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Ramirez, S. R.

Publications and source records attributed to Ramirez, S. R..

14 recordsLinked to original sources

Evolutionary contingency facilitates scent divergence in an emergent orchid population

Reproductive isolation can evolve rapidly even among populations with extensive genetic similarity, but the mechanisms underlying this divergence remain an open question in evolutionary biology. Here, we investigate the genetic basis of floral scent divergence, a key trait mediating differential pollinator attraction, in a group of nascent Gongora orchid lineages that occur in sympatry. We combined whole-genome resequencing and floral transcriptomics to characterize the transition from the monoterpene-emitting 'M chemotype' to the pollinator-isolated phenylpropanoid-emitting 'A chemotype' nested within it. While overall genetic differentiation was low, a few highly differentiated regions contained candidate genes in biosynthetic pathways. Of particular interest was a putative o-methyltransferase exhibiting evidence of a recent selective sweep in the A chemotype, with much higher expression in scent-emitting floral tissues of A than in M. Transcriptomic comparison with a more distantly related monoterpene-emitting lineage ('X chemotype') further revealed the coordinated and elevated expression of phenylpropanoid biosynthetic genes in M despite its absence of aromatic floral volatiles, including a putative key enzyme potentially involved in directing metabolic flux towards monolignol biosynthesis. Together, our results support a model in which pre-existing activity in a metabolic pathway may facilitate the evolution of a novel floral scent phenotype, potentially making transitions across the adaptive landscape of scent more accessible than others. We propose that such evolutionary contingency may help explain how divergent scent profiles, and consequently, reproductive isolation, can evolve rapidly via few genetic changes.

evolutionary biology↗

Exceptional diversification of floral form in a specialized orchid pollination system

Traits that facilitate specialized interactions, such as those in flowers that promote pollination, are often invoked as targets of stabilizing selection across macroevolutionary timescales. However, the diversity of pollination mechanisms across flowering plants begs further investigation into the generality of this pattern. We fit a model of multivariate character evolution on a dataset of 140 orchid species sampled across 65 genera from the diverse neotropical Cymbidieae clade to characterize the role of pollination mode on the pace of flower shape evolution. We find that, contrary to the expectation of pollinator-mediated stabilizing selection causing stasis, orchids pollinated by specialized scent-collecting male euglossine bees ("perfume flowers" sensu (1, 2)) exhibit elevated rates of floral evolution compared to plants utilizing other rewarding or deceptive mechanisms. This pattern is recapitulated across at least 5 independent origins of this pollination system amidst a complex backdrop of background rate evolution. The rapid rates of change we observed in perfume flowers may be facilitated by weak evolutionary coupling between functional regions in their flowers, allowing for independent trajectories of evolution. Our results provide novel insights into the capacity for pollinators to generate selective pressures on flowers at macroevolutionary scales, providing an engine for trait diversification in some of the worlds most floristically rich regions.

evolutionary biology↗

Regulatory Changes in the Fatty Acid Elongase eloF Underlie the Evolution of Sex-specific Pheromone Profiles in Drosophila prolongata

Pheromones play a key role in regulating sexual behavior throughout the animal kingdom. In Drosophila and other insects, many cuticular hydrocarbons (CHCs) are sexually dimorphic, and some are known to perform pheromonal functions. However, the genetic control of sex-specific CHC production is not understood outside of the model species D. melanogaster. A recent evolutionary change is found in D. prolongata, which, compared to its closest relatives, shows greatly increased sexual dimorphism in both CHCs and the chemosensory system responsible for their perception. A key transition involves a male-specific increase in the proportion of long-chain CHCs. Perfuming D. prolongata females with the male-biased CHCs reduces copulation success, suggesting that these compounds function as sex pheromones. The evolutionary change in CHC profiles correlates with a male-specific increase in the expression of multiple genes involved in CHC biosynthesis, including fatty acid elongases and reductases and other key enzymes. In particular, elongase F, which is responsible for producing female-specific pheromones in D. melanogaster, is strongly upregulated in D. prolongata males compared both to females and to males of the sibling species. Induced mutations in eloF reduce the amount of long-chain CHCs, resulting in a partial feminization of pheromone profiles in D. prolongata males while having minimal effect in females. Transgenic experiments show that sex-biased expression of eloF is caused in part by a putative transposable element insertion in its regulatory region. These results reveal one of the genetic mechanisms responsible for a recent evolutionary change in sexual communication.

evolutionary biology↗

Odorant receptors tuned to isothiocyanates in Drosophila melanogaster and their evolutionary expansion in herbivorous relatives

