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新型弗林纳病毒噬菌体 vWU2001 联合黏菌素对碳青霉烯类耐药鲍曼不动杆菌的增强抗菌作用。

Enhanced antibacterial effect of a novel Friunavirus phage vWU2001 in combination with colistin against carbapenem-resistant Acinetobacter baumannii.

机构信息

School of Science, Walailak University, Thasala, Nakhon Si Thammarat, 80161, Thailand.

Functional Proteomics Technology Laboratory, Functional Ingredients and Food Innovation Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Khlong Luang, Pathum Thani, 12120, Thailand.

出版信息

Sci Rep. 2022 Feb 16;12(1):2633. doi: 10.1038/s41598-022-06582-0.

DOI:10.1038/s41598-022-06582-0
PMID:35173237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8850435/
Abstract

The emergence of carbapenem-resistant Acinetobacter baumannii (CRAB) has been increasingly reported, leading to greater challenges in treating infections. With the development of phage therapy and phage-antibiotic combinations, it is promising to improve the treatment of bacterial infections. In the present study, a novel vB_AbaP_WU2001 (vWU2001) phage-specific CRAB with a genome of 40,792 bp was isolated. Genomic analysis disclosed that it belongs to the Autographiviridae family of the order Caudovirales. Phage vWU2001 had a broad host range with a high adsorption rate, short latent period, large burst size and good stability. The phage could reduce preformed biofilms and inhibit biofilm formation. The combination of phage vWU2001 and colistin had significantly higher bacterial growth inhibition activity than that of phage, or colistin alone. The efficacy of the combined treatment was also evaluated in Galleria mellonella. Evaluation of its therapeutic potential showed that the combination of phage and colistin resulted in a significantly greater increase in G. mellonella survival and in bacterial clearance, as compared with that of phage or colistin alone, indicating that the combination was synergistic against CRAB. The results demonstrated that phage vWU2001 has the potential to be developed as an antibacterial agent.

摘要

碳青霉烯类耐药鲍曼不动杆菌 (CRAB) 的出现日益受到关注,导致感染治疗面临更大的挑战。随着噬菌体治疗和噬菌体-抗生素联合疗法的发展,改善细菌感染的治疗前景广阔。本研究中,分离到一株新型 vB_AbaP_WU2001(vWU2001)噬菌体,可特异性杀灭 CRAB,其基因组大小为 40792bp。基因组分析表明,它属于尾病毒目 Autographiviridae 科。噬菌体 vWU2001 具有广泛的宿主范围、高吸附率、短潜伏期、大爆发量和良好的稳定性。噬菌体 vWU2001 可以减少预形成的生物膜并抑制生物膜形成。噬菌体 vWU2001 与多粘菌素联合使用时,对细菌生长的抑制活性明显高于单独使用噬菌体或多粘菌素。还在大蜡螟(Galleria mellonella)中评估了联合治疗的疗效。评估其治疗潜力的结果表明,与单独使用噬菌体或多粘菌素相比,噬菌体和多粘菌素联合使用可显著提高大蜡螟的存活率并清除细菌,表明联合治疗对 CRAB 具有协同作用。研究结果表明,噬菌体 vWU2001 具有作为抗菌剂开发的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f55/8850435/c552a3a1592f/41598_2022_6582_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f55/8850435/67ed0ad1c01e/41598_2022_6582_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f55/8850435/a029c32849a5/41598_2022_6582_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f55/8850435/5879455c156d/41598_2022_6582_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f55/8850435/a3afc93277c9/41598_2022_6582_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f55/8850435/3c80ea107ee4/41598_2022_6582_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f55/8850435/79e1dff8e3a7/41598_2022_6582_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f55/8850435/c552a3a1592f/41598_2022_6582_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f55/8850435/67ed0ad1c01e/41598_2022_6582_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f55/8850435/1ae375a71528/41598_2022_6582_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f55/8850435/a029c32849a5/41598_2022_6582_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f55/8850435/5879455c156d/41598_2022_6582_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f55/8850435/a3afc93277c9/41598_2022_6582_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f55/8850435/3c80ea107ee4/41598_2022_6582_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f55/8850435/79e1dff8e3a7/41598_2022_6582_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f55/8850435/c552a3a1592f/41598_2022_6582_Fig8_HTML.jpg

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