Group A Streptococcus (GAS) skin infections are caused by a diverse array of strain types and are highly prevalent in disadvantaged populations. The role of strain-specific immunity in preventing GAS infections is poorly understood, representing a critical knowledge gap in vaccine development. A recent GAS murine challenge study showed evidence that sterilising strain-specific and enduring immunity required two skin infections by the same GAS strain within three weeks. This mechanism of developing enduring immunity may be a significant impediment to the accumulation of immunity in populations. We used an agent-based mathematical model of GAS transmission to investigate the epidemiological consequences of enduring strain-specific immunity developing only after two infections with the same strain within a specified interval. Accounting for uncertainty when correlating murine timeframes to humans, we varied this maximum inter-infection interval from 3 to 420 weeks to assess its impact on prevalence and strain diversity, and considered additional scenarios where no maximum inter-infection interval was specified. Model outputs were compared with longitudinal GAS surveillance observations from northern Australia, a region with endemic infection. We also assessed the likely impact of a targeted strain-specific multivalent vaccine in this context. Our model produced patterns of transmission consistent with observations when the maximum inter-infection interval for developing enduring immunity was 19 weeks. Our vaccine analysis suggests that the leading multivalent GAS vaccine may have limited impact on the prevalence of GAS in populations in northern Australia if strain-specific PLOS COMPUTATIONAL BIOLOGY
GAS are under development, but their effective use will require better understanding of how immunity develops following infection. Evidence from an animal model of skin infection suggests that the generation of enduring strain-specific immunity requires two infections by the same strain within a short time frame. It is not clear if this mechanism of immune development operates in humans, nor how it would contribute to the persistence of GAS in populations and affect vaccine impact. We used a mathematical model of GAS transmission, calibrated to data collected in an Indigenous Australian community, to assess whether this mechanism of immune development is consistent with epidemiological observations, and to explore its implications for the impact of a vaccine.We found that it is plausible that repeat infections are required for the development of immunity in humans, and illustrate the difficulties associated with achieving sustained reductions in disease prevalence with a vaccine.
Randomized work stealing is used in distributed systems to increase performance and improve resource utilization. In this article, we consider randomized work stealing in a large system of homogeneous processors where parent jobs spawn child jobs that can feasibly be executed in parallel with the parent job. We analyse the performance of two work stealing strategies: one where only child jobs can be transferred across servers and the other where parent jobs are transferred. We define a mean-field model to derive the response time distribution in a large-scale system with Poisson arrivals and exponential parent and child job durations. We prove that the model has a unique fixed point that corresponds to the steady state of a structured Markov chain, allowing us to use matrix analytic methods to compute the unique fixed point. The accuracy of the mean-field model is validated using simulation. Using numerical examples, we illustrate the effect of different probe rates, load, and different child job size distributions on performance with respect to the two stealing strategies, individually, and compared to each other.
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