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Typing of Mycoplasma pneumoniae by nucleic acid sequence-based amplification, NASBA(R)
被引:19
|作者:
Ovyn, C
[1
]
vanStrijp, D
[1
]
Leven, M
[1
]
Ursi, D
[1
]
vanGemen, B
[1
]
Goossens, H
[1
]
机构:
[1] ORGANON TEKNIKA,BOXTEL 5280,NETHERLANDS
关键词:
Mycoplasma pneumoniae;
typing;
NASBA(R);
enzyme-linked gel assay (ELGA);
POLYMERASE CHAIN-REACTION;
RNA SEQUENCES;
IDENTIFICATION;
DISTINCTIONS;
INFECTIONS;
DNA;
D O I:
10.1006/mcpr.1996.0043
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Nucleic acid sequence-based amplification, NASBA(R), is an isothermal amplification technique for nucleic acids and was used for typing a collection of 24 Mycoplasma pneumoniae strains. A set of primers was chosen from the 16S rRNA sequence alignment of Mycoplasma species. The nucleotide sequences of the (-)RNA amplicons were determined for M. pneumoniae strains M15/83 (type 1) and FH (type 2), and revealed a one-point difference at the 16S rRNA level between the two types. Based on this result, two type-specific probes were constructed. The probes were hybridized in solution with the amplified nucleic acids of 24 M. pneumoniae strains In an enzyme linked gel assay (ELGA). The results obtained by NASBA-based typing are in agreement with the classification of the 24 M. pneumoniae strains into two types by other typing methods, confirming the reliability of this technique. (C) 1996 Academic Press Limited
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页码:319 / 324
页数:6
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