[1]甘昭平,梁亚萍,赵涛△,等.等位基因多重PCR技术快速诊断耐药结核病的应用研究*[J].陕西医学杂志,2018,(11):1438-1440,1444.
 Gan Zhaoping,Liang Yaping,Zhao Tao,et al.Application of allele multiple PCR in rapid diagnosis of drug-resistant tuberculosis[J].,2018,(11):1438-1440,1444.
点击复制

等位基因多重PCR技术快速诊断耐药结核病的应用研究*
分享到:

《陕西医学杂志》[ISSN:1000-7377/CN:61-1281/TN]

卷:
期数:
2018年11期
页码:
1438-1440,1444
栏目:
临床研究
出版日期:
2018-11-29

文章信息/Info

Title:
Application of allele multiple PCR in rapid diagnosis of drug-resistant tuberculosis
文章编号:
0.3969/j.issn.1000-7377.2018.11.021
作者:
甘昭平梁亚萍赵涛△王卓李静邹远妩
陕西省结核病防治院(西安 710100)
Author(s):
Gan ZhaopingLiang YapingZhao Taoet al.
Shaanxi Provincial Gan Zhaoping Tuberculosis Control and Prevention Hospital (Xi’an 710100)
关键词:
结核分枝杆菌结核 抗多种药物性广泛耐药结核@MAS-PCR
Keywords:
Mycobacterium tuberculosisTuberculosisuultidrug-resistantExtensively drug-resistant tuberculosis@MAS-PCR
分类号:
R521
文献标志码:
A
摘要:
目的:探讨MAS-PCR技术作为分子生物学方法对耐多药结核病(MDR-TB)与广泛耐药结核病(XDR-TB)快速诊断的临床实用价值,为MDR-TB与XDR-TB的诊断和监测提供新的技术手段。方法:利用MAS-PCR技术对108株结核分枝杆菌临床分离株(含MDR-TB、XDR-TB敏感菌株)进行检测验证,并与传统比例法药敏试验结果进行比较,评价MAS-PCR技术的实用性。结果:对108株临床分离株(36株MDR,其中7株XDR)进行了MAS-PCR检测。MAS-PCR与比例法药敏试验比较,异烟肼耐药的敏感性、特异性、准确性、阳性预测值、阴性预测值分别为75.0%(36/48)、100%(57/57)、86.1%(93/108)、100.0%(36/36)、82.6%(57/69);利福平耐药的敏感性、特异性、准确性、阳性预测值、阴性预测值分别为76.4%(42/55)、100%(53/53)、88.0%(95/108)、100.0%(42/42)、80.3%(53/66);卡那霉素耐药的敏感性、特异性、准确性、阳性预测值、阴性预测值分别为100.0%(11/12)、100.0%(96/96)、99.0%(107/108)、100.0%(11/11)、99.0%(96/97);氧氟沙星耐药的敏感性、特异性、准确性、阳性预测值、阴性预测值分别为75.0%(15/20)、98.9%(87/88)、94.4%(102/108)、93.8%(15/16)、94.6%(87/62);卷曲霉素耐药的敏感性、特异性、准确性、阳性预测值、阴性预测值分别为77.8%(7/9)、99.0%(98/99)、97.2%(105/108)、87.5%(7/8)、98.0%(98/100)。结论:MAS-PCR技术检测MDR-TB及XDR-TB耐药性简便、快速、准确性、特异性高,对MDR-TB及XDR-TB耐药早期诊断具有重要意义。
Abstract:
Objective:To discuss the clinical value of MAS-PCR as a molecular biological method for the rapid diagnosis of MDR-TB and XDR-TB, and to provide a new technical means for the diagnosis and detection of MDR-TB and XDR-TB.Methods:Testing 108 strains of mycobacterium tuberculosis clinical isolates from our hospital (including MDR-TB, XDR-TB, sensitive strains)with MAS-PCR technology,and comparing with the result of drug sensitivity by traditional proportional method,we evaluate the practicality of MAS-PCR technology.Results:108 clinical isolates (36 MDR,7 XDR) were detected by MAS-PCR. Compared with the drug sensitivity test of MAS-PCR and proportional method,the rates of the sensitivity, specificity, accuracy and positive predictive values of isoniazide resistance were 75.0% (36/48), 100%(57/57),86.1%(93/108),100.0%(36/36), and 82.6%(57/69),respectively. the rates of the sensitivity, specificity,accuracy, positive predictive value and negative predictive value of rifampicin resistance were 76.4% (42/55),100%(53/53),88.0%(95/108),100.0%(42/42),80.3%(53/66), respectively.The rates of the sensitivity,specificity,accuracy,positive predictive value,negative predictive value of kanamycin resistance were 100.0%(11/12),100.0%(96/96),99.0%(107/108),100.0%(11/11), 99.0(96/97). the rates of the sensitivity, specificity, accuracy, positive predictive value of ofloxacin resistance were 75.0% (15/20), 98.9% (87/88),94.4% (102/108),93.8% (15/16),and 94.6% (87/62),respectively. the rates of the sensitivity,specificity,accuracy, positive predictive value and negative predictive value of capreomycin resistance were 77.8%(7/9),99.0%(98/99),97.2%(105/108),87.5%(7/8) and 98.0%(98/100), respectively. Conclusion:The detection of MDR-TB and XDR-TB resistance by MAS-PCR is simple, rapid, accurate and specific, and is of great significance to the early diagnosis of MDR-TB and XDR-TB resistance.

