{"title":"Movement analysis of the bilophotrichous magnetotactic bacteria<i>Magnetofaba australis</i>strain IT-1.","authors":"Fernanda Abreu, Daniel Acosta-Avalos","doi":"10.1088/1478-3975/adf025","DOIUrl":null,"url":null,"abstract":"<p><p>Magnetotactic bacteria (MTB) are microorganisms that biomineralize intracellular magnetic nanoparticles inside a membrane vesicle/invagination. The set membrana + magnetic nanoparticle is known as magnetosome and generally magnetosomes are organized in linear chains in the cytoplasm, conferring a magnetic moment to the MTB. Due to their magnetic properties, MTB swim by following local magnetic field lines. This property makes MTB a suitable model to study bacterial movement. There are theoretical models to analyze the swimming of MTB, but the majority consider monotrichous bacteria. Only one model is related to the swimming of bilophotrichous bacteria, but they do not report the resultant trajectory parameters as a function of the magnetic field. Also, the literature lacks an experimental analysis of the trajectories of bilophotrichous MTB. The present study analyzes the movement of the bilphotrichous MTB<i>Magnetofaba australis</i>strain IT-1 exposed to different magnetic field intensities. The trajectories are composed of two oscillations, one of low frequency and large amplitude and another of high frequency and small amplitude. The amplitudes show a magnetic field dependency, and the frequencies show to be magnetic field independent. The analysis of the trajectory orientation relative to the magnetic field direction shows that magnetotaxis of<i>M. australis</i>for low magnetic fields is not as efficient as expected, perhaps due to living in a liquid culture medium rich in nutrients. As far as we know, this is the first time that these movement data have been obtained, and they will be important to validate future theoretical models of movement for bilophotrichous MTB.</p>","PeriodicalId":20207,"journal":{"name":"Physical biology","volume":" ","pages":""},"PeriodicalIF":1.6000,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physical biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1088/1478-3975/adf025","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Magnetotactic bacteria (MTB) are microorganisms that biomineralize intracellular magnetic nanoparticles inside a membrane vesicle/invagination. The set membrana + magnetic nanoparticle is known as magnetosome and generally magnetosomes are organized in linear chains in the cytoplasm, conferring a magnetic moment to the MTB. Due to their magnetic properties, MTB swim by following local magnetic field lines. This property makes MTB a suitable model to study bacterial movement. There are theoretical models to analyze the swimming of MTB, but the majority consider monotrichous bacteria. Only one model is related to the swimming of bilophotrichous bacteria, but they do not report the resultant trajectory parameters as a function of the magnetic field. Also, the literature lacks an experimental analysis of the trajectories of bilophotrichous MTB. The present study analyzes the movement of the bilphotrichous MTBMagnetofaba australisstrain IT-1 exposed to different magnetic field intensities. The trajectories are composed of two oscillations, one of low frequency and large amplitude and another of high frequency and small amplitude. The amplitudes show a magnetic field dependency, and the frequencies show to be magnetic field independent. The analysis of the trajectory orientation relative to the magnetic field direction shows that magnetotaxis ofM. australisfor low magnetic fields is not as efficient as expected, perhaps due to living in a liquid culture medium rich in nutrients. As far as we know, this is the first time that these movement data have been obtained, and they will be important to validate future theoretical models of movement for bilophotrichous MTB.
期刊介绍:
Physical Biology publishes articles in the broad interdisciplinary field bridging biology with the physical sciences and engineering. This journal focuses on research in which quantitative approaches – experimental, theoretical and modeling – lead to new insights into biological systems at all scales of space and time, and all levels of organizational complexity.
Physical Biology accepts contributions from a wide range of biological sub-fields, including topics such as:
molecular biophysics, including single molecule studies, protein-protein and protein-DNA interactions
subcellular structures, organelle dynamics, membranes, protein assemblies, chromosome structure
intracellular processes, e.g. cytoskeleton dynamics, cellular transport, cell division
systems biology, e.g. signaling, gene regulation and metabolic networks
cells and their microenvironment, e.g. cell mechanics and motility, chemotaxis, extracellular matrix, biofilms
cell-material interactions, e.g. biointerfaces, electrical stimulation and sensing, endocytosis
cell-cell interactions, cell aggregates, organoids, tissues and organs
developmental dynamics, including pattern formation and morphogenesis
physical and evolutionary aspects of disease, e.g. cancer progression, amyloid formation
neuronal systems, including information processing by networks, memory and learning
population dynamics, ecology, and evolution
collective action and emergence of collective phenomena.