Literature DB >> 33632122

Genomic insight into diet adaptation in the biological control agent Cryptolaemus montrouzieri.

Hao-Sen Li1, Yu-Hao Huang1, Mei-Lan Chen1,2, Zhan Ren1, Bo-Yuan Qiu1, Patrick De Clercq3, Gerald Heckel4, Hong Pang5.   

Abstract

BACKGROUND: The ladybird beetle Cryptolaemus montrouzieri Mulsant, 1853 (Coleoptera, Coccinellidae) is used worldwide as a biological control agent. It is a predator of various mealybug pests, but it also feeds on alternative prey and can be reared on artificial diets. Relatively little is known about the underlying genetic adaptations of its feeding habits.
RESULTS: We report the first high-quality genome sequence for C. montrouzieri. We found that the gene families encoding chemosensors and digestive and detoxifying enzymes among others were significantly expanded or contracted in C. montrouzieri in comparison to published genomes of other beetles. Comparisons of diet-specific larval development, survival and transcriptome profiling demonstrated that differentially expressed genes on unnatural diets as compared to natural prey were enriched in pathways of nutrient metabolism, indicating that the lower performance on the tested diets was caused by nutritional deficiencies. Remarkably, the C. montrouzieri genome also showed a significant expansion in an immune effector gene family. Some of the immune effector genes were dramatically downregulated when larvae were fed unnatural diets.
CONCLUSION: We suggest that the evolution of genes related to chemosensing, digestion, and detoxification but also immunity might be associated with diet adaptation of an insect predator. These findings help explain why this predatory ladybird has become a successful biological control agent and will enable the optimization of its mass rearing and use in biological control programs.

Entities:  

Keywords:  Biological control; Cryptolaemus montrouzieri; Evolution; Genome; Immunity; Ladybird; Prey adaptation

Mesh:

Substances:

Year:  2021        PMID: 33632122      PMCID: PMC7905881          DOI: 10.1186/s12864-021-07442-3

Source DB:  PubMed          Journal:  BMC Genomics        ISSN: 1471-2164            Impact factor:   3.969


  57 in total

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