In populations of Drosophila larvae, both, an aggregation and a dispersal behavior can be observed. However, the mechanisms coordinating larval locomotion in respect to other animals, especially in close proximity and during/after physical contacts are currently only little understood. Here we test whether relevant information is perceived before or during larva-larva contacts, analyze its influence on behavior and ask whether larvae avoid or pursue collisions. Employing frustrated total internal reflection-based imaging (FIM) we first found that larvae visually detect other moving larvae in a narrow perceptive field and respond with characteristic escape reactions. To decipher larval locomotion not only before but also during the collision we utilized a two color FIM approach (FIM2c), which allowed to faithfully extract the posture and motion of colliding animals. We show that during collision, larval locomotion freezes and sensory information is sampled during a KISS phase (german: Kollisions Induziertes Stopp Syndrom or english: collision induced stop syndrome). Interestingly, larvae react differently to living, dead or artificial larvae, discriminate other Drosophila species and have an increased bending probability for a short period after the collision terminates. Thus, Drosophila larvae evolved means to specify behaviors in response to other larvae.
Most animals move to find their prey or their appropriate mating partners, to avoid competition for resources or to engage in cooperation. The success of this goal-oriented locomotion strongly relies on the surrounding objects and animals. For example, avoiding collisions in densely populated areas requires an appropriate perception of the surrounding and complex locomotion maneuvers. In many insect clades such as Drosophila, females lay a large number of eggs close to a food source1 and thus hatching larvae have to cope with other moving larvae and to compete for limited resources. Drosophila larvae are attracted to areas already explored by other larvae via a pheromone triggered signaling pathway2. Larvae of different species release different cocktails of attractive pheromones2. Thereby, behavioral changes are instructed to route them to distinct areas in common food sources. This increases the relative density of conspecifics. It has also been shown that larvae aggregate to perform cooperative digging which may increase the feeding efficacy on solid food3,4,5. Moreover, larvae of two distinct Drosophila species avoid to pupate close to larvae of other species but preferentially pupate in the neighborhood of their conspecifics6.
How Drosophila larvae perceive other animals and communicate with each other is currently only partially understood. There is evidence that Drosophila larvae are able to interact with other larvae via visual or gustatory cues. For example, larvae are visually attracted to distinct motion of tethered siblings7. Larval vision is mostly mediated by the larval eyes called Bolwig’s organs that are located in small pouches flanking the cephalopharyngeal skeleton. The Bolwig’s organ comprises 12 photoreceptor neurons, four of which express the blue sensitive Rhodopsin (Rh) 5a and eight express the green sensitive Rh6 8. During feeding, larvae show negative phototaxis, which is reversed when wandering larvae leave the food and navigate towards a dry pupariation site9,10. Owing to the position of the Bolwig’s organs in the anteriorly directed pouches of the head, a preferential sensitivity to frontal light can be determined11.
During larval locomotion, go phases are interrupted by reorientation phases characterized by reduced locomotion velocity and intensive head bending. During this phase the Bolwig’s organs probe local light information to determine the direction of the successive run. To navigate away from direct illumination requires temporal procession of this sensory input12. In addition to the visual system, pheromone mediated communication systems have been described that ensure species-specific recognition of larvae2 but olfactory preference of individual larvae is not modulated by surrounding larvae13. All present studies, however, did not consider the influence of sensory input on posture and locomotion during collision since segmenting and thus quantifying individual animals in these situations is not trivial.
