Infertile worms resist infection-induced neurodegeneration

Infertile worms resist infection-induced neurodegeneration
Duke researchers have shown that infection with pathogenic bacteria causes neurodegeneration in the worm C. elegans. Infected animals displayed neural changes that are hallmarks of neurodegeneration in patients with illnesses like Alzheimer's disease. The green region in this worm is a wavy, branched and beaded neuron, indicating neurodegeneration. Credit: Alejandro Aballay lab, Duke University

The connections are still obscure, but mounting evidence points to a link between infections, the immune system, and neurodegenerative diseases like Alzheimer's, ALS, and Parkinson's.

Now, a team of Duke University researchers has shown that infection with live, pathogenic bacteria causes neurodegeneration in the worm C. elegans. Infected worms display a number of changes that are hallmarks of neurodegeneration in aging humans and patients with illnesses such as Alzheimer's disease.

The study, which appears online now and in print December 4, 2015 in the Journal of Biological Chemistry, also yielded a big surprise: infertile animals appear to be protected from neurodegeneration.

"In worms, there may be some type of signal from the or germline that plays a role in infection-induced neurodegeneration," said Alejandro Aballay, Ph.D., senior study author and associate professor of molecular genetics and microbiology at Duke University School of Medicine.

"That was definitely unexpected, though we know that infertility liberates energy that would have been spent on producing the germline and directs it toward tissue repair and other maintenance," Aballay said. "It will be interesting to figure out how the response to pathogens fits into this scheme."

In recent years, researchers have begun to notice a problematic relationship between pathogens and neurodegeneration. Multiple studies have shown that patients living with chronic infections are particularly susceptible to . What appears to happen is microbes infect a patient, alerting the immune system and unleashing inflammation, which progressively destroys neurons. This unintended side effect does not benefit the microorganism, and it certainly doesn't benefit the host.

Because it is so difficult to study this process in humans, Aballay's lab turned to the nematode worm, C. elegans, as a model. This 1-millimeter, transparent worm has a much simpler nervous system, consisting of only 302 neurons that represent most types of neurons in the mammalian brain. It also has a rudimentary immune system.

In the laboratory, these worms typically inhabit Petri dishes covered in a lawn of E. coli bacteria, which the animals graze all day. To infect the worms, Aballay and his colleagues simply replaced the worm's typical chow with the common bacterial pathogen Pseudomonas aeruginosa. They also tagged the animals' neurons with a fluorescent label so the researchers could visualize any neurodegenerative changes associated with infection.

The researchers witnessed a number of neural changes that are hallmarks of neurodegeneration. For example, they saw beaded neurons, nerve cells with little round outgrowths that give the appearance of beads. They also found areas where the neurons, which are normally straight like an arrow, were branched or wavy.

"Neurons are designed to act like a straightforward superhighway that sends signals from one cell to another," said Aballay. "These wavy neurons are more like a mountain route, where things go very slow and inefficiently because it turns and curves."

In humans, these changes would be accompanied by behavioral defects, perhaps making it harder to remember a name or where you put the car keys. In worms, the researchers found that these neural changes also had functional consequences. Normally, the animals would be able to sense and move toward their favorite treat—salt—but when their were affected, so was their ability to respond to the stimulus.

Next, the researchers wanted to determine if there were any genes that could protect against infection and neurodegeneration in worms. They mutated hundreds of worms, infected them with the same pathogen as before, and then looked to see if any were resistant to infection-induced neurodegeneration. The researchers found one particularly promising candidate, which contained a mutation in a gene called mes-1. Interestingly, all the with this mutation lacked the sex cells needed to produce offspring.

In additional genetic studies, Aballay and his colleagues found that another gene called DAF-16 was required for resistance to neurodegeneration in these mutant animals. Its human equivalent, a gene called FOXO6, is known to function at the intersection of pathways controlling immunity, longevity and stress responses.

"In the future, we plan to focus more on what is happening at the level of the neuron, to understand how the neuron senses pathogenic molecules or inflammatory cues, and how sensing those cues ultimately triggers ," said Aballay.

More information: Qiuli Wu et al. Genetic screen reveals link between maternal-effect sterile gene mes-1 and P. aeruginosa-Induced neurodegeneration in C. elegans, Journal of Biological Chemistry (2015). DOI: 10.1074/jbc.M115.674259

Journal information: Journal of Biological Chemistry

Provided by Duke University

Citation: Infertile worms resist infection-induced neurodegeneration (2015, November 23) retrieved 25 February 2024 from
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Explore further

Gene identified for immune system reset after infection


Feedback to editors