Discrimination of
View Patent ↗The present invention is directed to a novel method of discriminating a highly infectious bacterium Bacillus anthracis from a group of closely related microorganisms. Sequence variations in the 16S and 23S rRNA of the B. cereus subgroup including B. anthracis are utilized to construct an array that can detect these sequence variations through selective hybridizations. The identification and analysis of these sequence variations enables positive discrimination of isolates of the B. cereus group that includes B. anthracis . Discrimination of single base differences in rRNA was achieved with a microchip during analysis of B. cereus group isolates from both single and in mixed probes, as well as identification of polymorphic sites. Successful use of a microchip to determine the appropriate subgroup classification using eight reference microorganisms from the B. cereus group as a study set, was demonstrated.
1. A method for detecting an isolate of Bacillus anthracis in a sample, the method comprising:
(a) placing on a microchip a set of oligonucleotide probes targeted to rRNA sequences, wherein the set of oligonucleotide probes comprises the probe sequences as set forth in
(i) TTT GGG CTA TGT TCC GTT TC (SEQ ID NO: 57)
(ii) TTT GGG CTA GAT TCC GTT TC (SEQ ID NO: 58)
(iii) CAG CTC AGC CTT CAC GAT AA (SEQ ID NO: 97)
(iv) CAG CTC AGC CTT TAC GAT AA (SEQ ID NO: 98)
(v) TCT AGG GTT GTC AGA GGA TG (SEQ ID NO: 76)
(vi) TCT AGG GTT TTC AGA GGA TG (SEQ ID NO: 75)
(vii) CCG CTA ACT TCA TAA GAG CA (SEQ ID NO: 103)
(viii) CCG CTA ACT TCT TGA GAG CA (SEQ ID NO: 104)
(ix) reverse complement of GCTTCTCCTTCGGGAGCAGA (SEQ ID NO: 19);
(x) reverse complement of GCTTCcCCTTCGGGgGCAGA (SEQ ID NO: 20); and
(xi) CCC TCT GTG ACG AGC CTT TC (SEQ ID NO: 72)
and discriminates among the B. cereus subgroups;
(b) providing conditions for hybridization of the probes with nucleic acids from the sample; and
(c) analyzing hybridization signals in the microchip to detect Bacillus anthracis.
2. The method of claim 1 , wherein the oligonucleotide probes are directed to 16S rRNA and 23 S rRNA.
3. The method of claim 1 , wherein the nucleic acids are labeled.
4. The method of claim 3 , wherein the labels are fluorescent dyes.
5. The method of claim 1 , wherein oligonucleotide probes comprising sequences designated by SEQ ID NOS: 75 and 76 discriminate subgroups Anthracis, Cereus A and Mycoides B from subgroups Cereus B, Thuringiensis A, B and Mycoides A.
6. The method of claim 1 , wherein oligonucleotide probes targeted to nucleic acid sequences set forth in SEQ ID NOS: 103-104 discriminate subgroup Thuringiensis B from other subgroups of B. cereus group.
7. The method of claim 1 , wherein the oligonucleotide probes targeted to nucleic acid sequences as set forth in SEQ ID NOS: 97-98 discriminate subgroups Anthracis, Thuringiensis B and Mycoides from subgroups Cereus A, B.
8. The method of claim 1 , wherein the oligonucleotide probes targeted to nucleic acid sequences as set forth in SEQ ID NOS: 57-58 discriminate Mycoides A, B from subgroups Anthracis, Cereus A, B and Thuringiensis B.
9. A method for taxonomically classifying B. cereus group, said method comprising:
(a) placing on a microchip a set of oligonucleotide probes targeted to rRNA sequences, wherein the set of oligonucleotide probes comprises the probe sequences as set forth in
(i) TTT GGG CTA TGT TCC GTT TC (SEQ ID NO: 57)
(ii) TTT GGG CTA GAT TCC GTT TC (SEQ ID NO: 58)
(iii) CAG CTC AGC CTT CAC GAT AA (SEQ ID NO: 97)
(iv) CAG CTC AGC CTT TAC GAT AA (SEQ ID NO: 98)
(v) TCT AGG GTT GTC AGA GGA TG (SEQ ID NO: 76)
(vi) TCT AGG GTT TTC AGA GGA TG (SEQ ID NO: 75)
(vii) CCG CTA ACT TCA TAA GAG CA (SEQ ID NO: 103)
(viii) CCG CTA ACT TCT TGA GAG CA (SEQ ID NO: 104)
(ix) reverse complement of GCTTCTCCTTCGGGAGCAGA (SEQ ID NO: 19);
(x) reverse complement of GCTTCcCCTTCGGGgGCAGA (SEQ ID NO: 20); and
(xi) CCC TCT GTG ACG AGC CTT TC (SEQ ID NO: 72)
for B. cereus group isolates; and
(b) using the signature profiles of 16S and 23S rRNA sequences and phylogenetic trees to classify the various B. cereus group isolates.