Here, we asked whether Drosophila larvae have evolved means to change their locomotion behavior specifically in response to other larvae in dense populations. To study these aspects, automated tracking and analysis tools are required. In the last years several setups and algorithms have been established allowing high-throughput approaches, which unfortunately can only partially resolve colliding larvae14,15,16,17,18,19. To analyze what happens during and after a collision event, the identities and posture of the colliding animals must be traceable. A straightforward solution to this problem is to genetically mark one larva by green fluorescent protein (GFP) expression. We recently showed that frustrated total internal reflection (FTIR) provides an unprecedented high contrast view on crawling animals and developed the FTIR-based imaging (FIM) setup14. For a simultaneous analysis of multiple animals with different markers we developed FIM2c (FIM two color20). This technology now for the first time allows resolving interacting animals during a collision event in a multi-target imaging approach for high throughput experiments. Employing FIM2c, we analyzed larval collision behavior. Colliding larvae show a stereotypic behavioral sequence upon contact to scan the touched object. During a one to two seconds lasting KISS phase (German: Kollisions Induziertes Stopp Syndrom, or in English: collision induced stop syndrome) larvae sample the specimen and behave differently when the collision object is made of unrelated material, a dead or a living larva of the same or a related Drosophila species. Our studies support the hypothesis that Drosophila larvae perceive the presence of other larvae and reveal a stereotypic influence on behavior which has to be considered carefully in multi-animal tracking approaches.
Do larvae avoid or pursue collisions?
D. melanogaster larvae feed on moist substrates and leave the food during the third instar wandering stage. During their migratory path they often touch other animals. It was previously shown that larvae are able to use spatially and temporally coded visual stimuli to distinguish relatively complex visual patterns and for example respond to quivering larvae tethered above them7.
Therefore, we expected that larvae would react to other larvae if close enough to be visually recognized. To test this, we established the SLIT (Single Larva Impact Trench) assay to analyze directed larval locomotion towards each other (Fig. 1a, Supplementary Movie 1). When placed into a trench (3 mm wide and 2 mm deep), 62% of the larvae moved straight forward in this trench (n = 37). If a second larva is placed in the same trench, but facing in opposing direction, the two animals move towards each other. When we placed larvae in the 3 mm wide trench, they can easily pass each other. In the dark we detected an evasion reaction only in 15% of the events (n = 39 events with two larvae of which in 6 cases one larva evaded and no case with both larvae showing an evasion reaction [n = 39/6/0]) (Fig. 1b,c). Interestingly, under normal light conditions in 31% of the cases at least one larva showed an evasion reaction (Fig. 1c, n = 119/37/3). This suggests that larvae are capable to use visual information to avoid collisions.
To further increase the likelihood for a collision we placed the animals in a narrow trench (1.3 mm wide and 1.5 mm deep) which does not allow the larvae to pass each other without touching. In the dark we noted an evasion reaction in 24% of the cases (n = 67/16/2) whereas 48% of the larvae showed this reaction given normal illumination (Fig. 1b,c; n = 65/31/8). When we repeated these experiments with larvae crawling towards dead larvae in the dark, we detected in 15% of the events an evasion reaction (Fig. 1c, n = 26/4/0) whereas in the light we noted in 33% of the cases an evasion reaction (n = 24/8/0). This supports the hypothesis that larvae are capable to perceive moving larvae visually. To further validate this finding we utilized larvae expressing the cell death gene hid in all photoreceptor cells, which renders the Bolwig’s organ blind (GMR>hid)21. These larvae were compared to w1118 larvae, which share the same genetic background as the GMR>hid larvae and to Canton S larvae. When placed into the narrow trench, only 22% of the blind larvae (n = 70) showed an evasion reaction, whereas 42% of the Canton S (n = 69) and 43% of white1118 larvae (n = 69) showed an evasion reaction (Fig. 1c).
The evasion reaction was strongest when the animals were about 0.8 larval-lengths apart (Fig. 1d). It is known that larvae are sensitive to temperature gradients22 but since Drosophila is poikilothermic we expect that larvae will not influence the temperature of the environment. Therefore, we anticipate that larvae recognize either vibration signals caused by the moving animal or recognize visual cues. Importantly, larvae appear to incorporate information regarding their environment (wide or narrow trench) to initiate an escape response or not. Moreover, these data show that larvae are able to avoid collisions specifically.
