Evidence map›Paper›PMID 35506571›Full record

ArticleJournal of evolutionary biology2022

Negotiating mutualism: A locus for exploitation by rhizobia has a broad effect size distribution and context-dependent effects on legume hosts.

Camille E Wendlandt, Miles Roberts, Kyle T Nguyen, Marion L Graham, Zoie Lopez, Emily E Helliwell, Maren L Friesen, Joel S Griffitts, Paul Price, Stephanie S Porter

Open access · hybridAbstract read
In one paragraph

Article in Journal of evolutionary biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Camille E WendlandtSchool of Biological Sciences, Washington State University, Vancouver, Washington, USA.ORCID 0000-0001-7901-3442
Miles RobertsSchool of Biological Sciences, Washington State University, Vancouver, Washington, USA.ORCID 0000-0001-9854-701X
Kyle T NguyenSchool of Biological Sciences, Washington State University, Vancouver, Washington, USA.ORCID 0000-0001-8688-8175
Marion L GrahamBiology Department, Eastern Michigan University, Ypsilanti, Michigan, USA.ORCID 0000-0002-9445-9896
Zoie LopezSchool of Biological Sciences, Washington State University, Vancouver, Washington, USA.ORCID 0000-0002-6096-7323
Emily E HelliwellSchool of Biological Sciences, Washington State University, Vancouver, Washington, USA.ORCID 0000-0001-6340-7260
Maren L FriesenDepartment of Plant Pathology, Washington State University, Pullman, Washington, USA.ORCID 0000-0002-4274-8928
Joel S GriffittsDepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, Utah, USA.ORCID 0000-0003-1177-272X
Paul PriceBiology Department, Eastern Michigan University, Ypsilanti, Michigan, USA.ORCID 0000-0002-6001-3941
Stephanie S PorterSchool of Biological Sciences, Washington State University, Vancouver, Washington, USA.ORCID 0000-0002-1193-9705
Washington State University Vancouver · USEastern Michigan University · USBrigham Young University · USWashington State University · US

Funding

US National Science Foundation DEB-1355216US National Science Foundation DEB-1943239US National Science Foundation IOS-1755454
6 · The paper itself

Abstract

In mutualisms, variation at genes determining partner fitness provides the raw material upon which coevolutionary selection acts, setting the dynamics and pace of coevolution. However, we know little about variation in the effects of genes that underlie symbiotic fitness in natural mutualist populations. In some species of legumes that form root nodule symbioses with nitrogen-fixing rhizobial bacteria, hosts secrete nodule-specific cysteine-rich (NCR) peptides that cause rhizobia to differentiate in the nodule environment. However, rhizobia can cleave NCR peptides through the expression of genes like the plasmid-borne Host range restriction peptidase (hrrP), whose product degrades specific NCR peptides. Although hrrP activity can confer host exploitation by depressing host fitness and enhancing symbiont fitness, the effects of hrrP on symbiosis phenotypes depend strongly on the genotypes of the interacting partners. However, the effects of hrrP have yet to be characterised in a natural population context, so its contribution to variation in wild mutualist populations is unknown. To understand the distribution of effects of hrrP in wild rhizobia, we measured mutualism phenotypes conferred by hrrP in 12 wild Ensifer medicae strains. To evaluate context dependency of hrrP effects, we compared hrrP effects across two Medicago polymorpha host genotypes and across two experimental years for five E. medicae strains. We show for the first time in a natural population context that hrrP has a wide distribution of effect sizes for many mutualism traits, ranging from strongly positive to strongly negative. Furthermore, we show that hrrP effect size varies across host genotypes and experiment years, suggesting that researchers should be cautious about extrapolating the role of genes in natural populations from controlled laboratory studies of single genetic variants.

Indexed as

FabaceaeRhizobiumNegotiatingPeptidesSymbiosisVegetablesPeptidescooperationhrrPlegumepeptidaserhizobiasymbiosisworking balance hypothesis

Identifiers

PMID35506571
PMCPMC9325427
OpenAlexW4225426932

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.