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1 Bio 97 Pathogenetics ©2006 Lee Bardwell 2 Pathogenetics lecture outline - 1 • What are bacteria? • What are viruses? • Antibiotic resistance is a big problem – – – What is an antibiotic? Why don't antibiotics kill us? Why don't antibiotics kill viruses? • How do bacteria become resistant to antibiotic (biochemical mechanism)? ©2005 Lee Bardwell Genetics of pathogens - 2 3 • How do bacteria become resistant to antibiotic (genetic mechanism)? – – – What's a plasmid? What's a transposable element? How do these things move from cell to cell? • What are other ways for DNA to move from cell-to-cell? – – Transformation Viral Transduction ©2005 Lee Bardwell Bacterial life cycle Circular chrm s Bacteria • Prokaryotic • Unicellular • Haploid 4 Question Does the statement “loss-of-function alleles are often recessive” make sense when applied to bacteria? ©2005 Lee Bardwell 6 Viruses and Phages • Non-cellular micro-organism • Consist minimally of DNA or RNA genome and some protein • Infect host cells • Can replicate only within host cells • No intrinsic metabolism- relies on host for energy, precursor molecules • No ribosomes - relies on host for protein synthesis ©2005 Lee Bardwell Antibiotic resistance is a big problem in bacteria • Most bacteria isolated from clininal infection are resistant to multiple antibiotics • Some are resistant to all antibiotics in routine use • Some of what used to be the best antibiotics (very effective, few side effects) are now virtually useless ©2005 Lee Bardwell 7 What is an antibiotic ? • A substance that kills or halts the growth of a micro-organism (typically a bacterium) • Usually made by other microorganisms (fungi, other bacteria) • Examples • Pencillin • Streptomycin • Chloramphenicol ©2005 Lee Bardwell 8 Why don’t antibiotics kill us ? • Bacteria and humans share many core processes Bacteria polymerases resemble human polymerases Bacterial ribosomes resemble human ribosomes, etc. • But there are some things that are completely different bacteria have a peptidoglycan cell wall and we don’t • The best (least toxic to us) antibiotics target these “completely different” structures ©2005 Lee Bardwell 9 How do antibiotics kill bacteria ? Inhibition of bacterial cell-wall synthesis by certain* antibiotics QuickTime™ and a GIF decompressor are needed to see this picture. *penicillin, vancomycin, others NOTE: movies won’t work on downloads/pdfs 10 BONUS MATERIAL ! No need to memorize 11 BONUS MATERIAL ! No need to memorize 12 Inhibition of bacterial protein synthesis by macrolide* antibiotics QuickTime™ and a GIF decompressor are needed to see this picture. *erythromycin, azithromycin, others 13 Why don’t antibiotics kill viruses ? 14 How do bacteria become resistant ? They can acquire certain _____ that encode ______ that function to neutralize the antibiotic 15 DNA can move between bacteria • Many DNA sequences in bacteria are mobile – they can be transferred between individuals and even between species • Plasmids • Transposable Elements • Antibiotic resistance genes are often contained in these mobile elements • Other means of moving DNA between cells • Transformation • Viral Transduction 16 Plasmids Plasmids are circular DNA molecules that replicate independently of the bacterial chromosome • They often carry antibiotic resistance genes • They are used in genetic engineering as gene transfer vectors 17 18 19 F factor Plasmid • The F (fertility) factor plasmid is a lowcopy-number plasmid ~100 kb in length, and is present in 1–2 copies per cell • It replicates once per cell cycle and segregates to both daughter cells in cell division 20 F factor and Conjugation • Conjugation is a process in which DNA is transferred from bacterial donor cell to a recipient cell by cell-to-cell contact • The transfer is mediated by a tube-like structure called a pilus, formed between the cells, through which the plasmid DNA passes • The ~20 proteins that make up the pilus are encoded by the Ffactor plasmid 21 Mobility of smaller plasmids • Many small plasmids don’t have the genes necessary for pillus formation • They can recombine with F and tag along for the ride. 22 Transposable Elements • Transposable elements are DNA sequences that can jump from one position to another within a chrm, or from