V iral D etection M ethodologies Group-8 Introduction To Laboratory Medicine.

1. Viral Detection Methodologies Group-8 Introduction To Laboratory Medicine. Ug-3 ,6th Semester

2. Proudly Presented By: Viral Diagnosis Sheroze Ameen Kinza Waqar Sayeda Sarah Saleem Sameen Ruqia Sayeda Kashmala Zahra Uzma Batool

3. Three General Approaches for Laboratory Diagnosis of Viral Infections 1.Direct Examination - Microscopy - ELISA 2.Indirect Examination - Tissue Culture - Chick Embryo 3. Serology -Ab detection - Immunofluoresecence

4. Collection of Viral Specimens Nasal Tract Infection G.l Tract Infection Blood /Vesicular Infection Swabs , Sputum from Throat, Nasal Stool, rectal swab. Urine. Skin scraps, Blood Type Of Specimen Diarrheal and Entero -Viruses HSV, Rubella,Pox virus, Rabies, HBVHCV, HIV, CMV RSV, Influenza A, B Virus Type

5. Viral Specimen Storage & Bio-safety Personal protective equipment (PPE) • Store specimen at : • 4 °C to 8 °C for short periods of time • -20 °C to - 40 °C for long term storage Viral transport medium (VTM) collection vials Polyester Fiber-Tipped Applicator Viral transport medium (VTM) collection vials

6. Direct Methods of Virus Detection Direct Methods of Viral Detection Shehroze Ameen

7. ELISA

8. Microplate ELISA for HIV antibody: colouredwells indicate reactivity

9. Electron Microscopy • immune electron microscopy can increase specificity of EM • disadvantage: expensive, poor sensitivity due to high requirement of viral titres • Virus particles are detected and identified on the basis of morphology

10. Electron Microscopy 106virus particles per ml required for visualization, 50,000 - 60,000 magnification normally used. ADENO VIRUS ROTA VIRUS

11. Light Microscope • Replicating virus often produce histological changes in infected cells • Viral inclusion bodies are defined as replicating virus particles either in the nucleus or cytoplasm of infected cells

12. Light Microscope

13. RT, Reverse Trancriptase & Allele Specific PCR PCR allows the in vitro amplification of specific target DNA sequences by a factor  of 106 and is thus an extremely sensitive technique. It is based on an enzymatic  reaction involving the use of synthetic oligonucleotides flanking the target nucleic sequence  of interest. These oligonucleotides act as primers for the  thermostable  Taq polymerase

14. PCR Advantages of PCR: Extremely high sensitivity, may detect down to one viral genome per sample volume Easy to set up Fast turnaround time Disadvantages of PCR Extremely liable to contamination High degree of operator skill required Not easy to quantitate results A positive result may be difficult to interpret, especially with latent viruses such as CMV, where any seropositive person will have virus present in their blood irrespective whether they have disease or not.

15. INDIRECT METHODS FOR VIRAL DETECTION

16. Tissue Culturing Cells from man or animal are grown as a single layer(mono-layer) on the wall of the tubes or on one side of flat bottle. Cells are incubated at 37 degree Celsius. •Suspended in tissue culture media

17. Tissue Culturing Virus growth is recognized by: 1)Cytopathic effect:cell degeneration, Rounding, shrinkage 2) Haemadsorption Test : cells acquire the ability to stick to mammalian red blood cells. NEGRI BODIES SYNCYTIA INCLUSION BODIES

18. Problems With Tissue Culturing  Long period (up to 4 weeks) Poor Sensitivity Susceptible to contamination Not Applicable on all viruses

19. Chick Embryo Inoculation Chorioallantoic Membrane : Variola and Vaccinia Virus Allantoic Cavity : Influenza Virus and Paramyxo virus Amniotic Cavity: Primary isolation of Influenza virus 7-12 day old chick is used. Costs less, growth of virus is rapid and easy. The Inoculated eggs are kept at 37 degree for 48 hours till the virus replicates.

20. Serologic Tests

21. VIRALSEROLOGY Turn Around Time Specimen Tests Principle • Levels of IgG and IgMAb against viral antigens • 7-10 days • Serum Container Volume Tests Include HIV HSV HBV,HCV Rubella Measels CMV • 7ml • Red or • Gold • Top tube Storage • 4ºC

22. VIRAL SEROLOGY • Diagnosing • Primary +Re-Infection • 4 fold or more increase in titre of IgG or total antibody between acute and convalescent sera • Presence of IgM or IgG • Seroconversion • A single high titre of IgG (or total antibody) - very unreliable

23. HEMAGGLUTINATION TEST • Purpose : • -  To quantitate soluble antigens and HI titer in serum samples • -  Sensitive than CFT, simple, inexpensive, and rapid and is the method of • choice for • Assaying antibodies to any virus that causes hemagglutination • -  Commonly used for different  strains of influenza viruses, and parainfluenza • viruses • -  Hemagglutinins are used as antigens in influenza virus vaccines, thus • making HI the method of choice for measuring vaccine-induced antibodies

24. Label plates (8 or 12 wells/row) Add 50 ul PBS to all Wells Add 50 ulAAF to 1st well Mix & dilute (50 ul) – 1 st through last well Add 50 ul 0.5% washed rbcs to all wells 7. Mix by shaking plates 8. Read at 20 – 30 min PROCEDURE

25. Used For Detection of : • Influenza Virus A and B • Adeno Virus • Herpes Simplex Virus

26. Direct And Indirect Immunofluroesence • Reagents For Fixation: • Paraformaldehyde • PBS • BSA • Methanol

28. Limitations of serological Diagnosis Long length of time required for diagnosis Mild local infections such as HSVgenitalis may not produce a detectable humoral immune response Extensive antigenic cross-reactivity between related viruses e.g. HSV and VZV. Immunocompromised patients often give a reduced or absent humoral immune response. Patients given blood or blood products may give a false positive result due to the transfer of antibody.

29. THANK YOU !