Cargando…

Quantitative and Discrete Evolutionary Changes in the Egg-Laying Behavior of Single Drosophila Females

How a nervous system assembles and coordinates a suite of elementary behavioral steps into a complex behavior is not well understood. While often presented as a stereotyped sequence of events, even extensively studied behaviors such as fly courtship are rarely a strict repetition of the same steps i...

Descripción completa

Detalles Bibliográficos
Autores principales: Bräcker, Lasse B., Schmid, Christian A., Bolini, Verena A., Holz, Claudia A., Prud’homme, Benjamin, Sirota, Anton, Gompel, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6549446/
https://www.ncbi.nlm.nih.gov/pubmed/31191270
http://dx.doi.org/10.3389/fnbeh.2019.00118
_version_ 1783424011283202048
author Bräcker, Lasse B.
Schmid, Christian A.
Bolini, Verena A.
Holz, Claudia A.
Prud’homme, Benjamin
Sirota, Anton
Gompel, Nicolas
author_facet Bräcker, Lasse B.
Schmid, Christian A.
Bolini, Verena A.
Holz, Claudia A.
Prud’homme, Benjamin
Sirota, Anton
Gompel, Nicolas
author_sort Bräcker, Lasse B.
collection PubMed
description How a nervous system assembles and coordinates a suite of elementary behavioral steps into a complex behavior is not well understood. While often presented as a stereotyped sequence of events, even extensively studied behaviors such as fly courtship are rarely a strict repetition of the same steps in a predetermined sequence in time. We are focusing on oviposition, the act of laying an egg, in flies of the genus Drosophila to describe the elementary behavioral steps or microbehaviors that a single female fly undertakes prior to and during egg laying. We have analyzed the hierarchy and relationships in time of these microbehaviors in three closely related Drosophila species with divergent egg-laying preferences and uncovered cryptic differences in their behavioral patterns. Using high-speed imaging, we quantified in depth the oviposition behavior of single females of Drosophila suzukii, Drosophila biarmipes and Drosophila melanogaster in a novel behavioral assay. By computing transitions between microbehaviors, we identified a common ethogram structure underlying oviposition of all three species. Quantifying parameters such as relative time spent on a microbehavior and its average duration, however, revealed clear differences between species. In addition, we examined the temporal dynamics and probability of transitions to different microbehaviors relative to a central event of oviposition, ovipositor contact. Although the quantitative analysis highlights behavioral variability across flies, it reveals some interesting trends for each species in the mode of substrate sampling, as well as possible evolutionary differences. Larger datasets derived from automated video annotation will overcome this paucity of data in the future, and use the same framework to reappraise these observed differences. Our study reveals a common architecture to the oviposition ethogram of three Drosophila species, indicating its ancestral state. It also indicates that Drosophila suzukii’s behavior departs quantitatively and qualitatively from that of the outgroup species, in line with its known divergent ethology. Together, our results illustrate how a global shift in ethology breaks down in the quantitative reorganization of the elementary steps underlying a complex behavior.
format Online
Article
Text
id pubmed-6549446
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-65494462019-06-12 Quantitative and Discrete Evolutionary Changes in the Egg-Laying Behavior of Single Drosophila Females Bräcker, Lasse B. Schmid, Christian A. Bolini, Verena A. Holz, Claudia A. Prud’homme, Benjamin Sirota, Anton Gompel, Nicolas Front Behav Neurosci Neuroscience How a nervous system assembles and coordinates a suite of elementary behavioral steps into a complex behavior is not well understood. While often presented as a stereotyped sequence of events, even extensively studied behaviors such as fly courtship are rarely a strict repetition of the same steps in a predetermined sequence in time. We are focusing on oviposition, the act of laying an egg, in flies of the genus Drosophila to describe the elementary behavioral steps or microbehaviors that a single female fly undertakes prior to and during egg laying. We have analyzed the hierarchy and relationships in time of these microbehaviors in three closely related Drosophila species with divergent egg-laying preferences and uncovered cryptic differences in their behavioral patterns. Using high-speed imaging, we quantified in depth the oviposition behavior of single females of Drosophila suzukii, Drosophila biarmipes and Drosophila melanogaster in a novel behavioral assay. By computing transitions between microbehaviors, we identified a common ethogram structure underlying oviposition of all three species. Quantifying parameters such as relative time spent on a microbehavior and its average duration, however, revealed clear differences between species. In addition, we examined the temporal dynamics and probability of transitions to different microbehaviors relative to a central event of oviposition, ovipositor contact. Although the quantitative analysis highlights behavioral variability across flies, it reveals some interesting trends for each species in the mode of substrate sampling, as well as possible evolutionary differences. Larger datasets derived from automated video annotation will overcome this paucity of data in the future, and use the same framework to reappraise these observed differences. Our study reveals a common architecture to the oviposition ethogram of three Drosophila species, indicating its ancestral state. It also indicates that Drosophila suzukii’s behavior departs quantitatively and qualitatively from that of the outgroup species, in line with its known divergent ethology. Together, our results illustrate how a global shift in ethology breaks down in the quantitative reorganization of the elementary steps underlying a complex behavior. Frontiers Media S.A. 2019-05-29 /pmc/articles/PMC6549446/ /pubmed/31191270 http://dx.doi.org/10.3389/fnbeh.2019.00118 Text en Copyright © 2019 Bräcker, Schmid, Bolini, Holz, Prud’homme, Sirota and Gompel. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Bräcker, Lasse B.
Schmid, Christian A.
Bolini, Verena A.
Holz, Claudia A.
Prud’homme, Benjamin
Sirota, Anton
Gompel, Nicolas
Quantitative and Discrete Evolutionary Changes in the Egg-Laying Behavior of Single Drosophila Females
title Quantitative and Discrete Evolutionary Changes in the Egg-Laying Behavior of Single Drosophila Females
title_full Quantitative and Discrete Evolutionary Changes in the Egg-Laying Behavior of Single Drosophila Females
title_fullStr Quantitative and Discrete Evolutionary Changes in the Egg-Laying Behavior of Single Drosophila Females
title_full_unstemmed Quantitative and Discrete Evolutionary Changes in the Egg-Laying Behavior of Single Drosophila Females
title_short Quantitative and Discrete Evolutionary Changes in the Egg-Laying Behavior of Single Drosophila Females
title_sort quantitative and discrete evolutionary changes in the egg-laying behavior of single drosophila females
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6549446/
https://www.ncbi.nlm.nih.gov/pubmed/31191270
http://dx.doi.org/10.3389/fnbeh.2019.00118
work_keys_str_mv AT brackerlasseb quantitativeanddiscreteevolutionarychangesintheegglayingbehaviorofsingledrosophilafemales
AT schmidchristiana quantitativeanddiscreteevolutionarychangesintheegglayingbehaviorofsingledrosophilafemales
AT boliniverenaa quantitativeanddiscreteevolutionarychangesintheegglayingbehaviorofsingledrosophilafemales
AT holzclaudiaa quantitativeanddiscreteevolutionarychangesintheegglayingbehaviorofsingledrosophilafemales
AT prudhommebenjamin quantitativeanddiscreteevolutionarychangesintheegglayingbehaviorofsingledrosophilafemales
AT sirotaanton quantitativeanddiscreteevolutionarychangesintheegglayingbehaviorofsingledrosophilafemales
AT gompelnicolas quantitativeanddiscreteevolutionarychangesintheegglayingbehaviorofsingledrosophilafemales