Method for the direct detection of methicillin-resistant...

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

Reexamination Certificate

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C435S007100

Reexamination Certificate

active

07955796

ABSTRACT:
Described is a method for the detection and quantification of methicillin-resistantStaphylococcus aureusfrom a specimen comprising a) contacting the specimen with Anti-Protein A antibodies so as to adsorb methicillinresistantStaphylococcus aureusand/or methicillin-sensitiveStaphylococcus aureus, b) separating said antibodies to which methicillin-resistantStaphylococcus aureusand/or methicillin-sensitiveStaphylococcus aureushave been adsorbed from the specimen, c) lysing methicillin-resistantStaphylococcus aureusand/or methicillin-sensitiveStaphylococcus aureusadsorbed to said antibodies so as to release their DNA, d) combining the released DNA with (i) probes and/or primers which are specific for a target DNA sequence of the mecA gene of methicillin -resistantStaphylococcus aureusand/or of methicillin-resistantStaphylococcusepidermis, (ii) probes and/or primers which are specific for a target DNA sequence of methicillin-resistantStaphylococcus aureusother than a target DNA sequence of the mecA gene and (iii) probes and/or primers which are specific for a target DNA sequence of methicillin-resistantStaphylococcusepidermis other than a target DNA sequence of the mecA gene, whereby the target DNA sequences of methicillin-resistantStaphylococcus aureusand of methicillin-resistantStaphylococcusepidermis are not homologous, e) subjecting the combined released DNA and the specific probes and/or primers to conditions which permit amplification of said target DNA sequences, f) detecting the presence and amount of the amplified target DNA sequences as an indication of the presence and amount of methicillin-resistantStaphylococcus aureus, new primers and probes and diagnostic kits for the detection and quantification of MRSA.

REFERENCES:
patent: 5702895 (1997-12-01), Matsunaga et al.
patent: 0 625 575 (1994-11-01), None
patent: WO 92/05281 (1992-04-01), None
patent: WO 99/16780 (1999-04-01), None
Niemeyer et al. 1997. Analytical Biochem. vol. 246: pp. 140-145.
Sano et al. 1992. Science. vol. 258: pp. 120-122.
Towner et al. J. 1998. Med. Microbiol. vol. 47: pp. 607-613.
Francois et al. (J. Clin. Microbiol., 41:254-260, 2003).
BLAST alignment for Y14051, Aug. 13, 2009.
BLAST alignment for U23713, Aug. 13, 2009.
BLAST alignment for X17688, Aug. 13, 2009.
Nagahara et al., “A simple method for detection ofStaphylococcus aureususing anti-protein A igY,”Journal of the Food Hygenic Society of Japan(Oct. 1998), vol. 39, No. 5, pp. 318-323, Database Biosis 'Online!, Biosciences Information Service, Philadelphia, PA, US; Database accession No. PREV199900059917, XP002187201, ISSN: 0015-6426.
Wilkerson et al., “Comparison of five agglutination tests for identification ofStaphylococcus aureus,” Journal of Clinical Microbiology(1997), vol. 35, No. 1, pp. 148-151, XP001051889, ISSN: 0095-1137.
Ünal et al., “Detection of methycillin-resistant staphylococci by using the polymerase chain reaction,”Journal of Clinical Microbiology(Jul. 1992), vol. 30, No. 7, pp. 1685-1691, XP002099980, ISSN: 00951137.

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