Oligonucleotides for detection of Bacillus cereus group bacteria

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

435 912, 435 915, 536 231, 536 232, 536 237, 536 2432, 536 2433, C12Q 168, C12P 1934, C07H 2102, C07H 2104

Patent

active

060871040

ABSTRACT:
A method of detection is provided that permits differentiation of each of Bacillus cereus, Bacillus thuringiensis, and Bacillus anthracis from other microorganisms, using oligonucleotide primers for amplification of the target nucleotide sequences characteristic to Bacillus cereus, Bacillus thuringiensis, and Bacillus anthracis, consisting of the oligonucleotide (A) having a nucleotide sequence obtained from SEQ ID NO:1 and containing at least one site that can amplify a nucleotide sequence characteristic to Bacillus cereus, the oligonucleotide (B) having a nucleotide sequence obtained from SEQ ID NO:3 and containing at least one site that can amplify a nucleotide sequence characteristic to Bacillus thuringiensis, and the oligonucleotide (C) having a nucleotide sequence obtained from SEQ ID NO:5 and containing at least one site that can amplify a nucleotide sequence characteristic to Bacillus anthracis. Also provided are a method of detection of Bacillus cereus, Bacillus thuringiensis, and Bacillus anthracis by polymerase chain reaction (PCR) using a primer specific to the DNA gyrase sub-unit B (gyrB) gene and a method of detection of Bacillus cereus, Bacillus thuringiensis, and Bacillus anthracis in a sample by differentiation on the genetic level.

REFERENCES:
Abdel-Hameed, A. et al. Studies on Bacillus thuringiensis strains isolated from Swedish soils: insect toxicity and production of B. cereus-diarrhoeal-type enterotoxin, World J. Microbiology & Biotechnology vol. 10 (1994), p406-409.
Gonzalez, Jr., J.M. et al. Transfer of Bacillus thuringiensis plasmids coding for .delta.-endotoxin among strains of B. thuringiensis and B. cereus, Proc. pro. Natl. Acad. Sci. USA, vol. 79 (1982), p6951-6955.
Agata, N. et al. The bceT gene of Bacillus cereus encodes an enterotoxic protein, Microbiology 141 (1995), p983-988.
Yamamoto, S. et al. PCR Amplification and Direct Sequencing of gyrB Genes with Universal Primers and Their Application to the Detection and Taxonomic Analysis of Pseudomonas putida Strains, Applied & Environmental Microbiology, Mar. 1995, p1104-1109.
Beecher, D.J. et al. Identification and Analysis of the Antigens Detected by Two Commercial Bacillus cereus Diarrheal Enterotoxin Immunoassay Kits, Applied & Environmental Microbiology, Dec. 1994, p4614-4616.
Granum, P.E. et al. A survey of bacterial toxins involved in food poisoning: a suggestion for bacterial food poisoning toxin nomenclature, International Journal of Food Microbiology 28 (1995), p129-144.
Uchida, I. et al. Association of the Encapsulation of Bacillus anthracis with a 60 Megadalton Plasmid, Journal of General Microbiology 131 (1985), p363-367.
Saiki, R.K. et al. Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA Polymerase, Science vol. 239 (1988), p487-491.
Patra, G. et al. Isolation of a specific chromosomic DNA sequence of Bacillus anthracis and its possible use in diagnosis. FEMS Immuno. Med. Micro. 15:223-231, 1996.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Oligonucleotides for detection of Bacillus cereus group bacteria does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Oligonucleotides for detection of Bacillus cereus group bacteria, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Oligonucleotides for detection of Bacillus cereus group bacteria will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-540764

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.