Automated Microbial ID and AST Integration Workflow

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Solution Overview

Problem

Current systems for identifying microorganisms in biological samples and determining their antimicrobial susceptibility are labor-intensive and inefficient, making it difficult for healthcare professionals to rapidly react to emerging resistance or infections.

Innovation Solution

An automated system that integrates microbial identification using mass spectrometry with antimicrobial susceptibility testing, featuring a sample preparation station that prepares samples for both processes, ensuring the same isolate is used for both ID and AST, and a data management system for real-time data access and analysis.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If manual sample preparation and separate testing procedures are used for microbial identification and antimicrobial susceptibility testing, then data integrity between ID and AST can be maintained, but labor intensity and processing time increase significantly

Engineering Contradiction:
Improvedata integrityVSAvoidprocessing speed
Core Design Contradiction:
ReliabilityVSProductivity

Solution Approach 1:

The patent combines microbial identification (ID) and antimicrobial susceptibility testing (AST) into a single integrated workflow. The system automatically transfers the same microbial isolate from culture to both ID plates and AST panels without manual intervention, ensuring data integrity while eliminating duplicate sample preparation steps. This merging of previously separate procedures resolves the contradiction by maintaining reliability through automated consistency while dramatically improving productivity.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The automated system performs multiple functions using a single sample preparation process. The same isolate preparation step serves both ID and AST purposes simultaneously, and the system can handle various microbial types and multiple antimicrobial agents through standardized protocols. This multi-functionality allows the system to maintain data integrity across different test types while reducing overall processing time and labor requirements.

Inventive Principle:
Principle #6Universality (Multi-functionality)

2Measurement precision

If duplicate sample preparations are performed for ID and AST, then each test can be optimized independently, but time and resources are wasted

Engineering Contradiction:
Improvetest accuracyVSAvoidprocessing time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The system performs preliminary automated sample preparation by selecting and transferring a single microbial colony to a master culture tube before distributing samples to both ID and AST workflows. This preliminary action ensures that the same standardized isolate is used for both tests, maintaining measurement precision while eliminating the need for separate colony selection and preparation steps that would waste time and resources.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The automated system creates identical copies of the same microbial isolate from a single source colony, distributing the copied sample to both ID and AST plates. This copying approach ensures that both tests analyze the same microbial population, maintaining test accuracy while avoiding the time loss associated with independent sample preparations. The system maintains precision through automated, consistent replication rather than manual duplication.

Inventive Principle:
Principle #26Copying

3Productivity

If automated systems are implemented for integrated ID and AST, then productivity and data integrity improve, but device complexity increases

Engineering Contradiction:
ImprovethroughputVSAvoidsystem complexity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The automated system is segmented into distinct functional modules: a colony selection module, a sample transfer module, an ID processing module, and an AST processing module. Each module performs a specific function and can be independently maintained or calibrated. This segmentation allows the system to achieve high productivity through automation while managing complexity by dividing the overall system into manageable, specialized components that work together in a standardized workflow.

Inventive Principle:
Principle #1Segmentation

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

This system streamlines the process of identifying microorganisms and determining their susceptibility, improving patient care by providing timely and accurate data, reducing the need for duplicate sample preparations and ensuring data integrity.

Implementation Method 1

small quantities of microbes from a colony cultivated in the usual way in a nutrient medium are transferred to a mass spectrometric sample support plate known as a Maldi plate, and then subjected directly to mass spectrometric analysis

Methodology Applied
Scientific EffectMatrix Assisted Laser Desorption Ionization (MALDI):

Implementation Method 2

subjected directly to mass spectrometric analysis, generally by time-of-flight (TOF)

Methodology Applied
Scientific EffectTime-of-flight (TOF):

Data Source

PatentUS11371072B2Method and apparatus for identification of bacteria
Publication Date: 2022.06.28 BECTON DICKINSON & CO
  • US11371072B2 patent drawing
  • US11371072B2 patent drawing
  • US11371072B2 patent drawing

AI summary

An automated system for identifying in a biological sample microorganisms and their antimicrobial susceptibility (AST). The system provided an automated platform for preparing, from a single biological sample, inoculates for both ID and AST. The system loads a plate for ID testing as samples are being prepared for AST testing. The system tracks the sample and the inoculates from the samples to link the test results to the sample and the patients from whom the sample was obtained.