Skip to main content
Journal cover image

Programmed Allee effect in bacteria causes a tradeoff between population spread and survival.

Publication ,  Journal Article
Smith, R; Tan, C; Srimani, JK; Pai, A; Riccione, KA; Song, H; You, L
Published in: Proceedings of the National Academy of Sciences of the United States of America
February 2014

Dispersal is necessary for spread into new habitats, but it has also been shown to inhibit spread. Theoretical studies have suggested that the presence of a strong Allee effect may account for these counterintuitive observations. Experimental demonstration of this notion is lacking due to the difficulty in quantitative analysis of such phenomena in a natural setting. We engineered Escherichia coli to exhibit a strong Allee effect and examined how the Allee effect would affect the spread of the engineered bacteria. We showed that the Allee effect led to a biphasic dependence of bacterial spread on the dispersal rate: spread is promoted for intermediate dispersal rates but inhibited at low or high dispersal rates. The shape of this dependence is contingent upon the initial density of the source population. Moreover, the Allee effect led to a tradeoff between effectiveness of population spread and survival: increasing the number of target patches during dispersal allows more effective spread, but it simultaneously increases the risk of failing to invade or of going extinct. We also observed that total population growth is transiently maximized at an intermediate number of target patches. Finally, we demonstrate that fluctuations in cell growth may contribute to the paradoxical relationship between dispersal and spread. Our results provide direct experimental evidence that the Allee effect can explain the apparently paradoxical effects of dispersal on spread and have implications for guiding the spread of cooperative organisms.

Duke Scholars

Altmetric Attention Stats
Dimensions Citation Stats

Published In

Proceedings of the National Academy of Sciences of the United States of America

DOI

EISSN

1091-6490

ISSN

0027-8424

Publication Date

February 2014

Volume

111

Issue

5

Start / End Page

1969 / 1974

Related Subject Headings

  • Movement
  • Models, Biological
  • Microbial Viability
  • Genetic Engineering
  • Escherichia coli
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Smith, R., Tan, C., Srimani, J. K., Pai, A., Riccione, K. A., Song, H., & You, L. (2014). Programmed Allee effect in bacteria causes a tradeoff between population spread and survival. Proceedings of the National Academy of Sciences of the United States of America, 111(5), 1969–1974. https://doi.org/10.1073/pnas.1315954111
Smith, Robert, Cheemeng Tan, Jaydeep K. Srimani, Anand Pai, Katherine A. Riccione, Hao Song, and Lingchong You. “Programmed Allee effect in bacteria causes a tradeoff between population spread and survival.Proceedings of the National Academy of Sciences of the United States of America 111, no. 5 (February 2014): 1969–74. https://doi.org/10.1073/pnas.1315954111.
Smith R, Tan C, Srimani JK, Pai A, Riccione KA, Song H, et al. Programmed Allee effect in bacteria causes a tradeoff between population spread and survival. Proceedings of the National Academy of Sciences of the United States of America. 2014 Feb;111(5):1969–74.
Smith, Robert, et al. “Programmed Allee effect in bacteria causes a tradeoff between population spread and survival.Proceedings of the National Academy of Sciences of the United States of America, vol. 111, no. 5, Feb. 2014, pp. 1969–74. Epmc, doi:10.1073/pnas.1315954111.
Smith R, Tan C, Srimani JK, Pai A, Riccione KA, Song H, You L. Programmed Allee effect in bacteria causes a tradeoff between population spread and survival. Proceedings of the National Academy of Sciences of the United States of America. 2014 Feb;111(5):1969–1974.
Journal cover image

Published In

Proceedings of the National Academy of Sciences of the United States of America

DOI

EISSN

1091-6490

ISSN

0027-8424

Publication Date

February 2014

Volume

111

Issue

5

Start / End Page

1969 / 1974

Related Subject Headings

  • Movement
  • Models, Biological
  • Microbial Viability
  • Genetic Engineering
  • Escherichia coli