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来自牡蛎血淋巴的抗菌蛋白可提高传统抗生素的疗效。

Antimicrobial proteins from oyster hemolymph improve the efficacy of conventional antibiotics.

作者信息

Summer Kate, Guo Qi, Liu Lei, Barkla Bronwyn, Giles Sarah, Benkendorff Kirsten

机构信息

Faculty of Science and Engineering, Southern Cross University, Lismore, NSW, Australia.

Flinders Accelerator for Microbiome Exploration, College of Science and Engineering, Flinders University, Bedford Park, SA, Australia.

出版信息

PLoS One. 2025 Jan 21;20(1):e0312305. doi: 10.1371/journal.pone.0312305. eCollection 2025.

Abstract

Discovering new antibiotics and increasing the efficacy of existing antibiotics are priorities to address antimicrobial resistance. Antimicrobial proteins and peptides (AMPPs) are considered among the most promising antibiotic alternatives and complementary therapies. Here, we build upon previous work investigating the antibacterial activity of a semi-purified hemolymph protein extract (HPE) of the Australian oyster Saccostrea glomerata. HPE showed antimicrobial-biofilm inhibitory activity toward laboratory and clinical strains of Streptococcus pneumoniae and Streptococcus pyogenes at 4.4 and 24.1 μg/mL total protein, respectively. In combination assays, the effectiveness of conventional antibiotics (ampicillin, gentamicin, trimethoprim and ciprofloxacin) was improved between 2 to 32-fold in the presence of HPE (1-12 μg/mL) against a range of clinically important bacteria including Streptococcus spp., Pseudomonas aeruginosa, Moraxella catarrhalis, Klebsiella pneumoniae and Staphylococcus aureus. Effective HPE concentrations are comparable to AMPPs currently approved for use or in clinical trials pipelines. Proteomics analysis of HPE identified a number of proteins including abundant known AMPPs. It was non-toxic to A549 human lung cells up to 205 μg/mL, demonstrating safety well above effective concentrations. Activity was retained with storage at -80°C and ambient laboratory temperature (~24°C), but declined after treatment at either 37°C or 60°C (1 h). This study is in agreement with growing evidence that AMPPs show specificity and a high capacity for synergism with antibiotics. The discovery of HPE provides great opportunities for both pharmaceutical and aquaculture industry development.

摘要

发现新型抗生素并提高现有抗生素的疗效是应对抗菌药物耐药性的首要任务。抗菌蛋白和肽(AMPPs)被认为是最有前途的抗生素替代品和辅助治疗方法之一。在此,我们基于之前对澳大利亚牡蛎(Saccostrea glomerata)半纯化血淋巴蛋白提取物(HPE)抗菌活性的研究展开。HPE分别在总蛋白浓度为4.4 μg/mL和24.1 μg/mL时,对肺炎链球菌和化脓性链球菌的实验室菌株及临床菌株表现出抗微生物生物膜抑制活性。在联合试验中,在HPE(1 - 12 μg/mL)存在的情况下,传统抗生素(氨苄青霉素、庆大霉素、甲氧苄啶和环丙沙星)对一系列临床重要细菌(包括链球菌属、铜绿假单胞菌、卡他莫拉菌、肺炎克雷伯菌和金黄色葡萄球菌)的有效性提高了2至32倍。有效的HPE浓度与目前已批准使用或处于临床试验阶段的AMPPs相当。对HPE的蛋白质组学分析鉴定出了许多蛋白质,包括大量已知的AMPPs。在高达205 μg/mL的浓度下,它对A549人肺细胞无毒,表明其安全性远高于有效浓度。在 - 80°C和实验室环境温度(约24°C)下储存时,活性得以保留,但在37°C或60°C处理1小时后活性下降。这项研究与越来越多的证据一致,即AMPPs表现出特异性并具有与抗生素协同作用的高能力。HPE的发现为制药和水产养殖业的发展提供了巨大机遇。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db01/11750097/c81b5e1a1a12/pone.0312305.g001.jpg

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