Plants release defense volatile compounds that can deter herbivores. Among them are electrophilic toxins, such as isothiocyanates from mustard plants, that activate pain receptors by contact (i.e. taste) in many animals, including Drosophila melanogaster. While specialist insects have evolved strategies to tolerate toxicity and use mustard plants as hosts, it is unclear whether non-specialist insects detect and avoid electrophilic toxins via olfaction. To address this, and to understand if specialized insects co-opted these toxic compounds as hostplant olfactory cues, we leveraged closely related drosophilid species, including the microbe-feeding D. melanogaster and Scaptomyza pallida, and the mustard-feeding specialist S. flava. In olfactory assays, D. melanogaster exposed to allyl isothiocyanate volatiles were rapidly immobilized, demonstrating the high toxicity of this wasabi-derived compound to non-specialists. Through single sensillum electrophysiological recordings from olfactory organs and behavioral assays, we identified an Olfactory receptor (Or) necessary for volatile detection and behavioral aversion to allyl isothiocyanate in D. melanogaster. RNA sequencing and heterologous expression revealed that S. flava possess lineage-specific, triplicated homologs of this Or, and that each paralog exhibited broadened and distinct sensitivity to isothiocyanate compounds. Using AlphaFold2 modeling, site-directed mutagenesis and electrophysiological recordings, we identified two critical amino acid substitutions that changed the sensitivity of these paralogs from fruit-derived odors to isothiocyanates in the mustard specialist S. flava. Our findings show that non-specialists can detect electrophiles via olfaction, and that their olfactory systems can rapidly adapt to toxic hostplant niches through co-option and duplication of ancestral chemosensory genes with few amino acid changes.

evolutionary biology↗

Repeated loss of floral scent in independent transitions from bee to hummingbird pollination in spiral gingers

The repeated evolution of the same trait in different lineages provides powerful natural experiments to study the phenotypic and genotypic predictability of how traits are gained and lost. A fascinating example of this is the repeated evolution of hummingbird pollination in plant lineages in the Americas, a widespread and often unidirectional phenomenon. The spiral gingers in the genus Costus are ancestrally bee-pollinated, and hummingbird pollination has evolved multiple times independently in the tropical Americas. These pollinator transitions are accompanied by predictable morphological and color changes, but the changes in floral scent have not been described. In this study, we describe the floral scent composition of 30 species of Costus sampled across the phylogeny to understand how floral scent has evolved across the genus with respect to pollinator transitions. We then combine transcriptomics and genomics to identify genetic expression differences and gene family evolution associated with pollinator transitions. We show that hummingbird-pollinated species have mostly lost their floral scent, whereas bee-pollinated species exhibit either floral scent maintenance or in some cases, gains of more diverse scent profiles. We find the floral scent loss appears to be due to gene downregulation rather than pseudogenization. The remarkable consistency of scent loss in hummingbird-pollinated species highlights the shared strong selection pressures experienced by these lineages. Even species with more recent transitions from bee to hummingbird pollination exhibit scent loss, highlighting the rapid breakdown of scent production following pollinator transitions. This research highlights the capacity for rapid changes when selection pressures are strong through downregulation of floral scent genes. ResumenLa evolucion independiente de un rasgo en diferentes linajes ofrece la oportunidad de estudiar la predictibilidad de fenotipos y sus bases geneticas. Un ejemplo fascinante es la evolucion repetida de polinizacion por colibries en varios linajes de plantas en las Americas, un fenomeno generalizado y tipicamente unidireccional. Las especies de cana agria del genero Costus son polinizadas ancestralmente por abejas y la polinizacion por colibries ha evolucionado varias veces de forma independiente en America tropical. Cada transicion de polinizador ha sido acompanada de varios cambios morfologicos y colores predecibles, pero los cambios en el aroma floral no han sido descritos. En este estudio describimos la composicion del aroma floral de 30 especies de Costus para comprender como el aroma floral ha evolucionado con respecto a las transiciones de polinizadores. Combinamos transcriptomica y genomica en un clado de Costus para identificar diferencias en la expresion genetica y la evolucion de la familia de genes asociadas con las transiciones de polinizadores. Nuestros resultados muestran que las especies polinizadas por colibries han perdido en su mayoria su aroma floral, mientras que las especies polinizadas por abejas ya sea mantienen el aroma floral y, en algunos casos, muestran ganancias de perfiles de aroma mas diversos. La consistencia en la perdida de olor en especies polinizadas por colibries resalta las fuertes presiones de seleccion natural que experimentan estos linajes. Incluso las especies con transiciones mas recientes de polinizacion de abejas a colibries exhiben perdida de olor, lo que destaca la rapida interrupcion de la produccion de olores despues de las transiciones de los polinizadores. Tambien encontramos que la perdida de aroma floral parece estar controlada por regulacion genica negativa y no por la perdida de genes de produccion de aromas (e.g. pseudogenizacion). Esta investigacion destaca la rapidez de cambios a traves de la regulacion negativa de genes que controlan aromas florales cuando las presiones de seleccion son fuertes. Significance StatementThe independent evolution of the same trait in different lineages provides a natural experiment to investigate the predictability of evolution. A fascinating example is the evolution of hummingbird pollination, which has occurred many times across flowering plants, and often involves convergence in multiple traits. In this study, we combine comparative chemical ecology with genomics and transcriptomics to study floral scent evolution in the genus Costus. We show that species exhibit loss of floral scent following transitions to hummingbird pollination suggesting a shared strong selection pressure favoring scent loss. We demonstrate the floral scent loss appears to be due to gene downregulation. This research highlights the capacity for rapid changes when selection pressures are strong through downregulation of scent genes.

