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A high-throughput method for quantifying Drosophila fecundity.
Gomez, Andreana; Gonzalez, Sergio; Oke, Ashwini; Luo, Jiayu; Duong, Johnny B; Esquerra, Raymond M; Zimmerman, Thomas; Capponi, Sara; Fung, Jennifer C; Nystul, Todd G.
Afiliação
  • Gomez A; University of California, San Francisco, Department of Anatomy.
  • Gonzalez S; San Francisco State University, Department of Biology.
  • Oke A; Center for Cellular Construction, San Francisco, CA.
  • Luo J; San Francisco State University, Department of Chemistry and Biochemistry; University of California, San Francisco, OB/GYN Department.
  • Duong JB; IBM Almaden Research Center, San Jose, CA; University of California, San Francisco, Center for Reproductive Sciences.
  • Esquerra RM; San Francisco State University, Department of Biology.
  • Zimmerman T; Center for Cellular Construction, San Francisco, CA.
  • Capponi S; Center for Cellular Construction, San Francisco, CA.
  • Fung JC; San Francisco State University, Department of Chemistry and Biochemistry; University of California, San Francisco, OB/GYN Department.
  • Nystul TG; Center for Cellular Construction, San Francisco, CA.
bioRxiv ; 2024 Mar 30.
Article em En | MEDLINE | ID: mdl-38585877
ABSTRACT
Measurements of Drosophila fecundity are used in a wide variety of studies, such as investigations of stem cell biology, nutrition, behavior, and toxicology. In addition, because fecundity assays are performed on live flies, they are suitable for longitudinal studies such as investigations of aging or prolonged chemical exposure. However, standard Drosophila fecundity assays have been difficult to perform in a high-throughput manner because experimental factors such as the physiological state of the flies and environmental cues must be carefully controlled to achieve consistent results. In addition, exposing flies to a large number of different experimental conditions (such as chemical additives in the diet) and manually counting the number of eggs laid to determine the impact on fecundity is time-consuming. We have overcome these challenges by combining a new multiwell fly culture strategy with a novel 3D-printed fly transfer device to rapidly and accurately transfer flies from one plate to another; the RoboCam, a low-cost, custom built robotic camera to capture images of the wells automatically; and an image segmentation pipeline to automatically identify and quantify eggs. We show that this method is compatible with robust and consistent egg laying throughout the assay period; and demonstrate that the automated pipeline for quantifying fecundity is very accurate (r2 = 0.98 for the correlation between the automated egg counts and the ground truth) In addition, we show that this method can be used to efficiently detect the effects on fecundity induced by dietary exposure to chemicals. Taken together, this strategy substantially increases the efficiency and reproducibility of high throughput egg laying assays that require exposing flies to multiple different media conditions.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article