Molecular evidence of endogenous reactivation of Mycobacterium tuberculosis after 33 years of latent infection

被引:183
作者
Lillebaek, T
Dirksen, A
Baess, I
Strunge, B
Thomsen, VO
Andersen, ÅB
机构
[1] Statens Serum Inst, Int Reference Lab Mycobacteriol, Natl Inst Prevent & Control Infect Dis & Congenit, DK-2300 Copenhagen, Denmark
[2] Rigshosp Univ Hosp, Infect Dis Clin, Copenhagen, Denmark
[3] Gentofte Univ Hosp, Dept Pulm Med, Gentofte, Denmark
[4] Holstebro Hosp, Dept Pulm Med, Holstebro, Denmark
关键词
D O I
10.1086/338342
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Since Robert Koch described the cause of tuberculosis in 1882, the natural history of the disease after primary infection has been subject to debate. Only similar to10% of infected individuals develop active disease, which may appear years to decades after infection. Late onset has been attributed to the endogenous reactivation of dormant bacteria. However, this has not been documented by molecular means for latencies of more than a few years. In Denmark, we have recently recultured 205 freeze-dried Mycobacterium tuberculosis strains obtained from 1961 through 1967. These "historical" strains are analyzed by DNA restriction fragment-length polymorphism testing, and their DNA patterns are compared with those of 4008 recently obtained clinical specimens. This has, surprisingly, yielded molecular evidence of M. tuberculosis reactivation after 33 years of latent infection. A father and son who developed tuberculosis in 1961 and in 1994, respectively, were the only patients infected with strains that share an identical DNA pattern.
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页码:401 / 404
页数:4
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