Trajectory-driven computational analysis for element characterization in Trypanosoma cruzi video microscopy
Optical microscopy videos enable experts to analyze the motion of several biological elements. Particularly in blood samples infected with Trypanosoma cruzi (T. cruzi), microscopy videos reveal a dynamic scenario where the parasites' motions are conspicuous. While parasites have self-motion, ce...
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description | Optical microscopy videos enable experts to analyze the motion of several biological elements. Particularly in blood samples infected with Trypanosoma cruzi (T. cruzi), microscopy videos reveal a dynamic scenario where the parasites' motions are conspicuous. While parasites have self-motion, cells are inert and may assume some displacement under dynamic events, such as fluids and microscope focus adjustments. This paper analyzes the trajectory of T. cruzi and blood cells to discriminate between these elements by identifying the following motion patterns: collateral, fluctuating, and pan-tilt-zoom (PTZ). We consider two approaches: i) classification experiments for discrimination between parasites and cells; and ii) clustering experiments to identify the cell motion. We propose the trajectory step dispersion (TSD) descriptor based on standard deviation to characterize these elements, outperforming state-of-the-art descriptors. Our results confirm motion is valuable in discriminating T. cruzi of the cells. Since the parasites perform the collateral motion, their trajectory steps tend to randomness. The cells may assume fluctuating motion following a homogeneous and directional path or PTZ motion with trajectory steps in a restricted area. Thus, our findings may contribute to developing new computational tools focused on trajectory analysis, which can advance the study and medical diagnosis of Chagas disease. |
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Particularly in blood samples infected with Trypanosoma cruzi (T. cruzi), microscopy videos reveal a dynamic scenario where the parasites' motions are conspicuous. While parasites have self-motion, cells are inert and may assume some displacement under dynamic events, such as fluids and microscope focus adjustments. This paper analyzes the trajectory of T. cruzi and blood cells to discriminate between these elements by identifying the following motion patterns: collateral, fluctuating, and pan-tilt-zoom (PTZ). We consider two approaches: i) classification experiments for discrimination between parasites and cells; and ii) clustering experiments to identify the cell motion. We propose the trajectory step dispersion (TSD) descriptor based on standard deviation to characterize these elements, outperforming state-of-the-art descriptors. Our results confirm motion is valuable in discriminating T. cruzi of the cells. Since the parasites perform the collateral motion, their trajectory steps tend to randomness. The cells may assume fluctuating motion following a homogeneous and directional path or PTZ motion with trajectory steps in a restricted area. Thus, our findings may contribute to developing new computational tools focused on trajectory analysis, which can advance the study and medical diagnosis of Chagas disease.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0304716</identifier><identifier>PMID: 38829872</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Biology and Life Sciences ; Blood ; Blood cells ; Chagas disease ; Chagas Disease - parasitology ; Classification ; Clustering ; Computer applications ; Datasets ; Humans ; Image Processing, Computer-Assisted - methods ; Light microscopy ; Medical research ; Medicine and Health Sciences ; Medicine, Experimental ; Microscope and microscopy ; Microscopy ; Microscopy, Video - methods ; Motility ; Optical microscopy ; Parasites ; Physical Sciences ; Protozoa ; Research and Analysis Methods ; Software ; Trajectory analysis ; Trypanosoma cruzi ; Trypanosoma cruzi - physiology ; Vector-borne diseases ; Video</subject><ispartof>PloS one, 2024-06, Vol.19 (6), p.e0304716-e0304716</ispartof><rights>Copyright: © 2024 Martins et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</rights><rights>COPYRIGHT 2024 Public Library of Science</rights><rights>2024 Martins et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2024 Martins et al 2024 Martins et al</rights><rights>2024 Martins et al. 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Particularly in blood samples infected with Trypanosoma cruzi (T. cruzi), microscopy videos reveal a dynamic scenario where the parasites' motions are conspicuous. While parasites have self-motion, cells are inert and may assume some displacement under dynamic events, such as fluids and microscope focus adjustments. This paper analyzes the trajectory of T. cruzi and blood cells to discriminate between these elements by identifying the following motion patterns: collateral, fluctuating, and pan-tilt-zoom (PTZ). We consider two approaches: i) classification experiments for discrimination between parasites and cells; and ii) clustering experiments to identify the cell motion. We propose the trajectory step dispersion (TSD) descriptor based on standard deviation to characterize these elements, outperforming state-of-the-art descriptors. Our results confirm motion is valuable in discriminating T. cruzi of the cells. Since the parasites perform the collateral motion, their trajectory steps tend to randomness. The cells may assume fluctuating motion following a homogeneous and directional path or PTZ motion with trajectory steps in a restricted area. Thus, our findings may contribute to developing new computational tools focused on trajectory analysis, which can advance the study and medical diagnosis of Chagas disease.</description><subject>Biology and Life Sciences</subject><subject>Blood</subject><subject>Blood cells</subject><subject>Chagas disease</subject><subject>Chagas Disease - parasitology</subject><subject>Classification</subject><subject>Clustering</subject><subject>Computer applications</subject><subject>Datasets</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted - methods</subject><subject>Light microscopy</subject><subject>Medical research</subject><subject>Medicine and Health Sciences</subject><subject>Medicine, Experimental</subject><subject>Microscope and microscopy</subject><subject>Microscopy</subject><subject>Microscopy, Video - methods</subject><subject>Motility</subject><subject>Optical microscopy</subject><subject>Parasites</subject><subject>Physical Sciences</subject><subject>Protozoa</subject><subject>Research and Analysis Methods</subject><subject>Software</subject><subject>Trajectory analysis</subject><subject>Trypanosoma cruzi</subject><subject>Trypanosoma cruzi - 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Particularly in blood samples infected with Trypanosoma cruzi (T. cruzi), microscopy videos reveal a dynamic scenario where the parasites' motions are conspicuous. While parasites have self-motion, cells are inert and may assume some displacement under dynamic events, such as fluids and microscope focus adjustments. This paper analyzes the trajectory of T. cruzi and blood cells to discriminate between these elements by identifying the following motion patterns: collateral, fluctuating, and pan-tilt-zoom (PTZ). We consider two approaches: i) classification experiments for discrimination between parasites and cells; and ii) clustering experiments to identify the cell motion. We propose the trajectory step dispersion (TSD) descriptor based on standard deviation to characterize these elements, outperforming state-of-the-art descriptors. Our results confirm motion is valuable in discriminating T. cruzi of the cells. Since the parasites perform the collateral motion, their trajectory steps tend to randomness. The cells may assume fluctuating motion following a homogeneous and directional path or PTZ motion with trajectory steps in a restricted area. Thus, our findings may contribute to developing new computational tools focused on trajectory analysis, which can advance the study and medical diagnosis of Chagas disease.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>38829872</pmid><doi>10.1371/journal.pone.0304716</doi><tpages>e0304716</tpages><orcidid>https://orcid.org/0000-0003-1397-4528</orcidid><orcidid>https://orcid.org/0000-0002-4951-1536</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biology and Life Sciences Blood Blood cells Chagas disease Chagas Disease - parasitology Classification Clustering Computer applications Datasets Humans Image Processing, Computer-Assisted - methods Light microscopy Medical research Medicine and Health Sciences Medicine, Experimental Microscope and microscopy Microscopy Microscopy, Video - methods Motility Optical microscopy Parasites Physical Sciences Protozoa Research and Analysis Methods Software Trajectory analysis Trypanosoma cruzi Trypanosoma cruzi - physiology Vector-borne diseases Video |
title | Trajectory-driven computational analysis for element characterization in Trypanosoma cruzi video microscopy |
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