Unit 5 bacteria and viruses

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Unit 5 bacteria and viruses

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Laboratory Training for Field Epidemiologists Viral cultures Investigation strategies and methods May 2007 Laboratory Training for Field Epidemiologists Learning objectives Learning objectives At the end of the presentation, participants should: • Understand the principle of cultivating viruses • Understand the methods and problems with cultivating viruses Laboratory Training for Field Epidemiologists Techniques to identify viruses Techniques to identify viruses It can take a few hours to weeks to identify a virus Techniques include: • PCR (single round) or nested/semi-nested PCR • Real-time PCR • Direct electronic microscopy • Antigen capture • Isolation – Long process – Gold standard for viruses that can be cultured Laboratory Training for Field Epidemiologists Virus culture Virus culture Is based upon amplification of potentially infectious pathogens Implies intracellular replication of viruses in the cytoplasm or in the nucleus Is controlled by regulations (i.e. bio-safety level 2, 3 or 4) Allows for: • Identification • Further studies (e.g., Pathogenicity, antiviral sensitivity, research) Laboratory Training for Field Epidemiologists Virus culture Virus culture Long process • Not always possible for front-line diagnosis Primary objective for the diagnosis of an unknown disease No generic protocol Laboratory Training for Field Epidemiologists How to go about virus culture? How to go about virus culture? Obtain suitable specimens • Identified specimens with suitable information Evaluate of chances of success of the process before start Make sure transportation used cold chain • 4°C • -20°C • Dry ice (-79°C) Use suitable culture protocol • In vitro/in vivo cell cultures Laboratory Training for Field Epidemiologists Culture procedure Culture procedure Use of a variety of cell sources and techniques Treatment of the specimen prior to inoculation Follow-up Viral detection: • Non specific – Cytopathogenic effect (microscope) – Electronic microscopy identification (morphology) • Specific – Immunological detection: antigen detection, PCR, IFA… Viral load estimation (titration, plaque assay) Laboratory Training for Field Epidemiologists Limitations of cultures to Limitations of cultures to identify viruses identify viruses Absence of detection system for the agent Inappropriate culture systems Viruses that cannot be cultured A negative viral culture results does not mean that the agent is absent • Need of other tests • PCR can detect the viral genome in absence of the complete virus Laboratory Training for Field Epidemiologists Specimens used to culture viruses Specimens used to culture viruses Blood specimens • EDTA • Heparin • Serum Stool Throat swabs Naso-paryngeal aspirates Stools, rectal swabs Urine Saliva Cerebro-spinal fluid Biopsy • Skin (filoviridae) • Organs (fixation with formaldehyde 10%) Laboratory Training for Field Epidemiologists Potentially infectious specimen forms Potentially infectious specimen forms [...]... micro-organism Laboratory Training for Field Epidemiologists Investigation strategies and methods Developed by the Department of Epidemic and Pandemic Alert and Response of the World Health Organization with assistance from: European Program for Intervention Epidemiology Training Canadian Field Epidemiology Program Thailand Ministry of Health Institut Pasteur Laboratory Training for Field Epidemiologists . participants should: • Understand the principle of cultivating viruses • Understand the methods and problems with cultivating viruses Laboratory Training. Limitations of cultures to identify viruses identify viruses Absence of detection system for the agent Inappropriate culture systems Viruses that cannot be cultured A

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Mục lục

  • Slide 1

  • Learning objectives

  • Techniques to identify viruses

  • Virus culture

  • Slide 5

  • How to go about virus culture?

  • Culture procedure

  • Limitations of cultures to identify viruses

  • Specimens used to culture viruses

  • Potentially infectious specimen forms

  • Sequencing

  • Slide 12

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