evolutionary biology↗

Individual variation in male pheromone production in carpenter bees correlates with size and sexual maturity.

Sex pheromones are species-specific chemical signals that facilitate the location, identification, and selection of mating partners. These pheromones can vary between individuals, and act as signals of mate quality. Here, we investigate the variation of male pheromones in the mesosomal glands of the large carpenter bee Xylocopa sonorina, within a Northern California population. We tested the hypothesis that morphological traits are correlated with the observed variation in chemical blend composition of these bees. We also conducted behavioral assays to test whether these male pheromones act as long-range attractants to conspecifics. We found that larger males with darker mesosomal glands have a higher pheromone amount in their glands. Our analysis also shows initial evidence that this pheromone blend serves as a long-range attractant to both males and females. We show that both male body size and sexual maturation are important factors influencing pheromone abundance, and that this pheromone blend acts as a long-range attractant. We hypothesize that this recorded variation in male pheromone could be important for female choice.

evolutionary biology↗

The function of environmentally acquired perfume blends in male orchid bees

Perfume making by male orchid bees is a remarkable behavior giving rise to an entire pollination syndrome in the neotropics. Male orchid bees concoct and store perfume mixtures in specialized hind-leg pockets using volatiles acquired from multiple environmental sources, including orchids. However, the precise function and ultimate causes of this behavior have remained elusive. We supplemented male Euglossa dilemma reared from trap-nests with perfume loads harvested from wild conspecifics. In dual-choice experiments, males supplemented with perfumes mated with more females, and sired more offspring, than untreated, equal-aged, control males. Our results demonstrate that male-acquired perfumes function as chemical signals emitted during courtship and received by females when selecting mates. Sexual selection might be a key agent shaping the evolution of perfume signaling. One-Sentence SummaryThe possession of exogenous volatiles increase male mating success and paternity in orchid bees.

evolutionary biology↗

Seasonal stability and species specificity of environmentally acquired chemical mating signals in orchid bees

Traits that mediate reproductive isolation between species, such as those involved in mate choice and/or recognition, are predicted to experience stabilizing selection towards the species mean. Male orchid bees collect chemical compounds from many sources, such as plants and fungi, which they use as a perfume signal (pheromone) during courtship display. Environmentally acquired signals are more prone to variation as source availability can vary through space and time. Here, we investigate the seasonality and species-specificity of male perfumes across an entire year in three sympatric species of Euglossa orchid bees. Our analysis revealed considerable within-species variation in perfumes. However, species-specificity was maintained consistently throughout the year, suggesting that these perfumes could play an important role in reproductive isolation. Our analysis also identified strong correlations in the abundance of some compounds, possibly due to shared collection sources between species. Our study suggests that orchid bee perfumes are robust in the face of environmental changes in resource availability.

evolutionary biology↗

Experimental disruption of social structure reveals totipotency in the orchid bee, Euglossa dilemma

