New Tool to Aid Cystic Fibrosis Research
E.PathDash simplifies data analysis for cystic fibrosis research, enhancing treatment insights.
― 6 min read
Table of Contents
- Understanding the Impact on Lungs
- The Need for Better Research Tools
- Growth of Gene Expression Data
- E.PathDash: A New Tool for Researchers
- Features of E.PathDash
- Case Studies Demonstrating E.PathDash
- How E.PathDash Works
- Importance of Data Reproducibility
- Future Directions
- Conclusion
- Original Source
- Reference Links
Cystic fibrosis (CF) is a genetic illness that affects many people worldwide, with over 105,000 cases reported. It primarily impacts the lungs, leading to severe respiratory problems. The main cause of CF is a mutation in a specific gene known as the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The complications arising from this disease are mainly due to persistent infections in the lungs that are resistant to antibiotics.
Understanding the Impact on Lungs
CF significantly compromises lung function. Around 90% of health issues related to CF stem from lung complications. These complications often lead to chronic infections that are difficult to treat. The germs that cause these infections can be particularly stubborn. This makes research on how these germs respond to different treatments and conditions very important.
The Need for Better Research Tools
There are many studies conducted to explore how different drug treatments, genetic changes, and other factors affect the germs associated with CF. However, a lot of the data from these studies is not easy to access for further analysis. Only a small portion of the information gathered is available to other researchers. This limits the ability of scientists to build on previous work and discover new treatments or insights.
To address this, researchers have created an application that helps make it easier to analyze existing gene expression data from germs that are important to CF. This includes germs like Pseudomonas Aeruginosa and Staphylococcus aureus, which are often found in the lungs of people with CF.
Growth of Gene Expression Data
The production of data related to gene expressions has grown significantly over the years. This began with the creation of microarrays in the late 1990s and has continued to expand with advancements in technology and sequencing methods. Public repositories that store this data have emerged, making it easier for researchers to access the information. However, even with these repositories, many scientists still struggle to analyze RNA-sequencing data without special skills or extensive time involvement.
E.PathDash: A New Tool for Researchers
E.PathDash is an application designed to simplify the process of analyzing publicly available RNA-seq data linked to CF and other diseases. It allows users to perform pathway activation analysis quickly and efficiently. Instead of spending hours or days trying to analyze data, users can access and analyze information in seconds.
The application is particularly useful for microbiologists studying germs that cause persistent lung illnesses in people with CF. It includes data from numerous studies and samples, focusing on the most common pathogens associated with CF.
Features of E.PathDash
E.PathDash offers several key features that make it a valuable tool for research:
Quick Access to Data: Users can easily access a large collection of datasets, which include many studies and treatment comparisons.
User-Friendly Interface: The application provides a clear interface that guides users through the analysis process without needing extensive technical skills.
Pathway Activation Analysis: Users can analyze how specific biological pathways are activated or repressed based on the data available.
Downloadable Content: All results, including graphs and tables, can be downloaded for further study or use in other analyses.
Integration with Other Tools: The application is designed to work well with other Bioinformatics tools, allowing researchers to use the data in various ways.
Case Studies Demonstrating E.PathDash
To showcase the capabilities of E.PathDash, two case studies were conducted by scientists focused on CF research.
Case Study 1: Propanoate Metabolism in P. aeruginosa
In the first case study, a researcher sought to investigate how P. aeruginosa behaves in different environments, particularly in co-culture with another organism, Candida albicans. By using E.PathDash, the researcher was able to quickly analyze data related to propanoate metabolism. The findings showed that certain pathways associated with propanoate metabolism were activated when P. aeruginosa was in co-culture with C. albicans.
The researcher uncovered that genes related to propanoate metabolism had higher levels of expression in co-culture compared to when P. aeruginosa was grown alone. This led to insights suggesting that C. albicans might influence P. aeruginosa's metabolism.
Case Study 2: Effects of DNA-Gyrase Inhibitors on Biofilm Formation
In the second case study, another researcher explored how different classes of antibiotics, specifically DNA-gyrase inhibitors, affected biofilm formation in P. aeruginosa. Biofilms are clusters of germs that are resistant to treatment, making them difficult to eradicate.
Using E.PathDash, the researcher analyzed various datasets to compare the impact of different treatments on biofilm formation. The results indicated that one type of inhibitor was less effective than another in reducing biofilm formation, suggesting that understanding the specific effects of different antibiotics is crucial for treating infections in CF patients.
