| Literature DB >> 29215193 |
Tiffany M Lowe-Power1, Connor G Hendrich1, Edda von Roepenack-Lahaye2, Bin Li3, Dousheng Wu2, Raka Mitra4, Beth L Dalsing1, Patrizia Ricca2, Jacinth Naidoo5, David Cook6, Amy Jancewicz7, Patrick Masson7, Bart Thomma6, Thomas Lahaye2, Anthony J Michael3, Caitilyn Allen1.
Abstract
Ralstonia solanacearum thrives in plant xylem vessels and causes bacterial wilt disease despite the low nutrient content of xylem sap. We found that R. solanacearum manipulates its host to increase nutrients in tomato xylem sap, enabling it to grow better in sap from infected plants than in sap from healthy plants. Untargeted GC/MS metabolomics identified 22 metabolites enriched in R. solanacearum-infected sap. Eight of these could serve as sole carbon or nitrogen sources for R. solanacearum. Putrescine, a polyamine that is not a sole carbon or nitrogen source for R. solanacearum, was enriched 76-fold to 37 µM in R. solanacearum-infected sap. R. solanacearum synthesized putrescine via a SpeC ornithine decarboxylase. A ΔspeC mutant required ≥ 15 µM exogenous putrescine to grow and could not grow alone in xylem even when plants were treated with putrescine. However, co-inoculation with wildtype rescued ΔspeC growth, indicating R. solanacearum produced and exported putrescine to xylem sap. Intriguingly, treating plants with putrescine before inoculation accelerated wilt symptom development and R. solanacearum growth and systemic spread. Xylem putrescine concentration was unchanged in putrescine-treated plants, so the exogenous putrescine likely accelerated disease indirectly by affecting host physiology. These results indicate that putrescine is a pathogen-produced virulence metabolite.Entities:
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Year: 2017 PMID: 29215193 PMCID: PMC5903990 DOI: 10.1111/1462-2920.14020
Source DB: PubMed Journal: Environ Microbiol ISSN: 1462-2912 Impact factor: 5.491