Evidence map›Paper›PMID 41263491›Full record

ArticleGigaScience2025

A high-quality chromosome-level genome assembly of the oligophagous fruit fly Bactrocera tsuneonis (Diptera: Tephritidae) and insights into its host specificity.

Tengda Guo, Weisong Li, Yuan Zhang, Wenzhao Yang, Zhihong Li, Yujia Qin

Abstract read
In one paragraph

Article in GigaScience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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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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

1 citing paper in PubMed.

  1. 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

6 authors.

Tengda GuoState Key Laboratory of Agricultural and Forestry Biosecurity, MARA Key Laboratory of Surveillance and Management for Plant Quarantine Pests, College of Plant Protection, China Agricultural University, Beijing 100193, China.ORCID 0009-0002-6040-0906
Weisong LiState Key Laboratory of Agricultural and Forestry Biosecurity, MARA Key Laboratory of Surveillance and Management for Plant Quarantine Pests, College of Plant Protection, China Agricultural University, Beijing 100193, China.ORCID 0009-0000-3531-6783
Yuan ZhangState Key Laboratory of Agricultural and Forestry Biosecurity, MARA Key Laboratory of Surveillance and Management for Plant Quarantine Pests, College of Plant Protection, China Agricultural University, Beijing 100193, China.ORCID 0000-0001-6027-9064
Wenzhao YangState Key Laboratory of Agricultural and Forestry Biosecurity, MARA Key Laboratory of Surveillance and Management for Plant Quarantine Pests, College of Plant Protection, China Agricultural University, Beijing 100193, China.
Zhihong LiState Key Laboratory of Agricultural and Forestry Biosecurity, MARA Key Laboratory of Surveillance and Management for Plant Quarantine Pests, College of Plant Protection, China Agricultural University, Beijing 100193, China.ORCID 0000-0002-1281-2108
Yujia QinState Key Laboratory of Agricultural and Forestry Biosecurity, MARA Key Laboratory of Surveillance and Management for Plant Quarantine Pests, College of Plant Protection, China Agricultural University, Beijing 100193, China.ORCID 0000-0002-0903-9089

Funding

China Agricultural UniversityNational Key Research and Development Program of China 2022YFC2601500National Natural Science Foundation of China 32202288
6 · The paper itself

Abstract

backgroundBactrocera tsuneonis is a major pest of citrus, causing significant economic losses in fruit production. It exhibits a highly specialized host preference, primarily infesting citrus fruits. However, the genetic basis underlying its olfactory adaptation and host specificity remains largely unexplored. To elucidate the molecular mechanisms governing host selection in B. tsuneonis, we assembled a high-quality chromosome-level genome and performed comparative genomic, transcriptomic, and functional analyses of its chemosensory system.

resultsThe genome of B. tsuneonis was assembled to a total size of 339 Mb, with a contig N50 of 11.21 Mb and a scaffold N50 of 59.93 Mb. Comparative genomic analysis revealed significant contractions in chemosensory-related gene families, particularly in odorant-binding proteins (OBPs) and odorant receptors (ORs), perhaps suggesting an adaptation to a narrow host range. Transcriptome analysis demonstrated that BtsuOBP83a and BtsuOBP83b were highly expressed in the antennae, and most ORs were predominantly expressed in the antennae. Functional assays confirmed that BtsuOBP83a selectively binds to 2 citrus volatiles, trans-nerolidol and piperitone, with strong affinity. Molecular docking and molecular dynamics simulations further revealed that BtsuOR7a-6 and BtsuOR7a-4 specifically interact with these volatiles, suggesting their role in host odor recognition.

conclusionsOur high-quality genome of B. tsuneonis provides a valuable resource for genomic research and offers valuable insights into the genetic basis of its olfactory adaptation and host specificity. The findings highlight key molecular mechanisms underlying host selection and provide potential targets for behavior-based pest management strategies.

Indexed as

Chromosomes, InsectGenome, InsectHost SpecificityTephritidaeAnimalsGene Expression ProfilingGenomicsInsect ProteinsReceptors, OdorantTranscriptomeInsect Proteinsodorant-binding proteinReceptors, OdorantBactrocera tsuneoniscomparative genomicsgenomeolfactory proteinsoligophagous

Identifiers

PMID41263491
PMCPMC12723664

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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.