Cargando…

A soil bacterium alters sex determination and rhizoid development in gametophytes of the fern Ceratopteris richardii

Gametophytes of the fern Ceratopteris richardii develop into either hermaphrodites or males. As hermaphrodites develop, they secrete antheridiogen, or A(CE), into the environment, inducing male development in undifferentiated gametophytes. Hermaphrodites are composed of archegonia, antheridia, rhizo...

Descripción completa

Detalles Bibliográficos
Autores principales: Ganger, Michael T, Hiles, Rachel, Hallowell, Haley, Cooper, Lauren, McAllister, Nicole, Youngdahl, Doug, Alfieri, Jeremy, Ewing, Sarah J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474741/
https://www.ncbi.nlm.nih.gov/pubmed/31019671
http://dx.doi.org/10.1093/aobpla/plz012
_version_ 1783412657710170112
author Ganger, Michael T
Hiles, Rachel
Hallowell, Haley
Cooper, Lauren
McAllister, Nicole
Youngdahl, Doug
Alfieri, Jeremy
Ewing, Sarah J
author_facet Ganger, Michael T
Hiles, Rachel
Hallowell, Haley
Cooper, Lauren
McAllister, Nicole
Youngdahl, Doug
Alfieri, Jeremy
Ewing, Sarah J
author_sort Ganger, Michael T
collection PubMed
description Gametophytes of the fern Ceratopteris richardii develop into either hermaphrodites or males. As hermaphrodites develop, they secrete antheridiogen, or A(CE), into the environment, inducing male development in undifferentiated gametophytes. Hermaphrodites are composed of archegonia, antheridia, rhizoids and a notch meristem, while males consist of antheridia and rhizoids. Much of the research on sexual and morphological development concerns gametophytes grown in sterile environments. Using biochemical and molecular techniques we identify a soil bacterium and explore its effects on sexual and rhizoid development. Hermaphrodite and male gametophytes were exposed to this bacterium and the effects on sexual development, rhizoid length and rhizoid number were explored. The bacterium was identified as a pseudomonad, Pseudomonas nitroreducens. Gametophytes grown in the presence of the pseudomonad were more likely to develop into hermaphrodites across all gametophyte densities. Across all gametophyte sizes, hermaphrodites had rhizoids that were 2.95× longer in the presence of the pseudomonad while males had rhizoids that were 2.72× longer in the presence of the pseudomonad. Both hermaphrodite and male gametophytes developed fewer rhizoids in the presence of the pseudomonad. Control hermaphrodites produced 1.23× more rhizoids across all gametophyte sizes. For male gametophytes grown in the absence of the pseudomonad, the rate of increase in the number of rhizoids was greater with increasing size in the control than the rate of increase in males grown in the presence of the pseudomonad. The pseudomonad may be acting on gametophyte sexual development via several potential mechanisms: degradation of A(CE), changes in nutrient availability or phytohormone production. The pseudomonad may also increase rhizoid number through production of phytohormones or changes in nutrient availability.
format Online
Article
Text
id pubmed-6474741
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-64747412019-04-24 A soil bacterium alters sex determination and rhizoid development in gametophytes of the fern Ceratopteris richardii Ganger, Michael T Hiles, Rachel Hallowell, Haley Cooper, Lauren McAllister, Nicole Youngdahl, Doug Alfieri, Jeremy Ewing, Sarah J AoB Plants Research Article Gametophytes of the fern Ceratopteris richardii develop into either hermaphrodites or males. As hermaphrodites develop, they secrete antheridiogen, or A(CE), into the environment, inducing male development in undifferentiated gametophytes. Hermaphrodites are composed of archegonia, antheridia, rhizoids and a notch meristem, while males consist of antheridia and rhizoids. Much of the research on sexual and morphological development concerns gametophytes grown in sterile environments. Using biochemical and molecular techniques we identify a soil bacterium and explore its effects on sexual and rhizoid development. Hermaphrodite and male gametophytes were exposed to this bacterium and the effects on sexual development, rhizoid length and rhizoid number were explored. The bacterium was identified as a pseudomonad, Pseudomonas nitroreducens. Gametophytes grown in the presence of the pseudomonad were