Downy mildew disease
of quinoa caused by Peronospora variabilis is a serious threat which greatly
reduces yield. The identification of the source of the primary infection at the
early growth stages of quinoa is necessary to manage the spread of this
pathogen. Hence, a conventional detection method based on polymerase chain
reaction (PCR) was applied to detect the DNA of P. variabilis in the tissues of
the different organs of quinoa plants (radicle or root; cotyledon or leaf;
hypocotyl or stem) at the different growth stages (5-, 10-, 15- and 21-days old
plants) and in inflorescences (flowers and their axes) at 60 and 80 days old.
Twelve composite quinoa seedling samples were subdivided into different organs
at the different growth stages. P. variabilis was detected in cotyledon/leaf
tissues (10/12; 83%), hypocotyl/stem tissues (41.6%; 5/12) and radicle/root was
the least positive (1/12; 0.8%) for presence of the pathogen. Moreover, the PCR
showed that the pathogen was detected in the flowers and in their axes at the
ages of 60 and 80 days. The internal transcribed spacer (ITS) and cytochrome c
oxidase subunit 2 (COX2) regions were examined. Phylogenetic analyses confirmed
that P. variabilis (EGDM1) was the causal agent of downy mildew affecting
quinoa in Egypt and genetically similar to the United States and China lineage
(COX2 Maximum likelihood tree). Downy mildew pathogen was detected in different
organs of quinoa plant at early growth stages and inflorescences. Hence, the
pathogen can spread systemically in quinoa tissues.
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