Evidence map›Paper›PMID 37138224›Full record

ArticleBMC genomics2023

The transcriptome of Icerya aegyptiaca (Hemiptera: Monophlebidae) and comparison with neococcoids reveal genetic clues of evolution in the scale insects.

Xue-Fei Tang, Yu-Hao Huang, Yi-Fei Sun, Pei-Fang Zhang, Li-Zhi Huo, Hao-Sen Li, Hong Pang

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 2 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Xue-Fei Tang *State Key Laboratory of Biocontrol, School of Ecology, Sun Yat-Sen University, Shenzhen, China.
Yu-Hao Huang *State Key Laboratory of Biocontrol, School of Ecology, Sun Yat-Sen University, Shenzhen, China.
Yi-Fei SunState Key Laboratory of Biocontrol, School of Ecology, Sun Yat-Sen University, Shenzhen, China.
Pei-Fang ZhangState Key Laboratory of Biocontrol, School of Ecology, Sun Yat-Sen University, Shenzhen, China.
Li-Zhi HuoGuangzhou Institute of Forestry and Landscape Architecture, Guangzhou, China.
Hao-Sen LiState Key Laboratory of Biocontrol, School of Ecology, Sun Yat-Sen University, Shenzhen, China.
Hong PangState Key Laboratory of Biocontrol, School of Ecology, Sun Yat-Sen University, Shenzhen, China. lsshpang@mail.sysu.edu.cn.
Sun Yat-sen University · CNGuangdong Academy of Forestry · CN

Funding

Guangdong Basic and Applied Basic Research Foundation Grant No. 2021A1515011051 to HSLNational Natural Science Foundation of China Grant No. 31970439 to HPNational Natural Science Foundation of China No. 32172472 to HSLScience and Technology Planning Project of Guangzhou, China Grant No. 202102020818 to HSL
6 · The paper itself

Abstract

backgroundScale insects are worldwide sap-sucking parasites, which can be distinguished into neococcoids and non-neococcoids. Neococcoids are monophyletic with a peculiar reproductive system, paternal genome elimination (PGE). Different with neococcoids, Iceryini, a tribe in non-neococcoids including several damaging pests, has abdominal spiracles, compound eyes in males, relatively abundant wax, unique hermaphrodite system, and specific symbionts. However, the current studies on the gene resources and genomic mechanism of scale insects are mainly limited in the neococcoids, and lacked of comparison in an evolution frame.

resultWe sequenced and de novo assembled a transcriptome of Icerya aegyptiaca (Douglas), a worldwide pest of Iceryini, and used it as representative of non-neococcoids to compare with the genomes or transcriptomes of other six species from different families of neococcoids. We found that the genes under positive selection or negative selection intensification (simplified as "selected genes" below) in I. aegyptiaca included those related to neurogenesis and development, especially eye development. Some genes related to fatty acid biosynthesis were unique in its transcriptome with relatively high expression and not detected in neococcoids. These results may indicate a potential link to the unique structures and abundant wax of I. aegyptiaca compared with neococcoids. Meanwhile, genes related to DNA repair, mitosis, spindle, cytokinesis and oogenesis, were included in the selected genes in I. aegyptiaca, which is possibly associated with cell division and germ cell formation of the hermaphrodite system. Chromatin-related process were enriched from selected genes in neococcoids, along with some mitosis-related genes also detected, which may be related to their unique PGE system. Moreover, in neococcoid species, male-biased genes tend to undergo negative selection relaxation under the PGE system. We also found that the candidate horizontally transferred genes (HTGs) in the scale insects mainly derived from bacteria and fungi. bioD and bioB, the two biotin-synthesizing HTGs were exclusively found in the scale insects and neococcoids, respectively, which possibly show potential demand changes in the symbiotic relationships.

conclusionOur study reports the first I. aegyptiaca transcriptome and provides preliminary insights for the genetic change of structures, reproductive systems and symbiont relationships at an evolutionary aspect. This will provide a basis for further research and control of scale insects.

Indexed as

HemipteraAnimalsBacteriaMalePhylogenyTranscriptomeEvolutionIcerya aegyptiacaNeococcoidsScale insectsTranscriptome

Identifiers

PMID37138224
PMCPMC10158165
OpenAlexW4367856546

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LicenceCC BY
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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.