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Microorganisms. 2022 Jul 15;10(7):1436. doi: 10.3390/microorganisms10071436.
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Investigation of isoniazid and ethionamide cross-resistance by whole genome sequencing and association with poor treatment outcomes of multidrug-resistant tuberculosis patients in South Africa.通过全基因组测序研究异烟肼和乙硫异烟胺交叉耐药性及其与南非耐多药结核病患者治疗效果不佳的关联
Int J Mycobacteriol. 2016 Dec;5 Suppl 1:S36-S37. doi: 10.1016/j.ijmyco.2016.11.020. Epub 2016 Nov 25.
3
Genotypic Analysis of Genes Associated with Independent Resistance and Cross-Resistance to Isoniazid and Ethionamide in Mycobacterium tuberculosis Clinical Isolates.结核分枝杆菌临床分离株中与对异烟肼和乙硫异烟胺的独立耐药性及交叉耐药性相关基因的基因型分析
Antimicrob Agents Chemother. 2015 Dec;59(12):7805-10. doi: 10.1128/AAC.01028-15. Epub 2015 Sep 14.
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Molecular investigation of resistance to the antituberculous drug ethionamide in multidrug-resistant clinical isolates of Mycobacterium tuberculosis.结核分枝杆菌耐乙硫异烟胺的多药耐药临床分离株的耐药分子研究。
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EthR, a repressor of the TetR/CamR family implicated in ethionamide resistance in mycobacteria, octamerizes cooperatively on its operator.EthR是TetR/CamR家族的一种阻遏蛋白,与分枝杆菌对乙硫异烟胺的抗性有关,它在其操纵基因上协同形成八聚体。
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Correlation of mutations and ethionamide susceptibility: Experience from national reference center for tuberculosis.突变与乙硫异烟胺敏感性的相关性:来自国家结核病参考中心的经验
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1
The small-molecule SMARt751 reverses resistance to ethionamide in acute and chronic mouse models of tuberculosis.小分子 SMARt751 逆转了急性和慢性结核小鼠模型对乙硫异烟胺的耐药性。
Sci Transl Med. 2022 May 4;14(643):eaaz6280. doi: 10.1126/scitranslmed.aaz6280.
2
Integrating informatics tools and portable sequencing technology for rapid detection of resistance to anti-tuberculous drugs.整合信息学工具和便携式测序技术,用于快速检测抗结核药物耐药性。
Genome Med. 2019 Jun 24;11(1):41. doi: 10.1186/s13073-019-0650-x.
3
Bacterial Genome-Wide Association Identifies Novel Factors That Contribute to Ethionamide and Prothionamide Susceptibility in Mycobacterium tuberculosis.细菌全基因组关联分析鉴定了导致结核分枝杆菌对乙硫异烟胺和丙硫异烟胺敏感性的新因素。
mBio. 2019 Apr 23;10(2):e00616-19. doi: 10.1128/mBio.00616-19.
4
Detection of novel mutations associated with independent resistance and cross-resistance to isoniazid and prothionamide in Mycobacterium tuberculosis clinical isolates.检测与结核分枝杆菌临床分离株对异烟肼和丙硫异烟胺的独立耐药和交叉耐药相关的新突变。
Clin Microbiol Infect. 2019 Aug;25(8):1041.e1-1041.e7. doi: 10.1016/j.cmi.2018.12.008. Epub 2018 Dec 22.
5
Genome-wide analysis of multi- and extensively drug-resistant Mycobacterium tuberculosis.全基因组分析多药和广泛耐药结核分枝杆菌。
Nat Genet. 2018 Feb;50(2):307-316. doi: 10.1038/s41588-017-0029-0. Epub 2018 Jan 22.
6
Molecular detection methods of resistance to antituberculosis drugs in Mycobacterium tuberculosis.结核分枝杆菌耐药相关的分子检测方法。
Med Mal Infect. 2017 Sep;47(5):340-348. doi: 10.1016/j.medmal.2017.04.008. Epub 2017 Jun 17.
7
Reversion of antibiotic resistance in by spiroisoxazoline SMARt-420.通过螺噁唑啉 SMARt-420 逆转 的抗生素耐药性。
Science. 2017 Mar 17;355(6330):1206-1211. doi: 10.1126/science.aag1006. Epub 2017 Mar 16.
8
Genomic analysis of globally diverse Mycobacterium tuberculosis strains provides insights into the emergence and spread of multidrug resistance.对全球不同结核分枝杆菌菌株的基因组分析为深入了解多重耐药性的出现和传播提供了线索。
Nat Genet. 2017 Mar;49(3):395-402. doi: 10.1038/ng.3767. Epub 2017 Jan 16.
9
Investigation of isoniazid and ethionamide cross-resistance by whole genome sequencing and association with poor treatment outcomes of multidrug-resistant tuberculosis patients in South Africa.通过全基因组测序研究异烟肼和乙硫异烟胺交叉耐药性及其与南非耐多药结核病患者治疗效果不佳的关联
Int J Mycobacteriol. 2016 Dec;5 Suppl 1:S36-S37. doi: 10.1016/j.ijmyco.2016.11.020. Epub 2016 Nov 25.
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A Multilaboratory, Multicountry Study To Determine MIC Quality Control Ranges for Phenotypic Drug Susceptibility Testing of Selected First-Line Antituberculosis Drugs, Second-Line Injectables, Fluoroquinolones, Clofazimine, and Linezolid.一项多实验室、多国研究,以确定选定的一线抗结核药物、二线注射剂、氟喹诺酮类、氯法齐明和利奈唑胺的表型药敏试验的最低抑菌浓度(MIC)质量控制范围。
J Clin Microbiol. 2016 Dec;54(12):2963-2968. doi: 10.1128/JCM.01138-16. Epub 2016 Sep 21.