Larvae have a narrow field of perception
In the SLIT assay evasion behavior is provoked using thin trenches. We next assayed larval collision behavior when many larvae moved in community and movements are not constrained by a prefigured trench. For this we monitored the simultaneous locomotion of 12 larvae on an agar arena (9.5 cm diameter) flanked by a salt barrier to confine larval movements. We first focused on non-colliding animals. We defined a field of view for a larva (labeled as L1 in Fig. 1e) with the azimuth of ± α/2 and r = 10 mm (~2 larval lengths). An event is triggered for L1 if another larva enters the field of view (labeled as L2 in Fig. 1e). The bending behavior of L1 is then analyzed for several seconds to disclose a possible collision avoidance reaction. In a large field of view (α = 90°), almost no change in the mean bending probability can be detected (Fig. 1e,f, Supplementary Fig. 1). Upon narrowing of the field of view (α < 20°) there is a marked increase in the bending probability 4 seconds after the larvae entered the field of view (p = 0.002 comparing bending at t2sec and t4sec). Given that the average locomotion speed of a third instar larva is about one larval length in 5 seconds this corresponds well to the preferred reaction distance we found in the SLIT assay (Fig. 1a–d). Interestingly, no significant increase in the bending rate is noted when larvae approach a dead larva (Fig. 1f, Supplementary Fig. 1) suggesting that larvae do not react to the shape of the larvae but rather react to the changing contrast of a moving larva.
FIM2c allows simultaneous detection of images of different wavelengths
As pointed out above, larvae often collide but so far analysis of the collision event was not possible. To precisely study collisions we used a novel multi-color imaging system employing frustrated total internal reflection of infrared (IR) and ultraviolet (UV) light (FIM2c, Fig. 2)14,15,20. FIM2c allows to simultaneously image distinct genotypes (e.g. GFP+ and GFP−), so that two colliding animals can be analyzed (Fig. 2c–e). Due to the physical principles underlying FIM2c, larvae are imaged at a high signal-to-noise ratio (Supplementary Movie 2). Even internal organs can be determined within these free crawling assays by expressing GFP in a tissue- or cell type-specific manner. For example, we used the nrv2-Gal4 driver to express GFP in a small subset of glial cells. In the PNS, only three wrapping glial cells express nrv2-Gal4 in every abdominal peripheral nerve23,24 which can be detected using FIM imaging highlighting the sensitivity of FIM2c (Fig. 2g, Supplementary Movie 3). Last but not least using FIM2c collisions can be resolved and the animals can be studied in unprecedented detail within high throughput assays.
The influence of UV-irradiation on larval locomotion
To rule out possible side effects of UV-light on larval locomotion and thus possibly collision behavior, we first tested the effects of different UV-excitation strengths. Since the larval visual system is only composed of green- and blue- sensitive photoreceptor neurons (Rhodopsin 6 and Rhodopsin 5a), IR irradiation is not expected to affect behavior. Moreover, IR illumination does not affect the temperature on the tracking arena14. However, UV-LEDs emit light with a dominant wavelength of 470 nm, which might induce light avoidance behavior of Drosophila larvae25. In order to identify changes in larval locomotion, we determined aberrations in the run behavior by quantifying the accumulated distance after 90 seconds. In addition, the number of head sweeps was quantified to determine the probability for reorientation events26. We analyzed more than 100 animals each at different UV irradiations ranging from 0 to 240 lux and detected almost no change in the overall traveled distance (Fig. 2b). Similarly, the probability of reorientation events (bending angle ≥30° or ≥40°) did not change significantly. We only noted a slight increase in the number of reorientation events at higher UV irradiation levels (Fig. 2b). Whereas we measured almost no influence of constant UV-light on the locomotion of third instar larvae we did observe differences in larval reorientation during transitions from light on to light off or vice versa. In our experiments we subsequently used a constant lighting intensity of 100 lux. In conclusion, FIM2c allows to image genetically distinct larvae with nearly no effects on locomotion behavior.
