ArticleScientific reports2016
DTDP-rhamnosyl transferase RfbF, is a newfound receptor-related regulatory protein for phage phiYe-F10 specific for Yersinia enterocolitica serotype O:3.
Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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12 citing papers in PubMed, 16 citations in OpenAlex.
- From phenotype to receptor: validating physiological clustering ofJournal of virology · 2025Article
- Prevalence and genomic insights into Yersinia enterocolitica in Southeastern China (2008-2022).Applied microbiology and biotechnology · 2025Article
- Biological and genomic characterization of three psychrophilicFrontiers in microbiology · 2024Article
- Tailoring Effective Phage Cocktails for Long-Term Lysis ofPHAGE (New Rochelle, N.Y.) · 2023Article
- Phage vB_YenS_P400, a Novel Virulent Siphovirus ofMicroorganisms · 2022Article
- Properties of Two Broad Host Range Phages ofInternational journal of molecular sciences · 2021Article
- A LyticFrontiers in cellular and infection microbiology · 2021Article
- Review
- NovelFrontiers in microbiology · 2019Article
- Prevalence of Yersinia enterocolitica Bioserotype 3/O:3 among Children with Diarrhea, China, 2010-2015.Emerging infectious diseases · 2017Article
- Role of Low-Molecular-Mass Penicillin-Binding Proteins, NagZ and AmpR in AmpC β-lactamase Regulation ofFrontiers in cellular and infection microbiology · 2017Article
- Article
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11 authors at 4 institutions in 1 country.
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Abstract
Bacteriophages and their hosts are continuously engaged in evolutionary competition. Here we isolated a lytic phage phiYe-F10 specific for Yersinia enterocolitica serotype O:3. We firstly described the phage receptor was regulated by DTDP-rhamnosyl transferase RfbF, encoded within the rfb cluster that was responsible for the biosynthesis of the O antigens. The deletion of DTDP-rhamnosyl transferase RfbF of wild type O:3 strain caused failure in phiYe-F10 adsorption; however, the mutation strain retained agglutination with O:3 antiserum; and complementation of its mutant converted its sensitivity to phiYe-F10. Therefore, DTDP-rhamnosyl transferase RfbF was responsible for the phage infection but did not affect recognition of Y. enterocolitica O:3 antiserum. Further, the deletions in the putative O-antigen biosynthesis protein precursor and outer membrane protein had no effect on sensitivity to phiYe-F10 infection. However, adsorption of phages onto mutant HNF10-ΔO-antigen took longer time than onto the WT, suggesting that deletion of the putative O-antigen biosynthesis protein precursor reduced the infection efficiency.
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