Deciphering the molecular mechanisms of bacterial growth.

The Bernhardt lab studies how bacteria build and remodel their cell envelopes with the goal of enhancing our fundamental understanding of bacterial growth. The knowledge gained will enable the development of novel antibiotics to combat the global threat of drug resistant bacterial infections.

Affiliated with

Harvard Medical School Department of Microbiology Howard Hughes Medical Institute

About The Lab

Fundamental microbiology with translational relevance.

Core question

How do bacteria coordinate the assembly of their membranes, cell wall, and other surface layers to maintain cellular integrity and prevent the entry of antibiotics and other toxic compounds?

Why this matters

Many of our most effective antibiotics like penicillin and related drugs target the assembly of the bacterial cell wall. This wall and its associated surface layers also prevent antibiotic entry and contribute to the intrinsic drug resistance of bacteria. Defining the mechanisms of bacterial surface assembly therefore has the potential to identify new vulnerabilities in the bacterial growth program to target for antibiotic development and/or to resensitize resistant organisms to existing therapies.

How we work

We combine classical and modern bacterial genetics with biochemistry and advanced imaging methods across diverse bacterial species to uncover new insights into the mechanisms that promote bacterial growth and the integrity of their cell surface.

Education And Outreach

Community Phages Program

The lab runs the HMS Community Phages Program, which engages students in phage discovery and host-pathogen biology through hands-on research experiences.

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Team

Meet the team.

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Team directory

Browse the full directory for current lab members, research interests, and profile pages.

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Thomas Bernhardt

Professor in the Department of Microbiology at Harvard Medical School and Investigator of the Howard Hughes Medical Institute.

Thomas Bernhardt

The Bernhardt lab studies molecular mechanisms of bacterial growth and cell wall assembly to inform antibiotic discovery.

James Spencer

Laboratory Manager, Thomas Bernhardt Lab

James Spencer

Research operations lead for the Bernhardt and Abraham HHMI labs at HMS, overseeing finance, hiring, procurement, compliance, and lab infrastructure, and supporting HMS Community Phages.

Kathy Suarez

BBS Graduate Student

Kathy Suarez

I am interested in examining the function of cell wall synthesis in E. coli.

Betsy Hart

Postdoctoral Fellow

Betsy Hart

I am interested in cell envelope biogenesis in Corynebacterium glutamicum.

Johnathan Kepple

BPH Graduate Student

Johnathan Kepple

The general aim of my research is to understand the regulation of cell wall synthesis in the Gram-negative bacterium Pseudomonas aeruginosa.

Wanassa Beroual

Postdoctoral Fellow

Wanassa Beroual

I am interested in cell wall biogenesis in Corynebacterium glutamicum.

Anastacia Parks

Postdoctoral Fellow

Anastacia Parks

I am interested in understanding the role mannosylation plays in the membrane of Corynebacterium glutamicum.

Wilaysha Evans

ChemBio Graduate Student

Wilaysha Evans

I am most interested in understanding the mechanisms that underpin bacterial cell shape and division. More specifically, in the Bernhardt lab, I study some of the mechanisms by which cell wall integrity in Corynebacterium glutamicum is maintained.

Nilanjan Som

Postdoctoral Fellow

Nilanjan Som

I am interested in understanding the regulatory mechanisms that drive Gram-negative bacterial cell envelope expansion.

Tien Nguyen

MCO Graduate Student

Tien Nguyen

I am interested in studying the regulation of peptidoglycan hydrolysis during cell division in Escherichia coli, with a focus on mechanisms that control hydrolases and their activators for proper PG cleavage.

Dylan Burgin

BBS Graduate Student

Dylan Burgin

I am interested in studying the mechanisms that contribute to outer membrane integrity in Gram-negative bacteria.

Shailab Shrestha

Postdoctoral Fellow

Shailab Shrestha

I am interested in the biogenesis and maintenance of the Gram-negative cell envelope.

Vincent de Bakker

Postdoctoral Fellow

Vincent de Bakker

I work at the intersection of quantitative and fundamental microbiology. In that context, I'm currently implementing CRISPR interference techniques to study cell envelope biogenesis in Corynebacterium glutamicum.

Nazgul Sakenova

Postdoctoral Fellow

Nazgul Sakenova

I am interested in special protein localization and factors that determine it in Escherichia coli.

Abel Rodriguez

Undergraduate Researcher

Abel Rodriguez

I am interested in determining novel players in mycolic acid transport.

Eleanor Rand

Postdoctoral Fellow

Eleanor Rand

I am interested in using phages to learn more about their bacterial hosts. I also lead the Community Phages program (phages.hms.harvard.edu)!

Ophelia Lee

BBS Graduate Student

Ophelia Lee

I am interested in mycolic acid transport and regulation in Corynebacterium glutamicum.

