Evolution of the IS6110-based restriction fragment length polymorphism pattern during the transmission of Mycobacterium tuberculosis

被引:50
作者
Warren, RM
van der Spuy, GD
Richardson, M
Beyers, N
Booysen, C
Behr, MA
van Helden, PD
机构
[1] Univ Stellenbosch, MRC, Ctr Mol & Cellular Biol, Dept Med Biochem, ZA-7505 Tygerberg, South Africa
[2] Univ Stellenbosch, Fac Hlth Sci, Dept Paediat & Child Hlth, ZA-7505 Tygerberg, South Africa
[3] McGill Univ, Ctr Hlth, Dept Med, Montreal, PQ H3G 1A4, Canada
关键词
D O I
10.1128/JCM.40.4.1277-1282.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Interpretation of the molecular epidemiological data of Mycobacterium tuberculosis is dependent on the validity of the assumptions that have been made. It is assumed that the IS6110 banding pattern is sufficiently stable to define epidemiological events representing ongoing transmission. However, molecular epidemiological data also support the observation that the IS6110 banding pattern may change over time. Factors affecting this rate may include the nature and duration of disease in a host and the opportunity to experience different host environments during the transmission cycle. To estimate the rate of IS6110 change occurring during the process of transmission, M. tuberculosis isolates from epidemiologically linked patients were genotypically characterized by restriction fragment length polymorphism (RFLP) analysis. The identification of IS6110 banding pattern changes during ongoing transmission suggested that a rate could be estimated. IS6110 change was significantly associated with strains with >5 IS6110 elements (P = 0.013) and was not observed in low-copy-number isolates. The minimum rate of appearance of variant strains was calculated to be 0.14 variant cases per source-case per year. This data suggest that clustering of isolates based on identical RFLP patterns is expected to underestimate transmission in patients infected with high-copy-number isolates. A model based on the rate of appearance of both variant and invariant strains demonstrates that the genotypically defined population structure may change by 18.6% during the study period of approximately 6.5 years. The implications for the use of RFLP data for epidemiologic study are discussed.
引用
收藏
页码:1277 / 1282
页数:6
相关论文
共 27 条
[1]   TRANSMISSION OF TUBERCULOSIS IN NEW-YORK-CITY - AN ANALYSIS BY DNA-FINGERPRINTING AND CONVENTIONAL EPIDEMIOLOGIC METHODS [J].
ALLAND, D ;
KALKUT, GE ;
MOSS, AR ;
MCADAM, RA ;
HAHN, JA ;
BOSWORTH, W ;
DRUCKER, E ;
BLOOM, BR .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (24) :1710-1716
[2]   Transmission of Mycobacterium tuberculosis from patients smear-negative for acid-fast bacilli [J].
Behr, MA ;
Warren, SA ;
Salamon, H ;
Hopewell, PC ;
de Leon, AP ;
Daley, CL ;
Small, PM .
LANCET, 1999, 353 (9151) :444-449
[3]  
Beyers N, 1996, S AFR MED J, V86, P40
[4]   Origin and interstate spread of a New York City multidrug-resistant Mycobacterium tuberculosis clone family [J].
Bifani, PJ ;
Plikaytis, BB ;
Kapur, V ;
Stockbauer, K ;
Pan, X ;
Lutfey, ML ;
Moghazeh, SL ;
Eisner, W ;
Daniel, TM ;
Kaplan, MH ;
Crawford, JT ;
Musser, JM ;
Kreiswirth, BN .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 275 (06) :452-457
[5]   Impact of social interactions in the community on the transmission of tuberculosis in a high incidence area [J].
Classen, CN ;
Warren, R ;
Richardson, M ;
Hauman, JH ;
Gie, RP ;
Ellis, JHP ;
van Helden, PD ;
Beyers, N .
THORAX, 1999, 54 (02) :136-140
[6]   AN OUTBREAK OF TUBERCULOSIS WITH ACCELERATED PROGRESSION AMONG PERSONS INFECTED WITH THE HUMAN-IMMUNODEFICIENCY-VIRUS - AN ANALYSIS USING RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISMS [J].
DALEY, CL ;
SMALL, PM ;
SCHECTER, GF ;
SCHOOLNIK, GK ;
MCADAM, RA ;
JACOBS, WR ;
HOPEWELL, PC .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (04) :231-235
[7]   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
[8]   Genetic heterogeneity in Mycobacterium tuberculosis isolates reflected IS6110 restriction fragment length polymorphism patterns as low-intensity bands [J].
de Boer, AS ;
Kremer, K ;
Borgdorff, MW ;
de Haas, PEW ;
Heersma, HF ;
van Soolingen, D .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (12) :4478-4484
[9]   IS6110 transposition and evolutionary scenario of the direct repeat locus in a group of closely related Mycobacterium tuberculosis strains [J].
Fang, Z ;
Morrison, N ;
Watt, B ;
Doig, C ;
Forbes, KJ .
JOURNAL OF BACTERIOLOGY, 1998, 180 (08) :2102-2109
[10]   Differences in the prevalence of IS6110 insertion sites in Mycobacterium tuberculosis strains: low and high copy number of IS6110 [J].
Fomukong, N ;
Beggs, M ;
El Hajj, H ;
Templeton, G ;
Eisenach, K ;
Cave, MD .
TUBERCLE AND LUNG DISEASE, 1998, 78 (02) :109-116