• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
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
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
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 @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

广谱裂解噬菌体 vB_SenS_TUMS_E19 的特性分析及其对 的基因组分析及其在液态蛋中的效率评估。

Characterization and genome analysis of a broad host range lytic phage vB_SenS_TUMS_E19 against and its efficiency evaluation in the liquid egg.

机构信息

Department of Pharmaceutical Biotechnology, Faculty of Pharmacy & Biotechnology Research Center, Tehran University of Medical Sciences, Tehran, Iran.

Department of Food and Drug Control, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Can J Microbiol. 2024 Sep 1;70(9):358-369. doi: 10.1139/cjm-2024-0013. Epub 2024 Jul 4.

DOI:10.1139/cjm-2024-0013
PMID:38990097
Abstract

serovars are zoonotic bacterial that cause foodborne enteritis. Due to bacteria's antibiotic resistance, using bacteriophages for biocontrol and treatment is a new therapeutic approach. In this study, we isolated, characterized, and analyzed the genome of vB_SenS_TUMS_E19 (E19), a broad host range bacteriophage, and evaluated the influence of E19 on liquid eggs infected with serovar Enteritidis. Transmission electron microscopy showed that the isolated bacteriophage had a siphovirus morphotype. E19 showed rapid adsorption (92% in 5 min), a short latent period (18 min), a large burst size (156 PFU per cell), and a broad host range against different serovars. Whole-genome sequencing analysis indicated that the isolated phage had a 42 813 bp long genome with 49.8% G + C content. Neither tRNA genes nor those associated with antibiotic resistance, virulence factors, or lysogenic formation were detected in the genome. The efficacy of E19 was evaluated in liquid eggs inoculated with . Enteritidis at 4 and 25 °C, and results showed that it could effectively eradicate . Enteritidis in just 30 min and prevented its growth up to 72 h. Our findings indicate that E19 can be an alternative to a preservative to control in food samples and help prevent and treat salmonellosis.

摘要

血清型是一种引起食源性肠炎的人畜共患细菌。由于细菌对抗生素的耐药性,利用噬菌体进行生物防治和治疗是一种新的治疗方法。在本研究中,我们分离、鉴定并分析了 vB_SenS_TUMS_E19(E19)的基因组,E19 是一种广谱宿主范围的噬菌体,并评估了 E19 对感染肠炎沙门氏菌的液体蛋的影响。透射电子显微镜显示,分离的噬菌体具有长尾噬菌体形态。E19 表现出快速吸附(5 分钟内吸附率达 92%)、短潜伏期(18 分钟)、大爆发量(每个细胞 156 个 PFU)和对不同血清型的广泛宿主范围。全基因组测序分析表明,分离的噬菌体具有 42813bp 长的基因组,GC 含量为 49.8%。基因组中未检测到 tRNA 基因以及与抗生素抗性、毒力因子或溶原形成相关的基因。在 4 和 25°C 下用肠炎沙门氏菌接种的液体蛋中评估了 E19 的功效,结果表明,它可以在 30 分钟内有效根除肠炎沙门氏菌,并在 72 小时内阻止其生长。我们的研究结果表明,E19 可以作为防腐剂的替代品来控制食品样品中的肠炎沙门氏菌,并有助于预防和治疗沙门氏菌病。

