4.3 Article

Laser scanning cytometer-based assays for measuring host cell attachment and invasion by the human pathogen Toxoplasma gondii

期刊

CYTOMETRY PART A
卷 69A, 期 1, 页码 13-19

出版社

WILEY-BLACKWELL
DOI: 10.1002/cyto.a.20202

关键词

Toxoplasma gondii; invasion; attachment; laser scanning cytometer

资金

  1. NATIONAL CANCER INSTITUTE [P30CA022435] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R56AI054961, R01AI054961, R01AI063276] Funding Source: NIH RePORTER
  3. NCI NIH HHS [P30 CA22435, P30 CA022435] Funding Source: Medline
  4. NIAID NIH HHS [AI054961, R01 AI054961, R01 AI063276, AI063276, R56 AI054961] Funding Source: Medline

向作者/读者索取更多资源

Background: Toxoplasma gondii is among the most common protozoan parasites of humans. Both attachment to and invasion of host cells by T.gondii are necessary for infection, yet little is known about the molecular mechanisms underlying these processes. T.gondii's etiological importance and its role as a model organism for studying invasion in related parasites necessitate a means to quantitatively assay host cell attachment and invasion. Methods: We present here Laser Scanning Cytometer (LSC)-based assays of T.gondii invasion and attachment. The invasion assay involves automated counting of invaded and non-invaded parasites, differentially, labeled with distinct fluorochromes. The attachment assay compares the relative binding of differentially labeled parasites. The assays were evaluated using treatments known to decrease invasion or attachment. Results: The LSC-based assays are robust and reproducible, remove operator bias, and significantly increase the sample size that can be feasibly counted compared to other currently available microscope-based methods. In the first application of the new assays, we have shown that parasites attach to fixed and unfixed host cells using different mechanisms. Conclusions: The LSC-based assays represent useful new methods for quantitatively measuring attachment and invasion by T.gondii, and can be readily adapted to study similar processes in other host-pathogen systems. (c) 2005 International Society for Analytical Cytology.

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