Larval Drosophila encounter and feed on a diverse microbial community within fruit. In particular, free-living yeast microbes provide a source of dietary protein critical for development. However, successional changes to the fruit microbial community may alter host quality through impacts on relative protein content or yeast community composition. For many species of Drosophila, fitness benefits from yeast feeding vary between individual yeast species, indicating differences in yeast nutritional quality. To better understand these associations, we evaluated how five species of yeast impacted feeding preference and development in larval Drosophila suzukii. Larvae exhibited a strong attraction to the yeast Hanseniaspora uvarum in pairwise yeast feeding assays. However, larvae also performed most poorly on diets containing H. uvarum, a mismatch in preference and performance that suggests differences in yeast nutritional quality are not the primary factor driving larval feeding behavior. Together, these results demonstrate that yeast plays a critical role in D. suzukii’s ecology and that larvae may have developed specific yeast associations. Further inquiry, including systematic comparisons of Drosophila larval yeast associations more broadly, will be necessary to understand patterns of microbial resource use in larvae of D. suzukii and other frugivorous species.
Microorganisms can play a critical role in the nutritional ecology of insects and other animals1. Obligate symbionts, including bacteria and fungi that colonize the insect digestive tract, aid in the detoxification and digestion of phloem, wood, and other low-nutrient plant materials1,2,3,4. Some gut microbial symbionts also help their host synthesize essential amino acids5, vitamins6,7, or sterols8,9,10 otherwise lacking in the insect’s diet. In addition to obligate gut symbionts, insects can compensate for nutritional deficiencies within their food by supplementing their diets with free-living microbes, including bacteria, fungi, or yeast.
This latter category of nutritional interactions is particularly well documented within the genus Drosophila (Diptera: Drosophilidae). For many frugivorous species of Drosophila, yeasts provide a source of dietary protein otherwise absent from ripening fruit, a carbohydrate-rich resource11. While these carbohydrates are important for many aspects of adult Drosophila fitness, including their life span, fecundity, and survivorship12,13,14, yeast-associated protein also plays a critical role in fitness, particularly during the larval life stage. In general, Drosophila larvae exhibit lower survivorship in yeast-free or low yeast substrates15,16,17, and increasing the ratio of dietary protein to carbohydrates within the larval diet improves survivorship, reduces larval development time, and increases adult body mass18,19,20. Choice and no-choice behavioral studies suggest that Drosophila larvae preferentially feed on protein-rich food sources and will carefully regulate their food intake to consume protein quantities optimal for larval fitness19.
However, protein abundance within fruit and other fermenting larval substrates change over time, impacting nutritional quality for Drosophila larvae. During fermentation, the yeast microbial community undergoes a series of successional changes in both its species composition and density21. In particular, the protein to carbohydrate (P:C) ratio increases as fermentation progresses19,22. This microbial succession is frequently mirrored by sucessional colonization of different Drosophila species21, because individual Drosophila vary in their nutritional requirements22. Expanding our understand of the nutritional ecology of different Drosophila species may provide insight into larval resource partitioning and will also contribute to our knowledge of Drosophila suzukii Matsumura, a close relative of the model organism Drosophila melanogaster Meigen and a major agricultural pest in small fruit crops.
Drosophila suzukii is an invasive fruit fly that occupies a unique ecological niche among frugivorous Drosophila. Unlike other species, female D. suzukii possess a serrated ovipositor that enables them to lay eggs in ripening fruit23 during the early stages of fermentation. In contrast, most other frugivorous Drosophila species wait until fruit is decaying to deposit eggs. Consequentially, D. suzukii larvae develop under relatively protein-poor and carbohydrate-rich conditions, a nutritional niche that corresponds with larval performance in laboratory development assays. When reared on intermediate protein diets (e.g. 1:2 or 1:4 P:C ratio), larval D. suzukii exhibit faster development times, larger adult body sizes, and higher female ovariole numbers relative to Drosophila biarmipes Malloch19, a close relative of D. suzukii that colonizes decaying fruit. Furthermore, diets too rich in microbiota may have deleterious effects on larval D. suzukii fitness. The median lifespan of amicrobial D. suzukii reared on nutrient-rich sucrose-yeast diets (71 days) decreased when their natural microbiota was present (47 days). The presence of microbiota also decreased adult body size by 0.32 mg (female) and 0.11 mg (male), while slightly increasing the development period from 11.94 to 12.19 days17. In contrast, the microbiota/nutrient-rich diet combination does not appear to harm D. melanogaster; comparisons between amicrobial larvae and larvae containing their natural microbiota found no differences in larval development time24. These differences likely reflect adaptations by D. suzukii larvae to relatively nutrient-poor ripening fruit.
In addition to differences in yeast density, the composition and relative abundance of individual yeast species within a fruit changes over time. This can further impact fruit habitat suitability, as individual yeast species differentially impact larval fitness and development16,17. For example, D. melanogaster exhibit lower survivorship and smaller adult body mass when reared on diets containing the yeast Metschnikowia pulcherrima, compared with diets containing either Saccharomyces cerevisiae, Pichia toletana, or Kluyveromyces lactis25. Different quantities of heat-killed yeasts are needed, depending on species, to support development in larval D. melanogaster, suggesting that yeasts vary in their nutritional quality20. Indeed, the concentration and composition of key nutrients such as lipids, amino acids, mannoproteins, and fatty acids differ between yeast species26,27,28. In addition to variably impacting larval development, it is possible that these nutritional differences influence larval feeding behavior.
Larval Drosophila often exhibit distinct yeast feeding preferences25,29,30,31,32, though the level of selectivity can vary between species based on their host substrate. Drosophila that have a restricted host range tend to exhibit less selective feeding behavior. For example, larvae of the specialist cactophilic Drosophila nigrospiracula, Drosophila mettleri, and Drosophila pachea feed on yeast at the same frequency as yeast species occur within the larval substrate33. This behavior may indicate that larvae with a restricted host range cannot afford to evolve specialized microbe feeding behaviors, as microbial communities are ephemeral and often vary between conspecific host substrates33. In contrast, generalist Drosophila such as Drosophila mojavensis or D. melanogaster exhibit distinctive yeast feeding preferences in both field and laboratory settings30,33.
This selective foraging behavior may reflect perceived differences in yeast resource quality. The larval chemosensory system contains an array of gustatory and olfactory neural receptors34 that allow larvae to discriminate between food sources based on nutritional factors such as the identity and availability of sugars and amino acids35,36,37. Therefore, larval Drosophila may selectively feed on yeasts that best support their fitness, with specific Drosophila – yeast associations dependent on the fruit microbial community and stage of fruit decay typically encountered.
Previous field surveys indicate that D. suzukii larvae feed upon a distinct yeast fauna, with one species of yeast, Hanseniaspora uvarum, predominating in the gut38,39. Hanseniaspora uvarum is a widespread yeast species that occurs at high frequency in the early stages of fruit fermentation21,40 and can be antagonistic to other species of fungi, including yeast41. Therefore, larval feeding patterns may reflect H. uvarum’s abundant field density; alternatively, these patterns may indicate feeding preferences.
