PIPages
Labs

Rustem Ismagilov

California Institute of Technology, CA·Microbiology & Immunology

Microbes living inside human tissues and fluids influence immunity, barrier function and metabolism, yet they are extraordinarily hard to study where they actually reside. In a biopsy or a milk sample, human genetic material can outnumber microbial material a thousand to one, fragile microbial RNA degrades quickly, and reagent contamination can masquerade as a real organism.

Fields

Microbiology & Immunology

Biomedical Engineering

Chemistry

Topics

microbiome

metatranscriptomics

metagenomics

Grants
4 known grants, through Jun 2030

What they work on

  1. Optimize T-BEAM in germ-free tissue spiked with defined bacteria, targeting over 1,000-fold removal of host nucleic acids while preserving bacterial transcriptional profiles and RNA yield.
  2. Establish detection and quantification limits for T-BEAM in vivo using mice colonized by a single bacterial species and by hCom2, a defined human-derived gut community.
  3. Apply T-BEAM to biopsies from patients with subclinical perianal Crohn's disease and matched controls to find joint microbial and host expression patterns that predict radiological progression.
  4. Develop and validate MEM, a microbial enrichment and metagenomic sequencing method, using defined communities and milk-derived isolates to recover whole bacterial, archaeal and fungal genomes while excluding reagent contaminants.
  5. Apply MEM to repeated paired breast milk and stool samples from full-term and pre-term mother-infant dyads to assess milk microbiome stability and candidate transmission routes.
  6. Optimize FRAMES using differential lysis, RNase treatment and chemical fixation on vaginal swabs, verifying host RNA depletion and fungal transcript recovery by digital PCR and RNA sequencing.
  7. Use FRAMES across the menstrual cycle and in a recurrent vulvovaginal candidiasis cohort to identify Candida and human gene-expression signatures that separate benign colonization from disease.
  8. Create Viral-MEM for particle-independent viral enrichment from host-heavy tissue and Viral StochQuant for absolute, anchored viral quantification, validating both in vaginal swabs, saliva with small-intestine biopsies, and paired lower gastrointestinal biopsies.

More about the research

Four technology projects attack these measurement problems, each pairing a new sample-preparation and sequencing workflow with a human health question that the workflow is designed to answer.

Why it matters

Trustworthy measurements of what microbes are doing inside human tissue could expose targets for diagnostics and therapies in diseases where tissue-associated microbes are suspected but unproven, including inflammatory bowel disease, colorectal cancer, Parkinson's disease and periodontitis. Women with recurrent yeast infections could gain tests that distinguish colonization from disease, and infants, especially pre-term ones at risk of necrotizing enterocolitis and sepsis, could benefit from clearer evidence on milk-borne microbes and probiotic strain choice.

Known grants

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

Bacterial Metatranscriptomics from Human Tissues to Resolve Contributions of Host and Microbial Pathways to Health and Disease

NIH · Aug 2026 – Jun 2030

Technology for Longitudinal Whole-Genome Characterization of Term and Pre-Term Breast Milk Microbiomes

NIH · Aug 2026 – Jul 2028

Viral MEM: Viral Enrichment and Precise Stochastic Quantification with Microbial Context Preservation for Rigorous Virome Analysis of Challenging Human Samples

NIH · Sep 2024 – Jun 2028

Closest labs

June Louise Round

University of Utah, UT·Microbiology & Immunology

Catalog which commensal viruses in stool from healthy humans are bound by mucosal IgA and IgG antibodies, by purifying and sorting antibody-coated DNA and RNA viral particles.

Xin Li

University of Texas Southwestern Medical Center, TX·Microbiology & Immunology·Early-career

Determine how fungal stimulatory RNA (fsRNA), a newly identified fungal RNA, triggers innate immune responses in the intestine, using fungal genetic engineering and long-read RNA sequencing.

Karen Norris

University of Georgia, GA·Microbiology & Immunology

Test whether the NXT-2 vaccine, a lab-made peptide based on a fungal protein shared across species, triggers strong immune responses in nonhuman primates.

The school

California Institute of Technology: 18 labs on PI Pages, $445M a year on research, 200 research doctorates a year.

More about California Institute of Technology

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