Species-specific primer sets and identification of species-specific DNA sequences using genome fragment enrichment
View Patent ↗Targeted sequencing of genetic regions that differ between two DNA preparations uses genomic fragment enrichment. This method can be used to study genetic variation among closely related species and microbial communities.
1. A method for identifying differences between communities of microorganisms comprising:
a) obtaining labeled first genomic DNA fragments from a first community and hybridizing the first genomic DNA fragments with second genomic DNA fragments from a second community;
b) incubating the first and second genomic fragments with additional genomic fragments from the first community, said additional genomic fragments containing defined terminal sequence tags to form DNA hybrids;
c) capturing the resulting DNA hybrids formed with tags and PCR amplification of only the tagged fragments;
d) obtaining enriched amounts of sequences unique to the first community; and
e) identifying the enriched sequences to determine between said communities.
2. The method according to claim 1 wherein the tagged fragments are modified to work in real-time PCR assays.
3. The method according to claim 1 wherein the DNA is isolated from bacterial microorganisms.
4. The method according to claim 2 wherein a first and a second microorganism are identified, wherein the first microorganism is E. faecalis and the second microorganism is E. faecium.
5. The method according to claim 1 wherein the first genomic DNA is labeled with biotin.
6. The method according to claim 1 wherein the first community is associated with cows.
7. The method according to claim 1 wherein the first community is associated with chickens.
8. The method according to claim 1 wherein the first community is associated with humans.
9. A method for identifying genetic differences between two microbial genomes comprising:
a) obtaining labeled first genomic DNA fragments from a first microorganism and hybridizing the first genomic DNA fragments with second genomic DNA fragments from a second microorganism;
b) incubating the first and second genomic fragments with additional genomic fragments from the first microorganism, said additional genomic fragments containing defined terminal sequence tags;
c) capturing the resulting DNA hybrids formed with tags and PCR amplification of only the tagged fragments;
d) obtaining enriched amounts of sequences unique to the first microorganism; and
e) identifying the enriched sequences to determine the genetic differences between the two microbial genomes.
10. The method according to claim 9 wherein the tagged fragments are modified to work in real-time PCR.