Evidence map›Paper›PMID 40824427›Full record

ArticleCurrent microbiology2025

Characterization and Genome Comparison of Bacteriophage KKU62-1 Infecting Hypervirulent Streptococcus agalactiae ST283.

Wajeeorn Ouancharee, Jeerati Prompipak, Nirut Leela, Anusak Kerdsin, Hien Van Doan, Chanagun Chitmanat, Kiatichai Faksri, Nicha Charoensri

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Article in Current microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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.

Wajeeorn OuanchareeBiomedical Sciences, Graduate School, Khon Kaen University, Khon Kaen, Thailand.ORCID https://orcid.org/0009-0003-7350-4234
Jeerati PrompipakCentre for Research and Development of Medical Diagnostic Laboratories (CMDL), Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand.ORCID https://orcid.org/0000-0003-2887-4386
Nirut LeelaFaculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand.ORCID https://orcid.org/0009-0001-6778-5477
Anusak KerdsinFaculty of Public Health, Kasetsart University Chalermphrakiat Sakon Nakhon Province Campus, Sakon Nakhon, Thailand.ORCID https://orcid.org/0000-0003-1055-3656
Hien Van DoanDepartment of Animal and Aquatic Sciences, Faculty of Agriculture, Chiang Mai University, Chiang Mai, Thailand.ORCID http://orcid.org/0000-0003-1267-3328
Chanagun ChitmanatFaculty of Fisheries Technology and Aquatic Resources, Maejo University, Chiang Mai, Thailand.ORCID https://orcid.org/0000-0002-6700-6285
Kiatichai Faksri​Department of Microbiology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.ORCID http://orcid.org/0000-0001-5022-4182
Nicha CharoensriCentre for Research and Development of Medical Diagnostic Laboratories (CMDL), Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand. nicha@kku.ac.th.ORCID http://orcid.org/0000-0002-0679-9883

Funding

National Research Council of Thailand 29418
6 · The paper itself

Abstract

Streptococcus agalactiae is a multi-host pathogen affecting humans, cattle and aquatic animals. Phage therapy, recognized for its specificity and rapid bacterial killing, offers an alternative. This study aimed to characterize phage KKU62-1, which showed lytic activities against S. agalactiae. The phage with a hexagonal head and a long non-contractile tail was classified as a member of the Siphoviridae family. It exhibited stability at a wide pH (5-10) and thermal (4-40 °C) ranges. It demonstrated a short latent period (15 min) and a rise period of 75 min. Interestingly, KKU62-1 showed high specificity against a hypervirulent strain, S. agalactiae sequence type (ST)283 (78.9%). Its genome sequence was most similar to phage vB_Sags-UPM1 sharing 99.93% identity. Interestingly, a small distinct region with a low degree (41.84%) of identity in YopX family gene of KKU62-1 and vB_Sags-UPM1 was detected. The regions in KKU62-1 covered a 141-bp (Var-141), while in vB_Sags-UPM1 expanded a 138-bp (Var-138). These sequence variants were also found in some prophages of S. agalactiae, especially of the ST283. Additionally, this study was the first to explore the diversity (4 distinct types) of the YopX family gene among S. agalactiae and its phages. In conclusion, KKU62-1 and vB_Sags-UPM1 were almost identical phage, but a small recombination in the YopX family gene has made them apart.

Indexed as

BacteriophagesGenome, ViralSiphoviridaeStreptococcus agalactiaeStreptococcus PhagesAnimalsHost SpecificityPhylogenyVirulence

Identifiers

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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.