ArticleVirology journal2006
The ability of flagellum-specific Proteus vulgaris bacteriophage PV22 to interact with Campylobacter jejuni flagella in culture.
Article in Virology journal, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 18 citations in OpenAlex.
- A hybrid receptor binding protein enables phage F341 infection ofFrontiers in microbiology · 2024Article
- Flagellotropic Bacteriophages: Opportunities and Challenges for Antimicrobial Applications.International journal of molecular sciences · 2022Review
- The multi-drug efflux system AcrABZ-TolC is essential for infection ofJournal of virology · 2021Article
- Homologous Recombination in Core Genomes Facilitates Marine Bacterial Adaptation.Applied and environmental microbiology · 2018Article
- Architecture and gene repertoire of the flexible genome of the extreme acidophile Acidithiobacillus caldus.PloS one · 2013Article
- Genome and proteome analysis of 7-7-1, a flagellotropic phage infecting Agrobacterium sp H13-3.Virology journal · 2012Article
- Alternative mechanism for bacteriophage adsorption to the motile bacterium Caulobacter crescentus.Proceedings of the National Academy of Sciences of the United States of America · 2011Article
- Occurrence of Vibrio parahaemolyticus and its specific phages from shrimp ponds in east coast of India.Current microbiology · 2010Article
- Role of the Campylobacter jejuni Cj1461 DNA methyltransferase in regulating virulence characteristics.Journal of bacteriology · 2008Article
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Authors and funding
7 authors at 3 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundThere has been a recent resurgent interest in bacteriophage biology. Research was initiated to examine Campylobacter jejuni-specific bacteriophage in the Russian Federation to develop alternative control measures for this pathogen.
resultsA C. jejuni flagellum-specific phage PV22 from Proteus vulgaris was identified in sewage drainage. This phage interacted with C. jejuni by attachment to flagella followed by translocation of the phage to the polar region of the bacterium up to the point of DNA injection. Electron microscopic examination revealed adsorption of PV22 on C. jejuni flagella after a five minute incubation of the phage and bacteria. A different phenomenon was observed after incubating the mix under the same conditions, but for twenty minutes or longer. Phage accumulated primarily on the surface of cells at sites where flagella originated. Interestingly, PV22 did not inject DNA into C. jejuni and PV22 did not produce lytic plaques on medium containing C. jejuni cells. The constant of velocity for PV22 adsorption on cells was 7 x 10(-9) ml/min.
conclusionIt was demonstrated that a bacteriophage that productively infects P. vulgaris was able to bind C. jejuni and by a spot test that the growth of C. jejuni was reduced relative to control bacteria in the region of phage application. There may be two interesting applications of this effect. First, it may be possible to test phage PV22 as an antimicrobial agent to decrease C. jejuni colonization of the chicken intestine. Second, the phage could potentially be utilized for investigating biogenesis of C. jejuni flagella.
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