相似文献

1
Characterization and genome analysis of a broad host range lytic phage vB_SenS_TUMS_E19 against and its efficiency evaluation in the liquid egg.广谱裂解噬菌体 vB_SenS_TUMS_E19 的特性分析及其对 的基因组分析及其在液态蛋中的效率评估。
Can J Microbiol. 2024 Sep 1;70(9):358-369. doi: 10.1139/cjm-2024-0013. Epub 2024 Jul 4.
2
Isolation, characterization, and genome analysis of a broad host range Salmonella phage vB_SenS_TUMS_E4: a candidate bacteriophage for biocontrol.一种广谱沙门氏菌噬菌体 vB_SenS_TUMS_E4 的分离、鉴定和基因组分析:一种用于生物防治的候选噬菌体。
Vet Res Commun. 2023 Sep;47(3):1493-1503. doi: 10.1007/s11259-023-10105-1. Epub 2023 Apr 25.
3
Morphologic and genomic characterization of a broad host range Salmonella enterica serovar Pullorum lytic phage vB_SPuM_SP116.广泛宿主范围的肠炎沙门氏菌血清 Pullorum 裂解噬菌体 vB_SPuM_SP116 的形态学和基因组特征。
Microb Pathog. 2019 Nov;136:103659. doi: 10.1016/j.micpath.2019.103659. Epub 2019 Aug 6.
4
Characterization and whole-genome sequencing of broad-host-range Salmonella-specific bacteriophages for bio-control.广谱宿主范围沙门氏菌特异性噬菌体的特性及全基因组测序用于生物防治。
Microb Pathog. 2020 Jun;143:104119. doi: 10.1016/j.micpath.2020.104119. Epub 2020 Mar 10.
5
Biological and genomic characterization of a polyvalent phage PSH-1 against multidrug-resistant Salmonella Enteritidis.多价噬菌体 PSH-1 对多重耐药肠炎沙门氏菌的生物学和基因组特征分析。
BMC Microbiol. 2024 Sep 16;24(1):349. doi: 10.1186/s12866-024-03489-w.
6
Characterization of a Salmonella Enteritidis bacteriophage showing broad lytic activity against Gram-negative enteric bacteria.鉴定一株具有广泛裂解活性的肠炎沙门氏菌噬菌体,可裂解多种革兰氏阴性肠道细菌。
J Microbiol. 2018 Dec;56(12):917-925. doi: 10.1007/s12275-018-8310-1. Epub 2018 Oct 25.
7
Isolation, identification and some characteristics of two lytic bacteriophages against Salmonella enterica serovar Paratyphi B and S. enterica serovar Typhimurium from various food sources.从各种食物来源中分离、鉴定并研究两种针对副伤寒 B 血清型和鼠伤寒血清型沙门氏菌的裂解噬菌体的特性。
FEMS Microbiol Lett. 2021 Apr 25;368(7). doi: 10.1093/femsle/fnab037.
8
wksl3, a New biocontrol agent for Salmonella enterica serovars enteritidis and typhimurium in foods: characterization, application, sequence analysis, and oral acute toxicity study.wksl3,一种用于食品中肠炎沙门氏菌血清型肠炎和鼠伤寒的新型生物防治剂:特性描述、应用、序列分析和口服急性毒性研究。
Appl Environ Microbiol. 2013 Mar;79(6):1956-68. doi: 10.1128/AEM.02793-12. Epub 2013 Jan 18.
9
Characterization of the Salmonella bacteriophage vB_SenS-Ent1.肠沙门氏菌噬菌体 vB_SenS-Ent1 的特性研究。
J Gen Virol. 2012 Sep;93(Pt 9):2046-2056. doi: 10.1099/vir.0.043331-0. Epub 2012 Jun 13.
10
Genomic and functional characterization of five novel Salmonella-targeting bacteriophages.五种新型靶向沙门氏菌噬菌体的基因组和功能特征。
Virol J. 2021 Sep 8;18(1):183. doi: 10.1186/s12985-021-01655-4.

引用本文的文献

1
Bacteriophage PCSE1 as a Potential Strategy Against Enteritidis in Liquid Egg Products.噬菌体PCSE1作为一种应对液态蛋制品中肠炎沙门氏菌的潜在策略。
Antibiotics (Basel). 2025 Aug 8;14(8):811. doi: 10.3390/antibiotics14080811.
2
Isolation and characterization of a novel bacteriophage ST1749 and its effectiveness against Vibrio parahaemolyticus and Salmonella spp.新型噬菌体ST1749的分离、鉴定及其对副溶血性弧菌和沙门氏菌属的有效性
Virus Res. 2025 Jun;356:199579. doi: 10.1016/j.virusres.2025.199579. Epub 2025 Apr 27.
3
Evaluating the effectiveness and safety of a novel phage cocktail as a biocontrol of in biofilm, food products, and broiler chicken.
评估一种新型噬菌体鸡尾酒制剂在生物膜、食品和肉鸡中作为生物防治手段的有效性和安全性。
Front Microbiol. 2024 Nov 28;15:1505805. doi: 10.3389/fmicb.2024.1505805. eCollection 2024.