文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

小鼠腹腔注射溶菌性大肠杆菌噬菌体后免疫反应的比较分析

Comparative analysis of immune responses to intraperitoneal administration of lytic E. coli bacteriophages in mice.

作者信息

Alexyuk Madina S, Bogoyavlenskiy Andrey P, Zaitseva Irina A, Omirtaeva Elmira S, Moldakhanov Yergali S, Akanova Kuralay S, Anarkulova Elmira I, Berezin Vladimir E, Alexyuk Pavel G

机构信息

Research and Production Center for Microbiology and Virology, Almaty, Kazakhstan.

Research and Production Center for Microbiology and Virology, Almaty, Kazakhstan.

出版信息

Virus Res. 2025 Jul 19;359:199610. doi: 10.1016/j.virusres.2025.199610.


DOI:10.1016/j.virusres.2025.199610
PMID:40691898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12309589/
Abstract

With the global spread of bacterial resistance and the decreasing effectiveness of antibiotics, the relevance of phage therapy is constantly growing. However, for systemic use of bacteriophages in medical practice, a complete understanding of their interaction not only with bacterial cells but also with human and animal organisms in the context of co-administered therapy is required. This article presents the studies into the effects of lytic Escherichia coli bacteriophages on various immune response factors after their intraperitoneal administration in mice. It was found using Real-Time PCR and ELISA methods that the administration of the vB_EcoM_SCS4 and vB_EcoM_SCS57 phages did not increase the gene expression of TLR3, TLR9, IL-4, IL-5, IL-6 and the concentration of IL-2, IL-4, IL-5 and IL-6 in mice, but led to a multi-fold increase in the gene expression and concentration of IFNγ. Whereas, the injection of the vB_EcoS_SCS44 phage into mice increased the expression of the studied genes, except for the IL-5 gene, by 4 to 7 times and increased the concentration of IL-2, IL-4, IL-6 and IFNγ, except for IL-5, by 2 to 3 times. When determining the titer of virus-specific antibodies, it was found that after the administration of phages vB_EcoM_SCS4 and vB_EcoM_SCS57, the titer of IgA, IgG and IgM did not differ from that of the control animals, but the administration of phage vB_EcoS_SCS44 stimulated a twofold increase in the titer of phage-specific IgA, IgG, IgM.

摘要

随着细菌耐药性在全球范围内的传播以及抗生素有效性的降低,噬菌体疗法的相关性不断增加。然而,对于在医学实践中全身使用噬菌体,不仅需要全面了解它们与细菌细胞的相互作用,还需要了解在联合治疗背景下它们与人和动物机体的相互作用。本文介绍了溶菌性大肠杆菌噬菌体腹腔注射小鼠后对各种免疫反应因子影响的研究。使用实时荧光定量聚合酶链反应(Real-Time PCR)和酶联免疫吸附测定(ELISA)方法发现,vB_EcoM_SCS4和vB_EcoM_SCS57噬菌体的给药并未增加小鼠体内Toll样受体3(TLR3)、Toll样受体9(TLR9)、白细胞介素4(IL-4)、白细胞介素5(IL-5)、白细胞介素6(IL-6)的基因表达以及白细胞介素2(IL-2)、IL-4、IL-5和IL-6的浓度,但导致干扰素γ(IFNγ)的基因表达和浓度增加了数倍。而向小鼠注射vB_EcoS_SCS44噬菌体使所研究基因(白细胞介素5基因除外)的表达增加了4至7倍,并使IL-2、IL-4、IL-6和IFNγ(IL-5除外)的浓度增加了2至3倍。在测定病毒特异性抗体滴度时发现,给予噬菌体vB_EcoM_SCS4和vB_EcoM_SCS57后,免疫球蛋白A(IgA)、免疫球蛋白G(IgG)和免疫球蛋白M(IgM)的滴度与对照动物无差异,但给予噬菌体vB_EcoS_SCS44刺激了噬菌体特异性IgA、IgG、IgM滴度的两倍增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a74/12309589/e9a7494d86cd/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a74/12309589/5211a5a25ffa/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a74/12309589/63c4a2aae8f4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a74/12309589/1273f3761865/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a74/12309589/e9a7494d86cd/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a74/12309589/5211a5a25ffa/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a74/12309589/63c4a2aae8f4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a74/12309589/1273f3761865/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a74/12309589/e9a7494d86cd/gr3.jpg

