[一组耐药结核病患者的常规和分子诊断]。

Q4 Medicine
Pneumologia Pub Date : 2014-07-01
Roxana Mindru, Victor Spînu, Cristina Popa, Elena Botezatu, Ruxandra Spătaru
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引用次数: 0

摘要

在世界范围内,虽然敏感/易感结核病的发病率减少了,但耐药结核病的数量正在增加。细菌学诊断,遗传和表型,成为必不可少的流行病控制。耐药性表现为结核分枝杆菌基因组突变的表型表达。出现突变的利福平在rpoB区,异烟肼在katG区和ha区,乙胺丁醇- embb区,喹诺酮- gyra区,氨基甘氨酸和周期肽-rrs区。通过表型和遗传学方法对40例TB-DR患者的药敏试验(DST)结果进行一致性分析。我们按照生产厂家的说明对洛温斯坦-延森培养基进行药敏试验。间接遗传检测,INH和RIF为MTBDR +基因型,二线药物为MTBDRsl基因型。遗传方法与表型方法的一致性为95%,5%的患者对INH和RIF有不同的敏感性,但表型上他们是耐药的,这意味着他们有其他未被试纸检测到的突变。rpoB区最常见的突变是MUT3(52%),与W8带缺失相关。rpoB MUT1和MUT2A区域的突变分别为12.5%和15%。对于INH的高抗性,最常见的是mut1占95%,其次是INH -30%的INHMUTI抗性。对于二线药物,遗传方法和表型方法一致性最高的是EMB,占30%,从遗传学上讲,菌株在embB区没有突变,但在表型方法上具有耐药性。对于FQ、KAN、am和CAP,两种方法对所有检测菌株的一致性为100%。遗传方法灵敏度高,诊断速度快,可显著缩短诊断时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Conventional and molecular diagnosis in a group of patients with drug-resistant tuberculosis].

Worldwide, although the incidence of the sensitive/susceptible tuberculosis diminished, the number of drug resistant tuberculosis is growing. The bacteriological diagnosis, genetic and phenotypic, becomes essential for the epidemic control. The resistance appears as a phenotypic expression of mutations from M. tuberculosis genome. The mutations that appear for Rifampicin are in region rpoB, for Isoniazid in region katG and inhA, for Ethambutol-embB, Quinolone-gyrA, Aminoglicozid and Cyclical Peptides-rrs. To follow the concordance of results of drug sensitivity test (DST) through phenotypic and genetic method, we analyzed a group of 40 patients with TB-DR. We performed drug susceptibility testing on Lowenstein-Jensen medium according to the instructions of the manufacturer. The strains were tested indirect genetic too, Genotype MTBDR plus forl INH and RIF and Genotype MTBDRsl for the second line drugs. The concordance between genetic method and the phenotypic method is 95%, 5% from the patients have different sensitivity to INH and RIF, butphenotypical they are resistant, meaning that they have other mutations undetected by the strip. The most common mutation in region rpoB is MUT3 (52%) associating the absence of band W8. Mutations in the region rpoB MUT1 and MUT2A are 12.5%, and 15% respectively. For high resistance to INH, the mostcommon isMUT1 forkatG 95% and forlow resistance to INHMUTI from region inhA-30%. For the second line drugs, the most frequent concordance between genetic method andphenotypic method is for EMB, of 30%, geneticallyspeaking the strains display no mutation in region embB, but are resistantin phenotypic method. For FQ, KAN, AMKand CAP the concordance between the two methods is of 100% to all tested strains. In conclusion, genetic methods have high sensitivity, they are fast and shorten significantly the diagnosis time.

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来源期刊
Pneumologia
Pneumologia Medicine-Pulmonary and Respiratory Medicine
CiteScore
0.20
自引率
0.00%
发文量
10
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