Cargando…

Legionella pneumophila Infection of Drosophila S2 Cells Induces Only Minor Changes in Mitochondrial Dynamics

During infection of cells by Legionella pneumophila, the bacterium secretes a large number of effector proteins into the host cell cytoplasm, allowing it to alter many cellular processes and make the vacuole and the host cell into more hospitable environments for bacterial replication. One major cha...

Descripción completa

Detalles Bibliográficos
Autores principales: Sun, Elizabeth Wen, Wagner, Monica L., Maize, Amanda, Kemler, Doris, Garland-Kuntz, Elisabeth, Xu, Li, Luo, Zhao-Qing, Hollenbeck, Peter J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3640039/
https://www.ncbi.nlm.nih.gov/pubmed/23638172
http://dx.doi.org/10.1371/journal.pone.0062972
_version_ 1782476045659668480
author Sun, Elizabeth Wen
Wagner, Monica L.
Maize, Amanda
Kemler, Doris
Garland-Kuntz, Elisabeth
Xu, Li
Luo, Zhao-Qing
Hollenbeck, Peter J.
author_facet Sun, Elizabeth Wen
Wagner, Monica L.
Maize, Amanda
Kemler, Doris
Garland-Kuntz, Elisabeth
Xu, Li
Luo, Zhao-Qing
Hollenbeck, Peter J.
author_sort Sun, Elizabeth Wen
collection PubMed
description During infection of cells by Legionella pneumophila, the bacterium secretes a large number of effector proteins into the host cell cytoplasm, allowing it to alter many cellular processes and make the vacuole and the host cell into more hospitable environments for bacterial replication. One major change induced by infection is the recruitment of ER-derived vesicles to the surface of the vacuole, where they fuse with the vacuole membrane and prevent it from becoming an acidified, degradative compartment. However, the recruitment of mitochondria to the region of the vacuole has also been suggested by ultrastructural studies. In order to test this idea in a controlled and quantitative experimental system, and to lay the groundwork for a genome-wide screen for factors involved in mitochondrial recruitment, we examined the behavior of mitochondria during the early stages of Legionella pneumophila infection of Drosophila S2 cells. We found that the density of mitochondria near vacuoles formed by infection with wild type Legionella was not different from that found in dotA(–) mutant-infected cells during the first 4 hours after infection. We then examined 4 parameters of mitochondrial motility in infected cells: velocity of movement, duty cycle of movement, directional persistence and net direction. In the 4 hours following infection, most of these measures were indistinguishable between wild type and dotA(−).infection. However, wild type Legionella did induce a modest shift in the velocity distribution toward faster movement compared dotA(−) infection, and a small downward shift in the duty cycle distribution. In addition, wild type infection produced mitochondrial movement that was biased in the direction of the bacterial vacuole relative to dotA-, although not enough to cause a significant accumulation within 10 um of the vacuole. We conclude that in this host cell, mitochondria are not strongly recruited to the vacuole, nor is their motility dramatically affected.
format Online
Article
Text
id pubmed-3640039
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-36400392013-05-01 Legionella pneumophila Infection of Drosophila S2 Cells Induces Only Minor Changes in Mitochondrial Dynamics Sun, Elizabeth Wen Wagner, Monica L. Maize, Amanda Kemler, Doris Garland-Kuntz, Elisabeth Xu, Li Luo, Zhao-Qing Hollenbeck, Peter J. PLoS One Research Article During infection of cells by Legionella pneumophila, the bacterium secretes a large number of effector proteins into the host cell cytoplasm, allowing it to alter many cellular processes and make the vacuole and the host cell into more hospitable environments for bacterial replication. One major change induced by infection is the recruitment of ER-derived vesicles to the surface of the vacuole, where they fuse with the vacuole membrane and prevent it from becoming an acidified, degradative compartment. However, the recruitment of mitochondria to the region of the vacuole has also been suggested by ultrastructural studies. In order to test this idea in a controlled and quantitative experimental system, and to lay the groundwork for a genome-wide screen for factors involved in mitochondrial recruitment, we examined the behavior of mitochondria during the early stages of Legionella pneumophila infection of Drosophila S2 cells. We found that the density of mitochondria near vacuoles formed by infection with wild type Legionella was not different from that found in dotA(–) mutant-infected cells during the first 4 hours after infection. We then examined 4 parameters of mitochondrial motility in infected cells: velocity of movement, duty cycle of movement, directional persistence and net direction. In the 4 hours following infection, most of these measures were indistinguishable between wild type and dotA(−).infection. However, wild type Legionella did induce a modest shift in the velocity distribution toward faster movement compared dotA(−) infection, and a small downward shift in the duty cycle distribution. In addition, wild type infection produced mitochondrial movement that was biased in the direction of the bacterial vacuole relative to dotA-, although not enough to cause a significant accumulation within 10 um of the vacuole. We conclude that in this host cell, mitochondria are not strongly recruited to the vacuole, nor is their motility dramatically affected. Public Library of Science 2013-04-30 /pmc/articles/PMC3640039/ /pubmed/23638172 http://dx.doi.org/10.1371/journal.pone.0062972 Text en © 2013 Sun et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Sun, Elizabeth Wen
Wagner, Monica L.
Maize, Amanda
Kemler, Doris
Garland-Kuntz, Elisabeth
Xu, Li
Luo, Zhao-Qing
Hollenbeck, Peter J.
Legionella pneumophila Infection of Drosophila S2 Cells Induces Only Minor Changes in Mitochondrial Dynamics
title Legionella pneumophila Infection of Drosophila S2 Cells Induces Only Minor Changes in Mitochondrial Dynamics
title_full Legionella pneumophila Infection of Drosophila S2 Cells Induces Only Minor Changes in Mitochondrial Dynamics
title_fullStr Legionella pneumophila Infection of Drosophila S2 Cells Induces Only Minor Changes in Mitochondrial Dynamics
title_full_unstemmed Legionella pneumophila Infection of Drosophila S2 Cells Induces Only Minor Changes in Mitochondrial Dynamics
title_short Legionella pneumophila Infection of Drosophila S2 Cells Induces Only Minor Changes in Mitochondrial Dynamics
title_sort legionella pneumophila infection of drosophila s2 cells induces only minor changes in mitochondrial dynamics
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3640039/
https://www.ncbi.nlm.nih.gov/pubmed/23638172
http://dx.doi.org/10.1371/journal.pone.0062972
work_keys_str_mv AT sunelizabethwen legionellapneumophilainfectionofdrosophilas2cellsinducesonlyminorchangesinmitochondrialdynamics
AT wagnermonical legionellapneumophilainfectionofdrosophilas2cellsinducesonlyminorchangesinmitochondrialdynamics
AT maizeamanda legionellapneumophilainfectionofdrosophilas2cellsinducesonlyminorchangesinmitochondrialdynamics
AT kemlerdoris legionellapneumophilainfectionofdrosophilas2cellsinducesonlyminorchangesinmitochondrialdynamics
AT garlandkuntzelisabeth legionellapneumophilainfectionofdrosophilas2cellsinducesonlyminorchangesinmitochondrialdynamics
AT xuli legionellapneumophilainfectionofdrosophilas2cellsinducesonlyminorchangesinmitochondrialdynamics
AT luozhaoqing legionellapneumophilainfectionofdrosophilas2cellsinducesonlyminorchangesinmitochondrialdynamics
AT hollenbeckpeterj legionellapneumophilainfectionofdrosophilas2cellsinducesonlyminorchangesinmitochondrialdynamics