Gut microbiota facilitates the adaptation of <i>Apolygus lucorum</i> (Hemiptera: Miridae) to its host plant

The mirid bug, Apolygus lucorum Meyer-Dür, is a significant pest in cotton (Gossypium hirsutum L.) cultivation. Previous studies have shown that gut microbiota plays a crucial role in insect adaptation to host plants. However, the gut microbiota of A. lucorum and its role in insect adaptation remains unclear. In this study, we investigated the gut microbiota of A. lucorum and their contributions to the growth performance of the mirids on cotton plants. We analyzed gut microbial compositions of field-collected (FCAL) and laboratory-reared (LRAL) A. lucorum populations. High-throughput sequencing of the 16S rRNA gene revealed distinct gut microbial community structures between the two populations, with Delftia and Serratia serving as the dominant gut bacteria in the FCAL and LRAL populations, respectively. We confirmed that Delftia sp. W1 and Serratia marcescens R1 facilitate the growth of A. lucorum on cotton. The A. lucorum exhibits retarded growth on cotton by removal of these two strains, and its growth performance is restored upon recolonization with these strains. The capabilities of both strains in protein degradation are evident, with S. marcescens R1 exhibiting the most pronounced degradation ability. This study reveals the crucial role of gut microbiota in A. lucorum's adaptation to cotton. We identified two strains from the gut microbiota which contribute to protein digestion in A. lucorum. Our findings contribute to understanding the interaction mechanisms among insects, symbiotic bacteria, and plants, facilitating the development of insect symbiotic microbial resources.

Authors

Institutions

Publication Details

Journal
Journal of Economic Entomology
Published
2025-05-26
DOI
https://doi.org/10.1093/jee/toaf142
Citations
1
Primary Topic
Insect symbiosis and bacterial influences
Type
article
Field-Weighted Citation Impact
1.67
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Gut microbiota facilitates the adaptation of Apolygus lucorum (Hemiptera: Miridae) to its host plant

Yue Wu, Yu‐Pei Mu, Muyang Wang, Ying‐Bo Mao et al.
1 citations
Journal of Economic Entomology
Insect symbiosis and bacterial influences
1.67
article

Gut microbiota facilitates the adaptation of Apolygus lucorum (Hemiptera: Miridae) to its host plant

Yue Wu, Yu‐Pei Mu, Muyang Wang, Ying‐Bo Mao, Yin Tang, Jiajia Zhang, Xian Zhang, Wei Wang, Pai Li
article en
1 citations

Abstract

The mirid bug, Apolygus lucorum Meyer-Dür, is a significant pest in cotton (Gossypium hirsutum L.) cultivation. Previous studies have shown that gut microbiota plays a crucial role in insect adaptation to host plants. However, the gut microbiota of A. lucorum and its role in insect adaptation remains unclear. In this study, we investigated the gut microbiota of A. lucorum and their contributions to the growth performance of the mirids on cotton plants. We analyzed gut microbial compositions of field-collected (FCAL) and laboratory-reared (LRAL) A. lucorum populations. High-throughput sequencing of the 16S rRNA gene revealed distinct gut microbial community structures between the two populations, with Delftia and Serratia serving as the dominant gut bacteria in the FCAL and LRAL populations, respectively. We confirmed that Delftia sp. W1 and Serratia marcescens R1 facilitate the growth of A. lucorum on cotton. The A. lucorum exhibits retarded growth on cotton by removal of these two strains, and its growth performance is restored upon recolonization with these strains. The capabilities of both strains in protein degradation are evident, with S. marcescens R1 exhibiting the most pronounced degradation ability. This study reveals the crucial role of gut microbiota in A. lucorum's adaptation to cotton. We identified two strains from the gut microbiota which contribute to protein digestion in A. lucorum. Our findings contribute to understanding the interaction mechanisms among insects, symbiotic bacteria, and plants, facilitating the development of insect symbiotic microbial resources.

Journal of Economic EntomologyVol. 118(4)
East China University of Science and Technology (CN), Chinese Academy of Sciences (CN), Center for Excellence in Molecular Plant Sciences (CN)
Life in Land
Openalex Percentile: Top 17%
Insect symbiosis and bacterial influences
1.67
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.