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Mechanics of mucus in cystic fibrosis patients

Date:
October 28, 2020
Source:
University of Pittsburgh
Summary:
New research examines the properties of the mucus of cystic fibrosis (CF) patients and the role it plays in a pathogens' ability to survive. The new information could have important implications for CF treatment.
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If you've ever had a cold, you know that too much mucus can be an annoyance, but mucus plays a very important role in the body. The respiratory system creates mucus as part of the immune system, meant to trap inhaled bacteria, viruses, and dirt so they can be removed before causing infection. However, for people with the genetic disorder cystic fibrosis (CF), the mucus that their bodies produce is thicker and stickier, leading to an increased risk from infection and decreased ability to breathe over time.

New research led by the University of Pittsburgh's Swanson School of Engineering examines the properties of the mucus of CF patients and the role it plays in a pathogens' ability to survive. The new information could have important implications for CF treatment.

The researchers examined nonmucoid (PANT) and mucoid (PASL) strains of P. aeruginosa, a common pathogen that infects the lungs. P. aeruginosa adapts to the host environment mutating from a non-mucoid phenotype (PANT) to a mucoid phenotype (PASL). This mutation in P. aeruginosa creates a protective film of mucus around the bacteria thereby forming a more hydrated and slimy biofilm in the mucus.

"Think of the cells like grains of rice. PANT cells are like basmati rice, while PASL cells are like sushi rice: coated in such a way that they stick together when they're compressed," explained Tagbo Niepa, assistant professor of chemical and petroleum engineering, whose lab led the study. Niepa also has appointments in the Departments of Bioengineering, Civil and Environmental Engineering, and Mechanical Engineering and Materials Science. "We can measure how investigational drugs can alter the sticky nature of the coating that pathogens such as P. aeruginosa create upon mutation."

This mutation gives the mucus unique properties that contribute to increased antibiotic resistance. It also shields them against phagocytic cells, which help the immune system clear out dead or harmful cells by ingesting them.

In order to study these properties, the researchers used pendant drop elastometry to compress and expand the biofilm that the cells formed. They also assessed the transcriptional profile of the cells to correlate the film's mechanics to cell physiology.

"This is the first time that the pendant drop elastometry technique has been used to study the mechanics of these cells. We demonstrate that these techniques can be used to investigate the efficacy of mucolytic drugs -- drugs that are used to break down the film of mucus that the cells are making," noted Niepa. "This technique could be powerful for investigating those agents, to see if they have the anticipated effect."


Story Source:

Materials provided by University of Pittsburgh. Note: Content may be edited for style and length.


Journal Reference:

  1. Sricharani Rao Balmuri, Nicholas G. Waters, Jonas Hegemann, Jan Kierfeld, Tagbo H.R. Niepa. Material properties of interfacial films of mucoid and nonmucoid Pseudomonas aeruginosa isolates. Acta Biomaterialia, 2020; DOI: 10.1016/j.actbio.2020.10.010

Cite This Page:

University of Pittsburgh. "Mechanics of mucus in cystic fibrosis patients." ScienceDaily. ScienceDaily, 28 October 2020. <www.sciencedaily.com/releases/2020/10/201028124524.htm>.
University of Pittsburgh. (2020, October 28). Mechanics of mucus in cystic fibrosis patients. ScienceDaily. Retrieved October 13, 2024 from www.sciencedaily.com/releases/2020/10/201028124524.htm
University of Pittsburgh. "Mechanics of mucus in cystic fibrosis patients." ScienceDaily. www.sciencedaily.com/releases/2020/10/201028124524.htm (accessed October 13, 2024).

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