A novel male accessory gland peptide reduces female post-mating receptivity in the brown planthopper

Mating in insects commonly induces a profound change in the physiology and behavior of the female that serves to secure numerous and viable offspring, and to ensure paternity for the male by reducing receptivity of the female to further mating attempts. Here, we set out to characterize the post-mating response (PMR) in a pest insect, the brown planthopper Nilaparvata lugens and to identify a functional analog of sex peptide and/or other seminal fluid factors that contribute to the PMR in Drosophila. We find that N. lugens display a distinct PMR that lasts for about 4 days and includes a change in female behavior with decreased receptivity to males and increased oviposition. Extract from male accessory glands (MAG) injected into virgin females triggers a similar PMR, lasting about 24h. Since sex peptide does not exist in N. lugens, we screened for candidate mediators by performing a transcriptional and proteomics analysis of MAG extract. We identified a novel 51 amino acid peptide present only in the MAG and not in female N. lugens. This peptide, that we designate maccessin (macc), affects the female PMR. Females mated by males with macc knockdown display receptivity to wild type males in a second mating, which does not occur in controls. However, oviposition is not affected. Injection of recombinant macc reduces female receptivity, with no effect on oviposition. Thus, macc is an important seminal fluid peptide that affects the PMR of N. lugens. Our analysis suggests that the gene encoding the macc precursor is restricted to species closely related to N. lugens.

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Publication Details

Journal
PLoS Genetics
Published
2025-05-06
DOI
https://doi.org/10.1371/journal.pgen.1011699
Citations
7
Primary Topic
Neurobiology and Insect Physiology Research
Type
article
Field-Weighted Citation Impact
6.36

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article

A novel male accessory gland peptide reduces female post-mating receptivity in the brown planthopper

Y X Zhang, Shun‐Fan Wu, Dick R. Nässel, Cong‐Fen Gao et al.
7 citations
PLoS Genetics
Neurobiology and Insect Physiology Research
6.36
article

A novel male accessory gland peptide reduces female post-mating receptivity in the brown planthopper

Y X Zhang, Shun‐Fan Wu, Dick R. Nässel, Cong‐Fen Gao, Rongqiang Bu, Ning Zhang
article en
7 citations

Abstract

Mating in insects commonly induces a profound change in the physiology and behavior of the female that serves to secure numerous and viable offspring, and to ensure paternity for the male by reducing receptivity of the female to further mating attempts. Here, we set out to characterize the post-mating response (PMR) in a pest insect, the brown planthopper Nilaparvata lugens and to identify a functional analog of sex peptide and/or other seminal fluid factors that contribute to the PMR in Drosophila. We find that N. lugens display a distinct PMR that lasts for about 4 days and includes a change in female behavior with decreased receptivity to males and increased oviposition. Extract from male accessory glands (MAG) injected into virgin females triggers a similar PMR, lasting about 24h. Since sex peptide does not exist in N. lugens, we screened for candidate mediators by performing a transcriptional and proteomics analysis of MAG extract. We identified a novel 51 amino acid peptide present only in the MAG and not in female N. lugens. This peptide, that we designate maccessin (macc), affects the female PMR. Females mated by males with macc knockdown display receptivity to wild type males in a second mating, which does not occur in controls. However, oviposition is not affected. Injection of recombinant macc reduces female receptivity, with no effect on oviposition. Thus, macc is an important seminal fluid peptide that affects the PMR of N. lugens. Our analysis suggests that the gene encoding the macc precursor is restricted to species closely related to N. lugens.

PLoS GeneticsVol. 21(5)
Nanjing Agricultural University (CN), Stockholm University (SE)
National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 3%
Neurobiology and Insect Physiology Research
6.36
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