To better understand the nature of these interactions, we evaluated larval D. suzukii feeding preference and performance in response to diets prepared using five different species of yeast, including the model organism S. cerevisiae and natural yeast associates of larval D. suzukii38. We hypothesized that larvae would exhibit a significant preference for the yeast that best supported their fitness. While larvae did exhibit a strong preference for H. uvarum in laboratory preference assays, this preference negatively correlated with performance. Our results suggest larval D. suzukii yeast feeding preferences may be driven by factors beyond nutritional quality.
Larval development assays
We evaluated how three species of yeasts isolated from field collected D. suzukii larvae (H. uvarum, Pichia kluyveri, and Issatchenkia terricola) and diets without yeast (negative control) impacted fitness and development in larval D. suzukii (Supplementary Table S1). As a positive control, we also prepared diets using commerical Saccharomyces cerevisiae, because this species is frequently used as a model organism to study Drosophila – yeast interactions. To ensure the diet microbial community remained static and to remove confounding effects due to yeast growth rate, development assays were conducted with standardized amounts of frozen yeast and diets were autoclave sterilized to heat-kill all microbes. Diet treatments were monitored daily for both pupation and adult eclosion, and emergence data were used to calculate larval (1st instar larvae to pupa) survivorship and development time, pupal (pupa to adult) survivorship and development time, and total (1st instar larvae to adult) survivorship and development time. Thorax and wing length measurements were also taken to quantify the body size of any emerged adults. Diets were prepared on three separate occasions (N = 3) with 6 dishes per treatment for which subsamples were averaged prior to analysis.
Individual yeast species significantly affected larval survivorship (1st instar larvae to pupa; F3,6 = 6.688, P = 0.024). Larvae reared on a yeast-free diet (negative control) exhibited 0% survivorship across all replicates (Fig. 1), indicating that yeast is essential for D. suzukii development. Apart from the yeast-free control, the lowest rates of larval survivorship occurred on diets containing I. terricola (22.2 ± 2.5%; mean ± standard error), while there was higher larval survivorship on either S. cerevisiae (50.8 ± 8.2%) or H. uvarum (48.3 ± 8.4%) (Fig. 1A). Total survivorship patterns were similar (Fig. 1C; F3,6 = 6.466, P = 0.026), with the highest percentage of larvae sucessfully emerging as adults in response to either S. cerevisiae (48.1 ± 8.7%) or H. uvarum (36.4 ± 5.8%). In contrast, pupal survivorship (pupa to adult; F3,6 = 1.857, P = 0.238) was not impacted by diet treatments.
The fastest larval development period occurred on diets containing S. cerevisiae (1st instar larvae to pupa; F3,8 = 13.418, P = 0.002), with larvae taking 11.7 ± 0.6 days to pupate. Larvae reared on H. uvarum took 14.3 ± 0.2 days to reach the pupal stage, and the slowest larval development times occurred in response to either I. terricola or P. kluyveri (Fig. 2A, Supplementary Fig. S1A). Patterns in the total development times were similar (Fig. 2C; F3,8 = 12.799, P = 0.002), with the fastest larval to adult development times again occurring in response to S. cerevisiae (see also Supplementary Fig. S1B). We observed no significant differences in pupal development time among treatments (F3,6 = 3.369, P = 0.096; Fig. 2B).
Adult body size
The individual yeast diets significantly affected thorax length in both male (F3,6 = 9.880, P = 0.010) and female (F3,8 = 20.467, P < 0.001) D. suzukii (Table 1). The largest thorax lengths were observed in male (1.08 ± 0.01 mm) and female (1.24 ± 0.01 mm) flies reared on S. cerevisiae. In contrast, the smallest flies observed were those reared on a H. uvarum diet. Flies reared on either an I. terricola or a P. kluyveri based diet also exhibited a reduced body size relative to S. cerevisiae and were slightly larger than those observed from H. uvarum. Similar patterns emerged in the wing length of both male (F3, 6= 6.983, P = 0.022) and female (F3,8 = 17.462, P < 0.001) D. suzukii, with the largest wings occuring in flies reared on S. cerevisiae and the smallest wings in flies reared on H. uvarum (Table 1).
Diet nutritional analysis
To compare nutritional content between our experimental diets and the standard Drosophila diet used to maintain our laboratory stocks, we conducted proximate nutritional analysis on all diets used in this study and a standard diet prepared using freeze-dried S. cerevisiae (Supplementary Table S1). Nutrient analyses were repeated twice, using diets prepared on two separate dates.
We observed no major nutritional differences between any of our experimental diets, which were all prepared using yeast cells scraped from media plates. However, diets prepared without yeast (negative control) consistently had the lowest caloric content and fell below the detectable protein threshold in both replicates. In contrast, diets prepared using freeze-dried S. cerevisiae had higher caloric values (52.5 ± 0.5 calories per 100 grams diets; N = 2 replicates) relative to any other treatment. For example, diets prepared using wet H. uvarum cultures had the second highest caloric value at 43.0 ± 1.0 calories per 100 grams. We also observed higher relative amounts of ash (inorganic residue), carbohydrates, and protein within diets prepared using freeze-dried yeast cultures (Supplementary Table S2).
Larval yeast preference
We evaluated larval D. suzukii feeding preference for five species of yeast (H. uvarum, P. kluyveri, I. terricola, W. pijperi, and S. cerevisiae) through two-choice feeding assays. In each assay, larvae were placed on a large water-agar plate provisioned with two yeast options (colored red or blue) on opposite ends of the plate, and larval feeding preferences were assessed after one hour based on the color of the alimentary canal. For each set of two-choice tests, we conducted 12 replicate assays.
Overall, D. suzukii larvae preferred H. uvarum (T11 = 7.214, P < 0.001) and W. pijperi (T11 = 2.286, P = 0.043) over S. cerevisiae (Fig. 3). For example, 54.0% ± 2.3% (mean ± standard error) of the larvae assayed chose to feed on H. uvarum, compared with the 28.8% ± 2.3% that chose to feed on S. cerevisiae. Similarly, in comparisons between W. pijperi and S. cerevisiae, 46.0% ± 4.3% and 28.7% ± 3.6% of larvae assayed chose to feed on each yeast respectively (Fig. 3). However, larvae exhibited no significant feeding preferences in pairwise comparisons between S. cerevisiae and either P. kluyveri or I. terricola. Larvae also demonstrated no significant feeding preferences in pairwise comparisons of I. terricola, P. kluyveri, and W. pijperi (Supplementary Tables S3–S5).
Across all binary comparisons of larval feeding preference, H. uvarum elicited the strongest feeding response in D. suzukii (Fig. 4). In addition to demonstrating significant preferences for H. uvarum over S. cerevisiae, significantly more larvae chose to feed on H. uvarum over P. kluyveri (T11 = 7.468, P < 0.001), I. terricola (T11 = 8.601, P < 0.001), and W. pijperi (T11 = 3.042, P = 0.011).
