RT Conference Proceedings
T1 Disentangling the molecular mechanisms of disease suppression by endophytic Flavobacterium sp. 98
A1 Pan, Xinya
A1 Elsayed, Somayah S.
A1 van Wezel, Gilles P.
A1 Raaijmaker, Jos M.
A1 Carrión, Victor J.
K1 Endofitas - Congresos
AB Endophytic microorganisms that colonize and thrive inside plant tissues can provide protection to plants against pathogen infection. Among the beneficial endophytes, we previously showed that Flavobacterium sp. 98 (Fl98) protects sugar beet seedlings against the fungal root pathogen Rhizoctonia solani. To date, however, the underlying molecular mechanisms of disease control by Fl98 remain elusive. In this study, we investigated the role of biosynthetic gene cluster 298 (BGC298) in disease protection by Fl98. BGC298 was enriched in the endosphere microbiome of sugar beet seedlings grown in Rhizoctonia- suppressive soil and the BGC298 knockout mutant of Fl98 was less effective in disease control (Carrión et al., Science 366:606-612, 2019). Comparative metabolomics conducted here revealed that BGC298 is involved in regulating the biosynthesis of 5,6- dimethybenzimidazole (DMB), an antifungal compound that inhibits hyphal growth of R. solani. Subsequent site-directed mutagenesis of the DMB-synthase gene bluB abolished DMB production by Fl98. Greenhouse bioassays further showed that both mutants (ΔBGC298, ΔbluB) were compromised in protection of the sugar beet seedlings against infections by R. solani. Moreover, bioinformatic analyses suggested that bluB is widely distributed in the Flavobacterium clade, while BGC298 is less conserved and only present in a small subset of plant-associated Flavobacterium genomes. These findings revealed the pivotal role of BGC298 and DMB biosynthesis in plant protection by endophytic Flavobacterium sp. 98.
YR 2025
FD 2025-11-07
LK https://hdl.handle.net/10630/45621
UL https://hdl.handle.net/10630/45621
LA eng
NO Dutch Research Council (NWO)
NO OCENW.GROOT.2019.063
DS RIUMA. Repositorio Institucional de la Universidad de Málaga
RD 4 mar 2026