diagnosis of viruses Flashcards
(17 cards)
symptomology clinical categories
Jaundice, febrile polyarthritis, haemorrhagic fevers, SARI, encaphalitis, meningitis, rash, diarrhea, arboviruses, rodent feacal-oral
jaundice
Hep A - E and G. Yellow fever. Human cirrhosis virus (unclassified)
Febrile polyarthritis
(joint inflammation + fever) Dengue virus, ross river virus, O’nyong’nyong virus, Chikungunya virus
Haemorrhagic fevers
Yellow fever, Lass/Tacharibe viruses, Crimean-congo/Dugbe viruses, Ebola and Marburg virus
Severe acute respiratory infections
Influenza, SARS/MERS, Hantavirus, Adenovirus 14, Nipah/Hendra virus
Encaphalitis/meningitis
Cyclovirus Vietnam, West Nile virus, Tick-borne encephalitis virus, Lymphatic choriomeningitis virus, Rabies, Thogotoviruses
Rash
Herpes, roseolavirus, HPV, smallpox/cowpox, dengue fever, ross river virus, rubella, measles, hand-foot-mouth disease, erythrovirus,
Diarrhea
Noroviruses, rotaviruses, hand-foot and mouth disease
Arboviruses
Flaviviruses -> West nile, dengue, tick-borne encephalitis, yellow fever
Togaviridae -> all except rubella
Bunyavirdae -> dugbe, rift valley fever, crimean congo haemorrhagic fever
Orhtomyxoviridae -> dhori virus, thogoto virus
Rodent faecal-oral
Arenaviridae -> lassa viruses
Bunyaviridae -> hantavirus
Functional technique - Pfu
plaque forming units - quantifies the presence of a virus
Functional technique - haemagglutinin inhibition assay
serial dilution of virus added to wells and RBC’s added. The more virus is present, the greater the degree of agglutination
COVID-19 diagnosis through PCR
nasopharyngeal swab is collected
RNA is extracted from the deactivated virus
purified RNA is reverse transcribed to DNA and amplified by PCR
Positive patients cross the threshold line within 40,000 cycles (flourescence shows)
COVID-19 diagnosis through serologic test (lateral flow assay)
sample added to well with dilution phosphate saline solution
antibodies with specificity for COVID-19 bind to gold covid19 antigen coagulates in conjugate pad
sample enters testing well and covid-19 A-A complex binds to immobilised anti-human IgG/IgM antibodies on test strip
Rabbit antibody gold conjugate binds to immoblised anti-rabbit IgG antibodies on control strip
Sandwich ELISA
Quantifies presence of viral proteins antibody A at the bottom of the well - specific for antigen of virus being tested
test sample is added and any antigen binds to the antibody
everything washed
antibody B is added and binds to antigen being tested for
excess washed away
an enzyme conjugated secondary antiobdy is added - specificity for Ig from species of anitobdy B. binds only if antiobdy B is bound
chromogenic substrate of the enzyme is added and colour intesity after a fixed period of time determines the result of the test
Antibody capture ELISA
Quantifies presence of antibodies to a virus
Well is coated with a viral antigen
Test samples are added to the wells in serial dilutions
the unbound Ig is washed away and any antibody is detected by addition of a secondary antibody which is enzyme coupled
A positive result is detected by the enzyme converting the substrate into a coloured product
Neutralisation assay
Quantifies presence of functional antibodies to a virus