How E.PathDash Works
E.PathDash is designed to be intuitive, allowing users to filter data based on their specific interests. By selecting specific bacterial species and strains, users can access relevant datasets. The application consists of various dashboard pages where users can explore study data, view pathway activation analyses, and compare results across studies.
By using visual tools like boxplots and volcano plots, E.PathDash helps users understand their data better. These visual aids make it easier to see the differences in gene expressions and the impact of various treatments.
Importance of Data Reproducibility
One of the guiding principles behind tools like E.PathDash is to promote data fairness, which includes making data Findable, Accessible, Interoperable, and Reusable (FAIR). By improving accessibility and allowing for easy data reuse, researchers can build upon previous findings and collaborate more effectively.
Future Directions
While E.PathDash serves as a powerful tool for researchers, there are areas for improvement. One potential development could involve expanding the number of datasets available within the application. This would allow researchers to explore an even broader range of pathogens and treatments.
Another direction could be enhancing the analytical capabilities of the application. By refining the statistical methods used for pathway activation analysis, the tool could provide even more precise insights into the biological processes being examined.
Conclusion
Cystic fibrosis presents significant challenges for affected individuals and healthcare providers. Understanding the underlying biology and the germs that complicate lung function is critical for developing effective treatments. Tools like E.PathDash play an essential role in advancing research by providing easy access to complex data and enabling researchers to generate new hypotheses for further study.
By simplifying the process of data analysis and promoting data reusability, E.PathDash helps researchers uncover valuable insights that can lead to better treatments and a deeper understanding of cystic fibrosis and other related diseases. The ongoing development and enhancement of such tools will be vital in the quest to improve the lives of those living with conditions like cystic fibrosis.
Title: E.PathDash, pathway activation analysis of publicly available pathogen gene expression data
Abstract: E.PathDash facilitates re-analysis of gene expression data from pathogens clinically relevant to chronic respiratory diseases, including a total of 48 studies, 548 samples, and 404 unique treatment comparisons. The application enables users to assess broad biological stress responses at the KEGG pathway or Gene Ontology level and also provides data for individual genes. E.PathDash reduces the time required to gain access to data from multiple hours per dataset to seconds. Users can download high quality images such as volcano plots and boxplots, differential gene expression results and raw count data, making it fully interoperable with other tools. Importantly, users can rapidly toggle between experimental comparisons and different studies of the same phenomenon, enabling them to judge the extent to which observed responses are reproducible. As a proof of principle, we invited two cystic fibrosis scientists to use the application to explore scientific questions relevant to their specific research areas. Reassuringly, pathway activation analysis recapitulated results reported in original publications, but it also yielded new insights into pathogen responses to changes in their environments, validating the utility of the application. All software and data are freely accessible and the application is available at scangeo.dartmouth.edu/EPathDash. ImportanceChronic respiratory illnesses impose a high disease burden on our communities and people with respiratory diseases are susceptible to robust bacterial infections from pathogens, including Pseudomonas aeruginosa and Staphylococcus aureus, that contribute to morbidity and mortality. Public gene expression datasets generated from these and other pathogens are abundantly available and an important resource for synthesizing existing pathogenic research, leading to interventions that improve patient outcomes. However, it can take many hours or weeks to render publicly available datasets usable; significant time and skills are needed to clean, standardize, and apply reproducible and robust bioinformatic pipelines to the data. Through collaboration with two microbiologists we have shown that E.PathDash addresses this problem, enabling them to elucidate pathogen responses to a variety of over 400 experimental conditions and generate mechanistic hypotheses for cell-level behavior in response to disease-relevant exposures, all in a fraction of the time.
Authors: Lily Taub, T. H. Hampton, S. Sarkar, G. Doing, S. L. Neff, C. E. Finger, K. F. Fukutani, B. A. Stanton
Last Update: 2024-05-09 00:00:00
Language: English
Source URL: https://www.biorxiv.org/content/10.1101/2024.04.10.588749
Source PDF: https://www.biorxiv.org/content/10.1101/2024.04.10.588749.full.pdf
Licence: https://creativecommons.org/licenses/by-nc/4.0/
Changes: This summary was created with assistance from AI and may have inaccuracies. For accurate information, please refer to the original source documents linked here.
Thank you to biorxiv for use of its open access interoperability.