Evidence map›Paper›PMID 40731165›Full record

ArticleArchives of virology2025

Discovery of phage CSF, a novel generalist bacteriophage targeting multidrug-resistant and potentially pathogenic Staphylococcus spp. and Mammaliicoccus spp.

Faizan Ahmad, Vitor Emanuel Lanes Viana, Rafael Reis de Rezende, Samuel Sathler Martuchelle, Anderson Souza Cabral, Ana Luisa Andrade-Oliveira, Isabella Monteiro Carvalho, Sandy de Almada Estanislau, Nohman Rasheed, Poliane Alfenas Zerbini and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Archives of virology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

13 authors.

Faizan AhmadDepartmento de Bioquímica e Biologia Molecular, Universidade Federal de Viçosa, Viçosa, MG, Brazil.
Vitor Emanuel Lanes VianaDepartmento de Bioquímica e Biologia Molecular, Universidade Federal de Viçosa, Viçosa, MG, Brazil.
Rafael Reis de RezendeDepartmento de Microbiologia, Universidade Federal de Viçosa, Viçosa, MG, Brazil.ORCID http://orcid.org/0000-0001-7596-3619
Samuel Sathler MartuchelleDepartmento de Bioquímica e Biologia Molecular, Universidade Federal de Viçosa, Viçosa, MG, Brazil.
Anderson Souza CabralInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0000-0002-8997-8309
Ana Luisa Andrade-OliveiraInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.ORCID http://orcid.org/0009-0008-8173-9013
Isabella Monteiro CarvalhoInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Sandy de Almada EstanislauDepartmento de Bioquímica e Biologia Molecular, Universidade Federal de Viçosa, Viçosa, MG, Brazil.
Nohman RasheedDepartmento de Bioquímica e Biologia Molecular, Universidade Federal de Viçosa, Viçosa, MG, Brazil.
Poliane Alfenas ZerbiniDepartmento de Microbiologia, Universidade Federal de Viçosa, Viçosa, MG, Brazil.ORCID http://orcid.org/0000-0002-8203-5244
Monalessa Fábia PereiraDepartmento de Medicina, Universidade Federal de Lavras, Lavras, MG, Brazil.ORCID http://orcid.org/0000-0002-8134-8337
Marcia Giambiagi-deMarvalDepartmento de Medicina, Universidade Federal de Lavras, Lavras, MG, Brazil.ORCID http://orcid.org/0000-0002-6433-7521
Ciro César RossiDepartmento de Bioquímica e Biologia Molecular, Universidade Federal de Viçosa, Viçosa, MG, Brazil. ciro.rossi@ufv.br.ORCID http://orcid.org/0000-0003-3856-0882

Funding

Conselho Nacional das Fundações Estaduais de Amparo à Pesquisa 313528/2021-7, 304839/2022-1; 408564/2023-7; 309158/2023-0Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 23038.002486/2018-26Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/010.000172/2016; 010.00128/2016; E-26.210.875/2016, 101056/2018; 001463/2019; 211.554/2019; 201.071/2020,200.895/2021; E-26/204.925/2022; E-26/211.284/2021 and E-26/204.045/2024Fundação de Amparo à Pesquisa do Estado de Minas Gerais APQ-03498-22; APQ-01339-25
6 · The paper itself

Abstract

Antimicrobial resistance is escalating among Staphylococcus species, which are major pathogens affecting both humans and animals. As therapeutic options continue to narrow, phage therapy is re-emerging as a promising strategy to combat resistant strains. In this study, we isolated from pig farm effluents a bacteriophage named CSF, infecting a Staphylococcus xylosus strain. The CSF phage demonstrated a broad host range, lysing mecA-positive, multidrug-resistant strains across nine species of the genera Staphylococcus and Mammaliicoccus. Notably, it also inhibited biofilm formation in strains that it could not infect directly, and this activity persisted at low virus concentrations and in combination with antibiotics. The phage maintained its lytic activity under extreme conditions of temperature, pH, and UV exposure, underscoring its resilience for practical use. Sequencing of the viral genome revealed that it is 140 kb in length and has a genetic composition consistent with a lytic lifestyle. Phylogenetic analysis showed that phage CSF is related to members of the family Herelleviridae that are found globally, suggesting a widespread distribution of related viral lineages. Importantly, the phage genome was found to lack bacterial virulence or antimicrobial resistance genes, suggesting its safety for biotechnological applications. Intergenomic comparisons indicated that CSF should be classified as a member of a new genus, expanding the known diversity of bacteriophages. These findings demonstrate potential of CSF for phage therapy and other biotechnological applications.

Indexed as

BacteriophagesStaphylococcusStaphylococcus PhagesAnimalsAnti-Bacterial AgentsBiofilmsDrug Resistance, Multiple, BacterialGenome, ViralHost SpecificityPhage TherapyPhylogenySwineAnti-Bacterial Agents

Identifiers

What OpenQuestion holds

Textmetadata
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.