Skip to content
All posts

Vibrant Research Spotlight: Overcoming Limitations in Enteric Pathogen Testing

Gastrointestinal (GI) infections significantly impact public health, particularly in vulnerable populations like children, older adults, and immunocompromised individuals.  

Rapid and accurate identification of these infections is crucial, yet traditional diagnostic methods often fall short, leading to undiagnosed or late-diagnosed cases.  

To address this, our research team evaluated the efficacy of a novel DNA microarray-based Gastrointestinal Pathogens Panel. 

This article evaluates this advanced method for detecting gut pathogens through Vibrant Wellness research, allowing for earlier interventions and improved outcomes. 

GI infection

Table of Contents

Comprehensive Detection of Gut Pathogens: The Study

Tickborne Diseases  Advanced Detection Technology (800 x 1200 px) (1)-1

"Evaluation of the Vibrant DNA Microarray for the High-Throughput Multiplex Detection of Enteric Pathogens in Clinical Samples,” is a 2019 study published in BMC, conducted by the Vibrant research team. 

Our study sought to develop a more effective method for diagnosing gastrointestinal infections.  

Our goal was to evaluate the performance of the Gut Pathogens Panel, a DNA microarray-based qualitative multiplexed polymerase chain reaction (PCR) assay.  

We aimed to determine the panel’s efficacy in detecting 27 different enteric pathogens directly from stool samples, including bacteria, viruses, parasites, and fungi. 

Our research team utilized a variety of samples for a comprehensive analysis:  

  • 27 Quantitative Genomic DNAs: Obtained from reputable sources like the American Type Culture Collection (ATCC), ZeptoMetrix, and Waterborne. 
  • 212 Spiked Stool Specimens: Used to assess our panel's detection capabilities in controlled conditions. 
  • 1067 Clinical and Archived Stool Specimens: Collected over two years, these samples provided a real-world evaluation of the panel's performance. The specimens were transported in Cary-Blair transport media and tested in the Vibrant America Clinical Laboratory. 

Our team tested a total of 1055 stool samples in our CAP-accredited and CLIA-certified in-house lab. 

After sample collection, we used advanced DNA microarray technology to perform high-throughput, multiplex detection.  

DNA Microarray Technology for Enhanced Detection

The Gut Pathogens Panel utilizes DNA microarray technology to catch gastrointestinal infections and other pathogens accurately.

Think of it as a high-tech grid that can simultaneously detect the genetic material of multiple pathogens.  

The process involves: 

  1. Nucleic Acid Extraction: First, DNA and RNA are extracted from the stool samples. This step ensures that the genetic material of any pathogens present is isolated and ready for analysis. 
  2. Multiplex PCR Amplification: Next, the extracted nucleic acids are amplified using PCR (polymerase chain reaction). This step multiplies the DNA and RNA sequences, making detecting even the tiniest amounts of pathogens easier. 
  3. Hybridization: The amplified sequences are then placed on the microarray, where they bind to specific probes that match their genetic code. This is like matching puzzle pieces – only the right pieces (pathogen DNA/RNA) fit with the right probes on the array. 
  4. Labeling and Detection: Once the sequences are in place, they're labeled with a special enzyme that produces a light signal. The intensity of this signal is measured using a charge-coupled device (CCD) imaging system. The stronger the signal, the more of that particular pathogen is present in the sample.
Immunochip

Benefits of Vibrant Testing 

Vibrant’s technology provides several pivotal advantages over traditional testing methods: 

  • High-Throughput Capability: The microarray can process up to 96 patient samples per hour, saving time and resources. 
  • Multiplex Detection: This panel can detect 27 different pathogens in a single run, while traditional methods usually test for only one pathogen at a time. 
  • Sensitivity and Specificity: The study achieved an overall sensitivity of 95.9% and specificity of 100%, meaning it can accurately detect pathogens without many false positives or negatives. 
  • Rapid Results: Traditional methods can take days, but this technology delivers results much faster. Quick turnaround times mean you can deliver results to your patients sooner, improving outcomes. 