Larval collision phases
Despite the ability of larvae to induce evasion reactions, we still observe collisions. This prompted us to study locomotion behavior during larval collisions and ask whether relevant information might be transmitted during contact. We placed six white1118 larvae together with six larvae ubiquitously expressing GFP on an agar arena (9.5 cm diameter with salt barrier, ubiquitous GFP expression is mediated by the following genotype: daughterless-Gal4 (da-Gal4), UAS-CD8GFP) and allowed the larvae to crawl freely in the absence of stimuli for 7 minutes. Imaging was done using FIM2c (Fig. 2). Only collisions between single GFP-expressing and single non GFP-expressing animals with no overlays were counted as valid collisions. We extracted more than 1,400 resolved collisions in total. Larval collisions can be classified based on the duration of larval contacts and the duration of traceability before and after the collision. 25% of the collisions are very short and last less than 0.5 seconds whereas the other collisions last longer (Supplementary Fig. 2). Unless noted, we analyzed the behavior of the white1118 larvae involved in the collision and discarded the information relating to the GFP expressing animals.
In the following we extracted 358 distinct collisions from the overall 1,400 collisions that lasted >0.5 seconds with animals traceable and not involved in any other collisions ≥1 seconds before and after the analyzed collision (Figs 3, 4, 5). The median collision length in this set is 2.5 seconds (Supplementary Fig. 3a). Three distinct phases of a collision can be defined: (1) a pre-collision phase, (2) a collision phase and (3) a post-collision phase.
In the pre-collision phase, velocity and bending are unchanged from normal undisturbed locomotion (Fig. 3a,d blue lines). In this respect it should be noted that all situations analyzed lead to collisions (i.e. larvae successfully avoided a collision are not included here).
In the collision phase we noted a characteristic time window during which locomotion speed dropped significantly (p < 0.00001, for details see supplementary Fig. 4) but no increase in body bending can be measured (Fig. 3b,e, blue lines, Supplementary Movie 4). We named this period KISS phase (German: Kollisions Induziertes Stopp Syndrom, or in English: collision induced stop syndrome). The KISS phase lasted usually 1–2 seconds after which larvae even when still engaged in a collision event resumed their normal locomotion speed. After the KISS phase a slight increase in bending probability could be noted (Fig. 3b,e blue lines).
In the post-collision phase, locomotion speed gradually increased and we noted a short and significant increase in the bending probability (Fig. 3c,f blue lines, p < 0.0001, for details see supplementary Fig. 4), which initiates the reorientation behavior after the termination of the collision.
Larvae reveal different behaviors in the presence of different collision partners
The stereotypic reactions of larvae during as well as shortly after collisions indicate a significant change in behavior caused by the touch. To further investigate if this behavior changes due to different collision objects, we generated fluorescent artificial larvae (see Materials and Methods). In each trial, six of these artificial larvae were placed in the arena together with six unlabeled larvae (w1118) and their collision behavior was assayed. Before collision, bending probability and velocity remained constant as observed in collision of living Drosophila larvae (Fig. 3a,d, green line, n = 53 collision events). Interestingly, although collisions do not last longer, larval locomotion speed is still strongly reduced after the KISS phase (Fig. 3b,e, Supplementary Figs. 3a and 4, Supplementary Movie 5). The bending is again only slightly increased after the KISS phase during the collision event but dramatically increases in the beginning of the post-collision phase (Fig. 3c–f; p < 0.0001, see supplementary Fig. 4 for details). This change in behavior during and after the collision indicates that larvae sense a difference between artificial and living collision partners (statistical difference in velocity upon collision with living versus artificial larvae at t1.5sec p = 2 × 10−4, at t2.0sec p = 5 × 10−8). Most likely distinctive cues are sampled during the KISS phase and integrated into subsequent behavior.
To discriminate whether larvae use gustatory or haptic cues and to rule out the influence of locomotion, we confronted moving larvae with dead third instar larvae. We placed GFP expressing third instar larvae for 120 seconds in 60 °C hot air which is expected not to remove or disintegrate the long-chain fatty acid pheromones present on the larval cuticle2 and used the dead animals only for one recording. w1118 larvae colliding with dead larvae take longer to resume to their normal locomotion speed as compared to collisions with larvae that collide with living third instar larvae (Fig. 3b,e, difference living versus dead larvae at t1.5sec and at t2.0sec p = 2×10−6, see Supplementary Movie 6). Moreover, the length of collision time is increased (Supplementary Fig. 3a). In the beginning of the post-collision phase, the bending probability is in-between the measurement of animals colliding with artificial or living animals while the normal locomotion speed is resumed (Fig. 3e,f, red line, n = 175). These data demonstrate that larvae are able to discriminate their collision partner by gustatory and haptic cues independent of motility of the collision object. Again, this discrimination is likely to be sampled during the KISS period.
