Application of mycobacterial interspersed repetitive unit typing to Manitoba tuberculosis cases: Can restriction fragment length polymorphism be forgotten?

被引:37
作者
Blackwood, KS
Wolfe, JN
Kabani, AM
机构
[1] Natl Reference Ctr Mycobacteriol, Canadian Sci Ctr Human & Anim Hlth, Natl Microbiol Lab, Hlth Canada, Winnipeg, MB R3E 3R2, Canada
[2] Hlth Sci Ctr, Winnipeg, MB, Canada
关键词
D O I
10.1128/JCM.42.11.5001-5006.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Since 1993, all Mycobacterium tuberculosis isolates recovered in the province of Manitoba, Canada, have been genotyped by the standard IS6110-restriction fragment length polymorphism (RFLP) method for routine surveillance, prevention, and control purposes. To date, our laboratory has collected 1,290 isolates, from which we have identified approximately 390 unique fingerprint patterns or "types." Although the standard method is well known for being a lengthy and labor-intensive procedure, a more efficient alternative for typing tuberculosis isolates, the mycobacterial interspersed repetitive unit-variable number tandem repeat (MIRU-VNTR) method, has recently gained acceptance. Consequently, all isolates acquired in 2003 (n = 126) were typed by both methods in order to determine the utility of replacing the RFLP method with MIRU typing for all future isolates. Application of Hunter's discriminatory index to the available study population showed that the MIRU method was close in discriminatory power (D) to the RFLP method (D-MIRU = 0.831 to 0.984 versus D-RFLP = 0.821 to 0.997). Clustering of isolates by using MIRU data correlated with RELP-derived clustering, lending useful information for either an investigation or confirmation of an incidence of recent transmission. In addition, it was determined that each predominant RELP type in Manitoba had a corresponding, recognizable MIRU type. It is conceivable that in the future RFLP typing can be replaced with MIRU for real-time, ongoing tuberculosis surveillance in the province.
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页码:5001 / 5006
页数:6
相关论文
共 30 条
[1]   The IS6110 restriction fragment length polymorphism in particular multidrug-resistant Mycobacterium tuberculosis strains may evolve too fast for reliable use in outbreak investigation [J].
Alito, A ;
Morcillo, N ;
Scipioni, S ;
Dolmann, A ;
Romano, MI ;
Cataldi, A ;
van Soolingen, D .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (03) :788-791
[2]   Comparison of variable number tandem repeat and IS6110-restriction fragment length polymorphism analyses for discrimination of high- and low-copy-number IS6110 Mycobacterium tuberculosis isolates [J].
Barlow, REL ;
Gascoyne-Binzi, DM ;
Gillespie, SH ;
Dickens, A ;
Qamer, S ;
Hawkey, PM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (07) :2453-2457
[3]   Predictive value of contact investigation for identifying recent transmission of Mycobacterium tuberculosis [J].
Behr, MA ;
Hopewell, PC ;
Paz, EA ;
Kawamura, LM ;
Schecter, GF ;
Small, PM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 158 (02) :465-469
[4]   Conventional and molecular epidemiology of Tuberculosis in Manitoba [J].
Blackwood, KS ;
Al-Azem, A ;
Elliott, LJ ;
Hershfield, ES ;
Kabani, AM .
BMC INFECTIOUS DISEASES, 2003, 3 (1)
[5]  
Braden CR, 2002, EMERG INFECT DIS, V8, P1210
[6]   STABILITY OF DNA FINGERPRINT PATTERN PRODUCED WITH IS6110 IN STRAINS OF MYCOBACTERIUM-TUBERCULOSIS [J].
CAVE, MD ;
EISENACH, KD ;
TEMPLETON, G ;
SALFINGER, M ;
MAZUREK, G ;
BATES, JH ;
CRAWFORD, JT .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (01) :262-266
[7]   Variable-number-tandem repeat typing of mycobacterium tuberculosis isolates with low copy numbers of IS6110 by using mycobacterial interspersed repetitive units [J].
Cowan, LS ;
Mosher, L ;
Diem, L ;
Massey, JP ;
Crawford, JT .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (05) :1592-1602
[8]  
Crawford JT, 2003, INT J TUBERC LUNG D, V7, pS453
[9]   Analysis of rate of change of IS6110 RFLP patterns of Mycobacterium tuberculosis based on serial patient isolates [J].
de Boer, AS ;
Borgdorff, MW ;
de Haas, PEW ;
Nagelkerke, NJD ;
van Embden, JDA ;
van Soolingen, D .
JOURNAL OF INFECTIOUS DISEASES, 1999, 180 (04) :1238-1244
[10]   Genetic diversity in the Mycobacterium tuberculosis complex based on variable numbers of tandem DNA repeats [J].
Frothingham, R ;
Meeker-O'Connell, WA .
MICROBIOLOGY-UK, 1998, 144 :1189-1196