参考文献/References:

[1]Zhao Y,Xu S,Wang L,et al.National survey of drug-resistant tuberculosis in China[J].N Engl J Med, 2012,366(23):2161-2170.
[2]Iu GK,Tam YH,Ho PL,et al.Direct detection of isoniazid-resistant Mycobacterium tuberculosis in respiratory specimens by multiplex allele-specific polymerase chain reaction[J].Diagn Microbiol Infect Dis,2011,69(1):51-58.
[3]Evans J,Segal H.Novel multiplex allele-specific PCR assays for the detection of resistance to second-line drugs in Mycobacterium tuberculosis[J].J Antimicrob Chemother,2010,65(5):897-900.
[4]Hao LL,Xia Q,Lin N,et al.Multiplex allele-specific PCR combined with PCR-RFLP analysis for rapid detection of gyrA gene fluoroquinolone resistance mutations in Mycobacterium tuberculosis[J]. J Microbiol Methods,2012,88(1):175-178.
[5]梁亚萍,赵丽丽,高漫.124例耐多药结合分支杆菌基因突变特征分析[J].临床肺科杂志,2016,21(4):592-594.
[6]中国防痨协会基础委员会.结核病诊断实验室检验操作规程[M].北京:中国教育文化出版社,2006.
[7]陈燕.中国结核菌耐多药和广泛耐药相关基因突变特征及MAS-PCR研究[D].南华大学,2014.
[8]Ferrie R,Schwarz M,Robertson N,et al.Development multiplexing and application of ARMS tests for common mutations in the CFTR gene[J].American Journal of Human Genetics 1992,51(2):251-262
[9]梁亚萍,刘尚武,高漫.BACTET MGIT 960在二线抗结核药物药敏试验中的应用初探[J].陕西医学杂志,2012,41(11):1540-1541.
[10]孟祥红,匡铁吉,董梅.应用多重PCR方法快速鉴定结核分枝杆菌与非结核分枝杆菌[J].解放军医学杂志,2007,32(11):1177-1178.
[11]夏强,赵丽丽,刘志广,等.等位基因特异性多重PCR快速检测结核分枝杆菌喹诺酮耐药性的初步研究[J].医学研究杂志,2011,40(4):31-34.

备注/Memo

备注/Memo:
*陕西省卫生科研项目(2014D9)
更新日期/Last Update: 2018-11-30