Drosophila suzukii encounters a diverse microbial community within fruit that undergoes successional changes in both density and species composition21,42,43, allowing them to selectively feed on a wide variety of yeast microbes that play a critical role in their life history. Larvae exhibit a strong attraction to live yeast cultures, and yeasts are important components of D. suzukii’s diet. Similar to previous work16,17, we found that larvae reared in a completely yeast-free environment universally failed to pupate or eclose. Our ability to rescue larval development with heat-killed microbes confirms that yeasts provide D. suzukii larvae with a source of protein and essential nutrients not otherwise found in fruit or fly diets10,44,45. We initially hypothesized that larvae would preferentially feed on certain species of yeast based on perceived differences in resource quality. However, the mismatch between larval yeast preference and performance suggests that larvae do not discriminate between yeast species based on nutritional quality alone and instead there may be alternative mechanisms shaping D. suzukii’s yeast associations.
Results from this study suggest that D. suzukii larvae have developed a close association with H. uvarum. In binary laboratory choice assays, D. suzukii larvae preferentially fed on H. uvarum over alternative natural yeast associates as well as S. cerevisiae. This result is consistent with previous reports that H. uvarum predominates the culturable larval gut microbial community in geographically distant populations of D. suzukii38,39 and to the best of our knowledge, is the first evidence that larval D. suzukii exhibit feeding preferences for specific yeast species. Our studies suggest that larval feeding is not random; despite being confined to a single fruit throughout development, larval D. suzukii appear to deliberately seek out and feed on H. uvarum, indicating that there may be an association between these two organisms.
We initially hypothesized that D. suzukii preferentially fed on H. uvarum because it was a higher quality yeast that better supported larvae. Instead, larvae exhibited reduced performance on diets containing H. uvarum. Larvae reared on H. uvarum developed more slowly relative to diets containing S. cerevisiae, and adult body size was smaller compared to individuals reared on diets prepared with S. cerevisiae, P. kluyveri, or I. terricola. Surprisingly, the most robust fitness occurred on diets containing S. cerevisiae, with higher rates of surviorship and shorter developmental times relative to flies reared on diets containing natural yeast associates. Flies reared on S. cerevisiae based diets also had significantly larger adult body sizes, a trait that generally indicates higher levels of fecundity, survival, and mating success46. This higher performance on S. cerevisiae was surprising, because Drosophila rarely associate with this species of yeast in nature38,39,47 and larvae did not prefer S. cerevisiae in binary choice assays. It is possible that these results reflect phenotypic plasticity in resource use, with larvae able to exploit and perform well on diverse yeast resources despite specialization towards H. uvarum48. Similar plastic behavior may occur in adult D. suzukii during winter and early spring when ripe fruit is scarce in temperate climates; under no-choice laboratory conditions female D. suzukii will accept and oviposit into less optimal resources including mushroom, apple, and chicken-manure based diets49. The enhanced performance we observed could also result from laboratory colony selection effects. All flies used in this study came from a D. suzukii colony reared for over 50 generations on a standard S. cerevisiae based diet. Alternatively, the benefits conferred from S. cerevisiae may reflect commercial selection effects, because the particular strain of yeast used in this study was originally selected for making bread, which could impact protein content and secondary metabolite production. Since D. suzukii larvae do not frequently encounter S. cerevisiae in nature, they may not have recognized this particular yeast as a superior food source.
This mismatch in larval yeast preference and performance suggests that D. suzukii larvae do not discriminate between individual species of yeast based solely on the nutritional quality of the yeast. Yeast quantity, rather than quality, may be a more important determinant of larval fitness. In this study, D. suzukii larvae developed under protein-limited conditions. We prepared our fly diets following the standard recipe used to maintain our laboratory Drosophila stocks, changing only the species of yeast added. Instead of using dehydrated yeast, we harvested and weighed all our yeast directly from PDA plates, a step that likely reduced the nutritional value relative to the original, freeze-dried yeast recipe (Table S2). The protein content in our freeze-dried yeast diet averaged 2.42%, similar to protein concentrations (1.11% and 2.0%) in other published Drosophila diets11,17. In contrast, average protein concentration in our experimental diets ranged from 0.78–1.24%. Negative fitness impacts due to the limited protein conditions within our diets were likely compounded by the use of heat-killed microbes. By steam sterilizing our diets to avoid differences due to variable yeast growth rates50 and contamination by other microbes, we stopped microbial growth. This may have created yeast shortages typically not observed in the field where natural yeast growth or larval niche construction and yeast seeding would increase yeast abundance over time51,52.
Yeast shortages and the associated low dietary protein may have detrimentally impacted larval fitness, especially prolonging development. In this study, the fastest development time occurred in larvae reared on S. cerevisiae, with first instar larva to pupa development taking an average of 11.7 ± 0.6 days and first instar larva to adult devleopment taking an average of 16.9 ± 0.8 days. In contrast, other studies have observed that D. suzukii development times on S. cerevisiae-based fly diets takes 6.0–7.1 days for pupation16,53 and 11.9–12.8 days for adult emergence17,53 at temperature levels comparable to our study conditions16,17,53. Beyond development time, low protein conditions can negatively impact other aspects of larval fitness, including survivorship and adult body size18,19,20. Within carbohydrate-rich ripening fruit11, larval D. suzukii likely rely on the yeast microbial community to obtain sufficient protein for development.
Given the importance of dietary protein for development17, D. suzukii larvae may prioritize feeding on yeasts that are abundant and readily available over selectively seeking higher quality species. For example, D. suzukii larvae may preferentially feed on H. uvarum because it predominates yeast microbial communities during the early stages of fermentation, thus providing a more abundant source of protein. Previous studies have demonstrated that D. suzukii larvae provisioned with live cultures of H. uvarum generally experience a robust fitness phenotype relative to other yeast associates16,17. The higher performance observed in these studies likely reflects a higher yeast abundance when using live cultures, because Drosophila spp. larval feeding increases yeast abundance within their host substrates in field39 and laboratory experiments52, and live yeasts are able to continually grow during development assays. Microbial abundance positively correlates with larval growth rates in D. melanogaster, suggesting that a microbe’s ability to proliferate may be one of the most important predictors of its effect on larval fitness20. Therefore, D. suzukii larvae may benefit from H. uvarum’s widespread and competitive nature21,40, as it means that H. uvarum can quickly increase its density, providing larvae with a consistent and abundant source of protein.