相似文献

[1]
Comparative analysis of immune responses to intraperitoneal administration of lytic E. coli bacteriophages in mice.

Virus Res. 2025-7-19

[2]
Prescription of Controlled Substances: Benefits and Risks

2025-1

[3]
The virulent bacteriophage Henu8 as an antimicrobial synergist against .

Microbiol Spectr. 2025-7

[4]
Lytic bacteriophages targeting multidrug-resistant Pseudomonas aeruginosa in Moschus berezovskii: isolation, characterization, and therapeutic efficacy against bacteremia.

Virol J. 2025-8-19

[5]
Bacteriophage-enhanced doxycycline activity against Escherichia coli in chronic bacterial prostatitis.

Int J Antimicrob Agents. 2025-10

[6]
Physicochemical, genomic, and phenotypic characterization of phage BME3.

Microbiol Spectr. 2025-7

[7]
Isolation and characterization of phages ΦZC2 and ΦZC3 against carbapenem-resistant Acinetobacter baumannii, and efficacy of ΦZC3 on A549 cells.

Virol J. 2025-7-30

[8]
Characterization of a novel phage vB_EcoP_P64441 and its potential role in controlling uropathogenic Escherichia coli (UPEC) and biofilms formation.

Virology. 2025-8

[9]
Draft genome sequencing and activity data of the lytic vB_EcoM_AMO3598 bacteriophage effective against multi - drug resistant .

Data Brief. 2025-8-5

[10]
Efficacy of phage vB_Ps_ZCPS13 in controlling Pan-drug-resistant Pseudomonas aeruginosa from urinary tract infections (UTIs) and eradicating biofilms from urinary catheters.

Virol J. 2025-7-12

本文引用的文献

[1]
Genomic and Drug Resistance Profile of Bovine Multidrug-Resistant Isolated in Kazakhstan.

Pathogens. 2025-1-17

[2]
Novel intranasal phage-CaEDTA-ceftazidime/avibactam triple combination therapy demonstrates remarkable efficacy in treating Pseudomonas aeruginosa lung infection.

Biomed Pharmacother. 2023-10-28

[3]
A Comprehensive Review on Phage Therapy and Phage-Based Drug Development.

Antibiotics (Basel). 2024-9-11

[4]
Bacteriophage Bioengineering: A Transformative Approach for Targeted Drug Discovery and Beyond.

Pathogens. 2023-9-20

[5]
Isolation and Characterization of Jumbo Coliphage vB_EcoM_Lh1B as a Promising Therapeutic Agent against Chicken Colibacillosis.

Microorganisms. 2023-6-8

[6]
Liposomes-Based Drug Delivery Systems of Anti-Biofilm Agents to Combat Bacterial Biofilm Formation.

Antibiotics (Basel). 2023-5-8

[7]
Immunogenicity of bacteriophages.

Trends Microbiol. 2023-10

[8]
Current Clinical Landscape and Global Potential of Bacteriophage Therapy.

Viruses. 2023-4-21

[9]
Isolation and Characterization of Lytic Bacteriophages Active against Clinical Strains of and Development of a Phage Antimicrobial Cocktail.

Viruses. 2022-10-28

[10]
Prolongation of Fate of Bacteriophages In Vivo by Polylactic-Co-Glycolic-Acid/Alginate-Composite Encapsulation.

Antibiotics (Basel). 2022-9-17

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索