Evidence map›Paper›PMID 36609576›Full record

ArticleArchives of virology2023

Characterization of the novel temperate Staphylococcus haemolyticus phage IME1365_01.

Huanao Qiao, Yunjia Hu, Fengjuan Tian, Xiaoping An, Huahao Fan, Lihua Song, Mengzhe Li, Yigang Tong

Abstract read
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In one paragraph

Article in Archives of virology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.7field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Huanao QiaoCollege of Life Science and Technology, Beijing University of Chemical Technology, Beijing, China.
Yunjia HuCollege of Life Science and Technology, Beijing University of Chemical Technology, Beijing, China.
Fengjuan TianCollege of Life Science and Technology, Beijing University of Chemical Technology, Beijing, China.
Xiaoping AnCollege of Life Science and Technology, Beijing University of Chemical Technology, Beijing, China.
Huahao FanCollege of Life Science and Technology, Beijing University of Chemical Technology, Beijing, China.
Lihua SongCollege of Life Science and Technology, Beijing University of Chemical Technology, Beijing, China.
Mengzhe LiCollege of Life Science and Technology, Beijing University of Chemical Technology, Beijing, China. futurelmz123@163.com.ORCID http://orcid.org/0000-0002-4390-8989
Yigang TongCollege of Life Science and Technology, Beijing University of Chemical Technology, Beijing, China. tong.yigang@gmail.com.
Beijing University of Chemical Technology · CNBeijing University of Technology · CN

Funding

Fundamental Research Funds for Central Universities of the Central South University BUCTZY2022Fundamental Research Funds for Central Universities of the Central South University No. BUCTRC201917Funds for First-class Discipline Construction No. XK1805Key Project of Beijing University of Chemical Technology No. XK1803-06Military Biosecurity Research Program No. 20SWAQX27National Key Research and Development Program of China No. 2020YFC2005405
6 · The paper itself

Abstract

The presence of a novel functional prophage, IME1365_01, was predicted from bacterial high-throughput sequencing data and then successfully induced from Staphylococcus haemolyticus by mitomycin C treatment. Transmission electron microscopy showed that phage IME1365_01 has an icosahedral head (43 nm in diameter) and a long tail (172 nm long). This phage possesses a double-stranded DNA genome of 44,875 bp with a G+C content of 35.35%. A total of 63 putative open reading frames (ORFs) were identified in its genome. BLASTn analysis revealed that IME1365_01 is similar to Staphylococcus phage vB_SepS_E72, but with a genome homology coverage of only 26%. The phage genome does not have fixed termini. In ORF24 of phage IME1365_01, a conserved Toll-interleukin-1 receptor domain of the TIR_2 superfamily (accession no. c123749) is located at its N-terminus, and this might serve as a component of an anti-bacterial system. In conclusion, we developed a platform to obtain active temperate phage from prediction, identification, and induction from its bacterial host. After mass screening using this platform, numerous temperate phages and their innate anti-bacterial elements can provide extensive opportunities for therapy against bacterial (especially drug-resistant bacterial) infections.

Indexed as

BacteriophagesSiphoviridaeDNA, ViralGenome, ViralOpen Reading FramesSequence Analysis, DNAStaphylococcus haemolyticusStaphylococcus PhagesDNA, Viral

Identifiers

PMID36609576
OpenAlexW4313679375

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.