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Mechanically resolved imaging of bacteria using expansion microscopy.
Lim, Youngbin; Shiver, Anthony L; Khariton, Margarita; Lane, Keara M; Ng, Katharine M; Bray, Samuel R; Qin, Jian; Huang, Kerwyn Casey; Wang, Bo.
Affiliation
  • Lim Y; Department of Bioengineering, Stanford University, Stanford, California, United States of America.
  • Shiver AL; Department of Bioengineering, Stanford University, Stanford, California, United States of America.
  • Khariton M; Department of Bioengineering, Stanford University, Stanford, California, United States of America.
  • Lane KM; Department of Bioengineering, Stanford University, Stanford, California, United States of America.
  • Ng KM; Department of Bioengineering, Stanford University, Stanford, California, United States of America.
  • Bray SR; Department of Bioengineering, Stanford University, Stanford, California, United States of America.
  • Qin J; Department of Chemical Engineering, Stanford University, Stanford, California, United States of America.
  • Huang KC; Department of Bioengineering, Stanford University, Stanford, California, United States of America.
  • Wang B; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California, United States of America.
PLoS Biol ; 17(10): e3000268, 2019 10.
Article in En | MEDLINE | ID: mdl-31622337
Imaging dense and diverse microbial communities has broad applications in basic microbiology and medicine, but remains a grand challenge due to the fact that many species adopt similar morphologies. While prior studies have relied on techniques involving spectral labeling, we have developed an expansion microscopy method (µExM) in which bacterial cells are physically expanded prior to imaging. We find that expansion patterns depend on the structural and mechanical properties of the cell wall, which vary across species and conditions. We use this phenomenon as a quantitative and sensitive phenotypic imaging contrast orthogonal to spectral separation to resolve bacterial cells of different species or in distinct physiological states. Focusing on host-microbe interactions that are difficult to quantify through fluorescence alone, we demonstrate the ability of µExM to distinguish species through an in vitro defined community of human gut commensals and in vivo imaging of a model gut microbiota, and to sensitively detect cell-envelope damage caused by antibiotics or previously unrecognized cell-to-cell phenotypic heterogeneity among pathogenic bacteria as they infect macrophages.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Acetobacter / Muramidase / Lactobacillus plantarum / Escherichia coli / Microscopy Limits: Animals / Humans Language: En Journal: PLoS Biol Journal subject: BIOLOGIA Year: 2019 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Acetobacter / Muramidase / Lactobacillus plantarum / Escherichia coli / Microscopy Limits: Animals / Humans Language: En Journal: PLoS Biol Journal subject: BIOLOGIA Year: 2019 Document type: Article Affiliation country: United States Country of publication: United States