Beyond its ability to proliferate, there are a number of other factors that could mediate larval attraction to H. uvarum. For example, H. uvarum’s attractiveness may reflect yeast adaptations that enhance its fitness. Adult Drosophila disperse yeasts54,55, and more attractive yeast strains experience higher rates of dispersal56. Larval feeding may also confer competitive advantages to yeast by promoting yeast growth or genetic diversity51,52,57. Alternatively, some strains of H. uvarum produce “killer toxins” that may help larvae outcompete harmful plant pathogenic fungi58 or create an enemy-free space59, consequentially enhancing larval fitness through measures not quantified in this study. A similar competitive advantage has been proposed for D. melanogaster, with larvae parasitized by the wasp Asobara tabida preferentially feeding on yeast species that enhance their ability to melanotically encapsulate parasitic attacks60. It is also possible that H. uvarum confers additional fitness benefits during the adult life stage not quantified in this study such as adult survivorship61, adult cuticular pheromone production61, or reproductive outputs such as ovariole numbers19.
Hanseniaspora uvarum is a widespread yeast species frequently isolated from fermenting fruits and insects40, including adult Drosophila. A survey of Drosophila spp. yeast associations found that with a few exceptions, the H. uvarum species complex was the most abundant OTU isolated from the gut of adult flies47, suggesting a general feeding association between Drosophila and H. uvarum. Volatiles associated with H. uvarum are also highly attractive to multiple adult species, including D. suzukii and D. melanogaster62,63. While further work is necessary to fully understand the mechanism and nature of H. uvarum’s association with D. suzukii, it is clear that H. uvarum strongly impacts D. suzukii’s ecology, similar to other Drosophila.
The extent to which adult yeast associations overlap with the larval life-stage remains unclear. Adult flies are highly mobile insects, capable of visiting a diverse community of host plants, which provides them a different, broader feeding niche than larvae64. Field and laboratory surveys of cactophilic Drosophila yeast associations report differences between adult and larval yeast preferences29. For example, in laboratory assays, female Drosophila buzzati exhibited a significant preference for ovipositing and feeding on cactus inoculated with Pichia cactophila relative to Clavispora opuntiae65, while larvae exhibited high attraction to both yeast species66. In addition, surveys of adult feeding behavior on decaying oranges found that Drosophila spp., including D. melanogaster and D. pseudoobscura, fed more frequently on yeasts available at the surface of necrotic tissue compared to yeasts colonizing the interior fruit rot, suggesting a spatial separation between adult and larval feeding niches67.
Yeast associations and preferences have been fairly well surveyed within adult frugivorous Drosophila47,68,69,70,71. However, records of natural yeast associations within frugivorous larvae are more limited. Previous laboratory studies using D. melanogaster and cactophilic Drosophila larvae demonstrate that larvae have specific yeast preferences25,29,32, and these preferences vary between species. In pairwise yeast preference comparisons, D. buzzati and Drosophila aldrichi exhibited slight differences in their yeast preferences66. Also, within decaying oranges, D. arizonensi and D. melanogaster consumed H. uvarum at lower frequencies than it occurred in the orange microbial community33, a result that suggests larvae were avoiding H. uvarum, in contrast to the strong preference for H. uvarum we observed in D. suzukii. Within fermenting fruit, it therefore seems plausible that different species of Drosophila larvae develop different yeast preferences and associations, and that these associations shift across temporal niches within fermenting fruit. For example, D. suzukii larvae could develop closer associations with early stage fermentation communities compared to D. melanogaster and other late stage colonizers. Systematic comparisons of larval yeast preferences and surveys of larval yeast associations would be needed to test this hypothesis.
Because yeasts play such a critical role in D. suzukii’s ecology, there may be opportunities to exploit these interactions for more sustainable pest management72. Yeast associated volatiles could be integrated into monitoring programs for D. suzukii. Fermentation based-lures have already been developed, but current trapping systems remain difficult to use due to issues with trap selectivity and poor correlations between adult trap captures and larval infestation73,74. It may be possible to use yeast volatile components specifically attractive to D. suzukii63 to develop a more selective trapping system. Similarly, yeast-associated volatiles could also be incorporated into a push-pull system for D. suzukii75.
Recent research efforts have also focused on incorporating yeasts into feeding baits or biopesticides specific to D. suzukii. In laboratory trials, adult and larval D. suzukii exhibited reduced fitness after ingesting S. cerevisiae that was genetically modified to express double-stranded RNA76. Yeasts have also been tested as potential phagostimulants for insecticide applications, with variable efficacy. Adding yeast to either spinosad or cyanotraniliprole increased adult mortality and decreased larval infestation compared to treating with the insecticide alone77. However, efficacy varied between yeast species and insecticides, with highest efficacy observed when using S. cerevisiae and commercial formulations of the yeast Aureobasidium pullulans as phagostimulants77. Similarly, laboratory assays also reported that combinations of spinosad and H. uvarum increased D. suzukii mortality relative to the insecticide alone78. In contrast to these studies, recent field and laboratory assessments found that adding S. cerevisiae to various organic insecticides did not improve control of D. suzukii in either semi-field or laboratory assays, a difference that may reflect variation in D. suzukii’s physiological status between studies79.
There appears to be considerable variation in how D. suzukii interacts with yeasts throughout its life history. Both adult and larval D. suzukii exhibit specific yeast preferences, and during the adult life stage, different species of Drosophila vary in their response to specific yeast volatile components63. Furthermore, the physiological status of adult flies can also influence behavioral responses. For example, unmated or reproductively immature females exhibit a higher attraction towards yeast volatiles80,81, and winter and summer morph D. suzukii vary in their responses to fungal-associated volatiles82. Deepening our understanding of this interspecific and intraspecific variation may provide opportunities to develop more targeted management programs specific to D. suzukii.
Materials and Methods
A laboratory reared colony of D. suzukii was established using adults and larvae collected from raspberry fields (Germantown and Woodbine, MD, USA) as well as adults trapped in a residential riparian area (Beltsville, MD, USA) in 2014. Flies were reared for over 50 generations under a 16:8 hour light/dark cycle at 22 °C on a modified Bloomington Drosophila Stock Center cornmeal, molassess, and yeast medium (consisting of 84.4% v/v water, 9.6% v/v cornmeal, 5.5% w/v yeast, 4.6% v/v molasses, 0.5% w/v agar, 0.5% w/v proprionic acid, and 0.01% w/v methyl 4-hydroxybenzoate). Our colony recipe contains a higher concentration of yeast compared to the Bloomington recipe and uses different antifungals (proprionic acid and methyl 4-hydroxybenzoate instead of p-hydroxybenzoic acid methyl ester). However, all other ingredients and ratios were similar (Supplemental Table S1). The colony was infected with an unknown insect pathogen, which presented symptoms similar to Drosophila C Virus83; infected larvae typically exited the food at an early instar and developed a brownish-black coloration before dying. To minimize effects from this infection, fly bottles were carefully inspected prior to experiment, with flies only taken from bottles that did not exhibit active symptoms. Because development studies were completed using amicrobial larvae, we anticipate no confounding effects due to this infection.
