Evidence map›Paper›PMID 41042102›Full record

ArticleG3 (Bethesda, Md.)2026

Chromosome scale genomes of two invasive Adelges species enable virtual screening for selective adelgicides.

Adam M Glendening, Cole Stephens, Vidya S Vuruputoor, Tesko Chaganti, Meghan N Myles, David L Stern, Mohamed Abdelalim, Yu-Pu Juang, Saskia A Hogenhout, Thomas C Mathers and 4 more

Erratum issuedAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Adam M GlendeningDepartment of Ecology and Evolutionary Biology, University of Connecticut, Storrs, CT 06269, United States.ORCID 0009-0002-0508-6547
Cole StephensDepartment of Medicinal Chemistry, University of Michigan, Ann Arbor, MI 48109, United States.ORCID 0009-0002-5150-3401
Vidya S VuruputoorDepartment of Ecology and Evolutionary Biology, University of Connecticut, Storrs, CT 06269, United States.ORCID 0000-0002-5836-7054
Tesko ChagantiDepartment of Medicinal Chemistry, University of Michigan, Ann Arbor, MI 48109, United States.ORCID 0009-0003-3197-6241
Meghan N MylesDepartment of Ecology and Evolutionary Biology, University of Connecticut, Storrs, CT 06269, United States.ORCID 0009-0006-9268-8990
David L SternJanelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147, United States.ORCID 0000-0002-1847-6483
Mohamed AbdelalimDepartment of Medicinal Chemistry, University of Michigan, Ann Arbor, MI 48109, United States.ORCID 0000-0001-6338-787X
Yu-Pu JuangDepartment of Medicinal Chemistry, University of Michigan, Ann Arbor, MI 48109, United States.ORCID 0000-0002-9680-4307
Saskia A HogenhoutDepartment of Crop Genetics, John Innes Centre, Norwich Research Park, Norwich NR4 7UH, United Kingdom.ORCID 0000-0003-1371-5606
Thomas C MathersWellcome Sanger Institute, Cambridge CB10 1RQ  United Kingdom.ORCID 0000-0002-8637-3515
Nicole PauloskiDepartment of Molecular and Cell Biology, University of Connecticut, Storrs, CT 06269, United States.ORCID 0009-0004-6135-7078
Tim A CernakDepartment of Medicinal Chemistry, University of Michigan, Ann Arbor, MI 48109, United States.ORCID 0000-0001-5407-0643
Jill L WegrzynDepartment of Ecology and Evolutionary Biology, University of Connecticut, Storrs, CT 06269, United States.ORCID 0000-0001-5923-0888
Karl C FetterDepartment of Ecology and Evolutionary Biology, University of Connecticut, Storrs, CT 06269, United States.ORCID 0000-0002-9234-9300

Funding

Michigan Chemistry-Biology Interface Training ProgramT32GM132046 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Emily E Scott, Wenjing Wang · 2019 to 2026
$4.1M
BBSRC Institute Strategy Programmes BBS/E/J/000PR9797BBSRC Institute Strategy Programmes BBS/E/JI/230001BBiotechnology and Biological Sciences Research Council BB/R009481/1Biotechnology and Biological Sciences Research Council BB/V008544/1John Innes CentreJohn Innes FoundationNational Science Foundation DBI-2217100NIGMS NIH HHS T32 GM132046RaMP (Research and Mentoring for Postbaccalaureates)The Nature Conservancy 2T32GM132046-06Trees In PerilUK Research and InnovationUniversity of ConnecticutUSDA Postdoctoral Fellowship Program 2023-67012-40000
6 · The paper itself

Abstract

Two invasive adelgids are associated with widespread damage to several North American conifer species. Adelges tsugae, hemlock woolly adelgid, was introduced from Japan and reproduces parthenogenetically in North America, where it has rapidly decimated Tsuga canadensis and Tsuga caroliniana (eastern and Carolina hemlocks, respectively). Adelges abietis, eastern spruce gall adelgid, introduced from Europe, forms distinctive pineapple-shaped galls on several native spruce species. While not considered a major forest pest, it weakens trees and increases susceptibility to additional stressors. Broad-spectrum insecticides that are often used to control adelgid populations can have off-target impacts on beneficial insects. Whole-genome sequencing was performed on both species to aid in the development of targeted solutions that may minimize ecological impact. A. abietis was sequenced using barcoded linked-reads from 30 pooled individuals, with Hi-C scaffolding performed using data from a single individual collected from the same host plant. A. tsugae used long-read sequencing from pooled nymphs. The assembled A. tsugae and A. abietis genomes, pooled from several parthenogenetic females, are 220.75 and 253.16 Mb, respectively. Each consists of 8 autosomal chromosomes, as well as 2 sex chromosomes (X1/X2), supporting the XX-XO sex determination system. The genomes are over 96% complete based on BUSCO assessment. Genome annotation identified 11,424 and 12,060 protein-coding genes in A. tsugae and A. abietis, respectively. Comparative analysis of proteins across 31 hemipteran species and 14 arthropod outgroups identified 32,340 putative gene families. Gene family evolution analysis with CAFE revealed lineage-specific expansions in immune-related aminopeptidases (ERAP1) and juvenile hormone binding proteins (JHBP), contractions in juvenile hormone acid methyltransferases (JHAMT), and conservation of nicotinic acetylcholine receptors (nAChRs). These genes were explored as candidate families toward a long-term objective of developing adelgid-selective insecticides. Structural comparisons of proteins across 7 focal species (A. tsugae, A. abietis, Adelges cooleyi, Rhopalosiphum maidis, Apis mellifera, Danaus plexippus, and Drosophila melanogaster) revealed high conservation of nAChR and ERAP1, while JHAMT exhibited species-specific structural divergence. The potential of JHAMT as a lineage-specific target for pest control was explored through virtual screening of drugs and pesticides.

Indexed as

Chromosomes, PlantIntroduced SpeciesAnimalsGenome, PlantGenomicsadelgidsaminopeptidasesconservationforest tree healthgenome assemblyinvasive speciesjuvenile hormonereference genome

Identifiers

PMID41042102
PMCPMC12774606

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.