Immunoepidemiology of coccidiosis Don Klinkenberg Maite Severins Hans
Immuno-epidemiology of coccidiosis Don Klinkenberg Maite Severins Hans Heesterbeek
Coccidiosis • Caused by Eimeria spp • Protozoan • Intestinal infection – sometimes lesions – main problem: production loss • Seven species in chickens – location in the intestine – no cross-immunity
Parasite classification • After lecture notes by Kretschmar (micro/macro): Microparasite Macroparasite Eimeria Parasite lifespan Short Long Short Reproduction within host Rapid None Rapid (but dose effect) Transmission Direct Indirect Infection events One Multiple Immunity Complete Partial, slowly acquired Accumulative, slowly acquired Model type SIR type Parasite load ? ? ?
Essential characteristics • Transmission through environment • Dose-dependent infectivity • Slowly acquired immune response – stronger upon re-infection – reduces parasite excretion • Within-host dynamics!
This presentation • Model of within-host dynamics – relation between uptake and excretion of infectious material (oocysts) – interaction with immune system • Model of between-host dynamics (I) – coupling excretion and uptake of oocysts – interaction chickens and environment • Model of between-host dynamics (II)
Within-host model • Eimeria characteristics: – transmission through oocysts – Eimeria parasitises gut epithelial cells – limited number of asexual generations
Eimeria cycle Oocyst uptake (W) Sporozoites Oocyst excretion (Z) Schizont I (X(1)) Gamont Merozoites I (u(1)) Merozoites II (u(2)) Schizont II (X(2))
Eimeria cycle Oocyst uptake (W) Oocyst excretion (Z) Schizont I (X(1)) Schizont II (X(2))
Eimeria cycle Oocyst uptake (W) Schizont I (X(1)) Schizont II (X(2)) Oocyst excretion (Z)
Adding immunity • • Primarily T cell immunity Immunity evoked by schizonts Immunity inhibits schizont development Keeping the model simple: one immunity variable Y
Eimeria cycle with immunity Oocyst uptake (W) Oocyst excretion (Z) + Immunity (Y) – + Schizont II (X(2)) – Schizont I (X(1))
Eimeria cycle with immunity Oocyst uptake (W) Schizont I (X(1)) – Schizont II (X(2)) + + – Oocyst excretion (Z) Immunity (Y)
Eimeria cycle with immunity Oocyst uptake (W) Schizont I (X(1)) – Schizont II (X(2)) + + – Oocyst excretion (Z) Immunity (Y)
Eimeria cycle with immunity
Model summary • Discrete time • Two asexual schizont generations • T cell immunity against schizont development
Model analysis • Compare model experiments to data – relation single dose and excretion • saturation followed by decrease – excretion during trickle infections • excretion terminates after some time – immunising effect of trickle and single immunisation • trickle immunisation gives better protection
Single dose and excretion E. tenella
Model analysis • Model experiments – single dose and excretion • relation between W 0 and Z 4 – trickle infections – trickle vs single immunisation
Analysis: single dose
Analysis: single dose E. tenella
Analysis: single dose E. acervulina
Analysis: single dose E. maxima
Model analysis • Model experiments – single dose and excretion • relation between W 0 and Z 4 • b > 0 (naïve immunity growth) • m ≠ 1 (non-linear immune effectiveness) – trickle infections & immunisation • conclusions on g and a
Conclusions within-host model • Simple model of parasite input-output behaviour • Single immunity variable can explain experimental data • Solid basis for studying re-infection and between-host transmission
Between-host model • Relate excretion to uptake with oocyst level in environment V • Simplifying assumption: average chicken
Eimeria cycle Oocyst uptake (W) Oocyst excretion (Z) + Immunity (Y) – + Schizont II (X(2)) – Schizont I (X(1))
Eimeria cycle outside the chickens Environmental oocysts (V) × 1 × a 0 Oocyst excretion (Z) Oocyst uptake (W) × 1 × a 1 Immunity (Y) + Gamont (G) × l 2 – + Schizont II (X(2)) inside the chickens – Schizont I (X(1)) × l 1
Two new parameters • Per time step of ca. 2 days • Uptake rate a 0 – estimate from a single experiment: 0. 01 • Oocyst degradation rate – estimate from couple of articles: 0. 5
Interesting variables • Oocyst level in environment – decrease due to degradation (+ uptake) – increase due to excretion • Immunity level in average chicken – increase due to presence of schizonts – decrease by fixed rate • Number of infected cells as measure of damage – numbers of schizonts and gamonts
Basic dynamics
outside the chickens 4 5 Environmental oocysts (V) × 1 Oocyst excretion (Z) 3 Immunity (Y) Gamont (G) – + 2 2 × a 1 + 3 Schizont II (X(2)) inside the chickens 0 Oocyst uptake (W) × 1 × l 2 5 × a 0 – 1 Schizont I (X(1)) × l 1
Dynamics in single chicken cohort • First dose of each infection generation most important – major change compared to previous dose – fast decay of oocysts in environment • Dynamics can be described in terms of infection generations
Damage in single chicken cohort • Cumulative damage ≈ maximum damage logdmax logv 0
Conclusion on damage • Production damage is reflected by the maximum number of infected cells • Damage may take local minimum with intermediate oocyst level V 0 • Mechanism – maximum damage if a single infection generation dominates – minimum when generation dominance switches
Damage in single chicken cohort • Cumulative damage ≈ maximum damage logdmax 4 3 2 1 schizonts II gamonts logv 0
Discussion of the model • Single ‘average’ chicken • Deterministic model • No spatial effects
Different approach • Individual chickens • Stochastic model • Spatial model • Cost: – No continuous infection/immune level
Individual based model • Patches interact with walking chickens • Patches – oocyst level empty, low, medium, high (0; 103; 105; 107) – level rises if chicken excretes higher level – level falls after 14 days without excretion
Individual based model • Chickens – walk or ‘shuffle’ each hour – pick up maximum daily exposure (0, 101; 3; 5) – excrete once per day depending on • uptake -4 days • level of immunity (no, partial, full) • regulated by excretion templates – immunity level may increase depending on • time since first dose • number and level of doses
Example: fit to data (Galmes)
“damage” related to initial level
Local minimum • Mechanism? – High excretion due to serial medium doses • medium doses require serial low doses – If initial level is • high: early excretion of many medium, so serial medium doses before immunity • intermediate: early exposure for start-up immunity, but less serial medium exposure • low: many chicks are not immune while others already shed medium doses
More generalized mechanism for local minimum damage • Low initial level: exposure of naive chickens to large oocyst quantities excreted by first infection generation • Intermediate initial level: immunity builds up before large oocyst quantities are available • High initial level: large oocyst quantities available before immunity is reached • However: relation to level of mixing yet unclear
Our coccidiosis modellers • Deterministic continuous model – Don Klinkenberg, Hans Heesterbeek • Stochastic discrete model – Maite Severins, DK, HH • Stochastic continuous model (not shown) – Andriy Rychahivskyy, DK, HH
- Slides: 61