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一种免疫化学方法检测铜绿假单胞菌临床分离株产生的群体感应调节毒力因子 2-庚基-4-喹啉 N-氧化物(HQNO)。

An Immunochemical Approach to Detect the Quorum Sensing-Regulated Virulence Factor 2-Heptyl-4-Quinoline N-Oxide (HQNO) Produced by Pseudomonas aeruginosa Clinical Isolates.

机构信息

Nanobiotechnology for Diagnostics (Nb4D), Department of Surfactants and Nanotechnology, Institute for Advanced Chemistry of Catalonia (IQAC) of the Spanish Council for Scientific Research (CSIC), Barcelona, Spain.

CIBER de Bioingeniería, Biomateriales, y Nanomedicina (CIBER-BBN), Barcelona, Spain.

出版信息

Microbiol Spectr. 2022 Aug 31;10(4):e0107321. doi: 10.1128/spectrum.01073-21. Epub 2022 Jul 25.

DOI:10.1128/spectrum.01073-21
PMID:35876587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9431570/
Abstract

Understanding quorum sensing (QS) and its role in the development of pathogenesis may provide new avenues for diagnosing, surveillance, and treatment of infectious diseases. For this purpose, the availability of reliable and efficient analytical diagnostic tools suitable to specifically detect and quantify these essential QS small molecules and QS regulated virulence factors is crucial. Here, we reported the development and evaluation of antibodies and an enzyme-linked immunosorbent assay (ELISA) for HQNO (2-heptyl-4-quinoline N-oxide), a QS product of the PqsR system, which has been found to act as a major virulence factor that interferes with the growth of other microorganisms. Despite the nonimmunogenic character of HQNO, the antibodies produced showed high avidity and the microplate-based ELISA developed could detect HQNO in the low nM range. Hence, a limit of detection (LOD) of 0.60 ± 0.13 nM had been reached in Müeller Hinton (MH) broth, which was below previously reported levels using sophisticated equipment based on liquid chromatography coupled to mass spectrometry. The HQNO profile of release of different Pseudomonas aeruginosa clinical isolates analyzed using this ELISA showed significant differences depending on whether the clinical isolates belonged to patients with acute or chronic infections. These data point to the possibility of using HQNO as a specific biomarker to diagnose P. aeruginosa infections and for patient surveillance. Considering the role of HQNO in inhibiting the growth of coinfecting bacteria, the present ELISA will allow the investigation of these complex bacterial interactions underlying infections. Bacteria use quorum sensing (QS) as a communication mechanism that releases small signaling molecules which allow synchronizing a series of activities involved in the pathogenesis, such as the biosynthesis of virulence factors or the regulation of growth of other bacterial species. HQNO is a metabolite of the Pseudomonas aeruginosa-specific QS signaling molecule PQS (Pseudomonas quinolone signal). In this work, the development of highly specific antibodies and an immunochemical diagnostic technology (ELISA) for the detection and quantification of HQNO was reported. The ELISA allowed profiling of the release of HQNO by clinical bacterial isolates, showing its potential value for diagnosing and surveillance of P. aeruginosa infections. Moreover, the antibodies and the ELISA reported here may contribute to the knowledge of other underlying conditions related to the pathology, such as the role of the interactions with other bacteria of a particular microbiota environment.

摘要

理解群体感应(QS)及其在发病机制中的作用可能为诊断、监测和治疗传染病提供新的途径。为此,需要提供可靠和有效的分析诊断工具,以专门检测和定量这些必需的 QS 小分子和 QS 调节的毒力因子。在这里,我们报告了用于 HQNO(2-庚基-4-喹啉 N-氧化物)的抗体和酶联免疫吸附测定(ELISA)的开发和评估,HQNO 是 PqsR 系统的 QS 产物,已被发现作为一种主要的毒力因子,干扰其他微生物的生长。尽管 HQNO 没有免疫原性,但产生的抗体表现出高亲和力,并且开发的基于微孔板的 ELISA 可以在低 nM 范围内检测 HQNO。因此,在 Mueller Hinton(MH)肉汤中达到了检测限(LOD)为 0.60±0.13 nM,低于以前使用基于液相色谱-质谱联用的复杂设备报道的水平。使用这种 ELISA 分析不同铜绿假单胞菌临床分离株释放的 HQNO 图谱表明,根据临床分离株是否属于急性或慢性感染患者,存在显著差异。这些数据表明 HQNO 作为一种特定的生物标志物用于诊断铜绿假单胞菌感染和患者监测的可能性。考虑到 HQNO 在抑制共感染细菌生长中的作用,本 ELISA 将允许调查这些感染中复杂的细菌相互作用。细菌将群体感应(QS)用作一种通信机制,释放出允许同步参与发病机制的一系列活动的小分子信号,例如毒力因子的生物合成或其他细菌物种生长的调节。HQNO 是铜绿假单胞菌特异性 QS 信号分子 PQS(假单胞菌喹诺酮信号)的代谢物。在这项工作中,报道了用于检测和定量 HQNO 的高度特异性抗体和免疫化学诊断技术(ELISA)的开发。ELISA 允许对临床细菌分离株释放的 HQNO 进行分析,显示出其在诊断和监测铜绿假单胞菌感染方面的潜在价值。此外,本文报道的抗体和 ELISA 可能有助于了解与病理学相关的其他潜在情况,例如特定微生物群环境中与其他细菌相互作用的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193a/9431570/06bf13b9ac37/spectrum.01073-21-f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193a/9431570/14d3f5d5e5fb/spectrum.01073-21-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193a/9431570/5b8a678425c9/spectrum.01073-21-f002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193a/9431570/6ec82e9708c6/spectrum.01073-21-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193a/9431570/06bf13b9ac37/spectrum.01073-21-f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193a/9431570/14d3f5d5e5fb/spectrum.01073-21-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193a/9431570/5b8a678425c9/spectrum.01073-21-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193a/9431570/5073c00cb22a/spectrum.01073-21-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193a/9431570/6ec82e9708c6/spectrum.01073-21-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/193a/9431570/06bf13b9ac37/spectrum.01073-21-f005.jpg

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