用于结核分枝杆菌吡嗪酰胺抗菌药敏感性试验的简化吡嗪酰胺酶试验。

IF 6.1 2区 医学 Q1 MICROBIOLOGY
Hsin-Hua Chan, Yu-Chen Wang, Ruwen Jou
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引用次数: 0

摘要

吡嗪酰胺(PZA)可根除持续存在的结核分枝杆菌复合体(MTBC),是治疗结核病(TB)的重要一线药物。由于成本和技术方面的挑战,缺乏简单可靠的常规使用的基于培养的 PZA 抗菌药敏试验 (AST),阻碍了结核病的最终治疗策略。我们最初在结核病参比实验室开发了一种简化的色原吡嗪酰胺酶(PZase)检测方法,使用的是具有各种耐药性特征的 MTBC 分离物训练集,并在 10 个临床实验室使用连续的 BACTEC MGIT 960(MGIT)培养阳性培养物验证了其性能。以 pncA 基因 Sanger 测序结果为参考,并与 MGIT-PZA AST 进行比较。使用获得专利的内部实时 PCR 技术对牛分枝杆菌进行鉴别诊断。在 106 个训练分离株中,PZase 检验和 MGIT-PZA AST 与 Sanger 测序的一致性分别为 100.0% 和 99.1%。我们发现 32.1%(34/106)的分离株携带 pncA 突变,其中一个分离株携带沉默突变 S65S。为了进行验证,我们检测了 1,793 个临床分离株,其中包括 150 个来自同一病例标本的重复分离株和 16 个具有未定性耐药性(UDR)相关突变的分离株。除去重复分离株和 UDR 分离株,我们发现了 2.6%(43/1,627)的 PZA 耐药分离株,其中包括 1.3%(21/1,627)的 M. bovis 分离株。卡帕值为 0.851-1.000。此外,10家实验室进行的PZase检测的准确率为98.5%-100.0%。我们的简化 PZase 检测与 Sanger 测序和 MGIT-PZA AST 的一致性很高。将 PZase 检测纳入常规一线 AST 不费吹灰之力,这代表着实验室服务在终结结核病方面的进步:我们开发并验证了一种用于吡嗪酰胺(PZA)抗菌药物敏感性检测(AST)的简单吡嗪酰胺酶(PZase)检测方法。结果表明,PZase 检验与 pncA 基因测序和 MGIT-PZA AST 具有很高的一致性。将 PZase 检测纳入常规 AST 不费吹灰之力,而且还能改善结核病的实验室服务。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A simplified pyrazinamidase test for Mycobacterium tuberculosis pyrazinamide antimicrobial susceptibility testing.

Pyrazinamide (PZA) is an important first-line drug for tuberculosis (TB) treatment by eradicating the persisting Mycobacterium tuberculosis complex (MTBC). Due to cost and technical challenges, end TB strategies are hampered by the lack of a simple and reliable culture-based PZA antimicrobial susceptibility testing (AST) for routine use. We initially developed a simplified chromogenic pyrazinamidase (PZase) test in the TB reference laboratory using a training set MTBC isolates with various drug-resistant profiles, and validated its performance using consecutive BACTEC MGIT 960 (MGIT)-culture-positive culture in 10 clinical laboratories. The pncA gene Sanger sequencing results were used as the reference, and compared to the MGIT-PZA AST. Differential diagnosis of Mycobacterium bovis was conducted using patented in-house real-time PCR. Of the 106 training isolates, the PZase test and MGIT-PZA AST showed 100.0% and 99.1% concordance as compared to Sanger sequencing, respectively. We found 32.1% (34/106) isolates harbored pncA mutations, including one isolate with silent mutation S65S. For validation, 1,793 clinical isolates were tested including 150 duplicate isolates from specimens of the same cases and 16 isolates with uncharacterized drug resistance (UDR)-associated mutations. Excluding duplicated and UDR isolates, we identified 2.6% (43/1,627) PZA-resistant isolates, including 1.3% (21/1,627) M. bovis isolates. The kappa values were 0.851-1.000. In addition, the accuracy of the PZase test conducted by 10 laboratories was 98.5%-100.0%. Our simplified PZase test demonstrated high concordance with Sanger sequencing and MGIT-PZA AST. Integrating the PZase test into routine first-line AST is effortless and represents an improvement in laboratory services for ending TB.

Importance: We developed and validated a simple pyrazinamidase (PZase) test for pyrazinamide (PZA) antimicrobial susceptibility testing (AST). Our results demonstrated that the PZase test had high agreement with the pncA gene sequencing and MGIT-PZA AST. Integrating PZase test into routine AST is effortless and represents an improvement in laboratory services for ending TB.

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来源期刊
Journal of Clinical Microbiology
Journal of Clinical Microbiology 医学-微生物学
CiteScore
17.10
自引率
4.30%
发文量
347
审稿时长
3 months
期刊介绍: The Journal of Clinical Microbiology® disseminates the latest research concerning the laboratory diagnosis of human and animal infections, along with the laboratory's role in epidemiology and the management of infectious diseases.
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