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Insect social life is governed by chemicals. A great number of studies have demonstrated that the blend of hydrocarbons present on the cuticle (CHCs) plays a pivotal role in intra- and inter-specific communication. It is not surprising, therefore, that social parasites, specialized in exploiting the costly parental care provided by host workers, exploit the host chemical communication system too. Throughout their life cycle, social parasites intercept and break this CHC-based code. Recently, however, several polar compounds (mainly peptides) have been found in addition to CHCs both on the cuticle and on the comb surface of social insects, and their semiochemical role has been demonstrated in some circumstances. In the present study, we used the paper wasp social parasite-host system Polistes sulcifer (Zimmerman)-Polistes dominulus (Christ) to evaluate the relative importance of the CHCs and polar compounds in two different steps of the host exploitation process: host nest detection by the pre-usurping parasite and parasite chemical integration into the host colony. After separating the polar and apolar fractions of the host nest as well as those of pre- and post-usurpation parasites, we carried out laboratory assays based on the binary choice model. Our results show that nest polar compounds neither are used by the parasite to detect the host's nest nor play a role in parasite chemical integration into the host colony. In contrast, we demonstrate that CHCs are fundamental in both steps, thus confirming their primary role in social insect life and consequently in social parasite-host interactions.

A colony of social insects is like a fortress where access is allowed only to colony members. The epicuticular mixture of hydrocarbons has been widely reported to be involved in nestmate recognition in insects. However, recent studies have shown that polar compounds (mainly peptides) are also present, mixed with hydrocarbons, on the cuticle of various insects, including the paper wasps of the genus Polistes. As these polar compounds are variable among Polistes species and are perceived by the wasps, this cuticular fraction could also be involved in nestmate recognition. Through MALDI-TOF (Matrix-Assisted Laser Desorption Ionization Time of Flight) mass spectrometry analysis, we assessed, for the first time, the intercolonial variability of the cuticular polar fraction of Polistes dominulus in order to evaluate its reliability as source of nestmate recognition cues. We then tested through behavioral assays the importance of the 2 isolated fractions (apolar and polar) in nestmate recognition by presenting them separately to colonies of P. dominulus. Our results showed that the cuticular polar compounds are not colony specific and they are not used by paper wasps to discriminate nestmates from non-colony members. On the contrary, we confirmed that the isolated cuticular hydrocarbons are the chemical mediators prompting nestmate recognition in paper wasps.

During reproductive phase, larvae of male and female are intermingled in nest of social wasps. Workers care for and feed larvae that gives them an opportunity to bias investment with respect to sex, or even to kill some larvae, if they can distinguish between immature males and females. Cuticular hydrocarbon (CHC) mixtures are the most studied cues for species, nestmate, and caste recognition in social Hymenoptera. In this study, we investigate the paper wasp Polistes dominulus to see if male and female larvae show different patterns of CHCs and if workers are able to discriminate between male and female larvae on this basis. We performed gas chromatography-mass spectrometry analysis on cuticular extracts of larvae, and then we genotyped them to assign sex. We found sex-based variation in CHC-profiles sufficient for discrimination. However, our behavioral assays do not support the view that adults discriminate between male and female larvae within nests.

Insect social life is governed by chemicals. A great number of studies have demonstrated that the blend of hydrocarbons present on the cuticle (CHCs) plays a pivotal role in intra- and inter-specific communication. It is not surprising, therefore, that social parasites, specialized in exploiting the costly parental care provided by host workers, exploit the host chemical communication system too. Throughout their life cycle, social parasites intercept and break this CHC-based code. Recently, however, several polar compounds (mainly peptides) have been found in addition to CHCs both on the cuticle and on the comb surface of social insects, and their semiochemical role has been demonstrated in some circumstances. In the present study, we used the paper wasp social parasite-host system Polistes sulcifer (Zimmerman)-Polistes dominulus (Christ) to evaluate the relative importance of the CHC5 and polar compounds in two different steps of the host exploitation process: host nest detection by the pre-usurping parasite and parasite chemical integration into the host colony. After separating the polar and apolar fractions of the host nest as well as those of pre- and post-usurpation parasites, we carried out laboratory assays based on the binary choice model. Our results show that nest polar compounds neither are used by the parasite to detect the host's nest nor play a role in parasite chemical integration into the host colony. In contrast, we demonstrate that CHCs are fundamental in both steps, thus confirming their primary role in social insect life and consequently in social parasite-host interactions. [ABSTRACT FROM AUTHOR]

Simple Summary: Social insects use cuticular hydrocarbons for chemical recognition and communication. Cuticular hydrocarbons can also be exploited by parasites to their advantage for undermining host recognition systems. The small hive beetle (SHB) is a parasite of honey bee colonies but can also infest nests of other bee species. However, its chemical profile is still not known. For the first time, the present study investigated the SHB chemical profile and compared it with that of its honey bee host. The results show that the SHB has a low chemical profile that is similar to its honey bee host's. However, while honey bees had a clear colony-specific chemical profile, SHBs did not. The generic chemical profile of the SHB is most likely linked to its free-flying behaviour in the field as these parasites are known to switch between host colonies, possibly limiting the acquisition of a colony specific chemical profile. Our findings also suggest that SHBs do not exploit any finely tuned chemical strategy to conceal their presence inside host colonies and probably rely on behavioural adaptations. Cuticular hydrocarbons (CHCs) cover insects' bodies and play important roles in chemical communication, including nestmate recognition, for social insects. To enter colonies of a social host species, parasites may acquire host-specific CHCs or covertly maintain their own CHC profile by lowering its quantity. However, the chemical profile of small hive beetles (SHBs), Aethina tumida, which are parasites of honey bee, Apis mellifera, colonies, and other bee nests, is currently unknown. Here, adults of SHB and honey bee host workers were collected from the same field colonies and their CHC profiles were analysed using GC-MS. The chemical profiles of field-sampled SHBs were also compared with those of host-naive beetles reared in the laboratory. Laboratory-reared SHBs differed in their CHC profiles from field-sampled ones, which showed a more similar, but ten-fold lower, generic host CHC profile compared to host workers. While the data confirm colony-specific CHCs of honey bee workers, the profile of field-collected SHBs was not colony-specific. Adult SHBs often commute between different host colonies, thereby possibly preventing the acquisition of a colony-specific CHC profiles. An ester was exclusive to both groups of SHBs and might constitute an intraspecific recognition cue. Our data suggest that SHBs do not use any finely tuned chemical strategy to conceal their presence inside host colonies and instead probably rely on their hard exoskeleton and defence behaviours. [ABSTRACT FROM AUTHOR]

The article discusses research on the existence of a threshold for nest-mate chemical recognition in the social wasp Polistes dominulus. The study sought to test the hypothesis that cuticular semiochemicals mediate the aggression of resident female social wasps towards intruders such as predators or social parasites. It has observed various behavioural reactions in the resident foundress to various amounts of cuticular hydrocarbons (CHC) in a foreign female. The implications of the findings for social parasitism are tackled.