期刊论文详细信息
BMC Bioinformatics
BactImAS: a platform for processing and analysis of bacterial time-lapse microscopy movies
željka Maglica2  Darko Mekterović1  Igor Mekterović3 
[1]Division of Experimental Physics, Ruđer Bošković Institute, Bijenička cesta 54, 10000 Zagreb, Croatia
[2]School of Life Sciences, Swiss Federal Institute of Technology in Lausanne (EPFL), 1015 Lausanne, Switzerland
[3]Department of Applied Computing, Faculty of Electrical Engineering and Computing, University of Zagreb, Unska 3, 10000 Zagreb, Croatia
关键词: Database;    Data visualization;    Icy;    ImageJ;    Image analysis;    Mycobacteria;    Time-lapse microscopy;   
Others  :  1087541
DOI  :  10.1186/1471-2105-15-251
 received in 2014-07-06, accepted in 2014-07-17,  发布年份 2014
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【 摘 要 】

Background

The software available to date for analyzing image sequences from time-lapse microscopy works only for certain bacteria and under limited conditions. These programs, mostly MATLAB-based, fail for microbes with irregular shape, indistinct cell division sites, or that grow in closely packed microcolonies. Unfortunately, many organisms of interest have these characteristics, and analyzing their image sequences has been limited to time consuming manual processing.

Results

Here we describe BactImAS – a modular, multi-platform, open-source, Java-based software delivered both as a standalone program and as a plugin for Icy. The software is designed for extracting and visualizing quantitative data from bacterial time-lapse movies. BactImAS uses a semi-automated approach where the user defines initial cells, identifies cell division events, and, if necessary, manually corrects cell segmentation with the help of user-friendly GUI and incorporated ImageJ application. The program segments and tracks cells using a newly-developed algorithm designed for movies with difficult-to-segment cells that exhibit small frame-to-frame differences. Measurements are extracted from images in a configurable, automated fashion and an SQLite database is used to store, retrieve, and exchange all acquired data. Finally, the BactImAS can generate configurable lineage tree visualizations and export data as CSV files. We tested BactImAS on time-lapse movies of Mycobacterium smegmatis and achieved at least 10-fold reduction of processing time compared to manual analysis. We illustrate the power of the visualization tool by showing heterogeneity of both icl expression and cell growth atop of a lineage tree.

Conclusions

The presented software simplifies quantitative analysis of time-lapse movies overall and is currently the only available software for the analysis of mycobacteria-like cells. It will be of interest to the community of both end-users and developers of time-lapse microscopy software.