more likely to develop into hermaphrodites across all gametophyte densities. Across all gametophyte sizes, hermaphrodites had rhizoids that were 2.95× longer in the presence of the pseudomonad while males had rhizoids that were 2.72× longer in the presence of the pseudomonad. Both hermaphrodite and male gametophytes developed fewer rhizoids in the presence of the pseudomonad. Control hermaphrodites produced 1.23× more rhizoids across all gametophyte sizes. For male gametophytes grown in the absence of the pseudomonad, the rate of increase in the number of rhizoids was greater with increasing size in the control than the rate of increase in males grown in the presence of the pseudomonad. The pseudomonad may be acting on gametophyte sexual development via several potential mechanisms: degradation of A(CE), changes in nutrient availability or phytohormone production. The pseudomonad may also increase rhizoid number through production of phytohormones or changes in nutrient availability. Oxford University Press 2019-03-14 /pmc/articles/PMC6474741/ /pubmed/31019671 http://dx.doi.org/10.1093/aobpla/plz012 Text en © The Authors 2019. Published by Oxford University Press on behalf of the Annals of Botany Company. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ganger, Michael T
Hiles, Rachel
Hallowell, Haley
Cooper, Lauren
McAllister, Nicole
Youngdahl, Doug
Alfieri, Jeremy
Ewing, Sarah J
A soil bacterium alters sex determination and rhizoid development in gametophytes of the fern Ceratopteris richardii
title A soil bacterium alters sex determination and rhizoid development in gametophytes of the fern Ceratopteris richardii
title_full A soil bacterium alters sex determination and rhizoid development in gametophytes of the fern Ceratopteris richardii
title_fullStr A soil bacterium alters sex determination and rhizoid development in gametophytes of the fern Ceratopteris richardii
title_full_unstemmed A soil bacterium alters sex determination and rhizoid development in gametophytes of the fern Ceratopteris richardii
title_short A soil bacterium alters sex determination and rhizoid development in gametophytes of the fern Ceratopteris richardii
title_sort soil bacterium alters sex determination and rhizoid development in gametophytes of the fern ceratopteris richardii
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474741/
https://www.ncbi.nlm.nih.gov/pubmed/31019671
http://dx.doi.org/10.1093/aobpla/plz012
work_keys_str_mv AT gangermichaelt asoilbacteriumalterssexdeterminationandrhizoiddevelopmentingametophytesofthefernceratopterisrichardii
AT hilesrachel asoilbacteriumalterssexdeterminationandrhizoiddevelopmentingametophytesofthefernceratopterisrichardii
AT hallowellhaley asoilbacteriumalterssexdeterminationandrhizoiddevelopmentingametophytesofthefernceratopterisrichardii
AT cooperlauren asoilbacteriumalterssexdeterminationandrhizoiddevelopmentingametophytesofthefernceratopterisrichardii
AT mcallisternicole asoilbacteriumalterssexdeterminationandrhizoiddevelopmentingametophytesofthefernceratopterisrichardii
AT youngdahldoug asoilbacteriumalterssexdeterminationandrhizoiddevelopmentingametophytesofthefernceratopterisrichardii
AT alfierijeremy asoilbacteriumalterssexdeterminationandrhizoiddevelopmentingametophytesofthefernceratopterisrichardii
AT ewingsarahj asoilbacteriumalterssexdeterminationandrhizoiddevelopmentingametophytesofthefernceratopterisrichardii
AT gangermichaelt soilbacteriumalterssexdeterminationandrhizoiddevelopmentingametophytesofthefernceratopterisrichardii
AT hilesrachel soilbacteriumalterssexdeterminationandrhizoiddevelopmentingametophytesofthefernceratopterisrichardii
AT hallowellhaley soilbacteriumalterssexdeterminationandrhizoiddevelopmentingametophytesofthefernceratopterisrichardii
AT cooperlauren soilbacteriumalterssexdeterminationandrhizoiddevelopmentingametophytesofthefernceratopterisrichardii
AT mcallisternicole soilbacteriumalterssexdeterminationandrhizoiddevelopmentingametophytesofthefernceratopterisrichardii
AT youngdahldoug soilbacteriumalterssexdeterminationandrhizoiddevelopmentingametophytesofthefernceratopterisrichardii
AT alfierijeremy soilbacteriumalterssexdeterminationandrhizoiddevelopmentingametophytesofthefernceratopterisrichardii
AT ewingsarahj soilbacteriumalterssexdeterminationandrhizoiddevelopmentingametophytesofthefernceratopterisrichardii