Cargando…
Male Killing Spiroplasma Preferentially Disrupts Neural Development in the Drosophila melanogaster Embryo
Male killing bacteria such as Spiroplasma are widespread pathogens of numerous arthropods including Drosophila melanogaster. These maternally transmitted bacteria can bias host sex ratios toward the female sex in order to ‘selfishly’ enhance bacterial transmission. However, little is known about the...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3827344/ https://www.ncbi.nlm.nih.gov/pubmed/24236124 http://dx.doi.org/10.1371/journal.pone.0079368 |
_version_ | 1782291073943470080 |
---|---|
author | Martin, Jennifer Chong, Trisha Ferree, Patrick M. |
author_facet | Martin, Jennifer Chong, Trisha Ferree, Patrick M. |
author_sort | Martin, Jennifer |
collection | PubMed |
description | Male killing bacteria such as Spiroplasma are widespread pathogens of numerous arthropods including Drosophila melanogaster. These maternally transmitted bacteria can bias host sex ratios toward the female sex in order to ‘selfishly’ enhance bacterial transmission. However, little is known about the specific means by which these pathogens disrupt host development in order to kill males. Here we show that a male-killing Spiroplasma strain severely disrupts nervous tissue development in male but not female D. melanogaster embryos. The neuroblasts, or neuron progenitors, form properly and their daughter cells differentiate into neurons of the ventral nerve chord. However, the neurons fail to pack together properly and they produce highly abnormal axons. In contrast, non-neural tissue, such as mesoderm, and body segmentation appear normal during this time, although the entire male embryo becomes highly abnormal during later stages. Finally, we found that Spiroplasma is altogether absent from the neural tissue but localizes within the gut and the epithelium immediately surrounding the neural tissue, suggesting that the bacterium secretes a toxin that affects neural tissue development across tissue boundaries. Together these findings demonstrate the unique ability of this insect pathogen to preferentially affect development of a specific embryonic tissue to induce male killing. |
format | Online Article Text |
id | pubmed-3827344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38273442013-11-14 Male Killing Spiroplasma Preferentially Disrupts Neural Development in the Drosophila melanogaster Embryo Martin, Jennifer Chong, Trisha Ferree, Patrick M. PLoS One Research Article Male killing bacteria such as Spiroplasma are widespread pathogens of numerous arthropods including Drosophila melanogaster. These maternally transmitted bacteria can bias host sex ratios toward the female sex in order to ‘selfishly’ enhance bacterial transmission. However, little is known about the specific means by which these pathogens disrupt host development in order to kill males. Here we show that a male-killing Spiroplasma strain severely disrupts nervous tissue development in male but not female D. melanogaster embryos. The neuroblasts, or neuron progenitors, form properly and their daughter cells differentiate into neurons of the ventral nerve chord. However, the neurons fail to pack together properly and they produce highly abnormal axons. In contrast, non-neural tissue, such as mesoderm, and body segmentation appear normal during this time, although the entire male embryo becomes highly abnormal during later stages. Finally, we found that Spiroplasma is altogether absent from the neural tissue but localizes within the gut and the epithelium immediately surrounding the neural tissue, suggesting that the bacterium secretes a toxin that affects neural tissue development across tissue boundaries. Together these findings demonstrate the unique ability of this insect pathogen to preferentially affect development of a specific embryonic tissue to induce male killing. Public Library of Science 2013-11-13 /pmc/articles/PMC3827344/ /pubmed/24236124 http://dx.doi.org/10.1371/journal.pone.0079368 Text en © 2013 Martin 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 Martin, Jennifer Chong, Trisha Ferree, Patrick M. Male Killing Spiroplasma Preferentially Disrupts Neural Development in the Drosophila melanogaster Embryo |
title | Male Killing Spiroplasma Preferentially Disrupts Neural Development in the Drosophila melanogaster Embryo |
title_full | Male Killing Spiroplasma Preferentially Disrupts Neural Development in the Drosophila melanogaster Embryo |
title_fullStr | Male Killing Spiroplasma Preferentially Disrupts Neural Development in the Drosophila melanogaster Embryo |
title_full_unstemmed | Male Killing Spiroplasma Preferentially Disrupts Neural Development in the Drosophila melanogaster Embryo |
title_short | Male Killing Spiroplasma Preferentially Disrupts Neural Development in the Drosophila melanogaster Embryo |
title_sort | male killing spiroplasma preferentially disrupts neural development in the drosophila melanogaster embryo |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3827344/ https://www.ncbi.nlm.nih.gov/pubmed/24236124 http://dx.doi.org/10.1371/journal.pone.0079368 |
work_keys_str_mv | AT martinjennifer malekillingspiroplasmapreferentiallydisruptsneuraldevelopmentinthedrosophilamelanogasterembryo AT chongtrisha malekillingspiroplasmapreferentiallydisruptsneuraldevelopmentinthedrosophilamelanogasterembryo AT ferreepatrickm malekillingspiroplasmapreferentiallydisruptsneuraldevelopmentinthedrosophilamelanogasterembryo |