【 授权许可】

   
2014 Mekterovićet al.; licensee BioMed Central Ltd.

【 预 览 】
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【 参考文献 】
  • [1]Locke JC, Elowitz MB: Using movies to analyse gene circuit dynamics in single cells. Nat Rev Microbiol 2009, 7:383-392.
  • [2]Okumoto S, Jones A, Frommer WB: Quantitative imaging with fluorescent biosensors. Annu Rev Plant Biol 2012, 63:663-706.
  • [3]Coutu DL, Schroeder T: Probing cellular processes by long-term live imaging–historic problems and current solutions. J Cell Sci 2013, 126:3805-3815.
  • [4]Wakamoto Y, Dhar N, Chait R, Schneider K, Signorino-Gelo F, Leibler S, McKinney JD: Dynamic persistence of antibiotic-stressed mycobacteria. Science 2013, 339:91-95.
  • [5]Meijering E, Dzyubachyk O, Smal I: Methods for cell and particle tracking. Methods Enzymol 2012, 504:183-200.
  • [6]Young JW, Locke JC, Altinok A, Rosenfeld N, Bacarian T, Swain PS, Mjolsness E, Elowitz MB: Measuring single-cell gene expression dynamics in bacteria using fluorescence time-lapse microscopy. Nat Protoc 2012, 7:80-88.
  • [7]Sliusarenko O, Heinritz J, Emonet T, Jacobs-Wagner C: High-throughput, subpixel precision analysis of bacterial morphogenesis and intracellular spatio-temporal dynamics. Mol Microbiol 2011, 80:612-627.
  • [8]Wang Q, Niemi J, Tan C. M, You L, West M: Image segmentation and dynamic lineage analysis in single-cell fluorescence microscopy. Cytometry A 2010, 77:101-110.
  • [9]Klein J, Leupold S, Biegler I, Biedendieck R, Munch R, Jahn D: Tlm-tracker: software for cell segmentation, tracking and lineage analysis in time-lapse microscopy movies. Bioinformatics 2012, 28:2276-2277.
  • [10]Häkkinen A, Muthukrishnan AB, Mora A, Fonseca JM, Ribeiro AS: Cellaging: a tool to study segregation and partitioning in division in cell lineages of esherichia coli. Bioinformatics 2013, 29:1708-1709.
  • [11]Primet M, Demarez A, Taddei F, Lindner AB, Moisan L: Tracking of cells in a sequence of images using a low-dimension image representation. In Proceedings of the 5th IEEE International Symposium on Biomedical Imaging: From Nano to Macro (ISBI 2008): 14–17 May 2008; Paris. Edited by Olivo-Marin JC, Bloch I, Laine A. IEEE; 2008:995-998.
  • [12]Beilharz K, Novakova L, Fadda D, Branny P, Massidda O, Veening JW: Control of cell division in streptococcus pneumoniae by the conserved ser/thr protein kinase stkp. Proc Natl Acad Sci U S A 2012, 109:905-913.
  • [13]Lo Scrudato M, Blokesch M: The regulatory network of natural competence and transformation of vibrio cholerae. PLoS Genet 2012, 8:1002778.
  • [14]Vallet-Gely I, Boccard F: Chromosomal organization and segregation in pseudomonas aeruginosa. PLoS Genet 2013, 9:1003492.
  • [15]Paulson T: Epidemiology: a mortal foe. Nature 2013, 502:2-3.
  • [16]Santi I, Dhar N, Bousbaine D, Wakamoto Y, McKinney JD: Single-cell dynamics of the chromosome replication and cell division cycles in mycobacteria. Nat Commun 2013, 4:2470.
  • [17]Aldridge BB, Fernandez-Suarez M, Heller D, Ambravaneswaran V, Irimia D, Toner M, Fortune SM: Asymmetry and aging of mycobacterial cells lead to variable growth and antibiotic susceptibility. Science 2012, 335:100-104.
  • [18]Makarov V, Manina G, Mikusova K, Mollmann U, Ryabova O, Saint-Joanis B, Dhar N, Pasca MR, Buroni S, Lucarelli AP, Milano A, De Rossi E, Belanova M, Bobovska A, Dianiskova P, Kordulakova J, Sala C, Fullam E, Schneider P, McKinney JD, Brodin P, Christophe T, Waddell S, Butcher P, Albrethsen J, Rosenkrands I, Brosch R, Nandi V, Bharath S, Gaonkar S, et al.: Benzothiazinones kill mycobacterium tuberculosis by blocking arabinan synthesis. Science 2009, 324:801-804.
  • [19]Golchin SA, Stratford J, Curry RJ, McFadden J: A microfluidic system for long-term time-lapse microscopy studies of mycobacteria. Tuberculosis (Edinb) 2012, 92:489-496.
  • [20]Schneider CA, Rasband WS, Eliceiri KW: Nih image to imagej: 25 years of image analysis. Nat Methods 2012, 9:671-675.
  • [21]Carpenter AE, Kamentsky L, Eliceiri KW: A call for bioimaging software usability. Nat Methods 2012, 9:666-670.
  • [22]de Chaumont F, Dallongeville S, Chenouard N, Herve N, Pop S, Provoost T, Meas-Yedid V, Pankajakshan P, Lecomte T, Le Montagner Y, Lagache T, Dufour A, Olivo-Marin JC: Icy: an open bioimage informatics platform for extended reproducible research. Nat Methods 2012, 9:690-696.
  • [23]BactImAS [http://homer.zpr.fer.hr/bactimas/ webcite]
  • [24]Sobel [http://homepages.inf.ed.ac.uk/rbf/HIPR2/sobel.htm webcite]
  • [25]Ridler TW, Calvard S: Picture thresholding using an iterative selection method. IEEE Trans Syst Man Cybernet 1978, 8:630-632.
  • [26]Zhang Y, Suen CY: A fast parallel algorithm for thinning digital patterns. Commun ACM 1984, 27:236-239.
  • [27]SQuirreL SQL [http://www.squirrelsql.org/ webcite]
  • [28]Locke JC, Young JW, Fontes M, Hernandez Jimenez MJ, Elowitz MB: Stochastic pulse regulation in bacterial stress response. Science 2011, 334:366-369.
  • [29]Hempel AM, Cantlay S, Molle V, Wang SB, Naldrett MJ, Parker JL, Richards DM, Jung YG, Buttner MJ, Flardh K: The ser/thr protein kinase afsk regulates polar growth and hyphal branching in the filamentous bacteria streptomyces. Proc Natl Acad Sci U S A 2012, 109:2371-2379.
  • [30]McKinney JD, Honer zu Bentrup K, Munoz-Elias E, Miczak A, Chen B, Chan WT, Swenson D, Sacchettini JC, Jacobs WRJ, Russell DG: Persistence of mycobacterium tuberculosis in macrophages and mice requires the glyoxylate shunt enzyme isocitrate lyase. Nature 2000, 406:735-738.
  • [31]Munoz-Elias EJ, McKinney JD: Mycobacterium tuberculosis isocitrate lyases 1 and 2 are jointly required for in vivo growth and virulence. Nat Med 2005, 11:638-644.
  • [32]Micklinghoff JC, Breitinger KJ, Schmidt M, Geffers R, Eikmanns BJ, Bange FC: Role of the transcriptional regulator ramb (rv0465c) in the control of the glyoxylate cycle in mycobacterium tuberculosis. J Bacteriol 2009, 191:7260-7269.
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