one DNA molecule to another • Bacterial TE’s often contain antibiotic resistance genes • They can jump into plasmids, and move with ‘em • The smallest and simplest are 1–3 kb in length and encode the transposase protein required for transposition and one or more additional proteins that regulate the rate of transposition • TE’s are also found in eukaryotes, including humans 23 24 Bacterial Transformation • The process of genetic alteration by pure DNA is transformation • Recipient cells acquire genes from DNA outside the cell • DNA is taken up by cell and often recombines with genes on bacterial chromosome • Bacterial transformation showed that DNA is the genetic material (Avery, MacLeod, McCarty 1944) • Transformation may alter phenotype of recipient cells 25 Transduction • In the process of transduction, bacterial DNA is transferred from one bacterial cell to another by a phage • The transferred DNA may be integrated into the host chrm by recombination 26 Phage Life Cycle 27 In the process of transduction, bacterial DNA is transferred from one bacterial cell to another by a phage Fig. 7.16 28 The transferred DNA may be integrated into the host chrm by recombination Fig. 7.16 29 30 Bio 97 Brief review of diploid genetics ©2005 Lee Bardwell 31 Dominance, Recessiveness – Heterozygous genotype --> normal phenotype – The mutant allele is ___________ ©2001 Lee Bardwell 32 Dominance, Recessiveness – Heterozygous genotype --> disease phenotype – The mutant allele is ___________ ©2001 Lee Bardwell 33 Mutant (disease causing) alleles • Loss-of-function mutations --> allele encodes a protein that... – Is not made, or has a reduced function, or is nonfunctional • (e.g Hemophilia) Usually recessive • Gain-of-function mutations --> allele encodes a protein that... – has a new, disease-causing function • (e.g Huntington’s disease --> mutant protein forms toxic aggregates) Usually dominant ©2005 Lee Bardwell L.O.F. alleles 34 • In many cases, having only half the normal amount of a given protein is okay – Heterozygous genotype --> normal phenotype – The mutant (loss-of-function) allele is recessive ©2001 Lee Bardwell L.O.F. alleles II 35 • In some cases, having only half the normal amount of a given protein is NOT okay – Heterozygous genotype --> disease phenotype – Loss-of-function allele is dominant (= haploinsufficiency) ©2001 Lee Bardwell HUNTINGTON’S DISEASE Disease of the Day PHENOTYPE • PROGRESSIVE INVOLUTARY MOVEMENTS INCLUDING CHOREA (GREEK=DANCE), COGNITIVE DEFICITS, AND PSYCHIATRIC DISORDERS GENETICS • FREQUENCY = 1/10,000 (European origin) • AUTOSOMAL DOMINANT - COMPLETE PENETRANCE • LATE ONSET: 35-50 years of age 10-20 YEAR COURSE • ANTICIPATION -TRINUCLEOTIDE REPEAT EXPANSION (pp. 427-8) NO EFFECTIVE TREATMENT OR CURE HD is characterized by neuronal degeneration 37 HUNTINGTIN protein MATLEKLMKAFESLKSFQQQQQQQQQQQQQQQQQQQQQQQPPP PPPPPPPPQLPQPPPQAQPLLPQPQPPPPPPPPPPGPAVAEEPLHRP KKELSATKKDRVNHCLTICENIVAQSVRNSPEFQK… (3142 total aa’s) 350 kD protein 10-11 kb transcript The repeated trinucleotide is AGC which encodes Q (glutamine) ubiquitously expressed function unknown correlation between repeat size and age of onset Gene cloned by Huntington’s Disease Collaborative Research Group 1993 Most accepted current theory: The extended glutamine tracts are thought to promote the formation of toxic aggregates, leading to cell death 39 Ethical Issue Sex Selection Using genetic techniques To pick the sex of your kid 40 ©2005 Lee Bardwell Ethical Issue Sex Selection Using genetic techniques To pick the sex of your kid How ? • Sperm sorting – (X is heavier) 75% success if boy is desired, 90% if girl is desired • Preimplantation Genetic Diagnosis – In Vitro Fertilization – Determine sex of 4-8 cell embryos – Only implant the ones you want • Chorionic Villus Sampling - sample the placenta – Done at 8-9 weeks of gestation • Amniocentesis - sample the amniotic fluid – Done at 4-5 months 41 ©2005 Lee Bardwell Ethical Issue Sex Selection Picking the sex of your kid Why ? • To prevent the birth of sons to women carriers of X-linked recessive diseases • For family “balancing” • Because of economic and cultural pressures that lead to sons being more desirable 42 ©2005 Lee Bardwell Ethical Issue Sex Selection Picking the sex of your kid How do you feel about it ? 43 ©2005 Lee Bardwell