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首页> 外文期刊>Antimicrobial agents and chemotherapy. >Impact of Species Diversity on the Design of RNA-Based Diagnostics for Antibiotic Resistance in Neisseria gonorrhoeae
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Impact of Species Diversity on the Design of RNA-Based Diagnostics for Antibiotic Resistance in Neisseria gonorrhoeae

机译:物种多样性对Neisseria淋病性抗生素抗性抗生素诊断设计的影响

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摘要

Quantitative assessment of antibiotic-responsive RNA transcripts holds promise for a rapid point-of-care (POC) diagnostic tool for antimicrobial susceptibility testing. These assays aim to distinguish susceptible and resistant isolates by transcriptional differences upon drug exposure. However, an often-overlooked dimension of designing these tests is that the genetic diversity within a species may yield differential transcriptional regulation independent of resistance phenotype. Here, we use a phylogenetically diverse panel of Neisseria gonorrhoeae and transcriptome profiling coupled with reverse transcription-quantitative PCR to test this hypothesis, to identify azithromycin responsive transcripts and evaluate their potential diagnostic value, and to evaluate previously reported diagnostic markers for ciprofloxacin resistance (porB and rpmB). Transcriptome profiling confirmed evidence of genetic distance and population structure impacting transcriptional response to azithromycin. Taking this into account, we found azithromycin-responsive transcripts overrepresented in susceptible strains compared to resistant strains and selected four candidate diagnostic transcripts (rpsO, rplN, omp3, and NG01079) that were the most significantly differentially regulated between phenotypes across drug exposure. RNA signatures for these markers categorically predicted resistance in 19/20 cases, with the one incorrect categorical assignment for an isolate at the threshold of reduced susceptibility. Finally, we found that porB and rpmB expression were not uniformly diagnostic of ciprofloxacin resistance in a panel of isolates with unbiased phylogenetic sampling. Overall, our results suggest that RNA signatures as a diagnostic tool are promising for future POC diagnostics; however, development and testing should consider representative genetic diversity of the target pathogen.
机译:抗生素响应性RNA转录物的定量评估具有用于抗微生物易感性测试的快速护理(POC)诊断工具的承担。这些测定旨在通过对药物暴露的转录差来区分易感和抗性分离物。然而,经常被忽视的设计这些测试的维度是,物种内的遗传多样性可以屈服于无抗性表型的差异转录调节。在这里,我们使用具有逆转录定量PCR的细胞α淋病奈瑟耳肽和转录组分析的传递体分析,以测试该假设,以鉴定阿奇霉素响应性转录物并评估其潜在的诊断价值,并评估先前报告的环丙沙星抗性的诊断标志物(PORP和rpmb)。转录组分析证实了遗传距离和群体结构的证据,影响转录对阿奇霉素的反应。考虑到这一点,我们发现与抗性菌株相比,在易感菌株中发现了超过敏感菌株的阿奇霉素响应转录物,并选择了四种候选诊断转录物(RPSO,RPLN,OMP3和NG01079),其在药物暴露的表型之间是最显着的差异调节。对于这些标记的RNA签名在19/20案例中进行了分类预测的阻力,其中一个不正确的分类分配在降低易感性的阈值下的隔离分配。最后,我们发现Porb和RPMB表达并不均匀地诊断与无偏发育采样的分离物板中的环丙沙星抗性。总体而言,我们的结果表明RNA签名作为诊断工具是未来的POC诊断的承诺;然而,开发和测试应考虑靶病原体的代表性遗传多样性。

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