Experiments were conducted using five different species of yeast. Four of those species, Hanseniaspora uvarum, Pichia kluyveri, Issatchenkia terricola, and Wickerhamomyces pijperi, were isolated from the fecal pools (frass) of field-collected D. suzukii larvae38 with individual yeast species selected based on the strength of their association with D. suzukii. In particular, H. uvarum, P. kluyveri, and I. terricola, were isolated from multiple populations of D. suzukii in both Maryland and California38,39. A strain of Saccharomyces cerevisiae obtained from Red Star® Active Dry Yeast (LeSaffre Yeast Corporation, Milwaukee, WI, USA) was also included in laboratory assays as a positive control.
H. uvarum, P. kluyveri, I. terricola, and S. cerevisiae were used in all experiments described below, but W. pijperi was only included in the yeast preference assays. This species of yeast was only found in one field site in Maryland, but occured in 4 out of 12 larvae surveyed38. Given its strong prevelance at this single field site, we assayed larval yeast preference for W. pijperi. However, we excluded W. pijperi from the larval development assays due to labor constraints; larvae did not show a strong preference for that yeast and W. pijperi is not commonly associated with Drosophila spp.39,47.
Yeast impacts on larval growth and development
To evaluate yeast impacts on larval fitness and development, D. suzukii larvae were reared on the same colony diet described above using a standardized quantity of one of four yeast species: H. uvarum, P. kluyveri, I. terricola, and S. cerevisiae (see diet recipe in Supplementary Table S1). As a negative control, diets were also prepared with no yeast added. All diets were steam sterilized using an autoclave at 121 °C for 20 minutes prior to use in experiments; this step killed all microbes and ensured that yeast quantity remained constant throughout the experiment. Approximately 18 grams of diet were poured into small (60 × 15 mm) petri dishes and cooled overnight in a sterile biosafety cabinet.
After the overnight cooling period, 20 amicrobial first-instar larvae were then added to each petri dish (Supplementary Methods). This created a density of 1.1 larvae g−1 diet, which is slightly below the threshold at which larval D. suzukii begin exhibiting significant competition effects11. The entire experiment was repeated on three separate dates (N = 3 replicates). During each experimental replicate, we prepared six subsamples per treatment (six petri dishes of diet containing 20 D. suzukii larvae each). D. suzukii larvae were monitored daily, and we quantified survivorship, development time, and adult body size (wing and thorax measurements) as measures of larval fitness.
Diet plates with larvae were held in a 22 °C incubator on a 16:8 hour light/dark cycle and checked daily at approximately the same time that each experimental replicate was initiated (generally between 10 AM and 12 PM). Any pupae that emerged were transferred from the diet into an individual 1.5 mL microcentrifuge tube and then monitored daily for adult emergence. Transferring the pupa into individual tubes ensured that the adult flies did not become stuck within the diet, thus allowing us to measure adult body size. Once emerged, adult flies were held in their tubes for 24 hours to harden before being frozen and stored for future body size measurements.
To quantify adult body size, we measured the wing and thorax length for every adult D. suzukii that successfully emerged in our trials, using a Leica M80 microscope (Leica Microsystems, Wetzlar, Germany) with a reticle attached to the eyepiece. Measurements were adapted from previously described methods84,85. Briefly, to take thorax measurements, fine-tipped forceps were used to grasp each fly at the base of their legs, and the fly was oriented so its thorax was horizontal. Measurements were taken from the most anterior part of the mesothorax to the tip of the scutellum (Fig. 5A). Once thorax measurements were complete, the right wing was removed from the specimen and slide mounted. Two measurements were taken to quantify wing length: from the origin of the 4th longitudinal vein to the posterior cross vein (L1; Fig. 5B) and from the posterior cross vein to the intersection of the wing edge and the 4th longitudinal vein (L2; Fig. 5B). To minimize measurement biases and errors, all flies within a given replicate were measured by the same individual.
All statistical analysis were conducted using R.3.4.186. Data were averaged across subsamples within an individual trial (N = 3 replicate trials). Survivorship rates were calculated as the percentage of larvae that sucessfully pupated (larval survivorship), the percentage of pupae that sucessfully emerged as adults (pupal survivorship), and the percentage of larvae that sucessfully emerged as adults (total survivorship). For each category, data were analyzed using a linear mixed model, with the percent survivorship as the response variable, yeast treatment included as a categorical predictor, and replicate included as a random effect. Model residuals were checked for the assumptions of normality of variance and homogeneity of variance using Shapiro-Wilk and Levene’s tests. In all three analysis, assumptions were satisfied using untransformed data. Significant results were followed by pairwise mean comparisons using Tukey’s adjustment in the lsmeans package87.
Development time to pupation (larval development), time from pupation to adult eclosion (pupal development), and total development (1st instar larva to adult) were analyzed separately using a mixed-model ANOVA in the lme488 and lmerTest89 packages in R, with yeast treatment included as a main effect and trial replicate as a random effect. We confirmed data met the assumption of normality of variance with Shapiro-Wilk tests. However, weighted least squares methods [weighting factor: (treatment residual variance)−1] were used for larval and total development times due to difficulties satisfying the assumption of homogeneous variance. No weighting factor was required for analysis of pupal development time.
Body size measurements were also analyzed using a mixed-model ANOVA using the lme4 and lmerTest packages and models again included the yeast treatment as a fixed effect and trial replicate as a random effect. Data were transformed as necessary to meet assumptions of normality and homogeneity of variance. Due to difficulties satisfying assumptions of normality and homogeneity of variances, the analyses were conducted separately for male and female flies, with female wing and thorax measurements analyzed using weighted least squares [weighting factor: (treatment residual variance)−1]. Significant results were again followed by pairwise mean comparisons using Tukey’s adjustment in the lsmeans package87.
Quantifying diet quality
To compare the nutritional content of our experimental diets with the standard laboratory rearing diet, we conducted proximate nutrient analysis on each experimental diet as well as a diet prepared using freeze-dried S. cerevisiae. On two separate dates, diets were prepared using the same protocol described in 4.3. After autoclaving, all diets were poured into sterile 50 mL falcon tubes, refrigerated, and shipped to an off-site facility for analysis within three days of preparation. All analyses were conducted by Medallion Labs (General Mills D.B.A. Medallion Labs, Minneapolis, MN). Analysis were conducted 28 November 2018 and 9 January 2019 using standard testing protocols (Supplementary Methods).
Evaluating larval yeast preference
Using binary choice feeding assays, we evaluated larval D. suzukii’s preference for five species of yeast (described above). Bioassay arenas were constructed following methods adapted from previous larval Drosophila feeding assays32 (Supplementary Methods). Briefly, in each experimental replicate, larvae were presented with two yeast species stained red and blue with food coloring. After one hour, larvae were removed and visually scored for yeast feeding preferences.
Second-instar D. suzukii larvae were starved for one hour prior to starting the assay (Supplementary Methods). Forty larvae were then transferred to the center of one assay arena using an ethanol sterilized paintbrush and left in dark conditions for one hour, during which time they were free to crawl around and feed on either yeast option. At the end of the hour assay period, larvae were individually removed from the arena, and scored for feeding preference using a Leica M80 stereomicroscope based on the color of their abdomen (Fig. 5C–F). Each larva could be classified as either red, blue, purple (indicating that they fed on both yeasts), or white (indicating that no choice was made).
