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Conjugative DNA transfer, antibiotic resistance and MDR bacteria. With thanks to Steve Matson Who first created this lecture. Antibiotics – a medical miracle. The discovery of antibiotics changed the medical landscape. http://www.nature.com/nature/journal/v406/n6797.
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Conjugative DNA transfer, antibiotic resistance and MDR bacteria With thanks to Steve Matson Who first created this lecture
Antibiotics – a medical miracle The discovery of antibiotics changed the medical landscape http://www.nature.com/nature/journal/v406/n6797
Bacterial infection as cause of death plummeted • Life expectancy increased by 8 years between 1944 and 1972 Deaths in Scotland due to infectious disease per 100,0000 www.gro-scotland.gov.uk
Bacterial infection as cause of death plummeted • Life expectancy increased by 8 years between 1944 and 1972 Deaths in Scotland due to TB per 100,0000 www.gro-scotland.gov.uk
The antibiotic resistance problem • Drug resistant bacteria are very wide spread occurring throughout the world
The antibiotic resistance problem • Drug resistance happens quickly • One study observed an increase from 0% to 28% drug resistant E. coli in less than 5 years
The antibiotic resistance problem • In 2005 there were more deaths in the US from Methicillin resistant Staphylococcus aureus than from AIDS HIV 17,011 deaths MRSA Staph aureus 19,000 deaths Stats from CDC
The antibiotic resistance problem • 85% of the cases of MRSA Staph were acquired in hospitals or other health care settings HIV 17.011 deaths MRSA Staph aureus 19,000 deaths
And how drug resistant bugs arise evolution.berkeley.edu
And how drug resistant bugs arise evolution.berkeley.edu
And how drug resistant bugs arise evolution.berkeley.edu
And how drug resistant bugs arise evolution.berkeley.edu
How did that 1ststreptomysin resistant bug arise? • A simple error in DNA replication that produced a mutation • Occurs at low frequency • Mutation is on the chromosome • Mutation affects either ribosomal protein S12 or 16S rRNA to produce streptomycin resistance • Does not explain MDR bugs or high rate of spread
How do we solve this puzzle? • We know that drug resistance spreads at an alarming rate • Far too fast to be the result of single mutations in the chromosome that arise independently
How do we solve this puzzle? • We know that drug resistance spreads at an alarming rate • Far too fast to be the result of single mutations in the chromosome that arise independently • We also know that bacteria become resistant to more than a single drug • If this were the result of point mutations in the chromosome the rate would be even slower
The four waves of antibiotic resistance in Staph. aureus Vancomycin resistant
Plasmids are a key to combiningthem together in one bacterium
Plasmids are a key to combiningthem together in one bacterium A plasmid is an extra-chromosomal DNA molecule separate from the chromosomal DNA which is capable of replicating independently of the chromosomal DNA. In many cases, it is circular and double-stranded. Plasmids usually occur naturally in bacteria, but are sometimes found in eukaryotic organisms
To understand the rapid increase in multiple drug resistant strains of bacteria there are two questions we must answer. • 1– how are plasmids rapidly transferred in a bacterial population? • 2 – how do plasmids encode resistance to multiple drugs?
Bacterial conjugation • Driven by conjugative plasmids; 1st example =the fertility factor F • Mating only between cell with F (F+) and cell without F (F–) • Transfer of information is one-way from donor to recipient • Cells must be in close cell-cell contact for DNA transfer to occur
F Plasmid William Hayes • A 100 kb (single copy) with ~ 100 genes • Replicates using host machinery • Partitions to daughter cells
A selfish genetic element! • Encodes pillin which assembles into pili allowing cell contact • Only F+ cells have pili • F+ inhibited from contacting other F+ cells
Here’s how it happens • F+ donates single-stranded copy of F to F– cell (rolling circle) • F- cell converted to F+ by replication of ssDNA • F plasmid rapidly spreads through bacterial population
Bacterial conjugation is the primary mechanism which spreads antibiotic resistance among bacterial populations
Let’s look at the machine Tra I (H) = helicase Tra Y (R)= nicks donor DNA at oriT and remains covalently linked during transfer Tra D = links TraY to Type 4 secretion Machine = pillus
Look among existing drugsfor small moleculesthat inhibit the Relaxase (R) 1 nM 10 nM Proc Natl Acad Sci U S A. 2007 Jul 24;104(30):12282-7
These inhibit DNA transfer! Proc Natl Acad Sci U S A. 2007 Jul 24;104(30):12282-7
Plasmid transfer provides other drug targets Plasmids that replicate in similar ways (top, red and blue) compete for resources, and the losing plasmid is lost from the bacterial cell. J. Am. Chem. Soc., 2004, 126 (47), pp 15402–15404
Plasmid transfer provides a drug target An aminoglycoside that binds the small RNA causing plasmid incompatibility can mimic this natural process, causing elimination of a drug-resistance plasmid (bottom, green). J. Am. Chem. Soc., 2004, 126 (47), pp 15402–15404
Transposable Genetic Elements are also key to antibiotic resistance
Transposable Genetic Elements are also key to antibiotic resistance Transposable genetic elements (transposons) = DNA segments that can insert themselves at one or more sites in a genome. Remarkably, almost 50% of our chromosomes consist of transposable elements
Transposons can carry drug resistance genes onto “R plasmids”
The plasmid can then be transferred to another bacterium by conjugation!
R plasmids can become increasingly complex through natural selection
Wow! http://www.fbs.leeds.ac.uk/staff/profile.php?tag=ONeill_AJ
Research into this area iskey to combating TB andother bacterial infections! CDC