AI Article Synopsis

  • The text discusses the challenges posed by a problematic pathogen causing severe intestinal diseases, highlighting the need for alternative treatments to combat antibiotic resistance.
  • Researchers successfully induced and isolated five temperate bacteriophages from clinical isolates using a genotoxic agent, mitomycin C, but found that these phages had a narrow host range.
  • Characterization studies revealed that these phages have an icosahedral structure and a unique double-stranded DNA genome, showing potential for developing new therapeutic agents and detection methods against the targeted pathogen.

Article Abstract

is recognized as a problematic pathogen, causing severe enteric diseases including antibiotic-associated diarrhea and pseudomembranous colitis. The emergence of antibiotic resistant has driven a search for alternative anti-infection modalities. A promising strategy for controlling bacterial infection includes the use of bacteriophages and their gene products. Currently, knowledge of phages active against is still relatively limited by the fact that the isolation of phages for this organism is a technically demanding method since bacterial host themselves are difficult to culture. To isolate and characterize phages specific to , a genotoxic agent, mitomycin C, was used to induce temperate phages from 12 clinical isolates of . Five temperate phages consisting of ΦHR24, ΦHN10, ΦHN16-1, ΦHN16-2, and ΦHN50 were successfully induced and isolated. Spotting assays were performed against a panel of 92 isolates to screen for susceptible bacterial hosts. The results revealed that all the phages obtained in this work displayed a relatively narrow host range of 0-6.5% of the tested isolates. Electron microscopic characterization revealed that all isolated phages contained an icosahedral head connected to a long contractile tail, suggesting that they belonged to the family. Restriction enzyme analysis indicated that these phages possess unique double-stranded DNA genome. Further electron microscopic characterization revealed that the ΦHN10 absorbed to the bacterial surface via attachment to cell wall, potentially interacting with S-layer protein. Bacteriophages isolated from this study could lead to development of novel therapeutic agents and detection strategies for .

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6079236PMC
http://dx.doi.org/10.3389/fmicb.2018.01701DOI Listing

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