Evidence map›Paper›PMID 39325170›Full record

ArticleTAG. Theoretical and applied genetics. Theoretische und angewandte Genetik2024

Discovery of a major QTL for resistance to the guava root-knot nematode (Meloidogyne enterolobii) in 'Tanzania', an African landrace sweetpotato (Ipomoea batatas).

Simon Fraher, Tanner Schwarz, Chris Heim, Gabriel De Siqueira Gesteira, Marcelo Mollinari, Guilherme Da Silva Pereira, Zhao-Bang Zeng, Gina Brown-Guedira, Adrienne Gorny, G Craig Yencho

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Article in TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Simon FraherDepartment of Horticultural Science, North Carolina State University, 214 Kilgore Hall, Box 7609, Raleigh, NC, 27695, USA.ORCID http://orcid.org/0000-0003-0953-516X
Tanner SchwarzDepartment of Entomology and Plant Pathology, North Carolina State University, Raleigh, NC, 27695, USA.
Chris HeimDepartment of Horticultural Science, North Carolina State University, 214 Kilgore Hall, Box 7609, Raleigh, NC, 27695, USA.
Gabriel De Siqueira GesteiraDepartment of Horticultural Science, North Carolina State University, 214 Kilgore Hall, Box 7609, Raleigh, NC, 27695, USA.
Marcelo MollinariDepartment of Horticultural Science, North Carolina State University, 214 Kilgore Hall, Box 7609, Raleigh, NC, 27695, USA.
Guilherme Da Silva PereiraDepartment of Agronomy, Federal University of Viçosa, Viçosa, Minas Gerais, Brazil.
Zhao-Bang ZengDepartment of Horticultural Science, North Carolina State University, 214 Kilgore Hall, Box 7609, Raleigh, NC, 27695, USA.
Gina Brown-GuediraUSDA Agricultural Research Service, Plant Science Research Unit, Department of Crop and Soil Sciences, North Carolina State University, 2128 Plant Sciences Building, Raleigh, NC, USA.
Adrienne GornyDepartment of Entomology and Plant Pathology, North Carolina State University, Raleigh, NC, 27695, USA.
G Craig YenchoDepartment of Horticultural Science, North Carolina State University, 214 Kilgore Hall, Box 7609, Raleigh, NC, 27695, USA. spfraher@ncsu.edu.

Funding

Bill and Melinda Gates Foundation OPP1052983Bill and Melinda Gates Foundation OPP1213329National Institute of Food and Agriculture 2021-51181-35865National Institute of Food and Agriculture 2022-67013-36269
6 · The paper itself

Abstract

Sweetpotato, Ipomoea batatas (L.) Lam. (2n = 6x = 90), is among the world's most important food crops and is North Carolina's most important vegetable crop. The recent introduction of Meloidogyne enterolobii poses a significant economic threat to North Carolina's sweetpotato industry and breeding resistance into new varieties has become a high priority for the US sweetpotato industry. Previous studies have shown that 'Tanzania', a released African landrace, is resistant to M. enterolobii. We screened the biparental sweetpotato mapping population, 'Tanzania' x 'Beauregard', for resistance to M. enterolobii by inoculating 246 full-sibs with 10,000 eggs each under greenhouse conditions. 'Tanzania', the female parent, was highly resistant, while 'Beauregard' was highly susceptible. Our bioassays exhibited strong skewing toward resistance for three measures of resistance: reproductive factor, eggs per gram of root tissue, and root gall severity ratings. A 1:1 segregation for resistance suggested a major gene conferred M. enterolobii resistance. Using a random-effect multiple interval mapping model, we identified a single major QTL, herein designated as qIbMe-4.1, on linkage group 4 that explained 70% of variation in resistance to M. enterolobii. This study provides a new understanding of the genetic basis of M. enterolobii resistance in sweetpotato and represents a major step towards the identification of selectable markers for nematode resistance breeding.

Indexed as

Chromosome MappingDisease ResistanceIpomoea batatasPlant DiseasesQuantitative Trait LociTylenchoideaAnimalsGenetic MarkersPhenotypePlant RootsGenetic MarkersMarker-assisted breedingMeloidogyne enterolobiiQTLRoot-knot nematodesSweetpotato

Identifiers

PMID39325170
PMCPMC11427482

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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.