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1.
Proc Natl Acad Sci U S A ; 117(35): 21459-21468, 2020 09 01.
Article in English | MEDLINE | ID: mdl-32817436

ABSTRACT

Animal development has traditionally been viewed as an autonomous process directed by the host genome. But, in many animals, biotic and abiotic cues, like temperature and bacterial colonizers, provide signals for multiple developmental steps. Hydra offers unique features to encode these complex interactions of developmental processes with biotic and abiotic factors, and we used it here to investigate the impact of bacterial colonizers and temperature on the pattern formation process. In Hydra, formation of the head organizer involves the canonical Wnt pathway. Treatment with alsterpaullone (ALP) results in acquiring characteristics of the head organizer in the body column. Intriguingly, germfree Hydra polyps are significantly more sensitive to ALP compared to control polyps. In addition to microbes, ß-catenin-dependent pattern formation is also affected by temperature. Gene expression analyses led to the identification of two small secreted peptides, named Eco1 and Eco2, being up-regulated in the response to both Curvibacter sp., the main bacterial colonizer of Hydra, and low temperatures. Loss-of-function experiments revealed that Eco peptides are involved in the regulation of pattern formation and have an antagonistic function to Wnt signaling in Hydra.


Subject(s)
Hydra/genetics , Hydra/metabolism , beta Catenin/metabolism , Animals , Bacteria/metabolism , Body Patterning/genetics , Gene Expression Regulation, Developmental/genetics , Gene-Environment Interaction , Hydra/physiology , Peptides/metabolism , Temperature , Wnt Proteins/metabolism , Wnt Signaling Pathway/genetics , Wnt Signaling Pathway/physiology
2.
Proc Natl Acad Sci U S A ; 117(30): 17854-17863, 2020 07 28.
Article in English | MEDLINE | ID: mdl-32647059

ABSTRACT

Pacemaker neurons exert control over neuronal circuit function by their intrinsic ability to generate rhythmic bursts of action potential. Recent work has identified rhythmic gut contractions in human, mice, and hydra to be dependent on both neurons and the resident microbiota. However, little is known about the evolutionary origin of these neurons and their interaction with microbes. In this study, we identified and functionally characterized prototypical ANO/SCN/TRPM ion channel-expressing pacemaker cells in the basal metazoan Hydra by using a combination of single-cell transcriptomics, immunochemistry, and functional experiments. Unexpectedly, these prototypical pacemaker neurons express a rich set of immune-related genes mediating their interaction with the microbial environment. Furthermore, functional experiments gave a strong support to a model of the evolutionary emergence of pacemaker cells as neurons using components of innate immunity to interact with the microbial environment and ion channels to generate rhythmic contractions.


Subject(s)
Biological Clocks , Hydra/physiology , Microbiota , Neurons/physiology , Action Potentials , Animals , Biological Evolution , Cluster Analysis , Computational Biology/methods , Gene Expression Profiling , Gene Expression Regulation , Genome-Wide Association Study , Humans , Mice
3.
ISME J ; 9(7): 1543-56, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25514534

ABSTRACT

Epithelial surfaces of most animals are colonized by diverse microbial communities. Although it is generally agreed that commensal bacteria can serve beneficial functions, the processes involved are poorly understood. Here we report that in the basal metazoan Hydra, ectodermal epithelial cells are covered with a multilayered glycocalyx that provides a habitat for a distinctive microbial community. Removing this epithelial microbiota results in lethal infection by the filamentous fungus Fusarium sp. Restoring the complex microbiota in gnotobiotic polyps prevents pathogen infection. Although mono-associations with distinct members of the microbiota fail to provide full protection, additive and synergistic interactions of commensal bacteria are contributing to full fungal resistance. Our results highlight the importance of resident microbiota diversity as a protective factor against pathogen infections. Besides revealing insights into the in vivo function of commensal microbes in Hydra, our findings indicate that interactions among commensal bacteria are essential to inhibit pathogen infection.


Subject(s)
Bacteria/classification , Fungi/physiology , Hydra/microbiology , Animals , Epithelial Cells , Host-Pathogen Interactions , Symbiosis
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