A power-law dependence of bacterial invasion on mammalian host receptors

Pathogenic bacteria such as Listeria and Yersinia gain initial entry by binding to host target cells and stimulating their internalization. Bacterial uptake entails successive, increasingly strong associations between receptors on the surface of bacteria and hosts. Even with genetically identical ce...

Full description

Saved in:
Bibliographic Details
Published inPLoS computational biology Vol. 11; no. 4; p. e1004203
Main Authors Lee, Tae J, Wong, Jeffrey, Bae, Sena, Lee, Anna Jisu, Lopatkin, Allison, Yuan, Fan, You, Lingchong
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 01.04.2015
Public Library of Science (PLoS)
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Pathogenic bacteria such as Listeria and Yersinia gain initial entry by binding to host target cells and stimulating their internalization. Bacterial uptake entails successive, increasingly strong associations between receptors on the surface of bacteria and hosts. Even with genetically identical cells grown in the same environment, there are vast differences in the number of bacteria entering any given cell. To gain insight into this variability, we examined uptake dynamics of Escherichia coli engineered to express the invasin surface receptor from Yersinia, which enables uptake via mammalian host β1-integrins. Surprisingly, we found that the uptake probability of a single bacterium follows a simple power-law dependence on the concentration of integrins. Furthermore, the value of a power-law parameter depends on the particular host-bacterium pair but not on bacterial concentration. This power-law captures the complex, variable processes underlying bacterial invasion while also enabling differentiation of cell lines.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Conceived and designed the experiments: TJL LY JW SB. Performed the experiments: TJL SB. Analyzed the data: TJL JW SB AJL LY. Contributed reagents/materials/analysis tools: LY FY. Wrote the paper: TJL JW SB AJL AL FY LY. Implemented and analyzed the kinetic models: TJL JW.
Current address: Orthopedic Surgery, Brigham and Women’s Hospital and Harvard Medical School, Boston, Massachusetts, United States of America
The authors have declared that no competing interests exist.
ISSN:1553-7358
1553-734X
1553-7358
DOI:10.1371/journal.pcbi.1004203