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新型广谱裂解性噬菌体Phage_Pae01的特性及其对……的抗生物膜功效

Characterization of the novel broad-spectrum lytic phage Phage_Pae01 and its antibiofilm efficacy against .

作者信息

Shi Zhixin, Hong Xin, Li Zexuan, Zhang Meijuan, Zhou Jun, Zhao Zhe, Qiu Shengfeng, Liu Genyan

机构信息

Department of Laboratory Medicine, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.

National Key Clinical Department of Laboratory Medicine, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.

出版信息

Front Microbiol. 2024 Jul 17;15:1386830. doi: 10.3389/fmicb.2024.1386830. eCollection 2024.

DOI:10.3389/fmicb.2024.1386830
PMID:39091310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11292732/
Abstract

INTRODUCTION

is present throughout nature and is a common opportunistic pathogen in the human body. Carbapenem antibiotics are typically utilized as a last resort in the clinical treatment of multidrug-resistant infections caused by . The increase in carbapenem-resistant poses an immense challenge for the treatment of these infections. Bacteriophages have the potential to be used as antimicrobial agents for treating antibiotic-resistant bacteria.

METHODS AND RESULTS

In this study, a new virulent P. aeruginosa phage, Phage_Pae01, was isolated from hospital sewage and shown to have broad-spectrum antibacterial activity against clinical isolates (83.6%). These clinical strains included multidrug-resistant and carbapenem-resistant . Transmission electron microscopy revealed that the phage possessed an icosahedral head of approximately 80 nm and a long tail about 110  m, indicating that it belongs to the Myoviridae family of the order . Biological characteristic analysis revealed that Phage_Pae01 could maintain stable activity in the temperature range of 4~ 60°C and pH range of 4 ~ 10. According to the lysis kinetics of the phage, Phage_Pae01 demonstrated strong antibacterial activity. The optimal multiplicity of infection was 0.01. The genome of Phage_Pae01 has a total length of 93,182 bp and contains 176 open reading frames (ORFs). The phage genome does not contain genes related to virulence or antibiotic resistance. In addition, Phage_Pae01 effectively prevented the formation of biofilms and eliminated established biofilms. When Phage_Pae01 was combined with gentamicin, it significantly disrupted established biofilms.

CONCLUSION

We identified a novel phage and demonstrated its effective antimicrobial properties against in both the floating and biofilm states. These findings offer a promising approach for the treatment of drug-resistant bacterial infections in clinical settings.

摘要

引言

在自然界中普遍存在,是人体常见的机会性病原体。碳青霉烯类抗生素通常被用作治疗由其引起的多重耐药感染的临床最后手段。耐碳青霉烯类的增加给这些感染的治疗带来了巨大挑战。噬菌体有潜力被用作治疗抗生素耐药细菌的抗菌剂。

方法与结果

在本研究中,从医院污水中分离出一种新的强毒力铜绿假单胞菌噬菌体Phage_Pae01,它对临床分离株(83.6%)具有广谱抗菌活性。这些临床菌株包括多重耐药和耐碳青霉烯类的。透射电子显微镜显示该噬菌体具有一个约80纳米的二十面体头部和一条约110微米的长尾,表明它属于该目肌尾噬菌体科。生物学特性分析表明,Phage_Pae01在4至60°C的温度范围和4至10的pH范围内能保持稳定活性。根据噬菌体的裂解动力学,Phage_Pae01表现出很强的抗菌活性。最佳感染复数为0.01。Phage_Pae01的基因组全长93,182碱基对,包含176个开放阅读框(ORF)。该噬菌体基因组不包含与毒力或抗生素耐药性相关的基因。此外,Phage_Pae01有效阻止了生物膜的形成并消除已形成的生物膜。当Phage_Pae01与庆大霉素联合使用时,它显著破坏了已形成的生物膜。

结论

我们鉴定出一种新型噬菌体,并证明了其对浮游态和生物膜态的有效抗菌特性。这些发现为临床环境中耐药细菌感染的治疗提供了一种有前景的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af4/11292732/c3ad18801653/fmicb-15-1386830-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af4/11292732/c83b933d8a87/fmicb-15-1386830-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af4/11292732/a7b37c5a7a2f/fmicb-15-1386830-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af4/11292732/7ded756be6c6/fmicb-15-1386830-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af4/11292732/8768e5dc9a9b/fmicb-15-1386830-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af4/11292732/aa6194f624fa/fmicb-15-1386830-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af4/11292732/a22259e5bf2d/fmicb-15-1386830-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af4/11292732/23839a59d9e2/fmicb-15-1386830-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af4/11292732/c3ad18801653/fmicb-15-1386830-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af4/11292732/c83b933d8a87/fmicb-15-1386830-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af4/11292732/a7b37c5a7a2f/fmicb-15-1386830-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af4/11292732/7ded756be6c6/fmicb-15-1386830-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af4/11292732/8768e5dc9a9b/fmicb-15-1386830-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af4/11292732/aa6194f624fa/fmicb-15-1386830-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af4/11292732/a22259e5bf2d/fmicb-15-1386830-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af4/11292732/23839a59d9e2/fmicb-15-1386830-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af4/11292732/c3ad18801653/fmicb-15-1386830-g008.jpg

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