GENOMIC DIVERSITY IN Staphylococcus Aureus

<p><em>Staphylococcus aureus</em> chromosomal DNA from 125 methicillin-resistant and 10 methicillin-sensitive clinical isolates was digested with rare-cutting restriction endonucleases and subjected to pulsed-field gel electrophoresis (PFGE). Thirty-nine distinct genomic macrorestriction patterns (GPs) were identified using <em>Sma</em>I; 29 of these patterns are from methicillin-resistant <em>S. aureus</em> (MRSA).</p> <p>A dendrogram showing percent similarity among the patterns was constructed which revealed the considerable genomic diversity of the collection even though the isolates had been obtained during outbreaks. The majority of the MRSA formed one broad group with two outbreak subclasses. However, 8 of the 29 MRSA GPs (28%) were diverse.</p> <p>Digestion with <em>Csp</em>I, which clarified relationships among some <em>Sma</em>I patterns, showed that 5 strains had much larger genomes (3.5 to 3.8 Mb) than the average of our isolates (3.0 Mb). Duplications of large regions of their chromosomes may have occurred.</p> <p>Restriction fragment length polymorphisms (RFLPs) of the methicillin resistance gene, <em>mec</em>A, and the transposon, Tn554, were used to further type selected isolates. The association of the same <em>mec</em>A and Tn554 RFLPs with diverse MRSA indicates that <em>mec</em>A may have been horizontally transferred to diverse <em>S. aureus</em> strains on multiple occasions.</p> <p>In the process of examining genomic differences among the isolates, aberrantly migrating bands were observed. Evidence that these bands were supercoiled plasmids greater than 300 kb was obtained by linearizing the plasmids with S1 nuclease and determining their sizes with PFGE. The "S1-PFGE" method was developed in our laboratory as a general means of identifying and sizing very large plasmids that often escape detection.</p> <p>The <em>Sma</em>I genomic polymorphisms of two related isolates were attributed to the insertion of temperate bacteriophages both of which lacked <em>Sma</em>I sites. DNA of one of these isolates contained an additional <em>Sma</em>I site possibly created by point mutation.</p> <p>One MRSA isolate was serially propagated in antibiotic-free medium for 29 days. The serial culture showed a decline in the percentage of MRSA cells. PFGE analysis showed that the <em>mec</em>A gene had been deleted. Together, these observations indicate that <em>S. aureus</em>, particularly MRSA, may be more diverse than has been appreciated in the past.</p>

Name thesis:degree_name

Doctor of Philosophy (PhD)

Level thesis:degree_level

Dissertation

Discipline thesis:degree_discipline

Microbiology, Molecular Biology and Biochemistry

Year

1997

Author dc:creator

• Barton, Bret Max

Contributors dc:contributor

• Anthony J. Zuccarelli
• Barry L. Taylor
• Junichi Ryu
• David Hessinger
• Brad Hyman

• Microbiology
• Molecular Genetics
• Physiology
• Staphylococcus aureus -- genetics; Variation -- genetics; Staphylococcus Phages -- genetics; Genes, Bacterial.

Statement dc:rights

• This title appears here courtesy of the author, who has granted Loma Linda University a limited, non-exclusive right to make this publication available to the public. The author retains all other copyrights.

Language dc:language

English

Repository record dc:identifier

https://scholarsrepository.llu.edu/etd/1378

OAI identifier oai:identifier

oai:scholarsrepository.llu.edu:etd-2143