Nanobiotechnology for Diagnostics (Nb4D), Department of Surfactants and Nanobiotechnology, Institute for Advanced Chemistry of Catalonia (IQAC) of the Spanish Council for Scientific Research (CSIC), 08750 Barcelona, Spain.
CIBER de Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN), 28029 Madrid Spain.
ACS Infect Dis. 2022 Mar 11;8(3):645-656. doi: 10.1021/acsinfecdis.1c00670. Epub 2022 Feb 17.
An immunochemical strategy to detect and quantify AIP-IV, the quorum sensing (QS) signaling molecule produced by type IV, is reported here for the first time. Theoretical calculations and molecular modeling studies have assisted on the design and synthesis of a suitable peptide hapten (AIPIVS), allowing to obtain high avidity and specific antibodies toward this peptide despite its low molecular weight. The ELISA developed achieves an IC value of 2.80 ± 0.17 and an LOD of 0.19 ± 0.06 nM in complex media such as 1/2 Tryptic Soy Broth. Recognition of other AIPs (I-III) is negligible (cross-reactivity below 0.001%), regardless of the structural similarities. A pilot study with a set of clinical isolates from patients with airways infection or colonization demonstrates the potential of this ELISA to perform biomedical investigations related to the role of QS in pathogenesis and the association between dysfunctional or the type with unfavorable clinical outcomes. The AIP-IV levels could be quantified in the low nanomolar range in less than 1 h after inoculating IV-genotyped isolates in the culture broth, while those genotyped as I-III did not show any immunoreactivity after a 48 h growth, pointing to the possibility to use this technology for phenotyping . The research strategy here reported can be extended to the rest of the AIP types of , allowing the development of powerful multiplexed chips or point-of-care (PoC) diagnostic devices to unequivocally identify its presence and its type on samples from infected patients.
本文首次报道了一种用于检测和定量 IV 型群体感应(QS)信号分子 AIP-IV 的免疫化学策略。理论计算和分子建模研究辅助设计和合成了合适的肽半抗原(AIPIVS),尽管其分子量低,但仍能获得针对该肽的高亲和力和特异性抗体。开发的 ELISA 在复杂介质(如 1/2 胰蛋白酶大豆肉汤)中达到 2.80 ± 0.17 的 IC 值和 0.19 ± 0.06 nM 的 LOD。对其他 AIP(I-III)的识别可以忽略不计(交叉反应性低于 0.001%),无论结构相似性如何。一组来自呼吸道感染或定植患者的临床分离株的初步研究表明,该 ELISA 具有进行与 QS 在发病机制中的作用以及功能失调的相关性或与不利临床结果相关的生物医学研究的潜力。在接种 IV 型基因分型分离株到培养液中不到 1 小时后,AIP-IV 水平可以在低于纳摩尔级的范围内定量,而那些基因分型为 I-III 的在 48 小时生长后没有显示出任何免疫反应性,表明有可能使用该技术进行表型分析。本文报道的研究策略可以扩展到其他 AIP 类型,从而可以开发强大的多重芯片或即时护理(PoC)诊断设备,以明确识别感染患者样本中 AIP 的存在及其类型。