Claim · model-written summary
Most host mutations reduced host benefits in Medicago truncatula with Sinorhizobium meliloti.
- Taxon
- Medicago truncatula
Medicago truncatulae0
- Treatment
- mutationse1
- Interactor
- Sinorhizobium meliloti
Sinorhizobium melilotie0symbiont
- Outcome
- host benefitse1
- Direction
- reducede1
Not reportedComparator
Verbatim
e0“we inoculated 18 Medicago truncatula symbiotic mutants (including mutants that alter Nodule Cysteine-Rich (NCR) peptide production, plant defence, and nodule number regulation) with a mixture of 86 Sinorhizobium meliloti strains”
e1“Most mutations resulted in reduced host benefits, but the effects on rhizobial benefit (i.e. relative strain fitness) varied widely, revealing widespread host-by-strain fitness interactions”
Title
Sohini Guha; Regina B Bledsoe; Jeremy Sutherland; et al. The ISME Journal 2026. doi:10.1093/ismejo/wrag005
Other claims from this paper (10)
- Observation Effects of host mutations on relative strain fitness of rhizobia varied widely.
- Observation Host-by-strain fitness interactions in Medicago truncatula are widespread.
- Association Genome-wide association variants on rhizobial replicons pSymA and pSymB are important in mediating strain fitness responses to host mutations.
- Observation Nine rhizobial variants affected fitness across six or more host mutations.
- Observation Most top rhizobial variants affected fitness with one host mutation (limited effect variants).
- Observation Pervasive rhizobial variants occurred primarily on the symbiotic replicon pSymA.
- Observation Pervasive rhizobial variants include fixL and some metabolic genes.
- Association Variants with pervasive positive effects in mutant hosts tended to adversely affect strain fitness in wild-type hosts.
- Observation Competition assays confirmed a pervasive role for malonyl-CoA synthase among rhizobial candidates.
- Mechanism AlphaFold multimer modelling suggests that many rhizobial top candidates could interact with host NCR peptides.