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An Image Processing Tool for Automated Quantification of Bacterial Burdens in Zebrafish Larvae.
Yamaguchi, Naoya; Otsuna, Hideo; Eisenberg-Bord, Michal; Ramakrishnan, Lalita.
Affiliation
  • Yamaguchi N; Molecular Immunity Unit, Cambridge Institute of Therapeutic Immunology and Infectious Diseases, Department of Medicine, University of Cambridge, CB2 0AW Cambridge, UK.
  • Otsuna H; MRC Laboratory of Molecular Biology, CB2 0QH Cambridge, UK.
  • Eisenberg-Bord M; Equal contributions.
  • Ramakrishnan L; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, United States.
bioRxiv ; 2024 Aug 19.
Article in En | MEDLINE | ID: mdl-39229075
ABSTRACT
Zebrafish larvae are used to model the pathogenesis of multiple bacteria. This transparent model offers the unique advantage of allowing quantification of fluorescent bacterial burdens (fluorescent pixel counts FPC) in vivo by facile microscopical methods, replacing enumeration of bacteria using time-intensive plating of lysates on bacteriological media. Accurate FPC measurements require laborious manual image processing to mark the outside borders of the animals so as to delineate the bacteria inside the animals from those in the culture medium that they are in. Here, we have developed an automated ImageJ/Fiji-based macro that accurately detect the outside borders of Mycobacterium marinum-infected larvae.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: BioRxiv Year: 2024 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: BioRxiv Year: 2024 Document type: Article Country of publication: United States