Isolation of phages for phage therapy: a comparison of spot tests and efficiency of plating analyses for determination of host range and efficacy

PLoS One. 2015 Mar 11;10(3):e0118557. doi: 10.1371/journal.pone.0118557. eCollection 2015.

Abstract

Phage therapy, treating bacterial infections with bacteriophages, could be a future alternative to antibiotic treatment of bacterial infections. There are, however, several problems to be solved, mainly associated to the biology of phages, the interaction between phages and their bacterial hosts, but also to the vast variation of pathogenic bacteria which implies that large numbers of different phages are going to be needed. All of these phages must under present regulation of medical products undergo extensive clinical testing before they can be applied. It will consequently be of great economic importance that effective and versatile phages are selected and collected into phage libraries, i.e., the selection must be carried out in a way that it results in highly virulent phages with broad host ranges. We have isolated phages using the Escherichia coli reference (ECOR) collection and compared two methods, spot testing and efficiency of plating (EOP), which are frequently used to identify phages suitable for phage therapy. The analyses of the differences between the two methods show that spot tests often overestimate both the overall virulence and the host range and that the results are not correlated to the results of EOP assays. The conclusion is that single dilution spot tests cannot be used for identification and selection of phages to a phage library and should be replaced by EOP assays. The difference between the two methods can be caused by many factors. We have analysed if the differences and lack of correlation could be caused by lysis from without, bacteriocins in the phage lysate, or by the presence of prophages harbouring genes coding for phage resistance systems in the genomes of the bacteria in the ECOR collection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacteriolysis
  • Bacteriophages / physiology*
  • Bacteriophages / ultrastructure
  • Escherichia coli / virology
  • Host Specificity
  • Salmonella / virology
  • Virus Cultivation
  • Virus Latency

Grants and funding

This work was funded by the Olle Engqvist Foundation. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.