Four In Silico Designed and Validated qPCR Assays to Detect and Discriminate   and , Individually or as a Complex.

Biology (Basel)

Agriculture and Agri-Food Canada (AAFC), 960 Carling Avenue, Ottawa, ON K1A 0C6, Canada.

Published: December 2021

AI Article Synopsis

  • Several fungi in the genus are known to infect grass species like wheat, with a specific mention of a damaging pathogen causing Karnal bunt, which is heavily regulated in many countries.
  • Traditional identification of Karnal bunt relied on morphology, a tedious process complicated by the presence of similar species, but advances in molecular biology have introduced faster detection methods, albeit with some limitations.
  • This study developed four highly sensitive qPCR tests using unique genomic regions to effectively distinguish between Karnal bunt and related pathogens, ensuring accurate identification through rigorous testing against various genetic samples.

Article Abstract

Several fungi classified in the genus are well-known to infect grass species including wheat (). is a highly unwanted wheat pathogen causing Karnal bunt, subject to quarantine regulations in many countries. Historically, suspected Karnal bunt infections were identified by morphology, a labour-intensive process to rule out other tuberculate-spored species that may be found as contaminants in grain shipments, and the closely-related pathogen on ryegrass (). Molecular biology advances have brought numerous detection tools to discriminate congeners (PCR, qPCR, etc.). While those tests may help to identify more rapidly, they share weaknesses of targeting insufficiently variable markers or lacking sensitivity in a zero-tolerance context. A recent approach used comparative genomics to identify unique regions within target species, and qPCR assays were designed in silico. This study validated four qPCR tests based on single-copy genomic regions and with highly sensitive limits of detection (~200 fg), two to detect and separately, and two newly designed, targeting both species as a complex. The assays were challenged with reference DNA of the targets, their close relatives, other crop pathogens, the wheat host, and environmental specimens, ensuring a high level of specificity for accurate discrimination.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698337PMC
http://dx.doi.org/10.3390/biology10121295DOI Listing

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