Intra‐regional diversity of rice bacterial blight pathogen, Xanthomonas oryzae pv. oryzae , in the Andaman Islands, India: revelation by pathotyping and multilocus sequence typing

2020 ◽  
Author(s):  
K. Sakthivel ◽  
A. Kumar ◽  
R.K. Gautam ◽  
K. Manigundan ◽  
G.S. Laha ◽  
...  
Keyword(s):  
Multilocus Sequence Typing ◽  
Bacterial Blight ◽  
Xanthomonas Oryzae ◽  
Andaman Islands ◽  
Regional Diversity ◽  
Rice Bacterial Blight ◽  
Bacterial Blight Pathogen

scholarly journals An xa5 Resistance Gene-Breaking Indian Strain of the Rice Bacterial Blight Pathogen Xanthomonas oryzae pv. oryzae Is Nearly Identical to a Thai Strain

2020 ◽  
Vol 11 ◽  
Author(s):  
Sara C. D. Carpenter ◽  
Prashant Mishra ◽  
Chandrika Ghoshal ◽  
Prasanta K. Dash ◽  
Li Wang ◽  
...  
Keyword(s):  
Resistance Gene ◽  
Bacterial Blight ◽  
Xanthomonas Oryzae ◽  
Rice Bacterial Blight ◽  
Indian Strain ◽  
Bacterial Blight Pathogen

Biological control of rice bacterial blight by plant-associated bacteria producing 2,4-diacetylphloroglucinol

2006 ◽  
Vol 52 (1) ◽  
pp. 56-65 ◽  
Author(s):  
Palaniyandi Velusamy ◽  
J Ebenezar Immanuel ◽  
Samuel S Gnanamanickam ◽  
Linda Thomashow
Keyword(s):  
Biological Control ◽  
Pseudomonas Fluorescens ◽  
Bacterial Blight ◽  
Field Experiments ◽  
Screening Method ◽  
Xanthomonas Oryzae ◽  
Rice Bacterial Blight ◽  
Fluorescent Pseudomonas ◽  
Tn5 Mutants ◽  
Bacterial Blight Pathogen

Certain plant-associated strains of fluorescent Pseudomonas spp. are known to produce the antimicrobial antibiotic 2,4-diacetylphloroglucinol (DAPG). It has antibacterial, antifungal, antiviral, and antihelminthic properties and has played a significant role in the biological control of tobacco, wheat, and sugar beet diseases. It has never been reported from India and has not been implicated in the biological suppression of a major disease of the rice crop. Here, we report that a subpopulation of 27 strains of plant-associated Pseudomonas fluorescens screened in a batch of 278 strains of fluorescent pseudomonads produced DAPG. The DAPG production was detected by a PCR-based screening method that used primers Phl2a and Phl2b and amplified a 745-bp fragment characteristic of DAPG. HPLC,1H NMR, and IR analyses provided further evidence for its production. We report also that this compound inhibited the growth of the devastating rice bacterial blight pathogen Xanthomonas oryzae pv. oryzae in laboratory assays and suppressed rice bacterial blight up to 59%–64% in net-house and field experiments. Tn5 mutants defective in DAPG production (Phl–) of P. fluorescens PTB 9 were much less effective in their suppression of rice bacterial blight.Key words: biocontrol, 2,4-diacetylphloroglucinol, Pseudomonas fluorescens, rice, Xanthomonas oryzae pv. oryzae.

scholarly journals A strain of an emerging Indian pathotype of Xanthomonas oryzae pv. oryzae defeats the rice bacterial blight resistance gene xa13 without inducing a clade III SWEET gene and is nearly identical to a recent Thai isolate

2018 ◽  
Author(s):  
Sara C. D. Carpenter ◽  
Prashant Mishra ◽  
Chandrika Ghoshal ◽  
Prasanta Dash ◽  
Li Wang ◽  
...  
Keyword(s):  
Resistance Genes ◽  
Bacterial Blight ◽  
Xanthomonas Oryzae ◽  
Host Susceptibility ◽  
Transcription Activator ◽  
Rice Bacterial Blight ◽  
Indian Strain ◽  
Bacterial Blight Pathogen ◽  
Insight Into ◽  
S Genes

AbstractThe rice bacterial blight pathogen Xanthomonas oryzae pv. oryzae (Xoo) injects transcription activator-like effectors (TALEs) that bind and activate host ‘susceptibility’ (S) genes important for disease. Clade III SWEET genes are major S genes for bacterial blight. The resistance genes xa5, which reduces TALE activity generally, and xa13, a SWEET11 allele not recognized by the cognate TALE, have been effectively deployed. However, strains that defeat both resistance genes individually were recently reported in India and Thailand. To gain insight into the mechanism(s), we completely sequenced the genome of one such strain from each country and examined the encoded TALEs. Strikingly, the two strains are clones, sharing nearly identical TALE repertoires, including a TALE known to activate SWEET11 strongly enough to be effective even when diminished by xa5. We next investigated SWEET gene induction by the Indian strain. The Indian strain induced no clade III SWEET in plants harbouring xa13, indicating a pathogen adaptation that relieves dependence on these genes for susceptibility. The findings open a door to mechanistic understanding of the role SWEET genes play in susceptibility and illustrate the importance of complete genome sequence-based monitoring of Xoo populations in developing varieties with effective disease resistance.