Previous results demonstrated that larvae can use chemical signals to communicate with their neighbors2,6,27. Third instar larvae of Drosophila simulans, a closely related fly species, do not generate the chemical cues that are attractive to D. melanogaster2. We therefore assayed collisions between D. melanogaster and D. simulans. In this paradigm, we tested GFP expressing D. melanogaster during the collision with non GFP expressing D. simulans larvae (n = 179) and compared this to collisions with living w1118 larvae (n = 278). Note that Gal4 expressing animals are generally a little faster due to slightly increased body size (compare Figs 3d and 4d). As for all other collision events, velocity and bending probability were constant before the collisions (Fig. 4a,d, see supplementary Fig. 4 for statistical analysis). The KISS period was slightly prolonged and little later initiated when comparing velocity during collision of D. melanogaster GFP-expressing larvae with D. simulans or D. melanogaster larvae (Fig. 4e; pt1.5sec = 0.5; pt2.0sec = 0.009). In addition, the median collision length is prolonged comparing D. melanogaster – D. simulans with D. melanogaster – D. melanogaster collisions (Supplementary Fig. 3b). Interestingly, when Gal4 expressing D. melanogaster were confronted with dead w1118 larvae (n = 165), collision length was much longer when compared to collision with dead D. simulans larvae (n = 76; pt1.5sec = 0.018; pt2.0sec = 0.002; Supplementary Figs 3c,4,5). This suggests that the discrimination between different species can also be achieved during the KISS phase. Physical contact with larvae of different species or with dead larva of the same species increases the duration of the collision period, indicating an overall less aversive stimulation.
Three phases of larval locomotion when navigating in groups
Larval locomotion is usually classified into two distinct routines: After a phase of uninterrupted crawling the animals pause for self-induced reorientation28,29,30,31. FIM2c now allows to add the obstacle-induced COLLISION phase as a novel component of larval locomotion. Unrestricted locomotion is the GO phase where regular peristalsis ensures forward movement (Fig. 5). Here only micro head bends can be seen. GO phases usually last for several seconds and are followed by a REORIENTATION phase characterized by stronger bending at a reduced velocity. The REORIENTATION phase triggers a new GO phase. However, a GO phase can also be terminated by a collision event. In case the object appears in a relatively narrow field of view the larvae use primarily visual cues to avoid collisions. This is in contrast to a report that larvae preferentially move below a group of tethered but still living larvae7. After a COLLISION phase a larva cannot directly switch to the GO phase but rather initiates a REORIENTATION phase. The COLLISION phase almost always comprises a KISS phase which differs from a typical REORIENTATION phase. In a KISS phase the velocity is reduced as well but no body bending can be measured suggesting a sampling of sensory information.
Whenever animals move in dense populations recognition of interaction partners and environment is beneficial. For example, Drosophila larvae show a cooperative burrowing behavior and prefer to pupate with conspecific larvae1,2,3,4,5. Here we studied the interaction of larvae with their surroundings before and during collisions to unravel the behavioral programs controlling community influences. For the latter analysis we employed a novel multi-target tracking system and found that larvae recognize other larvae in a narrow perceptive field already before collision.
Our data demonstrate that larvae can react upon detection of moving animals in a small field of perception and may avoid collisions in dependency of lighting and motility of the opposed object. In case a collision occurs, the opponent is sampled during a short KISS phase characterized by a “frozen” body posture. During this time living D. melanogaster larvae are distinguished from inanimate matter, dead larvae, or other species. The fact that D. melanogaster can discriminate D. melanogaster and D. simulans suggests that gustatory cues are utilized. Likewise gustatory cues are used to establish social networks in adult Drosophila32. Since D. melanogaster can also discriminate living and dead and even artificial opponents we anticipate that haptic cues are sampled as well. If neither larva-like sensory nor haptic cues are present (e.g. artificial matter), the KISS phase and thus the sampling period is extended.
