Abstract
AbstractA simple method for PCR‐based plant clinical diagnosis of bacterial blight of geraniums caused by Xanthomonas campestris pv. pelargonii is described. The method entails maceration of infected tissues in water or 10mM Tris‐ HCI, pH 8.0 buffer, followed by treatment of the macerate with a commercially‐available extraction matrix (GeneReleaserTM) in which nucleic acid is released by brief microwave heating. Nucleic acid prepared in this manner served directly as template for PCR amplification with primers targeting a sequence in the genome of the bacterium. Using this protocol, it was possible to quickly identify X. campestris pv. pelargonii in infected geraniums, whereas amplification products were not obtained with nucleic acid preparations from noninfected plants, or from plants infected with the bacterial pathogens, Corynebacterium fascians or Pseudomonas cichorii.
Published Version (
Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call