HrcQ is necessary for Xanthomonas oryzae pv. oryzae HR-induction in non-host tobacco and pathogenicity in host rice

Abstract Bacterial blight, caused by Xanthomonas oryzae pv. oryzae ( Xoo ), is one of the most destructive diseases of rice ( Oryza sativa L.) worldwide. The type III secretion system (T3SS) of Xoo , encoded by the hrp ( h ypersensitive r esponse and p athogenicity) genes, plays critical roles in conferring pathogenicity in host rice and triggering a hypersensitive response (HR) in non-host plants. To investigate the major genes conferring the pathogenicity and avirulence of Xoo , we previously constructed a random Tn5-insertion mutant library of Xoo strain PXO99 A . We report here the isolation and characterization of a Tn5-insertion mutant PXM69. Tn5-insertion mutants were screened on indica rice JG30, which is highly susceptible to PXO99 A , by leaf-cutting inoculation. Four mutants with reduced virulence were obtained after two rounds of screening. Among them, the mutant PXM69 had completely lost virulence to the rice host and ability to elicit HR in non-host tobacco. Southern blotting analysis showed a single copy of a Tn5-insertion in the genome of PXM69. PCR walking and sequencing analysis revealed that the Tn5 transposon was inserted at nucleotide position 70,192–70,201 in the genome of PXO99 A , disrupting the type III hrc ( hrp -conserved) gene hrcQ , the first gene in the D operon of the hrp cluster in Xoo . To confirm the relationship between the Tn5-insertion and the avirulence phenotype of PXM69, we used the marker exchange mutagenesis to create a PXO99 A mutant, Δ hrcQ ::KAN, in which the hrcQ was disrupted by a kanamycin-encoding gene cassette at the same site as that of the Tn5-insertion. Δ hrcQ ::KAN showed the same phenotype as mutant PXM69. Reintroduction of the wild-type hrcQ gene partially complemented the pathogenic function of PXM69. RT-PCR and cellulase secretion assays showed that the Tn5-disruption of hrcQ did not affect transcription of downstream genes in the D operon and function of the type II secretion system. Our results provide new insights into the pathogenic functions of clustered hrp genes in Xoo .