1) wide spectrum of lytic activity of the bacteriophage preparation toward existing biotypes of the pathogen (achieved via polyvalent or complex nature of the preparation)
2) high virulence of single components of the preparation (i.e., separate phages composing the prep) and their high concentration (usually 10^7)
3) stability of lytic activity of the preparation with time
4) tolerance of the preparation to acidic gastric juices and, conversely, capability for easy dissolving in intestines (for preparations concerning which peroral use is anticipated; achieved usually by covering the tablets with acid-resistant coating
5) test on susceptibility of bacterial culture to bacteriophage preparation is strictly recommended. In case patient’s microflora is insensitive to phages from complex preparation,isolation of new virulent bacteriophages is needed (as well as following elevation of its activity towards this bacterial pathogen by adaptation)
6) phage therapy is considered as ONE of the components of complex treatment. In practice, phage therapy is very often combined with antibiotics and immunotherapy.
Therefore, success of bacteriophage therapy is defined by timeliness of treatment, susceptibility of patient’s microflora to the phage preparation utilized, and by optimal scheme of treatment (doses, mean of phage introduction, combination with other kinds of therapy).
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"In silico"
From Wikipedia
If the target host* of a phage therapy treatment is not an animal the term "biocontrol" (as in phage-mediated biocontrol of bacteria) is usually employed, rather than "phage therapy".
In silico
From:"Genomics,Proteomics and Clinical Bacteriology",N.Woodford and Alan P.Johnson
Phrase that emphasizes the fact that many molecular biologists spend increasing amounts of their time in front of a computer screen, generating hypotheses that can subsequently be tested and (hopefully) confirmed in the laboratory.
Phage Therapy is influenced by:
Phage therapy is influenced by:
Country : the epidemiological situation is different from country to country in terms of circulating bacteria and bacteriophages. Example: lytic phages from Italy may be no active on the same bacteria (genus and species) isolated from another country and vice versa.
Temporariness
Mutation rate
Phenotypical delay
Phage cocktail
My point of view
Country : the epidemiological situation is different from country to country in terms of circulating bacteria and bacteriophages. Example: lytic phages from Italy may be no active on the same bacteria (genus and species) isolated from another country and vice versa.
Temporariness
Mutation rate
Phenotypical delay
Phage cocktail
My point of view