Eusociality has evolved multiple times across the insect phylogeny. Social insects with greater levels of social complexity tend to exhibit specialized castes with low levels of individual phenotypic plasticity. In contrast, species with small, simple social groups may consist of totipotent individuals that can transition among behavioral and reproductive states as the social hierarchy shifts. However, recent work has shown that in some simple social groups, there can still be constraint on individual plasticity, caused by differences in maternal nourishment or initial social interaction. It is not well understood how and when these constraints arise during social evolution, ultimately leading to the evolution of nonreproductive workers. Some species of orchid bees can form social groups of a dominant and 1-2 subordinate helpers where all individuals are reproductive. Females can also disperse on emergence to start their own nest as a solitary foundress, which includes a nonreproductive nest guarding phase not typically expressed by subordinates. Little data exist to characterize the flexibility of orchid bees across these trajectories. Here, using the orchid bee Euglossa dilemma, we conduct an experiment assessing the plasticity of subordinate helpers, finding that they are highly flexible and capable of the behavioral, physiological, transcriptomic, and chemical changes seen in foundresses. Furthermore, we identify genes and gene networks associated with reproductive changes in E. dilemma that overlap with genes associated with worker physiology in eusocial species. Our results provide evidence that the lack of nonreproductive workers in E. dilemma is not due to a lack of subordinate plasticity.

evolutionary biology↗

The birth-and-death evolution of cytochrome P450 genes in bees

The birth-and-death model of multigene family evolution describes how families can expand by duplication and contract by gene deletion and formation of pseudogenes. The phylogenetic stability of a gene is thought to be related to the degree of functional importance. However, it is unclear how much evolution of a gene in a gene family is driven by adaptive versus neutral processes. The cytochrome P450s are one of the most diverse and well-studied multigene families, involved in both physiological and xenobiotic functions. Bees have a high toxin exposure due to their diet of nectar and pollen, as well as the resin-collecting behavior exhibited by some bees. Here, we describe the P450s of the orchid bee Euglossa dilemma. Orchid bees are a neotropical clade in which males form perfume bouquets used in courtship displays by collecting a diverse set of volatile compounds, resulting in high chemical compound exposure. We conducted phylogenetic and selection analyses across ten bee species encompassing three bee families. We do not find a relationship between the ecology of a bee species and its P450 repertoire. Our analyses reveal that P450 clades can be classified into stable and unstable clades, and that genes involved in xenobiotic metabolism are more likely to belong to unstable clades. Furthermore, we find that unstable clades are under more dynamic evolutionary pressures, with signals of adaptive evolution detected, suggesting that both gene duplication and positive selection driving sequence divergence have played a role in the diversification of bee P450s. Our works highlights the complexity of multigene family evolution which does not always follow generalized predictions. Significance statementGene family evolution is characterized by deletion and duplication, but it is unclear if this is driven by adaptive or neutral evolutionary processes. To investigate the dynamics of gene family evolution we analyze the P450s of ten bee species, a well-studied gene family involved in both physiological and detoxification roles. We find that genes involved in detoxification are more likely to belong to unstable clades, exhibit dynamic evolutionary pressures, and show signals of adaptive evolution. However, we do not find evidence for a relationship between resin collection or sociality, and the P450 repertoire of a bee species. Our findings highlight the complexity of multigene family evolution which does not always follow generalized predictions.

molecular biology↗

Selection and hybridization shaped the Africanized honey bee invasion of the Americas

Recent biological invasions offer natural laboratories to understand the genetics and ecology of adaptation, hybridization, and range limits. One of the most impressive and well-documented biological invasions of the 20th century began in 1957 when Apis mellifera scutellata honey bees swarmed out of managed experimental colonies in Brazil. This newly-imported subspecies, native to southern and eastern Africa, both hybridized with and out-competed previously-introduced European honey bee subspecies. Populations of scutellata-European hybrid honey bees rapidly expanded and spread across much of the Americas in less than 50 years. We use broad geographic sampling and whole genome sequencing of over 300 bees to map the distribution of scutellata ancestry where the northern and southern invasions have presently stalled, forming replicated hybrid zones with European bee populations in California and Argentina. California is much farther from Brazil, yet these hybrid zones occur at very similar latitudes, consistent with the invasion having reached a climate barrier. At these range limits, we observe genome-wide clines for scutellata ancestry, and parallel clines for wing length that span hundreds of kilometers, supporting a smooth transition from climates favoring scutellata-European hybrid bees to climates where they cannot survive winter. We find no large effect loci maintaining exceptionally steep ancestry transitions. Instead, we find most individual loci have concordant ancestry clines across South America, with a build-up of somewhat steeper clines in regions of the genome with low recombination rates, consistent with many loci of small effect contributing to climate-associated fitness trade-offs. Additionally, we find no substantial reductions in genetic diversity associated with rapid expansions nor complete dropout of scutellata ancestry at any individual loci on either continent, which suggests that the competitive fitness advantage of scutellata ancestry at lower latitudes has a polygenic basis and that scutellata-European hybrid bees maintained large population sizes during their invasion. To test for parallel selection across continents, we develop a null model that accounts for drift in ancestry frequencies during the rapid expansion. We identify several peaks within a larger genomic region where selection has pushed scutellata ancestry to high frequency hundreds of kilometers past the present cline centers in both North and South America and that may underlie high-fitness traits driving the invasion. Author SummaryCrop pollination around the world relies on native and introduced honey bee populations, which vary in their behaviors and climatic ranges. Scutellata-European hybrid honey bees (also known as Africanized honey bees) have been some of the most ecologically successful; originating in a 1950s experimental breeding program in Brazil, they rapidly came to dominate across most of the Americas. As a recent genetic mixture of multiple imported Apis mellifera subspecies, scutellata-European hybrid honey bees have a patchwork of ancestry across their genomes, which we leverage to identify loci with an excess of scutellata or European ancestry due to selection. We additionally use the natural replication in this invasion to compare outcomes between North and South America (California and Argentina). We identify several genomic regions with exceptionally high scutellata ancestry across continents and that may underlie favored scutellata-European hybrid honey bee traits (e.g. Varroa mite resistance). We find evidence that a climatic barrier has dramatically slowed the invasion at similar latitudes on both continents. At the current range limits, scutellata ancestry decreases over hundreds of kilometers, creating many bee populations with intermediate scutellata ancestry proportions that can be used to map the genetic basis of segregating traits (here, wing length) and call into question the biological basis for binary Africanized vs. European bee classifications.

