Pseudoperonospora cubensis, the causal agent of cucurbit downy mildew (CDM), is known to exhibit host specialization. The virulence of different isolates of the pathogen can be classified into pathotypes based on their compatibility with a differential set composed of specific cucurbit host types. However, the genetic basis of host specialization within P. cubensis is not yet known. Total genom...

Cucurbit downy mildew (Pseudoperonospora cubensis) is characterized by large variation in pathogenicity, specificity and host-parasite interactions. This report reviews the current state of understanding regarding interactions between P. cubensis and Cucurbitaceae, the genetic control of host reactions, and overall variation within the pathogen. A well-characterized set of differential Cucurbit...

Downy mildew caused by the oomycete pathogen Pseudoperonospora cubensis is a devastating foliar disease of cucurbits worldwide. We previously demonstrated that the wild melon line PI 124111F (PI) is highly resistant to all pathotypes of P. cubensis. That resistance was controlled genetically by two partially dominant, complementary loci. Here, we show that unlike other plant disease resistance ...

Pseudoperonospora cubensis, an obligate oomycete pathogen, is the causal agent of cucurbit downy mildew, a foliar disease of global economic importance. Similar to other oomycete plant pathogens, Ps. cubensis has a suite of RXLR and RXLR-like effector proteins, which likely function as virulence or avirulence determinants during the course of host infection. Using in silico analyses, we identif...

RNA sequencing (RNA-seq) and genotyping-by-sequencing (GBS) were used for single nucleotide polymorphism (SNP) identification from two economically important obligate plant pathogens, Pseudoperonospora cubensis and P. humuli. Twenty isolates of P. cubensis and 19 isolates of P. humuli were genotyped using RNA-seq and GBS. Principle components analysis (PCA) of each data set showed genetic separ...

the compatibility studies of pseudomonas fluorescens (pf1) with azoxystrobin at differ-ent concentrations viz., 100, 150, 200, 250 and 300 ppm revealed that it was compatible with all the concentrations of azoxystrobin tested and the growth of the bacterium was unaffected even at the maximum concentration of 300 ppm. the field experiment revealed a foliar application of pf1 (2.5 kg ha-1) and az...