Evidence map›Paper›PMID 40022128›Full record

ArticleBMC biology2025

Molecular evolution of dietary shifts in ladybird beetles (Coleoptera: Coccinellidae): from fungivory to carnivory and herbivory.

Yu-Hao Huang, Hermes E Escalona, Yi-Fei Sun, Pei-Fang Zhang, Xue-Yong Du, Sen-Rui Gong, Xue-Fei Tang, Yuan-Sen Liang, Dan Yang, Pei-Tao Chen and 13 more

Abstract read
In one paragraph

Article in BMC biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. 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

23 authors.

Yu-Hao HuangState Key Laboratory of Biocontrol, School of Ecology, Sun Yat-sen University, Shenzhen, 518107, China.
Hermes E EscalonaAustralian National Insect Collection, CSIRO, GPO Box 1700, Canberra, ACT, 2601, Australia.
Yi-Fei SunState Key Laboratory of Biocontrol, School of Ecology, Sun Yat-sen University, Shenzhen, 518107, China.
Pei-Fang ZhangState Key Laboratory of Biocontrol, School of Ecology, Sun Yat-sen University, Shenzhen, 518107, China.
Xue-Yong DuState Key Laboratory of Biocontrol, School of Ecology, Sun Yat-sen University, Shenzhen, 518107, China.
Sen-Rui GongState Key Laboratory of Biocontrol, School of Ecology, Sun Yat-sen University, Shenzhen, 518107, China.
Xue-Fei TangState Key Laboratory of Biocontrol, School of Ecology, Sun Yat-sen University, Shenzhen, 518107, China.
Yuan-Sen LiangState Key Laboratory of Biocontrol, School of Ecology, Sun Yat-sen University, Shenzhen, 518107, China.
Dan YangState Key Laboratory of Biocontrol, School of Ecology, Sun Yat-sen University, Shenzhen, 518107, China.
Pei-Tao ChenState Key Laboratory of Biocontrol, School of Ecology, Sun Yat-sen University, Shenzhen, 518107, China.
Huan-Ying YangState Key Laboratory of Biocontrol, School of Ecology, Sun Yat-sen University, Shenzhen, 518107, China.
Mei-Lan ChenSchool of Environmental and Life Sciences, Nanning Normal University, Nanning, 530001, China.
Bruno HüttelMax Planck Genome Centre Cologne, Max Planck Institute for Plant Breeding Research, Cologne, Germany.
Ondrej HlinkaCSIRO Information, Management and Technology, Pullenvale, QLD, Australia.
Xingmin WangCollege of Plant Protection, South China Agricultural University, Guangzhou, 510642, China.
Karen MeusemannLeibniz Institute for the Analysis of Biodiversity Change, Adenauerallee 127, Bonn, 53113, Germany.
Adam ŚlipińskiAustralian National Insect Collection, CSIRO, GPO Box 1700, Canberra, ACT, 2601, Australia.
Andreas ZwickAustralian National Insect Collection, CSIRO, GPO Box 1700, Canberra, ACT, 2601, Australia.
Robert M WaterhouseDepartment of Ecology and Evolution, University of Lausanne and Swiss Institute of Bioinformatics, Lausanne, 1015, Switzerland.
Bernhard MisofLeibniz Institute for the Analysis of Biodiversity Change, Adenauerallee 127, Bonn, 53113, Germany.
Oliver NiehuisDepartment of Evolutionary Biology and Ecology, Institute for Biology I (Zoology), University of Freiburg, Freiburg, 79104, Germany.
Hao-Sen LiState Key Laboratory of Biocontrol, School of Ecology, Sun Yat-sen University, Shenzhen, 518107, China. lihaosen3@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0003-3456-6603
Hong PangState Key Laboratory of Biocontrol, School of Ecology, Sun Yat-sen University, Shenzhen, 518107, China. lsshpang@mail.sysu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDietary shifts are major evolutionary steps that shape ecological niches and biodiversity. The beetle family Coccinellidae, commonly known as ladybirds, first transitioned from a fungivorous to an insectivorous and subsequently a plant diet. However, the molecular basis of this dietary diversification remained unexplored.

resultsWe investigated the molecular evolution of dietary shifts in ladybirds, focusing on the transitions from fungivory to carnivory (Coccinellidae) and from carnivory to herbivory (Epilachnini), by comparing 25 genomes and 62 transcriptomes of beetles. Our analysis shows that chemosensory gene families have undergone significant expansions at both nodes of diet change and were differentially expressed in feeding experiments, suggesting that they may be related to foraging. We found expansions of digestive and detoxifying gene families and losses of chitin-related digestive genes in the herbivorous ladybirds, and absence of most plant cell wall-degrading enzymes in the ladybirds dating from the transition to carnivory, likely indicating the effect of different digestion requirements on the gene repertoire. Immunity effector genes tend to emerge or have specific amino acid sequence compositions in carnivorous ladybirds and are downregulated under suboptimal dietary treatments, suggesting a potential function of these genes related to microbial symbionts in the sternorrhynchan prey.

conclusionsOur study provides a comprehensive comparative genomic analysis to address evolution of chemosensory, digestive, detoxifying, and immune genes associated with dietary shifts in ladybirds. Ladybirds can be considered a ubiquitous example of dietary shifts in insects, and thus a promising model system for evolutionary and applied biology.

Indexed as

CarnivoryColeopteraDietEvolution, MolecularHerbivoryAnimalsTranscriptomeChemosensationCoccinellidaeDetoxificationDigestionEvolutionFeeding habitGenomeImmunityLadybird beetleTranscriptome

Identifiers

PMID40022128
PMCPMC11871716

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.