Hyde1 Gene Product and T6SS Delivery for Plant Pathogen Control

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Solution Overview

Problem

The understanding of molecular mechanisms governing plant-microbe interactions is limited, hindering the ability to combat plant diseases and harness beneficial bacterial functions for agriculture, and there is a need to identify and characterize bacterial genes that help microbes thrive in the plant environment.

Innovation Solution

Utilization of a purified or isolated Hyde1 gene product, or a functional fragment thereof, and a modified host cell capable of expressing a Type VI secretion system (T6SS), Hyde1, to inhibit the growth of pathogenic bacteria by introducing a non-pathogenic bacterial strain expressing Hyde1 or Hyde2, which can limit or reduce the growth of pathogenic bacteria in environments.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Adaptability or versatility

If cultivation-independent methods (metagenome sequencing) are used to study plant-associated bacteria, then the ability to capture DNA of uncultivated organisms is improved, but the ability to perform functional validation of in silico predictions deteriorates

Engineering Contradiction:
Improveability to capture DNA of uncultivated organismsVSAvoidability to perform functional validation
Core Design Contradiction:
Adaptability or versatilityVSReliability

Solution Approach 1:

The research approach is segmented into two distinct phases: (1) cultivation-independent metagenome sequencing to discover and identify bacterial genes and functions in the plant environment, and (2) cultivation-dependent isolate-based methods to perform functional validation of the in silico predictions. This segmentation allows each method to excel at its specific task without compromise.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent uses cultivated bacterial isolates as an intermediary between the initial metagenomic discovery phase and the functional validation phase. These isolates serve as a bridge that connects the in silico predictions from metagenomics with experimental functional validation, enabling the translation of computational predictions into verified biological knowledge.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Reliability

If cultivated bacterial isolates are used for functional validation, then the ability to perform functional validation is improved, but the coverage of rare uncultivated organisms deteriorates

Engineering Contradiction:
Improveability to perform functional validationVSAvoidcoverage of rare uncultivated organisms
Core Design Contradiction:
ReliabilityVSAdaptability or versatility

Solution Approach 1:

The research methodology is divided into sequential segments where metagenomics first identifies genes and functions from the total bacterial community including rare uncultivated organisms, and then cultivated isolates are used to functionally validate specific predictions. This segmentation ensures both broad coverage and deep validation.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

Metagenome sequencing is performed as a preliminary action before isolate-based functional validation. This preliminary step identifies candidate genes and functions in the plant environment, which then guide subsequent targeted functional validation using cultivated isolates, ensuring that validation efforts focus on the most relevant discoveries.

Inventive Principle:
Principle #10Preliminary action

3Device complexity

If limited sequencing depth is used in metagenomics, then the cost and complexity are reduced, but the ability to access genomes of rare organisms deteriorates

Engineering Contradiction:
Improvesequencing depth and costVSAvoidability to access genomes of rare organisms
Core Design Contradiction:
Device complexityVSAdaptability or versatility

Solution Approach 1:

The patent applies partial sequencing depth to the metagenomic analysis, focusing on capturing sufficient data to identify common and dominant bacterial genes and functions in the plant environment. Rather than attempting to sequence every rare organism completely, the method performs partial action that is sufficient for discovery purposes, with the understanding that cultivated isolates will provide complete genomic information for validation.

Inventive Principle:
Principle #16Partial or excessive action

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 Hyde1 gene product effectively kills a broad array of plant pathogenic bacterial species, and modified bacterial cells can be used as biocontrol agents to treat plant diseases and reduce pathogenic bacterial growth in environments, such as intensive care units, by expressing Hyde1 or Hyde2 through the Type VI secretion system.

Implementation Method 1

a modified host cell comprises one or more genes encoding, and/or capable of expressing, a Type VI secretion system (T6SS), Hyde1, and/or Hyde2

Methodology Applied
Scientific EffectType VI secretion system (T6SS):

Data Source

PatentUS12378286B2Methods and compositions useful for inhibiting growth of certain bacteria
Publication Date: 2025.08.05 VIRGINIA TECH INTELLECTUAL PROPERTIES INC
  • US12378286B2 patent drawing
  • US12378286B2 patent drawing
  • US12378286B2 patent drawing

AI summary

The present invention provides for a composition comprising a purified or isolated Hyde1 gene product, or a functional fragment thereof; a modified host cell capable of expressing a Type VI secretion system (T6SS), Hyde1, and/or Hyde2, or a functional fragment thereof; a method of treating a disease caused all or in part by a bacterial cell, comprising administering a composition of the present invention to a subject in need thereof; and a method to limit or reduce growth of a pathogenic bacteria in an environment, comprising: introducing a non-pathogenic bacterial capable of expressing a Type VI secretion system (T6SS), Hyde1, and/or Hyde2, or functional fragment thereof, to an environment.