4.6 Article

Rapid imaging of mycoplasma in solution using Atmospheric Scanning Electron Microscopy (ASEM)

期刊

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2011.12.111

关键词

Mycoplasma mobile; Correlative microscopy; Environmental cell; Electron microscopy; Bacteria; Imaging

资金

  1. Japan Science and Technology Agency (JST)
  2. Ministry of Education, Culture, Sports, Science, and Technology (MEXT)
  3. Grant-in-Aid for Scientific Research on Innovative Areas, Structural Basis of Cell-Signaling Complexes Mediating Signal Perception, Transduction and Responses
  4. AIST
  5. Grants-in-Aid for Scientific Research [22121004] Funding Source: KAKEN

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Mycoplasma is a genus of bacterial pathogen that causes disease in vertebrates. In humans, the species Mycoplasma pneumoniae causes 15% or more of community-acquired pneumonia. Because this bacterium is tiny, corresponding in size to a large virus, diagnosis using optical microscopy is not easy. In current methods, chest X-rays are usually the first action, followed by serology, PCR amplification, and/or culture, but all of these are particularly difficult at an early stage of the disease. Using Myco plasma mobile as a model species, we directly observed mycoplasma in buffer with the newly developed Atmospheric Scanning Electron Microscope (ASEM). This microscope features an open sample dish with a pressure-resistant thin film window in its base, through which the SEM beam scans samples in solution, from below. Because of its 2-3 mu m-deep scanning capability, it can observe the whole internal structure of mycoplasma cells stained with metal solutions. Characteristic protein localizations were visualized using immuno-labeling. Cells were observed at low concentrations, because suspended cells concentrate in the observable zone by attaching to sialic acid on the silicon nitride (SiN) film surface within minutes. These results suggest the applicability of the ASEM for the study of mycoplasmas as well as for early-stage mycoplasma infection diagnosis. (C) 2011 Elsevier Inc. All rights reserved.

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