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Originally published as MBC in Press, 10.1091/mbc.E03-10-0747 on March 5, 2004

Vol. 15, Issue 5, 2164-2175, May 2004

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Listeria monocytogenes Actin-based Motility Varies Depending on Subcellular Location: A Kinematic Probe for Cytoarchitecture

Catherine I. Lacayo *, and Julie A. Theriot * {dagger} {ddagger}

* Department of Biochemistry, Stanford University, School of Medicine, Stanford, California 94305; {dagger} Department of Microbiology and Immunology, Stanford University, School of Medicine, Stanford, California 94305

Submitted October 17, 2003; Revised February 4, 2004; Accepted February 11, 2004
Monitoring Editor: Thomas Pollard

Intracellular Listeria monocytogenes actin-based motility is characterized by significant individual variability, which can be influenced by cytoarchitecture. L. monocytogenes was used as a probe to transmit information about structural variation among subcellular domains defined by mitochondrial density. By analyzing the movement of a large population of L. monocytogenes in PtK2 cells, we found that mean speed and trajectory curvature were significantly larger for bacteria moving in mitochondria-containing domains (generally perinuclear) than for bacteria moving in mitochondria-free domains (generally peripheral). Analysis of bacteria that traversed both mitochondria-containing and mitochondria-free domains revealed that these motile differences were not intrinsic to bacteria themselves. Disruption of mitochondrial respiration did not affect bacterial mean speed, speed persistence, or trajectory curvature. In contrast, microtubule depolymerization lead to decreased mean speed per bacterium and increased mean speed persistence of L. monocytogenes moving in mitochondria-free domains compared with untreated cells. L. monocytogenes were also observed to physically collide with mitochondria and push them away from the bacterial path of motion, causing bacteria to slow down before rapidly resuming their speed. Our results show that subcellular domains along with microtubule depolymerization may influence the actin cytoskeleton to affect L. monocytogenes speed, speed persistence, and trajectory curvature.


Article published online ahead of print. Mol. Biol. Cell 10.1091/mbc.E03–10–0747. Article and publication date are available at www.molbiolcell.org/cgi/doi/10.1091/mbc.E03–10–0747.

Online version of this article contains supporting material. Online version is available at www.molbiolcell.org.

{ddagger} Corresponding author. E-mail address: theriot{at}stanford.edu.




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