Evidence map›Paper›PMID 32183717›Full record

ArticleBMC genomics2020

Genome of the webworm Hyphantria cunea unveils genetic adaptations supporting its rapid invasion and spread.

Qi Chen, Hanbo Zhao, Ming Wen, Jiaxin Li, Haifeng Zhou, Jiatong Wang, Yuxin Zhou, Yulin Liu, Lixin Du, Hui Kang and 6 more

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in BMC genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 30 citations in OpenAlex.

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  7. Tracking Adaptive Pathways of Invasive Insects: Novel Insight from Genomics.International journal of molecular sciences · 2023
    Review
  8. Comparison of gut bacterial communities ofBiodiversity data journal · 2023
    Article
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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

16 authors at 3 institutions in 2 countries.

Qi ChenJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, China.
Hanbo ZhaoJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, China.
Ming WenJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, China.
Jiaxin LiJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, China.
Haifeng ZhouJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, China.
Jiatong WangJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, China.
Yuxin ZhouJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, China.
Yulin LiuJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, China.
Lixin DuJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, China.
Hui KangJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, China.
Jian ZhangSchool of Life Sciences, Changchun Normal University, Changchun, Jilin, China.
Rui CaoMeihekou Forest Pest Control Station, Changchun, Jilin, China.
Xiaoming XuGarden and Plant Protection Station of Changchun, Changchun, Jilin, China.
Jing-Jiang ZhouJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, China.
Bingzhong RenJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, China.
Yinliang WangJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, China. wangyl392@nenu.edu.cn.ORCID http://orcid.org/0000-0003-2207-3027
Northeast Normal University · CNChangchun Normal University · CNInstitute of Plant Protection · CN

Funding

Foundation of Xinjiang Uygur Autonomous Region No. 2017E0272Fund for Fostering Talents in Basic Science of the National Natural Science No. J1210070National Natural Science Foundation of China No. 31501890Natural Science Foundation of Jilin Province No. 20160204023NYNatural Science Foundation of Jilin Province No. 20170204003NYNatural Science Foundation of Jilin Province No. 20180101005JCNatural Science Foundation of Jilin Province No. 20190301047NYOpen Project Program of the Jilin Provincial Key Laboratory of Animal Resource Conservation and Utilization No. 130028684Open Project Program of the Jilin Provincial Key Laboratory of Animal Resource Conservation and Utilization No. 1300289103The Fundamental Research Funds for the Central Universities No. 11SSXT153The Fundamental Research Funds for the Central Universities No. 2412015KJ015The Fundamental Research Funds for the Central Universities No. 2412019FZ022Undergraduate teaching quality and teaching reform project of Northeast Normal University NO. 131004003
6 · The paper itself

Abstract

backgroundThe fall webworm Hyphantria cunea is an invasive and polyphagous defoliator pest that feeds on nearly any type of deciduous tree worldwide. The silk web of H. cunea aids its aggregating behavior, provides thermal regulation and is regarded as one of causes for its rapid spread. In addition, both chemosensory and detoxification genes are vital for host adaptation in insects.

resultsHere, a high-quality genome of H. cunea was obtained. Silk-web-related genes were identified from the genome, and successful silencing of the silk protein gene HcunFib-H resulted in a significant decrease in silk web shelter production. The CAFE analysis showed that some chemosensory and detoxification gene families, such as CSPs, CCEs, GSTs and UGTs, were expanded. A transcriptome analysis using the newly sequenced H. cunea genome showed that most chemosensory genes were specifically expressed in the antennae, while most detoxification genes were highly expressed during the feeding peak. Moreover, we found that many nutrient-related genes and one detoxification gene, HcunP450 (CYP306A1), were under significant positive selection, suggesting a crucial role of these genes in host adaptation in H. cunea. At the metagenomic level, several microbial communities in H. cunea gut and their metabolic pathways might be beneficial to H. cunea for nutrient metabolism and detoxification, and might also contribute to its host adaptation.

conclusionsThese findings explain the host and environmental adaptations of H. cunea at the genetic level and provide partial evidence for the cause of its rapid invasion and potential gene targets for innovative pest management strategies.

Indexed as

Introduced SpeciesAdaptation, PhysiologicalAnimalsBase SequenceGene Expression ProfilingGenomeMothsPhylogenyAdaptationFall webwormGene expansionGeneticsGenomeMetagenomeMolecular evolution

Identifiers

PMID32183717
PMCPMC7079503
OpenAlexW3010722454

What OpenQuestion holds

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LicenceCC BY
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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.