Please use this identifier to cite or link to this item: http://223.31.159.10:8080/jspui/handle/123456789/1259
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dc.contributor.authorDas, Joyati-
dc.contributor.authorKumar, Rahul-
dc.contributor.authorYadav, Sunil Kumar-
dc.contributor.authorJha, Gopaljee-
dc.date.accessioned2021-11-16T10:36:37Z-
dc.date.available2021-11-16T10:36:37Z-
dc.date.issued2022-
dc.identifier.citationEnvironmental Microbiology, 24(6): 2781-2796en_US
dc.identifier.issn1462-2920-
dc.identifier.otherhttps://doi.org/10.1111/1462-2920.15836-
dc.identifier.urihttps://sfamjournals.onlinelibrary.wiley.com/doi/10.1111/1462-2920.15836-
dc.identifier.urihttp://223.31.159.10:8080/jspui/handle/123456789/1259-
dc.descriptionAccepted date: 29 October 2021en_US
dc.description.abstractBacteria utilize RpoN, an alternative sigma factor (σ54) to grow in diverse habitats, including nitrogen-limiting conditions. Here, we report that a rice-associated mycophagous bacterium Burkholderia gladioli strain NGJ1 encodes two paralogues of rpoN viz. rpoN1 and rpoN2. Both of them are upregulated during 24 h of mycophagous interaction with Rhizoctonia solani, a polyphagous fungal pathogen. Disruption of either one of rpoNs renders the mutant NGJ1 bacterium defective in mycophagy, whereas ectopic expression of respective rpoN genes restores mycophagy in the complementing strains. NGJ1 requires rpoN1 and rpoN2 for efficient biocontrol to prevent R. solani to establish disease in rice and tomato. Further, we have identified 17 genes having RpoN regulatory motif in NGJ1, majority of them encode potential type III secretion system (T3SS) effectors, nitrogen assimilation, and cellular transport-related functions. Several of these RpoN regulated genes as well as certain previously reported T3SS apparatus (hrcC and hrcN) and effector (Bg_9562 and endo-β-1,3-glucanase) encoding genes are upregulated in NGJ1 but not in ΔrpoN1 or ΔrpoN2 mutant bacterium, during mycophagous interaction with R. solani. This highlights that RpoN1 and RpoN2 modulate T3SS, nitrogen assimilation as well as cellular transport systems in NGJ1 and thereby promote bacterial mycophagy.en_US
dc.description.sponsorshipThe work has been supported by NIPGR core research grant and NCR-cluster collaborative research grant. G.J. acknowledges Swarna Jayanti fellowship from Department of Science and Technology (DST), Ministry of Science and Technology, Govt. of India; J.D. and S.K.Y. acknowledge SRF fellowship from DBT, Govt. of India and R.K. acknowledges the SRA fellowship from CSIR, Govt. of India. The research funding from DBT, Government of India to support the G.J. lab is also gratefully acknowledged. The funders had no role in study design, data collection, and analysis, decision to publish, or preparation of the manuscript. The assistance of NIPGR central instrumentation facilities for DNA sequencing, qRT-PCR, and confocal imaging is acknowledged. The assistance of trainee student Mr. Balit Lather is also acknowledged. The authors are thankful to DBT-eLibrary Consortium (DelCON) for providing access to e-resources. G.J. planned the study and supervised the experiments. J.D. performed all the microbiology and molecular biology experiments in this study. R.K. created the ΔrpoN1/N2 double mutant and assisted J.D. in qRT-PCR analysis. S.K.Y. carried out the PtascanUI, gene neighbourhood, and phylogenetic analysis. G.J. and J.D. contributed to manuscript writing and all authors had approved the manuscript.en_US
dc.language.isoen_USen_US
dc.publisherJohn Wiley & Sonsen_US
dc.subjectBurkholderia gladiolien_US
dc.subjectrpoN1en_US
dc.subjectrpoN2en_US
dc.subjectmycophagous activityen_US
dc.titleThe alternative sigma factors, rpoN1 and rpoN2 are required for mycophagous activity of Burkholderia gladioli strain NGJ1en_US
dc.typeArticleen_US
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