Any larvae that died or went missing during the hour-long assay period were excluded from the analysis. Prior to analysis, the number of larvae that chose to feed on each yeast option within an assay arena were standardized using a preference index described in Eq. (1) 32:
Adjusted larval counts were analyzed using a paired t-test86, with each assay arena of 40 larvae treated as an experimental replicate. Data were graphically checked for outliers using both box plots and Q-Q normality plots, and the assumption that the sampling distribution of mean differences was normally distributed was assessed using Anderson Darling test for normality in R with the ‘nortest’ package90. Data is reported as the percentage of larvae that chose to feed on each yeast.
Preference assay controls
To ensure that food coloring did not impact larval performance, we alternated which color each yeast option was stained between replicates. Additionally, a series of control preference assays was also conducted, in which larvae were presented with the same species of yeast in both food colors. Food coloring did not impact larval preference for any of the yeasts assayed (Supplementary Table S6).
To confirm that our visual assessments of larval feeding matched their actual feeding behavior, we also performed a set of separate confirmation assays and sequence identified the gut microbial community for a subset of experimental larvae (Supplementary Methods); results indicated that larval yeast feeding corresponded with the color of their abdomen, with few exceptions (Supplementary Table S7).
The datasets generated during the current study are available from the corresponding author upon reasonable request.
Douglas, A. E. The microbial dimension in insect nutritional ecology. Funct. Ecol. 23, 38–47 (2009).
Wong, A. C., Dobson, A. J. & Douglas, A. E. Gut microbiota dictates the metabolic response of Drosophila to diet. J. Exp. Biol. 217, 1894–1901 (2014).
Hammer, T. J. & Bowers, M. D. Gut microbes may facilitate insect herbivory of chemically defended plants. Oecologia 179, 1–14 (2015).
Hansen, A. K. & Moran, N. A. The impact of microbial symbionts on host plant utilization by herbivorous insects. Mol. Ecol. 23, 1473–1496 (2014).
Shigenobu, S., Watanabe, H., Hattori, M., Sakaki, Y. & Ishikawa, H. Genome sequence of the endocellular bacterial symbiont of aphids Buchnera sp. APS. Nature 407, 81–86 (2000).
Douglas, A. E. The B vitamin nutrition of insects: the contributions of diet, microbiome and horizontally acquired genes. Curr. Opin. Insect Sci. 23, 65–69 (2017).
Salem, H. et al. Vitamin supplementation by gut symbionts ensures metabolic homeostasis in an insect host. P. Roy. Soc. B- Bio. Sci. 281, 20141838 (2014).
Nasir, H. & Noda, H. Yeast-like symbiotes as a sterol source in Anobiid beetles (Coleoptera, Anobiidae): possible metabolic pathways from fungal sterols to 7-dehydrocholesterol. Arch. Insect Biochem. Physiol. 52, 175–182 (2003).
Noda, H. & Koizumi, Y. Sterol biosynthesis by symbiotes: cytochrome P450 sterol C-22 desaturase genes from yeastlike symbiotes of rice planthoppers and anobiid beetles. Insect Biochem. Mol. Biol. 33, 649–658 (2003).
Bos, M., Burnet, B., Farrow, R. & Woods, R. A. Development of Drosophila on sterol mutants of the yeast Saccharomyces cerevisiae. Genet. Res. 28, 163–176 (1976).
Hardin, J. A., Kraus, D. A. & Burrack, H. J. Diet quality mitigates intraspecific larval competition in Drosophila suzukii. Entomol. Exp. Appl. 156, 59–65 (2015).
Rendon, D. et al. Interactions among morphotype, nutrition, and temperature impact fitness of an invasive fly. Ecol. Evol. 9, 2615–2628 (2019).
Tochen, S., Walton, V. M. & Lee, J. C. Impact of floral feeding on adult Drosophila suzukii survival and nutrient status. J. Pest Sci. (2004). 89, 793–802 (2016).
Lee, K. P. Dietary protein: Carbohydrate balance is a critical modulator of lifespan and reproduction in Drosophila melanogaster:a test using a chemically defined diet. J. Insect Physiol. 75, 12–19 (2015).
Becher, P. G. et al. Yeast, not fruit volatiles mediate Drosophila melanogaster attraction, oviposition and development. Funct. Ecol. 26, 822–828 (2012).
Bellutti, N. et al. Dietary yeast affects preference and performance in Drosophila suzukii. J. Pest Sci. (2004). 91, 651–660 (2017).
Bing, X., Gerlach, J., Loeb, G. & Buchon, N. Nutrient - dependant impact of microbes on Drosophila suzukii development. MBio 9, e02199–17 (2017).
Young, Y., Buckiewicz, N. & Long, T. A. F. Nutritional geometry and fitness consequences in Drosophila suzukii, the spotted-wing drosophila. Ecol. Evol. 8, 2842–2851 (2018).
Silva-Soares, N. F., Nogueira-Alves, A., Beldade, P. & Mirth, C. K. Adaptation to new nutritional environments: larval performance, foraging decisions, and adult oviposition choices in Drosophila suzukii. BMC Ecol. 17 (2017).
Keebaugh, E. S. et al. Microbial quantity impacts Drosophila nutrition, development, and lifespan. iScience 4, 247–259 (2018).
Morais, P. B., Martins, M. B., Klaczko, L. B., Mendonca-Hagler, L. C. & Hagler, A. N. Yeast succession in the amazon fruit Parahancornia amapa as resource partitioning among Drosophila spp. Appl. Environ. Microbiol. 61, 4251–4257 (1995).
Matavelli, C., Carvalho, M. J. A., Martins, N. E. & Mirth, C. K. Differences in larval nutritional requirements and female oviposition preference reflect the order of fruit colonization of Zaprionus indianus and Drosophila simulans. J. Insect Physiol. 82, 66–74 (2015).
Walsh, D. B. et al. Drosophila suzukii (Diptera: Drosophilidae): invasive pest of ripening soft fruit expanding its geographic range and damage potential. J. Integr. Pest Manag. 2, 1–7 (2011).
Storelli, G., Defaye, A., Erkosar, B., Hols, P. & Royet, J. Lactobacillus plantarum promotes Drosophila systemic growth by modulating hormonal signals through TOR-dependent nutrient sensing. Cell Metab. 14, 403–414 (2011).
Anagnostou, C., Dorsch, M. & Rohlfs, M. Influence of dietary yeasts on Drosophila melanogaster life-history traits. Entomol. Exp. Appl. 136, 1–11 (2010).
Lavrynenko, O. et al. The ecdysteroidome of Drosophila: influence of diet and development. Co. Biol. 142, 3758–3768 (2015).
Sitepu, I. R. et al. Manipulation of culture conditions alters lipid content and fatty acid profiles of a wide variety of known and new oleaginous yeast species. Bioresour. Technol. 144, 360–369 (2013).
