TY - JOUR
T1 - Retrotransposon-mediated evolutionary rewiring of a pathogen response orchestrates a resistance phenotype in an insect host
AU - Guo, Zhaojiang
AU - Guo, Le
AU - Bai, Yang
AU - Kang, Shi
AU - Sun, Dan
AU - Qin, Jianying
AU - Ye, Fan
AU - Wang, Shaoli
AU - Wu, Qingjun
AU - Xie, Wen
AU - Yang, Xin
AU - Crickmore, Neil
AU - Zhou, Xuguo
AU - Zhang, Youjun
N1 - Publisher Copyright:
Copyright © 2023 the Author(s).
PY - 2023
Y1 - 2023
N2 - Ongoing host–pathogen interactions can trigger a coevolutionary arms race, while genetic diversity within the host can facilitate its adaptation to pathogens. Here, we used the diamondback moth (Plutella xylostella) and its pathogen Bacillus thuringiensis (Bt) as a model for exploring an adaptive evolutionary mechanism. We found that insect host adaptation to the primary Bt virulence factors was tightly associated with a short interspersed nuclear element (SINE - named SE2) insertion into the promoter of the transcriptionally activated MAP4K4 gene. This retrotransposon insertion coopts and potentiates the effect of the transcription factor forkhead box O (FOXO) in inducing a hormone-modulated Mitogen-activated protein kinase (MAPK) signaling cascade, leading to an enhancement of a host defense mechanism against the pathogen. This work demonstrates that reconstructing a cis–trans interaction can escalate a host response mechanism into a more stringent resistance phenotype to resist pathogen infection, providing a new insight into the coevolutionary mechanism of host organisms and their microbial pathogens.
AB - Ongoing host–pathogen interactions can trigger a coevolutionary arms race, while genetic diversity within the host can facilitate its adaptation to pathogens. Here, we used the diamondback moth (Plutella xylostella) and its pathogen Bacillus thuringiensis (Bt) as a model for exploring an adaptive evolutionary mechanism. We found that insect host adaptation to the primary Bt virulence factors was tightly associated with a short interspersed nuclear element (SINE - named SE2) insertion into the promoter of the transcriptionally activated MAP4K4 gene. This retrotransposon insertion coopts and potentiates the effect of the transcription factor forkhead box O (FOXO) in inducing a hormone-modulated Mitogen-activated protein kinase (MAPK) signaling cascade, leading to an enhancement of a host defense mechanism against the pathogen. This work demonstrates that reconstructing a cis–trans interaction can escalate a host response mechanism into a more stringent resistance phenotype to resist pathogen infection, providing a new insight into the coevolutionary mechanism of host organisms and their microbial pathogens.
KW - Bacillus thuringiensis
KW - FOXO transcription factor
KW - Plutella xylostella
KW - genetic variation
KW - retrotransposon
UR - http://www.scopus.com/inward/record.url?scp=85151573480&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85151573480&partnerID=8YFLogxK
U2 - 10.1073/PNAS.2300439120
DO - 10.1073/PNAS.2300439120
M3 - Article
C2 - 36996102
AN - SCOPUS:85151573480
SN - 0027-8424
VL - 120
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 14
M1 - e2300439120
ER -