Calcium regulates the mycophagous ability of Burkholderia gladioli strain NGJ1 in a type III secretion system-dependent manner

dc.contributor.authorYadav, Sunil Kumar
dc.contributor.authorDas, Joyati
dc.contributor.authorKumar, Rahul
dc.contributor.authorJha, Gopaljee
dc.date.accessioned2020-07-28T10:22:27Z
dc.date.available2020-07-28T10:22:27Z
dc.date.issued2020
dc.descriptionAccepted date: 12 July 2020en_US
dc.description.abstractBackground: A rice associated bacterium Burkholderia gladioli strain NGJ1 demonstrates mycophagy, a phenomenon wherein bacteria feed on fungi. Previously, we have reported that NGJ1 utilizes type III secretion system (T3SS) to deliver a prophage tail-like protein (Bg_9562) into fungal cells to establish mycophagy. Results: In this study, we report that calcium ion concentration influences the mycophagous ability of NGJ1 on Rhizoctonia solani, an important fungal pathogen. The calcium limiting condition promotes mycophagy while high calcium environment prevents it. The expression of various T3SS apparatus encoding genes of NGJ1 was induced and secretion of several potential T3SS effector proteins (including Bg_9562) into extracellular milieu was triggered under calcium limiting condition. Using LC-MS/MS proteome analysis, we identified several calcium regulated T3SS effector proteins of NGJ1. The expression of genes encoding some of these effector proteins was upregulated during mycophagous interaction of NGJ1 with R. solani. Further, mutation of one of these genes (endo-β-1, 3- glucanase) rendered the mutant NGJ1 bacterium defective in mycophagy while complementation with full length copy of the gene restored its mycophagous activity. Conclusion: Our study provides evidence that low calcium environment triggers secretion of various T3SS effectors proteins into the extracellular milieu and suggests the importance of cocktail of these proteins in promoting mycophagyen_US
dc.description.sponsorshipWe acknowledge the central research facility (CRF) of IIT- Delhi and metabolomic facility of NIPGR (DBT grant no. BT/INF/22/SP28268/2018), New Delhi for help in ICPMS analysis. The authors are also thankful to DBT-eLibrary Consortium (DelCON) for providing access to e-resources. The assistance of NIPGR central instrumentation facilities for sequencing and qRT-PCR are acknowledged. We sincerely thank Dr. Ramesh V. Sonti and Dr. Srayan Ghosh for comments on the manuscript.en_US
dc.identifier.citationBMC Microbiology 20(1): 216en_US
dc.identifier.issn1471-2180
dc.identifier.otherhttps://doi.org/10.1186/s12866-020-01897-2
dc.identifier.urihttps://bmcmicrobiol.biomedcentral.com/articles/10.1186/s12866-020-01897-2
dc.identifier.urihttps://ndkr-library.nipgr.ac.in/handle/123456789/1079
dc.language.isoen_USen_US
dc.publisherBioMed Central Ltden_US
dc.subjectMycophagyen_US
dc.subjectBacterial-fungal interactionen_US
dc.subjectT3SSen_US
dc.subjectEffectorsen_US
dc.subjectEndo-β-1en_US
dc.subject3- glucanaseen_US
dc.titleCalcium regulates the mycophagous ability of Burkholderia gladioli strain NGJ1 in a type III secretion system-dependent manneren_US
dc.typeArticleen_US

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