Freeland, J. C. & Gale, E. F. The amino-acid composition of certain bacteria and yeasts. Biochem J. 41, 135–138 (1947).
Cooper, D. M. Food preference of larval and adult Drosophila. Evolution 14, 41–55 (1960).
Fogleman, J. C., Starmer, W. T. & Heed, W. B. Larval selectivity for yeast species by Drosophila mojavensis in natural substrates. Proc. Natl. Acad. Sci. 78, 4435–4439 (1981).
Lindsay, S. L. Food Preferences of Drosophila larvae. Am. Nat. 92, 279–285 (1958).
Hoang, D., Kopp, A. & Chandler, J. A. Interactions between Drosophila and its natural yeast symbionts - Is Saccharomyces cerevisiae a good model for studying the fly-yeast relationship? PeerJ 3, e1116 (2015).
Fogleman, J. C., Starmer, W. T. & Heed, W. B. Comparisons of yeast florae from natural substrates and larval guts of southwestern Drosophila. Oecologia 52, 187–191 (1982).
Joseph, R. M. & Carlson, J. R. Drosophila chemoreceptors: a molecular interface between the chemical world and the brain. Trends Genet. 31, 683–695 (2015).
Rohwedder, A. et al. Nutritional value-dependent and nutritional value-independent effects on Drosophila melanogaster larval behavior. Chem. Senses 37, 711–721 (2012).
Apostolopoulou, A. A., Rist, A. & Thum, A. S. Taste processing in Drosophila larvae. Front. Integr. Neurosci. 9, 1–9 (2015).
Bjordal, M., Arquier, N., Kniazeff, J., Pin, J. P. & Léopold, P. Sensing of amino acids in a dopaminergic circuitry promotes rejection of an incomplete diet in Drosophila. Cell 156, 510–521 (2014).
Lewis, M. T., Koivunen, E. E., Swett, C. L. & Hamby, K. A. Associations between Drosophila suzukii (Diptera: Drosophilidae) and fungi in raspberries. Environ. Entomol. 48, 68–79 (2019).
Hamby, K. A., Hernández, A., Boundy-Mills, K. & Zalom, F. G. Associations of yeasts with spotted-wing Drosophila (Drosophila suzukii; Diptera: Drosophilidae) in cherries and raspberries. Appl. Environ. Microbiol. 78, 4869–4873 (2012).
Cadez, N. & Smith, M. T. In The yeasts - a taxonomic study (eds Kurtzman, C. P., Fell, J. W. & Boekhout, T.) 421–434 (Elsevier, 2011).
Liu, H. M. et al. Control of gray mold of grape by Hanseniaspora uvarum and its effects on postharvest quality parameters. Ann. Microbiol. 60, 31–35 (2010).
Duarte, W. F., Dias, D. R., De Melo Pereira, G. V., Gervásio, I. M. & Schwan, R. F. Indigenous and inoculated yeast fermentation of gabiroba (Campomanesia pubescens) pulp for fruit wine production. J. Ind. Microbiol. Biotechnol. 36, 557–569 (2009).
Fleet, G. H. Yeast interactions and wine flavour. Int. J. Food Microbiol. 86, 11–22 (2003).
Fanson, B. G. & Taylor, P. W. Additive and interactive effects of nutrient classes on longevity, reproduction, and diet consumption in the Queensland fruit fly (Bactrocera tryoni). J. Insect Physiol. 58, 327–334 (2012).
Skorupa, D. A., Dervisefendic, A., Zwiener, J. & Pletcher, S. D. Dietary composition specifies consumption, obesity and lifespan in Drosophila melanogaster. Aging Cell 7, 478–490 (2008).
Kingsolver, J. G. & Huey, R. B. Size, temperature, and fitness: three rules. Evol. Ecol. Res. 10, 251–268 (2008).
Chandler, J. A., Eisen, J. A. & Kopp, A. Yeast communities of diverse Drosophila species: comparison of two symbiont groups in the same hosts. Appl. Environ. Microbiol. 78, 7327–7336 (2012).
Richards, C. L., Bossdorf, O., Muth, N. Z., Gurevitch, J. & Pigliucci, M. Jack of all trades, master of some? On the role of phenotypic plasticity in plant invasions. Ecol. Lett. 9, 981–993 (2006).
Stockton, D. G., Brown, R. & Loeb, G. M. Not berry hungry? Discovering the hidden food sources of a small fruit specialist, Drosophila suzukii. Ecol. Entomol., https://doi.org/10.1111/een.12766 (2019).
Williams, K. M., Liu, P. & Fay, J. C. Evolution of ecological dominance of yeast species in high-sugar environments. Evolution 69, 2079–2093 (2015).
Witzgall, P. et al. This is not an apple-yeast mutualism in codling moth. J. Chem. Ecol. 38, 949–957 (2012).
Stamps, J. A., Yang, L. H., Morales, V. M. & Boundy-Mills, K. L. Drosophila regulate yeast density and increase yeast community similarity in a natural substrate. PLoS One 7 (2012).
Emiljanowicz, L. M., Ryan, G. D., Langille, A. & Newman, J. Development, reproductive output and population growth of the fruit fly pest Drosophila suzukii (Diptera: Drosophilidae) on artificial diet. J. Econ. Entomol 107, 1392–1398 (2014).
Lam, S. S. T. H. & Howell, K. S. Drosophila - associated yeast species in vineyard ecosystems. FEMS Microbiol. Lett. 362, fvn170 (2015).
Buser, C. C., Newcomb, R. D., Gaskett, A. C. & Goddard, M. R. Niche construction initiates the evolution of mutualistic interactions. Ecol. Lett. 17, 1257–1264 (2014).
Christiaens, J. F. et al. The fungal aroma gene ATF1 promotes dispersal of yeast cells through insect vectors. Cell Rep. 9, 425–432 (2014).
Reuter, M., Bell, G. & Greig, D. Increased outbreeding in yeast in response to dispersal by an insect vector. Curr. Biol. 17, 81–83 (2007).
Magliani, W., Conti, S., Gerloni, M., Bertolotti, D. & Polonelli, L. Yeast killer systems. Clin. Microbiol. Rev. 10, 369–400 (1997).
Thompson, J. N. Evolutionary ecology of the relationship between oviposition preference and performance of offspring in phytophagous insects. Entomol. Exp. Appl. 3–14 (1988).
Anagnostou, C., LeGrand, E. A. & Rohlfs, M. Friendly food for fitter flies? - Influence of dietary microbial species on food choice and parasitoid resistance in Drosophila. Oikos 119, 533–541 (2010).
Grangeteau, C. et al. Yeast quality in juvenile diet affects Drosophila melanogaster adult life traits. Sci. Rep. 8, 13070 (2018).
Batista, M. R. D. et al. Differential attraction of drosophilids to banana baits inoculated with Saccharomyces cerevisiae and Hanseniaspora uvarum within a Neotropical forest remnant. PeerJ 5, e3063 (2017).