聚合酶链反应测序策略如何能带来新数据以改善乙硫异烟胺耐药性的诊断。

How a PCR Sequencing Strategy Can Bring New Data to Improve the Diagnosis of Ethionamide Resistance.

作者信息

Maitre Thomas, Morel Florence, Brossier Florence, Sougakoff Wladimir, Jaffre Jéremy, Cheng Sokleaph, Veziris Nicolas, Aubry Alexandra

机构信息

Centre National de Référence des Mycobactéries et de la Résistance des Mycobactéries aux Antituberculeux, Hôpital Pitié-Salpêtrière, AP-HP (Assistance Publique Hôpitaux de Paris), Sorbonne-Université, F-75013 Paris, France.

Centre d'Immunologie et des Maladies Infectieuses, Sorbonne Université, INSERM, U1135, Cimi-Paris, F-75013 Paris, France.

出版信息

Microorganisms. 2022 Jul 15;10(7):1436. doi: 10.3390/microorganisms10071436.

DOI:10.3390/microorganisms10071436
PMID:35889155
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9316172/
Abstract

Ethionamide (ETH) is a second-line antituberculosis drug. ETH resistance (ETH-R) is mainly related to the mutations of the monooxygenase-activating ETH (EthA), the ETH target (InhA), and the promoter. Nonetheless, diagnosing ETH-R is still challenging. We assessed the strategy used for detecting ETH-R at the French National Reference Center for Mycobacteria in 497 MDR-TB isolates received from 2008 to 2016. The genotypic ETH's resistance detection was performed by sequencing , , the intergenic region, and the promoter in the 497 multidrug-resistant isolates, whereas the phenotypic ETH susceptibility testing (PST) was performed using the reference proportion method. Mutations were found in up to 76% of the 387 resistant isolates and in up to 28% of the 110 susceptible isolates. Our results do not support the role of mutations in ETH resistance. Altogether, the positive predictive value of our genotypic strategy to diagnose ETH-R was improved when only considering the variants included in the WHO catalogue and in other databases, such as TB-Profiler. Therefore, our work will help to update the list of mutations that could be graded as being associated with resistance to improve ETH-R diagnosis.

摘要

乙硫异烟胺(ETH)是一种二线抗结核药物。乙硫异烟胺耐药(ETH-R)主要与单加氧酶激活乙硫异烟胺(EthA)、乙硫异烟胺靶点(InhA)及启动子的突变有关。尽管如此,诊断ETH-R仍然具有挑战性。我们评估了法国国家分枝杆菌参考中心对2008年至2016年收到的497株耐多药结核分枝杆菌分离株检测ETH-R所采用的策略。对497株耐多药分离株的、基因间区域及启动子进行测序,以进行乙硫异烟胺耐药性的基因分型检测,而采用参考比例法进行乙硫异烟胺药敏表型检测(PST)。在387株耐药分离株中,高达76%发现有突变,在110株敏感分离株中,高达28%发现有突变。我们的结果不支持突变在乙硫异烟胺耐药中的作用。总体而言,当仅考虑世界卫生组织目录及其他数据库(如TB-Profiler)中包含的变异时,我们用于诊断ETH-R的基因分型策略的阳性预测值得到了提高。因此,我们的工作将有助于更新可被归类为与耐药相关的突变列表,以改进ETH-R的诊断。