
Immune lag is a major cost of prokaryotic adaptive immunity during viral outbreaks
Author(s) -
Jake L. Weissman,
Ellinor Alseth,
Sean Meaden,
Edze R. Westra,
Jed A. Fuhrman
Publication year - 2021
Publication title -
proceedings - royal society. biological sciences/proceedings - royal society. biological sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.342
H-Index - 253
eISSN - 1471-2954
pISSN - 0962-8452
DOI - 10.1098/rspb.2021.1555
Subject(s) - biology , crispr , immune system , acquired immune system , immunity , virology , virus , host (biology) , computational biology , immunology , genetics , gene
Clustered regularly interspaced short palindromic repeat (CRISPR)-Cas adaptive immune systems enable bacteria and archaea to efficiently respond to viral pathogens by creating a genomic record of previous encounters. These systems are broadly distributed across prokaryotic taxa, yet are surprisingly absent in a majority of organisms, suggesting that the benefits of adaptive immunity frequently do not outweigh the costs. Here, combining experiments and models, we show that a delayed immune response which allows viruses to transiently redirect cellular resources to reproduction, which we call ‘immune lag’, is extremely costly during viral outbreaks, even to completely immune hosts. Critically, the costs of lag are only revealed by examining the early, transient dynamics of a host–virus system occurring immediately after viral challenge. Lag is a basic parameter of microbial defence, relevant to all intracellular, post-infection antiviral defence systems, that has to-date been largely ignored by theoretical and experimental treatments of host-phage systems.