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Nosema ceranae is a microsporidium pathogen widely spread around the world. Negative effects on foraging behavior and longevity of EHB colonies have been associated with this pathogen as well as possible population losses, but its effects have not been studied in tropical adapted honey bees. We studied the interaction between this pathogen and Africanized honey bees (AHB) in the Yucatan peninsula of Mexico where N. ceranae has only been detected since 2008. Non-infected and artificially infected workers with two different spore concentrations were introduced in observation hives to evaluate the onset and duration of foraging and longevity. The results showed precocious foraging, a reduction of the duration of foraging and a decrease in the longevity of infected bees compared with non-infected ones. However, the results indicate that although negative effects can be caused by N. ceranae in AHB, these were of a moderate magnitude compared with similar reports on EHB in temperate areas. Further research is necessary to evaluate the long-term effect of N. ceranae on AHBs in relation to colony dynamics to better understand the absence of significant colony losses associated with this pathogen in tropical and subtropical Mexico.Nosema ceranae / foraging behavior / longevity / Nosemosis / Africanized bees

Eusocial insect queens are remarkable in their ability to maximise both fecundity and longevity, thus escaping the typical trade-off between these two traits. In species exhibiting complex eusocial behaviour, several mechanisms have been proposed to underlie the remoulding of the trade-off, such as reshaping of the juvenile hormone pathway, or caste-specific susceptibility to oxidative stress. However, it remains a challenge to disentangle the molecular mechanisms underlying the remoulding of the trade-off in eusocial insects from caste-specific physiological attributes that have subsequently arisen due to their different life histories. Socially plastic species such as the orchid bee Euglossa viridissima represent excellent models to address the role of sociality per se in longevity as they allow direct comparisons of solitary and social individuals within a common genetic background. We present data on gene expression and juvenile hormone levels from young and old bees, from both solitary and social nests. We found 940 genes to be differentially expressed with age in solitary females, versus only 14 genes in social dominant females, and seven genes in subordinate females. We performed a weighted gene co-expression network analysis to further highlight candidate genes related to ageing in this species. Primary “ageing gene” candidates were related to protein synthesis, gene expression, immunity and venom production. Remarkably, juvenile hormone titres did not vary with age or social status. These results represent an important step in understanding the proximate mechanisms underlying the remodeling of the fecundity/longevity trade-off that accompanies the evolutionary transition from solitary life to eusociality.Significance statementThe remarkably long lifespan of the queens of eusocial insects despite their high reproductive output suggests that they are not subject to the widespread trade-off between fecundity and longevity that governs solitary animal life histories, yet surprisingly little is known of the molecular mechanisms underpinning their longevity. Using a socially plastic bee in which some individuals of a population are social whilst others are solitary, we identified hundreds of candidate genes and related gene networks that are involved in the remoulding of the fecundity/longevity tradeoff. As well as identifying candidate ageing genes, our data suggest that even in incipient stages of sociality there is a marked reprogramming of ageing; long live the queen.

Eusocial insect queens are remarkable in their ability to maximise both fecundity and longevity, thus escaping the typical trade-off between these two traits. Several mechanisms have been proposed to underlie the remoulding of the trade-off, such as reshaping of the juvenile hormone pathway, or caste-specific susceptibility to oxidative stress. However, it remains a challenge to disentangle the molecular mechanisms underlying the remoulding of the trade-off in eusocial insects from caste-specific physiological attributes that have subsequently arisen. The socially polymorphic orchid bee Euglossa viridissima represents an excellent model to address the role of sociality per se in longevity as it allows direct comparisons of solitary and social individuals within a common genetic background. We investigated gene expression and juvenile hormone levels in young and old bees from both solitary and social nests. We found 902 genes to be differentially expressed with age in solitary females, including genes involved in oxidative stress, versus only 100 genes in social dominant females, and 13 genes in subordinate females. A weighted gene co-expression network analysis further highlights pathways related to ageing in this species, including the TOR pathway. Eleven genes involved in translation, apoptosis and DNA repair show concurrent age-related expression changes in solitary but not in social females, representing potential differences based on social status. Juvenile hormone titres did not vary with age or social status. Our results represent an important step in understanding the proximate mechanisms underlying the remodelling of the fecundity/longevity trade-off that accompanies the evolutionary transition from solitary life to eusociality.

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