Scheidler, N. H., Liu, C., Hamby, K. A., Zalom, F. G. & Syed, Z. Volatile codes: correlation of olfactory signals and reception in Drosophila-yeast chemical communication. Sci. Rep. 5, 14059 (2015).
Morais, P. B., Rosa, C. A., Hagler, A. N. & Mendonca-Hagler, L. C. Yeast communities of the cactus Pilosocereus arrabidae as resources for larval and adult stages of Drosophila serido. Antonie Van Leeuwenhoek 66, 313–317 (1994).
Vacek, D. C., East, P. D., Barker, J. S. F. & Soliman, M. H. Feeding and oviposition preferences of Drosophila buxxatii for microbial species isolated from its natural environment. Biol. J. Linn. Soc. 24, 175–187 (1985).
Barker, J. S. F., Vacek, D. C. & East, P. D. Attraction of larvae of Drosophila buzzatii and Drosophila aldrichi to yeast species isolated from their natural environments. Aust. J. Zool. 36, 53–56 (1988).
Vacek, D. C., Starmer, W. T. & Heed, W. B. Relevance of the ecology of citrus yeasts to the diet of Drosophila. Microb. Ecol. 5, 43–49 (1979).
Morais, B., Hagler, N., Rosa, C. A. & Mendonca-hagler, L. C. Yeasts associated with Drosophila in tropical forests of Rio de Janeiro, Brazil. Can. J. Microbiol. 38, 1150–1155 (1992).
Palanca, L., Gaskett, A. C., Günther, C. S., Newcomb, R. D. & Goddard, M. R. Quantifying variation in the ability of yeasts to attract Drosophila melanogaster. PLoS One 8, 1–10 (2013).
Gilbert, D. G. Dispersal of yeasts and bacteria by Drosophila in a temperate forest. Oecologia 46, 135–137 (1980).
Quan, A. S. & Eisen, M. B. The ecology of the Drosophila - yeast mutualism in wineries. PLoS One 13, e0196440 (2018).
Hamby, K. A. & Becher, P. G. Current knowledge of interactions between Drosophila suzukii and microbes, and their potential utility for pest management. J. Pest Sci. (2004). 89, 621–630 (2016).
Burrack, H. J. et al. Multistate comparison of attractants for monitoring Drosophila suzukii (Diptera: Drosophilidae) in blueberries and caneberries. Environ. Entomol. 44, 704–712 (2015).
Hamby, K. A., Bolda, M. P., Sheehan, M. E. & Zalom, F. G. Seasonal monitoring for Drosophila suzukii (Diptera: Drosophilidae) in California commercial raspberries. Environ. Entomol. 43, 1008–1018 (2014).
Wallingford, A. K., Cha, D. H., Linn, C. E., Wolfin, M. S. & Loeb, G. M. Robust manipulations of pest insect behavior using repellents and practical application for integrated pest management. Environ. Entomol. 46, 1041–1050 (2017).
Murphy, K. A., Tabuloc, C. A., Cervantes, K. R. & Chiu, J. C. Ingestion of genetically modified yeast symbiont reduces fitness of an insect pest via RNA interference. Sci. Rep. 6, 1–13 (2016).
Knight, A. L., Basoalto, E., Yee, W., Hilton, R. & Kurtzman, C. P. Adding yeasts with sugar to increase the number of effective insecticide classes to manage Drosophila suzukii (Matsumura) (Diptera: Drosophilidae) in cherry. Pest Manag. Sci. 72, 1482–1490 (2015).
Mori, B. A. et al. Enhanced yeast feeding following mating facilitates control of the invasive fruit pest Drosophila suzukii. J. Appl. Ecol. 170–177, https://doi.org/10.1111/1365-2664.12688 (2016).
Roubos, C. R. et al. Impact of phagostimulants on effectiveness of OMRI‐listed insecticides used for control of spotted-wing drosophila (Drosophila suzukii Matsumura). J. Appl. Entomol. 143, 609–625 (2019).
Wong, J. S., Wallingford, A. K., Loeb, G. M. & Lee, J. C. Physiological status of Drosophila suzukii (Diptera: Drosophilidae) affects their response to attractive odours. J. Appl. Entomol. 142, 473–482 (2018).
Swoboda-Bhattarai, K. A., McPhie, D. R. & Burrack, H. J. Reproductive status of Drosophila suzukii (Diptera: Drosophilidae) females influences attraction to fermentation-based baits and ripe fruits. J. Econ. Entomol. 110, 1648–1652 (2017).
Kirkpatrick, D. M. et al. Comparative antennal and behavioral responses of summer and winter morph Drosophila suzukii (Diptera: Drosophilidae) to ecologically relevant volatiles. Environ. Entomol. 47, 700–706 (2018).
Ashburner, M., Golic, K. G. & Hawley, R. S. Drosophila: a laboratory handbook. (Cold Spring Harbor Laboratory Press, 2005).
Robertson, F. W. & Reeve, E. Studies in quantitative inheritance - I. The effects of selection of wing and thorax length in Drosophila melanogaster. J. Genet. 50, 414–448 (1952).
Shearer, P. W. et al. Seasonal cues induce phenotypic plasticity of Drosophila suzukii to enhance winter survival. BMC Ecol. 16, 11 (2016).
Team, R. C. R: A language and environment for statistical computing. (R Foundation for Statistical Computing, 2017).
Lenth, R. V. Least-squares means: the R Package lsmeans. J. Stat. Softw. 69, 1–33 (2016).
Bates, D., Maechler, M., Bolker, B. & Walker, S. Fitting linear mixed-effects models using lme4. J. Stat. Softw. 67, 1–48 (2015).
Kuznetsova, A., Brockhoff, P. B. & Christensen, R. H. B. lmerTest: tests in linear mixed effects models. (R package version 2.0–33, 2016).
Gross, J. & Ligges, U. Nortest: Tests for Normality. R package version 1.0–4. Available at, https://cran.r-project.org/package=nortest (2015).
This work was supported by funding from the University of Maryland Research and Scholarship Awards. We also would like to thank Galen Dively, Kathryn Everts, Megan Fritz, Raymond St. Leger, and Torsten Schӧneberg as well as anonymous reviewers and the editor for comments that improved the quality of this manuscript. Members of the Hamby lab, particularly Adrienne Beerman, Elizabeth Hines, Logan Miller, and Melissa Naugle, also helped with data collection.
The authors declare no competing interests.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Lewis, M.T., Hamby, K.A. Differential Impacts of Yeasts on Feeding Behavior and Development in Larval Drosophila suzukii (Diptera:Drosophilidae). Sci Rep 9, 13370 (2019). https://doi.org/10.1038/s41598-019-48863-1
Separate and combined Hanseniaspora uvarum and Metschnikowia pulcherrima metabolic volatiles are attractive to Drosophila suzukii in the laboratory and field
Scientific Reports (2021)
Resource use by individual Drosophila suzukii reveals a flexible preference for oviposition into healthy fruits
Scientific Reports (2020)
Journal of Pest Science (2020)