Evidence map›Paper›PMID 32677941›Full record

ArticleBMC biology2020

Differential loss of effector genes in three recently expanded pandemic clonal lineages of the rice blast fungus.

Sergio M Latorre, C Sarai Reyes-Avila, Angus Malmgren, Joe Win, Sophien Kamoun, Hernán A Burbano

Abstract read
In one paragraph

Article in BMC biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–field-weighted citation impact
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

39 citing papers in PubMed.

  1. Review
  2. How to frustrate a plant pathogen.The Plant journal : for cell and molecular biology · 2026
    Review
  3. Article
  4. Article
  5. TheProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Host-Adaptive Divergence Shapes the Genetic Architecture ofJournal of fungi (Basel, Switzerland) · 2025
    Article
  7. Article
  8. Article
  9. Genomic profiles ofFrontiers in plant science · 2025
    Article
  10. Current research in microbial sciences · 2025
    Article
  11. Review
  12. Regional Variability of Chestnut (Plants (Basel, Switzerland) · 2024
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Pyricularia oryzae: Lab star and field scourge.Molecular plant pathology · 2024
    Review
  19. Article
  20. The roles ofFrontiers in plant science · 2024
    Review
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

6 authors.

Sergio M LatorreResearch Group for Ancient Genomics and Evolution, Max Planck Institute for Developmental Biology, Tuebingen, Germany.
C Sarai Reyes-AvilaThe Sainsbury Laboratory, University of East Anglia, Norwich Research Park, Norwich, UK.
Angus MalmgrenThe Sainsbury Laboratory, University of East Anglia, Norwich Research Park, Norwich, UK.
Joe WinThe Sainsbury Laboratory, University of East Anglia, Norwich Research Park, Norwich, UK.
Sophien KamounThe Sainsbury Laboratory, University of East Anglia, Norwich Research Park, Norwich, UK. sophien.kamoun@tsl.ac.uk.
Hernán A BurbanoResearch Group for Ancient Genomics and Evolution, Max Planck Institute for Developmental Biology, Tuebingen, Germany. hernan.burbano@tuebingen.mpg.de.ORCID 0000-0003-3433-719X

Funding

Biotechnology and Biological Sciences Research CouncilGatsby Charitable Foundation GCFH2020 European Research Council 743165
6 · The paper itself

Abstract

backgroundUnderstanding the mechanisms and timescales of plant pathogen outbreaks requires a detailed genome-scale analysis of their population history. The fungus Magnaporthe (Syn. Pyricularia) oryzae-the causal agent of blast disease of cereals- is among the most destructive plant pathogens to world agriculture and a major threat to the production of rice, wheat, and other cereals. Although M. oryzae is a multihost pathogen that infects more than 50 species of cereals and grasses, all rice-infecting isolates belong to a single genetically defined lineage. Here, we combined the two largest genomic datasets to reconstruct the genetic history of the rice-infecting lineage of M. oryzae based on 131 isolates from 21 countries.

resultsThe global population of the rice blast fungus consists mainly of three well-defined genetic groups and a diverse set of individuals. Multiple population genetic tests revealed that the rice-infecting lineage of the blast fungus probably originated from a recombining diverse group in Southeast Asia followed by three independent clonal expansions that took place over the last ~ 200 years. Patterns of allele sharing identified a subpopulation from the recombining diverse group that introgressed with one of the clonal lineages before its global expansion. Remarkably, the four genetic lineages of the rice blast fungus vary in the number and patterns of presence and absence of candidate effector genes. These genes encode secreted proteins that modulate plant defense and allow pathogen colonization. In particular, clonal lineages carry a reduced repertoire of effector genes compared with the diverse group, and specific combinations of presence and absence of effector genes define each of the pandemic clonal lineages.

conclusionsOur analyses reconstruct the genetic history of the rice-infecting lineage of M. oryzae revealing three clonal lineages associated with rice blast pandemics. Each of these lineages displays a specific pattern of presence and absence of effector genes that may have shaped their adaptation to the rice host and their evolutionary history.

Indexed as

Biological EvolutionGenetic VariationAscomycotaGenes, FungalGenome, FungalPlant DiseasesCerealsEffectorsFungiGenomesInfectious diseasesPandemicsPathogensPlantsPopulation historyRice

Identifiers

PMID32677941
PMCPMC7364606

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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.