NLM DIR Seminar Schedule
UPCOMING SEMINARS
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June 3, 2025 MG Hirsch
Interactions among subclones and immunity controls melanoma progression -
June 10, 2025 Aleksandra Foerster
TBD -
June 17, 2025 Yoshitaka Inoue
TBD -
June 19, 2025 Ermin Hodzic
TBD -
June 24, 2025 Leslie Ronish
TBD
RECENT SEMINARS
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May 29, 2025 Harutyun Sahakyan
In silico evolution of globular protein folds from random sequences -
May 20, 2025 Ajith Pankajam
A roadmap from single cell to knowledge graph -
May 2, 2025 Pascal Mutz
Characterization of covalently closed cirular RNAs detected in (meta)transcriptomic data -
May 2, 2025 Dr. Lang Wu
Integration of multi-omics data in epidemiologic research -
April 22, 2025 Stanley Liang, PhD
Large Vision Model for medical knowledge adaptation
Scheduled Seminars on March 4, 2025
In-person: Building 38A/B2N14 NCBI Library or Meeting Link
Contact NLMDIRSeminarScheduling@mail.nih.gov with questions about this seminar.
Abstract:
Prokaryotes can acquire antivirus immunity via two fundamentally distinct types of processes: direct interaction with the virus as in CRISPR-Cas adaptive immunity systems and horizontal transfer of defense genes which is the main route of transmission of innate immunity systems. These routes of defense evolution are not mutually exclusive and may operate simultaneously, but empirical observations suggest that at least in some bacterial and archaeal species, one or the other dominates the defense landscape. We hypothesized that the observed dichotomy is due to the different life-history tradeoffs characteristic of these organisms. To test this hypothesis, we analyzed a mathematical model of a well-mixed population of prokaryotes under a stochastically changing viral load. Optimization of the long-term growth rate of the population reveals two contrasting modes of defense evolution. In a stable, predictable and fluctuating, unpredictable environments with a moderate viral load, adaptive immunity and horizontal transfer of defense genes become the optimal routes of immunity acquisition, respectively. In the HGT-dominant mode, we observe a universal distribution of the fraction of microbes possessing different immune repertoires. Under very low virus load, the cost of immunity exceeds its benefits such that the optimal state of a prokaryote is carrying no defense systems at all. By contrast, under very high virus load, horizontal spread of defense systems dominates regardless of the stability of the environments. These findings seem to explain some consistently observed but enigmatic patterns in the spread of antivirus defense systems among prokaryotes such as the ubiquity of adaptive immunity in hyperthermophiles contrasting their patchy distribution among mesophiles.