090010: Single Nucleotide Polymorphism (SNP) Genotyping of E. Coli 0157:H7
        
            Case ID:
            
            TEC2009-0010
            
        
                    
        
            Web Published:
            7/21/2014
        
                    
        
            Description:
            E. coli 
O157:H7 is a major health problem causing infection in more than 70,000 patients 
a year in the United States. These infections may be both in large outbreaks as 
well as isolated sporadic infections in small numbers of individuals. The Center 
for Disease Control (CDC) typically uses Pulse Field Gel Electrophoresis (PFGE) 
for identifying an E. coli outbreak, but it is neither a rapid nor inexpensive 
method. Enzyme immunoassay (EIA) is used in clinics, but the test is too 
expensive and does not provide rapid results. A need exists for a quick 
real-time assay that will detect single nucleotides.
 
Michigan 
State University’s technology utilizes SNP (single nucleotide polymorphism) to 
classify the O157 strains into clade groupings. The classification into clades 
is based upon the presence (or absence) of 96 SNPs that vary among the O157 
subtypes. Some of these clades were found to be more epidemiologically relevant 
because they cause more disease than others. In particular, the frequency and 
distribution of the Shiga toxin genes were found to be important in the 
progression of the disease and in the types of disease reported. The SNP method 
is more useful in circumstances of outbreak investigations over current methods 
because it can directly translate into populating genetics and phylogenetic 
analysis, thus pinpointing genotypes that can cause disease. As such, it could 
be useful in determining the precise nature of a patient’s infection, allowing 
for effective and timely treatment.
 
Benefits
* Rapid, precise, and inexpensive diagnosis of 
E. coli infection: The SNP genotyping approach is able to provide for a 
quick real-time assay capable of detecting single nucleotides. 
* Directly pinpoints genotype that causes 
disease: The SNP method is useful in outbreak investigations because it 
can directly translate into populating genetics and phylogenetic analysis, thus 
pinpointing genotypes that can cause disease and allowing for effective and 
timely treatment.
*Pathogen tracking: Allows pathogen 
strain tracking across time and geography 
* Compatible: Works with rapid SNP 
Stream analysis, so it could be expanded to other strains. 
 
Applications 
* 
Clinical testing kits for pathogen infection 
* CDC or 
state lab outbreak tracking 
* Food 
supply monitoring 
 
IP Protection 
Status
Patent 
pending
         
        Patent Information:
                    
        
            
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            For Information, Contact:
            Randy Ramharack
            Technology Manager
            Michigan State University - Test
            517-355-2186
            ramharac@msu.edu