Sex Pheromone of the Papaya Mealybug

Sex pheromones of mealybugs are reported from more than 20 species and have generally been shown to be monoterpene alcohols esterified with short-chain carboxylic acids. Here, however, we discovered and isolated an alcohol without an acid moiety as a pheromone compound released from adult females of the papaya mealybug, Paracoccus marginatus. By means of gas chromatography - mass spectrometry and nuclear magnetic resonance spectroscopy analyses, the structure was identified to be trans-2-(2-isopropenyl-1-methylcyclobutyl)ethanol, a monoterpene with a unique cyclobutene skeleton, commonly known as fragranol. We then completely separated synthetic (±)-fragranol into each enantiomer by means of preparative high-performance liquid chromatography using a chiral resolution column, and (-)-(1S,2S)-fragranol was definitely confirmed to be the natural pheromone and to attract many males in the field when used as a pheromone trap lure. (±)-Fragranol showed attractiveness comparable to that of the pure (-)-(1S,2S)-enantiomer. This study provides not only useful information for the monitoring and management of P. marginatus but also an interesting exception underlining the great diversity of mealybug pheromone structures.

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Publication Details

Journal
Journal of Chemical Ecology
Published
2025-02-01
DOI
https://doi.org/10.1007/s10886-025-01574-6
Citations
1
Primary Topic
Research on scale insects
Type
article
Field-Weighted Citation Impact
1.67

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article

Sex Pheromone of the Papaya Mealybug

Yuma Sugawara, Takumi Uesato, Jun Tabata
1 citations
Journal of Chemical Ecology
Research on scale insects
1.67
article

Sex Pheromone of the Papaya Mealybug

Yuma Sugawara, Takumi Uesato, Jun Tabata
article en
1 citations

Abstract

Sex pheromones of mealybugs are reported from more than 20 species and have generally been shown to be monoterpene alcohols esterified with short-chain carboxylic acids. Here, however, we discovered and isolated an alcohol without an acid moiety as a pheromone compound released from adult females of the papaya mealybug, Paracoccus marginatus. By means of gas chromatography - mass spectrometry and nuclear magnetic resonance spectroscopy analyses, the structure was identified to be trans-2-(2-isopropenyl-1-methylcyclobutyl)ethanol, a monoterpene with a unique cyclobutene skeleton, commonly known as fragranol. We then completely separated synthetic (±)-fragranol into each enantiomer by means of preparative high-performance liquid chromatography using a chiral resolution column, and (-)-(1S,2S)-fragranol was definitely confirmed to be the natural pheromone and to attract many males in the field when used as a pheromone trap lure. (±)-Fragranol showed attractiveness comparable to that of the pure (-)-(1S,2S)-enantiomer. This study provides not only useful information for the monitoring and management of P. marginatus but also an interesting exception underlining the great diversity of mealybug pheromone structures.

Journal of Chemical EcologyVol. 51(1)
National Agriculture and Food Research Organization (JP), University of Tsukuba (JP), Okinawa Prefectural Agricultural Research Center (JP), Okinawa Prefecture (JP)
National Agriculture and Food Research Organization, Japan Society for the Promotion of Science
Zero hunger
Openalex Percentile: Top 22%
Research on scale insects
1.67
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