Evidence map›Paper›PMID 36494564›Full record

ArticleScientific reports2022

Biological properties of Staphylococcus virus ΦSA012 for phage therapy.

Jumpei Fujiki, Tomohiro Nakamura, Keisuke Nakamura, Keita Nishida, Yurika Amano, Yusaku Watanabe, Satoshi Gondaira, Masaru Usui, Masaru Shimizu, Kazuhiko Miyanaga and 10 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Phage cocktails containing a dual-receptorApplied and environmental microbiology · 2026
    Article
  2. Article
  3. Article
  4. Phage therapy: a promising approach forJournal of virology · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Bacteriophage therapy for drug-resistantFrontiers in cellular and infection microbiology · 2024
    Review
  13. Article
  14. Review
  15. 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

20 authors at 6 institutions in 1 country.

Jumpei FujikiLaboratory of Veterinary Biochemistry, Rakuno Gakuen University School of Veterinary Medicine, Ebetsu, Hokkaido, Japan.
Tomohiro NakamuraLaboratory of Veterinary Biochemistry, Rakuno Gakuen University School of Veterinary Medicine, Ebetsu, Hokkaido, Japan.
Keisuke NakamuraLaboratory of Veterinary Biochemistry, Rakuno Gakuen University School of Veterinary Medicine, Ebetsu, Hokkaido, Japan.
Keita NishidaLaboratory of Veterinary Biochemistry, Rakuno Gakuen University School of Veterinary Medicine, Ebetsu, Hokkaido, Japan.
Yurika AmanoLaboratory of Veterinary Biochemistry, Rakuno Gakuen University School of Veterinary Medicine, Ebetsu, Hokkaido, Japan.
Yusaku WatanabeLaboratory of Veterinary Biochemistry, Rakuno Gakuen University School of Veterinary Medicine, Ebetsu, Hokkaido, Japan.
Satoshi GondairaLaboratory of Animal Health, Rakuno Gakuen University School of Veterinary Medicine, Ebetsu, Hokkaido, Japan.
Masaru UsuiLaboratory of Food Microbiology and Food Safety, Rakuno Gakuen University School of Veterinary Medicine, Ebetsu, Hokkaido, Japan.
Masaru ShimizuDepartment of Anesthesiology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Kazuhiko MiyanagaDivision of Bacteriology, Department of Infection and Immunology, School of Medicine, Jichi Medical University, Shimotsuke, Tochigi, Japan.
Shinya WatanabeDivision of Bacteriology, Department of Infection and Immunology, School of Medicine, Jichi Medical University, Shimotsuke, Tochigi, Japan.
Tomohito IwasakiDepartment of Food Science and Human Wellness, College of Agriculture, Food and Environment Science, Rakuno Gakuen University, Ebetsu, Japan.
Kotaro KigaResearch Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, Japan.
Tomoko HanawaDepartment of Infectious Diseases, Kyorin University School of Medicine, Mitaka, Tokyo, Japan.
Hidetoshi HiguchiLaboratory of Animal Health, Rakuno Gakuen University School of Veterinary Medicine, Ebetsu, Hokkaido, Japan.
Teiji SawaDepartment of Anesthesiology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Yasunori TanjiPhage Therapy Institute, Waseda University, Tokyo, Japan.
Yutaka TamuraLaboratory of Food Microbiology and Food Safety, Rakuno Gakuen University School of Veterinary Medicine, Ebetsu, Hokkaido, Japan.
Longzhu CuiDivision of Bacteriology, Department of Infection and Immunology, School of Medicine, Jichi Medical University, Shimotsuke, Tochigi, Japan.
Hidetomo IwanoLaboratory of Veterinary Biochemistry, Rakuno Gakuen University School of Veterinary Medicine, Ebetsu, Hokkaido, Japan. h-iwano@rakuno.ac.jp.
Rakuno Gakuen University · JPJichi Medical University · JPKyoto Prefectural University of Medicine · JPNational Institute of Infectious Diseases · JPKyorin University · JPWaseda University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Staphylococcus virus ΦSA012 has a wide host range and efficient lytic activity. Here, we assessed the biological stability of ΦSA012 against temperature, freeze-thawing, and pH to clinically apply the phage. In addition, inoculation of ΦSA012 through i.p. and i.v. injections into mice revealed that phages were reached the limit of detection in serum and accumulated notably spleens without inflammation at 48 h post-inoculation. Furthermore, inoculation of ΦSA012 through s.c. injections in mice significantly induced IgG, which possesses neutralizing activity against ΦSA012 and other Staphylococcus viruses, ΦSA039 and ΦMR003, but not Pseudomonas viruses ΦS12-3 and ΦR18 or Escherichia viruses T1, T4, and T7 in vitro. Immunoelectron microscopic analysis showed that purified anti-phage IgG recognizes the long-tail fiber of staphylococcus viruses. Although S. aureus inoculation resulted in a 25% survival rate in a mouse i.p. model, ΦSA012 inoculation (i.p.) improved the survival rate to 75%; however, the survival rate of ΦSA012-immunized mice decreased to less than non-immunized mice with phage i.v. injection at a MOI of 100. These results indicated that ΦSA012 possesses promise for use against staphylococcal infections but we should carefully address the appropriate dose and periods of phage administration. Our findings facilitate understandings of staphylococcus viruses for phage therapy.

Indexed as

Phage TherapyStaphylococcal InfectionsAnimalsImmunoglobulin GMiceMyoviridaeStaphylococcusStaphylococcus aureusStaphylococcus PhagesImmunoglobulin G

Identifiers

PMID36494564
PMCPMC9734660
OpenAlexW4311676487

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.