James Warner

Postdoctoral Fellow

James Warner

I want to understand how the pathogen Staphylococcus aureus coordinates the synthesis of its cell envelope to escape antibiotic killing.

Taran Bauer

BBS Graduate Student

Taran Bauer

I am interested in uncovering the downstream regulatory mechanisms of the envelope stress response and how this relates to lipid transport. My larger goal is to uncover novel functions of the envelope stress signal to characterize how E. coli and other species maintain membrane integrity.

Research In Motion

A dividing bacterial cell in real time.

Featured video shows bacterial growth, division, and envelope stress responses as they happen.

Featured Video

Inside the Bernhardt Lab research program

A short video overview of how the lab studies bacterial envelope growth and division, and why these mechanisms matter for antimicrobial strategy.

Captions are enabled in the player.

Watch on YouTube
Read video transcript

The Bernhardt Lab investigates how bacteria build, maintain, and remodel their cell envelopes during growth and division. The video highlights live-cell microscopy and genetics approaches used to map where and when envelope machinery is active.

It explains how coupling synthesis with regulated hydrolysis is essential for accurate cytokinesis, how stress-response pathways protect envelope integrity, and why these mechanisms create opportunities to identify vulnerable nodes for antibiotic development.

The featured examples span model organisms and clinically important pathogens, connecting basic envelope biology to broader antimicrobial strategy and resistance-focused research.

Transcript reviewed March 16, 2026.

Live-cell dynamics Fluorescence architecture Cryo-ET + EM Division-site dynamics

Publication Archive

Selected Bernhardt Lab Publications

  1. The aPBP-type cell wall synthase PBP1b plays a specialized role in fortifying the Escherichia coli division site against osmotic rupture

    Shows that PBP1b fortifies the division site against osmotic rupture during cytokinesis.

    bioRxiv (2025)

  2. The mycomembrane proteins PorH and ProtX are inserted at polar growth zones and linked to the cell wall

    Links PorH and ProtX insertion to polar growth and cell-wall connectivity in the corynebacterial mycomembrane.

    bioRxiv (2025)

  3. Using fluorescently labeled wheat germ agglutinin to track lipopolysaccharide transport to the outer membrane in Escherichia coli

    Introduces a direct live-cell readout for lipopolysaccharide trafficking into the outer membrane.

    mBio (2025)

  4. Synthesis of lipid-linked precursors of the bacterial cell wall is governed by a feedback control mechanism in Pseudomonas aeruginosa

    Reveals feedback control over lipid-linked precursor synthesis in Pseudomonas aeruginosa cell-wall biogenesis.

    Nature Microbiology (2024)

  5. A role for the Gram-negative outer membrane in bacterial shape determination

    Demonstrates that the Gram-negative outer membrane contributes directly to bacterial shape determination.

    PNAS (2023)

  6. Phage resistance profiling identifies new genes required for biogenesis and modification of the corynebacterial cell envelope

    Uses phage resistance profiling to uncover new genes required for corynebacterial envelope biogenesis and modification.

    eLife (2022)

View Complete PubMed Bibliography

Featured Alumni

Where Bernhardt lab alumni are now.

Browse Full Alumni Directory

Roles are based on Bernhardt lab records and public institutional profiles (updated March 17, 2026). Request an update or removal. Include your name, entry URL, and requested correction/removal.

Contact

Thomas Bernhardt Lab

Department of Microbiology
Harvard Medical School
Boston, MA 02115

Email: thomas_bernhardt [at] hms.harvard.edu

Contact The Lab

Harvard Medical School, 77 Avenue Louis Pasteur, Boston.

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Training opportunities

If you are looking for training opportunities at any level, please contact us about potential openings.

  • Postdoctoral fellows
  • Graduate students
  • Undergraduate researchers

A short note about your interests, training stage, and timing is helpful.

Collaborators

Collaborator Network

The Bernhardt Lab works with complementary HMS and Harvard groups across microbiology, chemistry, structure, and single-molecule biophysics.

Lab Arcade

Envelope Escape: Stress Test Chamber

Move with WASD or the arrow keys, drag on touch, and press Space to induce the envelope stress response.

Envelope Stress Assay
Score 0
Time 0:00
Dominant pressure Homeostatic load

Sparse hazards. Gather envelope factors and stabilize PG assembly.

Integrity 100%
Assembly 0 / 4
Response 0%

Envelope Stress Assay

Keep the envelope intact.

Collect envelope biogenesis factors, restore PG assembly, and outlast phages, beta-lactam pulses, and autolysin breaches.

Balanced envelope-biogenesis profile for learning the flow.

Collect envelope assembly units, then induce the stress response when the meter is full.

  • Difficulty rises slowly, so clean movement matters more than memorizing patterns.
Species trait Envelope homeostasis

Envelope factors charge the stress-response meter a little faster.

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