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Table 1 Summary of model assumptions trialled for norovirus, where each model was fitted to age-specific incidence data in England. Models A0–B20 were taken forward to estimate incidence of norovirus between 2020 and 2022

From: Predicted norovirus resurgence in 2021–2022 due to the relaxation of nonpharmaceutical interventions associated with COVID-19 restrictions in England: a mathematical modeling study

Model

A0

A20

B0

B20

D0

D20

E0

F0

Assumptions

 First infection

Always symptomatic

Always symptomatic

Always symptomatic

Always symptomatic

50% asymptomatic

50% asymptomatic

50% asymptomatic

Always symptomatic

 Duration of Asymptomatic infectiousness (days)

15

15

20

20

15

15

15

15

 Asymptomatic infectiousness relative to symptomatic

0.05

0.05

0.05

0.05

0.05

0.05

0.5

1

 Under-reporting assumed in fitted data (%)

0

20

0

20

0

20

0

0

Results

 Probability of transmission given a contact (qs)

0.1892696

0.2070616

0.1693301

0.1824529

0.2183579

0.2193598

0.374627

0.1909186

 Log-likelihood of age-specific incidence when fitted to data from England [15]

−77.94

−190.03

−72.10

−107.46

−667.77

−850.36

−1458.08

−1454.57

 R0 (at endemic equilibrium)

1.81

2.03

1.81

2.01

1.94

1.62

>10

>10

 Shedding prevalence (at endemic equilibrium) (%)

0.18

0.25

0.303

0.41

0.718

0.70

59.44

59.77

 Sero-prevalence (at endemic equilibrium) (%)

24.64

30.55

24.54

29.92

27.73

37.80

20.49

20.17

 Comments

Good fit; used for 2020–2022 projections

Good fit; used for 2020–2022 projections

Good fit; used for 2020–2022 projections

Good fit; used for 2020–2022 projections

Poor fit to data, incidence in younger ages was under-estimated and incidence in older ages was over-estimated

Poor fit to data, incidence in younger ages was under-estimated and incidence in older ages was over-estimated

Poor fit to the incidence data (high incidence in adults) and unrealistic R0, but better comparison with expected seroprevalence and shedding

Poor fit to the incidence data (high incidence in adults) and unrealistic R0, but better comparison with expected seroprevalence and shedding