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ProcCluster® 和盐酸普鲁卡因可抑制 和 生长,并在与甲型流感病毒和 共同感染时发挥抗菌作用。

ProcCluster® and procaine hydrochloride inhibit the growth of species and exert antimicrobial properties during coinfection with influenza A viruses and .

机构信息

Section of Experimental Virology, Institute of Medical Microbiology, Center for Molecular Biomedicine (CMB), Jena University Hospital, Jena, Germany.

Department of Molecular and Applied Microbiology, Leibniz Institute for Natural Product Research and Infection Biology - Hans-Knoell-Institute, Jena, Germany.

出版信息

Front Cell Infect Microbiol. 2024 Oct 15;14:1445428. doi: 10.3389/fcimb.2024.1445428. eCollection 2024.

Abstract

INTRODUCTION

Influenza-associated pulmonary aspergillosis is associated with high mortality rates and limited treatment options. The current standard practice involves treating each pathogen separately. However, the use of antifungal drugs can lead to serious side effects, and the presence of triazole-resistant strains can complicate antifungal therapy. In addition, drug-resistant influenza viruses are becoming an increasing concern in clinics. A drug that affects fungal and viral propagation could overcome these disadvantages. Thus, we conducted a study to examine the antifungal and antiviral properties of ProcCluster® and procaine hydrochloride (HCl), which are prodrugs derived from the local anesthetic procaine.

METHODS

Conidia of different strains, and were treated with the test substances in a human cell-free system and antifungal properties were analyzed either by fluorescence microscopy or absorption measurements. Changes in metabolic activity and intracellular Ca distribution during treatment of with ProcCluster® were observed using fluorescence microscopy. In addition, antifungal and antiviral properties of ProcCluster® and procaine HCl were investigated during coinfection of lung epithelial cells with and influenza A viruses (IAV). Analysis was performed by fluorescence microscopy, standard plaque assay and Western blot assay.

RESULTS

Both substances inhibited the growth of the fungus, even when applied after germination or in the presence of purified IAV particles. ProcCluster® remained effective against triazole-resistant strains. However, the addition of CaCl reversed the antifungal effect, indicating that ProcCluster® inhibited fungal growth by disrupting fungal Ca homeostasis. Furthermore, studies showed that ProcCluster® and procaine HCl reduced the pathogen load of IAV and during coinfection. Finally, the combination of ProcCluster® with the antiviral drug favipiravir exhibited increased antipathogenic activity, particularly against IAV replication.

DISCUSSION

This research highlights ProcCluster® and procaine HCl as substances with anti-infective properties against various pathogens.

摘要

简介

流感相关性肺曲霉病与高死亡率和有限的治疗选择相关。目前的标准做法是分别治疗每种病原体。然而,抗真菌药物的使用会导致严重的副作用,并且三唑耐药菌株的存在会使抗真菌治疗复杂化。此外,临床中越来越关注耐药性流感病毒。一种既能影响真菌又能影响病毒繁殖的药物可以克服这些缺点。因此,我们进行了一项研究,以检验 ProcCluster®和普鲁卡因盐酸盐(Procaine HCl)的抗真菌和抗病毒特性,这两种前药均源自局部麻醉药普鲁卡因。

方法

用测试物质处理不同菌株的分生孢子,在无细胞的人体系中分析抗真菌特性,或通过荧光显微镜或吸收测量。用荧光显微镜观察 ProcCluster®处理 时代谢活性和细胞内 Ca 分布的变化。此外,还研究了 ProcCluster®和普鲁卡因 HCl 在肺上皮细胞与 和流感 A 病毒(IAV)共感染时的抗真菌和抗病毒特性。通过荧光显微镜、标准噬菌斑测定和 Western blot 分析进行分析。

结果

两种物质均抑制了真菌的生长,即使在发芽后或存在纯化的 IAV 颗粒时应用也是如此。ProcCluster®对三唑耐药菌株仍然有效。然而,添加 CaCl2 逆转了抗真菌作用,表明 ProcCluster®通过破坏真菌的 Ca 稳态来抑制真菌生长。此外,研究表明 ProcCluster®和普鲁卡因 HCl 在共感染时减少了 IAV 和 的病原体负荷。最后,ProcCluster®与抗病毒药物法匹拉韦联合使用表现出增强的抗病原体活性,特别是对 IAV 复制的抑制作用。

讨论

本研究强调 ProcCluster®和普鲁卡因 HCl 是具有针对各种病原体的抗感染特性的物质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e923/11518849/47da6c8ff02d/fcimb-14-1445428-g001.jpg

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