Probe, probe set, probe-immobilized carrier, and genetic testing method

• US 8,207,319 B2
• Filed: 03/30/2007
• Issued: 06/26/2012
• Est. Priority Date: 03/31/2006
• Status: Active Grant

• Current Assignee: Canon Kabushiki Kaisha (Canon Inc.)
• Original Assignee: Canon Kabushiki Kaisha (Canon Inc.)
• Inventors: Kuribayashi, Hideto, Fukui, Toshifumi
• Primary Examiner(s): Salmon, Katherine
• Application Number:
  US12/294,910
• Publication Number:
  US 20090305260A1
• Time in Patent Office: 1,915 Days
• Field of Search: None
• US Class Current: 536/23.1
• CPC Class Codes: C12Q 1/689 for bacteria
• CPC Class Codes: C12Q 2600/16 Primer sets for multiplex assays

Abstract

A nucleic acid probe for classification of pathogenic bacterial species is capable of collectively detecting bacterial strains of the same species and differentially detecting them from other bacterial species. Any one of the base sequences of SEQ ID NOS. 59 to 61 or a combination of at least two of them is used for detecting the gene of an infectious disease pathogenic bacterium.

Claims

1. A probe set for detecting the internal transcribed spacer (ITS) region of the DNA of infectious disease pathogenic bacterium, Porphyromonas gingivalis, comprising three probes consisting of the following base sequences (1) to (3) respectively:

(1) TTATAGCTGTAAGATAGGCATGCGTCCC (SEQ ID NO.

     59) or the complementary sequence thereof;

(2) AACGGGCGATACGAGTATTGCATTGA (SEQ ID NO.

     60) or the complementary sequence thereof; and

(3) ATATACCGTCAAGCTTCCACAGCGA (SEQ ID NO.

     61) or the complementary sequence thereof.

2. A probe-immobilized carrier, wherein the probe set of claim 1 is arranged on a solid-phase carrier.

3. A probe-immobilized carrier according to claim 2, wherein the probe-immobilized carrier further comprises at least one probe comprising any one of the base sequences of SEQ ID NOS. 35 to 58 and 62 to 67 immobilized at a position spaced from the probe set.

4. A kit for detecting the internal transcribed spacer (ITS) region of the DNA of Porphyromonas gingivalis, comprising:

the probe set of claim 1 and a reagent for detecting a reaction between the probe set and a target nucleic acid.

5. A kit according to claim 4, wherein the reagent comprises a primer set for amplifying the ITS region of the DNA of Porphyromonas gingivalis, and wherein the primer set comprises:

an oligonucleotide comprising a base sequence of 5′

gcgataggcttaacacatgcaag 3′

(SEQ ID NO;

     18); and

at least one of the oligonucleotides from the group consisting of;

an oligonucleotide comprising a base sequence of 5′

atccagccgcaccttccgatac 3′

(SEQ ID NO;

     22); and

an oligonucleotide comprising a base sequence of 5′

atccagccgcacgttcccgtac 3′

(SEQ ID NO;

     28).

6. A gene detection kit, comprising:

the probe-immobilized carrier of claim 3; and

a reagent for detecting a reaction between the probe set and a target nucleic acid, wherein the reagent comprises a primer set, and wherein the primer set comprises;

an oligonucleotide comprising a base sequence of 5′

gcgataggcttaacacatgcaag 3′

(SEQ ID NO;

     18); and

at least one of the oligonucleotides from the group consisting of;

an oligonucleotide comprising a base sequence of 5′

atccagccgcaccttccgatac 3′

(SEQ ID NO;

     22); and

an oligonucleotide comprising a base sequence of 5′

atccagccgcacgttcccgtac 3′

(SEQ ID NO;

     28).

7. A probe set according to claim 1, wherein the probe set shows a hybridization intensity weak enough to avoid cross-hybridization with the 16S rRNA coding region of any bacterium selected from Anaerococcus prevotii, Bacteroides fragilis, Bacteroides thetaiotaomicron, Clostridium difficile, Clostridium perfringens, Eggerthella lenta, Fusobacterium necrophorum, Peptoniphilus asaccharolyticus, Porphyromonas asaccharolytica, Enterococcus avium, and Providencia rettgeri.

