Computational classification of different wild-type zebrafish strains based on their variation in light-induced locomotor response.

Journal: Computers in biology and medicine
Published Date:

Abstract

Zebrafish larvae display a rapid and characteristic swimming behaviour after abrupt light onset or offset. This light-induced locomotor response (LLR) has been widely used for behavioural research and drug screening. However, the locomotor responses have long been shown to be different between different wild-type (WT) strains. Thus, it is critical to define the differences in the WT LLR to facilitate accurate interpretation of behavioural data. In this investigation, we used support vector machine (SVM) models to classify LLR data collected from three WT strains: AB, TL and TLAB (a hybrid of AB and TL), during early embryogenesis, from 3 to 9 days post-fertilisation (dpf). We analysed both the complete dataset and a subset of the data during the first 30after light change. This initial period of activity is substantially driven by vision, and is also known as the visual motor response (VMR). The analyses have resulted in three major conclusions: First, the LLR is different between the three WT strains, and at different developmental stages. Second, the distinguishable information in the VMR is comparable to, if not better than, the full dataset for classification purposes. Third, the distinguishable information of WT strains in the light-onset response differs from that in the light-offset response. While the classification accuracies were higher for the light-offset than light-onset response when using the complete LLR dataset, a reverse trend was observed when using a shorter VMR dataset. Together, our results indicate that one should use caution when extrapolating interpretations of LLR/VMR obtained from one WT strain to another.

Authors

  • Yuan Gao
    Engineering Research Center of EMR and Intelligent Expert System, Ministry of Education, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, College of Biomedical Engineering and Instrument Science, Zhejiang University, Hangzhou Zhejiang Province, China.
  • Gaonan Zhang
    Department of Biological Sciences, Purdue University, 915W. State Street, West Lafayette, IN 47907, USA.
  • Beth Jelfs
    Department of Electronic Engineering, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong.
  • Robert Carmer
    Department of Electronic Engineering, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong; Department of Statistics, Purdue University, 250N. University Street, West Lafayette, IN 47907, USA.
  • Prahatha Venkatraman
    Department of Biological Sciences, Purdue University, 915W. State Street, West Lafayette, IN 47907, USA.
  • Mohammad Ghadami
    Department of Electronic Engineering, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong.
  • Skye A Brown
    Department of Biological Sciences, Purdue University, 915W. State Street, West Lafayette, IN 47907, USA.
  • Chi Pui Pang
    Department of Ophthalmology and Visual Sciences, Chinese University of Hong Kong, Hong Kong.
  • Yuk Fai Leung
    Department of Biological Sciences, Purdue University, 915W. State Street, West Lafayette, IN 47907, USA; Department of Biochemistry and Molecular Biology, Indiana University School of Medicine-Lafayette, 625 Harrison Street, West Lafayette, IN 47907, USA. Electronic address: yfleung@purdue.edu.
  • Rosa H M Chan
    Department of Electronic Engineering, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong. Electronic address: rosachan@cityu.edu.hk.
  • Mingzhi Zhang
    Joint Shantou International Eye Center, Shantou University & the Chinese University of Hong Kong, Shantou, China. Electronic address: zmz@jsiec.org.