When Meghan Martin 21, a biochemistry and American Sign Language double major, was a sophomore in high school, she began experiencing intense, chronic pain. An avid runner and soccer player, she was crippled by cramps, nausea, and back spasms that left her unable to participate in the sports she loved.
Ive always been really active, but I would go to practice, and then I would come home and have to lay down because my back would be spasming so badly, Martin says. I would start throwing up because I was so nauseous and in so much pain.
Initially when she sought help, her doctor told her it was just period cramps and that she should take aspirin and get additional rest. Her mother, however, sensed there was something more going on. After some online research, she found that her daughter was exhibiting symptoms characteristic of endometriosis, a chronic disease in which tissue similar to the tissue that normally lines the inside of the uterus grows outside the uterine cavity.
The only way to know for sure if Martin had the disorder, however, was for her to undergo surgery.
When I heard I had to get surgery to figure this out I was like No, I dont want to do this, Martin says. Ive had surgery before for other things, but it was my senior year of high school at that point. I was thinking, This sounds ridiculous, Ive never even heard of endometriosis.
Today, approximately 1 in 10 women worldwide are affected by endometriosis during their reproductive years, yet invasive laparoscopic surgery is the only current technique used to diagnoseand then treatthe disease. Because of a lack of awareness of the condition and of research in the field, many women can experience a delay in diagnosis of up to 11 years from the onset of symptoms. That can mean several years of pelvic pain, severe cramps, and possible infertility while endometrial-like tissue grows outside of the uterus.
Problem-solving with synthetic biology to create an endometriosis test
Early in 2020, Rochester
launched a class composed of 12 undergraduates to compete in a worldwide synthetic biology competition with the goal to solve a real-world problem using innovative biological ideas. (Synthetic biology involves creating new biological parts or systems using materials already found in nature.) During the iGEM competitionthis year held November 1421the undergraduates present to a panel of judges the projects they have designed and implemented.
Martin was a member of Rochesters iGEM team and, based on her own experience, suggested the group tackle as their project the difficult problem of endometriosis diagnosis.
I thought of endometriosis because it was a big problem for me, and I knew it was an area that didnt have a lot of significant research, but that needed significant research, she says.
Rochesters iGEM team is advised by Anne S. Meyer, an associate professor of biology, who served as an advisor for iGEM teams at Delft University in the Netherlands, where she taught before coming to Rochester. Under her direction, the Delft University iGEM teams received many notable awards, including the grand prize at the iGEM competition in 2015.
iGEM is so unique as a research experience for undergraduates, since the students come up with a project of their own choosing, Meyer says. iGEM projects only run for nine months, which is a very short time to brainstorm, plan, and execute a brand-new scientific project.
COVID-19 presents a unique challenge
After deciding that endometriosis would be the subject of their project, the Rochester iGEM team spent the following months developing a novel endometriosis test for diagnosing the disease.
When COVID-19 hit at the beginning of the year, the team was met with additional challenges as they were forced to conduct the majority of their research online and hold meetings via Zoom. They also did not have access to labs to test their designs.
One of the other challenges we faced was that we were supposed to have in-person wet lab all summer to develop and optimize our design, but we didnt get into the wet lab until the fall, Martin says. We have all our initial testing done, but we havent had a chance to put together this whole assay
Although the pandemic changed many of the testing plans, the group developed detailed written protocols for running experiments and troubleshooting problems that might arise.
A novel endometriosis test
The device developed by the Rochester iGEM team is based on detecting six biomarkers in menstrual fluid that are indicative of endometriosis.
The team created a new type of menstrual cup to collect samples of menstrual fluid from endometriosis patients and a lateral flow assaysimilar to a pregnancy test stickthat changes color based on either the presence or absence of the six biomarkers in the menstrual sample. This involved using a strain of Escherichia coli (E. coli) bacteria to produce the antibodies needed to detect each biomarker.
The synthetic biology part came in when we created this plug-and-play antibody system, Martin says. You need two antibodies to detect each biomarker, and this would normally be the most expensive part of the test. Instead, we used bacteria to produce antibodies in an inexpensive way.
The team also developed an imaging station to determine the actual quantity of biomarkers in a sample using only a cell phone camera.
The group envisions doctors providing patients with the menstrual cup. The patient would take the cup home and collect a menstrual sample during her next period. The patient would then bring the sample back to the doctor, and the doctor would run the endometriosis test.
This inexpensive, noninvasive endometriosis test could potentially complement or even replace surgery as a diagnostic, making it more accessible to women around the world.
Rochesters team additionally developed endometriosis education tools for physicians and the general public to increase awareness of the disease and encourage further research. One of these tools is a predictive model with 42 variables that can be used to conduct a self-assessment before consulting a doctor or as a clinical tool to supplement a physical test. The teams educational materials, which they had translated into many different languages, are all available in an open-access format.
We learned many endometriosis patients were not aware of their illness until years later because not only do the patients lack awareness themselves, but also the physicians were not educated about the disease, says Heather Shi 22, a microbiology and health, behavior, and society major, who is a member of Rochesters iGEM team.
A really rewarding experience
Today Martins health is much improved. After undergoing laparoscopic surgery during her senior year of high school, her back pain and intense cramping went away only two weeks after surgery. But she considers herself one of the lucky ones.
Going into it, I thought it was an unnecessary surgery, she says. I didnt think I had endometriosis, and I was going to have to spend weeks recovering from surgery for no reason. In my case, I was fortunate to have the results and actually get the endometriosis tissue removed.
She hopes Rochesters iGEM project may eventually help relieve some of this stress for others.
The most rewarding thing for me about this project is spreading awareness about the disease, Martin says. Usually when I first approach people about endometriosis, people dont know about it. The fact that I get to work on a disease that personally affected me, and still be able to make strides in the research and learn about the disease and educate others has been really rewarding.