Quantitative Detection of Mycoplasma DNA Using Competitive PCR

作者: Maninder K. Sidhu , Mei-June Liao , Abbas Rashidbaigi

DOI: 10.1007/978-1-4612-4164-5_15

关键词:

摘要: Mycoplasma are free-living pleomorphic prokaryotes that can pass through regular bacteriological filters. These organisms have a small genome with low G + C content, and lack the rigid peptidoglycan cell wall of eubacteria. There more than 80 species known to date, major culture contaminants human, bovine, or porcine origin being: orale, M. fermentants, hyorhinus, arginini, salivarium, Acholeplasma laidlawii (McGarrity et al., 1985). More 15–30% all lines used contaminated mycoplasma (Mowles 1988; Gignac 1991). grow in supernatant attached extracellular surface membranes. The growth these microorganisms may not necessarily destroy cells but produces significant changes medium composition, which leads alterations host metabolism, thus rendering infected unacceptable for use any research diagnostic procedure. Cell infections by various species, as well their effects, documented. Some effects on cultures include induction suppression enzymes cytokines, alteration antigenicity, interference viral expression, chromosomal breaks. A few also been reported produce transformation (Macpherson Russel, 1966).

参考文章(23)
CC Uphoff, S Brauer, D Grunicke, SM Gignac, RA MacLeod, H Quentmeier, K Steube, M Tümmler, M Voges, B Wagner, None, Sensitivity and specificity of five different mycoplasma detection assays. Leukemia. ,vol. 6, pp. 335- 341 ,(1992)
J. D. Lifson, M. Piatak, B. Williams, Ka-Cheung Luk, Quantitative competitive polymerase chain reaction for accurate quantitation of HIV DNA and RNA species BioTechniques. ,vol. 14, pp. 70- 81 ,(1993)
F J van Kuppeveld, K E Johansson, J M Galama, J Kissing, G Bölske, J T van der Logt, W J Melchers, Detection of mycoplasma contamination in cell cultures by a mycoplasma group-specific PCR. Applied and Environmental Microbiology. ,vol. 60, pp. 149- 152 ,(1994) , 10.1128/AEM.60.1.149-152.1994
A C Thomsen, Occurrence of mycoplasmas in urinary tracts of patients with acute pyelonephritis. Journal of Clinical Microbiology. ,vol. 8, pp. 84- 88 ,(1978) , 10.1128/JCM.8.1.84-88.1978
Hitoshi Kotani, Gary Butler, Diane Heggan, Gerard J. McGarrity, ELIMINATION OF MYCOPLASMAS FROM CELL CULTURES BY A NOVEL SOFT AGAR TECHNIQUE In Vitro Cellular & Developmental Biology – Plant. ,vol. 27, pp. 509- 513 ,(1991) , 10.1007/BF02631153
H. M. Foy, G. E. Kenny, M. K. Cooney, I. D. Allan, Long-Term Epidemiology of Infections with Mycoplasma pneumoniae The Journal of Infectious Diseases. ,vol. 139, pp. 681- 687 ,(1979) , 10.1093/INFDIS/139.6.681
Julia M. Inamine, Timothy P. Denny, Steven Loechel, Ulrike Schaper, Chien-hui Huang, Kenneth F. Bolt, Ping-chuan Hu, Nucleotide sequence of the P1 attachment-protein gene of Mycoplasma pneumoniae Gene. ,vol. 64, pp. 217- 229 ,(1988) , 10.1016/0378-1119(88)90337-X
Anne Hopert, Cord C. Uphoff, Manfred Wirth, Hansjörg Hauser, Hans G. Drexler, Specifity and sensitivity of polymerase chain reaction (PCR) in comparison with other methods for the detection of mycoplasma contamination in cell lines Journal of Immunological Methods. ,vol. 164, pp. 91- 100 ,(1993) , 10.1016/0022-1759(93)90279-G
Maninder K. Sidhu, Abbas Rashidbaigi, Douglas Testa, Mei-June Liao, Competitor internal standards for quantitative detection of mycoplasma DNA Fems Microbiology Letters. ,vol. 128, pp. 207- 211 ,(1995) , 10.1111/J.1574-6968.1995.TB07524.X