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Dissection of the in vitro developmental program of Hammondia hammondi reveals a link between stress sensitivity and life cycle flexibility in Toxoplasma gondii

Most eukaryotic parasites are obligately heteroxenous, requiring sequential infection of different host species in order to survive. Toxoplasma gondii is a rare exception to this rule, having a uniquely facultative heteroxenous life cycle. To understand the origins of this phenomenon, we compared de...

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Autores principales: Sokol, Sarah L, Primack, Abby S, Nair, Sethu C, Wong, Zhee S, Tembo, Maiwase, Verma, Shiv K, Cerqueira-Cezar, Camila K, Dubey, JP, Boyle, Jon P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5963921/
https://www.ncbi.nlm.nih.gov/pubmed/29785929
http://dx.doi.org/10.7554/eLife.36491
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author Sokol, Sarah L
Primack, Abby S
Nair, Sethu C
Wong, Zhee S
Tembo, Maiwase
Verma, Shiv K
Cerqueira-Cezar, Camila K
Dubey, JP
Boyle, Jon P
author_facet Sokol, Sarah L
Primack, Abby S
Nair, Sethu C
Wong, Zhee S
Tembo, Maiwase
Verma, Shiv K
Cerqueira-Cezar, Camila K
Dubey, JP
Boyle, Jon P
author_sort Sokol, Sarah L
collection PubMed
description Most eukaryotic parasites are obligately heteroxenous, requiring sequential infection of different host species in order to survive. Toxoplasma gondii is a rare exception to this rule, having a uniquely facultative heteroxenous life cycle. To understand the origins of this phenomenon, we compared development and stress responses in T. gondii to those of its its obligately heteroxenous relative, Hammondia hammondi and have identified multiple H. hammondi growth states that are distinct from those in T. gondii. Of these, the most dramatic difference was that H. hammondi was refractory to stressors that robustly induce cyst formation in T. gondii, and this was reflected most dramatically in its unchanging transcriptome after stress exposure. We also found that H. hammondi could be propagated in vitro for up to 8 days post-excystation, and we exploited this to generate the first ever transgenic H. hammondi line. Overall our data show that H. hammondi zoites grow as stringently regulated, unique life stages that are distinct from T. gondii tachyzoites, and implicate stress sensitivity as a potential developmental innovation that increased the flexibility of the T. gondii life cycle.
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spelling pubmed-59639212018-05-24 Dissection of the in vitro developmental program of Hammondia hammondi reveals a link between stress sensitivity and life cycle flexibility in Toxoplasma gondii Sokol, Sarah L Primack, Abby S Nair, Sethu C Wong, Zhee S Tembo, Maiwase Verma, Shiv K Cerqueira-Cezar, Camila K Dubey, JP Boyle, Jon P eLife Microbiology and Infectious Disease Most eukaryotic parasites are obligately heteroxenous, requiring sequential infection of different host species in order to survive. Toxoplasma gondii is a rare exception to this rule, having a uniquely facultative heteroxenous life cycle. To understand the origins of this phenomenon, we compared development and stress responses in T. gondii to those of its its obligately heteroxenous relative, Hammondia hammondi and have identified multiple H. hammondi growth states that are distinct from those in T. gondii. Of these, the most dramatic difference was that H. hammondi was refractory to stressors that robustly induce cyst formation in T. gondii, and this was reflected most dramatically in its unchanging transcriptome after stress exposure. We also found that H. hammondi could be propagated in vitro for up to 8 days post-excystation, and we exploited this to generate the first ever transgenic H. hammondi line. Overall our data show that H. hammondi zoites grow as stringently regulated, unique life stages that are distinct from T. gondii tachyzoites, and implicate stress sensitivity as a potential developmental innovation that increased the flexibility of the T. gondii life cycle. eLife Sciences Publications, Ltd 2018-05-22 /pmc/articles/PMC5963921/ /pubmed/29785929 http://dx.doi.org/10.7554/eLife.36491 Text en http://creativecommons.org/publicdomain/zero/1.0/ http://creativecommons.org/publicdomain/zero/1.0/This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (http://creativecommons.org/publicdomain/zero/1.0/) .
spellingShingle Microbiology and Infectious Disease
Sokol, Sarah L
Primack, Abby S
Nair, Sethu C
Wong, Zhee S
Tembo, Maiwase
Verma, Shiv K
Cerqueira-Cezar, Camila K
Dubey, JP
Boyle, Jon P
Dissection of the in vitro developmental program of Hammondia hammondi reveals a link between stress sensitivity and life cycle flexibility in Toxoplasma gondii
title Dissection of the in vitro developmental program of Hammondia hammondi reveals a link between stress sensitivity and life cycle flexibility in Toxoplasma gondii
title_full Dissection of the in vitro developmental program of Hammondia hammondi reveals a link between stress sensitivity and life cycle flexibility in Toxoplasma gondii
title_fullStr Dissection of the in vitro developmental program of Hammondia hammondi reveals a link between stress sensitivity and life cycle flexibility in Toxoplasma gondii
title_full_unstemmed Dissection of the in vitro developmental program of Hammondia hammondi reveals a link between stress sensitivity and life cycle flexibility in Toxoplasma gondii
title_short Dissection of the in vitro developmental program of Hammondia hammondi reveals a link between stress sensitivity and life cycle flexibility in Toxoplasma gondii
title_sort dissection of the in vitro developmental program of hammondia hammondi reveals a link between stress sensitivity and life cycle flexibility in toxoplasma gondii
topic Microbiology and Infectious Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5963921/
https://www.ncbi.nlm.nih.gov/pubmed/29785929
http://dx.doi.org/10.7554/eLife.36491
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