1887

Abstract

PFGE is the ‘gold standard’ method for bacterial subtyping. However, many strains are non-typable by this approach because of DNA degradation by nucleases action.

To evaluate a modified PFGE protocol for typing nosocomial isolates of .

Twenty- five isolates previously exposed to DNA degradation were used to optimize an extraction method for elimination of DNases activity before applying Xba1 enzyme. Introducing of sodium dodecyl sulfate (SDS) in different concentrations to the extraction buffer was evaluated for protecting genomic DNA molecule from degradation by nucleases.

Addition of 3 % SDS in combination with 3 % N-lauryl sarcosine to the extraction buffer was found to reduce the previously experienced nuclease activity. Pre-examination of plug quality prior to the digestion phase could efficiently reduce the expense of the wasted enzyme.

We have successfully devised a PFGE protocol that enhanced the typeability of nosocomial .

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/content/journal/jmm/10.1099/jmm.0.001093
2019-10-29
2019-11-20
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