This microarray technology provides an unprecedented platform that can be universally applied for similar testing that requires high throughput and low cost, helping optimize diagnostic processes and produce better results. 

Results & Clinical Significance

Screen Shot 2024-06-27 at 11.25.10 AM

Our study demonstrates the GI Pathogens panel’s unique ability to detect multiple enteric pathogens quickly and accurately.  

One standout finding is the test’s ability to detect polymicrobial infections. In the study, 20.2% of samples that turned out positive contained multiple pathogens, which traditional testing methods often miss.   

Identifying these co-infections is crucial because it can significantly impact treatment decisions and patient outcomes. 

The panel’s ability to rapidly and accurately detect gut pathogens allows you to quickly determine the cause of an infection and begin the appropriate treatment sooner.  

This can not only help your patients recover faster but also reduces the risk of complications and the spread of disease. 

Additionally, the comprehensive nature of the Gut Pathogens Panel means you can rely on a single test to diagnose a wide range of pathogens.  

This reduces the need for multiple tests while ensuring no potential pathogens are overlooked. 

The panel’s high accuracy rates and ability to detect multiple pathogens simultaneously make it a valuable tool for diagnosing and managing gastrointestinal infections. 

Drawbacks of Conventional Testing

petri dish testing

Traditional methods for detecting enteric pathogens, such as culture, microscopy, and antigen-based tests, present significant limitations.  

Culture methods are often low yield and less accurate, especially for antibiotic-treated samples, and have long turnaround times.  

Microscopy, while cost-effective, requires highly skilled personnel and is labor-intensive, making it unsuitable for rapid diagnosis.  

Antigen-based tests, although advanced, do not detect all relevant pathogens, leading to potential misdiagnoses

Current molecular tests like PCR offer improved sensitivity and specificity but are limited by the number of detectable targets and can be costly and complex.  

These issues can result in delayed or inaccurate diagnoses. Thus, more innovative tools are necessary to provide comprehensive, rapid, and accurate pathogen detection. 

Advanced Diagnostic Testing: The GI Pathogens Panel

GI infections

To gain the earliest assessment of common autoimmune disorders, you can utilize Vibrant’s Connective Tissue Disorders panel. 

The Gut Pathogens Panel detects the nucleic acids of 27 different pathogens, covering bacteria, viruses, parasites, and fungi.  

Some of the key pathogens include: 

  • Bacteria: E. coli (various strains), Salmonella, Campylobacter, and Helicobacter pylori. 
  • Viruses: Norovirus, Rotavirus, Adenovirus, and Astrovirus. 
  • Parasites: Giardia lamblia, Cryptosporidium, Entamoeba histolytica, and Cyclospora cayetanensis. 
  • Fungi: Candida spp. and Microsporidium spp.   

By measuring DNA and RNA, this intricate panel directly detects enteric pathogens, giving you a complete picture of your patient’s GI status. 

A Step Forward in Diagnostic Testing

DNA test tube

The Gut Pathogens Panel exemplifies the potential of advanced diagnostic tools to transform the detection and management of major ailments. 

Vibrant's DNA microarray technology marks a step forward in detecting enteric pathogens. 

By overcoming the limitations of traditional methods, this platform enhances diagnostic accuracy, reduces turnaround time, and improves patient care.  

As we continue to improve our methods and aim for even greater goals, tools like this panel will play a crucial role in enhancing patient care, supporting effective disease management, and contributing to better health outcomes. 


Give your patients the care they deserve


Regulatory Statement:

The general wellness test intended uses relate to sustaining or offering general improvement to functions associated with a general state of health while making reference to diseases or conditions. This test has been laboratory developed and its performance characteristics determined by Vibrant America LLC and Vibrant Genomics, a CLIA-certified and CAP-accredited laboratory performing the test. The lab tests referenced have not been cleared or approved by the U.S. Food and Drug Administration (FDA). Although FDA does not currently clear or approve laboratory-developed tests in the U.S., certification of the laboratory is required under CLIA to ensure the quality and validity of the test