Evidence map›Paper›PMID 39403866›Full record

ArticlePlant biotechnology journal2024

Edited eukaryotic translation initiation factors confer resistance against maize lethal necrosis.

Zhengyu Wen, Fengzhong Lu, Mark Jung, Sabrina Humbert, Lisa Marshall, Craig Hastings, Emily Wu, Todd Jones, Mario Pacheco, Ivan Martinez and 5 more

Abstract read
In one paragraph

Article in Plant biotechnology journal, 2024. 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
–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

5 citing papers in PubMed.

  1. Article
  2. Targeted knockout of a host peroxisomal peptidase confers field resistance to maize lethal necrosis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    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

15 authors.

Zhengyu WenInternational Maize and Wheat Improvement Center, Texcoco, Mexico.
Fengzhong LuInternational Maize and Wheat Improvement Center, Texcoco, Mexico.
Mark JungCorteva Agriscience, Johnston, Iowa, USA.
Sabrina HumbertCorteva Agriscience, Johnston, Iowa, USA.
Lisa MarshallCorteva Agriscience, Johnston, Iowa, USA.
Craig HastingsCorteva Agriscience, Johnston, Iowa, USA.
Emily WuCorteva Agriscience, Johnston, Iowa, USA.
Todd JonesCorteva Agriscience, Johnston, Iowa, USA.
Mario PachecoInternational Maize and Wheat Improvement Center, Texcoco, Mexico.
Ivan MartinezInternational Maize and Wheat Improvement Center, Texcoco, Mexico.
L M SureshInternational Maize and Wheat Improvement Center, Nairobi, Kenya.
Yoseph BeyeneInternational Maize and Wheat Improvement Center, Nairobi, Kenya.
Prasanna BoddupalliInternational Maize and Wheat Improvement Center, Nairobi, Kenya.
Kevin PixleyInternational Maize and Wheat Improvement Center, Texcoco, Mexico.
Kanwarpal S DhuggaInternational Maize and Wheat Improvement Center, Texcoco, Mexico.ORCID 0000-0003-2477-3422

Funding

Bill and Melinda Gates Foundation OPP1193833Gates Foundation INV-007833
6 · The paper itself

Abstract

Maize lethal necrosis (MLN), which is caused by maize chlorotic mottle virus along with a potyvirus, has threatened the food security of smallholders in sub-Saharan Africa. Mutations in eukaryotic translation initiation factors (eIFs), which also facilitate virus genome translation, are known to confer variable resistance against viruses. Following phylogenetic analysis, we selected two eIF4E proteins from maize as the most likely candidates to facilitate MLN infection. A knockout (KO) of each of the corresponding genes in elite but MLN-susceptible maize lines conferred only partial protection. Our inability to knockout both the genes together suggested that at least one was required for survival. When we edited (ED) the eIF4E genes in Mini Maize, however, the plants with the eif4e1-KO became highly resistant, whereas those with the eif4e2-KO remained susceptible. Neither of the causal viruses could be detected in the MLN-inoculated eif4e1-KO plants. The eIF4E2 cDNA in Mini Maize lacked the entire 4th exon, causing a 22-amino acid in-frame deletion, which shortened the protein to 198 amino acids. When we introduced mutations in the 4th exon of the eIF4E2 gene in two elite, MLN-susceptible lines pre-edited for an eif4e1-KO, we obtained as strong resistance against MLN as in eif4e1-KO Mini Maize. The MLN-inoculated lines with eif4e1-KO/eIF4E2-exon-4ED performed as well as the uninoculated wild-type lines. We demonstrate that the C-terminal 38 amino acids of eIF4E2 are dispensable for normal plant growth but are required for the multiplication of MLN viruses. Our discovery has wide applications across plant species for developing virus-resistant varieties.

Indexed as

Disease ResistancePlant DiseasesPlant ProteinsTombusviridaeZea maysEukaryotic Initiation Factor-4EEukaryotic Initiation FactorsGene EditingPhylogenyPlants, Genetically ModifiedPotyvirusEukaryotic Initiation Factor-4EEukaryotic Initiation Factorsmaize chlorotic mottle virusPlant ProteinseIF4Efood securitygene editingmaize lethal necrosis or MLNsub‐Saharan Africavirus resistance

Identifiers

PMID39403866
PMCPMC11606411

What Socratic 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 Socratic graph.