micro-plaque assay of influenza virus sensitivity ... - · pdf filemikhail matrosovich and...
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Mikhail Matrosovich and Tatyana MatrosovichMikhail Matrosovich and Tatyana Matrosovich
VIRGIL Antiviral CourseVIRGIL Antiviral Course33--6 October 20066 October 2006
MicroMicro--plaque assay of influenza virus plaque assay of influenza virus sensitivity to neuraminidase inhibitorssensitivity to neuraminidase inhibitors
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Influenza virus receptors: sialic acidsInfluenza virus receptors: sialic acids
HA binds to sialic acid (Sia)HA binds to sialic acid (Sia)
1
Neu5Ac
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Functions of influenza virus neuraminidase (NA)Functions of influenza virus neuraminidase (NA)
Early in infection: Early in infection: Late in infection:Late in infection:
Removes Removes receptors from receptors from virus progeny virus progeny and cell and cell surfacesurface
Promotes virus Promotes virus release and release and spreadspread
Destroys Destroys mucin mucin inhibitors inhibitors and decoy and decoy receptorsreceptors
Promotes Promotes virus entry virus entry into cellinto cell
Neu5Ac
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Inhibition of NA impaires virus release and spreadInhibition of NA impaires virus release and spread
Normal virus release (top) Normal virus release (top) and release in the presence of and release in the presence of NA inhibitor (bottom) NA inhibitor (bottom) From Gubareva et al., 2000From Gubareva et al., 2000
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Plaque reduction assayPlaque reduction assay
NA inhibitor decreases size of plaques produced NA inhibitor decreases size of plaques produced by influenza virusby influenza virusFrom Bantia et al., 1998From Bantia et al., 1998
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Pitfalls of plaque assaysPitfalls of plaque assays
1. Assays in 1. Assays in MDCK cellsMDCK cells do not correlate with virus do not correlate with virus sensitivity to NA inhibitors in vivosensitivity to NA inhibitors in vivo
2. Plaque assays under agar overlays are cumbersome 2. Plaque assays under agar overlays are cumbersome and cannot be performed in 96and cannot be performed in 96--well plateswell plates
New assay solves these problemsNew assay solves these problems
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I. Viral sensitivity to NAI in MDCK cells do not I. Viral sensitivity to NAI in MDCK cells do not correlate with sensitivity in vivocorrelate with sensitivity in vivo
Viruses with drugViruses with drug--sensitive NA can be sensitive NA can be resistantresistant
Viruses with drugViruses with drug--resistant resistant mutations in HA and NA can mutations in HA and NA can display sensitivitydisplay sensitivity
Laboratory cells do not mimic receptors in human airway epitheliLaboratory cells do not mimic receptors in human airway epitheliumumM.MatrosovichM.Matrosovich
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How to model influenza virus receptors of human How to model influenza virus receptors of human airway tissues in a laboratory cell line?airway tissues in a laboratory cell line?
Cell line with high Cell line with high concentration of 6concentration of 6--linked linked sialic acids is requiredsialic acids is required
Laboratory cells
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Preparation of a cell line for resistance assay: Preparation of a cell line for resistance assay: overexpression of SIAT1 in MDCK cellsoverexpression of SIAT1 in MDCK cells
SIAT1SIAT1 (beta(beta--galactoside a2,6galactoside a2,6--sialyltransferase) generates 6sialyltransferase) generates 6--
linked sialic acid receptors recognized by human influenza viruslinked sialic acid receptors recognized by human influenza viruseses
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Influenza viruses are more sensitive to Influenza viruses are more sensitive to NA NA inhibitor in MDCKinhibitor in MDCK--SIAT1 cells than in MDCK cells:SIAT1 cells than in MDCK cells:
A/Sydney/5/97 (H3N2)A/Sydney/5/97 (H3N2)
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Viral plaque assaysViral plaque assays
General cellular stain ImmunoGeneral cellular stain Immuno--stainingstainingdetects destroyed cellsdetects destroyed cells detects infected cellsdetects infected cells
Under liquid medium, Under liquid medium, the plaques are not the plaques are not localised and cannot localised and cannot be countedbe counted
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Known overlaysKnown overlays
-- Gels (agar, Gels (agar, agaroseagarose) ) Time and labor consuming; heated agar can damage Time and labor consuming; heated agar can damage cells; cannot be used in 96cells; cannot be used in 96--well plateswell plates
-- ““SemiSemi--liquidliquid”” overlays (solutions of overlays (solutions of methylcellulose, methylcellulose, tragacanthtragacanth gum, etc)gum, etc)High High viscousityviscousity ----> particularly difficult to handle > particularly difficult to handle in in microplatemicroplate formatformat
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Our approach: Our approach: ThixotropicThixotropic gelsgels
The viscosity decreases as shear rate increasesThe viscosity decreases as shear rate increases
(Examples: yogurt, ketchup)(Examples: yogurt, ketchup)
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AvicelAvicelTMTM (FMC (FMC BioPolymerBioPolymer))
-- Microcrystalline water insoluble celluloseMicrocrystalline water insoluble cellulose