In a recent report it was shown that larvae are attracted to moving objects in a light dependent manner7. Here we presented evidence that larvae rather tend to avoid other living animals provided they move in a narrow “field of view”. This corresponds to the structure the Bolwig’s organs embedded in anterior pouches in the head, which preferentially detect light coming from the front11. Since larvae react differently to living and dead larvae in the trench we anticipate that larvae integrate the changes of visual information over time rather than process complex images. In the SLIT assay we provoked collisions by forcing larvae to move onto each other in a precast trench. Surprisingly, larvae react different when moving in a narrow or a wide trench. This could indicate that the “field of view” is indeed very narrow and in the wide trench larvae do not see each other as often as in the narrow trench. Alternatively, larvae also integrate environmental features since pursuing a collision in a trench too small for two larvae to pass results in an increase of collision avoidance behavior. A related correlation of body size and the environment has been observed to modulate adult walking flies or stick insects that need to bridge a gap or in block climbing cockroaches33,34,35. Thus, knowledge on body size can be calculated by the insect brain and may already be present in third instar larvae.
To further test this hypothesis, advanced imaging technologies such as FIM2c as introduced here are of great advantage. Although the resolution and the signal-to-noise ratio of most imaging setups is sufficient for tracking, the segmentation of individual animals shape fails during a collision event. In combination with sophisticated optogenetic or thermogenetic tools36,37,38,39,40 FIM2c allows to use UV-light to modify neuronal activity in a temporally controlled manner while simultaneously recording larval behavior (data not shown). Higher sensitivity cameras may even allow the detection of GCaMP signals in groups of behaving animals.
The expression of fluorescent markers has been previously used to classify populations of adult Drosophila flies within the same experiment41. The Fluorescence Behavioral Imaging (FBI) tracker employs transgenic fluorescence and imaging hardware to discriminate courtship partner choice in genetically mixed groups of Drosophila but behavior during collisions cannot be addressed by this setup. The idTracker19 generates a characteristic optical fingerprint from each animal which allows to maintain identity before and after the collision. However, the method is not able to resolve the locomotion pattern during the collision event. We have now established a database with 1,400 fully resolved collisions and we envision that this ground truth will facilitate further mathematical modeling, including advanced representations like Eigenworms and Sequential Monte Carlo methods may lead to stable assignment of identity and posture resolution during collision events18,42,43.
In conclusion, we have demonstrated that Drosophila larvae react to others and can avoid collisions in a lighting dependent manner. However, larvae exhibit reactions only when moving animals appear in a narrow “field of view”. In case collisions occur we identified a stereotyped response pattern initiated by a KISS phase that eventually leads to the discrimination of living or dead animals and allows the detection of conspecific larvae. This suggests, that larvae sample their surroundings for information about other animals while navigating. Most likely this information is instructive for behavior also in the natural habitat. Considering the observed community effects, the population density has to be taken in account when performing larval locomotion assays. Moreover, the fact that larvae behave different in a wide or a narrow trench suggests that cues regarding larval environment feed into the execution of complex motor programs.
Material and Methods
Drosophila culture and strains
Drosophila larvae were raised on standard food at 25 °C in a 12 h dark-light cycle with 65% humidity. For imaging only third instar wandering stage larvae were collected 116 hours after egg laying. The following genotypes were used: D. simulans, D. melanogaster white1118, Canton S, daughterless-Gal4 (daGal4) driving expression in all tissues, nervana-Gal4 (nrv2Gal4) driving expression in the peripheral wrapping glial cells, GMR-Gal4 driving expression in all photoreceptor neurons, UAS-Hid (to drive expression of the proapoptotic gene head involution defective (hid). UAS-CD8GFP (to drive expression of a membrane tethered GFP). All fly strains were obtained from the Bloomington stock collection.