8. A probe set according to claim 1, wherein the probe set shows a hybridization intensity weak enough to avoid cross-hybridization with the 16S rRNA coding region of any bacterium selected from Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Serratia marcescens, Streptococcus pneumoniae, Haemophilus influenzae, Enterobacter cloacae, Enterococcus faecalis, Staphylococcus haemolyticus, Staphylococcus hominis, Staphylococcus saprophyticus, Streptococcus agalactiae, Streptococcus mutans, Streptococcus pyogenes, Streptococcus sanguinis, Enterococcus avium, Enterococcus faecium, Pseudomonas fluorescens, Pseudomonas putida, Burkholderia cepacia, Stenotrophomonas maltophilia, Acinetobacter baumannii, Acinetobacter calcoaceticus, Achromobacter xylosoxidans, Vibrio vulnificus, Salmonella choleraesuis, Citrobacter freundii, Klebsiella oxytoca, Enterobacter aerogenes, Hafnia alvei, Serratia liquefaciens, Proteus mirabilis, Proteus vulgaris, Morganella morganii, Providencia rettgeri, Aeromonas hydrophila, Aeromonas sobria, Gardnerella vaginalis, Corynebacterium diphtheriae, Legionella pneumophila, Bacillus cereus, Bacillus subtilis, Mycobacterium kansasii, Mycobacterium intracellulare, Mycobacterium chelonae, Nocardia asteroids, Bacteroides fragilis, Bacteroides thetaiotaomicron, Clostridium difficile, Clostridium perfrigens, Eggerthella lenta, Fusobacterium necrophorum, Fusobacterium nucleatum, Lactobacillus acidophilus, Anaerococcus prevotii, Peptoniphilus asaccharolyticus, Porphyromonas asaccharolytica, Prevotella denticola, and Propionibacterium acnes.

12. A method of detecting the internal transcribed spacer (ITS) region of Porphyromonas gingivalis in an analyte by using a probe-immobilized carrier, comprising the steps of:

(i) reacting the analyte with a probe-immobilized carrier according to claim 2; and

(ii) detecting the presence or absence of a hybridization reaction of the probe set on the probe-immobilized carrier with a nucleic acid in the analyte, or detecting the strength of a hybridization reaction of the probe set on the probe-immobilized carrier with the nucleic acid in the analyte, wherein the presence of the hybridization reaction or the strength of the hybridization reaction indicates the presence of the ITS region of Porphyromonas gingivalis in the analyte.

13. A method according to claim 12, further comprising the step of carrying out PCR amplification of the nucleic acid in the analyte by using a primer set, wherein the primer set comprises:

an oligonucleotide comprising a base sequence of 5′

gcgataggcttaacacatgcaag 3′

(SEQ ID NO;

     18); and

at least one of the oligonucleotides from the group consisting of;

an oligonucleotide comprising a base sequence of 5′

atccagccgcaccttccgatac 3′

(SEQ ID NO;

     22); and

an oligonucleotide comprising a base sequence of 5′

atccagccgcacgttcccgtac 3′

(SEQ ID NO;

     28).

9. A probe set for detecting the internal transcribed spacer (ITS) region of the DNA of infectious disease pathogenic bacterium, Porphyromonas gingivalis, comprising the following three probes (A) to (C), wherein the probe set does not comprise any other probes to detect the ITS region of the DNA of Porphyromonas gingivalis:

(A) a probe consisting of a base sequence of TTATAGCTGTAAGATAGGCATGCGTCCC (SEQ ID NO.

     59);

(B) a probe consisting of a base sequence of AACGGGCGATACGAGTATTGCATTGA (SEQ ID NO.

     60); and

(C) a probe consisting of a base sequence of ATATACCGTCAAGCTTCCACAGCGA (SEQ ID NO.

     61).

10. A probe-immobilized carrier, comprising the probe set of claim 9, wherein the three probes are arranged on a solid-phase carrier at intervals from each other.

11. A probe-immobilized carrier according to claim 10, wherein the probe-immobilized carrier further comprises at least one probe comprising any one of the base sequences of SEQ ID NOS. 35 to 58 and 62 to 67 immobilized at a position spaced from the probe set.