尿路感染患者尿液样本中的两种新型噬菌体--克雷伯氏菌噬菌体 GADU21 和埃希氏菌噬菌体 GADU22。

IF 1.9 4区 医学 Q3 GENETICS & HEREDITY
Virus Genes Pub Date : 2024-04-01 Epub Date: 2024-01-18 DOI:10.1007/s11262-024-02052-z
Hanife Salih Doğan, Abdulkerim Karaynir, Ülkü İrem Yilmaz, Bilgin Bahadır Başgöz, Tuğrul Hoşbul, Bülent Bozdoğan
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引用次数: 0

摘要

噬菌体存在于包括体液在内的各种细菌存在的地方。本研究旨在从尿路感染患者的尿液样本中分离噬菌体。对 10 份尿液样本进行培养以分离细菌,并将其作为抗分离细菌的噬菌体来源。从 10 份培养结果呈阳性的尿液样本中分离出了 3 个噬菌体(33%),并对其中两个噬菌体进行了进一步研究。克雷伯氏菌噬菌体 GADU21 和大肠埃希氏菌噬菌体 GADU22 分别感染了肺炎克雷伯氏菌和大肠埃希氏菌。在进行宿主范围分析的 14 个受测菌种中,克雷伯菌噬菌体 GADU21 可感染肺炎克雷伯菌和奇异变形杆菌两种菌种,而大肠埃希菌噬菌体 GADU22 可感染柔性志贺氏菌、宋内志贺氏菌和大肠埃希菌四种菌种。在每种噬菌体的不同指示菌分离物中,GADU21 感染了 20 个肺炎克雷伯菌分离物中的一半,而 GADU22 感染了 20 个大肠杆菌分离物中的 85%。GADU21 和 GADU22 的基因组大小和 GC 比率分别为 75,968 bp 和 44.4%,以及 168,023 bp 和 35.3%。GADU21 和 GADU22 都是溶菌,没有抗生素抗性基因和毒力基因。GADU21 与克雷伯氏菌噬菌体 vB_KpP_FBKp27 同源,但该噬菌体只覆盖了基因组的 88%。GADU21 基因组未被覆盖的部分包括尾纤蛋白和 HNH 内切酶的基因。GADU22 与埃希氏噬菌体 vB_Eco_OMNI12 的同源性为 94.8%,并含有免疫蛋白基因。系统进化分析表明,GADU21 和 GADU22 分别属于裂殖病毒科、Efbeekayvirus 属和 Straboviridae 科、Tevenvirinae 属。VIRIDIC 分析将这些噬菌体归入了新的物种群。我们的研究证明了利用受感染体液作为噬菌体来源来分离新型噬菌体的可能性。GADU21 是首次报道从人类体液中分离出的克雷伯氏菌噬菌体。这些噬菌体的基因组中没有毒力基因和抗生素耐药性基因,因此有可能成为抗感染的治疗工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Two novel phages, Klebsiella phage GADU21 and Escherichia phage GADU22, from the urine samples of patients with urinary tract infection.

Two novel phages, Klebsiella phage GADU21 and Escherichia phage GADU22, from the urine samples of patients with urinary tract infection.

Phages are found in a wide variety of places where bacteria exist including body fluids. The aim of the present study was to isolate phages from the urine samples of patients with urinary tract infection. The 10 urine samples were cultured to isolate bacteria and also used as phage sources against the isolated bacteria. From 10 urine samples with positive cultures, 3 phages were isolated (33%) and two of them were further studied. The Klebsiella phage GADU21 and Escherichia phage GADU22 phages infected Klebsiella pneumonia and Escherichia coli, respectively. Among the tested 14 species for host range analysis, the Klebsiella phage GADU21 was able to infect two species which are Klebsiella pneumonia and Proteus mirabilis, and Escherichia phage GADU22 was able to infect four species which are Shigella flexneri, Shigella sonnei and Escherichia coli. Among different isolates of the indicator bacteria for each phage, GADU21 infected half of the tested 20 Klebsiella pneumonia isolates while GADU22 infected 85% of the tested 20 E. coli isolates. The genome sizes and GC ratios were 75,968 bp and 44.4%, and 168,023 bp and 35.3% for GADU21 and GADU22, respectively. GADU21 and GADU22 were both lytic and had no antibiotic resistance and virulence genes. GADU21 was homologue with Klebsiella phage vB_KpP_FBKp27 but only 88% of the genome was covered by this phage. The non-covered parts of the GADU21 genome included genes for tail-fiber-proteins and HNH-endonuclease. GADU22 had 94.8% homology with Escherichia phage vB_Eco_OMNI12 and had genes for immunity proteins. Phylogenetic analysis showed GADU21 and GADU22 were members of Schitoviridae family and Efbeekayvirus genus and Straboviridae family and Tevenvirinae genus, respectively. VIRIDIC analysis classified these phages in new species clusters. Our study demonstrated the possibility to use infected body fluids as phage sources to isolate novel phages. GADU21 is the first reported Klebsiella phage isolated from human body fluid. The absence of virulence and antibiotic resistance genes in their genomes makes the phages a potential therapeutic tool against infections.

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来源期刊
Virus Genes
Virus Genes 医学-病毒学
CiteScore
3.30
自引率
0.00%
发文量
76
审稿时长
3 months
期刊介绍: Viruses are convenient models for the elucidation of life processes. The study of viruses is again on the cutting edge of biological sciences: systems biology, genomics, proteomics, metagenomics, using the newest most powerful tools. Huge amounts of new details on virus interactions with the cell, other pathogens and the hosts – animal (including human), insect, fungal, plant, bacterial, and archaeal - and their role in infection and disease are forthcoming in perplexing details requiring analysis and comments. Virus Genes is dedicated to the publication of studies on the structure and function of viruses and their genes, the molecular and systems interactions with the host and all applications derived thereof, providing a forum for the analysis of data and discussion of its implications, and the development of new hypotheses.
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