evolutionary biology↗

Olfactory receptors tuned to volatile mustard oils in drosophilid flies

The diversity of herbivorous insects is attributed to their propensity to specialize on toxic plants. In an evolutionary twist, toxins betray the identity of their bearers when herbivores co-opt them as cues for host-plant finding, but the mechanisms underlying this process are poorly understood. We focused on Scaptomyza flava, an herbivorous drosophilid specialized on isothiocyanate (ITC)-producing (Brassicaceae) plants, and identified Or67b paralogs that were triplicated as mustard-specific herbivory evolved. Using heterologous systems for the expression of olfactory receptors, we found that S. flava Or67bs, but not homologs from microbe-feeding relatives, responded selectively to ITCs, each paralog detecting different ITC subsets. Consistent with this, S. flava was attracted to ITCs, as was Drosophila melanogaster expressing S. flava Or67b3 in the homologous Or67b olfactory circuit. Thus, our results show that plant toxins were likely co-opted as olfactory attractants through gene duplication and functional specialization (neofunctionalization and subfunctionalization) in drosophilid flies.

evolutionary biology↗

An olfactory receptor gene underlies reproductive isolation in perfume-collecting orchid bees

Speciation is facilitated by the evolution of reproductive barriers that prevent or reduce hybridization among diverging lineages. However, the genetic mechanisms that control the evolution of reproductive barriers remain elusive, particularly in natural populations. We identify a gene associated with divergence in chemical courtship signaling in a pair of nascent orchid bee lineages. Male orchid bees collect perfume compounds from flowers and other sources to subsequently expose during courtship display, thereby conveying information on species identity. We show that these two lineages exhibit differentiated perfume blends and that this change is associated with the rapid evolution of a single odorant receptor gene. Our study suggests that reproductive isolation evolved through divergence of a major barrier gene involved in chemically mediated pre-mating isolation via genetic coupling.

evolutionary biology↗

The Evolutionary Dynamics Of The Odorant Receptor Gene Family In Corbiculate Bees

Insects rely on chemical information to locate food, choose mates, and detect potential predators. It has been hypothesized that adaptive changes in the olfactory system facilitated the diversification of numerous insect lineages. For instance, evolutionary changes of Odorant Receptor (OR) genes often occur in parallel with modifications in life history strategies. Corbiculate bees display a diverse array of behaviors that are controlled through olfaction, including varying degrees of social organization, and manifold associations with floral resources. Here we investigated the molecular mechanisms driving the evolution of the OR gene family in corbiculate bees in comparison to other chemosensory gene families. Our results indicate that the genomic organization of the OR gene family has remained highly conserved for approximately 80 million years, despite exhibiting major changes in repertoire size among bee lineages. Moreover, the evolution of OR genes appears to be driven mostly by lineage-specific gene duplications in few genomic regions that harbor large numbers of OR genes. A selection analysis revealed that OR genes evolve under positive selection, with the strongest signals detected in recently duplicated copies. Our results indicate that chromosomal translocations had a minimal impact on OR evolution, and instead local molecular mechanisms appear to be main drivers of OR repertoire size. Our results provide empirical support to the longstanding hypothesis that positive selection shaped the diversification of the OR gene family. Together, our results shed new light on the molecular mechanisms underlying the evolution of olfaction in insects.

evolutionary biology↗