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Unit 1 How to Fight an Infection

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Unit 1 How to Fight an Infection. Bioinformatics. The collection, classification, storage, and analysis of biochemical and biological information using computers especially as applied i n molecular genetics and genomics Sue and the outbreak of Neiserria meningitidis - PowerPoint PPT Presentation

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Page 1: Unit 1 How to Fight an Infection

Unit 1 How to Fight an Infection

Page 2: Unit 1 How to Fight an Infection

Bioinformatics

• The collection, classification, storage, and analysis of biochemical and biological information using computers especially as applied in molecular genetics and genomics

• Sue and the outbreak of Neiserria meningitidis – We collected information from individuals to try to

track the infection

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BLAST

• We identified the possible organisms infecting the college students with BLAST

• http://blast.ncbi.nlm.nih.gov/Blast.cgi– Provides you with a match to your sequence of

DNA.– The higher the percentage, the greater the match

that it is that organism.

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ELISA

• Enzyme-linked immunosorbant assay– Quantitative and Qualitative results– http://www.sumanasinc.com/webcontent/animati

ons/content/ELISA.html

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Attack of the Superbugs

• 1.2.2 - This activity investigates the mechanisms by which DNA from one bacterial cell is transferred to another bacterial cell.– This process is called CONJUGATION.

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Attack of the Superbugs

• To see if we can induce conjugation making an antibiotic resistant bacterium

• We are using two strains of Escherichia coli– Strain 1 – has a gene on its DNA that codes for

streptomycin resistance– Strain 2 – has a gene found on the plasmid DNA

that codes for ampicillin resistance.

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Results• We had growth on three plates.

• If conjugation had not occurred, we would not have seen growth on the plate with strep and amp in it. Plasmid was conjugated.

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Transduction and Transformation

• Transduction is the process by which DNA is transferred from one bacterium to another by a virus

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• Bacterial transformation is the process by which bacterial cells take up naked DNA molecules from the surrounding media.– Not sure how this occurs.

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Antibiotic Resistance

• Lab showed how bacteria can establish antibiotic resistance.

• Bad!

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Hearing Loss

• Put a pic of the ear on your sheet with structures labeled– Sensionuerial vs conductive• Related to the use of Sue’s use of antibiotics due to

Neiserria meningitidis

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• Conductive hearing problems are those that disrupt the conduction of sound through the outer and middle ear.

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Conductive Hearing Loss

• Affects hearing before the sound reaches the cochlea and the nerve receptors of the inner ear.

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Sensorineural deafness

• Sensorineural deafness is decreased hearing or hearing loss that occurs from damage to the inner ear, the auditory nerve, or the brain.

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• Sensorineural hearing loss is most often due to a loss of hair cells (sensory receptors in the inner ear).

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Treatment

• Cochlear Implant• Hearing Aid

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Causes of Conduction Deafness

• Otitis Media• Middle ear infection• Chronic suppurative otitis media –

1.Peferation of the tympanic membrane

2. Bacterial infection

l

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Otosclerosis

• Ossicles of the middle ear harden and become less able to vibrate.

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Otosclerosis

• Approximately one-third of all persons with impaired hearing have this condition.

• Hereditary• Damage to the ossicles, e.g. by serious infection or

head injury. • Perforated (pierced) eardrum, which can be caused

by an untreated ear infection (chronic suppurative otitis media), head injury or a blow to the ear, or from poking something in your ear.

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Interventions

• Hearing aids -usually effective for conductive hearing loss.

http://www.nlm.nih.gov/medlineplus/ency/imagepages/8685.htm

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Vaccines – 3 major, out of 6

• Types of Vaccines– Attenuated – live virus, slightly weakened,

changed so that you get an immune response but not the disease

– Killed – virus is dead but still elicites an immune response

– Toxoid - vaccine is designed to trigger an immune response to a toxin produced by a bacterium or virus, not to the organism itself.