General setup and preparations
Tracking experiments were performed on 0.8% agar in deionized H2O. For collision analysis the tracking surface is surrounded by a 2.5% agar barrier in 3M NaCl to keep animals confined to the tracking surface. All experiments were performed under room light conditions or in darkness. In the FIM2c setup infrared LEDs (HP HSDL-4230) and ultraviolet LEDs (LC503FBL1-15P-A3) were installed. The latter light sources have a dominant wavelength of 470 nm. For imaging a stereo-camera system is used (two Basler acA2040–25 gm cameras) with appropriate lenses (KOWA LM35HC). Besides the IR long pass filter (Schneider Kreuznach IF093), a custom GFP bandpass filter is mounted to the so-called GFP camera (AHF BrightLine HC 536/40). Recording and data analysis was carried out using a Fujitsu 520Celsius workstation. A new FIMTrack software module was created to match the requirements of FIM2c (Supplementary Fig. 6; software available at: http://fim.uni-muenster.de). Note, that other and more than two colors can be integrated. Quantitative data visualization was done by custom-made MATLAB scripts. The non-parametrical Wilcoxon-Mann-Whitney-Test implemented in MATLAB was used as statistical test since a Gaussian distribution cannot be assumed.
FIM2c specific principles of illumination and recording
In the FIM2c setup, light from both light sources enters the acrylic glass and is completely reflected at the glass / agar / air boundary as long as the angle of incidence is below the critical angle14,15,20. At the agar / larva transition light of both wavelengths enters the semi-translucent animal. The scattered infrared light is captured by an IR camera as described previously14. The UV light that enters the animals excites GFP which is detected by the GFP camera. This principle, as well as resultant images from both views, is given in Fig. 2a. Both cameras are monochrome cameras resulting in two monochrome detections, namely all animals in the IR image and GFP emissions in the GFP image. These measurements are merged into a RGB image whereas the red channel is used to store the IR image and the green channel is used to store the GFP image20.
2-Color collision resolution algorithm
The following conditions must be satisfied in order to resolve collisions within the FIM2c system: Only two larvae participate within the collision, and one of the two animals must express GFP. In contrast to the algorithm described14, too big contours are not rejected and instead, the larvae participating in this collision are determined20. All larvae from time t − 1 having at least one point within the collision contour at time t are identified as participants. Collisions are assumed to be resolvable as long as only two larvae are involved in the collision and one of the two larvae is a GFP larva (bGFP = true). The other larva has to be a non-GFP expressing animal (bGFP = false). All collisions that are not satisfying both conditions are rejected. Resolvable collision contours are processed by first splitting the 2-color image into the red and green channel to segment the contour of the GFP expressing animal. All pixels within this collision contour are assumed to belong to the GFP larvae, all other pixels belong to the other animal. Afterwards, these contours can be used to calculate all features as described14,20. The result viewer tool from FIMTrack was used to validate the contour detection during collision resolution (>1,000 collisions).
Generation of artificial larvae
We melted plastic hot sticks (Pattex PTK 56) and mixed it with fluorescein (Sigma). Threads of approximately 0.5 mm diameter were pulled out of the melted plastic and were cut into 5 mm long artificial larvae which after washing, were used in all experiments.
Single larvae impact trench (SLIT) assay
To obtain trenches in the tracking arena we positioned thin and wide glass negatives of the desired trench into an agar slab casting tray. The slits were 5 cm long and 3 × 2 or 1.3 × 1.5 mm in diameter respectively. Several slabs were cut from casks each containing one trench and simultaneously imaged.
How to cite this article: Otto, N. et al. Interactions among Drosophila larvae before and during collision. Sci. Rep. 6, 31564; doi: 10.1038/srep31564 (2016).
We are thankful to B. Gerber (Magdeburg) for discussions throughout the project and J. Hermann for help with the construction of the FIM2c setup. We thank J. Krüger and J. Kappel for help with data acquisition. We are grateful to M. Bechtold, G. Steffes and K. Yildirim for critical reading of the manuscript. We also thank anonymous reviewers for their constructive input. This work was supported by a CIM-IMPRS PhD fellowship to N.O. and through grants of the Deutsche Forschungsgemeinschaft to C.K. (SFB 629 B6, SFB 1009).
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