内溶解素 NC5 可改善小鼠模型中尤伯杯链球菌乳腺炎的早期氯唑西林治疗。

IF 3.9 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied Microbiology and Biotechnology Pub Date : 2024-12-01 Epub Date: 2024-01-10 DOI:10.1007/s00253-023-12820-w
Niels Vander Elst, Julie Bellemans, Rob Lavigne, Yves Briers, Evelyne Meyer
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引用次数: 0

摘要

小牛链球菌经常引起牛乳腺炎,这是一种传染性乳房疾病,对奶牛的经济影响很大。传统抗生素(如氯西林)作为一种独立疗法,有时在消除小牛链球菌方面效果有限。为了应对这一挑战,本研究的目的是调查 VersaTile 工程内溶菌素 NC5 在小鼠模型中作为氯唑西林的辅助疗法治疗牛尤伯杯氏菌乳腺炎的情况。NC5 之前是根据其细胞内杀灭和生物膜根除活性筛选出来的。为了对这一补充策略进行临床前概念验证,哺乳期小鼠在瘤内感染了牛尤伯杯氏菌野外分离株,随后接受氯唑西林(30.0 μg)与低剂量(23.5 μg)或高剂量(235.0 μg)NC5 联合治疗。对照组包括抗生素单药治疗组和安慰剂治疗组。结果发现两类反应者:快速反应者(17 人),治疗 4 小时后出现反应;慢速反应者(10 人),治疗 4 小时后各组均无明显反应。与安慰剂治疗相比,大剂量联合疗法对快速反应者的乳腺炎特征有以下影响:(i) 细菌量减少 13,000 倍(4.11 ± 0.78 Δlog10;p < 0.001);(ii) 中性粒细胞浸润减少 5.7 倍(p > 0.05);(iii) 主要促炎趋化因子 IL-8 减少 13 倍(p < 0.01)。这些乳腺炎特征通常与内溶素的添加量呈剂量反应关系。目前的体内研究补充了我们的体外数据,并提供了 NC5 作为乳房内氯唑西林治疗辅助药物的临床前概念证明。要点- 对工程内溶菌素 NC5 作为氯唑西林治疗的辅助药物进行了临床前评估。- 观察到两种类型的小鼠(反应慢和反应快)。- 附加治疗可减少细菌量、中性粒细胞流入量和促炎介质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endolysin NC5 improves early cloxacillin treatment in a mouse model of Streptococcus uberis mastitis.

Streptococcus uberis frequently causes bovine mastitis, an infectious udder disease with significant economic implications for dairy cows. Conventional antibiotics, such as cloxacillin, sometimes have limited success in eliminating S. uberis as a stand-alone therapy. To address this challenge, the study objective was to investigate the VersaTile engineered endolysin NC5 as a supplemental therapy to cloxacillin in a mouse model of bovine S. uberis mastitis. NC5 was previously selected based on its intracellular killing and biofilm eradicating activity. To deliver preclinical proof-of-concept of this supplemental strategy, lactating mice were intramammarily infected with a bovine S. uberis field isolate and subsequently treated with cloxacillin (30.0 μg) combined with either a low (23.5 μg) or high (235.0 μg) dose of NC5. An antibiotic monotherapy group, as well as placebo treatment, was included as controls. Two types of responders were identified: fast (n = 17), showing response after 4-h treatment, and slow (n = 10), exhibiting no clear response at 4 h post-treatment across all groups. The high-dose combination therapy in comparison with placebo treatment impacted the hallmarks of mastitis in the fast responders by reducing (i) the bacterial load 13,000-fold (4.11 ± 0.78 Δlog10; p < 0.001), (ii) neutrophil infiltration 5.7-fold (p > 0.05), and (iii) the key pro-inflammatory chemokine IL-8 13-fold (p < 0.01). These mastitis hallmarks typically followed a dose response dependent on the amount of endolysin added. The current in vivo study complements our in vitro data and provides preclinical proof-of-concept of NC5 as an adjunct to intramammary cloxacillin treatment. KEY POINTS: • Engineered endolysin NC5 was preclinically evaluated as add-on to cloxacillin treatment. • Two types of mice (slow and fast responding) were observed. • The add-on treatment decreased bacterial load, neutrophil influx, and pro-inflammatory mediators.

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来源期刊
Applied Microbiology and Biotechnology
Applied Microbiology and Biotechnology 工程技术-生物工程与应用微生物
CiteScore
10.00
自引率
4.00%
发文量
535
审稿时长
2 months
期刊介绍: Applied Microbiology and Biotechnology focusses on prokaryotic or eukaryotic cells, relevant enzymes and proteins; applied genetics and molecular biotechnology; genomics and proteomics; applied microbial and cell physiology; environmental biotechnology; process and products and more. The journal welcomes full-length papers and mini-reviews of new and emerging products, processes and technologies.
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