Page 22: Unit 1 How to Fight an Infection

Unit 2 How To Screen What Is in Your Genes

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Genetic Testing

• Genetic testing is the use of molecular methods to determine if someone has a genetic disorder, will develop one, or is a carrier of a genetic illness and involves sampling a person’s DNA and examining the chromosomes or genes for abnormalities.

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• 2.1.1. Genetic Counselor• 2.1.2 Screening our own genes - PTC gene– PCR• http://www.sumanasinc.com/webcontent/animations/

content/pcr.html• Know the steps and the temps for each step

• 2.1.3 Restriction Enzymes– What are they– Sticky vs blunt- SNPs

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2.2

• Gene Therapy– Gene therapy is the practice of inserting functional

genes into a person’s genome to replace faulty genes

– Viral Vectors vs Non-viral• Viral – can be engineered, enters cells easily but can

cause an immune response• Non-viral – plasmids, don’t enters cells as easily

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2.3

• Reproductive Technology– in vitro fertilization (IVF) – preimplantation genetic diagnosis (PGD)

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Unit 3 How to Conquer Cancer

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3.1• Regulation in the cell cycle

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• Proto-oncognes become oncogenes through a disruption in the cell cycle.

• Normally, cells will detect a mutation or that a certain point in the cell cycle has been disrupted and cause the cell to undergo apoptosis

• Oncogenes lead to cancerous cells

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DNA Microarray - What Are They?

• Technology in which the activity (whether a gene is turned on or off) of thousands of genes can be measured.

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• mRNA is attached to the wells• Conjucated with cDNA (complimentary) along

with a flourescent tag.• Color that is emited is detected.• Detects for the level of expression of mRNA

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3.2 Cancer Screens and 3.3 Treating Cancer

• Why do we do screens?• How do we treat cancer?– Radiation– Chemotherapy– Biofeedback therapy

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3.4 Building a Better Cancer Treatment

• Personalized Medicine– SNPS, haplotypes– How do you determine which medication to give

looking at SNPs?

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Clinical Trials

• Random• Double Blind **• Orphan• Single Blind

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Nanotechnology

• What can nanotechnology do?• How can we use it in cancer?

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Unit 4 How To Prevail When Organs Fail

• GFP Lab– Why hdyrophobic column– Why CaCl2 and heat shock– Why lysozyme– Why binding buffer

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ESRD and Organ Transplantation

• Know the tests that are used to diagnose ESRD

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Kidney Vs Heart Transplant

• Both are used for patients that are ill and in need of an organ.

• Both must utilize tissue typing.• Both can have organ rejection.

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Heart Transplant More extreme of a surgery

Kidney = laproscopicHeart = opening entire chest cavity

Blood has to be rerouted during surgery to a bypass machineKidney = just clamp the vessels to the kidney that is to be

removed Longer recovery time Needs to be performed ASAP vs wait time on a

kidney – WHY?

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Transplantation of Other Tissues Which of the following can we currently transplant?

HeartIntestineKidneyLiverPancreasLungBone/TendonsCorneaSkin

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• Which of the following organs is the only organ that can regenerate itself?– Heart– Intestine– Kidney– Liver– Pancreas– Lung

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The Liver!

• A portion of a liver can be transplanted and can grow while the donor ‘s original liver can grow back to normal as well.

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Those Involved Anesthesiologist

Provides medicine to put patient under during surgery Transplant Surgeon

Specializes in the transplant of a certain organ Preoperative Nurse

Works with the surgeon handing her tools and provides help when needed

PharmacistProvides ant-rejection medication to patient after surgery

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Xenotransplantation

• Using animal parts for humans– Plenty of animals, plenty of parts

• Problem – we can reject the organ (HLA)– Introduction of animal viruses into humans

• Problem – clone the animals – can lead to inferior structures

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Tissue Engineering

• Using patients cells to grow organs and tissues in the lab– Could grow a replacement organ??– Bladder would be easier than intestines – due to

the multiple functions of intestines• What are some negatives?http://science.howstuffworks.com/genetic-science/cloned-organ-transplant.htm