C2MI Nucleotide Sequences for Early Disease Marker Detection

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current methods fail to effectively identify specific nucleotide sequences associated with diseases such as cancer, atherosclerosis, diabetes, and CNS disorders, limiting diagnostic and therapeutic options.

Innovation Solution

Isolation and analysis of circular DNA genomes from cow milk samples using abutting PCR primers to amplify full-length circular DNA molecules, identifying C2MI sequences with similarity to plasmids of Acinetobacter baumannii, which are used as markers for disease diagnosis and potential therapeutic targets.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If conventional metagenomic analysis methods are used to identify infectious agents, then known agents can be detected, but novel or unknown infectious agents remain unidentified

Engineering Contradiction:
Improvedetection accuracyVSAvoidability to detect novel agents
Core Design Contradiction:
ReliabilityVSAdaptability or versatility

Solution Approach 1:

The patent applies preliminary action by performing in silico comparisons and metagenomic analyses before actual sample testing to identify potential novel infectious agents. This preparatory computational work enables the detection of unknown agents by establishing reference frameworks and identification criteria in advance, resolving the contradiction between reliable detection of known agents and the ability to discover novel ones.

Inventive Principle:
Principle #10Preliminary action

2Reliability

If focus is placed on identifying known infectious entities, then detection reliability is maintained, but identification of novel infectious agents is neglected

Engineering Contradiction:
Improvedetection consistencyVSAvoidnovel agent identification
Core Design Contradiction:
ReliabilityVSLoss of information

Solution Approach 1:

The patent applies parameter changes by modifying the analytical parameters of metagenomic studies - shifting from traditional targeted detection of known agents to broader genomic sequencing and comparison parameters that capture novel infectious entities. This includes using updated databases, expanded taxonomic coverage, and modified identification thresholds, enabling simultaneous maintenance of reliable known agent detection while discovering novel pathogens.

Inventive Principle:
Principle #35Parameter changes

3Device complexity

If strict demarcation between infectious agent groups is maintained, then classification clarity is preserved, but phylogenetic relationships and chimeric genomes cannot be properly analyzed

Engineering Contradiction:
Improveclassification simplicityVSAvoidphylogenetic analysis capability
Core Design Contradiction:
Device complexityVSAdaptability or versatility

Solution Approach 1:

The patent applies segmentation by dividing the analysis into distinct functional modules: genomic sequencing, in silico comparison, phylogenetic tree construction, and chimeric genome detection. This segmented approach allows clear classification of known agents while simultaneously enabling complex phylogenetic analyses and identification of chimeric genomes, resolving the contradiction between classification simplicity and analytical versatility.

Inventive Principle:
Principle #1Segmentation

Data Source

PatentUS20220025371A1CMI sequences as an early marker for the future development of cancer, atherosclerosis, diabetes and diseases of the CNS and as a target for the treatment and prevention of these diseases
Publication Date: 2022.01.27 DEUTES KREBSFORSCHUNGSZENT STIFTUNG DES OFFENTLICHEN RECHTS
  • US20220025371A1 patent drawing
  • US20220025371A1 patent drawing
  • US20220025371A1 patent drawing

AI summary

Described are CMI (Cow Milk Isolate) nucleotide sequences as well as probes and primers comprising part of said nucleotide sequences and antibodies against polypeptides encoded by said nucleotide sequences. Said compounds are useful as early markers for the future development of cancer, diabetes, atherosclerosis and diseases of the CNS (Multiple sclerosis MS, Prion-linked diseases, amyotrophic lateral sclerosis, transmissible spongiforme encephalitis, Parkinson's disease, Alzheimer disease) and should represent targets for treatment and prevention.