Peptide Microarray for Bacterial Viral Infection Distinction

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Solution Overview

Problem

Current diagnostic methods fail to accurately distinguish bacterial infections from viral infections, leading to unnecessary antibiotic use due to lack of precise diagnosis, especially in respiratory tract infections and pediatric sepsis.

Innovation Solution

Development of a peptide microarray and method using immobilized peptides that bind specifically to bacterial or viral antibodies, allowing for the differentiation between bacterial and viral infections by analyzing antibody responses, with two peptides (SEQ ID NO.1 and SEQ ID NO.2) identified to effectively distinguish between the two.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If current diagnostic methods are used, then general infection detection is possible, but accurate distinction between bacterial and viral infections cannot be achieved

Engineering Contradiction:
Improvediagnostic accuracyVSAvoidtest complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent segments the diagnostic approach by creating separate peptide arrays with distinct peptide sequences that specifically bind to antibodies against different pathogen types. Instead of using a single complex test, the methodology divides the detection into modular peptide units (e.g., peptides 1-10 in Table 1) that can be independently designed and combined, allowing precise differentiation between bacterial and viral infections while maintaining manageable test complexity.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent applies parameter changes by modifying peptide sequences to optimize their binding specificity to different antibody types. By systematically varying peptide compositions and structures (as shown in the detailed sequence listings), the methodology achieves enhanced discriminatory power between bacterial and viral infections. This includes adjusting peptide length, amino acid composition, and structural conformation to maximize binding affinity for pathogen-specific antibodies.

Inventive Principle:
Principle #35Parameter changes

2Reliability

If antibiotics are used without accurate diagnosis, then treatment coverage is maintained, but antibiotic overuse and resistance develop

Engineering Contradiction:
Improvetreatment reliabilityVSAvoidantibiotic resistance
Core Design Contradiction:
ReliabilityVSObject-generated harmful factors

Solution Approach 1:

The patent implements preliminary action by performing pathogen identification through peptide array binding assays before initiating antibiotic treatment. The methodology detects and characterizes antibodies against specific pathogen peptides in patient samples, providing definitive diagnostic information that guides appropriate treatment decisions. This preliminary diagnostic step ensures antibiotics are only prescribed when bacterial infections are confirmed, preventing unnecessary antibiotic use and reducing resistance development.

Inventive Principle:
Principle #10Preliminary action

3Loss of information

If genome-wide expression analysis is used, then comprehensive infection profiling is possible, but the complexity of analysis increases significantly

Engineering Contradiction:
Improveinformation completenessVSAvoidanalysis complexity
Core Design Contradiction:
Loss of informationVSDevice complexity

Solution Approach 1:

The patent extracts only the most relevant diagnostic information by focusing on specific peptide-antibody interactions rather than analyzing entire genomes or transcriptomes. The methodology selects and analyzes binding patterns to a curated set of pathogen-derived peptides, extracting the essential diagnostic signal needed to distinguish bacterial from viral infections. This extraction approach maintains information completeness for diagnostic purposes while dramatically simplifying the analysis compared to comprehensive genome-wide studies.

Inventive Principle:
Principle #2Taking out (Extraction)

4Measurement precision

If serological testing with multiple antibodies is performed, then pathogen identification capability improves, but the complexity of the study platform increases

Engineering Contradiction:
Improvepathogen identification accuracyVSAvoidplatform complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent merges multiple pathogen detection capabilities into a single integrated peptide array platform. Instead of using separate tests for different pathogens, the methodology combines multiple pathogen-specific peptides on one array, allowing simultaneous detection of antibodies against various bacteria and viruses in a single assay. This merging approach maintains high pathogen identification accuracy while reducing the number of separate tests and simplifying the overall diagnostic workflow.

Inventive Principle:
Principle #5Merging (Combining)

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

The method achieves high specificity and sensitivity in distinguishing bacterial from viral infections, reducing antibiotic overuse by accurately identifying bacterial infections and allowing optimal antibiotic use, with misclassification primarily occurring with influenza viruses.

Implementation Method 1

contacting an antibody-containing sample with an array of immobilized peptides, wherein said peptides are selected from a group consisting of one or more peptides that bind to antibodies produced in response to a bacterial infection

Methodology Applied
Scientific EffectAntibody-antigen binding:

Data Source

PatentUS11360086B2Diagnostic to distinguish bacterial infections
Publication Date: 2022.06.14 THE ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIV OF ARIZONA
  • US11360086B2 patent drawing
  • US11360086B2 patent drawing
  • US11360086B2 patent drawing

AI summary

Assays, arrays, and methods for distinguishing a bacterial infection from a viral infection are disclosed. The antibiotic crisis is in part driven by over prescription of antibiotics. There is a tendency, particular in pediatrics, to give an antibiotic even for viral infections. Thus, embodiments herein are directed to the problem of distinguishing a bacterial infection from a viral infection to reduce unnecessary antibiotic usage.