PIPages
Labs

Jay Lennon

Indiana University, IN·Microbiology & Immunology

When growth conditions turn bad, many microbes go dormant, entering a reversible state of very low metabolic activity. Dormancy has long been seen as a way to survive starvation, extreme temperatures or antimicrobial drugs, but it also changes how microbes interact with the viruses that infect them.

Fields

Microbiology & Immunology

Ecology & Evolution

Biology

Topics

microbial dormancy

sporulation

bacterial spores

Grants
1 known grant, through Dec 2030

What they work on

  1. Test competing models of how phage genomes become entrapped in Bacillus subtilis spores, using CRISPR editing of viral auxiliary sporulation genes and single-cell assays to assess suppression of the lytic cycle and chromosome segregation.
  2. Determine how entrapment changes spore development by profiling host and virus gene expression with single-cell transcriptomics and analyzing cell morphology with AI-informed methods.
  3. Track the fate of infected spores, or "virospores," in a microfluidic platform to quantify entrapment dynamics and its fitness consequences for both bacterium and phage.
  4. Integrate experimental data with mechanistic models to explain how viruses and hosts make infection and dormancy decisions in fluctuating, uncertain environments.

More about the research

Dormancy can shield a cell from infection, yet some viruses have evolved ways around this defense, which raises the question of how these two strategies coevolve.

Why it matters

Dormant microbial stages make infections hard to clear, since both spores and quiescent cells can evade treatment. Clarifying how viral genomes hide inside spores and reawaken could inform phage therapy, which uses viruses to kill bacteria, for chronic infections caused by spore-forming bacteria and other microbes with quiescent life stages, and it extends basic theory about host–pathogen coevolution.

Known grants

From NIH and NSF research grants. Labs often have other funding we can't see.

Cell dormancy and virus entrapment

NIH · Mar 2026 – Dec 2030

Closest labs

Paul Kirchberger

Oklahoma State University, OK·Microbiology & Immunology

Compare the mechanisms of superinfection exclusion, by which a resident prophage blocks other viruses, across independently evolved microvirus prophages, a putative defense system and lytic microviruses that may have supplied its evolutionary precursors.

Elizabeth Libby

Northeastern University, MA·Microbiology & Immunology

Quantitatively dissect how conserved Hanks-type serine/threonine kinase–phosphatase systems in Bacillus subtilis are wired, and how that architecture generates rare single cells with extreme phenotypes such as antibiotic resistance.

Seunghyun Sim

University of California-Irvine, CA·Chemistry·Early-career

Build a high-throughput screen for enzyme activity using fluorescence-activated cell sorting, an instrument that sorts single particles by brightness, together with engineered chemical probes that fluoresce only when the displayed enzyme turns over its substrate.

The school

Indiana University: 21 labs on PI Pages, $897M a year on research, 438 research doctorates a year.

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