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本文引用的文献

1
Genetic heterogeneity in Mycobacterium tuberculosis isolates reflected in IS6110 restriction fragment length polymorphism patterns as low-intensity bands.结核分枝杆菌分离株中的基因异质性在IS6110限制性片段长度多态性模式中表现为低强度条带。
J Clin Microbiol. 2000 Dec;38(12):4478-84. doi: 10.1128/JCM.38.12.4478-4484.2000.
2
Stability of IS6110 restriction fragment length polymorphism patterns of Mycobacterium tuberculosis strains in actual chains of transmission.结核分枝杆菌菌株IS6110限制性片段长度多态性模式在实际传播链中的稳定性。
J Clin Microbiol. 2000 Jul;38(7):2563-7. doi: 10.1128/JCM.38.7.2563-2567.2000.
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Genetic distances for the study of infectious disease epidemiology.用于传染病流行病学研究的遗传距离。
Am J Epidemiol. 2000 Feb 1;151(3):324-34. doi: 10.1093/oxfordjournals.aje.a010209.
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Interpreting DNA fingerprint clusters of Mycobacterium tuberculosis. European Concerted Action on Molecular Epidemiology and Control of Tuberculosis.解读结核分枝杆菌的DNA指纹图谱簇。欧洲分子流行病学与结核病控制联合行动。
Int J Tuberc Lung Dis. 1999 Dec;3(12):1055-60.
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Exogenous reinfection as a cause of recurrent tuberculosis after curative treatment.外源性再感染作为治愈性治疗后复发性结核病的一个病因。
N Engl J Med. 1999 Oct 14;341(16):1174-9. doi: 10.1056/NEJM199910143411602.
6
Analysis of rate of change of IS6110 RFLP patterns of Mycobacterium tuberculosis based on serial patient isolates.基于系列患者分离株的结核分枝杆菌IS6110限制性片段长度多态性模式变化率分析
J Infect Dis. 1999 Oct;180(4):1238-44. doi: 10.1086/314979.
7
Stability of Mycobacterium tuberculosis IS6110 restriction fragment length polymorphism patterns and spoligotypes determined by analyzing serial isolates from patients with drug-resistant tuberculosis.通过分析耐多药结核病患者的系列分离株确定结核分枝杆菌IS6110限制性片段长度多态性模式和间隔寡核苷酸分型的稳定性。
J Clin Microbiol. 1999 Feb;37(2):409-12. doi: 10.1128/JCM.37.2.409-412.1999.
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Stability of Mycobacterium tuberculosis DNA genotypes.结核分枝杆菌DNA基因型的稳定性
J Infect Dis. 1998 Apr;177(4):1107-11. doi: 10.1086/517406.
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Unexpectedly high strain diversity of Mycobacterium tuberculosis in a high-incidence community.在一个高发病率社区中,结核分枝杆菌出现意外高的菌株多样性。
S Afr Med J. 1996 Jan;86(1):45-9.
10
The use of a geographical information system (GIS) to evaluate the distribution of tuberculosis in a high-incidence community.利用地理信息系统(GIS)评估高发病率社区的结核病分布情况。
S Afr Med J. 1996 Jan;86(1):40-1, 44.

持续性结核分枝杆菌病患者中IS6110条带模式稳定性的计算

Calculation of the stability of the IS6110 banding pattern in patients with persistent Mycobacterium tuberculosis disease.

作者信息

Warren R M, van der Spuy G D, Richardson M, Beyers N, Borgdorff M W, Behr M A, van Helden P D

机构信息

MRC Centre for Molecular and Cellular Biology, Department of Medical Biochemistry, Faculty of Health Sciences, University of Stellenbosch, Tygerberg 7505, South Africa.

出版信息

J Clin Microbiol. 2002 May;40(5):1705-8. doi: 10.1128/JCM.40.5.1705-1708.2002.

DOI:10.1128/JCM.40.5.1705-1708.2002
PMID:11980946
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC130951/
Abstract

The interpretation of molecular epidemiologic data of Mycobacterium tuberculosis infection is dependent on the understanding of the stability and evolutionary characteristics of the DNA fingerprinting marker used to classify clinical isolates. This study investigated the stability of the IS6110 banding pattern in serial tuberculosis isolates collected from patients resident in an area with a high incidence of tuberculosis. Evolutionary changes were observed in 4% of the strains, and a half-life (t(1/2)) of 8.74 years was calculated, assuming a constant rate of change over time. This rate may be composed of a high rate of change seen during the early disease phase (t(1/2) = 0.57 years) and a low rate of change seen in the late disease phase (t(1/2) = 10.69 years). The early rate probably reflects change occurring during active growth prior to therapy, while the low late rate may reflect change occurring during or after treatment. We demonstrate that the calculation of these rates is strongly influenced by the time interval between onset of disease and sputum sampling. These calculations are further complicated by partial replacement of the original strain population, resulting in the sporadic appearance of clonal variants in sputum specimens. Therefore, the true extent of genetic diversity may be underestimated within each host, thereby influencing molecular epidemiological data used to establish transmission chains.

摘要

结核分枝杆菌感染分子流行病学数据的解读取决于对用于分类临床分离株的DNA指纹识别标记的稳定性和进化特征的理解。本研究调查了从结核病高发地区居民中收集的系列结核分离株中IS6110条带模式的稳定性。在4%的菌株中观察到进化变化,假设随时间变化率恒定,计算出半衰期(t(1/2))为8.74年。该变化率可能由疾病早期阶段观察到的高变化率(t(1/2)=0.57年)和疾病晚期阶段观察到的低变化率(t(1/2)=10.69年)组成。早期变化率可能反映治疗前活跃生长期间发生的变化,而晚期低变化率可能反映治疗期间或治疗后发生的变化。我们证明,这些变化率的计算受到疾病发作与痰液采样之间时间间隔的强烈影响。由于原始菌株群体的部分替代,导致痰液标本中克隆变体的零星出现,这些计算进一步复杂化。因此,每个宿主内遗传多样性的真实程度可能被低估,从而影响用于建立传播链的分子流行病学数据。