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Cysteine synthases CYSL-1 and CYSL-2 mediate C. elegans heritable adaptation to P. vranovensis infection

Published version
Peer-reviewed

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Authors

Burton, nick 
Riccio, Cristian 
Dallaire, Alexandra  ORCID logo  https://orcid.org/0000-0003-1097-7766
Jenkins, Benjamin 

Abstract

Parental exposure to pathogens can prime offspring immunity in diverse organisms. The mechanisms by which this heritable priming occurs are largely unknown. Here we report that the soil bacteria Pseudomonas vranovensis is a natural pathogen of the nematode Caenorhabditis elegans and that parental exposure of animals to P. vranovensis promotes offspring resistance to infection. Furthermore, we demonstrate a multigenerational enhancement of progeny survival when three consecutive generations of animals are exposed to P. vranovensis. By investigating the mechanisms by which animals heritably adapt to P. vranovensis infection, we found that parental infection by P. vranovensis results in increased expression of the cysteine synthases cysl-1 and cysl-2 and the regulator of hypoxia inducible factor rhy-1 in progeny, and that these three genes are required for adaptation to P. vranovensis. These observations establish a CYSL-1, CYSL-2, and RHY-1 dependent mechanism by which animals heritably adapt to infection.

Description

Keywords

Adaptation, Physiological, Animals, Caenorhabditis elegans, Caenorhabditis elegans Proteins, Cysteine Synthase, Embryo, Nonmammalian, Gene Expression Regulation, Developmental, Inheritance Patterns, Models, Biological, Pseudomonas

Journal Title

Nature Communications

Conference Name

Journal ISSN

2041-1723
2041-1723

Volume Title

Publisher

Springer Nature
Sponsorship
Biotechnology and Biological Sciences Research Council (BB/M027252/1)
Wellcome Trust (104640/Z/14/Z)
Wellcome Trust (092096/Z/10/Z)
Cancer Research UK (C6946/A24843)
Cancer Research Uk (None)
Cancer Research UK (18583)
Biotechnology and Biological Sciences Research Council (BB/M027252/2)
MRC (MC_UU_00014/5)
Medical Research Council (MC_UU_12012/5)
Medical Research Council (MC_PC_12012)
BBSRC grant BB/M027252/1