Assessing the antiviral activity of antimicrobial peptides Caerin1.1 against PRRSV in Vitro and in Vivo

IF 2.4 2区 农林科学 Q3 MICROBIOLOGY
Shengnan Ruan , Xuexiang Yu , Hao Wu , Mingkai Lei , Xugang Ku , Ahmed H. Ghonaim , Wentao Li , Yunbo Jiang , Qigai He
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Abstract

The Porcine reproductive and respiratory syndrome (PRRS) causes severe financial losses to the global swine industry. Due to continuous virus evolution, the protection against the PRRS provided by current vaccines is limited. In order to find new antiviral strategies, this study investigated the antiviral potential of antimicrobial peptides (AMPs) against PRRSV. Given the diversity of PRRSV strains and the limited effectiveness of existing vaccines in controlling PRRSV, this study evaluated the inhibitory effects of KLAK, Cecropin B, Piscidin1, and Caerin1.1 on 3 strains of PRRSV (lineage 5 classical strain, lineage 8 highly pathogenic strain, and lineage 1 NADC30-like strain). Caerin1.1 exhibited significant dose-dependent antiviral activity, with an effective concentration (EC50) of 7.5 μM. Caerin1.1 effectively inhibited PRRSV replication when added before or in early infection but showed reduced effectiveness when added in late infection, indicating its potential involvement in targeting early transcription mechanisms of viral RNA polymerase and significantly upregulating cytokine gene expression. In the NADC30 strain-based animal infection model, Caerin1.1 treatment significantly reduced lung viral loads and inflammation in the lungs of PRRSV-infected pigs, with a mortality rate of 0 % (0/5) in the treated group compared to 66.67 % (4/6) in the untreated group, indicating a reduction in the mortality rate. Additionally, compared with the untreated group, the Caerin1.1-treated group showed significant improvements, such as lighter fever, more daily weight gain, less clinical symptoms, less viral load in blood, and less virus oral shedding (P < 0.05). These findings reveal the potential of antimicrobial peptides as PRRSV therapeutic agents and suggest that Caerin1.1 is a promising candidate for a novel anti-PRRSV drug.

评估抗菌肽 Caerin1.1 对体外和体内 PRRSV 的抗病毒活性。
猪繁殖与呼吸综合征(PRRS)给全球养猪业造成了严重的经济损失。由于病毒不断进化,目前的疫苗对 PRRS 的保护有限。为了寻找新的抗病毒策略,本研究调查了抗菌肽(AMPs)对 PRRSV 的抗病毒潜力。鉴于 PRRSV 株系的多样性以及现有疫苗对 PRRSV 的控制效果有限,本研究评估了 KLAK、Cecropin B、Piscidin1 和 Caerin1.1 对 3 株 PRRSV(5 系经典株、8 系高致病性株和 1 系 NADC30-like 株)的抑制作用。Caerin1.1 具有显著的剂量依赖性抗病毒活性,有效浓度(EC50)为 7.5 μM。在感染前或感染早期加入 Caerin1.1 能有效抑制 PRRSV 的复制,但在感染晚期加入 Caerin1.1 则效果减弱,这表明 Caerin1.1 可能参与了针对病毒 RNA 聚合酶早期转录机制的作用,并能显著上调细胞因子基因的表达。在基于 NADC30 株的动物感染模型中,Caerin1.1 治疗可显著降低 PRRSV 感染猪肺部病毒载量和炎症,治疗组死亡率为 0 %(0/5),而未治疗组死亡率为 66.67 %(4/6),表明死亡率有所降低。此外,与未治疗组相比,Caerin1.1 治疗组有明显改善,如发热减轻、日增重增加、临床症状减轻、血液中病毒载量减少、病毒口腔脱落减少(P < 0.05)。这些发现揭示了抗菌肽作为PRRSV治疗剂的潜力,并表明Caerin1.1是一种新型抗PRRSV药物的理想候选物。
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来源期刊
Veterinary microbiology
Veterinary microbiology 农林科学-兽医学
CiteScore
5.90
自引率
6.10%
发文量
221
审稿时长
52 days
期刊介绍: Veterinary Microbiology is concerned with microbial (bacterial, fungal, viral) diseases of domesticated vertebrate animals (livestock, companion animals, fur-bearing animals, game, poultry, fish) that supply food, other useful products or companionship. In addition, Microbial diseases of wild animals living in captivity, or as members of the feral fauna will also be considered if the infections are of interest because of their interrelation with humans (zoonoses) and/or domestic animals. Studies of antimicrobial resistance are also included, provided that the results represent a substantial advance in knowledge. Authors are strongly encouraged to read - prior to submission - the Editorials (''Scope or cope'' and ''Scope or cope II'') published previously in the journal. The Editors reserve the right to suggest submission to another journal for those papers which they feel would be more appropriate for consideration by that journal. Original research papers of high quality and novelty on aspects of control, host response, molecular biology, pathogenesis, prevention, and treatment of microbial diseases of animals are published. Papers dealing primarily with immunology, epidemiology, molecular biology and antiviral or microbial agents will only be considered if they demonstrate a clear impact on a disease. Papers focusing solely on diagnostic techniques (such as another PCR protocol or ELISA) will not be published - focus should be on a microorganism and not on a particular technique. Papers only reporting microbial sequences, transcriptomics data, or proteomics data will not be considered unless the results represent a substantial advance in knowledge. Drug trial papers will be considered if they have general application or significance. Papers on the identification of microorganisms will also be considered, but detailed taxonomic studies do not fall within the scope of the journal. Case reports will not be published, unless they have general application or contain novel aspects. Papers of geographically limited interest, which repeat what had been established elsewhere will not be considered. The readership of the journal is global.
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