Evidence map›Paper›PMID 30383872›Full record

ArticlePloS one2018

Multiple recombination events between two cytochrome P450 loci contribute to global pyrethroid resistance in Helicoverpa armigera.

Thomas K Walsh, Nicole Joussen, Kai Tian, Angela McGaughran, Craig J Anderson, Xinghui Qiu, Seung-Joon Ahn, Lisa Bird, Nena Pavlidi, John Vontas and 10 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 68 citations in OpenAlex.

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  15. Exposure ofInsects · 2021
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  20. Mitochondrial DNA genomes of five majorEcology and evolution · 2019
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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

20 authors at 12 institutions in 8 countries.

Thomas K WalshBlack Mountain Laboratories, Commonwealth Scientific and Industrial Research Organisation, Acton, Australian Capital Territory, Australia.
Nicole JoussenDepartment of Entomology, Max Planck Institute for Chemical Ecology, Jena, Germany.
Kai TianState Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Angela McGaughranBlack Mountain Laboratories, Commonwealth Scientific and Industrial Research Organisation, Acton, Australian Capital Territory, Australia.
Craig J AndersonBlack Mountain Laboratories, Commonwealth Scientific and Industrial Research Organisation, Acton, Australian Capital Territory, Australia.ORCID 0000-0002-2832-9313
Xinghui QiuState Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Seung-Joon AhnHorticultural and Herbal Crop Environment Division, National Institute of Horticultural and Herbal Science, Suwon, Korea.ORCID 0000-0002-5980-106X
Lisa BirdTamworth Agricultural Institute, New South Wales Department of Primary Industry, Calala, New South Wales, Australia.
Nena PavlidiDepartment of Biology, University of Crete, Rethymno, Greece.
John VontasLaboratory of Pesticide Science, Agricultural University of Athens, Athens, Greece.ORCID 0000-0002-8704-2574
Jaeeun RyuBlack Mountain Laboratories, Commonwealth Scientific and Industrial Research Organisation, Acton, Australian Capital Territory, Australia.ORCID 0000-0003-1463-7742
Akhtar RasoolInsect Molecular Biology Laboratory, National Institute for Biotechnology and Genetic Engineering, Faisalabad, Pakistan.
Isabella Barony MacedoFaculdade de Farmácia, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.ORCID 0000-0002-3802-0977
Wee Tek TayBlack Mountain Laboratories, Commonwealth Scientific and Industrial Research Organisation, Acton, Australian Capital Territory, Australia.
Yongjun ZhangInstitute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, China.
Mary E A WhitehouseAustralian Cotton Research Institute, Narrabri, New South Wales, Australia.
Pierre Jean SilvieAgroécologie et intensification durable des cultures annuelles, Centre de coopération internationale en recherche agronomique pour le développement, Montpellier, France.
Sharon DownesAustralian Cotton Research Institute, Narrabri, New South Wales, Australia.
Lori NemecAustralian Cotton Research Institute, Narrabri, New South Wales, Australia.
David G HeckelDepartment of Entomology, Max Planck Institute for Chemical Ecology, Jena, Germany.ORCID 0000-0001-8991-2150
Commonwealth Scientific and Industrial Research Organisation · AUCotton Research and Development Corporation · AUChinese Academy of Sciences · CNMax Planck Institute for Chemical Ecology · DEAgricultural University of Athens · GRCentre de Coopération Internationale en Recherche Agronomique pour le Développement · FRInstitute of Plant Protection · CNNational Institute for Biotechnology and Genetic Engineering · PKNew South Wales Department of Primary Industries · AUUniversidade Federal de Minas Gerais · BRUniversity of Crete · GRUniversity of Stirling · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cotton bollworm, Helicoverpa armigera (Hübner) is one of the most serious insect pest species to evolve resistance against many insecticides from different chemical classes. This species has evolved resistance to the pyrethroid insecticides across its native range and is becoming a truly global pest after establishing in South America and having been recently recorded in North America. A chimeric cytochrome P450 gene, CYP337B3, has been identified as a resistance mechanism for resistance to fenvalerate and cypermethrin. Here we show that this resistance mechanism is common around the world with at least eight different alleles. It is present in South America and has probably introgressed into its closely related native sibling species, Helicoverpa zea. The different alleles of CYP337B3 are likely to have arisen independently in different geographic locations from selection on existing diversity. The alleles found in Brazil are those most commonly found in Asia, suggesting a potential origin for the incursion of H. armigera into the Americas.

Indexed as

AllelesAnimalsCytochrome P-450 Enzyme SystemGenetic LociInsecticide ResistanceInsecticidesMothsPyrethrinsRecombination, GeneticCytochrome P-450 Enzyme SystemInsecticidesPyrethrins

Identifiers

PMID30383872
PMCPMC6211633
OpenAlexW2898796699

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.