Divakar Badal, Aloke Kumar, Varsha Singh, Danny Raj M
{"title":"动态的流体景观有助于细菌的传播","authors":"Divakar Badal, Aloke Kumar, Varsha Singh, Danny Raj M","doi":"arxiv-2309.05351","DOIUrl":null,"url":null,"abstract":"Microbial interactions regulate their spread and survival in competitive\nenvironments. It is not clear if the physical parameters of the environment\nregulate the outcome of these interactions. In this work, we show that the\nopportunistic pathogen Pseudomonas aeruginosa occupies a larger area on the\nsubstratum in the presence of yeast such as Cryptococcus neoformans , than\nwithout it. At the microscopic level, bacterial cells show an enhanced activity\nin the vicinity of yeast cells. We observe this behaviour even when the live\nyeast cells are replaced with heat-killed cells or with spherical glass beads\nof similar morphology, which suggests that the observed behaviour is not\nspecific to the biology of microbes. Upon careful investigation, we find that a\nfluid pool is formed around yeast cells which facilitates the swimming of the\nflagellated P. aeruginosa , causing their enhanced motility. Using mathematical\nmodeling we demonstrate how this local enhancement of bacterial motility leads\nto the enhanced spread observed at the level of the plate. We find that the\ndynamics of the fluid landscape around the bacteria, mediated by the growing\nyeast lawn, affects the spreading. For instance, when the yeast lawn grows\nfaster, a bacterial colony prefers a lower initial loading of yeast cells for\noptimum enhancement in the spread. We confirm our predictions using Candida\nalbicans and C. neoformans, at different initial compositions. In summary, our\nwork shows the importance of considering the dynamically changing physical\nenvironment while studying bacterial motility in complex environments.","PeriodicalId":501321,"journal":{"name":"arXiv - QuanBio - Cell Behavior","volume":"12 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A dynamic fluid landscape mediates the spread of bacteria\",\"authors\":\"Divakar Badal, Aloke Kumar, Varsha Singh, Danny Raj M\",\"doi\":\"arxiv-2309.05351\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Microbial interactions regulate their spread and survival in competitive\\nenvironments. It is not clear if the physical parameters of the environment\\nregulate the outcome of these interactions. In this work, we show that the\\nopportunistic pathogen Pseudomonas aeruginosa occupies a larger area on the\\nsubstratum in the presence of yeast such as Cryptococcus neoformans , than\\nwithout it. At the microscopic level, bacterial cells show an enhanced activity\\nin the vicinity of yeast cells. We observe this behaviour even when the live\\nyeast cells are replaced with heat-killed cells or with spherical glass beads\\nof similar morphology, which suggests that the observed behaviour is not\\nspecific to the biology of microbes. Upon careful investigation, we find that a\\nfluid pool is formed around yeast cells which facilitates the swimming of the\\nflagellated P. aeruginosa , causing their enhanced motility. Using mathematical\\nmodeling we demonstrate how this local enhancement of bacterial motility leads\\nto the enhanced spread observed at the level of the plate. We find that the\\ndynamics of the fluid landscape around the bacteria, mediated by the growing\\nyeast lawn, affects the spreading. For instance, when the yeast lawn grows\\nfaster, a bacterial colony prefers a lower initial loading of yeast cells for\\noptimum enhancement in the spread. We confirm our predictions using Candida\\nalbicans and C. neoformans, at different initial compositions. In summary, our\\nwork shows the importance of considering the dynamically changing physical\\nenvironment while studying bacterial motility in complex environments.\",\"PeriodicalId\":501321,\"journal\":{\"name\":\"arXiv - QuanBio - Cell Behavior\",\"volume\":\"12 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-09-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"arXiv - QuanBio - Cell Behavior\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/arxiv-2309.05351\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Cell Behavior","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2309.05351","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A dynamic fluid landscape mediates the spread of bacteria
Microbial interactions regulate their spread and survival in competitive
environments. It is not clear if the physical parameters of the environment
regulate the outcome of these interactions. In this work, we show that the
opportunistic pathogen Pseudomonas aeruginosa occupies a larger area on the
substratum in the presence of yeast such as Cryptococcus neoformans , than
without it. At the microscopic level, bacterial cells show an enhanced activity
in the vicinity of yeast cells. We observe this behaviour even when the live
yeast cells are replaced with heat-killed cells or with spherical glass beads
of similar morphology, which suggests that the observed behaviour is not
specific to the biology of microbes. Upon careful investigation, we find that a
fluid pool is formed around yeast cells which facilitates the swimming of the
flagellated P. aeruginosa , causing their enhanced motility. Using mathematical
modeling we demonstrate how this local enhancement of bacterial motility leads
to the enhanced spread observed at the level of the plate. We find that the
dynamics of the fluid landscape around the bacteria, mediated by the growing
yeast lawn, affects the spreading. For instance, when the yeast lawn grows
faster, a bacterial colony prefers a lower initial loading of yeast cells for
optimum enhancement in the spread. We confirm our predictions using Candida
albicans and C. neoformans, at different initial compositions. In summary, our
work shows the importance of considering the dynamically changing physical
environment while studying bacterial motility in complex environments.