Simple bioreactor makes ‘gut check’ more practical

NEWS RELEASE

Jeff Falk
713-348-6775
jfalk@rice.edu

Mike Williams
713-348-6728
mikewilliams@rice.edu

Rice, Baylor device mimics intestines to show how invading bacteria cause disease

HOUSTON – (Jan. 7, 2021) – Rice University and Baylor College of Medicine researchers have found a way to mimic conditions in intestines, giving them a mechanical model for the real-time growth of bacterial infections.

In a new study, they demonstrate a lab tool that simplifies simulations of the human intestine, making it more practical to find treatments for diseases like infectious diarrhea.

The team led by bioengineer Jane Grande-Allen of Rice’s Brown School of Engineering developed transparent millifluidic perfusion cassettes (mPCs) that are easy to fabricate and operate and compatible with common microscopic and biochemical analysis.

Illustration by Rice University/Baylor College of Medicine

The cassettes allow even non-bioengineers to perform the kind of studies typically done with a 96-well petri dish, with the added benefit of fluid flow over seeded epithelial cells infected with bacteria. The cassettes also have micro-scale ports for input and output, allowing not only for fluid flow but also for sampling of the environment.

The study led by Grande-Allen, Rice’s Isabel C. Cameron Professor of Bioengineering, and lead author and Rice and Baylor M.D./Ph.D. alumnus Reid Wilson, currently a resident at Oregon Health and Science University, appears in the Annals of Biomedical Engineering.

Replicating the complicated human gut is a challenge for researchers, said co-author Anthony Maresso, an associate professor of molecular virology and microbiology at Baylor. “Devices like these are often not user-friendly and practical for biologists like myself,” he said. “This one was designed to be easy to use by scientists with less engineering know-how. The hope is it will lower barriers between engineers and medical researchers.”

Grande-Allen said making a microfluidic system that doesn’t leak can be technically challenging. “In this case, we needed to mimic the rate of fluid throughout the intestine that, especially compared to blood, is really slow,” she said.

Molds of the devices, about the size of standard 96-well plates, were created with a 3D printer and used to form the clear polymer cassettes. The mPCs were seeded with human intestinal enteroids (HIEs), cultures that contain the major cell types native to the intestinal epithelium. When fluid containing bacteria flowed through, it formed a biofilm on the cells, a phenomenon not seen in static platforms.

Researchers can easily evaluate how well bacteria adhere to and infect the cells, both visually and by sampling through the ports on either end. Static plates allow bacteria to overgrow the cells and limit experiments to a few hours, but the slow flow through mPCs allows extended observation and more realistic results, Grande-Allen said.

Testing the device led the researchers to find the first direct evidence that aggregative adherence fimbriae, sticky appendages found on most infectious enteroaggregative Escherichia coli (EAEC), are necessary for the bacteria to form a biofilm.

“Our intention was to slowly flush the bacterial toxins to keep them from harming the cells,” Grande-Allen said. “That allowed more cells to survive so we could watch the process of infection. We were completely surprised to see that it also dramatically changed the nature of the film that formed.”

The transparent mPC bioreactors developed by Rice University and Baylor College of Medicine allow for easy imaging of interactions between intestinal cell cultures and bacteria or other pathogens. These microscope images show stained epithelial cells infected with enteroaggregative Escherichia coli with and without flow through the mPCs after 8 hours. The images show bacteria inserted without flow aggregated into small clusters (left), but formed biofilms when flow was present (center and right). The scale bars are 30 microns.

The devices also keep HIE cultures alive by replenishing oxygen and nutrients in the mPC chamber, allowing for better evaluation of realistic interactions between the cells and invading pathogens, Grande-Allen said.

She said mPCs will facilitate research on many such interactions. “This will allow the systematic examination of a lot of different combinations, good and bad, and how flow changes the dynamics of this environment,” she said.

Co-authors of the paper are graduate student Sarah Hewes and alumnus Takanori Iida of Rice, and postdoctoral associate Anubama Rajan, graduate student Shih-Ching Lin, senior research assistant Carolyn Bomidi and Mary Estes, a distinguished service professor of molecular virology and microbiology, all at Baylor.

The National Institutes of Health and the Cancer Prevention and Research Institute of Texas supported the research.

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Read the abstract at https://link.springer.com/article/10.1007/s10439-020-02705-8.

Follow Rice News and Media Relations via Twitter @RiceUNews.

Related materials:

Grande-Allen Integrative Matrix Mechanics Lab: https://grandegroup.blogs.rice.edu

Anthony Maresso Lab: https://www.bcm.edu/research/labs-and-centers/faculty-labs/anthony-maresso-lab

Department of Bioengineering: https://bioengineering.rice.edu

George R. Brown School of Engineering: https://engineering.rice.edu

Images for download:

https://news2.rice.edu/files/2020/12/1221_INTESTINE-1-WEB.jpg

Researchers at Rice University and Baylor College of Medicine developed millifluidic perfusion cassettes (mPCs) that mimic conditions in the intestines to evaluate infections like those that cause diarrhea. The devices formed from 3D-printed molds (top right) were seeded with   intestinal enteroid cultures (IECs) and infected with pathogens for 24 hours or more to see how infections take hold. (Credit: Illustration by Rice University/Baylor College of Medicine)

https://news2.rice.edu/files/2020/12/1221_INTESTINE-2-WEB.jpg

The transparent mPC bioreactors developed by Rice University and Baylor College of Medicine allow for easy imaging of interactions between intestinal cell cultures and bacteria or other pathogens. These microscope images show stained epithelial cells infected with enteroaggregative Escherichia coli with and without flow through the mPCs after 8 hours. The images show bacteria inserted without flow aggregated into small clusters (left), but formed biofilms when flow was present (center and right). The scale bars are 30 microns. (Credit: Baylor College of Medicine/Rice University)

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