.doi.org/10.3390/toxins11030179DOI Listing

Publication Analysis

Top Keywords

qpcr assay
16
biocontrol strategy
16
maize lines
16
assay measure
8
measure biomass
8
maize
8
biomass maize
8
strategy limit
8
aflatoxin production
8
gaf4 kdv1
8

Similar Publications

Heritable fragile bone disorders (FBDs), ranging from multifactorial to rare monogenic conditions, are characterized by an elevated fracture risk. Validating causative genes and understanding their mechanisms remain challenging. We assessed a semi-high throughput zebrafish screening platform for rapid in vivo functional testing of candidate FBD genes.

View Article and Find Full Text PDF

Recent advances in molecular science have significantly enlightened our mechanistic understanding of spinocerebellar ataxia type 7. To further close remaining gaps, we performed a multi-omics analysis using SCA7 mice. Entire brain tissue samples were collected from 12-week-old mice, and RNA sequencing, methylation analysis, and proteomic analysis were performed.

View Article and Find Full Text PDF

Detection of spp. DNA in gynaecological samples by quantitative real-time polymerase chain reaction (qPCR) is considered to be the reference diagnostic test for female genital schistosomiasis (FGS). However, qPCR needs expensive laboratory procedures and highly trained technicians.

View Article and Find Full Text PDF

Introduction: Schistosomiasis (Bilharzia), a neglected tropical disease caused by parasites, afflicts over 240 million people globally, disproportionately impacting Sub-Saharan Africa. Current diagnostic tests, despite their utility, suffer from limitations like low sensitivity. Polymerase chain reaction (PCR) and quantitative real-time PCR (qPCR) remain the most common and sensitive nucleic acid amplification tests.

View Article and Find Full Text PDF

Dirofilariasis, caused by the nematode spp., poses significant challenges in diagnosis due to its diverse clinical manifestations and complex life cycle. This comprehensive literature review focuses on the evolution of diagnostic methodologies, spanning from traditional morphological analyses to modern emerging techniques in the context of dirofilariasis diagnosis.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!