A Comparative Assessment of Ribosomal DNA Polymorphisms in Methicillin Resistant Staphylococcus Aureus (MRSA) Epidemiology
Chromosomal DNA from 19 strains of methicillin resistant Staphylococcus Aureus (MRSA) which included 13 strains from different geographical locations in England and 6 strains from St George's Hospital (SGH), London, with MRSA NCTC 119040 and Oxford S. aureus were digested with the restriction e...
Saved in:
Published in | African journal of biomedical research Vol. 10; no. 2 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Published |
Nigeria
Ibadan Biomedical Communications Group
06.08.2009
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Chromosomal DNA from 19 strains of methicillin resistant Staphylococcus
Aureus (MRSA) which included 13 strains from different geographical
locations in England and 6 strains from St George's Hospital
(SGH), London, with MRSA NCTC 119040 and Oxford S. aureus were digested
with the restriction endonucleases, HindIII and HaeIII. Southern blot
hybridisation was carried out on the DNA digests transferred onto
membrane using radioactive probe prepared from 16S and 23S rRNA from
Escherichia coli . The pattern of bands which depended on restriction
fragment length polymorphisms was used as a measure of minor genomic
variation within the MRSA strains. Phage typing, biotyping,
antibiogram, and plasmid profile analysis were also carried out on all
the strains for comparison. Four and five different patterns were
obtained for HindIII and HaeIII, respectively for representative
isolates from different geographical locations in England for that
year. Three different patterns were identified among the MRSA strains
from SGH, London, using HaeIII. None of the epidemiological markers
used in this study gave results that correlated with each other.
Ribosomal DNA polymorphisms have proved to be a very useful technique
for studying the epidemiology of MRSA in hospitals when used along with
other epidemiological markers. |
---|---|
ISSN: | 1119-5096 |