scholarly journals The RpfB-Dependent Quorum Sensing Signal Turnover System Is Required for Adaptation and Virulence in Rice Bacterial Blight Pathogen Xanthomonas oryzae pv. oryzae

2016 ◽  
Vol 29 (3) ◽  
pp. 220-230 ◽  
Author(s):  
Xing-Yu Wang ◽  
Lian Zhou ◽  
Jun Yang ◽  
Guang-Hai Ji ◽  
Ya-Wen He
Keyword(s):  
Quorum Sensing ◽  
Bacterial Blight ◽  
Xanthomonas Campestris ◽  
Deletion Mutant ◽  
Extracellular Polysaccharide ◽  
Xanthomonas Oryzae ◽  
Rice Bacterial Blight ◽  
Double Deletion ◽  
Diffusible Signal Factor ◽  
Bacterial Blight Pathogen

Xanthomonas oryzae pv. oryzae, the bacterial blight pathogen of rice, produces diffusible signal factor (DSF) family quorum sensing signals to regulate virulence. The biosynthesis and perception of DSF family signals require components of the rpf (regulation of pathogenicity factors) cluster. In this study, we report that RpfB plays an essential role in DSF family signal turnover in X. oryzae pv. oryzae PXO99A. The production of DSF family signals was boosted by deletion of the rpfB gene and was abolished by its overexpression. The RpfC/RpfG-mediated DSF signaling system negatively regulates rpfB expression via the global transcription regulator Clp, whose activity is reversible in the presence of cyclic diguanylate monophosphate. These findings indicate that the DSF family signal turnover system in PXO99A is generally consistent with that in Xanthomonas campestris pv. campestris. Moreover, this study has revealed several specific roles of RpfB in PXO99A. First, the rpfB deletion mutant produced high levels of DSF family signals but reduced extracellular polysaccharide production, extracellular amylase activity, and attenuated pathogenicity. Second, the rpfB/rpfC double-deletion mutant was partially deficient in xanthomonadin production. Taken together, the RpfB-dependent DSF family signal turnover system is a conserved and naturally presenting signal turnover system in Xanthomonas spp., which plays unique roles in X. oryzae pv. oryzae adaptation and pathogenesis.

Understanding the variability of rice bacterial blight pathogen, Xanthomonas oryzae pv. oryzae in Andhra Pradesh, India

2021 ◽  
Author(s):  
Arra Yugander ◽  
Md Ershad ◽  
Pitchiah P. Muthuraman ◽  
Vellaisamy Prakasam ◽  
Duraisamy Ladhalakshmi ◽  
...  
Keyword(s):  
Bacterial Blight ◽  
Andhra Pradesh ◽  
Xanthomonas Oryzae ◽  
Rice Bacterial Blight ◽  
Bacterial Blight Pathogen

scholarly journals Transgenic Expression of the Functional Fragment Hpa110-42 of the Harpin Protein Hpa1 Imparts Enhanced Resistance to Powdery Mildew in Wheat

Plant Disease ◽  
2014 ◽  
Vol 98 (4) ◽  
pp. 448-455 ◽  
Author(s):  
Defu Wang ◽  
Yajun Wang ◽  
Maoqiang Fu ◽  
Shuyuan Mu ◽  
Bing Han ◽  
...  
Keyword(s):  
Powdery Mildew ◽  
Bacterial Blight ◽  
Fungal Species ◽  
Effective Control ◽  
Transgenic Expression ◽  
Rice Bacterial Blight ◽  
Harpin Protein ◽  
Transgenic Lines ◽  
Bacterial Blight Pathogen ◽  
Pathogen Populations

Powdery mildew, one of devastating diseases of wheat worldwide, is caused by Erysiphe graminis f. sp. tritici, a fungal species with constant population changes, which often poses challenges in disease management with host resistance. Transgenic approaches that utilize broad-spectrum resistance may limit changes of pathogen populations and contribute to effective control of the disease. The harpin protein Hpa1, produced by the rice bacterial blight pathogen, can induce resistance to bacterial blight and blast in rice. The fragment comprising residues 10 through 42 of Hpa1, Hpa110-42, is reportedly three- to eightfold more effective than the full-length protein. This study evaluated the transgenic expression of the Hpa110-42 gene for resistance to powdery mildew in wheat caused by E. graminis f. sp. tritici. Nine Hpa110-42 transgenic wheat lines were generated. The genomic integration of Hpa110-42 was confirmed, and expression of the transgene was detected at different levels in the individual transgenic lines. Following inoculation with the E. graminis f. sp. tritici isolate Egt15 in the greenhouse, five transgenic lines had significantly higher levels of resistance to powdery mildew compared with nontransformed plants. Thus, transgenic expression of Hpa110-42 conferred resistance to one isolate of E. graminis f. sp. tritici in wheat in the greenhouse.

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