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A gloved hand holds a labelled specimen bag reading 'Haematobium eggs in 1x PBS, UCSF, Brian Graham'
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SCOPE Lab note · San Francisco

Securing parasitic egg samples in San Francisco

June 14, 2025 · 7 min read
UCSF · Graham Lab

Sometimes the most extraordinary samples come from the most unexpected connections. Through a friend of a friend, we found the lab of Dr. Brian Graham at UCSF — who handed our team one of the stranger gifts in global health research: a vial of Schistosoma haematobium eggs.

This is the story of the S. haematobium eggs we collected at UCSF, carried to another Bay Area lab, and brought all the way back to Houston — and what we plan to do with them. Because they’re killed eggs, they let us study the precise evidence of infection safely, with no risk of live infection and none of the upkeep of a live animal model. That single sample moves us toward our larger goal: accessible diagnostics for rural communities, validated against the exact specimen our tools — like the Foldscope — need to be ready to detect.

For the unfamiliar, S. haematobium is the parasite behind schistosomiasis — also called snail fever, or bilharzia. Its eggs are normally only encountered in clinical samples from infected patients, which makes them critical for diagnostic development yet difficult to obtain in a controlled laboratory setting. Our vial has since been divided into aliquots bound for two research hubs: the Prakash Lab at Stanford’s Shriram Center for Bioengineering, and Dr. Lee’s lab at UTHealth in Houston.

From a many-people-CC’d email thread to a (totally-not) high-security handoff of a globally significant pathogen, this small episode is what frugal science really runs on: serendipity, community, and scientific generosity.

The connector

A friend who connected the dots

Maya Grayck — my dear friend and coworker in Clyde Wright’s lab at CU Anschutz from 2021 to 2023 — joined our team and this project in March. We’re glad to have her for many reasons, but one stands out: without her knack for connecting dots across states, institutions, and labs, we simply would not have access to these samples.

Maya crouches outdoors, looking through a small green Foldscope microscope held to one eye
Maya peers through the Foldscope for the very first time.

In March, Maya got up to speed on a Zoom call with Jim Cybulski, Manu Prakash, and the Health in Your Hands team — and within a few days she realized our worlds overlapped in an unexpected way. Her mother, Dr. Eva Nozik — mentor and friend to so many — had just studied pulmonary hypertension from chronic schistosomiasis in a murine model, alongside Brian Graham, who keeps schisto specimens in his lab at UCSF.

Screenshot of the journal article in Lung Cellular and Molecular Physiology
The paper that connected the dots for us. Read it on PubMed →

Eva is the kind of physician-scientist who studies — at the highest level — just about every nuance of an organ system, so I should have known we’d be seeking her sage advice eventually, given schistosomiasis can reach the lungs: her area of expertise. At that point, I was still naive to that clinical consequence.

Medical illustration of the lungs and pulmonary artery affected by schistosomiasis
Chronic infection can drive pulmonary hypertension.
Diagram of the schistosome life cycle through freshwater snails and a human host
The schistosome life cycle, start to finish.
The science

Why these eggs, specifically?

A fair question we kept getting: why not just use the eggs already in Dr. Lee’s lab — aren’t those good enough? Both S. mansoni and S. haematobium are parasitic flatworms that cause schistosomiasis, but they differ in where they settle in the body, what their eggs look like, and how the disease presents.

S. mansoni

Already in the lab
Target
Intestinal tract & liver
Eggs in
Stool
Presents
Intestinal & hepatic disease

S. haematobium

What we needed
Target
Urogenital system
Eggs in
Urine
Presents
Hematuria; long-term bladder damage & cancer risk

This distinction is critical for diagnostic development. Urine-based diagnostics — especially the low-cost, field-deployable kind we’re building — must be tested using S. haematobium eggs specifically, since they differ in size, shape, and localization from S. mansoni eggs.

Chart comparing the relative size of Schistosoma japonicum, mansoni and haematobium eggs on light microscopy
Relative size of Schistosoma eggs on light microscopy — haematobium’s terminal-spined egg at right.
The mission

A tiny rented car, a big errand

In early April, Maya joined myself, Phillip, and Nehali on a trip to Stanford. Anesta Kothari and Hope Leng — who are working on a low-cost molecular test for schistosomiasis — coached us on how to ask for the eggs and how to transport them. We opted for frozen samples on dry ice.

Maya stands smiling in front of a wall reading 'UCSF Pride Hall'
Maya, en route to secure the eggs.

A couple of days in — realizing time was running short — I asked Phillip and Maya whether they’d take our tiny rented car and run the mission to UCSF without me, while I stayed on campus, another coffee in hand, prototyping and testing the microfluidic trap we were developing. They accepted the mission.

*More on that microfluidic trap in a separate lab note — read it here →
Maya and Phillip stand among tall windswept cypress trees
Maya and Phil between stops on the Bay Area run.
Phillip smiles holding a small styrofoam shipping box on dry ice
Mission complete. Phil returns to the Prakash Lab, eggs on dry ice.
What's next

What we’ll do with them

Here’s the mile-high view of what our Stanford collaborators and friends plan to use the samples for — three reasons these specific eggs matter to the work ahead.

Why we want these eggs in the lab

1

Develop a workable field diagnostic

Prove out a urine-based method a community health worker can run with a Foldscope — far from any formal lab.

2

Build a sustainable workflow

Move from one-off samples toward a repeatable, affordable sample-prep and testing pipeline that holds up in the field.

3

Test Vaibhav's PlanktoScope

Run these samples through an automated imaging setup to help train its model. See the project →

Workflow diagram: freshwater exposure, urine collection, filtration, Foldscope reading, prevalence data
An accessible workflow for diagnosing schistosomiasis — from freshwater exposure to prevalence data. Courtesy of the Prakash Lab.

We’ve joined forces with Vaibhav Shokeen for the current study, and we’re thrilled to be meeting in five weeks in Nigeria. In the next lab note, you’ll see how we use these samples to help train his automated model. More to come — stay tuned, my friends.

A polaroid photo held up in a lab shows five researchers standing together
Hope, Anesta, Manu, Will, and Jim in the Prakash Lab.
Filed under SCOPE
Focus Schistosomiasis · Place San Francisco → Stanford → Houston
Thank you

You’ve launched us into 40%-funded territory.

Thank you for seeing the vision — a future with accessible diagnostic solutions to this neglected tropical disease. Please feel free to share these lab notes with any friends, family, or colleagues who’d want a look behind the scenes of what this work takes.

40% funded