Molecular methods for Mycobacterium tuberculosis strain typing:: a users guide

被引:56
作者
Kanduma, E
McHugh, TD
Gillespie, SH
机构
[1] UCL, Dept Med Microbiol, London NW3 2PF, England
[2] Kilimanjaro Christian Med Coll, Clin Lab, Moshi, Tanzania
关键词
FRAGMENT-LENGTH-POLYMORPHISM; MULTIDRUG-RESISTANT TUBERCULOSIS; 16S-23S SPACER REGION; FIELD GEL-ELECTROPHORESIS; POLYMERASE-CHAIN-REACTION; REPETITIVE DNA-SEQUENCES; NUMBER-TANDEM REPEAT; INSERTION-SEQUENCE; PULMONARY TUBERCULOSIS; CROSS-CONTAMINATION;
D O I
10.1046/j.1365-2672.2003.01918.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
There are now a wide range of techniques available to type Mycobacterium tuberculosis, the problem is to chose the correct technique. For large scale epidemiological studies the portability and standardization of IS6110 restriction fragment length polymorphism (RFLP) means that this remains the gold standard technique. In the next few years the internationally standard mycobacterial interspersed repetitive unit (MIRU) may come to challenge this primacy. Low copy number stains remain a problem and these can by typed by either polymorphic Guanine cytosine-rich repetitive sequence (PGRS) or MIRU-variable numbers of tandem repeat (VNTR). To confirm whether strains are part of a true cluster PGRS remains the method of choice. For local outbreaks and investigations of laboratory cross contamination where speed is of greatest importance suspect strains should be initially investigated using a PCR-based method The superior reproducibility and discrimination of MIRU-VNTR means that these methods should be favoured. If matches are found, then further confirmation of identity can be achieved using IS6110 RFLP or PGRS if the strains prove to have a low IS6110 copy number.
引用
收藏
页码:781 / 791
页数:11
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