Modeling light propagation through bacterial colonies and its correlation with forward scattering patterns

被引:31
作者
Bae, Euiwon [1 ]
Bai, Nan [1 ]
Aroonnual, Amornrat [2 ]
Robinson, J. Paul [3 ,4 ]
Bhunia, Arun K. [2 ]
Hirleman, E. Daniel [1 ]
机构
[1] Purdue Univ, Sch Mech Engn, W Lafayette, IN 47906 USA
[2] Purdue Univ, Dept Food Sci, Mol Food Microbiol Lab, W Lafayette, IN 47906 USA
[3] Purdue Univ, Dept Basic Med Sci, W Lafayette, IN 47906 USA
[4] Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47906 USA
关键词
bacterial colony; diffraction; phase modulation; NEMATIC-LIQUID-CRYSTAL; SELF-PHASE MODULATION; INDUCED DIFFRACTION RINGS; MAMMALIAN-CELL COLONIES; LASER-BEAM; THIN-FILM;
D O I
10.1117/1.3463003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Bacterial colonies play an important role in the isolation and identification of bacterial species, and plating on a petri dish is still regarded as the gold standard for confirming the cause of an outbreak situation. A bacterial colony consists of millions of densely packed individual bacteria along with matrices such as extracellular materials. When a laser is directed through a colony, complicated structures encode their characteristic signatures, which results in unique forward scattering patterns. We investigate the connection between the morphological parameters of a bacterial colony and corresponding forward scattering patterns to understand bacterial growth morphology. A colony elevation is modeled with a Gaussian profile, which is defined with two critical parameters: center thickness and diameter. Then, applying the scalar diffraction theory, we compute an amplitude modulation via light attenuation from multiple layers of bacteria while a phase modulation is computed from the colony profile. Computational results indicate that center thickness plays a critical role in the total number of diffraction rings while the magnitude of the slope of a colony determines the maximum diffraction angle. Experimental validation is performed by capturing the scattering patterns, monitoring colony diameters via phase contrast microscope, and acquiring the colony profiles via confocal displacement meter. (C) 2010 Society of Photo-Optical Instrumentation Engineers. [DOI: 10.1117/1.3463003]
引用
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页数:11
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