-- Particles (~0,2 uM) Particles (~0,2 uM) form a network of weak form a network of weak hydrogen bonds that hydrogen bonds that account for thixotropic account for thixotropic properties of Avicel properties of Avicel dispersionsdispersions
-- Low viscosityLow viscosity (~ 100(~ 100--200 mPa.s at 1,5% 200 mPa.s at 1,5% Compare to 3000 mPa.s for 1,5% solution of Compare to 3000 mPa.s for 1,5% solution of methylcellulose)methylcellulose)
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AvicelAvicelTMTM (FMC (FMC BioPolymerBioPolymer))
Standardised commercial product:Standardised commercial product:Widely used as vehicle for the preparation of Widely used as vehicle for the preparation of pharmaceutical suspensions and emulsions pharmaceutical suspensions and emulsions
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Plaque assays under Avicel Plaque assays under Avicel vsvs agar agar influenza virus A/Memphis/14/96 (H1N1)influenza virus A/Memphis/14/96 (H1N1)
-- Plaques are bigger; size can be controlledPlaques are bigger; size can be controlled
-- As low as 0.3% ( ! ) of Avicel is still sufficient to localize As low as 0.3% ( ! ) of Avicel is still sufficient to localize plaquesplaques
-- More plaques under Avicel than under agarMore plaques under Avicel than under agar
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Avicel vs. methylcellulose, MDCKAvicel vs. methylcellulose, MDCK--SIAT1 cellsSIAT1 cells
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Plaque formation by different human and avian virusesPlaque formation by different human and avian viruses
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Assay variants in 96Assay variants in 96--well platewell plate
Viral inoculumViral inoculumwas removedwas removedbefore addingbefore addingAvicel overlayAvicel overlay------------------------------------------------------ ------------------------------------------------------------------------------------------------------------Avicel overlayAvicel overlaywas added w/o was added w/o removing removing inoculuminoculum
No need to remove viral inoculum: easier to No need to remove viral inoculum: easier to perform, lower chances of crossperform, lower chances of cross--contaminationcontamination
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Detecting drugDetecting drug--resistant virusesresistant virusesMDCKMDCK--SIAT1, 96SIAT1, 96--well formatwell format
The viruses were kindly provided by The viruses were kindly provided by Robert WebsterRobert Webster
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Step 1. Step 1. Seed MDCKSeed MDCK--SIAT1 cells in 96SIAT1 cells in 96--well platewell plate
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Step 2. Step 2. Wash the cells 3Wash the cells 3--4 times with serum4 times with serum--free mediumfree medium
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Step 3. Step 3. Add 10Add 10--fold serial dilutions of the drug, 50 ul/wellfold serial dilutions of the drug, 50 ul/well
Drug concentration, Drug concentration, uMuM
H G F E D C B A
1
2
3
4
5
6
7
8
9
10
11
12
0 0 0.00
40.
040.
44 40 40
0
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Step 4. Step 4. Add 3Add 3--fold serial dilutions of the virus, 50 ul/wellfold serial dilutions of the virus, 50 ul/well
Drug concentration, Drug concentration, uMuM
H G F E D C B A
1
2
3
4
5
6
7
8
9
10
11
12
0 0 0.00
40.
040.
44 40 40
0
Dilution 1Dilution 1
Dilution 3Dilution 3
Dilution 9Dilution 9
Dilution 27Dilution 27
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Step 5. Step 5. Mix, incubate 1Mix, incubate 1--2 h for initiation of infection2 h for initiation of infection
Drug Drug
H G F E D C B A
1
2
3
4
5
6
7
8
9
10
11
12
0 0 0.00
40.
040.
44 40 40
0
VIRUSVIRUS
Dilution 1Dilution 1
Dilution 3Dilution 3
Dilution 9Dilution 9
Dilution 27Dilution 27
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Step 6. Step 6. Add Avicel overlay medium, 100 ul/wellAdd Avicel overlay medium, 100 ul/well
Drug Drug
H G F E D C B A
1
2
3
4
5
6
7
8
9
10
11
12
0 0 0.00
40.
040.
44 40 40
0
VIRUSVIRUS
Dilution 1Dilution 1
Dilution 3Dilution 3
Dilution 9Dilution 9
Dilution 27Dilution 27
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Step 7. Step 7. Incubate for 20Incubate for 20--48 h to allow formation of plaques 48 h to allow formation of plaques
Drug Drug
H G F E D C B A
1
2
3
4
5
6
7
8
9
10
11
12
0 0 0.00
40.
040.
44 40 40
0
VIRUSVIRUS
Dilution 1Dilution 1
Dilution 3Dilution 3
Dilution 9Dilution 9
Dilution 27Dilution 27
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Step 8. Step 8. Fix and immunostain to visualise plaques:Fix and immunostain to visualise plaques:
-- remove overlay medium, incubate with 4% paraformaldehyde,remove overlay medium, incubate with 4% paraformaldehyde,30 min at 4 oC30 min at 4 oC
-- permeabilize the cells with 0.5% Tritonpermeabilize the cells with 0.5% Triton--XX--100, 10 min100, 10 min-- incubate with primary antibodies (antiincubate with primary antibodies (anti--NPNP--A or A or --NPNP--B), 1 hB), 1 h-- incubate with HRPincubate with HRP--labeled secondary antibodies, 1 hlabeled secondary antibodies, 1 h-- incubate with precipitateincubate with precipitate--forming peroxidase substrate, forming peroxidase substrate,
30 min30 min-- let dry and analyselet dry and analyse
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VIRUSVIRUS
Dilution 1Dilution 1
Dilution 3Dilution 3
Dilution 9Dilution 9
Dilution 27Dilution 27
Drug concentration, Drug concentration, uMuM M.MatrosovichM.Matrosovich
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PostPost--treatment virus is NAItreatment virus is NAI--resistentresistent
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